ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
NECFGCCN_00001 | 2.7e-105 | pat | 2.3.1.183 | M | N-acetyltransferase | |
NECFGCCN_00002 | 0.0 | dld | 1.1.5.12 | C | Catalyzes the oxidation of D-lactate to pyruvate | |
NECFGCCN_00003 | 0.0 | bglX | 3.2.1.21 | GH3 | G | Belongs to the glycosyl hydrolase 3 family |
NECFGCCN_00004 | 1.9e-164 | yehZ | M | Periplasmic glycine betaine choline-binding (lipo)protein of an ABC-type transport system (osmoprotectant binding protein) | ||
NECFGCCN_00005 | 5.4e-201 | yehY | P | permease | ||
NECFGCCN_00006 | 1.5e-172 | yehX | E | abc transporter atp-binding protein | ||
NECFGCCN_00007 | 7.6e-124 | yehW | P | permease | ||
NECFGCCN_00008 | 5.7e-10 | yohO | S | UPF0387 membrane protein YohO | ||
NECFGCCN_00009 | 2.1e-305 | yehU | 2.7.13.3 | T | Histidine kinase | |
NECFGCCN_00010 | 2.2e-128 | yehT | KT | Response regulator of the LytR AlgR family | ||
NECFGCCN_00011 | 1.8e-78 | yehS | S | protein conserved in bacteria | ||
NECFGCCN_00012 | 0.0 | metG | 6.1.1.10, 6.1.1.20 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
NECFGCCN_00013 | 5.2e-209 | mrp | D | Binds and transfers iron-sulfur (Fe-S) clusters to target apoproteins. Can hydrolyze ATP | ||
NECFGCCN_00014 | 8.9e-51 | yjaB_1 | 2.3.1.210 | K | N-acetyltransferase | |
NECFGCCN_00015 | 8.5e-56 | yohN | S | Nickel cobalt homeostasis protein RcnB | ||
NECFGCCN_00016 | 2.4e-164 | K | Transcriptional regulator | |||
NECFGCCN_00017 | 2.9e-238 | yicO | S | permease | ||
NECFGCCN_00018 | 0.0 | ade | 3.5.4.2 | F | adenine deaminase | |
NECFGCCN_00019 | 2.2e-149 | K | Transcriptional regulator | |||
NECFGCCN_00020 | 1.3e-67 | uspA2 | T | Universal stress protein | ||
NECFGCCN_00021 | 1.2e-132 | thiM | 2.7.1.50 | H | Catalyzes the phosphorylation of the hydroxyl group of 4-methyl-5-beta-hydroxyethylthiazole (THZ) | |
NECFGCCN_00022 | 1e-142 | thiD | 2.7.1.49, 2.7.4.7 | H | phosphomethylpyrimidine kinase | |
NECFGCCN_00023 | 5.1e-198 | fbaB | 4.1.2.13 | G | Catalyzes the formation of glycerone phosphate and D-glyceraldehyde 3-phosphate from D-fructose 1,6-bisphosphate | |
NECFGCCN_00024 | 1.4e-120 | P | Major facilitator superfamily | |||
NECFGCCN_00025 | 4.9e-126 | 2.7.1.176 | O | Zeta toxin | ||
NECFGCCN_00026 | 9.7e-80 | nprA | K | Cro/C1-type HTH DNA-binding domain | ||
NECFGCCN_00027 | 1.2e-34 | |||||
NECFGCCN_00028 | 2.9e-48 | XK27_00545 | U | This gene contains a nucleotide ambiguity which may be the result of a sequencing error | ||
NECFGCCN_00029 | 5.1e-63 | P | arsenate reductase (glutaredoxin) activity | |||
NECFGCCN_00030 | 1.4e-62 | XK27_00590 | ||||
NECFGCCN_00031 | 8.8e-107 | S | type VI secretion protein | |||
NECFGCCN_00032 | 4.2e-253 | S | type VI secretion protein | |||
NECFGCCN_00033 | 1.3e-96 | S | Type IV VI secretion system | |||
NECFGCCN_00034 | 3.4e-106 | abiGI | K | Transcriptional regulator, AbiEi antitoxin | ||
NECFGCCN_00035 | 0.0 | mhpA | 1.14.13.127 | CH | Catalyzes the insertion of one atom of molecular oxygen into position 2 of the phenyl ring of 3-(3- hydroxyphenyl)propionate (3-HPP) and hydroxycinnamic acid (3HCI) | |
NECFGCCN_00036 | 3.5e-166 | mhpB | 1.13.11.16 | S | Catalyzes the non-heme iron(II)-dependent oxidative cleavage of 2,3-dihydroxyphenylpropionic acid and 2,3- dihydroxicinnamic acid into 2-hydroxy-6-ketononadienedioate and 2- hydroxy-6-ketononatrienedioate, respectively | |
NECFGCCN_00037 | 2.7e-168 | mhpC | 3.7.1.14, 3.7.1.17 | I | Alpha/beta hydrolase family | |
NECFGCCN_00038 | 4.4e-149 | mhpD | 4.2.1.80 | Q | hydratase | |
NECFGCCN_00039 | 2e-169 | mhpF | 1.2.1.10 | Q | Catalyzes the conversion of acetaldehyde to acetyl-CoA, using NAD( ) and coenzyme A. Is the final enzyme in the meta- cleavage pathway for the degradation of aromatic compounds | |
NECFGCCN_00040 | 3.4e-183 | mhpE | 4.1.3.39 | E | Catalyzes the retro-aldol cleavage of 4-hydroxy-2- oxopentanoate to pyruvate and acetaldehyde. Is involved in the meta-cleavage pathway for the degradation of aromatic compounds | |
NECFGCCN_00041 | 8.5e-141 | mhpT | EGP | Major facilitator Superfamily | ||
NECFGCCN_00042 | 1.2e-137 | yfiH | S | Multi-copper polyphenol oxidoreductase laccase | ||
NECFGCCN_00043 | 1.4e-292 | MA20_21580 | 2.8.1.11 | P | sulfurtransferase | |
NECFGCCN_00044 | 1.1e-112 | S | Cysteine dioxygenase type I | |||
NECFGCCN_00045 | 3.7e-149 | K | Transcriptional regulator | |||
NECFGCCN_00046 | 3.4e-205 | ssuD_2 | 1.14.14.5 | C | Alkanesulfonate monooxygenase | |
NECFGCCN_00047 | 5.2e-53 | ydbM | I | acyl-CoA dehydrogenase | ||
NECFGCCN_00048 | 4.1e-44 | S | Nucleotidyl transferase AbiEii toxin, Type IV TA system | |||
NECFGCCN_00049 | 7.9e-185 | |||||
NECFGCCN_00050 | 1.9e-81 | FNV0100 | F | Belongs to the Nudix hydrolase family | ||
NECFGCCN_00051 | 8.2e-73 | XK27_01300 | P | Protein conserved in bacteria | ||
NECFGCCN_00052 | 9.4e-107 | ynjF | 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
NECFGCCN_00053 | 5.1e-69 | nudG | 3.6.1.55, 3.6.1.65 | L | belongs to the nudix hydrolase family | |
NECFGCCN_00054 | 3.3e-258 | gdhA | 1.4.1.4 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
NECFGCCN_00055 | 1.3e-179 | qor | 1.6.5.5 | C | COG0604 NADPH quinone reductase and related Zn-dependent oxidoreductases | |
NECFGCCN_00056 | 0.0 | topB | 5.99.1.2 | L | Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone | |
NECFGCCN_00057 | 2.4e-195 | selD | 2.7.9.3 | F | Synthesizes selenophosphate from selenide and ATP | |
NECFGCCN_00058 | 1.8e-136 | pho | 3.1.3.2 | I | Acid phosphatase | |
NECFGCCN_00059 | 0.0 | pflB | 2.3.1.54 | C | formate acetyltransferase' | |
NECFGCCN_00060 | 2.8e-202 | dinB | 2.7.7.7 | L | Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII | |
NECFGCCN_00061 | 1e-34 | |||||
NECFGCCN_00062 | 1.3e-151 | yxeM | ET | ABC-type amino acid transport signal transduction systems, periplasmic component domain | ||
NECFGCCN_00063 | 1.4e-162 | yxeN | P | ABC transporter (Permease | ||
NECFGCCN_00064 | 6.1e-129 | tcyN | 3.6.3.21 | E | abc transporter atp-binding protein | |
NECFGCCN_00065 | 1.2e-76 | S | dextransucrase activity | |||
NECFGCCN_00066 | 1.8e-240 | norM | V | Multidrug efflux pump | ||
NECFGCCN_00068 | 8.8e-181 | msrA | 1.8.4.11, 1.8.4.12 | O | Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine | |
NECFGCCN_00069 | 1.1e-229 | brnQ | E | Component of the transport system for branched-chain amino acids | ||
NECFGCCN_00070 | 1.7e-181 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
NECFGCCN_00071 | 4e-59 | S | Protein of unknown function (DUF3290) | |||
NECFGCCN_00072 | 2.8e-106 | S | Protein of unknown function (DUF421) | |||
NECFGCCN_00073 | 1.1e-16 | csbD | S | CsbD-like | ||
NECFGCCN_00074 | 2.2e-109 | S | Carbohydrate-binding domain-containing protein Cthe_2159 | |||
NECFGCCN_00075 | 1.6e-67 | prkC | 2.7.11.1 | KLT | serine threonine protein kinase | |
NECFGCCN_00076 | 2.6e-135 | stp | 3.1.3.16 | T | phosphatase | |
NECFGCCN_00077 | 5e-93 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
NECFGCCN_00078 | 6.5e-146 | nasE | P | ABC-type nitrate sulfonate bicarbonate transport system permease component | ||
NECFGCCN_00079 | 4e-242 | nasF | P | COG0715 ABC-type nitrate sulfonate bicarbonate transport systems periplasmic components | ||
NECFGCCN_00080 | 7.5e-190 | nasR | K | Nitrate and nitrite sensing domain protein | ||
NECFGCCN_00081 | 6.6e-57 | ychN | P | conserved protein involved in intracellular sulfur reduction | ||
NECFGCCN_00082 | 3.3e-39 | S | Protein involved in biological_process | |||
NECFGCCN_00083 | 3.6e-128 | chaC | P | Catalyzes the cleavage of glutathione into 5-oxo-L- proline and a Cys-Gly dipeptide. Acts specifically on glutathione, but not on other gamma-glutamyl peptides | ||
NECFGCCN_00084 | 1.9e-36 | chaB | S | Cation transport regulator | ||
NECFGCCN_00085 | 4e-185 | chaA | P | Calcium Proton | ||
NECFGCCN_00086 | 2.2e-159 | kdsA | 2.5.1.55 | M | Belongs to the KdsA family | |
NECFGCCN_00087 | 1.2e-149 | ychA | S | Transglutaminase-like superfamily | ||
NECFGCCN_00088 | 7.3e-65 | sirB2 | S | Invasion gene expression up-regulator SirB | ||
NECFGCCN_00089 | 4.8e-146 | prmC | 2.1.1.297, 2.1.1.298 | J | Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif | |
NECFGCCN_00090 | 8.4e-196 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
NECFGCCN_00091 | 9.4e-223 | hemA | 1.2.1.70 | H | Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA) | |
NECFGCCN_00092 | 4.5e-114 | lolB | M | Plays a critical role in the incorporation of lipoproteins in the outer membrane after they are released by the LolA protein | ||
NECFGCCN_00093 | 8.6e-69 | ispE | 2.1.1.182, 2.7.1.148 | F | Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol | |
NECFGCCN_00094 | 3.9e-107 | hisB | 1.1.1.23, 2.6.1.9, 3.1.3.15, 4.2.1.19 | E | imidazoleglycerol-phosphate dehydratase | |
NECFGCCN_00095 | 1.1e-231 | hisD | 1.1.1.23, 1.1.1.308 | E | Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine | |
NECFGCCN_00096 | 8e-117 | hisG | 2.4.2.17 | E | Catalyzes the condensation of ATP and 5-phosphoribose 1- diphosphate to form N'-(5'-phosphoribosyl)-ATP (PR-ATP). Has a crucial role in the pathway because the rate of histidine biosynthesis seems to be controlled primarily by regulation of HisG enzymatic activity | |
NECFGCCN_00097 | 4.8e-182 | hisZ | 2.4.2.17, 6.1.1.21 | E | Required for the first step of histidine biosynthesis. May allow the feedback regulation of ATP phosphoribosyltransferase activity by histidine | |
NECFGCCN_00098 | 1.1e-189 | hisC | 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
NECFGCCN_00099 | 1.8e-53 | nasD | 3.6.3.36 | P | (ABC) transporter | |
NECFGCCN_00100 | 3.6e-186 | desK | 2.7.13.3 | T | Histidine kinase | |
NECFGCCN_00101 | 3.3e-101 | desR | K | COG2197 Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
NECFGCCN_00102 | 5.8e-55 | S | TM2 domain | |||
NECFGCCN_00103 | 3.7e-162 | rluA | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
NECFGCCN_00104 | 0.0 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
NECFGCCN_00105 | 2.8e-24 | secE | U | Belongs to the SecE SEC61-gamma family | ||
NECFGCCN_00106 | 3.5e-82 | ywbD | 2.1.1.191 | J | Methyltransferase | |
NECFGCCN_00107 | 1.1e-116 | aroD | 1.1.1.25, 4.2.1.10 | E | Involved in the third step of the chorismate pathway, which leads to the biosynthesis of aromatic amino acids. Catalyzes the cis-dehydration of 3-dehydroquinate (DHQ) and introduces the first double bond of the aromatic ring to yield 3- dehydroshikimate | |
NECFGCCN_00108 | 6.3e-154 | aroE | 1.1.1.25 | E | Involved in the biosynthesis of the chorismate, which leads to the biosynthesis of aromatic amino acids. Catalyzes the reversible NADPH linked reduction of 3-dehydroshikimate (DHSA) to yield shikimate (SA) | |
NECFGCCN_00109 | 1.7e-201 | aroB | 2.7.1.71, 4.2.3.4 | E | Catalyzes the conversion of 3-deoxy-D-arabino- heptulosonate 7-phosphate (DAHP) to dehydroquinate (DHQ) | |
NECFGCCN_00110 | 1.4e-217 | aroC | 4.2.3.5 | E | Catalyzes the anti-1,4-elimination of the C-3 phosphate and the C-6 proR hydrogen from 5-enolpyruvylshikimate-3-phosphate (EPSP) to yield chorismate, which is the branch point compound that serves as the starting substrate for the three terminal pathways of aromatic amino acid biosynthesis. This reaction introduces a second double bond into the aromatic ring system | |
NECFGCCN_00111 | 2e-205 | tyrA | 1.3.1.12, 1.3.1.43 | E | prephenate dehydrogenase | |
NECFGCCN_00112 | 1.2e-52 | yheA | S | Belongs to the UPF0342 family | ||
NECFGCCN_00113 | 7e-170 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
NECFGCCN_00114 | 1.3e-232 | aroA | 1.3.1.12, 1.3.1.43, 2.5.1.19 | E | Catalyzes the transfer of the enolpyruvyl moiety of phosphoenolpyruvate (PEP) to the 5-hydroxyl of shikimate-3- phosphate (S3P) to produce enolpyruvyl shikimate-3-phosphate and inorganic phosphate | |
NECFGCCN_00115 | 2.7e-77 | aroK | 1.1.1.25, 2.7.1.71, 4.2.1.10, 4.2.3.4 | F | Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate | |
NECFGCCN_00116 | 1.4e-153 | pheA | 4.2.1.51 | E | Prephenate dehydratase | |
NECFGCCN_00118 | 1.3e-130 | D | Lytic transglycosylase with a strong preference for naked glycan strands that lack stem peptides | |||
NECFGCCN_00119 | 2.9e-15 | dnaX | 2.4.99.16, 2.7.7.7 | GH13 | D | cell septum assembly |
NECFGCCN_00124 | 1.4e-37 | yclQ | P | ABC-type enterochelin transport system, periplasmic component | ||
NECFGCCN_00125 | 2.4e-40 | pspC | KT | PspC domain | ||
NECFGCCN_00126 | 5.5e-59 | livG | E | Part of the ABC transporter complexes LivFGHMJ and LivFGHMK involved in the high-affinity transport of branched-chain amino acids | ||
NECFGCCN_00127 | 2.3e-22 | niaR | S | small molecule binding protein (contains 3H domain) | ||
NECFGCCN_00128 | 4.5e-86 | |||||
NECFGCCN_00129 | 7.1e-201 | ffh | 3.6.5.4 | U | Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Binds to the hydrophobic signal sequence of the ribosome-nascent chain (RNC) as it emerges from the ribosomes. The SRP-RNC complex is then targeted to the cytoplasmic membrane where it interacts with the SRP receptor FtsY | |
NECFGCCN_00130 | 1.5e-166 | sufD | O | FeS assembly protein SufD | ||
NECFGCCN_00131 | 2.2e-131 | sufC | O | FeS assembly ATPase SufC | ||
NECFGCCN_00132 | 2e-293 | sufB | O | FeS assembly protein SufB | ||
NECFGCCN_00133 | 9.8e-67 | sufA | S | Is able to transfer iron-sulfur clusters to apo- ferredoxin. Multiple cycles of 2Fe2S cluster formation and transfer are observed, suggesting that IscA acts catalytically. Recruits intracellular free iron so as to provide iron for the assembly of transient iron-sulfur cluster in IscU in the presence of IscS, L-cysteine and the thioredoxin reductase system | ||
NECFGCCN_00134 | 2.6e-18 | |||||
NECFGCCN_00135 | 3e-34 | S | DoxX | |||
NECFGCCN_00136 | 8.7e-52 | K | transcriptional regulator | |||
NECFGCCN_00137 | 5.7e-222 | lldD | 1.1.2.3 | C | Catalyzes the conversion of L-lactate to pyruvate. Is coupled to the respiratory chain | |
NECFGCCN_00138 | 0.0 | czcA | V | Belongs to the resistance-nodulation-cell division (RND) (TC 2.A.6) family | ||
NECFGCCN_00139 | 9.1e-90 | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | |||
NECFGCCN_00140 | 0.0 | salB | V | Lanthionine synthetase C-like protein | ||
NECFGCCN_00141 | 0.0 | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | |||
NECFGCCN_00142 | 4.2e-122 | V | ABC transporter | |||
NECFGCCN_00143 | 0.0 | yfeA | T | MASE1 | ||
NECFGCCN_00144 | 1.1e-204 | nupC | F | Belongs to the concentrative nucleoside transporter (CNT) (TC 2.A.41) family | ||
NECFGCCN_00145 | 1.1e-210 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
NECFGCCN_00146 | 5.5e-27 | ypeC | S | Protein of unknown function (DUF2502) | ||
NECFGCCN_00147 | 1.1e-181 | yghZ | C | reductase | ||
NECFGCCN_00148 | 1.6e-307 | ipdC | 4.1.1.74 | GH | Belongs to the TPP enzyme family | |
NECFGCCN_00149 | 8.9e-210 | yfeO | P | ion-transport protein | ||
NECFGCCN_00150 | 5.6e-183 | glk | 2.7.1.2 | F | Belongs to the bacterial glucokinase family | |
NECFGCCN_00151 | 6.9e-133 | ypdB | K | response regulator | ||
NECFGCCN_00152 | 4.7e-311 | ypdA | 2.7.13.3 | T | Histidine kinase | |
NECFGCCN_00153 | 3.2e-236 | yfdZ | 2.6.1.83 | E | aminotransferase | |
NECFGCCN_00154 | 2.7e-203 | cynX | P | transporter | ||
NECFGCCN_00155 | 3.2e-72 | guaD | 3.5.4.33 | FJ | deaminase | |
NECFGCCN_00156 | 1.1e-140 | cynR | K | transcriptional regulator | ||
NECFGCCN_00157 | 2.6e-142 | |||||
NECFGCCN_00158 | 6e-85 | 5.3.1.9 | G | Cupin 2, conserved barrel domain protein | ||
NECFGCCN_00160 | 3.3e-156 | yfdC | P | Formate nitrite | ||
NECFGCCN_00161 | 1.1e-146 | vacJ | M | Lipoprotein | ||
NECFGCCN_00162 | 4e-256 | fadL | I | long-chain fatty acid transport protein | ||
NECFGCCN_00163 | 9.4e-46 | yfcZ | S | protein conserved in bacteria | ||
NECFGCCN_00164 | 9.1e-237 | fadI | 2.3.1.16 | I | Catalyzes the final step of fatty acid oxidation in which acetyl-CoA is released and the CoA ester of a fatty acid two carbons shorter is formed | |
NECFGCCN_00165 | 0.0 | fadJ | 1.1.1.157, 1.1.1.35, 4.2.1.17, 5.1.2.3, 5.3.3.8 | I | Involved in the aerobic and anaerobic degradation of long-chain fatty acids via beta-oxidation cycle. Catalyzes the formation of 3-oxoacyl-CoA from enoyl-CoA via L-3-hydroxyacyl-CoA. It can also use D-3-hydroxyacyl-CoA and cis-3-enoyl-CoA as substrate | |
NECFGCCN_00166 | 5.8e-88 | sixA | T | phosphohistidine phosphatase | ||
NECFGCCN_00167 | 2.2e-99 | yfcN | S | Belongs to the UPF0115 family | ||
NECFGCCN_00168 | 3.1e-184 | prmB | 2.1.1.297, 2.1.1.298 | J | Specifically methylates the 50S ribosomal protein L3 on a specific glutamine residue | |
NECFGCCN_00169 | 1.5e-205 | aroC | 4.2.3.5 | E | Catalyzes the anti-1,4-elimination of the C-3 phosphate and the C-6 proR hydrogen from 5-enolpyruvylshikimate-3-phosphate (EPSP) to yield chorismate, which is the branch point compound that serves as the starting substrate for the three terminal pathways of aromatic amino acid biosynthesis. This reaction introduces a second double bond into the aromatic ring system | |
NECFGCCN_00170 | 3.8e-156 | mepA | M | Murein endopeptidase that cleaves the D-alanyl-meso-2,6- diamino-pimelyl amide bond that connects peptidoglycan strands. Likely plays a role in the removal of murein from the sacculus | ||
NECFGCCN_00171 | 9.2e-139 | yfcA | S | membrane transporter protein | ||
NECFGCCN_00172 | 1.6e-105 | yfcM | S | protein conserved in bacteria | ||
NECFGCCN_00173 | 3.3e-43 | yfcL | S | YfcL protein | ||
NECFGCCN_00174 | 0.0 | mnmC | 2.1.1.61, 2.1.1.72, 2.4.2.29, 4.2.1.151 | J | Catalyzes the last two steps in the biosynthesis of 5- methylaminomethyl-2-thiouridine (mnm(5)s(2)U) at the wobble position (U34) in tRNA. Catalyzes the FAD-dependent demodification of cmnm(5)s(2)U34 to nm(5)s(2)U34, followed by the transfer of a methyl group from S-adenosyl-L-methionine to nm(5)s(2)U34, to form mnm(5)s(2)U34 | |
NECFGCCN_00175 | 1.2e-227 | fabB | 2.3.1.41 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP | |
NECFGCCN_00176 | 8.1e-257 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
NECFGCCN_00177 | 2.6e-157 | rgfB | 3.1.3.90 | L | Endonuclease/Exonuclease/phosphatase family | |
NECFGCCN_00178 | 0.0 | ptsG | 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | pts system | |
NECFGCCN_00179 | 1e-26 | ptsG | 2.7.1.199, 2.7.1.208 | G | pts system | |
NECFGCCN_00180 | 6.4e-160 | mleP2 | S | Transporter, auxin efflux carrier (AEC) family protein | ||
NECFGCCN_00181 | 1.7e-45 | S | membrane | |||
NECFGCCN_00182 | 0.0 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
NECFGCCN_00183 | 1.5e-231 | lacY | G | Major facilitator superfamily | ||
NECFGCCN_00184 | 5e-56 | rhaM | 5.1.3.32 | G | Involved in the anomeric conversion of L-rhamnose | |
NECFGCCN_00185 | 8.3e-210 | fucO | 1.1.1.1 | C | alcohol dehydrogenase | |
NECFGCCN_00186 | 1.1e-173 | rhaQ | U | Belongs to the binding-protein-dependent transport system permease family | ||
NECFGCCN_00187 | 1.5e-175 | rhaP | U | Belongs to the binding-protein-dependent transport system permease family | ||
NECFGCCN_00188 | 8.5e-279 | rbsA | 3.6.3.17 | P | import. Responsible for energy coupling to the transport system | |
NECFGCCN_00189 | 1.2e-172 | rhaS | G | (ABC) transporter | ||
NECFGCCN_00190 | 8.8e-161 | rhaD | 4.1.1.104, 4.1.2.17, 4.1.2.19, 4.2.1.109, 5.1.3.4 | H | Catalyzes the reversible cleavage of L-rhamnulose-1- phosphate to dihydroxyacetone phosphate (DHAP) and L-lactaldehyde | |
NECFGCCN_00191 | 1e-248 | rhaA | 2.7.1.5, 5.3.1.14 | G | L-rhamnose isomerase | |
NECFGCCN_00192 | 1.5e-280 | rhaB | 2.7.1.17, 2.7.1.189, 2.7.1.5, 2.7.1.51, 5.3.1.14 | F | Involved in the catabolism of L-rhamnose (6-deoxy-L- mannose). Catalyzes the transfer of the gamma-phosphate group from ATP to the 1-hydroxyl group of L-rhamnulose to yield L-rhamnulose 1-phosphate | |
NECFGCCN_00193 | 1.8e-158 | rhaS | K | Activates expression of the rhaBAD and rhaT operons | ||
NECFGCCN_00194 | 2e-160 | rhaR | K | Activates expression of the rhaSR operon in response to L-rhamnose | ||
NECFGCCN_00195 | 4e-187 | rhaT | U | Uptake of L-rhamnose across the boundary membrane with the concomitant transport of protons into the cell (symport system) | ||
NECFGCCN_00196 | 2.2e-116 | sodA | 1.15.1.1 | C | Destroys radicals which are normally produced within the cells and which are toxic to biological systems | |
NECFGCCN_00197 | 4e-127 | yiiM | C | protein conserved in bacteria | ||
NECFGCCN_00198 | 5.4e-240 | T | PhoQ Sensor | |||
NECFGCCN_00199 | 3.1e-127 | K | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
NECFGCCN_00200 | 9.3e-81 | cpxP | NPTU | Repressor of the Cpx envelope stress response pathway which occurs via periplasmic interactions with CpxA | ||
NECFGCCN_00201 | 8.1e-160 | fieF | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
NECFGCCN_00202 | 1.1e-183 | pfkA | 2.7.1.11 | F | Catalyzes the phosphorylation of D-fructose 6-phosphate, the first committing step of glycolysis. Uses inorganic phosphate (PPi) as phosphoryl donor instead of ATP like common ATP-dependent phosphofructokinases (ATP-PFKs), which renders the reaction reversible, and can thus function both in glycolysis and gluconeogenesis. Consistently, PPi-PFK can replace the enzymes of both the forward (ATP-PFK) and reverse (fructose-bisphosphatase (FBPase)) reactions | |
NECFGCCN_00203 | 2.9e-87 | rraA | H | Catalyzes the aldol cleavage of 4-hydroxy-4-methyl-2- oxoglutarate (HMG) into 2 molecules of pyruvate. Also contains a secondary oxaloacetate (OAA) decarboxylase activity due to the common pyruvate enolate transition state formed following C-C bond cleavage in the retro-aldol and decarboxylation reactions | ||
NECFGCCN_00204 | 1.1e-164 | menA | 2.5.1.74 | H | Belongs to the MenA family. Type 1 subfamily | |
NECFGCCN_00205 | 1.1e-242 | hslU | O | this subunit has chaperone activity. The binding of ATP and its subsequent hydrolysis by HslU are essential for unfolding of protein substrates subsequently hydrolyzed by HslV. HslU recognizes the N-terminal part of its protein substrates and unfolds these before they are guided to HslV for hydrolysis | ||
NECFGCCN_00206 | 4.2e-92 | hslV | 3.4.25.2 | O | Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery | |
NECFGCCN_00207 | 1.1e-110 | ftsN | D | Essential cell division protein that activates septal peptidoglycan synthesis and constriction of the cell. Acts on both sides of the membrane, via interaction with FtsA in the cytoplasm and interaction with the FtsQBL complex in the periplasm. These interactions may induce a conformational switch in both FtsA and FtsQBL, leading to septal peptidoglycan synthesis by FtsI and associated synthases | ||
NECFGCCN_00208 | 5.4e-192 | cytR | K | transcriptional | ||
NECFGCCN_00209 | 0.0 | priA | L | Involved in the restart of stalled replication forks. Recognizes and binds the arrested nascent DNA chain at stalled replication forks. It can open the DNA duplex, via its helicase activity, and promote assembly of the primosome and loading of the major replicative helicase DnaB onto DNA | ||
NECFGCCN_00210 | 3e-36 | rpmE | J | Binds the 23S rRNA | ||
NECFGCCN_00211 | 1.8e-53 | metJ | K | This regulatory protein, when combined with SAM (S- adenosylmethionine) represses the expression of the methionine regulon and of enzymes involved in SAM synthesis | ||
NECFGCCN_00212 | 1.5e-214 | metB | 2.5.1.48, 4.4.1.1, 4.4.1.8 | E | Catalyzes the formation of L-homocysteine from O- succinyl-L-homoserine (OSHS) and hydrogen sulfide | |
NECFGCCN_00213 | 0.0 | metL | 1.1.1.3, 2.7.2.4 | E | belongs to the aspartokinase family | |
NECFGCCN_00214 | 2e-73 | tnp3503b | 2.7.7.7 | L | Transposase | |
NECFGCCN_00215 | 2.2e-277 | soxB | 3.1.3.5, 3.6.1.45 | F | 5'-nucleotidase, C-terminal domain | |
NECFGCCN_00216 | 5.3e-57 | MA20_13090 | 4.1.1.44 | S | decarboxylase | |
NECFGCCN_00217 | 1.3e-152 | K | transcriptional regulator | |||
NECFGCCN_00218 | 9.4e-169 | metF | 1.5.1.20 | E | Methylenetetrahydrofolate reductase | |
NECFGCCN_00219 | 7e-124 | yijE | EG | EamA-like transporter family | ||
NECFGCCN_00220 | 1.2e-205 | gldA | 1.1.1.6 | C | glycerol dehydrogenase | |
NECFGCCN_00221 | 2.6e-115 | tal | 2.2.1.2 | H | Belongs to the transaldolase family. Type | |
NECFGCCN_00222 | 2.3e-152 | yijO | K | transcriptional regulator | ||
NECFGCCN_00223 | 7e-121 | adcA | S | periplasmic or secreted protein | ||
NECFGCCN_00224 | 7.4e-46 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
NECFGCCN_00225 | 2.5e-18 | folE | 3.5.4.16 | F | gtp cyclohydrolase | |
NECFGCCN_00226 | 5.9e-146 | folP | 2.5.1.15, 2.7.6.3 | H | Catalyzes the condensation of para-aminobenzoate (pABA) with 6-hydroxymethyl-7,8-dihydropterin diphosphate (DHPt-PP) to form 7,8-dihydropteroate (H2Pte), the immediate precursor of folate derivatives | |
NECFGCCN_00227 | 1.7e-292 | amy | 3.2.1.1 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
NECFGCCN_00228 | 5e-60 | folB | 1.13.11.81, 2.5.1.15, 2.7.6.3, 4.1.2.25, 5.1.99.8 | H | Catalyzes the conversion of 7,8-dihydroneopterin to 6- hydroxymethyl-7,8-dihydropterin | |
NECFGCCN_00230 | 3.3e-66 | S | DoxX family | |||
NECFGCCN_00231 | 0.0 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
NECFGCCN_00232 | 2.5e-186 | ltaE | 4.1.2.48 | E | Threonine aldolase | |
NECFGCCN_00233 | 4e-270 | ybjT | GM | Epimerase dehydratase | ||
NECFGCCN_00234 | 7.9e-196 | ybjS | 1.1.1.133, 5.1.3.13 | M | 3-beta hydroxysteroid dehydrogenase | |
NECFGCCN_00235 | 2e-157 | amiD | 3.5.1.28 | V | N-acetylmuramoyl-L-alanine amidase | |
NECFGCCN_00236 | 2e-192 | 2.7.7.65 | T | Diguanylate cyclase | ||
NECFGCCN_00237 | 9.1e-09 | yahO | S | Protein of unknown function (DUF1471) | ||
NECFGCCN_00238 | 4.6e-91 | ybjP | M | Induced during stationary phase and by acivicin (a glutamine analog) | ||
NECFGCCN_00239 | 9.8e-132 | artP | E | Arginine ABC transporter, ATP-binding protein | ||
NECFGCCN_00240 | 5.8e-135 | artI | ET | belongs to the bacterial solute-binding protein 3 family | ||
NECFGCCN_00241 | 8.2e-115 | artQ | P | arginine transporter permease subunit ArtQ | ||
NECFGCCN_00242 | 2.6e-107 | artM | P | (ABC) transporter | ||
NECFGCCN_00243 | 2.1e-134 | artJ | ET | belongs to the bacterial solute-binding protein 3 family | ||
NECFGCCN_00244 | 1.6e-253 | T | PhoQ Sensor | |||
NECFGCCN_00245 | 3.4e-129 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
NECFGCCN_00246 | 1.3e-212 | rumB | 2.1.1.189, 2.1.1.190 | J | Catalyzes the formation of 5-methyl-uridine at position 747 (m5U747) in 23S rRNA | |
NECFGCCN_00247 | 8.7e-84 | ybjO | S | Membrane | ||
NECFGCCN_00248 | 1e-148 | potI | P | ABC-type spermidine putrescine transport system, permease component II | ||
NECFGCCN_00249 | 1.5e-175 | potH | P | ABC-type spermidine putrescine transport system, permease component I | ||
NECFGCCN_00250 | 1.6e-221 | potG | P | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | ||
NECFGCCN_00251 | 3.4e-216 | potF | P | Required for the activity of the bacterial periplasmic transport system of putrescine | ||
NECFGCCN_00252 | 5e-84 | ybjN | S | sensory transduction regulator | ||
NECFGCCN_00253 | 4.6e-163 | rimK | 6.3.1.17, 6.3.2.32, 6.3.2.41 | F | Belongs to the RimK family | |
NECFGCCN_00254 | 2.2e-131 | nfsA | 1.5.1.38, 1.5.1.39 | C | Nitroreductase | |
NECFGCCN_00255 | 1.7e-42 | ybjC | S | Protein of unknown function (DUF1418) | ||
NECFGCCN_00256 | 1.8e-46 | grxA | 1.17.4.1 | O | Glutaredoxin | |
NECFGCCN_00257 | 3.8e-66 | ybjM | S | Putative inner membrane protein of Enterobacteriaceae | ||
NECFGCCN_00258 | 5.2e-301 | ybjL | P | transport protein | ||
NECFGCCN_00259 | 1.7e-94 | ybjK | K | transcriptional regulator | ||
NECFGCCN_00260 | 7.1e-212 | ybjJ | G | Major facilitator superfamily | ||
NECFGCCN_00261 | 1.2e-151 | ybjI | 3.1.3.102, 3.1.3.104, 3.1.3.23 | C | Hydrolase | |
NECFGCCN_00262 | 3.2e-223 | mdfA | EGP | multi-drug | ||
NECFGCCN_00263 | 3.6e-108 | ybjG | 3.6.1.27 | I | Phosphatase | |
NECFGCCN_00264 | 1.1e-141 | deoR | K | transcriptional | ||
NECFGCCN_00265 | 2.5e-225 | dacC | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
NECFGCCN_00266 | 1.4e-115 | yliJ | 2.5.1.18 | O | Glutathione S-Transferase | |
NECFGCCN_00267 | 2.9e-207 | yliI | G | glucose sorbosone | ||
NECFGCCN_00268 | 3.7e-61 | bssR | S | disruption of this gene in Escherichia coli led to effects on biofilm formation, alteration in expression of a number of genes and mutations in bssS led to defects in indole transport and autoinducer-2 uptake and processing | ||
NECFGCCN_00269 | 6.8e-226 | lacY | G | Major facilitator superfamily | ||
NECFGCCN_00270 | 1.5e-258 | rimO | 2.8.4.4 | J | Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein S12 | |
NECFGCCN_00271 | 5e-08 | N | PFAM Uncharacterised protein family UPF0150 | |||
NECFGCCN_00272 | 2.9e-111 | serB | 3.1.3.3 | E | phosphoserine phosphatase | |
NECFGCCN_00273 | 8.1e-255 | ezrA | D | modulates the frequency and position of FtsZ ring formation. Inhibits FtsZ ring formation at polar sites. Interacts either with FtsZ or with one of its binding partners to promote depolymerization | ||
NECFGCCN_00274 | 7.1e-239 | tyrS | 6.1.1.1 | J | Catalyzes the attachment of tyrosine to tRNA(Tyr) in a two-step reaction tyrosine is first activated by ATP to form Tyr- AMP and then transferred to the acceptor end of tRNA(Tyr) | |
NECFGCCN_00275 | 1.7e-41 | gltL | 3.6.3.21 | E | (ABC) transporter | |
NECFGCCN_00276 | 0.0 | U | Hemolysin activation secretion protein | |||
NECFGCCN_00277 | 9.6e-197 | U | Large exoproteins involved in heme utilization or adhesion | |||
NECFGCCN_00278 | 6.4e-87 | ybeL | 1.17.4.1, 4.6.1.1 | J | Zinc-ribbon containing domain | |
NECFGCCN_00279 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
NECFGCCN_00280 | 3.6e-84 | lptE | M | Together with LptD, is involved in the assembly of lipopolysaccharide (LPS) at the surface of the outer membrane. Required for the proper assembly of LptD. Binds LPS and may serve as the LPS recognition site at the outer membrane | ||
NECFGCCN_00281 | 4e-187 | holA | 2.7.7.7 | L | dna polymerase III delta subunit | |
NECFGCCN_00282 | 2.9e-119 | nadD | 2.7.7.18, 3.5.4.4, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
NECFGCCN_00283 | 4.7e-114 | cobC | 3.1.3.73 | G | Belongs to the phosphoglycerate mutase family | |
NECFGCCN_00284 | 5.7e-52 | rsfS | 2.7.7.18 | J | Functions as a ribosomal silencing factor. Interacts with ribosomal protein L14 (rplN), blocking formation of intersubunit bridge B8. Prevents association of the 30S and 50S ribosomal subunits and the formation of functional ribosomes, thus repressing translation | |
NECFGCCN_00285 | 8.9e-86 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
NECFGCCN_00286 | 0.0 | mrdA | 3.4.16.4 | M | Catalyzes cross-linking of the peptidoglycan cell wall | |
NECFGCCN_00287 | 8.3e-199 | mrdB | M | Peptidoglycan polymerase that is essential for cell wall elongation | ||
NECFGCCN_00288 | 6.5e-154 | rlpA | M | Lytic transglycosylase with a strong preference for naked glycan strands that lack stem peptides | ||
NECFGCCN_00289 | 2e-228 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
NECFGCCN_00290 | 2.9e-41 | ybeD | S | Belongs to the UPF0250 family | ||
NECFGCCN_00291 | 4.6e-117 | lipB | 2.3.1.181 | H | Catalyzes the transfer of endogenously produced octanoic acid from octanoyl-acyl-carrier-protein onto the lipoyl domains of lipoate-dependent enzymes. Lipoyl-ACP can also act as a substrate although octanoyl-ACP is likely to be the physiological substrate | |
NECFGCCN_00292 | 4.4e-150 | ybeF | K | transcriptional regulator | ||
NECFGCCN_00293 | 2.2e-187 | lipA | 2.8.1.8 | H | Catalyzes the radical-mediated insertion of two sulfur atoms into the C-6 and C-8 positions of the octanoyl moiety bound to the lipoyl domains of lipoate-dependent enzymes, thereby converting the octanoylated domains into lipoylated derivatives | |
NECFGCCN_00294 | 1.2e-18 | tatE | U | Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. TatE shares overlapping functions with TatA | ||
NECFGCCN_00295 | 5.1e-134 | ybeM | 3.5.1.3 | S | Nitrilase cyanide hydratase and apolipoprotein N-acyltransferase | |
NECFGCCN_00296 | 1.2e-64 | crcB | D | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
NECFGCCN_00297 | 4.3e-32 | cspE | K | SMART Cold shock protein | ||
NECFGCCN_00298 | 5.4e-100 | pagP | 2.3.1.251 | M | Transfers a palmitate residue from the sn-1 position of a phospholipid to the N-linked hydroxymyristate on the proximal unit of lipid A or its precursors | |
NECFGCCN_00299 | 2.8e-236 | dcuC | C | C4-dicarboxylate | ||
NECFGCCN_00300 | 4.2e-152 | rna | 3.1.27.1, 3.1.27.6 | J | Belongs to the RNase T2 family | |
NECFGCCN_00301 | 1.6e-67 | rnk | K | regulator of nucleoside diphosphate kinase | ||
NECFGCCN_00302 | 2.3e-72 | uspG | T | Belongs to the universal stress protein A family | ||
NECFGCCN_00303 | 1.3e-295 | ahpF | O | alkyl hydroperoxide reductase | ||
NECFGCCN_00304 | 1e-104 | ahpC | 1.11.1.15 | O | C-terminal domain of 1-Cys peroxiredoxin | |
NECFGCCN_00305 | 7.2e-138 | dsbG | 5.3.4.1 | O | Required for disulfide bond formation in some periplasmic proteins. Acts by transferring its disulfide bond to other proteins and is reduced in the process | |
NECFGCCN_00306 | 1.4e-159 | ybdO | K | transcriptional regulator | ||
NECFGCCN_00307 | 4.8e-248 | ybdN | S | phosphoadenosine phosphosulfate | ||
NECFGCCN_00308 | 2.6e-109 | ibrB | K | ParB-like nuclease domain | ||
NECFGCCN_00309 | 6.8e-220 | ybdL | 2.6.1.17, 2.6.1.88 | E | aminotransferase | |
NECFGCCN_00310 | 3.1e-127 | mtnC | 3.1.3.77 | E | Bifunctional enzyme that catalyzes the enolization of 2,3-diketo-5-methylthiopentyl-1-phosphate (DK-MTP-1-P) into the intermediate 2-hydroxy-3-keto-5-methylthiopentenyl-1-phosphate (HK-MTPenyl-1-P), which is then dephosphorylated to form the acireductone 1,2-dihydroxy-3-keto-5-methylthiopentene (DHK- MTPene) | |
NECFGCCN_00311 | 2.5e-103 | mtnD | 1.13.11.53, 1.13.11.54 | S | Catalyzes 2 different reactions between oxygene and the acireductone 1,2-dihydroxy-3-keto-5-methylthiopentene (DHK-MTPene) depending upon the metal bound in the active site. Fe-containing acireductone dioxygenase (Fe-ARD) produces formate and 2-keto-4- methylthiobutyrate (KMTB), the alpha-ketoacid precursor of methionine in the methionine recycle pathway. Ni-containing acireductone dioxygenase (Ni-ARD) produces methylthiopropionate, carbon monoxide and formate, and does not lie on the methionine recycle pathway | |
NECFGCCN_00312 | 0.0 | dorA | 1.7.2.3, 1.8.5.3 | C | Belongs to the prokaryotic molybdopterin-containing oxidoreductase family | |
NECFGCCN_00313 | 9.6e-183 | G | (ABC) transporter | |||
NECFGCCN_00314 | 4.3e-294 | rbsA | 3.6.3.17 | P | (ABC) transporter | |
NECFGCCN_00315 | 1.5e-170 | alsC_1 | G | Belongs to the binding-protein-dependent transport system permease family | ||
NECFGCCN_00316 | 5.3e-176 | G | Belongs to the binding-protein-dependent transport system permease family | |||
NECFGCCN_00317 | 2.3e-173 | ydjH | 2.7.1.15 | G | belongs to the carbohydrate kinase PfkB family | |
NECFGCCN_00318 | 5.9e-191 | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | ||
NECFGCCN_00319 | 1.8e-181 | lyx_2 | 2.7.1.17, 2.7.1.189, 2.7.1.215, 2.7.1.5, 2.7.1.51 | G | Belongs to the FGGY kinase family | |
NECFGCCN_00320 | 1e-296 | V | abc transporter atp-binding protein | |||
NECFGCCN_00321 | 0.0 | V | abc transporter atp-binding protein | |||
NECFGCCN_00322 | 4.5e-187 | XK27_10075 | S | abc transporter atp-binding protein | ||
NECFGCCN_00324 | 5.8e-11 | |||||
NECFGCCN_00325 | 1.8e-105 | cfa | 2.1.1.317, 2.1.1.79 | M | synthase | |
NECFGCCN_00326 | 1.3e-139 | 2.1.1.79 | S | Plasmid partition ParA protein | ||
NECFGCCN_00327 | 1.3e-245 | S | NAD FAD-binding protein | |||
NECFGCCN_00328 | 2.9e-128 | sdh | S | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | ||
NECFGCCN_00329 | 4.7e-81 | 5.3.3.1 | S | transcriptional regulator | ||
NECFGCCN_00330 | 1.3e-136 | K | Transcriptional regulator | |||
NECFGCCN_00331 | 8.6e-101 | blc | M | Outer Membrane Lipoprotein | ||
NECFGCCN_00332 | 3.6e-55 | ysdA | K | Membrane | ||
NECFGCCN_00333 | 0.0 | cusA | P | Belongs to the resistance-nodulation-cell division (RND) (TC 2.A.6) family | ||
NECFGCCN_00334 | 1.2e-225 | cusB | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | ||
NECFGCCN_00335 | 2e-50 | cusF | S | Copper binding periplasmic protein CusF | ||
NECFGCCN_00336 | 3.8e-241 | cusC | M | RND efflux system, outer membrane lipoprotein | ||
NECFGCCN_00337 | 1.5e-121 | KT | Transcriptional regulatory protein, C terminal | |||
NECFGCCN_00338 | 6.6e-257 | cusS | 2.7.13.3 | T | member of a two-component regulatory system | |
NECFGCCN_00339 | 2.1e-31 | S | Protein of unknown function (DUF1778) | |||
NECFGCCN_00340 | 1.6e-62 | Z012_05445 | 2.3.1.189 | K | acetyltransferase | |
NECFGCCN_00341 | 5.6e-227 | ycfD | 1.14.11.47 | S | Cupin 4 family protein | |
NECFGCCN_00342 | 2.8e-126 | proV | E | abc transporter atp-binding protein | ||
NECFGCCN_00343 | 2.1e-150 | C | alcohol dehydrogenase | |||
NECFGCCN_00344 | 5.4e-64 | mgrA | K | Transcriptional regulator, MarR family | ||
NECFGCCN_00345 | 8.8e-133 | budA | 4.1.1.5 | H | Belongs to the alpha-acetolactate decarboxylase family | |
NECFGCCN_00346 | 6.4e-41 | rof | K | Suppresses temperature-sensitive mutations in essential genes by modulating rho-dependent transcription termination | ||
NECFGCCN_00347 | 7.3e-29 | yaeP | S | Belongs to the UPF0253 family | ||
NECFGCCN_00348 | 5.5e-95 | yaeQ | S | protein conserved in bacteria | ||
NECFGCCN_00349 | 2.7e-46 | yaeJ | J | chain release factor | ||
NECFGCCN_00350 | 1.4e-135 | cutF | MP | Copper homeostasis | ||
NECFGCCN_00351 | 2e-136 | yaeF | M | cysteine-type peptidase activity | ||
NECFGCCN_00352 | 0.0 | proS | 6.1.1.15 | J | Catalyzes the attachment of proline to tRNA(Pro) in a two-step reaction proline is first activated by ATP to form Pro- AMP and then transferred to the acceptor end of tRNA(Pro). As ProRS can inadvertently accommodate and process non-cognate amino acids such as alanine and cysteine, to avoid such errors it has two additional distinct editing activities against alanine. One activity is designated as 'pretransfer' editing and involves the tRNA(Pro)-independent hydrolysis of activated Ala-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Ala-tRNA(Pro). The misacylated Cys- tRNA(Pro) is not edited by ProRS | |
NECFGCCN_00353 | 2.4e-130 | yaeB | P | PFAM Uncharacterised protein family UPF0066 | ||
NECFGCCN_00354 | 8.1e-67 | rcsF | M | colanic acid biosynthetic process | ||
NECFGCCN_00355 | 9.9e-149 | metQ | P | Belongs to the NlpA lipoprotein family | ||
NECFGCCN_00356 | 4e-76 | metI | P | ABC-type metal ion transport system permease component | ||
NECFGCCN_00357 | 2.1e-188 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
NECFGCCN_00358 | 1.8e-104 | gmhB | 3.1.3.15, 3.1.3.82, 3.1.3.83, 4.2.1.19, 6.3.2.10 | E | D,D-heptose 1,7-bisphosphate phosphatase | |
NECFGCCN_00359 | 3.6e-54 | phoE | M | Belongs to the Gram-negative porin family | ||
NECFGCCN_00360 | 2.7e-157 | dprA | LU | DNA protecting protein DprA | ||
NECFGCCN_00362 | 1.2e-174 | yubA | S | permease | ||
NECFGCCN_00363 | 1.9e-92 | rimM | J | An accessory protein needed during the final step in the assembly of 30S ribosomal subunit, possibly for assembly of the head region. Probably interacts with S19. Essential for efficient processing of 16S rRNA. May be needed both before and after RbfA during the maturation of 16S rRNA. It has affinity for free ribosomal 30S subunits but not for 70S ribosomes | ||
NECFGCCN_00364 | 1e-156 | yjjH | S | Calcineurin-like phosphoesterase | ||
NECFGCCN_00365 | 2.5e-130 | nfrA | 1.5.1.38, 1.5.1.39 | C | nitroreductase | |
NECFGCCN_00366 | 0.0 | pacL | 3.6.3.8 | P | cation transport ATPase | |
NECFGCCN_00367 | 1.7e-66 | ywiB | S | Domain of unknown function (DUF1934) | ||
NECFGCCN_00368 | 5.9e-136 | XK27_00115 | 2.3.1.128 | K | Acetyltransferase GNAT family | |
NECFGCCN_00369 | 7.8e-146 | yidA | S | hydrolases of the HAD superfamily | ||
NECFGCCN_00370 | 2.9e-179 | murM | 2.3.2.10, 2.3.2.16 | V | protein involved in methicillin resistance | |
NECFGCCN_00371 | 1.5e-56 | S | Protein of unknown function (DUF454) | |||
NECFGCCN_00372 | 2.7e-154 | vicX | 3.1.26.11 | S | Metal-dependent hydrolases of the beta-lactamase superfamily I | |
NECFGCCN_00373 | 6.2e-233 | vicK | 2.7.13.3 | T | Histidine kinase | |
NECFGCCN_00374 | 1.9e-127 | KT | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
NECFGCCN_00375 | 6.1e-66 | rnfC | C | Part of a membrane complex involved in electron transport | ||
NECFGCCN_00376 | 1.2e-11 | rnfC | C | Belongs to the 4Fe4S bacterial-type ferredoxin family. RnfC subfamily | ||
NECFGCCN_00377 | 1.3e-40 | rnfC | C | Part of a membrane complex involved in electron transport | ||
NECFGCCN_00378 | 1.6e-89 | rnfB | 1.12.98.1 | C | Part of a membrane complex involved in electron transport | |
NECFGCCN_00379 | 6.5e-94 | rnfA | C | Part of a membrane complex involved in electron transport | ||
NECFGCCN_00380 | 2.5e-66 | ydgK | S | Membrane | ||
NECFGCCN_00381 | 5.6e-32 | cnu | S | positive regulation of protein complex disassembly | ||
NECFGCCN_00382 | 1e-270 | bglC | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
NECFGCCN_00383 | 2.5e-12 | blr | ||||
NECFGCCN_00384 | 4.3e-189 | ydgJ | 1.1.1.371 | S | oxidoreductase | |
NECFGCCN_00385 | 2.2e-182 | add | 3.5.4.4 | F | Catalyzes the hydrolytic deamination of adenine to hypoxanthine. Plays an important role in the purine salvage pathway and in nitrogen catabolism | |
NECFGCCN_00386 | 4.9e-192 | ynfM_2 | EGP | Major facilitator Superfamily | ||
NECFGCCN_00387 | 9.5e-80 | yybR_1 | K | transcriptional regulator | ||
NECFGCCN_00389 | 3.2e-89 | L | Transposase | |||
NECFGCCN_00390 | 5.8e-174 | S | hydrolase | |||
NECFGCCN_00391 | 0.0 | U | protein secretion | |||
NECFGCCN_00392 | 8.4e-196 | pepQ | 3.4.13.9 | E | Belongs to the peptidase M24B family | |
NECFGCCN_00393 | 1.9e-181 | ccpA | K | Catabolite control protein A | ||
NECFGCCN_00394 | 4.7e-191 | yyaQ | S | YjbR | ||
NECFGCCN_00395 | 9e-193 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
NECFGCCN_00396 | 8.7e-78 | yueI | S | Protein of unknown function (DUF1694) | ||
NECFGCCN_00397 | 7.4e-247 | eno | 4.2.1.11 | G | Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis | |
NECFGCCN_00399 | 2.5e-283 | murE | 3.4.16.4, 6.3.2.10, 6.3.2.13 | M | Catalyzes the addition of meso-diaminopimelic acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
NECFGCCN_00400 | 0.0 | ftsI | 3.4.16.4 | M | Catalyzes cross-linking of the peptidoglycan cell wall at the division septum | |
NECFGCCN_00401 | 1.5e-59 | ftsL | D | Essential cell division protein. May link together the upstream cell division proteins, which are predominantly cytoplasmic, with the downstream cell division proteins, which are predominantly periplasmic | ||
NECFGCCN_00402 | 4.8e-171 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
NECFGCCN_00403 | 5e-81 | mraZ | K | Negatively regulates its own expression and that of the subsequent genes in the proximal part of the division and cell wall (dcw) gene cluster. Acts by binding directly to DNA. May also regulate the expression of genes outside the dcw cluster | ||
NECFGCCN_00404 | 1.2e-188 | fruR | 3.2.1.26 | GH32 | K | Transcriptional |
NECFGCCN_00405 | 3.1e-81 | ilvH | 2.2.1.6 | E | acetolactate synthase | |
NECFGCCN_00406 | 0.0 | ilvI | 2.2.1.6 | H | acetolactate synthase | |
NECFGCCN_00407 | 1.8e-178 | leuO | K | transcriptional regulator | ||
NECFGCCN_00408 | 9.7e-286 | leuA | 2.3.3.13 | E | Catalyzes the condensation of the acetyl group of acetyl-CoA with 3-methyl-2-oxobutanoate (2-oxoisovalerate) to form 3-carboxy-3-hydroxy-4-methylpentanoate (2-isopropylmalate) | |
NECFGCCN_00409 | 5.9e-205 | leuB | 1.1.1.85 | CE | Catalyzes the oxidation of 3-carboxy-2-hydroxy-4- methylpentanoate (3-isopropylmalate) to 3-carboxy-4-methyl-2- oxopentanoate. The product decarboxylates to 4-methyl-2 oxopentanoate | |
NECFGCCN_00410 | 5.3e-267 | leuC | 4.2.1.33, 4.2.1.35 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
NECFGCCN_00411 | 1.9e-112 | leuD | 4.2.1.33, 4.2.1.35 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
NECFGCCN_00412 | 0.0 | 1.3.1.34 | C | COG1902 NADH flavin oxidoreductases, Old Yellow Enzyme family | ||
NECFGCCN_00413 | 3.1e-161 | aroE | 1.1.1.25, 1.1.1.282, 1.3.5.4 | E | The actual biological function of YdiB remains unclear, nor is it known whether 3-dehydroshikimate or quinate represents the natural substrate. Catalyzes the reversible NAD-dependent reduction of both 3-dehydroshikimate (DHSA) and 3-dehydroquinate to yield shikimate (SA) and quinate, respectively. It can use both NAD or NADP for catalysis, however it has higher catalytic efficiency with NAD | |
NECFGCCN_00414 | 8.8e-210 | ydiM | G | transport protein | ||
NECFGCCN_00415 | 1.5e-130 | aroD | 1.1.1.25, 4.2.1.10 | E | Involved in the third step of the chorismate pathway, which leads to the biosynthesis of aromatic amino acids. Catalyzes the cis-dehydration of 3-dehydroquinate (DHQ) and introduces the first double bond of the aromatic ring to yield 3- dehydroshikimate | |
NECFGCCN_00416 | 4.6e-163 | yybE | K | Transcriptional regulator | ||
NECFGCCN_00417 | 2.1e-233 | G | transporter | |||
NECFGCCN_00418 | 1e-207 | setA | EGP | Major facilitator Superfamily | ||
NECFGCCN_00419 | 4.4e-18 | S | Inhibitor of glucose uptake transporter SgrT | |||
NECFGCCN_00420 | 0.0 | sgrR | K | Activates the small RNA gene sgrS under glucose- phosphate stress conditions as well as yfdZ. Represses its own transcription under both stress and non-stress conditions. Might act as a sensor of the intracellular accumulation of phosphoglucose by binding these molecules in its C-terminal solute-binding domain | ||
NECFGCCN_00421 | 1.8e-181 | tbpA | P | thiamine ABC transporter | ||
NECFGCCN_00422 | 1.3e-290 | thiP | P | with TbpA and ThiQ functions in transport of thiamine and thiamine pyrophosphate into the cell | ||
NECFGCCN_00423 | 7e-119 | thiQ | P | Part of the ABC transporter complex ThiBPQ involved in thiamine import. Responsible for energy coupling to the transport system | ||
NECFGCCN_00424 | 7.9e-124 | yabI | 3.6.1.27 | I | membrane-associated protein | |
NECFGCCN_00425 | 2.6e-168 | araC | K | transcriptional regulator | ||
NECFGCCN_00426 | 0.0 | araB | 2.7.1.16 | C | Belongs to the ribulokinase family | |
NECFGCCN_00427 | 3.9e-300 | araA | 5.3.1.4 | G | Catalyzes the conversion of L-arabinose to L-ribulose | |
NECFGCCN_00428 | 5.1e-130 | araD | 4.1.1.104, 4.1.2.17, 4.1.2.19, 4.2.1.109, 5.1.3.4 | G | Catalyzes the isomerization of L-ribulose 5-phosphate to D-xylulose 5-phosphate | |
NECFGCCN_00429 | 0.0 | polB | 2.7.7.7 | L | DNA polymerase | |
NECFGCCN_00430 | 0.0 | rapA | K | Transcription regulator that activates transcription by stimulating RNA polymerase (RNAP) recycling in case of stress conditions such as supercoiled DNA or high salt concentrations. Probably acts by releasing the RNAP, when it is trapped or immobilized on tightly supercoiled DNA. Does not activate transcription on linear DNA. Probably not involved in DNA repair | ||
NECFGCCN_00431 | 2.3e-63 | tdcF | 3.5.99.10 | J | endoribonuclease L-PSP | |
NECFGCCN_00432 | 2.6e-123 | queC | 6.3.4.20 | F | Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) | |
NECFGCCN_00433 | 8.2e-81 | queD | 4.1.2.50, 4.2.3.12 | H | synthase | |
NECFGCCN_00434 | 4.6e-134 | queE | 1.97.1.4, 4.3.99.3 | H | Catalyzes the complex heterocyclic radical-mediated conversion of 6-carboxy-5,6,7,8-tetrahydropterin (CPH4) to 7- carboxy-7-deazaguanine (CDG), a step common to the biosynthetic pathways of all 7-deazapurine-containing compounds | |
NECFGCCN_00435 | 1.4e-94 | queF | 1.7.1.13 | S | Belongs to the GTP cyclohydrolase I family. QueF type 1 subfamily | |
NECFGCCN_00436 | 5e-85 | fimF | NU | Fimbrial protein | ||
NECFGCCN_00437 | 0.0 | fimD | NU | Usher protein | ||
NECFGCCN_00438 | 5.4e-119 | fimC | M | chaperone | ||
NECFGCCN_00439 | 3.2e-95 | fimI | NU | Fimbrial protein | ||
NECFGCCN_00440 | 2.6e-84 | fimA | NU | Fimbrial protein | ||
NECFGCCN_00441 | 0.0 | 3.4.17.14, 3.5.1.28 | NU | GBS Bsp-like repeat | ||
NECFGCCN_00442 | 1.5e-213 | mltA | GH102 | M | Murein-degrading enzyme. May play a role in recycling of muropeptides during cell elongation and or cell division | |
NECFGCCN_00443 | 9.3e-147 | ygdL | 2.7.7.73, 2.7.7.80 | H | Dinucleotide-utilizing enzymes involved in molybdopterin and thiamine biosynthesis family 1 | |
NECFGCCN_00444 | 3.5e-68 | csdE | 2.8.1.7, 4.4.1.16 | S | cysteine desulfurase, sulfur acceptor subunit CsdE | |
NECFGCCN_00445 | 9e-223 | csdA | 2.8.1.7, 4.4.1.16 | E | Cysteine desulfurases mobilize the sulfur from L- cysteine to yield L-alanine, an essential step in sulfur metabolism for biosynthesis of a variety of sulfur-containing biomolecules. Component of the suf operon, which is activated and required under specific conditions such as oxidative stress and iron limitation. Acts as a potent selenocysteine lyase in vitro, that mobilizes selenium from L-selenocysteine. Selenocysteine lyase activity is however unsure in vivo | |
NECFGCCN_00446 | 6.7e-34 | ygdI | S | Lipoprotein | ||
NECFGCCN_00447 | 1.3e-168 | gcvA | K | transcriptional regulator | ||
NECFGCCN_00448 | 2.5e-65 | ygdD | S | Small membrane protein | ||
NECFGCCN_00449 | 2.1e-218 | rlmM | 2.1.1.186 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA methyltransferase RlmE family. RlmM subfamily | |
NECFGCCN_00450 | 3.1e-130 | fucR | K | transcriptional regulator | ||
NECFGCCN_00451 | 1.9e-71 | fucU | 5.1.3.29 | G | Involved in the anomeric conversion of L-fucose | |
NECFGCCN_00452 | 8.3e-268 | fucK | 2.7.1.17, 2.7.1.189, 2.7.1.5, 2.7.1.51 | F | Belongs to the FGGY kinase family | |
NECFGCCN_00453 | 0.0 | fucI | 5.3.1.25, 5.3.1.3 | G | Converts the aldose L-fucose into the corresponding ketose L-fuculose | |
NECFGCCN_00454 | 6.9e-245 | fucP | G | transporter | ||
NECFGCCN_00455 | 4.7e-117 | fucA | 4.1.1.104, 4.1.2.17, 4.1.2.19, 4.2.1.109, 5.1.3.4 | G | Catalyzes the cleavage of L-fuculose 1-phosphate to glycerone phosphate and L-lactaldehyde | |
NECFGCCN_00456 | 2e-211 | fucO | 1.1.1.1, 1.1.1.77, 1.1.99.37, 1.2.98.1 | C | alcohol dehydrogenase | |
NECFGCCN_00457 | 1.6e-140 | xni | 2.7.7.7 | L | Has flap endonuclease activity. During DNA replication, flap endonucleases cleave the 5'-overhanging flap structure that is generated by displacement synthesis when DNA polymerase encounters the 5'-end of a downstream Okazaki fragment | |
NECFGCCN_00458 | 0.0 | flbD | T | COG2204 Response regulator containing CheY-like receiver, AAA-type ATPase, and DNA-binding domains | ||
NECFGCCN_00459 | 1.8e-223 | ssuD | 1.14.14.5 | C | Catalyzes the desulfonation of aliphatic sulfonates | |
NECFGCCN_00460 | 1.8e-82 | S | oxidoreductase | |||
NECFGCCN_00461 | 5.7e-49 | S | oxidoreductase | |||
NECFGCCN_00462 | 0.0 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
NECFGCCN_00463 | 8.5e-145 | trxB1 | 1.18.1.2, 1.19.1.1 | C | Ferredoxin--NADP reductase | |
NECFGCCN_00465 | 8.6e-72 | hit | FG | Diadenosine tetraphosphate (Ap4A) hydrolase and other HIT family hydrolases | ||
NECFGCCN_00466 | 9.9e-132 | ecsA | V | abc transporter atp-binding protein | ||
NECFGCCN_00467 | 1.9e-176 | ecsB | U | Bacterial ABC transporter protein EcsB | ||
NECFGCCN_00468 | 9.5e-55 | ytmP | 2.7.1.89 | M | Phosphotransferase | |
NECFGCCN_00469 | 2e-18 | K | HxlR-like helix-turn-helix | |||
NECFGCCN_00470 | 2.9e-265 | 1.1.3.15 | C | Fad linked oxidase | ||
NECFGCCN_00471 | 2.3e-137 | P | ABC-type nitrate sulfonate bicarbonate transport system permease component | |||
NECFGCCN_00472 | 5e-148 | P | ABC-type nitrate sulfonate bicarbonate transport system, ATPase component | |||
NECFGCCN_00473 | 1.4e-184 | P | ABC-type nitrate sulfonate bicarbonate transport systems, periplasmic components | |||
NECFGCCN_00474 | 3.4e-171 | 3.5.2.10 | S | Creatininase | ||
NECFGCCN_00475 | 1e-81 | 3.5.99.10 | J | translation initiation inhibitor, yjgF family | ||
NECFGCCN_00476 | 1.1e-237 | codA | 3.5.4.1 | F | Cytosine deaminase and related metal-dependent hydrolases | |
NECFGCCN_00477 | 7.3e-175 | vanB | C | Flavodoxin reductases (Ferredoxin-NADPH reductases) family 1 | ||
NECFGCCN_00478 | 6e-163 | K | Transcriptional regulator | |||
NECFGCCN_00479 | 8.5e-187 | P | COG0715 ABC-type nitrate sulfonate bicarbonate transport systems, periplasmic components | |||
NECFGCCN_00480 | 3.8e-133 | F | COG0402 Cytosine deaminase and related metal-dependent hydrolases | |||
NECFGCCN_00481 | 0.0 | entF | 6.3.2.14 | Q | amino acid activation for nonribosomal peptide biosynthetic process | |
NECFGCCN_00482 | 6.9e-147 | fepC | 3.6.3.34 | HP | (ABC) transporter | |
NECFGCCN_00483 | 1.9e-170 | fepG | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
NECFGCCN_00484 | 1.6e-172 | fepD | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
NECFGCCN_00485 | 1.4e-267 | yfmM | S | abc transporter atp-binding protein | ||
NECFGCCN_00486 | 1.3e-39 | 3.6.3.8 | P | cation transport ATPase | ||
NECFGCCN_00487 | 1.2e-97 | 1.6.5.2 | S | NADPH-quinone reductase (modulator of drug activity B) | ||
NECFGCCN_00488 | 2.4e-99 | K | Transcriptional regulator | |||
NECFGCCN_00489 | 1.6e-129 | artI | ET | belongs to the bacterial solute-binding protein 3 family | ||
NECFGCCN_00490 | 4.4e-100 | orn | L | 3'-to-5' exoribonuclease specific for small oligoribonucleotides | ||
NECFGCCN_00491 | 1.1e-195 | rsgA | 3.1.3.100 | S | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Helps release RbfA from mature subunits. May play a role in the assembly of ribosomal proteins into the subunit. Circularly permuted GTPase that catalyzes slow GTP hydrolysis, GTPase activity is stimulated by the 30S ribosomal subunit | |
NECFGCCN_00492 | 3.7e-179 | psd | 4.1.1.65 | I | Catalyzes the formation of phosphatidylethanolamine (PtdEtn) from phosphatidylserine (PtdSer) | |
NECFGCCN_00493 | 0.0 | yjeP | M | mechanosensitive ion channel | ||
NECFGCCN_00494 | 2.6e-272 | yjeM | E | amino acid | ||
NECFGCCN_00495 | 6e-185 | epmA | J | With EpmB is involved in the beta-lysylation step of the post-translational modification of translation elongation factor P (EF-P). Catalyzes the ATP-dependent activation of (R)-beta-lysine produced by EpmB, forming a lysyl-adenylate, from which the beta- lysyl moiety is then transferred to the epsilon-amino group of a conserved specific lysine residue in EF-P | ||
NECFGCCN_00496 | 0.0 | frdA | 1.3.5.1, 1.3.5.4 | C | Belongs to the FAD-dependent oxidoreductase 2 family. FRD SDH subfamily | |
NECFGCCN_00497 | 1.7e-144 | frdB | 1.3.5.1, 1.3.5.4 | C | Belongs to the succinate dehydrogenase fumarate reductase iron-sulfur protein family | |
NECFGCCN_00498 | 1.9e-68 | frdC | C | Seems to be involved in the anchoring of the catalytic components of the fumarate reductase complex to the cytoplasmic membrane | ||
NECFGCCN_00499 | 3.4e-61 | frdD | C | Seems to be involved in the anchoring of the catalytic components of the fumarate reductase complex to the cytoplasmic membrane | ||
NECFGCCN_00500 | 2.8e-99 | blc | M | Outer Membrane Lipoprotein | ||
NECFGCCN_00501 | 3e-45 | sugE | U | multidrug resistance protein | ||
NECFGCCN_00502 | 4e-16 | ecnB | S | Entericidin EcnA/B family | ||
NECFGCCN_00503 | 8.8e-104 | efp | J | Involved in peptide bond synthesis. Alleviates ribosome stalling that occurs when 3 or more consecutive Pro residues or the sequence PPG is present in a protein, possibly by augmenting the peptidyl transferase activity of the ribosome. Modification of Lys-34 is required for alleviation | ||
NECFGCCN_00504 | 1.3e-193 | kamA | 5.4.3.2 | C | lysine 2,3-aminomutase | |
NECFGCCN_00505 | 1.5e-81 | K | transcriptional regulator | |||
NECFGCCN_00506 | 2.6e-79 | NU | cell adhesion | |||
NECFGCCN_00507 | 1.8e-119 | M | Pili assembly chaperone PapD, C-terminal domain | |||
NECFGCCN_00508 | 0.0 | safC | NU | Usher protein | ||
NECFGCCN_00509 | 2.4e-59 | NU | Fimbrial protein | |||
NECFGCCN_00511 | 1.1e-162 | M | Secretion Protein | |||
NECFGCCN_00512 | 0.0 | V | COG2274 ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | |||
NECFGCCN_00513 | 1.2e-133 | yjeJ | S | YjeJ-like | ||
NECFGCCN_00514 | 1.2e-58 | yjeI | S | Membrane | ||
NECFGCCN_00515 | 2e-97 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
NECFGCCN_00516 | 0.0 | uvrC | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrC both incises the 5' and 3' sides of the lesion. The N-terminal half is responsible for the 3' incision and the C-terminal half is responsible for the 5' incision | ||
NECFGCCN_00517 | 6.2e-115 | uvrY | K | response regulator | ||
NECFGCCN_00518 | 2.8e-29 | yecF | S | Protein of unknown function (DUF2594) | ||
NECFGCCN_00519 | 4.4e-132 | vjbR | K | Transcriptional | ||
NECFGCCN_00520 | 2e-132 | yecC | 3.6.3.21 | E | (ABC) transporter | |
NECFGCCN_00521 | 3.8e-114 | yecS | P | amino acid ABC transporter | ||
NECFGCCN_00522 | 8e-177 | dcyD | 4.4.1.15 | E | Catalyzes the alpha,beta-elimination reaction of D- cysteine and of several D-cysteine derivatives. It could be a defense mechanism against D-cysteine | |
NECFGCCN_00523 | 4e-142 | fliY | ET | Belongs to the bacterial solute-binding protein 3 family | ||
NECFGCCN_00524 | 3.2e-294 | amyA | 3.2.1.1 | GH13 | G | Cytoplasmic alpha-amylase |
NECFGCCN_00525 | 1.2e-68 | yedD | S | (Lipo)protein | ||
NECFGCCN_00526 | 7.2e-107 | rcsA | K | Component of the Rcs signaling system, which controls transcription of numerous genes. Binds, with RcsB, to the RcsAB box to regulate expression of genes | ||
NECFGCCN_00527 | 4.1e-29 | dsrB | S | Dextransucrase DSRB | ||
NECFGCCN_00528 | 8.2e-21 | yodD | S | Protein of unknown function (DUF2525) | ||
NECFGCCN_00529 | 2.7e-302 | yedQ | 2.7.7.65 | T | Diguanylate cyclase | |
NECFGCCN_00530 | 1.9e-132 | yedI | S | protein conserved in bacteria | ||
NECFGCCN_00531 | 2.5e-156 | yedA | EG | of the drug metabolite transporter (DMT) superfamily | ||
NECFGCCN_00532 | 6.6e-87 | vsr | L | May nick specific sequences that contain T G mispairs resulting from m5C-deamination | ||
NECFGCCN_00533 | 1.6e-263 | dcm | 2.1.1.37 | H | Methyl-transferase | |
NECFGCCN_00534 | 5.2e-122 | yedJ | S | Metal-dependent phosphohydrolase | ||
NECFGCCN_00535 | 4.2e-46 | yedR | ||||
NECFGCCN_00536 | 1.4e-212 | ompS1 | M | Belongs to the Gram-negative porin family | ||
NECFGCCN_00538 | 8.2e-148 | mtfA | C | Belongs to the MtfA family | ||
NECFGCCN_00539 | 4e-114 | ET | ABC transporter | |||
NECFGCCN_00540 | 9.4e-136 | ET | Belongs to the bacterial solute-binding protein 3 family | |||
NECFGCCN_00541 | 2.8e-210 | arcT | 2.6.1.1 | E | Aminotransferase | |
NECFGCCN_00542 | 6.1e-135 | gltS | ET | Belongs to the bacterial solute-binding protein 3 family | ||
NECFGCCN_00543 | 3.2e-20 | rpsU | J | Belongs to the bacterial ribosomal protein bS21 family | ||
NECFGCCN_00544 | 4.2e-49 | mscL | M | Channel that opens in response to stretch forces in the membrane lipid bilayer. May participate in the regulation of osmotic pressure changes within the cell | ||
NECFGCCN_00545 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
NECFGCCN_00546 | 4e-201 | sigA | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released. This sigma factor is the primary sigma factor during exponential growth | ||
NECFGCCN_00547 | 3.4e-55 | yitW | K | metal-sulfur cluster biosynthetic enzyme | ||
NECFGCCN_00548 | 4e-170 | yfdH | GT2 | M | COG0463, glycosyltransferases involved in cell wall biogenesis | |
NECFGCCN_00549 | 3.1e-257 | S | Glucosyl transferase GtrII | |||
NECFGCCN_00550 | 2.9e-159 | rfbD | 1.1.1.133, 5.1.3.13 | M | Catalyzes the reduction of dTDP-6-deoxy-L-lyxo-4- hexulose to yield dTDP-L-rhamnose | |
NECFGCCN_00551 | 3.9e-221 | amrA | S | membrane protein involved in the export of O-antigen and teichoic acid | ||
NECFGCCN_00552 | 1.6e-174 | M | Glycosyltransferase, group 2 family protein | |||
NECFGCCN_00553 | 1.2e-121 | mta | K | Transcriptional | ||
NECFGCCN_00554 | 1.4e-29 | S | Protein of unknown function (DUF3021) | |||
NECFGCCN_00555 | 1.3e-73 | K | COG3279 Response regulator of the LytR AlgR family | |||
NECFGCCN_00556 | 9.3e-134 | cylB | V | ABC-2 type transporter | ||
NECFGCCN_00557 | 3.2e-153 | cylA | V | abc transporter atp-binding protein | ||
NECFGCCN_00558 | 2e-149 | V | COG2274 ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | |||
NECFGCCN_00559 | 6.2e-39 | repB | S | Replication regulatory protein RepB | ||
NECFGCCN_00560 | 3.9e-11 | repA1 | S | This protein is essential for plasmid replication | ||
NECFGCCN_00561 | 5.3e-181 | repA | S | IncFII RepA protein family | ||
NECFGCCN_00562 | 6e-41 | |||||
NECFGCCN_00563 | 9.3e-44 | insN | L | silverDB | ||
NECFGCCN_00564 | 4.4e-141 | XK27_10035 | V | abc transporter atp-binding protein | ||
NECFGCCN_00565 | 7.7e-230 | pepT | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
NECFGCCN_00566 | 0.0 | rnjA | S | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
NECFGCCN_00567 | 1.5e-33 | ykzG | S | Belongs to the UPF0356 family | ||
NECFGCCN_00568 | 9e-119 | yeaZ | 2.3.1.234 | O | COG1214, inactive homolog of metal-dependent proteases | |
NECFGCCN_00569 | 4.8e-73 | rimI | 2.3.1.128 | K | This enzyme acetylates the N-terminal alanine of ribosomal protein S18 | |
NECFGCCN_00570 | 1.1e-184 | tsaD | 2.3.1.234 | O | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaE and TsaB. TsaD likely plays a direct catalytic role in this reaction | |
NECFGCCN_00571 | 1.7e-112 | azlC | E | AzlC protein | ||
NECFGCCN_00572 | 4.4e-47 | azlD | S | branched-chain amino acid | ||
NECFGCCN_00573 | 0.0 | recD2 | 3.1.11.5 | L | DNA-dependent ATPase and ATP-dependent 5'-3' DNA helicase. Has no activity on blunt DNA or DNA with 3'-overhangs, requires at least 10 bases of 5'-ssDNA for helicase activity | |
NECFGCCN_00574 | 6.1e-106 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
NECFGCCN_00575 | 4.8e-64 | rnhC | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
NECFGCCN_00576 | 0.0 | gidA | D | NAD-binding protein involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA-cmnm(5)s(2)U34 | ||
NECFGCCN_00577 | 1.4e-21 | |||||
NECFGCCN_00578 | 2.7e-32 | T | Phage conjugal plasmid C-4 type zinc finger protein, TraR family | |||
NECFGCCN_00579 | 1.6e-30 | S | Domain of unknown function (DUF4222) | |||
NECFGCCN_00580 | 8.1e-229 | Z012_07715 | L | Belongs to the 'phage' integrase family | ||
NECFGCCN_00581 | 1.4e-12 | hipO | 3.5.1.47 | E | COG1473 Metal-dependent amidase aminoacylase carboxypeptidase | |
NECFGCCN_00582 | 9.8e-97 | tktB | 2.2.1.1 | G | Transketolase | |
NECFGCCN_00583 | 1.5e-178 | 2.2.1.1 | G | Transketolase | ||
NECFGCCN_00584 | 1.7e-214 | rhlE | 3.6.4.13 | JKL | DEAD-box RNA helicase involved in | |
NECFGCCN_00585 | 0.0 | dinG | 3.6.4.12 | KL | helicase | |
NECFGCCN_00586 | 3.8e-31 | gluA | 3.6.3.21 | E | (ABC) transporter | |
NECFGCCN_00587 | 2.3e-159 | fliY | ET | ABC transporter substrate-binding protein | ||
NECFGCCN_00588 | 9.3e-115 | yncG | 2.5.1.18 | O | Glutathione S-Transferase | |
NECFGCCN_00589 | 4.6e-35 | pptA | 5.3.2.6 | S | Belongs to the 4-oxalocrotonate tautomerase family | |
NECFGCCN_00590 | 1e-42 | K | Helix-turn-helix domain | |||
NECFGCCN_00591 | 2.6e-26 | |||||
NECFGCCN_00592 | 3.1e-255 | lamB | M | Maltoporin (phage lambda and maltose receptor) | ||
NECFGCCN_00593 | 6.6e-246 | G | COG2211 Na melibiose symporter and related transporters | |||
NECFGCCN_00594 | 1.3e-293 | ram2 | 3.2.1.40 | G | Bacterial alpha-L-rhamnosidase 6 hairpin glycosidase domain | |
NECFGCCN_00595 | 3.7e-135 | K | transcriptional regulator | |||
NECFGCCN_00596 | 3.5e-108 | yddH | S | Flavin reductase | ||
NECFGCCN_00598 | 4.7e-123 | phnT | 3.6.3.30 | P | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | |
NECFGCCN_00599 | 2.4e-173 | ftpB | P | ABC transporter substrate-binding protein | ||
NECFGCCN_00600 | 1.9e-284 | ftpA | P | ABC-type Fe3 transport system permease component | ||
NECFGCCN_00601 | 8.7e-164 | nhoA | 2.3.1.118, 2.3.1.5 | Q | Belongs to the arylamine N-acetyltransferase family | |
NECFGCCN_00602 | 4.2e-26 | glnQ2 | 3.6.3.21 | E | (ABC) transporter | |
NECFGCCN_00603 | 7.4e-72 | S | Protein of unknown function (DUF1062) | |||
NECFGCCN_00604 | 1.5e-57 | E | glyoxalase bleomycin resistance protein dioxygenase | |||
NECFGCCN_00605 | 2.7e-182 | cmr | EGP | Major facilitator Superfamily | ||
NECFGCCN_00606 | 9.9e-55 | 4.4.1.5 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | ||
NECFGCCN_00607 | 6.9e-207 | P | Major facilitator superfamily | |||
NECFGCCN_00608 | 5e-213 | oxlT | P | COG0477 Permeases of the major facilitator superfamily | ||
NECFGCCN_00609 | 6.1e-120 | yrrM | 2.1.1.104 | S | O-Methyltransferase | |
NECFGCCN_00610 | 8.6e-167 | prsA | 3.1.3.16, 5.2.1.8 | O | peptidyl-prolyl cis-trans isomerase activity | |
NECFGCCN_00611 | 1.7e-84 | yxjI | S | LURP-one-related | ||
NECFGCCN_00612 | 0.0 | alaS | 6.1.1.7 | J | Catalyzes the attachment of alanine to tRNA(Ala) in a two-step reaction alanine is first activated by ATP to form Ala- AMP and then transferred to the acceptor end of tRNA(Ala). Also edits incorrectly charged Ser-tRNA(Ala) and Gly-tRNA(Ala) via its editing domain | |
NECFGCCN_00613 | 8.8e-162 | K | sequence-specific DNA binding | |||
NECFGCCN_00614 | 5.9e-09 | |||||
NECFGCCN_00615 | 1.3e-105 | K | Transcriptional regulator | |||
NECFGCCN_00616 | 8.2e-120 | L | Molecular Function DNA binding, Biological Process DNA recombination | |||
NECFGCCN_00617 | 4.8e-45 | L | transposase activity | |||
NECFGCCN_00618 | 9e-08 | S | Enterocin A Immunity | |||
NECFGCCN_00619 | 1.4e-62 | S | oxidoreductase | |||
NECFGCCN_00620 | 1e-173 | iolE | 4.2.1.44 | G | Xylose isomerase domain protein TIM barrel | |
NECFGCCN_00621 | 1.1e-176 | K | Transcriptional regulator, LacI family | |||
NECFGCCN_00622 | 2.5e-41 | S | Protein of unknown function (DUF1778) | |||
NECFGCCN_00623 | 1.2e-80 | S | Acetyltransferase (GNAT) domain | |||
NECFGCCN_00625 | 2e-78 | XK27_01265 | S | ECF-type riboflavin transporter, S component | ||
NECFGCCN_00626 | 3.6e-141 | pdxK | 2.7.1.35 | H | Belongs to the pyridoxine kinase family | |
NECFGCCN_00627 | 1.6e-83 | S | ECF-type riboflavin transporter, S component | |||
NECFGCCN_00629 | 0.0 | nifJ | 1.2.7.1 | C | Oxidoreductase required for the transfer of electrons from pyruvate to flavodoxin | |
NECFGCCN_00630 | 1.3e-274 | lpdA | 1.8.1.4 | C | Dehydrogenase | |
NECFGCCN_00631 | 1.2e-143 | S | Domain of unknown function (DUF4123) | |||
NECFGCCN_00632 | 0.0 | S | protein conserved in bacteria | |||
NECFGCCN_00633 | 0.0 | clpV | O | Belongs to the ClpA ClpB family | ||
NECFGCCN_00634 | 5.7e-91 | hcp | S | Type VI secretion system effector | ||
NECFGCCN_00635 | 6e-310 | M | Belongs to the ompA family | |||
NECFGCCN_00636 | 1.2e-51 | livG | E | Part of the ABC transporter complexes LivFGHMJ and LivFGHMK involved in the high-affinity transport of branched-chain amino acids | ||
NECFGCCN_00637 | 5.6e-223 | livM | U | Belongs to the binding-protein-dependent transport system permease family | ||
NECFGCCN_00638 | 2e-158 | livH | E | Belongs to the binding-protein-dependent transport system permease family | ||
NECFGCCN_00639 | 1e-212 | livJ | E | With LivFGHM is involved in the high affinity leucine transport | ||
NECFGCCN_00640 | 0.0 | pflB | 2.3.1.54 | C | formate acetyltransferase | |
NECFGCCN_00641 | 6e-219 | ackA | 2.7.2.1, 2.7.2.15 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
NECFGCCN_00642 | 2.8e-241 | tdcC | E | Involved in the import of threonine and serine into the cell, with the concomitant import of a proton (symport system) | ||
NECFGCCN_00643 | 8.8e-184 | tdcB | 4.3.1.15, 4.3.1.19 | E | Catalyzes the anaerobic formation of alpha-ketobutyrate and ammonia from threonine in a two-step reaction. The first step involved a dehydration of threonine and a production of enamine intermediates (aminocrotonate), which tautomerizes to its imine form (iminobutyrate). Both intermediates are unstable and short- lived. The second step is the nonenzymatic hydrolysis of the enamine imine intermediates to form 2-ketobutyrate and free ammonia. In the low water environment of the cell, the second step is accelerated by RidA | |
NECFGCCN_00644 | 1.4e-170 | tdcA | K | Transcriptional regulator | ||
NECFGCCN_00645 | 4.7e-143 | P | ABC-type phosphate phosphonate transport system periplasmic component | |||
NECFGCCN_00646 | 9e-192 | I | fatty acid desaturase | |||
NECFGCCN_00647 | 2.5e-47 | U | family outer membrane protein | |||
NECFGCCN_00648 | 1.8e-35 | U | Large exoproteins involved in heme utilization or adhesion | |||
NECFGCCN_00651 | 1.5e-37 | U | family outer membrane protein | |||
NECFGCCN_00652 | 8.3e-24 | U | Large exoproteins involved in heme utilization or adhesion | |||
NECFGCCN_00653 | 0.0 | fhaC | U | hemolysin activation secretion protein | ||
NECFGCCN_00654 | 1.3e-114 | cstA | T | Carbon starvation protein | ||
NECFGCCN_00655 | 3.9e-136 | 3.5.1.32 | S | amidohydrolase | ||
NECFGCCN_00656 | 0.0 | fdhF | 1.17.1.10, 1.17.1.9, 1.17.99.7 | C | Belongs to the prokaryotic molybdopterin-containing oxidoreductase family | |
NECFGCCN_00657 | 9.5e-208 | ybiC | 1.5.1.21 | C | Belongs to the LDH2 MDH2 oxidoreductase family | |
NECFGCCN_00658 | 7.1e-203 | afuA | P | ABC transporter substrate-binding protein | ||
NECFGCCN_00659 | 2.4e-11 | cysW_1 | P | Binding-protein-dependent transport system inner membrane component | ||
NECFGCCN_00660 | 1.7e-57 | cysW_1 | P | ABC-type Fe3 transport system permease component | ||
NECFGCCN_00661 | 3e-119 | E | phosphoserine phosphatase | |||
NECFGCCN_00662 | 5.6e-126 | EG | COG0697 Permeases of the drug metabolite transporter (DMT) superfamily | |||
NECFGCCN_00663 | 4.7e-87 | nlpC | 3.4.17.13 | M | lipoprotein nlpC | |
NECFGCCN_00664 | 3.4e-116 | S | dextransucrase activity | |||
NECFGCCN_00665 | 2.8e-168 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
NECFGCCN_00666 | 3.2e-124 | ftsE | D | cell division ATP-binding protein FtsE | ||
NECFGCCN_00667 | 2.6e-164 | ftsX | D | Part of the ABC transporter FtsEX involved in asymmetric cellular division facilitating the initiation of sporulation | ||
NECFGCCN_00668 | 2e-208 | queG | 1.17.99.6 | C | Catalyzes the conversion of epoxyqueuosine (oQ) to queuosine (Q), which is a hypermodified base found in the wobble positions of tRNA(Asp), tRNA(Asn), tRNA(His) and tRNA(Tyr) | |
NECFGCCN_00669 | 9.7e-267 | nnrD | 4.2.1.136, 5.1.99.6 | H | Bifunctional enzyme that catalyzes the epimerization of the S- and R-forms of NAD(P)HX and the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. This allows the repair of both epimers of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration | |
NECFGCCN_00670 | 4.5e-82 | yjeE | S | ATPase or kinase | ||
NECFGCCN_00671 | 4.2e-221 | amiB | 3.5.1.28 | M | N-acetylmuramoyl-L-alanine amidase | |
NECFGCCN_00672 | 0.0 | mutL | L | This protein is involved in the repair of mismatches in DNA. It is required for dam-dependent methyl-directed DNA mismatch repair. May act as a molecular matchmaker , a protein that promotes the formation of a stable complex between two or more DNA-binding proteins in an ATP-dependent manner without itself being part of a final effector complex | ||
NECFGCCN_00673 | 1.7e-176 | miaA | 2.5.1.75 | F | Catalyzes the transfer of a dimethylallyl group onto the adenine at position 37 in tRNAs that read codons beginning with uridine, leading to the formation of N6-(dimethylallyl)adenosine (i(6)A) | |
NECFGCCN_00674 | 1.3e-29 | hfq | J | RNA chaperone that binds small regulatory RNA (sRNAs) and mRNAs to facilitate mRNA translational regulation in response to envelope stress, environmental stress and changes in metabolite concentrations. Also binds with high specificity to tRNAs | ||
NECFGCCN_00675 | 8e-238 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
NECFGCCN_00676 | 1.3e-163 | hflK | O | HflC and HflK could encode or regulate a protease | ||
NECFGCCN_00677 | 8.1e-118 | hflC | O | HflC and HflK could regulate a protease | ||
NECFGCCN_00678 | 7.8e-128 | mak | 2.7.1.4, 2.7.1.59 | GK | ROK family | |
NECFGCCN_00679 | 1e-48 | celC | 2.7.1.196, 2.7.1.205 | G | PTS system, cellobiose-specific IIA component | |
NECFGCCN_00680 | 3.3e-242 | celB | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
NECFGCCN_00681 | 1.4e-50 | gmuB | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
NECFGCCN_00682 | 9.1e-235 | celB | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
NECFGCCN_00683 | 1.2e-268 | lamB | G | maltoporin | ||
NECFGCCN_00684 | 0.0 | 2.1.1.72, 3.1.4.46, 3.2.1.1 | GH13 | G | Pkd domain containing protein | |
NECFGCCN_00685 | 1.3e-281 | bgl | 3.2.1.21, 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
NECFGCCN_00686 | 0.0 | fhlA | KT | transcriptional regulator | ||
NECFGCCN_00687 | 0.0 | ctpF | P | ATPase, P-type (transporting), HAD superfamily, subfamily IC | ||
NECFGCCN_00688 | 5.4e-234 | ybhC | 3.1.1.11, 4.2.2.2 | G | Pectinesterase | |
NECFGCCN_00689 | 1.3e-219 | hutI | 3.5.2.7 | Q | Imidazolone-5-propionate hydrolase | |
NECFGCCN_00690 | 2.2e-176 | hutG | 3.5.3.8 | E | Catalyzes the conversion of N-formimidoyl-L-glutamate to L-glutamate and formamide | |
NECFGCCN_00691 | 1e-125 | hutC | K | histidine utilization repressor | ||
NECFGCCN_00692 | 0.0 | hutU | 4.2.1.49 | E | Catalyzes the conversion of urocanate to 4-imidazolone- 5-propionate | |
NECFGCCN_00693 | 3.2e-70 | dmsB | C | reductase chain B | ||
NECFGCCN_00694 | 2e-135 | ssuB2 | P | (ABC) transporter | ||
NECFGCCN_00695 | 1.3e-182 | ssuC2 | P | ABC-type nitrate sulfonate bicarbonate transport system permease component | ||
NECFGCCN_00696 | 1.2e-191 | P | ABC-type nitrate sulfonate bicarbonate transport | |||
NECFGCCN_00697 | 6.7e-15 | |||||
NECFGCCN_00699 | 2.8e-68 | pinE | L | Site-specific recombinases, DNA invertase Pin homologs | ||
NECFGCCN_00700 | 1.2e-25 | pinE | L | Site-specific recombinases, DNA invertase Pin homologs | ||
NECFGCCN_00701 | 7e-182 | L | Belongs to the 'phage' integrase family | |||
NECFGCCN_00702 | 6e-181 | abgT | H | transporter | ||
NECFGCCN_00703 | 2.1e-271 | abgB | 3.5.1.32 | S | amidohydrolase | |
NECFGCCN_00704 | 4.2e-242 | abgA | 3.5.1.32 | S | Protein involved in hydrolase activity and metabolic process | |
NECFGCCN_00705 | 2.1e-160 | abgR | K | transcriptional regulator | ||
NECFGCCN_00707 | 1.2e-127 | U | TraM recognition site of TraD and TraG | |||
NECFGCCN_00709 | 2.3e-48 | vex3 | V | Efflux ABC transporter, permease protein | ||
NECFGCCN_00710 | 1.5e-115 | K | Response regulator receiver domain protein | |||
NECFGCCN_00711 | 4.2e-08 | bcrA | V | abc transporter atp-binding protein | ||
NECFGCCN_00712 | 2.4e-290 | V | ABC transporter transmembrane region | |||
NECFGCCN_00713 | 3.2e-51 | |||||
NECFGCCN_00715 | 4.8e-63 | yqeB | S | Pyrimidine dimer DNA glycosylase | ||
NECFGCCN_00716 | 6.4e-61 | S | Protein of unknown function (DUF1722) | |||
NECFGCCN_00717 | 7.6e-20 | S | Bacterial lipoprotein | |||
NECFGCCN_00718 | 7.5e-10 | |||||
NECFGCCN_00719 | 1.4e-128 | V | CAAX protease self-immunity | |||
NECFGCCN_00720 | 3e-45 | |||||
NECFGCCN_00721 | 1.4e-75 | K | TetR family transcriptional regulator | |||
NECFGCCN_00724 | 1.1e-56 | rplS | J | This protein is located at the 30S-50S ribosomal subunit interface and may play a role in the structure and function of the aminoacyl-tRNA binding site | ||
NECFGCCN_00725 | 1.6e-211 | XK27_05110 | P | Chloride transporter ClC family | ||
NECFGCCN_00726 | 2.8e-39 | pheA | 1.3.1.12, 2.3.1.79, 4.2.1.51, 5.4.99.5 | E | Chorismate mutase | |
NECFGCCN_00727 | 4e-276 | clcA | P | Chloride transporter, ClC family | ||
NECFGCCN_00728 | 1e-75 | fld | C | Flavodoxin | ||
NECFGCCN_00729 | 2.2e-18 | XK27_08880 | ||||
NECFGCCN_00730 | 4.7e-126 | XK27_08875 | O | Zinc-dependent metalloprotease | ||
NECFGCCN_00731 | 2.8e-148 | estA | CE1 | S | Esterase | |
NECFGCCN_00732 | 1.3e-309 | rnjB | S | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
NECFGCCN_00733 | 8.9e-136 | XK27_08845 | S | abc transporter atp-binding protein | ||
NECFGCCN_00734 | 2.6e-147 | XK27_08840 | S | Belongs to the binding-protein-dependent transport system permease family | ||
NECFGCCN_00735 | 4e-176 | XK27_08835 | S | ABC transporter substrate binding protein | ||
NECFGCCN_00736 | 1.7e-18 | S | Domain of unknown function (DUF4649) | |||
NECFGCCN_00737 | 4.2e-87 | Q | the current gene model (or a revised gene model) may contain a frame shift | |||
NECFGCCN_00738 | 7.8e-233 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
NECFGCCN_00739 | 0.0 | pulA | 3.2.1.41 | CBM48,GH13 | G | belongs to the glycosyl hydrolase 13 family |
NECFGCCN_00740 | 0.0 | glgB | 2.4.1.18, 3.2.1.141, 3.2.1.20 | CBM48,GH13,GH31 | G | Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position |
NECFGCCN_00741 | 6.4e-186 | glgC | 2.7.7.27 | H | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
NECFGCCN_00742 | 4.9e-178 | glgD | 2.4.1.21, 2.7.7.27 | GT5 | G | glucose-1-phosphate adenylyltransferase |
NECFGCCN_00743 | 1e-281 | glgA | 2.4.1.21 | GT5 | G | Synthesizes alpha-1,4-glucan chains using ADP-glucose |
NECFGCCN_00744 | 0.0 | glgP | 2.4.1.1 | GT35 | G | Phosphorylase is an important allosteric enzyme in carbohydrate metabolism. Enzymes from different sources differ in their regulatory mechanisms and in their natural substrates. However, all known phosphorylases share catalytic and structural properties |
NECFGCCN_00745 | 1.8e-101 | 2.3.1.128 | K | Acetyltransferase GNAT Family | ||
NECFGCCN_00746 | 2.3e-284 | S | Protein of unknown function (DUF3114) | |||
NECFGCCN_00748 | 0.0 | gshF | 6.3.2.2, 6.3.2.29, 6.3.2.30, 6.3.2.4 | H | Belongs to the glutamate--cysteine ligase type 1 family | |
NECFGCCN_00749 | 8.2e-18 | bglC | K | Transcriptional regulator | ||
NECFGCCN_00750 | 1.2e-242 | mnmE | S | Exhibits a very high intrinsic GTPase hydrolysis rate. Involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA- cmnm(5)s(2)U34 | ||
NECFGCCN_00751 | 2.9e-165 | gltI | ET | ABC-type amino acid transport signal transduction systems periplasmic component domain | ||
NECFGCCN_00752 | 5.1e-136 | gltJ | P | amino acid ABC transporter | ||
NECFGCCN_00753 | 1.2e-112 | gltK | P | With GltJLPS and GadC for glutamate and GltJLP, DctA and DcuAB for aspartate is involved in the transport of glutamate and aspartate | ||
NECFGCCN_00754 | 1.4e-19 | gltL | 3.6.3.21 | E | (ABC) transporter | |
NECFGCCN_00757 | 7.8e-154 | ydgD | M | Belongs to the peptidase S1B family | ||
NECFGCCN_00758 | 3e-51 | mdtI | U | Catalyzes the excretion of spermidine | ||
NECFGCCN_00759 | 4.2e-51 | mdtJ | U | Catalyzes the excretion of spermidine | ||
NECFGCCN_00760 | 2.7e-143 | tqsA | T | permease | ||
NECFGCCN_00761 | 2.3e-41 | mdcA | 2.3.1.187 | I | malonate decarboxylase, alpha subunit | |
NECFGCCN_00762 | 4.5e-89 | K | transcriptional regulator | |||
NECFGCCN_00763 | 1.6e-36 | yneF | S | UPF0154 protein | ||
NECFGCCN_00764 | 7.6e-149 | murI | 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
NECFGCCN_00765 | 2.1e-182 | rdgB | 3.6.1.66, 5.1.1.3 | F | Pyrophosphatase that catalyzes the hydrolysis of nucleoside triphosphates to their monophosphate derivatives, with a high preference for the non-canonical purine nucleotides XTP (xanthosine triphosphate), dITP (deoxyinosine triphosphate) and ITP. Seems to function as a house-cleaning enzyme that removes non-canonical purine nucleotides from the nucleotide pool, thus preventing their incorporation into DNA RNA and avoiding chromosomal lesions | |
NECFGCCN_00766 | 8.1e-96 | XK27_09740 | S | Phosphoesterase | ||
NECFGCCN_00767 | 7.1e-86 | ykuL | S | CBS domain | ||
NECFGCCN_00768 | 3.1e-128 | xerD | L | tyrosine recombinase. Not involved in the cutting and rejoining of the recombining DNA molecules on dif(SL) site | ||
NECFGCCN_00769 | 3.8e-120 | scpA | D | Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpB that pull DNA away from mid-cell into both cell halves | ||
NECFGCCN_00770 | 3.1e-96 | scpB | D | Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpA that pull DNA away from mid-cell into both cell halves | ||
NECFGCCN_00771 | 3.4e-132 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
NECFGCCN_00772 | 9.5e-118 | nfnB | 1.5.1.34 | C | Nitroreductase | |
NECFGCCN_00773 | 1.2e-66 | ybdF | S | YjbR | ||
NECFGCCN_00774 | 8.8e-99 | K | transcriptional regulator | |||
NECFGCCN_00775 | 1.6e-218 | romA | S | Zn-dependent hydrolases of the beta-lactamase fold | ||
NECFGCCN_00776 | 1e-59 | ramA | K | Transcriptional regulator | ||
NECFGCCN_00777 | 5.9e-36 | ybdJ | S | membrane | ||
NECFGCCN_00778 | 1.5e-07 | |||||
NECFGCCN_00779 | 8.2e-48 | ctpF | P | ATPase, P-type (transporting), HAD superfamily, subfamily IC | ||
NECFGCCN_00780 | 6.7e-87 | ytsP | 1.8.4.14 | T | GAF domain-containing protein | |
NECFGCCN_00781 | 1.4e-44 | dsbA | O | Thiol disulfide interchange protein | ||
NECFGCCN_00782 | 2e-157 | phoH | T | PhoH-like protein | ||
NECFGCCN_00783 | 1.9e-247 | efeB | P | peroxidase | ||
NECFGCCN_00784 | 7.4e-203 | efeO | P | periplasmic lipoprotein involved in iron transport | ||
NECFGCCN_00785 | 9.2e-126 | efeU | P | Iron Permease | ||
NECFGCCN_00786 | 8.8e-202 | nupC | F | Belongs to the concentrative nucleoside transporter (CNT) (TC 2.A.41) family | ||
NECFGCCN_00787 | 9.5e-74 | J | Protein of unknown function (DUF3574) | |||
NECFGCCN_00788 | 4.2e-278 | putP | E | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
NECFGCCN_00789 | 0.0 | putA | 1.2.1.88, 1.3.8.7, 1.5.5.2 | C | Oxidizes proline to glutamate for use as a carbon and nitrogen source | |
NECFGCCN_00790 | 9.6e-65 | S | Lysozyme inhibitor LprI | |||
NECFGCCN_00791 | 4.2e-110 | rutR | K | transcriptional regulator | ||
NECFGCCN_00792 | 1.3e-207 | rutA | 1.14.99.46 | C | Catalyzes the pyrimidine ring opening between N-3 and C- 4 by an unusual flavin hydroperoxide-catalyzed mechanism to yield ureidoacrylate peracid. It cleaves pyrmidine rings directly by adding oxygen atoms, making a toxic ureidoacrylate peracid product which can be spontaneously reduced to ureidoacrylate | |
NECFGCCN_00793 | 4.3e-132 | rutB | 3.5.1.110 | Q | In vivo, quickly hydrolyzes the ureidoacrylate peracid to avoid toxicity, but can also hydrolyzes ureidoacrylate that is formed spontaneously from ureidoacrylate peracid. One of the products of hydrolysis, carbamate, hydrolyzes spontaneously, thereby releasing one of the pyrimidine rings nitrogen atoms as ammonia and one of its carbons as CO2 | |
NECFGCCN_00794 | 1.4e-68 | rutC | 3.5.99.10 | J | May reduce aminoacrylate peracid to aminoacrylate. Required to remove a toxic intermediate produce by the pyrimidine nitrogen degradation | |
NECFGCCN_00795 | 2e-138 | rutD | I | May increase the rate of spontaneous hydrolysis of aminoacrylate to malonic semialdehyde. Required to remove a toxic intermediate produce in the pyrimidine nitrogen degradation | ||
NECFGCCN_00796 | 1.6e-111 | rutE | C | May reduce toxic product malonic semialdehyde to 3- hydroxypropionic acid, which is excreted | ||
NECFGCCN_00797 | 2.2e-90 | rutF | 1.5.1.36 | C | Catalyzes the reduction of FMN to FMNH2 which is used to reduce pyrimidine by RutA via the Rut pathway | |
NECFGCCN_00798 | 5.6e-234 | rutG | F | Xanthine uracil | ||
NECFGCCN_00799 | 5.2e-22 | agrA | KT | response regulator | ||
NECFGCCN_00800 | 2.8e-227 | topA | 5.99.1.2 | L | Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone | |
NECFGCCN_00801 | 1.6e-83 | mutF | V | AAA domain, putative AbiEii toxin, Type IV TA system | ||
NECFGCCN_00802 | 6.3e-54 | V | ABC-2 family transporter protein | |||
NECFGCCN_00804 | 4.6e-120 | KT | Transcriptional regulatory protein, C terminal | |||
NECFGCCN_00805 | 1.5e-94 | malQ | 2.4.1.25 | GH77 | G | 4-alpha-glucanotransferase |
NECFGCCN_00806 | 0.0 | glgP | 2.4.1.1 | GT35 | G | Phosphorylase is an important allosteric enzyme in carbohydrate metabolism. Enzymes from different sources differ in their regulatory mechanisms and in their natural substrates. However, all known phosphorylases share catalytic and structural properties |
NECFGCCN_00807 | 8.4e-159 | dam | 2.1.1.72 | L | Site-specific DNA-methyltransferase (Adenine-specific) | |
NECFGCCN_00808 | 1.7e-48 | manO | S | Protein conserved in bacteria | ||
NECFGCCN_00809 | 5.9e-158 | manN | G | PTS system mannose fructose sorbose family IID component | ||
NECFGCCN_00810 | 5.7e-133 | manY | G | pts system | ||
NECFGCCN_00811 | 6.2e-39 | manL | 2.7.1.191 | G | pts system | |
NECFGCCN_00812 | 1.9e-46 | S | PerC transcriptional activator | |||
NECFGCCN_00813 | 1.6e-92 | K | Bacterial regulatory proteins, luxR family | |||
NECFGCCN_00814 | 0.0 | H | Exports the biofilm adhesin polysaccharide poly-beta- 1,6-N-acetyl-D-glucosamine (PGA) across the outer membrane. The PGA transported seems to be partially N-deacetylated since N- deacetylation of PGA by PgaB is needed for PGA export through the PgaA porin | |||
NECFGCCN_00815 | 0.0 | pgaB | G | Polysaccharide deacetylase | ||
NECFGCCN_00816 | 1e-256 | pgaC | GT2 | M | Poly-beta-1,6-N-acetyl-D-glucosamine synthase | |
NECFGCCN_00817 | 4.4e-74 | pgaD | S | PgaD-like protein | ||
NECFGCCN_00818 | 1.3e-132 | O | Dsba oxidoreductase | |||
NECFGCCN_00819 | 2.6e-103 | yoaE_3 | P | COG0861 Membrane protein TerC possibly involved in tellurium resistance | ||
NECFGCCN_00820 | 6.5e-173 | cbpA | O | displays overlapping activities with DnaJ, but functions under different conditions, probably acting as a molecular chaperone in an adaptive response to environmental stresses other than heat shock. Lacks autonomous chaperone activity | ||
NECFGCCN_00821 | 7.5e-49 | cbpM | K | Interacts with CbpA and inhibits both the DnaJ-like co- chaperone activity and the DNA binding activity of CbpA. Together with CbpA, modulates the activity of the DnaK chaperone system. Does not inhibit the co-chaperone activity of DnaJ | ||
NECFGCCN_00822 | 7.4e-98 | ywbL | P | COG0672 High-affinity Fe2 Pb2 permease | ||
NECFGCCN_00823 | 1.5e-124 | tatC | U | Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes | ||
NECFGCCN_00824 | 1.9e-23 | tatA | U | protein secretion | ||
NECFGCCN_00826 | 8.8e-212 | msmX | P | Belongs to the ABC transporter superfamily | ||
NECFGCCN_00827 | 2.2e-151 | malG | P | ABC transporter (Permease | ||
NECFGCCN_00828 | 4.8e-249 | malF | P | ABC transporter (Permease | ||
NECFGCCN_00829 | 3.9e-229 | malX | G | ABC transporter | ||
NECFGCCN_00830 | 9.4e-47 | osmY_1 | S | Periplasmic or secreted lipoprotein | ||
NECFGCCN_00831 | 2.3e-104 | yqaB | S | Phosphatase | ||
NECFGCCN_00832 | 4.7e-73 | yqaA | S | Membrane | ||
NECFGCCN_00833 | 8.7e-303 | gshA | 6.3.2.2 | H | Belongs to the glutamate--cysteine ligase type 1 family. Type 1 subfamily | |
NECFGCCN_00834 | 4.7e-96 | luxS | 4.4.1.21 | H | Involved in the synthesis of autoinducer 2 (AI-2) which is secreted by bacteria and is used to communicate both the cell density and the metabolic potential of the environment. The regulation of gene expression in response to changes in cell density is called quorum sensing. Catalyzes the transformation of S-ribosylhomocysteine (RHC) to homocysteine (HC) and 4,5- dihydroxy-2,3-pentadione (DPD) | |
NECFGCCN_00835 | 2.3e-139 | K | AraC family transcriptional regulator | |||
NECFGCCN_00836 | 0.0 | leuA | 2.3.3.13 | E | Catalyzes the condensation of the acetyl group of acetyl-CoA with 3-methyl-2-oxobutanoate (2-oxoisovalerate) to form 3-carboxy-3-hydroxy-4-methylpentanoate (2-isopropylmalate) | |
NECFGCCN_00837 | 1.2e-277 | emrB | EGP | Major facilitator Superfamily | ||
NECFGCCN_00838 | 3.6e-208 | emrA | V | multidrug resistance efflux pump | ||
NECFGCCN_00839 | 4.5e-94 | mprA | K | Transcriptional | ||
NECFGCCN_00840 | 1.9e-50 | ygaH | S | L-valine transmembrane transporter activity | ||
NECFGCCN_00841 | 6.8e-112 | ygaZ | E | branched-chain amino acid | ||
NECFGCCN_00842 | 1.4e-181 | proX | E | glycine, betaine | ||
NECFGCCN_00843 | 1.5e-168 | proW | P | ABC-type proline glycine betaine transport system, permease component | ||
NECFGCCN_00844 | 2.4e-220 | proV | 3.6.3.32 | E | glycine, betaine | |
NECFGCCN_00845 | 3.6e-182 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
NECFGCCN_00846 | 0.0 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
NECFGCCN_00847 | 1.7e-72 | nrdI | F | Probably involved in ribonucleotide reductase function | ||
NECFGCCN_00848 | 3.3e-39 | nrdH | O | Glutaredoxin-like protein NrdH | ||
NECFGCCN_00849 | 1.1e-69 | S | Antioxidant protein with alkyl hydroperoxidase activity. Required for the reduction of the AhpC active site cysteine residues and for the regeneration of the AhpC enzyme activity | |||
NECFGCCN_00850 | 6.7e-243 | gabR_2 | K | Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | ||
NECFGCCN_00851 | 1.1e-56 | ygaM | S | ribosome binding | ||
NECFGCCN_00852 | 7.4e-64 | ygaC | S | Protein of unknown function (DUF2002) | ||
NECFGCCN_00853 | 1.4e-75 | alaE | U | L-alanine exporter AlaE | ||
NECFGCCN_00855 | 4.9e-53 | stpA | S | Belongs to the histone-like protein H-NS family | ||
NECFGCCN_00856 | 2.2e-07 | |||||
NECFGCCN_00857 | 4.7e-176 | lpxO | O | Aspartyl Asparaginyl beta-hydroxylase | ||
NECFGCCN_00858 | 3.6e-78 | ygaP | P | SMART Rhodanese domain protein | ||
NECFGCCN_00859 | 3.1e-47 | ygaV | K | transcriptional regulator | ||
NECFGCCN_00860 | 3.3e-101 | azoR | I | Catalyzes the reductive cleavage of azo bond in aromatic azo compounds to the corresponding amines. Requires NADH, but not NADPH, as an electron donor for its activity | ||
NECFGCCN_00861 | 3.5e-155 | K | transcriptional regulator | |||
NECFGCCN_00862 | 0.0 | acoR | KQ | transcriptional regulator | ||
NECFGCCN_00863 | 5e-295 | aldA | 1.2.1.3 | C | belongs to the aldehyde dehydrogenase family | |
NECFGCCN_00864 | 3.6e-68 | NU | Fimbrial protein | |||
NECFGCCN_00865 | 1.3e-117 | NU | chaperone | |||
NECFGCCN_00866 | 0.0 | fimD_3 | NU | Usher protein | ||
NECFGCCN_00867 | 3.1e-190 | NU | Fimbrial protein | |||
NECFGCCN_00868 | 2.3e-78 | etfD | NU | Fimbrial protein | ||
NECFGCCN_00869 | 3.4e-232 | fimD | NU | Fimbrial biogenesis outer membrane usher protein | ||
NECFGCCN_00870 | 2.9e-69 | M | chaperone | |||
NECFGCCN_00871 | 1.3e-51 | NU | Fimbrial protein | |||
NECFGCCN_00872 | 1.8e-21 | rcsV | K | helix_turn_helix, Lux Regulon | ||
NECFGCCN_00873 | 1e-135 | pheC | 4.2.1.51, 4.2.1.91 | ET | Belongs to the bacterial solute-binding protein 3 family | |
NECFGCCN_00874 | 2.1e-103 | |||||
NECFGCCN_00875 | 1.4e-136 | IQ | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
NECFGCCN_00876 | 5.2e-178 | ghrA | 1.1.1.79, 1.1.1.81 | EH | D-isomer specific 2-hydroxyacid dehydrogenase | |
NECFGCCN_00877 | 1.2e-134 | fucA_2 | 4.1.1.104, 4.1.2.17, 4.1.2.19, 4.2.1.109, 5.1.3.4 | G | COG0235 Ribulose-5-phosphate 4-epimerase and related epimerases and aldolases | |
NECFGCCN_00878 | 6.3e-274 | 3.6.3.21 | E | (ABC) transporter | ||
NECFGCCN_00879 | 6.1e-143 | ET | Amino acid ABC transporter substrate-binding protein | |||
NECFGCCN_00880 | 1.5e-208 | efe_1 | C | Belongs to the iron ascorbate-dependent oxidoreductase family | ||
NECFGCCN_00881 | 2.9e-167 | G | Xylose isomerase | |||
NECFGCCN_00882 | 1.4e-183 | speB | 3.5.3.11, 3.5.3.7 | E | Belongs to the arginase family | |
NECFGCCN_00883 | 4.2e-172 | gbuR | K | transcriptional regulator | ||
NECFGCCN_00884 | 4.7e-82 | ywnA | K | transcriptional regulator | ||
NECFGCCN_00885 | 0.0 | mexF | V | Belongs to the resistance-nodulation-cell division (RND) (TC 2.A.6) family | ||
NECFGCCN_00886 | 1.5e-211 | mexE | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | ||
NECFGCCN_00887 | 1.6e-58 | marA | K | sequence-specific DNA binding | ||
NECFGCCN_00888 | 1.2e-104 | K | Flavin Reductase | |||
NECFGCCN_00889 | 6.9e-164 | K | Transcriptional regulator | |||
NECFGCCN_00890 | 5.3e-147 | S | nucleotidyltransferase activity | |||
NECFGCCN_00892 | 3.4e-88 | smpB | J | Required for rescue of stalled ribosomes mediated by trans-translation. Binds to transfer-messenger RNA (tmRNA), required for stable association of tmRNA with ribosomes. tmRNA and SmpB together mimic tRNA shape, replacing the anticodon stem-loop with SmpB. tmRNA is encoded by the ssrA gene | ||
NECFGCCN_00893 | 3e-75 | ratA | I | oligoketide cyclase lipid transport protein | ||
NECFGCCN_00894 | 6.2e-45 | rnfH | S | Belongs to the UPF0125 (RnfH) family | ||
NECFGCCN_00895 | 8.3e-57 | bamE | M | Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane | ||
NECFGCCN_00896 | 2.8e-307 | recN | L | May be involved in recombinational repair of damaged DNA | ||
NECFGCCN_00897 | 2.3e-167 | nadK | 2.7.1.23 | F | Involved in the regulation of the intracellular balance of NAD and NADP, and is a key enzyme in the biosynthesis of NADP. Catalyzes specifically the phosphorylation on 2'-hydroxyl of the adenosine moiety of NAD to yield NADP | |
NECFGCCN_00898 | 9.2e-96 | grpE | O | Participates actively in the response to hyperosmotic and heat shock by preventing the aggregation of stress-denatured proteins, in association with DnaK and GrpE. It is the nucleotide exchange factor for DnaK and may function as a thermosensor. Unfolded proteins bind initially to DnaJ | ||
NECFGCCN_00899 | 1.3e-224 | yfjD | P | Mg2 and Co2 transporter CorB | ||
NECFGCCN_00900 | 5.6e-141 | ypjD | S | cytochrome C assembly protein | ||
NECFGCCN_00901 | 1.7e-230 | ffh | 3.6.5.4 | U | Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Binds to the hydrophobic signal sequence of the ribosome-nascent chain (RNC) as it emerges from the ribosomes. The SRP-RNC complex is then targeted to the cytoplasmic membrane where it interacts with the SRP receptor FtsY. Interaction with FtsY leads to the transfer of the RNC complex to the Sec translocase for insertion into the membrane, the hydrolysis of GTP by both Ffh and FtsY, and the dissociation of the SRP-FtsY complex into the individual components | |
NECFGCCN_00902 | 4.1e-37 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
NECFGCCN_00903 | 7.2e-103 | rimM | J | An accessory protein needed during the final step in the assembly of 30S ribosomal subunit, possibly for assembly of the head region. Probably interacts with S19. Essential for efficient processing of 16S rRNA. May be needed both before and after RbfA during the maturation of 16S rRNA. It has affinity for free ribosomal 30S subunits but not for 70S ribosomes | ||
NECFGCCN_00904 | 5.3e-144 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
NECFGCCN_00905 | 4.2e-56 | rplS | J | This protein is located at the 30S-50S ribosomal subunit interface and may play a role in the structure and function of the aminoacyl-tRNA binding site | ||
NECFGCCN_00906 | 4.5e-74 | copB | P | Protein of unknown function (DUF2946) | ||
NECFGCCN_00907 | 1.7e-246 | S | Iron-regulated membrane protein | |||
NECFGCCN_00908 | 3e-84 | yfiB | M | Belongs to the ompA family | ||
NECFGCCN_00909 | 7.2e-220 | yfiN | 2.7.7.65 | T | Diguanylate cyclase | |
NECFGCCN_00910 | 1.3e-90 | yfiR | S | bacterial-type flagellum-dependent swarming motility | ||
NECFGCCN_00911 | 5.9e-202 | aroF | 2.5.1.54 | E | Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) | |
NECFGCCN_00912 | 4.2e-206 | tyrA | 1.3.1.12, 1.3.1.13, 1.3.1.43, 5.4.99.5 | E | T-protein | |
NECFGCCN_00913 | 1.5e-174 | yvrE | 3.1.1.15 | G | gluconolactonase | |
NECFGCCN_00914 | 2.8e-213 | pheA | 1.3.1.12, 2.3.1.79, 2.5.1.54, 4.2.1.51, 5.4.99.5 | E | chorismate mutase | |
NECFGCCN_00915 | 2.6e-55 | hpf | J | Sigma 54 modulation protein | ||
NECFGCCN_00916 | 3.5e-137 | bamD | GH23 | M | Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane | |
NECFGCCN_00917 | 1e-184 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
NECFGCCN_00918 | 1.2e-140 | yfiH | S | Belongs to the multicopper oxidase YfiH RL5 family | ||
NECFGCCN_00919 | 0.0 | clpB | O | Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE | ||
NECFGCCN_00920 | 6e-258 | trkH | P | Cation transport protein | ||
NECFGCCN_00921 | 1.2e-244 | trkA | P | Potassium transporter peripheral membrane component | ||
NECFGCCN_00922 | 1.8e-95 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
NECFGCCN_00923 | 3.5e-89 | ribU | U | Mediates riboflavin uptake, may also transport FMN and roseoflavin. Probably a riboflavin-binding protein that interacts with the energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates. The substrates themselves are bound by transmembrane, not extracytoplasmic soluble proteins | ||
NECFGCCN_00924 | 2.4e-89 | bcrC | 3.6.1.27 | I | Membrane-associated phospholipid phosphatase | |
NECFGCCN_00925 | 6e-155 | K | sequence-specific DNA binding | |||
NECFGCCN_00926 | 0.0 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
NECFGCCN_00927 | 3.2e-53 | yhaI | L | Membrane | ||
NECFGCCN_00928 | 8.2e-244 | S | Domain of unknown function (DUF4173) | |||
NECFGCCN_00929 | 6.8e-95 | ureI | S | AmiS/UreI family transporter | ||
NECFGCCN_00930 | 7.6e-46 | ureA | 3.5.1.5 | E | Belongs to the urease gamma subunit family | |
NECFGCCN_00931 | 7.8e-54 | ureB | 3.5.1.5 | E | Belongs to the urease beta subunit family | |
NECFGCCN_00932 | 0.0 | ureC | 3.5.1.5 | E | Belongs to the metallo-dependent hydrolases superfamily. Urease alpha subunit family | |
NECFGCCN_00933 | 6.6e-78 | ureE | O | enzyme active site formation | ||
NECFGCCN_00934 | 1.7e-128 | ureF | O | Required for maturation of urease via the functional incorporation of the urease nickel metallocenter | ||
NECFGCCN_00935 | 9.5e-112 | ureG | KO | Facilitates the functional incorporation of the urease nickel metallocenter. This process requires GTP hydrolysis, probably effectuated by UreG | ||
NECFGCCN_00936 | 1.7e-159 | ureD | O | Required for maturation of urease via the functional incorporation of the urease nickel metallocenter | ||
NECFGCCN_00937 | 4.3e-175 | cbiM | P | PDGLE domain | ||
NECFGCCN_00938 | 7.1e-11 | |||||
NECFGCCN_00939 | 1.2e-89 | K | Bacterial regulatory proteins, tetR family | |||
NECFGCCN_00940 | 4.2e-164 | GM | NmrA-like family | |||
NECFGCCN_00941 | 1.5e-163 | S | Beta-lactamase | |||
NECFGCCN_00942 | 4.1e-167 | mexT | K | transcriptional regulator | ||
NECFGCCN_00943 | 5.8e-166 | K | Transcriptional regulator | |||
NECFGCCN_00944 | 2.5e-87 | yrdA | S | COG0663 Carbonic anhydrases acetyltransferases, isoleucine patch superfamily | ||
NECFGCCN_00945 | 5.7e-42 | yrdB | S | Protein of unknown function (DUF1488) | ||
NECFGCCN_00946 | 8.4e-148 | aroE | 1.1.1.25 | E | Involved in the biosynthesis of the chorismate, which leads to the biosynthesis of aromatic amino acids. Catalyzes the reversible NADPH linked reduction of 3-dehydroshikimate (DHSA) to yield shikimate (SA) | |
NECFGCCN_00947 | 3.1e-104 | tsaC | 2.7.7.87 | J | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Catalyzes the conversion of L-threonine, HCO(3)(-) CO(2) and ATP to give threonylcarbamoyl-AMP (TC-AMP) as the acyladenylate intermediate, with the release of diphosphate | |
NECFGCCN_00948 | 1.3e-80 | yrdD | L | dNA topoisomerase | ||
NECFGCCN_00949 | 1.2e-82 | smg | S | Belongs to the Smg family | ||
NECFGCCN_00950 | 4.9e-199 | dprA | LU | Rossmann fold nucleotide-binding protein involved in DNA uptake | ||
NECFGCCN_00951 | 9.2e-35 | |||||
NECFGCCN_00952 | 1.5e-158 | gcvA_4 | K | Transcriptional regulator, LysR family | ||
NECFGCCN_00953 | 4.9e-85 | |||||
NECFGCCN_00954 | 1.2e-128 | ytnP | S | Beta-lactamase | ||
NECFGCCN_00956 | 6.8e-72 | yqeI | K | Transcriptional regulatory protein, C terminal | ||
NECFGCCN_00957 | 4.4e-89 | |||||
NECFGCCN_00958 | 4.8e-23 | S | Protein of unknown function (DUF1471) | |||
NECFGCCN_00959 | 1.2e-117 | cynT | 4.2.1.1 | P | Reversible hydration of carbon dioxide | |
NECFGCCN_00960 | 1.8e-102 | E | threonine efflux protein | |||
NECFGCCN_00961 | 2.6e-135 | glpR_5 | K | Transcriptional Regulator, DeoR family | ||
NECFGCCN_00962 | 1.3e-63 | yyaH | 4.4.1.5 | E | bleomycin resistance protein | |
NECFGCCN_00963 | 4.1e-124 | cat | 2.3.1.28 | V | This enzyme is an effector of chloramphenicol resistance in bacteria | |
NECFGCCN_00964 | 0.0 | oppA5 | E | ABC transporter substrate-binding protein | ||
NECFGCCN_00965 | 4.5e-146 | ydaO | E | amino acid | ||
NECFGCCN_00967 | 0.0 | asnB | 6.3.5.4 | E | asparagine synthase, glutamine-hydrolyzing | |
NECFGCCN_00968 | 2.2e-142 | nagD | G | HAD-superfamily hydrolase, subfamily IIA | ||
NECFGCCN_00969 | 3.2e-228 | nagC | 2.1.1.303 | K | Regulates the synthesis of glucosamine and N-acetylglucosamine by acting as a repressor of the nagEBACD operon and both a repressor and activator of the glmSU operon | |
NECFGCCN_00970 | 3.4e-219 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
NECFGCCN_00971 | 3.2e-152 | nagB | 3.1.1.31, 3.5.99.6 | G | Catalyzes the reversible isomerization-deamination of glucosamine 6-phosphate (GlcN6P) to form fructose 6-phosphate (Fru6P) and ammonium ion | |
NECFGCCN_00972 | 4.1e-125 | nagE | 2.7.1.192, 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | Phosphotransferase System | |
NECFGCCN_00973 | 1.5e-135 | acoA | 1.2.4.1, 1.2.4.4 | C | Dehydrogenase E1 component | |
NECFGCCN_00974 | 6.4e-182 | acoB | 1.2.4.1, 1.2.4.4 | C | COG0022 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, beta subunit | |
NECFGCCN_00975 | 2.6e-135 | citZ | 2.3.3.1 | C | Belongs to the citrate synthase family | |
NECFGCCN_00976 | 1.7e-218 | icd | 1.1.1.42 | C | Isocitrate dehydrogenase | |
NECFGCCN_00977 | 3e-38 | ptsH | G | phosphocarrier protein Hpr | ||
NECFGCCN_00978 | 0.0 | ptsI | 2.7.3.9 | G | General (non sugar-specific) component of the phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS). This major carbohydrate active-transport system catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. Enzyme I transfers the phosphoryl group from phosphoenolpyruvate (PEP) to the phosphoryl carrier protein (HPr) | |
NECFGCCN_00979 | 6.6e-265 | gapN | 1.2.1.9 | C | Belongs to the aldehyde dehydrogenase family | |
NECFGCCN_00980 | 9.7e-160 | XK27_05670 | S | Putative esterase | ||
NECFGCCN_00981 | 3.5e-153 | XK27_05675 | S | Esterase | ||
NECFGCCN_00982 | 1.7e-223 | XK27_05680 | 6.3.2.2, 6.3.2.4 | M | carbamoylphosphate synthase large subunit | |
NECFGCCN_00983 | 3.3e-176 | yfmL | 3.6.4.13 | L | DEAD DEAH box helicase | |
NECFGCCN_00984 | 3.1e-113 | udk | 2.7.1.48 | F | Cytidine monophosphokinase | |
NECFGCCN_00985 | 1.1e-214 | ubiF | CH | ubiquinone biosynthesis hydroxylase, UbiH UbiF VisC COQ6 | ||
NECFGCCN_00986 | 7.7e-274 | miaB | 2.8.4.3 | J | Catalyzes the methylthiolation of N6- (dimethylallyl)adenosine (i(6)A), leading to the formation of 2- methylthio-N6-(dimethylallyl)adenosine (ms(2)i(6)A) at position 37 in tRNAs that read codons beginning with uridine | |
NECFGCCN_00987 | 4.8e-151 | ybeZ | T | phosphate starvation-inducible protein PhoH | ||
NECFGCCN_00988 | 3.6e-111 | sodA | 1.15.1.1 | C | radicals which are normally produced within the cells and which are toxic to biological systems | |
NECFGCCN_00989 | 3.5e-162 | 3.5.2.6 | V | D-alanyl-D-alanine carboxypeptidase | ||
NECFGCCN_00990 | 2.4e-100 | pilD | 3.4.23.43 | NOU | Type II secretory pathway prepilin signal peptidase PulO and related peptidases | |
NECFGCCN_00991 | 1.5e-78 | dps | P | Belongs to the Dps family | ||
NECFGCCN_00992 | 3.4e-79 | perR | P | Belongs to the Fur family | ||
NECFGCCN_00993 | 4.2e-27 | yqgQ | S | protein conserved in bacteria | ||
NECFGCCN_00994 | 5.6e-175 | glk | 2.7.1.2 | G | Glucokinase | |
NECFGCCN_00995 | 0.0 | typA | T | GTP-binding protein TypA | ||
NECFGCCN_00996 | 7.7e-80 | S | CAAX amino terminal protease family protein | |||
NECFGCCN_00997 | 4.9e-137 | ssuC | 1.14.14.5 | P | ABC-type nitrate sulfonate bicarbonate transport system permease component | |
NECFGCCN_00998 | 5.5e-214 | ssuD | 1.14.14.5 | C | Catalyzes the desulfonation of aliphatic sulfonates | |
NECFGCCN_00999 | 8e-174 | ssuA | P | ABC transporter | ||
NECFGCCN_01000 | 1.4e-101 | ssuE | 1.5.1.38 | S | fmn reductase | |
NECFGCCN_01001 | 6.9e-192 | pyrD | 1.3.1.14, 1.3.5.2 | F | Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor | |
NECFGCCN_01002 | 2.5e-100 | zapC | D | Contributes to the efficiency of the cell division process by stabilizing the polymeric form of the cell division protein FtsZ. Acts by promoting interactions between FtsZ protofilaments and suppressing the GTPase activity of FtsZ | ||
NECFGCCN_01003 | 1.5e-211 | ycbX | 1.17.1.1 | C | Mosc domain protein beta barrel domain protein | |
NECFGCCN_01004 | 4.9e-133 | rlmL | 2.1.1.173, 2.1.1.191, 2.1.1.264, 2.1.1.72 | J | Specifically methylates the guanine in position 2445 (m2G2445) and the guanine in position 2069 (m7G2069) of 23S rRNA | |
NECFGCCN_01005 | 2.2e-63 | 3.1.3.27, 3.1.3.4, 3.1.3.81, 3.6.1.27 | I | phosphatidate phosphatase activity | ||
NECFGCCN_01006 | 4.3e-144 | cof | S | Sucrose-6F-phosphate phosphohydrolase | ||
NECFGCCN_01007 | 1.5e-130 | glcR | K | transcriptional regulator (DeoR family) | ||
NECFGCCN_01008 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
NECFGCCN_01009 | 7.9e-71 | K | transcriptional | |||
NECFGCCN_01010 | 1.7e-229 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
NECFGCCN_01011 | 5.1e-262 | argH | 4.3.2.1 | E | Argininosuccinate lyase | |
NECFGCCN_01012 | 3.8e-54 | rnpA | 3.1.26.5 | J | RNaseP catalyzes the removal of the 5'-leader sequence from pre-tRNA to produce the mature 5'-terminus. It can also cleave other RNA substrates such as 4.5S RNA. The protein component plays an auxiliary but essential role in vivo by binding to the 5'-leader sequence and broadening the substrate specificity of the ribozyme | |
NECFGCCN_01013 | 2.4e-139 | yidC | U | Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins | ||
NECFGCCN_01014 | 7.4e-212 | vex1 | V | Efflux ABC transporter, permease protein | ||
NECFGCCN_01015 | 5.5e-197 | mdcA | 2.3.1.187 | I | Malonate decarboxylase | |
NECFGCCN_01016 | 9.8e-119 | V | CAAX protease self-immunity | |||
NECFGCCN_01017 | 5e-145 | fecD | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
NECFGCCN_01018 | 7.1e-133 | fecE | 3.6.3.34 | HP | ABC transporter | |
NECFGCCN_01019 | 5.5e-173 | fatB | P | COG0614 ABC-type Fe3 -hydroxamate transport system, periplasmic component | ||
NECFGCCN_01020 | 2.1e-123 | ybbA | S | Putative esterase | ||
NECFGCCN_01021 | 3.7e-157 | yegS | 2.7.1.107 | I | Diacylglycerol kinase | |
NECFGCCN_01022 | 1.4e-221 | scrA | 2.7.1.192, 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | PTS system sucrose-specific | |
NECFGCCN_01023 | 8.1e-284 | scrB | 3.2.1.26 | GH32 | G | invertase |
NECFGCCN_01024 | 2.1e-188 | scrR | 3.2.1.26 | GH32 | K | Sucrose operon repressor |
NECFGCCN_01026 | 9.2e-158 | purU | 2.7.7.72, 3.5.1.10 | F | Catalyzes the hydrolysis of 10-formyltetrahydrofolate (formyl-FH4) to formate and tetrahydrofolate (FH4) | |
NECFGCCN_01027 | 3e-86 | ychJ | S | Belongs to the UPF0225 family | ||
NECFGCCN_01028 | 8.9e-167 | rssA | M | esterase of the alpha-beta hydrolase superfamily | ||
NECFGCCN_01029 | 2.2e-177 | T | Regulates the turnover of the sigma S factor (RpoS) by promoting its proteolysis in exponentially growing cells. Acts by binding and delivering RpoS to the ClpXP protease. RssB is not co- degraded with RpoS, but is released from the complex and can initiate a new cycle of RpoS recognition and degradation | |||
NECFGCCN_01030 | 4.4e-166 | galU | 2.7.7.9 | M | Utp--glucose-1-phosphate uridylyltransferase | |
NECFGCCN_01031 | 8.7e-61 | hns | K | Belongs to the histone-like protein H-NS family | ||
NECFGCCN_01032 | 2.9e-93 | tdk | 2.7.1.21 | F | thymidine kinase | |
NECFGCCN_01033 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
NECFGCCN_01034 | 1.8e-108 | ychE | U | UPF0056 membrane protein | ||
NECFGCCN_01035 | 0.0 | oppA | E | ABC transporter substrate-binding protein | ||
NECFGCCN_01036 | 1.7e-152 | oppB | P | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
NECFGCCN_01037 | 1.6e-144 | oppC | P | COG1173 ABC-type dipeptide oligopeptide nickel transport systems permease components | ||
NECFGCCN_01038 | 1.6e-188 | oppD | 3.6.3.24 | P | Belongs to the ABC transporter superfamily | |
NECFGCCN_01039 | 7.6e-191 | oppF | P | Belongs to the ABC transporter superfamily | ||
NECFGCCN_01040 | 1.1e-142 | kch | J | COG1226 Kef-type K transport systems | ||
NECFGCCN_01041 | 1.2e-57 | yciU | S | Belongs to the UPF0263 family | ||
NECFGCCN_01042 | 9.7e-280 | cls | 2.7.8.8 | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | |
NECFGCCN_01043 | 1.2e-26 | yciY | ||||
NECFGCCN_01044 | 1.8e-97 | yceI | S | Belongs to the UPF0312 family | ||
NECFGCCN_01045 | 1.2e-46 | yciI | T | YciI from Haemophilus influenzae presents crystal structure similarity to a muconolactone isomerase, but does not seem to catalyze any of the | ||
NECFGCCN_01046 | 9.3e-77 | tonB | U | Interacts with outer membrane receptor proteins that carry out high-affinity binding and energy dependent uptake into the periplasmic space of specific substrates. It could act to transduce energy from the cytoplasmic membrane to specific energy- requiring processes in the outer membrane, resulting in the release into the periplasm of ligands bound by these outer membrane proteins | ||
NECFGCCN_01047 | 8.9e-172 | yniA | G | Fructosamine kinase | ||
NECFGCCN_01048 | 2.6e-40 | ydiZ | S | endoribonuclease activity | ||
NECFGCCN_01049 | 2.1e-166 | pfkB | 2.7.1.11, 2.7.1.56 | H | belongs to the carbohydrate kinase PfkB family | |
NECFGCCN_01050 | 2.5e-138 | ydiY | M | Salt-induced outer membrane protein | ||
NECFGCCN_01051 | 5.9e-30 | |||||
NECFGCCN_01052 | 0.0 | thrS | 6.1.1.3 | J | Catalyzes the attachment of threonine to tRNA(Thr) in a two-step reaction L-threonine is first activated by ATP to form Thr-AMP and then transferred to the acceptor end of tRNA(Thr) | |
NECFGCCN_01053 | 1.2e-71 | infC | J | IF-3 binds to the 30S ribosomal subunit and shifts the equilibrum between 70S ribosomes and their 50S and 30S subunits in favor of the free subunits, thus enhancing the availability of 30S subunits on which protein synthesis initiation begins | ||
NECFGCCN_01054 | 9.5e-29 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
NECFGCCN_01055 | 2.4e-54 | rplT | J | Binds directly to 23S ribosomal RNA and is necessary for the in vitro assembly process of the 50S ribosomal subunit. It is not involved in the protein synthesizing functions of that subunit | ||
NECFGCCN_01056 | 3.8e-187 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
NECFGCCN_01057 | 9.7e-149 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
NECFGCCN_01058 | 1.2e-65 | K | Transcriptional regulator | |||
NECFGCCN_01060 | 4.8e-204 | pepA | 3.4.11.7 | G | COG1363 Cellulase M and related proteins | |
NECFGCCN_01061 | 5.2e-131 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
NECFGCCN_01062 | 4e-100 | S | CAAX amino terminal protease family protein | |||
NECFGCCN_01064 | 7.3e-110 | V | CAAX protease self-immunity | |||
NECFGCCN_01065 | 8.8e-27 | lanR | K | sequence-specific DNA binding | ||
NECFGCCN_01066 | 1.4e-220 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
NECFGCCN_01067 | 1.5e-175 | ytxK | 2.1.1.72 | L | DNA methylase | |
NECFGCCN_01068 | 2.4e-13 | comGF | U | Putative Competence protein ComGF | ||
NECFGCCN_01069 | 3.8e-70 | comGF | U | Competence protein ComGF | ||
NECFGCCN_01070 | 1.1e-15 | NU | Type II secretory pathway pseudopilin | |||
NECFGCCN_01071 | 7.1e-69 | cglD | NU | Competence protein | ||
NECFGCCN_01072 | 1.1e-42 | comGC | U | Required for transformation and DNA binding | ||
NECFGCCN_01073 | 1.7e-143 | comGA | NU | Type II secretory pathway, ATPase PulE Tfp pilus assembly pathway, ATPase PilB | ||
NECFGCCN_01074 | 4.6e-174 | comGA | NU | Type II secretory pathway, ATPase PulE Tfp pilus assembly pathway, ATPase PilB | ||
NECFGCCN_01075 | 1.6e-49 | bta | 1.8.1.8 | CO | cell redox homeostasis | |
NECFGCCN_01076 | 0.0 | glmS | 2.6.1.16 | M | Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source | |
NECFGCCN_01077 | 6.6e-59 | phnA | P | Alkylphosphonate utilization operon protein PhnA | ||
NECFGCCN_01078 | 1.4e-105 | artQ | P | ABC transporter (Permease | ||
NECFGCCN_01079 | 7.5e-112 | glnQ | 3.6.3.21 | E | abc transporter atp-binding protein | |
NECFGCCN_01080 | 5.9e-09 | aatB | ET | ABC transporter substrate-binding protein | ||
NECFGCCN_01081 | 8.4e-165 | VPA0243 | S | protein conserved in bacteria | ||
NECFGCCN_01082 | 7.7e-17 | |||||
NECFGCCN_01083 | 3.7e-157 | K | transcriptional regulator | |||
NECFGCCN_01084 | 1.4e-130 | scoA | 2.8.3.5 | I | COG1788 Acyl CoA acetate 3-ketoacid CoA transferase, alpha subunit | |
NECFGCCN_01085 | 4.4e-115 | scoB | 2.8.3.5 | I | COG2057 Acyl CoA acetate 3-ketoacid CoA transferase beta subunit | |
NECFGCCN_01086 | 1.2e-208 | atoB | 2.3.1.9 | I | Catalyzes the final step of fatty acid oxidation in which acetyl-CoA is released and the CoA ester of a fatty acid two carbons shorter is formed | |
NECFGCCN_01087 | 5.7e-161 | hbd2 | 1.1.1.157, 1.1.1.35, 4.2.1.17, 5.1.2.3, 5.3.3.8 | I | 3-hydroxyacyl-coa dehydrogenase | |
NECFGCCN_01088 | 6.7e-246 | yxjC | EG | COG2610 H gluconate symporter and related permeases | ||
NECFGCCN_01089 | 4.7e-140 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
NECFGCCN_01090 | 3.9e-159 | budR | K | transcriptional regulator | ||
NECFGCCN_01091 | 1.9e-149 | budA | 4.1.1.5 | Q | Alpha-acetolactate decarboxylase | |
NECFGCCN_01092 | 0.0 | alsS | 2.2.1.6 | EH | Belongs to the TPP enzyme family | |
NECFGCCN_01093 | 9.7e-138 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
NECFGCCN_01094 | 7.2e-66 | ykkB | J | Acetyltransferase (GNAT) domain | ||
NECFGCCN_01095 | 1.4e-34 | Q | hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides | |||
NECFGCCN_01096 | 8.1e-96 | 3.1.1.85 | S | Alpha beta hydrolase | ||
NECFGCCN_01097 | 2.9e-103 | yvgN | S | Reductase | ||
NECFGCCN_01098 | 5.2e-77 | ykgD | K | Cupin | ||
NECFGCCN_01100 | 8.6e-298 | O | MreB/Mbl protein | |||
NECFGCCN_01102 | 1.2e-114 | M | Pilin isopeptide linkage domain protein | |||
NECFGCCN_01103 | 6.3e-102 | V | Psort location CytoplasmicMembrane, score | |||
NECFGCCN_01106 | 5.2e-14 | |||||
NECFGCCN_01107 | 1.2e-225 | dcuS | 2.7.13.3 | T | protein histidine kinase activity | |
NECFGCCN_01108 | 3.7e-233 | 2.7.13.3 | T | protein histidine kinase activity | ||
NECFGCCN_01109 | 0.0 | rexB | 3.1.21.3, 3.6.4.12 | L | The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination | |
NECFGCCN_01110 | 0.0 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
NECFGCCN_01111 | 3.6e-126 | S | Protein of unknown function (DUF554) | |||
NECFGCCN_01112 | 1.5e-132 | ecsA_2 | V | abc transporter atp-binding protein | ||
NECFGCCN_01113 | 8.7e-266 | XK27_00765 | ||||
NECFGCCN_01114 | 2.6e-141 | proB | 2.7.2.11 | E | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
NECFGCCN_01115 | 3.5e-222 | proA | 1.2.1.41 | E | Catalyzes the NADPH-dependent reduction of L-glutamate 5-phosphate into L-glutamate 5-semialdehyde and phosphate. The product spontaneously undergoes cyclization to form 1-pyrroline-5- carboxylate | |
NECFGCCN_01116 | 4.3e-58 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
NECFGCCN_01117 | 2e-263 | adhB | C | Cytochrome c | ||
NECFGCCN_01118 | 0.0 | 1.1.99.3 | E | Choline dehydrogenase and related flavoproteins | ||
NECFGCCN_01119 | 4.5e-140 | 1.1.99.3 | S | Gluconate 2-dehydrogenase | ||
NECFGCCN_01120 | 8.4e-63 | E | glyoxalase bleomycin resistance protein dioxygenase | |||
NECFGCCN_01121 | 3.2e-95 | potA_1 | 3.6.3.30 | P | Belongs to the ABC transporter superfamily | |
NECFGCCN_01122 | 1.8e-40 | XK27_08130 | K | Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | ||
NECFGCCN_01123 | 3.3e-38 | L | HTH-like domain | |||
NECFGCCN_01124 | 2.5e-12 | S | Cobalamin synthesis protein cobW C-terminal domain | |||
NECFGCCN_01125 | 7e-46 | nifJ | 1.2.7.1 | C | Oxidoreductase required for the transfer of electrons from pyruvate to flavodoxin | |
NECFGCCN_01126 | 6.9e-98 | nifJ | 1.2.7.1 | C | Oxidoreductase required for the transfer of electrons from pyruvate to flavodoxin | |
NECFGCCN_01127 | 6e-39 | ydbJ | S | Lipoprotein | ||
NECFGCCN_01128 | 1.6e-73 | hslJ | O | Heat shock protein | ||
NECFGCCN_01129 | 1.6e-185 | ldhA | 1.1.1.28 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
NECFGCCN_01130 | 2e-75 | dedA | 3.6.1.27 | S | FtsZ-dependent cytokinesis | |
NECFGCCN_01131 | 1.3e-294 | yfiB1 | V | abc transporter atp-binding protein | ||
NECFGCCN_01132 | 1.4e-108 | pvaA | M | lytic transglycosylase activity | ||
NECFGCCN_01133 | 5.9e-48 | leuC | 4.2.1.33, 4.2.1.35 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
NECFGCCN_01134 | 7.1e-38 | ysdA | L | Membrane | ||
NECFGCCN_01135 | 3.6e-188 | leuB | 1.1.1.85 | CE | Catalyzes the oxidation of 3-carboxy-2-hydroxy-4- methylpentanoate (3-isopropylmalate) to 3-carboxy-4-methyl-2- oxopentanoate. The product decarboxylates to 4-methyl-2 oxopentanoate | |
NECFGCCN_01136 | 5.5e-289 | leuA | 2.3.3.13 | E | Catalyzes the condensation of the acetyl group of acetyl-CoA with 3-methyl-2-oxobutanoate (2-oxoisovalerate) to form 3-carboxy-3-hydroxy-4-methylpentanoate (2-isopropylmalate) | |
NECFGCCN_01137 | 2.1e-131 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
NECFGCCN_01138 | 1.2e-45 | cpsE | M | Exopolysaccharide biosynthesis polyprenyl glycosylphosphotransferase | ||
NECFGCCN_01139 | 1.5e-34 | |||||
NECFGCCN_01140 | 5.4e-33 | S | Protein of unknown function (DUF1648) | |||
NECFGCCN_01141 | 3.8e-114 | P | FtsX-like permease family | |||
NECFGCCN_01142 | 1.2e-24 | ligA | 6.5.1.2 | L | DNA ligase that catalyzes the formation of phosphodiester linkages between 5'-phosphoryl and 3'-hydroxyl groups in double-stranded DNA using NAD as a coenzyme and as the energy source for the reaction. It is essential for DNA replication and repair of damaged DNA | |
NECFGCCN_01143 | 1.5e-203 | ligA | 6.5.1.2 | L | DNA ligase that catalyzes the formation of phosphodiester linkages between 5'-phosphoryl and 3'-hydroxyl groups in double-stranded DNA using NAD as a coenzyme and as the energy source for the reaction. It is essential for DNA replication and repair of damaged DNA | |
NECFGCCN_01144 | 1.1e-102 | zipA | D | Essential cell division protein that stabilizes the FtsZ protofilaments by cross-linking them and that serves as a cytoplasmic membrane anchor for the Z ring. Also required for the recruitment to the septal ring of downstream cell division proteins | ||
NECFGCCN_01145 | 7.6e-143 | cysZ | U | High affinity, high specificity proton-dependent sulfate transporter, which mediates sulfate uptake. Provides the sulfur source for the cysteine synthesis pathway | ||
NECFGCCN_01146 | 4.3e-175 | cysK | 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
NECFGCCN_01147 | 1.1e-37 | ptsH | G | Phosphocarrier protein Hpr | ||
NECFGCCN_01148 | 0.0 | ptsI | 2.7.1.121, 2.7.3.9 | G | General (non sugar-specific) component of the phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS). This major carbohydrate active-transport system catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. Enzyme I transfers the phosphoryl group from phosphoenolpyruvate (PEP) to the phosphoryl carrier protein (HPr) | |
NECFGCCN_01149 | 6.7e-87 | crr | G | pts system | ||
NECFGCCN_01150 | 2.2e-35 | |||||
NECFGCCN_01151 | 3e-143 | pdxK | 2.7.1.35 | H | Pyridoxal kinase involved in the salvage pathway of pyridoxal 5'-phosphate (PLP). Catalyzes the phosphorylation of pyridoxal to PLP | |
NECFGCCN_01152 | 4.2e-234 | ptsJ | K | Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | ||
NECFGCCN_01153 | 7.1e-68 | yybH | S | SnoaL-like domain | ||
NECFGCCN_01154 | 1e-165 | cysM | 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
NECFGCCN_01155 | 9.1e-206 | cysA | 3.6.3.25, 3.6.3.29 | P | Part of the ABC transporter complex CysAWTP involved in sulfate thiosulfate import. Responsible for energy coupling to the transport system | |
NECFGCCN_01156 | 1.5e-158 | cysW | P | (ABC) transporter | ||
NECFGCCN_01157 | 4e-145 | cysT | P | sulfate ABC transporter | ||
NECFGCCN_01158 | 5.3e-192 | cysP | P | Thiosulfate transporter subunit | ||
NECFGCCN_01159 | 1.5e-169 | yfeX | P | peroxidase | ||
NECFGCCN_01160 | 2.6e-103 | yfeY | S | Protein of unknown function (DUF1131) | ||
NECFGCCN_01161 | 1.6e-79 | yfeZ | S | Protein of unknown function (DUF2919) | ||
NECFGCCN_01162 | 2.4e-77 | ypeA | K | Belongs to the acetyltransferase family. YpeA subfamily | ||
NECFGCCN_01163 | 4.4e-155 | amiA | 3.5.1.28 | M | N-acetylmuramoyl-L-alanine amidase | |
NECFGCCN_01164 | 1.4e-180 | hemF | 1.3.3.3 | H | Involved in the heme biosynthesis. Catalyzes the aerobic oxidative decarboxylation of propionate groups of rings A and B of coproporphyrinogen-III to yield the vinyl groups in protoporphyrinogen-IX | |
NECFGCCN_01165 | 3.8e-201 | eutR | K | transcriptional regulator | ||
NECFGCCN_01166 | 6.9e-73 | eutK | CQ | ethanolamine utilization protein | ||
NECFGCCN_01167 | 1.4e-113 | eutL | E | Carboxysome structural protein involved in ethanolamine utilization | ||
NECFGCCN_01168 | 1.1e-143 | eutC | 4.3.1.7 | E | Belongs to the EutC family | |
NECFGCCN_01169 | 1.6e-260 | eutB | 4.3.1.7 | E | With EutC catalyzes the formation of acetaldehyde and ammonia from ethanolamine | |
NECFGCCN_01170 | 4.1e-251 | eutA | E | ethanolamine utilization protein | ||
NECFGCCN_01171 | 1.6e-219 | eutH | E | ethanolamine utilization protein | ||
NECFGCCN_01172 | 2e-247 | merA | 1.16.1.1 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
NECFGCCN_01173 | 3e-135 | mvk | 1.1.1.88, 2.3.3.10, 2.7.1.36 | I | mevalonate kinase | |
NECFGCCN_01174 | 2.9e-168 | mvaD | 4.1.1.33 | I | diphosphomevalonate decarboxylase | |
NECFGCCN_01175 | 3.5e-164 | mvaK2 | 2.7.1.36, 2.7.1.43, 2.7.4.2 | I | phosphomevalonate kinase | |
NECFGCCN_01176 | 6.2e-185 | fni | 1.1.1.88, 5.3.3.2 | C | Involved in the biosynthesis of isoprenoids. Catalyzes the 1,3-allylic rearrangement of the homoallylic substrate isopentenyl (IPP) to its allylic isomer, dimethylallyl diphosphate (DMAPP) | |
NECFGCCN_01177 | 0.0 | mgtA | 3.6.3.2 | P | COG0474 Cation transport ATPase | |
NECFGCCN_01178 | 9.6e-245 | glmU | 2.3.1.157, 2.7.7.23 | M | Catalyzes the last two sequential reactions in the de novo biosynthetic pathway for UDP-N-acetylglucosamine (UDP- GlcNAc). The C-terminal domain catalyzes the transfer of acetyl group from acetyl coenzyme A to glucosamine-1-phosphate (GlcN-1-P) to produce N-acetylglucosamine-1-phosphate (GlcNAc-1-P), which is converted into UDP-GlcNAc by the transfer of uridine 5- monophosphate (from uridine 5-triphosphate), a reaction catalyzed by the N-terminal domain | |
NECFGCCN_01179 | 1.2e-94 | nudF | 3.6.1.13 | L | AdP-ribose pyrophosphatase | |
NECFGCCN_01180 | 2.1e-23 | |||||
NECFGCCN_01181 | 5.2e-110 | ugpC | P | Belongs to the ABC transporter superfamily | ||
NECFGCCN_01182 | 1.2e-246 | yesO | G | ABC transporter substrate-binding protein | ||
NECFGCCN_01183 | 5.5e-245 | rafY | S | Porin-like glycoporin RafY | ||
NECFGCCN_01184 | 2.2e-292 | cscA | 3.2.1.26 | GH32 | G | invertase |
NECFGCCN_01185 | 4.7e-227 | lacY_2 | P | Major facilitator superfamily | ||
NECFGCCN_01186 | 1.8e-184 | cscR | K | Transcriptional | ||
NECFGCCN_01187 | 5.9e-258 | araE | EGP | Major facilitator Superfamily | ||
NECFGCCN_01188 | 7.3e-138 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
NECFGCCN_01189 | 3.7e-237 | ogl | 4.2.2.6 | U | oligogalacturonate lyase | |
NECFGCCN_01190 | 1.4e-132 | lptD | M | oligogalacturonate-specific porin | ||
NECFGCCN_01191 | 6.2e-12 | G | mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase activity | |||
NECFGCCN_01192 | 3.6e-32 | yhcA | V | abc transporter atp-binding protein | ||
NECFGCCN_01193 | 8.1e-133 | E | PFAM secretory lipase | |||
NECFGCCN_01194 | 1.6e-48 | evgA | 3.1.4.52 | T | helix_turn_helix, Lux Regulon | |
NECFGCCN_01195 | 2e-55 | S | Fusaric acid resistance protein-like | |||
NECFGCCN_01196 | 0.0 | evgS | 2.7.13.3 | T | PhoQ Sensor | |
NECFGCCN_01197 | 2.3e-52 | evgA | 3.1.4.52 | K | response regulator | |
NECFGCCN_01198 | 7.9e-19 | |||||
NECFGCCN_01199 | 1.7e-75 | M | Pili assembly chaperone PapD, C-terminal domain | |||
NECFGCCN_01200 | 9.9e-12 | NU | Fimbrial protein | |||
NECFGCCN_01201 | 4.3e-47 | NU | Fimbrial protein | |||
NECFGCCN_01202 | 4.1e-85 | M | Pili assembly chaperone PapD, C-terminal domain | |||
NECFGCCN_01203 | 9.3e-85 | M | Pili assembly chaperone PapD, C-terminal domain | |||
NECFGCCN_01204 | 0.0 | fimD_3 | NU | outer membrane usher protein | ||
NECFGCCN_01206 | 5.3e-36 | |||||
NECFGCCN_01207 | 3.6e-112 | pagO | EG | EamA-like transporter family | ||
NECFGCCN_01208 | 3.3e-31 | hdeA | M | Required for optimal acid stress protection. Exhibits a chaperone-like activity only at low pH by suppressing non- specifically the aggregation of denaturated periplasmic proteins | ||
NECFGCCN_01209 | 5.6e-77 | dppF | 3.6.3.30 | EP | abc transporter atp-binding protein | |
NECFGCCN_01210 | 7.9e-106 | oppD | P | abc transporter atp-binding protein | ||
NECFGCCN_01211 | 4.6e-122 | dppC | P | ABC transporter (permease) | ||
NECFGCCN_01212 | 1.4e-152 | dppB | P | COG0601 ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
NECFGCCN_01213 | 5.3e-255 | appA_2 | E | ABC transporter substrate-binding protein | ||
NECFGCCN_01214 | 2.8e-129 | yut | E | urea transporter | ||
NECFGCCN_01215 | 6.6e-104 | ureD | O | Required for maturation of urease via the functional incorporation of the urease nickel metallocenter | ||
NECFGCCN_01216 | 1.8e-102 | ureG | F | Facilitates the functional incorporation of the urease nickel metallocenter. This process requires GTP hydrolysis, probably effectuated by UreG | ||
NECFGCCN_01217 | 4.5e-73 | ureF | O | Required for maturation of urease via the functional incorporation of the urease nickel metallocenter | ||
NECFGCCN_01218 | 3.6e-53 | ureE | O | Involved in urease metallocenter assembly. Binds nickel. Probably functions as a nickel donor during metallocenter assembly | ||
NECFGCCN_01219 | 7.6e-300 | ureC | 3.5.1.5 | E | Belongs to the metallo-dependent hydrolases superfamily. Urease alpha subunit family | |
NECFGCCN_01220 | 1e-43 | ureB | 3.5.1.5 | E | Urease beta subunit | |
NECFGCCN_01221 | 6.7e-42 | ureA | 3.5.1.5 | E | Belongs to the urease gamma subunit family | |
NECFGCCN_01222 | 2.4e-194 | P | Psort location CytoplasmicMembrane, score 10.00 | |||
NECFGCCN_01223 | 2e-20 | hdeB | M | Required for optimal acid stress protection, which is important for survival of enteric bacteria in the acidic environment of the host stomach. Exhibits a chaperone-like activity at acidic pH by preventing the aggregation of many different periplasmic proteins | ||
NECFGCCN_01224 | 4.4e-29 | hdeD | S | Acid-resistance membrane protein | ||
NECFGCCN_01225 | 5.6e-246 | emrY | P | Fungal trichothecene efflux pump (TRI12) | ||
NECFGCCN_01226 | 3.5e-83 | emrA | V | HlyD membrane-fusion protein of T1SS | ||
NECFGCCN_01227 | 1.6e-90 | evgA | 3.1.4.52 | T | helix_turn_helix, Lux Regulon | |
NECFGCCN_01228 | 1e-138 | evgS | 2.7.13.3 | T | PhoQ Sensor | |
NECFGCCN_01229 | 1.4e-45 | ccrB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
NECFGCCN_01230 | 6.7e-47 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
NECFGCCN_01231 | 8.9e-56 | |||||
NECFGCCN_01232 | 5.2e-19 | ttgC | MU | CyaE is necessary for transport of calmodulin-sensitive adenylate cyclase-hemolysin (cyclolysin) | ||
NECFGCCN_01233 | 4.5e-142 | ycgG | T | EAL domain | ||
NECFGCCN_01234 | 6.7e-36 | lgrD | Q | Polysaccharide biosynthesis protein | ||
NECFGCCN_01235 | 1.2e-133 | 4.1.1.44 | S | decarboxylase | ||
NECFGCCN_01236 | 3.2e-50 | C | Aldo keto reductase | |||
NECFGCCN_01237 | 5.8e-112 | C | Aldo keto reductase | |||
NECFGCCN_01238 | 5.3e-93 | kefF | S | Flavodoxin-like fold | ||
NECFGCCN_01239 | 4.1e-55 | S | Protein conserved in bacteria | |||
NECFGCCN_01240 | 7.3e-161 | Z012_07430 | K | Transcriptional regulator | ||
NECFGCCN_01242 | 1.9e-109 | S | Protein of unknown function (DUF1349) | |||
NECFGCCN_01243 | 2.2e-42 | S | protein conserved in bacteria | |||
NECFGCCN_01244 | 1e-51 | arsR | K | transcriptional regulator | ||
NECFGCCN_01245 | 5.3e-229 | arsB | P | Involved in arsenical resistance. Thought to form the channel of an arsenite pump | ||
NECFGCCN_01246 | 9.6e-71 | arsC | 1.20.4.1 | P | arsenate reductase | |
NECFGCCN_01247 | 1e-287 | dtpT | U | Proton-dependent permease that transports di- and tripeptides | ||
NECFGCCN_01248 | 1.4e-47 | yoaC | S | Domain of unknown function (DUF1889) | ||
NECFGCCN_01249 | 2.2e-255 | mdtP | MU | RND efflux system, outer membrane lipoprotein | ||
NECFGCCN_01250 | 0.0 | mdtO | S | Resistance protein | ||
NECFGCCN_01251 | 7.5e-178 | mdtN | V | multidrug resistance | ||
NECFGCCN_01252 | 4.2e-43 | ytcA | S | Uncharacterised protein family | ||
NECFGCCN_01253 | 4.5e-38 | yjdI | 1.6.3.4 | S | Divergent 4Fe-4S mono-cluster | |
NECFGCCN_01254 | 3.4e-45 | yjdJ | S | GCN5-related N-acetyl-transferase | ||
NECFGCCN_01255 | 1.2e-245 | T | EAL domain | |||
NECFGCCN_01256 | 4.6e-163 | fimH | NU | Fimbrial protein | ||
NECFGCCN_01257 | 2.7e-149 | ydaM | 2.7.7.65 | T | Diguanylate cyclase | |
NECFGCCN_01258 | 1.3e-254 | guaD | 3.5.4.3 | F | Guanine deaminase | |
NECFGCCN_01259 | 3.7e-235 | pucI | FH | uracil, thiamine, allantoin | ||
NECFGCCN_01260 | 2.6e-160 | ulaE | 5.1.3.22 | G | 3-epimerase | |
NECFGCCN_01261 | 4.5e-126 | ulaF | 4.1.1.104, 4.1.2.17, 4.1.2.19, 4.2.1.109, 5.1.3.4 | G | Catalyzes the isomerization of L-ribulose 5-phosphate to D-xylulose 5-phosphate | |
NECFGCCN_01262 | 1.2e-211 | yajR_1 | EGP | Major facilitator Superfamily | ||
NECFGCCN_01263 | 8e-42 | yjfY | S | Protein of unknown function (DUF1471) | ||
NECFGCCN_01264 | 1e-66 | rpsF | 4.3.1.19 | J | Binds together with S18 to 16S ribosomal RNA | |
NECFGCCN_01265 | 3.6e-54 | priB | L | Binds single-stranded DNA at the primosome assembly site (PAS) | ||
NECFGCCN_01266 | 1.3e-34 | rpsR | J | Binds as a heterodimer with protein S6 to the central domain of the 16S rRNA, where it helps stabilize the platform of the 30S subunit | ||
NECFGCCN_01267 | 3e-70 | rplI | J | Binds to the 23S rRNA | ||
NECFGCCN_01268 | 9.8e-94 | ytfB | M | Opacity-associated protein A | ||
NECFGCCN_01269 | 2.1e-111 | fklB | 5.2.1.8 | G | Peptidyl-prolyl cis-trans | |
NECFGCCN_01270 | 4.6e-255 | cycA | E | amino acid | ||
NECFGCCN_01271 | 1.2e-120 | ytfE | D | Di-iron-containing protein involved in the repair of iron-sulfur clusters | ||
NECFGCCN_01272 | 2.9e-179 | ytfF | EG | Permeases of the drug metabolite transporter (DMT) superfamily | ||
NECFGCCN_01273 | 1.2e-157 | K | transcriptional regulator | |||
NECFGCCN_01274 | 2e-144 | ytfG | 1.6.5.2 | GM | NmrA family | |
NECFGCCN_01275 | 1.4e-62 | ytfH | K | Transcriptional regulator | ||
NECFGCCN_01276 | 0.0 | cpdB | 3.1.3.5, 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
NECFGCCN_01277 | 1.7e-139 | cysQ | 3.1.3.7 | P | 3'(2'),5'-bisphosphate nucleotidase | |
NECFGCCN_01278 | 6.7e-96 | ytfJ | S | transcriptional regulator | ||
NECFGCCN_01279 | 1.2e-29 | ytfK | S | Protein of unknown function (DUF1107) | ||
NECFGCCN_01280 | 6.2e-173 | araC_3 | K | regulates the araBAD and araFGH operons and other genes involved in the transport and catabolism of L-arabinose | ||
NECFGCCN_01281 | 0.0 | lacZ3 | 3.2.1.23 | G | beta-galactosidase | |
NECFGCCN_01282 | 1.3e-229 | P | Major facilitator superfamily | |||
NECFGCCN_01283 | 4.2e-221 | ytfL | P | Hemolysins and related proteins containing CBS domains | ||
NECFGCCN_01284 | 1.6e-122 | msrA | 1.8.4.11 | O | Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine | |
NECFGCCN_01285 | 0.0 | ytfM | M | COG0729 Outer membrane protein | ||
NECFGCCN_01286 | 0.0 | ytfN | M | protein conserved in bacteria | ||
NECFGCCN_01287 | 2.1e-63 | ytfP | S | AIG2 family | ||
NECFGCCN_01288 | 3.8e-25 | |||||
NECFGCCN_01289 | 1.4e-98 | ppa | 3.6.1.1 | C | Catalyzes the hydrolysis of inorganic pyrophosphate (PPi) forming two phosphate ions | |
NECFGCCN_01290 | 4.8e-171 | ytfQ | G | Periplasmic binding protein LacI transcriptional regulator | ||
NECFGCCN_01291 | 1.4e-281 | ytfR | 3.6.3.17 | P | import. Responsible for energy coupling to the transport system | |
NECFGCCN_01292 | 4.7e-172 | ytfT | G | Belongs to the binding-protein-dependent transport system permease family | ||
NECFGCCN_01293 | 9.8e-175 | yjfF | G | Belongs to the binding-protein-dependent transport system permease family | ||
NECFGCCN_01294 | 4.9e-190 | fbp | 3.1.3.11 | G | D-fructose-1,6-bisphosphate 1-phosphohydrolase class 1 | |
NECFGCCN_01295 | 2.4e-272 | murC | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Reutilizes the intact tripeptide L-alanyl-gamma-D- glutamyl-meso-diaminopimelate by linking it to UDP-N- acetylmuramate | |
NECFGCCN_01296 | 2.4e-95 | 2.3.1.128 | K | Acetyltransferase GNAT Family | ||
NECFGCCN_01297 | 3.1e-231 | IV02_08475 | G | Thioredoxin | ||
NECFGCCN_01298 | 1.4e-95 | H | ergothioneine biosynthetic process | |||
NECFGCCN_01299 | 1.3e-99 | PP2730 | S | Protein of unknown function (DUF3833) | ||
NECFGCCN_01300 | 5.3e-186 | ybgA | S | Conserved Protein | ||
NECFGCCN_01301 | 2.4e-43 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
NECFGCCN_01302 | 4.5e-36 | ylqC | L | Belongs to the UPF0109 family | ||
NECFGCCN_01303 | 9.7e-236 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
NECFGCCN_01304 | 4.5e-52 | higA-2 | K | Helix-turn-helix domain | ||
NECFGCCN_01305 | 1.2e-58 | S | RelE family toxin-antitoxin system | |||
NECFGCCN_01306 | 6.4e-205 | nepI | EGP | Major facilitator Superfamily | ||
NECFGCCN_01307 | 6.4e-148 | phnX | 2.6.1.37, 3.1.3.18, 3.11.1.1 | S | Belongs to the HAD-like hydrolase superfamily. PhnX family | |
NECFGCCN_01308 | 2.8e-210 | phnW | 2.5.1.49, 2.6.1.37, 3.11.1.1 | H | Belongs to the class-V pyridoxal-phosphate-dependent aminotransferase family. PhnW subfamily | |
NECFGCCN_01309 | 1.1e-135 | phnR | K | UTRA | ||
NECFGCCN_01310 | 2.1e-188 | phnS | P | Bacterial extracellular solute-binding protein | ||
NECFGCCN_01311 | 1.4e-206 | phnT | P | Belongs to the ABC transporter superfamily | ||
NECFGCCN_01312 | 2.4e-145 | phnU | P | Binding-protein-dependent transport system inner membrane component | ||
NECFGCCN_01313 | 4.2e-136 | phnV | P | TIGRFAM 2-aminoethylphosphonate ABC transport system, membrane component PhnV | ||
NECFGCCN_01314 | 1.5e-280 | xylB | 2.7.1.17, 2.7.1.189, 2.7.1.5, 2.7.1.51 | G | xylulose kinase | |
NECFGCCN_01315 | 1.6e-263 | mtlD | 1.1.1.11, 1.1.1.17, 1.1.1.57, 1.1.1.58 | G | Belongs to the mannitol dehydrogenase family | |
NECFGCCN_01316 | 5.8e-177 | smoC | K | transcriptional regulator | ||
NECFGCCN_01317 | 8.4e-174 | 3.2.1.26 | GH32 | K | transcriptional regulator | |
NECFGCCN_01318 | 5.9e-132 | rbtD | 1.1.1.56 | S | COG4221 Short-chain alcohol dehydrogenase of | |
NECFGCCN_01319 | 2.6e-278 | rtlK | 2.7.1.47 | C | Belongs to the ribulokinase family | |
NECFGCCN_01320 | 8.9e-57 | EGP | Major facilitator superfamily | |||
NECFGCCN_01322 | 1.7e-211 | 2.7.13.3 | T | protein histidine kinase activity | ||
NECFGCCN_01324 | 1.3e-100 | agrA | KT | phosphorelay signal transduction system | ||
NECFGCCN_01325 | 1.4e-09 | |||||
NECFGCCN_01326 | 2.2e-254 | dnaA | L | it binds specifically double-stranded DNA at a 9 bp consensus (dnaA box) 5'-TTATC CA A CA A-3'. DnaA binds to ATP and to acidic phospholipids | ||
NECFGCCN_01327 | 2.4e-30 | yozG | K | Transcriptional regulator | ||
NECFGCCN_01331 | 0.0 | recG | 3.6.4.12 | L | Critical role in recombination and DNA repair. Helps process Holliday junction intermediates to mature products by catalyzing branch migration. Has a DNA unwinding activity characteristic of a DNA helicase with a 3'- to 5'- polarity. Unwinds branched duplex DNA (Y-DNA) | |
NECFGCCN_01332 | 1.2e-181 | alr | 5.1.1.1, 5.1.1.5 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
NECFGCCN_01333 | 1.7e-60 | acpS | 2.7.6.3, 2.7.8.7, 5.1.1.1 | I | Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein | |
NECFGCCN_01334 | 2.5e-197 | aroF | 2.5.1.54 | E | Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) | |
NECFGCCN_01335 | 5.5e-197 | aroF | 2.5.1.54 | E | Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) | |
NECFGCCN_01336 | 0.0 | secA | U | Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. Has a central role in coupling the hydrolysis of ATP to the transfer of proteins into and across the cell membrane, serving as an ATP-driven molecular motor driving the stepwise translocation of polypeptide chains across the membrane | ||
NECFGCCN_01338 | 3.7e-187 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
NECFGCCN_01339 | 2e-171 | scrK | 2.7.1.2, 2.7.1.4 | GK | Fructokinase | |
NECFGCCN_01340 | 0.0 | scrA | 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | pts system | |
NECFGCCN_01341 | 2.6e-285 | scrB | 3.2.1.26, 3.2.1.80 | GH32 | G | invertase |
NECFGCCN_01342 | 7.5e-180 | scrR | K | Transcriptional regulator | ||
NECFGCCN_01343 | 8.1e-73 | nusB | K | Involved in transcription antitermination. Required for transcription of ribosomal RNA (rRNA) genes. Binds specifically to the boxA antiterminator sequence of the ribosomal RNA (rrn) operons | ||
NECFGCCN_01344 | 1.7e-61 | yqhY | S | protein conserved in bacteria | ||
NECFGCCN_01345 | 7.1e-98 | efp | J | Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase | ||
NECFGCCN_01346 | 3.3e-85 | comEB | 3.5.4.12 | F | ComE operon protein 2 | |
NECFGCCN_01347 | 5.4e-187 | pepP | 3.4.11.9, 3.4.13.9 | E | Belongs to the peptidase M24B family | |
NECFGCCN_01349 | 9.5e-33 | blpT | ||||
NECFGCCN_01352 | 0.0 | uvrA | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrA is an ATPase and a DNA-binding protein. A damage recognition complex composed of 2 uvrA and 2 uvrB subunits scans DNA for abnormalities. When the presence of a lesion has been verified by uvrB, the uvrA molecules dissociate | ||
NECFGCCN_01353 | 4.2e-167 | corA | P | COG0598 Mg2 and Co2 transporters | ||
NECFGCCN_01354 | 8.5e-122 | XK27_01040 | S | Protein of unknown function (DUF1129) | ||
NECFGCCN_01356 | 1.7e-35 | rpsR | J | Binds as a heterodimer with protein S6 to the central domain of the 16S rRNA, where it helps stabilize the platform of the 30S subunit | ||
NECFGCCN_01357 | 2.5e-81 | ssb | L | Plays an important role in DNA replication, recombination and repair. Binds to ssDNA and to an array of partner proteins to recruit them to their sites of action during DNA metabolism | ||
NECFGCCN_01358 | 3e-47 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
NECFGCCN_01360 | 8.1e-157 | K | Helix-turn-helix XRE-family like proteins | |||
NECFGCCN_01361 | 1.2e-278 | V | ABC transporter transmembrane region | |||
NECFGCCN_01362 | 3.3e-17 | lacL | 3.2.1.23 | G | -beta-galactosidase | |
NECFGCCN_01363 | 1.5e-48 | lacL | 3.2.1.23 | G | -beta-galactosidase | |
NECFGCCN_01364 | 3.7e-47 | lacL | 3.2.1.23 | G | -beta-galactosidase | |
NECFGCCN_01365 | 0.0 | lacS | G | transporter | ||
NECFGCCN_01366 | 7.5e-177 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
NECFGCCN_01367 | 4.5e-64 | S | dextransucrase activity | |||
NECFGCCN_01368 | 3.8e-117 | M | Pili assembly chaperone PapD, C-terminal domain | |||
NECFGCCN_01369 | 5e-91 | NU | COG3539 P pilus assembly protein, pilin FimA | |||
NECFGCCN_01370 | 3.2e-113 | K | response regulator | |||
NECFGCCN_01372 | 1.8e-248 | gltA | 2.3.3.1 | H | Belongs to the citrate synthase family | |
NECFGCCN_01373 | 3.9e-23 | |||||
NECFGCCN_01374 | 7.2e-68 | hiuH | 3.5.2.17, 4.1.1.97 | S | Belongs to the transthyretin family. 5-hydroxyisourate hydrolase subfamily | |
NECFGCCN_01375 | 3.1e-28 | T | Sh3 type 3 domain protein | |||
NECFGCCN_01376 | 7.2e-62 | manO | S | protein conserved in bacteria | ||
NECFGCCN_01377 | 1.5e-228 | serS | 6.1.1.11 | J | Catalyzes the attachment of serine to tRNA(Ser). Is also able to aminoacylate tRNA(Sec) with serine, to form the misacylated tRNA L-seryl-tRNA(Sec), which will be further converted into selenocysteinyl-tRNA(Sec) | |
NECFGCCN_01378 | 1.2e-101 | |||||
NECFGCCN_01379 | 9.7e-247 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
NECFGCCN_01380 | 1.3e-165 | dnaI | L | Primosomal protein DnaI | ||
NECFGCCN_01381 | 5.9e-211 | dnaB | L | Replication initiation and membrane attachment | ||
NECFGCCN_01382 | 3e-81 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
NECFGCCN_01383 | 7.6e-261 | T | PhoQ Sensor | |||
NECFGCCN_01384 | 3.9e-66 | spxA_2 | 1.20.4.1 | P | Belongs to the ArsC family | |
NECFGCCN_01385 | 6.8e-204 | recA | L | Can catalyze the hydrolysis of ATP in the presence of single-stranded DNA, the ATP-dependent uptake of single-stranded DNA by duplex DNA, and the ATP-dependent hybridization of homologous single-stranded DNAs. It interacts with LexA causing its activation and leading to its autocatalytic cleavage | ||
NECFGCCN_01386 | 3.5e-202 | glpQ | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
NECFGCCN_01387 | 8.1e-249 | glpT | G | transporter | ||
NECFGCCN_01388 | 3.8e-309 | glpA | 1.1.5.3 | C | Belongs to the FAD-dependent glycerol-3-phosphate dehydrogenase family | |
NECFGCCN_01389 | 9.1e-42 | WQ51_02910 | S | Protein of unknown function, DUF536 | ||
NECFGCCN_01390 | 2.4e-104 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
NECFGCCN_01391 | 2.3e-125 | K | transcriptional regulator, MerR family | |||
NECFGCCN_01392 | 0.0 | V | ABC transporter (Permease | |||
NECFGCCN_01393 | 2.6e-123 | acrB | V | Belongs to the resistance-nodulation-cell division (RND) (TC 2.A.6) family | ||
NECFGCCN_01394 | 2.2e-72 | yjdL | U | Proton-dependent permease that transports di- and tripeptides | ||
NECFGCCN_01395 | 0.0 | cadA | 4.1.1.17, 4.1.1.18, 4.1.1.19 | E | decarboxylase | |
NECFGCCN_01396 | 3.9e-243 | cadB | E | antiporter | ||
NECFGCCN_01397 | 3.8e-266 | cadC | K | transcriptional | ||
NECFGCCN_01398 | 3.5e-42 | S | Protein of unknown function (DUF1471) | |||
NECFGCCN_01399 | 3.9e-178 | lpxL | 2.3.1.241, 2.3.1.242, 2.3.1.243 | M | Catalyzes the transfer of laurate from lauroyl-acyl carrier protein (ACP) to Kdo(2)-lipid IV(A) to form Kdo(2)- (lauroyl)-lipid IV(A) | |
NECFGCCN_01400 | 4.3e-166 | S | acetyltransferase | |||
NECFGCCN_01401 | 4.4e-194 | NU | cell adhesion | |||
NECFGCCN_01402 | 0.0 | Z012_00755 | NU | Usher protein | ||
NECFGCCN_01403 | 1.6e-191 | rsmC | 2.1.1.172, 2.1.1.174 | J | Specifically methylates the guanine in position 1207 of 16S rRNA in the 30S particle | |
NECFGCCN_01404 | 7.7e-73 | holD | 2.7.7.7 | L | DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity. The exact function of the psi subunit is | |
NECFGCCN_01405 | 3.7e-73 | rimI | 2.3.1.128, 2.3.1.234 | K | This enzyme acetylates the N-terminal alanine of ribosomal protein S18 | |
NECFGCCN_01406 | 4.1e-124 | yjjG | 3.1.3.102, 3.1.3.104, 3.1.3.5, 3.8.1.2 | S | HAD-superfamily hydrolase, subfamily IA, variant 3 | |
NECFGCCN_01407 | 6.3e-309 | prfC | J | Increases the formation of ribosomal termination complexes and stimulates activities of RF-1 and RF-2. It binds guanine nucleotides and has strong preference for UGA stop codons. It may interact directly with the ribosome. The stimulation of RF- 1 and RF-2 is significantly reduced by GTP and GDP, but not by GMP | ||
NECFGCCN_01408 | 3.9e-97 | osmY | S | Periplasmic or secreted lipoprotein | ||
NECFGCCN_01409 | 1.6e-18 | ytjA | S | UPF0391 membrane protein | ||
NECFGCCN_01410 | 6.9e-40 | cah | 4.2.1.1 | P | carbonic anhydrase | |
NECFGCCN_01411 | 9e-75 | yjcF | S | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
NECFGCCN_01413 | 1.2e-29 | K | Helix-turn-helix XRE-family like proteins | |||
NECFGCCN_01414 | 1.6e-50 | S | Toxin-antitoxin system, toxin component, RelE family | |||
NECFGCCN_01415 | 0.0 | 3.2.1.25 | G | Belongs to the glycosyl hydrolase 2 family | ||
NECFGCCN_01416 | 3.8e-27 | 3.2.1.25 | G | Belongs to the glycosyl hydrolase 2 family | ||
NECFGCCN_01417 | 2.5e-158 | akr5f | S | reductase | ||
NECFGCCN_01418 | 1.3e-152 | opdE | EGP | Major facilitator Superfamily | ||
NECFGCCN_01419 | 1.9e-192 | S | Hydrolases of the alpha beta superfamily | |||
NECFGCCN_01420 | 7.9e-152 | K | Transcriptional regulator | |||
NECFGCCN_01421 | 2e-32 | |||||
NECFGCCN_01422 | 7.7e-67 | E | lactoylglutathione lyase activity | |||
NECFGCCN_01423 | 0.0 | mppA | E | ABC transporter substrate-binding protein | ||
NECFGCCN_01424 | 1.5e-137 | mpaA | E | Murein peptide amidase A | ||
NECFGCCN_01425 | 2.8e-174 | ycjG | 5.1.1.20 | M | Belongs to the mandelate racemase muconate lactonizing enzyme family | |
NECFGCCN_01426 | 2.8e-85 | tpx | 1.11.1.15 | O | Thiol-specific peroxidase that catalyzes the reduction of hydrogen peroxide and organic hydroperoxides to water and alcohols, respectively. Plays a role in cell protection against oxidative stress by detoxifying peroxides | |
NECFGCCN_01427 | 1.4e-176 | abrB | S | Ammonia monooxygenase | ||
NECFGCCN_01428 | 2.1e-293 | tyrR | K | Transcriptional regulator of aromatic amino acids metabolism | ||
NECFGCCN_01429 | 2.1e-217 | celF | 3.2.1.86 | GT4 | G | Catalyzes the fromation of N-acetyl-D-glucosamine and N-acetyl-D-glucosamine-6-phosphate from diacetylchitobiose-6-phosphate |
NECFGCCN_01430 | 5.8e-134 | K | transcriptional regulator | |||
NECFGCCN_01431 | 2.2e-67 | ycjF | S | UPF0283 membrane protein | ||
NECFGCCN_01435 | 8.2e-193 | purR | K | Is the main repressor of the genes involved in the de novo synthesis of purine nucleotides, regulating purB, purC, purEK, purF, purHD, purL, purMN and guaBA expression. PurR is allosterically activated to bind its cognate DNA by binding the purine corepressors, hypoxanthine or guanine, thereby effecting transcription repression | ||
NECFGCCN_01436 | 4.3e-178 | ydhB | K | Transcriptional regulator | ||
NECFGCCN_01437 | 1.8e-207 | ydhC | EGP | Member of the major facilitator superfamily (MFS) | ||
NECFGCCN_01438 | 1.2e-229 | cfa | 2.1.1.317, 2.1.1.79 | M | synthase | |
NECFGCCN_01439 | 1.2e-112 | ribE | 2.5.1.9 | H | Riboflavin synthase | |
NECFGCCN_01440 | 9.6e-229 | mdtK | V | Multidrug efflux pump | ||
NECFGCCN_01441 | 2.4e-136 | cnhA | 3.5.1.3 | S | Nitrilase cyanide hydratase and apolipoprotein N-acyltransferase | |
NECFGCCN_01442 | 5.9e-35 | mtnE | 2.6.1.83 | E | mutations do not affect methionine salvage in vivo however | |
NECFGCCN_01443 | 4e-43 | S | Sugar efflux transporter for intercellular exchange | |||
NECFGCCN_01446 | 3e-102 | |||||
NECFGCCN_01448 | 0.0 | clpL | O | ATP-dependent Clp protease ATP-binding subunit | ||
NECFGCCN_01449 | 1e-43 | yoeB | S | Addiction module toxin, Txe YoeB family | ||
NECFGCCN_01450 | 7.8e-39 | yefM | 2.3.1.15 | D | Antitoxin component of a toxin-antitoxin (TA) module | |
NECFGCCN_01451 | 1e-201 | ylbM | S | Belongs to the UPF0348 family | ||
NECFGCCN_01452 | 4.9e-139 | yqeM | Q | Methyltransferase domain protein | ||
NECFGCCN_01453 | 7.7e-58 | rsfS | J | Functions as a ribosomal silencing factor. Interacts with ribosomal protein L14 (rplN), blocking formation of intersubunit bridge B8. Prevents association of the 30S and 50S ribosomal subunits and the formation of functional ribosomes, thus repressing translation | ||
NECFGCCN_01454 | 2.5e-86 | entB | 3.5.1.19 | Q | Isochorismatase family | |
NECFGCCN_01455 | 5.8e-106 | nadD | 2.7.6.3, 2.7.7.18 | H | HD superfamily hydrolase involved in NAD metabolism | |
NECFGCCN_01456 | 1e-116 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
NECFGCCN_01457 | 7.7e-49 | yhbY | J | RNA-binding protein | ||
NECFGCCN_01458 | 1.6e-213 | yqeH | S | in Bacillus subtilis this enzyme appears to be involved in 30S ribosomal RNA subunit biogenesis | ||
NECFGCCN_01459 | 3e-98 | yqeG | S | hydrolase of the HAD superfamily | ||
NECFGCCN_01460 | 4.1e-127 | arnC | M | group 2 family protein | ||
NECFGCCN_01461 | 8.2e-120 | liaI | S | membrane | ||
NECFGCCN_01462 | 6.8e-75 | XK27_02470 | K | LytTr DNA-binding domain protein | ||
NECFGCCN_01463 | 1.7e-296 | KT | response to antibiotic | |||
NECFGCCN_01464 | 1.4e-98 | 3.6.3.34 | HP | COG1120 ABC-type cobalamin Fe3 -siderophores transport systems, ATPase components | ||
NECFGCCN_01465 | 8.6e-213 | P | Major facilitator superfamily | |||
NECFGCCN_01466 | 2.8e-196 | metE | 2.1.1.14 | E | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | |
NECFGCCN_01467 | 1.1e-175 | S | Domain of unknown function (DUF1852) | |||
NECFGCCN_01469 | 1.8e-187 | phoH | T | phosphate starvation-inducible protein PhoH | ||
NECFGCCN_01473 | 0.0 | metG | 6.1.1.10, 6.1.1.20 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
NECFGCCN_01474 | 5.2e-161 | S | reductase | |||
NECFGCCN_01475 | 4e-107 | K | transcriptional regulator (lysR family) | |||
NECFGCCN_01477 | 1.6e-271 | cioA | 1.10.3.14 | C | oxidase, subunit | |
NECFGCCN_01478 | 8.2e-165 | katN | P | Mn-containing catalase | ||
NECFGCCN_01479 | 2.5e-86 | yciE | S | protein conserved in bacteria | ||
NECFGCCN_01480 | 2.1e-77 | yciF | S | protein conserved in bacteria | ||
NECFGCCN_01483 | 9.5e-233 | ybdR | 1.1.1.14 | E | COG1063 Threonine dehydrogenase and related Zn-dependent dehydrogenases | |
NECFGCCN_01484 | 2.6e-38 | MA20_39405 | S | protein conserved in bacteria | ||
NECFGCCN_01485 | 3.4e-52 | yqjZ | S | Antibiotic biosynthesis monooxygenase | ||
NECFGCCN_01486 | 1.6e-53 | M | domain protein | |||
NECFGCCN_01487 | 7.7e-123 | K | DNA-binding helix-turn-helix protein | |||
NECFGCCN_01488 | 1.6e-157 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
NECFGCCN_01489 | 1.9e-145 | XK27_08050 | O | HflC and HflK could regulate a protease | ||
NECFGCCN_01490 | 1.5e-70 | gloA | 4.4.1.5 | E | Lactoylglutathione lyase | |
NECFGCCN_01491 | 2.7e-227 | sufS | 2.8.1.7, 4.4.1.16 | E | Cysteine desulfurases mobilize the sulfur from L- cysteine to yield L-alanine, an essential step in sulfur metabolism for biosynthesis of a variety of sulfur-containing biomolecules. Component of the suf operon, which is activated and required under specific conditions such as oxidative stress and iron limitation. Acts as a potent selenocysteine lyase in vitro, that mobilizes selenium from L-selenocysteine. Selenocysteine lyase activity is however unsure in vivo | |
NECFGCCN_01492 | 4.2e-71 | sufE | 2.8.1.7, 4.4.1.16 | S | PFAM Fe-S metabolism associated SufE | |
NECFGCCN_01493 | 1.8e-176 | ycfS | M | ErfK YbiS YcfS YnhG family protein | ||
NECFGCCN_01494 | 1.3e-16 | lpp | M | Lipoprotein leucine-zipper | ||
NECFGCCN_01495 | 1.2e-258 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
NECFGCCN_01496 | 2e-29 | ydhZ | S | fumarate hydratase activity | ||
NECFGCCN_01497 | 2.4e-110 | nicS | K | transcriptional regulator | ||
NECFGCCN_01498 | 1.3e-193 | ilvC | 1.1.1.86 | H | Involved in the biosynthesis of branched-chain amino acids (BCAA). Catalyzes an alkyl-migration followed by a ketol- acid reduction of (S)-2-acetolactate (S2AL) to yield (R)-2,3- dihydroxy-isovalerate. In the isomerase reaction, S2AL is rearranged via a Mg-dependent methyl migration to produce 3- hydroxy-3-methyl-2-ketobutyrate (HMKB). In the reductase reaction, this 2-ketoacid undergoes a metal-dependent reduction by NADPH to yield (R)-2,3-dihydroxy-isovalerate | |
NECFGCCN_01499 | 2.2e-76 | ilvN | 2.2.1.6 | E | Acetolactate synthase | |
NECFGCCN_01500 | 0.0 | ilvB | 2.2.1.6 | EH | Acetolactate synthase | |
NECFGCCN_01501 | 0.0 | ilvD | 4.2.1.9 | E | Belongs to the IlvD Edd family | |
NECFGCCN_01502 | 4.2e-303 | yloV | S | kinase related to dihydroxyacetone kinase | ||
NECFGCCN_01503 | 1.4e-57 | asp | S | cog cog1302 | ||
NECFGCCN_01504 | 3.3e-223 | norN | V | Mate efflux family protein | ||
NECFGCCN_01505 | 2.8e-274 | thrC | 4.2.3.1 | E | Threonine synthase | |
NECFGCCN_01508 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
NECFGCCN_01509 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
NECFGCCN_01510 | 2.5e-258 | treC | 3.2.1.93 | GH13 | G | COG0366 Glycosidases |
NECFGCCN_01511 | 1.5e-95 | ywlG | S | Belongs to the UPF0340 family | ||
NECFGCCN_01514 | 1.4e-179 | bioF | 2.3.1.47, 2.8.1.6 | H | Catalyzes the decarboxylative condensation of pimeloyl- acyl-carrier protein and L-alanine to produce 8-amino-7- oxononanoate (AON), acyl-carrier protein , and carbon dioxide | |
NECFGCCN_01515 | 1.9e-130 | bioC | 2.1.1.197 | H | Converts the free carboxyl group of a malonyl-thioester to its methyl ester by transfer of a methyl group from S-adenosyl- L-methionine (SAM). It allows to synthesize pimeloyl-ACP via the fatty acid synthetic pathway | |
NECFGCCN_01516 | 2e-121 | bioD | 6.3.3.3 | H | Catalyzes a mechanistically unusual reaction, the ATP- dependent insertion of CO2 between the N7 and N8 nitrogen atoms of 7,8-diaminopelargonic acid (DAPA) to form an ureido ring | |
NECFGCCN_01517 | 7.5e-132 | urtE | E | ABC transporter ATP-binding protein | ||
NECFGCCN_01518 | 0.0 | uvrB | L | damaged site, the DNA wraps around one UvrB monomer. DNA wrap is dependent on ATP binding by UvrB and probably causes local melting of the DNA helix, facilitating insertion of UvrB beta-hairpin between the DNA strands. Then UvrB probes one DNA strand for the presence of a lesion. If a lesion is found the UvrA subunits dissociate and the UvrB-DNA preincision complex is formed. This complex is subsequently bound by UvrC and the second UvrB is released. If no lesion is found, the DNA wraps around the other UvrB subunit that will check the other stand for damage | ||
NECFGCCN_01520 | 3.3e-192 | basS | 2.7.13.3 | T | Sensor protein basS | |
NECFGCCN_01521 | 1.4e-119 | T | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
NECFGCCN_01522 | 8.3e-296 | eptA | 2.7.8.42, 2.7.8.43 | S | membrane-associated metal-dependent hydrolase | |
NECFGCCN_01523 | 1.7e-162 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
NECFGCCN_01524 | 1e-190 | moaA | 4.1.99.22 | H | Catalyzes the cyclization of GTP to (8S)-3',8-cyclo-7,8- dihydroguanosine 5'-triphosphate | |
NECFGCCN_01525 | 1.6e-88 | moaB | 2.7.7.75 | H | May be involved in the biosynthesis of molybdopterin | |
NECFGCCN_01526 | 2.2e-82 | moaC | 4.6.1.17 | H | Catalyzes the conversion of (8S)-3',8-cyclo-7,8- dihydroguanosine 5'-triphosphate to cyclic pyranopterin monophosphate (cPMP) | |
NECFGCCN_01527 | 2.2e-35 | moaD | 2.7.7.77, 2.8.1.12 | H | Involved in sulfur transfer in the conversion of molybdopterin precursor Z to molybdopterin | |
NECFGCCN_01528 | 1.4e-80 | moaE | 2.8.1.12 | H | Molybdopterin converting factor, large subunit | |
NECFGCCN_01529 | 1.6e-118 | ybhL | S | Belongs to the BI1 family | ||
NECFGCCN_01530 | 2.5e-138 | 2.4.2.3 | F | Phosphorylase superfamily | ||
NECFGCCN_01531 | 5.2e-44 | gph | 3.1.3.18 | S | HAD hydrolase, family IA, variant 1 | |
NECFGCCN_01533 | 1.6e-15 | L | Transposase, IS605 OrfB family | |||
NECFGCCN_01534 | 2.2e-101 | |||||
NECFGCCN_01536 | 1.5e-201 | htrA | 3.4.21.107 | O | Trypsin-like serine proteases, typically periplasmic, contain C-terminal PDZ domain' | |
NECFGCCN_01537 | 1.6e-132 | parB | K | Belongs to the ParB family | ||
NECFGCCN_01538 | 2.2e-148 | rrmJ | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
NECFGCCN_01539 | 4e-156 | ispA | 2.5.1.1, 2.5.1.10, 2.5.1.29, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
NECFGCCN_01540 | 4.6e-29 | xseB | 3.1.11.6 | L | Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides | |
NECFGCCN_01541 | 2.8e-233 | xseA | 3.1.11.6 | L | Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides | |
NECFGCCN_01543 | 3.2e-112 | nth | 4.2.99.18 | L | DNA repair enzyme that has both DNA N-glycosylase activity and AP-lyase activity. The DNA N-glycosylase activity releases various damaged pyrimidines from DNA by cleaving the N- glycosidic bond, leaving an AP (apurinic apyrimidinic) site. The AP-lyase activity cleaves the phosphodiester bond 3' to the AP site by a beta-elimination, leaving a 3'-terminal unsaturated sugar and a product with a terminal 5'-phosphate | |
NECFGCCN_01544 | 2.7e-123 | dnaD | ||||
NECFGCCN_01545 | 6.7e-181 | metA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to L- homoserine, forming acetyl-L-homoserine | |
NECFGCCN_01546 | 4.9e-93 | apt | 2.4.2.7 | F | Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis | |
NECFGCCN_01547 | 2.4e-104 | recJ | L | Single-strand DNA-specific exonuclease, C terminal domain | ||
NECFGCCN_01548 | 7.2e-89 | fruA | 3.2.1.1, 3.2.1.26, 3.2.1.65, 3.2.1.80 | GH13,GH32 | G | Belongs to the glycosyl hydrolase 32 family |
NECFGCCN_01549 | 2.5e-77 | urtC | E | Belongs to the binding-protein-dependent transport system permease family | ||
NECFGCCN_01550 | 5.5e-144 | urtD | E | abc transporter atp-binding protein | ||
NECFGCCN_01551 | 5.4e-127 | urtE | E | ABC transporter ATP-binding protein | ||
NECFGCCN_01552 | 4.4e-80 | K | Transcriptional | |||
NECFGCCN_01553 | 1.6e-208 | ydeE | EGP | Major facilitator Superfamily | ||
NECFGCCN_01554 | 2.1e-152 | eamA | EG | of the drug metabolite transporter (DMT) superfamily | ||
NECFGCCN_01555 | 2.5e-30 | marB | S | Multiple antibiotic resistance | ||
NECFGCCN_01556 | 1.8e-65 | marA | K | Transcriptional activator of genes involved in the multiple antibiotic resistance (Mar) phenotype | ||
NECFGCCN_01557 | 5e-75 | marR | K | transcriptional regulator | ||
NECFGCCN_01559 | 3.4e-115 | marC | U | UPF0056 membrane protein | ||
NECFGCCN_01560 | 9.3e-204 | sotB | EGP | Major facilitator Superfamily | ||
NECFGCCN_01561 | 3.3e-25 | yddE | S | phenazine biosynthesis protein PhzF | ||
NECFGCCN_01562 | 1.1e-81 | yfnA | E | amino acid | ||
NECFGCCN_01563 | 6.8e-51 | XK27_01300 | S | ASCH | ||
NECFGCCN_01564 | 3.7e-24 | sasH | 3.1.3.5, 3.6.1.45 | F | Belongs to the 5'-nucleotidase family | |
NECFGCCN_01565 | 2.5e-66 | sasH | 3.1.3.5, 3.6.1.45 | F | Belongs to the 5'-nucleotidase family | |
NECFGCCN_01566 | 8.5e-63 | glnR | K | Transcriptional regulator | ||
NECFGCCN_01567 | 2.5e-86 | S | Fusaric acid resistance protein-like | |||
NECFGCCN_01568 | 1.7e-221 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
NECFGCCN_01569 | 2.4e-114 | |||||
NECFGCCN_01570 | 7.1e-181 | gap | 1.2.1.12 | C | Glyceraldehyde 3-phosphate dehydrogenase, C-terminal domain | |
NECFGCCN_01571 | 0.0 | fusA | J | Catalyzes the GTP-dependent ribosomal translocation step during translation elongation. During this step, the ribosome changes from the pre-translocational (PRE) to the post- translocational (POST) state as the newly formed A-site-bound peptidyl-tRNA and P-site-bound deacylated tRNA move to the P and E sites, respectively. Catalyzes the coordinated movement of the two tRNA molecules, the mRNA and conformational changes in the ribosome | ||
NECFGCCN_01572 | 3.9e-81 | rpsG | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the head domain of the 30S subunit. Is located at the subunit interface close to the decoding center, probably blocks exit of the E-site tRNA | ||
NECFGCCN_01573 | 2.3e-69 | rpsL | J | Interacts with and stabilizes bases of the 16S rRNA that are involved in tRNA selection in the A site and with the mRNA backbone. Located at the interface of the 30S and 50S subunits, it traverses the body of the 30S subunit contacting proteins on the other side and probably holding the rRNA structure together. The combined cluster of proteins S8, S12 and S17 appears to hold together the shoulder and platform of the 30S subunit | ||
NECFGCCN_01574 | 4e-142 | purR | 2.4.2.7 | F | operon repressor | |
NECFGCCN_01575 | 2.2e-176 | cbf | S | 3'-5' exoribonuclease yhaM | ||
NECFGCCN_01576 | 6.3e-147 | rmuC | S | RmuC domain protein | ||
NECFGCCN_01577 | 2.8e-102 | tag | 3.2.2.20 | L | 3-methyladenine DNA glycosylase | |
NECFGCCN_01578 | 3e-102 | ruvA | 3.6.4.12 | L | The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing. RuvA stimulates, in the presence of DNA, the weak ATPase activity of RuvB | |
NECFGCCN_01580 | 0.0 | mutL | L | This protein is involved in the repair of mismatches in DNA. It is required for dam-dependent methyl-directed DNA mismatch repair. May act as a molecular matchmaker , a protein that promotes the formation of a stable complex between two or more DNA-binding proteins in an ATP-dependent manner without itself being part of a final effector complex | ||
NECFGCCN_01582 | 1.6e-68 | K | LytTr DNA-binding domain | |||
NECFGCCN_01583 | 2.5e-77 | S | Protein of unknown function (DUF3021) | |||
NECFGCCN_01584 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
NECFGCCN_01585 | 3.4e-53 | ymcA | 3.6.3.21 | S | Belongs to the UPF0342 family | |
NECFGCCN_01586 | 3.4e-68 | argR | K | Regulates arginine biosynthesis genes | ||
NECFGCCN_01587 | 0.0 | argS | 6.1.1.19 | J | Catalyzes a two-step reaction, first charging an arginine molecule by linking its carboxyl group to the alpha-phosphate of ATP, followed by transfer of the aminoacyl-adenylate to its tRNA | |
NECFGCCN_01588 | 9.6e-247 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
NECFGCCN_01589 | 1.9e-33 | |||||
NECFGCCN_01590 | 2.8e-217 | L | Reverse transcriptase (RNA-dependent DNA polymerase) | |||
NECFGCCN_01591 | 5.2e-198 | purK | 6.3.4.18 | F | Catalyzes the ATP-dependent conversion of 5- aminoimidazole ribonucleotide (AIR) and HCO(3)(-) to N5- carboxyaminoimidazole ribonucleotide (N5-CAIR) | |
NECFGCCN_01592 | 9.1e-81 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
NECFGCCN_01593 | 2.7e-238 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
NECFGCCN_01594 | 2.1e-20 | D | Plasmid stabilization system | |||
NECFGCCN_01595 | 3.3e-14 | XK27_10545 | ||||
NECFGCCN_01596 | 1.5e-155 | S | CHAP domain | |||
NECFGCCN_01597 | 3.2e-101 | S | abc transporter atp-binding protein | |||
NECFGCCN_01598 | 4.7e-25 | M | Right handed beta helix region | |||
NECFGCCN_01599 | 9.4e-77 | dexB | 3.2.1.10, 3.2.1.70 | GH13 | G | COG0366 Glycosidases |
NECFGCCN_01600 | 8.9e-152 | galR | K | Transcriptional regulator | ||
NECFGCCN_01601 | 1e-57 | yqeF | 2.3.1.9 | I | Catalyzes the final step of fatty acid oxidation in which acetyl-CoA is released and the CoA ester of a fatty acid two carbons shorter is formed | |
NECFGCCN_01602 | 1.2e-155 | allS_3 | K | Transcriptional regulator | ||
NECFGCCN_01603 | 4.1e-75 | YPO2978 | S | PFAM transmembrane pair domain protein | ||
NECFGCCN_01604 | 2.3e-218 | yqeG | E | transporter | ||
NECFGCCN_01605 | 4e-156 | ydbC | 1.1.1.65 | C | oxidoreductase | |
NECFGCCN_01606 | 2.1e-126 | ycgR | M | Acts as a flagellar brake, regulating swimming and swarming in a bis-(3'-5') cyclic diguanylic acid (c-di-GMP)- dependent manner. Binds 1 c-di-GMP dimer per subunit. Increasing levels of c-di-GMP lead to decreased motility | ||
NECFGCCN_01607 | 2.3e-91 | rcsV | K | COG2197 Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
NECFGCCN_01608 | 7.9e-126 | yhjH | 3.1.4.52 | T | Diguanylate phosphodiesterase | |
NECFGCCN_01609 | 1.4e-118 | NU | Fimbrial protein | |||
NECFGCCN_01610 | 7.3e-178 | NU | Fimbrial protein | |||
NECFGCCN_01611 | 0.0 | htrE | NU | Outer membrane usher protein | ||
NECFGCCN_01612 | 2.3e-125 | focC | M | Pili and flagellar-assembly chaperone, PapD N-terminal domain | ||
NECFGCCN_01613 | 4.2e-104 | NU | Fimbrial protein | |||
NECFGCCN_01614 | 3.8e-28 | S | Protein of unknown function (DUF1471) | |||
NECFGCCN_01615 | 5.6e-153 | pecM | EG | of the drug metabolite transporter (DMT) superfamily | ||
NECFGCCN_01616 | 6.5e-82 | K | transcriptional regulator | |||
NECFGCCN_01617 | 5.8e-148 | nicO | U | Belongs to the NiCoT transporter (TC 2.A.52) family | ||
NECFGCCN_01618 | 2.1e-111 | fimB | K | FimB is one of the 2 regulatory proteins which control the phase variation of type 1 fimbriae in E.coli. These proteins mediate the periodic inversion of a 300bp DNA segment that harbors the promoter for the fimbrial structural gene, fimA. FimB switches fimA on | ||
NECFGCCN_01619 | 1.6e-106 | fimE | K | FimE is one of the 2 regulatory proteins which control the phase variation of type 1 fimbriae in E.coli. These proteins mediate the periodic inversion of a 300bp DNA segment that harbors the promoter for the fimbrial structural gene, fimA. FimE switches fimA off | ||
NECFGCCN_01620 | 8.9e-173 | P | (ABC) transporter | |||
NECFGCCN_01621 | 1.2e-46 | ydbM | I | acyl-CoA dehydrogenase | ||
NECFGCCN_01622 | 6.9e-78 | S | reductase | |||
NECFGCCN_01624 | 8.6e-287 | ahpF | O | alkyl hydroperoxide reductase | ||
NECFGCCN_01625 | 4.2e-106 | ahpC | 1.11.1.15 | O | alkyl hydroperoxide reductase | |
NECFGCCN_01626 | 7.4e-138 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
NECFGCCN_01627 | 1e-182 | tsf | J | Associates with the EF-Tu.GDP complex and induces the exchange of GDP to GTP. It remains bound to the aminoacyl-tRNA.EF- Tu.GTP complex up to the GTP hydrolysis stage on the ribosome | ||
NECFGCCN_01628 | 1.6e-82 | S | Putative small multi-drug export protein | |||
NECFGCCN_01629 | 2e-74 | ctsR | K | Belongs to the CtsR family | ||
NECFGCCN_01630 | 0.0 | clpC | O | Belongs to the ClpA ClpB family | ||
NECFGCCN_01631 | 6.7e-229 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
NECFGCCN_01632 | 9.9e-225 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
NECFGCCN_01633 | 0.0 | pnp | 2.7.7.8 | J | Involved in mRNA degradation. Catalyzes the phosphorolysis of single-stranded polyribonucleotides processively in the 3'- to 5'-direction | |
NECFGCCN_01634 | 3.1e-122 | dacA | 2.7.7.85 | S | Catalyzes the condensation of 2 ATP molecules into cyclic di-AMP (c-di-AMP), a second messenger used to regulate differing processes in different bacteria | |
NECFGCCN_01635 | 1.1e-162 | ybbR | S | Protein conserved in bacteria | ||
NECFGCCN_01636 | 9.7e-250 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
NECFGCCN_01637 | 5.1e-27 | gtrA | S | GtrA-like protein | ||
NECFGCCN_01639 | 2e-88 | ybhB | S | PFAM PEBP family protein | ||
NECFGCCN_01640 | 6.9e-245 | bioA | 2.6.1.62 | H | Catalyzes the transfer of the alpha-amino group from S- adenosyl-L-methionine (SAM) to 7-keto-8-aminopelargonic acid (KAPA) to form 7,8-diaminopelargonic acid (DAPA). It is the only animotransferase known to utilize SAM as an amino donor | |
NECFGCCN_01641 | 1.4e-195 | bioB | 2.8.1.6 | H | Catalyzes the conversion of dethiobiotin (DTB) to biotin by the insertion of a sulfur atom into dethiobiotin via a radical- based mechanism | |
NECFGCCN_01642 | 2.7e-202 | proB | 2.7.2.11 | E | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
NECFGCCN_01643 | 6.1e-214 | proA | 1.2.1.41 | E | Catalyzes the NADPH-dependent reduction of L-glutamate 5-phosphate into L-glutamate 5-semialdehyde and phosphate. The product spontaneously undergoes cyclization to form 1-pyrroline-5- carboxylate | |
NECFGCCN_01645 | 6.8e-67 | intS | L | Belongs to the 'phage' integrase family | ||
NECFGCCN_01648 | 4.2e-140 | I | radical SAM domain protein | |||
NECFGCCN_01649 | 6.9e-50 | |||||
NECFGCCN_01650 | 2e-165 | T | Nacht domain | |||
NECFGCCN_01651 | 4.5e-192 | T | Restriction endonuclease | |||
NECFGCCN_01653 | 0.0 | pknK | 2.7.11.1 | K | Positively regulates the transcription of the maltose regulon whose gene products are responsible for uptake and catabolism of malto-oligosaccharides. Binds and recognizes a DNA motif (called the malT box) 5'-GGA TG GA-3' | |
NECFGCCN_01654 | 4.8e-179 | acoA | C | dehydrogenase e1 component | ||
NECFGCCN_01655 | 3e-187 | acoB | C | COG0022 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, beta subunit | ||
NECFGCCN_01656 | 1.6e-253 | acoC | 2.3.1.12 | C | COG0508 Pyruvate 2-oxoglutarate dehydrogenase complex, dihydrolipoamide acyltransferase (E2) component, and related enzymes | |
NECFGCCN_01657 | 9e-251 | lpdA | 1.8.1.4 | C | COG1249 Pyruvate 2-oxoglutarate dehydrogenase complex, dihydrolipoamide dehydrogenase (E3) component, and related enzymes | |
NECFGCCN_01658 | 1.7e-35 | S | Putative zinc ribbon domain | |||
NECFGCCN_01659 | 4e-139 | 4.1.2.13 | G | Involved in the degradation of phospho-AI-2, thereby terminating induction of the lsr operon and closing the AI-2 signaling cycle. Catalyzes the transfer of an acetyl moiety from 3-hydroxy-5-phosphonooxypentane-2,4-dione to CoA to form glycerone phosphate and acetyl-CoA | ||
NECFGCCN_01660 | 2.1e-94 | glpP | K | Glycerol-3-phosphate responsive antiterminator | ||
NECFGCCN_01661 | 1.7e-271 | 2.7.1.53 | G | Belongs to the FGGY kinase family | ||
NECFGCCN_01662 | 9e-128 | IQ | reductase | |||
NECFGCCN_01663 | 4.4e-167 | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | ||
NECFGCCN_01664 | 1.9e-223 | gatC | G | system Galactitol-specific IIC component | ||
NECFGCCN_01665 | 1.6e-117 | 2.5.1.18 | O | Glutathione S-Transferase | ||
NECFGCCN_01666 | 4e-136 | M | Methyltransferase domain | |||
NECFGCCN_01667 | 1.6e-39 | yjhX | S | Belongs to the UPF0386 family | ||
NECFGCCN_01668 | 2.1e-185 | csiD | C | May be involved in the control of utilization of gamma- aminobutyric acid | ||
NECFGCCN_01669 | 1.4e-237 | lhgO | S | L-2-hydroxyglutarate oxidase LhgO | ||
NECFGCCN_01670 | 3.5e-274 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | belongs to the aldehyde dehydrogenase family | |
NECFGCCN_01671 | 1e-240 | gabT | 2.6.1.19, 2.6.1.22, 2.6.1.48 | E | Belongs to the class-III pyridoxal-phosphate-dependent aminotransferase family | |
NECFGCCN_01672 | 3.9e-254 | gabP | E | Gamma-aminobutyrate | ||
NECFGCCN_01673 | 2.6e-118 | csiR | K | Transcriptional | ||
NECFGCCN_01674 | 1.6e-50 | |||||
NECFGCCN_01675 | 2.8e-165 | K | Transcriptional regulator | |||
NECFGCCN_01676 | 6.4e-190 | pld1 | 1.1.1.122 | C | Aldo Keto reductase | |
NECFGCCN_01677 | 7.7e-138 | IQ | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
NECFGCCN_01678 | 1.6e-70 | S | Polyketide cyclase / dehydrase and lipid transport | |||
NECFGCCN_01679 | 1.5e-23 | S | Protein of unknown function (DUF1471) | |||
NECFGCCN_01680 | 8.7e-74 | crl | K | Binds to the sigma-S subunit of RNA polymerase, activating expression of sigma-S-regulated genes. Stimulates RNA polymerase holoenzyme formation and may bind to several other sigma factors, such as sigma-70 and sigma-32 | ||
NECFGCCN_01681 | 2.9e-248 | frsA | S | Belongs to the UPF0255 family | ||
NECFGCCN_01682 | 8.2e-84 | gpt | 2.4.2.22 | F | Acts on guanine, xanthine and to a lesser extent hypoxanthine | |
NECFGCCN_01683 | 6.3e-279 | pepD | E | aminoacyl-histidine dipeptidase | ||
NECFGCCN_01684 | 2e-74 | yafP | 5.3.1.16 | K | SOS response | |
NECFGCCN_01685 | 1.5e-197 | dinB | 2.7.7.7 | L | Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII | |
NECFGCCN_01686 | 7.5e-147 | ugpQ_1 | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
NECFGCCN_01688 | 5.7e-31 | KT | response to antibiotic | |||
NECFGCCN_01689 | 1e-215 | hemN | H | Involved in the biosynthesis of porphyrin-containing compound | ||
NECFGCCN_01690 | 1.1e-141 | fat | 3.1.2.21 | I | Acyl-ACP thioesterase | |
NECFGCCN_01691 | 8.8e-139 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
NECFGCCN_01692 | 1.8e-116 | ylfI | S | tigr01906 | ||
NECFGCCN_01693 | 3.3e-135 | hisK | 3.1.3.15 | E | Histidinol phosphatase and related hydrolases of the PHP family | |
NECFGCCN_01695 | 0.0 | cadA | 3.6.3.3, 3.6.3.5 | P | COG2217 Cation transport ATPase | |
NECFGCCN_01696 | 1.6e-61 | smtB | K | Transcriptional regulator | ||
NECFGCCN_01697 | 2.4e-51 | zupT | P | Mediates zinc uptake. May also transport other divalent cations | ||
NECFGCCN_01698 | 2.4e-75 | P | Mediates zinc uptake. May also transport other divalent cations | |||
NECFGCCN_01699 | 1.2e-42 | ydaL | S | protein conserved in bacteria | ||
NECFGCCN_01700 | 5.6e-144 | pcaR | K | transcriptional regulator | ||
NECFGCCN_01701 | 2.7e-123 | pcaI | 2.8.3.6 | I | COG1788 Acyl CoA acetate 3-ketoacid CoA transferase, alpha subunit | |
NECFGCCN_01702 | 3.4e-123 | pcaJ | 2.8.3.6 | I | COG2057 Acyl CoA acetate 3-ketoacid CoA transferase, beta subunit | |
NECFGCCN_01703 | 7.4e-84 | pcaF | 2.3.1.16, 2.3.1.174, 2.3.1.223, 2.3.1.9 | I | Catalyzes the final step of fatty acid oxidation in which acetyl-CoA is released and the CoA ester of a fatty acid two carbons shorter is formed | |
NECFGCCN_01704 | 2.5e-89 | frdC | 1.3.5.4 | C | NADH flavin oxidoreductase | |
NECFGCCN_01705 | 3.3e-127 | frdC | 1.3.5.4 | C | NADH flavin oxidoreductase | |
NECFGCCN_01706 | 1e-119 | frdC | 1.3.5.4 | C | NADH flavin | |
NECFGCCN_01707 | 2.8e-245 | ttdT | P | transporter | ||
NECFGCCN_01708 | 7.4e-283 | E | amino acid | |||
NECFGCCN_01709 | 4.9e-97 | S | Protein of unknown function (DUF3156) | |||
NECFGCCN_01710 | 4.9e-215 | hdaH | BQ | COG0123 Deacetylases, including yeast histone deacetylase and acetoin utilization protein | ||
NECFGCCN_01713 | 1.3e-11 | mliC | S | Membrane-bound lysozyme-inhibitor of c-type lysozyme | ||
NECFGCCN_01714 | 2.8e-82 | def | 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions | |
NECFGCCN_01715 | 6.5e-230 | dinF | V | Mate efflux family protein | ||
NECFGCCN_01716 | 6.4e-54 | S | Psort location CytoplasmicMembrane, score | |||
NECFGCCN_01717 | 3.1e-204 | yeaN | P | transporter | ||
NECFGCCN_01718 | 3.7e-73 | XK27_04435 | 3.5.4.5 | J | Acetyltransferase GNAT family | |
NECFGCCN_01719 | 1.5e-141 | S | hydrolases or acyltransferases (alpha beta hydrolase superfamily) | |||
NECFGCCN_01720 | 5.9e-55 | |||||
NECFGCCN_01721 | 8.7e-60 | |||||
NECFGCCN_01722 | 1.1e-49 | |||||
NECFGCCN_01723 | 1e-257 | yheS_2 | S | ATPase components of ABC transporters with duplicated ATPase domains | ||
NECFGCCN_01724 | 2e-217 | EGP | Transmembrane secretion effector | |||
NECFGCCN_01725 | 4.3e-22 | |||||
NECFGCCN_01726 | 5.1e-20 | copA | 3.6.3.54 | P | P-type ATPase | |
NECFGCCN_01727 | 9.2e-160 | T | Diguanylate cyclase | |||
NECFGCCN_01728 | 1.3e-66 | recC | 3.1.11.5 | L | A helicase nuclease that prepares dsDNA breaks (DSB) for recombinational DNA repair. Binds to DSBs and unwinds DNA via a highly rapid and processive ATP-dependent bidirectional helicase activity. Unwinds dsDNA until it encounters a Chi (crossover hotspot instigator) sequence from the 3' direction. Cuts ssDNA a few nucleotides 3' to the Chi site. The properties and activities of the enzyme are changed at Chi. The Chi-altered holoenzyme produces a long 3'-ssDNA overhang and facilitates RecA-binding to the ssDNA for homologous DNA recombination and repair. Holoenzyme degrades any linearized DNA that is unable to undergo homologous recombination. In the holoenzyme this subunit recognizes the wild- type Chi sequence, and when added to isolated RecB increases its ATP-dependent helicase processivity | |
NECFGCCN_01729 | 0.0 | ptrA | 3.4.24.55, 3.4.24.56 | O | Belongs to the peptidase M16 family | |
NECFGCCN_01730 | 0.0 | recB | 3.1.11.5, 3.6.4.12 | L | A helicase nuclease that prepares dsDNA breaks (DSB) for recombinational DNA repair. Binds to DSBs and unwinds DNA via a highly rapid and processive ATP-dependent bidirectional helicase activity. Unwinds dsDNA until it encounters a Chi (crossover hotspot instigator) sequence from the 3' direction. Cuts ssDNA a few nucleotides 3' to the Chi site. The properties and activities of the enzyme are changed at Chi. The Chi-altered holoenzyme produces a long 3'-ssDNA overhang and facilitates RecA-binding to the ssDNA for homologous DNA recombination and repair. Holoenzyme degrades any linearized DNA that is unable to undergo homologous recombination. In the holoenzyme this subunit contributes ATPase, 3'-5' helicase, exonuclease activity and loads RecA onto ssDNA | |
NECFGCCN_01731 | 0.0 | recD | 3.1.11.5 | L | A helicase nuclease that prepares dsDNA breaks (DSB) for recombinational DNA repair. Binds to DSBs and unwinds DNA via a highly rapid and processive ATP-dependent bidirectional helicase activity. Unwinds dsDNA until it encounters a Chi (crossover hotspot instigator) sequence from the 3' direction. Cuts ssDNA a few nucleotides 3' to the Chi site. The properties and activities of the enzyme are changed at Chi. The Chi-altered holoenzyme produces a long 3'-ssDNA overhang and facilitates RecA-binding to the ssDNA for homologous DNA recombination and repair. Holoenzyme degrades any linearized DNA that is unable to undergo homologous recombination. In the holoenzyme this subunit has ssDNA-dependent ATPase and 5'-3' helicase activity. When added to pre-assembled RecBC greatly stimulates nuclease activity and augments holoenzyme processivity. Negatively regulates the RecA-loading ability of RecBCD | |
NECFGCCN_01733 | 3.3e-250 | argA | 2.3.1.1, 2.7.2.8 | E | Belongs to the acetyltransferase family. ArgA subfamily | |
NECFGCCN_01734 | 2.8e-227 | amiC | 3.5.1.28 | M | N-acetylmuramoyl-L-alanine amidase | |
NECFGCCN_01735 | 8.9e-198 | cobD | 4.1.1.81 | E | decarboxylates L-threonine-O-3-phosphate to yield (R)-1-amino-2-propanol O-2-phosphate, the precursor for the linkage between the nucleotide loop and the corrin ring in cobalamin | |
NECFGCCN_01736 | 1.8e-159 | pduX | 2.7.1.177 | Q | GHMP kinase | |
NECFGCCN_01737 | 7.7e-222 | ackA | 2.7.2.1, 2.7.2.15 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
NECFGCCN_01738 | 2.3e-75 | pduV | E | utilization protein | ||
NECFGCCN_01739 | 3.8e-57 | pduU | E | propanediol utilization protein | ||
NECFGCCN_01740 | 2.2e-91 | pduT | CQ | propanediol utilization protein | ||
NECFGCCN_01741 | 2.3e-243 | rnfC | C | NADH dehydrogenase | ||
NECFGCCN_01742 | 3.6e-202 | pduQ | C | alcohol dehydrogenase | ||
NECFGCCN_01743 | 3.7e-244 | pduP | 1.2.1.87 | C | Aldehyde dehydrogenase | |
NECFGCCN_01744 | 1.2e-175 | pduO | 2.5.1.17 | S | adenosyltransferase | |
NECFGCCN_01745 | 8.2e-39 | pduN | CQ | ethanolamine utilization protein | ||
NECFGCCN_01746 | 9.7e-75 | pduM | S | propanediol utilization protein | ||
NECFGCCN_01747 | 1.3e-108 | pduL | 2.3.1.222, 2.3.1.8 | Q | Involved in 1,2-propanediol (1,2-PD) degradation by catalyzing the conversion of propanoyl-CoA to propanoyl-phosphate | |
NECFGCCN_01748 | 1.2e-60 | pduK | CQ | BMC | ||
NECFGCCN_01749 | 2.2e-39 | pduJ | CQ | Carbon dioxide concentrating mechanism carboxysome shell protein | ||
NECFGCCN_01750 | 1.5e-56 | pduH | S | Dehydratase medium subunit | ||
NECFGCCN_01751 | 0.0 | pduG | D | dehydratase | ||
NECFGCCN_01752 | 3e-90 | pduE | 4.2.1.28, 4.2.1.30 | Q | Dehydratase Small Subunit | |
NECFGCCN_01753 | 1.1e-119 | pduD | 4.2.1.28, 4.2.1.30 | Q | dehydratase, medium subunit | |
NECFGCCN_01754 | 0.0 | pduC | 4.2.1.28, 4.2.1.30 | E | Dehydratase large subunit | |
NECFGCCN_01755 | 5.2e-142 | pduB | E | may be involved in the formation of the polyhedral organelles involved in propanediol degradation | ||
NECFGCCN_01756 | 8.2e-42 | pduA | CQ | Carbon dioxide concentrating mechanism carboxysome shell protein | ||
NECFGCCN_01757 | 4.9e-148 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
NECFGCCN_01758 | 7.2e-45 | pocR | K | transcriptional regulator AraC family | ||
NECFGCCN_01759 | 8e-114 | pocR | K | transcriptional regulator AraC family | ||
NECFGCCN_01760 | 6.6e-262 | cbiA | 6.3.5.11, 6.3.5.9 | H | Catalyzes the ATP-dependent amidation of the two carboxylate groups at positions a and c of hydrogenobyrinate, using either L-glutamine or ammonia as the nitrogen source | |
NECFGCCN_01761 | 1.2e-182 | cobD | 6.3.1.10 | H | Converts cobyric acid to cobinamide by the addition of aminopropanol on the F carboxylic group | |
NECFGCCN_01762 | 1.7e-111 | cbiC | 5.4.99.60, 5.4.99.61 | H | Precorrin-8X methylmutase | |
NECFGCCN_01763 | 9.7e-211 | cbiD | 2.1.1.195 | H | Catalyzes the methylation of C-1 in cobalt-precorrin-5B to form cobalt-precorrin-6A | |
NECFGCCN_01764 | 9.1e-107 | cbiE | 2.1.1.132, 2.1.1.289 | H | Catalyzes the methylation of C-5 in cobalt-precorrin-6Y to form cobalt-precorrin-7W-a | |
NECFGCCN_01765 | 7.9e-97 | cbiT | 2.1.1.132, 2.1.1.196 | H | precorrin-6y C5,15-methyltransferase | |
NECFGCCN_01766 | 7e-144 | cobM | 1.3.1.76, 2.1.1.131, 2.1.1.133, 2.1.1.271, 3.7.1.12, 4.99.1.4 | H | Precorrin-4 C(11)-methyltransferase | |
NECFGCCN_01767 | 4.4e-189 | cbiG | 2.1.1.131, 2.1.1.133, 2.1.1.271, 3.7.1.12 | H | Cobalamin biosynthesis protein CbiG | |
NECFGCCN_01768 | 3.5e-129 | cobJ | 2.1.1.131, 2.1.1.133, 2.1.1.271, 3.7.1.12, 6.3.5.10 | H | precorrin-3B C17-methyltransferase | |
NECFGCCN_01769 | 3.2e-144 | cobK | 1.3.1.106, 1.3.1.54, 2.1.1.195 | H | reductase | |
NECFGCCN_01770 | 1.7e-145 | cbiK | 4.99.1.3 | H | Catalyzes the insertion of Co(2 ) into sirohydrochlorin | |
NECFGCCN_01771 | 1.9e-127 | cobI | 2.1.1.130, 2.1.1.151, 4.99.1.3 | H | Belongs to the precorrin methyltransferase family | |
NECFGCCN_01772 | 6.4e-131 | cbiM | P | Part of the energy-coupling factor (ECF) transporter complex CbiMNOQ involved in cobalt import | ||
NECFGCCN_01773 | 4.2e-22 | cbiN | P | Part of the energy-coupling factor (ECF) transporter complex CbiMNOQ involved in cobalt import | ||
NECFGCCN_01774 | 1.1e-116 | cbiQ | P | cobalt transport protein | ||
NECFGCCN_01775 | 1.1e-150 | cbiO | 2.1.1.195 | P | Responsible for energy coupling to the transport system | |
NECFGCCN_01776 | 3.2e-286 | cobQ | 6.3.5.10 | H | Catalyzes amidations at positions B, D, E, and G on adenosylcobyrinic A,C-diamide. NH(2) groups are provided by glutamine, and one molecule of ATP is hydrogenolyzed for each amidation | |
NECFGCCN_01777 | 8.5e-96 | cobU | 2.7.1.156, 2.7.7.62, 6.3.5.10 | H | Catalyzes ATP-dependent phosphorylation of adenosylcobinamide and addition of GMP to adenosylcobinamide phosphate | |
NECFGCCN_01778 | 6.3e-188 | cobT | 2.4.2.21, 6.3.5.11, 6.3.5.9 | F | Catalyzes the synthesis of alpha-ribazole-5'-phosphate from nicotinate mononucleotide (NAMN) and 5,6- dimethylbenzimidazole (DMB) | |
NECFGCCN_01779 | 1.5e-164 | pbpG | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
NECFGCCN_01780 | 1.9e-101 | yohC | S | Membrane | ||
NECFGCCN_01781 | 8e-89 | yohD | S | Membrane | ||
NECFGCCN_01782 | 7.1e-259 | mdtQ | MU | RND efflux system, outer membrane lipoprotein | ||
NECFGCCN_01783 | 4.3e-277 | bglB | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
NECFGCCN_01784 | 0.0 | bglF | 2.7.1.192, 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | Phosphotransferase System | |
NECFGCCN_01785 | 2.4e-150 | bglG | K | antiterminator | ||
NECFGCCN_01786 | 3.8e-270 | oprB | M | COG3659 Carbohydrate-selective porin | ||
NECFGCCN_01787 | 1.7e-176 | dusC | J | Catalyzes the synthesis of 5,6-dihydrouridine (D), a modified base found in the D-loop of most tRNAs, via the reduction of the C5-C6 double bond in target uridines. Specifically modifies U16 in tRNAs | ||
NECFGCCN_01788 | 2.4e-63 | lrgA | S | UPF0299 membrane protein | ||
NECFGCCN_01789 | 9.4e-108 | yohK | M | effector of murein hydrolase | ||
NECFGCCN_01790 | 1.7e-162 | cdd | 3.5.4.5 | F | This enzyme scavenges exogenous and endogenous cytidine and 2'-deoxycytidine for UMP synthesis | |
NECFGCCN_01791 | 1.3e-131 | sanA | S | Vancomycin high temperature exclusion protein | ||
NECFGCCN_01792 | 4.5e-175 | mglC | G | Belongs to the binding-protein-dependent transport system permease family | ||
NECFGCCN_01793 | 5.9e-288 | mglA | 3.6.3.17 | P | import. Responsible for energy coupling to the transport system | |
NECFGCCN_01794 | 2e-183 | mglB | G | Wtih MglAC is involved in the transport of beta-methylgalactoside | ||
NECFGCCN_01795 | 8.8e-187 | galS | K | transcriptional regulator | ||
NECFGCCN_01796 | 3.5e-216 | yeiB | S | Membrane | ||
NECFGCCN_01797 | 9.1e-116 | folE | 2.7.6.3, 3.5.4.16 | F | GTP cyclohydrolase | |
NECFGCCN_01798 | 1.3e-159 | yeiG | 3.1.2.12 | CE1 | S | Serine hydrolase involved in the detoxification of formaldehyde |
NECFGCCN_01799 | 0.0 | cirA | P | Receptor | ||
NECFGCCN_01800 | 4.9e-160 | ppaC | 3.6.1.1 | C | inorganic pyrophosphatase | |
NECFGCCN_01801 | 9.9e-107 | S | Domain of unknown function (DUF1803) | |||
NECFGCCN_01802 | 7.8e-102 | ygaC | J | Belongs to the UPF0374 family | ||
NECFGCCN_01803 | 5.9e-135 | recX | 2.4.1.337 | GT4 | S | Regulatory protein RecX |
NECFGCCN_01804 | 4.5e-247 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
NECFGCCN_01805 | 1.4e-192 | asnA | 6.3.1.1 | E | aspartate--ammonia ligase | |
NECFGCCN_01806 | 1.7e-257 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
NECFGCCN_01807 | 0.0 | narG | 1.7.5.1 | C | Belongs to the prokaryotic molybdopterin-containing oxidoreductase family | |
NECFGCCN_01808 | 6.6e-173 | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | |||
NECFGCCN_01809 | 3.4e-166 | bcrA | V | abc transporter atp-binding protein | ||
NECFGCCN_01810 | 4.6e-216 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
NECFGCCN_01811 | 3.6e-174 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
NECFGCCN_01812 | 0.0 | recJ | L | Single-stranded-DNA-specific exonuclease | ||
NECFGCCN_01813 | 3.1e-130 | dsbC | 5.3.4.1 | O | Required for disulfide bond formation in some periplasmic proteins. Acts by transferring its disulfide bond to other proteins and is reduced in the process | |
NECFGCCN_01814 | 3e-162 | xerD | D | recombinase XerD | ||
NECFGCCN_01815 | 3.5e-99 | fldB | C | Low-potential electron donor to a number of redox enzymes | ||
NECFGCCN_01816 | 2e-73 | ygfX | S | Membrane | ||
NECFGCCN_01817 | 1.5e-45 | sdhE | 1.3.5.1, 1.3.5.4 | S | An FAD assembly protein, which accelerates covalent attachment of the cofactor into other proteins. Plays an essential role in the assembly of succinate dehydrogenase (SDH, respiratory complex II), an enzyme complex that is a component of both the tricarboxylic acid cycle and the electron transport chain, and which couples the oxidation of succinate to fumarate with the reduction of ubiquinone (coenzyme Q) to ubiquinol. Required for flavinylation (covalent attachment of FAD) of the flavoprotein subunit SdhA of SDH | |
NECFGCCN_01818 | 3.2e-178 | ygfZ | S | Folate-binding protein involved in regulating the level of ATP-DnaA and in the modification of some tRNAs. It is probably a key factor in regulatory networks that act via tRNA modification, such as initiation of chromosomal replication | ||
NECFGCCN_01819 | 1.4e-113 | yqfA | S | protein, hemolysin III | ||
NECFGCCN_01820 | 2.4e-47 | yqfB | S | Belongs to the UPF0267 family | ||
NECFGCCN_01821 | 6.4e-131 | ybbH_1 | K | transcriptional regulator | ||
NECFGCCN_01822 | 2.8e-292 | bglA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
NECFGCCN_01823 | 3.1e-54 | scsA | S | resistance, protein | ||
NECFGCCN_01824 | 1.3e-98 | comFC | K | competence protein | ||
NECFGCCN_01825 | 1.6e-94 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
NECFGCCN_01826 | 7.9e-140 | yecS_2 | E | amino acid ABC transporter | ||
NECFGCCN_01827 | 7.4e-138 | glnH | ET | ABC transporter substrate-binding protein | ||
NECFGCCN_01828 | 7.6e-158 | K | transcriptional regulator | |||
NECFGCCN_01829 | 1.7e-176 | P | periplasmic binding protein | |||
NECFGCCN_01830 | 8.5e-177 | feuC | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
NECFGCCN_01831 | 1.9e-149 | viuD | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
NECFGCCN_01832 | 6.9e-150 | yusV | 3.6.3.34 | HP | (ABC) transporter | |
NECFGCCN_01833 | 0.0 | fecA | P | Receptor | ||
NECFGCCN_01834 | 1.3e-248 | S | LVIVD repeat | |||
NECFGCCN_01835 | 6.3e-196 | G | Sugar ABC Transporter | |||
NECFGCCN_01836 | 4e-168 | rbsC_3 | G | Belongs to the binding-protein-dependent transport system permease family | ||
NECFGCCN_01837 | 1.5e-280 | mglA_3 | 3.6.3.17 | G | (ABC) transporter | |
NECFGCCN_01838 | 5.7e-200 | gldA | 1.1.1.1, 1.1.1.6 | C | Iron-containing alcohol dehydrogenase | |
NECFGCCN_01839 | 1.1e-125 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
NECFGCCN_01840 | 3.3e-49 | relE | DJ | nuclease activity | ||
NECFGCCN_01841 | 1.5e-68 | K | transcriptional regulator | |||
NECFGCCN_01842 | 2.4e-32 | ybdD | S | Pfam:DUF466 | ||
NECFGCCN_01843 | 2.9e-185 | cstA | T | Carbon starvation protein | ||
NECFGCCN_01844 | 4.5e-291 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
NECFGCCN_01845 | 2.2e-73 | rplI | J | binds to the 23S rRNA | ||
NECFGCCN_01846 | 6.5e-246 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
NECFGCCN_01847 | 1.8e-47 | veg | S | Biofilm formation stimulator VEG | ||
NECFGCCN_01848 | 5.8e-109 | rpsD | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the body of the 30S subunit | ||
NECFGCCN_01849 | 1.1e-10 | |||||
NECFGCCN_01850 | 7.7e-53 | ypaA | M | Membrane | ||
NECFGCCN_01851 | 2.3e-93 | XK27_06935 | K | transcriptional regulator | ||
NECFGCCN_01852 | 5.4e-26 | S | Protein of unknown function (DUF4089) | |||
NECFGCCN_01853 | 1.6e-299 | ywrD | 2.3.2.2, 3.4.19.13 | M | Gamma-glutamyltransferase | |
NECFGCCN_01854 | 1.6e-149 | K | transcriptional regulator | |||
NECFGCCN_01855 | 6.2e-140 | IV02_26540 | ET | belongs to the bacterial solute-binding protein 3 family | ||
NECFGCCN_01856 | 1.2e-115 | P | amino acid ABC transporter | |||
NECFGCCN_01857 | 6.4e-114 | yecS_3 | P | amino acid ABC transporter | ||
NECFGCCN_01858 | 9.9e-132 | glnQ_2 | 3.6.3.21 | E | amino acid ABC transporter, ATP-binding protein | |
NECFGCCN_01859 | 1.1e-242 | pucG | 2.6.1.112, 2.6.1.44, 2.6.1.45, 2.6.1.51 | E | Serine-pyruvate aminotransferase archaeal aspartate aminotransferase | |
NECFGCCN_01860 | 1.3e-21 | motX | S | Sel1-like repeats. | ||
NECFGCCN_01861 | 6.7e-215 | araT | 2.6.1.1 | E | Aminotransferase | |
NECFGCCN_01862 | 9.5e-175 | prs | 2.7.6.1 | F | Involved in the biosynthesis of the central metabolite phospho-alpha-D-ribosyl-1-pyrophosphate (PRPP) via the transfer of pyrophosphoryl group from ATP to 1-hydroxyl of ribose-5-phosphate (Rib-5-P) | |
NECFGCCN_01863 | 1.9e-84 | usp | 3.5.1.28 | CBM50 | S | CHAP domain |
NECFGCCN_01864 | 1e-82 | mreD | M | rod shape-determining protein MreD | ||
NECFGCCN_01865 | 2e-58 | mreC | M | Involved in formation and maintenance of cell shape | ||
NECFGCCN_01866 | 1.8e-128 | L | Belongs to the 'phage' integrase family | |||
NECFGCCN_01868 | 3e-180 | iroB | CG | Protein of unknown function (DUF1205) | ||
NECFGCCN_01870 | 4.8e-131 | iroD | P | enterochelin esterase | ||
NECFGCCN_01875 | 4e-176 | mchC | S | Uncharacterized ACR, YdiU/UPF0061 family | ||
NECFGCCN_01876 | 6e-77 | mchD | S | RTX toxin acyltransferase family | ||
NECFGCCN_01877 | 2.8e-198 | mclA | M | Secretion Protein | ||
NECFGCCN_01878 | 0.0 | mchF | V | COG2274 ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
NECFGCCN_01880 | 1.3e-64 | CP_0355 | S | CAAX protease self-immunity | ||
NECFGCCN_01881 | 0.0 | ileS | 6.1.1.5 | J | amino acids such as valine, to avoid such errors it has two additional distinct tRNA(Ile)-dependent editing activities. One activity is designated as 'pretransfer' editing and involves the hydrolysis of activated Val-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Val-tRNA(Ile) | |
NECFGCCN_01882 | 5.5e-137 | divIVA | D | Cell division initiation protein | ||
NECFGCCN_01883 | 1.1e-136 | ylmH | S | conserved protein, contains S4-like domain | ||
NECFGCCN_01884 | 9.1e-83 | sepF | D | cell septum assembly | ||
NECFGCCN_01885 | 8.1e-120 | ylmE | S | Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis | ||
NECFGCCN_01886 | 6.2e-233 | ftsZ | D | Essential cell division protein that forms a contractile ring structure (Z ring) at the future cell division site. The regulation of the ring assembly controls the timing and the location of cell division. One of the functions of the FtsZ ring is to recruit other cell division proteins to the septum to produce a new cell wall between the dividing cells. Binds GTP and shows GTPase activity | ||
NECFGCCN_01887 | 1e-222 | ftsA | D | Cell division protein that is involved in the assembly of the Z ring. May serve as a membrane anchor for the Z ring | ||
NECFGCCN_01888 | 2.2e-133 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
NECFGCCN_01889 | 3.1e-198 | murG | 2.4.1.227 | GT28 | M | Cell wall formation. Catalyzes the transfer of a GlcNAc subunit on undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide (lipid intermediate I) to form undecaprenyl-pyrophosphoryl-MurNAc- (pentapeptide)GlcNAc (lipid intermediate II) |
NECFGCCN_01890 | 9e-248 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
NECFGCCN_01891 | 9.8e-43 | hipB | K | Antitoxin component of a type II toxin-antitoxin (TA) system. Neutralizes the toxic effect of cognate toxin HipA. Also neutralizes the toxic effect of non- cognate toxin YjjJ. Binds to operator sites with the consensus sequence 5-'TATCCN(8)GGATA-3' to repress the hipBA operon promoter | ||
NECFGCCN_01892 | 2.8e-246 | hipA | 2.7.11.1 | S | protein related to capsule biosynthesis enzymes | |
NECFGCCN_01893 | 1.1e-250 | yddW | S | Lipoprotein | ||
NECFGCCN_01894 | 2.1e-180 | NU | Fimbrial protein | |||
NECFGCCN_01895 | 0.0 | NU | Usher protein | |||
NECFGCCN_01896 | 5e-125 | NU | pilus organization | |||
NECFGCCN_01897 | 1e-91 | phfS | NU | cell adhesion | ||
NECFGCCN_01899 | 4e-147 | map | 3.4.11.18 | E | Methionine aminopeptidase | |
NECFGCCN_01900 | 2.7e-32 | S | ParD-like antitoxin of type II bacterial toxin-antitoxin system | |||
NECFGCCN_01901 | 8.2e-38 | |||||
NECFGCCN_01902 | 0.0 | T | Diguanylate cyclase | |||
NECFGCCN_01903 | 1.9e-148 | besA | S | hydrolase of the alpha beta superfamily | ||
NECFGCCN_01905 | 9.1e-34 | |||||
NECFGCCN_01906 | 7.9e-76 | fruB_2 | G | phosphotransferase system, IIa | ||
NECFGCCN_01907 | 9.3e-259 | iolT | EGP | Major facilitator Superfamily | ||
NECFGCCN_01908 | 4.7e-257 | 3.2.1.122, 3.2.1.22, 3.2.1.86 | GH4,GT4 | G | 6-phospho-alpha-glucosidase | |
NECFGCCN_01909 | 7.3e-270 | 2.7.1.192, 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | PTS system | ||
NECFGCCN_01910 | 1.2e-123 | K | UTRA | |||
NECFGCCN_01911 | 1.6e-113 | S | membrane transporter protein | |||
NECFGCCN_01912 | 1.6e-27 | MA20_06395 | K | transcriptional regulator | ||
NECFGCCN_01913 | 1.4e-30 | copZ | 2.7.7.77 | P | Heavy metal-associated domain protein | |
NECFGCCN_01914 | 0.0 | copA | 3.6.3.54 | P | P-type ATPase | |
NECFGCCN_01915 | 1.6e-73 | copY | K | negative regulation of transcription, DNA-templated | ||
NECFGCCN_01917 | 4.5e-180 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dihydroxyacetone kinase | |
NECFGCCN_01918 | 2.6e-95 | dhaL | 2.7.1.121 | S | Dihydroxyacetone kinase | |
NECFGCCN_01919 | 7.9e-129 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
NECFGCCN_01920 | 1.7e-57 | S | there are four paralogs in L.lactis | |||
NECFGCCN_01921 | 2.5e-148 | gsiD | P | transport | ||
NECFGCCN_01922 | 1.9e-164 | gsiC | P | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
NECFGCCN_01923 | 1.6e-296 | gsiB | E | Extracellular solute-binding protein, family 5 | ||
NECFGCCN_01924 | 0.0 | gsiA | P | ATPase activity | ||
NECFGCCN_01925 | 1.6e-171 | iaaA | 3.4.19.5, 3.5.1.1 | E | asparaginase | |
NECFGCCN_01926 | 6.4e-232 | moeA | 2.10.1.1 | H | molybdopterin | |
NECFGCCN_01927 | 7.5e-135 | moeB | 2.7.7.73, 2.7.7.80 | H | COG0476 Dinucleotide-utilizing enzymes involved in molybdopterin and thiamine biosynthesis family 2 | |
NECFGCCN_01928 | 1.5e-169 | ybiY | 1.97.1.4 | O | Pyruvate formate lyase-activating protein | |
NECFGCCN_01929 | 0.0 | ybiW | 2.3.1.54 | C | Glycine radical enzyme that catalyzes the cleavage of a C-N bond in choline, producing trimethylamine (TMA) and acetaldehyde | |
NECFGCCN_01930 | 5.4e-147 | supH | 3.1.3.102, 3.1.3.104, 3.1.3.23 | C | Hydrolase | |
NECFGCCN_01931 | 6.5e-248 | ybiU | S | Protein of unknown function (DUF1479) | ||
NECFGCCN_01932 | 1.8e-197 | cytR_1 | K | Periplasmic binding protein LacI transcriptional regulator | ||
NECFGCCN_01933 | 6.2e-246 | exuT_1 | G | Major facilitator superfamily | ||
NECFGCCN_01934 | 0.0 | yicI | 3.2.1.20 | GH31 | G | Belongs to the glycosyl hydrolase 31 family |
NECFGCCN_01935 | 0.0 | gyrB | 5.99.1.3 | L | A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner | |
NECFGCCN_01936 | 1e-105 | 3.1.3.18 | S | IA, variant 1 | ||
NECFGCCN_01937 | 1.9e-116 | lrgB | M | Inhibits the expression or activity of extracellular murein hydrolases by interacting, possibly with LrgA, with the holin-like proteins CidA and or CidB. The LrgAB and CidAB proteins may affect the proton motive force of the membrane. May be involved in programmed cell death (PCD), possibly triggering PCD in response to antibiotics and environmental stresses | ||
NECFGCCN_01938 | 5.9e-56 | lrgA | S | Effector of murein hydrolase LrgA | ||
NECFGCCN_01940 | 5.4e-59 | arsC | 1.20.4.1 | P | Belongs to the ArsC family | |
NECFGCCN_01941 | 1.7e-71 | ogt | 2.1.1.63, 3.2.2.20 | L | methylated-DNA-[protein]-cysteine S-methyltransferase activity | |
NECFGCCN_01942 | 4.5e-219 | serA | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
NECFGCCN_01943 | 3.1e-101 | wecD | M | Acetyltransferase (GNAT) domain | ||
NECFGCCN_01944 | 5.1e-209 | serC | 2.6.1.52 | E | Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine | |
NECFGCCN_01945 | 3e-63 | GK | ROK family | |||
NECFGCCN_01946 | 4.6e-29 | Z012_07620 | 2.7.1.180 | S | protein conserved in bacteria | |
NECFGCCN_01947 | 1.6e-235 | nqrF | 1.6.5.8 | C | NQR complex catalyzes the reduction of ubiquinone-1 to ubiquinol by two successive reactions, coupled with the transport of Na( ) ions from the cytoplasm to the periplasm. The first step is catalyzed by NqrF, which accepts electrons from NADH and reduces ubiquinone-1 to ubisemiquinone by a one-electron transfer pathway | |
NECFGCCN_01948 | 7.3e-101 | nqrE | 1.6.5.8 | C | NQR complex catalyzes the reduction of ubiquinone-1 to ubiquinol by two successive reactions, coupled with the transport of Na( ) ions from the cytoplasm to the periplasm. NqrA to NqrE are probably involved in the second step, the conversion of ubisemiquinone to ubiquinol | |
NECFGCCN_01949 | 1.7e-108 | nqrD | 1.6.5.8 | C | NQR complex catalyzes the reduction of ubiquinone-1 to ubiquinol by two successive reactions, coupled with the transport of Na( ) ions from the cytoplasm to the periplasm. NqrA to NqrE are probably involved in the second step, the conversion of ubisemiquinone to ubiquinol | |
NECFGCCN_01950 | 2.2e-140 | nqrC | 1.6.5.8 | C | NQR complex catalyzes the reduction of ubiquinone-1 to ubiquinol by two successive reactions, coupled with the transport of Na( ) ions from the cytoplasm to the periplasm. NqrA to NqrE are probably involved in the second step, the conversion of ubisemiquinone to ubiquinol | |
NECFGCCN_01951 | 1.1e-234 | nqrB | 1.6.5.8 | C | NQR complex catalyzes the reduction of ubiquinone-1 to ubiquinol by two successive reactions, coupled with the transport of Na( ) ions from the cytoplasm to the periplasm. NqrA to NqrE are probably involved in the second step, the conversion of ubisemiquinone to ubiquinol | |
NECFGCCN_01952 | 1.9e-250 | nqrA | 1.6.5.8 | C | NQR complex catalyzes the reduction of ubiquinone-1 to ubiquinol by two successive reactions, coupled with the transport of Na( ) ions from the cytoplasm to the periplasm. NqrA to NqrE are probably involved in the second step, the conversion of ubisemiquinone to ubiquinol | |
NECFGCCN_01953 | 2e-140 | yafK | S | ErfK YbiS YcfS YnhG family protein | ||
NECFGCCN_01954 | 1.6e-153 | yafJ | S | glutamine amidotransferase | ||
NECFGCCN_01955 | 4.5e-103 | gmhA | 5.3.1.28 | G | Catalyzes the isomerization of sedoheptulose 7-phosphate in D-glycero-D-manno-heptose 7-phosphate | |
NECFGCCN_01956 | 0.0 | fadE | I | acyl-CoA dehydrogenase | ||
NECFGCCN_01957 | 3.7e-145 | yafV | 3.5.1.3 | S | Hydrolase | |
NECFGCCN_01958 | 5e-94 | eamB | E | LysE type translocator | ||
NECFGCCN_01959 | 6.3e-157 | yfiE | K | Transcriptional regulator | ||
NECFGCCN_01961 | 4.2e-30 | |||||
NECFGCCN_01963 | 1.7e-22 | S | dextransucrase activity | |||
NECFGCCN_01964 | 5.5e-10 | S | dextransucrase activity | |||
NECFGCCN_01965 | 4.1e-68 | pcaC | 1.1.1.31, 3.1.1.24, 4.1.1.44 | S | 4-carboxymuconolactone decarboxylase | |
NECFGCCN_01966 | 3.3e-138 | pcaD | 3.1.1.24, 3.4.11.5, 4.1.1.44 | S | 3-oxoadipate enol-lactonase | |
NECFGCCN_01967 | 7.5e-211 | pcaB | 5.5.1.2 | F | 3-carboxy-cis,cis-muconate cycloisomerase | |
NECFGCCN_01968 | 8.5e-87 | lrp | K | Transcriptional regulator | ||
NECFGCCN_01969 | 1.7e-182 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
NECFGCCN_01970 | 0.0 | cydD | V | (ABC) transporter | ||
NECFGCCN_01971 | 5.4e-298 | cydC | V | (ABC) transporter | ||
NECFGCCN_01972 | 2.9e-133 | aat | 2.3.2.6 | O | Functions in the N-end rule pathway of protein degradation where it conjugates Leu, Phe and, less efficiently, Met from aminoacyl-tRNAs to the N-termini of proteins containing an N-terminal arginine or lysine | |
NECFGCCN_01973 | 2.4e-33 | infA | J | One of the essential components for the initiation of protein synthesis. Stabilizes the binding of IF-2 and IF-3 on the 30S subunit to which N-formylmethionyl-tRNA(fMet) subsequently binds. Helps modulate mRNA selection, yielding the 30S pre- initiation complex (PIC). Upon addition of the 50S ribosomal subunit IF-1, IF-2 and IF-3 are released leaving the mature 70S translation initation complex | ||
NECFGCCN_01974 | 0.0 | clpA | O | Belongs to the ClpA ClpB family | ||
NECFGCCN_01975 | 8e-54 | clpS | S | Involved in the modulation of the specificity of the ClpAP-mediated ATP-dependent protein degradation | ||
NECFGCCN_01976 | 8.1e-37 | cspD | K | Cold shock | ||
NECFGCCN_01977 | 0.0 | macB | V | Part of the tripartite efflux system MacAB-TolC. MacB is a non-canonical ABC transporter that contains transmembrane domains (TMD), which form a pore in the inner membrane, and an ATP-binding domain (NBD), which is responsible for energy generation. Confers resistance against macrolides | ||
NECFGCCN_01978 | 3e-93 | macA | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | ||
NECFGCCN_01979 | 7.8e-59 | macA | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | ||
NECFGCCN_01980 | 0.0 | ybjD | L | ATP-dependent endonuclease of the OLD family | ||
NECFGCCN_01981 | 1e-122 | aqpZ | G | Channel that permits osmotically driven movement of water in both directions. It is involved in the osmoregulation and in the maintenance of cell turgor during volume expansion in rapidly growing cells. It mediates rapid entry or exit of water in response to abrupt changes in osmolarity | ||
NECFGCCN_01982 | 4.2e-148 | ybjE | S | membrane | ||
NECFGCCN_01983 | 0.0 | hcp | 1.7.99.1 | C | Catalyzes the reduction of hydroxylamine to form NH(3) and H(2)O | |
NECFGCCN_01984 | 2.8e-182 | hcr | C | oxidoreductase | ||
NECFGCCN_01985 | 1.7e-27 | mmuP | E | amino acid | ||
NECFGCCN_01986 | 3.9e-110 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
NECFGCCN_01987 | 2.6e-225 | clpX | O | ATP-dependent specificity component of the Clp protease. It directs the protease to specific substrates. Can perform chaperone functions in the absence of ClpP | ||
NECFGCCN_01988 | 9.7e-22 | |||||
NECFGCCN_01989 | 2.9e-90 | folA | 1.5.1.3, 1.5.1.47, 2.1.1.45, 3.5.4.12 | H | Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis | |
NECFGCCN_01990 | 2.7e-165 | thyA | 2.1.1.45 | F | Catalyzes the reductive methylation of 2'-deoxyuridine- 5'-monophosphate (dUMP) to 2'-deoxythymidine-5'-monophosphate (dTMP) while utilizing 5,10-methylenetetrahydrofolate (mTHF) as the methyl donor and reductant in the reaction, yielding dihydrofolate (DHF) as a by-product. This enzymatic reaction provides an intracellular de novo source of dTMP, an essential precursor for DNA biosynthesis | |
NECFGCCN_01991 | 5.8e-211 | mvaS | 2.3.3.10 | I | synthase | |
NECFGCCN_01992 | 1.6e-70 | paaG | 5.3.3.18 | I | Enoyl-CoA hydratase/isomerase | |
NECFGCCN_01993 | 8e-255 | paaH | 1.1.1.157, 1.1.1.35, 4.2.1.17, 5.1.2.3, 5.3.3.8 | C | 3-hydroxyacyl-CoA dehydrogenase | |
NECFGCCN_01994 | 1e-72 | paaI | Q | Phenylacetic acid degradation protein PaaD | ||
NECFGCCN_01995 | 1.5e-217 | paaJ | 2.3.1.16, 2.3.1.174, 2.3.1.223, 2.3.1.9 | I | Catalyzes the final step of fatty acid oxidation in which acetyl-CoA is released and the CoA ester of a fatty acid two carbons shorter is formed | |
NECFGCCN_01996 | 3.9e-256 | paaK | 6.2.1.30 | H | Catalyzes the activation of phenylacetic acid (PA) to phenylacetyl-CoA (PA-CoA) | |
NECFGCCN_01997 | 2.1e-174 | paaX | K | phenylacetic acid degradation operon negative regulatory protein | ||
NECFGCCN_01998 | 8.2e-84 | paaY | S | Phenylacetic acid degradation protein PaaY | ||
NECFGCCN_01999 | 1.8e-74 | S | Glutathione-dependent formaldehyde-activating | |||
NECFGCCN_02000 | 2e-106 | azoR | C | Catalyzes the reductive cleavage of azo bond in aromatic azo compounds to the corresponding amines. Requires NADH, but not NADPH, as an electron donor for its activity | ||
NECFGCCN_02001 | 0.0 | hrpA | 3.6.4.13 | L | ATP-dependent helicase hrpA | |
NECFGCCN_02002 | 1.7e-125 | mdmC | 2.1.1.104 | H | Methyltransferase domain | |
NECFGCCN_02003 | 1.7e-185 | oprM | M | membrane | ||
NECFGCCN_02004 | 2.9e-140 | hlyD | V | Secretion protein | ||
NECFGCCN_02005 | 6.5e-134 | EGP | Major facilitator Superfamily | |||
NECFGCCN_02006 | 7.5e-22 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
NECFGCCN_02007 | 1.7e-89 | U | ABC-2 type transporter | |||
NECFGCCN_02008 | 7.4e-92 | V | AAA domain, putative AbiEii toxin, Type IV TA system | |||
NECFGCCN_02009 | 3.4e-97 | ulaD | 4.1.1.85, 4.1.2.43 | G | Catalyzes the decarboxylation of 3-keto-L-gulonate-6-P into L-xylulose-5-P. Is involved in the anaerobic L-ascorbate utilization | |
NECFGCCN_02010 | 6.6e-81 | ulaC | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | Phosphotransferase System | |
NECFGCCN_02011 | 4e-50 | ulaB | 2.7.1.194, 2.7.1.200 | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS), a major carbohydrate active transport system, catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. The enzyme II UlaABC PTS system is involved in ascorbate transport | |
NECFGCCN_02012 | 4.2e-256 | ulaA | 2.7.1.194 | G | pts system | |
NECFGCCN_02013 | 2e-218 | ulaG | S | Probably catalyzes the hydrolysis of L-ascorbate-6-P into 3-keto-L-gulonate-6-P. Is essential for L-ascorbate utilization under anaerobic conditions | ||
NECFGCCN_02014 | 3.4e-135 | ulaR | K | transcriptional regulator | ||
NECFGCCN_02015 | 6.1e-134 | yjfP | S | esterase activity towards palmitoyl-CoA and pNP-butyrate in vitro | ||
NECFGCCN_02016 | 3.1e-50 | bsmA | S | In Escherichia coli, mutation of this gene affects biofilm maturation, stress response, and motility | ||
NECFGCCN_02017 | 4.4e-40 | yjfN | S | Protein of unknown function (DUF1471) | ||
NECFGCCN_02018 | 0.0 | aidB | I | acyl-CoA dehydrogenase | ||
NECFGCCN_02019 | 1.4e-130 | rlmB | 2.1.1.185, 2.1.1.34 | J | Specifically methylates the ribose of guanosine 2251 in 23S rRNA | |
NECFGCCN_02020 | 0.0 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
NECFGCCN_02021 | 3.9e-72 | nsrR | K | Nitric oxide-sensitive repressor of genes involved in protecting the cell against nitrosative stress. May require iron for activity | ||
NECFGCCN_02022 | 4.2e-250 | purA | 6.3.4.4 | F | Plays an important role in the de novo pathway of purine nucleotide biosynthesis. Catalyzes the first committed step in the biosynthesis of AMP from IMP | |
NECFGCCN_02023 | 3.5e-28 | yjeT | S | protein conserved in bacteria | ||
NECFGCCN_02024 | 3.1e-28 | |||||
NECFGCCN_02025 | 7.3e-92 | ameR | K | transcriptional regulator | ||
NECFGCCN_02026 | 1e-179 | GM | COG0451 Nucleoside-diphosphate-sugar epimerases | |||
NECFGCCN_02027 | 7.6e-158 | K | transcriptional regulator | |||
NECFGCCN_02028 | 4.9e-182 | P | ABC transporter substrate-binding protein | |||
NECFGCCN_02029 | 8.1e-156 | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | |||
NECFGCCN_02031 | 3.3e-95 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
NECFGCCN_02032 | 3.8e-199 | G | COG0457 FOG TPR repeat | |||
NECFGCCN_02033 | 1.9e-124 | V | abc transporter atp-binding protein | |||
NECFGCCN_02035 | 3.9e-42 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
NECFGCCN_02036 | 1.8e-47 | celC | 2.7.1.196, 2.7.1.205 | G | PTS system, cellobiose-specific IIA component | |
NECFGCCN_02037 | 1.7e-246 | celB | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
NECFGCCN_02038 | 7.4e-52 | celA | 2.7.1.196, 2.7.1.205 | G | Phosphotransferase system, lactose cellobiose-specific IIB subunit | |
NECFGCCN_02039 | 6.2e-171 | ascG_1 | K | transcriptional regulator | ||
NECFGCCN_02040 | 1.1e-253 | EGP | Major facilitator Superfamily | |||
NECFGCCN_02041 | 2e-249 | ligB | 1.13.11.57, 1.13.11.8 | S | Extradiol catechol dioxygenase that catalyzes the oxidative cleavage of substituted catechols | |
NECFGCCN_02042 | 1e-226 | K | transcriptional regulator | |||
NECFGCCN_02043 | 3.4e-140 | MA20_26640 | 4.2.1.83 | S | PFAM LmbE family protein | |
NECFGCCN_02044 | 1.2e-129 | ligK | 4.1.3.17 | H | methyltransferase | |
NECFGCCN_02045 | 6.4e-204 | fldA | 5.3.2.8 | P | protein conserved in bacteria | |
NECFGCCN_02046 | 9.5e-150 | fldX | 1.1.1.31 | I | 3-hydroxyisobutyrate dehydrogenase and related beta-hydroxyacid dehydrogenases | |
NECFGCCN_02047 | 8.1e-45 | |||||
NECFGCCN_02048 | 1.6e-155 | yicL | EG | transporter | ||
NECFGCCN_02049 | 1.2e-08 | L | Integrase core domain | |||
NECFGCCN_02050 | 6.1e-142 | acoC | 2.3.1.12, 2.3.1.61 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
NECFGCCN_02051 | 4.6e-175 | acoB | C | dehydrogenase E1 component | ||
NECFGCCN_02052 | 9e-166 | acoA | C | Acetoin dehydrogenase E1 component subunit alpha | ||
NECFGCCN_02053 | 4.3e-173 | pdhD | 1.8.1.4 | C | Dehydrogenase | |
NECFGCCN_02056 | 1.4e-11 | K | Helix-turn-helix XRE-family like proteins | |||
NECFGCCN_02057 | 3.7e-08 | WQ51_05790 | S | protein containing a divergent version of the methyl-accepting chemotaxis-like domain | ||
NECFGCCN_02058 | 1.7e-145 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
NECFGCCN_02059 | 3.4e-100 | hprK | F | Catalyzes the ATP- as well as the pyrophosphate- dependent phosphorylation of a specific serine residue in HPr, a phosphocarrier protein of the phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS). HprK P also catalyzes the pyrophosphate-producing, inorganic phosphate-dependent dephosphorylation (phosphorolysis) of seryl-phosphorylated HPr (P- Ser-HPr). The two antagonistic activities of HprK P are regulated by several intracellular metabolites, which change their concentration in response to the absence or presence of rapidly metabolisable carbon sources (glucose, fructose, etc.) in the growth medium. Therefore, by controlling the phosphorylation state of HPr, HPrK P is a sensor enzyme that plays a major role in the regulation of carbon metabolism and sugar transport it mediates carbon catabolite repression (CCR), and regulates PTS-catalyzed carbohydrate uptake and inducer exclusion | ||
NECFGCCN_02060 | 4.7e-100 | phrB | 4.1.99.3 | L | Belongs to the DNA photolyase family | |
NECFGCCN_02061 | 2.1e-49 | dtpD | U | Proton-dependent permease that transports di- and tripeptides | ||
NECFGCCN_02062 | 4.2e-98 | ynjA | S | Antioxidant protein with alkyl hydroperoxidase activity. Required for the reduction of the AhpC active site cysteine residues and for the regeneration of the AhpC enzyme activity | ||
NECFGCCN_02063 | 1.1e-122 | ydjZ | S | TVP38 TMEM64 family inner membrane protein ydjZ | ||
NECFGCCN_02064 | 4e-108 | ydjX | P | SNARE associated Golgi protein | ||
NECFGCCN_02065 | 1.2e-159 | xthA | 3.1.11.2 | L | Exodeoxyribonuclease III | |
NECFGCCN_02066 | 7.9e-235 | argD | 2.6.1.11, 2.6.1.17, 2.6.1.81 | E | aminotransferase | |
NECFGCCN_02067 | 8.3e-201 | astA | 1.2.1.71, 2.3.1.109 | E | arginine N-succinyltransferase | |
NECFGCCN_02068 | 1.3e-279 | astD | 1.2.1.71 | C | Catalyzes the NAD-dependent reduction of succinylglutamate semialdehyde into succinylglutamate | |
NECFGCCN_02069 | 2.4e-245 | astB | 3.5.3.23 | E | Catalyzes the hydrolysis of N(2)-succinylarginine into N(2)-succinylornithine, ammonia and CO(2) | |
NECFGCCN_02070 | 4.4e-188 | astE | 3.5.1.96 | E | Belongs to the AspA AstE family. Succinylglutamate desuccinylase subfamily | |
NECFGCCN_02071 | 6.8e-81 | spy | NPTU | P pilus assembly Cpx signaling pathway, periplasmic inhibitor zinc-resistance associated protein | ||
NECFGCCN_02072 | 4e-164 | cho | 2.7.7.7 | L | Nuclease subunit of the excinuclease complex | |
NECFGCCN_02073 | 7.9e-154 | nadE | 6.3.1.5 | F | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
NECFGCCN_02074 | 1.8e-56 | osmE | J | activator of ntr-like gene protein | ||
NECFGCCN_02075 | 3.2e-50 | chbB | 2.7.1.196, 2.7.1.205 | G | protein IIA transfers a phosphoryl group to IIB which then transfers the phosphoryl group to the sugar | |
NECFGCCN_02076 | 4.7e-236 | celB | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
NECFGCCN_02077 | 5.7e-53 | celC | 2.7.1.196, 2.7.1.205 | G | Phosphotransferase System | |
NECFGCCN_02078 | 5.1e-153 | chbR | K | transcriptional regulator | ||
NECFGCCN_02079 | 3.9e-259 | chbF | 3.2.1.86 | GT4 | G | Catalyzes the fromation of N-acetyl-D-glucosamine and N-acetyl-D-glucosamine-6-phosphate from diacetylchitobiose-6-phosphate |
NECFGCCN_02080 | 7.8e-132 | chbG | 2.7.1.196, 2.7.1.205, 3.5.1.105 | G | Involved in the degradation of chitin. ChbG is essential for growth on the acetylated chitooligosaccharides chitobiose and chitotriose but is dispensable for growth on cellobiose and chitosan dimer, the deacetylated form of chitobiose. Deacetylation of chitobiose-6-P and chitotriose-6-P is necessary for both the activation of the chb promoter by the regulatory protein ChbR and the hydrolysis of phosphorylated beta-glucosides by the phospho- beta-glucosidase ChbF. Catalyzes the removal of only one acetyl group from chitobiose-6-P to yield monoacetylchitobiose-6-P, the inducer of ChbR and the substrate of ChbF | |
NECFGCCN_02081 | 0.0 | katE | 1.11.1.6 | C | serves to protect cells from the toxic effects of hydrogen peroxide | |
NECFGCCN_02082 | 6.2e-41 | cedA | D | Cell division activator CedA | ||
NECFGCCN_02083 | 1e-230 | ydjN | U | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
NECFGCCN_02084 | 2.4e-112 | ydjM | S | membrane-bound metal-dependent | ||
NECFGCCN_02085 | 2.7e-132 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
NECFGCCN_02086 | 5.3e-116 | yniC | 3.1.3.23 | S | HAD-superfamily hydrolase subfamily IA, variant 3 | |
NECFGCCN_02087 | 8.1e-91 | yniB | S | Membrane | ||
NECFGCCN_02088 | 1.9e-68 | yciA | I | acyl-CoA thioester hydrolase | ||
NECFGCCN_02089 | 0.0 | P | Receptor | |||
NECFGCCN_02090 | 2.2e-229 | mtnK | 2.7.1.100 | F | Catalyzes the phosphorylation of methylthioribose into methylthioribose-1-phosphate | |
NECFGCCN_02091 | 1.6e-183 | mtnA | 4.2.1.109, 5.3.1.23 | E | Catalyzes the interconversion of methylthioribose-1- phosphate (MTR-1-P) into methylthioribulose-1-phosphate (MTRu-1- P) | |
NECFGCCN_02092 | 1.8e-242 | appA | 3.1.3.10, 3.1.3.2, 3.1.3.26 | S | Acid phosphatase | |
NECFGCCN_02093 | 2.2e-249 | uhpC_2 | G | transporter | ||
NECFGCCN_02094 | 6e-154 | 3.1.3.25 | G | inositol monophosphatase | ||
NECFGCCN_02095 | 1.6e-188 | K | transcriptional regulator | |||
NECFGCCN_02096 | 2.3e-237 | codA | 3.5.4.1, 3.5.4.21 | F | cytosine deaminase | |
NECFGCCN_02097 | 4.6e-230 | QT | transcriptional regulator | |||
NECFGCCN_02100 | 3.8e-177 | wbbI | M | transferase activity, transferring glycosyl groups | ||
NECFGCCN_02101 | 1e-184 | sacB | GT2,GT4 | M | Stealth protein CR2, conserved region 2 | |
NECFGCCN_02102 | 2.2e-215 | glf | 5.4.99.9 | M | UDP-galactopyranose mutase | |
NECFGCCN_02103 | 2.2e-244 | epsU | S | Polysaccharide biosynthesis protein | ||
NECFGCCN_02104 | 1.5e-126 | cps3F | ||||
NECFGCCN_02105 | 4.5e-49 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
NECFGCCN_02106 | 1.5e-46 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
NECFGCCN_02107 | 3.3e-129 | ydaF_2 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | ||
NECFGCCN_02108 | 5e-63 | WQ51_03320 | S | cog cog4835 | ||
NECFGCCN_02109 | 2.8e-146 | XK27_08360 | S | EDD domain protein, DegV family | ||
NECFGCCN_02110 | 2.5e-138 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
NECFGCCN_02111 | 1.1e-220 | cca | 2.7.7.19, 2.7.7.72 | J | Catalyzes the addition and repair of the essential 3'- terminal CCA sequence in tRNAs without using a nucleic acid template. Adds these three nucleotides in the order of C, C, and A to the tRNA nucleotide-73, using CTP and ATP as substrates and producing inorganic pyrophosphate | |
NECFGCCN_02112 | 0.0 | yfmR | S | abc transporter atp-binding protein | ||
NECFGCCN_02113 | 1.7e-26 | U | response to pH | |||
NECFGCCN_02114 | 3.7e-129 | 3.6.1.13, 3.6.1.55 | F | AdP-ribose pyrophosphatase | ||
NECFGCCN_02115 | 1e-209 | nadD | 2.7.1.22, 2.7.7.1, 2.7.7.18, 3.6.1.55 | H | adenylyltransferase | |
NECFGCCN_02116 | 9e-256 | gdhA | 1.4.1.4 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
NECFGCCN_02118 | 6.6e-161 | dnaX | 2.7.7.7 | L | DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
NECFGCCN_02119 | 2.2e-38 | ybaB | L | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
NECFGCCN_02120 | 3e-110 | recR | L | May play a role in DNA repair. It seems to be involved in an RecBC-independent recombinational process of DNA repair. It may act with RecF and RecO | ||
NECFGCCN_02121 | 0.0 | htpG | O | Molecular chaperone. Has ATPase activity | ||
NECFGCCN_02122 | 1.1e-115 | adk | 2.7.4.3 | F | Catalyzes the reversible transfer of the terminal phosphate group between ATP and AMP. Plays an important role in cellular energy homeostasis and in adenine nucleotide metabolism | |
NECFGCCN_02123 | 2.8e-182 | hemH | 4.99.1.1, 4.99.1.9 | H | Catalyzes the ferrous insertion into protoporphyrin IX | |
NECFGCCN_02124 | 1.5e-255 | gsk | 2.7.1.20, 2.7.1.73, 2.7.1.92 | G | COG0524 Sugar kinases, ribokinase family | |
NECFGCCN_02125 | 2.9e-296 | ybaL | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
NECFGCCN_02126 | 3.7e-216 | fsr | P | fosmidomycin resistance protein | ||
NECFGCCN_02127 | 0.0 | ushA | 3.1.3.5, 3.6.1.45 | F | Belongs to the 5'-nucleotidase family | |
NECFGCCN_02128 | 4.7e-82 | ybaK | S | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
NECFGCCN_02129 | 4.3e-149 | ybaP | S | protein conserved in bacteria | ||
NECFGCCN_02130 | 0.0 | copA | 3.6.3.54 | P | P-type atpase | |
NECFGCCN_02131 | 3.8e-72 | cueR | K | Transcriptional regulator | ||
NECFGCCN_02132 | 5.7e-77 | ybbJ | OU | Membrane protein implicated in regulation of membrane protease activity | ||
NECFGCCN_02133 | 6.8e-122 | qmcA | O | COG0330 Membrane protease subunits stomatin prohibitin homologs | ||
NECFGCCN_02134 | 1.4e-119 | ybbL | S | abc transporter atp-binding protein | ||
NECFGCCN_02135 | 6.8e-131 | ybbM | S | transport system permease component | ||
NECFGCCN_02136 | 6.1e-149 | ybbN | O | Thioredoxin | ||
NECFGCCN_02137 | 8.8e-139 | ybbO | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | ||
NECFGCCN_02138 | 2.1e-115 | tesA | 3.1.1.5 | E | COG2755 Lysophospholipase L1 and related esterases | |
NECFGCCN_02139 | 0.0 | ybbP | Q | ABC-type transport system involved in lysophospholipase L1 biosynthesis permease component | ||
NECFGCCN_02140 | 1.8e-225 | omp | M | Membrane | ||
NECFGCCN_02141 | 3.1e-220 | rgpAc | GT4 | M | group 1 family protein | |
NECFGCCN_02142 | 4.8e-76 | S | Domain of Unknown Function with PDB structure (DUF3862) | |||
NECFGCCN_02143 | 5.4e-92 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
NECFGCCN_02144 | 6.7e-251 | yeeF | E | Amino Acid | ||
NECFGCCN_02145 | 2.6e-134 | yeeY | K | transcriptional regulator | ||
NECFGCCN_02146 | 9e-158 | yeeZ | GM | COG0451 Nucleoside-diphosphate-sugar epimerases | ||
NECFGCCN_02147 | 7e-164 | hisG | 2.4.2.17 | F | Catalyzes the condensation of ATP and 5-phosphoribose 1- diphosphate to form N'-(5'-phosphoribosyl)-ATP (PR-ATP). Has a crucial role in the pathway because the rate of histidine biosynthesis seems to be controlled primarily by regulation of HisG enzymatic activity | |
NECFGCCN_02148 | 6.3e-230 | hisD | 1.1.1.23, 1.1.1.308 | E | Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine | |
NECFGCCN_02149 | 1e-193 | hisC | 1.1.1.23, 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
NECFGCCN_02150 | 1.7e-209 | hisB | 1.1.1.23, 2.6.1.9, 3.1.3.15, 3.1.3.82, 3.1.3.83, 4.2.1.19 | E | Histidine biosynthesis bifunctional protein HisB | |
NECFGCCN_02151 | 1e-110 | hisH | E | IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisH subunit provides the glutamine amidotransferase activity that produces the ammonia necessary to HisF for the synthesis of IGP and AICAR | ||
NECFGCCN_02152 | 7.4e-135 | hisA | 5.3.1.16 | E | 1-(5-phosphoribosyl)-5- (5-phosphoribosylamino)methylideneamino imidazole-4-carboxamide isomerase | |
NECFGCCN_02153 | 2.4e-144 | hisF | 3.5.4.19, 3.6.1.31 | E | IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisF subunit catalyzes the cyclization activity that produces IGP and AICAR from PRFAR using the ammonia provided by the HisH subunit | |
NECFGCCN_02154 | 8.1e-108 | hisI | 3.5.4.19, 3.5.4.25, 3.6.1.31, 5.3.1.16 | E | Catalyzes the hydrolysis of the adenine ring of phosphoribosyl-AMP | |
NECFGCCN_02155 | 1.4e-136 | M | Glycosyltransferases involved in cell wall biogenesis | |||
NECFGCCN_02156 | 1.8e-185 | wbbO | 2.4.1.52 | GT4 | M | glycosyl transferase group 1 |
NECFGCCN_02157 | 1.3e-112 | cps3B | S | Glycosyl Transferase | ||
NECFGCCN_02158 | 9.3e-201 | glf | 5.4.99.9 | M | UDP-galactopyranose mutase | |
NECFGCCN_02159 | 3.9e-305 | wbbM | M | Glycosyl Transferase | ||
NECFGCCN_02160 | 1.6e-129 | rfbB | 3.6.3.38, 3.6.3.40 | GM | ABC-type polysaccharide polyol phosphate transport system ATPase component | |
NECFGCCN_02161 | 3.9e-131 | rfbA | GM | Transport permease protein | ||
NECFGCCN_02162 | 1.3e-190 | capI | 5.1.3.6 | M | epimerase dehydratase | |
NECFGCCN_02163 | 1.4e-217 | ugd | 1.1.1.22 | M | Belongs to the UDP-glucose GDP-mannose dehydrogenase family | |
NECFGCCN_02164 | 2.3e-246 | manB | 5.4.2.2, 5.4.2.8 | G | phosphomannomutase | |
NECFGCCN_02165 | 1e-254 | cpsB | 2.7.7.13, 5.3.1.8 | GM | Belongs to the mannose-6-phosphate isomerase type 2 family | |
NECFGCCN_02166 | 1e-262 | gnd | 1.1.1.343, 1.1.1.44 | H | Catalyzes the oxidative decarboxylation of 6- phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NADP to NADPH | |
NECFGCCN_02167 | 9.2e-179 | wcaJ | M | Bacterial sugar transferase | ||
NECFGCCN_02168 | 2.6e-22 | 2.3.1.157, 2.3.1.79, 2.7.7.23 | S | Bacterial transferase hexapeptide (six repeats) | ||
NECFGCCN_02169 | 7.3e-08 | S | outer membrane | |||
NECFGCCN_02170 | 2.3e-111 | wzxC | S | biosynthesis protein | ||
NECFGCCN_02171 | 1e-46 | |||||
NECFGCCN_02172 | 3e-82 | M | transferase activity, transferring glycosyl groups | |||
NECFGCCN_02173 | 2.5e-86 | G | glycosyl transferase group 1 | |||
NECFGCCN_02174 | 1.2e-72 | cps4F | 2.4.1.306 | GT4 | M | Glycosyl transferase 4-like domain |
NECFGCCN_02175 | 1e-285 | wzc | D | protein involved in exopolysaccharide biosynthesis | ||
NECFGCCN_02176 | 2e-11 | etp | 3.1.3.48 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
NECFGCCN_02177 | 1.2e-208 | V | SLBB domain | |||
NECFGCCN_02178 | 5.1e-265 | S | Capsule assembly protein Wzi | |||
NECFGCCN_02179 | 1e-105 | I | COG0671 Membrane-associated phospholipid phosphatase | |||
NECFGCCN_02180 | 4.6e-163 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
NECFGCCN_02181 | 8.8e-282 | yegH | P | membrane protein, terc | ||
NECFGCCN_02182 | 0.0 | asmA | M | Protein involved in outer membrane biogenesis | ||
NECFGCCN_02183 | 1e-107 | dcd | 3.5.4.13 | F | Belongs to the dCTP deaminase family | |
NECFGCCN_02184 | 3.9e-116 | udk | 2.7.1.48 | F | Cytidine monophosphokinase | |
NECFGCCN_02185 | 9e-153 | alkA | 3.2.2.21 | L | 3-methyladenine DNA glycosylase 8-oxoguanine DNA glycosylase | |
NECFGCCN_02186 | 3.9e-251 | yegD | O | Belongs to the heat shock protein 70 family | ||
NECFGCCN_02187 | 0.0 | T | PhoQ Sensor | |||
NECFGCCN_02188 | 2.9e-120 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
NECFGCCN_02189 | 2.1e-14 | |||||
NECFGCCN_02190 | 4.7e-103 | K | response regulator | |||
NECFGCCN_02191 | 2.9e-219 | gltP | U | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
NECFGCCN_02192 | 3.6e-203 | mdtA | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | ||
NECFGCCN_02193 | 9.8e-26 | mdtB | V | Belongs to the resistance-nodulation-cell division (RND) (TC 2.A.6) family | ||
NECFGCCN_02194 | 5.8e-46 | mdtB | V | Belongs to the resistance-nodulation-cell division (RND) (TC 2.A.6) family | ||
NECFGCCN_02195 | 3.6e-28 | |||||
NECFGCCN_02197 | 9e-81 | |||||
NECFGCCN_02198 | 1.8e-58 | S | protein conserved in bacteria | |||
NECFGCCN_02199 | 7.7e-77 | K | Acetyltransferase (GNAT) family | |||
NECFGCCN_02200 | 5.2e-41 | S | Protein of unknown function (DUF1778) | |||
NECFGCCN_02201 | 3.8e-56 | |||||
NECFGCCN_02202 | 6.9e-184 | 1.6.5.5 | C | Zinc-binding dehydrogenase | ||
NECFGCCN_02203 | 1.8e-188 | lacI | K | Periplasmic binding protein LacI transcriptional regulator | ||
NECFGCCN_02204 | 0.0 | lacZ | 3.2.1.23 | G | Belongs to the glycosyl hydrolase 2 family | |
NECFGCCN_02205 | 4.8e-219 | lacY | P | LacY proton/sugar symporter | ||
NECFGCCN_02206 | 5.3e-43 | L | cog cog1662 | |||
NECFGCCN_02207 | 5.3e-46 | L | PFAM Insertion element protein | |||
NECFGCCN_02208 | 2.6e-32 | S | Protein of unknown function (DUF2534) | |||
NECFGCCN_02209 | 6.9e-307 | oprC | P | Receptor | ||
NECFGCCN_02210 | 2.5e-89 | pat | 2.3.1.183 | M | acetyltransferase | |
NECFGCCN_02211 | 4e-270 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
NECFGCCN_02212 | 0.0 | uvrC | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrC both incises the 5' and 3' sides of the lesion. The N-terminal half is responsible for the 3' incision and the C-terminal half is responsible for the 5' incision | ||
NECFGCCN_02213 | 1e-125 | yjjG | 3.1.3.102, 3.1.3.104, 3.1.3.5, 3.8.1.2 | E | hydrolase | |
NECFGCCN_02214 | 2.1e-120 | sdaAB | 4.3.1.17 | E | L-serine dehydratase | |
NECFGCCN_02215 | 7.6e-147 | sdaAA | 4.3.1.17 | E | L-serine dehydratase | |
NECFGCCN_02216 | 5.3e-90 | XK27_08140 | K | Bacterial regulatory proteins, tetR family | ||
NECFGCCN_02217 | 2.3e-99 | ypgQ | F | HD superfamily hydrolase | ||
NECFGCCN_02218 | 7.5e-128 | S | CAAX amino terminal protease family | |||
NECFGCCN_02219 | 3.2e-110 | cutC | P | Participates in the control of copper homeostasis | ||
NECFGCCN_02221 | 4.1e-21 | S | Domain of unknown function (DUF4767) | |||
NECFGCCN_02222 | 1.9e-21 | S | Domain of unknown function (DUF4300) | |||
NECFGCCN_02223 | 2.2e-108 | yvyE | 3.4.13.9 | S | YigZ family | |
NECFGCCN_02224 | 7e-167 | cysK | 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
NECFGCCN_02225 | 2.5e-110 | acuB | S | CBS domain | ||
NECFGCCN_02226 | 5.6e-124 | livF | E | COG0410 ABC-type branched-chain amino acid transport systems, ATPase component | ||
NECFGCCN_02227 | 4e-136 | livG | E | COG0411 ABC-type branched-chain amino acid transport systems, ATPase component | ||
NECFGCCN_02228 | 1.4e-138 | livM | E | Belongs to the binding-protein-dependent transport system permease family | ||
NECFGCCN_02229 | 1.2e-144 | livH | E | Belongs to the binding-protein-dependent transport system permease family | ||
NECFGCCN_02230 | 8.5e-210 | livJ | E | COG0683 ABC-type branched-chain amino acid transport systems, periplasmic component | ||
NECFGCCN_02231 | 1.9e-46 | ylbG | S | UPF0298 protein | ||
NECFGCCN_02232 | 2.4e-72 | ylbF | S | Belongs to the UPF0342 family | ||
NECFGCCN_02233 | 3.7e-105 | clpP | 3.4.21.92 | OU | Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins | |
NECFGCCN_02234 | 5.7e-112 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
NECFGCCN_02235 | 0.0 | sacB | 2.4.1.10, 2.4.1.9, 3.2.1.26 | GH32,GH68 | G | Belongs to the glycosyl hydrolase 68 family |
NECFGCCN_02236 | 2.9e-262 | XK27_07020 | S | Belongs to the UPF0371 family | ||
NECFGCCN_02238 | 4.7e-130 | dtpA | U | Proton-dependent permease that transports di- and tripeptides | ||
NECFGCCN_02240 | 1.2e-117 | nth | 4.2.99.18 | L | DNA repair enzyme that has both DNA N-glycosylase activity and AP-lyase activity. The DNA N-glycosylase activity releases various damaged pyrimidines from DNA by cleaving the N- glycosidic bond, leaving an AP (apurinic apyrimidinic) site. The AP-lyase activity cleaves the phosphodiester bond 3' to the AP site by a beta-elimination, leaving a 3'-terminal unsaturated sugar and a product with a terminal 5'-phosphate | |
NECFGCCN_02241 | 1.6e-118 | rnfE | 2.3.1.243, 4.2.99.18 | C | Part of a membrane complex involved in electron transport | |
NECFGCCN_02242 | 4.6e-114 | rnfG | C | Part of a membrane complex involved in electron transport | ||
NECFGCCN_02243 | 1.1e-192 | rnfD | 1.6.5.8 | C | Part of a membrane complex involved in electron transport | |
NECFGCCN_02244 | 8.7e-41 | L | InsA N-terminal domain | |||
NECFGCCN_02245 | 7.3e-78 | Q | Escherichia coli O157 H7 ortholog z1925 | |||
NECFGCCN_02246 | 2.3e-12 | K | luxR family | |||
NECFGCCN_02248 | 1.2e-107 | pagO | EG | EamA-like transporter family | ||
NECFGCCN_02250 | 0.0 | iroN | P | This protein is involved in the initial step of iron uptake by binding ferrienterobactin (Fe-ENT), an iron chelatin siderophore that allows E.coli to extract iron from the environment. FepA also acts as a receptor for colicins B and D | ||
NECFGCCN_02251 | 1.7e-197 | iroD | P | Domain of unknown function (DUF3327) | ||
NECFGCCN_02252 | 0.0 | iroC | V | Involved in lipid A export and possibly also in glycerophospholipid export and for biogenesis of the outer membrane. Transmembrane domains (TMD) form a pore in the inner membrane and the ATP-binding domain (NBD) is responsible for energy generation | ||
NECFGCCN_02253 | 1.1e-198 | iroB | CG | Protein of unknown function (DUF1205) | ||
NECFGCCN_02254 | 3.6e-109 | ibrB | K | ParB-like nuclease domain | ||
NECFGCCN_02255 | 2.2e-240 | ibrA | S | Domain of unknown function (DUF3440) | ||
NECFGCCN_02256 | 3.8e-20 | L | PFAM transposase IS66 | |||
NECFGCCN_02257 | 1.8e-17 | hokB | S | Hok/gef family | ||
NECFGCCN_02261 | 1.5e-118 | S | PAAR repeat-containing protein | |||
NECFGCCN_02263 | 1.6e-12 | L | Transposase | |||
NECFGCCN_02264 | 6.9e-192 | mcrB | L | restriction endonuclease | ||
NECFGCCN_02265 | 7.8e-47 | ykfI | S | Toxic component of a toxin-antitoxin (TA) system. Overexpression results in inhibition of growth in liquid cultures and a decrease in colony formation | ||
NECFGCCN_02266 | 2e-55 | yeeU | S | CbeA_antitoxin, type IV, cytoskeleton bundling-enhancing factor A | ||
NECFGCCN_02267 | 2.5e-92 | radC | L | RadC-like JAB domain | ||
NECFGCCN_02268 | 4.1e-80 | S | Antirestriction protein | |||
NECFGCCN_02269 | 7.4e-152 | S | Domain of unknown function (DUF932) | |||
NECFGCCN_02270 | 1.8e-70 | ykfB | ||||
NECFGCCN_02271 | 9.2e-24 | |||||
NECFGCCN_02273 | 8.2e-131 | yfjR | K | WYL domain | ||
NECFGCCN_02274 | 1.3e-151 | S | GTP-binding protein | |||
NECFGCCN_02275 | 4.7e-15 | pdl | 3.1.1.3 | I | Lipase (class 3) | |
NECFGCCN_02276 | 6.7e-162 | |||||
NECFGCCN_02277 | 3.7e-105 | S | Inovirus Gp2 | |||
NECFGCCN_02278 | 1.5e-29 | K | Prophage CP4-57 regulatory protein (AlpA) | |||
NECFGCCN_02279 | 4.3e-112 | |||||
NECFGCCN_02280 | 8.3e-37 | S | Inovirus Gp2 | |||
NECFGCCN_02281 | 0.0 | L | DEAD-like helicases superfamily | |||
NECFGCCN_02282 | 9e-310 | |||||
NECFGCCN_02283 | 4e-219 | |||||
NECFGCCN_02284 | 0.0 | L | DNA helicase | |||
NECFGCCN_02285 | 0.0 | L | COG1205 Distinct helicase family with a unique C-terminal domain including a metal-binding cysteine cluster | |||
NECFGCCN_02286 | 0.0 | V | Type II restriction enzyme, methylase subunits | |||
NECFGCCN_02287 | 0.0 | hepA | K | Transcription regulator that activates transcription by stimulating RNA polymerase (RNAP) recycling in case of stress conditions such as supercoiled DNA or high salt concentrations. Probably acts by releasing the RNAP, when it is trapped or immobilized on tightly supercoiled DNA. Does not activate transcription on linear DNA. Probably not involved in DNA repair | ||
NECFGCCN_02288 | 0.0 | L | Helicase conserved C-terminal domain | |||
NECFGCCN_02289 | 0.0 | |||||
NECFGCCN_02290 | 1.4e-21 | |||||
NECFGCCN_02291 | 2.7e-262 | U | nuclear chromosome segregation | |||
NECFGCCN_02292 | 4.6e-118 | M | OmpA family | |||
NECFGCCN_02293 | 5.9e-189 | V | HNH nucleases | |||
NECFGCCN_02294 | 9.5e-231 | intB | L | Belongs to the 'phage' integrase family | ||
NECFGCCN_02296 | 1.8e-119 | ybcF | 4.2.1.1 | P | Reversible hydration of carbon dioxide | |
NECFGCCN_02297 | 9.8e-256 | ychM | 4.2.1.1 | P | transporter | |
NECFGCCN_02298 | 3.3e-194 | yjgB | 1.1.1.1 | S | alcohol dehydrogenase | |
NECFGCCN_02299 | 1.2e-157 | MA20_28410 | P | Binding-protein-dependent transport systems inner membrane component | ||
NECFGCCN_02300 | 8.4e-20 | MA20_28405 | P | Binding-protein-dependent transport systems inner membrane component | ||
NECFGCCN_02301 | 1.2e-126 | MA20_28405 | P | Binding-protein-dependent transport systems inner membrane component | ||
NECFGCCN_02302 | 2.6e-165 | cpdA | 2.1.2.2, 3.1.4.53 | S | Hydrolyzes cAMP to 5'-AMP. Plays an important regulatory role in modulating the intracellular concentration of cAMP, thereby influencing cAMP-dependent processes | |
NECFGCCN_02303 | 1.1e-195 | 3.6.3.20 | P | Belongs to the ABC transporter superfamily | ||
NECFGCCN_02304 | 2.2e-246 | MA20_28400 | G | Extracellular solute-binding protein | ||
NECFGCCN_02305 | 1.7e-178 | iolE | 4.2.1.44 | G | Catalyzes the dehydration of inosose (2-keto-myo- inositol, 2KMI or 2,4,6 3,5-pentahydroxycyclohexanone) to 3D- (3,5 4)-trihydroxycyclohexane-1,2-dione (D-2,3-diketo-4-deoxy-epi- inositol) | |
NECFGCCN_02306 | 5.3e-172 | iolH | G | Sugar phosphate isomerases epimerases | ||
NECFGCCN_02307 | 9e-192 | iolG | 1.1.1.18, 1.1.1.369 | S | Involved in the oxidation of myo-inositol (MI) to 2- keto-myo-inositol (2KMI or 2-inosose) | |
NECFGCCN_02308 | 0.0 | iolD | 3.7.1.22 | E | Belongs to the TPP enzyme family | |
NECFGCCN_02309 | 0.0 | iolC | 2.7.1.92 | G | 5-dehydro-2-deoxygluconokinase | |
NECFGCCN_02310 | 4.7e-149 | Z012_10240 | K | transcriptional regulator | ||
NECFGCCN_02311 | 9.6e-128 | adcB | P | ABC transporter (Permease | ||
NECFGCCN_02312 | 5.4e-135 | adcC | 3.6.3.35 | P | ABC transporter, ATP-binding protein | |
NECFGCCN_02313 | 5e-70 | adcR | K | transcriptional | ||
NECFGCCN_02314 | 2.8e-182 | dus | J | Catalyzes the synthesis of 5,6-dihydrouridine (D), a modified base found in the D-loop of most tRNAs, via the reduction of the C5-C6 double bond in target uridines | ||
NECFGCCN_02315 | 3.6e-157 | hslO | O | Redox regulated molecular chaperone. Protects both thermally unfolding and oxidatively damaged proteins from irreversible aggregation. Plays an important role in the bacterial defense system toward oxidative stress | ||
NECFGCCN_02316 | 2.7e-26 | |||||
NECFGCCN_02317 | 4.1e-189 | sufB | O | assembly protein SufB | ||
NECFGCCN_02318 | 3.2e-53 | gstR | K | transcriptional regulator | ||
NECFGCCN_02319 | 1.1e-273 | bmr3 | EGP | Major facilitator Superfamily | ||
NECFGCCN_02320 | 1.3e-114 | K | Transcriptional regulator | |||
NECFGCCN_02321 | 3.2e-71 | K | histone acetyltransferase HPA2 and related acetyltransferases | |||
NECFGCCN_02322 | 1.6e-197 | mexA | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | ||
NECFGCCN_02323 | 0.0 | mexB | V | Belongs to the resistance-nodulation-cell division (RND) (TC 2.A.6) family | ||
NECFGCCN_02324 | 4.1e-240 | ibeB | M | RND efflux system, outer membrane lipoprotein | ||
NECFGCCN_02325 | 2.8e-197 | tcaB | EGP | Major facilitator Superfamily | ||
NECFGCCN_02326 | 4.6e-131 | murQ | 4.2.1.126 | H | Specifically catalyzes the cleavage of the D-lactyl ether substituent of MurNAc 6-phosphate, producing GlcNAc 6- phosphate and D-lactate. Together with AnmK, is also required for the utilization of anhydro-N-acetylmuramic acid (anhMurNAc) either imported from the medium or derived from its own cell wall murein, and thus plays a role in cell wall recycling | |
NECFGCCN_02327 | 2e-111 | murP | 2.7.1.192, 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS), a major carbohydrate active transport system, catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. This system is involved in N-acetylmuramic acid (MurNAc) transport, yielding cytoplasmic MurNAc-6-P. Is | |
NECFGCCN_02328 | 5.9e-55 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
NECFGCCN_02329 | 1.1e-25 | amt | P | Ammonium Transporter | ||
NECFGCCN_02330 | 1e-103 | mur1 | 3.4.17.14, 3.5.1.28 | NU | amidase activity | |
NECFGCCN_02331 | 2.6e-95 | S | HD domain | |||
NECFGCCN_02332 | 1e-143 | XK27_04800 | S | Sucrose-6F-phosphate phosphohydrolase | ||
NECFGCCN_02333 | 4e-61 | S | Bacterial inner membrane protein | |||
NECFGCCN_02335 | 1.1e-107 | 3.4.17.14, 3.5.1.28 | NU | amidase activity | ||
NECFGCCN_02336 | 3.5e-294 | nptA | P | COG1283 Na phosphate symporter | ||
NECFGCCN_02337 | 2.2e-218 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
NECFGCCN_02338 | 7.7e-116 | cpsD | D | COG0489 ATPases involved in chromosome partitioning | ||
NECFGCCN_02339 | 1.6e-110 | cps4C | M | biosynthesis protein | ||
NECFGCCN_02340 | 6.8e-133 | cpsB | 3.1.3.48 | GM | Capsular polysaccharide biosynthesis protein | |
NECFGCCN_02341 | 1.2e-248 | cps4A | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
NECFGCCN_02342 | 4.9e-128 | deoD | 2.4.2.1, 2.4.2.28 | F | purine nucleoside phosphorylase | |
NECFGCCN_02343 | 6.9e-130 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
NECFGCCN_02344 | 4.9e-81 | copY | K | Copper transport repressor, CopY TcrY family | ||
NECFGCCN_02345 | 0.0 | 3.6.3.4 | P | P-type ATPase | ||
NECFGCCN_02347 | 1.2e-101 | cadD | P | cadmium resistance | ||
NECFGCCN_02348 | 4.5e-55 | cadX | K | transcriptional regulator, ArsR family | ||
NECFGCCN_02349 | 1.7e-42 | yiiE | S | protein homotetramerization | ||
NECFGCCN_02350 | 1.2e-18 | |||||
NECFGCCN_02351 | 1.5e-29 | K | Helix-turn-helix domain | |||
NECFGCCN_02353 | 2e-149 | srtB | 3.4.22.70 | S | Sortase family | |
NECFGCCN_02354 | 2.5e-233 | capA | M | Bacterial capsule synthesis protein | ||
NECFGCCN_02355 | 8e-39 | gcvR | T | UPF0237 protein | ||
NECFGCCN_02356 | 9.6e-242 | XK27_08635 | S | UPF0210 protein | ||
NECFGCCN_02357 | 8.9e-130 | ais | G | Phosphoglycerate mutase | ||
NECFGCCN_02358 | 2e-138 | vanY | 3.4.17.14 | M | D-alanyl-D-alanine carboxypeptidase | |
NECFGCCN_02359 | 1.2e-100 | acmA | 3.2.1.17, 3.4.17.14, 3.5.1.28 | NU | Muramidase (Flagellum-specific) | |
NECFGCCN_02360 | 3.7e-185 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
NECFGCCN_02361 | 9.1e-63 | grpE | O | Participates actively in the response to hyperosmotic and heat shock by preventing the aggregation of stress-denatured proteins, in association with DnaK and GrpE. It is the nucleotide exchange factor for DnaK and may function as a thermosensor. Unfolded proteins bind initially to DnaJ | ||
NECFGCCN_02363 | 0.0 | dnaK | O | Heat shock 70 kDa protein | ||
NECFGCCN_02365 | 2.6e-187 | dnaJ | O | ATP binding to DnaK triggers the release of the substrate protein, thus completing the reaction cycle. Several rounds of ATP-dependent interactions between DnaJ, DnaK and GrpE are required for fully efficient folding. Also involved, together with DnaK and GrpE, in the DNA replication of plasmids through activation of initiation proteins | ||
NECFGCCN_02366 | 1.3e-139 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
NECFGCCN_02367 | 3.4e-135 | thiD | 2.7.1.35, 2.7.1.49, 2.7.4.7 | H | phosphomethylpyrimidine kinase | |
NECFGCCN_02368 | 1.5e-80 | hmpT | S | cog cog4720 | ||
NECFGCCN_02369 | 6.8e-53 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
NECFGCCN_02370 | 6.5e-34 | nrdH | O | Glutaredoxin | ||
NECFGCCN_02371 | 3.1e-245 | pepB | 3.4.11.1, 3.4.11.23 | E | Probably plays an important role in intracellular peptide degradation | |
NECFGCCN_02372 | 6.4e-33 | iscX | S | Iron-sulphur cluster assembly | ||
NECFGCCN_02373 | 8.7e-59 | fdx | C | Ferredoxin, 2Fe-2S type, ISC system | ||
NECFGCCN_02374 | 0.0 | hscA | O | Chaperone involved in the maturation of iron-sulfur cluster-containing proteins. Has a low intrinsic ATPase activity which is markedly stimulated by HscB. Involved in the maturation of IscU | ||
NECFGCCN_02375 | 1.4e-87 | hscB | O | Co-chaperone involved in the maturation of iron-sulfur cluster-containing proteins. Seems to help targeting proteins to be folded toward HscA | ||
NECFGCCN_02376 | 2.1e-54 | iscA | S | Is able to transfer iron-sulfur clusters to apo- ferredoxin. Multiple cycles of 2Fe2S cluster formation and transfer are observed, suggesting that IscA acts catalytically. Recruits intracellular free iron so as to provide iron for the assembly of transient iron-sulfur cluster in IscU in the presence of IscS, L-cysteine and the thioredoxin reductase system | ||
NECFGCCN_02377 | 5e-66 | iscU | C | A scaffold on which IscS assembles Fe-S clusters. It is likely that Fe-S cluster coordination is flexible as the role of this complex is to build and then hand off Fe-S clusters | ||
NECFGCCN_02378 | 6.1e-227 | iscS | 2.8.1.7 | E | Master enzyme that delivers sulfur to a number of partners involved in Fe-S cluster assembly, tRNA modification or cofactor biosynthesis. Catalyzes the removal of elemental sulfur atoms from cysteine to produce alanine. Functions as a sulfur delivery protein for Fe-S cluster synthesis onto IscU, an Fe-S scaffold assembly protein, as well as other S acceptor proteins | |
NECFGCCN_02379 | 2.3e-84 | iscR | 2.8.1.7 | K | Regulates the transcription of several operons and genes involved in the biogenesis of Fe-S clusters and Fe-S-containing proteins | |
NECFGCCN_02380 | 7.6e-132 | trmJ | 2.1.1.200, 3.5.1.19, 6.1.1.16 | J | Catalyzes the formation of 2'O-methylated cytidine (Cm32) or 2'O-methylated uridine (Um32) at position 32 in tRNA | |
NECFGCCN_02381 | 6.8e-150 | suhB | 3.1.3.25 | G | Inositol monophosphatase | |
NECFGCCN_02383 | 4.8e-166 | yohM | P | Belongs to the NiCoT transporter (TC 2.A.52) family | ||
NECFGCCN_02384 | 1.2e-117 | MA20_06510 | 2.7.4.1 | S | transport system periplasmic component | |
NECFGCCN_02385 | 6.6e-173 | csiE | K | Stationary phase inducible protein CsiE | ||
NECFGCCN_02386 | 6.8e-50 | csiE | K | Stationary phase inducible protein CsiE | ||
NECFGCCN_02387 | 1.4e-201 | hcaT | 1.5.1.2 | EGP | Major facilitator Superfamily | |
NECFGCCN_02388 | 1.6e-141 | yphB | 5.1.3.3 | G | Aldose 1-epimerase | |
NECFGCCN_02389 | 4.6e-311 | E | Extracellular solute-binding protein, family 5 | |||
NECFGCCN_02390 | 7.3e-230 | M | Belongs to the mandelate racemase muconate lactonizing enzyme family | |||
NECFGCCN_02391 | 6.4e-106 | hisE | 3.1.3.23 | G | TIGRFAM HAD-superfamily hydrolase, subfamily IA, variant 3 | |
NECFGCCN_02392 | 7.1e-133 | EGP | Major facilitator Superfamily | |||
NECFGCCN_02393 | 0.0 | 2.4.1.5 | GH13 | M | KxYKxGKxW signal domain protein | |
NECFGCCN_02394 | 7.1e-227 | rodA | D | Belongs to the SEDS family | ||
NECFGCCN_02395 | 2.1e-222 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
NECFGCCN_02396 | 9.9e-112 | galT | 2.7.7.12 | G | UDPglucose--hexose-1-phosphate uridylyltransferase | |
NECFGCCN_02397 | 2.7e-174 | rnz | 3.1.26.11 | S | Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA | |
NECFGCCN_02398 | 2.2e-134 | XK27_05435 | 1.1.1.100 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
NECFGCCN_02399 | 7.5e-21 | Q | Methyltransferase domain | |||
NECFGCCN_02400 | 1.3e-64 | GnaT | 2.5.1.16 | K | acetyltransferase | |
NECFGCCN_02401 | 3e-22 | recJ | L | Single-strand DNA-specific exonuclease, C terminal domain | ||
NECFGCCN_02402 | 7.2e-26 | recJ | L | Single-strand DNA-specific exonuclease, C terminal domain | ||
NECFGCCN_02403 | 1.6e-171 | ydhF | S | Aldo keto reductase | ||
NECFGCCN_02404 | 1.5e-98 | K | WHG domain | |||
NECFGCCN_02405 | 1.5e-121 | V | abc transporter atp-binding protein | |||
NECFGCCN_02406 | 2.1e-165 | apaH | 3.6.1.41 | T | Hydrolyzes diadenosine 5',5'''-P1,P4-tetraphosphate to yield ADP | |
NECFGCCN_02407 | 1.8e-65 | apaG | P | protein affecting Mg2 Co2 transport | ||
NECFGCCN_02408 | 3.4e-149 | ksgA | 2.1.1.182 | J | Specifically dimethylates two adjacent adenosines (A1518 and A1519) in the loop of a conserved hairpin near the 3'-end of 16S rRNA in the 30S particle. May play a critical role in biogenesis of 30S subunits | |
NECFGCCN_02409 | 2.1e-185 | pdxA | 1.1.1.262, 1.1.1.408, 1.1.1.409 | H | Catalyzes the NAD(P)-dependent oxidation of 4- (phosphohydroxy)-L-threonine (HTP) into 2-amino-3-oxo-4- (phosphohydroxy)butyric acid which spontaneously decarboxylates to form 3-amino-2-oxopropyl phosphate (AHAP) | |
NECFGCCN_02410 | 8.6e-232 | surA | 5.2.1.8 | M | Chaperone involved in the correct folding and assembly of outer membrane proteins. Recognizes specific patterns of aromatic residues and the orientation of their side chains, which are found more frequently in integral outer membrane proteins. May act in both early periplasmic and late outer membrane-associated steps of protein maturation | |
NECFGCCN_02411 | 0.0 | lptD | M | Together with LptE, is involved in the assembly of lipopolysaccharide (LPS) at the surface of the outer membrane | ||
NECFGCCN_02412 | 4.8e-151 | djlA | O | Regulatory DnaK co-chaperone. Direct interaction between DnaK and DjlA is needed for the induction of the wcaABCDE operon, involved in the synthesis of a colanic acid polysaccharide capsule, possibly through activation of the RcsB RcsC phosphotransfer signaling pathway. The colanic acid capsule may help the bacterium survive conditions outside the host | ||
NECFGCCN_02413 | 3.4e-121 | dpiA | K | transcriptional regulatory protein | ||
NECFGCCN_02414 | 5e-293 | citA | 2.7.13.3 | T | signal transduction histidine kinase regulating citrate malate metabolism | |
NECFGCCN_02415 | 9.1e-248 | cimH | U | Uptake of citrate across the boundary membrane with the concomitant uptake of a sodium ion (symport system) | ||
NECFGCCN_02416 | 3.9e-101 | citG | 2.4.2.52, 2.7.7.61 | HI | Apo-citrate lyase phosphoribosyl-dephospho-CoA transferase | |
NECFGCCN_02417 | 4.3e-58 | rluA | 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
NECFGCCN_02418 | 6.8e-167 | togN | P | PFAM binding-protein-dependent transport systems inner membrane component | ||
NECFGCCN_02419 | 5e-162 | ycjO | P | Binding-protein-dependent transport systems inner membrane component | ||
NECFGCCN_02420 | 7.9e-57 | kdgF | S | PFAM Cupin 2, conserved barrel domain protein | ||
NECFGCCN_02421 | 1.7e-128 | ygeA | 5.1.1.13 | M | Belongs to the aspartate glutamate racemases family | |
NECFGCCN_02422 | 2e-166 | lysR | K | transcriptional regulator | ||
NECFGCCN_02423 | 5.3e-242 | lysA | 2.7.2.4, 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
NECFGCCN_02424 | 2.4e-189 | ascG | K | Transcriptional regulator | ||
NECFGCCN_02425 | 4.8e-241 | licC | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
NECFGCCN_02426 | 5.2e-294 | celH | 3.2.1.21, 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
NECFGCCN_02427 | 2.5e-141 | uxuR | K | Transcriptional | ||
NECFGCCN_02428 | 4.9e-87 | mshD | 2.3.1.189 | S | PFAM GCN5-related N-acetyltransferase | |
NECFGCCN_02429 | 1.6e-185 | galR | K | transcriptional regulator | ||
NECFGCCN_02430 | 0.0 | aas | 2.3.1.40, 6.2.1.20 | I | Plays a role in lysophospholipid acylation. Transfers fatty acids to the 1-position via an enzyme-bound acyl-ACP intermediate in the presence of ATP and magnesium. Its physiological function is to regenerate phosphatidylethanolamine from 2-acyl-glycero-3-phosphoethanolamine (2-acyl-GPE) formed by transacylation reactions or degradation by phospholipase A1 | |
NECFGCCN_02431 | 1.6e-200 | lplT | 2.3.1.40, 6.2.1.20 | U | Catalyzes the facilitated diffusion of 2-acyl-glycero-3- phosphoethanolamine (2-acyl-GPE) into the cell | |
NECFGCCN_02432 | 1.5e-194 | tas | C | Aldo keto reductase | ||
NECFGCCN_02433 | 2.7e-32 | ygdR | S | (Lipo)protein | ||
NECFGCCN_02434 | 1e-120 | ygdQ | P | membrane protein, terc | ||
NECFGCCN_02435 | 2e-126 | mutH | L | Sequence-specific endonuclease that cleaves unmethylated GATC sequences. It is involved in DNA mismatch repair | ||
NECFGCCN_02436 | 6.4e-20 | |||||
NECFGCCN_02437 | 1.5e-100 | nudH | L | Accelerates the degradation of transcripts by removing pyrophosphate from the 5'-end of triphosphorylated RNA, leading to a more labile monophosphorylated state that can stimulate subsequent ribonuclease cleavage | ||
NECFGCCN_02438 | 0.0 | ptsP | 2.7.3.9 | T | Belongs to the PEP-utilizing enzyme family | |
NECFGCCN_02439 | 2.6e-171 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
NECFGCCN_02440 | 1.1e-157 | thyA | 2.1.1.45 | F | Catalyzes the reductive methylation of 2'-deoxyuridine- 5'-monophosphate (dUMP) to 2'-deoxythymidine-5'-monophosphate (dTMP) while utilizing 5,10-methylenetetrahydrofolate (mTHF) as the methyl donor and reductant in the reaction, yielding dihydrofolate (DHF) as a by-product. This enzymatic reaction provides an intracellular de novo source of dTMP, an essential precursor for DNA biosynthesis | |
NECFGCCN_02441 | 6.2e-76 | ppdA | NU | prepilin peptidase dependent protein A | ||
NECFGCCN_02442 | 1.3e-94 | ppdB | U | prepilin peptidase dependent protein | ||
NECFGCCN_02443 | 7.6e-65 | ygdB | S | Protein of unknown function (DUF2509) | ||
NECFGCCN_02444 | 5.5e-50 | ppdC | NU | Prepilin peptidase dependent protein c | ||
NECFGCCN_02445 | 4.8e-43 | M | Putative cell wall binding repeat | |||
NECFGCCN_02446 | 1e-07 | S | dextransucrase activity | |||
NECFGCCN_02448 | 1.5e-189 | ET | ankyrin repeat | |||
NECFGCCN_02449 | 0.0 | eptB | 2.7.8.42, 2.7.8.43 | S | membrane-associated metal-dependent hydrolase | |
NECFGCCN_02450 | 3.2e-188 | yhjX | P | Major facilitator superfamily | ||
NECFGCCN_02451 | 6.9e-113 | yhjY | N | outer membrane autotransporter | ||
NECFGCCN_02452 | 3.7e-105 | tag | 3.2.2.20 | L | glycosylase | |
NECFGCCN_02453 | 8.1e-81 | yiaC | 2.3.1.1, 2.3.1.210 | K | acetyltransferase | |
NECFGCCN_02454 | 0.0 | bisC | 1.7.2.3, 1.8.5.3 | C | Belongs to the prokaryotic molybdopterin-containing oxidoreductase family | |
NECFGCCN_02455 | 1.8e-87 | yiaD | M | Belongs to the ompA family | ||
NECFGCCN_02456 | 7.4e-186 | ptxS | K | transcriptional regulator | ||
NECFGCCN_02457 | 6.8e-136 | kguE | 2.7.1.45 | G | Xylose isomerase domain protein TIM barrel | |
NECFGCCN_02458 | 4e-170 | kdgK | 2.7.1.13, 2.7.1.45 | G | 2-dehydro-3-deoxygluconokinase | |
NECFGCCN_02459 | 7e-242 | G | Major facilitator superfamily | |||
NECFGCCN_02460 | 6.4e-179 | ghrB | 1.1.1.215, 1.1.1.26, 1.1.1.43, 1.1.1.79, 1.1.1.81 | CH | Catalyzes the NADPH-dependent reduction of glyoxylate and hydroxypyruvate into glycolate and glycerate, respectively | |
NECFGCCN_02461 | 2.3e-125 | yiaF | S | exported protein | ||
NECFGCCN_02462 | 9.7e-234 | G | transporter | |||
NECFGCCN_02463 | 5.6e-46 | yiaG | K | transcriptional regulator | ||
NECFGCCN_02464 | 3.1e-33 | cspA | K | SMART Cold shock protein | ||
NECFGCCN_02465 | 3.9e-282 | yheS_2 | S | ATPase components of ABC transporters with duplicated ATPase domains | ||
NECFGCCN_02466 | 1.7e-23 | S | PFAM Hok gef | |||
NECFGCCN_02467 | 0.0 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
NECFGCCN_02468 | 1e-178 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
NECFGCCN_02469 | 1.9e-44 | ysaB | S | YsaB-like lipoprotein | ||
NECFGCCN_02470 | 2.9e-182 | wecH | S | Responsible for the incorporation of O-acetyl groups into the enterobacterial common antigen (ECA) trisaccharide repeat units | ||
NECFGCCN_02471 | 2.1e-76 | yiaA | S | Membrane | ||
NECFGCCN_02472 | 4.2e-62 | yiaA | S | Membrane | ||
NECFGCCN_02473 | 1.3e-276 | xylB | 2.7.1.17, 2.7.1.189, 2.7.1.5, 2.7.1.51 | G | xylulose kinase | |
NECFGCCN_02474 | 3.6e-265 | xylA | 5.3.1.5 | G | Belongs to the xylose isomerase family | |
NECFGCCN_02475 | 3.5e-180 | xylF | G | D-xylose ABC transporter periplasmic substrate-binding protein | ||
NECFGCCN_02476 | 1.2e-288 | xylG | 3.6.3.17 | P | import. Responsible for energy coupling to the transport system | |
NECFGCCN_02477 | 4.2e-10 | xylH | G | Belongs to the binding-protein-dependent transport system permease family | ||
NECFGCCN_02478 | 8e-90 | 2.4.1.60 | S | Glycosyltransferase group 2 family protein | ||
NECFGCCN_02479 | 1.1e-108 | |||||
NECFGCCN_02480 | 0.0 | rgpF | GT2,GT4 | M | Glycosyltransferase like family 2 | |
NECFGCCN_02481 | 3.6e-219 | M | Psort location CytoplasmicMembrane, score | |||
NECFGCCN_02482 | 3.2e-223 | GT4 | M | transferase activity, transferring glycosyl groups | ||
NECFGCCN_02483 | 5e-223 | rgpA | GT4 | M | Domain of unknown function (DUF1972) | |
NECFGCCN_02484 | 4.8e-171 | rgpB | GT2 | M | Glycosyltransferase, group 2 family protein | |
NECFGCCN_02485 | 9.8e-141 | rgpC | GM | Transport permease protein | ||
NECFGCCN_02486 | 1.9e-120 | K | sequence-specific DNA binding | |||
NECFGCCN_02487 | 2.9e-151 | V | ABC transporter, ATP-binding protein | |||
NECFGCCN_02488 | 8e-94 | S | ABC-2 family transporter protein | |||
NECFGCCN_02490 | 1.3e-39 | ytxH | S | General stress protein | ||
NECFGCCN_02491 | 2.1e-64 | estA | E | GDSL-like Lipase/Acylhydrolase | ||
NECFGCCN_02492 | 1.4e-99 | |||||
NECFGCCN_02493 | 1.5e-273 | sulP | P | Sulfate permease and related transporters (MFS superfamily) | ||
NECFGCCN_02494 | 1e-232 | nirB | 1.7.1.15 | C | Belongs to the nitrite and sulfite reductase 4Fe-4S domain family | |
NECFGCCN_02495 | 1.7e-74 | nirB | 1.7.1.15 | C | Belongs to the nitrite and sulfite reductase 4Fe-4S domain family | |
NECFGCCN_02496 | 2.4e-233 | tcdB | S | dextransucrase activity | ||
NECFGCCN_02497 | 0.0 | S | dextransucrase activity | |||
NECFGCCN_02498 | 1.4e-21 | I | phospholipase d transphosphatidylase | |||
NECFGCCN_02499 | 1.7e-167 | K | transcriptional | |||
NECFGCCN_02500 | 2.5e-256 | EGP | Major facilitator superfamily | |||
NECFGCCN_02501 | 1.4e-223 | ybdG | M | Mechanosensitive Ion channel | ||
NECFGCCN_02502 | 6.1e-169 | cytR | 5.1.1.1 | K | Periplasmic binding protein LacI transcriptional regulator | |
NECFGCCN_02503 | 4.7e-70 | |||||
NECFGCCN_02504 | 1.1e-217 | S | oxidoreductase | |||
NECFGCCN_02505 | 2.2e-198 | iolE | G | AP endonuclease | ||
NECFGCCN_02506 | 6.2e-227 | yegT | G | Broad-specificity transporter of purine and pyrimidine nucleosides. Driven by a proton motive force | ||
NECFGCCN_02507 | 1.2e-247 | pheP | E | PFAM amino acid permease-associated region | ||
NECFGCCN_02508 | 0.0 | fcuA | P | receptor | ||
NECFGCCN_02509 | 2.8e-199 | S | amine dehydrogenase activity | |||
NECFGCCN_02510 | 4.4e-272 | feaB | 1.2.1.39 | C | belongs to the aldehyde dehydrogenase family | |
NECFGCCN_02511 | 1.1e-253 | ordL | E | oxidoreductase | ||
NECFGCCN_02512 | 1.5e-64 | S | enzyme of the cupin superfamily | |||
NECFGCCN_02513 | 4.3e-217 | hscC | O | Belongs to the heat shock protein 70 family | ||
NECFGCCN_02514 | 1.1e-162 | yocS | S | Transporter | ||
NECFGCCN_02515 | 1.5e-107 | plsY | 2.3.1.15, 3.5.1.104 | I | Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP | |
NECFGCCN_02516 | 2.1e-13 | L | Helix-hairpin-helix DNA-binding motif class 1 | |||
NECFGCCN_02517 | 2.2e-30 | S | Domain of unknown function (DUF1912) | |||
NECFGCCN_02518 | 1.5e-169 | mmuM | 1.5.1.20, 2.1.1.10 | H | Homocysteine | |
NECFGCCN_02519 | 2.4e-101 | mmuP | E | amino acid | ||
NECFGCCN_02520 | 5.6e-106 | codA | 3.5.4.1 | F | cytosine deaminase | |
NECFGCCN_02521 | 5.6e-217 | tsgA | G | Protein tsgA homolog | ||
NECFGCCN_02522 | 2.7e-100 | ppiA | 5.2.1.8 | M | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
NECFGCCN_02523 | 8e-21 | yhfG | S | Protein of unknown function (DUF2559) | ||
NECFGCCN_02524 | 4.2e-112 | fic | D | cell filamentation protein Fic | ||
NECFGCCN_02525 | 1.7e-99 | pabA | 2.4.2.18, 2.6.1.85, 4.1.3.27 | EH | anthranilate synthase | |
NECFGCCN_02526 | 6.7e-234 | argD | 2.6.1.11, 2.6.1.17, 2.6.1.81 | E | aminotransferase | |
NECFGCCN_02527 | 0.0 | yhfK | S | integral membrane protein, YccS YhfK family | ||
NECFGCCN_02528 | 1.9e-115 | crp | K | COG0664 cAMP-binding proteins - catabolite gene activator and regulatory subunit of cAMP-dependent protein kinases | ||
NECFGCCN_02529 | 2.8e-67 | yhfA | O | Redox protein regulator of disulfide bond formation | ||
NECFGCCN_02530 | 9.5e-166 | prkB | 2.7.1.19 | G | Phosphoribulokinase | |
NECFGCCN_02531 | 2.8e-34 | yheU | S | Belongs to the UPF0270 family | ||
NECFGCCN_02532 | 2.7e-204 | yheT | S | hydrolase of the alpha beta-hydrolase fold | ||
NECFGCCN_02533 | 1.3e-292 | yheS | S | ABC transporter | ||
NECFGCCN_02534 | 2.5e-103 | kefG | S | Regulatory subunit of a potassium efflux system that confers protection against electrophiles. Required for full activity of KefB | ||
NECFGCCN_02535 | 0.0 | kefB | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
NECFGCCN_02536 | 1.2e-31 | yheV | S | nucleic-acid-binding protein containing a Zn-ribbon domain | ||
NECFGCCN_02537 | 4.7e-76 | slyD | 5.2.1.8 | G | Peptidyl-prolyl cis-trans | |
NECFGCCN_02538 | 1.3e-31 | slyX | S | Belongs to the SlyX family | ||
NECFGCCN_02539 | 6.6e-140 | fkpA | 5.2.1.8 | M | Peptidyl-prolyl cis-trans | |
NECFGCCN_02540 | 8.3e-131 | yheO | S | protein conserved in bacteria | ||
NECFGCCN_02541 | 7.2e-65 | tusD | P | Part of a sulfur-relay system required for 2-thiolation of 5-methylaminomethyl-2-thiouridine (mnm(5)s(2)U) at tRNA wobble positions. Accepts sulfur from TusA and transfers it in turn to TusE | ||
NECFGCCN_02542 | 2.6e-61 | tusC | P | Belongs to the DsrF TusC family | ||
NECFGCCN_02543 | 1.4e-44 | tusB | P | Part of a sulfur-relay system required for 2-thiolation of 5-methylaminomethyl-2-thiouridine (mnm(5)s(2)U) at tRNA wobble positions | ||
NECFGCCN_02544 | 1.2e-64 | rpsL | J | Interacts with and stabilizes bases of the 16S rRNA that are involved in tRNA selection in the A site and with the mRNA backbone. Located at the interface of the 30S and 50S subunits, it traverses the body of the 30S subunit contacting proteins on the other side and probably holding the rRNA structure together. The combined cluster of proteins S8, S12 and S17 appears to hold together the shoulder and platform of the 30S subunit | ||
NECFGCCN_02545 | 1.1e-78 | rpsG | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the head domain of the 30S subunit. Is located at the subunit interface close to the decoding center, probably blocks exit of the E-site tRNA | ||
NECFGCCN_02546 | 0.0 | fusA | J | Catalyzes the GTP-dependent ribosomal translocation step during translation elongation. During this step, the ribosome changes from the pre-translocational (PRE) to the post- translocational (POST) state as the newly formed A-site-bound peptidyl-tRNA and P-site-bound deacylated tRNA move to the P and E sites, respectively. Catalyzes the coordinated movement of the two tRNA molecules, the mRNA and conformational changes in the ribosome | ||
NECFGCCN_02547 | 2.9e-28 | hpk9 | 2.7.13.3 | T | protein histidine kinase activity | |
NECFGCCN_02548 | 1.1e-74 | fumB | 4.2.1.2 | C | Catalyzes the reversible hydration of fumarate to (S)- malate | |
NECFGCCN_02549 | 3.5e-183 | plsX | 2.3.1.15 | I | Catalyzes the reversible formation of acyl-phosphate (acyl-PO(4)) from acyl- acyl-carrier-protein (acyl-ACP). This enzyme utilizes acyl-ACP as fatty acyl donor, but not acyl-CoA | |
NECFGCCN_02550 | 3.1e-29 | acpP1 | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
NECFGCCN_02551 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
NECFGCCN_02552 | 6.5e-35 | S | Immunity protein 41 | |||
NECFGCCN_02553 | 0.0 | M | Putative cell wall binding repeat | |||
NECFGCCN_02554 | 1.3e-51 | uraH | 3.5.2.17 | P | Belongs to the transthyretin family. 5-hydroxyisourate hydrolase subfamily | |
NECFGCCN_02555 | 4.8e-77 | uraD | 3.5.3.4, 4.1.1.97 | S | Ohcu decarboxylase | |
NECFGCCN_02556 | 3.6e-252 | pbuX | F | xanthine | ||
NECFGCCN_02557 | 1.1e-222 | hpxO | 1.14.13.113 | CH | COG0654 2-polyprenyl-6-methoxyphenol hydroxylase and related FAD-dependent oxidoreductases | |
NECFGCCN_02558 | 2.5e-164 | K | transcriptional regulator | |||
NECFGCCN_02559 | 4e-211 | vanA | P | Phenylpropionate dioxygenase and related ring-hydroxylating dioxygenases large terminal subunit | ||
NECFGCCN_02560 | 2.1e-182 | vanB | C | Flavodoxin reductases (Ferredoxin-NADPH reductases) family 1 | ||
NECFGCCN_02561 | 1.7e-185 | amaB | 3.5.1.6, 3.5.1.87, 3.5.3.9 | E | the allantoate amidohydrolase from Escherichia coli forms a dimer and binds zinc ions for catalytic activity and catalyzes the conversion of allantoate to (S)-ureidoglycolate and ammonia | |
NECFGCCN_02562 | 1.5e-172 | 1.13.12.16, 1.3.1.9 | S | COG2070 Dioxygenases related to 2-nitropropane dioxygenase | ||
NECFGCCN_02563 | 8.9e-167 | K | transcriptional regulator | |||
NECFGCCN_02564 | 1.3e-11 | |||||
NECFGCCN_02565 | 6.3e-207 | namA | 1.6.99.1 | C | COG1902 NADH flavin oxidoreductases, Old Yellow Enzyme family | |
NECFGCCN_02566 | 5.4e-292 | ydhS | S | FAD-NAD(P)-binding | ||
NECFGCCN_02567 | 1.1e-220 | jen | EGP | Major facilitator Superfamily | ||
NECFGCCN_02568 | 7.9e-163 | Z012_01315 | EG | Permeases of the drug metabolite transporter (DMT) superfamily | ||
NECFGCCN_02569 | 8.8e-209 | S | Iron-containing redox enzyme | |||
NECFGCCN_02570 | 2.9e-102 | K | Bacterial regulatory proteins, tetR family | |||
NECFGCCN_02571 | 8.1e-91 | 2.3.1.128 | J | Acetyltransferase (GNAT) domain | ||
NECFGCCN_02572 | 2.6e-220 | P | Major facilitator superfamily | |||
NECFGCCN_02574 | 1.6e-191 | gntR | K | transcriptional regulator | ||
NECFGCCN_02575 | 1e-67 | cmtB | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | Phosphotransferase System | |
NECFGCCN_02576 | 4.8e-36 | ulaB | 2.7.1.194, 2.7.1.200 | G | Phosphotransferase System | |
NECFGCCN_02577 | 3.4e-212 | ulaA | 2.7.1.194 | S | transporter subunit | |
NECFGCCN_02578 | 5.8e-126 | alsE | 5.1.3.1 | G | 3-epimerase | |
NECFGCCN_02579 | 2e-77 | frvA | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | PTS IIA-like nitrogen-regulatory protein PtsN | |
NECFGCCN_02580 | 1.1e-44 | fruA | 2.7.1.202 | G | PTS system fructose-specific IIB | |
NECFGCCN_02581 | 2.7e-165 | G | and phosphoenolpyruvate-dependent sugar phosphotransferase system | |||
NECFGCCN_02582 | 5.5e-107 | yrhP | E | threonine efflux protein | ||
NECFGCCN_02583 | 8.3e-73 | ygaU | GH23 | S | peptidoglycan-binding protein | |
NECFGCCN_02584 | 1e-241 | pgtP | G | transporter | ||
NECFGCCN_02585 | 2.4e-194 | pgtC | P | ABC-type Fe3 transport system, periplasmic component | ||
NECFGCCN_02586 | 0.0 | pgtB | 2.7.13.3 | T | His Kinase A (phosphoacceptor) domain | |
NECFGCCN_02587 | 9.4e-199 | pgtA | T | Response regulator containing CheY-like receiver AAA-type ATPase and DNA-binding domains | ||
NECFGCCN_02588 | 7.9e-59 | yqkA | S | GrpB protein | ||
NECFGCCN_02589 | 2e-166 | K | LysR substrate binding domain | |||
NECFGCCN_02590 | 3e-184 | C | aldo keto reductase | |||
NECFGCCN_02591 | 2.6e-219 | C | Aldo/keto reductase family | |||
NECFGCCN_02592 | 3.2e-133 | glcR_2 | K | transcriptional regulator | ||
NECFGCCN_02593 | 3.3e-189 | 2.7.1.17, 2.7.1.189, 2.7.1.5, 2.7.1.51, 2.7.1.53 | G | xylulose kinase | ||
NECFGCCN_02594 | 3.2e-36 | fucR | K | transcriptional regulator | ||
NECFGCCN_02595 | 1.5e-113 | alsE | 5.1.3.1 | G | 3-epimerase | |
NECFGCCN_02596 | 2e-161 | rbsK | 2.7.1.15, 2.7.1.4 | G | Catalyzes the phosphorylation of ribose at O-5 in a reaction requiring ATP and magnesium. The resulting D-ribose-5- phosphate can then be used either for sythesis of nucleotides, histidine, and tryptophan, or as a component of the pentose phosphate pathway | |
NECFGCCN_02597 | 3.2e-237 | fucP | G | transporter | ||
NECFGCCN_02598 | 1.1e-65 | 4.4.1.5 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | ||
NECFGCCN_02599 | 4.6e-296 | MA20_27905 | 6.2.1.26, 6.2.1.3 | IQ | AMP-binding enzyme C-terminal domain | |
NECFGCCN_02600 | 8.9e-303 | ydiF | 2.8.3.1 | I | CoA transferase having broad substrate specificity for short-chain acyl-CoA thioesters with the activity decreasing when the length of the carboxylic acid chain exceeds four carbons | |
NECFGCCN_02601 | 2.7e-129 | IQ | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
NECFGCCN_02602 | 1.3e-120 | bktB | 2.3.1.9 | I | Catalyzes the final step of fatty acid oxidation in which acetyl-CoA is released and the CoA ester of a fatty acid two carbons shorter is formed | |
NECFGCCN_02603 | 2.5e-225 | malE | G | Bacterial extracellular solute-binding protein | ||
NECFGCCN_02604 | 2.7e-205 | malK | P | Part of the ABC transporter complex MalEFGK involved in maltose maltodextrin import. Responsible for energy coupling to the transport system | ||
NECFGCCN_02605 | 2.8e-254 | lamB | M | involved in the transport of maltose and maltodextrins | ||
NECFGCCN_02606 | 1.9e-156 | malM | S | maltose operon periplasmic | ||
NECFGCCN_02607 | 5.6e-86 | ubiC | 4.1.3.40 | H | Removes the pyruvyl group from chorismate, with concomitant aromatization of the ring, to provide 4- hydroxybenzoate (4HB) for the ubiquinone pathway | |
NECFGCCN_02608 | 1.2e-141 | ubiA | 2.5.1.39 | H | Catalyzes the prenylation of para-hydroxybenzoate (PHB) with an all-trans polyprenyl group. Mediates the second step in the final reaction sequence of ubiquinone-8 (UQ-8) biosynthesis, which is the condensation of the polyisoprenoid side chain with PHB, generating the first membrane-bound Q intermediate 3- octaprenyl-4-hydroxybenzoate | |
NECFGCCN_02609 | 0.0 | plsB | 2.3.1.15 | I | Belongs to the GPAT DAPAT family | |
NECFGCCN_02610 | 1.1e-57 | dgkA | 2.7.1.107 | M | Recycling of diacylglycerol produced during the turnover of membrane phospholipid | |
NECFGCCN_02611 | 2e-106 | lexA | 3.4.21.88 | K | Represses a number of genes involved in the response to DNA damage (SOS response), including recA and lexA. Binds to the 16 bp palindromic sequence 5'-CTGTATATATATACAG-3'. In the presence of single-stranded DNA, RecA interacts with LexA causing an autocatalytic cleavage which disrupts the DNA-binding part of LexA, leading to derepression of the SOS regulon and eventually DNA repair | |
NECFGCCN_02612 | 5.6e-226 | dinF | V | COG0534 Na -driven multidrug efflux pump | ||
NECFGCCN_02613 | 2.6e-32 | yjbJ | S | Belongs to the UPF0337 (CsbD) family | ||
NECFGCCN_02614 | 1.9e-92 | zur | P | belongs to the Fur family | ||
NECFGCCN_02615 | 2.4e-97 | manC | S | conserved protein, contains double-stranded beta-helix domain | ||
NECFGCCN_02616 | 3e-181 | dusA | J | Catalyzes the synthesis of 5,6-dihydrouridine (D), a modified base found in the D-loop of most tRNAs, via the reduction of the C5-C6 double bond in target uridines. Specifically modifies U20 and U20a in tRNAs | ||
NECFGCCN_02617 | 1.2e-30 | pspG | S | Phage Shock Protein G | ||
NECFGCCN_02618 | 9.4e-178 | qor | 1.6.5.5 | C | COG0604 NADPH quinone reductase and related Zn-dependent oxidoreductases | |
NECFGCCN_02619 | 2.7e-263 | dnaB | 3.6.4.12 | L | it exhibits DNA-dependent ATPase activity and contains distinct active sites for ATP binding, DNA binding, and interaction with DnaC protein, primase, and other prepriming proteins | |
NECFGCCN_02620 | 6e-202 | alr | 5.1.1.1 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
NECFGCCN_02621 | 3e-226 | tyrB | 2.6.1.1, 2.6.1.57 | E | aminotransferase | |
NECFGCCN_02622 | 9.6e-132 | aphA | 3.1.3.2 | S | Belongs to the class B bacterial acid phosphatase family | |
NECFGCCN_02623 | 3.3e-76 | yjbQ | S | Secondary thiamine-phosphate synthase enzyme | ||
NECFGCCN_02624 | 3e-57 | yjbR | S | protein conserved in bacteria | ||
NECFGCCN_02625 | 0.0 | uvrA | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrA is an ATPase and a DNA-binding protein. A damage recognition complex composed of 2 UvrA and 2 UvrB subunits scans DNA for abnormalities. When the presence of a lesion has been verified by UvrB, the UvrA molecules dissociate | ||
NECFGCCN_02626 | 1.8e-58 | ssb | L | Plays an important role in DNA replication, recombination and repair. Binds to ssDNA and to an array of partner proteins to recruit them to their sites of action during DNA metabolism | ||
NECFGCCN_02627 | 1.1e-251 | VP0557 | M | Murein-degrading enzyme that degrades murein glycan strands and insoluble, high-molecular weight murein sacculi, with the concomitant formation of a 1,6-anhydromuramoyl product. Lytic transglycosylases (LTs) play an integral role in the metabolism of the peptidoglycan (PG) sacculus. Their lytic action creates space within the PG sacculus to allow for its expansion as well as for the insertion of various structures such as secretion systems and flagella | ||
NECFGCCN_02628 | 3.9e-42 | L | Transposase | |||
NECFGCCN_02629 | 1.6e-168 | L | COG2801 Transposase and inactivated derivatives | |||
NECFGCCN_02630 | 0.0 | fepA | P | Receptor | ||
NECFGCCN_02631 | 7.6e-64 | K | Transcriptional regulator | |||
NECFGCCN_02632 | 0.0 | E | Tannase and feruloyl esterase | |||
NECFGCCN_02634 | 0.0 | bamA | M | Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane | ||
NECFGCCN_02635 | 5.8e-61 | iraM | S | Inhibits RpoS proteolysis by regulating RssB activity, thereby increasing the stability of the sigma stress factor RpoS during magnesium starvation | ||
NECFGCCN_02636 | 1.4e-133 | 3.1.3.25 | G | inositol monophosphatase | ||
NECFGCCN_02637 | 3.6e-172 | K | transcriptional regulator | |||
NECFGCCN_02638 | 3e-139 | MA20_22080 | S | of the beta-lactamase superfamily III | ||
NECFGCCN_02639 | 1.3e-185 | 3.6.3.30 | P | Part of the ABC transporter complex FbpABC involved in Fe(3 ) ions import. Responsible for energy coupling to the transport system | ||
NECFGCCN_02640 | 9.1e-217 | S | extracellular solute-binding protein, family 1 | |||
NECFGCCN_02641 | 9.2e-118 | P | Binding-protein-dependent transport systems inner membrane component | |||
NECFGCCN_02642 | 4.7e-149 | P | Binding-protein-dependent transport systems inner membrane component | |||
NECFGCCN_02643 | 1.6e-42 | yjcB | S | membrane | ||
NECFGCCN_02645 | 4.9e-301 | yjcC | 3.1.4.52 | T | signal transduction protein containing sensor and EAL | |
NECFGCCN_02646 | 1.2e-55 | soxS | K | transcriptional regulator | ||
NECFGCCN_02647 | 1.7e-81 | soxR | K | redox-sensitive transcriptional activator SoxR | ||
NECFGCCN_02648 | 1.7e-122 | gstA | 2.5.1.18 | O | Belongs to the GST superfamily | |
NECFGCCN_02649 | 4.7e-228 | yjcD | S | permease | ||
NECFGCCN_02650 | 3.3e-292 | yjcE | P | NhaP-type Na H and K H antiporters | ||
NECFGCCN_02651 | 4.6e-160 | ywbI | K | transcriptional regulator | ||
NECFGCCN_02652 | 3e-61 | cidA | S | LrgA family | ||
NECFGCCN_02653 | 5.7e-113 | ywbG | M | effector of murein hydrolase | ||
NECFGCCN_02654 | 1.7e-88 | NU | Fimbrial protein | |||
NECFGCCN_02655 | 2.8e-120 | sthB | M | chaperone | ||
NECFGCCN_02656 | 0.0 | NU | Usher protein | |||
NECFGCCN_02657 | 5.1e-80 | NU | Fimbrial protein | |||
NECFGCCN_02658 | 1.8e-190 | phfB | NU | Fimbrial protein | ||
NECFGCCN_02659 | 8.1e-299 | actP | S | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
NECFGCCN_02660 | 4.5e-49 | yjcH | S | Membrane | ||
NECFGCCN_02661 | 0.0 | acsA | 6.2.1.1 | I | Catalyzes the conversion of acetate into acetyl-CoA (AcCoA), an essential intermediate at the junction of anabolic and catabolic pathways. AcsA undergoes a two-step reaction. In the first half reaction, AcsA combines acetate with ATP to form acetyl-adenylate (AcAMP) intermediate. In the second half reaction, it can then transfer the acetyl group from AcAMP to the sulfhydryl group of CoA, forming the product AcCoA | |
NECFGCCN_02662 | 3.5e-228 | gltP | U | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
NECFGCCN_02663 | 1.9e-121 | yjcO | S | Sel1 repeat | ||
NECFGCCN_02664 | 1.6e-137 | pepN | 3.4.11.2 | E | aminopeptidase | |
NECFGCCN_02665 | 1.8e-22 | parE | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
NECFGCCN_02666 | 1e-91 | Z012_04635 | K | Helix-turn-helix XRE-family like proteins | ||
NECFGCCN_02668 | 4.7e-51 | L | COG1943 Transposase and inactivated derivatives | |||
NECFGCCN_02669 | 9.3e-272 | G | Protein of unknown function (DUF3131) | |||
NECFGCCN_02670 | 5.6e-74 | VPA1107 | C | nitric oxide dioxygenase activity | ||
NECFGCCN_02671 | 0.0 | T | PhoQ Sensor | |||
NECFGCCN_02672 | 2e-79 | rplM | J | This protein is one of the early assembly proteins of the 50S ribosomal subunit, although it is not seen to bind rRNA by itself. It is important during the early stages of 50S assembly | ||
NECFGCCN_02673 | 7.5e-11 | endA | S | DNA/RNA non-specific endonuclease | ||
NECFGCCN_02674 | 3.7e-145 | feaB | 1.2.1.39 | C | belongs to the aldehyde dehydrogenase family | |
NECFGCCN_02675 | 1.5e-34 | panE | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
NECFGCCN_02676 | 2.9e-126 | 5.2.1.8 | O | peptidylprolyl isomerase | ||
NECFGCCN_02677 | 1.2e-168 | speE | 2.5.1.16 | E | Catalyzes the irreversible transfer of a propylamine group from the amino donor S-adenosylmethioninamine (decarboxy- AdoMet) to putrescine (1,4-diaminobutane) to yield spermidine | |
NECFGCCN_02678 | 6.3e-148 | speD | 2.5.1.16, 4.1.1.50 | E | Catalyzes the decarboxylation of S-adenosylmethionine to S-adenosylmethioninamine (dcAdoMet), the propylamine donor required for the synthesis of the polyamines spermine and spermidine from the diamine putrescine | |
NECFGCCN_02679 | 1.8e-62 | yacL | S | Belongs to the UPF0231 family | ||
NECFGCCN_02680 | 0.0 | acnB | 4.2.1.3, 4.2.1.99 | C | Belongs to the aconitase IPM isomerase family | |
NECFGCCN_02681 | 2.2e-192 | yacH | S | Protein of unknown function (DUF3300) | ||
NECFGCCN_02682 | 2e-138 | flgK | N | Protein of unknown function (DUF2950) | ||
NECFGCCN_02683 | 1.9e-30 | |||||
NECFGCCN_02684 | 1e-270 | lpdA | 1.8.1.4 | C | COG1249 Pyruvate 2-oxoglutarate dehydrogenase complex, dihydrolipoamide dehydrogenase (E3) component, and related enzymes | |
NECFGCCN_02685 | 3.8e-284 | aceF | 2.3.1.12 | C | The pyruvate dehydrogenase complex catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2) | |
NECFGCCN_02686 | 0.0 | aceE | 1.2.4.1 | C | Component of the pyruvate dehydrogenase (PDH) complex, that catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2) | |
NECFGCCN_02687 | 1.1e-136 | pdhR | K | pyruvate dehydrogenase complex | ||
NECFGCCN_02688 | 1.1e-245 | aroP | E | amino acid | ||
NECFGCCN_02689 | 1.9e-264 | yicJ | G | COG2211 Na melibiose symporter and related transporters | ||
NECFGCCN_02690 | 2.4e-194 | abf | G | Belongs to the glycosyl hydrolase 43 family | ||
NECFGCCN_02691 | 7.4e-155 | ampE | 6.3.1.10 | V | regulatory protein AmpE | |
NECFGCCN_02692 | 1.9e-106 | ampD | 3.5.1.28 | V | Negative regulator of beta-lactamase expression | |
NECFGCCN_02693 | 2.2e-165 | nadC | 2.4.2.19 | H | Belongs to the NadC ModD family | |
NECFGCCN_02694 | 1.9e-74 | ppdD | NU | Belongs to the N-Me-Phe pilin family | ||
NECFGCCN_02695 | 6.9e-251 | hofB | NU | Type II secretory pathway, ATPase PulE Tfp pilus assembly pathway, ATPase PilB | ||
NECFGCCN_02696 | 8.4e-205 | hofC | U | type II secretion system | ||
NECFGCCN_02697 | 6.1e-137 | guaC | 1.1.1.205, 1.7.1.7 | F | Catalyzes the irreversible NADPH-dependent deamination of GMP to IMP. It functions in the conversion of nucleobase, nucleoside and nucleotide derivatives of G to A nucleotides, and in maintaining the intracellular balance of A and G nucleotides | |
NECFGCCN_02698 | 1.6e-39 | guaC | 1.1.1.205, 1.7.1.7 | F | Catalyzes the irreversible NADPH-dependent deamination of GMP to IMP. It functions in the conversion of nucleobase, nucleoside and nucleotide derivatives of G to A nucleotides, and in maintaining the intracellular balance of A and G nucleotides | |
NECFGCCN_02699 | 1.6e-103 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
NECFGCCN_02700 | 4.4e-135 | zapD | D | Cell division factor that enhances FtsZ-ring assembly. Directly interacts with FtsZ and promotes bundling of FtsZ protofilaments, with a reduction in FtsZ GTPase activity | ||
NECFGCCN_02701 | 2.6e-31 | yacG | 2.7.1.24 | S | Inhibits all the catalytic activities of DNA gyrase by preventing its interaction with DNA. Acts by binding directly to the C-terminal domain of GyrB, which probably disrupts DNA binding by the gyrase | |
NECFGCCN_02702 | 2.1e-64 | mutT | 3.6.1.55, 3.6.1.65 | L | belongs to the nudix hydrolase family | |
NECFGCCN_02703 | 0.0 | secA | U | Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. Has a central role in coupling the hydrolysis of ATP to the transfer of proteins into and across the cell membrane, serving both as a receptor for the preprotein-SecB complex and as an ATP-driven molecular motor driving the stepwise translocation of polypeptide chains across the membrane | ||
NECFGCCN_02704 | 1.3e-82 | secM | S | Regulates secA expression by translational coupling of the secM secA operon. Translational pausing at a specific Pro residue 5 residues before the end of the protein may allow disruption of a mRNA repressor helix that normally suppresses secA translation initiation | ||
NECFGCCN_02705 | 5.9e-174 | lpxC | 3.5.1.108, 4.2.1.59 | M | Catalyzes the hydrolysis of UDP-3-O-myristoyl-N- acetylglucosamine to form UDP-3-O-myristoylglucosamine and acetate, the committed step in lipid A biosynthesis | |
NECFGCCN_02706 | 4.6e-208 | ftsZ | D | Essential cell division protein that forms a contractile ring structure (Z ring) at the future cell division site. The regulation of the ring assembly controls the timing and the location of cell division. One of the functions of the FtsZ ring is to recruit other cell division proteins to the septum to produce a new cell wall between the dividing cells. Binds GTP and shows GTPase activity | ||
NECFGCCN_02707 | 8.8e-237 | ftsA | D | Cell division protein that is involved in the assembly of the Z ring. May serve as a membrane anchor for the Z ring | ||
NECFGCCN_02708 | 1.5e-152 | ftsQ | 6.3.2.4 | D | Essential cell division protein. May link together the upstream cell division proteins, which are predominantly cytoplasmic, with the downstream cell division proteins, which are predominantly periplasmic. May control correct divisome assembly | |
NECFGCCN_02709 | 3.8e-165 | ddl | 1.3.1.98, 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
NECFGCCN_02710 | 4.1e-278 | murC | 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
NECFGCCN_02711 | 1.2e-194 | murG | 2.4.1.227 | GT28 | M | Cell wall formation. Catalyzes the transfer of a GlcNAc subunit on undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide (lipid intermediate I) to form undecaprenyl-pyrophosphoryl-MurNAc- (pentapeptide)GlcNAc (lipid intermediate II) |
NECFGCCN_02712 | 4.3e-223 | ftsW | 2.4.1.227 | GT28 | M | Peptidoglycan polymerase that is essential for cell division |
NECFGCCN_02713 | 2.4e-245 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
NECFGCCN_02714 | 6e-202 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
NECFGCCN_02715 | 8.8e-229 | murF | 6.3.2.10 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
NECFGCCN_02716 | 1.2e-126 | XK27_08080 | 3.1.1.53 | G | Exopolysaccharide biosynthesis protein | |
NECFGCCN_02717 | 9.3e-234 | gatA | 3.5.1.4, 3.5.1.84, 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Gln-tRNA(Gln) through the transamidation of misacylated Glu-tRNA(Gln) in organisms which lack glutaminyl-tRNA synthetase. The reaction takes place in the presence of glutamine and ATP through an activated gamma-phospho-Glu-tRNA(Gln) | |
NECFGCCN_02718 | 4.5e-67 | ybeY | S | Protein of unknown function (DUF3225) | ||
NECFGCCN_02719 | 2.7e-65 | XK27_03610 | K | Acetyltransferase (GNAT) domain | ||
NECFGCCN_02720 | 2.9e-207 | asd | 1.2.1.11 | E | Semialdehyde dehydrogenase, NAD binding domain | |
NECFGCCN_02721 | 7.3e-103 | K | transcriptional regulator | |||
NECFGCCN_02722 | 1.3e-153 | V | multidrug resistance efflux pump | |||
NECFGCCN_02723 | 2.6e-291 | EGP | the major facilitator superfamily | |||
NECFGCCN_02724 | 6.1e-230 | fabF | 2.3.1.179 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP | |
NECFGCCN_02725 | 3.7e-67 | 3.4.13.21 | S | protein conserved in bacteria | ||
NECFGCCN_02726 | 1.8e-66 | |||||
NECFGCCN_02727 | 6.4e-111 | MA20_01125 | K | AraC-like ligand binding domain | ||
NECFGCCN_02728 | 8.6e-130 | yfeJ | 6.3.5.2 | F | Glutamine amidotransferase | |
NECFGCCN_02729 | 1.4e-111 | S | Alpha beta hydrolase | |||
NECFGCCN_02730 | 4.5e-11 | |||||
NECFGCCN_02731 | 7.9e-140 | ripA_2 | K | transcriptional regulator | ||
NECFGCCN_02732 | 1.1e-133 | S | membrane transporter protein | |||
NECFGCCN_02733 | 1.9e-188 | puuE | 3.5.1.41, 3.5.2.5 | G | deacetylase | |
NECFGCCN_02734 | 8.8e-128 | hyuE | 5.1.99.3 | E | racemase | |
NECFGCCN_02735 | 9e-130 | yncC | K | transcriptional regulator | ||
NECFGCCN_02736 | 2.9e-137 | S | Replication-relaxation | |||
NECFGCCN_02738 | 2.3e-301 | L | Recombinase | |||
NECFGCCN_02739 | 6.5e-154 | endA | F | DNA RNA non-specific endonuclease | ||
NECFGCCN_02740 | 7.2e-26 | epuA | S | DNA-directed RNA polymerase subunit beta | ||
NECFGCCN_02741 | 3.8e-232 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
NECFGCCN_02743 | 8.1e-193 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
NECFGCCN_02744 | 1.1e-134 | G | Domain of unknown function (DUF4832) | |||
NECFGCCN_02745 | 9.2e-84 | S | membrane | |||
NECFGCCN_02746 | 3e-96 | P | VTC domain | |||
NECFGCCN_02747 | 1.2e-112 | cotH | M | CotH kinase protein | ||
NECFGCCN_02748 | 5.5e-56 | yedA | EG | of the drug metabolite transporter (DMT) superfamily | ||
NECFGCCN_02749 | 3.3e-46 | pqqL | S | Peptidase, M16 | ||
NECFGCCN_02750 | 2.2e-46 | FrpB2 | P | receptor | ||
NECFGCCN_02751 | 2e-29 | FrpB2 | P | receptor | ||
NECFGCCN_02752 | 6.5e-173 | EGP | Major facilitator Superfamily | |||
NECFGCCN_02753 | 4.1e-309 | iucA | 6.3.2.38 | Q | Siderophore biosynthesis protein | |
NECFGCCN_02754 | 4.9e-184 | iucB | 2.3.1.102, 6.3.2.38 | J | Siderophore biosynthesis protein | |
NECFGCCN_02755 | 0.0 | iucC | 6.3.2.39 | Q | Siderophore biosynthesis protein | |
NECFGCCN_02756 | 1.3e-230 | iucD | 1.14.13.59 | Q | L-lysine 6-monooxygenase (NADPH-requiring) | |
NECFGCCN_02757 | 0.0 | iutA | M | TonB dependent receptor | ||
NECFGCCN_02758 | 2.2e-09 | S | Protein of unknown function (DUF1471) | |||
NECFGCCN_02759 | 2.4e-77 | K | Transcriptional regulator | |||
NECFGCCN_02760 | 6.1e-57 | S | Protein of unknown function, DUF417 | |||
NECFGCCN_02761 | 1.4e-22 | 4.1.1.44 | S | Antioxidant protein with alkyl hydroperoxidase activity. Required for the reduction of the AhpC active site cysteine residues and for the regeneration of the AhpC enzyme activity | ||
NECFGCCN_02762 | 4.8e-66 | S | Electron transfer DM13 | |||
NECFGCCN_02763 | 1.2e-44 | |||||
NECFGCCN_02764 | 1.9e-78 | pin | L | Resolvase, N terminal domain | ||
NECFGCCN_02765 | 0.0 | L | Domain of unknown function (DUF4158) | |||
NECFGCCN_02766 | 4.8e-100 | S | dextransucrase activity | |||
NECFGCCN_02767 | 2.8e-97 | yddQ | P | Binding-protein-dependent transport systems inner membrane component | ||
NECFGCCN_02768 | 2.3e-148 | oppD | 3.6.3.24 | EP | (ABC) transporter | |
NECFGCCN_02769 | 1.1e-122 | gsiA_3 | 3.6.3.24 | EP | (ABC) transporter | |
NECFGCCN_02770 | 1.9e-52 | S | Antibiotic biosynthesis monooxygenase | |||
NECFGCCN_02771 | 1.3e-87 | btuE | 1.11.1.9 | O | Belongs to the glutathione peroxidase family | |
NECFGCCN_02772 | 7.2e-98 | |||||
NECFGCCN_02773 | 2.4e-226 | yhbH | S | Belongs to the UPF0229 family | ||
NECFGCCN_02774 | 0.0 | prkA | T | Serine Protein Kinase | ||
NECFGCCN_02775 | 2e-143 | mipA | M | MltA-interacting protein | ||
NECFGCCN_02776 | 6.3e-154 | yeaE | 1.1.1.21 | S | Aldo keto | |
NECFGCCN_02777 | 9e-172 | yeaD | 4.2.1.9, 5.1.3.15 | G | Belongs to the glucose-6-phosphate 1-epimerase family | |
NECFGCCN_02778 | 1.6e-185 | gapA | 1.2.1.12, 1.2.1.72 | C | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
NECFGCCN_02779 | 6.5e-80 | msrB | 1.8.4.12 | O | Belongs to the MsrB Met sulfoxide reductase family | |
NECFGCCN_02780 | 1.7e-44 | yeaC | S | protein conserved in bacteria | ||
NECFGCCN_02781 | 1.2e-63 | yajD | 2.1.1.148 | L | endonuclease | |
NECFGCCN_02782 | 6.2e-235 | chiA1 | 3.2.1.14 | GH18 | G | chitinase |
NECFGCCN_02783 | 2.1e-117 | pncA | 2.7.11.1, 3.5.1.19 | Q | Nicotinamidase | |
NECFGCCN_02784 | 5.9e-191 | ansA | 3.5.1.1 | EJ | COG0252 L-asparaginase archaeal Glu-tRNAGln amidotransferase subunit D | |
NECFGCCN_02785 | 0.0 | sppA | OU | Signal peptide peptidase | ||
NECFGCCN_02786 | 6.4e-99 | ydjA | C | Nitroreductase | ||
NECFGCCN_02787 | 6.9e-184 | 1.1.1.18, 1.1.1.369 | E | 2-dehydrogenase | ||
NECFGCCN_02788 | 1e-190 | K | Transcriptional | |||
NECFGCCN_02789 | 9.4e-164 | mocB | G | ABC-type sugar transport system periplasmic component | ||
NECFGCCN_02790 | 1.4e-278 | mglA_1 | 3.6.3.17 | P | import. Responsible for energy coupling to the transport system | |
NECFGCCN_02791 | 1.9e-176 | rbsC1 | G | Belongs to the binding-protein-dependent transport system permease family | ||
NECFGCCN_02792 | 9.4e-55 | fumA | 4.2.1.2 | C | Catalyzes the reversible hydration of fumarate to (S)- malate | |
NECFGCCN_02793 | 1.5e-166 | O | Belongs to the peptidase S8 family | |||
NECFGCCN_02794 | 3.4e-09 | S | pathogenesis | |||
NECFGCCN_02796 | 5.2e-150 | cbiO2 | P | ABC transporter, ATP-binding protein | ||
NECFGCCN_02797 | 7.8e-157 | P | ATPase activity | |||
NECFGCCN_02798 | 4.8e-132 | cbiQ | P | cobalt transport | ||
NECFGCCN_02799 | 2.4e-91 | 2.7.7.65 | T | Psort location CytoplasmicMembrane, score | ||
NECFGCCN_02800 | 8e-135 | S | Phenazine biosynthesis protein | |||
NECFGCCN_02801 | 2.6e-22 | proWX | P | ABC transporter | ||
NECFGCCN_02802 | 1e-210 | metK | 2.5.1.6 | H | Catalyzes the formation of S-adenosylmethionine (AdoMet) from methionine and ATP. The overall synthetic reaction is composed of two sequential steps, AdoMet formation and the subsequent tripolyphosphate hydrolysis which occurs prior to release of AdoMet from the enzyme | |
NECFGCCN_02803 | 1.6e-171 | birA | 6.3.4.15 | HK | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
NECFGCCN_02804 | 1e-179 | dnaX | 2.7.7.7 | L | DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
NECFGCCN_02805 | 9.3e-09 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
NECFGCCN_02806 | 6.2e-111 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
NECFGCCN_02808 | 5.2e-27 | S | unusual protein kinase | |||
NECFGCCN_02809 | 3.2e-38 | S | granule-associated protein | |||
NECFGCCN_02810 | 1.2e-285 | bglH | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
NECFGCCN_02811 | 2.4e-108 | S | hmm pf01594 | |||
NECFGCCN_02812 | 6.5e-64 | acrF | V | Belongs to the resistance-nodulation-cell division (RND) (TC 2.A.6) family | ||
NECFGCCN_02813 | 7.1e-33 | yhdV | S | Protein involved in biological_process | ||
NECFGCCN_02814 | 2.5e-77 | fruA | 3.2.1.1, 3.2.1.26, 3.2.1.65, 3.2.1.80 | GH13,GH32 | G | Belongs to the glycosyl hydrolase 32 family |
NECFGCCN_02815 | 1.1e-25 | fruA | 3.2.1.1, 3.2.1.26, 3.2.1.65, 3.2.1.80 | GH13,GH32 | G | Belongs to the glycosyl hydrolase 32 family |
NECFGCCN_02816 | 4.6e-99 | fruA | 3.2.1.1, 3.2.1.26, 3.2.1.65, 3.2.1.80 | GH13,GH32 | G | Belongs to the glycosyl hydrolase 32 family |
NECFGCCN_02817 | 1.7e-51 | fruA | 3.2.1.1, 3.2.1.26, 3.2.1.65, 3.2.1.80 | GH13,GH32 | G | Belongs to the glycosyl hydrolase 32 family |
NECFGCCN_02818 | 1e-162 | yjlA | EG | membrane | ||
NECFGCCN_02819 | 1.5e-158 | garR | 1.1.1.60 | I | Catalyzes the reduction of tatronate semialdehyde to D- glycerate | |
NECFGCCN_02820 | 1.6e-140 | garL | 4.1.2.20, 4.1.2.52, 4.1.2.53 | G | Belongs to the HpcH HpaI aldolase family | |
NECFGCCN_02821 | 3.2e-221 | garP | G | transporter | ||
NECFGCCN_02823 | 3.6e-280 | garD | 4.2.1.42, 4.2.1.7 | G | Catalyzes the dehydration of galactarate to form 5- dehydro-4-deoxy-D-glucarate | |
NECFGCCN_02824 | 1.4e-156 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
NECFGCCN_02825 | 0.0 | lpoA | M | Regulator of peptidoglycan synthesis that is essential for the function of penicillin-binding protein 1A (PBP1a) | ||
NECFGCCN_02826 | 2e-67 | yraN | L | Belongs to the UPF0102 family | ||
NECFGCCN_02827 | 4.1e-104 | gmhA | 2.7.1.167, 2.7.1.33, 2.7.7.70, 5.3.1.28 | G | Catalyzes the isomerization of sedoheptulose 7-phosphate in D-glycero-D-manno-heptose 7-phosphate | |
NECFGCCN_02828 | 1.4e-80 | yraP | S | Periplasmic or secreted lipoprotein | ||
NECFGCCN_02829 | 2.1e-183 | yraQ | S | permease | ||
NECFGCCN_02830 | 3.6e-109 | yraR | GM | Nucleoside-diphosphate-sugar epimerases | ||
NECFGCCN_02831 | 8.4e-96 | yfkM | 3.5.1.124 | S | intracellular protease | |
NECFGCCN_02832 | 6.3e-81 | yhbP | S | Belongs to the UPF0306 family | ||
NECFGCCN_02833 | 8.9e-45 | yhbQ | L | endonuclease containing a URI domain | ||
NECFGCCN_02834 | 1.7e-90 | yhbS | S | acetyltransferase | ||
NECFGCCN_02835 | 2.5e-89 | yhbT | I | lipid carrier protein | ||
NECFGCCN_02836 | 2.2e-190 | yhbU | O | Peptidase U32 | ||
NECFGCCN_02837 | 8.1e-165 | yhbV | O | protease | ||
NECFGCCN_02838 | 1.5e-191 | yhbW | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | ||
NECFGCCN_02839 | 9.3e-223 | mtr | E | Amino Acid | ||
NECFGCCN_02840 | 2.8e-282 | deaD | 3.6.4.13 | F | DEAD-box RNA helicase involved in various cellular processes at low temperature, including ribosome biogenesis, mRNA degradation and translation initiation | |
NECFGCCN_02841 | 6.3e-165 | nlpI | S | May be involved in cell division | ||
NECFGCCN_02842 | 0.0 | pnp | 2.7.7.8 | J | Involved in mRNA degradation. Catalyzes the phosphorolysis of single-stranded polyribonucleotides processively in the 3'- to 5'-direction | |
NECFGCCN_02843 | 1.5e-40 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
NECFGCCN_02844 | 1.8e-173 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
NECFGCCN_02845 | 2.6e-65 | rbfA | J | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Associates with free 30S ribosomal subunits (but not with 30S subunits that are part of 70S ribosomes or polysomes). Required for efficient processing of 16S rRNA. May interact with the 5'-terminal helix region of 16S rRNA | ||
NECFGCCN_02846 | 0.0 | infB | J | One of the essential components for the initiation of protein synthesis. Protects formylmethionyl-tRNA from spontaneous hydrolysis and promotes its binding to the 30S ribosomal subunits. Also involved in the hydrolysis of GTP during the formation of the 70S ribosomal complex | ||
NECFGCCN_02847 | 2e-272 | nusA | K | Participates in both transcription termination and antitermination | ||
NECFGCCN_02848 | 1e-72 | rimP | S | Required for maturation of 30S ribosomal subunits | ||
NECFGCCN_02849 | 4.3e-169 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
NECFGCCN_02850 | 1.3e-146 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
NECFGCCN_02851 | 4.2e-237 | XK27_04775 | S | hemerythrin HHE cation binding domain | ||
NECFGCCN_02852 | 1e-34 | M1-755 | P | Hemerythrin HHE cation binding domain protein | ||
NECFGCCN_02853 | 1.1e-110 | hsdS2 | 2.1.1.72 | V | Type I restriction modification DNA specificity domain | |
NECFGCCN_02854 | 4.2e-86 | tpx | 1.11.1.15 | O | Thiol-specific peroxidase that catalyzes the reduction of hydrogen peroxide and organic hydroperoxides to water and alcohols, respectively. Plays a role in cell protection against oxidative stress by detoxifying peroxides | |
NECFGCCN_02855 | 2.8e-137 | S | haloacid dehalogenase-like hydrolase | |||
NECFGCCN_02856 | 7e-56 | nrdD_1 | 1.1.98.6, 1.17.4.1 | F | Ribonucleoside-triphosphate reductase | |
NECFGCCN_02858 | 1.7e-108 | 6.3.2.2 | H | gamma-glutamylcysteine synthetase | ||
NECFGCCN_02860 | 1.3e-165 | fba | 4.1.2.13, 4.1.2.29 | G | aldolase | |
NECFGCCN_02861 | 8.2e-168 | IQ | Dehydrogenases with different specificities (Related to short-chain alcohol dehydrogenases) | |||
NECFGCCN_02863 | 1.9e-27 | |||||
NECFGCCN_02864 | 7.2e-73 | yciE | S | protein conserved in bacteria | ||
NECFGCCN_02866 | 4.5e-311 | 3.2.1.1, 5.4.99.16 | GH13 | G | COG0366 Glycosidases | |
NECFGCCN_02867 | 9.5e-178 | yxnA | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | ||
NECFGCCN_02869 | 1.3e-65 | S | Protein involved in biological_process | |||
NECFGCCN_02870 | 1.7e-74 | |||||
NECFGCCN_02871 | 3.4e-65 | ydeI | Q | PFAM Bacterial OB fold (BOF) protein | ||
NECFGCCN_02873 | 3.2e-74 | osmC | O | redox protein regulator of disulfide bond formation | ||
NECFGCCN_02874 | 2.2e-154 | M | protein conserved in bacteria | |||
NECFGCCN_02875 | 7.4e-113 | ET | COG0834 ABC-type amino acid transport signal transduction systems periplasmic component domain | |||
NECFGCCN_02876 | 6.8e-146 | fieF | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
NECFGCCN_02877 | 2.2e-168 | S | Membrane | |||
NECFGCCN_02878 | 0.0 | cbbbC | C | Belongs to the prokaryotic molybdopterin-containing oxidoreductase family | ||
NECFGCCN_02879 | 5.7e-158 | oxyR_3 | K | transcriptional regulator | ||
NECFGCCN_02880 | 1.1e-189 | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | |||
NECFGCCN_02881 | 4.4e-291 | 3.2.1.40 | G | Bacterial alpha-L-rhamnosidase C-terminal domain | ||
NECFGCCN_02882 | 1.3e-128 | K | Transcriptional regulator | |||
NECFGCCN_02884 | 3.9e-120 | I | PFAM Alpha beta hydrolase fold-3 domain protein | |||
NECFGCCN_02885 | 1.9e-39 | 2.7.1.196, 2.7.1.205 | G | Phosphotransferase System | ||
NECFGCCN_02886 | 4.8e-35 | celC | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIA subunit | |
NECFGCCN_02887 | 9.7e-261 | lacY | P | Sugar (and other) transporter | ||
NECFGCCN_02888 | 2.6e-86 | mgtC | S | MgtC SapB transporter | ||
NECFGCCN_02889 | 2.9e-177 | S | AFG1-like ATPase | |||
NECFGCCN_02890 | 0.0 | katG | 1.11.1.21 | P | Bifunctional enzyme with both catalase and broad- spectrum peroxidase activity | |
NECFGCCN_02891 | 4.8e-139 | K | Transcriptional regulator | |||
NECFGCCN_02892 | 2.7e-52 | S | Putative inner membrane exporter, YdcZ | |||
NECFGCCN_02893 | 5.2e-57 | S | Putative inner membrane exporter, YdcZ | |||
NECFGCCN_02894 | 0.0 | mrdA | 3.4.16.4 | M | Catalyzes cross-linking of the peptidoglycan cell wall | |
NECFGCCN_02895 | 6.4e-131 | guaA | 6.3.5.2 | F | glutamine amidotransferase | |
NECFGCCN_02896 | 3.1e-77 | lysA | 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
NECFGCCN_02897 | 1.6e-235 | pepT | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
NECFGCCN_02898 | 8.3e-52 | potA | 3.6.3.31 | P | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | |
NECFGCCN_02899 | 1.9e-155 | murI | 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
NECFGCCN_02900 | 0.0 | btuB | P | Involved in the active translocation of vitamin B12 (cyanocobalamin) across the outer membrane to the periplasmic space. It derives its energy for transport by interacting with the trans-periplasmic membrane protein TonB | ||
NECFGCCN_02901 | 2.6e-208 | trmA | 2.1.1.190, 2.1.1.35 | J | Dual-specificity methyltransferase that catalyzes the formation of 5-methyluridine at position 54 (m5U54) in all tRNAs, and that of position 341 (m5U341) in tmRNA (transfer-mRNA) | |
NECFGCCN_02902 | 5.5e-59 | yijD | S | membrane | ||
NECFGCCN_02903 | 3.9e-108 | fabR | K | Represses the transcription of fabB, involved in unsaturated fatty acid (UFA) biosynthesis. By controlling UFA production, FabR directly influences the physical properties of the membrane bilayer | ||
NECFGCCN_02904 | 2.2e-273 | sthA | 1.6.1.1 | C | Conversion of NADPH, generated by peripheral catabolic pathways, to NADH, which can enter the respiratory chain for energy generation | |
NECFGCCN_02905 | 3.6e-171 | oxyR | K | Transcriptional regulator | ||
NECFGCCN_02906 | 2e-255 | argH | 2.3.1.1, 4.3.2.1 | E | argininosuccinate lyase | |
NECFGCCN_02907 | 6.3e-137 | argB | 2.3.1.1, 2.7.2.8 | E | Catalyzes the ATP-dependent phosphorylation of N-acetyl- L-glutamate | |
NECFGCCN_02908 | 2.6e-191 | argC | 1.2.1.38 | E | Catalyzes the NADPH-dependent reduction of N-acetyl-5- glutamyl phosphate to yield N-acetyl-L-glutamate 5-semialdehyde | |
NECFGCCN_02909 | 1.6e-208 | argE | 3.5.1.16 | E | Belongs to the peptidase M20A family. ArgE subfamily | |
NECFGCCN_02910 | 6.2e-243 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
NECFGCCN_02911 | 0.0 | S | bacteriocin-associated integral membrane protein | |||
NECFGCCN_02912 | 2.1e-19 | S | Bacteriocin (Lactococcin_972) | |||
NECFGCCN_02913 | 1.1e-57 | |||||
NECFGCCN_02914 | 0.0 | ctpE | P | E1-E2 ATPase | ||
NECFGCCN_02915 | 1.8e-195 | epd | 1.2.1.12, 1.2.1.72 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
NECFGCCN_02916 | 9e-212 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
NECFGCCN_02917 | 5.6e-208 | fbaA | 4.1.2.13 | G | Fructose-bisphosphate aldolase, class II | |
NECFGCCN_02918 | 7.5e-131 | mscS | M | Mechanosensitive Ion channel | ||
NECFGCCN_02919 | 6.4e-111 | argO | S | Involved in the export of arginine. Important to control the intracellular level of arginine and the correct balance between arginine and lysine | ||
NECFGCCN_02920 | 1.7e-118 | yggE | S | Protein of unknown function (DUF541) | ||
NECFGCCN_02921 | 8.8e-167 | argP | K | Controls the transcription of genes involved in arginine and lysine metabolism | ||
NECFGCCN_02922 | 9.9e-115 | rpiA | 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
NECFGCCN_02923 | 3.3e-228 | serA | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
NECFGCCN_02924 | 9.6e-109 | fthC | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
NECFGCCN_02925 | 2.7e-44 | zapA | D | Activator of cell division through the inhibition of FtsZ GTPase activity, therefore promoting FtsZ assembly into bundles of protofilaments necessary for the formation of the division Z ring. It is recruited early at mid-cell but it is not essential for cell division | ||
NECFGCCN_02926 | 5.1e-107 | ygfB | S | Belongs to the UPF0149 family | ||
NECFGCCN_02927 | 4.2e-250 | pepP | 3.4.11.9 | E | aminopeptidase | |
NECFGCCN_02928 | 2.3e-215 | ubiH | CH | hydroxylase | ||
NECFGCCN_02929 | 4e-223 | visC | CH | ubiquinone biosynthesis hydroxylase, UbiH UbiF VisC COQ6 | ||
NECFGCCN_02930 | 5.5e-211 | gcvT | 2.1.2.10 | H | The glycine cleavage system catalyzes the degradation of glycine | |
NECFGCCN_02931 | 3.6e-64 | gcvH | E | The glycine cleavage system catalyzes the degradation of glycine. The H protein shuttles the methylamine group of glycine from the P protein to the T protein | ||
NECFGCCN_02932 | 0.0 | gcvP | 1.4.4.2 | E | The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor | |
NECFGCCN_02933 | 1.2e-129 | IQ | Dehydrogenases with different specificities (Related to short-chain alcohol dehydrogenases) | |||
NECFGCCN_02934 | 1.6e-85 | scsD | CO | COG0526 Thiol-disulfide isomerase and thioredoxins | ||
NECFGCCN_02935 | 5.4e-107 | bdbD | O | DSBA-like thioredoxin domain | ||
NECFGCCN_02936 | 8.2e-236 | dsbD | 1.8.1.8 | CO | Disulphide bond corrector protein DsbC | |
NECFGCCN_02937 | 4.8e-55 | murQ | 4.2.1.126 | S | Specifically catalyzes the cleavage of the D-lactyl ether substituent of MurNAc 6-phosphate, producing GlcNAc 6- phosphate and D-lactate | |
NECFGCCN_02938 | 0.0 | mqo | 1.1.5.4 | C | malate quinone oxidoreductase | |
NECFGCCN_02939 | 8e-163 | mdcR | K | Transcriptional regulator | ||
NECFGCCN_02940 | 2.5e-153 | mdcH | 2.3.1.39 | I | malonyl CoA-acyl carrier protein transacylase | |
NECFGCCN_02941 | 2.4e-110 | mdcG | 2.7.7.66 | H | Phosphoribosyl-dephospho-CoA transferase MdcG | |
NECFGCCN_02942 | 5.4e-162 | mdcF | S | auxin efflux carrier | ||
NECFGCCN_02943 | 7e-139 | mdcE | 4.1.1.87 | I | malonate decarboxylase gamma subunit | |
NECFGCCN_02944 | 2e-149 | mdcD | 4.1.1.87 | I | Beta subunit | |
NECFGCCN_02945 | 3.4e-46 | mdcC | C | Subunit of malonate decarboxylase, it is an acyl carrier protein to which acetyl and malonyl thioester residues are bound via a 2'-(5''-phosphoribosyl)-3'-dephospho-CoA prosthetic group and turn over during the catalytic mechanism | ||
NECFGCCN_02946 | 3.1e-26 | mdcB | 2.4.2.52 | H | Involved in the formation of 2-(5''-phosphoribosyl)-3'- dephosphocoenzyme-A, the prosthetic group of the acyl-carrier protein of the malonate decarboxylase | |
NECFGCCN_02949 | 2.6e-154 | ydiJ | C | Fad linked oxidase | ||
NECFGCCN_02950 | 1.2e-97 | ydiJ | C | Fad linked oxidase | ||
NECFGCCN_02951 | 2.7e-197 | ydiK | S | ydiK promoter presents a PurR sequence, suggesting that its expression is purine-regulated | ||
NECFGCCN_02952 | 0.0 | ppsA | 2.7.9.2 | H | Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate | |
NECFGCCN_02953 | 5.2e-153 | ydiA | 2.7.11.33, 2.7.4.28 | S | Bifunctional serine threonine kinase and phosphorylase involved in the regulation of the phosphoenolpyruvate synthase (PEPS) by catalyzing its phosphorylation dephosphorylation | |
NECFGCCN_02954 | 5e-30 | aroH | 2.5.1.54 | E | Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) | |
NECFGCCN_02955 | 2.6e-68 | cysW_1 | P | ABC-type Fe3 transport system permease component | ||
NECFGCCN_02956 | 1.5e-112 | thiN | 2.7.6.2 | H | thiamine pyrophosphokinase | |
NECFGCCN_02957 | 7.8e-120 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
NECFGCCN_02958 | 1.7e-159 | rsgA | 3.1.3.100 | G | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Helps release RbfA from mature subunits. May play a role in the assembly of ribosomal proteins into the subunit. Circularly permuted GTPase that catalyzes slow GTP hydrolysis, GTPase activity is stimulated by the 30S ribosomal subunit | |
NECFGCCN_02960 | 2.4e-153 | ksgA | 2.1.1.182 | J | Specifically dimethylates two adjacent adenosines (A1518 and A1519) in the loop of a conserved hairpin near the 3'-end of 16S rRNA in the 30S particle. May play a critical role in biogenesis of 30S subunits | |
NECFGCCN_02961 | 1.1e-98 | rnmV | 3.1.26.8 | J | Required for correct processing of both the 5' and 3' ends of 5S rRNA precursor. Cleaves both sides of a double-stranded region yielding mature 5S rRNA in one step | |
NECFGCCN_02962 | 6.8e-142 | tatD | L | Hydrolase, tatd | ||
NECFGCCN_02963 | 1.1e-23 | yccU | S | CoA-binding protein | ||
NECFGCCN_02964 | 1.9e-300 | ybiT | S | COG0488 ATPase components of ABC transporters with duplicated ATPase domains | ||
NECFGCCN_02965 | 6e-127 | 3.1.3.48 | T | Protein tyrosine serine phosphatase | ||
NECFGCCN_02966 | 1.6e-172 | ybiS | M | ErfK YbiS YcfS YnhG family protein | ||
NECFGCCN_02967 | 1.2e-126 | gmuR | K | GntR family | ||
NECFGCCN_02968 | 1.1e-272 | pbg6 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
NECFGCCN_02969 | 1.5e-195 | ybiR | P | Citrate transporter | ||
NECFGCCN_02970 | 3.3e-80 | mntR | K | transcriptional regulator | ||
NECFGCCN_02971 | 5.8e-16 | |||||
NECFGCCN_02972 | 1.7e-301 | ybiP | 2.7.8.42, 2.7.8.43 | S | membrane-associated metal-dependent hydrolase | |
NECFGCCN_02973 | 8.6e-90 | ompX | M | PFAM virulence-related outer membrane protein | ||
NECFGCCN_02974 | 4.2e-153 | rhtA | S | permease DMT superfamily | ||
NECFGCCN_02975 | 6.7e-87 | dps | P | During stationary phase, binds the chromosome non- specifically, forming a highly ordered and stable dps-DNA co- crystal within which chromosomal DNA is condensed and protected from diverse damages. It protects DNA from oxidative damage by sequestering intracellular Fe(2 ) ion and storing it in the form of Fe(3 ) oxyhydroxide mineral, which can be released after reduction. One hydrogen peroxide oxidizes two Fe(2 ) ions, which prevents hydroxyl radical production by the Fenton reaction | ||
NECFGCCN_02976 | 1.1e-135 | glnH | ET | belongs to the bacterial solute-binding protein 3 family | ||
NECFGCCN_02977 | 7.1e-113 | glnP | P | (ABC) transporter | ||
NECFGCCN_02978 | 9.1e-130 | glnQ | E | (ABC) transporter | ||
NECFGCCN_02979 | 0.0 | ybiO | M | mechanosensitive ion channel | ||
NECFGCCN_02980 | 9e-175 | rlmF | 2.1.1.181 | J | Specifically methylates the adenine in position 1618 of 23S rRNA | |
NECFGCCN_02981 | 6.4e-116 | IV02_24660 | S | Conserved protein domain typically associated with flavoprotein oxygenases DIM6 NTAB family | ||
NECFGCCN_02982 | 5.8e-34 | mcbA | S | colanic acid metabolic process | ||
NECFGCCN_02983 | 4.4e-45 | ybiI | T | DnaK suppressor protein | ||
NECFGCCN_02984 | 1.8e-35 | ybiJ | S | protein involved in | ||
NECFGCCN_02985 | 3.1e-133 | ybiB | 2.4.2.18 | E | Glycosyl transferase | |
NECFGCCN_02986 | 2.4e-41 | livF | P | Branched-chain amino acid transport | ||
NECFGCCN_02987 | 3.8e-26 | |||||
NECFGCCN_02988 | 5e-145 | fliY_2 | ET | Belongs to the bacterial solute-binding protein 3 family | ||
NECFGCCN_02989 | 4e-142 | glnQ | 3.6.3.21 | E | (ABC) transporter | |
NECFGCCN_02990 | 1.1e-130 | glnM | P | (ABC) transporter | ||
NECFGCCN_02991 | 5.3e-119 | glnP | P | (ABC) transporter | ||
NECFGCCN_02992 | 3.3e-132 | ecpE | NU | Part of the ecpRABCDE operon, which encodes the E.coli common pilus (ECP). ECP is found in both commensal and pathogenic strains and plays a dual role in early-stage biofilm development and host cell recognition (By similarity) | ||
NECFGCCN_02993 | 0.0 | yagW | S | Part of the ecpRABCDE operon, which encodes the E.coli common pilus (ECP). ECP is found in both commensal and pathogenic strains and plays a dual role in early-stage biofilm development and host cell recognition. Tip pilus adhesin, which is required for assembly of EcpA into fibers (By similarity) | ||
NECFGCCN_02994 | 0.0 | ecpC | NU | Part of the ecpRABCDE operon, which encodes the E.coli common pilus (ECP). ECP is found in both commensal and pathogenic strains and plays a dual role in early-stage biofilm development and host cell recognition (By similarity) | ||
NECFGCCN_02995 | 3e-119 | ecpB | M | Part of the ecpRABCDE operon, which encodes the E.coli common pilus (ECP). ECP is found in both commensal and pathogenic strains and plays a dual role in early-stage biofilm development and host cell recognition (By similarity) | ||
NECFGCCN_02996 | 9.2e-96 | matB | S | Part of the ecpRABCDE operon, which encodes the E.coli common pilus (ECP). ECP is found in both commensal and pathogenic strains and plays a dual role in early-stage biofilm development and host cell recognition. Major subunit of the fimbria | ||
NECFGCCN_02997 | 1.9e-92 | matA | K | Part of the ecpRABCDE operon, which encodes the E.coli common pilus (ECP). ECP is found in both commensal and pathogenic strains and plays a dual role in early-stage biofilm development and host cell recognition | ||
NECFGCCN_02998 | 4.6e-149 | phnC | 3.6.3.28 | P | Part of the ABC transporter complex PhnCDE involved in phosphonates import. Responsible for energy coupling to the transport system | |
NECFGCCN_02999 | 9.3e-175 | phnD | P | Phosphonate ABC transporter | ||
NECFGCCN_03000 | 4.7e-157 | phnE_2 | P | Phosphonate ABC transporter | ||
NECFGCCN_03001 | 5.7e-158 | phnE | 3.6.1.63 | P | Phosphonate ABC transporter | |
NECFGCCN_03002 | 1.2e-58 | Z012_04635 | K | Transcriptional activator, Rgg GadR MutR family | ||
NECFGCCN_03003 | 3.7e-197 | yjbB | G | Permeases of the major facilitator superfamily | ||
NECFGCCN_03004 | 2.3e-300 | prfC | J | Increases the formation of ribosomal termination complexes and stimulates activities of RF-1 and RF-2. It binds guanine nucleotides and has strong preference for UGA stop codons. It may interact directly with the ribosome. The stimulation of RF- 1 and RF-2 is significantly reduced by GTP and GDP, but not by GMP | ||
NECFGCCN_03005 | 3.1e-116 | ywaF | S | Integral membrane protein (intg_mem_TP0381) | ||
NECFGCCN_03006 | 9.2e-256 | murF | 6.3.2.10 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
NECFGCCN_03010 | 3.3e-155 | cjaA | ET | ABC transporter substrate-binding protein | ||
NECFGCCN_03011 | 3.4e-135 | glnQ | 3.6.3.21 | E | abc transporter atp-binding protein | |
NECFGCCN_03012 | 5.1e-106 | P | ABC transporter (Permease | |||
NECFGCCN_03013 | 8.6e-114 | papP | P | ABC transporter (Permease | ||
NECFGCCN_03014 | 3e-190 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
NECFGCCN_03015 | 1.5e-86 | zntB | P | Zinc transport protein zntB | ||
NECFGCCN_03016 | 2.7e-121 | glcR | K | transcriptional regulator | ||
NECFGCCN_03017 | 3.9e-188 | ydgJ | 1.1.1.371 | S | oxidoreductase | |
NECFGCCN_03018 | 4.2e-29 | |||||
NECFGCCN_03019 | 4.9e-118 | |||||
NECFGCCN_03020 | 4.8e-93 | P | ABC transporter (permease) | |||
NECFGCCN_03021 | 1e-182 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
NECFGCCN_03022 | 7.8e-146 | metQ_2 | P | NLPA lipoprotein | ||
NECFGCCN_03023 | 4.8e-221 | ykrV3 | 2.6.1.83 | E | Aminotransferase class I and II | |
NECFGCCN_03024 | 2.3e-73 | 1.6.5.5 | C | COG0604 NADPH quinone reductase and related Zn-dependent oxidoreductases | ||
NECFGCCN_03025 | 3.8e-22 | plnP | V | CAAX protease self-immunity | ||
NECFGCCN_03026 | 0.0 | S | dextransucrase activity | |||
NECFGCCN_03027 | 3e-182 | K | Probable Zinc-ribbon domain | |||
NECFGCCN_03028 | 1.2e-56 | gepA | S | Protein of unknown function (DUF4065) | ||
NECFGCCN_03030 | 2e-80 | M | Pilin isopeptide linkage domain protein | |||
NECFGCCN_03031 | 2.4e-66 | XK27_09825 | V | abc transporter atp-binding protein | ||
NECFGCCN_03032 | 5.7e-119 | yvfS | V | Transporter | ||
NECFGCCN_03033 | 9.5e-37 | |||||
NECFGCCN_03034 | 9.4e-74 | nifU | C | SUF system FeS assembly protein, NifU family | ||
NECFGCCN_03035 | 5.9e-238 | sufS | 2.8.1.7, 4.4.1.16 | E | Catalyzes the removal of elemental sulfur and selenium atoms from L-cysteine, L-cystine, L-selenocysteine, and L- selenocystine to produce L-alanine | |
NECFGCCN_03036 | 1.5e-233 | sufD | O | assembly protein SufD | ||
NECFGCCN_03037 | 1.7e-137 | sufC | O | ABC-type transport system involved in Fe-S cluster assembly, ATPase component | ||
NECFGCCN_03038 | 5.7e-182 | tagO | 2.7.8.33, 2.7.8.35 | M | transferase | |
NECFGCCN_03039 | 6.6e-123 | mecA | NOT | Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis | ||
NECFGCCN_03040 | 2.4e-17 | S | Protein of unknown function (DUF3021) | |||
NECFGCCN_03041 | 1.5e-152 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
NECFGCCN_03042 | 4.3e-270 | glnP | P | ABC transporter | ||
NECFGCCN_03045 | 3.4e-53 | gutM | K | Glucitol operon activator | ||
NECFGCCN_03046 | 1.3e-137 | srlR | K | Transcriptional | ||
NECFGCCN_03047 | 8.1e-174 | gutQ | 5.3.1.13 | M | Arabinose 5-phosphate isomerase | |
NECFGCCN_03048 | 2.9e-282 | norR | KT | transcriptional regulator | ||
NECFGCCN_03049 | 1.6e-202 | norV | 1.6.3.4 | C | uses NADH to detoxify nitric oxide (NO), protecting several 4Fe-4S NO-sensitive enzymes. Has at least 2 reductase partners, only one of which (NorW, flavorubredoxin reductase) has been identified. NO probably binds to the di-iron center | |
NECFGCCN_03050 | 1.3e-277 | urtB | E | Belongs to the binding-protein-dependent transport system permease family | ||
NECFGCCN_03051 | 1.2e-246 | urtA | E | COG0683 ABC-type branched-chain amino acid transport systems, periplasmic component | ||
NECFGCCN_03052 | 2.3e-217 | yxjG | 2.1.1.14 | E | methionine synthase | |
NECFGCCN_03053 | 4.8e-72 | XK27_05625 | P | Rhodanese | ||
NECFGCCN_03054 | 3.1e-198 | ftrA | K | Transcriptional regulator containing an amidase domain and an AraC-type DNA-binding HTH domain | ||
NECFGCCN_03055 | 3.1e-33 | S | Domain of unknown function (DUF4177) | |||
NECFGCCN_03056 | 2.7e-76 | K | Acetyltransferase (GNAT) domain | |||
NECFGCCN_03058 | 3.2e-101 | lacI | K | binds specific sites in lac operon resulting in DNA looping between the operators | ||
NECFGCCN_03059 | 1.8e-31 | dksA1 | T | Transcription factor that acts by binding directly to the RNA polymerase (RNAP). Required for negative regulation of rRNA expression and positive regulation of several amino acid biosynthesis promoters. Also required for regulation of fis expression | ||
NECFGCCN_03060 | 1e-246 | dacA1 | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
NECFGCCN_03061 | 1.6e-247 | pbuO | S | permease | ||
NECFGCCN_03062 | 1e-75 | ydiB | 2.7.1.221, 5.1.1.1 | M | ATPase or kinase | |
NECFGCCN_03063 | 1.1e-87 | XK27_05885 | 2.3.1.82 | M | phosphinothricin N-acetyltransferase activity | |
NECFGCCN_03064 | 7.4e-212 | brpA | K | Transcriptional | ||
NECFGCCN_03065 | 2.3e-81 | rimP | S | Required for maturation of 30S ribosomal subunits | ||
NECFGCCN_03066 | 3.5e-195 | nusA | K | Participates in both transcription termination and antitermination | ||
NECFGCCN_03067 | 1e-47 | ylxR | K | Nucleic-acid-binding protein implicated in transcription termination | ||
NECFGCCN_03068 | 0.0 | infB | J | One of the essential components for the initiation of protein synthesis. Protects formylmethionyl-tRNA from spontaneous hydrolysis and promotes its binding to the 30S ribosomal subunits. Also involved in the hydrolysis of GTP during the formation of the 70S ribosomal complex | ||
NECFGCCN_03069 | 8.6e-57 | rbfA | J | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Associates with free 30S ribosomal subunits (but not with 30S subunits that are part of 70S ribosomes or polysomes). Required for efficient processing of 16S rRNA. May interact with the 5'-terminal helix region of 16S rRNA | ||
NECFGCCN_03070 | 1.2e-97 | yvdD | 3.2.2.10 | S | Belongs to the LOG family | |
NECFGCCN_03071 | 1.7e-268 | murE | 6.3.2.13, 6.3.2.7 | M | to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
NECFGCCN_03072 | 1.2e-64 | glyA | 2.1.2.1 | E | Catalyzes the reversible interconversion of serine and glycine with tetrahydrofolate (THF) serving as the one-carbon carrier. This reaction serves as the major source of one-carbon groups required for the biosynthesis of purines, thymidylate, methionine, and other important biomolecules. Also exhibits THF- independent aldolase activity toward beta-hydroxyamino acids, producing glycine and aldehydes, via a retro-aldol mechanism | |
NECFGCCN_03073 | 2.8e-76 | ywlC | 2.7.7.87, 3.1.3.48 | J | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine | |
NECFGCCN_03074 | 4.4e-144 | prmB | 2.1.1.297, 2.1.1.298 | J | Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif | |
NECFGCCN_03075 | 1.1e-190 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
NECFGCCN_03076 | 2.1e-47 | tdk | 2.7.1.21 | F | thymidine kinase | |
NECFGCCN_03077 | 5.6e-228 | noxE | P | NADH oxidase | ||
NECFGCCN_03078 | 3e-50 | zntB | P | Zinc transport protein zntB | ||
NECFGCCN_03079 | 1.2e-255 | dbpA | 3.6.4.13 | JKL | DEAD-box RNA helicase involved in the assembly of the 50S ribosomal subunit. Has an RNA-dependent ATPase activity, which is specific for 23S rRNA, and a 3' to 5' RNA helicase activity that uses the energy of ATP hydrolysis to destabilize and unwind short rRNA duplexes | |
NECFGCCN_03080 | 1.6e-179 | ttcA | 6.3.4.19 | J | Catalyzes the ATP-dependent 2-thiolation of cytidine in position 32 of tRNA, to form 2-thiocytidine (s(2)C32). The sulfur atoms are provided by the cysteine cysteine desulfurase (IscS) system | |
NECFGCCN_03081 | 3.1e-72 | uspF | T | Belongs to the universal stress protein A family | ||
NECFGCCN_03082 | 1.5e-32 | S | KTSC domain | |||
NECFGCCN_03083 | 1.5e-58 | ompN | M | Belongs to the Gram-negative porin family | ||
NECFGCCN_03084 | 2.7e-157 | 5.2.1.8 | G | hydrolase | ||
NECFGCCN_03085 | 6.1e-114 | 1.14.14.5 | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | ||
NECFGCCN_03086 | 1.1e-196 | MA20_36090 | S | Protein of unknown function (DUF2974) | ||
NECFGCCN_03087 | 1.9e-133 | sdh | 1.1.1.276, 1.1.1.313, 1.1.1.381 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
NECFGCCN_03088 | 0.0 | hsdR | 3.1.21.3 | L | Subunit R is required for both nuclease and ATPase activities, but not for modification | |
NECFGCCN_03089 | 3e-98 | cfa | 2.1.1.317, 2.1.1.79 | M | synthase | |
NECFGCCN_03090 | 1.6e-86 | outB | S | Type II secretion system protein B | ||
NECFGCCN_03091 | 5.2e-60 | outS | S | TIGRFAM lipoprotein, PulS OutS family | ||
NECFGCCN_03092 | 0.0 | mrcB | 2.4.1.129, 3.4.16.4 | GT51 | M | Cell wall formation. Synthesis of cross-linked peptidoglycan from the lipid intermediates. The enzyme has a penicillin-insensitive transglycosylase N-terminal domain (formation of linear glycan strands) and a penicillin-sensitive transpeptidase C-terminal domain (cross-linking of the peptide subunits) |
NECFGCCN_03093 | 0.0 | fhuA | P | Receptor | ||
NECFGCCN_03094 | 1.1e-144 | fhuC | 3.6.3.34 | HP | ABC-type cobalamin Fe3 -siderophores transport systems, ATPase components | |
NECFGCCN_03095 | 2.7e-160 | fhuD | P | ABC-type Fe3 -hydroxamate transport system, periplasmic component | ||
NECFGCCN_03096 | 0.0 | fhuB | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
NECFGCCN_03097 | 1.2e-61 | F | COG0402 Cytosine deaminase and related metal-dependent hydrolases | |||
NECFGCCN_03098 | 4.4e-191 | C | Belongs to the iron ascorbate-dependent oxidoreductase family | |||
NECFGCCN_03099 | 9.7e-161 | K | transcriptional regulator | |||
NECFGCCN_03100 | 1.5e-230 | EGP | Permeases of the major facilitator superfamily | |||
NECFGCCN_03101 | 6.6e-07 | K | luxR family | |||
NECFGCCN_03102 | 6.2e-90 | S | DinB family | |||
NECFGCCN_03103 | 1.2e-49 | cigR | S | response to cobalt ion | ||
NECFGCCN_03104 | 9.3e-178 | gsiA_8 | P | Belongs to the ABC transporter superfamily | ||
NECFGCCN_03105 | 1.6e-174 | oppD | 3.6.3.24 | P | Belongs to the ABC transporter superfamily | |
NECFGCCN_03106 | 5e-168 | appC | P | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
NECFGCCN_03107 | 4.8e-70 | appB | P | ABC-type dipeptide oligopeptide nickel transport systems, permease | ||
NECFGCCN_03108 | 8.3e-51 | S | LemA family | |||
NECFGCCN_03109 | 1.6e-76 | punA | 2.4.2.1 | F | The purine nucleoside phosphorylases catalyze the phosphorolytic breakdown of the N-glycosidic bond in the beta- (deoxy)ribonucleoside molecules, with the formation of the corresponding free purine bases and pentose-1-phosphate | |
NECFGCCN_03110 | 5.6e-209 | seuB | I | acyl-CoA dehydrogenase | ||
NECFGCCN_03111 | 2.8e-255 | ygcS | EGP | Major facilitator superfamily | ||
NECFGCCN_03112 | 3e-159 | metQ_1 | P | ABC transporter substrate-binding protein | ||
NECFGCCN_03113 | 4e-122 | metI | U | ABC transporter (permease) | ||
NECFGCCN_03114 | 1.3e-182 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
NECFGCCN_03115 | 9.6e-277 | soxA | 1.14.14.28 | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | |
NECFGCCN_03116 | 9.3e-75 | S | oxidoreductase | |||
NECFGCCN_03117 | 1e-28 | L | cog cog3677 | |||
NECFGCCN_03118 | 1.6e-79 | Q | DSBA-like thioredoxin domain | |||
NECFGCCN_03119 | 1.7e-189 | IQ | PFAM AMP-dependent synthetase and ligase | |||
NECFGCCN_03120 | 1.6e-43 | fcy21 | F | Belongs to the purine-cytosine permease (2.A.39) family | ||
NECFGCCN_03121 | 4.7e-83 | T | signal transduction protein containing sensor and EAL | |||
NECFGCCN_03122 | 5.8e-15 | L | Integrase core domain | |||
NECFGCCN_03123 | 5.7e-139 | S | X-Pro dipeptidyl-peptidase (S15 family) | |||
NECFGCCN_03124 | 3.4e-85 | tnpR | L | Resolvase, N terminal domain | ||
NECFGCCN_03125 | 2.2e-131 | L | Transposase | |||
NECFGCCN_03126 | 6.1e-243 | L | Tn3 transposase DDE domain | |||
NECFGCCN_03127 | 1.8e-20 | S | Protein of unknown function (DUF1173) | |||
NECFGCCN_03130 | 1.4e-56 | dsbC | 5.3.4.1 | O | Required for disulfide bond formation in some periplasmic proteins. Acts by transferring its disulfide bond to other proteins and is reduced in the process | |
NECFGCCN_03131 | 4.5e-56 | M | lytic transglycosylase activity | |||
NECFGCCN_03132 | 1.3e-27 | L | membrane | |||
NECFGCCN_03133 | 4.5e-21 | |||||
NECFGCCN_03134 | 1.3e-130 | S | Putative helicase | |||
NECFGCCN_03135 | 2e-224 | tgt | 2.4.2.29 | F | Catalyzes the base-exchange of a guanine (G) residue with the queuine precursor 7-aminomethyl-7-deazaguanine (PreQ1) at position 34 (anticodon wobble position) in tRNAs with GU(N) anticodons (tRNA-Asp, -Asn, -His and -Tyr). Catalysis occurs through a double-displacement mechanism. The nucleophile active site attacks the C1' of nucleotide 34 to detach the guanine base from the RNA, forming a covalent enzyme-RNA intermediate. The proton acceptor active site deprotonates the incoming PreQ1, allowing a nucleophilic attack on the C1' of the ribose to form the product. After dissociation, two additional enzymatic reactions on the tRNA convert PreQ1 to queuine (Q), resulting in the hypermodified nucleoside queuosine (7-(((4,5-cis-dihydroxy-2- cyclopenten-1-yl)amino)methyl)-7-deazaguanosine) | |
NECFGCCN_03136 | 3.8e-66 | foxA | P | Receptor | ||
NECFGCCN_03137 | 2.2e-53 | foxA | P | Receptor | ||
NECFGCCN_03138 | 1.9e-112 | emtA | GH23 | M | Murein-degrading enzyme. May play a role in recycling of muropeptides during cell elongation and or cell division. Preferentially cleaves at a distance of more than two disaccharide units from the ends of the glycan chain | |
NECFGCCN_03139 | 1.5e-169 | ldcA | 3.4.17.13 | V | proteins, homologs of microcin C7 resistance protein MccF | |
NECFGCCN_03140 | 0.0 | nhaP2 | P | K( ) H( ) antiporter that extrudes potassium in exchange for external protons and maintains the internal concentration of potassium under toxic levels | ||
NECFGCCN_03141 | 1.4e-203 | alr | 5.1.1.1 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
NECFGCCN_03142 | 2e-252 | dadA | 1.4.5.1 | E | Oxidative deamination of D-amino acids | |
NECFGCCN_03143 | 5.7e-307 | spoVR | S | SpoVR family | ||
NECFGCCN_03144 | 5.5e-135 | fadR | K | Multifunctional regulator of fatty acid metabolism | ||
NECFGCCN_03145 | 1.5e-252 | nhaB | P | Na( ) H( ) antiporter that extrudes sodium in exchange for external protons | ||
NECFGCCN_03146 | 1.2e-97 | dsbB | O | Required for disulfide bond formation in some periplasmic proteins. Acts by oxidizing the DsbA protein | ||
NECFGCCN_03147 | 1.1e-61 | P | protein domain, possibly involved in tellurite resistance | |||
NECFGCCN_03148 | 5.5e-85 | ycgN | S | Belongs to the UPF0260 family | ||
NECFGCCN_03149 | 1.9e-121 | ycgM | Q | COG0179 2-keto-4-pentenoate hydratase 2-oxohepta-3-ene-1,7-dioic acid hydratase (catechol pathway) | ||
NECFGCCN_03150 | 2.1e-45 | ycgL | S | YcgL domain-containing protein | ||
NECFGCCN_03151 | 3.4e-113 | minC | D | Cell division inhibitor that blocks the formation of polar Z ring septums. Rapidly oscillates between the poles of the cell to destabilize FtsZ filaments that have formed before they mature into polar Z rings. Prevents FtsZ polymerization | ||
NECFGCCN_03152 | 1.1e-144 | minD | D | Belongs to the ParA family | ||
NECFGCCN_03153 | 3.9e-41 | minE | D | Prevents the cell division inhibition by proteins MinC and MinD at internal division sites while permitting inhibition at polar sites. This ensures cell division at the proper site by restricting the formation of a division septum at the midpoint of the long axis of the cell | ||
NECFGCCN_03154 | 2.2e-207 | rnd | 3.1.13.5 | J | Exonuclease involved in the 3' processing of various precursor tRNAs. Initiates hydrolysis at the 3'-terminus of an RNA molecule and releases 5'-mononucleotides | |
NECFGCCN_03155 | 0.0 | fadD | 6.2.1.3 | IQ | COG0318 Acyl-CoA synthetases (AMP-forming) AMP-acid ligases II | |
NECFGCCN_03156 | 3.9e-99 | yeaY | M | Outer Membrane Lipoprotein | ||
NECFGCCN_03157 | 8.5e-125 | yeaZ | 2.3.1.234 | O | COG1214 Inactive homolog of metal-dependent proteases | |
NECFGCCN_03158 | 0.0 | dinG | 3.6.4.12 | KL | helicase | |
NECFGCCN_03159 | 1.5e-57 | yoaB | J | Translation Initiation Inhibitor YjgF Family | ||
NECFGCCN_03160 | 1.1e-21 | yoaH | S | Belongs to the UPF0181 family | ||
NECFGCCN_03161 | 6.7e-251 | pabB | 2.6.1.85 | EH | Part of a heterotetrameric complex that catalyzes the two-step biosynthesis of anthranilate, an intermediate in the biosynthesis of L-tryptophan. In the first step, the glutamine- binding beta subunit (TrpG) of anthranilate synthase (AS) provides the glutamine amidotransferase activity which generates ammonia as a substrate that, along with chorismate, is used in the second step, catalyzed by the large alpha subunit of AS (TrpE) to produce anthranilate. In the absence of TrpG, TrpE can synthesize anthranilate directly from chorismate and high concentrations of ammonia | |
NECFGCCN_03162 | 1.2e-103 | nudL | L | NUDIX hydrolase | ||
NECFGCCN_03163 | 2.9e-262 | sdaA | 4.3.1.17 | E | l-serine dehydratase | |
NECFGCCN_03164 | 2e-262 | adrB | 3.1.4.52 | T | EAL domain | |
NECFGCCN_03165 | 4.1e-276 | yoaE | P | membrane protein, terc | ||
NECFGCCN_03166 | 2.2e-163 | manX | 2.7.1.191 | G | pts system | |
NECFGCCN_03167 | 3.4e-133 | manY | G | pts system | ||
NECFGCCN_03168 | 3.5e-157 | manZ | G | PTS system mannose fructose sorbose family IID component | ||
NECFGCCN_03169 | 7.7e-74 | yobD | S | UPF0266 membrane protein | ||
NECFGCCN_03170 | 5.2e-96 | mntP | P | Probably functions as a manganese efflux pump | ||
NECFGCCN_03171 | 4.1e-147 | rrmA | 2.1.1.187 | Q | Methyl-transferase | |
NECFGCCN_03172 | 0.0 | ftsI | 3.4.16.4 | M | Catalyzes cross-linking of the peptidoglycan cell wall at the division septum | |
NECFGCCN_03173 | 1.1e-32 | cspC | K | Cold shock | ||
NECFGCCN_03174 | 6.4e-42 | yebO | S | YebO-like protein | ||
NECFGCCN_03175 | 5.9e-33 | yobH | S | YobH-like protein | ||
NECFGCCN_03176 | 3.3e-141 | kdgR | K | transcriptional regulator | ||
NECFGCCN_03177 | 5e-238 | yebQ | EGP | Major facilitator superfamily | ||
NECFGCCN_03178 | 2.1e-152 | htpX | O | Belongs to the peptidase M48B family | ||
NECFGCCN_03179 | 0.0 | prc | 3.4.21.102 | M | Belongs to the peptidase S41A family | |
NECFGCCN_03180 | 2e-86 | proQ | T | RNA chaperone with significant RNA binding, RNA strand exchange and RNA duplexing activities | ||
NECFGCCN_03181 | 4e-85 | yebR | 1.8.4.14 | T | GAF domain-containing protein | |
NECFGCCN_03182 | 4.1e-234 | yebS | S | paraquat-inducible protein A | ||
NECFGCCN_03183 | 0.0 | yebT | Q | paraquat-inducible protein b | ||
NECFGCCN_03184 | 8.1e-260 | rsmF | 2.1.1.176, 2.1.1.178 | J | Specifically methylates the cytosine at position 1407 (m5C1407) of 16S rRNA | |
NECFGCCN_03185 | 3.4e-41 | yebV | S | Protein of unknown function (DUF1480) | ||
NECFGCCN_03186 | 2.6e-31 | yebW | S | Protein of unknown function (DUF1482) | ||
NECFGCCN_03187 | 1.1e-118 | pphA | 3.1.3.16 | T | Serine Threonine protein | |
NECFGCCN_03188 | 7.9e-164 | virK | S | protein conserved in bacteria | ||
NECFGCCN_03190 | 1.3e-54 | yebY | S | Protein of unknown function (DUF2511) | ||
NECFGCCN_03191 | 9.2e-145 | yebZ | P | copper resistance protein | ||
NECFGCCN_03192 | 1e-55 | yobA | S | Resistance protein | ||
NECFGCCN_03193 | 1.3e-34 | holE | 2.7.7.7 | L | DNA polymerase III | |
NECFGCCN_03194 | 1.1e-124 | exoX | L | 3'-5' exonuclease activity on single or double-strand DNA | ||
NECFGCCN_03195 | 0.0 | ptrB | 3.4.21.83 | E | Protease II | |
NECFGCCN_03196 | 3.6e-101 | yebE | S | Protein of unknown function (DUF533) | ||
NECFGCCN_03197 | 3.7e-36 | yebG | S | protein conserved in bacteria | ||
NECFGCCN_03198 | 5e-210 | purT | 2.1.2.2 | F | Involved in the de novo purine biosynthesis. Catalyzes the transfer of formate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR). Formate is provided by PurU via hydrolysis of 10-formyl-tetrahydrofolate | |
NECFGCCN_03199 | 1.4e-113 | eda | 4.1.2.14, 4.1.3.42 | G | Aldolase | |
NECFGCCN_03200 | 0.0 | edd | 4.2.1.12 | EG | Belongs to the IlvD Edd family | |
NECFGCCN_03201 | 6.8e-289 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
NECFGCCN_03202 | 2.1e-147 | hexR | K | transcriptional regulator | ||
NECFGCCN_03203 | 4.3e-264 | pyk | 2.7.1.40 | G | Belongs to the pyruvate kinase family | |
NECFGCCN_03204 | 1.9e-187 | lpxM | 2.3.1.241, 2.3.1.242, 2.3.1.243 | M | Catalyzes the transfer of myristate from myristoyl-acyl carrier protein (ACP) to Kdo(2)-(lauroyl)-lipid IV(A) to form Kdo(2)-lipid A | |
NECFGCCN_03205 | 2.6e-247 | yebA | M | COG0739 Membrane proteins related to metalloendopeptidases | ||
NECFGCCN_03206 | 4.4e-156 | znuA | P | ABC-type Zn2 transport system, periplasmic component surface adhesin | ||
NECFGCCN_03207 | 6.8e-136 | znuC | P | Part of the ABC transporter complex ZnuABC involved in zinc import. Responsible for energy coupling to the transport system | ||
NECFGCCN_03208 | 2.9e-113 | znuB | P | ABC 3 transport family | ||
NECFGCCN_03209 | 9.6e-186 | ruvB | 3.6.4.12 | L | The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing | |
NECFGCCN_03210 | 1.3e-105 | ruvA | 3.6.4.12 | L | The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing. RuvA stimulates, in the presence of DNA, the weak ATPase activity of RuvB | |
NECFGCCN_03211 | 1.1e-87 | ruvC | 3.1.22.4 | L | Nuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves the cruciform structure in supercoiled DNA by nicking to strands with the same polarity at sites symmetrically opposed at the junction in the homologous arms and leaves a 5'-terminal phosphate and a 3'-terminal hydroxyl group | |
NECFGCCN_03212 | 3.7e-126 | yebC | K | transcriptional regulatory protein | ||
NECFGCCN_03213 | 4.2e-77 | nudB | 2.3.1.181, 3.6.1.13, 3.6.1.55, 3.6.1.67 | L | dihydroneopterin triphosphate | |
NECFGCCN_03214 | 0.0 | aspS | 6.1.1.12 | J | L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp) | |
NECFGCCN_03215 | 2.8e-102 | yecD | Q | Hydrolase | ||
NECFGCCN_03216 | 5.8e-157 | yecE | S | Protein of unknown function DUF72 | ||
NECFGCCN_03217 | 4.9e-69 | yecN | S | relative of glutathione S-transferase, MAPEG superfamily | ||
NECFGCCN_03218 | 6.1e-137 | cmoA | Q | Catalyzes the conversion of S-adenosyl-L-methionine (SAM) to carboxy-S-adenosyl-L-methionine (Cx-SAM) | ||
NECFGCCN_03219 | 1e-195 | cmoB | J | Catalyzes carboxymethyl transfer from carboxy-S- adenosyl-L-methionine (Cx-SAM) to 5-hydroxyuridine (ho5U) to form 5-carboxymethoxyuridine (cmo5U) at position 34 in tRNAs | ||
NECFGCCN_03220 | 5e-131 | cutC | P | Participates in the control of copper homeostasis | ||
NECFGCCN_03221 | 6.6e-107 | yecM | S | protein conserved in bacteria | ||
NECFGCCN_03222 | 0.0 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
NECFGCCN_03223 | 1.7e-223 | yesR | 3.2.1.172 | GH105 | S | Glycosyl Hydrolase Family 88 |
NECFGCCN_03224 | 7.5e-286 | G | Major Facilitator | |||
NECFGCCN_03225 | 2.6e-68 | uspC | T | Required for resistance to DNA-damaging agents | ||
NECFGCCN_03226 | 6.8e-278 | otsA | 2.4.1.15, 2.4.1.347 | GT20 | G | Probably involved in the osmoprotection via the biosynthesis of trehalose. Catalyzes the transfer of glucose from UDP-glucose (UDP-Glc) to D-glucose 6-phosphate (Glc-6-P) to form trehalose-6-phosphate. Acts with retention of the anomeric configuration of the UDP-sugar donor |
NECFGCCN_03227 | 1.6e-140 | otsB | 2.4.1.15, 2.4.1.347, 3.1.3.12 | GT20 | G | Removes the phosphate from trehalose 6-phosphate to produce free trehalose |
NECFGCCN_03228 | 1.4e-157 | araH | G | Belongs to the binding-protein-dependent transport system permease family | ||
NECFGCCN_03229 | 2.5e-286 | araG | 3.6.3.17 | P | Part of the ABC transporter complex AraFGH involved in arabinose import. Responsible for energy coupling to the transport system | |
NECFGCCN_03230 | 6e-185 | araF | G | l-arabinose-binding periplasmic protein | ||
NECFGCCN_03231 | 1.7e-85 | ftnA | 1.16.3.2 | P | Iron-storage protein | |
NECFGCCN_03232 | 6.7e-279 | yihO3 | G | Major Facilitator | ||
NECFGCCN_03233 | 4.6e-36 | yecJ | S | Protein of unknown function (DUF2766) | ||
NECFGCCN_03234 | 3.4e-253 | EGP | Major facilitator Superfamily | |||
NECFGCCN_03235 | 6.6e-116 | YPO1991 | 5.3.1.26, 5.3.1.6 | G | isomerase | |
NECFGCCN_03236 | 3.9e-87 | ftnA | 1.16.3.2 | P | Iron-storage protein | |
NECFGCCN_03237 | 2.3e-29 | yecH | S | Protein of unknown function (DUF2492) | ||
NECFGCCN_03238 | 1.2e-195 | tyrP | E | amino acid | ||
NECFGCCN_03239 | 3.6e-120 | yecA | C | Belongs to the UPF0149 family | ||
NECFGCCN_03240 | 3.6e-144 | dapA5 | 4.3.3.7 | EM | Belongs to the DapA family | |
NECFGCCN_03244 | 1.3e-74 | GM | domain, Protein | |||
NECFGCCN_03245 | 1.6e-263 | uvrX | 2.7.7.7 | L | Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII | |
NECFGCCN_03246 | 2.2e-45 | |||||
NECFGCCN_03247 | 1.6e-23 | S | dextransucrase activity | |||
NECFGCCN_03249 | 2.5e-28 | S | dextransucrase activity | |||
NECFGCCN_03250 | 1.6e-41 | S | dextransucrase activity | |||
NECFGCCN_03251 | 2.6e-123 | prkC | 2.7.11.1 | KLT | serine threonine protein kinase | |
NECFGCCN_03252 | 1.2e-103 | kcsA | P | Ion transport protein | ||
NECFGCCN_03253 | 8.6e-117 | yvqF | S | Membrane | ||
NECFGCCN_03254 | 1.9e-170 | vraS | 2.7.13.3 | T | Histidine kinase | |
NECFGCCN_03255 | 1.4e-113 | vraR | K | Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
NECFGCCN_03256 | 6.5e-115 | S | ABC-type transport system involved in multi-copper enzyme maturation, permease component | |||
NECFGCCN_03257 | 7.1e-164 | feaR | K | transcriptional regulator | ||
NECFGCCN_03258 | 5.7e-47 | ydbL | S | protein conserved in bacteria | ||
NECFGCCN_03259 | 4.3e-23 | ynbE | S | (Lipo)protein | ||
NECFGCCN_03260 | 0.0 | ydbH | S | Dicarboxylate transport | ||
NECFGCCN_03261 | 6.3e-39 | hup | L | Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions | ||
NECFGCCN_03262 | 1.7e-94 | ypmS | S | Protein conserved in bacteria | ||
NECFGCCN_03263 | 1.4e-156 | ypmR | E | COG2755 Lysophospholipase L1 and related esterases | ||
NECFGCCN_03264 | 4.4e-144 | DegV | S | DegV family | ||
NECFGCCN_03265 | 3.9e-301 | recN | L | May be involved in recombinational repair of damaged DNA | ||
NECFGCCN_03266 | 7.9e-70 | yccU | 2.5.1.49 | S | CoA-binding protein | |
NECFGCCN_03267 | 2.3e-81 | mgsA | 4.2.3.3 | G | Methylglyoxal synthase | |
NECFGCCN_03268 | 0.0 | helD | 3.6.4.12 | L | DNA helicase | |
NECFGCCN_03269 | 2.1e-76 | yccF | S | Membrane | ||
NECFGCCN_03270 | 0.0 | yccS | S | Membrane | ||
NECFGCCN_03271 | 2.4e-99 | sxy | K | regulator of competence-specific genes | ||
NECFGCCN_03272 | 2e-83 | sulA | D | Component of the SOS system and an inhibitor of cell division. Accumulation of SulA causes rapid cessation of cell division and the appearance of long, non-septate filaments. In the presence of GTP, binds a polymerization-competent form of FtsZ in a 1 1 ratio, thus inhibiting FtsZ polymerization and therefore preventing it from participating in the assembly of the Z ring. This mechanism prevents the premature segregation of damaged DNA to daughter cells during cell division | ||
NECFGCCN_03273 | 6e-194 | ompA | M | Belongs to the ompA family | ||
NECFGCCN_03274 | 2.5e-77 | matP | D | Required for spatial organization of the terminus region of the chromosome (Ter macrodomain) during the cell cycle. Prevents early segregation of duplicated Ter macrodomains during cell division. Binds specifically to matS, which is a 13 bp signature motif repeated within the Ter macrodomain | ||
NECFGCCN_03275 | 0.0 | ycbZ | O | Belongs to the peptidase S16 family | ||
NECFGCCN_03276 | 1.1e-97 | fabA | 4.2.1.59, 5.3.3.14 | I | Necessary for the introduction of cis unsaturation into fatty acids. Catalyzes the dehydration of (3R)-3-hydroxydecanoyl- ACP to E-(2)-decenoyl-ACP and then its isomerization to Z-(3)- decenoyl-ACP. Can catalyze the dehydratase reaction for beta- hydroxyacyl-ACPs with saturated chain lengths up to 16 0, being most active on intermediate chain length | |
NECFGCCN_03277 | 2.9e-99 | ymbA | S | protein conserved in bacteria | ||
NECFGCCN_03278 | 0.0 | pqiB | Q | paraquat-inducible protein b | ||
NECFGCCN_03279 | 1.3e-235 | pqiA | S | paraquat-inducible protein A | ||
NECFGCCN_03280 | 0.0 | uup | S | ABC transporter C-terminal domain | ||
NECFGCCN_03281 | 6.4e-240 | rlmL | 2.1.1.173, 2.1.1.191, 2.1.1.264, 2.1.1.72 | J | Specifically methylates the guanine in position 2445 (m2G2445) and the guanine in position 2069 (m7G2069) of 23S rRNA | |
NECFGCCN_03283 | 7.9e-64 | entF | 6.3.2.14 | Q | amino acid activation for nonribosomal peptide biosynthetic process | |
NECFGCCN_03284 | 2.7e-54 | entF | 6.3.2.14 | Q | amino acid activation for nonribosomal peptide biosynthetic process | |
NECFGCCN_03285 | 9.1e-35 | ybdZ | P | PFAM MbtH domain protein | ||
NECFGCCN_03286 | 7.3e-241 | fes | P | esterase | ||
NECFGCCN_03287 | 7.5e-121 | mtnN | 3.2.2.9 | F | Catalyzes the irreversible cleavage of the glycosidic bond in both 5'-methylthioadenosine (MTA) and S- adenosylhomocysteine (SAH AdoHcy) to adenine and the corresponding thioribose, 5'-methylthioribose and S-ribosylhomocysteine, respectively | |
NECFGCCN_03288 | 5.3e-289 | dgt | 3.1.5.1 | F | dGTPase preferentially hydrolyzes dGTP over the other canonical NTPs | |
NECFGCCN_03289 | 4.9e-252 | degP | 1.3.1.74, 3.4.21.107 | M | Belongs to the peptidase S1C family | |
NECFGCCN_03290 | 4.1e-215 | cdaR | KT | regulator | ||
NECFGCCN_03291 | 3.2e-65 | yaeH | S | Belongs to the UPF0325 family | ||
NECFGCCN_03292 | 7.2e-123 | dapD | 2.3.1.117, 2.3.1.89 | E | Belongs to the transferase hexapeptide repeat family | |
NECFGCCN_03293 | 0.0 | glnD | 2.7.7.59 | O | Modifies, by uridylylation and deuridylylation, the PII regulatory proteins (GlnB and homologs), in response to the nitrogen status of the cell that GlnD senses through the glutamine level. Under low glutamine levels, catalyzes the conversion of the PII proteins and UTP to PII-UMP and PPi, while under higher glutamine levels, GlnD hydrolyzes PII-UMP to PII and UMP (deuridylylation). Thus, controls uridylylation state and activity of the PII proteins, and plays an important role in the regulation of nitrogen | |
NECFGCCN_03294 | 2.5e-149 | map | 3.4.11.18 | E | Methionine aminopeptidase | |
NECFGCCN_03295 | 1.3e-131 | rpsB | J | ribosomal protein | ||
NECFGCCN_03296 | 6.1e-149 | tsf | J | Associates with the EF-Tu.GDP complex and induces the exchange of GDP to GTP. It remains bound to the aminoacyl-tRNA.EF- Tu.GTP complex up to the GTP hydrolysis stage on the ribosome | ||
NECFGCCN_03297 | 1.6e-129 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
NECFGCCN_03298 | 2.2e-75 | frr | J | Responsible for the release of ribosomes from messenger RNA at the termination of protein biosynthesis. May increase the efficiency of translation by recycling ribosomes from one round of translation to another | ||
NECFGCCN_03299 | 2.9e-213 | dxr | 1.1.1.267 | I | Catalyzes the NADP-dependent rearrangement and reduction of 1-deoxy-D-xylulose-5-phosphate (DXP) to 2-C-methyl-D-erythritol 4-phosphate (MEP) | |
NECFGCCN_03300 | 9.5e-141 | uppS | 2.5.1.31 | H | Catalyzes the sequential condensation of isopentenyl diphosphate (IPP) with (2E,6E)-farnesyl diphosphate (E,E-FPP) to yield (2Z,6Z,10Z,14Z,18Z,22Z,26Z,30Z,34E,38E)-undecaprenyl diphosphate (di-trans,octa-cis-UPP). UPP is the precursor of glycosyl carrier lipid in the biosynthesis of bacterial cell wall polysaccharide components such as peptidoglycan and lipopolysaccharide | |
NECFGCCN_03301 | 4.4e-146 | cdsA | 2.7.7.41 | I | Belongs to the CDS family | |
NECFGCCN_03302 | 4.6e-252 | rseP | 3.4.21.107 | M | zinc metalloprotease | |
NECFGCCN_03303 | 0.0 | bamA | M | Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane | ||
NECFGCCN_03304 | 9.6e-75 | skp | M | Belongs to the skp family | ||
NECFGCCN_03305 | 4.9e-113 | lpxD | 2.3.1.191 | M | as the acyl donor. Is involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell | |
NECFGCCN_03306 | 8.4e-81 | fabZ | 4.2.1.59 | I | Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs | |
NECFGCCN_03307 | 9.1e-83 | lpxA | 2.3.1.129 | M | involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell | |
NECFGCCN_03308 | 1.1e-214 | lpxB | 2.4.1.182 | GT19 | M | Condensation of UDP-2,3-diacylglucosamine and 2,3- diacylglucosamine-1-phosphate to form lipid A disaccharide, a precursor of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell |
NECFGCCN_03309 | 2.2e-105 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
NECFGCCN_03310 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase | |
NECFGCCN_03311 | 4.2e-175 | accA | 2.1.3.15, 6.4.1.2 | I | Component of the acetyl coenzyme A carboxylase (ACC) complex. First, biotin carboxylase catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the carboxyltransferase to acetyl-CoA to form malonyl-CoA | |
NECFGCCN_03312 | 0.0 | ldcC | 4.1.1.17, 4.1.1.18, 4.1.1.19 | E | decarboxylase | |
NECFGCCN_03313 | 3e-71 | yaeR | E | glyoxalase bleomycin resistance protein dioxygenase | ||
NECFGCCN_03314 | 1.4e-40 | tilS | 6.3.4.19 | D | Ligates lysine onto the cytidine present at position 34 of the AUA codon-specific tRNA(Ile) that contains the anticodon CAU, in an ATP-dependent manner. Cytidine is converted to lysidine, thus changing the amino acid specificity of the tRNA from methionine to isoleucine | |
NECFGCCN_03315 | 1.9e-50 | yjdL | U | Proton-dependent permease that transports di- and tripeptides | ||
NECFGCCN_03316 | 1.6e-216 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
NECFGCCN_03317 | 7.9e-27 | narH | 1.7.5.1 | C | nitrate reductase beta subunit | |
NECFGCCN_03318 | 2e-113 | narJ | 1.7.5.1 | C | nitrate reductase molybdenum cofactor assembly chaperone | |
NECFGCCN_03319 | 2.2e-125 | narI | 1.7.5.1 | C | nitrate reductase, gamma subunit | |
NECFGCCN_03320 | 7.5e-52 | sseB | S | enhanced serine sensitivity protein SseB | ||
NECFGCCN_03322 | 2.6e-163 | sseA | 2.8.1.1, 2.8.1.2 | P | sulfurtransferase | |
NECFGCCN_03323 | 6.2e-196 | yfhM | P | Large extracellular alpha-helical protein | ||
NECFGCCN_03324 | 8.2e-142 | yfhM | P | Large extracellular alpha-helical protein | ||
NECFGCCN_03325 | 3.9e-154 | czcD | P | cation diffusion facilitator family transporter | ||
NECFGCCN_03326 | 5.9e-189 | hemH | 4.99.1.1, 4.99.1.9 | H | Catalyzes the ferrous insertion into protoporphyrin IX | |
NECFGCCN_03327 | 9.5e-189 | adhB | 1.1.1.1, 1.1.1.14 | E | Dehydrogenase | |
NECFGCCN_03329 | 1.4e-32 | |||||
NECFGCCN_03330 | 2.8e-97 | |||||
NECFGCCN_03331 | 8.1e-57 | S | ABC-2 type transporter | |||
NECFGCCN_03332 | 5.7e-158 | V | AAA domain, putative AbiEii toxin, Type IV TA system | |||
NECFGCCN_03334 | 9.5e-139 | C | Iron-sulfur cluster-binding domain | |||
NECFGCCN_03335 | 2e-76 | pqqC | 1.3.3.11 | I | radical SAM domain protein | |
NECFGCCN_03336 | 7.6e-44 | yphJ | 4.1.1.44 | I | decarboxylase | |
NECFGCCN_03337 | 1.1e-133 | tam | 2.1.1.144, 2.1.1.197 | S | Catalyzes the S-adenosylmethionine monomethyl esterification of trans-aconitate | |
NECFGCCN_03338 | 9.6e-46 | |||||
NECFGCCN_03339 | 2.7e-203 | EGP | MFS-type transporter | |||
NECFGCCN_03340 | 8.1e-70 | yycE | 3.4.21.26, 5.3.1.24 | E | PFAM Glyoxalase bleomycin resistance protein dioxygenase | |
NECFGCCN_03341 | 2.7e-200 | yjiJ | EGP | Major facilitator Superfamily | ||
NECFGCCN_03342 | 2.1e-149 | gltR_2 | K | LysR substrate binding domain | ||
NECFGCCN_03343 | 1.2e-70 | S | Protein involved in biological_process | |||
NECFGCCN_03345 | 8.7e-60 | S | Type VI secretion system effector | |||
NECFGCCN_03346 | 5.1e-144 | gspL | U | involved in a type II secretion system (T2SS, formerly general secretion pathway, GSP) for the export of proteins | ||
NECFGCCN_03347 | 7.1e-78 | gspM | U | involved in a type II secretion system (T2SS, formerly general secretion pathway, GSP) for the export of proteins | ||
NECFGCCN_03348 | 1.4e-37 | S | Type II secretion system (T2SS), protein N | |||
NECFGCCN_03349 | 1.1e-144 | pppA | 3.4.23.43 | NOU | Cleaves type-4 fimbrial leader sequence and methylates the N-terminal (generally Phe) residue | |
NECFGCCN_03350 | 0.0 | hrpB | 3.6.4.13 | L | ATP-dependent helicase | |
NECFGCCN_03351 | 2.9e-96 | ligT | 3.1.4.58, 3.5.1.42 | J | Hydrolyzes RNA 2',3'-cyclic phosphodiester to an RNA 2'- phosphomonoester | |
NECFGCCN_03352 | 4.3e-132 | sfsA | S | Belongs to the SfsA family | ||
NECFGCCN_03353 | 3.5e-79 | dksA | T | Transcription factor that acts by binding directly to the RNA polymerase (RNAP). Required for negative regulation of rRNA expression and positive regulation of several amino acid biosynthesis promoters. Also required for regulation of fis expression | ||
NECFGCCN_03354 | 3.9e-167 | gluQ | J | Catalyzes the tRNA-independent activation of glutamate in presence of ATP and the subsequent transfer of glutamate onto a tRNA(Asp). Glutamate is transferred on the 2-amino-5-(4,5- dihydroxy-2-cyclopenten-1-yl) moiety of the queuosine in the wobble position of the QUC anticodon | ||
NECFGCCN_03355 | 9.1e-256 | pcnB | 2.7.7.19, 2.7.7.72 | H | Adds poly(A) tail to the 3' end of many RNAs, which usually targets these RNAs for decay. Plays a significant role in the global control of gene expression, through influencing the rate of transcript degradation, and in the general RNA quality control | |
NECFGCCN_03356 | 2.3e-81 | folK | 2.7.6.3, 4.1.2.25 | H | 2-amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase | |
NECFGCCN_03357 | 2.7e-143 | panB | 2.1.2.11 | H | Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is transferred onto alpha-ketoisovalerate to form ketopantoate | |
NECFGCCN_03358 | 5.3e-153 | panC | 6.3.2.1 | H | Catalyzes the condensation of pantoate with beta-alanine in an ATP-dependent reaction via a pantoyl-adenylate intermediate | |
NECFGCCN_03359 | 1.6e-64 | panD | 4.1.1.11 | H | Catalyzes the pyruvoyl-dependent decarboxylation of aspartate to produce beta-alanine | |
NECFGCCN_03360 | 5.8e-233 | yadE | 3.5.1.41 | G | Polysaccharide deacetylase | |
NECFGCCN_03361 | 4.2e-77 | yadI | G | IIa component | ||
NECFGCCN_03362 | 4.8e-137 | yadH | V | Transport Permease Protein | ||
NECFGCCN_03363 | 5.4e-167 | yadG | V | (ABC) transporter | ||
NECFGCCN_03364 | 6e-128 | can | 4.2.1.1 | P | Reversible hydration of carbon dioxide | |
NECFGCCN_03365 | 6.1e-94 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
NECFGCCN_03366 | 0.0 | gcd | 1.1.5.2 | G | Dehydrogenase | |
NECFGCCN_03367 | 4.4e-286 | cueO | Q | Multi-copper | ||
NECFGCCN_03368 | 2.3e-57 | yacC | S | Type II secretion system pilotin lipoprotein (PulS_OutS) | ||
NECFGCCN_03369 | 1.5e-57 | |||||
NECFGCCN_03370 | 1.4e-23 | S | oxidoreductase | |||
NECFGCCN_03373 | 4.3e-49 | dgs | 2.4.1.208 | GT4 | M | Glycosyltransferase, group 1 family protein |
NECFGCCN_03374 | 1e-243 | mgs | 2.4.1.337 | GT4 | M | Glycosyltransferase, group 1 family protein |
NECFGCCN_03375 | 1.7e-13 | |||||
NECFGCCN_03376 | 4.2e-55 | thrS | 6.1.1.3 | J | Catalyzes the attachment of threonine to tRNA(Thr) in a two-step reaction L-threonine is first activated by ATP to form Thr-AMP and then transferred to the acceptor end of tRNA(Thr) | |
NECFGCCN_03377 | 1.2e-18 | thrS | 6.1.1.3 | J | Catalyzes the attachment of threonine to tRNA(Thr) in a two-step reaction L-threonine is first activated by ATP to form Thr-AMP and then transferred to the acceptor end of tRNA(Thr) | |
NECFGCCN_03378 | 2.4e-178 | hemB | 4.2.1.24 | H | Belongs to the ALAD family | |
NECFGCCN_03379 | 1.1e-222 | ampH | 3.4.16.4 | V | This protein has no known enzymatic function | |
NECFGCCN_03380 | 9.8e-97 | 3.5.1.19 | Q | Isochorismatase | ||
NECFGCCN_03381 | 5.5e-228 | sbmA | I | In Escherichia coli SbmA is involved in uptake of microcin J25 | ||
NECFGCCN_03382 | 3e-201 | yaiW | S | Lipoprotein | ||
NECFGCCN_03383 | 3.7e-48 | yaiY | S | Protein of unknown function (DUF2755) | ||
NECFGCCN_03384 | 6.1e-31 | yaiZ | S | Protein of unknown function (DUF2754) | ||
NECFGCCN_03385 | 5e-204 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
NECFGCCN_03386 | 5.6e-121 | S | extensin | |||
NECFGCCN_03387 | 3.8e-213 | pmrA | EGP | Major facilitator Superfamily | ||
NECFGCCN_03388 | 2.5e-37 | iraP | S | Inhibits RpoS proteolysis by regulating RssB activity, thereby increasing the stability of the sigma stress factor RpoS especially during phosphate starvation, but also in stationary phase and during nitrogen starvation. Its effect on RpoS stability is due to its interaction with RssB, which probably blocks the interaction of RssB with RpoS, and the consequent delivery of the RssB-RpoS complex to the ClpXP protein degradation pathway | ||
NECFGCCN_03389 | 3.4e-261 | phoA | 3.1.3.1, 3.1.3.39 | P | Belongs to the alkaline phosphatase family | |
NECFGCCN_03390 | 2.1e-25 | psiF | S | Phosphate starvation-inducible protein, PSIF | ||
NECFGCCN_03391 | 4e-142 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
NECFGCCN_03392 | 1.1e-77 | yaiI | S | Belongs to the UPF0178 family | ||
NECFGCCN_03393 | 2.2e-83 | yba2 | S | protein conserved in bacteria | ||
NECFGCCN_03394 | 1.5e-92 | aroK | 2.7.1.71, 4.2.3.4 | F | Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate | |
NECFGCCN_03395 | 1.2e-28 | yaiA | S | YaiA protein | ||
NECFGCCN_03396 | 1.4e-108 | aroM | E | AroM protein | ||
NECFGCCN_03397 | 8.5e-47 | ppnP | 2.4.2.1, 2.4.2.2 | S | Catalyzes the phosphorolysis of diverse nucleosides, yielding D-ribose 1-phosphate and the respective free bases. Can use uridine, adenosine, guanosine, cytidine, thymidine, inosine and xanthosine as substrates. Also catalyzes the reverse reactions | |
NECFGCCN_03398 | 5.8e-166 | rdgC | L | May be involved in recombination | ||
NECFGCCN_03399 | 2.2e-173 | mak | 2.7.1.4, 2.7.1.59 | GK | ROK family | |
NECFGCCN_03400 | 0.0 | sbcC | L | SbcCD cleaves DNA hairpin structures. These structures can inhibit DNA replication and are intermediates in certain DNA recombination reactions. The complex acts as a 3'- 5' double strand exonuclease that can open hairpins. It also has a 5' single-strand endonuclease activity | ||
NECFGCCN_03401 | 5.3e-223 | sbcD | L | SbcCD cleaves DNA hairpin structures. These structures can inhibit DNA replication and are intermediates in certain DNA recombination reactions. The complex acts as a 3'- 5' double strand exonuclease that can open hairpins. It also has a 5' single-strand endonuclease activity | ||
NECFGCCN_03402 | 2.8e-128 | K | phosphate regulon transcriptional regulatory protein PhoB | |||
NECFGCCN_03403 | 3.5e-233 | phoR | 2.7.13.3 | T | Histidine kinase | |
NECFGCCN_03404 | 7.7e-234 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
NECFGCCN_03405 | 1.6e-252 | proY | E | Cryptic permease that may be involved in the transport of proline across the inner membrane | ||
NECFGCCN_03406 | 0.0 | malZ | 3.2.1.20 | GH31 | G | Belongs to the glycosyl hydrolase 13 family |
NECFGCCN_03407 | 3e-170 | K | transcriptional regulator | |||
NECFGCCN_03409 | 2.4e-118 | Q | Hydrolase | |||
NECFGCCN_03410 | 1.3e-99 | S | Antibiotic biosynthesis monooxygenase | |||
NECFGCCN_03411 | 0.0 | nfdA | S | metal-dependent hydrolase with the TIM-barrel fold | ||
NECFGCCN_03412 | 4e-156 | fbaA | 4.1.2.13, 4.1.2.29 | G | Aldolase | |
NECFGCCN_03413 | 1.2e-180 | rbsK | 2.7.1.15 | G | Phosphorylates 6-deoxy-6-sulfo-D-fructose (SF) to 6- deoxy-6-sulfo-D-fructose 1-phosphate (SFP) | |
NECFGCCN_03414 | 1.3e-252 | ulaA | 2.7.1.194 | G | protein conserved in bacteria | |
NECFGCCN_03415 | 8.9e-44 | 2.7.1.194, 2.7.1.200 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
NECFGCCN_03416 | 9.1e-72 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
NECFGCCN_03417 | 3.4e-114 | ahpC | 1.11.1.15 | O | alkyl hydroperoxide reductase | |
NECFGCCN_03418 | 4.6e-108 | acpH | 3.1.4.14 | S | Converts holo-ACP to apo-ACP by hydrolytic cleavage of the phosphopantetheine prosthetic group from ACP | |
NECFGCCN_03419 | 7.7e-202 | queA | 2.4.2.29, 2.4.99.17 | J | Transfers and isomerizes the ribose moiety from AdoMet to the 7-aminomethyl group of 7-deazaguanine (preQ1-tRNA) to give epoxyqueuosine (oQ-tRNA) | |
NECFGCCN_03420 | 3.6e-226 | tgt | 2.4.2.29 | F | Catalyzes the base-exchange of a guanine (G) residue with the queuine precursor 7-aminomethyl-7-deazaguanine (PreQ1) at position 34 (anticodon wobble position) in tRNAs with GU(N) anticodons (tRNA-Asp, -Asn, -His and -Tyr). Catalysis occurs through a double-displacement mechanism. The nucleophile active site attacks the C1' of nucleotide 34 to detach the guanine base from the RNA, forming a covalent enzyme-RNA intermediate. The proton acceptor active site deprotonates the incoming PreQ1, allowing a nucleophilic attack on the C1' of the ribose to form the product. After dissociation, two additional enzymatic reactions on the tRNA convert PreQ1 to queuine (Q), resulting in the hypermodified nucleoside queuosine (7-(((4,5-cis-dihydroxy-2- cyclopenten-1-yl)amino)methyl)-7-deazaguanosine) | |
NECFGCCN_03421 | 7.8e-52 | yajC | U | Preprotein translocase subunit | ||
NECFGCCN_03422 | 0.0 | secD | U | Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. SecDF uses the proton motive force (PMF) to complete protein translocation after the ATP-dependent function of SecA | ||
NECFGCCN_03423 | 3.8e-171 | secF | U | Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. SecDF uses the proton motive force (PMF) to complete protein translocation after the ATP-dependent function of SecA | ||
NECFGCCN_03424 | 9.8e-64 | S | glyoxalase bleomycin resistance protein dioxygenase | |||
NECFGCCN_03425 | 5.9e-118 | K | transcriptional regulator | |||
NECFGCCN_03426 | 1.6e-176 | tsx | M | nucleoside-specific channel-forming protein | ||
NECFGCCN_03427 | 9e-82 | yajI | M | Lipoprotein | ||
NECFGCCN_03428 | 1.7e-78 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
NECFGCCN_03429 | 9.8e-208 | ribD | 1.1.1.193, 3.5.4.26 | H | Converts 2,5-diamino-6-(ribosylamino)-4(3h)-pyrimidinone 5'-phosphate into 5-amino-6-(ribosylamino)-2,4(1h,3h)- pyrimidinedione 5'-phosphate | |
NECFGCCN_03430 | 9e-78 | ribH | 2.5.1.78 | H | Catalyzes the formation of 6,7-dimethyl-8- ribityllumazine by condensation of 5-amino-6-(D- ribitylamino)uracil with 3,4-dihydroxy-2-butanone 4-phosphate. This is the penultimate step in the biosynthesis of riboflavin | |
NECFGCCN_03431 | 4.7e-70 | nusB | K | Involved in transcription antitermination. Required for transcription of ribosomal RNA (rRNA) genes. Binds specifically to the boxA antiterminator sequence of the ribosomal RNA (rrn) operons | ||
NECFGCCN_03432 | 2.1e-185 | thiL | 2.7.4.16 | H | Catalyzes the ATP-dependent phosphorylation of thiamine- monophosphate (TMP) to form thiamine-pyrophosphate (TPP), the active form of vitamin B1 | |
NECFGCCN_03433 | 4.3e-94 | pgpA | 3.1.3.27 | I | Lipid phosphatase which dephosphorylates phosphatidylglycerophosphate (PGP) to phosphatidylglycerol (PG) | |
NECFGCCN_03434 | 1.3e-182 | yajO | 1.1.1.91 | C | Aldo keto reductase | |
NECFGCCN_03435 | 0.0 | dxs | 2.2.1.7 | H | Catalyzes the acyloin condensation reaction between C atoms 2 and 3 of pyruvate and glyceraldehyde 3-phosphate to yield 1-deoxy-D-xylulose-5-phosphate (DXP) | |
NECFGCCN_03436 | 1.1e-159 | ispA | 2.5.1.1, 2.5.1.10, 2.5.1.29, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
NECFGCCN_03437 | 2.9e-35 | xseB | 3.1.11.6 | L | Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides | |
NECFGCCN_03438 | 6.7e-273 | thiI | 2.8.1.4 | H | Catalyzes the ATP-dependent transfer of a sulfur to tRNA to produce 4-thiouridine in position 8 of tRNAs, which functions as a near-UV photosensor. Also catalyzes the transfer of sulfur to the sulfur carrier protein ThiS, forming ThiS-thiocarboxylate. This is a step in the synthesis of thiazole, in the thiamine biosynthesis pathway. The sulfur is donated as persulfide by IscS | |
NECFGCCN_03439 | 4.2e-83 | S | Activator of Hsp90 ATPase 1 family protein | |||
NECFGCCN_03440 | 2.1e-103 | thiJ | 2.7.11.1, 3.5.1.124 | S | TIGRFAM DJ-1 family protein | |
NECFGCCN_03441 | 3.4e-166 | panE | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
NECFGCCN_03442 | 5.7e-83 | yajQ | S | Belongs to the UPF0234 family | ||
NECFGCCN_03443 | 7.2e-245 | yajR | EGP | Major facilitator Superfamily | ||
NECFGCCN_03444 | 1.2e-232 | S | oxidoreductase | |||
NECFGCCN_03445 | 1.7e-238 | EGP | Major facilitator Superfamily | |||
NECFGCCN_03446 | 1.1e-144 | G | Xylose isomerase | |||
NECFGCCN_03447 | 2e-129 | C | Succinate dehydrogenase fumarate reductase, flavoprotein subunit | |||
NECFGCCN_03448 | 2.8e-90 | yafM | L | Transposase and inactivated derivatives | ||
NECFGCCN_03449 | 2.1e-16 | Q | Methyltransferase domain protein | |||
NECFGCCN_03450 | 2.7e-39 | MA20_06245 | S | yiaA/B two helix domain | ||
NECFGCCN_03451 | 1e-310 | uup | S | abc transporter atp-binding protein | ||
NECFGCCN_03452 | 3.2e-12 | ycdA | S | Domain of unknown function (DUF4352) | ||
NECFGCCN_03453 | 1.1e-100 | ybhL | S | Belongs to the BI1 family | ||
NECFGCCN_03454 | 7.3e-94 | XK27_09705 | 6.1.1.14 | S | HD superfamily hydrolase | |
NECFGCCN_03455 | 3.9e-128 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
NECFGCCN_03456 | 2e-45 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
NECFGCCN_03457 | 3.4e-166 | yidC | U | Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins | ||
NECFGCCN_03458 | 1.2e-77 | greA | K | Necessary for efficient RNA polymerase transcription elongation past template-encoded arresting sites. The arresting sites in DNA have the property of trapping a certain fraction of elongating RNA polymerases that pass through, resulting in locked ternary complexes. Cleavage of the nascent transcript by cleavage factors such as GreA or GreB allows the resumption of elongation from the new 3'terminus. GreA releases sequences of 2 to 3 nucleotides | ||
NECFGCCN_03459 | 3e-292 | mltG | ADL | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
NECFGCCN_03460 | 4.2e-86 | XK27_09675 | K | histone acetyltransferase HPA2 and related acetyltransferases | ||
NECFGCCN_03461 | 1.3e-254 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
NECFGCCN_03462 | 4.8e-22 | |||||
NECFGCCN_03463 | 0.0 | snf | 2.7.11.1 | L | Superfamily II DNA RNA helicases, SNF2 family' | |
NECFGCCN_03464 | 1.1e-276 | mapZ | D | Early cell division protein that marks the future cell division site and supports proper FtsZ ring positioning | ||
NECFGCCN_03465 | 1.5e-222 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
NECFGCCN_03466 | 2.2e-38 | gpsB | D | Divisome component that associates with the complex late in its assembly, after the Z-ring is formed, and is dependent on DivIC and PBP2B for its recruitment to the divisome. Together with EzrA, is a key component of the system that regulates PBP1 localization during cell cycle progression. Its main role could be the removal of PBP1 from the cell pole after pole maturation is completed. Also contributes to the recruitment of PBP1 to the division complex. Not essential for septum formation | ||
NECFGCCN_03467 | 8.3e-93 | ypsA | S | Belongs to the UPF0398 family | ||
NECFGCCN_03468 | 4.3e-109 | recU | L | Endonuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves mobile four-strand junctions by introducing symmetrical nicks in paired strands. Promotes annealing of linear ssDNA with homologous dsDNA. Required for DNA repair, homologous recombination and chromosome segregation | ||
NECFGCCN_03469 | 0.0 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
NECFGCCN_03470 | 1.6e-252 | pepC | 3.4.22.40 | E | aminopeptidase | |
NECFGCCN_03471 | 2.4e-72 | yhaI | S | Protein of unknown function (DUF805) | ||
NECFGCCN_03472 | 5e-148 | nadE | 6.3.1.5 | H | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
NECFGCCN_03473 | 3.7e-271 | pncB | 6.3.4.21 | H | Catalyzes the synthesis of beta-nicotinate D- ribonucleotide from nicotinate and 5-phospho-D-ribose 1-phosphate at the expense of ATP | |
NECFGCCN_03474 | 1.5e-125 | macB_2 | V | FtsX-like permease family | ||
NECFGCCN_03475 | 1.8e-68 | ispE | 2.1.1.182, 2.7.1.148 | F | Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol | |
NECFGCCN_03476 | 4.3e-172 | prs | 2.7.6.1 | F | Involved in the biosynthesis of the central metabolite phospho-alpha-D-ribosyl-1-pyrophosphate (PRPP) via the transfer of pyrophosphoryl group from ATP to 1-hydroxyl of ribose-5-phosphate (Rib-5-P) | |
NECFGCCN_03477 | 1.5e-268 | sulP | P | COG0659 Sulfate permease and related transporters (MFS superfamily) | ||
NECFGCCN_03478 | 5.1e-90 | nolA | K | transcriptional regulator | ||
NECFGCCN_03479 | 1.2e-201 | P | Major facilitator superfamily | |||
NECFGCCN_03481 | 2.7e-139 | C | Iron-sulfur cluster-binding domain | |||
NECFGCCN_03482 | 6e-250 | 3.1.6.1 | P | Sulfatase | ||
NECFGCCN_03483 | 2.2e-311 | guaA | 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
NECFGCCN_03484 | 5e-268 | guaB | 1.1.1.205 | F | Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate- limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth | |
NECFGCCN_03485 | 5.5e-192 | xseA | 3.1.11.6 | L | Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides | |
NECFGCCN_03486 | 3.4e-27 | yfgJ | S | bacterial-type flagellum-dependent swarming motility | ||
NECFGCCN_03487 | 5.8e-181 | S | Protein involved in oxidoreductase activity | |||
NECFGCCN_03488 | 8.3e-279 | der | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | ||
NECFGCCN_03489 | 1.7e-173 | bamB | M | Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane | ||
NECFGCCN_03490 | 7.1e-107 | yfgM | S | protein conserved in bacteria | ||
NECFGCCN_03491 | 1.5e-244 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
NECFGCCN_03492 | 6e-205 | ispG | 1.17.7.1, 1.17.7.3 | I | Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate | |
NECFGCCN_03493 | 1.1e-130 | rodZ | S | Cytoskeletal protein that is involved in cell-shape control through regulation of the length of the long axis | ||
NECFGCCN_03494 | 3.3e-222 | rlmN | 2.1.1.192 | J | Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs | |
NECFGCCN_03495 | 3.9e-173 | GM | NmrA-like family | |||
NECFGCCN_03496 | 2.1e-26 | ybiJ | S | Protein of unknown function (DUF1471) | ||
NECFGCCN_03497 | 5.6e-158 | K | AraC-type transcriptional regulator N-terminus | |||
NECFGCCN_03498 | 1.6e-132 | IQ | short-chain dehydrogenase | |||
NECFGCCN_03499 | 6.6e-102 | yjgJ | K | tetR family | ||
NECFGCCN_03500 | 5.5e-127 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
NECFGCCN_03501 | 5.4e-81 | |||||
NECFGCCN_03502 | 6.9e-90 | tssJ | S | Type VI secretion | ||
NECFGCCN_03503 | 1.1e-206 | S | type VI secretion protein | |||
NECFGCCN_03504 | 0.0 | tssF | S | Type VI secretion | ||
NECFGCCN_03505 | 3.9e-298 | S | type VI secretion-associated protein | |||
NECFGCCN_03506 | 0.0 | N | type VI secretion protein | |||
NECFGCCN_03507 | 1.1e-211 | |||||
NECFGCCN_03508 | 1.7e-46 | S | PAAR motif | |||
NECFGCCN_03509 | 0.0 | S | Uncharacterized alpha/beta hydrolase domain (DUF2235) | |||
NECFGCCN_03510 | 9.1e-76 | M | Putative cell wall binding repeat | |||
NECFGCCN_03511 | 1e-47 | S | dextransucrase activity | |||
NECFGCCN_03512 | 1e-12 | S | dextransucrase activity | |||
NECFGCCN_03513 | 8.3e-171 | mprF | 2.3.2.3 | S | Membrane | |
NECFGCCN_03514 | 4.7e-243 | clsB | 2.7.8.8 | I | Catalyzes the phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | |
NECFGCCN_03515 | 1.5e-146 | ybhP | L | Endonuclease Exonuclease Phosphatase | ||
NECFGCCN_03516 | 3.8e-70 | ybhQ | S | inner membrane protein YbhQ | ||
NECFGCCN_03517 | 3.7e-199 | ybhR | V | Transport Permease Protein | ||
NECFGCCN_03518 | 5e-199 | ybhS | V | ABC-type multidrug transport system, permease component | ||
NECFGCCN_03519 | 0.0 | ybhF | V | (ABC) transporter | ||
NECFGCCN_03520 | 6.9e-120 | ybhG | M | Secretion protein | ||
NECFGCCN_03521 | 5.2e-116 | ybiH | K | Transcriptional regulator | ||
NECFGCCN_03522 | 4.2e-164 | K | transcriptional regulator | |||
NECFGCCN_03523 | 1.1e-248 | G | Major Facilitator Superfamily | |||
NECFGCCN_03524 | 2e-127 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
NECFGCCN_03525 | 3.9e-52 | S | dextransucrase activity | |||
NECFGCCN_03526 | 3.2e-89 | abiGI | K | Transcriptional regulator, AbiEi antitoxin | ||
NECFGCCN_03527 | 1.5e-192 | P | periplasmic binding protein | |||
NECFGCCN_03528 | 3.5e-172 | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | |||
NECFGCCN_03529 | 4.7e-129 | fecE | 3.6.3.34 | HP | (ABC) transporter | |
NECFGCCN_03530 | 1.7e-131 | 5.3.3.7 | P | Molybdenum ABC transporter, periplasmic molybdate-binding protein | ||
NECFGCCN_03531 | 9.2e-59 | aroE | 1.1.1.25, 4.2.1.10 | E | shikimate | |
NECFGCCN_03532 | 6.7e-99 | xpt | 2.4.2.22, 2.4.2.7 | F | Converts the preformed base xanthine, a product of nucleic acid breakdown, to xanthosine 5'-monophosphate (XMP), so it can be reused for RNA or DNA synthesis | |
NECFGCCN_03533 | 1.9e-223 | pbuX | F | xanthine permease | ||
NECFGCCN_03534 | 1.2e-269 | V | (ABC) transporter | |||
NECFGCCN_03535 | 8.9e-83 | cobQ | S | glutamine amidotransferase | ||
NECFGCCN_03536 | 8e-168 | murD | 3.4.21.10, 6.3.2.13, 6.3.2.9 | M | Mur ligase, middle domain protein | |
NECFGCCN_03537 | 0.0 | ynfE | 1.8.5.3, 1.97.1.9 | C | Belongs to the prokaryotic molybdopterin-containing oxidoreductase family | |
NECFGCCN_03538 | 1.9e-40 | ynfD | S | membrane | ||
NECFGCCN_03539 | 7.6e-129 | ynfC | M | Uncharacterised protein family (UPF0257) | ||
NECFGCCN_03540 | 1.3e-102 | speG | 2.3.1.57 | J | Catalyzes the formation of N(1)- and N(8)-acetylspermidine from spermidine | |
NECFGCCN_03541 | 2.3e-54 | ynfB | S | Belongs to the UPF0482 family | ||
NECFGCCN_03542 | 3.1e-53 | ynfA | S | UPF0060 membrane protein | ||
NECFGCCN_03543 | 3e-232 | yjjL | G | Major facilitator superfamily | ||
NECFGCCN_03544 | 1.5e-264 | mtlK | 1.1.1.11, 1.1.1.17, 1.1.1.289, 1.1.1.57, 1.1.1.58, 1.1.1.67, 2.7.1.17 | G | Belongs to the mannitol dehydrogenase family | |
NECFGCCN_03545 | 1.1e-69 | uspF | T | Universal stress protein | ||
NECFGCCN_03546 | 8.1e-120 | ydfH | K | transcriptional regulator | ||
NECFGCCN_03547 | 1.8e-136 | ydfG | 1.1.1.313, 1.1.1.381 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
NECFGCCN_03548 | 0.0 | dcp | 3.4.15.5, 3.4.24.70 | E | PFAM peptidase M3A and M3B, thimet oligopeptidase F | |
NECFGCCN_03549 | 3.5e-51 | |||||
NECFGCCN_03550 | 4.6e-109 | K | transcriptional regulator | |||
NECFGCCN_03551 | 5.7e-110 | yedK | S | SOS response associated peptidase (SRAP) | ||
NECFGCCN_03553 | 7.6e-80 | K | LuxR family transcriptional regulator | |||
NECFGCCN_03555 | 2.9e-76 | ibp | O | Belongs to the small heat shock protein (HSP20) family | ||
NECFGCCN_03556 | 9.5e-81 | cinA | 3.5.1.42 | S | Competence-damaged protein | |
NECFGCCN_03557 | 8.5e-205 | T | EAL domain | |||
NECFGCCN_03559 | 7e-138 | ykgA | K | transcriptional regulator | ||
NECFGCCN_03560 | 3.4e-226 | ygbN | EG | Gluconate | ||
NECFGCCN_03561 | 3.2e-144 | ygbM | 5.3.1.22, 5.3.1.35 | G | Belongs to the hyi family | |
NECFGCCN_03562 | 8.4e-79 | pcaF | 2.3.1.16, 2.3.1.174, 2.3.1.223, 2.3.1.9 | I | Catalyzes the final step of fatty acid oxidation in which acetyl-CoA is released and the CoA ester of a fatty acid two carbons shorter is formed | |
NECFGCCN_03563 | 6.1e-24 | S | dextransucrase activity | |||
NECFGCCN_03564 | 3.1e-156 | pdxS | 4.3.3.6 | H | Catalyzes the formation of pyridoxal 5'-phosphate from ribose 5-phosphate (RBP), glyceraldehyde 3-phosphate (G3P) and ammonia. The ammonia is provided by the PdxT subunit. Can also use ribulose 5-phosphate and dihydroxyacetone phosphate as substrates, resulting from enzyme-catalyzed isomerization of RBP and G3P, respectively | |
NECFGCCN_03565 | 6.2e-100 | pdxT | 4.3.3.6 | H | Catalyzes the hydrolysis of glutamine to glutamate and ammonia as part of the biosynthesis of pyridoxal 5'-phosphate. The resulting ammonia molecule is channeled to the active site of PdxS | |
NECFGCCN_03566 | 1.7e-35 | S | the current gene model (or a revised gene model) may contain a frame shift | |||
NECFGCCN_03568 | 1.4e-15 | S | HipA-like C-terminal domain | |||
NECFGCCN_03569 | 2.9e-33 | XK27_00500 | L | SNF2 family N-terminal domain | ||
NECFGCCN_03571 | 4.1e-192 | murB | 1.3.1.98 | M | cell wall formation | |
NECFGCCN_03572 | 5.7e-180 | birA | 2.7.1.33, 6.3.4.15 | H | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a biotin-operon repressor. In the presence of ATP, BirA activates biotin to form the BirA-biotinyl-5'-adenylate (BirA-bio- 5'-AMP or holoBirA) complex. HoloBirA can either transfer the biotinyl moiety to the biotin carboxyl carrier protein (BCCP) subunit of acetyl-CoA carboxylase, or bind to the biotin operator site and inhibit transcription of the operon | |
NECFGCCN_03573 | 7.7e-174 | coaA | 2.7.1.33 | F | pantothenic acid kinase | |
NECFGCCN_03575 | 1e-26 | galT | 2.7.7.12 | G | UDPglucose--hexose-1-phosphate uridylyltransferase | |
NECFGCCN_03576 | 9e-101 | galT | 2.7.7.12 | G | UDPglucose--hexose-1-phosphate uridylyltransferase | |
NECFGCCN_03577 | 4.8e-151 | galK | 2.7.1.6 | G | Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) | |
NECFGCCN_03578 | 5.8e-16 | xylG | 3.6.3.17 | S | ABC transporter, ATP-binding protein | |
NECFGCCN_03579 | 6.8e-190 | tcsA | S | membrane | ||
NECFGCCN_03580 | 2.9e-24 | deoC | 4.1.2.4, 5.4.2.8 | F | Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate | |
NECFGCCN_03581 | 2.8e-152 | K | transcriptional regulator | |||
NECFGCCN_03582 | 4.3e-155 | S | COG0491 Zn-dependent hydrolases, including glyoxylases | |||
NECFGCCN_03583 | 4.1e-18 | rpsV | J | 30S ribosomal protein subunit S22 family | ||
NECFGCCN_03584 | 0.0 | maeA | 1.1.1.38 | C | Malic enzyme | |
NECFGCCN_03586 | 0.0 | tlrC | S | ABC transporter | ||
NECFGCCN_03587 | 1.3e-171 | K | Transcriptional regulator | |||
NECFGCCN_03588 | 7.1e-104 | ppa | 3.6.1.1 | C | Catalyzes the hydrolysis of inorganic pyrophosphate (PPi) forming two phosphate ions | |
NECFGCCN_03589 | 4.2e-189 | adhP | 1.1.1.1 | S | alcohol dehydrogenase | |
NECFGCCN_03590 | 0.0 | E | Extracellular solute-binding protein | |||
NECFGCCN_03591 | 2.7e-150 | P | PFAM binding-protein-dependent transport systems inner membrane component | |||
NECFGCCN_03592 | 2.8e-130 | P | COG1173 ABC-type dipeptide oligopeptide nickel transport systems permease components | |||
NECFGCCN_03593 | 2.3e-282 | P | ATPase activity | |||
NECFGCCN_03594 | 1.6e-185 | MA20_00170 | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | ||
NECFGCCN_03595 | 1.4e-195 | O | Antioxidant protein with alkyl hydroperoxidase activity. Required for the reduction of the AhpC active site cysteine residues and for the regeneration of the AhpC enzyme activity | |||
NECFGCCN_03596 | 4.9e-202 | araJ | EGP | Major facilitator Superfamily | ||
NECFGCCN_03597 | 3.7e-73 | E | Lactoylglutathione lyase and related lyases | |||
NECFGCCN_03598 | 2.3e-153 | ppk2 | 2.7.4.1 | H | polyphosphate kinase | |
NECFGCCN_03599 | 7.8e-25 | |||||
NECFGCCN_03600 | 2.6e-55 | S | CcdB protein | |||
NECFGCCN_03601 | 5.4e-121 | fdnI | C | formate dehydrogenase | ||
NECFGCCN_03602 | 5.7e-174 | fdnH | C | formate dehydrogenase | ||
NECFGCCN_03603 | 2.6e-202 | fdnG | 1.17.1.9, 1.17.5.3 | C | Belongs to the prokaryotic molybdopterin-containing oxidoreductase family | |
NECFGCCN_03604 | 1.1e-141 | |||||
NECFGCCN_03605 | 3.1e-26 | |||||
NECFGCCN_03606 | 1e-48 | S | Phage-related protein | |||
NECFGCCN_03607 | 1.2e-43 | K | sequence-specific DNA binding | |||
NECFGCCN_03608 | 7.6e-21 | S | the current gene model (or a revised gene model) may contain a frame shift | |||
NECFGCCN_03609 | 5.6e-32 | ybfA | S | Membrane | ||
NECFGCCN_03610 | 1.1e-303 | kdpA | 3.6.3.12 | P | Part of the high-affinity ATP-driven potassium transport (or Kdp) system, which catalyzes the hydrolysis of ATP coupled with the electrogenic transport of potassium into the cytoplasm. This subunit binds and transports the potassium across the cytoplasmic membrane | |
NECFGCCN_03611 | 0.0 | kdpB | 3.6.3.12 | P | Part of the high-affinity ATP-driven potassium transport (or Kdp) system, which catalyzes the hydrolysis of ATP coupled with the electrogenic transport of potassium into the cytoplasm. This subunit is responsible for energy coupling to the transport system | |
NECFGCCN_03612 | 4.9e-94 | kdpC | 3.6.3.12 | P | Part of the high-affinity ATP-driven potassium transport (or Kdp) system, which catalyzes the hydrolysis of ATP coupled with the electrogenic transport of potassium into the cytoplasm. This subunit acts as a catalytic chaperone that increases the ATP- binding affinity of the ATP-hydrolyzing subunit KdpB by the formation of a transient KdpB KdpC ATP ternary complex | |
NECFGCCN_03613 | 0.0 | T | PhoQ Sensor | |||
NECFGCCN_03614 | 1.2e-123 | K | response regulator | |||
NECFGCCN_03615 | 6.2e-73 | |||||
NECFGCCN_03616 | 0.0 | pgm | 5.4.2.2 | G | Phosphoglucomutase | |
NECFGCCN_03617 | 1.1e-100 | seqA | L | Negative regulator of replication initiation, which contributes to regulation of DNA replication and ensures that replication initiation occurs exactly once per chromosome per cell cycle. Binds to pairs of hemimethylated GATC sequences in the oriC region, thus preventing assembly of replication proteins and re- initiation at newly replicated origins. Repression is relieved when the region becomes fully methylated | ||
NECFGCCN_03618 | 4.1e-104 | ybfF | S | Alpha beta hydrolase | ||
NECFGCCN_03619 | 5e-42 | ybfE | S | CopG domain protein DNA-binding domain protein | ||
NECFGCCN_03620 | 1.5e-100 | fldA | C | Low-potential electron donor to a number of redox enzymes | ||
NECFGCCN_03621 | 4e-83 | fur | K | belongs to the Fur family | ||
NECFGCCN_03622 | 1.2e-70 | citA | EGP | Is involved in the uptake of citrate and the transport of protons into the cell | ||
NECFGCCN_03623 | 4.2e-53 | ybfN | S | YbfN-like lipoprotein | ||
NECFGCCN_03624 | 2.4e-280 | chiP | S | Outer membrane porin | ||
NECFGCCN_03626 | 0.0 | glnS | 6.1.1.18 | J | Catalyzes a two-step reaction, first charging a glutamine molecule by linking its carboxyl group to the alpha-phosphate of ATP, followed by transfer of the aminoacyl-adenylate to its tRNA | |
NECFGCCN_03627 | 7.4e-71 | nagE | 2.7.1.192, 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | Phosphotransferase System | |
NECFGCCN_03628 | 3.2e-109 | fdoG | 1.17.1.9, 1.17.5.3 | C | Sulfate ABC transporter substrate-binding protein | |
NECFGCCN_03629 | 4.4e-152 | fdhD | C | Required for formate dehydrogenase (FDH) activity. Acts as a sulfur carrier protein that transfers sulfur from IscS to the molybdenum cofactor prior to its insertion into FDH | ||
NECFGCCN_03630 | 3.8e-15 | S | Protein of unknown function (DUF1471) | |||
NECFGCCN_03631 | 5.3e-181 | pfkA | 2.7.1.11, 2.7.1.90 | F | Catalyzes the phosphorylation of D-fructose 6-phosphate to fructose 1,6-bisphosphate by ATP, the first committing step of glycolysis | |
NECFGCCN_03632 | 2.2e-48 | ptxB | 2.7.1.194, 2.7.1.200 | G | Phosphotransferase system, lactose cellobiose-specific IIB subunit | |
NECFGCCN_03633 | 1.7e-246 | ulaA | 2.7.1.194 | G | protein conserved in bacteria | |
NECFGCCN_03634 | 8.4e-151 | 4.1.2.13 | G | Aldolase | ||
NECFGCCN_03635 | 7.3e-40 | |||||
NECFGCCN_03636 | 7.3e-74 | ulaC | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | PTS IIA-like nitrogen-regulatory protein PtsN | |
NECFGCCN_03637 | 3.2e-104 | adk | 2.7.4.3 | F | adenylate kinase activity | |
NECFGCCN_03638 | 6.3e-46 | S | Branched-chain amino acid transport | |||
NECFGCCN_03639 | 4.8e-112 | azlC | E | branched-chain amino acid | ||
NECFGCCN_03640 | 7.7e-97 | sinR | K | Transcriptional regulator | ||
NECFGCCN_03641 | 3.6e-185 | aglR | K | PFAM Periplasmic binding protein LacI transcriptional regulator | ||
NECFGCCN_03642 | 9.8e-65 | thiT | S | Thiamine transporter | ||
NECFGCCN_03643 | 9.4e-133 | vncS | 2.7.13.3 | T | Histidine kinase | |
NECFGCCN_03644 | 3.4e-49 | 3.6.1.55 | F | NUDIX domain | ||
NECFGCCN_03646 | 1.5e-23 | csrA | J | Could accelerate the degradation of some genes transcripts potentially through selective RNA binding | ||
NECFGCCN_03647 | 5.5e-12 | |||||
NECFGCCN_03648 | 0.0 | alaS | 6.1.1.7 | J | Catalyzes the attachment of alanine to tRNA(Ala) in a two-step reaction alanine is first activated by ATP to form Ala- AMP and then transferred to the acceptor end of tRNA(Ala). Also edits incorrectly charged Ser-tRNA(Ala) and Gly-tRNA(Ala) via its editing domain | |
NECFGCCN_03649 | 5.6e-86 | recX | 2.4.1.337 | GT4 | S | Regulatory protein recX |
NECFGCCN_03650 | 1.6e-191 | recA | L | Can catalyze the hydrolysis of ATP in the presence of single-stranded DNA, the ATP-dependent uptake of single-stranded DNA by duplex DNA, and the ATP-dependent hybridization of homologous single-stranded DNAs. It interacts with LexA causing its activation and leading to its autocatalytic cleavage | ||
NECFGCCN_03651 | 4.9e-82 | ygaD | 3.5.1.42 | J | Belongs to the CinA family | |
NECFGCCN_03652 | 4.5e-155 | mntA | 3.2.1.78 | GH26 | P | Belongs to the bacterial solute-binding protein 9 family |
NECFGCCN_03653 | 3.9e-143 | znuB | P | ABC-type Mn2 Zn2 transport systems permease components | ||
NECFGCCN_03654 | 4.4e-118 | znuC | P | (ABC) transporter | ||
NECFGCCN_03656 | 1.3e-159 | folD | 1.5.1.5, 3.5.4.9 | F | Catalyzes the oxidation of 5,10- methylenetetrahydrofolate to 5,10-methenyltetrahydrofolate and then the hydrolysis of 5,10-methenyltetrahydrofolate to 10- formyltetrahydrofolate | |
NECFGCCN_03657 | 1.3e-31 | yaaA | S | Ribosome-associated protein | ||
NECFGCCN_03658 | 3.9e-270 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
NECFGCCN_03659 | 1.4e-89 | ppiB | 2.7.11.1, 5.2.1.8 | G | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
NECFGCCN_03660 | 8.5e-136 | lpxH | 3.6.1.54 | S | Hydrolyzes the pyrophosphate bond of UDP-2,3- diacylglucosamine to yield 2,3-diacylglucosamine 1-phosphate (lipid X) and UMP by catalyzing the attack of water at the alpha-P atom. Involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell | |
NECFGCCN_03661 | 1.1e-45 | |||||
NECFGCCN_03662 | 2e-86 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
NECFGCCN_03663 | 2.4e-203 | purK | 6.3.4.18 | F | Catalyzes the ATP-dependent conversion of 5- aminoimidazole ribonucleotide (AIR) and HCO(3)(-) to N5- carboxyaminoimidazole ribonucleotide (N5-CAIR) | |
NECFGCCN_03664 | 2.2e-204 | selU | H | Catalyzes the transfer of selenium from selenophosphate for conversion of 2-thiouridine to 2-selenouridine at the wobble position in tRNA | ||
NECFGCCN_03665 | 7.8e-32 | D | Antitoxin component of a toxin-antitoxin (TA) module | |||
NECFGCCN_03666 | 1.2e-61 | doc | S | Death ON curing protein | ||
NECFGCCN_03667 | 2.2e-58 | L | Helix-turn-helix domain | |||
NECFGCCN_03668 | 2.4e-136 | IQ | Acetoin reductase | |||
NECFGCCN_03670 | 0.0 | lepA | M | Required for accurate and efficient protein synthesis under certain stress conditions. May act as a fidelity factor of the translation reaction, by catalyzing a one-codon backward translocation of tRNAs on improperly translocated ribosomes. Back- translocation proceeds from a post-translocation (POST) complex to a pre-translocation (PRE) complex, thus giving elongation factor G a second chance to translocate the tRNAs correctly. Binds to ribosomes in a GTP-dependent manner | ||
NECFGCCN_03672 | 0.0 | S | Domain of unknown function (DUF5107) | |||
NECFGCCN_03673 | 1.3e-221 | yphH | 2.7.1.2 | GK | ROK family | |
NECFGCCN_03674 | 6.4e-68 | yphA | S | SURF4 family | ||
NECFGCCN_03675 | 4.2e-239 | glyA | 2.1.2.1 | E | Catalyzes the reversible interconversion of serine and glycine with tetrahydrofolate (THF) serving as the one-carbon carrier. This reaction serves as the major source of one-carbon groups required for the biosynthesis of purines, thymidylate, methionine, and other important biomolecules. Also exhibits THF- independent aldolase activity toward beta-hydroxyamino acids, producing glycine and aldehydes, via a retro-aldol mechanism | |
NECFGCCN_03676 | 1.6e-227 | hmp | 1.14.12.17 | C | Is involved in NO detoxification in an aerobic process, termed nitric oxide dioxygenase (NOD) reaction that utilizes O(2) and NAD(P)H to convert NO to nitrate, which protects the bacterium from various noxious nitrogen compounds. Therefore, plays a central role in the inducible response to nitrosative stress | |
NECFGCCN_03677 | 2e-55 | glnB | K | Belongs to the P(II) protein family | ||
NECFGCCN_03678 | 5.8e-247 | yfhA | T | COG2204 Response regulator containing CheY-like receiver, AAA-type ATPase, and DNA-binding domains | ||
NECFGCCN_03679 | 7.9e-123 | yfhG | NU | YfhG lipoprotein | ||
NECFGCCN_03680 | 9e-246 | T | PhoQ Sensor | |||
NECFGCCN_03681 | 0.0 | purL | 6.3.5.3 | F | Phosphoribosylformylglycinamidine synthase involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate | |
NECFGCCN_03682 | 1.3e-306 | mltF | M | Murein-degrading enzyme that degrades murein glycan strands and insoluble, high-molecular weight murein sacculi, with the concomitant formation of a 1,6-anhydromuramoyl product. Lytic transglycosylases (LTs) play an integral role in the metabolism of the peptidoglycan (PG) sacculus. Their lytic action creates space within the PG sacculus to allow for its expansion as well as for the insertion of various structures such as secretion systems and flagella | ||
NECFGCCN_03683 | 1.1e-89 | tadA | 3.4.17.13, 3.5.4.1, 3.5.4.3, 3.5.4.33, 3.8.1.5 | FJ | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
NECFGCCN_03684 | 1.5e-115 | yfhB | 3.1.3.27 | E | HAD superfamily (Subfamily IF) hydrolase, YfhB | |
NECFGCCN_03685 | 3.5e-149 | yfhH | K | Transcriptional regulator | ||
NECFGCCN_03686 | 4.6e-47 | yfhL | C | Ferredoxin | ||
NECFGCCN_03687 | 1.3e-63 | acpS | 2.7.8.7, 3.2.1.52 | I | Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein | |
NECFGCCN_03688 | 4.6e-129 | pdxJ | 2.6.99.2 | H | Catalyzes the complicated ring closure reaction between the two acyclic compounds 1-deoxy-D-xylulose-5-phosphate (DXP) and 3-amino-2-oxopropyl phosphate (1-amino-acetone-3-phosphate or AAP) to form pyridoxine 5'-phosphate (PNP) and inorganic phosphate | |
NECFGCCN_03689 | 2.7e-137 | recO | 2.6.99.2 | L | Involved in DNA repair and RecF pathway recombination | |
NECFGCCN_03690 | 1.1e-167 | era | S | An essential GTPase that binds both GDP and GTP, with rapid nucleotide exchange. Plays a role in 16S rRNA processing and 30S ribosomal subunit biogenesis and possibly also in cell cycle regulation and energy metabolism | ||
NECFGCCN_03691 | 1.6e-123 | rnc | 3.1.26.3 | J | Digests double-stranded RNA. Involved in the processing of primary rRNA transcript to yield the immediate precursors to the large and small rRNAs (23S and 16S). Processes some mRNAs, and tRNAs when they are encoded in the rRNA operon. Processes pre- crRNA and tracrRNA of type II CRISPR loci if present in the organism | |
NECFGCCN_03692 | 1.5e-188 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
NECFGCCN_03693 | 0.0 | lepA | M | Required for accurate and efficient protein synthesis under certain stress conditions. May act as a fidelity factor of the translation reaction, by catalyzing a one-codon backward translocation of tRNAs on improperly translocated ribosomes. Back- translocation proceeds from a post-translocation (POST) complex to a pre-translocation (PRE) complex, thus giving elongation factor G a second chance to translocate the tRNAs correctly. Binds to ribosomes in a GTP-dependent manner | ||
NECFGCCN_03695 | 7.5e-80 | rseC | T | Positive regulator of | ||
NECFGCCN_03696 | 1.4e-173 | rseB | T | Negative regulator of sigma E activity | ||
NECFGCCN_03697 | 5.9e-104 | rseA | T | An anti-sigma factor for extracytoplasmic function (ECF) sigma factor sigma-E (RpoE). ECF sigma factors are held in an inactive form by an anti-sigma factor until released by regulated intramembrane proteolysis (RIP). RIP occurs when an extracytoplasmic signal triggers a concerted proteolytic cascade to transmit information and elicit cellular responses. The membrane-spanning regulatory substrate protein is first cut periplasmically (site-1 protease, S1P, DegS), then within the membrane itself (site-2 protease, S2P, RseP), while cytoplasmic proteases finish degrading the anti-sigma factor, liberating sigma-E | ||
NECFGCCN_03698 | 4.2e-101 | rpoE | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
NECFGCCN_03699 | 0.0 | nadB | 1.3.5.4, 1.4.3.16 | H | Catalyzes the oxidation of L-aspartate to iminoaspartate | |
NECFGCCN_03700 | 1.8e-133 | yfiC | 2.1.1.223, 2.1.1.72 | J | Specifically methylates the adenine in position 37 of tRNA(1)(Val) (anticodon cmo5UAC) | |
NECFGCCN_03701 | 1.1e-224 | srmB | 3.6.4.13 | JKL | DEAD-box RNA helicase involved in the assembly of the 50S ribosomal subunit at low temperature. Exhibits RNA-stimulated ATP hydrolysis and RNA unwinding activity | |
NECFGCCN_03702 | 6.4e-66 | grcA | 1.14.13.236 | S | Acts as a radical domain for damaged PFL and possibly other radical proteins | |
NECFGCCN_03703 | 4.5e-134 | ung | 3.2.2.27 | L | Excises uracil residues from the DNA which can arise as a result of misincorporation of dUMP residues by DNA polymerase or due to deamination of cytosine | |
NECFGCCN_03704 | 8.4e-188 | yfiF | 2.1.1.185, 2.1.1.34 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
NECFGCCN_03705 | 1.3e-78 | trxC | 1.8.1.8 | O | Thioredoxin | |
NECFGCCN_03706 | 1.2e-123 | yfiP | S | DTW domain containing protein | ||
NECFGCCN_03707 | 0.0 | yfiQ | 6.2.1.13 | C | Acyl-CoA synthetase (NDP forming) | |
NECFGCCN_03708 | 1.3e-262 | pssA | 2.7.8.8 | I | Catalyzes de novo synthesis of phosphatidylserine from CDP-diacylglycerol and L-serine which leads eventually to the production of phosphatidylethanolamine | |
NECFGCCN_03709 | 6.2e-54 | yfiM | S | Required for high salt suppression of motility | ||
NECFGCCN_03710 | 7.6e-236 | kgtP | EGP | transporter | ||
NECFGCCN_03711 | 3.6e-26 | lctO | C | Catalyzes the conversion of L-lactate to pyruvate. Is coupled to the respiratory chain | ||
NECFGCCN_03712 | 2.5e-78 | Q | Escherichia coli O157 H7 ortholog z1925 | |||
NECFGCCN_03713 | 5.6e-78 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
NECFGCCN_03714 | 2.1e-45 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
NECFGCCN_03715 | 5.7e-201 | V | permease protein | |||
NECFGCCN_03716 | 7.5e-121 | macB | V | ABC transporter, ATP-binding protein | ||
NECFGCCN_03717 | 2.6e-180 | acrA | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | ||
NECFGCCN_03718 | 7.6e-127 | 2.1.1.223 | S | Putative SAM-dependent methyltransferase | ||
NECFGCCN_03719 | 0.0 | carB | 6.3.5.5 | F | carbamoyl-phosphate synthetase ammonia chain | |
NECFGCCN_03720 | 4.6e-210 | carA | 6.3.5.5 | F | carbamoyl-phosphate synthetase glutamine chain | |
NECFGCCN_03721 | 1.5e-172 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
NECFGCCN_03722 | 1.8e-221 | pyrP | F | uracil Permease | ||
NECFGCCN_03724 | 1.8e-87 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
NECFGCCN_03725 | 9.1e-16 | 2.4.1.21 | GT5 | M | Right handed beta helix region | |
NECFGCCN_03726 | 2.9e-174 | spd | F | DNA RNA non-specific endonuclease | ||
NECFGCCN_03727 | 7.7e-92 | lemA | S | LemA family | ||
NECFGCCN_03728 | 4e-135 | htpX | O | Belongs to the peptidase M48B family | ||
NECFGCCN_03729 | 1.7e-119 | sirR | K | iron dependent repressor | ||
NECFGCCN_03730 | 2.1e-171 | sitA | P | Belongs to the bacterial solute-binding protein 9 family | ||
NECFGCCN_03731 | 8.7e-132 | mtsC | P | ABC-type Mn2 Zn2 transport systems, permease components | ||
NECFGCCN_03732 | 5.6e-127 | sitB | 3.6.3.35 | P | ABC transporter, ATP-binding protein | |
NECFGCCN_03733 | 9.8e-56 | S | Psort location CytoplasmicMembrane, score | |||
NECFGCCN_03734 | 1.8e-63 | S | Domain of unknown function (DUF4430) | |||
NECFGCCN_03736 | 0.0 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
NECFGCCN_03737 | 1.2e-85 | ybeY | 2.6.99.2, 3.5.4.5 | J | Single strand-specific metallo-endoribonuclease involved in late-stage 70S ribosome quality control and in maturation of the 3' terminus of the 16S rRNA | |
NECFGCCN_03738 | 1.3e-168 | corC | P | Mg2 and Co2 transporter CorC | ||
NECFGCCN_03739 | 2.7e-280 | lnt | GT2 | M | Transfers the fatty acyl group on membrane lipoproteins | |
NECFGCCN_03740 | 3.6e-196 | nadA | 2.5.1.72 | H | Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate | |
NECFGCCN_03741 | 1.1e-127 | pnuC | H | nicotinamide mononucleotide transporter | ||
NECFGCCN_03742 | 2.1e-166 | zitB | P | cation diffusion facilitator family transporter | ||
NECFGCCN_03743 | 5.6e-35 | ybgS | S | YbgS-like protein | ||
NECFGCCN_03744 | 1.9e-200 | aroG | 2.5.1.54 | E | Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) | |
NECFGCCN_03745 | 2e-143 | gpmA | 5.4.2.11 | G | Belongs to the phosphoglycerate mutase family. BPG- dependent PGAM subfamily | |
NECFGCCN_03746 | 5.4e-200 | galM | 2.7.1.6, 5.1.3.3 | G | converts alpha-aldose to the beta-anomer | |
NECFGCCN_03747 | 7.8e-216 | galK | 2.7.1.6 | G | Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) | |
NECFGCCN_03748 | 5.4e-208 | galT | 2.7.7.12 | H | galactose-1-phosphate uridylyltransferase | |
NECFGCCN_03749 | 1.3e-198 | galE | 5.1.3.2 | M | udp-glucose 4-epimerase | |
NECFGCCN_03750 | 4.8e-279 | modF | 3.6.3.21, 3.6.3.34 | P | ABC-type molybdenum transport system ATPase component photorepair protein PhrA | |
NECFGCCN_03751 | 2.6e-138 | modE | H | Transcriptional regulator | ||
NECFGCCN_03752 | 1.4e-16 | acrZ | U | drug transmembrane transporter activity | ||
NECFGCCN_03753 | 6.3e-137 | modA | 5.3.3.7 | P | ABC transporter, periplasmic molybdate-binding protein | |
NECFGCCN_03754 | 4.1e-119 | modB | 3.6.3.29 | P | ABC-type molybdate transport system, permease component | |
NECFGCCN_03755 | 1.1e-189 | modC | 3.6.3.29 | P | Part of the ABC transporter complex ModABC involved in molybdenum import. Responsible for energy coupling to the transport system | |
NECFGCCN_03756 | 6e-146 | ybhA | S | hydrolases of the HAD superfamily | ||
NECFGCCN_03757 | 4e-192 | pgl | 3.1.1.31 | G | Catalyzes the hydrolysis of 6-phosphogluconolactone to 6-phosphogluconate | |
NECFGCCN_03758 | 1.9e-38 | ariR | S | Two-component-system connector protein AriR | ||
NECFGCCN_03759 | 8.3e-40 | |||||
NECFGCCN_03760 | 8.1e-38 | ycgZ | S | Two-component-system connector protein YcgZ | ||
NECFGCCN_03761 | 9e-223 | ycgF | T | EAL domain | ||
NECFGCCN_03762 | 3.5e-137 | ycgE | K | Transcriptional regulator | ||
NECFGCCN_03763 | 4e-101 | K | helix_turn_helix, Lux Regulon | |||
NECFGCCN_03764 | 6e-29 | |||||
NECFGCCN_03765 | 1.9e-89 | |||||
NECFGCCN_03766 | 8.3e-171 | S | enterobacterial common antigen metabolic process | |||
NECFGCCN_03767 | 0.0 | czcA | V | Belongs to the resistance-nodulation-cell division (RND) (TC 2.A.6) family | ||
NECFGCCN_03768 | 2.7e-186 | ttgA | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | ||
NECFGCCN_03770 | 1.8e-69 | uspF | T | Required for resistance to DNA-damaging agents | ||
NECFGCCN_03771 | 1e-61 | ctpF | P | ATPase, P-type (transporting), HAD superfamily, subfamily IC | ||
NECFGCCN_03772 | 1.8e-275 | yjiR | K | Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | ||
NECFGCCN_03773 | 9.3e-22 | yjiS | S | Domain of unknown function (DUF1127) | ||
NECFGCCN_03774 | 6.8e-78 | slyA | K | Transcriptional regulator | ||
NECFGCCN_03775 | 2.3e-193 | yiaV | V | Secretion Protein | ||
NECFGCCN_03776 | 6.3e-188 | S | Protein of unknown function (DUF2955) | |||
NECFGCCN_03777 | 3.2e-29 | S | Protein of unknown function (DUF3343) | |||
NECFGCCN_03778 | 2e-135 | yjiL | I | 4 iron, 4 sulfur cluster binding | ||
NECFGCCN_03779 | 7.5e-219 | yjiM | E | cellular response to DNA damage stimulus | ||
NECFGCCN_03780 | 1.8e-34 | S | Uncharacterized conserved protein (DUF2164) | |||
NECFGCCN_03781 | 3.5e-222 | mdtM | EGP | Major facilitator Superfamily | ||
NECFGCCN_03782 | 5.3e-229 | yjiN | S | Membrane | ||
NECFGCCN_03783 | 2.8e-109 | rhtC | E | PFAM Lysine exporter protein (LYSE YGGA) | ||
NECFGCCN_03784 | 3.4e-149 | msmR | K | transcriptional regulator | ||
NECFGCCN_03785 | 1.1e-151 | yfaD | S | Transposase | ||
NECFGCCN_03786 | 1.2e-255 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.24, 1.2.1.79 | C | belongs to the aldehyde dehydrogenase family | |
NECFGCCN_03787 | 9.1e-98 | S | YfaZ precursor | |||
NECFGCCN_03788 | 7.5e-180 | yjiA | S | cobalamin synthesis protein | ||
NECFGCCN_03789 | 7.7e-34 | yjiX | S | Selenoprotein, putative | ||
NECFGCCN_03790 | 3.4e-194 | cstA | T | Carbon starvation protein | ||
NECFGCCN_03791 | 2.3e-13 | |||||
NECFGCCN_03792 | 9.5e-283 | ypwA | 3.4.17.19 | E | Broad specificity carboxypetidase that releases amino acids sequentially from the C-terminus, including neutral, aromatic, polar and basic residues | |
NECFGCCN_03793 | 2.9e-224 | ynfM | EGP | Major facilitator Superfamily | ||
NECFGCCN_03794 | 1.9e-161 | ynfL | K | transcriptional regulator | ||
NECFGCCN_03795 | 9.7e-225 | mlc | GK | Mlc, controls the expression of genes involved in the phosphotransferase and phosphoenolpyruvate systems, regulates genes involved in the uptake of sugars | ||
NECFGCCN_03796 | 1.9e-124 | bioD | 6.3.3.3 | H | Catalyzes a mechanistically unusual reaction, the ATP- dependent insertion of CO2 between the N7 and N8 nitrogen atoms of 7,8-diaminopelargonic acid (DAPA) to form an ureido ring | |
NECFGCCN_03797 | 6e-225 | clcB | P | Probably acts as an electrical shunt for an outwardly- directed proton pump that is linked to amino acid decarboxylation, as part of the extreme acid resistance (XAR) response | ||
NECFGCCN_03798 | 1.8e-107 | dmsD | S | Required for biogenesis assembly of DMSO reductase, but not for the interaction of the DmsA signal peptide with the Tat system. May be part of a chaperone cascade complex that facilitates a folding-maturation pathway for the substrate protein | ||
NECFGCCN_03799 | 2.7e-141 | dmsC | S | Dimethyl sulfoxide reductase | ||
NECFGCCN_03800 | 4.8e-31 | 2.4.1.5 | GH13 | M | KxYKxGKxW signal domain protein | |
NECFGCCN_03802 | 2.5e-78 | S | dextransucrase activity | |||
NECFGCCN_03803 | 2.8e-19 | S | dextransucrase activity | |||
NECFGCCN_03804 | 1.1e-20 | S | dextransucrase activity | |||
NECFGCCN_03805 | 5.2e-121 | xylH | G | Belongs to the binding-protein-dependent transport system permease family | ||
NECFGCCN_03806 | 1.4e-225 | xylR | 5.3.1.12 | K | transcriptional regulator | |
NECFGCCN_03807 | 1.3e-102 | bax | GH73 | S | FlgJ-related protein | |
NECFGCCN_03808 | 0.0 | malS | 3.2.1.1 | GH13 | G | alpha-amylase |
NECFGCCN_03809 | 9.9e-249 | avtA | 2.6.1.66 | E | Valine--pyruvate aminotransferase | |
NECFGCCN_03810 | 4.4e-88 | ysaA | C | electron transport | ||
NECFGCCN_03811 | 9.4e-155 | yiaJ | K | transcriptional regulator | ||
NECFGCCN_03812 | 9.2e-189 | dlgD | 1.1.1.130, 1.5.1.21 | C | Catalyzes the reduction of 2,3-diketo-L-gulonate in the presence of NADH, to form 3-keto-L-gulonate | |
NECFGCCN_03813 | 2.4e-83 | yiaL | G | Domain of unknown function (DUF386) | ||
NECFGCCN_03814 | 4e-170 | L | Domain of unknown function (DUF4862) | |||
NECFGCCN_03815 | 3.2e-242 | G | Major facilitator superfamily | |||
NECFGCCN_03816 | 2.8e-290 | lyx | 2.7.1.17, 2.7.1.189, 2.7.1.5, 2.7.1.51, 2.7.1.53 | G | Belongs to the FGGY kinase family | |
NECFGCCN_03817 | 1.9e-118 | sgbH | 4.1.1.85, 4.1.2.43 | G | decarboxylase | |
NECFGCCN_03818 | 2.2e-162 | sgbU | 5.1.3.22 | G | 3-epimerase | |
NECFGCCN_03819 | 1.6e-131 | araD | 4.1.1.104, 4.1.2.17, 4.1.2.19, 4.2.1.109, 5.1.3.4 | G | Catalyzes the isomerization of L-ribulose 5-phosphate to D-xylulose 5-phosphate | |
NECFGCCN_03820 | 0.0 | selB | J | Translation elongation factor | ||
NECFGCCN_03821 | 7.1e-240 | selA | 2.9.1.1 | J | Converts seryl-tRNA(Sec) to selenocysteinyl-tRNA(Sec) required for selenoprotein biosynthesis | |
NECFGCCN_03822 | 5.4e-107 | yibF | 2.5.1.18 | O | Glutathione S-Transferase | |
NECFGCCN_03823 | 0.0 | mtlA | 2.7.1.197, 2.7.1.202 | G | PTS system mannitol-specific | |
NECFGCCN_03824 | 2.9e-210 | mtlD | 1.1.1.17 | C | Mannitol-1-Phosphate 5-Dehydrogenase | |
NECFGCCN_03825 | 1.3e-102 | mtlR | K | Mannitol repressor | ||
NECFGCCN_03826 | 5.9e-35 | yibT | S | response to butan-1-ol | ||
NECFGCCN_03827 | 2.7e-53 | yibL | S | Protein of unknown function (DUF2810) | ||
NECFGCCN_03828 | 8.4e-288 | lldP | C | L-lactate permease | ||
NECFGCCN_03829 | 1.2e-135 | lldR | K | Represses the lctPRD operon | ||
NECFGCCN_03830 | 1.9e-225 | lldD | 1.1.2.3 | C | Catalyzes the conversion of L-lactate to pyruvate. Is coupled to the respiratory chain | |
NECFGCCN_03831 | 1.8e-86 | trmL | 2.1.1.207 | J | Methylates the ribose at the nucleotide 34 wobble position in the two leucyl isoacceptors tRNA(Leu)(CmAA) and tRNA(Leu)(cmnm5UmAA). Catalyzes the methyl transfer from S- adenosyl-L-methionine to the 2'-OH of the wobble nucleotide | |
NECFGCCN_03832 | 2.5e-152 | cysE | 2.3.1.30 | E | serine acetyltransferase | |
NECFGCCN_03833 | 5.1e-187 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
NECFGCCN_03834 | 2.4e-83 | secB | U | One of the proteins required for the normal export of preproteins out of the cell cytoplasm. It is a molecular chaperone that binds to a subset of precursor proteins, maintaining them in a translocation-competent state. It also specifically binds to its receptor SecA | ||
NECFGCCN_03835 | 3.3e-42 | grxC | O | Has a glutathione-disulfide oxidoreductase activity in the presence of NADPH and glutathione reductase. Reduces low molecular weight disulfides and proteins | ||
NECFGCCN_03836 | 8e-73 | yibN | 2.8.1.1, 2.8.1.2 | P | rhodanese-related sulfurtransferase | |
NECFGCCN_03837 | 5.6e-294 | gpmI | 5.4.2.12 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
NECFGCCN_03838 | 9.3e-138 | envC | D | peptidase | ||
NECFGCCN_03839 | 2.1e-166 | yibQ | S | protein conserved in bacteria | ||
NECFGCCN_03840 | 5.1e-150 | M | COG0463 Glycosyltransferases involved in cell wall biogenesis | |||
NECFGCCN_03841 | 2e-199 | tdh | 1.1.1.103 | C | Catalyzes the NAD( )-dependent oxidation of L-threonine to 2-amino-3-ketobutyrate | |
NECFGCCN_03842 | 2.8e-224 | kbl | 2.3.1.29, 2.3.1.47 | H | Catalyzes the decarboxylative condensation of pimeloyl- acyl-carrier protein and L-alanine to produce 8-amino-7- oxononanoate (AON), acyl-carrier protein , and carbon dioxide | |
NECFGCCN_03843 | 3.3e-180 | hldD | 5.1.3.20 | GM | Catalyzes the interconversion between ADP-D-glycero- beta-D-manno-heptose and ADP-L-glycero-beta-D-manno-heptose via an epimerization at carbon 6 of the heptose | |
NECFGCCN_03844 | 2.8e-204 | rfaF | GT9 | M | heptosyltransferase | |
NECFGCCN_03845 | 1.9e-178 | rfaC | GT9 | M | lipopolysaccharide heptosyltransferase I | |
NECFGCCN_03846 | 1.1e-172 | rfaZ | GT73 | S | lipopolysaccharide core region biosynthetic process | |
NECFGCCN_03847 | 1.8e-212 | M | O-Antigen ligase | |||
NECFGCCN_03848 | 6.9e-198 | waaU | M | Glycosyltransferase family 9 (heptosyltransferase) | ||
NECFGCCN_03849 | 6.6e-192 | walW | G | Lipopolysaccharide biosynthesis protein | ||
NECFGCCN_03850 | 3.3e-141 | livG | E | Part of the ABC transporter complexes LivFGHMJ and LivFGHMK involved in the high-affinity transport of branched-chain amino acids | ||
NECFGCCN_03851 | 2.6e-186 | livM | E | Belongs to the binding-protein-dependent transport system permease family | ||
NECFGCCN_03852 | 6.8e-151 | livH | E | Belongs to the binding-protein-dependent transport system permease family | ||
NECFGCCN_03853 | 1e-207 | livK | E | With LivFGHM is involved in the high affinity leucine transport | ||
NECFGCCN_03854 | 9.5e-141 | eutC | 4.3.1.7 | E | Belongs to the EutC family | |
NECFGCCN_03855 | 1.7e-262 | eutB | 4.3.1.7 | E | With EutC catalyzes the formation of acetaldehyde and ammonia from ethanolamine | |
NECFGCCN_03856 | 1.1e-248 | eat | E | amino acid | ||
NECFGCCN_03857 | 5.5e-264 | mmuP | E | amino acid | ||
NECFGCCN_03858 | 8.1e-171 | mmuM | 1.5.1.20, 2.1.1.10 | H | homocysteine | |
NECFGCCN_03859 | 3.6e-174 | tauA | P | taurine ABC transporter | ||
NECFGCCN_03860 | 1.9e-138 | tauB | 3.6.3.36 | P | Part of the ABC transporter complex TauABC involved in taurine import. Responsible for energy coupling to the transport system | |
NECFGCCN_03861 | 6.5e-132 | tauC | P | ABC-type nitrate sulfonate bicarbonate transport system permease component | ||
NECFGCCN_03862 | 1.4e-166 | tauD | 1.14.11.17 | Q | taurine catabolism dioxygenase | |
NECFGCCN_03863 | 0.0 | I | Acyltransferase | |||
NECFGCCN_03864 | 8.6e-63 | fepB | P | Periplasmic binding protein | ||
NECFGCCN_03865 | 1.8e-72 | fepB | P | Periplasmic binding protein | ||
NECFGCCN_03866 | 3.3e-214 | entC | 5.4.4.2 | HQ | Isochorismate synthase | |
NECFGCCN_03867 | 1.1e-308 | entE | 2.7.7.58, 6.3.2.14 | Q | 2,3-dihydroxybenzoate-AMP ligase | |
NECFGCCN_03868 | 2e-160 | entB | 3.3.2.1, 6.3.2.14 | Q | Phosphopantetheine attachment site | |
NECFGCCN_03869 | 2.1e-129 | IQ | PFAM Short-chain dehydrogenase reductase SDR | |||
NECFGCCN_03870 | 2.9e-72 | entH | 3.1.2.28 | Q | Required for optimal enterobactin synthesis. Acts as a proofreading enzyme that prevents EntB misacylation by hydrolyzing the thioester bound existing between EntB and wrongly charged molecules | |
NECFGCCN_03871 | 7.9e-123 | T | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
NECFGCCN_03872 | 3.1e-90 | yceD | K | metal-binding, possibly nucleic acid-binding protein | ||
NECFGCCN_03873 | 5.5e-127 | rsmG | 2.1.1.170 | J | Ribosomal RNA small subunit methyltransferase G | |
NECFGCCN_03874 | 9.8e-234 | P | COG0168 Trk-type K transport systems, membrane components | |||
NECFGCCN_03875 | 4.8e-117 | ktrA | P | COG0569 K transport systems, NAD-binding component | ||
NECFGCCN_03876 | 3.2e-147 | cbiQ | P | cobalt transport | ||
NECFGCCN_03877 | 8.7e-309 | ykoD | P | abc transporter atp-binding protein | ||
NECFGCCN_03878 | 2.3e-93 | S | UPF0397 protein | |||
NECFGCCN_03879 | 6e-157 | salL | 2.5.1.63, 2.5.1.94 | S | S-adenosyl-l-methionine hydroxide adenosyltransferase | |
NECFGCCN_03880 | 1.3e-210 | sstT | E | Involved in the import of serine and threonine into the cell, with the concomitant import of sodium (symport system) | ||
NECFGCCN_03881 | 1.2e-99 | metI | P | ABC transporter (Permease | ||
NECFGCCN_03882 | 6.4e-188 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
NECFGCCN_03883 | 2.3e-262 | dapE | 3.5.1.18 | E | COG0624, acetylornithine deacetylase succinyl-diaminopimelate desuccinylase and related deacylases | |
NECFGCCN_03884 | 1.9e-164 | metQ | M | Belongs to the NlpA lipoprotein family | ||
NECFGCCN_03885 | 6.3e-138 | ET | ABC transporter substrate-binding protein | |||
NECFGCCN_03886 | 2.6e-80 | fasA | KT | Response regulator of the LytR AlgR family | ||
NECFGCCN_03887 | 2.2e-23 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
NECFGCCN_03888 | 1.4e-19 | |||||
NECFGCCN_03890 | 1.4e-162 | repB | K | Belongs to the ParB family | ||
NECFGCCN_03891 | 3.1e-228 | parA | D | COG1192 ATPases involved in chromosome partitioning | ||
NECFGCCN_03892 | 9e-184 | repA | S | RePlication protein | ||
NECFGCCN_03893 | 1.9e-138 | L | Phage integrase family | |||
NECFGCCN_03894 | 3.8e-08 | |||||
NECFGCCN_03896 | 8e-114 | pscB | M | CHAP domain protein | ||
NECFGCCN_03897 | 2.5e-191 | glnA | 6.3.1.2 | E | glutamine synthetase | |
NECFGCCN_03898 | 4.1e-50 | hisE | 3.5.4.19, 3.6.1.31, 5.3.1.16 | E | phosphoribosyl-ATP diphosphatase activity | |
NECFGCCN_03899 | 3.6e-60 | hisI | 3.5.4.19, 3.5.4.25, 3.6.1.31, 5.3.1.16 | E | Catalyzes the hydrolysis of the adenine ring of phosphoribosyl-AMP | |
NECFGCCN_03900 | 4.7e-137 | hisF | 3.5.4.19, 3.6.1.31 | E | IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisF subunit catalyzes the cyclization activity that produces IGP and AICAR from PRFAR using the ammonia provided by the HisH subunit | |
NECFGCCN_03901 | 7.7e-129 | hisA | 5.3.1.16 | E | 1-(5-phosphoribosyl)-5- 5-phosphoribosylamino)methylideneamino imidazole-4-carboxamide isomerase | |
NECFGCCN_03902 | 3.3e-12 | hisH | E | IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisH subunit provides the glutamine amidotransferase activity that produces the ammonia necessary to HisF for the synthesis of IGP and AICAR | ||
NECFGCCN_03903 | 0.0 | fdhF | 1.17.1.10, 1.17.1.9, 1.17.99.7 | C | Belongs to the prokaryotic molybdopterin-containing oxidoreductase family | |
NECFGCCN_03904 | 4.4e-76 | fdhF | 1.17.1.10, 1.17.1.9, 1.17.99.7 | C | Spermidine putrescine ABC transporter substrate-binding protein | |
NECFGCCN_03905 | 3.7e-123 | K | response regulator | |||
NECFGCCN_03906 | 3.1e-136 | K | Transcriptional regulator, AbiEi antitoxin N-terminal domain | |||
NECFGCCN_03907 | 2e-166 | S | Nucleotidyl transferase AbiEii toxin, Type IV TA system | |||
NECFGCCN_03908 | 1.5e-186 | 2.7.1.15, 2.7.1.4 | G | PfkB domain protein | ||
NECFGCCN_03909 | 1.7e-168 | rbsB | G | PFAM Periplasmic binding protein LacI transcriptional regulator | ||
NECFGCCN_03910 | 1.8e-168 | MA20_14255 | P | Belongs to the binding-protein-dependent transport system permease family | ||
NECFGCCN_03911 | 9.4e-278 | rbsA | 3.6.3.17 | P | import. Responsible for energy coupling to the transport system | |
NECFGCCN_03912 | 0.0 | virA | T | Histidine kinase | ||
NECFGCCN_03913 | 8.2e-18 | |||||
NECFGCCN_03914 | 2.3e-147 | phnP | 3.1.4.55 | S | Carbon-phosphorus lyase complex accessory protein | |
NECFGCCN_03915 | 1.7e-99 | phnN | 2.7.4.23 | F | Catalyzes the phosphorylation of ribose 1,5-bisphosphate to 5-phospho-D-ribosyl alpha-1-diphosphate (PRPP) | |
NECFGCCN_03916 | 5.9e-208 | phnM | 3.6.1.63 | P | phosphonate metabolism protein PhnM | |
NECFGCCN_03917 | 6e-123 | phnL | 2.7.8.37 | P | phosphonate C-P lyase system protein PhnL | |
NECFGCCN_03918 | 1.9e-138 | phnK | 4.7.1.1 | P | phosphonate C-P lyase system protein PhnK | |
NECFGCCN_03919 | 5.1e-164 | phnJ | 4.7.1.1 | H | Catalyzes the breakage of the C-P bond in alpha-D-ribose 1-methylphosphonate 5-phosphate (PRPn) forming alpha-D-ribose | |
NECFGCCN_03920 | 1.7e-196 | phnI | 2.7.8.37 | P | Phosphonate | |
NECFGCCN_03921 | 1.5e-101 | phnH | 2.7.8.37 | P | phosphonate C-P lyase system protein PhnH | |
NECFGCCN_03922 | 1.1e-77 | phnG | 2.7.8.37 | P | Phosphonate C-P lyase system protein PhnG | |
NECFGCCN_03923 | 4.5e-129 | phnF | K | Transcriptional regulator | ||
NECFGCCN_03924 | 5.2e-80 | phnB | S | PFAM Glyoxalase bleomycin resistance protein dioxygenase | ||
NECFGCCN_03925 | 2.5e-58 | phnA | P | Alkylphosphonate utilization operon protein PhnA | ||
NECFGCCN_03926 | 1.1e-270 | proP | EGP | transporter | ||
NECFGCCN_03927 | 1.3e-176 | melR | 2.1.1.63, 3.1.31.1, 3.2.2.21 | K | melibiose operon regulatory protein | |
NECFGCCN_03928 | 4.8e-265 | melA | 3.2.1.122, 3.2.1.22, 3.2.1.86 | GH4,GT4 | G | Catalyses the hydrolysis of terminal non-reducing alpha-D-galactose residues in alpha-D-galactosides |
NECFGCCN_03929 | 7.2e-256 | melB | G | COG2211 Na melibiose symporter and related transporters | ||
NECFGCCN_03931 | 2.7e-177 | O | PFAM StbA family protein | |||
NECFGCCN_03932 | 1.3e-42 | S | Plasmid stability protein | |||
NECFGCCN_03933 | 2.7e-57 | S | overlaps another CDS with the same product name | |||
NECFGCCN_03934 | 3.7e-235 | L | viral genome integration into host DNA | |||
NECFGCCN_03935 | 7.3e-256 | |||||
NECFGCCN_03936 | 2.4e-202 | |||||
NECFGCCN_03937 | 1.1e-60 | K | Peptidase S24-like | |||
NECFGCCN_03938 | 4.2e-08 | L | Transposase | |||
NECFGCCN_03939 | 3.5e-160 | 3.1.21.3 | V | type I restriction modification DNA specificity domain | ||
NECFGCCN_03940 | 6.1e-137 | MA20_32445 | O | PFAM 20S proteasome, A and B subunits | ||
NECFGCCN_03941 | 4.6e-154 | MA20_32430 | E | Transglutaminase | ||
NECFGCCN_03942 | 5.2e-170 | MA20_32425 | S | protein conserved in bacteria | ||
NECFGCCN_03943 | 5.2e-286 | gcs2 | S | Circularly permuted ATP-grasp type 2 | ||
NECFGCCN_03944 | 0.0 | treA | 3.2.1.28 | GH37 | G | Provides the cells with the ability to utilize trehalose at high osmolarity by splitting it into glucose molecules that can subsequently be taken up by the phosphotransferase-mediated uptake system |
NECFGCCN_03945 | 1.6e-148 | foxA | P | Receptor | ||
NECFGCCN_03946 | 9.5e-46 | pfkB | 2.7.1.11, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
NECFGCCN_03947 | 0.0 | fruA | 2.7.1.202 | G | phosphotransferase system | |
NECFGCCN_03948 | 9e-256 | gor | 1.8.1.7 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
NECFGCCN_03949 | 1e-224 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
NECFGCCN_03951 | 5.4e-209 | iscS2 | 2.8.1.7 | E | Cysteine sulfinate desulfinase cysteine desulfurase and related enzymes | |
NECFGCCN_03952 | 2.2e-224 | thiI | 2.8.1.4 | H | Catalyzes the ATP-dependent transfer of a sulfur to tRNA to produce 4-thiouridine in position 8 of tRNAs, which functions as a near-UV photosensor. Also catalyzes the transfer of sulfur to the sulfur carrier protein ThiS, forming ThiS-thiocarboxylate. This is a step in the synthesis of thiazole, in the thiamine biosynthesis pathway. The sulfur is donated as persulfide by IscS | |
NECFGCCN_03953 | 5.3e-289 | gtf1 | 2.4.1.52 | GT4 | M | An N-acetylglucosaminyl transferase that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon |
NECFGCCN_03954 | 4.1e-253 | gtf2 | M | A stabilizing protein that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon. Stabilizes the glycosylation activity of Gtf1 | ||
NECFGCCN_03955 | 2.4e-90 | ligA | 6.5.1.2 | L | DNA ligase that catalyzes the formation of phosphodiester linkages between 5'-phosphoryl and 3'-hydroxyl groups in double-stranded DNA using NAD as a coenzyme and as the energy source for the reaction. It is essential for DNA replication and repair of damaged DNA | |
NECFGCCN_03956 | 1.4e-33 | ypeB | 2.7.7.7 | S | protein conserved in bacteria | |
NECFGCCN_03957 | 1.1e-176 | yfeH | S | Bile acid sodium symporter | ||
NECFGCCN_03958 | 9.2e-167 | yfeR | K | transcriptional regulator | ||
NECFGCCN_03959 | 2.5e-112 | cysE | 2.3.1.30 | E | serine acetyltransferase | |
NECFGCCN_03960 | 4.4e-255 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
NECFGCCN_03961 | 2.7e-67 | mrnC | J | Involved in correct processing of both the 5' and 3' ends of 23S rRNA precursor. Processes 30S rRNA precursor transcript even in absence of ribonuclease 3 (Rnc) | ||
NECFGCCN_03963 | 3.7e-134 | trmH | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
NECFGCCN_03964 | 6e-91 | yacP | S | RNA-binding protein containing a PIN domain | ||
NECFGCCN_03965 | 5e-282 | yciQ | S | Predicted membrane protein (DUF2207) | ||
NECFGCCN_03966 | 1.1e-82 | lemA | S | LemA family | ||
NECFGCCN_03967 | 7.1e-65 | panZ | K | Controls both the activation and catalytic activity of PanD in a coenzyme A (CoA)-dependent fashion | ||
NECFGCCN_03968 | 1.3e-208 | livK | E | With LivFGHM is involved in the high affinity leucine transport | ||
NECFGCCN_03969 | 2.6e-145 | livH | E | Belongs to the binding-protein-dependent transport system permease family | ||
NECFGCCN_03970 | 1.2e-214 | livM | E | Belongs to the binding-protein-dependent transport system permease family | ||
NECFGCCN_03971 | 7.9e-140 | livG | E | Part of the ABC transporter complexes LivFGHMJ and LivFGHMK involved in the high-affinity transport of branched-chain amino acids | ||
NECFGCCN_03972 | 9.3e-127 | livF | P | Branched-chain amino acid transport | ||
NECFGCCN_03973 | 7.9e-90 | |||||
NECFGCCN_03974 | 1.1e-172 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
NECFGCCN_03975 | 2.4e-45 | ftsL | D | cell division protein FtsL | ||
NECFGCCN_03976 | 0.0 | ftsI | 3.4.16.4 | M | penicillin-binding protein | |
NECFGCCN_03977 | 4.5e-183 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
NECFGCCN_03978 | 1.1e-219 | cshB | 3.6.4.13 | JKL | DEAD-box RNA helicase. May work in conjunction with the cold shock proteins to ensure proper initiation of transcription at low and optimal temperatures | |
NECFGCCN_03979 | 1e-257 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
NECFGCCN_03980 | 5.7e-63 | yutD | J | protein conserved in bacteria | ||
NECFGCCN_03981 | 1.8e-223 | rlmN | 2.1.1.192 | J | Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs | |
NECFGCCN_03982 | 9.7e-89 | XK27_09885 | V | Glycopeptide antibiotics resistance protein | ||
NECFGCCN_03984 | 0.0 | mdlA | V | abc transporter atp-binding protein | ||
NECFGCCN_03985 | 0.0 | mdlB | V | abc transporter atp-binding protein | ||
NECFGCCN_03992 | 5.9e-43 | spiA | K | sequence-specific DNA binding | ||
NECFGCCN_03994 | 3.9e-07 | |||||
NECFGCCN_03995 | 0.0 | pepX | 3.4.14.11 | E | Removes N-terminal dipeptides sequentially from polypeptides having unsubstituted N-termini provided that the penultimate residue is proline | |
NECFGCCN_03996 | 5.6e-150 | gla | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
NECFGCCN_03997 | 1.5e-94 | V | CAAX protease self-immunity | |||
NECFGCCN_03998 | 4.7e-137 | cppA | E | CppA N-terminal | ||
NECFGCCN_03999 | 1.1e-170 | ampC | V | COG1680 Beta-lactamase class C and other penicillin binding proteins | ||
NECFGCCN_04000 | 1.9e-219 | mnmA | 2.8.1.13 | J | Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 | |
NECFGCCN_04001 | 7.8e-305 | S | Bacterial membrane protein, YfhO | |||
NECFGCCN_04002 | 9.3e-63 | isaA | GH23 | M | Immunodominant staphylococcal antigen A | |
NECFGCCN_04003 | 2.5e-61 | lytE | M | LysM domain protein | ||
NECFGCCN_04004 | 2.2e-132 | ecfT | P | Transmembrane (T) component of an energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
NECFGCCN_04005 | 1.4e-150 | ecfA2 | 3.6.3.55 | P | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | |
NECFGCCN_04006 | 2.7e-149 | ecfA1 | P | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
NECFGCCN_04007 | 5.9e-89 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
NECFGCCN_04008 | 9.2e-129 | S | sequence-specific DNA binding | |||
NECFGCCN_04009 | 4.3e-231 | ymfH | S | Peptidase M16 | ||
NECFGCCN_04010 | 4.3e-228 | ymfF | S | Peptidase M16 | ||
NECFGCCN_04011 | 1.9e-57 | yaaA | S | S4 domain protein YaaA | ||
NECFGCCN_04012 | 4.8e-199 | recF | L | it is required for DNA replication and normal SOS inducibility. RecF binds preferentially to single-stranded, linear DNA. It also seems to bind ATP | ||
NECFGCCN_04013 | 1.1e-273 | guaB | 1.1.1.205 | F | Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate- limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth | |
NECFGCCN_04014 | 2.5e-189 | trpS | 6.1.1.2 | J | Tryptophanyl-tRNA synthetase | |
NECFGCCN_04015 | 7.1e-153 | yvjA | S | membrane | ||
NECFGCCN_04016 | 1.1e-305 | ybiT | S | abc transporter atp-binding protein | ||
NECFGCCN_04017 | 0.0 | XK27_10405 | S | Bacterial membrane protein YfhO | ||
NECFGCCN_04018 | 2.9e-147 | |||||
NECFGCCN_04019 | 1.2e-104 | L | NgoPII restriction endonuclease | |||
NECFGCCN_04020 | 1e-20 | XK27_10050 | K | Peptidase S24-like | ||
NECFGCCN_04021 | 2.1e-94 | ispZ | D | probably involved in intracellular septation | ||
NECFGCCN_04022 | 2.4e-117 | yciC | S | UPF0259 membrane protein | ||
NECFGCCN_04023 | 9.7e-76 | ykgJ | S | Fe-S-cluster oxidoreductase | ||
NECFGCCN_04024 | 1.1e-118 | ompW | M | outer membrane protein W | ||
NECFGCCN_04025 | 5.7e-126 | ybiX | S | PkhD-type hydroxylase | ||
NECFGCCN_04026 | 0.0 | fiu | P | receptor | ||
NECFGCCN_04027 | 7.9e-94 | IQ | short-chain dehydrogenase | |||
NECFGCCN_04029 | 3.7e-163 | 1.6.5.5 | C | alcohol dehydrogenase | ||
NECFGCCN_04030 | 2.7e-77 | K | Transcriptional | |||
NECFGCCN_04031 | 2.4e-147 | trpA | 4.2.1.20 | E | The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate | |
NECFGCCN_04032 | 4.8e-148 | trpB | 4.2.1.20 | E | The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine | |
NECFGCCN_04033 | 6.8e-139 | IQ | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
NECFGCCN_04034 | 7.2e-59 | srlB | 2.7.1.198 | G | PTS system glucitol sorbitol-specific | |
NECFGCCN_04035 | 1.2e-151 | srlE | 2.7.1.198 | G | PTS system glucitol sorbitol-specific | |
NECFGCCN_04036 | 1.4e-101 | srlA | G | PTS system glucitol sorbitol-specific | ||
NECFGCCN_04037 | 6e-210 | mltB | GH103 | M | Lytic murein transglycosylase | |
NECFGCCN_04038 | 2.3e-53 | S | Cupin 2, conserved barrel domain protein | |||
NECFGCCN_04039 | 9.6e-45 | IV02_09080 | S | conserved protein | ||
NECFGCCN_04040 | 4.7e-196 | efe | C | Belongs to the iron ascorbate-dependent oxidoreductase family | ||
NECFGCCN_04041 | 8.6e-145 | metQ | M | Belongs to the nlpA lipoprotein family | ||
NECFGCCN_04042 | 1.3e-121 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
NECFGCCN_04043 | 1.1e-31 | metI | P | ABC-type metal ion transport system permease component | ||
NECFGCCN_04044 | 9.4e-231 | ygbK | 2.7.1.217 | S | Putative nucleotide-binding of sugar-metabolising enzyme | |
NECFGCCN_04045 | 1.2e-73 | ygbJ | 1.1.1.411 | I | Dehydrogenase | |
NECFGCCN_04046 | 4.5e-70 | ygbJ | 1.1.1.411 | I | Dehydrogenase | |
NECFGCCN_04047 | 2.4e-133 | lacR | K | DeoR C terminal sensor domain | ||
NECFGCCN_04048 | 4e-37 | penP | 3.5.2.6 | V | Beta-lactamase | |
NECFGCCN_04049 | 3.4e-97 | hemG | 1.3.5.3 | CH | Protoporphyrinogen oxidase | |
NECFGCCN_04050 | 1.3e-271 | trkH | P | Low-affinity potassium transport system. Interacts with trk system potassium uptake protein TrkA | ||
NECFGCCN_04051 | 4.3e-104 | yigZ | 2.1.1.45, 3.4.13.9 | S | YigZ family | |
NECFGCCN_04052 | 2e-263 | pepQ | 3.4.11.9, 3.4.13.9 | E | Splits dipeptides with a prolyl residue in the C- terminal position | |
NECFGCCN_04053 | 0.0 | fadB | 1.1.1.157, 1.1.1.35, 4.2.1.17, 5.1.2.3, 5.3.3.8 | I | Involved in the aerobic and anaerobic degradation of long-chain fatty acids via beta-oxidation cycle. Catalyzes the formation of 3-oxoacyl-CoA from enoyl-CoA via L-3-hydroxyacyl-CoA. It can also use D-3-hydroxyacyl-CoA and cis-3-enoyl-CoA as substrate | |
NECFGCCN_04054 | 2.1e-213 | fadA | 2.3.1.16 | I | Catalyzes the final step of fatty acid oxidation in which acetyl-CoA is released and the CoA ester of a fatty acid two carbons shorter is formed | |
NECFGCCN_04055 | 2.8e-128 | fre | 1.16.1.3, 1.17.1.1, 1.5.1.41 | C | PFAM Oxidoreductase FAD NAD(P)-binding | |
NECFGCCN_04056 | 1.7e-292 | ubiD | 4.1.1.61, 4.1.1.98 | H | Catalyzes the decarboxylation of 3-octaprenyl-4-hydroxy benzoate to 2-octaprenylphenol, an intermediate step in ubiquinone biosynthesis | |
NECFGCCN_04057 | 8.4e-87 | rfaH | K | Enhances distal genes transcription elongation in a specialized subset of operons that encode extracytoplasmic components. RfaH is recruited into a multi-component RNA polymerase complex by the ops element, which is a short conserved DNA sequence located downstream of the main promoter of these operons. Once bound, RfaH suppresses pausing and inhibits Rho- dependent and intrinsic termination at a subset of sites. Termination signals are bypassed, which allows complete synthesis of long RNA chains | ||
NECFGCCN_04058 | 3.5e-143 | tatD | L | 3'-5' exonuclease that prefers single-stranded DNA and RNA. May play a role in the H(2)O(2)-induced DNA damage repair | ||
NECFGCCN_04059 | 8.6e-134 | tatC | U | Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. Together with TatB, TatC is part of a receptor directly interacting with Tat signal peptides | ||
NECFGCCN_04060 | 1.1e-66 | tatB | U | Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. Together with TatC, TatB is part of a receptor directly interacting with Tat signal peptides. TatB may form an oligomeric binding site that transiently accommodates folded Tat precursor proteins before their translocation | ||
NECFGCCN_04061 | 1.7e-30 | tatA | U | Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. TatA could form the protein-conducting channel of the Tat system | ||
NECFGCCN_04062 | 0.0 | ubiB | S | Is probably a protein kinase regulator of UbiI activity which is involved in aerobic coenzyme Q (ubiquinone) biosynthesis | ||
NECFGCCN_04063 | 2.5e-104 | yigP | S | protein conserved in bacteria | ||
NECFGCCN_04064 | 1.3e-139 | ubiE | 2.1.1.163, 2.1.1.201 | H | Methyltransferase required for the conversion of demethylmenaquinol (DMKH2) to menaquinol (MKH2) and the conversion of 2-polyprenyl-6-methoxy-1,4-benzoquinol (DDMQH2) to 2- polyprenyl-3-methyl-6-methoxy-1,4-benzoquinol (DMQH2) | |
NECFGCCN_04065 | 1.6e-255 | rmuC | V | DNA Recombination protein RmuC | ||
NECFGCCN_04066 | 6.2e-137 | udp | 2.4.2.3 | F | Catalyzes the reversible phosphorylytic cleavage of uridine and deoxyuridine to uracil and ribose- or deoxyribose-1- phosphate. The produced molecules are then utilized as carbon and energy sources or in the rescue of pyrimidine bases for nucleotide synthesis | |
NECFGCCN_04067 | 1.1e-155 | ysgA | 3.1.1.45 | Q | Dienelactone hydrolase | |
NECFGCCN_04068 | 0.0 | metE | 2.1.1.14 | E | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | |
NECFGCCN_04069 | 7.4e-180 | metR | K | transcriptional regulator | ||
NECFGCCN_04070 | 7e-164 | yigM | EG | COG0697 Permeases of the drug metabolite transporter (DMT) superfamily | ||
NECFGCCN_04071 | 2e-154 | yigL | S | Hydrolase | ||
NECFGCCN_04072 | 2.8e-198 | pldB | 3.1.1.5 | I | Lysophospholipase | |
NECFGCCN_04073 | 3e-105 | rhtB | E | efflux protein | ||
NECFGCCN_04074 | 2.2e-152 | S | Transposase | |||
NECFGCCN_04075 | 1.9e-107 | rhtC | E | threonine efflux protein | ||
NECFGCCN_04076 | 8.7e-133 | recQ | 3.6.4.12 | L | DNA helicase | |
NECFGCCN_04077 | 1.4e-08 | S | dextransucrase activity | |||
NECFGCCN_04078 | 2.1e-186 | S | dextransucrase activity | |||
NECFGCCN_04079 | 2.1e-38 | supH | 3.1.3.102, 3.1.3.104 | S | Sucrose-6F-phosphate phosphohydrolase | |
NECFGCCN_04080 | 2.3e-81 | supH | 3.1.3.102, 3.1.3.104 | S | Sucrose-6F-phosphate phosphohydrolase | |
NECFGCCN_04081 | 4.1e-107 | pgm | G | Belongs to the phosphoglycerate mutase family | ||
NECFGCCN_04082 | 5.4e-107 | G | Belongs to the phosphoglycerate mutase family | |||
NECFGCCN_04083 | 2.8e-108 | G | Belongs to the phosphoglycerate mutase family | |||
NECFGCCN_04084 | 1.3e-24 | I | phospholipase d transphosphatidylase | |||
NECFGCCN_04085 | 6.6e-168 | coiA | 3.6.4.12 | S | Competence protein | |
NECFGCCN_04086 | 8.1e-274 | 2.7.13.3, 2.7.7.7, 5.4.99.21 | D | Lytic transglycosylase with a strong preference for naked glycan strands that lack stem peptides | ||
NECFGCCN_04087 | 1.2e-103 | S | CAAX amino terminal protease family protein | |||
NECFGCCN_04089 | 7.8e-25 | WQ51_00785 | ||||
NECFGCCN_04090 | 0.0 | ltaS | 2.7.8.20 | M | Belongs to the LTA synthase family | |
NECFGCCN_04091 | 9.9e-48 | cdd | 2.4.2.4, 3.5.4.5 | F | cytidine deaminase activity | |
NECFGCCN_04092 | 2.3e-131 | potC | P | ABC-type spermidine putrescine transport system, permease component II | ||
NECFGCCN_04093 | 4.1e-139 | potB | P | ABC-type spermidine putrescine transport system, permease component I | ||
NECFGCCN_04094 | 5.2e-212 | potA | 3.6.3.30, 3.6.3.31 | P | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | |
NECFGCCN_04095 | 2.1e-168 | murB | 1.3.1.98 | M | cell wall formation | |
NECFGCCN_04096 | 6.4e-81 | hycA | E | seems to prevent binding of FhlA transcriptional activator to the activator sequence of hyc operon | ||
NECFGCCN_04097 | 2.6e-58 | hypA | S | Probably plays a role in a hydrogenase nickel cofactor insertion step | ||
NECFGCCN_04098 | 2.8e-165 | hypB | KO | Hydrogenase accessory protein HypB | ||
NECFGCCN_04099 | 1.9e-43 | hypC | O | Hydrogenase assembly chaperone hypC hupF | ||
NECFGCCN_04100 | 7.6e-216 | hypD | O | Belongs to the HypD family | ||
NECFGCCN_04101 | 2.8e-185 | hypE | O | hydrogenase expression formation protein HypE | ||
NECFGCCN_04102 | 0.0 | gltD | 1.4.1.13, 1.4.1.14 | C | Glutamate synthase | |
NECFGCCN_04103 | 9.6e-109 | nudK | 3.6.1.13 | L | GDP-mannose pyrophosphatase | |
NECFGCCN_04104 | 8.7e-198 | ypfG | S | Protein of unknown function (DUF1176) | ||
NECFGCCN_04105 | 0.0 | tkt | 2.2.1.1 | G | Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate | |
NECFGCCN_04106 | 1.1e-175 | tal | 2.2.1.2 | G | Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway | |
NECFGCCN_04107 | 0.0 | maeB | 1.1.1.38, 1.1.1.40, 2.3.1.8 | C | Malic enzyme | |
NECFGCCN_04108 | 2.9e-54 | eutS | E | ethanolamine utilization protein | ||
NECFGCCN_04109 | 2.7e-85 | eutP | E | ethanolamine utilization protein EutP | ||
NECFGCCN_04110 | 4.6e-123 | eutQ | E | Ethanolamine utilization protein eutQ | ||
NECFGCCN_04111 | 1.2e-143 | eutT | 2.5.1.17 | E | Cobalamin adenosyltransferase | |
NECFGCCN_04112 | 3.2e-181 | pta | 1.1.1.40, 2.3.1.8 | C | belongs to the CobB CobQ family | |
NECFGCCN_04113 | 2.6e-43 | eutM | CQ | BMC domain | ||
NECFGCCN_04114 | 6.6e-47 | eutN | CQ | Ethanolamine utilization protein eutN | ||
NECFGCCN_04115 | 9.1e-251 | eutE | 1.2.1.87 | C | Aldehyde dehydrogenase | |
NECFGCCN_04116 | 5.2e-153 | eutJ | E | Ethanolamine utilization protein EutJ | ||
NECFGCCN_04117 | 1.9e-105 | eutG | C | alcohol dehydrogenase | ||
NECFGCCN_04118 | 1e-212 | L | AAA ATPase domain | |||
NECFGCCN_04120 | 9.7e-41 | S | Periplasmic Protein | |||
NECFGCCN_04121 | 9.4e-24 | |||||
NECFGCCN_04123 | 1.7e-39 | M | Mycolic acid cyclopropane synthetase | |||
NECFGCCN_04126 | 1.4e-40 | S | Pyocin activator protein PrtN | |||
NECFGCCN_04127 | 1.4e-72 | abgT | H | transporter | ||
NECFGCCN_04129 | 9.8e-94 | ogt | 2.1.1.63 | L | Involved in the cellular defense against the biological effects of O6-methylguanine (O6-MeG) and O4-methylthymine (O4-MeT) in DNA. Repairs the methylated nucleobase in DNA by stoichiometrically transferring the methyl group to a cysteine residue in the enzyme. This is a suicide reaction the enzyme is irreversibly inactivated | |
NECFGCCN_04130 | 5.6e-138 | fnr | K | COG0664 cAMP-binding proteins - catabolite gene activator and regulatory subunit of cAMP-dependent protein kinases | ||
NECFGCCN_04131 | 2.7e-182 | uspE | T | universal stress protein | ||
NECFGCCN_04132 | 9.3e-25 | ydiH | S | Domain of unknown function | ||
NECFGCCN_04133 | 4.5e-250 | pntB | 1.6.1.2 | C | The transhydrogenation between NADH and NADP is coupled to respiration and ATP hydrolysis and functions as a proton pump across the membrane | |
NECFGCCN_04134 | 5.8e-275 | pntA | 1.6.1.2 | C | The transhydrogenation between NADH and NADP is coupled to respiration and ATP hydrolysis and functions as a proton pump across the membrane | |
NECFGCCN_04135 | 2e-169 | ydgH | S | Protein of unknown function (DUF1471) | ||
NECFGCCN_04136 | 6.2e-244 | ydgI | E | Arginine ornithine antiporter | ||
NECFGCCN_04137 | 1e-128 | IQ | reductase | |||
NECFGCCN_04138 | 1e-51 | ydgC | S | membrane protein required for alginate biosynthesis | ||
NECFGCCN_04139 | 5e-128 | K | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
NECFGCCN_04140 | 7.4e-64 | |||||
NECFGCCN_04141 | 3.5e-241 | T | PhoQ Sensor | |||
NECFGCCN_04142 | 2.1e-166 | tus | L | Trans-acting protein required for termination of DNA replication. Binds to DNA replication terminator sequences (terA to terF) to prevent the passage of replication forks. The termination efficiency will be affected by the affinity of this protein for the terminator sequence | ||
NECFGCCN_04143 | 8.7e-262 | fumC | 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
NECFGCCN_04144 | 2.8e-277 | ynjC | P | transport system permease component | ||
NECFGCCN_04145 | 8e-106 | ynjD | S | ABC transporter | ||
NECFGCCN_04146 | 1e-76 | ynjE | 2.8.1.11 | M | sulfurtransferase | |
NECFGCCN_04147 | 1.4e-80 | ynjE | 2.8.1.11 | M | sulfurtransferase | |
NECFGCCN_04148 | 1.2e-33 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
NECFGCCN_04149 | 9.1e-90 | yfaZ | S | YfaZ precursor | ||
NECFGCCN_04150 | 7.5e-148 | S | Transposase | |||
NECFGCCN_04151 | 2.9e-75 | nudI | L | Catalyzes the hydrolysis of nucleoside triphosphates, with a preference for pyrimidine deoxynucleoside triphosphates (dUTP, dTTP and dCTP) | ||
NECFGCCN_04152 | 2.4e-240 | menE | 4.2.1.113, 6.2.1.26 | IQ | O-succinylbenzoic acid--CoA ligase | |
NECFGCCN_04153 | 1.4e-170 | menC | 4.2.1.113 | H | Converts 2-succinyl-6-hydroxy-2,4-cyclohexadiene-1- carboxylate (SHCHC) to 2-succinylbenzoate (OSB) | |
NECFGCCN_04154 | 9.4e-166 | menB | 4.1.3.36 | H | Converts o-succinylbenzoyl-CoA (OSB-CoA) to 1,4- dihydroxy-2-naphthoyl-CoA (DHNA-CoA) | |
NECFGCCN_04155 | 1.3e-131 | menH | 4.2.99.20 | H | Catalyzes a proton abstraction reaction that results in 2,5-elimination of pyruvate from 2-succinyl-5-enolpyruvyl-6- hydroxy-3-cyclohexene-1-carboxylate (SEPHCHC) and the formation of 2-succinyl-6-hydroxy-2,4-cyclohexadiene-1-carboxylate (SHCHC) | |
NECFGCCN_04156 | 0.0 | menD | 2.2.1.9 | H | Catalyzes the thiamine diphosphate-dependent decarboxylation of 2-oxoglutarate and the subsequent addition of the resulting succinic semialdehyde-thiamine pyrophosphate anion to isochorismate to yield 2-succinyl-5-enolpyruvyl-6-hydroxy-3- cyclohexene-1-carboxylate (SEPHCHC) | |
NECFGCCN_04157 | 1.8e-237 | menF | 5.4.4.2 | H | Catalyzes the conversion of chorismate to isochorismate | |
NECFGCCN_04158 | 7.2e-80 | elaA | S | Acyltransferase | ||
NECFGCCN_04159 | 4.8e-176 | rnz | 3.1.26.11 | S | Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA | |
NECFGCCN_04160 | 3.2e-259 | nuoN | 1.6.5.3 | C | NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient | |
NECFGCCN_04161 | 8e-285 | nuoM | 1.6.5.3 | C | NADH ubiquinone | |
NECFGCCN_04162 | 0.0 | nuoL | 1.6.5.3 | CP | NADH ubiquinone | |
NECFGCCN_04163 | 2.1e-27 | nuoK | 1.6.5.3 | C | NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient | |
NECFGCCN_04164 | 1.2e-89 | nuoJ | 1.6.5.3 | C | Belongs to the complex I subunit 6 family | |
NECFGCCN_04165 | 2.9e-88 | nuoI | 1.6.5.3 | C | NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient | |
NECFGCCN_04166 | 8.1e-182 | nuoH | 1.6.5.3 | C | NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient. This subunit may bind ubiquinone | |
NECFGCCN_04167 | 0.0 | nuoG | 1.6.5.3 | C | NADH-quinone oxidoreductase | |
NECFGCCN_04168 | 1.2e-268 | nuoF | 1.6.5.3 | C | NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain | |
NECFGCCN_04169 | 8.1e-93 | nuoE | 1.6.5.3 | C | NADH dehydrogenase | |
NECFGCCN_04170 | 0.0 | nuoC | 1.6.5.3 | C | NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient | |
NECFGCCN_04171 | 5.5e-129 | nuoB | 1.6.5.3 | C | NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient | |
NECFGCCN_04172 | 7.2e-77 | nuoA | 1.6.5.3 | C | NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient | |
NECFGCCN_04173 | 4.1e-159 | lrhA | K | Transcriptional regulator | ||
NECFGCCN_04174 | 2e-238 | alaA | 2.6.1.2, 2.6.1.66 | E | in Corynebacterium glutamicum this protein can use glutamate, 2-aminobutyrate, and aspartate as amino donors and pyruvate as the acceptor' | |
NECFGCCN_04175 | 7.6e-106 | yfbR | 3.1.3.89 | S | Catalyzes the strictly specific dephosphorylation of 2'- deoxyribonucleoside 5'-monophosphates | |
NECFGCCN_04176 | 0.0 | yfbS | P | COG0471 Di- and tricarboxylate transporters | ||
NECFGCCN_04177 | 5.2e-116 | yfbT | 3.1.3.23 | S | Phosphatase | |
NECFGCCN_04178 | 1.4e-89 | yfbU | S | Belongs to the UPF0304 family | ||
NECFGCCN_04179 | 6.9e-83 | yfbV | S | UPF0208 membrane protein | ||
NECFGCCN_04180 | 3.5e-227 | ackA | 2.7.2.1, 2.7.2.15 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
NECFGCCN_04181 | 0.0 | pta | 1.1.1.40, 2.3.1.8 | C | belongs to the CobB CobQ family | |
NECFGCCN_04182 | 3e-101 | yfcD | 2.7.6.2, 5.3.3.2 | I | NUDIX hydrolase | |
NECFGCCN_04183 | 2.9e-99 | yfcE | S | Phosphoesterase | ||
NECFGCCN_04184 | 1.7e-108 | yfcF | 2.5.1.18 | O | Glutathione S-transferase | |
NECFGCCN_04185 | 2.9e-116 | yfcG | O | Belongs to the GST superfamily | ||
NECFGCCN_04186 | 1.2e-61 | folX | 1.13.11.81, 4.1.2.25, 5.1.99.7, 5.1.99.8 | H | Catalyzes the formation of dihydromonapterin triphosphate from dihydroneopterin triphosphate | |
NECFGCCN_04187 | 2.7e-171 | yfcH | CH | epimerase | ||
NECFGCCN_04188 | 4.4e-89 | J | PFAM GCN5-related N-acetyltransferase | |||
NECFGCCN_04189 | 8.8e-139 | hisP | 3.6.3.21 | E | abc transporter atp-binding protein | |
NECFGCCN_04190 | 7.9e-126 | hisM | P | ABC transporter (permease) | ||
NECFGCCN_04191 | 5.8e-118 | hisQ | P | (ABC) transporter | ||
NECFGCCN_04192 | 4.4e-138 | hisJ | ET | belongs to the bacterial solute-binding protein 3 family | ||
NECFGCCN_04193 | 8.1e-140 | argT | ET | belongs to the bacterial solute-binding protein 3 family | ||
NECFGCCN_04194 | 2.3e-96 | ubiX | 2.5.1.129 | H | Flavin prenyltransferase that catalyzes the synthesis of the prenylated FMN cofactor (prenyl-FMN) for 4-hydroxy-3- polyprenylbenzoic acid decarboxylase UbiD. The prenyltransferase is metal-independent and links a dimethylallyl moiety from dimethylallyl monophosphate (DMAP) to the flavin N5 and C6 atoms of FMN | |
NECFGCCN_04195 | 2.6e-291 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
NECFGCCN_04196 | 3.5e-85 | cvpA | S | Colicin v production | ||
NECFGCCN_04197 | 1e-90 | dedD | D | Non-essential cell division protein that could be required for efficient cell constriction | ||
NECFGCCN_04198 | 2.5e-231 | folC | 6.3.2.12, 6.3.2.17 | H | Functions in two distinct reactions of the de novo folate biosynthetic pathway. Catalyzes the addition of a glutamate residue to dihydropteroate (7,8-dihydropteroate or H2Pte) to form dihydrofolate (7,8-dihydrofolate monoglutamate or H2Pte-Glu). Also catalyzes successive additions of L-glutamate to tetrahydrofolate or 10-formyltetrahydrofolate or 5,10-methylenetetrahydrofolate, leading to folylpolyglutamate derivatives | |
NECFGCCN_04199 | 4.5e-172 | accD | 2.1.3.15, 6.4.1.2 | I | Component of the acetyl coenzyme A carboxylase (ACC) complex. Biotin carboxylase (BC) catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the transcarboxylase to acetyl-CoA to form malonyl- CoA | |
NECFGCCN_04200 | 3.8e-114 | dedA | I | Pfam SNARE associated Golgi protein | ||
NECFGCCN_04201 | 7.8e-154 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
NECFGCCN_04202 | 2.2e-182 | asd | 1.2.1.11 | E | Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate | |
NECFGCCN_04203 | 3.3e-211 | pdxB | 1.1.1.290 | H | Catalyzes the oxidation of erythronate-4-phosphate to 3- hydroxy-2-oxo-4-phosphonooxybutanoate | |
NECFGCCN_04204 | 3e-168 | flk | N | Acts as a regulator of flagellar gene expression by modulating the protein level of the anti sigma factor FlgM upon sensing ring completion or hook elongation. Flk could inhibit FlgM secretion by acting as a braking system for the flagellar- associated type III secretion | ||
NECFGCCN_04205 | 2.2e-151 | yfcJ | EGP | Major facilitator Superfamily | ||
NECFGCCN_04206 | 2.4e-199 | pmrB | EGP | Major facilitator Superfamily | ||
NECFGCCN_04207 | 6.6e-140 | ccmI | O | cytochrome complex assembly | ||
NECFGCCN_04208 | 1.7e-73 | ccmH | P | subunit of a heme lyase | ||
NECFGCCN_04209 | 3e-104 | dsbE | CO | Thiol disulfide interchange protein | ||
NECFGCCN_04210 | 0.0 | ccmF | O | Cytochrome c-type biogenesis protein | ||
NECFGCCN_04211 | 5.5e-80 | ccmE | O | Heme chaperone required for the biogenesis of c-type cytochromes. Transiently binds heme delivered by CcmC and transfers the heme to apo-cytochromes in a process facilitated by CcmF and CcmH | ||
NECFGCCN_04212 | 5.8e-30 | ccmD | U | Required for the export of heme to the periplasm for the biogenesis of c-type cytochromes | ||
NECFGCCN_04213 | 3e-112 | ccmC | U | Required for the export of heme to the periplasm for the biogenesis of c-type cytochromes | ||
NECFGCCN_04214 | 3.5e-104 | ccmB | 3.6.3.41 | U | Required for the export of heme to the periplasm for the biogenesis of c-type cytochromes | |
NECFGCCN_04215 | 1.6e-56 | secE | U | Essential subunit of the Sec protein translocation channel SecYEG. Clamps together the 2 halves of SecY. May contact the channel plug during translocation | ||
NECFGCCN_04216 | 7.4e-100 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
NECFGCCN_04217 | 2.8e-70 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
NECFGCCN_04218 | 7.1e-119 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
NECFGCCN_04219 | 7.8e-80 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
NECFGCCN_04220 | 3.2e-46 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
NECFGCCN_04221 | 0.0 | rpoB | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
NECFGCCN_04222 | 0.0 | rpoC | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
NECFGCCN_04223 | 1.2e-242 | dcuB | S | Responsible for the transport of C4-dicarboxylates from the periplasm across the inner membrane | ||
NECFGCCN_04224 | 5e-48 | celC | 2.7.1.196, 2.7.1.205 | G | Phosphotransferase System | |
NECFGCCN_04225 | 7e-47 | chbB | 2.7.1.196, 2.7.1.205 | G | Phosphotransferase System | |
NECFGCCN_04226 | 8.6e-287 | T | Diguanylate cyclase | |||
NECFGCCN_04227 | 7.4e-219 | thiH | 4.1.99.19 | C | In Escherichia coli this enzyme functions in thiamine biosynthesis along with thiFSGI and iscS | |
NECFGCCN_04228 | 5.5e-133 | thiG | 2.8.1.10 | H | Catalyzes the rearrangement of 1-deoxy-D-xylulose 5- phosphate (DXP) to produce the thiazole phosphate moiety of thiamine. Sulfur is provided by the thiocarboxylate moiety of the carrier protein ThiS. In vitro, sulfur can be provided by H(2)S | |
NECFGCCN_04229 | 6.6e-30 | thiS | 2.8.1.10 | H | thiamine biosynthesis protein ThiS | |
NECFGCCN_04230 | 2.3e-131 | thiF | 2.7.7.73, 2.7.7.80 | H | COG0476 Dinucleotide-utilizing enzymes involved in molybdopterin and thiamine biosynthesis family 2 | |
NECFGCCN_04231 | 8.3e-111 | thiE | 2.5.1.3, 2.7.1.49, 2.7.4.7 | H | Condenses 4-methyl-5-(beta-hydroxyethyl)thiazole monophosphate (THZ-P) and 2-methyl-4-amino-5-hydroxymethyl pyrimidine pyrophosphate (HMP-PP) to form thiamine monophosphate (TMP) | |
NECFGCCN_04232 | 0.0 | thiC | 4.1.99.17 | H | Catalyzes the synthesis of the hydroxymethylpyrimidine phosphate (HMP-P) moiety of thiamine from aminoimidazole ribotide (AIR) in a radical S-adenosyl-L-methionine (SAM)-dependent reaction | |
NECFGCCN_04233 | 3.2e-89 | rsd | K | Binds RpoD and negatively regulates RpoD-mediated transcription activation by preventing the interaction between the primary sigma factor RpoD with the catalytic core of the RNA polymerase and with promoter DNA. May be involved in replacement of the RNA polymerase sigma subunit from RpoD to RpoS during the transition from exponential growth to the stationary phase | ||
NECFGCCN_04234 | 2e-151 | nudC | 1.3.7.1, 3.6.1.22 | L | nadh pyrophosphatase | |
NECFGCCN_04235 | 7e-203 | hemE | 4.1.1.37 | H | Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III | |
NECFGCCN_04236 | 3.3e-126 | nfi | 3.1.21.7 | L | DNA repair enzyme involved in the repair of deaminated bases. Selectively cleaves double-stranded DNA at the second phosphodiester bond 3' to a deoxyinosine leaving behind the intact lesion on the nicked DNA | |
NECFGCCN_04237 | 4.4e-106 | yjaG | S | Protein of unknown function (DUF416) | ||
NECFGCCN_04238 | 9.6e-40 | hupA | L | Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions | ||
NECFGCCN_04239 | 3.2e-116 | yjaH | S | Protein of unknown function (DUF1481) | ||
NECFGCCN_04240 | 1.2e-47 | zraP | NPTU | Binds zinc. Could be an important component of the zinc- balancing mechanism | ||
NECFGCCN_04241 | 2.9e-241 | zraS | 2.7.13.3 | T | Member of the two-component regulatory system ZraS ZraR. May function as a membrane-associated protein kinase that phosphorylates ZraR in response to high concentrations of zinc or lead in the medium | |
NECFGCCN_04242 | 2.4e-237 | zraR | T | COG2204 Response regulator containing CheY-like receiver, AAA-type ATPase, and DNA-binding domains | ||
NECFGCCN_04243 | 9.9e-244 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
NECFGCCN_04244 | 5e-298 | purH | 2.1.2.3, 3.5.4.10 | F | bifunctional purine biosynthesis protein purh | |
NECFGCCN_04246 | 6.4e-30 | bfd | P | Bacterioferritin-associated ferredoxin | ||
NECFGCCN_04247 | 2.5e-83 | bfr | 1.16.3.1 | P | Iron-storage protein, whose ferroxidase center binds Fe(2 ) ions, oxidizes them by dioxygen to Fe(3 ), and participates in the subsequent Fe(3 ) oxide mineral core formation within the central cavity of the protein complex | |
NECFGCCN_04248 | 5.9e-78 | hopD | 3.4.23.43 | NOU | Cleaves type-4 fimbrial leader sequence and methylates the N-terminal (generally Phe) residue | |
NECFGCCN_04249 | 2e-49 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
NECFGCCN_04250 | 1.7e-111 | rplC | J | One of the primary rRNA binding proteins, it binds directly near the 3'-end of the 23S rRNA, where it nucleates assembly of the 50S subunit | ||
NECFGCCN_04251 | 8e-103 | rplD | J | Forms part of the polypeptide exit tunnel | ||
NECFGCCN_04252 | 2.4e-47 | |||||
NECFGCCN_04253 | 6e-154 | rplB | J | One of the primary rRNA binding proteins. Required for association of the 30S and 50S subunits to form the 70S ribosome, for tRNA binding and peptide bond formation. It has been suggested to have peptidyltransferase activity | ||
NECFGCCN_04254 | 1.9e-46 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
NECFGCCN_04255 | 2.3e-51 | rplV | J | The globular domain of the protein is located near the polypeptide exit tunnel on the outside of the subunit, while an extended beta-hairpin is found that lines the wall of the exit tunnel in the center of the 70S ribosome | ||
NECFGCCN_04256 | 6.5e-125 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
NECFGCCN_04257 | 2.1e-70 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
NECFGCCN_04258 | 2e-23 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
NECFGCCN_04259 | 1.2e-39 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
NECFGCCN_04260 | 1e-63 | |||||
NECFGCCN_04261 | 1.2e-49 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
NECFGCCN_04262 | 4.9e-96 | rplE | J | This is 1 of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance. In the 70S ribosome it contacts protein S13 of the 30S subunit (bridge B1b), connecting the 2 subunits | ||
NECFGCCN_04263 | 1.3e-48 | rpsN | J | Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site | ||
NECFGCCN_04264 | 8.1e-64 | rpsH | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA central domain where it helps coordinate assembly of the platform of the 30S subunit | ||
NECFGCCN_04265 | 2.3e-93 | rplF | J | This protein binds to the 23S rRNA, and is important in its secondary structure. It is located near the subunit interface in the base of the L7 L12 stalk, and near the tRNA binding site of the peptidyltransferase center | ||
NECFGCCN_04266 | 4.3e-48 | |||||
NECFGCCN_04267 | 1.3e-85 | |||||
NECFGCCN_04268 | 3.7e-24 | rpmD | J | Ribosomal protein L30 | ||
NECFGCCN_04269 | 7.8e-60 | rplO | J | binds to the 23S rRNA | ||
NECFGCCN_04270 | 2.5e-242 | secY | U | The central subunit of the protein translocation channel SecYEG. Consists of two halves formed by TMs 1-5 and 6-10. These two domains form a lateral gate at the front which open onto the bilayer between TMs 2 and 7, and are clamped together by SecE at the back. The channel is closed by both a pore ring composed of hydrophobic SecY resides and a short helix (helix 2A) on the extracellular side of the membrane which forms a plug. The plug probably moves laterally to allow the channel to open. The ring and the pore may move independently | ||
NECFGCCN_04271 | 2.5e-13 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
NECFGCCN_04272 | 5.1e-57 | rpsM | J | Located at the top of the head of the 30S subunit, it contacts several helices of the 16S rRNA. In the 70S ribosome it contacts the 23S rRNA (bridge B1a) and protein L5 of the 50S subunit (bridge B1b), connecting the 2 subunits | ||
NECFGCCN_04273 | 5.9e-67 | rpsK | J | Located on the platform of the 30S subunit, it bridges several disparate RNA helices of the 16S rRNA. Forms part of the Shine-Dalgarno cleft in the 70S ribosome | ||
NECFGCCN_04274 | 1.3e-108 | rpsD | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the body of the 30S subunit | ||
NECFGCCN_04275 | 1.1e-181 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
NECFGCCN_04276 | 8.8e-63 | rplQ | J | Ribosomal protein L17 | ||
NECFGCCN_04277 | 6e-61 | yhdN | S | PFAM DnaJ homologue, subfamily C, member 28, conserved domain | ||
NECFGCCN_04278 | 1.3e-64 | zntR | K | transcriptional regulator | ||
NECFGCCN_04279 | 4.1e-30 | arfA | S | Domain of unknown function | ||
NECFGCCN_04280 | 1.8e-66 | mscL | M | Channel that opens in response to stretch forces in the membrane lipid bilayer. May participate in the regulation of osmotic pressure changes within the cell | ||
NECFGCCN_04281 | 1.5e-253 | trkA | P | found to be peripherally associated with the inner membrane in Escherichia coli | ||
NECFGCCN_04282 | 2.6e-244 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
NECFGCCN_04283 | 4.8e-171 | fmt | 2.1.1.176, 2.1.2.9 | J | Attaches a formyl group to the free amino group of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by promoting its recognition by IF2 and preventing the misappropriation of this tRNA by the elongation apparatus | |
NECFGCCN_04284 | 8.8e-84 | def | 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions | |
NECFGCCN_04285 | 4.5e-149 | dipZ | CO | cytochrome c biogenesis protein | ||
NECFGCCN_04286 | 3.7e-37 | pepN | 3.4.11.2 | E | aminopeptidase | |
NECFGCCN_04287 | 1.4e-29 | pepN | 3.4.11.2 | E | aminopeptidase | |
NECFGCCN_04288 | 1.3e-38 | pepN | 3.4.11.2 | E | aminopeptidase | |
NECFGCCN_04289 | 3.2e-113 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
NECFGCCN_04290 | 3.9e-139 | pstB | 3.6.3.27 | P | Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system | |
NECFGCCN_04291 | 1.5e-149 | pstB | 3.6.3.27 | P | Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system | |
NECFGCCN_04292 | 9.1e-156 | pstA | P | phosphate transport system permease | ||
NECFGCCN_04293 | 1.4e-156 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
NECFGCCN_04294 | 1e-63 | pstS | P | phosphate | ||
NECFGCCN_04295 | 3.9e-28 | pstS | P | phosphate | ||
NECFGCCN_04296 | 5.5e-100 | S | oxidoreductase | |||
NECFGCCN_04297 | 9.5e-189 | S | Protein of unknown function (DUF4056) | |||
NECFGCCN_04298 | 1.1e-95 | cybB | C | Cytochrome B561 | ||
NECFGCCN_04299 | 1.4e-41 | frmR | S | protein conserved in bacteria | ||
NECFGCCN_04300 | 1.4e-217 | frmA | 1.1.1.1, 1.1.1.284 | C | Belongs to the zinc-containing alcohol dehydrogenase family. Class-III subfamily | |
NECFGCCN_04301 | 0.0 | quiA | 1.1.5.8 | G | Dehydrogenase | |
NECFGCCN_04302 | 3.5e-166 | pcaQ | K | transcriptional regulator | ||
NECFGCCN_04303 | 7.6e-117 | pcaG | 1.13.11.3 | Q | protocatechuate 3,4-dioxygenase | |
NECFGCCN_04304 | 5.5e-146 | pcaH | 1.13.11.3 | Q | protocatechuate 3,4-dioxygenase | |
NECFGCCN_04305 | 1.1e-250 | ydcJ | S | protein conserved in bacteria | ||
NECFGCCN_04306 | 9e-289 | pnbA | CE10 | I | Belongs to the type-B carboxylesterase lipase family | |
NECFGCCN_04307 | 3.8e-196 | 1.1.1.90 | C | COG1062 Zn-dependent alcohol dehydrogenases, class III | ||
NECFGCCN_04308 | 0.0 | mdoD | P | Involved in the biosynthesis of osmoregulated periplasmic glucans (OPGs) | ||
NECFGCCN_04309 | 1.8e-96 | rimL | J | COG1670 Acetyltransferases, including N-acetylases of ribosomal proteins | ||
NECFGCCN_04310 | 2.3e-120 | ydcK | 5.4.2.9 | JM | COG1208 Nucleoside-diphosphate-sugar pyrophosphorylase involved in lipopolysaccharide biosynthesis translation initiation factor 2B, gamma epsilon subunits eIF-2Bgamma eIF-2Bepsilon | |
NECFGCCN_04311 | 3.4e-175 | tehA | P | PFAM C4-dicarboxylate transporter malic acid transport protein | ||
NECFGCCN_04312 | 1.4e-104 | tehB | 2.1.1.265 | Q | Tellurite resistance protein TehB | |
NECFGCCN_04313 | 1e-119 | ydcL | S | Protein of unknown function (DUF3313) | ||
NECFGCCN_04314 | 8.6e-162 | BP3797 | EG | of the drug metabolite transporter (DMT) superfamily | ||
NECFGCCN_04315 | 8.6e-167 | tetD | K | AraC family transcriptional regulator | ||
NECFGCCN_04316 | 9.1e-180 | ydcO | Q | protein involved in benzoate metabolism | ||
NECFGCCN_04317 | 3.8e-99 | ydcN | K | transcriptional regulator | ||
NECFGCCN_04318 | 0.0 | ydcP | O | peptidase U32 | ||
NECFGCCN_04319 | 1.9e-28 | yncJ | S | Protein of unknown function (DUF2554) | ||
NECFGCCN_04320 | 2e-197 | vanY | 3.4.17.14, 3.5.1.28, 4.1.1.105, 4.1.1.28 | GH23 | M | D-alanyl-D-alanine carboxypeptidase |
NECFGCCN_04322 | 4.7e-188 | O | ATPase (AAA | |||
NECFGCCN_04323 | 0.0 | O | Subtilase family | |||
NECFGCCN_04325 | 4.8e-288 | mscS | M | Mechanosensitive ion channel | ||
NECFGCCN_04326 | 2.3e-56 | fumB | 4.2.1.2, 4.2.1.32 | C | Catalyzes the reversible hydration of fumarate to (S)- malate | |
NECFGCCN_04327 | 8.7e-125 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
NECFGCCN_04328 | 2e-35 | puuA | 6.3.1.11, 6.3.1.2 | E | glutamine synthetase | |
NECFGCCN_04329 | 5.6e-146 | puuD | 3.5.1.94 | E | Gamma-glutamyl-gamma-aminobutyrate hydrolase | |
NECFGCCN_04330 | 1.6e-94 | puuR | K | Helix-turn-helix domain | ||
NECFGCCN_04331 | 6.4e-279 | puuC | 1.2.1.3, 1.2.1.54, 1.2.1.99 | C | belongs to the aldehyde dehydrogenase family | |
NECFGCCN_04332 | 3.7e-251 | puuB | E | oxidoreductase | ||
NECFGCCN_04333 | 2.7e-174 | dmlR | K | Transcriptional regulator | ||
NECFGCCN_04334 | 1.9e-211 | dmlA | 1.1.1.83, 1.1.1.93, 4.1.1.73 | CE | Tartrate dehydrogenase | |
NECFGCCN_04335 | 9.9e-294 | yeaV | M | Belongs to the BCCT transporter (TC 2.A.15) family | ||
NECFGCCN_04336 | 7.8e-229 | yeaW | 1.14.13.239 | P | COG4638 Phenylpropionate dioxygenase and related ring-hydroxylating dioxygenases, large terminal subunit | |
NECFGCCN_04337 | 9e-270 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | belongs to the aldehyde dehydrogenase family | |
NECFGCCN_04338 | 2.1e-169 | yeaX | 1.14.13.238, 1.14.13.239 | C | Flavodoxin reductases (Ferredoxin-NADPH reductases) family 1 | |
NECFGCCN_04339 | 0.0 | ptsA | 2.7.1.121, 2.7.1.194, 2.7.1.200, 2.7.1.202, 2.7.3.9 | G | General (non sugar-specific) component of the phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS). This major carbohydrate active-transport system catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. Enzyme I transfers the phosphoryl group from phosphoenolpyruvate (PEP) to the phosphoryl carrier protein (HPr) | |
NECFGCCN_04340 | 6.2e-191 | frwC | G | pts system | ||
NECFGCCN_04341 | 6e-49 | frwB | G | FrwB with FrwC, FrwD and PtsA forms a PEP-dependent sugar phosphotransferase system (PTS) permease which may phosphorylate and transport sugars into the cell | ||
NECFGCCN_04342 | 0.0 | pflD | 2.3.1.54 | C | Glycine radical enzyme that catalyzes the cleavage of a C-N bond in choline, producing trimethylamine (TMA) and acetaldehyde | |
NECFGCCN_04343 | 9.2e-169 | pflC | 1.97.1.4 | O | glycyl-radical enzyme activating protein family | |
NECFGCCN_04344 | 1.6e-55 | fruA | 2.7.1.202, 2.7.1.56 | G | pts system | |
NECFGCCN_04345 | 1.9e-146 | Q | Protein involved in biosynthesis of mitomycin antibiotics polyketide fumonisin | |||
NECFGCCN_04346 | 2.5e-155 | K | transcriptional regulator | |||
NECFGCCN_04347 | 1.1e-169 | T | (GGDEF) domain | |||
NECFGCCN_04348 | 1.2e-186 | fbpC | 3.6.3.30 | P | Part of the ABC transporter complex FbpABC involved in Fe(3 ) ions import. Responsible for energy coupling to the transport system | |
NECFGCCN_04349 | 4.7e-280 | sfuB | P | ABC-type Fe3 transport system permease component | ||
NECFGCCN_04350 | 1.9e-189 | fbpA | P | ABC-type Fe3 transport system, periplasmic component | ||
NECFGCCN_04351 | 5.8e-259 | ycgG | T | Diguanylate phosphodiesterase | ||
NECFGCCN_04352 | 6.2e-52 | rsbV | T | Belongs to the anti-sigma-factor antagonist family | ||
NECFGCCN_04353 | 0.0 | 2.4.1.1 | GT35 | G | Phosphorylase is an important allosteric enzyme in carbohydrate metabolism. Enzymes from different sources differ in their regulatory mechanisms and in their natural substrates. However, all known phosphorylases share catalytic and structural properties | |
NECFGCCN_04355 | 1e-309 | oppA-1 | E | ABC transporter substrate-binding protein | ||
NECFGCCN_04356 | 2.1e-93 | yccA | S | Belongs to the BI1 family | ||
NECFGCCN_04357 | 6.8e-56 | tusE | P | part of a sulfur-relay system | ||
NECFGCCN_04358 | 6.4e-47 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
NECFGCCN_04359 | 2.7e-135 | ybcM | K | transcriptional regulator | ||
NECFGCCN_04360 | 5.4e-98 | ybcL | S | PFAM PEBP family protein | ||
NECFGCCN_04361 | 2.4e-231 | rlmI | 2.1.1.191 | J | Specifically methylates the cytosine at position 1962 (m5C1962) of 23S rRNA | |
NECFGCCN_04362 | 8.8e-53 | hspQ | S | Involved in the degradation of certain denaturated proteins, including DnaA, during heat shock stress | ||
NECFGCCN_04363 | 1.9e-137 | |||||
NECFGCCN_04364 | 0.0 | murF | 6.3.2.10 | M | PFAM Glycosyl transferase, group 1 | |
NECFGCCN_04365 | 1.8e-210 | M | TIGRFAM type I secretion membrane fusion protein, HlyD | |||
NECFGCCN_04366 | 0.0 | V | ABC transporter, transmembrane region | |||
NECFGCCN_04367 | 4.2e-235 | MU | Outer membrane efflux protein | |||
NECFGCCN_04368 | 9.6e-215 | pic | 3.4.24.40 | Q | von willebrand factor, type A | |
NECFGCCN_04369 | 0.0 | pulA | 3.2.1.41 | CBM48,GH13 | G | Belongs to the glycosyl hydrolase 13 family |
NECFGCCN_04370 | 7.6e-128 | gspC | U | General secretion pathway protein C | ||
NECFGCCN_04371 | 0.0 | gspD | NU | General Secretion Pathway protein | ||
NECFGCCN_04372 | 1.1e-273 | gspE | NU | Type II secretory pathway, ATPase PulE Tfp pilus assembly pathway, ATPase PilB | ||
NECFGCCN_04373 | 1.8e-199 | gspF | U | general secretion pathway protein | ||
NECFGCCN_04374 | 4.9e-75 | gspG | U | General Secretion Pathway protein | ||
NECFGCCN_04375 | 7.5e-86 | gspH | NU | general secretion pathway protein | ||
NECFGCCN_04376 | 2.5e-59 | NU | general secretion pathway protein | |||
NECFGCCN_04377 | 4.8e-100 | gspJ | U | General secretion pathway protein J | ||
NECFGCCN_04378 | 5.3e-44 | gspK | U | COG3156 Type II secretory pathway component PulK | ||
NECFGCCN_04379 | 1e-21 | |||||
NECFGCCN_04380 | 1.6e-248 | S | dextransucrase activity | |||
NECFGCCN_04382 | 0.0 | 2.4.1.5 | GH13 | M | KxYKxGKxW signal domain protein | |
NECFGCCN_04383 | 8.7e-265 | yeeO | V | Mate efflux family protein | ||
NECFGCCN_04384 | 1.2e-221 | XK27_05470 | E | Methionine synthase | ||
NECFGCCN_04385 | 1.2e-70 | ndk | 2.7.4.6 | F | Major role in the synthesis of nucleoside triphosphates other than ATP. The ATP gamma phosphate is transferred to the NDP beta phosphate via a ping-pong mechanism, using a phosphorylated active-site intermediate | |
NECFGCCN_04386 | 6e-85 | btuE | 1.11.1.9 | O | Belongs to the glutathione peroxidase family | |
NECFGCCN_04387 | 1.1e-176 | 4.1.1.37 | H | Uroporphyrinogen decarboxylase (URO-D) | ||
NECFGCCN_04388 | 1.8e-164 | ET | ABC transporter substrate-binding protein | |||
NECFGCCN_04389 | 1e-109 | ytmL | P | ABC transporter (Permease | ||
NECFGCCN_04390 | 5.4e-113 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
NECFGCCN_04391 | 1.2e-77 | ypmB | S | Protein conserved in bacteria | ||
NECFGCCN_04392 | 6.3e-213 | aspB | 2.6.1.1, 2.6.1.14 | E | Aminotransferase | |
NECFGCCN_04393 | 5.4e-261 | asnS | 6.1.1.22 | J | Catalyzes a two-step reaction, first charging an asparagine molecule by linking its carboxyl group to the alpha-phosphate of ATP, followed by transfer of the aminoacyl-adenylate to its tRNA | |
NECFGCCN_04394 | 9.8e-228 | pdp | 2.4.2.2, 2.4.2.4 | F | Catalyzes the reversible phosphorolysis of thymidine, deoxyuridine and their analogues to their respective bases and 2-deoxyribose 1-phosphate | |
NECFGCCN_04395 | 1.1e-101 | rsmC | 2.1.1.172 | J | Methyltransferase small domain protein | |
NECFGCCN_04396 | 1.2e-169 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
NECFGCCN_04397 | 2.8e-154 | E | Alpha/beta hydrolase of unknown function (DUF915) | |||
NECFGCCN_04398 | 6.4e-227 | pts13C | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
NECFGCCN_04399 | 3.7e-111 | drgA | C | nitroreductase | ||
NECFGCCN_04400 | 1.5e-102 | yoaK | S | Protein of unknown function (DUF1275) | ||
NECFGCCN_04401 | 7.1e-158 | yvgN | C | reductase | ||
NECFGCCN_04402 | 1.3e-207 | S | Tetratricopeptide repeat | |||
NECFGCCN_04403 | 5.8e-131 | clpB | O | C-terminal, D2-small domain, of ClpB protein | ||
NECFGCCN_04404 | 2e-44 | |||||
NECFGCCN_04405 | 2e-53 | I | mechanosensitive ion channel activity | |||
NECFGCCN_04406 | 2.1e-25 | |||||
NECFGCCN_04407 | 5.5e-17 | M | LysM domain | |||
NECFGCCN_04408 | 1.4e-119 | cmk | 1.17.7.4, 2.5.1.19, 2.7.1.26, 2.7.4.25, 2.7.7.2, 6.3.2.1 | F | Belongs to the cytidylate kinase family. Type 1 subfamily | |
NECFGCCN_04409 | 1e-85 | infC | J | IF-3 binds to the 30S ribosomal subunit and shifts the equilibrum between 70S ribosomes and their 50S and 30S subunits in favor of the free subunits, thus enhancing the availability of 30S subunits on which protein synthesis initiation begins | ||
NECFGCCN_04410 | 8.1e-28 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
NECFGCCN_04411 | 1.5e-56 | rplT | J | Binds directly to 23S ribosomal RNA and is necessary for the in vitro assembly process of the 50S ribosomal subunit. It is not involved in the protein synthesizing functions of that subunit | ||
NECFGCCN_04412 | 1.1e-75 | XK27_03610 | K | Gnat family | ||
NECFGCCN_04413 | 5.6e-89 | yybC | ||||
NECFGCCN_04414 | 4.9e-27 | dmpI | 5.3.2.6 | G | Belongs to the 4-oxalocrotonate tautomerase family | |
NECFGCCN_04415 | 4.1e-267 | pepV | 3.5.1.18 | E | Dipeptidase | |
NECFGCCN_04416 | 2e-106 | ung2 | 3.2.2.27 | L | Uracil-DNA glycosylase | |
NECFGCCN_04418 | 2.8e-13 | V | Glucan-binding protein C | |||
NECFGCCN_04419 | 1.2e-26 | V | Glucan-binding protein C | |||
NECFGCCN_04424 | 7e-17 | zur | K | Belongs to the Fur family | ||
NECFGCCN_04425 | 4.5e-16 | S | Protein of unknown function (DUF2969) | |||
NECFGCCN_04426 | 1.7e-198 | ilvE | 2.6.1.42 | E | Aminotransferase | |
NECFGCCN_04427 | 0.0 | parC | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
NECFGCCN_04428 | 1.1e-35 | codA | 3.5.4.1 | F | cytosine deaminase | |
NECFGCCN_04430 | 0.0 | nirB | 1.7.1.15 | C | Belongs to the nitrite and sulfite reductase 4Fe-4S domain family | |
NECFGCCN_04431 | 1.7e-54 | nirD | 1.7.1.15 | P | Nitrite reductase | |
NECFGCCN_04432 | 3.7e-257 | cysG | 1.3.1.76, 2.1.1.107, 2.1.1.131, 3.7.1.12, 4.2.1.75, 4.99.1.3, 4.99.1.4 | H | Multifunctional enzyme that catalyzes the SAM-dependent methylations of uroporphyrinogen III at position C-2 and C-7 to form precorrin-2 via precorrin-1. Then it catalyzes the NAD- dependent ring dehydrogenation of precorrin-2 to yield sirohydrochlorin. Finally, it catalyzes the ferrochelation of sirohydrochlorin to yield siroheme | |
NECFGCCN_04433 | 2.9e-190 | trpS | 6.1.1.2 | J | Tryptophanyl-tRNA synthetase | |
NECFGCCN_04434 | 2.4e-141 | gph | 3.1.3.18 | G | Phosphoglycolate phosphatase | |
NECFGCCN_04435 | 1.5e-121 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
NECFGCCN_04436 | 2.2e-156 | dam | 2.1.1.72 | L | Site-specific DNA-methyltransferase (Adenine-specific) | |
NECFGCCN_04437 | 1.6e-108 | damX | D | Cell division protein DamX | ||
NECFGCCN_04438 | 7.4e-200 | aroB | 2.7.1.71, 4.2.3.4 | E | Catalyzes the conversion of 3-deoxy-D-arabino- heptulosonate 7-phosphate (DAHP) to dehydroquinate (DHQ) | |
NECFGCCN_04439 | 1.9e-89 | aroK | 2.7.1.71, 4.2.3.4 | F | Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate | |
NECFGCCN_04440 | 6.2e-211 | pilQ | U | (Type IV) pilus | ||
NECFGCCN_04441 | 7.5e-23 | |||||
NECFGCCN_04442 | 2.5e-60 | hofN | NU | carbon utilization | ||
NECFGCCN_04443 | 4.1e-131 | hofM | NU | Pilus assembly protein | ||
NECFGCCN_04444 | 0.0 | mrcA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
NECFGCCN_04445 | 3.6e-97 | nudE | L | Hydrolase | ||
NECFGCCN_04446 | 0.0 | yrfF | S | Intracellular growth attenuator | ||
NECFGCCN_04447 | 3.7e-133 | yrfG | 3.1.3.5 | E | Hydrolase | |
NECFGCCN_04448 | 4e-66 | hslR | J | Belongs to the HSP15 family | ||
NECFGCCN_04449 | 3.4e-163 | hslO | O | Redox regulated molecular chaperone. Protects both thermally unfolding and oxidatively damaged proteins from irreversible aggregation. Plays an important role in the bacterial defense system toward oxidative stress | ||
NECFGCCN_04450 | 0.0 | pckA | 4.1.1.49 | H | Involved in the gluconeogenesis. Catalyzes the conversion of oxaloacetate (OAA) to phosphoenolpyruvate (PEP) through direct phosphoryl transfer between the nucleoside triphosphate and OAA | |
NECFGCCN_04451 | 1e-254 | T | PhoQ Sensor | |||
NECFGCCN_04452 | 5.7e-132 | K | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
NECFGCCN_04453 | 7.5e-85 | greB | K | Necessary for efficient RNA polymerase transcription elongation past template-encoded arresting sites. The arresting sites in DNA have the property of trapping a certain fraction of elongating RNA polymerases that pass through, resulting in locked ternary complexes. Cleavage of the nascent transcript by cleavage factors such as GreA or GreB allows the resumption of elongation from the new 3'terminus. GreB releases sequences of up to 9 nucleotides in length | ||
NECFGCCN_04454 | 0.0 | yhgF | K | accessory protein | ||
NECFGCCN_04455 | 2.3e-34 | feoA | P | Fe2 transport system protein A | ||
NECFGCCN_04456 | 0.0 | feoB | P | Transporter of a GTP-driven Fe(2 ) uptake system | ||
NECFGCCN_04457 | 3.7e-35 | feoC | K | metal cluster binding | ||
NECFGCCN_04458 | 1.9e-40 | yahO | S | Protein of unknown function (DUF1471) | ||
NECFGCCN_04459 | 3.8e-142 | bioH | 2.1.1.197, 3.1.1.85 | S | The physiological role of BioH is to remove the methyl group introduced by BioC when the pimeloyl moiety is complete. It allows to synthesize pimeloyl-ACP via the fatty acid synthetic pathway through the hydrolysis of the ester bonds of pimeloyl-ACP esters | |
NECFGCCN_04460 | 4.1e-124 | comF | S | Competence protein | ||
NECFGCCN_04461 | 2.8e-105 | nfuA | C | Involved in iron-sulfur cluster biogenesis. Binds a 4Fe- 4S cluster, can transfer this cluster to apoproteins, and thereby intervenes in the maturation of Fe S proteins. Could also act as a scaffold chaperone for damaged Fe S proteins | ||
NECFGCCN_04462 | 4.7e-225 | gntT | EG | Gluconate | ||
NECFGCCN_04463 | 0.0 | malQ | 2.4.1.25 | GH77 | G | 4-alpha-glucanotransferase |
NECFGCCN_04464 | 0.0 | malP | 2.4.1.1 | GT35 | G | Phosphorylase is an important allosteric enzyme in carbohydrate metabolism. Enzymes from different sources differ in their regulatory mechanisms and in their natural substrates. However, all known phosphorylases share catalytic and structural properties |
NECFGCCN_04465 | 0.0 | malT | K | Positively regulates the transcription of the maltose regulon whose gene products are responsible for uptake and catabolism of malto-oligosaccharides. Binds and recognizes a DNA motif (called the malT box) 5'-GGA TG GA-3' | ||
NECFGCCN_04466 | 1.8e-136 | glpR | K | transcriptional regulator | ||
NECFGCCN_04467 | 4.2e-155 | glpG | S | Rhomboid-type serine protease that catalyzes intramembrane proteolysis | ||
NECFGCCN_04468 | 3.3e-58 | glpE | 2.8.1.1 | P | Catalyzes, although with low efficiency, the sulfur transfer reaction from thiosulfate to cyanide | |
NECFGCCN_04469 | 1.7e-295 | glpD | 1.1.5.3 | C | Belongs to the FAD-dependent glycerol-3-phosphate dehydrogenase family | |
NECFGCCN_04470 | 2.2e-60 | S | protein conserved in bacteria | |||
NECFGCCN_04471 | 0.0 | glgP | 2.4.1.1 | GT35 | G | Phosphorylase is an important allosteric enzyme in carbohydrate metabolism. Enzymes from different sources differ in their regulatory mechanisms and in their natural substrates. However, all known phosphorylases share catalytic and structural properties |
NECFGCCN_04472 | 1.5e-280 | glgA | 2.4.1.21 | GT5 | G | Synthesizes alpha-1,4-glucan chains using ADP-glucose |
NECFGCCN_04473 | 1.5e-252 | glgC | 2.7.7.27 | H | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
NECFGCCN_04474 | 0.0 | glgX | 3.2.1.196, 3.2.1.68 | CBM48,GH13 | G | Belongs to the glycosyl hydrolase 13 family |
NECFGCCN_04475 | 0.0 | glgB | 2.4.1.18 | CBM48,GH13 | G | Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position |
NECFGCCN_04476 | 3.6e-210 | asd | 1.2.1.11 | E | Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate | |
NECFGCCN_04477 | 6.4e-238 | gntU | EG | Gluconate | ||
NECFGCCN_04478 | 2e-94 | gntK | 2.7.1.12 | F | Gluconokinase | |
NECFGCCN_04479 | 2.8e-185 | gntR | K | Transcriptional | ||
NECFGCCN_04480 | 5.5e-132 | yhhW | S | Belongs to the pirin family | ||
NECFGCCN_04481 | 4.7e-196 | yhhX | 1.1.1.371 | S | oxidoreductase | |
NECFGCCN_04482 | 5.4e-89 | M | COG1664 Integral membrane protein CcmA involved in cell shape determination | |||
NECFGCCN_04483 | 9e-89 | yhhY | 2.3.1.178 | J | acetyltransferase | |
NECFGCCN_04484 | 0.0 | ggt | 2.3.2.2, 3.4.19.13 | M | Gamma-glutamyltransferase | |
NECFGCCN_04485 | 1.1e-23 | yhhA | S | Protein of unknown function (DUF2756) | ||
NECFGCCN_04486 | 1e-139 | ugpQ | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
NECFGCCN_04487 | 2.8e-199 | ugpC | 3.6.3.20 | P | Belongs to the ABC transporter superfamily | |
NECFGCCN_04488 | 7.9e-149 | ugpE | P | probably responsible for the translocation of the substrate across the membrane | ||
NECFGCCN_04489 | 1.8e-159 | ugpA | P | With UgpEC is involved in the uptake of glycerol-3-phosphate | ||
NECFGCCN_04490 | 1.1e-255 | ugpB | G | ABC transporter substrate-binding protein | ||
NECFGCCN_04491 | 6.7e-107 | VM57_08315 | 3.2.2.10 | S | Belongs to the LOG family | |
NECFGCCN_04493 | 1.5e-64 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
NECFGCCN_04494 | 1e-17 | malI | K | Transcriptional regulator | ||
NECFGCCN_04495 | 6.4e-269 | ydgA | S | protein conserved in bacteria | ||
NECFGCCN_04496 | 1.4e-217 | manA | 1.14.13.81, 5.3.1.8, 5.4.2.8 | G | Belongs to the mannose-6-phosphate isomerase type 1 family | |
NECFGCCN_04497 | 3.7e-176 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
NECFGCCN_04498 | 8.2e-44 | mprF | 2.3.2.3 | J | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms | |
NECFGCCN_04499 | 7.2e-96 | 2.4.1.83 | GT2 | M | COG0463, glycosyltransferases involved in cell wall biogenesis | |
NECFGCCN_04500 | 0.0 | bcsA | 2.4.1.12 | GT2 | M | COG1215 Glycosyltransferases, probably involved in cell wall biogenesis |
NECFGCCN_04501 | 0.0 | |||||
NECFGCCN_04502 | 1.3e-93 | NU | Protein of unknown function (DUF3131) | |||
NECFGCCN_04503 | 0.0 | 2.4.1.12 | GT2 | M | Cellulose synthase | |
NECFGCCN_04504 | 6.5e-229 | S | OpgC protein | |||
NECFGCCN_04505 | 5.6e-177 | |||||
NECFGCCN_04506 | 1.7e-229 | 3.1.3.3 | T | response regulator | ||
NECFGCCN_04507 | 7.2e-53 | rsbV | T | Belongs to the anti-sigma-factor antagonist family | ||
NECFGCCN_04508 | 4.3e-80 | 2.7.11.1 | T | Anti-sigma regulatory factor (Ser Thr protein kinase) | ||
NECFGCCN_04509 | 9.4e-18 | |||||
NECFGCCN_04510 | 3.1e-159 | K | transcriptional regulator | |||
NECFGCCN_04511 | 3.2e-125 | IQ | KR domain | |||
NECFGCCN_04512 | 2.4e-148 | S | HD superfamily | |||
NECFGCCN_04513 | 2e-103 | pfpI | 3.5.1.124 | S | Intracellular protease | |
NECFGCCN_04514 | 1.3e-82 | tssB | S | type VI secretion protein | ||
NECFGCCN_04515 | 1.2e-83 | S | type VI secretion protein | |||
NECFGCCN_04516 | 3.2e-30 | 3.5.1.28 | M | N-Acetylmuramoyl-L-alanine amidase | ||
NECFGCCN_04517 | 0.0 | U | Type IV secretory system Conjugative DNA transfer | |||
NECFGCCN_04518 | 2.6e-127 | mobC | K | Transcriptional regulator | ||
NECFGCCN_04519 | 1.5e-164 | L | Domain of unknown function (DUF1738) | |||
NECFGCCN_04520 | 1.9e-132 | K | PGAP1-like protein | |||
NECFGCCN_04521 | 9.5e-17 | |||||
NECFGCCN_04522 | 6.2e-213 | L | ATPase involved in DNA repair | |||
NECFGCCN_04523 | 4.1e-15 | |||||
NECFGCCN_04525 | 0.0 | pcrA1 | 3.6.4.12 | L | PFAM UvrD REP helicase | |
NECFGCCN_04526 | 8.2e-289 | L | AAA ATPase domain | |||
NECFGCCN_04527 | 7.4e-95 | |||||
NECFGCCN_04528 | 1.7e-66 | yjgH | J | Translation Initiation Inhibitor YjgF Family | ||
NECFGCCN_04529 | 9.1e-159 | K | transcriptional regulator | |||
NECFGCCN_04530 | 1.2e-174 | erfK | S | Catalyzes th removal of D-alanine and attachment of the murein lipoprotein to the peptidoglycan tetrapeptide chain | ||
NECFGCCN_04531 | 5.3e-178 | cbl | K | transcriptional regulator | ||
NECFGCCN_04532 | 3.5e-158 | nac | K | transcriptional regulator | ||
NECFGCCN_04533 | 1.1e-175 | P | ABC-type nitrate sulfonate bicarbonate transport systems periplasmic components | |||
NECFGCCN_04534 | 6.3e-257 | sdaB | 4.3.1.17 | E | l-serine dehydratase | |
NECFGCCN_04535 | 1.7e-227 | sdaC | E | Serine transporter | ||
NECFGCCN_04536 | 2.5e-261 | ygdH | 3.2.2.10 | S | Rossmann fold nucleotide-binding protein | |
NECFGCCN_04537 | 4.7e-162 | queF | 1.7.1.13 | K | Catalyzes the NADPH-dependent reduction of 7-cyano-7- deazaguanine (preQ0) to 7-aminomethyl-7-deazaguanine (preQ1) | |
NECFGCCN_04538 | 2.3e-93 | syd | S | regulation of protein complex assembly | ||
NECFGCCN_04539 | 2e-55 | yqcC | 3.5.1.28, 5.1.3.13, 5.4.99.26 | S | protein conserved in bacteria | |
NECFGCCN_04540 | 6.7e-150 | truC | 5.4.99.26 | J | Pseudouridine synthase | |
NECFGCCN_04541 | 1e-78 | yqcA | C | flavodoxin binds one FMN molecule, which serves as a redox-active prosthetic group | ||
NECFGCCN_04542 | 6.5e-254 | gudP | G | transporter | ||
NECFGCCN_04543 | 4.3e-266 | gudD | 4.2.1.40 | M | Belongs to the mandelate racemase muconate lactonizing enzyme family | |
NECFGCCN_04544 | 1.5e-263 | gudD | 4.2.1.40 | M | Belongs to the mandelate racemase muconate lactonizing enzyme family | |
NECFGCCN_04545 | 9.1e-201 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
NECFGCCN_04546 | 0.0 | barA | 2.7.13.3 | T | PhoQ Sensor | |
NECFGCCN_04547 | 4.5e-244 | rlmD | 2.1.1.190 | J | Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA | |
NECFGCCN_04548 | 0.0 | relA | 2.7.6.5, 3.1.7.2 | KT | In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance | |
NECFGCCN_04549 | 2.5e-144 | mazG | 3.6.1.66, 3.6.1.9 | C | nucleoside triphosphate pyrophosphohydrolase | |
NECFGCCN_04550 | 0.0 | pyrG | 6.3.4.2 | F | Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen. Regulates intracellular CTP levels through interactions with the four ribonucleotide triphosphates | |
NECFGCCN_04551 | 3.1e-237 | eno | 4.2.1.11 | G | Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis | |
NECFGCCN_04552 | 1.2e-205 | hetM | GM | Male sterility protein | ||
NECFGCCN_04553 | 1.9e-129 | queE | 1.97.1.4, 4.3.99.3 | H | Catalyzes the complex heterocyclic radical-mediated conversion of 6-carboxy-5,6,7,8-tetrahydropterin (CPH4) to 7- carboxy-7-deazaguanine (CDG), a step common to the biosynthetic pathways of all 7-deazapurine-containing compounds | |
NECFGCCN_04554 | 5.9e-69 | queD | 4.1.2.50, 4.2.3.12 | H | synthase | |
NECFGCCN_04555 | 0.0 | cysJ | 1.8.1.2 | P | Component of the sulfite reductase complex that catalyzes the 6-electron reduction of sulfite to sulfide. This is one of several activities required for the biosynthesis of L- cysteine from sulfate. The flavoprotein component catalyzes the electron flow from NADPH - FAD - FMN to the hemoprotein component | |
NECFGCCN_04556 | 0.0 | cysI | 1.7.7.1, 1.8.1.2, 1.8.7.1 | C | Component of the sulfite reductase complex that catalyzes the 6-electron reduction of sulfite to sulfide. This is one of several activities required for the biosynthesis of L- cysteine from sulfate | |
NECFGCCN_04557 | 1.7e-136 | cysH | 1.8.4.10, 1.8.4.8 | C | Belongs to the PAPS reductase family. CysH subfamily | |
NECFGCCN_04558 | 1.3e-185 | iap | S | Peptidase family M28 | ||
NECFGCCN_04559 | 1.5e-253 | cysG | 1.3.1.76, 2.1.1.107, 2.1.1.131, 3.7.1.12, 4.2.1.75, 4.99.1.3, 4.99.1.4 | H | Multifunctional enzyme that catalyzes the SAM-dependent methylations of uroporphyrinogen III at position C-2 and C-7 to form precorrin-2 via precorrin-1. Then it catalyzes the NAD- dependent ring dehydrogenation of precorrin-2 to yield sirohydrochlorin. Finally, it catalyzes the ferrochelation of sirohydrochlorin to yield siroheme | |
NECFGCCN_04560 | 4e-175 | cysD | 1.8.4.10, 1.8.4.8, 2.7.7.4 | H | sulfate adenylyltransferase), subunit 2 | |
NECFGCCN_04561 | 1.7e-268 | cysN | 2.7.1.25, 2.7.7.4 | H | Belongs to the TRAFAC class translation factor GTPase superfamily. Classic translation factor GTPase family. CysN NodQ subfamily | |
NECFGCCN_04562 | 2.7e-111 | cysC | 2.7.1.25 | F | Catalyzes the synthesis of activated sulfate | |
NECFGCCN_04563 | 3.2e-50 | ygbE | S | membrane | ||
NECFGCCN_04564 | 1.7e-51 | ftsB | D | Essential cell division protein. May link together the upstream cell division proteins, which are predominantly cytoplasmic, with the downstream cell division proteins, which are predominantly periplasmic | ||
NECFGCCN_04565 | 4.9e-128 | ispD | 2.7.7.60 | I | Catalyzes the formation of 4-diphosphocytidyl-2-C- methyl-D-erythritol from CTP and 2-C-methyl-D-erythritol 4- phosphate (MEP) | |
NECFGCCN_04566 | 1.8e-86 | ispF | 2.1.1.228, 2.7.7.60, 4.6.1.12 | I | Involved in the biosynthesis of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP), two major building blocks of isoprenoid compounds. Catalyzes the conversion of 4- diphosphocytidyl-2-C-methyl-D-erythritol 2-phosphate (CDP-ME2P) to 2-C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-CPP) with a corresponding release of cytidine 5-monophosphate (CMP) | |
NECFGCCN_04567 | 1.9e-197 | truD | 5.4.99.27 | J | Responsible for synthesis of pseudouridine from uracil- 13 in transfer RNAs | |
NECFGCCN_04568 | 1.6e-132 | surE | 3.1.3.5 | S | Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates | |
NECFGCCN_04569 | 5.2e-113 | pcm | 2.1.1.77 | J | Catalyzes the methyl esterification of L-isoaspartyl residues in peptides and proteins that result from spontaneous decomposition of normal L-aspartyl and L-asparaginyl residues. It plays a role in the repair and or degradation of damaged proteins | |
NECFGCCN_04570 | 1.5e-134 | nlpD | DM | COG0739 Membrane proteins related to metalloendopeptidases | ||
NECFGCCN_04571 | 5.5e-178 | rpoS | K | RNA polymerase sigma | ||
NECFGCCN_04572 | 7.5e-59 | S | protein conserved in bacteria | |||
NECFGCCN_04573 | 9.3e-212 | EGP | Major facilitator Superfamily | |||
NECFGCCN_04574 | 1.6e-152 | ptxR | K | transcriptional regulator | ||
NECFGCCN_04575 | 4.9e-64 | hosA | K | Transcriptional regulator | ||
NECFGCCN_04576 | 3.4e-106 | ubiX | 2.5.1.129 | H | Flavin prenyltransferase that catalyzes the synthesis of the prenylated FMN cofactor (prenyl-FMN) for 4-hydroxy-3- polyprenylbenzoic acid decarboxylase UbiD. The prenyltransferase is metal-independent and links a dimethylallyl moiety from dimethylallyl monophosphate (DMAP) to the flavin N5 and C6 atoms of FMN | |
NECFGCCN_04577 | 6.6e-281 | yclC | 4.1.1.61 | H | Decarboxylase involved in the decarboxylation and detoxification of phenolic derivatives under both aerobic and anaerobic conditions. It is able to catalyze the reversible decarboxylation of 4-hydroxybenzoate and vanillate | |
NECFGCCN_04578 | 4.4e-41 | bsdD | 4.1.1.61 | S | 4-hydroxybenzoate decarboxylase | |
NECFGCCN_04579 | 1.1e-16 | hokE | S | Hok/gef family | ||
NECFGCCN_04580 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
NECFGCCN_04581 | 4.4e-146 | hmuV | 1.14.15.20, 3.6.3.33, 3.6.3.34 | P | Part of the ABC transporter complex HmuTUV involved in hemin import. Responsible for energy coupling to the transport system | |
NECFGCCN_04582 | 3.6e-161 | hmuU | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
NECFGCCN_04583 | 2.6e-141 | hmuT | P | ABC-type hemin transport system, periplasmic component | ||
NECFGCCN_04584 | 9.8e-194 | hmuS | P | hemin transport protein | ||
NECFGCCN_04585 | 0.0 | hpuB | P | Receptor | ||
NECFGCCN_04586 | 2.2e-50 | O | protein conserved in bacteria | |||
NECFGCCN_04587 | 0.0 | 2.2.1.6 | EH | COG0028 Thiamine pyrophosphate-requiring enzymes acetolactate synthase, pyruvate dehydrogenase (cytochrome), glyoxylate carboligase, phosphonopyruvate decarboxylase | ||
NECFGCCN_04588 | 1.9e-135 | ywkB | S | transporter | ||
NECFGCCN_04589 | 5.2e-159 | K | LysR substrate binding domain | |||
NECFGCCN_04590 | 1.5e-58 | ygbA | S | Nitrous oxide-stimulated promoter | ||
NECFGCCN_04591 | 4.2e-142 | sitD | P | COG1108 ABC-type Mn2 Zn2 transport systems permease components | ||
NECFGCCN_04592 | 1e-148 | sitC | P | iron transport system membrane protein | ||
NECFGCCN_04593 | 1.9e-147 | sitB | P | (ABC) transporter | ||
NECFGCCN_04594 | 2.6e-169 | psaA | P | Belongs to the bacterial solute-binding protein 9 family | ||
NECFGCCN_04595 | 1.2e-169 | K | transcriptional regulator | |||
NECFGCCN_04596 | 2e-16 | 2.7.13.3 | T | signal transduction protein with a C-terminal ATPase domain | ||
NECFGCCN_04597 | 2.1e-20 | 6.1.1.6 | S | Psort location CytoplasmicMembrane, score | ||
NECFGCCN_04599 | 2e-28 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
NECFGCCN_04600 | 7.2e-71 | |||||
NECFGCCN_04601 | 3e-170 | iolE | 4.2.1.44 | G | Catalyzes the dehydration of inosose (2-keto-myo- inositol, 2KMI or 2,4,6 3,5-pentahydroxycyclohexanone) to 3D- (3,5 4)-trihydroxycyclohexane-1,2-dione (D-2,3-diketo-4-deoxy-epi- inositol) | |
NECFGCCN_04602 | 1.9e-225 | S | oxidoreductase | |||
NECFGCCN_04603 | 1.6e-196 | dhdh | S | oxidoreductase | ||
NECFGCCN_04604 | 2.3e-303 | guaA | 2.3.1.128, 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
NECFGCCN_04605 | 7.7e-126 | gntR1 | K | transcriptional | ||
NECFGCCN_04606 | 2e-55 | ylxM | S | Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY ffh. May be a regulatory protein | ||
NECFGCCN_04607 | 4.9e-174 | yeiH | S | membrane | ||
NECFGCCN_04609 | 4.5e-91 | adk | 2.7.4.3 | F | topology modulation protein | |
NECFGCCN_04610 | 5.5e-247 | purA | 6.3.4.4 | F | Plays an important role in the de novo pathway of purine nucleotide biosynthesis. Catalyzes the first committed step in the biosynthesis of AMP from IMP | |
NECFGCCN_04611 | 2.6e-79 | ptpA | 3.1.3.48 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
NECFGCCN_04612 | 2.8e-35 | XK27_09805 | S | MORN repeat protein | ||
NECFGCCN_04613 | 0.0 | XK27_09800 | I | Acyltransferase | ||
NECFGCCN_04614 | 1e-187 | ruvB | 3.6.4.12 | L | The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing | |
NECFGCCN_04615 | 2.9e-48 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
NECFGCCN_04616 | 2.4e-110 | rplC | J | One of the primary rRNA binding proteins, it binds directly near the 3'-end of the 23S rRNA, where it nucleates assembly of the 50S subunit | ||
NECFGCCN_04617 | 5.7e-104 | rplD | J | Forms part of the polypeptide exit tunnel | ||
NECFGCCN_04618 | 2.4e-44 | rplW | J | One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome | ||
NECFGCCN_04619 | 6.8e-153 | rplB | J | One of the primary rRNA binding proteins. Required for association of the 30S and 50S subunits to form the 70S ribosome, for tRNA binding and peptide bond formation. It has been suggested to have peptidyltransferase activity | ||
NECFGCCN_04620 | 8.3e-47 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
NECFGCCN_04621 | 7.3e-53 | rplV | J | The globular domain of the protein is located near the polypeptide exit tunnel on the outside of the subunit, while an extended beta-hairpin is found that lines the wall of the exit tunnel in the center of the 70S ribosome | ||
NECFGCCN_04622 | 1.6e-117 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
NECFGCCN_04623 | 1.1e-71 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
NECFGCCN_04624 | 3.5e-26 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
NECFGCCN_04625 | 6e-39 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
NECFGCCN_04626 | 3.9e-60 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
NECFGCCN_04627 | 1.4e-47 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
NECFGCCN_04628 | 1.6e-94 | rplE | J | This is 1 of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance. In the 70S ribosome it contacts protein S13 of the 30S subunit (bridge B1b), connecting the 2 subunits | ||
NECFGCCN_04629 | 1.2e-67 | rpsH | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA central domain where it helps coordinate assembly of the platform of the 30S subunit | ||
NECFGCCN_04630 | 6.6e-93 | rplF | J | This protein binds to the 23S rRNA, and is important in its secondary structure. It is located near the subunit interface in the base of the L7 L12 stalk, and near the tRNA binding site of the peptidyltransferase center | ||
NECFGCCN_04631 | 1.3e-79 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
NECFGCCN_04632 | 1.9e-23 | rpmD | J | ribosomal protein l30 | ||
NECFGCCN_04633 | 5.7e-58 | rplO | J | binds to the 23S rRNA | ||
NECFGCCN_04634 | 3e-232 | secY | U | The central subunit of the protein translocation channel SecYEG. Consists of two halves formed by TMs 1-5 and 6-10. These two domains form a lateral gate at the front which open onto the bilayer between TMs 2 and 7, and are clamped together by SecE at the back. The channel is closed by both a pore ring composed of hydrophobic SecY resides and a short helix (helix 2A) on the extracellular side of the membrane which forms a plug. The plug probably moves laterally to allow the channel to open. The ring and the pore may move independently | ||
NECFGCCN_04635 | 2.1e-114 | adk | 2.7.4.3 | F | Catalyzes the reversible transfer of the terminal phosphate group between ATP and AMP. Plays an important role in cellular energy homeostasis and in adenine nucleotide metabolism | |
NECFGCCN_04636 | 2.7e-32 | infA | J | One of the essential components for the initiation of protein synthesis. Stabilizes the binding of IF-2 and IF-3 on the 30S subunit to which N-formylmethionyl-tRNA(fMet) subsequently binds. Helps modulate mRNA selection, yielding the 30S pre- initiation complex (PIC). Upon addition of the 50S ribosomal subunit IF-1, IF-2 and IF-3 are released leaving the mature 70S translation initation complex | ||
NECFGCCN_04637 | 4e-57 | rpsM | J | Located at the top of the head of the 30S subunit, it contacts several helices of the 16S rRNA. In the 70S ribosome it contacts the 23S rRNA (bridge B1a) and protein L5 of the 50S subunit (bridge B1b), connecting the 2 subunits | ||
NECFGCCN_04638 | 4e-170 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
NECFGCCN_04639 | 4.4e-62 | rplQ | J | ribosomal protein l17 | ||
NECFGCCN_04640 | 5.1e-261 | yjcE | P | NhaP-type Na H and K H antiporters | ||
NECFGCCN_04641 | 1.3e-120 | nemR | K | transcriptional regulator | ||
NECFGCCN_04642 | 5.3e-173 | yhdH | C | COG0604 NADPH quinone reductase and related Zn-dependent oxidoreductases | ||
NECFGCCN_04643 | 2.5e-156 | S | Nucleoside recognition family protein | |||
NECFGCCN_04644 | 1.3e-296 | 3.1.1.1 | I | Serine aminopeptidase, S33 | ||
NECFGCCN_04645 | 2.4e-29 | pmrD | S | Polymyxin resistance protein PmrD | ||
NECFGCCN_04646 | 7.4e-288 | amn | 3.2.2.4 | F | Catalyzes the hydrolysis of the N-glycosidic bond of AMP to form adenine and ribose 5-phosphate. Involved in regulation of AMP concentrations | |
NECFGCCN_04647 | 1.1e-144 | zupT | P | Mediates zinc uptake. May also transport other divalent cations | ||
NECFGCCN_04648 | 2.2e-145 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
NECFGCCN_04649 | 2.3e-78 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
NECFGCCN_04650 | 1.2e-117 | manM | G | pts system | ||
NECFGCCN_04651 | 4.5e-118 | manL | 2.7.1.191 | G | pts system | |
NECFGCCN_04652 | 1e-159 | accD | 2.1.3.15, 6.4.1.2 | I | Component of the acetyl coenzyme A carboxylase (ACC) complex. Biotin carboxylase (BC) catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the transcarboxylase to acetyl-CoA to form malonyl- CoA | |
NECFGCCN_04653 | 8.3e-257 | accC | 6.3.4.14, 6.4.1.2 | I | An AccC homodimer forms the biotin carboxylase subunit of the acetyl CoA carboxylase, an enzyme that catalyzes the formation of malonyl-CoA, which in turn controls the rate of fatty acid metabolism | |
NECFGCCN_04654 | 1.5e-71 | fabZ | 3.5.1.108, 4.2.1.59 | I | Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs | |
NECFGCCN_04655 | 2.5e-54 | accB | 2.3.1.12, 4.1.1.3 | I | first, biotin carboxylase catalyzes the carboxylation of the carrier protein and then the transcarboxylase transfers the carboxyl group to form malonyl-CoA | |
NECFGCCN_04656 | 5.7e-233 | fabF | 2.3.1.179 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP | |
NECFGCCN_04657 | 6.2e-126 | IQ | reductase | |||
NECFGCCN_04658 | 1.8e-162 | fabD | 2.3.1.39 | I | Malonyl CoA-acyl carrier protein transacylase | |
NECFGCCN_04659 | 1.2e-172 | fabK | 1.3.1.9 | S | 2-Nitropropane dioxygenase | |
NECFGCCN_04660 | 3.3e-30 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
NECFGCCN_04661 | 6.4e-171 | fabH | 2.3.1.180 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids | |
NECFGCCN_04662 | 5.2e-72 | marR | K | Transcriptional regulator, MarR family | ||
NECFGCCN_04663 | 6.2e-140 | phaB | 5.3.3.14, 5.3.3.18 | I | Belongs to the enoyl-CoA hydratase isomerase family | |
NECFGCCN_04664 | 1.5e-32 | dnaX | 2.7.7.7 | L | DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
NECFGCCN_04665 | 1.8e-98 | apt | 2.4.2.7 | F | Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis | |
NECFGCCN_04666 | 1.3e-63 | ybaN | S | Membrane | ||
NECFGCCN_04667 | 3e-74 | priC | L | primosomal replication protein | ||
NECFGCCN_04668 | 1.9e-12 | ybaM | S | Protein of unknown function (DUF2496) | ||
NECFGCCN_04669 | 1.6e-147 | yadD | S | Putative transposase, YhgA-like | ||
NECFGCCN_04670 | 0.0 | kefA | M | mechanosensitive ion channel | ||
NECFGCCN_04671 | 1.4e-113 | acrR | K | transcriptional regulator | ||
NECFGCCN_04672 | 1.3e-213 | acrA | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | ||
NECFGCCN_04673 | 6.9e-122 | narJ | 1.7.5.1 | C | Nitrate reductase | |
NECFGCCN_04674 | 2.7e-123 | narI | 1.7.5.1 | C | nitrate reductase, gamma subunit | |
NECFGCCN_04675 | 8.9e-151 | yxxF | EG | Multidrug DMT transporter permease | ||
NECFGCCN_04676 | 5.7e-74 | lrpC | K | AsnC family transcriptional regulator | ||
NECFGCCN_04677 | 7.3e-245 | proY | E | Amino acid permease-associated region | ||
NECFGCCN_04678 | 2.3e-232 | hutH | 3.5.2.7, 4.3.1.3 | E | PFAM Phenylalanine histidine ammonia-lyase | |
NECFGCCN_04679 | 2.2e-159 | cvfB | S | Protein conserved in bacteria | ||
NECFGCCN_04680 | 1.7e-91 | frr | J | Responsible for the release of ribosomes from messenger RNA at the termination of protein biosynthesis. May increase the efficiency of translation by recycling ribosomes from one round of translation to another | ||
NECFGCCN_04681 | 1.7e-131 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
NECFGCCN_04682 | 6.8e-210 | sptS | 2.7.13.3 | T | Histidine kinase | |
NECFGCCN_04683 | 6e-115 | T | response regulator | |||
NECFGCCN_04684 | 9.7e-112 | 2.7.6.5 | S | Region found in RelA / SpoT proteins | ||
NECFGCCN_04685 | 1.3e-111 | K | Acetyltransferase (GNAT) family | |||
NECFGCCN_04686 | 0.0 | lmrA2 | V | abc transporter atp-binding protein | ||
NECFGCCN_04687 | 7.5e-311 | lmrA1 | V | abc transporter atp-binding protein | ||
NECFGCCN_04688 | 1.4e-72 | K | DNA-binding transcription factor activity | |||
NECFGCCN_04689 | 3.9e-69 | def_1 | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins | |
NECFGCCN_04690 | 1.7e-264 | S | Psort location CytoplasmicMembrane, score | |||
NECFGCCN_04691 | 5.7e-240 | nylA | 3.5.1.4 | J | Belongs to the amidase family | |
NECFGCCN_04692 | 4.4e-112 | pyrE | 2.4.2.10, 4.1.1.23 | F | Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) | |
NECFGCCN_04693 | 5.5e-124 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
NECFGCCN_04694 | 2.1e-174 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
NECFGCCN_04695 | 5e-145 | pyrK | C | Responsible for channeling the electrons from the oxidation of dihydroorotate from the FMN redox center in the PyrD type B subunit to the ultimate electron acceptor NAD( ) | ||
NECFGCCN_04696 | 5.2e-93 | thiJ | 2.7.11.1, 3.5.1.124 | S | DJ-1 family | |
NECFGCCN_04697 | 4.4e-133 | S | TraX protein | |||
NECFGCCN_04698 | 2.6e-13 | FbpA | K | RNA-binding protein homologous to eukaryotic snRNP | ||
NECFGCCN_04699 | 1.8e-24 | |||||
NECFGCCN_04701 | 1.2e-140 | modF | 3.6.3.21, 3.6.3.34 | P | abc transporter atp-binding protein | |
NECFGCCN_04702 | 3.2e-237 | hlyX | S | COG1253 Hemolysins and related proteins containing CBS domains | ||
NECFGCCN_04703 | 1.4e-08 | MU | outer membrane autotransporter barrel domain protein | |||
NECFGCCN_04704 | 2e-157 | pflA | 1.97.1.4 | C | Activation of pyruvate formate-lyase under anaerobic conditions by generation of an organic free radical, using S- adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine | |
NECFGCCN_04706 | 9e-75 | XK27_03180 | T | universal stress protein | ||
NECFGCCN_04707 | 7.6e-238 | alaA | 2.6.1.2, 2.6.1.66 | E | Aminotransferase | |
NECFGCCN_04708 | 8.1e-140 | codY | K | DNA-binding protein that represses the expression of many genes that are induced as cells make the transition from rapid exponential growth to stationary phase. It is a GTP-binding protein that senses the intracellular GTP concentration as an indicator of nutritional limitations. At low GTP concentration it no longer binds GTP and stop to act as a transcriptional repressor | ||
NECFGCCN_04709 | 5.8e-100 | pncA | Q | isochorismatase | ||
NECFGCCN_04710 | 1.9e-103 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
NECFGCCN_04711 | 2.9e-42 | livF | P | Branched-chain amino acid transport | ||
NECFGCCN_04712 | 7.5e-166 | yjiE | K | transcriptional regulator | ||
NECFGCCN_04713 | 0.0 | pckA | 4.1.1.49 | H | Involved in the gluconeogenesis. Catalyzes the conversion of oxaloacetate (OAA) to phosphoenolpyruvate (PEP) through direct phosphoryl transfer between the nucleoside triphosphate and OAA | |
NECFGCCN_04714 | 1e-84 | ats | 2.3.1.57 | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | |
NECFGCCN_04715 | 2.2e-168 | K | transcriptional regulator | |||
NECFGCCN_04716 | 3.3e-231 | citA | EGP | Is involved in the uptake of citrate and the transport of protons into the cell | ||
NECFGCCN_04717 | 1.6e-138 | 5.3.3.7 | P | ABC transporter substrate-binding protein | ||
NECFGCCN_04718 | 6.5e-28 | ybhD | K | transcriptional regulator | ||
NECFGCCN_04719 | 3.6e-188 | pfkA | 2.7.1.11 | F | Catalyzes the phosphorylation of D-fructose 6-phosphate to fructose 1,6-bisphosphate by ATP, the first committing step of glycolysis | |
NECFGCCN_04720 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase | |
NECFGCCN_04721 | 0.0 | dmsA | 1.8.5.3, 1.97.1.9 | C | Belongs to the prokaryotic molybdopterin-containing oxidoreductase family | |
NECFGCCN_04722 | 9.7e-41 | pepD | E | Dipeptidase | ||
NECFGCCN_04723 | 1.3e-160 | whiA | K | May be required for sporulation | ||
NECFGCCN_04724 | 6.2e-182 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
NECFGCCN_04725 | 2e-163 | rapZ | S | Displays ATPase and GTPase activities | ||
NECFGCCN_04726 | 5.3e-136 | yejC | S | cyclic nucleotide-binding protein | ||
NECFGCCN_04727 | 1.1e-25 | D | nuclear chromosome segregation | |||
NECFGCCN_04728 | 3.5e-51 | D | nuclear chromosome segregation | |||
NECFGCCN_04729 | 2.6e-27 | D | nuclear chromosome segregation | |||
NECFGCCN_04730 | 3.7e-63 | XK27_02560 | S | cog cog2151 | ||
NECFGCCN_04731 | 0.0 | ilvD | 4.2.1.9 | E | Belongs to the IlvD Edd family | |
NECFGCCN_04732 | 6.3e-221 | ytfP | S | Flavoprotein | ||
NECFGCCN_04734 | 2e-120 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
NECFGCCN_04735 | 3.6e-47 | ytmP | 2.7.1.89 | M | Phosphotransferase | |
NECFGCCN_04736 | 5.6e-186 | wcoF | M | Glycosyltransferase, group 1 family protein | ||
NECFGCCN_04737 | 1.2e-09 | fruR | K | transcriptional | ||
NECFGCCN_04739 | 7e-262 | mloB | K | Transcriptional regulator | ||
NECFGCCN_04740 | 3.4e-65 | |||||
NECFGCCN_04741 | 2e-13 | |||||
NECFGCCN_04742 | 2.4e-61 | |||||
NECFGCCN_04743 | 1e-198 | L | Replication initiation factor | |||
NECFGCCN_04745 | 5.2e-281 | L | DNA integration | |||
NECFGCCN_04746 | 2e-231 | |||||
NECFGCCN_04747 | 4.3e-127 | P | ATPases associated with a variety of cellular activities | |||
NECFGCCN_04748 | 6.7e-19 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
NECFGCCN_04749 | 1.5e-25 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
NECFGCCN_04750 | 3.6e-218 | metE | 2.1.1.14 | E | Methionine synthase | |
NECFGCCN_04751 | 6.1e-08 | 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | pts system | ||
NECFGCCN_04752 | 7.5e-59 | 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | pts system | ||
NECFGCCN_04753 | 4e-237 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
NECFGCCN_04755 | 0.0 | aspS | 6.1.1.12 | J | Catalyzes the attachment of L-aspartate to tRNA(Asp) in a two-step reaction L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp) | |
NECFGCCN_04756 | 1e-128 | XK27_01785 | S | cog cog1284 | ||
NECFGCCN_04757 | 3.5e-118 | yaaA | S | Belongs to the UPF0246 family | ||
NECFGCCN_04758 | 1.3e-113 | nrdG | 1.97.1.4 | O | Activation of anaerobic ribonucleoside-triphosphate reductase under anaerobic conditions by generation of an organic free radical, using S-adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine | |
NECFGCCN_04759 | 1.1e-84 | XK27_10930 | K | acetyltransferase | ||
NECFGCCN_04760 | 7.5e-14 | |||||
NECFGCCN_04761 | 0.0 | nrdD | 1.1.98.6 | F | Ribonucleoside-triphosphate reductase | |
NECFGCCN_04762 | 1.1e-287 | ccs | S | the current gene model (or a revised gene model) may contain a frame shift | ||
NECFGCCN_04763 | 2.1e-43 | yrzB | S | Belongs to the UPF0473 family | ||
NECFGCCN_04764 | 1.8e-69 | yqgF | L | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
NECFGCCN_04765 | 6.3e-44 | yrzL | S | Belongs to the UPF0297 family | ||
NECFGCCN_04766 | 8.4e-27 | rpmB | J | Belongs to the bacterial ribosomal protein bL28 family | ||
NECFGCCN_04767 | 3.5e-233 | rarA | L | ATPase related to the helicase subunit of the Holliday junction resolvase | ||
NECFGCCN_04769 | 9.4e-214 | int | L | Phage integrase family | ||
NECFGCCN_04770 | 1.4e-18 | S | Domain of unknown function (DUF3173) | |||
NECFGCCN_04771 | 1.5e-109 | L | Replication initiation factor | |||
NECFGCCN_04772 | 5.5e-89 | K | sequence-specific DNA binding | |||
NECFGCCN_04773 | 4.2e-43 | C | Succinate dehydrogenase fumarate reductase, flavoprotein subunit | |||
NECFGCCN_04774 | 1.8e-25 | C | Succinate dehydrogenase fumarate reductase, flavoprotein subunit | |||
NECFGCCN_04775 | 3.4e-52 | S | NIPSNAP family containing protein | |||
NECFGCCN_04776 | 0.0 | C | Succinate dehydrogenase fumarate reductase, flavoprotein subunit | |||
NECFGCCN_04777 | 1.8e-142 | aroE | 1.1.1.25, 4.2.1.10 | E | shikimate dehydrogenase | |
NECFGCCN_04778 | 1.2e-135 | pcaR | K | Transcriptional regulator | ||
NECFGCCN_04779 | 1.2e-07 | |||||
NECFGCCN_04780 | 1.1e-161 | cyoE | 2.5.1.141 | O | Converts heme B (protoheme IX) to heme O by substitution of the vinyl group on carbon 2 of heme B porphyrin ring with a hydroxyethyl farnesyl side group | |
NECFGCCN_04781 | 9.6e-26 | cyoD | C | PFAM Cytochrome C oxidase subunit IV | ||
NECFGCCN_04782 | 2.9e-113 | cyoC | C | oxidase subunit | ||
NECFGCCN_04783 | 0.0 | cyoB | 1.10.3.10, 1.10.3.12, 1.9.3.1 | C | Cytochrome c oxidase is the component of the respiratory chain that catalyzes the reduction of oxygen to water. Subunits 1- 3 form the functional core of the enzyme complex. CO I is the catalytic subunit of the enzyme. Electrons originating in cytochrome c are transferred via the copper A center of subunit 2 and heme A of subunit 1 to the bimetallic center formed by heme A3 and copper B | |
NECFGCCN_04784 | 8.4e-176 | cyoA | 1.10.3.10, 1.10.3.12 | C | Subunits I and II form the functional core of the enzyme complex. Electrons originating in cytochrome c are transferred via heme a and Cu(A) to the binuclear center formed by heme a3 and Cu(B) | |
NECFGCCN_04785 | 1.6e-266 | ampG | EGP | Major facilitator Superfamily | ||
NECFGCCN_04786 | 2.1e-97 | yajG | M | Lipoprotein | ||
NECFGCCN_04787 | 5.1e-53 | bolA | T | Belongs to the BolA IbaG family | ||
NECFGCCN_04788 | 6e-233 | tig | D | Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation. Functions as a peptidyl-prolyl cis-trans isomerase | ||
NECFGCCN_04789 | 6.1e-114 | clpP | 3.4.21.92 | OU | Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins | |
NECFGCCN_04790 | 4e-237 | clpX | O | ATP-dependent specificity component of the Clp protease. It directs the protease to specific substrates. Can perform chaperone functions in the absence of ClpP | ||
NECFGCCN_04791 | 0.0 | lon | 3.4.21.53 | O | ATP-dependent serine protease that mediates the selective degradation of mutant and abnormal proteins as well as certain short-lived regulatory proteins. Required for cellular homeostasis and for survival from DNA damage and developmental changes induced by stress. Degrades polypeptides processively to yield small peptide fragments that are 5 to 10 amino acids long. Binds to DNA in a double-stranded, site-specific manner | |
NECFGCCN_04792 | 4.8e-39 | hupB | L | Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions | ||
NECFGCCN_04793 | 6.3e-308 | ppiD | 5.2.1.8 | O | peptidylprolyl isomerase | |
NECFGCCN_04794 | 1.6e-53 | ybaV | 3.1.26.11 | L | Competence protein ComEA | |
NECFGCCN_04795 | 1.2e-67 | tesC | S | Thioesterase | ||
NECFGCCN_04796 | 8e-131 | queC | 6.3.4.20 | F | Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) | |
NECFGCCN_04797 | 0.0 | ybaE | S | ABC transporter substrate-binding protein | ||
NECFGCCN_04798 | 1.2e-157 | cof | S | Catalyzes the hydrolysis of 4-amino-2-methyl-5- hydroxymethylpyrimidine pyrophosphate (HMP-PP) to 4-amino-2- methyl-5-hydroxymethylpyrimidine phosphate (HMP-P) | ||
NECFGCCN_04799 | 1.3e-198 | cysK_2 | 2.5.1.47 | E | cysteine synthase | |
NECFGCCN_04800 | 1.8e-78 | ybaO | K | transcriptional regulator | ||
NECFGCCN_04801 | 2.9e-302 | mdlA | V | Involved in lipid A export and possibly also in glycerophospholipid export and for biogenesis of the outer membrane. Transmembrane domains (TMD) form a pore in the inner membrane and the ATP-binding domain (NBD) is responsible for energy generation | ||
NECFGCCN_04802 | 0.0 | mdlB | V | Involved in lipid A export and possibly also in glycerophospholipid export and for biogenesis of the outer membrane. Transmembrane domains (TMD) form a pore in the inner membrane and the ATP-binding domain (NBD) is responsible for energy generation | ||
NECFGCCN_04803 | 1.1e-53 | glnK | K | Belongs to the P(II) protein family | ||
NECFGCCN_04804 | 2e-236 | amtB | P | Ammonium transporter | ||
NECFGCCN_04805 | 2.6e-163 | tesB | I | Acyl-CoA thioesterase | ||
NECFGCCN_04806 | 4e-68 | ybaY | S | protein conserved in bacteria | ||
NECFGCCN_04807 | 1.3e-53 | ybaZ | 2.1.1.63 | L | methylated DNA-protein cysteine methyltransferase | |
NECFGCCN_04808 | 4.6e-62 | |||||
NECFGCCN_04809 | 6.1e-36 | |||||
NECFGCCN_04810 | 3e-36 | |||||
NECFGCCN_04811 | 2.3e-265 | K | Transcriptional regulator | |||
NECFGCCN_04812 | 4e-102 | S | Membrane | |||
NECFGCCN_04813 | 3.9e-124 | rcnA | U | Belongs to the NiCoT transporter (TC 2.A.52) family | ||
NECFGCCN_04814 | 3.3e-40 | rcnR | S | protein conserved in bacteria | ||
NECFGCCN_04815 | 1e-295 | ylaB | 3.1.4.52 | T | signal transduction protein containing sensor and EAL | |
NECFGCCN_04816 | 1.2e-210 | ganK | P | Belongs to the ABC transporter superfamily | ||
NECFGCCN_04817 | 1.5e-228 | cycB | G | Functions in the MalKFGE ABC transporter complex to transport maltose into the cell by using ATP hydrolysis | ||
NECFGCCN_04818 | 2.8e-246 | malC | P | transport | ||
NECFGCCN_04819 | 2.7e-149 | ganQ | P | transport | ||
NECFGCCN_04820 | 1.7e-237 | ganB | 3.2.1.89 | G | Arabinogalactan endo-beta-1,4-galactanase | |
NECFGCCN_04821 | 0.0 | bglY | 3.2.1.23 | G | beta-galactosidase | |
NECFGCCN_04822 | 8.5e-48 | 2.7.1.192, 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | Phosphotransferase System | ||
NECFGCCN_04823 | 2.4e-250 | lamB | M | involved in the transport of maltose and maltodextrins | ||
NECFGCCN_04824 | 5e-193 | lacI | K | binds specific sites in lac operon resulting in DNA looping between the operators | ||
NECFGCCN_04825 | 2.6e-42 | rpmE2 | J | Ribosomal protein L31 | ||
NECFGCCN_04826 | 7e-18 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
NECFGCCN_04827 | 1.2e-129 | ydaF_2 | J | Acetyltransferases including N-acetylases of ribosomal proteins | ||
NECFGCCN_04828 | 2.4e-246 | gabR_4 | K | Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | ||
NECFGCCN_04829 | 3.3e-80 | ylaC | S | Membrane | ||
NECFGCCN_04830 | 7.2e-90 | maa | 2.3.1.79 | S | acetyltransferase, isoleucine patch superfamily | |
NECFGCCN_04831 | 1.4e-33 | hha | S | Haemolysin expression modulating protein | ||
NECFGCCN_04832 | 2e-67 | tomB | S | Biofilm formation regulator YbaJ | ||
NECFGCCN_04833 | 1.7e-70 | acrB | V | Belongs to the resistance-nodulation-cell division (RND) (TC 2.A.6) family | ||
NECFGCCN_04834 | 1.2e-249 | 2.6.1.55 | E | Belongs to the class-III pyridoxal-phosphate-dependent aminotransferase family | ||
NECFGCCN_04835 | 2.1e-137 | sdh | 1.1.1.276, 1.1.1.313, 1.1.1.381 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
NECFGCCN_04836 | 1.7e-134 | glnQ | 3.6.3.21 | E | abc transporter atp-binding protein | |
NECFGCCN_04837 | 2.5e-113 | E | (ABC) transporter | |||
NECFGCCN_04838 | 1.8e-105 | E | (ABC) transporter | |||
NECFGCCN_04839 | 2.9e-159 | ET | ABC transporter substrate-binding protein | |||
NECFGCCN_04840 | 3.1e-286 | gabR_2 | K | Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | ||
NECFGCCN_04841 | 6.2e-249 | K | Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | |||
NECFGCCN_04842 | 3.4e-153 | ydeK | EG | transporter | ||
NECFGCCN_04843 | 3e-245 | amaB | 3.5.1.6, 3.5.1.87, 3.5.3.9 | E | the allantoate amidohydrolase from Escherichia coli forms a dimer and binds zinc ions for catalytic activity and catalyzes the conversion of allantoate to (S)-ureidoglycolate and ammonia | |
NECFGCCN_04844 | 1.6e-185 | dppD | 3.6.3.24 | P | Belongs to the ABC transporter superfamily | |
NECFGCCN_04845 | 1.4e-192 | MA20_19370 | E | Belongs to the ABC transporter superfamily | ||
NECFGCCN_04846 | 1.2e-155 | MA20_19380 | EP | N-terminal TM domain of oligopeptide transport permease C | ||
NECFGCCN_04847 | 2.6e-172 | MA20_19385 | EP | Binding-protein-dependent transport system inner membrane component | ||
NECFGCCN_04848 | 0.0 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | |||
NECFGCCN_04849 | 6.2e-218 | ybdK | H | ATP-dependent carboxylate-amine ligase which exhibits weak glutamate--cysteine ligase activity | ||
NECFGCCN_04850 | 2.8e-118 | yigE | S | Phosphodiester glycosidase | ||
NECFGCCN_04851 | 0.0 | bepG | V | Belongs to the resistance-nodulation-cell division (RND) (TC 2.A.6) family | ||
NECFGCCN_04852 | 3.4e-149 | bepF | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | ||
NECFGCCN_04853 | 0.0 | ctpF | P | ATPase, P-type (transporting), HAD superfamily, subfamily IC | ||
NECFGCCN_04854 | 1e-164 | recC | 3.1.11.5 | L | A helicase nuclease that prepares dsDNA breaks (DSB) for recombinational DNA repair. Binds to DSBs and unwinds DNA via a highly rapid and processive ATP-dependent bidirectional helicase activity. Unwinds dsDNA until it encounters a Chi (crossover hotspot instigator) sequence from the 3' direction. Cuts ssDNA a few nucleotides 3' to the Chi site. The properties and activities of the enzyme are changed at Chi. The Chi-altered holoenzyme produces a long 3'-ssDNA overhang and facilitates RecA-binding to the ssDNA for homologous DNA recombination and repair. Holoenzyme degrades any linearized DNA that is unable to undergo homologous recombination. In the holoenzyme this subunit recognizes the wild- type Chi sequence, and when added to isolated RecB increases its ATP-dependent helicase processivity | |
NECFGCCN_04856 | 4.7e-279 | gltX | 6.1.1.17, 6.1.1.24 | J | Catalyzes the attachment of glutamate to tRNA(Glu) in a two-step reaction glutamate is first activated by ATP to form Glu-AMP and then transferred to the acceptor end of tRNA(Glu) | |
NECFGCCN_04857 | 3.1e-63 | yfeD | L | Putative transcription regulator (DUF1323) | ||
NECFGCCN_04858 | 1.9e-56 | yfeC | L | Negative Regulator | ||
NECFGCCN_04859 | 0.0 | 3.5.1.28 | NU | amidase activity | ||
NECFGCCN_04861 | 7.7e-76 | aroH | 2.5.1.54 | E | Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) | |
NECFGCCN_04862 | 1.4e-31 | hemP | P | Hemin uptake protein | ||
NECFGCCN_04863 | 5.1e-281 | ydiU | S | Belongs to the UPF0061 (SELO) family | ||
NECFGCCN_04864 | 1e-86 | nlpC | 3.4.17.13 | M | COG0791 Cell wall-associated hydrolases (invasion-associated proteins) | |
NECFGCCN_04865 | 3.8e-131 | btuD | 3.6.3.33 | P | Part of the ABC transporter complex BtuCDF involved in vitamin B12 import. Responsible for energy coupling to the transport system | |
NECFGCCN_04866 | 2.9e-99 | btuE | 1.11.1.9 | O | Belongs to the glutathione peroxidase family | |
NECFGCCN_04867 | 2.1e-143 | metQ | P | Belongs to the NlpA lipoprotein family | ||
NECFGCCN_04868 | 8.3e-174 | btuC | H | Part of the ABC transporter complex BtuCDF involved in vitamin B12 import. Involved in the translocation of the substrate across the membrane | ||
NECFGCCN_04869 | 2.1e-242 | S | antiporter activity | |||
NECFGCCN_04870 | 6.5e-165 | VPA0331 | K | Transcriptional regulator | ||
NECFGCCN_04871 | 6.5e-232 | dadA2 | 1.4.5.1 | C | D-amino acid dehydrogenase | |
NECFGCCN_04872 | 2.2e-55 | J | Translation Initiation Inhibitor YjgF Family | |||
NECFGCCN_04873 | 8.1e-48 | himA | K | This protein is one of the two subunits of integration host factor, a specific DNA-binding protein that functions in genetic recombination as well as in transcriptional and translational control | ||
NECFGCCN_04874 | 2e-169 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
NECFGCCN_04875 | 1.8e-24 | accA | 2.1.3.15, 6.4.1.2 | I | Component of the acetyl coenzyme A carboxylase (ACC) complex. First, biotin carboxylase catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the carboxyltransferase to acetyl-CoA to form malonyl-CoA | |
NECFGCCN_04876 | 4.7e-90 | luxS | 4.4.1.21 | H | Involved in the synthesis of autoinducer 2 (AI-2) which is secreted by bacteria and is used to communicate both the cell density and the metabolic potential of the environment. The regulation of gene expression in response to changes in cell density is called quorum sensing. Catalyzes the transformation of S-ribosylhomocysteine (RHC) to homocysteine (HC) and 4,5- dihydroxy-2,3-pentadione (DPD) | |
NECFGCCN_04877 | 2.4e-207 | rny | D | Endoribonuclease that initiates mRNA decay | ||
NECFGCCN_04878 | 3.3e-26 | fruR | K | transcriptional | ||
NECFGCCN_04879 | 7.7e-83 | mobB | 2.10.1.1, 2.7.7.77 | H | molybdopterin-guanine dinucleotide biosynthesis protein | |
NECFGCCN_04880 | 1.3e-105 | mobA | 2.10.1.1, 2.7.7.77 | H | Transfers a GMP moiety from GTP to Mo-molybdopterin (Mo- MPT) cofactor (Moco or molybdenum cofactor) to form Mo- molybdopterin guanine dinucleotide (Mo-MGD) cofactor | |
NECFGCCN_04881 | 7e-43 | yihD | S | protein conserved in bacteria | ||
NECFGCCN_04882 | 2.5e-194 | srkA | F | A protein kinase that phosphorylates Ser and Thr residues. Probably acts to suppress the effects of stress linked to accumulation of reactive oxygen species. Probably involved in the extracytoplasmic stress response | ||
NECFGCCN_04883 | 1.1e-112 | dsbA | O | Thiol disulfide interchange protein | ||
NECFGCCN_04884 | 3.1e-167 | yihG | I | Acyltransferase | ||
NECFGCCN_04885 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
NECFGCCN_04886 | 8.9e-113 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
NECFGCCN_04887 | 8.8e-63 | yihI | S | A GTPase-activating protein (GAP) that modifies Der EngA GTPase function. May play a role in ribosome biogenesis | ||
NECFGCCN_04888 | 1.5e-261 | hemN | 1.3.98.3 | H | Belongs to the anaerobic coproporphyrinogen-III oxidase family | |
NECFGCCN_04890 | 2.2e-268 | glnG | T | COG2204 Response regulator containing CheY-like receiver, AAA-type ATPase, and DNA-binding domains | ||
NECFGCCN_04891 | 6.2e-196 | glnL | 2.7.13.3 | T | Signal transduction histidine kinase, nitrogen specific | |
NECFGCCN_04892 | 1.1e-275 | glnA | 5.4.4.3, 6.3.1.2 | E | glutamine synthetase | |
NECFGCCN_04893 | 0.0 | typA | T | GTP-binding protein TypA | ||
NECFGCCN_04894 | 7.4e-109 | yihX | 3.1.3.10 | S | hydrolase | |
NECFGCCN_04895 | 6.4e-138 | rbn | K | UPF0761 membrane protein | ||
NECFGCCN_04896 | 9.6e-74 | dtd | J | rejects L-amino acids rather than detecting D-amino acids in the active site. By recycling D-aminoacyl-tRNA to D-amino acids and free tRNA molecules, this enzyme counteracts the toxicity associated with the formation of D-aminoacyl-tRNA entities in vivo and helps enforce protein L-homochirality | ||
NECFGCCN_04897 | 8.8e-184 | yiiD | K | Putative thioesterase (yiiD_Cterm) | ||
NECFGCCN_04898 | 3.8e-165 | aes | I | Alpha beta hydrolase | ||
NECFGCCN_04899 | 1.2e-36 | yiiE | K | Ribbon-helix-helix protein, copG family | ||
NECFGCCN_04900 | 3.2e-65 | vapC | S | Toxic component of a toxin-antitoxin (TA) module. An RNase | ||
NECFGCCN_04901 | 4.4e-177 | fdhE | O | Necessary for formate dehydrogenase activity | ||
NECFGCCN_04902 | 5e-116 | fdoI | C | formate dehydrogenase | ||
NECFGCCN_04903 | 2.3e-183 | fdoH | C | formate dehydrogenase | ||
NECFGCCN_04904 | 1.3e-212 | fdoG | 1.17.1.9, 1.17.5.3 | C | Belongs to the prokaryotic molybdopterin-containing oxidoreductase family | |
NECFGCCN_04905 | 0.0 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
NECFGCCN_04906 | 4.1e-83 | mutT | 3.6.1.55 | F | Nudix family | |
NECFGCCN_04908 | 6.4e-19 | |||||
NECFGCCN_04909 | 2.1e-114 | ycaK | 1.6.5.2 | C | Flavodoxin-like fold | |
NECFGCCN_04910 | 7.8e-88 | MA20_25245 | K | Gnat family | ||
NECFGCCN_04911 | 0.0 | uvrB | L | damaged site, the DNA wraps around one UvrB monomer. DNA wrap is dependent on ATP binding by UvrB and probably causes local melting of the DNA helix, facilitating insertion of UvrB beta-hairpin between the DNA strands. Then UvrB probes one DNA strand for the presence of a lesion. If a lesion is found the UvrA subunits dissociate and the UvrB-DNA preincision complex is formed. This complex is subsequently bound by UvrC and the second UvrB is released. If no lesion is found, the DNA wraps around the other UvrB subunit that will check the other stand for damage | ||
NECFGCCN_04913 | 9.6e-164 | S | CAAX amino terminal protease family protein | |||
NECFGCCN_04914 | 0.0 | glnP | P | ABC-type amino acid transport signal transduction systems periplasmic component domain | ||
NECFGCCN_04915 | 3.3e-135 | glnQ | 3.6.3.21 | E | abc transporter atp-binding protein | |
NECFGCCN_04916 | 1.7e-17 | XK27_00735 | ||||
NECFGCCN_04917 | 8.8e-248 | obg | S | An essential GTPase which binds GTP, GDP and possibly (p)ppGpp with moderate affinity, with high nucleotide exchange rates and a fairly low GTP hydrolysis rate. Plays a role in control of the cell cycle, stress response, ribosome biogenesis and in those bacteria that undergo differentiation, in morphogenesis control | ||
NECFGCCN_04918 | 3.9e-128 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
NECFGCCN_04919 | 9.8e-10 | O | ADP-ribosylglycohydrolase | |||
NECFGCCN_04920 | 5.6e-62 | paaI | Q | protein possibly involved in aromatic compounds catabolism | ||
NECFGCCN_04921 | 3.5e-61 | ycaO | O | OsmC-like protein | ||
NECFGCCN_04922 | 5.1e-77 | |||||
NECFGCCN_04923 | 2e-122 | S | ABC-2 family transporter protein | |||
NECFGCCN_04924 | 2.6e-11 | L | Belongs to the 'phage' integrase family | |||
NECFGCCN_04925 | 0.0 | S | Phosphatase | |||
NECFGCCN_04926 | 3.1e-77 | znuC | P | ATPases associated with a variety of cellular activities | ||
NECFGCCN_04927 | 6e-112 | znuB | P | ABC 3 transport family | ||
NECFGCCN_04928 | 3e-120 | 3.2.1.78 | GH26 | P | Zinc-uptake complex component A periplasmic | |
NECFGCCN_04929 | 2e-177 | zinT | S | amine dehydrogenase activity | ||
NECFGCCN_04931 | 8.9e-191 | E | Glycine D-amino acid oxidases (Deaminating) | |||
NECFGCCN_04932 | 5.9e-31 | |||||
NECFGCCN_04933 | 3.1e-176 | hemB | 4.2.1.24 | H | Belongs to the ALAD family | |
NECFGCCN_04934 | 1.4e-229 | pyrC | 3.5.2.3 | F | Amidohydrolase family | |
NECFGCCN_04935 | 4.5e-59 | S | Succinylglutamate desuccinylase / Aspartoacylase family | |||
NECFGCCN_04936 | 0.0 | thrS | 6.1.1.3 | J | Catalyzes the attachment of threonine to tRNA(Thr) in a two-step reaction L-threonine is first activated by ATP to form Thr-AMP and then transferred to the acceptor end of tRNA(Thr) | |
NECFGCCN_04937 | 6.8e-122 | psaA | P | Belongs to the bacterial solute-binding protein 9 family | ||
NECFGCCN_04938 | 9.8e-96 | sitB | P | ATPases associated with a variety of cellular activities | ||
NECFGCCN_04939 | 5.6e-126 | sitC | P | ABC 3 transport family | ||
NECFGCCN_04940 | 2.6e-104 | sitD | P | Iron transport protein, inner membrane component SitD | ||
NECFGCCN_04941 | 4.7e-66 | I | Protein of unknown function (DUF1460) | |||
NECFGCCN_04942 | 3.3e-134 | queD | 1.1.1.42 | H | COG0720 6-pyruvoyl-tetrahydropterin synthase | |
NECFGCCN_04943 | 2.3e-96 | ccmM | S | COG0663 Carbonic anhydrases acetyltransferases, isoleucine patch superfamily | ||
NECFGCCN_04944 | 4.4e-116 | folE2 | 3.5.4.16 | S | Converts GTP to 7,8-dihydroneopterin triphosphate | |
NECFGCCN_04946 | 9e-184 | cioB | 1.10.3.14 | C | oxidase subunit | |
NECFGCCN_04947 | 3.8e-265 | cioA | 1.10.3.14 | C | oxidase, subunit | |
NECFGCCN_04949 | 2.3e-262 | ydcR | 2.7.7.65 | K | Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | |
NECFGCCN_04950 | 5.3e-225 | ydcS | E | Spermidine putrescine ABC transporter substrate-binding protein | ||
NECFGCCN_04951 | 6.1e-180 | ydcT | 3.6.3.31 | P | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | |
NECFGCCN_04952 | 1.1e-162 | ydcU | P | ABC transporter (Permease | ||
NECFGCCN_04953 | 1e-142 | ydcV | P | ABC transporter (permease) | ||
NECFGCCN_04954 | 9.2e-267 | prr | 1.2.1.19, 1.2.1.3 | C | belongs to the aldehyde dehydrogenase family | |
NECFGCCN_04956 | 8.7e-11 | |||||
NECFGCCN_04958 | 2.2e-21 | ydcX | S | Toxin GhoT_OrtT | ||
NECFGCCN_04959 | 1.4e-125 | S | Alpha beta hydrolase | |||
NECFGCCN_04960 | 1.4e-259 | vdh | 1.2.1.28 | C | belongs to the aldehyde dehydrogenase family | |
NECFGCCN_04961 | 0.0 | dppA | E | ABC-Type Dipeptide Transport System Periplasmic Component | ||
NECFGCCN_04962 | 7e-31 | ydcY | S | Protein of unknown function (DUF2526) | ||
NECFGCCN_04963 | 3.1e-67 | ydcZ | S | membrane | ||
NECFGCCN_04964 | 5.2e-95 | yncA | 2.3.1.183 | M | acetyltransferase | |
NECFGCCN_04965 | 3.4e-103 | K | transcriptional regulator | |||
NECFGCCN_04966 | 6e-199 | yncB | S | nadp-dependent | ||
NECFGCCN_04967 | 1.9e-175 | rihA | G | Belongs to the IUNH family | ||
NECFGCCN_04968 | 7.1e-44 | yiiS | S | Protein of unknown function (DUF406) | ||
NECFGCCN_04969 | 2.2e-251 | nfdA_2 | S | metal-dependent hydrolase with the TIM-barrel fold | ||
NECFGCCN_04970 | 0.0 | yncD | P | receptor | ||
NECFGCCN_04971 | 7.3e-168 | yncE | S | DNA binding | ||
NECFGCCN_04972 | 3.5e-32 | ygdR | S | (Lipo)protein | ||
NECFGCCN_04973 | 6.9e-270 | ansP | E | Involved in the transporte of L-asparagine | ||
NECFGCCN_04974 | 1.2e-155 | dmlR_3 | K | Transcriptional regulator | ||
NECFGCCN_04975 | 1.3e-99 | adk | 2.7.4.3 | F | adenylate kinase | |
NECFGCCN_04976 | 8.4e-182 | ytmO | C | Luciferase Family | ||
NECFGCCN_04977 | 2.4e-206 | yxeP | 3.5.1.32 | S | amidohydrolase | |
NECFGCCN_04978 | 6.9e-253 | moxC | C | monooxygenase | ||
NECFGCCN_04979 | 2e-169 | fliY_4 | ET | ABC transporter substrate-binding protein | ||
NECFGCCN_04980 | 3.8e-90 | K | N-acetyltransferase | |||
NECFGCCN_04981 | 3.9e-157 | P | amino acid ABC transporter | |||
NECFGCCN_04982 | 4.5e-12 | gluA | 3.6.3.21 | E | (ABC) transporter | |
NECFGCCN_04983 | 2.6e-10 | |||||
NECFGCCN_04986 | 6.3e-57 | trpB | 4.2.1.20 | E | The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine | |
NECFGCCN_04988 | 3.4e-141 | hdfR | K | Negatively regulates the transcription of the flagellar master operon flhDC by binding to the upstream region of the operon | ||
NECFGCCN_04989 | 2.2e-46 | yifE | S | protein conserved in bacteria | ||
NECFGCCN_04990 | 1.5e-158 | comM | O | ATPase with chaperone activity | ||
NECFGCCN_04991 | 4.8e-100 | comM | O | ATPase with chaperone activity | ||
NECFGCCN_04992 | 0.0 | ilvG | 2.2.1.6 | H | acetolactate synthase | |
NECFGCCN_04993 | 3.2e-37 | ilvM | 2.2.1.6 | S | acetolactate synthase | |
NECFGCCN_04994 | 1.3e-176 | ilvE | 2.6.1.21, 2.6.1.42 | E | Belongs to the class-IV pyridoxal-phosphate-dependent aminotransferase family | |
NECFGCCN_04995 | 0.0 | ilvD | 4.2.1.9 | EG | Belongs to the IlvD Edd family | |
NECFGCCN_04996 | 1.1e-294 | ilvA | 4.3.1.15, 4.3.1.19 | E | Catalyzes the anaerobic formation of alpha-ketobutyrate and ammonia from threonine in a two-step reaction. The first step involved a dehydration of threonine and a production of enamine intermediates (aminocrotonate), which tautomerizes to its imine form (iminobutyrate). Both intermediates are unstable and short- lived. The second step is the nonenzymatic hydrolysis of the enamine imine intermediates to form 2-ketobutyrate and free ammonia. In the low water environment of the cell, the second step is accelerated by RidA | |
NECFGCCN_04997 | 7.5e-166 | ilvY | K | transcriptional regulator | ||
NECFGCCN_04998 | 5.7e-280 | ilvC | 1.1.1.86 | EH | Involved in the biosynthesis of branched-chain amino acids (BCAA). Catalyzes an alkyl-migration followed by a ketol- acid reduction of (S)-2-acetolactate (S2AL) to yield (R)-2,3- dihydroxy-isovalerate. In the isomerase reaction, S2AL is rearranged via a Mg-dependent methyl migration to produce 3- hydroxy-3-methyl-2-ketobutyrate (HMKB). In the reductase reaction, this 2-ketoacid undergoes a metal-dependent reduction by NADPH to yield (R)-2,3-dihydroxy-isovalerate | |
NECFGCCN_04999 | 3.8e-47 | ppiC | 5.2.1.8 | G | peptidylprolyl isomerase | |
NECFGCCN_05000 | 2.3e-44 | ppiC | 5.2.1.8 | G | PPIC-type PPIASE domain | |
NECFGCCN_05001 | 0.0 | rep | 3.6.4.12 | L | it can initiate unwinding at a nick in the DNA. It binds to the single-stranded DNA and acts in a progressive fashion along the DNA in the 3' to 5' direction | |
NECFGCCN_05002 | 5.5e-119 | S | Protein of unknown function (DUF554) | |||
NECFGCCN_05003 | 4.7e-193 | 4.1.1.46 | S | metal-dependent hydrolase of the TIM-barrel fold | ||
NECFGCCN_05004 | 4.1e-167 | K | Transcriptional regulator | |||
NECFGCCN_05005 | 1.5e-259 | gppA | 3.6.1.11, 3.6.1.40 | FP | Catalyzes the conversion of pppGpp to ppGpp. Guanosine pentaphosphate (pppGpp) is a cytoplasmic signaling molecule which together with ppGpp controls the stringent response , an adaptive process that allows bacteria to respond to amino acid starvation, resulting in the coordinated regulation of numerous cellular activities | |
NECFGCCN_05006 | 1.1e-239 | rhlB | 3.6.4.13 | JKL | DEAD-box RNA helicase involved in | |
NECFGCCN_05007 | 4.7e-57 | trxA | O | Belongs to the thioredoxin family | ||
NECFGCCN_05008 | 8.2e-235 | rho | K | Facilitates transcription termination by a mechanism that involves Rho binding to the nascent RNA, activation of Rho's RNA-dependent ATPase activity, and release of the mRNA from the DNA template | ||
NECFGCCN_05009 | 4.6e-181 | wecA | 2.7.8.33, 2.7.8.35, 5.1.3.14 | M | Catalyzes the transfer of the GlcNAc-1-phosphate moiety from UDP-GlcNAc onto the carrier lipid undecaprenyl phosphate (C55-P), yielding GlcNAc-pyrophosphoryl-undecaprenyl (GlcNAc-PP- C55) | |
NECFGCCN_05010 | 1.9e-189 | wzzE | M | Modulates the polysaccharide chain length of enterobacterial common antigen (ECA) | ||
NECFGCCN_05011 | 1.5e-208 | wecB | 5.1.3.14 | M | Catalyzes the reversible epimerization at C-2 of UDP-N- acetylglucosamine (UDP-GlcNAc) and thereby provides bacteria with UDP-N-acetylmannosamine (UDP-ManNAc), the activated donor of ManNAc residues | |
NECFGCCN_05012 | 5.7e-236 | wecC | 1.1.1.336 | M | Belongs to the UDP-glucose GDP-mannose dehydrogenase family | |
NECFGCCN_05013 | 3.1e-203 | rffG | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
NECFGCCN_05014 | 2.5e-169 | rfbA | 2.7.7.24 | H | Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis | |
NECFGCCN_05015 | 3.5e-115 | wecD | 2.3.1.210 | K | Catalyzes the acetylation of dTDP-fucosamine (dTDP-4- amino-4,6-dideoxy-D-galactose) to dTDP-Fuc4NAc, which is utilized in the biosynthesis of the enterobacterial common antigen (ECA) | |
NECFGCCN_05016 | 1.2e-197 | wecE | 2.6.1.59 | E | Catalyzes the synthesis of dTDP-4-amino-4,6-dideoxy-D- galactose (dTDP-Fuc4N) from dTDP-4-keto-6-deoxy-D-glucose (dTDP-D- Glc4O) and L-glutamate | |
NECFGCCN_05017 | 4.6e-222 | wzxE | U | Mediates the transbilayer movement of Und-PP-GlcNAc- ManNAcA-Fuc4NAc (lipid III) from the inner to the outer leaflet of the cytoplasmic membrane during the assembly of enterobacterial common antigen (ECA) | ||
NECFGCCN_05018 | 7.5e-205 | rffT | 2.4.1.325 | GT56 | C | Catalyzes the synthesis of Und-PP-GlcNAc-ManNAcA-Fuc4NAc (Lipid III), the third lipid-linked intermediate involved in ECA synthesis |
NECFGCCN_05019 | 1.5e-250 | wzyE | S | Probably involved in the polymerization of enterobacterial common antigen (ECA) trisaccharide repeat units | ||
NECFGCCN_05020 | 7.1e-138 | rffM | 2.4.1.180, 2.4.1.187 | GT26 | M | Catalyzes the synthesis of Und-PP-GlcNAc-ManNAcA (Lipid II), the second lipid-linked intermediate involved in enterobacterial common antigen (ECA) synthesis |
NECFGCCN_05021 | 4.2e-256 | yifK | E | 'involved in the transport across the cytoplasmic membrane of D-alanine, D-serine and glycine' | ||
NECFGCCN_05024 | 6.8e-178 | yegQ | O | Peptidase U32 | ||
NECFGCCN_05025 | 7.5e-252 | yegQ | O | Peptidase U32 | ||
NECFGCCN_05026 | 7.5e-52 | S | CHY zinc finger | |||
NECFGCCN_05027 | 7.9e-86 | bioY | S | biotin synthase | ||
NECFGCCN_05029 | 1.1e-33 | XK27_12190 | S | protein conserved in bacteria | ||
NECFGCCN_05030 | 2.4e-232 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
NECFGCCN_05031 | 4.8e-11 | |||||
NECFGCCN_05032 | 3.1e-13 | |||||
NECFGCCN_05033 | 5.4e-286 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
NECFGCCN_05034 | 4.3e-32 | M | LysM domain | |||
NECFGCCN_05035 | 1.1e-18 | V | Glucan-binding protein C | |||
NECFGCCN_05037 | 7.1e-83 | S | RES domain protein | |||
NECFGCCN_05038 | 1.6e-76 | S | Protein of unknown function (DUF2384) | |||
NECFGCCN_05039 | 2.8e-23 | umuC | 2.7.7.7 | L | Binds processed UmuD protein to form functional DNA pol V (UmuD'2UmuC) | |
NECFGCCN_05040 | 7.7e-10 | fecB | P | Periplasmic binding protein | ||
NECFGCCN_05041 | 0.0 | fecA | P | receptor | ||
NECFGCCN_05042 | 5.5e-84 | fecR | PT | Fe2 -dicitrate sensor, membrane component | ||
NECFGCCN_05043 | 8.7e-82 | fecI | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
NECFGCCN_05044 | 1e-94 | yedA | EG | of the drug metabolite transporter (DMT) superfamily | ||
NECFGCCN_05045 | 6.9e-107 | wrbA | 1.6.5.2 | S | Belongs to the WrbA family | |
NECFGCCN_05046 | 2e-35 | yccJ | S | YccJ-like protein | ||
NECFGCCN_05047 | 1.9e-236 | agp | 3.1.3.10 | S | Acid phosphatase | |
NECFGCCN_05048 | 3e-78 | K | transcriptional regulator | |||
NECFGCCN_05049 | 7.9e-135 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
NECFGCCN_05050 | 3.3e-30 | |||||
NECFGCCN_05051 | 9.4e-11 | |||||
NECFGCCN_05052 | 4.5e-258 | puuP | E | Amino Acid | ||
NECFGCCN_05054 | 7.5e-120 | puuA | 6.3.1.11, 6.3.1.2 | E | glutamine synthetase | |
NECFGCCN_05055 | 6.2e-169 | yeiH | S | Membrane | ||
NECFGCCN_05056 | 9.3e-127 | mur1 | 3.4.17.14, 3.5.1.28 | NU | muramidase | |
NECFGCCN_05057 | 6.1e-93 | XK27_05000 | S | metal cluster binding | ||
NECFGCCN_05058 | 0.0 | V | ABC transporter (permease) | |||
NECFGCCN_05059 | 7.1e-133 | macB2 | V | ABC transporter, ATP-binding protein | ||
NECFGCCN_05060 | 6.5e-166 | T | Histidine kinase | |||
NECFGCCN_05061 | 3.3e-115 | pgm6 | 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase | |
NECFGCCN_05062 | 1.1e-80 | ybaK | S | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
NECFGCCN_05063 | 1.9e-137 | XK27_00880 | 3.4.17.14, 3.5.1.28 | M | Glycosyl hydrolase, family 25 | |
NECFGCCN_05064 | 3.8e-44 | gatB | 6.1.1.12, 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | |
NECFGCCN_05065 | 1.9e-267 | gatA | 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Gln-tRNA(Gln) through the transamidation of misacylated Glu-tRNA(Gln) in organisms which lack glutaminyl-tRNA synthetase. The reaction takes place in the presence of glutamine and ATP through an activated gamma-phospho-Glu-tRNA(Gln) | |
NECFGCCN_05066 | 1.4e-47 | gatC | 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | |
NECFGCCN_05067 | 1.3e-54 | tagE | 2.4.1.52 | GT4 | M | transferase activity, transferring glycosyl groups |
NECFGCCN_05068 | 2.7e-193 | ascB | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
NECFGCCN_05070 | 4.1e-107 | dtpB | U | Proton-dependent permease that transports di- and tripeptides | ||
NECFGCCN_05071 | 2e-135 | rsmJ | 2.1.1.242 | J | Specifically methylates the guanosine in position 1516 of 16S rRNA | |
NECFGCCN_05072 | 0.0 | prlC | 3.4.15.5, 3.4.24.70 | E | oligopeptidase | |
NECFGCCN_05073 | 2.6e-228 | phoC | I | phosphoesterase, PA-phosphatase | ||
NECFGCCN_05074 | 3.2e-158 | rlmJ | 2.1.1.266 | H | Specifically methylates the adenine in position 2030 of 23S rRNA | |
NECFGCCN_05075 | 1.2e-263 | gor | 1.8.1.7 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
NECFGCCN_05076 | 6.7e-121 | gst8 | 2.5.1.18 | O | Glutathione S-Transferase | |
NECFGCCN_05077 | 9.9e-206 | eutG | 1.1.1.1, 4.3.3.7 | C | alcohol dehydrogenase | |
NECFGCCN_05078 | 0.0 | treF | 3.2.1.28 | GH37 | G | Provides the cells with the ability to utilize trehalose at high osmolarity by splitting it into glucose molecules that can subsequently be taken up by the phosphotransferase-mediated uptake system |
NECFGCCN_05079 | 3.3e-100 | J | Acetyltransferases, including N-acetylases of ribosomal proteins | |||
NECFGCCN_05080 | 8.4e-134 | IQ | short-chain dehydrogenase | |||
NECFGCCN_05081 | 8.9e-167 | yhjC | K | transcriptional regulator | ||
NECFGCCN_05082 | 7.5e-186 | yhjD | S | Membrane | ||
NECFGCCN_05083 | 3e-235 | yhjE | EGP | Major facilitator superfamily | ||
NECFGCCN_05084 | 0.0 | yhjG | M | protein involved in outer membrane biogenesis | ||
NECFGCCN_05085 | 4.7e-171 | kdgK | 2.7.1.45 | G | COG0524 Sugar kinases, ribokinase family | |
NECFGCCN_05086 | 1.9e-283 | yhjJ | S | Peptidase, M16 | ||
NECFGCCN_05087 | 1e-224 | dctA | U | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
NECFGCCN_05088 | 0.0 | yhjK | T | the EAL-domain portion of HmsP from Y. pestis shows phosphodiesterase activity which is required for the inhibition of biofilm formation | ||
NECFGCCN_05089 | 0.0 | M | Cellulose synthase | |||
NECFGCCN_05090 | 2.3e-212 | bcsZ | 3.2.1.4 | GH5,GH8,GH9 | G | Belongs to the glycosyl hydrolase 8 (cellulase D) family |
NECFGCCN_05091 | 0.0 | bcsB | M | Cellulose synthase | ||
NECFGCCN_05092 | 0.0 | bcsA | 2.4.1.12 | GT2 | M | Cellulose synthase |
NECFGCCN_05093 | 3.7e-131 | yhjQ | D | Cellulose synthase | ||
NECFGCCN_05094 | 5.8e-28 | yhjR | S | Cellulose biosynthesis protein BcsR | ||
NECFGCCN_05095 | 4.5e-291 | bcsE | S | cellulose biosynthesis protein BcsE | ||
NECFGCCN_05096 | 1.5e-26 | bcsF | S | Cellulose biosynthesis protein BcsF | ||
NECFGCCN_05097 | 2.6e-281 | kbaA | 2.7.8.42, 2.7.8.43 | S | cellulose synthase operon protein YhjU | |
NECFGCCN_05098 | 1.6e-193 | celC | 3.2.1.4 | GH8 | G | Belongs to the glycosyl hydrolase 8 (cellulase D) family |
NECFGCCN_05099 | 3.6e-57 | bcsD | S | cellulose synthase | ||
NECFGCCN_05100 | 1.7e-11 | bcsD | S | cellulose synthase | ||
NECFGCCN_05101 | 0.0 | M | Cellulose synthase | |||
NECFGCCN_05102 | 0.0 | bcsB | NU | cellulose synthase | ||
NECFGCCN_05103 | 0.0 | bcsA | 2.4.1.12 | GT2 | M | Cellulose synthase |
NECFGCCN_05104 | 1.5e-144 | yhjQ | D | cellulose synthase operon protein YhjQ | ||
NECFGCCN_05105 | 2.4e-42 | S | Cellulose biosynthesis protein BcsO | |||
NECFGCCN_05106 | 1.7e-190 | dppF | P | Belongs to the ABC transporter superfamily | ||
NECFGCCN_05107 | 1.7e-182 | dppD | 3.6.3.24 | P | Belongs to the ABC transporter superfamily | |
NECFGCCN_05108 | 2.1e-131 | dppC | P | PFAM binding-protein-dependent transport systems inner membrane component | ||
NECFGCCN_05109 | 1.7e-185 | dppB | P | PFAM binding-protein-dependent transport systems inner membrane component | ||
NECFGCCN_05110 | 0.0 | dppA | E | ABC-Type Dipeptide Transport System Periplasmic Component | ||
NECFGCCN_05111 | 8.5e-108 | dtpA | U | Proton-dependent permease that transports di- and tripeptides | ||
NECFGCCN_05112 | 1.3e-105 | gst | 2.5.1.18 | O | Belongs to the GST superfamily | |
NECFGCCN_05113 | 3.5e-160 | pdxY | 2.7.1.35 | H | Pyridoxal kinase involved in the salvage pathway of pyridoxal 5'-phosphate (PLP). Catalyzes the phosphorylation of pyridoxal to PLP | |
NECFGCCN_05114 | 2.1e-246 | tyrS | 6.1.1.1 | J | Catalyzes the attachment of tyrosine to tRNA(Tyr) in a two-step reaction tyrosine is first activated by ATP to form Tyr- AMP and then transferred to the acceptor end of tRNA(Tyr) | |
NECFGCCN_05115 | 9e-124 | pdxH | 1.4.3.5 | H | Catalyzes the oxidation of either pyridoxine 5'- phosphate (PNP) or pyridoxamine 5'-phosphate (PMP) into pyridoxal 5'-phosphate (PLP) | |
NECFGCCN_05116 | 3.1e-54 | mliC | S | membrane-bound lysozyme inhibitor of c-type lysozyme | ||
NECFGCCN_05117 | 1.1e-211 | anmK | 2.7.1.170, 4.2.1.126 | F | Catalyzes the specific phosphorylation of 1,6-anhydro-N- acetylmuramic acid (anhMurNAc) with the simultaneous cleavage of the 1,6-anhydro ring, generating MurNAc-6-P. Is required for the utilization of anhMurNAc either imported from the medium or derived from its own cell wall murein, and thus plays a role in cell wall recycling | |
NECFGCCN_05118 | 1.3e-52 | slyB | M | Outer Membrane Lipoprotein | ||
NECFGCCN_05119 | 7.3e-197 | T | Diguanylate cyclase | |||
NECFGCCN_05120 | 6.8e-72 | slyA | K | Transcription regulator that can specifically activate or repress expression of target genes | ||
NECFGCCN_05121 | 4.3e-36 | ydhI | S | Protein of unknown function (DUF1656) | ||
NECFGCCN_05122 | 1.9e-137 | ydhJ | V | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | ||
NECFGCCN_05123 | 0.0 | ydhK | S | Fusaric acid resistance protein | ||
NECFGCCN_05124 | 1.3e-90 | sodC | 1.15.1.1 | P | Destroys radicals which are normally produced within the cells and which are toxic to biological systems | |
NECFGCCN_05125 | 1.8e-167 | ydhF | S | Aldo Keto reductase | ||
NECFGCCN_05126 | 4.2e-39 | ydhL | S | Fe-S protein | ||
NECFGCCN_05127 | 4.5e-106 | nemR | K | transcriptional regulator | ||
NECFGCCN_05128 | 2.6e-205 | nemA | C | nadh flavin | ||
NECFGCCN_05129 | 2.4e-71 | gloA | 4.4.1.5 | E | Catalyzes the conversion of hemimercaptal, formed from methylglyoxal and glutathione, to S-lactoylglutathione | |
NECFGCCN_05130 | 2.4e-121 | rnt | L | Trims short 3' overhangs of a variety of RNA species, leaving a one or two nucleotide 3' overhang. Responsible for the end-turnover of tRNA specifically removes the terminal AMP residue from uncharged tRNA (tRNA-C-C-A). Also appears to be involved in tRNA biosynthesis | ||
NECFGCCN_05131 | 3.3e-61 | grxD | C | Belongs to the glutaredoxin family. Monothiol subfamily | ||
NECFGCCN_05132 | 2.2e-122 | ydhO | 3.2.1.14, 3.4.17.13 | GH18 | M | COG0791 Cell wall-associated hydrolases (invasion-associated proteins) |
NECFGCCN_05133 | 5.3e-73 | K | Transcriptional regulator | |||
NECFGCCN_05134 | 1.4e-109 | sodB | 1.15.1.1, 3.1.11.6 | C | Destroys radicals which are normally produced within the cells and which are toxic to biological systems | |
NECFGCCN_05135 | 2.7e-36 | |||||
NECFGCCN_05136 | 1.3e-45 | S | Protein of unknown function with HXXEE motif | |||
NECFGCCN_05137 | 7.7e-64 | dltA | 6.1.1.13 | Q | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
NECFGCCN_05138 | 1.1e-60 | |||||
NECFGCCN_05139 | 1.5e-189 | bdhA | 1.1.1.303, 1.1.1.4 | E | Dehydrogenase | |
NECFGCCN_05141 | 6.2e-51 | spd | F | DNA RNA non-specific endonuclease | ||
NECFGCCN_05142 | 5.6e-247 | serS | 6.1.1.11 | J | Catalyzes the attachment of serine to tRNA(Ser). Is also able to aminoacylate tRNA(Sec) with serine, to form the misacylated tRNA L-seryl-tRNA(Sec), which will be further converted into selenocysteinyl-tRNA(Sec) | |
NECFGCCN_05143 | 4.2e-253 | rarA | L | ATPase related to the helicase subunit of the Holliday junction resolvase | ||
NECFGCCN_05144 | 2.3e-113 | lolA | M | Participates in the translocation of lipoproteins from the inner membrane to the outer membrane. Only forms a complex with a lipoprotein if the residue after the N-terminal Cys is not an aspartate (The Asp acts as a targeting signal to indicate that the lipoprotein should stay in the inner membrane) | ||
NECFGCCN_05145 | 0.0 | ftsK | D | PFAM cell divisionFtsK SpoIIIE | ||
NECFGCCN_05146 | 2.5e-65 | copY | K | Copper transport repressor, CopY TcrY family | ||
NECFGCCN_05147 | 5.8e-230 | ycdB | P | peroxidase | ||
NECFGCCN_05148 | 5.1e-143 | ycdO | P | periplasmic lipoprotein involved in iron transport | ||
NECFGCCN_05149 | 0.0 | pulA | 3.2.1.1, 3.2.1.41 | CBM48,GH13 | G | belongs to the glycosyl hydrolase 13 family |
NECFGCCN_05150 | 6.5e-19 | agrA | KT | phosphorelay signal transduction system | ||
NECFGCCN_05151 | 2.4e-112 | leuD | 4.2.1.33, 4.2.1.35 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
NECFGCCN_05152 | 1.1e-143 | leuC | 4.2.1.33, 4.2.1.35 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
NECFGCCN_05153 | 6.7e-270 | uvrX | 2.7.7.7 | L | Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII | |
NECFGCCN_05154 | 1.8e-44 | |||||
NECFGCCN_05155 | 4.2e-189 | adhP | 1.1.1.1 | C | alcohol dehydrogenase | |
NECFGCCN_05156 | 2.1e-48 | G | COG0477 Permeases of the major facilitator superfamily | |||
NECFGCCN_05157 | 2e-163 | vllY | 1.13.11.27 | E | 4-hydroxyphenylpyruvate dioxygenase | |
NECFGCCN_05158 | 4.5e-52 | K | transcriptional regulator, PadR family | |||
NECFGCCN_05159 | 3.4e-58 | XK27_06920 | S | Protein of unknown function (DUF1700) | ||
NECFGCCN_05160 | 2.7e-101 | S | Putative adhesin | |||
NECFGCCN_05161 | 1.2e-138 | XK27_06930 | V | domain protein | ||
NECFGCCN_05162 | 7.6e-69 | cpoB | 3.5.1.28 | D | Mediates coordination of peptidoglycan synthesis and outer membrane constriction during cell division | |
NECFGCCN_05163 | 3.6e-75 | pal | M | Belongs to the ompA family | ||
NECFGCCN_05164 | 3e-155 | tolB | U | involved in the tonB-independent uptake of proteins | ||
NECFGCCN_05165 | 8.7e-46 | tolA | M | Membrane protein involved in colicin uptake | ||
NECFGCCN_05166 | 1.2e-68 | tolR | U | biopolymer transport protein | ||
NECFGCCN_05167 | 2.9e-117 | tolQ | U | MotA TolQ ExbB proton channel | ||
NECFGCCN_05168 | 1.6e-67 | ybgC | S | Thioesterase | ||
NECFGCCN_05169 | 2.8e-45 | ybgE | S | cyd operon protein YbgE | ||
NECFGCCN_05170 | 3.1e-11 | ybgT | 1.10.3.14 | S | Cyd operon protein YbgT | |
NECFGCCN_05171 | 5e-215 | cydB | 1.10.3.14 | C | cytochrome d ubiquinol oxidase, subunit | |
NECFGCCN_05172 | 1.1e-294 | cydA | 1.10.3.14 | C | oxidase, subunit | |
NECFGCCN_05173 | 8.6e-159 | sucD | 6.2.1.5 | C | Succinyl-CoA synthetase functions in the citric acid cycle (TCA), coupling the hydrolysis of succinyl-CoA to the synthesis of either ATP or GTP and thus represents the only step of substrate-level phosphorylation in the TCA. The alpha subunit of the enzyme binds the substrates coenzyme A and phosphate, while succinate binding and nucleotide specificity is provided by the beta subunit | |
NECFGCCN_05174 | 1.2e-216 | sucC | 6.2.1.5 | F | Succinyl-CoA synthetase functions in the citric acid cycle (TCA), coupling the hydrolysis of succinyl-CoA to the synthesis of either ATP or GTP and thus represents the only step of substrate-level phosphorylation in the TCA. The beta subunit provides nucleotide specificity of the enzyme and binds the substrate succinate, while the binding sites for coenzyme A and phosphate are found in the alpha subunit | |
NECFGCCN_05175 | 2.4e-207 | sucB | 2.3.1.61 | C | The 2-oxoglutarate dehydrogenase complex catalyzes the overall conversion of 2-oxoglutarate to succinyl-CoA and CO(2) | |
NECFGCCN_05176 | 0.0 | sucA | 1.2.4.2, 4.1.1.71 | C | Dehydrogenase E1 component | |
NECFGCCN_05177 | 3.7e-139 | sdhB | 1.3.5.1, 1.3.5.4 | C | Belongs to the succinate dehydrogenase fumarate reductase iron-sulfur protein family | |
NECFGCCN_05178 | 0.0 | sdhA | 1.3.5.1, 1.3.5.4 | C | Belongs to the FAD-dependent oxidoreductase 2 family. FRD SDH subfamily | |
NECFGCCN_05179 | 3.3e-53 | sdhD | C | Succinate dehydrogenase hydrophobic membrane anchor subunit | ||
NECFGCCN_05180 | 1.2e-65 | sdhC | C | succinate dehydrogenase | ||
NECFGCCN_05181 | 7e-250 | gltA | 2.3.3.1 | C | Belongs to the citrate synthase family | |
NECFGCCN_05182 | 2e-138 | nei | 4.2.99.18 | L | Involved in base excision repair of DNA damaged by oxidation or by mutagenic agents. Acts as DNA glycosylase that recognizes and removes damaged bases. Has a preference for oxidized pyrimidines, such as thymine glycol, 5,6-dihydrouracil and 5,6-dihydrothymine. Has AP (apurinic apyrimidinic) lyase activity and introduces nicks in the DNA strand. Cleaves the DNA backbone by beta-delta elimination to generate a single-strand break at the site of the removed base with both 3'- and 5'- phosphates | |
NECFGCCN_05183 | 6.9e-113 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
NECFGCCN_05184 | 4.3e-178 | S | Protein of unknown function (DUF979) | |||
NECFGCCN_05185 | 4.5e-129 | S | Protein of unknown function (DUF969) | |||
NECFGCCN_05186 | 8.5e-131 | ybgL | S | Belongs to the UPF0271 (lamB) family | ||
NECFGCCN_05187 | 1.4e-178 | ybgK | 3.5.1.54, 6.3.4.6 | E | Allophanate hydrolase subunit 2 | |
NECFGCCN_05188 | 2.4e-121 | kipI | 3.5.1.54 | E | Allophanate hydrolase subunit 1 | |
NECFGCCN_05189 | 5e-139 | ybgI | 3.5.4.16 | S | metal-binding protein | |
NECFGCCN_05190 | 1.6e-123 | dtpD | U | Proton-dependent permease that transports di- and tripeptides | ||
NECFGCCN_05191 | 2.3e-23 | dtpD | U | Proton-dependent permease that transports di- and tripeptides | ||
NECFGCCN_05192 | 2.8e-235 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
NECFGCCN_05193 | 2.9e-119 | ung | 3.2.2.27 | L | Excises uracil residues from the DNA which can arise as a result of misincorporation of dUMP residues by DNA polymerase or due to deamination of cytosine | |
NECFGCCN_05194 | 7.6e-184 | pelG | M | Putative exopolysaccharide Exporter (EPS-E) | ||
NECFGCCN_05195 | 1e-273 | pelF | GT4 | M | Domain of unknown function (DUF3492) | |
NECFGCCN_05196 | 0.0 | S | Uncharacterised protein conserved in bacteria (DUF2194) | |||
NECFGCCN_05197 | 2.7e-147 | |||||
NECFGCCN_05198 | 3.7e-206 | 5.1.3.2 | GM | Psort location CytoplasmicMembrane, score | ||
NECFGCCN_05199 | 7e-172 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
NECFGCCN_05200 | 7.5e-152 | nadK | 2.7.1.23 | H | Involved in the regulation of the intracellular balance of NAD and NADP, and is a key enzyme in the biosynthesis of NADP. Catalyzes specifically the phosphorylation on 2'-hydroxyl of the adenosine moiety of NAD to yield NADP | |
NECFGCCN_05201 | 2.1e-120 | yjbM | 2.7.6.5 | S | Gtp pyrophosphokinase | |
NECFGCCN_05202 | 2.4e-101 | yjbK | S | Adenylate cyclase | ||
NECFGCCN_05203 | 8.7e-176 | prs | 2.7.6.1 | F | Involved in the biosynthesis of the central metabolite phospho-alpha-D-ribosyl-1-pyrophosphate (PRPP) via the transfer of pyrophosphoryl group from ATP to 1-hydroxyl of ribose-5-phosphate (Rib-5-P) | |
NECFGCCN_05204 | 9.8e-208 | iscS | 2.8.1.7 | E | Cysteine desulfurase | |
NECFGCCN_05205 | 8.2e-60 | XK27_04120 | S | Putative amino acid metabolism | ||
NECFGCCN_05206 | 1.9e-118 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
NECFGCCN_05207 | 4.4e-129 | puuD | T | peptidase C26 | ||
NECFGCCN_05208 | 9e-119 | radC | E | Belongs to the UPF0758 family | ||
NECFGCCN_05209 | 2.3e-53 | |||||
NECFGCCN_05210 | 4.2e-198 | yhhJ | V | ABC-type multidrug transport system, permease component | ||
NECFGCCN_05211 | 0.0 | rbbA | V | (ABC) transporter | ||
NECFGCCN_05212 | 5.3e-134 | yhiI | M | Secretion protein | ||
NECFGCCN_05213 | 2e-266 | dosC | 2.7.7.65 | T | Diguanylate cyclase | |
NECFGCCN_05214 | 1.9e-181 | trpS | 6.1.1.2 | J | Tryptophanyl-tRNA synthetase | |
NECFGCCN_05215 | 1.6e-169 | lsrB_2 | G | (ABC) transporter | ||
NECFGCCN_05216 | 1.1e-233 | 3.6.3.17 | G | ABC transporter | ||
NECFGCCN_05217 | 5.3e-157 | U | Branched-chain amino acid transport system / permease component | |||
NECFGCCN_05218 | 3.2e-154 | U | Branched-chain amino acid transport system / permease component | |||
NECFGCCN_05219 | 1.7e-153 | nqo1 | 1.6.5.2 | S | NADPH dehydrogenase | |
NECFGCCN_05220 | 6.7e-154 | syrM1 | K | transcriptional regulator | ||
NECFGCCN_05221 | 1.3e-75 | fosB | 2.5.1.18 | E | Glutathione transferase | |
NECFGCCN_05222 | 5e-10 | S | Protein of unknown function (DUF4059) | |||
NECFGCCN_05223 | 2.1e-171 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
NECFGCCN_05224 | 2.5e-92 | rsmD | 2.1.1.171 | L | Methyltransferase | |
NECFGCCN_05225 | 5e-87 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
NECFGCCN_05226 | 6e-186 | ylbL | T | Belongs to the peptidase S16 family | ||
NECFGCCN_05227 | 1e-181 | yhcC | S | radical SAM protein | ||
NECFGCCN_05228 | 9.4e-95 | ytqB | 2.1.1.176 | J | (SAM)-dependent | |
NECFGCCN_05230 | 0.0 | yjcE | P | NhaP-type Na H and K H antiporters | ||
NECFGCCN_05231 | 1.6e-79 | L | reverse transcriptase | |||
NECFGCCN_05232 | 2.8e-122 | ydiJ | C | Fad linked oxidase | ||
NECFGCCN_05233 | 3.2e-71 | menI | 3.1.2.28 | Q | Catalyzes the hydrolysis of 1,4-dihydroxy-2-naphthoyl- CoA (DHNA-CoA) to 1,4-dihydroxy-2-naphthoate (DHNA) | |
NECFGCCN_05234 | 7e-37 | yeaQ | S | transglycosylase associated protein | ||
NECFGCCN_05235 | 2.4e-292 | yfhM | P | Large extracellular alpha-helical protein | ||
NECFGCCN_05236 | 0.0 | pbpC | 2.4.1.129 | GT51 | M | penicillin-binding protein 1C |
NECFGCCN_05237 | 8.5e-75 | ndk | 2.7.4.6 | F | Major role in the synthesis of nucleoside triphosphates other than ATP. The ATP gamma phosphate is transferred to the NDP beta phosphate via a ping-pong mechanism, using a phosphorylated active-site intermediate | |
NECFGCCN_05238 | 7.9e-132 | srtA | 3.4.22.70 | M | Sortase (surface protein transpeptidase) | |
NECFGCCN_05239 | 8.3e-100 | gyrA | 5.99.1.3 | L | A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner | |
NECFGCCN_05240 | 4.9e-38 | S | oxidoreductase | |||
NECFGCCN_05241 | 6.2e-48 | XK27_09445 | S | Domain of unknown function (DUF1827) | ||
NECFGCCN_05242 | 2.2e-84 | mutT | 3.5.4.33, 3.6.1.13, 3.6.1.55 | L | Belongs to the Nudix hydrolase family | |
NECFGCCN_05243 | 0.0 | clpE | O | Belongs to the ClpA ClpB family | ||
NECFGCCN_05244 | 2e-180 | argF | 2.1.3.3 | E | Reversibly catalyzes the transfer of the carbamoyl group from carbamoyl phosphate (CP) to the N(epsilon) atom of ornithine (ORN) to produce L-citrulline | |
NECFGCCN_05245 | 1e-34 | ykuJ | S | protein conserved in bacteria | ||
NECFGCCN_05246 | 1.7e-117 | WQ51_01820 | P | Binding-protein-dependent transport system inner membrane component | ||
NECFGCCN_05247 | 9.3e-130 | glnQ | 3.6.3.21 | E | abc transporter atp-binding protein | |
NECFGCCN_05248 | 1.6e-77 | feoA | P | FeoA domain protein | ||
NECFGCCN_05249 | 0.0 | feoB | P | transporter of a GTP-driven Fe(2 ) uptake system | ||
NECFGCCN_05250 | 8.6e-08 | |||||
NECFGCCN_05251 | 6.1e-148 | I | Alpha/beta hydrolase family | |||
NECFGCCN_05252 | 3.1e-153 | folD | 1.5.1.5, 3.5.4.9 | F | Catalyzes the oxidation of 5,10- methylenetetrahydrofolate to 5,10-methenyltetrahydrofolate and then the hydrolysis of 5,10-methenyltetrahydrofolate to 10- formyltetrahydrofolate | |
NECFGCCN_05253 | 1.6e-155 | yjjU | I | esterase of the alpha-beta hydrolase superfamily | ||
NECFGCCN_05254 | 1.1e-125 | yjjV | L | Deoxyribonuclease | ||
NECFGCCN_05255 | 3.5e-209 | nupX | F | Belongs to the concentrative nucleoside transporter (CNT) (TC 2.A.41) family | ||
NECFGCCN_05256 | 6.8e-139 | deoC | 4.1.2.4 | F | Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate | |
NECFGCCN_05257 | 1.3e-238 | deoA | 2.4.2.2, 2.4.2.4 | F | The enzymes which catalyze the reversible phosphorolysis of pyrimidine nucleosides are involved in the degradation of these compounds and in their utilization as carbon and energy sources, or in the rescue of pyrimidine bases for nucleotide synthesis | |
NECFGCCN_05258 | 6.1e-243 | deoB | 5.4.2.7 | G | Phosphotransfer between the C1 and C5 carbon atoms of pentose | |
NECFGCCN_05259 | 2.9e-132 | ytgP | S | Membrane protein involved in the export of O-antigen and teichoic acid | ||
NECFGCCN_05260 | 0.0 | pacL | 3.6.3.8, 3.6.3.9 | P | cation transport ATPase | |
NECFGCCN_05261 | 1.2e-25 | metB | 2.5.1.48, 4.4.1.8 | E | cystathionine | |
NECFGCCN_05262 | 2.6e-155 | metB | 2.5.1.48, 4.4.1.8 | E | cystathionine | |
NECFGCCN_05263 | 3e-223 | malY | 4.4.1.8 | E | COG1168 Bifunctional PLP-dependent enzyme with beta-cystathionase and maltose regulon repressor activities | |
NECFGCCN_05264 | 1.1e-40 | 3.2.1.26, 3.2.1.65 | GH32 | G | Belongs to the glycosyl hydrolase 32 family | |
NECFGCCN_05265 | 2.6e-147 | 1.13.11.2 | S | glyoxalase | ||
NECFGCCN_05266 | 1.6e-97 | dppB_1 | P | Binding-protein-dependent transport systems inner membrane component | ||
NECFGCCN_05267 | 1.1e-161 | P | Binding-protein-dependent transport systems inner membrane component | |||
NECFGCCN_05268 | 8e-157 | oppD | 3.6.3.24 | EP | (ABC) transporter | |
NECFGCCN_05269 | 1.1e-136 | 3.6.3.24 | EP | (ABC) transporter | ||
NECFGCCN_05270 | 9.5e-169 | yegS | 2.7.1.107 | I | the in vivo substrate is | |
NECFGCCN_05271 | 3.2e-269 | yegQ | O | protease | ||
NECFGCCN_05272 | 2.3e-133 | K | response regulator | |||
NECFGCCN_05273 | 7.3e-259 | T | PhoQ Sensor | |||
NECFGCCN_05274 | 5.7e-253 | mdtD | EGP | Major facilitator superfamily | ||
NECFGCCN_05275 | 0.0 | mdtC | V | Belongs to the resistance-nodulation-cell division (RND) (TC 2.A.6) family | ||
NECFGCCN_05276 | 3.4e-62 | yhaI | J | Protein of unknown function (DUF805) | ||
NECFGCCN_05277 | 1.1e-162 | mvaA | 1.1.1.34, 1.1.1.88, 2.3.1.9 | C | Belongs to the HMG-CoA reductase family | |
NECFGCCN_05278 | 3e-78 | K | hmm pf08876 | |||
NECFGCCN_05279 | 1.2e-118 | yqfA | K | protein, Hemolysin III | ||
NECFGCCN_05280 | 6.7e-198 | S | Protein of unknown function (DUF3114) | |||
NECFGCCN_05281 | 7.7e-86 | S | hydrolases or acyltransferases (alpha beta hydrolase superfamily) | |||
NECFGCCN_05282 | 5.1e-202 | rpsA | 1.17.7.4 | J | ribosomal protein S1 | |
NECFGCCN_05285 | 6.4e-39 | pchB | 2.5.1.19, 4.2.1.10, 4.2.99.21, 5.4.99.5 | E | Chorismate mutase type II | |
NECFGCCN_05286 | 2e-255 | trpE | 4.1.3.27 | EH | Part of a heterotetrameric complex that catalyzes the two-step biosynthesis of anthranilate, an intermediate in the biosynthesis of L-tryptophan. In the first step, the glutamine- binding beta subunit (TrpG) of anthranilate synthase (AS) provides the glutamine amidotransferase activity which generates ammonia as a substrate that, along with chorismate, is used in the second step, catalyzed by the large alpha subunit of AS (TrpE) to produce anthranilate. In the absence of TrpG, TrpE can synthesize anthranilate directly from chorismate and high concentrations of ammonia | |
NECFGCCN_05287 | 3e-104 | trpG | 2.4.2.18, 2.6.1.85, 4.1.3.27 | EH | anthranilate | |
NECFGCCN_05288 | 8.7e-179 | trpD | 2.4.2.18, 4.1.3.27 | F | Catalyzes the transfer of the phosphoribosyl group of 5- phosphorylribose-1-pyrophosphate (PRPP) to anthranilate to yield N-(5'-phosphoribosyl)-anthranilate (PRA) | |
NECFGCCN_05289 | 3.6e-132 | trpC | 4.1.1.48, 5.3.1.24 | E | Belongs to the TrpC family | |
NECFGCCN_05290 | 4.3e-98 | trpF | 4.1.1.48, 4.2.1.160, 4.2.1.20, 5.3.1.24 | E | belongs to the TrpF family | |
NECFGCCN_05291 | 7.6e-230 | trpB | 4.2.1.20, 5.3.1.24 | E | The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine | |
NECFGCCN_05292 | 5.1e-142 | trpA | 4.2.1.20 | E | The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate | |
NECFGCCN_05294 | 8.1e-51 | parE | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
NECFGCCN_05296 | 0.0 | S | dextransucrase activity | |||
NECFGCCN_05297 | 2.1e-137 | tcyC2 | 3.6.3.21 | E | abc transporter atp-binding protein | |
NECFGCCN_05298 | 3e-40 | L | COG1943 Transposase and inactivated derivatives | |||
NECFGCCN_05301 | 4.7e-33 | ssb | L | Plays an important role in DNA replication, recombination and repair. Binds to ssDNA and to an array of partner proteins to recruit them to their sites of action during DNA metabolism | ||
NECFGCCN_05302 | 7.6e-23 | fruR | K | transcriptional | ||
NECFGCCN_05303 | 3e-44 | M | domain protein | |||
NECFGCCN_05304 | 3.8e-212 | salK | 2.7.13.3 | T | Histidine kinase | |
NECFGCCN_05305 | 3e-102 | salR | K | helix_turn_helix, Lux Regulon | ||
NECFGCCN_05306 | 2.1e-86 | vanY | 3.4.17.14, 3.5.1.28 | M | D-alanyl-D-alanine carboxypeptidase | |
NECFGCCN_05307 | 1.9e-116 | gltJ | P | ABC transporter (Permease | ||
NECFGCCN_05308 | 1.1e-110 | tcyB_2 | P | ABC transporter (permease) | ||
NECFGCCN_05309 | 2e-19 | L | transposase activity | |||
NECFGCCN_05310 | 1.9e-13 | |||||
NECFGCCN_05311 | 3.2e-121 | glnQ | 3.6.3.21 | E | abc transporter atp-binding protein | |
NECFGCCN_05312 | 2.6e-124 | btuF | P | (ABC) transporter | ||
NECFGCCN_05313 | 9.3e-43 | L | Integrase core domain | |||
NECFGCCN_05314 | 4.2e-83 | L | Integrase core domain | |||
NECFGCCN_05315 | 2.2e-212 | tkt | 2.2.1.1 | G | Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate | |
NECFGCCN_05317 | 2e-132 | agrA | KT | Response regulator of the LytR AlgR family | ||
NECFGCCN_05318 | 2.8e-192 | S | cobalamin synthesis protein | |||
NECFGCCN_05319 | 5.1e-256 | lamB | G | Maltoporin (phage lambda and maltose receptor) | ||
NECFGCCN_05320 | 0.0 | imd | 3.2.1.94 | GH27 | S | cellulase activity |
NECFGCCN_05321 | 1.4e-60 | M | NlpC/P60 family | |||
NECFGCCN_05322 | 5.7e-64 | |||||
NECFGCCN_05323 | 3.2e-75 | |||||
NECFGCCN_05325 | 1.8e-84 | M | tape measure protein | |||
NECFGCCN_05327 | 2.6e-07 | |||||
NECFGCCN_05328 | 1.8e-80 | K | BRO family, N-terminal domain | |||
NECFGCCN_05329 | 4.5e-78 | ant | K | BRO family, N-terminal domain | ||
NECFGCCN_05331 | 1.5e-110 | K | Helix-turn-helix domain | |||
NECFGCCN_05332 | 8.2e-31 | |||||
NECFGCCN_05333 | 5.9e-34 | |||||
NECFGCCN_05334 | 5.1e-43 | gepA | S | Protein of unknown function (DUF4065) | ||
NECFGCCN_05335 | 1.1e-119 | |||||
NECFGCCN_05336 | 6e-132 | N | domain, Protein | |||
NECFGCCN_05337 | 3.5e-64 | |||||
NECFGCCN_05338 | 1.9e-51 | |||||
NECFGCCN_05339 | 7.7e-61 | |||||
NECFGCCN_05340 | 8.6e-26 | |||||
NECFGCCN_05341 | 1.1e-62 | |||||
NECFGCCN_05342 | 2.5e-30 | |||||
NECFGCCN_05343 | 2.6e-186 | S | Linocin_M18 bacteriocin protein | |||
NECFGCCN_05344 | 7.8e-68 | |||||
NECFGCCN_05345 | 1.7e-225 | S | protein conserved in bacteria | |||
NECFGCCN_05347 | 3.1e-159 | S | head morphogenesis protein, SPP1 gp7 | |||
NECFGCCN_05348 | 6.1e-266 | S | Protein of unknown function (DUF1073) | |||
NECFGCCN_05349 | 3.8e-292 | S | Terminase | |||
NECFGCCN_05350 | 2.3e-82 | xtmA | L | terminase, small subunit | ||
NECFGCCN_05351 | 1.6e-10 | S | Uncharacterized small protein (DUF2158) | |||
NECFGCCN_05353 | 1.3e-44 | |||||
NECFGCCN_05354 | 7.7e-88 | S | Phage lysozyme | |||
NECFGCCN_05355 | 2.1e-32 | essD | S | Bacteriophage P21 holin S | ||
NECFGCCN_05360 | 5.2e-92 | |||||
NECFGCCN_05361 | 5e-16 | ylcG | ||||
NECFGCCN_05362 | 7.4e-64 | rusA | 3.1.22.4 | L | Endonuclease that resolves Holliday junction intermediates made during homologous genetic recombination and DNA repair. Exhibits sequence and structure-selective cleavage of four-way DNA junctions, where it introduces symmetrical nicks in two strands of the same polarity at the 5' side of dinucleotides. Corrects the defects in genetic recombination and DNA repair associated with inactivation of ruvAB or ruvC | |
NECFGCCN_05363 | 1e-47 | S | phage protein | |||
NECFGCCN_05364 | 4.4e-09 | S | NINE Protein | |||
NECFGCCN_05365 | 1.6e-106 | S | Protein of unknown function (DUF1367) | |||
NECFGCCN_05367 | 2e-23 | D | Protein of unknown function (DUF551) | |||
NECFGCCN_05368 | 1.1e-15 | |||||
NECFGCCN_05370 | 1.6e-28 | |||||
NECFGCCN_05371 | 8.4e-107 | yhdJ | 2.1.1.72 | L | DNA methylase | |
NECFGCCN_05372 | 2.3e-57 | S | exonuclease activity | |||
NECFGCCN_05373 | 1.3e-13 | |||||
NECFGCCN_05374 | 2.8e-16 | |||||
NECFGCCN_05375 | 8.7e-78 | S | DNA replication initiation | |||
NECFGCCN_05376 | 1.7e-43 | K | Helix-turn-helix domain | |||
NECFGCCN_05377 | 3.3e-30 | S | Bacteriophage CII protein | |||
NECFGCCN_05378 | 1.1e-28 | S | Putative antitoxin of bacterial toxin-antitoxin system, YdaS/YdaT | |||
NECFGCCN_05379 | 1.2e-88 | K | Peptidase S24-like | |||
NECFGCCN_05381 | 3.2e-10 | S | Predicted membrane protein (DUF2335) | |||
NECFGCCN_05382 | 2.2e-25 | |||||
NECFGCCN_05385 | 8.1e-31 | |||||
NECFGCCN_05386 | 2.4e-41 | |||||
NECFGCCN_05388 | 3.6e-48 | |||||
NECFGCCN_05389 | 5.4e-54 | L | YqaJ-like viral recombinase domain | |||
NECFGCCN_05390 | 1.4e-69 | |||||
NECFGCCN_05391 | 2.7e-120 | KT | Belongs to the MT-A70-like family | |||
NECFGCCN_05392 | 6.8e-28 | |||||
NECFGCCN_05393 | 2.2e-273 | ycjX | S | COG3106 Predicted ATPase | ||
NECFGCCN_05394 | 2.9e-31 | pspD | S | Phage Shock Protein | ||
NECFGCCN_05395 | 7.9e-58 | pspC | KT | phage shock protein C | ||
NECFGCCN_05396 | 1.4e-33 | pspB | S | Phage shock protein B | ||
NECFGCCN_05397 | 4.7e-64 | pspA | KT | Phage shock protein A | ||
NECFGCCN_05398 | 2.1e-177 | pspF | K | transcriptional activator | ||
NECFGCCN_05399 | 2.9e-225 | norB | G | Quinolone resistance protein | ||
NECFGCCN_05400 | 1.9e-222 | 3.5.1.32 | S | amidohydrolase | ||
NECFGCCN_05401 | 0.0 | K | helix_turn_helix, arabinose operon control protein | |||
NECFGCCN_05402 | 9.9e-152 | K | transcriptional | |||
NECFGCCN_05403 | 7.4e-153 | GM | Nad-dependent epimerase dehydratase | |||
NECFGCCN_05404 | 0.0 | sapA | E | ABC transporter substrate-binding protein | ||
NECFGCCN_05405 | 1.8e-173 | sapB | P | peptide transport system, permease | ||
NECFGCCN_05406 | 4.7e-160 | sapC | V | peptide transport system, permease | ||
NECFGCCN_05407 | 1e-192 | sapD | P | ATPase activity | ||
NECFGCCN_05408 | 2.9e-148 | sapF | P | ATPase activity | ||
NECFGCCN_05409 | 1.2e-242 | fcy21 | U | Belongs to the purine-cytosine permease (2.A.39) family | ||
NECFGCCN_05410 | 1.5e-81 | ves | S | protein conserved in bacteria | ||
NECFGCCN_05411 | 1.7e-142 | fabI | 1.3.1.10, 1.3.1.9 | I | Enoyl- acyl-carrier-protein reductase NADH | |
NECFGCCN_05412 | 1.7e-146 | yciW | S | protein conserved in bacteria | ||
NECFGCCN_05413 | 0.0 | rnb | 3.1.13.1 | J | Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3' to 5' direction | |
NECFGCCN_05414 | 2.2e-24 | yciZ | S | Belongs to the UPF0509 family | ||
NECFGCCN_05415 | 1.6e-132 | yciT | K | transcriptional regulator | ||
NECFGCCN_05416 | 7.6e-27 | osmB | M | Lipoprotein | ||
NECFGCCN_05417 | 1.6e-52 | yciH | J | Translation Initiation Factor | ||
NECFGCCN_05418 | 5.3e-125 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
NECFGCCN_05419 | 9.3e-217 | lapB | G | Modulates cellular lipopolysaccharide (LPS) levels by regulating LpxC, which is involved in lipid A biosynthesis. May act by modulating the proteolytic activity of FtsH towards LpxC. May also coordinate assembly of proteins involved in LPS synthesis at the plasma membrane | ||
NECFGCCN_05420 | 3.9e-45 | lapA | S | Involved in the assembly of lipopolysaccharide (LPS) | ||
NECFGCCN_05421 | 3.3e-138 | pgpB | 3.1.3.27, 3.1.3.4, 3.1.3.81, 3.6.1.27 | I | phosphatidylglycerophosphatase | |
NECFGCCN_05422 | 7.9e-111 | ribA | 3.5.4.25 | F | Catalyzes the conversion of GTP to 2,5-diamino-6- ribosylamino-4(3H)-pyrimidinone 5'-phosphate (DARP), formate and pyrophosphate | |
NECFGCCN_05423 | 0.0 | acnA | 4.2.1.3 | C | Catalyzes the isomerization of citrate to isocitrate via cis-aconitate | |
NECFGCCN_05424 | 6.6e-23 | |||||
NECFGCCN_05425 | 3.6e-182 | cysB | K | transcriptional regulator | ||
NECFGCCN_05426 | 0.0 | topA | 5.99.1.2 | L | Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone | |
NECFGCCN_05427 | 2.3e-40 | yciN | S | Protein of unknown function (DUF2498) | ||
NECFGCCN_05428 | 2.2e-180 | sohB | OU | peptidase | ||
NECFGCCN_05429 | 1.5e-141 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
NECFGCCN_05430 | 1.4e-107 | cobO | 2.5.1.17 | H | Required for both de novo synthesis of the corrin ring for the assimilation of exogenous corrinoids. Participates in the adenosylation of a variety of incomplete and complete corrinoids | |
NECFGCCN_05431 | 1.7e-165 | rluB | 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
NECFGCCN_05432 | 1.1e-84 | K | LysR substrate binding domain | |||
NECFGCCN_05433 | 5.2e-98 | yijE | EG | EamA-like transporter family | ||
NECFGCCN_05434 | 1.9e-115 | yciO | 2.7.7.87 | J | Belongs to the SUA5 family | |
NECFGCCN_05435 | 7.5e-163 | trpH | 3.1.3.97 | S | Metal-dependent phosphoesterases (PHP family) | |
NECFGCCN_05436 | 7.2e-289 | trpE | 4.1.3.27 | EH | Part of a heterotetrameric complex that catalyzes the two-step biosynthesis of anthranilate, an intermediate in the biosynthesis of L-tryptophan. In the first step, the glutamine- binding beta subunit (TrpG) of anthranilate synthase (AS) provides the glutamine amidotransferase activity which generates ammonia as a substrate that, along with chorismate, is used in the second step, catalyzed by the large alpha subunit of AS (TrpE) to produce anthranilate. In the absence of TrpG, TrpE can synthesize anthranilate directly from chorismate and high concentrations of ammonia | |
NECFGCCN_05437 | 3.3e-289 | trpD | 2.4.2.18, 2.6.1.85, 4.1.3.27 | F | Catalyzes the transfer of the phosphoribosyl group of 5- phosphorylribose-1-pyrophosphate (PRPP) to anthranilate to yield N-(5'-phosphoribosyl)-anthranilate (PRA) | |
NECFGCCN_05438 | 7.4e-172 | trpF | 4.1.1.48, 4.2.1.160, 4.2.1.20, 5.3.1.24 | E | Belongs to the TrpC family | |
NECFGCCN_05439 | 3.4e-59 | K | sequence-specific DNA binding | |||
NECFGCCN_05440 | 3.3e-98 | S | Carbohydrate-binding domain-containing protein Cthe_2159 | |||
NECFGCCN_05441 | 2.8e-177 | XK27_08075 | M | glycosyl transferase family 2 | ||
NECFGCCN_05442 | 0.0 | 2.4.1.5 | GH13 | M | KxYKxGKxW signal domain protein | |
NECFGCCN_05443 | 1.6e-20 | 2.4.1.5 | GH13 | M | KxYKxGKxW signal domain protein | |
NECFGCCN_05444 | 0.0 | pabB | 2.6.1.85, 4.1.3.27, 4.1.3.38 | EH | component I | |
NECFGCCN_05446 | 0.0 | metE | 2.1.1.14 | E | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | |
NECFGCCN_05447 | 1.1e-164 | metF | 1.5.1.20 | E | reductase | |
NECFGCCN_05448 | 0.0 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase | |
NECFGCCN_05449 | 1.7e-91 | panT | S | ECF transporter, substrate-specific component | ||
NECFGCCN_05450 | 1.7e-91 | coaBC | 4.1.1.36, 6.3.2.5 | H | Catalyzes two steps in the biosynthesis of coenzyme A. In the first step cysteine is conjugated to 4'-phosphopantothenate to form 4-phosphopantothenoylcysteine, in the latter compound is decarboxylated to form 4'-phosphopantotheine | |
NECFGCCN_05451 | 1.9e-116 | coaB | 4.1.1.36, 6.3.2.5 | H | Phosphopantothenate-cysteine ligase | |
NECFGCCN_05452 | 0.0 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
NECFGCCN_05453 | 5.1e-187 | L | Transposase | |||
NECFGCCN_05454 | 6e-41 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
NECFGCCN_05455 | 9.6e-62 | yjqA | S | Bacterial PH domain | ||
NECFGCCN_05456 | 1.8e-151 | corA | P | CorA-like protein | ||
NECFGCCN_05457 | 1.7e-253 | cshA | 3.6.4.13 | JKL | DEAD-box RNA helicase possibly involved in RNA degradation. Unwinds dsRNA in both 5'- and 3'-directions, has RNA- dependent ATPase activity | |
NECFGCCN_05458 | 1e-41 | yazA | L | endonuclease containing a URI domain | ||
NECFGCCN_05459 | 1.2e-127 | yabB | 2.1.1.223 | L | Methyltransferase | |
NECFGCCN_05460 | 4.6e-142 | nodB3 | G | deacetylase | ||
NECFGCCN_05461 | 1.1e-141 | plsC | 2.3.1.51 | I | Acyltransferase | |
NECFGCCN_05462 | 1.4e-87 | comEA | L | COG1555 DNA uptake protein and related DNA-binding proteins | ||
NECFGCCN_05463 | 0.0 | comEC | S | Competence protein ComEC | ||
NECFGCCN_05464 | 2.3e-229 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
NECFGCCN_05465 | 3.5e-97 | XK27_07830 | 2.3.1.128 | J | Acetyltransferase GNAT Family | |
NECFGCCN_05466 | 7.3e-231 | ytoI | K | transcriptional regulator containing CBS domains | ||
NECFGCCN_05467 | 1.1e-166 | map | 3.4.11.18 | E | Removes the N-terminal methionine from nascent proteins. The N-terminal methionine is often cleaved when the second residue in the primary sequence is small and uncharged (Met-Ala-, Cys, Gly, Pro, Ser, Thr, or Val). Requires deformylation of the N(alpha)-formylated initiator methionine before it can be hydrolyzed | |
NECFGCCN_05468 | 5.7e-150 | rbn | E | Belongs to the UPF0761 family | ||
NECFGCCN_05469 | 2.8e-85 | ccl | S | cog cog4708 | ||
NECFGCCN_05470 | 0.0 | ligA | 6.5.1.2 | L | DNA ligase that catalyzes the formation of phosphodiester linkages between 5'-phosphoryl and 3'-hydroxyl groups in double-stranded DNA using NAD as a coenzyme and as the energy source for the reaction. It is essential for DNA replication and repair of damaged DNA | |
NECFGCCN_05471 | 2.4e-184 | yegS | 2.7.1.107 | I | Sphingosine kinase and enzymes related to eukaryotic diacylglycerol kinase | |
NECFGCCN_05474 | 9.4e-170 | yfjR | K | regulation of single-species biofilm formation | ||
NECFGCCN_05476 | 1.2e-69 | S | QueT transporter | |||
NECFGCCN_05477 | 5.9e-157 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
NECFGCCN_05479 | 8.2e-194 | S | dextransucrase activity | |||
NECFGCCN_05480 | 1.5e-141 | S | ABC-2 family transporter protein | |||
NECFGCCN_05481 | 4.2e-90 | S | ABC-2 family transporter protein | |||
NECFGCCN_05482 | 0.0 | 2.4.1.5 | GH13 | M | KxYKxGKxW signal domain protein | |
NECFGCCN_05483 | 2.7e-23 | |||||
NECFGCCN_05484 | 7.6e-90 | coaE | 2.7.1.24, 3.2.2.23, 4.2.99.18 | GH23 | H | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A |
NECFGCCN_05485 | 3.9e-145 | fpg | 3.2.2.23, 4.2.99.18 | L | Involved in base excision repair of DNA damaged by oxidation or by mutagenic agents. Acts as DNA glycosylase that recognizes and removes damaged bases. Has a preference for oxidized purines, such as 7,8-dihydro-8-oxoguanine (8-oxoG). Has AP (apurinic apyrimidinic) lyase activity and introduces nicks in the DNA strand. Cleaves the DNA backbone by beta-delta elimination to generate a single-strand break at the site of the removed base with both 3'- and 5'-phosphates | |
NECFGCCN_05486 | 2.9e-165 | era | M | An essential GTPase that binds both GDP and GTP, with rapid nucleotide exchange. Plays a role in 16S rRNA processing and 30S ribosomal subunit biogenesis and possibly also in cell cycle regulation and energy metabolism | ||
NECFGCCN_05487 | 4.4e-65 | dgkA | 2.7.1.107, 2.7.1.66 | M | Diacylglycerol kinase | |
NECFGCCN_05488 | 1.3e-87 | ybeY | 2.6.99.2, 3.5.4.5 | S | Single strand-specific metallo-endoribonuclease involved in late-stage 70S ribosome quality control and in maturation of the 3' terminus of the 16S rRNA | |
NECFGCCN_05489 | 3.4e-144 | licT | K | antiterminator | ||
NECFGCCN_05490 | 1.3e-105 | recR | L | May play a role in DNA repair. It seems to be involved in an RecBC-independent recombinational process of DNA repair. It may act with RecF and RecO | ||
NECFGCCN_05491 | 0.0 | pbp2b | 3.4.16.4 | M | penicillin-binding protein | |
NECFGCCN_05492 | 1.7e-12 | 2.7.13.3 | T | GHKL domain | ||
NECFGCCN_05493 | 1.7e-58 | 2.7.13.3 | T | GHKL domain | ||
NECFGCCN_05494 | 4.7e-23 | L | COG3547 Transposase and inactivated derivatives | |||
NECFGCCN_05495 | 1.2e-24 | yrpB | 1.13.12.16, 1.3.1.9 | S | 2-nitropropane dioxygenase | |
NECFGCCN_05496 | 1.8e-248 | 3.5.1.28 | NU | GBS Bsp-like repeat | ||
NECFGCCN_05497 | 5e-125 | yieP | K | transcriptional regulator | ||
NECFGCCN_05498 | 3.6e-247 | hsrA | EGP | Major facilitator superfamily | ||
NECFGCCN_05499 | 7.4e-183 | rbsR | K | Is the main repressor of the genes involved in the de novo synthesis of purine nucleotides, regulating purB, purC, purEK, purF, purHD, purL, purMN and guaBA expression. PurR is allosterically activated to bind its cognate DNA by binding the purine corepressors, hypoxanthine or guanine, thereby effecting transcription repression | ||
NECFGCCN_05500 | 1.4e-151 | rbsK | 2.7.1.15 | H | Catalyzes the phosphorylation of ribose at O-5 in a reaction requiring ATP and magnesium. The resulting D-ribose-5- phosphate can then be used either for sythesis of nucleotides, histidine, and tryptophan, or as a component of the pentose phosphate pathway | |
NECFGCCN_05501 | 2.9e-154 | rbsB | G | Periplasmic | ||
NECFGCCN_05502 | 2.8e-150 | rbsC | P | Belongs to the binding-protein-dependent transport system permease family | ||
NECFGCCN_05503 | 3.2e-278 | rbsA | 3.6.3.17 | P | import. Responsible for energy coupling to the transport system | |
NECFGCCN_05504 | 2.3e-69 | rbsD | 5.4.99.62 | G | Catalyzes the interconversion of beta-pyran and beta- furan forms of D-ribose | |
NECFGCCN_05505 | 0.0 | kup | P | transport of potassium into the cell | ||
NECFGCCN_05506 | 1.1e-281 | ravA | S | Functions as an ATPase. May play a role in metal insertion (metal-chelatase) or as a chaperone | ||
NECFGCCN_05507 | 8.1e-271 | viaA | S | VWA domain protein interacting with AAA ATPase | ||
NECFGCCN_05508 | 5e-187 | asnA | 6.3.1.1 | E | aspartate--ammonia ligase | |
NECFGCCN_05509 | 1.5e-77 | asnC | K | transcriptional | ||
NECFGCCN_05510 | 1e-75 | mioC | C | flavodoxin binds one FMN molecule, which serves as a redox-active prosthetic group | ||
NECFGCCN_05511 | 0.0 | gidA | D | NAD-binding protein involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA-cmnm(5)s(2)U34 | ||
NECFGCCN_05512 | 1.1e-110 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of guanine in position 527 of 16S rRNA | |
NECFGCCN_05513 | 2.1e-56 | atpI | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. Subunit I associates with the membrane and may be involved with cation translocation | ||
NECFGCCN_05514 | 5.4e-147 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
NECFGCCN_05515 | 1.7e-32 | atpE | C | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
NECFGCCN_05516 | 4.1e-54 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
NECFGCCN_05517 | 2.9e-88 | atpH | C | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
NECFGCCN_05518 | 1.2e-285 | atpA | 3.6.3.14 | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit | |
NECFGCCN_05519 | 2.4e-153 | atpG | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The gamma chain is believed to be important in regulating ATPase activity and the flow of protons through the CF(0) complex | ||
NECFGCCN_05520 | 1.2e-258 | atpD | 3.6.3.14 | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The catalytic sites are hosted primarily by the beta subunits | |
NECFGCCN_05521 | 3.1e-69 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
NECFGCCN_05522 | 1.2e-236 | glmU | 2.3.1.157, 2.7.7.23 | M | Catalyzes the last two sequential reactions in the de novo biosynthetic pathway for UDP-N-acetylglucosamine (UDP- GlcNAc). The C-terminal domain catalyzes the transfer of acetyl group from acetyl coenzyme A to glucosamine-1-phosphate (GlcN-1-P) to produce N-acetylglucosamine-1-phosphate (GlcNAc-1-P), which is converted into UDP-GlcNAc by the transfer of uridine 5- monophosphate (from uridine 5-triphosphate), a reaction catalyzed by the N-terminal domain | |
NECFGCCN_05523 | 0.0 | glmS | 2.6.1.16 | M | Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source | |
NECFGCCN_05524 | 1.7e-193 | pstS | P | Part of the ABC transporter complex PstSACB involved in phosphate import | ||
NECFGCCN_05525 | 1.2e-169 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
NECFGCCN_05526 | 2.9e-154 | pstA | P | phosphate transport system permease | ||
NECFGCCN_05527 | 1.1e-146 | pstB | 3.6.3.27 | P | Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system | |
NECFGCCN_05528 | 4.9e-131 | phoU | P | Part of the phosphate (Pho) regulon, which plays a key role in phosphate homeostasis. PhoU is essential for the repression of the Pho regulon at high phosphate conditions | ||
NECFGCCN_05529 | 0.0 | bglH | M | PFAM porin LamB type | ||
NECFGCCN_05530 | 1.5e-214 | yieL | P | Belongs to the glycosyl hydrolase 13 family | ||
NECFGCCN_05531 | 3.3e-124 | nagB | 3.1.1.31, 3.5.99.6 | G | glucosamine-6-phosphate deaminase activity | |
NECFGCCN_05532 | 2.2e-122 | yieH | S | HAD-superfamily hydrolase subfamily IA, variant 3 | ||
NECFGCCN_05533 | 1.1e-229 | yieG | S | permease | ||
NECFGCCN_05534 | 1.8e-101 | yieF | S | NAD(P)H-dependent FMN reductase | ||
NECFGCCN_05535 | 3.1e-125 | yieE | 2.7.8.7 | H | Phosphopantetheinyl transferase | |
NECFGCCN_05536 | 7e-186 | yidZ | K | HTH-type transcriptional regulator YidZ | ||
NECFGCCN_05537 | 7e-196 | mdtL | EGP | Major facilitator Superfamily | ||
NECFGCCN_05538 | 2.2e-75 | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | |||
NECFGCCN_05539 | 6.8e-251 | mnmE | J | Exhibits a very high intrinsic GTPase hydrolysis rate. Involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA- cmnm(5)s(2)U34 | ||
NECFGCCN_05540 | 2.3e-298 | yidC | U | Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins. Aids folding of multispanning membrane proteins | ||
NECFGCCN_05541 | 2.8e-54 | rnpA | 3.1.26.5 | J | RNaseP catalyzes the removal of the 5'-leader sequence from pre-tRNA to produce the mature 5'-terminus. It can also cleave other RNA substrates such as 4.5S RNA. The protein component plays an auxiliary but essential role in vivo by binding to the 5'-leader sequence and broadening the substrate specificity of the ribozyme | |
NECFGCCN_05542 | 5.5e-264 | dnaA | L | it binds specifically double-stranded DNA at a 9 bp consensus (dnaA box) 5'-TTATC CA A CA A-3'. DnaA binds to ATP and to acidic phospholipids | ||
NECFGCCN_05543 | 2e-205 | dnaN | 2.7.7.7 | L | Confers DNA tethering and processivity to DNA polymerases and other proteins. Acts as a clamp, forming a ring around DNA (a reaction catalyzed by the clamp-loading complex) which diffuses in an ATP-independent manner freely and bidirectionally along dsDNA. Initially characterized for its ability to contact the catalytic subunit of DNA polymerase III (Pol III), a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria | |
NECFGCCN_05544 | 3.2e-203 | recF | L | it is required for DNA replication and normal SOS inducibility. RecF binds preferentially to single-stranded, linear DNA. It also seems to bind ATP | ||
NECFGCCN_05545 | 0.0 | gyrB | 5.99.1.3 | L | A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner | |
NECFGCCN_05546 | 3.5e-146 | yidA | S | member of the haloacid dehalogenase-like hydrolases superfamily and Cof family of proteins | ||
NECFGCCN_05547 | 3.8e-193 | |||||
NECFGCCN_05548 | 1.7e-215 | M | Outer membrane protein protective antigen OMA87 | |||
NECFGCCN_05549 | 3e-122 | dgoR | K | FCD domain | ||
NECFGCCN_05550 | 2.7e-160 | dgoK | 2.7.1.58 | G | 2-keto-3-deoxy-galactonokinase | |
NECFGCCN_05551 | 6.2e-111 | dgoA | 4.1.2.14, 4.1.2.21, 4.1.3.42 | G | KDPG and KHG aldolase | |
NECFGCCN_05552 | 1.5e-227 | dgoD | 4.2.1.6 | H | Catalyzes the dehydration of D-galactonate to 2-keto-3- deoxy-D-galactonate | |
NECFGCCN_05553 | 3.6e-246 | dgoT | G | Major facilitator superfamily | ||
NECFGCCN_05554 | 1.5e-241 | yidR | U | Biopolymer transporter Tol | ||
NECFGCCN_05555 | 2.4e-53 | yidQ | S | (Lipo)protein | ||
NECFGCCN_05556 | 2.5e-71 | ibpA | O | Associates with aggregated proteins, together with IbpB, to stabilize and protect them from irreversible denaturation and extensive proteolysis during heat shock and oxidative stress. Aggregated proteins bound to the IbpAB complex are more efficiently refolded and reactivated by the ATP-dependent chaperone systems ClpB and DnaK DnaJ GrpE. Its activity is ATP- independent | ||
NECFGCCN_05557 | 2.9e-75 | ibpB | O | Associates with aggregated proteins, together with IbpA, to stabilize and protect them from irreversible denaturation and extensive proteolysis during heat shock and oxidative stress. Aggregated proteins bound to the IbpAB complex are more efficiently refolded and reactivated by the ATP-dependent chaperone systems ClpB and DnaK DnaJ GrpE. Its activity is ATP- independent | ||
NECFGCCN_05558 | 6.1e-114 | dinD | S | DNA-damage-inducible protein d | ||
NECFGCCN_05559 | 7.6e-289 | yidE | U | transport protein | ||
NECFGCCN_05560 | 6.3e-134 | yidP | K | transcriptional regulator | ||
NECFGCCN_05561 | 4.3e-305 | glvC | 2.7.1.192, 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | PTS system | |
NECFGCCN_05562 | 2.2e-262 | aglB | 3.2.1.122, 3.2.1.22, 3.2.1.86 | GH4,GT4 | G | 6-phospho-alpha-glucosidase |
NECFGCCN_05563 | 4.2e-48 | yidH | S | Membrane | ||
NECFGCCN_05564 | 5e-60 | yidG | S | Membrane | ||
NECFGCCN_05565 | 1.9e-78 | yidF | K | radical SAM | ||
NECFGCCN_05566 | 2.1e-249 | dsdA | 4.3.1.18 | E | Belongs to the serine threonine dehydratase family. DsdA subfamily | |
NECFGCCN_05567 | 2.1e-228 | dsdX | EG | Gluconate | ||
NECFGCCN_05568 | 1.5e-172 | dsdC | K | transcriptional regulator | ||
NECFGCCN_05569 | 8.8e-215 | emrD | EGP | Major facilitator Superfamily | ||
NECFGCCN_05570 | 2.7e-141 | EG | of the drug metabolite transporter (DMT) superfamily | |||
NECFGCCN_05571 | 1.7e-81 | K | Acetyltransferase (GNAT) domain | |||
NECFGCCN_05574 | 0.0 | ilvB | 2.2.1.6 | H | acetolactate synthase | |
NECFGCCN_05575 | 1.6e-48 | ilvN | 2.2.1.6 | E | acetolactate synthase | |
NECFGCCN_05576 | 1.9e-104 | uhpA | K | response regulator | ||
NECFGCCN_05577 | 2.5e-275 | uhpB | 2.7.13.3 | T | Histidine kinase | |
NECFGCCN_05578 | 2.4e-253 | uhpC | G | transporter | ||
NECFGCCN_05579 | 4.5e-258 | uhpT | G | PFAM Major facilitator superfamily | ||
NECFGCCN_05580 | 1.3e-78 | yicN | S | Protein of unknown function (DUF1198) | ||
NECFGCCN_05581 | 4.3e-30 | radC | E | Belongs to the UPF0758 family | ||
NECFGCCN_05586 | 8.6e-09 | S | ERF superfamily | |||
NECFGCCN_05587 | 7.1e-30 | pi112 | 3.6.4.12 | L | PDDEXK-like domain of unknown function (DUF3799) | |
NECFGCCN_05588 | 7.6e-38 | gltX | 6.1.1.17, 6.1.1.24 | J | Catalyzes the attachment of glutamate to tRNA(Glu) in a two-step reaction glutamate is first activated by ATP to form Glu-AMP and then transferred to the acceptor end of tRNA(Glu) | |
NECFGCCN_05589 | 9.1e-223 | amiA | E | ABC transporter, substrate-binding protein, family 5 | ||
NECFGCCN_05590 | 4.6e-118 | V | Type III restriction enzyme, res subunit | |||
NECFGCCN_05594 | 1.1e-175 | xylG | 3.6.3.17 | S | ABC transporter, ATP-binding protein | |
NECFGCCN_05595 | 5.1e-177 | yufP | S | Belongs to the binding-protein-dependent transport system permease family | ||
NECFGCCN_05596 | 1.1e-167 | yufQ | S | Belongs to the binding-protein-dependent transport system permease family | ||
NECFGCCN_05597 | 5.6e-115 | ycbL | 3.1.2.6 | S | COG0491 Zn-dependent hydrolases, including glyoxylases | |
NECFGCCN_05598 | 2.8e-260 | cbs | 2.5.1.47, 4.2.1.22 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
NECFGCCN_05599 | 3.5e-216 | metC | 2.5.1.48, 4.4.1.1, 4.4.1.8 | E | Catalyzes the formation of L-homocysteine from O- succinyl-L-homoserine (OSHS) and hydrogen sulfide | |
NECFGCCN_05600 | 2.2e-165 | K | transcriptional regulator | |||
NECFGCCN_05601 | 2.1e-103 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
NECFGCCN_05602 | 1.1e-51 | |||||
NECFGCCN_05603 | 2e-15 | |||||
NECFGCCN_05605 | 1.6e-219 | lysN | EK | Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | ||
NECFGCCN_05606 | 0.0 | gsp | 3.5.1.78, 6.3.1.8 | E | Glutathionylspermidine synthase | |
NECFGCCN_05607 | 9.9e-108 | 5.3.4.1 | O | Required for disulfide bond formation in some periplasmic proteins. Acts by transferring its disulfide bond to other proteins and is reduced in the process | ||
NECFGCCN_05608 | 3.1e-169 | yghU | O | Belongs to the GST superfamily | ||
NECFGCCN_05609 | 2.4e-49 | yghW | S | response to butan-1-ol | ||
NECFGCCN_05610 | 9.4e-169 | yghX | 3.1.1.45 | Q | Dienelactone hydrolase | |
NECFGCCN_05611 | 1.5e-83 | yqhA | S | UPF0114 protein | ||
NECFGCCN_05612 | 4.6e-232 | G | Belongs to the glycosyl hydrolase 43 family | |||
NECFGCCN_05613 | 2.7e-242 | yicJ | G | COG2211 Na melibiose symporter and related transporters | ||
NECFGCCN_05614 | 6.3e-62 | exbD | U | Biopolymer transport protein, ExbD | ||
NECFGCCN_05615 | 8.4e-123 | exbB | U | tonB-system energizer ExbB | ||
NECFGCCN_05616 | 3.8e-07 | |||||
NECFGCCN_05617 | 7.2e-225 | metC | 2.5.1.48, 4.4.1.1, 4.4.1.11, 4.4.1.8 | E | cystathionine beta-lyase | |
NECFGCCN_05618 | 3.3e-118 | yghB | S | Pfam SNARE associated Golgi protein | ||
NECFGCCN_05619 | 1.1e-161 | yqhC | K | transcriptional regulator | ||
NECFGCCN_05620 | 4.9e-218 | yqhD | C | alcohol dehydrogenase | ||
NECFGCCN_05621 | 1.2e-157 | dkgA | 1.1.1.346 | S | reductase | |
NECFGCCN_05622 | 1.7e-85 | M | Acetyltransferase (GNAT) domain | |||
NECFGCCN_05623 | 0.0 | ygiQ | C | UPF0313 protein | ||
NECFGCCN_05624 | 9.7e-277 | ftsP | D | Cell division protein that is required for growth during stress conditions. May be involved in protecting or stabilizing the divisomal assembly under conditions of stress | ||
NECFGCCN_05625 | 4e-125 | plsC | 2.3.1.51, 3.1.3.3 | I | Belongs to the 1-acyl-sn-glycerol-3-phosphate acyltransferase family | |
NECFGCCN_05626 | 0.0 | parC | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
NECFGCCN_05627 | 9.2e-169 | ygiV | K | transcriptional regulator | ||
NECFGCCN_05628 | 1.5e-54 | ygiW | S | Bacterial OB fold (BOF) protein | ||
NECFGCCN_05629 | 1.5e-118 | K | response regulator | |||
NECFGCCN_05630 | 1.1e-234 | qseC | 2.7.13.3 | T | Histidine kinase | |
NECFGCCN_05631 | 1.1e-109 | mdaB | S | modulator of drug activity B | ||
NECFGCCN_05632 | 1.5e-52 | ygiN | S | monooxygenase | ||
NECFGCCN_05633 | 0.0 | parE | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
NECFGCCN_05634 | 1.1e-104 | yqiA | S | esterase | ||
NECFGCCN_05635 | 4.6e-162 | cpdA | 2.1.2.2, 3.1.4.53 | S | Hydrolyzes cAMP to 5'-AMP. Plays an important regulatory role in modulating the intracellular concentration of cAMP, thereby influencing cAMP-dependent processes | |
NECFGCCN_05636 | 7.6e-76 | yqiB | S | protein conserved in bacteria | ||
NECFGCCN_05637 | 1.2e-112 | nudF | 3.6.1.13 | L | COG0494 NTP pyrophosphohydrolases including oxidative damage repair enzymes | |
NECFGCCN_05638 | 7.1e-238 | tolC | MU | type I secretion outer membrane protein, TolC | ||
NECFGCCN_05639 | 4.8e-117 | ygiB | S | Belongs to the UPF0441 family | ||
NECFGCCN_05640 | 2.3e-228 | ygiC | 3.5.1.78, 6.3.1.8 | E | Glutathionylspermidine synthase | |
NECFGCCN_05641 | 2.7e-151 | ygiD | 1.13.11.8 | S | dioxygenase | |
NECFGCCN_05642 | 5.2e-115 | zupT | P | Mediates zinc uptake. May also transport other divalent cations | ||
NECFGCCN_05643 | 2.8e-117 | ribB | 3.5.4.25, 4.1.99.12 | H | Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate | |
NECFGCCN_05644 | 1.1e-38 | yqiC | S | protein conserved in bacteria | ||
NECFGCCN_05645 | 1.7e-30 | glgS | S | positive regulation of cellular carbohydrate metabolic process | ||
NECFGCCN_05646 | 3.5e-266 | hldE | 2.7.1.167, 2.7.7.70 | H | Catalyzes the ADP transfer from ATP to D-glycero-beta-D- manno-heptose 1-phosphate, yielding ADP-D-glycero-beta-D-manno- heptose | |
NECFGCCN_05647 | 0.0 | glnE | 2.7.7.42, 2.7.7.89 | H | Involved in the regulation of glutamine synthetase GlnA, a key enzyme in the process to assimilate ammonia. When cellular nitrogen levels are high, the C-terminal adenylyl transferase (AT) inactivates GlnA by covalent transfer of an adenylyl group from ATP to specific tyrosine residue of GlnA, thus reducing its activity. Conversely, when nitrogen levels are low, the N-terminal adenylyl removase (AR) activates GlnA by removing the adenylyl group by phosphorolysis, increasing its activity. The regulatory region of GlnE binds the signal transduction protein PII (GlnB) which indicates the nitrogen status of the cell | |
NECFGCCN_05648 | 4.5e-236 | ygiF | 3.6.1.25 | S | Adenylate cyclase | |
NECFGCCN_05649 | 1.4e-110 | ygiM | T | sh3 domain protein | ||
NECFGCCN_05650 | 8.6e-237 | cca | 2.7.7.19, 2.7.7.72 | F | Catalyzes the addition and repair of the essential 3'- terminal CCA sequence in tRNAs without using a nucleic acid template. Adds these three nucleotides in the order of C, C, and A to the tRNA nucleotide-73, using CTP and ATP as substrates and producing inorganic pyrophosphate. Also shows phosphatase, 2'- nucleotidase and 2',3'-cyclic phosphodiesterase activities. These phosphohydrolase activities are probably involved in the repair of the tRNA 3'-CCA terminus degraded by intracellular RNases | |
NECFGCCN_05651 | 1.1e-142 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
NECFGCCN_05652 | 2.1e-64 | folB | 1.13.11.81, 4.1.2.25, 5.1.99.7, 5.1.99.8 | H | Catalyzes the conversion of 7,8-dihydroneopterin to 6- hydroxymethyl-7,8-dihydropterin | |
NECFGCCN_05653 | 1.4e-110 | plsY | 2.3.1.15 | I | Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP | |
NECFGCCN_05655 | 7.9e-154 | ureD | O | Required for maturation of urease via the functional incorporation of the urease nickel metallocenter | ||
NECFGCCN_05656 | 4e-47 | ureA | 3.5.1.5 | E | Belongs to the urease gamma subunit family | |
NECFGCCN_05657 | 1.9e-55 | ureB | 3.5.1.5 | E | Belongs to the urease beta subunit family | |
NECFGCCN_05658 | 0.0 | ureC | 3.5.1.5 | E | Belongs to the metallo-dependent hydrolases superfamily. Urease alpha subunit family | |
NECFGCCN_05659 | 2e-72 | ureE | O | Involved in urease metallocenter assembly. Binds nickel. Probably functions as a nickel donor during metallocenter assembly | ||
NECFGCCN_05660 | 6.7e-125 | ureF | O | Required for maturation of urease via the functional incorporation of the urease nickel metallocenter | ||
NECFGCCN_05661 | 7.8e-114 | ureG | KO | Facilitates the functional incorporation of the urease nickel metallocenter. This process requires GTP hydrolysis, probably effectuated by UreG | ||
NECFGCCN_05662 | 7.8e-299 | F | Belongs to the purine-cytosine permease (2.A.39) family | |||
NECFGCCN_05663 | 3.2e-189 | tsaD | 2.3.1.234 | J | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaE and TsaB. TsaD likely plays a direct catalytic role in this reaction | |
NECFGCCN_05664 | 1.6e-29 | rpsU | J | Belongs to the bacterial ribosomal protein bS21 family | ||
NECFGCCN_05665 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
NECFGCCN_05666 | 0.0 | rpoD | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released. This sigma factor is the primary sigma factor during exponential growth | ||
NECFGCCN_05667 | 1.5e-91 | mug | 3.2.2.28, 6.3.3.2 | L | Excises ethenocytosine and uracil, which can arise by alkylation or deamination of cytosine, respectively, from the corresponding mispairs with guanine in ds-DNA. It is capable of hydrolyzing the carbon-nitrogen bond between the sugar-phosphate backbone of the DNA and the mispaired base. The complementary strand guanine functions in substrate recognition. Required for DNA damage lesion repair in stationary-phase cells | |
NECFGCCN_05669 | 3.3e-40 | |||||
NECFGCCN_05670 | 4.5e-09 | hdeB | M | Required for optimal acid stress protection, which is important for survival of enteric bacteria in the acidic environment of the host stomach. Exhibits a chaperone-like activity at acidic pH by preventing the aggregation of many different periplasmic proteins | ||
NECFGCCN_05671 | 4.9e-108 | evgA | 3.1.4.52 | K | response regulator | |
NECFGCCN_05672 | 0.0 | evgS | 2.7.13.3 | T | PhoQ Sensor | |
NECFGCCN_05673 | 2.1e-98 | yfdX | S | YfdX protein | ||
NECFGCCN_05674 | 2.5e-98 | hdeD | S | Acid-resistance membrane protein | ||
NECFGCCN_05675 | 2.7e-51 | hdeB | M | Required for optimal acid stress protection, which is important for survival of enteric bacteria in the acidic environment of the host stomach. Exhibits a chaperone-like activity at acidic pH by preventing the aggregation of many different periplasmic proteins | ||
NECFGCCN_05676 | 4.2e-144 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
NECFGCCN_05677 | 0.0 | O | glycerol dehydratase | |||
NECFGCCN_05678 | 1.1e-71 | pduE | 4.2.1.28, 4.2.1.30 | Q | Dehydratase Small Subunit | |
NECFGCCN_05679 | 7.7e-103 | dhaC | 4.2.1.28, 4.2.1.30 | Q | dehydratase, medium subunit | |
NECFGCCN_05680 | 2.3e-311 | dhaB | 4.2.1.28, 4.2.1.30 | E | Dehydratase large subunit | |
NECFGCCN_05681 | 8.9e-69 | pduO | S | protein possibly involved in utilization of glycolate and propanediol | ||
NECFGCCN_05682 | 8.4e-218 | dhaT | 1.1.1.1, 1.1.1.202 | C | alcohol dehydrogenase | |
NECFGCCN_05683 | 2e-61 | S | Dehydratase medium subunit | |||
NECFGCCN_05684 | 6.1e-91 | MMAB | 2.5.1.17 | S | adenosyltransferase | |
NECFGCCN_05685 | 0.0 | dhaR | KQ | Positively regulates the dhaKLM operon from a sigma-70 promoter | ||
NECFGCCN_05686 | 5.5e-203 | gldA | 1.1.1.6 | C | glycerol dehydrogenase | |
NECFGCCN_05687 | 3.5e-202 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dihydroxyacetone kinase | |
NECFGCCN_05688 | 6.8e-113 | dhaL | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | S | Dihydroxyacetone kinase | |
NECFGCCN_05689 | 2.5e-248 | dhaM | 2.7.1.121, 2.7.1.202, 2.7.3.9 | G | Belongs to the PEP-utilizing enzyme family | |
NECFGCCN_05690 | 2.2e-296 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dihydroxyacetone kinase | |
NECFGCCN_05691 | 5.2e-147 | yqjH | 1.16.1.9 | P | Siderophore-interacting protein | |
NECFGCCN_05692 | 5.2e-93 | yqjI | K | transcriptional regulator | ||
NECFGCCN_05693 | 7.3e-261 | patA | 2.6.1.11, 2.6.1.17, 2.6.1.82 | H | Catalyzes the aminotransferase reaction from putrescine to 2-oxoglutarate, leading to glutamate and 4-aminobutanal, which spontaneously cyclizes to form 1-pyrroline. Is also able to transaminate cadaverine and, in lower extent, spermidine, but not ornithine | |
NECFGCCN_05694 | 3.2e-49 | lsrG | 5.3.1.32 | S | Involved in the degradation of phospho-AI-2, thereby terminating induction of the lsr operon and closing the AI-2 signaling cycle. Catalyzes the conversion of (4S)-4-hydroxy-5- phosphonooxypentane-2,3-dione (P-DPD) to 3-hydroxy-5- phosphonooxypentane-2,4-dione (P-HPD) | |
NECFGCCN_05695 | 3.3e-166 | lsrF | 2.3.1.245, 4.1.2.13 | H | Involved in the degradation of phospho-AI-2, thereby terminating induction of the lsr operon and closing the AI-2 signaling cycle. Catalyzes the transfer of an acetyl moiety from 3-hydroxy-5-phosphonooxypentane-2,4-dione to CoA to form glycerone phosphate and acetyl-CoA | |
NECFGCCN_05696 | 2e-183 | lsrB | G | Periplasmic binding protein domain | ||
NECFGCCN_05697 | 2.1e-172 | lsrD | P | Branched-chain amino acid transport system / permease component | ||
NECFGCCN_05698 | 1.2e-178 | lsrC | U | Belongs to the binding-protein-dependent transport system permease family | ||
NECFGCCN_05699 | 6e-269 | lsrA | 3.6.3.17 | P | Part of the ABC transporter complex LsrABCD involved in autoinducer 2 (AI-2) import. Responsible for energy coupling to the transport system | |
NECFGCCN_05700 | 2e-172 | lsrR | K | transcriptional regulator | ||
NECFGCCN_05701 | 3.3e-305 | lsrK | 2.7.1.17, 2.7.1.189, 2.7.1.5 | G | Catalyzes the phosphorylation of autoinducer-2 (AI-2) to phospho-AI-2, which subsequently inactivates the transcriptional regulator LsrR and leads to the transcription of the lsr operon. Phosphorylates the ring-open form of (S)-4,5-dihydroxypentane-2,3- dione (DPD), which is the precursor to all AI-2 signaling molecules, at the C5 position | |
NECFGCCN_05702 | 0.0 | fadH | 1.3.1.34 | C | COG1902 NADH flavin oxidoreductases, Old Yellow Enzyme family | |
NECFGCCN_05703 | 1.1e-214 | rlmG | 2.1.1.172, 2.1.1.174 | J | Specifically methylates the guanine in position 1835 (m2G1835) of 23S rRNA | |
NECFGCCN_05704 | 9.7e-92 | S | B3 4 domain | |||
NECFGCCN_05705 | 4.2e-72 | puuR_1 | K | Helix-turn-helix domain | ||
NECFGCCN_05706 | 6.2e-85 | ygjP | S | WLM domain | ||
NECFGCCN_05707 | 9.1e-181 | ygjR | S | oxidoreductase | ||
NECFGCCN_05708 | 9.6e-167 | alx | P | membrane protein, terc | ||
NECFGCCN_05709 | 3.2e-215 | sstT | E | Involved in the import of serine and threonine into the cell, with the concomitant import of sodium (symport system) | ||
NECFGCCN_05710 | 6e-97 | ygjV | S | Membrane | ||
NECFGCCN_05711 | 4.7e-290 | uxaA | 4.2.1.7 | G | Catalyzes the dehydration of galactarate to form 5- dehydro-4-deoxy-D-glucarate | |
NECFGCCN_05712 | 6.7e-278 | uxaC | 5.3.1.12 | G | glucuronate isomerase | |
NECFGCCN_05713 | 1.6e-241 | exuT | G | Major facilitator superfamily | ||
NECFGCCN_05714 | 1.6e-143 | exuR | K | Transcriptional | ||
NECFGCCN_05715 | 2.5e-118 | yqjA | S | Inner membrane protein yqjA | ||
NECFGCCN_05716 | 1.2e-64 | mzrA | S | Modulates the activity of the EnvZ OmpR two-component regulatory system, probably by directly modulating EnvZ enzymatic activity and increasing stability of phosphorylated OmpR | ||
NECFGCCN_05717 | 9.3e-38 | yqjC | S | Protein of unknown function (DUF1090) | ||
NECFGCCN_05718 | 1.2e-41 | yqjD | S | Membrane protein YqjD | ||
NECFGCCN_05719 | 2.8e-56 | yqjE | S | Membrane | ||
NECFGCCN_05720 | 2.2e-45 | yqjK | S | Membrane | ||
NECFGCCN_05721 | 2.5e-65 | yqjF | S | membrane | ||
NECFGCCN_05722 | 7.7e-188 | yqjG | 1.8.5.7, 2.5.1.18 | O | Glutathione S-Transferase | |
NECFGCCN_05723 | 6e-69 | yhaH | S | Membrane | ||
NECFGCCN_05724 | 3.5e-163 | yhaJ | K | transcriptional regulator | ||
NECFGCCN_05725 | 1.6e-123 | yhaK | S | Belongs to the pirin family | ||
NECFGCCN_05726 | 5.4e-17 | yhaL | ||||
NECFGCCN_05727 | 1.8e-53 | NPTU | COG3678 P pilus assembly Cpx signaling pathway, periplasmic inhibitor zinc-resistance associated protein | |||
NECFGCCN_05730 | 4.9e-110 | yhfC | S | Putative membrane peptidase family (DUF2324) | ||
NECFGCCN_05731 | 4.2e-43 | czrA | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
NECFGCCN_05732 | 1.4e-14 | S | integral membrane protein | |||
NECFGCCN_05733 | 3.4e-25 | mccF | V | LD-carboxypeptidase | ||
NECFGCCN_05734 | 1.3e-204 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
NECFGCCN_05735 | 2.1e-23 | |||||
NECFGCCN_05736 | 2.8e-251 | P | 50S ribosome-binding GTPase | |||
NECFGCCN_05737 | 7.2e-190 | P | N,N-dimethylaniline monooxygenase activity | |||
NECFGCCN_05738 | 3.1e-22 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
NECFGCCN_05739 | 2.5e-123 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
NECFGCCN_05742 | 4.3e-85 | yfjR | K | regulation of single-species biofilm formation | ||
NECFGCCN_05743 | 8.4e-23 | |||||
NECFGCCN_05744 | 2.4e-130 | recQ | 3.6.4.12 | L | DNA helicase | |
NECFGCCN_05745 | 1.6e-168 | pldA | 3.1.1.32, 3.1.1.4 | M | Phospholipase | |
NECFGCCN_05746 | 4.7e-79 | yigI | Q | protein possibly involved in aromatic compounds catabolism | ||
NECFGCCN_05747 | 2.8e-165 | rarD | S | Rard protein | ||
NECFGCCN_05748 | 2.5e-175 | corA | P | Mediates influx of magnesium ions | ||
NECFGCCN_05749 | 0.0 | uvrD | 3.6.4.12 | L | it can initiate unwinding at a nick in the DNA. It binds to the single-stranded DNA and acts in a progressive fashion along the DNA in the 3' to 5' direction | |
NECFGCCN_05750 | 7.4e-132 | yigB | 3.1.3.10, 3.1.3.102, 3.1.3.104 | S | Hydrolase | |
NECFGCCN_05751 | 2.2e-165 | xerC | D | Belongs to the 'phage' integrase family. XerC subfamily | ||
NECFGCCN_05752 | 1.2e-126 | yigA | S | protein conserved in bacteria | ||
NECFGCCN_05753 | 4.1e-158 | dapF | 5.1.1.7 | E | Catalyzes the stereoinversion of LL-2,6- diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso- DAP), a precursor of L-lysine and an essential component of the bacterial peptidoglycan | |
NECFGCCN_05754 | 2.3e-31 | yifL | N | Prokaryotic lipoprotein-attachment site | ||
NECFGCCN_05755 | 3.2e-58 | cyaY | 1.16.3.1 | P | Belongs to the frataxin family | |
NECFGCCN_05756 | 0.0 | cyaA | 4.6.1.1 | F | Adenylate cyclase | |
NECFGCCN_05757 | 3.3e-167 | hemC | 2.1.1.107, 2.5.1.61, 4.2.1.75 | H | Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps | |
NECFGCCN_05758 | 6.5e-131 | hemD | 2.1.1.107, 2.5.1.61, 4.2.1.75 | H | Uroporphyrinogen-III synthase | |
NECFGCCN_05759 | 1.6e-176 | hemX | 2.1.1.107, 4.2.1.75 | H | enzyme of heme biosynthesis | |
NECFGCCN_05760 | 1.6e-219 | hemY | H | enzyme of heme biosynthesis | ||
NECFGCCN_05761 | 1.7e-07 | |||||
NECFGCCN_05762 | 9.7e-132 | pip | 1.11.1.10 | S | Alpha beta hydrolase | |
NECFGCCN_05763 | 7.9e-191 | FbpA | K | RNA-binding protein homologous to eukaryotic snRNP | ||
NECFGCCN_05764 | 1e-35 | 6.3.2.4 | M | D-ala D-ala ligase C-terminus | ||
NECFGCCN_05766 | 6.8e-78 | yjaB | K | Acetyltransferase | ||
NECFGCCN_05767 | 3.8e-181 | metAS | 2.3.1.46 | E | Transfers a succinyl group from succinyl-CoA to L- homoserine, forming succinyl-L-homoserine | |
NECFGCCN_05768 | 0.0 | aceB | 2.3.3.9 | C | Involved in the glycolate utilization. Catalyzes the condensation and subsequent hydrolysis of acetyl-coenzyme A (acetyl-CoA) and glyoxylate to form malate and CoA | |
NECFGCCN_05769 | 1e-248 | aceA | 4.1.3.1 | C | Isocitrate lyase | |
NECFGCCN_05770 | 0.0 | aceK | 2.7.11.5 | F | Bifunctional enzyme which can phosphorylate or dephosphorylate isocitrate dehydrogenase (IDH) on a specific serine residue. This is a regulatory mechanism which enables bacteria to bypass the Krebs cycle via the glyoxylate shunt in response to the source of carbon. When bacteria are grown on glucose, IDH is fully active and unphosphorylated, but when grown on acetate or ethanol, the activity of IDH declines drastically concomitant with its phosphorylation | |
NECFGCCN_05771 | 3.5e-149 | iclR | K | transcriptional regulator | ||
NECFGCCN_05772 | 0.0 | metH | 2.1.1.13 | E | methionine synthase | |
NECFGCCN_05773 | 1.9e-284 | yjbB | P | Na Pi-Cotransporter | ||
NECFGCCN_05774 | 1.2e-143 | aroE | 1.1.1.25 | E | shikimate | |
NECFGCCN_05775 | 1.3e-245 | sorE | E | L-sorbose 1-phosphate reductase | ||
NECFGCCN_05776 | 5e-148 | sorM | G | IID component | ||
NECFGCCN_05777 | 5.2e-134 | sorA | G | pts system | ||
NECFGCCN_05778 | 2.7e-88 | sorB | 2.7.1.191, 2.7.1.206 | G | iib component | |
NECFGCCN_05779 | 1.4e-71 | sorF | 2.7.1.191, 2.7.1.206 | G | IIa component | |
NECFGCCN_05780 | 9.5e-136 | IQ | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
NECFGCCN_05781 | 2.2e-179 | sorC | K | transcriptional regulator | ||
NECFGCCN_05782 | 6.9e-164 | rluF | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
NECFGCCN_05783 | 2.1e-39 | yjbD | S | YjbD family (DUF3811) | ||
NECFGCCN_05784 | 4.9e-160 | yocS | S | Bile acid sodium symporter | ||
NECFGCCN_05785 | 1.9e-242 | lysC | 1.1.1.3, 2.7.2.4, 4.1.1.20 | E | Belongs to the aspartokinase family | |
NECFGCCN_05786 | 0.0 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
NECFGCCN_05787 | 5.7e-77 | 2.3.1.79 | S | UDP-3-O-(3-hydroxymyristoyl) glucosamine N-acyltransferase | ||
NECFGCCN_05788 | 4.4e-62 | 2.3.1.57 | K | acetyltransferase | ||
NECFGCCN_05789 | 9.9e-59 | tdcF | 3.5.99.10 | J | PFAM Endoribonuclease L-PSP | |
NECFGCCN_05790 | 7.3e-47 | S | Branched-chain amino acid transport protein (AzlD) | |||
NECFGCCN_05791 | 5.7e-111 | E | AzlC protein | |||
NECFGCCN_05792 | 1.4e-34 | yhaM | S | Belongs to the UPF0597 family | ||
NECFGCCN_05793 | 1.3e-43 | yhaM | S | Belongs to the UPF0597 family | ||
NECFGCCN_05794 | 6.3e-106 | yhaM | S | Belongs to the UPF0597 family | ||
NECFGCCN_05795 | 3.4e-65 | psiE | S | Protein PsiE homolog | ||
NECFGCCN_05796 | 1.2e-160 | malG | P | transport | ||
NECFGCCN_05797 | 6.4e-290 | malF | P | transport | ||
NECFGCCN_05798 | 4.5e-18 | 3.1.4.4 | I | phospholipase D activity | ||
NECFGCCN_05799 | 1.4e-133 | dnaQ | 2.7.7.7, 3.1.26.4 | L | DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. The epsilon subunit contain the editing function and is a proofreading 3'-5' exonuclease | |
NECFGCCN_05800 | 1.6e-87 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
NECFGCCN_05801 | 4.8e-139 | yafS | Q | Methyl-transferase | ||
NECFGCCN_05802 | 8.6e-147 | gloB | 3.1.2.6 | S | Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid | |
NECFGCCN_05803 | 3.7e-257 | mltD | M | COG0741 Soluble lytic murein transglycosylase and related regulatory proteins (some contain LysM invasin domains) | ||
NECFGCCN_05804 | 1.5e-135 | yafE | Q | methyltransferase | ||
NECFGCCN_05805 | 1.2e-149 | yafD | S | UPF0294 protein | ||
NECFGCCN_05806 | 2.3e-202 | ytbD | EGP | Major facilitator Superfamily | ||
NECFGCCN_05807 | 7.3e-161 | yafC | K | Transcriptional regulator | ||
NECFGCCN_05808 | 1.4e-142 | dkgB | 1.1.1.346 | S | reductase | |
NECFGCCN_05809 | 1.4e-119 | potA | 3.6.3.31 | P | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | |
NECFGCCN_05810 | 1.5e-150 | potB | P | ABC-type spermidine putrescine transport system, permease component I | ||
NECFGCCN_05811 | 1.9e-133 | potC | P | ABC-type spermidine putrescine transport system, permease component II | ||
NECFGCCN_05812 | 2.9e-201 | potD | P | Required for the activity of the bacterial periplasmic transport system of putrescine | ||
NECFGCCN_05813 | 0.0 | 1.2.1.5 | C | COG1012 NAD-dependent aldehyde dehydrogenases | ||
NECFGCCN_05814 | 3.4e-310 | 6.2.1.44 | IQ | COG0318 Acyl-CoA synthetases (AMP-forming) AMP-acid ligases II | ||
NECFGCCN_05815 | 4.2e-261 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type | |
NECFGCCN_05816 | 1.2e-104 | arcR | T | Winged helix-turn-helix DNA binding | ||
NECFGCCN_05817 | 5.6e-79 | S | YfaZ precursor | |||
NECFGCCN_05818 | 1.6e-59 | |||||
NECFGCCN_05820 | 2.1e-49 | secG | U | Preprotein translocase, subunit SecG | ||
NECFGCCN_05821 | 2.7e-252 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
NECFGCCN_05822 | 6.5e-151 | folP | 2.5.1.15 | H | Catalyzes the condensation of para-aminobenzoate (pABA) with 6-hydroxymethyl-7,8-dihydropterin diphosphate (DHPt-PP) to form 7,8-dihydropteroate (H2Pte), the immediate precursor of folate derivatives | |
NECFGCCN_05823 | 0.0 | ftsH | O | Acts as a processive, ATP-dependent zinc metallopeptidase for both cytoplasmic and membrane proteins. Plays a role in the quality control of integral membrane proteins | ||
NECFGCCN_05824 | 1e-113 | ftsJ | 2.1.1.166 | J | Specifically methylates the uridine in position 2552 of 23S rRNA at the 2'-O position of the ribose in the fully assembled 50S ribosomal subunit | |
NECFGCCN_05825 | 4.8e-49 | yhbY | J | CRS1 / YhbY (CRM) domain | ||
NECFGCCN_05826 | 1.4e-81 | greA | K | Necessary for efficient RNA polymerase transcription elongation past template-encoded arresting sites. The arresting sites in DNA have the property of trapping a certain fraction of elongating RNA polymerases that pass through, resulting in locked ternary complexes. Cleavage of the nascent transcript by cleavage factors such as GreA or GreB allows the resumption of elongation from the new 3'terminus. GreA releases sequences of 2 to 3 nucleotides | ||
NECFGCCN_05827 | 4.8e-239 | dacB | 3.4.16.4 | M | D-alanyl-D-alanine carboxypeptidase | |
NECFGCCN_05828 | 1.7e-194 | obg | S | An essential GTPase which binds GTP, GDP and possibly (p)ppGpp with moderate affinity, with high nucleotide exchange rates and a fairly low GTP hydrolysis rate. Plays a role in control of the cell cycle, stress response, ribosome biogenesis and in those bacteria that undergo differentiation, in morphogenesis control | ||
NECFGCCN_05829 | 1.9e-170 | yhbE | EG | Permeases of the drug metabolite transporter (DMT) superfamily | ||
NECFGCCN_05830 | 8.2e-41 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
NECFGCCN_05831 | 1.8e-50 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
NECFGCCN_05832 | 4.6e-177 | ispB | 2.5.1.30, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
NECFGCCN_05833 | 2e-45 | sfsB | K | transcriptional regulator | ||
NECFGCCN_05834 | 6.3e-235 | murA | 2.5.1.7 | M | Belongs to the EPSP synthase family. MurA subfamily | |
NECFGCCN_05835 | 2.8e-41 | yrbA | K | Belongs to the BolA IbaG family | ||
NECFGCCN_05836 | 4.1e-41 | mlaB | S | NTP binding protein (Contains STAS domain) | ||
NECFGCCN_05837 | 8.1e-114 | mlaC | Q | ABC-type transport system involved in resistance to organic solvents auxiliary component | ||
NECFGCCN_05838 | 3.5e-97 | mlaD | Q | ABC-type transport system involved in resistance to organic solvents periplasmic component | ||
NECFGCCN_05839 | 3.9e-134 | mlaE | Q | COG0767 ABC-type transport system involved in resistance to organic solvents, permease component | ||
NECFGCCN_05840 | 3.7e-148 | mlaF | Q | (ABC) transporter | ||
NECFGCCN_05841 | 2.5e-162 | yrbG | P | antiporter | ||
NECFGCCN_05842 | 2.9e-182 | kdsD | 5.3.1.13 | M | Arabinose 5-phosphate isomerase | |
NECFGCCN_05843 | 3.8e-99 | kdsC | 3.1.3.45 | S | Involved in the biosynthesis of lipopolysaccharides (LPSs). Catalyzes the hydrolysis of 3-deoxy-D-manno-octulosonate 8-phosphate (KDO 8-P) to 3-deoxy-D-manno-octulosonate (KDO) and inorganic phosphate | |
NECFGCCN_05844 | 1.4e-101 | lptC | S | Involved in the assembly of lipopolysaccharide (LPS). Required for the translocation of LPS from the inner membrane to the outer membrane. Facilitates the transfer of LPS from the inner membrane to the periplasmic protein LptA. Could be a docking site for LptA | ||
NECFGCCN_05845 | 6.1e-94 | lptA | T | Involved in the assembly of lipopolysaccharide (LPS). Required for the translocation of LPS from the inner membrane to the outer membrane. May form a bridge between the inner membrane and the outer membrane, via interactions with LptC and LptD, thereby facilitating LPS transfer across the periplasm | ||
NECFGCCN_05846 | 2.4e-130 | lptB | S | abc transporter atp-binding protein | ||
NECFGCCN_05847 | 7.6e-253 | rpoN | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
NECFGCCN_05848 | 9.5e-46 | hpf | J | sigma (54) modulation protein | ||
NECFGCCN_05849 | 6.3e-82 | ptsN | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | PTS IIA-like nitrogen-regulatory protein PtsN | |
NECFGCCN_05850 | 1.9e-158 | rapZ | S | Modulates the synthesis of GlmS, by affecting the processing and stability of the regulatory small RNA GlmZ. When glucosamine-6-phosphate (GlcN6P) concentrations are high in the cell, RapZ binds GlmZ and targets it to cleavage by RNase E. Consequently, GlmZ is inactivated and unable to activate GlmS synthesis. Under low GlcN6P concentrations, RapZ is sequestered and inactivated by an other regulatory small RNA, GlmY, preventing GlmZ degradation and leading to synthesis of GlmS | ||
NECFGCCN_05851 | 6.7e-41 | ptsO | 2.7.1.121, 2.7.1.202, 2.7.3.9 | H | PTS HPr component phosphorylation site | |
NECFGCCN_05852 | 2.8e-131 | mtgA | 2.4.1.129, 3.4.16.4 | GT51 | M | Peptidoglycan polymerase that catalyzes glycan chain elongation from lipid-linked precursors |
NECFGCCN_05853 | 2.1e-109 | elbB | Q | Displays glyoxalase activity, catalyzing the conversion of glyoxal to glycolate | ||
NECFGCCN_05854 | 0.0 | arcB | 2.7.13.3 | T | PhoQ Sensor | |
NECFGCCN_05855 | 2.5e-208 | uxuA | 4.2.1.8 | G | Catalyzes the dehydration of D-mannonate | |
NECFGCCN_05856 | 1.1e-186 | rspB | 1.1.1.380 | C | Dehydrogenase | |
NECFGCCN_05857 | 1.6e-222 | G | Major facilitator superfamily | |||
NECFGCCN_05858 | 1e-173 | yhcC | S | radical SAM protein | ||
NECFGCCN_05859 | 0.0 | gltB | 1.4.1.13, 1.4.1.14, 1.4.7.1 | E | Glutamate synthase | |
NECFGCCN_05860 | 2.7e-279 | gltD | 1.4.1.13, 1.4.1.14 | C | Glutamate synthase | |
NECFGCCN_05861 | 4e-114 | nanE | 2.7.1.60, 5.1.3.9 | G | Converts N-acetylmannosamine-6-phosphate (ManNAc-6-P) to N-acetylglucosamine-6-phosphate (GlcNAc-6-P) | |
NECFGCCN_05862 | 5.5e-78 | sspB | S | stringent starvation protein b | ||
NECFGCCN_05863 | 1.3e-116 | sspA | O | stringent starvation protein A | ||
NECFGCCN_05864 | 4.7e-64 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
NECFGCCN_05865 | 3.4e-91 | rplM | J | This protein is one of the early assembly proteins of the 50S ribosomal subunit, although it is not seen to bind rRNA by itself. It is important during the early stages of 50S assembly | ||
NECFGCCN_05866 | 1.3e-210 | zapE | D | Reduces the stability of FtsZ polymers in the presence of ATP | ||
NECFGCCN_05867 | 3.3e-65 | yhcB | S | Cytochrome D ubiquinol oxidase, subunit | ||
NECFGCCN_05868 | 2.2e-241 | degQ | 1.3.1.74, 3.4.21.107 | M | Belongs to the peptidase S1C family | |
NECFGCCN_05869 | 8.5e-193 | degS | 3.4.21.107 | M | Belongs to the peptidase S1C family | |
NECFGCCN_05870 | 1.9e-167 | mdh | 1.1.1.37 | C | Catalyzes the reversible oxidation of malate to oxaloacetate | |
NECFGCCN_05871 | 3.4e-77 | argR | K | Regulates arginine biosynthesis genes | ||
NECFGCCN_05872 | 1.3e-38 | yhcN | S | Protein of unknown function (DUF1471) | ||
NECFGCCN_05873 | 7.5e-37 | bhsA_1 | S | Protein of unknown function (DUF1471) | ||
NECFGCCN_05874 | 1.1e-43 | yhcO | K | inhibitor | ||
NECFGCCN_05875 | 0.0 | aaeB | U | Forms an efflux pump with AaeA. Could function as a metabolic relief valve, allowing to eliminate certain compounds when they accumulate to high levels in the cell | ||
NECFGCCN_05876 | 4.4e-161 | aaeA | V | P-hydroxybenzoic acid efflux pump subunit AaeA | ||
NECFGCCN_05877 | 2.6e-29 | aaeX | S | Protein of unknown function (DUF1656) | ||
NECFGCCN_05878 | 1.7e-168 | aaeR | K | Transcriptional regulator | ||
NECFGCCN_05879 | 3.5e-266 | tldD | S | 'responsible for the proteolytic maturation of the E. coli pMccB17 plasmid-encoded microcin B17, an exported protein that targets the essential topoisomerase II DNA gyrase | ||
NECFGCCN_05880 | 0.0 | yhdP | D | Membrane | ||
NECFGCCN_05881 | 4.2e-275 | rng | J | Involved in the processing of the 5'-end of 16S rRNA | ||
NECFGCCN_05882 | 3.6e-92 | maf | 2.1.1.190 | D | Maf-like protein | |
NECFGCCN_05883 | 3.7e-82 | mreD | M | Involved in formation of the rod shape of the cell. May also contribute to regulation of formation of penicillin-binding proteins | ||
NECFGCCN_05884 | 2.8e-177 | mreC | M | Involved in formation and maintenance of cell shape | ||
NECFGCCN_05885 | 2.3e-190 | mreB | D | TIGRFAM Cell shape determining protein MreB Mrl | ||
NECFGCCN_05886 | 0.0 | csrD | T | GGDEF domain | ||
NECFGCCN_05887 | 1.5e-194 | msrP | C | Part of the MsrPQ system that repairs oxidized periplasmic proteins containing methionine sulfoxide residues (Met-O), using respiratory chain electrons. Thus protects these proteins from oxidative-stress damage caused by reactive species of oxygen and chlorine generated by the host defense mechanisms. MsrPQ is essential for the maintenance of envelope integrity under bleach stress, rescuing a wide series of structurally unrelated periplasmic proteins from methionine oxidation. The catalytic subunit MsrP is non-stereospecific, being able to reduce both (R-) and (S-) diastereoisomers of methionine sulfoxide | ||
NECFGCCN_05888 | 4.9e-100 | msrQ | C | Part of the MsrPQ system that repairs oxidized periplasmic proteins containing methionine sulfoxide residues (Met-O), using respiratory chain electrons. Thus protects these proteins from oxidative-stress damage caused by reactive species of oxygen and chlorine generated by the host defense mechanisms. MsrPQ is essential for the maintenance of envelope integrity under bleach stress, rescuing a wide series of structurally unrelated periplasmic proteins from methionine oxidation. MsrQ provides electrons for reduction to the reductase catalytic subunit MsrP, using the quinone pool of the respiratory chain | ||
NECFGCCN_05889 | 1.5e-74 | aroQ | 3.4.13.9, 4.2.1.10 | E | Catalyzes a trans-dehydration via an enolate intermediate | |
NECFGCCN_05890 | 2.9e-60 | accB | 2.3.1.12, 4.1.1.3 | I | first, biotin carboxylase catalyzes the carboxylation of the carrier protein and then the transcarboxylase transfers the carboxyl group to form malonyl-CoA | |
NECFGCCN_05891 | 5.1e-259 | accC | 6.3.4.14, 6.4.1.2 | I | An AccC homodimer forms the biotin carboxylase subunit of the acetyl CoA carboxylase, an enzyme that catalyzes the formation of malonyl-CoA, which in turn controls the rate of fatty acid metabolism | |
NECFGCCN_05892 | 2e-36 | yhdT | S | Membrane | ||
NECFGCCN_05893 | 6.3e-223 | panF | H | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
NECFGCCN_05894 | 1.5e-166 | prmA | J | Ribosomal protein L11 methyltransferase | ||
NECFGCCN_05895 | 1.5e-183 | dusB | J | Catalyzes the synthesis of 5,6-dihydrouridine (D), a modified base found in the D-loop of most tRNAs, via the reduction of the C5-C6 double bond in target uridines | ||
NECFGCCN_05896 | 4.4e-46 | fis | K | Activates ribosomal RNA transcription. Plays a direct role in upstream activation of rRNA promoters | ||
NECFGCCN_05897 | 1.5e-102 | ttgR | K | acrEF envCD operon | ||
NECFGCCN_05898 | 3.7e-202 | acrE | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | ||
NECFGCCN_05899 | 2.1e-90 | acrF | V | Belongs to the resistance-nodulation-cell division (RND) (TC 2.A.6) family | ||
NECFGCCN_05900 | 9.8e-52 | acrF | V | Belongs to the resistance-nodulation-cell division (RND) (TC 2.A.6) family | ||
NECFGCCN_05901 | 1.4e-90 | acrF | V | Belongs to the resistance-nodulation-cell division (RND) (TC 2.A.6) family | ||
NECFGCCN_05902 | 2.4e-51 | zmpB | M | signal peptide protein, YSIRK family | ||
NECFGCCN_05903 | 1.9e-36 | zmpB | M | signal peptide protein, YSIRK family | ||
NECFGCCN_05904 | 9.8e-83 | zmpB | M | signal peptide protein, YSIRK family | ||
NECFGCCN_05905 | 4.3e-56 | zmpB | M | signal peptide protein, YSIRK family | ||
NECFGCCN_05906 | 8.1e-34 | zmpB | M | M26 IgA1-specific Metallo-endopeptidase C-terminal region | ||
NECFGCCN_05907 | 2.5e-273 | V | ABC transporter | |||
NECFGCCN_05908 | 6.1e-126 | yeeN | K | transcriptional regulatory protein | ||
NECFGCCN_05909 | 1.7e-46 | yajC | U | protein transport | ||
NECFGCCN_05910 | 5.9e-140 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
NECFGCCN_05911 | 4.6e-143 | cdsA | 2.7.7.41 | S | Belongs to the CDS family | |
NECFGCCN_05912 | 5e-232 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
NECFGCCN_05913 | 0.0 | proS | 6.1.1.15 | J | Catalyzes the attachment of proline to tRNA(Pro) in a two-step reaction proline is first activated by ATP to form Pro- AMP and then transferred to the acceptor end of tRNA(Pro). As ProRS can inadvertently accommodate and process non-cognate amino acids such as alanine and cysteine, to avoid such errors it has two additional distinct editing activities against alanine. One activity is designated as 'pretransfer' editing and involves the tRNA(Pro)-independent hydrolysis of activated Ala-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Ala-tRNA(Pro). The misacylated Cys- tRNA(Pro) is not edited by ProRS | |
NECFGCCN_05914 | 0.0 | WQ51_06230 | S | ABC transporter | ||
NECFGCCN_05915 | 2.3e-142 | cmpC | S | abc transporter atp-binding protein | ||
NECFGCCN_05916 | 4.9e-42 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
NECFGCCN_05917 | 3.8e-285 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
NECFGCCN_05918 | 2.5e-130 | E | Glyoxalase-like domain | |||
NECFGCCN_05919 | 2.4e-170 | alkR | K | Transcriptional regulator | ||
NECFGCCN_05920 | 7.8e-147 | nepI | EGP | Major facilitator Superfamily | ||
NECFGCCN_05921 | 8.7e-28 | K | DNA-binding transcription factor activity | |||
NECFGCCN_05922 | 6.2e-222 | opuD | M | Belongs to the BCCT transporter (TC 2.A.15) family | ||
NECFGCCN_05923 | 1.3e-20 | S | Antitoxin component of a toxin-antitoxin (TA) module | |||
NECFGCCN_05924 | 4.5e-10 | S | Domain of unknown function (DUF3173) | |||
NECFGCCN_05925 | 1.5e-219 | L | Belongs to the 'phage' integrase family | |||
NECFGCCN_05926 | 1.4e-79 | entS | EGP | Exports the siderophore enterobactin out of the cell | ||
NECFGCCN_05928 | 4.1e-37 | U | domain, Protein | |||
NECFGCCN_05929 | 2.3e-29 | |||||
NECFGCCN_05930 | 7.5e-139 | U | Large exoproteins involved in heme utilization or adhesion | |||
NECFGCCN_05931 | 1.1e-133 | nahR | K | transcriptional regulator | ||
NECFGCCN_05932 | 3.5e-247 | EGP | Major facilitator superfamily | |||
NECFGCCN_05934 | 7.4e-116 | nlpD | DM | COG0739 Membrane proteins related to metalloendopeptidases | ||
NECFGCCN_05935 | 6.2e-102 | idi | 5.3.3.2 | I | Catalyzes the 1,3-allylic rearrangement of the homoallylic substrate isopentenyl (IPP) to its highly electrophilic allylic isomer, dimethylallyl diphosphate (DMAPP) | |
NECFGCCN_05936 | 1e-22 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
NECFGCCN_05937 | 6.2e-38 | hpk9 | 2.7.13.3 | T | protein histidine kinase activity | |
NECFGCCN_05938 | 2.3e-224 | fasC | T | protein histidine kinase activity | ||
NECFGCCN_05939 | 8.2e-116 | mtnB | 3.1.3.87, 4.1.1.104, 4.1.2.17, 4.1.2.19, 4.2.1.109, 5.1.3.4 | E | Catalyzes the dehydration of methylthioribulose-1- phosphate (MTRu-1-P) into 2,3-diketo-5-methylthiopentyl-1- phosphate (DK-MTP-1-P) | |
NECFGCCN_05940 | 7.7e-36 | codB | F | permease | ||
NECFGCCN_05941 | 8.1e-120 | rpiA | 2.7.1.12, 2.7.1.15, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
NECFGCCN_05942 | 0.0 | 3.5.1.28 | M | domain protein | ||
NECFGCCN_05943 | 1.4e-136 | S | N-acetylphosphatidylethanolamine-hydrolysing phospholipas activity | |||
NECFGCCN_05944 | 2.7e-89 | maa | 2.3.1.79 | GK | Maltose O-acetyltransferase | |
NECFGCCN_05945 | 6.9e-66 | rmaI | K | Transcriptional regulator, MarR family | ||
NECFGCCN_05946 | 1.3e-238 | EGP | Major facilitator Superfamily | |||
NECFGCCN_05947 | 7.8e-132 | XK27_00785 | S | CAAX protease self-immunity | ||
NECFGCCN_05948 | 7.4e-118 | mleR | K | malolactic fermentation system | ||
NECFGCCN_05949 | 1.2e-47 | K | Helix-turn-helix | |||
NECFGCCN_05950 | 5e-309 | sfcA | 1.1.1.38, 4.1.1.101 | C | malic enzyme | |
NECFGCCN_05951 | 2.9e-160 | mleP | S | Sodium Bile acid symporter family | ||
NECFGCCN_05952 | 3.7e-99 | NU | Protein of unknown function (DUF3131) | |||
NECFGCCN_05953 | 1.7e-108 | G | Protein of unknown function (DUF3131) | |||
NECFGCCN_05954 | 1.2e-09 | S | NTF2 fold immunity protein | |||
NECFGCCN_05955 | 5.1e-113 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
NECFGCCN_05956 | 4.3e-189 | yeeE | S | Sulphur transport | ||
NECFGCCN_05957 | 8.3e-37 | yeeD | O | sulfur carrier activity | ||
NECFGCCN_05958 | 1.9e-65 | ssb_2 | L | Plays an important role in DNA replication, recombination and repair. Binds to ssDNA and to an array of partner proteins to recruit them to their sites of action during DNA metabolism | ||
NECFGCCN_05959 | 5.1e-90 | tadA | 3.5.4.1, 3.5.4.33 | FJ | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
NECFGCCN_05963 | 3.5e-157 | rrmA | 2.1.1.187 | Q | methyltransferase | |
NECFGCCN_05964 | 1.4e-128 | S | HAD hydrolase, family IA, variant | |||
NECFGCCN_05965 | 5.3e-58 | dapD | 2.3.1.117, 2.3.1.89 | E | Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate | |
NECFGCCN_05966 | 2.2e-218 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
NECFGCCN_05967 | 1.2e-94 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
NECFGCCN_05968 | 4.1e-116 | gluP | 3.4.21.105 | O | membrane protein (homolog of Drosophila rhomboid) | |
NECFGCCN_05969 | 1.9e-169 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
NECFGCCN_05970 | 7e-184 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
NECFGCCN_05971 | 3.3e-95 | XK27_08585 | S | Psort location CytoplasmicMembrane, score | ||
NECFGCCN_05972 | 4.8e-140 | fnt | P | Formate nitrite transporter | ||
NECFGCCN_05973 | 2.7e-21 | XK27_09615 | C | reductase | ||
NECFGCCN_05974 | 4.2e-52 | XK27_09615 | C | reductase | ||
NECFGCCN_05975 | 2.7e-35 | XK27_09615 | C | reductase | ||
NECFGCCN_05976 | 6.3e-108 | XK27_09620 | S | FMN reductase (NADPH) activity | ||
NECFGCCN_05977 | 1e-75 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | This enzyme is involved in nucleotide metabolism it produces dUMP, the immediate precursor of thymidine nucleotides and it decreases the intracellular concentration of dUTP so that uracil cannot be incorporated into DNA | |
NECFGCCN_05978 | 4.4e-77 | 3.5.1.19 | Q | hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides | ||
NECFGCCN_05979 | 1.4e-226 | radA | O | DNA-dependent ATPase involved in processing of recombination intermediates, plays a role in repairing DNA breaks. Stimulates the branch migration of RecA-mediated strand transfer reactions, allowing the 3' invading strand to extend heteroduplex DNA faster. Binds ssDNA in the presence of ADP but not other nucleotides, has ATPase activity that is stimulated by ssDNA and various branched DNA structures, but inhibited by SSB. Does not have RecA's homology-searching function | ||
NECFGCCN_05980 | 1.6e-126 | WQ51_05710 | S | Mitochondrial biogenesis AIM24 | ||
NECFGCCN_05981 | 3.5e-88 | cah | 4.2.1.1 | P | Reversible hydration of carbon dioxide | |
NECFGCCN_05982 | 1.2e-50 | S | Protein of unknown function (DUF3397) | |||
NECFGCCN_05983 | 3.7e-70 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
NECFGCCN_05984 | 1.2e-118 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
NECFGCCN_05986 | 3.3e-41 | xisC | L | viral genome integration into host DNA | ||
NECFGCCN_05988 | 3.6e-14 | |||||
NECFGCCN_05990 | 5.4e-41 | trsE | S | COG0433 Predicted ATPase | ||
NECFGCCN_05991 | 5.8e-49 | yczG | K | transcriptional regulator | ||
NECFGCCN_05992 | 0.0 | fusA | J | Catalyzes the GTP-dependent ribosomal translocation step during translation elongation. During this step, the ribosome changes from the pre-translocational (PRE) to the post- translocational (POST) state as the newly formed A-site-bound peptidyl-tRNA and P-site-bound deacylated tRNA move to the P and E sites, respectively. Catalyzes the coordinated movement of the two tRNA molecules, the mRNA and conformational changes in the ribosome | ||
NECFGCCN_05993 | 2.4e-245 | 4.1.3.27, 4.2.99.21, 5.4.4.2 | EH | chorismate binding enzyme | ||
NECFGCCN_05994 | 8.1e-222 | ybtX | EGP | Major Facilitator Superfamily | ||
NECFGCCN_05995 | 0.0 | ybtQ | V | ABC transporter transmembrane region | ||
NECFGCCN_05996 | 0.0 | ybtP | V | ABC transporter transmembrane region | ||
NECFGCCN_05997 | 3.5e-185 | ybtA | K | helix_turn_helix, arabinose operon control protein | ||
NECFGCCN_05998 | 0.0 | mbtB | Q | protein Irp2 TR Q9Z399 (EMBL AL031866) (2041 aa) fasta scores E() 0 | ||
NECFGCCN_05999 | 0.0 | ppsE | IQ | PKS_KR | ||
NECFGCCN_06000 | 0.0 | ppsE | IQ | PKS_KR | ||
NECFGCCN_06001 | 8.5e-220 | pchG | Q | protein ybtU TR Q9Z3C6 (EMBL AL031866) (365 aa) fasta scores E() | ||
NECFGCCN_06002 | 5.7e-157 | irp4 | 3.1.2.21 | Q | Thioesterase domain | |
NECFGCCN_06003 | 2.4e-300 | irp5 | Q | AMP-binding enzyme C-terminal domain | ||
NECFGCCN_06004 | 0.0 | fyuA | P | Receptor | ||
NECFGCCN_06005 | 1e-101 | yoqH | M | LysM domain | ||
NECFGCCN_06006 | 1.9e-26 | K | Prophage CP4-57 regulatory protein (AlpA) | |||
NECFGCCN_06008 | 4.3e-106 | S | Protein of unknown function (DUF2857) | |||
NECFGCCN_06009 | 2.6e-25 | |||||
NECFGCCN_06010 | 6.5e-96 | virB1 | M | COG0741 Soluble lytic murein transglycosylase and related regulatory proteins (some contain LysM invasin domains) | ||
NECFGCCN_06011 | 3.7e-37 | virB2 | S | TrbC/VIRB2 family | ||
NECFGCCN_06012 | 0.0 | lvhB4 | U | CagE, TrbE, VirB family, component of type IV transporter system | ||
NECFGCCN_06013 | 5.9e-89 | virB5 | U | type IV secretion | ||
NECFGCCN_06014 | 6.8e-29 | |||||
NECFGCCN_06015 | 1.1e-150 | triE | U | TrbL/VirB6 plasmid conjugal transfer protein | ||
NECFGCCN_06016 | 1.9e-15 | |||||
NECFGCCN_06017 | 1.6e-120 | virB8 | U | VirB8 protein | ||
NECFGCCN_06018 | 3.2e-164 | virB9 | U | Conjugal transfer protein | ||
NECFGCCN_06019 | 5.1e-205 | virB10 | U | Bacterial conjugation TrbI-like protein | ||
NECFGCCN_06020 | 3.1e-200 | virB11 | NU | Type II/IV secretion system protein | ||
NECFGCCN_06021 | 2.3e-50 | kikA | S | TrbM | ||
NECFGCCN_06022 | 2.2e-48 | |||||
NECFGCCN_06023 | 2.9e-273 | sbcB | 3.1.11.1 | L | Exonucleolytic cleavage in the 3'- to 5'-direction to yield nucleoside 5'-phosphates | |
NECFGCCN_06024 | 1.1e-222 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
NECFGCCN_06025 | 5.3e-86 | sbmC | L | Inhibits the supercoiling activity of DNA gyrase. Acts by inhibiting DNA gyrase at an early step, prior to (or at the step of) binding of DNA by the gyrase. It protects cells against toxins that target DNA gyrase, by inhibiting activity of these toxins and reducing the formation of lethal double-strand breaks in the cell | ||
NECFGCCN_06026 | 1.3e-196 | yeeA | S | Membrane | ||
NECFGCCN_06027 | 7.1e-50 | yeeX | S | Belongs to the UPF0265 family | ||
NECFGCCN_06028 | 3.2e-122 | cobS | 2.7.8.26 | H | Joins adenosylcobinamide-GDP and alpha-ribazole to generate adenosylcobalamin (Ado-cobalamin). Also synthesizes adenosylcobalamin 5'-phosphate from adenosylcobinamide-GDP and alpha-ribazole 5'-phosphate | |
NECFGCCN_06029 | 4.3e-184 | cobT | 2.4.2.21, 6.3.5.11, 6.3.5.9 | F | Catalyzes the synthesis of alpha-ribazole-5'-phosphate from nicotinate mononucleotide (NAMN) and 5,6- dimethylbenzimidazole (DMB) | |
NECFGCCN_06030 | 6.6e-212 | 3.3.1.1 | H | May play a key role in the regulation of the intracellular concentration of adenosylhomocysteine | ||
NECFGCCN_06031 | 1.1e-125 | T | CBS-domain-containing membrane protein | |||
NECFGCCN_06032 | 5.5e-65 | S | tautomerase | |||
NECFGCCN_06033 | 2.2e-171 | K | transcriptional regulator | |||
NECFGCCN_06034 | 7.9e-129 | lipL | 2.3.1.200, 2.3.1.204 | H | Lipoate-protein ligase | |
NECFGCCN_06035 | 6.3e-238 | shiA | EGP | Major facilitator superfamily | ||
NECFGCCN_06036 | 3.9e-63 | S | protein conserved in bacteria | |||
NECFGCCN_06037 | 0.0 | T | Diguanylate cyclase | |||
NECFGCCN_06038 | 6e-60 | yeaR | P | Domain of unknown function (DUF1971) | ||
NECFGCCN_06039 | 3e-43 | yoaG | S | Domain of unknown function (DUF1869) | ||
NECFGCCN_06040 | 9.4e-156 | K | transcriptional regulator | |||
NECFGCCN_06041 | 3.8e-78 | |||||
NECFGCCN_06042 | 8e-162 | cpo | 1.11.1.10 | I | Alpha beta hydrolase | |
NECFGCCN_06043 | 6.2e-182 | T | Diguanylate cyclase | |||
NECFGCCN_06044 | 4.7e-194 | KLT | serine threonine protein kinase | |||
NECFGCCN_06045 | 0.0 | M | family 8 | |||
NECFGCCN_06046 | 1.9e-212 | secY2 | U | Part of the accessory SecA2 SecY2 system specifically required for export of | ||
NECFGCCN_06047 | 3.6e-288 | asp1 | S | Accessory Sec system protein Asp1 | ||
NECFGCCN_06048 | 0.0 | ftsH | O | Acts as a processive, ATP-dependent zinc metallopeptidase for both cytoplasmic and membrane proteins. Plays a role in the quality control of integral membrane proteins | ||
NECFGCCN_06049 | 2e-97 | hpt | 2.4.2.8, 6.3.4.19 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
NECFGCCN_06050 | 6.9e-212 | tilS | 2.4.2.8, 6.3.4.19 | D | Ligates lysine onto the cytidine present at position 34 of the AUA codon-specific tRNA(Ile) that contains the anticodon CAU, in an ATP-dependent manner. Cytidine is converted to lysidine, thus changing the amino acid specificity of the tRNA from methionine to isoleucine | |
NECFGCCN_06051 | 3.9e-232 | XK27_09285 | 3.5.2.6 | V | Beta-lactamase enzyme family | |
NECFGCCN_06053 | 8.7e-60 | divIC | D | Septum formation initiator | ||
NECFGCCN_06054 | 2.2e-39 | yabO | J | Ribosome-associated heat shock protein implicated in the recycling of the 50S subunit (S4 paralog) | ||
NECFGCCN_06055 | 0.0 | mfd | L | Couples transcription and DNA repair by recognizing RNA polymerase (RNAP) stalled at DNA lesions. Mediates ATP-dependent release of RNAP and its truncated transcript from the DNA, and recruitment of nucleotide excision repair machinery to the damaged site | ||
NECFGCCN_06056 | 5.2e-104 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
NECFGCCN_06057 | 1.1e-203 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
NECFGCCN_06058 | 3.2e-29 | yyzM | S | Protein conserved in bacteria | ||
NECFGCCN_06059 | 4.7e-193 | narG | 1.7.5.1 | C | Belongs to the prokaryotic molybdopterin-containing oxidoreductase family | |
NECFGCCN_06060 | 7.8e-134 | narG | 1.7.5.1 | C | Belongs to the prokaryotic molybdopterin-containing oxidoreductase family | |
NECFGCCN_06061 | 1e-113 | S | flavin-nucleotide-binding protein structurally related to pyridoxine 5'-phosphate oxidase | |||
NECFGCCN_06062 | 2.3e-89 | S | 50S ribosomal protein L21 | |||
NECFGCCN_06063 | 1.8e-90 | S | Antioxidant protein with alkyl hydroperoxidase activity. Required for the reduction of the AhpC active site cysteine residues and for the regeneration of the AhpC enzyme activity | |||
NECFGCCN_06064 | 2.5e-161 | ykgD | K | Transcriptional | ||
NECFGCCN_06065 | 5.4e-147 | metQ | M | Belongs to the nlpA lipoprotein family | ||
NECFGCCN_06066 | 5.5e-158 | EG | of the drug metabolite transporter (DMT) superfamily | |||
NECFGCCN_06067 | 3.1e-101 | aspA | 3.6.1.13 | L | Belongs to the Nudix hydrolase family | |
NECFGCCN_06068 | 1.3e-145 | yddR | S | Zn-dependent hydrolases of the beta-lactamase fold | ||
NECFGCCN_06069 | 7e-178 | adpA | K | Transcriptional regulator containing an amidase domain and an AraC-type DNA-binding HTH domain | ||
NECFGCCN_06070 | 3.1e-203 | yahK | 1.1.1.1 | S | alcohol dehydrogenase | |
NECFGCCN_06071 | 1.4e-122 | arcR | T | Winged helix-turn-helix DNA binding | ||
NECFGCCN_06072 | 2.4e-44 | S | Antibiotic biosynthesis monooxygenase | |||
NECFGCCN_06073 | 7.1e-181 | C | Belongs to the zinc-containing alcohol dehydrogenase family. Quinone oxidoreductase subfamily | |||
NECFGCCN_06074 | 4.9e-84 | MA20_18690 | S | Belongs to the UPF0311 family | ||
NECFGCCN_06076 | 4.2e-264 | yicJ | G | COG2211 Na melibiose symporter and related transporters | ||
NECFGCCN_06077 | 0.0 | yicI | 3.2.1.177 | GH31 | G | Belongs to the glycosyl hydrolase 31 family |
NECFGCCN_06078 | 9.4e-135 | K | Sugar isomerase | |||
NECFGCCN_06079 | 9.2e-256 | celF | 3.2.1.86 | GT4 | G | Glycoside hydrolase |
NECFGCCN_06080 | 1.6e-296 | 2.7.1.192, 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | PTS system | ||
NECFGCCN_06081 | 0.0 | yicH | M | AsmA Family | ||
NECFGCCN_06082 | 4.2e-248 | xanP | F | xanthine | ||
NECFGCCN_06083 | 9.9e-206 | gltS | P | Catalyzes the sodium-dependent transport of glutamate | ||
NECFGCCN_06084 | 4e-18 | S | NADPH-dependent FMN reductase | |||
NECFGCCN_06087 | 1e-179 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
NECFGCCN_06088 | 2.2e-79 | yafM | L | Transposase IS200 like | ||
NECFGCCN_06089 | 1.9e-195 | ftsY | U | Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Acts as a receptor for the complex formed by the signal recognition particle (SRP) and the ribosome-nascent chain (RNC) | ||
NECFGCCN_06090 | 5.6e-144 | XK27_02985 | S | overlaps another CDS with the same product name | ||
NECFGCCN_06091 | 6.9e-147 | supH | S | overlaps another CDS with the same product name | ||
NECFGCCN_06092 | 2.1e-61 | yvoA_1 | K | Transcriptional | ||
NECFGCCN_06093 | 5.9e-118 | skfE | V | abc transporter atp-binding protein | ||
NECFGCCN_06094 | 9.3e-128 | V | Psort location CytoplasmicMembrane, score | |||
NECFGCCN_06095 | 3.6e-171 | oppF | P | Belongs to the ABC transporter superfamily | ||
NECFGCCN_06096 | 1.3e-201 | oppD | P | Belongs to the ABC transporter superfamily | ||
NECFGCCN_06097 | 3.5e-166 | amiD | P | ABC transporter (Permease | ||
NECFGCCN_06098 | 9.3e-278 | amiC | P | ABC transporter (Permease | ||
NECFGCCN_06099 | 6.2e-306 | amiA | E | ABC transporter, substrate-binding protein, family 5 | ||
NECFGCCN_06100 | 9.6e-104 | amiA | E | ABC transporter, substrate-binding protein, family 5 | ||
NECFGCCN_06101 | 3.7e-72 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
NECFGCCN_06102 | 1.4e-303 | hsdM | 2.1.1.72 | V | type I restriction-modification system | |
NECFGCCN_06103 | 1.7e-42 | K | Helix-turn-helix domain | |||
NECFGCCN_06104 | 4.7e-56 | S | Phage derived protein Gp49-like (DUF891) | |||
NECFGCCN_06105 | 9.4e-39 | hsdS | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | |
NECFGCCN_06106 | 1.4e-245 | rsmF | 2.1.1.176, 2.1.1.178 | J | NOL1 NOP2 sun family protein | |
NECFGCCN_06107 | 2.1e-140 | suhB | 3.1.3.25 | G | Belongs to the inositol monophosphatase superfamily | |
NECFGCCN_06108 | 4.3e-43 | yktA | S | Belongs to the UPF0223 family | ||
NECFGCCN_06109 | 8e-49 | T | peptidase | |||
NECFGCCN_06110 | 4.4e-133 | E | Alpha beta hydrolase | |||
NECFGCCN_06112 | 1.1e-195 | ald | 1.4.1.1 | C | Belongs to the AlaDH PNT family | |
NECFGCCN_06113 | 5.1e-251 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
NECFGCCN_06114 | 2e-97 | mip | S | hydroperoxide reductase activity | ||
NECFGCCN_06115 | 1.1e-200 | I | acyl-CoA dehydrogenase | |||
NECFGCCN_06116 | 5.3e-154 | ydiA | P | C4-dicarboxylate transporter malic acid transport protein | ||
NECFGCCN_06117 | 4.3e-08 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
NECFGCCN_06118 | 1.5e-113 | S | VIT family | |||
NECFGCCN_06119 | 1e-142 | deoD_1 | 2.4.2.3 | F | Phosphorylase superfamily | |
NECFGCCN_06120 | 2.7e-24 | |||||
NECFGCCN_06121 | 1.2e-196 | yceA | S | Belongs to the UPF0176 family | ||
NECFGCCN_06122 | 7.7e-24 | nagB | 3.1.1.31, 3.5.99.6 | G | Catalyzes the reversible isomerization-deamination of glucosamine 6-phosphate (GlcN6P) to form fructose 6-phosphate (Fru6P) and ammonium ion | |
NECFGCCN_06123 | 1.8e-122 | nagB | 3.1.1.31, 3.5.99.6 | G | Catalyzes the reversible isomerization-deamination of glucosamine 6-phosphate (GlcN6P) to form fructose 6-phosphate (Fru6P) and ammonium ion | |
NECFGCCN_06124 | 4.3e-197 | queA | 2.4.99.17 | J | Transfers and isomerizes the ribose moiety from AdoMet to the 7-aminomethyl group of 7-deazaguanine (preQ1-tRNA) to give epoxyqueuosine (oQ-tRNA) | |
NECFGCCN_06125 | 0.0 | lmrA | V | abc transporter atp-binding protein | ||
NECFGCCN_06126 | 2.2e-296 | mdlB | V | abc transporter atp-binding protein | ||
NECFGCCN_06127 | 1.7e-108 | XK27_00915 | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | ||
NECFGCCN_06128 | 3.7e-17 | yjdB | S | Domain of unknown function (DUF4767) | ||
NECFGCCN_06129 | 1.1e-164 | tehB | 2.1.1.265 | PQ | tellurite resistance protein tehb | |
NECFGCCN_06130 | 1.9e-90 | eutG | C | alcohol dehydrogenase | ||
NECFGCCN_06131 | 3.8e-182 | add | 3.5.4.4 | F | Catalyzes the hydrolytic deamination of adenine to hypoxanthine. Plays an important role in the purine salvage pathway and in nitrogen catabolism | |
NECFGCCN_06132 | 1.9e-152 | gst | O | Glutathione S-transferase | ||
NECFGCCN_06133 | 2.5e-175 | nrnA | 3.1.13.3, 3.1.3.7 | S | domain protein | |
NECFGCCN_06134 | 7.6e-296 | glpK | 2.7.1.30 | F | Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate | |
NECFGCCN_06135 | 4.2e-158 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
NECFGCCN_06136 | 6.3e-11 | zapB | 2.1.1.80, 3.1.1.61 | D | Non-essential, abundant cell division factor that is required for proper Z-ring formation. It is recruited early to the divisome by direct interaction with FtsZ, stimulating Z-ring assembly and thereby promoting cell division earlier in the cell cycle. Its recruitment to the Z-ring requires functional FtsA or ZipA | |
NECFGCCN_06137 | 1.4e-189 | sbp | P | sulfate ABC transporter | ||
NECFGCCN_06138 | 5.8e-143 | cdh | 3.6.1.26 | I | CDP-diacylglycerol | |
NECFGCCN_06139 | 4.8e-238 | P | Citrate transporter | |||
NECFGCCN_06140 | 3.7e-137 | tpiA | 5.3.1.1 | G | Involved in the gluconeogenesis. Catalyzes stereospecifically the conversion of dihydroxyacetone phosphate (DHAP) to D-glyceraldehyde-3-phosphate (G3P) | |
NECFGCCN_06141 | 5.5e-96 | yiiQ | S | Protein of unknown function (DUF1454) | ||
NECFGCCN_06142 | 1.2e-76 | yiiR | S | Membrane | ||
NECFGCCN_06143 | 2e-124 | fpr | 1.18.1.2, 1.19.1.1 | C | COG1018 Flavodoxin reductases (ferredoxin-NADPH reductases) family 1 | |
NECFGCCN_06144 | 4.8e-185 | glpX | 2.2.1.1, 3.1.3.11, 3.1.3.37 | G | Fructose-1,6-bisphosphatase | |
NECFGCCN_06145 | 0.0 | recG | 3.6.4.12 | L | Critical role in recombination and DNA repair. Helps process Holliday junction intermediates to mature products by catalyzing branch migration. Has a DNA unwinding activity characteristic of a DNA helicase with a 3'- to 5'- polarity. Unwinds branched duplex DNA (Y-DNA) | |
NECFGCCN_06146 | 9.3e-124 | trmH | 2.1.1.185, 2.1.1.34 | J | Catalyzes the 2'-O methylation of guanosine at position 18 in tRNA | |
NECFGCCN_06147 | 0.0 | spoT | 2.7.6.5, 3.1.7.2 | KT | In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance | |
NECFGCCN_06148 | 1.6e-34 | rpoZ | 2.7.7.6 | K | Promotes RNA polymerase assembly. Latches the N- and C- terminal regions of the beta' subunit thereby facilitating its interaction with the beta and alpha subunits | |
NECFGCCN_06149 | 2.3e-112 | gmk | 2.7.4.8, 4.1.1.23 | F | Essential for recycling GMP and indirectly, cGMP | |
NECFGCCN_06150 | 0.0 | ligB | 6.5.1.2 | L | Catalyzes the formation of phosphodiester linkages between 5'-phosphoryl and 3'-hydroxyl groups in double-stranded DNA using NAD as a coenzyme and as the energy source for the reaction | |
NECFGCCN_06151 | 3e-105 | yicG | S | Membrane | ||
NECFGCCN_06152 | 2.6e-217 | clcA_2 | P | Chloride channel | ||
NECFGCCN_06153 | 4.5e-194 | ada | 2.1.1.63, 3.2.2.21 | FL | Involved in the cellular defense against the biological effects of O6-methylguanine (O6-MeG) and O4-methylthymine (O4-MeT) in DNA. Repairs the methylated nucleobase in DNA by stoichiometrically transferring the methyl group to a cysteine residue in the enzyme. This is a suicide reaction the enzyme is irreversibly inactivated | |
NECFGCCN_06154 | 1e-112 | G | COG2513 PEP phosphonomutase and related enzymes | |||
NECFGCCN_06155 | 1e-151 | yicC | S | Stress-induced protein | ||
NECFGCCN_06156 | 3.3e-279 | I | Acyltransferase | |||
NECFGCCN_06157 | 8.1e-158 | V | HlyD family secretion protein | |||
NECFGCCN_06158 | 1.2e-38 | ybhF | V | (ABC) transporter | ||
NECFGCCN_06159 | 1.2e-115 | ybhF | V | (ABC) transporter | ||
NECFGCCN_06160 | 2.2e-191 | ybhS | V | ABC-type multidrug transport system, permease component | ||
NECFGCCN_06161 | 5.5e-127 | rph | 2.7.7.56, 3.6.1.66 | J | Phosphorolytic exoribonuclease that removes nucleotide residues following the -CCA terminus of tRNA and adds nucleotides to the ends of RNA molecules by using nucleoside diphosphates as substrates | |
NECFGCCN_06162 | 2.8e-114 | pyrE | 2.4.2.10 | F | Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) | |
NECFGCCN_06163 | 8.8e-171 | gnl | 3.1.1.17 | G | SMP-30/Gluconolaconase/LRE-like region | |
NECFGCCN_06164 | 2.5e-101 | slmA | D | Required for nucleoid occlusion (NO) phenomenon, which prevents Z-ring formation and cell division over the nucleoid. Acts as a DNA-associated cell division inhibitor that binds simultaneously chromosomal DNA and FtsZ, and disrupts the assembly of FtsZ polymers. SlmA-DNA-binding sequences (SBS) are dispersed on non-Ter regions of the chromosome, preventing FtsZ polymerization at these regions | ||
NECFGCCN_06165 | 5.5e-80 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | This enzyme is involved in nucleotide metabolism it produces dUMP, the immediate precursor of thymidine nucleotides and it decreases the intracellular concentration of dUTP so that uracil cannot be incorporated into DNA | |
NECFGCCN_06166 | 7.2e-220 | coaBC | 4.1.1.36, 6.3.2.5 | H | Catalyzes two steps in the biosynthesis of coenzyme A. In the first step cysteine is conjugated to 4'-phosphopantothenate to form 4-phosphopantothenoylcysteine, in the latter compound is decarboxylated to form 4'-phosphopantotheine | |
NECFGCCN_06167 | 2.7e-112 | radC | E | Belongs to the UPF0758 family | ||
NECFGCCN_06168 | 6.6e-37 | rpmB | J | Belongs to the bacterial ribosomal protein bL28 family | ||
NECFGCCN_06169 | 1.9e-22 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
NECFGCCN_06170 | 4.1e-155 | fpg | 3.2.2.23, 4.2.99.18 | L | Involved in base excision repair of DNA damaged by oxidation or by mutagenic agents. Acts as DNA glycosylase that recognizes and removes damaged bases. Has a preference for oxidized purines, such as 7,8-dihydro-8-oxoguanine (8-oxoG). Has AP (apurinic apyrimidinic) lyase activity and introduces nicks in the DNA strand. Cleaves the DNA backbone by beta-delta elimination to generate a single-strand break at the site of the removed base with both 3'- and 5'-phosphates | |
NECFGCCN_06171 | 3e-81 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
NECFGCCN_06172 | 1.5e-141 | waaE | GT2 | M | Glycosyl transferase | |
NECFGCCN_06173 | 3.8e-240 | kdtA | 2.4.99.12, 2.4.99.13, 2.4.99.14, 2.4.99.15 | GT30 | M | Transferase |
NECFGCCN_06174 | 4.8e-190 | wgaB | 2.4.2.53 | GT2 | M | Glycosyl transferase, family 2 |
NECFGCCN_06175 | 1.1e-203 | rfaB | 2.4.1.291 | GT4 | M | glycosyl transferase group 1 |
NECFGCCN_06176 | 4.8e-218 | rfaG | GT4 | M | Catalyzes the addition of the first glucose residue to the LPS core | |
NECFGCCN_06177 | 3.4e-09 | |||||
NECFGCCN_06178 | 5.6e-160 | iolB | 5.3.1.30 | G | 5-deoxyglucuronate isomerase | |
NECFGCCN_06179 | 2.1e-290 | mmsA | 1.2.1.18, 1.2.1.27 | C | Methylmalonate-semialdehyde dehydrogenase | |
NECFGCCN_06180 | 1.1e-150 | iolI | 5.3.99.11 | G | isomerase | |
NECFGCCN_06181 | 4.5e-280 | yjgR | S | ATP-binding protein | ||
NECFGCCN_06182 | 2.2e-196 | lptG | S | permease | ||
NECFGCCN_06183 | 2.9e-196 | lptF | S | Permease | ||
NECFGCCN_06184 | 3.7e-290 | pepA | 3.4.11.1, 3.4.11.23 | E | Presumably involved in the processing and regular turnover of intracellular proteins. Catalyzes the removal of unsubstituted N-terminal amino acids from various peptides | |
NECFGCCN_06185 | 1.3e-78 | holC | 2.7.7.7 | L | DNA polymerase III chi subunit | |
NECFGCCN_06186 | 0.0 | valS | 6.1.1.9 | J | amino acids such as threonine, to avoid such errors, it has a posttransfer editing activity that hydrolyzes mischarged Thr-tRNA(Val) in a tRNA-dependent manner | |
NECFGCCN_06187 | 6.4e-90 | yjgM | K | Acetyltransferase | ||
NECFGCCN_06188 | 2.6e-143 | miaE | FJ | Hydroxylase for synthesis of 2-methylthio-cis-ribozeatin in tRNA | ||
NECFGCCN_06189 | 4.3e-63 | rraB | S | Globally modulates RNA abundance by binding to RNase E (Rne) and regulating its endonucleolytic activity. Can modulate Rne action in a substrate-dependent manner by altering the composition of the degradosome | ||
NECFGCCN_06190 | 1.7e-187 | argF | 2.1.3.3 | E | Reversibly catalyzes the transfer of the carbamoyl group from carbamoyl phosphate (CP) to the N(epsilon) atom of ornithine (ORN) to produce L-citrulline | |
NECFGCCN_06191 | 9.6e-77 | tabA | G | Toxin-antitoxin biofilm protein TabA | ||
NECFGCCN_06192 | 9.5e-172 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
NECFGCCN_06193 | 5.9e-82 | pyrI | 2.1.3.2 | F | Involved in allosteric regulation of aspartate carbamoyltransferase | |
NECFGCCN_06194 | 8.8e-63 | ridA | 3.5.99.10 | J | Endoribonuclease | |
NECFGCCN_06195 | 0.0 | mgtA | 3.6.3.2 | P | ATPase, P-type (transporting), HAD superfamily, subfamily IC | |
NECFGCCN_06196 | 2.2e-171 | treR | K | trehalose | ||
NECFGCCN_06197 | 8.8e-262 | treB | 2.7.1.192, 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | pts system | |
NECFGCCN_06198 | 0.0 | treC | 3.2.1.93 | GH13 | G | COG0366 Glycosidases |
NECFGCCN_06199 | 3.3e-242 | licC | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
NECFGCCN_06200 | 5.1e-240 | celF | 3.2.1.86 | GT4 | G | Family 4 glycosyl hydrolase |
NECFGCCN_06201 | 8.2e-40 | celA | 2.7.1.196, 2.7.1.205 | G | Phosphotransferase System | |
NECFGCCN_06202 | 3.7e-118 | hexR | K | Transcriptional regulator | ||
NECFGCCN_06203 | 0.0 | nrdD | 1.1.98.6 | F | Ribonucleoside-triphosphate reductase | |
NECFGCCN_06204 | 5e-89 | nrdG | 1.97.1.4 | O | Activation of anaerobic ribonucleoside-triphosphate reductase under anaerobic conditions by generation of an organic free radical, using S-adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine | |
NECFGCCN_06205 | 1.6e-45 | relE | DJ | Cytotoxic translational repressor of toxin-antitoxin stability system | ||
NECFGCCN_06206 | 2.2e-35 | relB | L | bifunctional antitoxin of the RelE-RelB toxin-antitoxin system transcriptional repressor | ||
NECFGCCN_06207 | 0.0 | licR | 2.7.1.197 | GK | transcriptional antiterminator | |
NECFGCCN_06208 | 1.7e-194 | ykgB | 3.1.1.31 | G | COG2706 3-carboxymuconate cyclase | |
NECFGCCN_06209 | 3.1e-133 | 4.1.2.14 | S | 2-dehydro-3-deoxyphosphooctonate aldolase | ||
NECFGCCN_06210 | 4.8e-202 | selA | 2.9.1.1 | E | selenium transferase | |
NECFGCCN_06211 | 8.5e-207 | dho | 3.5.2.3 | S | Amidohydrolase family | |
NECFGCCN_06212 | 1.4e-110 | S | Membrane | |||
NECFGCCN_06213 | 4.7e-140 | S | Membrane | |||
NECFGCCN_06214 | 3.2e-44 | S | Domain of unknown function (DUF4312) | |||
NECFGCCN_06215 | 5e-60 | S | Glycine-rich SFCGS | |||
NECFGCCN_06216 | 2.6e-53 | S | PRD domain protein | |||
NECFGCCN_06217 | 1.4e-60 | cybC | C | Cytochrome b(562) | ||
NECFGCCN_06218 | 8.4e-254 | pmbA | S | Protease involved in proteolytic processing of the antibiotic Microcin B17 and in sensitivity to the DNA gyrase inhibitor LetD | ||
NECFGCCN_06219 | 3.3e-95 | yjgA | S | Belongs to the UPF0307 family | ||
NECFGCCN_06220 | 1.7e-164 | O | protein import | |||
NECFGCCN_06221 | 1.9e-217 | mutY | L | A G-specific adenine glycosylase | ||
NECFGCCN_06223 | 1.7e-37 | |||||
NECFGCCN_06225 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
NECFGCCN_06226 | 0.0 | mutS2 | L | Endonuclease that is involved in the suppression of homologous recombination and may therefore have a key role in the control of bacterial genetic diversity | ||
NECFGCCN_06227 | 2.4e-90 | cvpA | S | toxin biosynthetic process | ||
NECFGCCN_06228 | 1.4e-26 | zapA | D | Activator of cell division through the inhibition of FtsZ GTPase activity, therefore promoting FtsZ assembly into bundles of protofilaments necessary for the formation of the division Z ring. It is recruited early at mid-cell but it is not essential for cell division | ||
NECFGCCN_06229 | 8.5e-40 | L | Integrase core domain | |||
NECFGCCN_06230 | 3.6e-67 | agcS | E | (Alanine) symporter | ||
NECFGCCN_06231 | 2.1e-159 | acoC | 2.3.1.12 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
NECFGCCN_06232 | 8.2e-199 | gldA | 1.1.1.6 | C | glycerol dehydrogenase | |
NECFGCCN_06233 | 1.3e-145 | XK27_10475 | S | oxidoreductase | ||
NECFGCCN_06234 | 5.1e-173 | apbE | 2.7.1.180 | H | Flavin transferase that catalyzes the transfer of the FMN moiety of FAD and its covalent binding to the hydroxyl group of a threonine residue in a target flavoprotein | |
NECFGCCN_06235 | 9.1e-130 | dcuR | K | Transcriptional Regulatory protein | ||
NECFGCCN_06236 | 5e-293 | dcuS | 2.7.13.3 | T | signal transduction histidine kinase regulating citrate malate metabolism | |
NECFGCCN_06237 | 1.5e-13 | |||||
NECFGCCN_06238 | 1.2e-101 | narG | 1.7.5.1 | C | Belongs to the prokaryotic molybdopterin-containing oxidoreductase family | |
NECFGCCN_06239 | 1.2e-234 | narU | P | nitrate nitrite transporter | ||
NECFGCCN_06240 | 2.9e-88 | ybjK | K | transcriptional regulator | ||
NECFGCCN_06241 | 7.3e-214 | smvA | EGP | Major facilitator superfamily | ||
NECFGCCN_06242 | 2.2e-132 | pcaR | K | transcriptional regulator | ||
NECFGCCN_06243 | 1.7e-196 | catB | 5.5.1.1 | M | Belongs to the mandelate racemase muconate lactonizing enzyme family | |
NECFGCCN_06244 | 1.2e-43 | catC | 5.3.3.4 | Q | Muconolactone delta-isomerase | |
NECFGCCN_06245 | 2.8e-168 | catA | 1.13.11.1 | Q | catechol 1,2-dioxygenase | |
NECFGCCN_06246 | 2e-258 | benA | 1.14.12.10 | P | COG4638 Phenylpropionate dioxygenase and related ring-hydroxylating dioxygenases, large terminal subunit | |
NECFGCCN_06247 | 1.1e-91 | benB | 1.14.12.10 | Q | COG5517 Small subunit of phenylpropionate dioxygenase | |
NECFGCCN_06248 | 2.1e-188 | pyrK | 1.16.1.3, 1.3.1.14, 1.5.1.41, 3.5.2.3 | C | COG0543 2-polyprenylphenol hydroxylase and related flavodoxin oxidoreductases | |
NECFGCCN_06249 | 1e-131 | IQ | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
NECFGCCN_06250 | 2.8e-149 | yddG | EG | of the drug metabolite transporter (DMT) superfamily | ||
NECFGCCN_06251 | 8.5e-110 | fdnG | 1.17.1.9, 1.17.5.3 | C | Sulfate ABC transporter substrate-binding protein | |
NECFGCCN_06252 | 9.9e-258 | narK | P | nitrate nitrite transporter | ||
NECFGCCN_06253 | 0.0 | narX | 2.7.13.3 | T | Histidine kinase | |
NECFGCCN_06254 | 2.2e-111 | narL | K | response regulator | ||
NECFGCCN_06255 | 3.3e-269 | ychO | 3.2.1.14 | GH18 | M | entry into host |
NECFGCCN_06256 | 0.0 | nasA | 1.6.99.3, 1.7.7.2 | C | Catalytic subunit of the nitrate reductase (NAP). Only expressed at high levels during aerobic growth. NapAB complex receives electrons from the membrane-anchored tetraheme protein NapC. Essential function for nitrate assimilation and may have a role in anaerobic metabolism | |
NECFGCCN_06257 | 5e-159 | nirB | 1.7.1.15 | C | Belongs to the nitrite and sulfite reductase 4Fe-4S domain family | |
NECFGCCN_06258 | 3.8e-102 | S | COG1853 Conserved protein domain typically associated with flavoprotein oxygenases, DIM6 NTAB family | |||
NECFGCCN_06261 | 1.4e-14 | coiA | 3.6.4.12 | S | Competence protein | |
NECFGCCN_06262 | 7.5e-16 | T | peptidase | |||
NECFGCCN_06263 | 6e-158 | rarD | S | Transporter | ||
NECFGCCN_06264 | 2.6e-141 | thrB | 2.7.1.39 | E | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
NECFGCCN_06265 | 2.6e-236 | hom | 1.1.1.3, 2.7.2.4 | E | homoserine dehydrogenase | |
NECFGCCN_06266 | 6.3e-133 | yxkH | G | deacetylase | ||
NECFGCCN_06267 | 3.9e-204 | argD | 2.6.1.11, 2.6.1.17 | E | acetylornithine aminotransferase | |
NECFGCCN_06268 | 2.2e-123 | argB | 2.7.2.8 | E | Belongs to the acetylglutamate kinase family. ArgB subfamily | |
NECFGCCN_06269 | 6.2e-216 | argJ | 2.3.1.1, 2.3.1.35, 2.7.2.8 | E | Catalyzes two activities which are involved in the cyclic version of arginine biosynthesis the synthesis of N- acetylglutamate from glutamate and acetyl-CoA as the acetyl donor, and of ornithine by transacetylation between N(2)-acetylornithine and glutamate | |
NECFGCCN_06270 | 7e-184 | argC | 1.2.1.38 | E | Catalyzes the NADPH-dependent reduction of N-acetyl-5- glutamyl phosphate to yield N-acetyl-L-glutamate 5-semialdehyde | |
NECFGCCN_06271 | 6.2e-67 | mtnE | 2.6.1.83 | E | mutations do not affect methionine salvage in vivo however | |
NECFGCCN_06272 | 2.2e-165 | asp2 | 3.4.11.5 | S | Accessory Sec system protein Asp2 | |
NECFGCCN_06273 | 9.4e-77 | asp3 | S | Accessory Sec system protein Asp3 | ||
NECFGCCN_06274 | 0.0 | secA2 | U | Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. Has a central role in coupling the hydrolysis of ATP to the transfer of proteins into and across the cell membrane, serving as an ATP-driven molecular motor driving the stepwise translocation of polypeptide chains across the membrane | ||
NECFGCCN_06275 | 5.7e-283 | gtf1 | 2.4.1.52 | GT4 | M | An N-acetylglucosaminyl transferase that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon |
NECFGCCN_06276 | 6.1e-244 | gtf2 | M | A stabilizing protein that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon. Stabilizes the glycosylation activity of Gtf1 | ||
NECFGCCN_06277 | 2.6e-17 | S | Accessory secretory protein Sec Asp4 | |||
NECFGCCN_06278 | 3.6e-16 | S | Accessory secretory protein Sec, Asp5 | |||
NECFGCCN_06279 | 4e-184 | nss | M | transferase activity, transferring glycosyl groups | ||
NECFGCCN_06280 | 1.2e-54 | yabA | L | Involved in initiation control of chromosome replication | ||
NECFGCCN_06281 | 2.5e-25 | yaaT | S | stage 0 sporulation protein | ||
NECFGCCN_06282 | 1.1e-62 | pepF | E | oligoendopeptidase F | ||
NECFGCCN_06283 | 4.2e-89 | hpaC | 1.5.1.36 | C | 4-hydroxyphenylacetate 3-monooxygenase, reductase subunit | |
NECFGCCN_06284 | 0.0 | hpaB | 1.14.14.9 | C | 4-hydroxyphenylacetate 3-hydroxylase C terminal | |
NECFGCCN_06285 | 1.7e-170 | hpaA | K | 4-hydroxyphenylacetate catabolism regulatory protein hpaA | ||
NECFGCCN_06286 | 4.2e-253 | EGP | Major facilitator superfamily | |||
NECFGCCN_06287 | 9.4e-144 | hpaI | 4.1.2.20, 4.1.2.52 | G | HpcH/HpaI aldolase/citrate lyase family | |
NECFGCCN_06288 | 1.2e-151 | hpaH | Q | 2-oxohepta-3-ene-1,7-dioic acid hydratase | ||
NECFGCCN_06289 | 1.3e-66 | hpcD | 4.1.1.68, 5.3.3.10 | E | 5-carboxymethyl-2-hydroxymuconate isomerase | |
NECFGCCN_06290 | 1.3e-167 | hpaD | 1.13.11.15 | S | 3,4-dihydroxyphenylacetate 2,3-dioxygenase | |
NECFGCCN_06291 | 4.5e-285 | hpaE | 1.2.1.60 | C | Belongs to the aldehyde dehydrogenase family | |
NECFGCCN_06292 | 8.4e-142 | hpaG | 4.1.1.68 | Q | 4-hydroxyphenylacetate degradation bifunctional isomerase | |
NECFGCCN_06293 | 2.8e-114 | hpaG1 | 4.1.1.68 | Q | isomerase | |
NECFGCCN_06294 | 4.8e-73 | hpaR | K | Homoprotocatechuate degradative operon repressor | ||
NECFGCCN_06295 | 1e-19 | ooxA | C | HI0933-like protein | ||
NECFGCCN_06296 | 1.4e-20 | ooxA | C | HI0933-like protein | ||
NECFGCCN_06297 | 1.3e-185 | allD | 1.1.1.338, 1.5.1.21 | C | Belongs to the LDH2 MDH2 oxidoreductase family | |
NECFGCCN_06298 | 1e-229 | dsd | 4.3.1.18 | E | Putative serine dehydratase domain | |
NECFGCCN_06299 | 2.3e-278 | dan | 3.5.1.81, 3.5.1.82 | Q | N-acyl-D-aspartate D-glutamate deacylase | |
NECFGCCN_06300 | 1.4e-68 | tdcF | J | translation initiation inhibitor, yjgF family | ||
NECFGCCN_06301 | 1.5e-267 | VVA1143 | E | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
NECFGCCN_06302 | 5.6e-158 | dgoK | 2.7.1.58 | G | 2-keto-3-deoxy-galactonokinase | |
NECFGCCN_06303 | 9.7e-93 | dgoA | 4.1.2.14, 4.1.2.21, 4.1.3.42 | G | KDPG and KHG aldolase | |
NECFGCCN_06304 | 1.7e-146 | hexR | K | transcriptional regulator | ||
NECFGCCN_06305 | 7.5e-89 | S | Acetyltransferase | |||
NECFGCCN_06306 | 7.7e-141 | K | N-acetyltransferase | |||
NECFGCCN_06307 | 0.0 | K | transcriptional regulator | |||
NECFGCCN_06308 | 1.5e-68 | G | PTS sugar transporter | |||
NECFGCCN_06309 | 5.3e-78 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | ||
NECFGCCN_06310 | 5.6e-117 | G | PTS system | |||
NECFGCCN_06311 | 1.2e-152 | G | PTS mannose transporter subunit IID | |||
NECFGCCN_06312 | 3.4e-181 | M | glucosamine--fructose-6-phosphate aminotransferase | |||
NECFGCCN_06313 | 6.4e-190 | agaS | M | Glucosamine--fructose-6-phosphate aminotransferase | ||
NECFGCCN_06314 | 2.1e-147 | S | Transposase | |||
NECFGCCN_06315 | 0.0 | mdoB | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
NECFGCCN_06316 | 1.1e-54 | yjjA | S | Glycoprotein Receptor | ||
NECFGCCN_06317 | 9.1e-133 | dnaC | L | DNA replication protein | ||
NECFGCCN_06318 | 2.1e-94 | dnaT | L | it is also involved in inducing stable DNA replication during SOS response. It forms, in concert with dnaB protein and other prepriming proteins dnaC, N, N', N'' a prepriming protein complex on the specific site of the template DNA recognized by protein N' | ||
NECFGCCN_06319 | 2.5e-80 | yjjB | S | UPF0442 protein | ||
NECFGCCN_06320 | 3.4e-138 | yjjP | S | Membrane | ||
NECFGCCN_06321 | 2e-227 | pobA | 1.14.13.2 | CH | Catalyzes the formation of protocatechuate from 4-hydroxybenzoate | |
NECFGCCN_06322 | 1.9e-161 | pobR | K | transcriptional regulator | ||
NECFGCCN_06323 | 1.5e-127 | yjjQ | K | regulator | ||
NECFGCCN_06324 | 3.4e-118 | bglJ | K | transcriptional | ||
NECFGCCN_06325 | 1.2e-79 | ywhH | S | Prolyl-tRNA synthetase | ||
NECFGCCN_06326 | 5.5e-245 | celB | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
NECFGCCN_06327 | 9e-139 | fhuF | S | Iron reductase | ||
NECFGCCN_06328 | 9e-187 | hmsT | 2.7.7.65 | T | Diguanylate cyclase | |
NECFGCCN_06329 | 1.8e-34 | yjjZ | S | Protein of unknown function (DUF1435) | ||
NECFGCCN_06330 | 2.8e-82 | cstA | T | Carbon starvation protein | ||
NECFGCCN_06331 | 2.2e-21 | M | Pilin isopeptide linkage domain protein | |||
NECFGCCN_06332 | 1.7e-170 | 3.1.21.4 | L | Recognizes the double-stranded unmethylated sequence GATC and cleaves before G-1 | ||
NECFGCCN_06333 | 4e-107 | |||||
NECFGCCN_06334 | 1e-87 | dpnA | 2.1.1.72 | L | Belongs to the N(4) N(6)-methyltransferase family | |
NECFGCCN_06335 | 2.9e-83 | V | ABC transporter | |||
NECFGCCN_06336 | 1.1e-261 | xylA | 5.3.1.5 | G | Belongs to the xylose isomerase family | |
NECFGCCN_06337 | 1e-273 | xynT | G | transporter | ||
NECFGCCN_06338 | 0.0 | xynB | 3.2.1.37 | GH43 | G | Belongs to the glycosyl hydrolase 43 family |
NECFGCCN_06339 | 1.5e-72 | L | endonuclease | |||
NECFGCCN_06340 | 3.6e-53 | L | transposase | |||
NECFGCCN_06341 | 1.7e-140 | GM | Polysaccharide pyruvyl transferase | |||
NECFGCCN_06342 | 2.8e-278 | tuaC | 2.4.1.21 | GT4,GT5 | M | glycosyl transferase family |
NECFGCCN_06343 | 1.2e-39 | peb1A | ET | Belongs to the bacterial solute-binding protein 3 family | ||
NECFGCCN_06344 | 1.6e-48 | 1.1.1.1 | C | nadph quinone reductase | ||
NECFGCCN_06345 | 4.4e-152 | I | Alpha/beta hydrolase family | |||
NECFGCCN_06346 | 0.0 | purL | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
NECFGCCN_06347 | 7.8e-274 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
NECFGCCN_06348 | 2.5e-189 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
NECFGCCN_06349 | 1.1e-98 | purN | 2.1.2.2 | F | Catalyzes the transfer of a formyl group from 10- formyltetrahydrofolate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR) and tetrahydrofolate | |
NECFGCCN_06350 | 9.6e-294 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
NECFGCCN_06353 | 6.9e-91 | ybhD | K | transcriptional regulator | ||
NECFGCCN_06354 | 9.5e-83 | csp | K | Cold-Shock Protein | ||
NECFGCCN_06355 | 4.5e-127 | rluA | 5.4.99.28, 5.4.99.29 | J | Pseudouridine synthase | |
NECFGCCN_06356 | 1.8e-65 | yaiL | S | protein conserved in bacteria | ||
NECFGCCN_06357 | 4.1e-61 | S | Gamma-glutamyl cyclotransferase, AIG2-like | |||
NECFGCCN_06358 | 1.1e-245 | S | type VI secretion protein | |||
NECFGCCN_06359 | 5.2e-116 | S | Type VI secretion system protein ImpK | |||
NECFGCCN_06360 | 0.0 | oprF_2 | M | Belongs to the ompA family | ||
NECFGCCN_06361 | 0.0 | S | Uncharacterized protein conserved in bacteria (DUF2345) | |||
NECFGCCN_06362 | 1.9e-61 | I | phospholipase d transphosphatidylase | |||
NECFGCCN_06363 | 2.8e-46 | I | phospholipase d transphosphatidylase | |||
NECFGCCN_06364 | 4.8e-123 | ydfF | K | transcriptional regulator | ||
NECFGCCN_06365 | 8.1e-243 | icd | 1.1.1.42 | C | TIGRFAM isocitrate dehydrogenase, NADP-dependent | |
NECFGCCN_06366 | 8e-117 | rluE | 5.4.99.19, 5.4.99.20, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
NECFGCCN_06367 | 5.1e-86 | nudJ | L | Belongs to the Nudix hydrolase family. NudJ subfamily | ||
NECFGCCN_06368 | 2.2e-226 | mnmA | 2.8.1.13 | J | Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 | |
NECFGCCN_06369 | 2.9e-111 | hflD | 4.3.2.2 | S | High frequency lysogenization protein hflD homolog | |
NECFGCCN_06370 | 1.7e-262 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
NECFGCCN_06371 | 8.2e-63 | G | mannose-6-phosphate isomerase | |||
NECFGCCN_06372 | 8.9e-150 | K | AraC family transcriptional regulator | |||
NECFGCCN_06373 | 1.9e-121 | K | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
NECFGCCN_06374 | 1.3e-271 | T | PhoQ Sensor | |||
NECFGCCN_06375 | 5.1e-228 | ycfD | 1.14.11.47 | S | Cupin 4 family protein | |
NECFGCCN_06376 | 4.2e-82 | pqqF | O | Belongs to the peptidase M16 family | ||
NECFGCCN_06377 | 1.7e-39 | pqqF | O | Belongs to the peptidase M16 family | ||
NECFGCCN_06378 | 3.6e-221 | pqqE | S | Pyrroloquinoline quinone biosynthesis protein E | ||
NECFGCCN_06379 | 2e-45 | pqqD | S | With PqqC converts a biosynthetic intermediate to pyrroloquinoline quinone | ||
NECFGCCN_06380 | 1.2e-17 | pqqC | 1.3.3.11 | H | Ring cyclization and eight-electron oxidation of 3a-(2- amino-2-carboxyethyl)-4,5-dioxo-4,5,6,7,8,9-hexahydroquinoline- 7,9-dicarboxylic-acid to PQQ | |
NECFGCCN_06381 | 5.3e-106 | pqqC | 1.3.3.11 | H | Ring cyclization and eight-electron oxidation of 3a-(2- amino-2-carboxyethyl)-4,5-dioxo-4,5,6,7,8,9-hexahydroquinoline- 7,9-dicarboxylic-acid to PQQ | |
NECFGCCN_06382 | 1.9e-180 | pqqB | 3.1.4.55 | CO | May be involved in the transport of PQQ or its precursor to the periplasm | |
NECFGCCN_06383 | 1.1e-186 | 3.4.13.19 | E | Zn-dependent dipeptidase, microsomal dipeptidase | ||
NECFGCCN_06384 | 9.1e-189 | S | Alpha beta hydrolase | |||
NECFGCCN_06385 | 3.1e-133 | K | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
NECFGCCN_06386 | 6e-236 | T | PhoQ Sensor | |||
NECFGCCN_06387 | 2e-33 | secG | U | Preprotein translocase subunit SecG | ||
NECFGCCN_06388 | 0.0 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
NECFGCCN_06389 | 6.6e-81 | smpB | O | the 2 termini fold to resemble tRNA(Ala) and it encodes a tag peptide , a short internal open reading frame. During trans-translation Ala- aminoacylated tmRNA acts like a tRNA, entering the A-site of stalled ribosomes, displacing the stalled mRNA. The ribosome then switches to translate the ORF on the tmRNA | ||
NECFGCCN_06390 | 6.9e-275 | ppiB | 5.2.1.8 | G | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
NECFGCCN_06391 | 1.3e-63 | yugI | 5.3.1.9 | J | RNA binding protein, contains ribosomal protein S1 domain | |
NECFGCCN_06392 | 7.9e-157 | rssA | S | Phospholipase, patatin family | ||
NECFGCCN_06393 | 2.4e-102 | estA | E | Lysophospholipase L1 and related esterases | ||
NECFGCCN_06394 | 3.9e-90 | gmk | 2.7.4.8 | F | Essential for recycling GMP and indirectly, cGMP | |
NECFGCCN_06395 | 3.6e-46 | rpoZ | 2.7.7.6 | K | DNA-directed 5'-3' RNA polymerase activity | |
NECFGCCN_06396 | 0.0 | priA | L | Involved in the restart of stalled replication forks. Recognizes and binds the arrested nascent DNA chain at stalled replication forks. It can open the DNA duplex, via its helicase activity, and promote assembly of the primosome and loading of the major replicative helicase DnaB onto DNA | ||
NECFGCCN_06397 | 3.4e-169 | fmt | 2.1.2.9 | J | Attaches a formyl group to the free amino group of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by promoting its recognition by IF2 and preventing the misappropriation of this tRNA by the elongation apparatus | |
NECFGCCN_06398 | 3.8e-93 | panE | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
NECFGCCN_06399 | 4.8e-171 | qor | 1.6.5.5 | C | alcohol dehydrogenase | |
NECFGCCN_06400 | 0.0 | tynA | 1.4.3.21 | Q | amine oxidase | |
NECFGCCN_06401 | 0.0 | paaN | 1.2.1.91, 3.3.2.12 | CI | MaoC like domain | |
NECFGCCN_06402 | 1.1e-180 | paaA | 1.14.13.149 | S | Phenylacetic acid catabolic protein | |
NECFGCCN_06403 | 8.3e-50 | paaB | Q | Phenylacetic acid degradation B | ||
NECFGCCN_06404 | 1.4e-141 | paaC | 1.14.13.149 | S | Phenylacetic acid catabolic protein | |
NECFGCCN_06405 | 1.7e-95 | paaD | S | Iron-sulfur cluster assembly protein | ||
NECFGCCN_06406 | 4.7e-199 | paaE | C | Oxidoreductase FAD-binding domain | ||
NECFGCCN_06407 | 3.9e-131 | paaF | 4.2.1.17 | I | Enoyl-CoA hydratase/isomerase | |
NECFGCCN_06408 | 1.7e-07 | |||||
NECFGCCN_06409 | 7.3e-81 | K | acetyltransferase | |||
NECFGCCN_06410 | 4.5e-269 | uxaB | 1.1.1.11, 1.1.1.17, 1.1.1.57, 1.1.1.58 | G | Belongs to the mannitol dehydrogenase family. UxaB subfamily | |
NECFGCCN_06411 | 9.5e-84 | ttr | K | histone acetyltransferase HPA2 and related acetyltransferases | ||
NECFGCCN_06412 | 7.3e-256 | yneF | T | Diguanylate cyclase | ||
NECFGCCN_06413 | 1.2e-61 | yneG | S | Domain of unknown function (DUF4186) | ||
NECFGCCN_06414 | 3.4e-169 | glsA | 3.5.1.2 | E | Belongs to the glutaminase family | |
NECFGCCN_06415 | 1.1e-259 | sad | 1.2.1.16, 1.2.1.20, 1.2.1.24, 1.2.1.79 | C | belongs to the aldehyde dehydrogenase family | |
NECFGCCN_06416 | 2.6e-163 | yneJ | K | Transcriptional regulator | ||
NECFGCCN_06417 | 3.3e-83 | ysnE | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
NECFGCCN_06418 | 3.1e-170 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
NECFGCCN_06419 | 4.9e-134 | K | transcriptional regulator | |||
NECFGCCN_06420 | 4.2e-178 | pdxA | 1.1.1.262, 1.1.1.408, 1.1.1.409 | H | Catalyzes the NAD(P)-dependent oxidation of 4- (phosphohydroxy)-L-threonine (HTP) into 2-amino-3-oxo-4- (phosphohydroxy)butyric acid which spontaneously decarboxylates to form 3-amino-2-oxopropyl phosphate (AHAP) | |
NECFGCCN_06421 | 2.1e-211 | ygbK | 2.7.1.219, 2.7.1.220 | G | type III effector | |
NECFGCCN_06422 | 4.7e-197 | dhaT | C | alcohol dehydrogenase | ||
NECFGCCN_06423 | 1.8e-156 | dapA_2 | 4.3.3.7 | EM | Belongs to the DapA family | |
NECFGCCN_06424 | 4.7e-247 | E | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | |||
NECFGCCN_06425 | 6.7e-207 | 3.2.1.51 | GH29 | G | BNR repeat-like domain | |
NECFGCCN_06426 | 5.9e-53 | yjgK | G | Domain of unknown function (DUF386) | ||
NECFGCCN_06427 | 2.8e-88 | IQ | NAD dependent epimerase/dehydratase family | |||
NECFGCCN_06428 | 3e-72 | yddE | S | phenazine biosynthesis protein PhzF | ||
NECFGCCN_06429 | 2.8e-144 | KLT | Protein tyrosine kinase | |||
NECFGCCN_06430 | 3.7e-98 | |||||
NECFGCCN_06432 | 7.8e-171 | L | DNA integration | |||
NECFGCCN_06434 | 8e-22 | S | PAAR motif | |||
NECFGCCN_06435 | 2.8e-107 | |||||
NECFGCCN_06436 | 1e-138 | N | type VI secretion protein | |||
NECFGCCN_06437 | 0.0 | N | type VI secretion protein | |||
NECFGCCN_06438 | 0.0 | vasA | S | Type VI secretion | ||
NECFGCCN_06439 | 2.3e-198 | S | type VI secretion protein | |||
NECFGCCN_06440 | 1.4e-90 | S | Type VI secretion lipoprotein, VasD, EvfM, TssJ, VC_A0113 | |||
NECFGCCN_06441 | 3.6e-76 | S | Type VI secretion system | |||
NECFGCCN_06442 | 7.8e-218 | M | ImpA domain protein | |||
NECFGCCN_06443 | 3e-162 | G | ABC-type sugar transport system periplasmic component | |||
NECFGCCN_06445 | 2.2e-204 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
NECFGCCN_06446 | 2.1e-108 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
NECFGCCN_06447 | 4.5e-45 | ychH | S | cellular response to cadmium ion | ||
NECFGCCN_06448 | 1.3e-68 | S | cog cog4699 | |||
NECFGCCN_06449 | 0.0 | rpoC | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
NECFGCCN_06450 | 0.0 | rpoB | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
NECFGCCN_06451 | 0.0 | pbp1B | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
NECFGCCN_06452 | 1.6e-103 | btuF | P | Part of the ABC transporter complex BtuCDF involved in vitamin B12 import. Binds vitamin B12 and delivers it to the periplasmic surface of BtuC | ||
NECFGCCN_06453 | 3.4e-109 | yadS | S | membrane | ||
NECFGCCN_06454 | 1.1e-59 | erpA | C | iron--sulfur cluster insertion protein erpA | ||
NECFGCCN_06455 | 1.2e-256 | clcA | P | Probably acts as an electrical shunt for an outwardly- directed proton pump that is linked to amino acid decarboxylation, as part of the extreme acid resistance (XAR) response | ||
NECFGCCN_06456 | 5.7e-244 | hemL | 5.4.3.8 | H | Glutamate-1-semialdehyde aminotransferase | |
NECFGCCN_06458 | 6.8e-170 | ansA | 3.5.1.1 | EJ | COG0252 L-asparaginase archaeal Glu-tRNAGln amidotransferase subunit D | |
NECFGCCN_06459 | 1.8e-259 | XK27_03190 | S | hydrolases of the HAD superfamily | ||
NECFGCCN_06460 | 3.5e-07 | |||||
NECFGCCN_06462 | 0.0 | S | cellulase activity | |||
NECFGCCN_06463 | 1.9e-70 | |||||
NECFGCCN_06464 | 3.8e-84 | S | Domain of unknown function (DUF1833) | |||
NECFGCCN_06465 | 3.5e-90 | |||||
NECFGCCN_06466 | 0.0 | M | tape measure protein | |||
NECFGCCN_06467 | 8.3e-08 | S | YebO-like protein | |||
NECFGCCN_06468 | 1.2e-46 | S | Protein of unknown function (DUF4035) | |||
NECFGCCN_06469 | 3.7e-55 | S | tail assembly chaperone | |||
NECFGCCN_06470 | 2.6e-83 | |||||
NECFGCCN_06472 | 1.1e-53 | S | Structural component (Phage or Prophage Related) | |||
NECFGCCN_06473 | 8.6e-70 | S | Bacteriophage HK97-gp10, putative tail-component | |||
NECFGCCN_06474 | 3.6e-44 | S | head-tail adaptor | |||
NECFGCCN_06475 | 2.3e-29 | S | Phage gp6-like head-tail connector protein | |||
NECFGCCN_06476 | 2.1e-182 | S | TIGRFAM Phage major capsid protein, HK97 | |||
NECFGCCN_06477 | 8.2e-100 | S | Prohead protease | |||
NECFGCCN_06478 | 7.8e-214 | S | TIGRFAM Phage portal protein, HK97 | |||
NECFGCCN_06480 | 1.1e-264 | K | terminase | |||
NECFGCCN_06481 | 4.7e-69 | L | Phage terminase, small subunit | |||
NECFGCCN_06482 | 2.9e-57 | L | HNH endonuclease | |||
NECFGCCN_06483 | 1.8e-17 | |||||
NECFGCCN_06484 | 5.8e-44 | S | Domain of unknown function (DUF4747) | |||
NECFGCCN_06486 | 2.3e-105 | GH19 | S | Chitinase class I | ||
NECFGCCN_06487 | 5.3e-41 | S | Putative 3TM holin, Phage_holin_3 | |||
NECFGCCN_06488 | 3.6e-64 | S | Putative phage holin | |||
NECFGCCN_06490 | 2.2e-81 | S | Protein of unknown function (DUF1133) | |||
NECFGCCN_06491 | 4.2e-138 | ydfU | V | Protein of unknown function (DUF968) | ||
NECFGCCN_06492 | 3.2e-49 | rusA | 3.1.22.4 | L | Endodeoxyribonuclease RusA | |
NECFGCCN_06493 | 1.8e-110 | dam | 2.1.1.37, 2.1.1.72 | H | Site-specific DNA-methyltransferase (Adenine-specific) | |
NECFGCCN_06494 | 2e-99 | S | DNA replication | |||
NECFGCCN_06495 | 5.8e-25 | S | Domain of unknown function (DUF4222) | |||
NECFGCCN_06496 | 4.7e-63 | |||||
NECFGCCN_06497 | 5.7e-26 | cro | S | DNA-binding transcriptional regulator Cro | ||
NECFGCCN_06498 | 1.2e-112 | c2 | K | Helix-turn-helix domain | ||
NECFGCCN_06500 | 3.4e-114 | |||||
NECFGCCN_06502 | 2.2e-57 | |||||
NECFGCCN_06503 | 5.5e-31 | S | Membrane | |||
NECFGCCN_06504 | 4.9e-12 | S | CsbD-like | |||
NECFGCCN_06505 | 6.5e-117 | dgdR | K | transcriptional regulator | ||
NECFGCCN_06506 | 1.4e-22 | dgdR | K | transcriptional regulator | ||
NECFGCCN_06507 | 1.7e-271 | ddc | 2.6.1.76, 4.1.1.86 | E | decarboxylase | |
NECFGCCN_06508 | 1.9e-269 | dat | 2.6.1.76 | E | Belongs to the class-III pyridoxal-phosphate-dependent aminotransferase family | |
NECFGCCN_06509 | 6.8e-170 | Z012_04120 | P | COG0715 ABC-type nitrate sulfonate bicarbonate transport systems periplasmic components | ||
NECFGCCN_06510 | 5.5e-114 | Z012_04125 | P | ABC-type nitrate sulfonate bicarbonate transport system permease component | ||
NECFGCCN_06511 | 2.1e-126 | ssuB_2 | P | ABC-type nitrate sulfonate bicarbonate transport system ATPase component | ||
NECFGCCN_06512 | 1.1e-121 | tenA | 3.5.99.2 | K | Catalyzes an amino-pyrimidine hydrolysis reaction at the C5' of the pyrimidine moiety of thiamine compounds, a reaction that is part of a thiamine salvage pathway | |
NECFGCCN_06515 | 1e-73 | cioB | 1.10.3.14 | C | oxidase subunit | |
NECFGCCN_06516 | 9.8e-10 | |||||
NECFGCCN_06518 | 8.6e-100 | 4.2.99.18 | L | oxidized base lesion DNA N-glycosylase activity | ||
NECFGCCN_06519 | 2.8e-120 | 3.1.4.52 | T | EAL domain | ||
NECFGCCN_06520 | 2.1e-290 | 4.1.1.98 | H | 3-octaprenyl-4-hydroxybenzoate carboxy-lyase | ||
NECFGCCN_06521 | 3.2e-153 | K | transcriptional regulator | |||
NECFGCCN_06522 | 0.0 | ytrP | 2.7.7.65 | T | Diguanylate cyclase | |
NECFGCCN_06523 | 6e-219 | rpfG | T | metal-dependent phosphohydrolase, HD | ||
NECFGCCN_06524 | 2.4e-184 | ansB | 3.5.1.1 | EJ | Belongs to the asparaginase 1 family | |
NECFGCCN_06525 | 1.3e-178 | lpxL | 2.3.1.241, 2.3.1.242, 2.3.1.243 | M | Catalyzes the transfer of laurate from lauroyl-acyl carrier protein (ACP) to Kdo(2)-lipid IV(A) to form Kdo(2)- (lauroyl)-lipid IV(A) | |
NECFGCCN_06526 | 6.2e-106 | leuE | E | Efflux Protein | ||
NECFGCCN_06527 | 1.3e-38 | ynaJ | S | Protein of unknown function (DUF2534) | ||
NECFGCCN_06528 | 1.6e-08 | yoaK | ||||
NECFGCCN_06529 | 4.3e-186 | yeaP | 2.7.7.65 | T | Diguanylate cyclase | |
NECFGCCN_06530 | 2.1e-38 | yoaF | ||||
NECFGCCN_06531 | 1.2e-61 | yeaO | S | MarR family transcriptional regulator | ||
NECFGCCN_06532 | 1.8e-87 | ybbK | S | Purine nucleoside phosphorylase | ||
NECFGCCN_06533 | 8.2e-128 | pyrG2 | 6.3.4.2 | F | CTP synthase | |
NECFGCCN_06534 | 8e-208 | yeaN | P | Major facilitator superfamily | ||
NECFGCCN_06535 | 5.3e-147 | yeaM | K | Transcriptional regulator | ||
NECFGCCN_06536 | 5.9e-71 | yeaL | S | UPF0756 membrane protein | ||
NECFGCCN_06537 | 1.6e-85 | yeaK | S | YbaK prolyl-tRNA synthetase associated | ||
NECFGCCN_06538 | 4.8e-210 | waaU | M | Glycosyltransferase family 9 (heptosyltransferase) | ||
NECFGCCN_06539 | 8.9e-37 | msgA | S | Virulence protein msgA | ||
NECFGCCN_06540 | 8.9e-61 | umuD | KT | Belongs to the peptidase S24 family | ||
NECFGCCN_06541 | 6.1e-214 | umuC | 2.7.7.7 | L | DNA polymerase | |
NECFGCCN_06542 | 1.7e-165 | K | transcriptional regulator | |||
NECFGCCN_06543 | 7.8e-124 | IQ | Dehydrogenases with different specificities (Related to short-chain alcohol dehydrogenases) | |||
NECFGCCN_06544 | 1.9e-115 | EGP | Major Facilitator Superfamily | |||
NECFGCCN_06545 | 4.1e-48 | EGP | Major Facilitator Superfamily | |||
NECFGCCN_06546 | 8.2e-157 | K | transcriptional regulator | |||
NECFGCCN_06547 | 4.4e-45 | rpmE2 | J | 50S ribosomal protein L31 | ||
NECFGCCN_06548 | 2.3e-215 | mntH | P | Mn2 and Fe2 transporters of the NRAMP family | ||
NECFGCCN_06549 | 2.2e-35 | dltC | 6.1.1.13 | IQ | Carrier protein involved in the D-alanylation of lipoteichoic acid (LTA). The loading of thioester-linked D-alanine onto DltC is catalyzed by D-alanine--D-alanyl carrier protein ligase DltA. The DltC-carried D-alanyl group is further transferred to cell membrane phosphatidylglycerol (PG) by forming an ester bond, probably catalyzed by DltD. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
NECFGCCN_06550 | 3.7e-243 | dltD | M | Protein involved in D-alanine esterification of lipoteichoic acid and wall teichoic acid (D-alanine transfer protein) | ||
NECFGCCN_06551 | 4.3e-07 | |||||
NECFGCCN_06554 | 9e-07 | |||||
NECFGCCN_06556 | 6.3e-70 | badR | K | Transcriptional regulator, marr family | ||
NECFGCCN_06557 | 1.2e-35 | XK27_02060 | S | Transglycosylase associated protein | ||
NECFGCCN_06558 | 6.6e-237 | pepS | E | COG2309 Leucyl aminopeptidase (aminopeptidase T) | ||
NECFGCCN_06559 | 0.0 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
NECFGCCN_06560 | 5.4e-92 | paiA | 2.3.1.57 | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | |
NECFGCCN_06561 | 3.9e-198 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
NECFGCCN_06562 | 2.3e-22 | WQ51_00220 | K | Helix-turn-helix domain | ||
NECFGCCN_06563 | 7.7e-81 | S | Protein of unknown function (DUF3278) | |||
NECFGCCN_06564 | 0.0 | smc | D | Required for chromosome condensation and partitioning | ||
NECFGCCN_06565 | 2.9e-38 | rnc | 3.1.26.3 | J | Digests double-stranded RNA. Involved in the processing of primary rRNA transcript to yield the immediate precursors to the large and small rRNAs (23S and 16S). Processes some mRNAs, and tRNAs when they are encoded in the rRNA operon. Processes pre- crRNA and tracrRNA of type II CRISPR loci if present in the organism | |
NECFGCCN_06566 | 8.4e-142 | P | molecular chaperone | |||
NECFGCCN_06567 | 7.6e-94 | XK27_05505 | S | Psort location CytoplasmicMembrane, score | ||
NECFGCCN_06569 | 2.9e-47 | Z012_11195 | L | Helix-turn-helix domain | ||
NECFGCCN_06570 | 8.9e-38 | Z012_11195 | L | Putative transposase DNA-binding domain | ||
NECFGCCN_06571 | 4.1e-97 | Z012_11195 | L | Putative transposase DNA-binding domain | ||
NECFGCCN_06572 | 5.6e-180 | umuC | 2.7.7.7 | L | Binds processed UmuD protein to form functional DNA pol V (UmuD'2UmuC) | |
NECFGCCN_06573 | 2e-42 | umuC | 2.7.7.7 | L | Binds processed UmuD protein to form functional DNA pol V (UmuD'2UmuC) | |
NECFGCCN_06574 | 2e-76 | L | Peptidase S24-like | |||
NECFGCCN_06575 | 7.8e-285 | 2.7.7.49 | L | Reverse transcriptase (RNA-dependent DNA polymerase) | ||
NECFGCCN_06576 | 1e-21 | |||||
NECFGCCN_06577 | 3.9e-41 | S | Antirestriction protein | |||
NECFGCCN_06578 | 7.1e-37 | 2.7.7.7 | L | DNA polymerase | ||
NECFGCCN_06579 | 9.8e-44 | |||||
NECFGCCN_06580 | 3.3e-152 | S | Psort location Cytoplasmic, score 8.96 | |||
NECFGCCN_06582 | 3.8e-87 | M | invasion protein IagB | |||
NECFGCCN_06583 | 2.1e-61 | S | TraM protein, DNA-binding | |||
NECFGCCN_06584 | 1.9e-80 | |||||
NECFGCCN_06585 | 3.8e-55 | S | TraA | |||
NECFGCCN_06586 | 1.7e-56 | traL | S | TraL protein | ||
NECFGCCN_06587 | 2e-100 | traE | S | TraE protein | ||
NECFGCCN_06588 | 2.4e-133 | traK | 1.16.1.9 | P | TraK protein | |
NECFGCCN_06589 | 2.9e-236 | tolA | 2.7.13.3 | NU | transfer protein TraB | |
NECFGCCN_06590 | 7e-104 | S | Type IV conjugative transfer system lipoprotein (TraV) | |||
NECFGCCN_06592 | 6.8e-36 | |||||
NECFGCCN_06593 | 1e-11 | |||||
NECFGCCN_06594 | 1.7e-72 | |||||
NECFGCCN_06596 | 3.2e-60 | |||||
NECFGCCN_06597 | 0.0 | traG | U | F pilus assembly Type-IV secretion system for plasmid transfer | ||
NECFGCCN_06598 | 2.2e-61 | S | Type-F conjugative transfer system protein (TrbI_Ftype) | |||
NECFGCCN_06599 | 1.7e-116 | traW | S | Type-F conjugative transfer system protein TraW | ||
NECFGCCN_06600 | 5.7e-65 | |||||
NECFGCCN_06601 | 2.3e-200 | traU | S | PFAM TraU | ||
NECFGCCN_06603 | 3.9e-116 | trbC | S | Type-F conjugative transfer system pilin assembly protein | ||
NECFGCCN_06604 | 0.0 | traN | S | F plasmid TraN appears to recognize OmpA in the recipient cell | ||
NECFGCCN_06605 | 3.2e-37 | S | Conjugal transfer protein TrbE | |||
NECFGCCN_06606 | 8.2e-36 | |||||
NECFGCCN_06607 | 3e-56 | |||||
NECFGCCN_06608 | 2.3e-139 | traF | CO | Type IV secretion system pilus assembly protein | ||
NECFGCCN_06609 | 1.4e-37 | S | Type-F conjugative transfer system pilin chaperone (TraQ) | |||
NECFGCCN_06610 | 6.9e-101 | CO | F plasmid transfer operon protein | |||
NECFGCCN_06611 | 1.2e-76 | |||||
NECFGCCN_06612 | 8.8e-251 | traH | S | PFAM Conjugative relaxosome accessory transposon protein | ||
NECFGCCN_06613 | 0.0 | S | TraG-like protein, N-terminal region | |||
NECFGCCN_06614 | 2.3e-62 | S | TraG-like protein, N-terminal region | |||
NECFGCCN_06616 | 1.1e-114 | ylpA | S | TraT complement resistance | ||
NECFGCCN_06617 | 0.0 | traD | U | Type IV secretion system coupling protein | ||
NECFGCCN_06618 | 0.0 | traI | L | ATP-dependent exoDNAse (exonuclease V) alpha subunit - helicase superfamily I member | ||
NECFGCCN_06619 | 2.5e-135 | S | TraX protein | |||
NECFGCCN_06620 | 4.2e-96 | finO | T | Fertility inhibition protein N terminal | ||
NECFGCCN_06621 | 7.2e-56 | |||||
NECFGCCN_06622 | 3.1e-12 | CP_0355 | S | CAAX protease self-immunity | ||
NECFGCCN_06623 | 6.8e-173 | S | Microcin H47 secretion protein | |||
NECFGCCN_06625 | 1.1e-11 | S | ABC-2 family transporter protein | |||
NECFGCCN_06627 | 1.4e-07 | L | Psort location Cytoplasmic, score 8.96 | |||
NECFGCCN_06629 | 3.7e-26 | soj | D | ATPases involved in chromosome partitioning | ||
NECFGCCN_06631 | 8.4e-11 | bipA | S | protein secretion | ||
NECFGCCN_06632 | 3e-31 | bipA | S | protein secretion | ||
NECFGCCN_06633 | 3.7e-148 | lcnDR2 | V | Domain of unknown function (DUF4135) | ||
NECFGCCN_06634 | 1.2e-44 | yfaE | C | Ferredoxin | ||
NECFGCCN_06635 | 1.5e-216 | nrdB | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
NECFGCCN_06636 | 0.0 | nrdA | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
NECFGCCN_06637 | 1.2e-137 | ubiG | 2.1.1.222, 2.1.1.64 | H | O-methyltransferase that catalyzes the 2 O-methylation steps in the ubiquinone biosynthetic pathway | |
NECFGCCN_06638 | 0.0 | gyrA | 5.99.1.3 | L | A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner | |
NECFGCCN_06639 | 0.0 | rcsC | 2.7.13.3 | T | PhoQ Sensor | |
NECFGCCN_06640 | 4.1e-113 | rcsB | K | Component of the Rcs signaling system, which controls transcription of numerous genes. RcsB is the response regulator that binds to regulatory DNA regions | ||
NECFGCCN_06641 | 0.0 | rcsD | 2.7.13.3, 4.6.1.1 | T | Component of the Rcs signaling system, which controls transcription of numerous genes. RcsD is a phosphotransfer intermediate between the sensor kinase RcsC and the response regulator RcsB. It acquires a phosphoryl group from RcsC and transfers it to RcsB | |
NECFGCCN_06642 | 1.6e-194 | ompC | M | Belongs to the Gram-negative porin family | ||
NECFGCCN_06643 | 5.3e-195 | apbE | 2.7.1.180 | H | Flavin transferase that catalyzes the transfer of the FMN moiety of FAD and its covalent binding to the hydroxyl group of a threonine residue in a target flavoprotein | |
NECFGCCN_06644 | 1.8e-190 | ada | 2.1.1.63, 3.2.2.21 | FL | Involved in the cellular defense against the biological effects of O6-methylguanine (O6-MeG) and O4-methylthymine (O4-MeT) in DNA. Repairs the methylated nucleobase in DNA by stoichiometrically transferring the methyl group to a cysteine residue in the enzyme. This is a suicide reaction the enzyme is irreversibly inactivated | |
NECFGCCN_06645 | 9.1e-121 | alkB | 1.14.11.33 | L | Alkylated DNA repair protein | |
NECFGCCN_06646 | 3.7e-304 | yojI | PQ | Cyclic peptide transporter | ||
NECFGCCN_06647 | 1.2e-263 | mgtE | P | Acts as a magnesium transporter | ||
NECFGCCN_06648 | 5.1e-189 | P | COG0659 Sulfate permease and related transporters (MFS superfamily) | |||
NECFGCCN_06649 | 0.0 | mqo | 1.1.5.4 | C | malate quinone oxidoreductase | |
NECFGCCN_06650 | 3.9e-84 | eco | M | General inhibitor of pancreatic serine proteases inhibits chymotrypsin, trypsin, elastases, factor X, kallikrein as well as a variety of other proteases | ||
NECFGCCN_06651 | 1.8e-193 | ydiK_1 | S | permease | ||
NECFGCCN_06653 | 0.0 | yejM | S | Hydrolase of alkaline phosphatase superfamily | ||
NECFGCCN_06654 | 9.3e-32 | yejL | S | Belongs to the UPF0352 family | ||
NECFGCCN_06655 | 3.8e-182 | ndpA | S | Nucleoid-associated protein | ||
NECFGCCN_06656 | 4.6e-124 | glcR | 3.6.4.12 | K | transcriptional regulator | |
NECFGCCN_06657 | 1.1e-107 | nudK | 3.6.1.13 | L | Nudix-type nucleoside diphosphatase, YffH AdpP family | |
NECFGCCN_06658 | 5e-248 | nylB | V | Beta-lactamase | ||
NECFGCCN_06659 | 1.7e-154 | K | Transcriptional regulator | |||
NECFGCCN_06660 | 6.7e-44 | rplY | J | This is one of the proteins that binds to the 5S RNA in the ribosome where it forms part of the central protuberance | ||
NECFGCCN_06661 | 0.0 | yejH | L | Type III restriction protein res subunit | ||
NECFGCCN_06662 | 5.1e-133 | rsuA | 5.4.99.19, 5.4.99.20, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
NECFGCCN_06663 | 1e-210 | bcr | EGP | Major facilitator Superfamily | ||
NECFGCCN_06664 | 4.3e-61 | yejG | S | YejG-like protein | ||
NECFGCCN_06665 | 4.9e-285 | yejF | P | ATPase activity | ||
NECFGCCN_06666 | 1.8e-176 | yejE | P | ABC transporter (Permease | ||
NECFGCCN_06667 | 1.3e-199 | yejB | P | ABC transporter (permease) | ||
NECFGCCN_06668 | 0.0 | yejA | E | ABC-type oligopeptide transport system, periplasmic component | ||
NECFGCCN_06669 | 3.7e-285 | rtn | T | Involved in resistance to the phages N4 and lambda | ||
NECFGCCN_06670 | 5.6e-98 | spr | 3.4.17.13 | M | COG0791 Cell wall-associated hydrolases (invasion-associated proteins) | |
NECFGCCN_06671 | 9e-122 | lpxT | 2.7.4.29 | I | Involved in the modification of the lipid A domain of lipopolysaccharides (LPS). Transfers a phosphate group from undecaprenyl pyrophosphate (C55-PP) to lipid A to form lipid A 1- diphosphate. Contributes to the recycling of undecaprenyl phosphate (C55-P) | |
NECFGCCN_06672 | 1.4e-173 | yeiR | S | cobalamin synthesis protein, P47K | ||
NECFGCCN_06673 | 1.1e-278 | mtlK | 1.1.1.11, 1.1.1.17, 1.1.1.289, 1.1.1.57, 1.1.1.58, 1.1.1.67, 2.7.1.17 | G | Belongs to the mannitol dehydrogenase family | |
NECFGCCN_06674 | 2.1e-232 | uxuA | 4.2.1.8 | G | Catalyzes the dehydration of D-mannonate | |
NECFGCCN_06675 | 4.4e-103 | efp | J | Elongation factor P | ||
NECFGCCN_06676 | 1.4e-139 | L | Cleaves both 3' and 5' ssDNA extremities of branched DNA structures | |||
NECFGCCN_06677 | 1e-210 | setB | EGP | Major facilitator Superfamily | ||
NECFGCCN_06678 | 2.2e-186 | fruB | 2.7.1.121, 2.7.1.202, 2.7.3.9 | G | Bifunctional PTS system fructose-specific transporter subunit IIA HPr protein | |
NECFGCCN_06679 | 1.1e-175 | fruK | 2.7.1.11, 2.7.1.56 | H | belongs to the carbohydrate kinase PfkB family | |
NECFGCCN_06680 | 1.6e-270 | fruA | 2.7.1.202 | G | PTS system, fructose subfamily, IIC subunit | |
NECFGCCN_06681 | 2e-160 | nfo | 3.1.21.2 | L | Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin | |
NECFGCCN_06682 | 5e-185 | yeiH | S | Belongs to the UPF0324 family | ||
NECFGCCN_06683 | 3.6e-157 | yeiE | K | transcriptional regulator | ||
NECFGCCN_06684 | 2.7e-277 | lysP | E | amino acid | ||
NECFGCCN_06685 | 8.5e-31 | |||||
NECFGCCN_06686 | 9.4e-21 | |||||
NECFGCCN_06688 | 2.8e-157 | XK27_09825 | V | abc transporter atp-binding protein | ||
NECFGCCN_06692 | 8.4e-67 | anK3 | G | response to abiotic stimulus | ||
NECFGCCN_06693 | 1e-45 | malI | K | Transcriptional regulator | ||
NECFGCCN_06694 | 3.3e-297 | malX | 2.7.1.192, 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | PTS system | |
NECFGCCN_06695 | 1e-223 | malY | 4.4.1.8 | E | Bifunctional PLP-dependent enzyme with beta-cystathionase and maltose regulon repressor activities | |
NECFGCCN_06696 | 2.5e-189 | corA | P | transporter | ||
NECFGCCN_06697 | 4.2e-32 | ydfZ_1 | S | selenium-binding protein YdfZ | ||
NECFGCCN_06698 | 1e-89 | |||||
NECFGCCN_06699 | 5.6e-48 | MA20_23345 | S | membrane | ||
NECFGCCN_06700 | 3.5e-227 | yedE | S | transporter component | ||
NECFGCCN_06701 | 1.2e-38 | yedF | O | Belongs to the sulfur carrier protein TusA family | ||
NECFGCCN_06702 | 2.1e-59 | ycgX | S | Phage envelope protein | ||
NECFGCCN_06703 | 1.1e-22 | yqaE | S | homolog of Blt101 | ||
NECFGCCN_06704 | 7.5e-183 | gap | 1.2.1.12, 1.2.1.72 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
NECFGCCN_06705 | 1.1e-270 | aldA | 1.2.1.21, 1.2.1.22 | C | belongs to the aldehyde dehydrogenase family | |
NECFGCCN_06706 | 2.7e-143 | ydcF | S | DUF218 domain | ||
NECFGCCN_06707 | 4.9e-238 | proP | EGP | Major facilitator superfamily | ||
NECFGCCN_06708 | 5.8e-261 | cycA | E | amino acid | ||
NECFGCCN_06709 | 1.5e-183 | astE | 3.5.1.96 | E | Belongs to the AspA AstE family. Succinylglutamate desuccinylase subfamily | |
NECFGCCN_06710 | 1.3e-254 | astB | 3.5.3.23 | E | Catalyzes the hydrolysis of N(2)-succinylarginine into N(2)-succinylornithine, ammonia and CO(2) | |
NECFGCCN_06711 | 4.1e-270 | astD | 1.2.1.71 | C | Catalyzes the NAD-dependent reduction of succinylglutamate semialdehyde into succinylglutamate | |
NECFGCCN_06712 | 2.7e-188 | astA | 2.3.1.109 | E | arginine N-succinyltransferase | |
NECFGCCN_06713 | 5.8e-230 | argD | 2.6.1.11, 2.6.1.17, 2.6.1.81 | E | aminotransferase | |
NECFGCCN_06714 | 6.1e-246 | gdhA | 1.4.1.3, 1.4.1.4 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
NECFGCCN_06715 | 1.1e-176 | C | Aldo keto reductase | |||
NECFGCCN_06716 | 3.6e-158 | K | Transcriptional regulator | |||
NECFGCCN_06717 | 1.7e-62 | marR1 | K | transcriptional regulator | ||
NECFGCCN_06718 | 9.8e-88 | folA | 1.5.1.3 | H | Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis | |
NECFGCCN_06719 | 0.0 | kefC | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
NECFGCCN_06720 | 2e-102 | kefF | C | Regulatory subunit of a potassium efflux system that confers protection against electrophiles. Required for full activity of KefC. Shows redox enzymatic activity, but this enzymatic activity is not required for activation of KefC | ||
NECFGCCN_06721 | 4.4e-33 | ygdi3 | S | (LipO)protein | ||
NECFGCCN_06722 | 0.0 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthetase ammonia chain | |
NECFGCCN_06723 | 2.2e-218 | carA | 6.3.5.5 | F | Belongs to the CarA family | |
NECFGCCN_06724 | 7.9e-146 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
NECFGCCN_06725 | 2.6e-158 | citG | 2.4.2.52, 2.7.7.61 | H | 2-(5''-triphosphoribosyl)-3'-dephosphocoenzyme-A synthase | |
NECFGCCN_06726 | 9.4e-286 | citF | 2.8.3.10 | H | Citrate lyase alpha subunit | |
NECFGCCN_06727 | 9.9e-155 | citE | 4.1.3.25, 4.1.3.34 | G | Belongs to the HpcH HpaI aldolase family | |
NECFGCCN_06728 | 3.8e-42 | citD | 4.1.3.34 | C | Covalent carrier of the coenzyme of citrate lyase | |
NECFGCCN_06729 | 4.1e-192 | citC | 6.2.1.22 | H | Acetylation of prosthetic group (2-(5''-phosphoribosyl)- 3'-dephosphocoenzyme-A) of the gamma subunit of citrate lyase | |
NECFGCCN_06730 | 4.8e-217 | citS | P | Uptake of citrate across the boundary membrane with the concomitant uptake of a sodium ion (symport system) | ||
NECFGCCN_06731 | 1.6e-28 | oadG | 4.1.1.3 | C | oxaloacetate decarboxylase gamma chain | |
NECFGCCN_06732 | 8.4e-294 | oadA | 2.3.1.12, 4.1.1.3, 6.4.1.1 | CI | Oxaloacetate | |
NECFGCCN_06733 | 1.8e-224 | oadB | 4.1.1.3 | C | Na -transporting methylmalonyl-CoA oxaloacetate decarboxylase, beta subunit | |
NECFGCCN_06734 | 1.1e-242 | citA | 2.7.13.3 | T | Signal transduction histidine kinase regulating citrate malate metabolism | |
NECFGCCN_06735 | 1.7e-117 | citB | K | transcriptional regulatory protein | ||
NECFGCCN_06736 | 4.8e-111 | alaS_2 | 6.1.1.7 | S | Alanyl-tRNA synthetase | |
NECFGCCN_06737 | 2.9e-168 | K | transcriptional regulator | |||
NECFGCCN_06738 | 1.4e-57 | yhaI | S | Protein of unknown function (DUF805) | ||
NECFGCCN_06739 | 1.5e-169 | rihC | 3.2.2.1 | F | Belongs to the IUNH family | |
NECFGCCN_06740 | 1e-173 | ispH | 1.17.7.4, 2.7.4.25 | IM | Catalyzes the conversion of 1-hydroxy-2-methyl-2-(E)- butenyl 4-diphosphate (HMBPP) into a mixture of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP). Acts in the terminal step of the DOXP MEP pathway for isoprenoid precursor biosynthesis | |
NECFGCCN_06741 | 1.9e-77 | fkpB | 5.2.1.8 | G | Peptidyl-prolyl cis-trans | |
NECFGCCN_06742 | 3.7e-90 | lspA | 3.4.23.36 | M | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
NECFGCCN_06743 | 0.0 | ileS | 6.1.1.5 | J | amino acids such as valine, to avoid such errors it has two additional distinct tRNA(Ile)-dependent editing activities. One activity is designated as 'pretransfer' editing and involves the hydrolysis of activated Val-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Val-tRNA(Ile) | |
NECFGCCN_06744 | 3e-173 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
NECFGCCN_06745 | 9.1e-30 | |||||
NECFGCCN_06746 | 9.5e-169 | nhaR | K | transcriptional regulator | ||
NECFGCCN_06747 | 8.6e-205 | nhaA | P | Na( ) H( ) antiporter that extrudes sodium in exchange for external protons | ||
NECFGCCN_06748 | 9.8e-179 | dnaJ | O | ATP binding to DnaK triggers the release of the substrate protein, thus completing the reaction cycle. Several rounds of ATP-dependent interactions between DnaJ, DnaK and GrpE are required for fully efficient folding. Also involved, together with DnaK and GrpE, in the DNA replication of plasmids through activation of initiation proteins | ||
NECFGCCN_06749 | 0.0 | dnaK | O | Heat shock 70 kDa protein | ||
NECFGCCN_06750 | 1.1e-63 | yaaI | S | Belongs to the UPF0412 family | ||
NECFGCCN_06751 | 1.9e-130 | yaaW | S | protein conserved in bacteria | ||
NECFGCCN_06752 | 4.2e-98 | yaaH | S | GPR1 FUN34 yaaH family protein | ||
NECFGCCN_06753 | 4.2e-226 | tphA | EGP | Major facilitator superfamily | ||
NECFGCCN_06754 | 3.1e-104 | mog | 2.7.7.75, 2.8.1.12 | H | Molybdenum cofactor | |
NECFGCCN_06755 | 6.1e-174 | tal | 2.2.1.2 | G | Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway | |
NECFGCCN_06756 | 1.5e-256 | yaaJ | E | alanine symporter | ||
NECFGCCN_06757 | 7.2e-141 | yaaA | S | Belongs to the UPF0246 family | ||
NECFGCCN_06758 | 3.8e-10 | |||||
NECFGCCN_06759 | 1.4e-245 | thrC | 4.2.3.1 | E | Threonine synthase | |
NECFGCCN_06760 | 7.5e-177 | thrB | 2.7.1.39 | E | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
NECFGCCN_06761 | 0.0 | thrA | 1.1.1.3, 2.7.2.4 | E | belongs to the aspartokinase family | |
NECFGCCN_06762 | 2.1e-115 | trmJ | 2.1.1.200 | J | Catalyzes the formation of 2'O-methylated cytidine (Cm32) or 2'O-methylated uridine (Um32) at position 32 in tRNA | |
NECFGCCN_06763 | 5.1e-133 | K | Two component transcriptional regulator, winged helix family | |||
NECFGCCN_06764 | 4.2e-245 | creD | V | Inner membrane protein involved in colicin E2 resistance | ||
NECFGCCN_06765 | 4.4e-261 | T | PhoQ Sensor | |||
NECFGCCN_06766 | 2.5e-124 | KT | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
NECFGCCN_06767 | 4.2e-83 | creA | S | protein conserved in bacteria | ||
NECFGCCN_06768 | 4.3e-166 | rob | K | Binds to the right arm of the replication origin oriC | ||
NECFGCCN_06769 | 1.4e-118 | gpmB | 5.4.2.12 | G | Belongs to the phosphoglycerate mutase family | |
NECFGCCN_06770 | 3.4e-86 | yjjX | F | Phosphatase that hydrolyzes non-canonical purine nucleotides such as XTP and ITP to their respective diphosphate derivatives. Probably excludes non-canonical purines from DNA precursor pool, thus preventing their incorporation into DNA and avoiding chromosomal lesions | ||
NECFGCCN_06771 | 3e-51 | trpR | K | This protein is an aporepressor. When complexed with L- tryptophan it binds the operator region of the trp operon (5'- ACTAGT-'3') and prevents the initiation of transcription. The complex also regulates trp repressor biosynthesis by binding to its regulatory region | ||
NECFGCCN_06772 | 0.0 | slt | GH23 | M | Soluble lytic murein transglycosylase and related regulatory proteins (some contain LysM invasin domains) | |
NECFGCCN_06773 | 0.0 | yjjK | 3.6.3.25 | S | abc transporter atp-binding protein | |
NECFGCCN_06774 | 5.2e-242 | nadR | 2.7.1.22, 2.7.7.1 | H | transcriptional regulator | |
NECFGCCN_06775 | 2e-258 | radA | O | DNA-dependent ATPase involved in processing of recombination intermediates, plays a role in repairing DNA breaks. Stimulates the branch migration of RecA-mediated strand transfer reactions, allowing the 3' invading strand to extend heteroduplex DNA faster. Binds ssDNA in the presence of ADP but not other nucleotides, has ATPase activity that is stimulated by ssDNA and various branched DNA structures, but inhibited by SSB. Does not have RecA's homology-searching function | ||
NECFGCCN_06776 | 6.9e-181 | serB | 3.1.3.3 | E | phosphoserine phosphatase | |
NECFGCCN_06777 | 1e-111 | smp | 2.4.1.15, 2.4.1.347, 2.7.13.3, 6.3.1.20 | GT20 | S | membrane protein affecting hemolysin expression |
NECFGCCN_06778 | 9.6e-194 | lplA | 6.3.1.20 | H | Catalyzes both the ATP-dependent activation of exogenously supplied lipoate to lipoyl-AMP and the transfer of the activated lipoyl onto the lipoyl domains of lipoate-dependent enzymes | |
NECFGCCN_06779 | 1.5e-132 | deoD | 2.4.2.1, 2.4.2.28 | F | Purine nucleoside phosphorylase | |
NECFGCCN_06780 | 1.1e-114 | yqgA | S | Membrane | ||
NECFGCCN_06781 | 0.0 | speC | 4.1.1.17, 4.1.1.18, 4.1.1.19 | E | decarboxylase | |
NECFGCCN_06782 | 3.5e-230 | nupG | G | Broad-specificity transporter of purine and pyrimidine nucleosides. Driven by a proton motive force | ||
NECFGCCN_06783 | 2.4e-203 | mltC | GH23 | M | Murein-degrading enzyme. May play a role in recycling of muropeptides during cell elongation and or cell division | |
NECFGCCN_06784 | 6.3e-47 | yggX | C | Could be a mediator in iron transactions between iron acquisition and iron-requiring processes, such as synthesis and or repair of Fe-S clusters in biosynthetic enzymes | ||
NECFGCCN_06785 | 1.8e-206 | mutY | L | a g-specific adenine glycosylase | ||
NECFGCCN_06786 | 1.8e-138 | trmB | 2.1.1.297, 2.1.1.33, 2.4.99.12, 2.4.99.13, 2.4.99.14, 2.4.99.15 | GT30 | J | catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA |
NECFGCCN_06787 | 1e-56 | yggL | S | protein conserved in bacteria | ||
NECFGCCN_06788 | 5.7e-124 | yggN | S | Protein of unknown function (DUF2884) | ||
NECFGCCN_06789 | 3.2e-207 | P | Belongs to the binding-protein-dependent transport system permease family | |||
NECFGCCN_06790 | 6.2e-143 | 3.6.3.17 | P | Part of the ABC transporter complex RbsABC involved in ribose import. Responsible for energy coupling to the transport system | ||
NECFGCCN_06791 | 1.2e-191 | G | PFAM Periplasmic binding protein LacI transcriptional regulator | |||
NECFGCCN_06792 | 7.4e-219 | hemN | H | Involved in the biosynthesis of porphyrin-containing compound | ||
NECFGCCN_06793 | 4.1e-104 | rdgB | 3.6.1.66, 5.1.1.3 | F | Pyrophosphatase that catalyzes the hydrolysis of nucleoside triphosphates to their monophosphate derivatives, with a high preference for the non-canonical purine nucleotides XTP (xanthosine triphosphate), dITP (deoxyinosine triphosphate) and ITP. Seems to function as a house-cleaning enzyme that removes non-canonical purine nucleotides from the nucleotide pool, thus preventing their incorporation into DNA RNA and avoiding chromosomal lesions | |
NECFGCCN_06794 | 2.1e-45 | yggU | S | Belongs to the UPF0235 family | ||
NECFGCCN_06795 | 9.1e-93 | yggT | S | integral membrane protein | ||
NECFGCCN_06796 | 1.1e-124 | yggS | E | Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis | ||
NECFGCCN_06797 | 2.2e-171 | yggR | NU | twitching motility protein | ||
NECFGCCN_06798 | 5.7e-115 | corR | K | Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
NECFGCCN_06799 | 1e-72 | yqgF | L | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
NECFGCCN_06800 | 7.4e-103 | yqgE | K | Belongs to the UPF0301 (AlgH) family | ||
NECFGCCN_06801 | 1.8e-181 | gshB | 6.3.2.2, 6.3.2.3 | H | Belongs to the prokaryotic GSH synthase family | |
NECFGCCN_06802 | 2.6e-132 | rsmE | 2.1.1.193 | J | Specifically methylates the N3 position of the uracil ring of uridine 1498 (m3U1498) in 16S rRNA. Acts on the fully assembled 30S ribosomal subunit | |
NECFGCCN_06803 | 4.1e-127 | endA | 3.1.21.1 | L | endonuclease I | |
NECFGCCN_06804 | 6.5e-81 | sprT | S | Belongs to the SprT family | ||
NECFGCCN_06805 | 1.9e-256 | galP | EGP | Major facilitator Superfamily | ||
NECFGCCN_06806 | 7.6e-211 | metK | 2.5.1.6 | H | Catalyzes the formation of S-adenosylmethionine (AdoMet) from methionine and ATP. The overall synthetic reaction is composed of two sequential steps, AdoMet formation and the subsequent tripolyphosphate hydrolysis which occurs prior to release of AdoMet from the enzyme | |
NECFGCCN_06807 | 0.0 | speA | 4.1.1.19 | H | Catalyzes the biosynthesis of agmatine from arginine | |
NECFGCCN_06808 | 2e-177 | speB | 3.5.3.11 | E | Belongs to the arginase family | |
NECFGCCN_06809 | 5.7e-193 | EGP | Major facilitator Superfamily | |||
NECFGCCN_06810 | 7.6e-60 | ndoA | 1.7.1.15 | C | Rieske [2Fe-2S] domain | |
NECFGCCN_06811 | 1.2e-54 | |||||
NECFGCCN_06812 | 1.7e-206 | carAa | P | Rieske [2Fe-2S] domain | ||
NECFGCCN_06813 | 4.5e-132 | IQ | KR domain | |||
NECFGCCN_06814 | 2.3e-142 | K | helix_turn_helix isocitrate lyase regulation | |||
NECFGCCN_06815 | 2.1e-179 | todE | C | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | ||
NECFGCCN_06816 | 3.1e-223 | andAa | 1.18.1.3, 1.7.1.15 | P | Pyridine nucleotide-disulphide oxidoreductase | |
NECFGCCN_06817 | 2.5e-228 | sauU | G | Major Facilitator Superfamily | ||
NECFGCCN_06818 | 5.5e-100 | G | WxcM-like, C-terminal | |||
NECFGCCN_06819 | 7.4e-138 | I | Alpha/beta hydrolase family | |||
NECFGCCN_06820 | 1.4e-139 | IQ | KR domain | |||
NECFGCCN_06821 | 3.1e-128 | nadX | 1.4.1.21 | H | Specifically catalyzes the NAD or NADP-dependent dehydrogenation of L-aspartate to iminoaspartate | |
NECFGCCN_06822 | 1.8e-281 | aldA | 1.2.1.3, 1.2.1.8 | C | Aldehyde dehydrogenase family | |
NECFGCCN_06823 | 5.7e-305 | 2.2.1.6, 4.1.1.75 | C | Thiamine pyrophosphate enzyme, central domain | ||
NECFGCCN_06824 | 8.5e-243 | oprD | S | outer membrane porin, OprD family | ||
NECFGCCN_06825 | 3.9e-131 | yggG | O | metalloprotease | ||
NECFGCCN_06826 | 0.0 | mdtB | V | Belongs to the resistance-nodulation-cell division (RND) (TC 2.A.6) family | ||
NECFGCCN_06827 | 1.1e-34 | mdtC | V | Belongs to the resistance-nodulation-cell division (RND) (TC 2.A.6) family | ||
NECFGCCN_06829 | 0.0 | sbcC | L | ATPase involved in DNA repair | ||
NECFGCCN_06830 | 1.4e-220 | sbcD | L | SbcCD cleaves DNA hairpin structures. These structures can inhibit DNA replication and are intermediates in certain DNA recombination reactions. The complex acts as a 3'- 5' double strand exonuclease that can open hairpins. It also has a 5' single-strand endonuclease activity | ||
NECFGCCN_06831 | 0.0 | GM | domain, Protein | |||
NECFGCCN_06832 | 4.7e-207 | deoB | 5.4.2.7 | G | Phosphotransfer between the C1 and C5 carbon atoms of pentose | |
NECFGCCN_06833 | 6.9e-73 | S | Protein of unknown function (DUF1697) | |||
NECFGCCN_06834 | 1.3e-171 | glpB | 1.1.5.3 | C | Conversion of glycerol 3-phosphate to dihydroxyacetone. Uses fumarate or nitrate as electron acceptor | |
NECFGCCN_06835 | 7.2e-225 | glpC | 1.1.5.3 | C | dehydrogenase subunit C | |
NECFGCCN_06836 | 8e-143 | rhmA | 4.1.2.20, 4.1.2.52, 4.1.2.53 | G | Belongs to the HpcH HpaI aldolase family | |
NECFGCCN_06837 | 6.9e-229 | rhmT | G | Major facilitator superfamily | ||
NECFGCCN_06838 | 1.7e-237 | rhmD | 4.2.1.90 | M | Catalyzes the dehydration of L-rhamnonate to 2-keto-3- deoxy-L-rhamnonate (KDR) | |
NECFGCCN_06839 | 3.5e-143 | rhmR | K | Transcriptional regulator | ||
NECFGCCN_06840 | 1.1e-161 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
NECFGCCN_06841 | 4.8e-76 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
NECFGCCN_06842 | 4.7e-168 | fhuR | K | transcriptional regulator (lysR family) | ||
NECFGCCN_06844 | 1.6e-44 | |||||
NECFGCCN_06845 | 5.8e-69 | K | Helix-turn-helix | |||
NECFGCCN_06849 | 1.3e-139 | ppiA | 5.2.1.8 | O | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
NECFGCCN_06850 | 0.0 | pts33BCA | 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | pts system | |
NECFGCCN_06851 | 9.2e-09 | uvrX | 2.7.7.7 | L | Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII | |
NECFGCCN_06852 | 4.5e-250 | cycA | E | permease | ||
NECFGCCN_06853 | 1.7e-38 | ynzC | S | UPF0291 protein | ||
NECFGCCN_06854 | 2.8e-288 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
NECFGCCN_06855 | 0.0 | acrD | V | Belongs to the resistance-nodulation-cell division (RND) (TC 2.A.6) family | ||
NECFGCCN_06856 | 1.7e-60 | yffB | 1.20.4.1 | P | Belongs to the ArsC family | |
NECFGCCN_06857 | 1.3e-218 | dapE | 3.5.1.18 | E | Catalyzes the hydrolysis of N-succinyl-L,L- diaminopimelic acid (SDAP), forming succinate and LL-2,6- diaminoheptanedioate (DAP), an intermediate involved in the bacterial biosynthesis of lysine and meso-diaminopimelic acid, an essential component of bacterial cell walls | |
NECFGCCN_06858 | 2.5e-32 | ypfN | S | Uncharacterised protein family (UPF0370) | ||
NECFGCCN_06859 | 8.2e-128 | ypfH | S | Phospholipase Carboxylesterase | ||
NECFGCCN_06860 | 0.0 | tmcA | 2.3.1.193, 2.3.1.57 | J | Catalyzes the formation of N(4)-acetylcytidine (ac(4)C) at the wobble position of tRNA(Met), by using acetyl-CoA as an acetyl donor and ATP (or GTP) | |
NECFGCCN_06861 | 3.3e-150 | ypfJ | S | zinc metallopeptidase | ||
NECFGCCN_06862 | 1.3e-133 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
NECFGCCN_06863 | 4e-187 | bamC | M | Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane | ||
NECFGCCN_06864 | 1.2e-163 | dapA | 2.5.1.72, 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
NECFGCCN_06865 | 3.7e-102 | gcvR | E | glycine cleavage system | ||
NECFGCCN_06866 | 1.1e-88 | bcp | 1.11.1.15 | O | PFAM alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen | |
NECFGCCN_06867 | 1.3e-172 | perM | S | permease | ||
NECFGCCN_06868 | 7e-270 | bepA | S | Functions as both a chaperone and a metalloprotease. Maintains the integrity of the outer membrane by promoting either the assembly or the elimination of outer membrane proteins, depending on their folding state | ||
NECFGCCN_06869 | 6.3e-55 | arsC | 1.20.4.1 | P | arsenate reductase | |
NECFGCCN_06870 | 1.1e-148 | S | Transposase | |||
NECFGCCN_06871 | 4.7e-128 | hda | L | Mediates the interaction of DNA replication inititator protein DnaA with DNA polymerase subunit beta sliding clamp (dnaN). Stimulates hydrolysis of ATP-DnaA to ADP-DnaA, rendering DnaA inactive for reinititation, a process called regulatory inhibition of DnaA or RIDA | ||
NECFGCCN_06872 | 6e-225 | uraA | F | Xanthine uracil | ||
NECFGCCN_06873 | 5.3e-110 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
NECFGCCN_06874 | 3.1e-291 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
NECFGCCN_06875 | 7.5e-166 | bglK | 2.7.1.85 | GK | ROK family | |
NECFGCCN_06876 | 1.7e-198 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
NECFGCCN_06877 | 6e-117 | purN | 2.1.2.2 | F | Catalyzes the transfer of a formyl group from 10- formyltetrahydrofolate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR) and tetrahydrofolate | |
NECFGCCN_06878 | 0.0 | ppk | 2.7.4.1 | H | Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) | |
NECFGCCN_06879 | 3.7e-290 | ppx | 3.6.1.11, 3.6.1.40 | FP | Catalyzes the conversion of pppGpp to ppGpp. Guanosine pentaphosphate (pppGpp) is a cytoplasmic signaling molecule which together with ppGpp controls the stringent response , an adaptive process that allows bacteria to respond to amino acid starvation, resulting in the coordinated regulation of numerous cellular activities | |
NECFGCCN_06880 | 0.0 | yfgF | T | cyclic-guanylate-specific phosphodiesterase activity | ||
NECFGCCN_06881 | 6.8e-23 | yfgG | S | Protein of unknown function (DUF2633) | ||
NECFGCCN_06882 | 4.9e-29 | cysL_1 | K | transcriptional regulator | ||
NECFGCCN_06883 | 2.8e-45 | glnQ | E | abc transporter atp-binding protein | ||
NECFGCCN_06884 | 3.6e-181 | D | nuclear chromosome segregation | |||
NECFGCCN_06885 | 1.3e-81 | V | VanZ like family | |||
NECFGCCN_06886 | 5.4e-43 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
NECFGCCN_06887 | 6e-170 | yhjX | P | Major Facilitator | ||
NECFGCCN_06888 | 2.9e-103 | fnr5 | K | Catabolite gene activator and regulatory subunit of cAMP-dependent protein kinases | ||
NECFGCCN_06889 | 5.6e-112 | def | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions | |
NECFGCCN_06890 | 1.4e-234 | ilvA | 4.3.1.19 | E | Catalyzes the anaerobic formation of alpha-ketobutyrate and ammonia from threonine in a two-step reaction. The first step involved a dehydration of threonine and a production of enamine intermediates (aminocrotonate), which tautomerizes to its imine form (iminobutyrate). Both intermediates are unstable and short- lived. The second step is the nonenzymatic hydrolysis of the enamine imine intermediates to form 2-ketobutyrate and free ammonia. In the low water environment of the cell, the second step is accelerated by RidA | |
NECFGCCN_06891 | 0.0 | dex | 3.2.1.11 | GH66 | G | Glycosyl hydrolase family 66 |
NECFGCCN_06892 | 1.3e-73 | dtd | J | rejects L-amino acids rather than detecting D-amino acids in the active site. By recycling D-aminoacyl-tRNA to D-amino acids and free tRNA molecules, this enzyme counteracts the toxicity associated with the formation of D-aminoacyl-tRNA entities in vivo and helps enforce protein L-homochirality | ||
NECFGCCN_06893 | 0.0 | relA | 2.7.6.5 | KT | In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance | |
NECFGCCN_06894 | 3.1e-83 | nrdI | F | Belongs to the NrdI family | ||
NECFGCCN_06895 | 0.0 | cpdB | 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
NECFGCCN_06896 | 6.5e-131 | rsmE | 2.1.1.193 | J | Specifically methylates the N3 position of the uracil ring of uridine 1498 (m3U1498) in 16S rRNA. Acts on the fully assembled 30S ribosomal subunit | |
NECFGCCN_06897 | 4.3e-176 | prmA | J | Ribosomal protein L11 methyltransferase | ||
NECFGCCN_06898 | 8.4e-84 | XK27_03960 | S | Protein of unknown function (DUF3013) | ||
NECFGCCN_06899 | 2.4e-308 | pyrG | 6.3.4.2 | F | Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen. Regulates intracellular CTP levels through interactions with the four ribonucleotide triphosphates | |
NECFGCCN_06900 | 1.3e-70 | rpoE | K | Participates in both the initiation and recycling phases of transcription. In the presence of the delta subunit, RNAP displays an increased specificity of transcription, a decreased affinity for nucleic acids, and an increased efficiency of RNA synthesis because of enhanced recycling | ||
NECFGCCN_06901 | 5.2e-229 | tig | D | Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation. Functions as a peptidyl-prolyl cis-trans isomerase | ||
NECFGCCN_06902 | 7.9e-135 | ykuT | M | mechanosensitive ion channel | ||
NECFGCCN_06903 | 3.3e-86 | sigH | K | DNA-templated transcription, initiation | ||
NECFGCCN_06904 | 2.4e-161 | rfbA | 2.7.7.24 | M | Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis | |
NECFGCCN_06905 | 9.9e-255 | S | phospholipase Carboxylesterase | |||
NECFGCCN_06906 | 8.5e-176 | mocA | 1.1.1.91 | C | oxidoreductases (related to aryl-alcohol dehydrogenases) | |
NECFGCCN_06907 | 5.7e-146 | hisJ_2 | ET | Belongs to the bacterial solute-binding protein 3 family | ||
NECFGCCN_06908 | 1.7e-221 | hipO | 3.5.1.32 | S | amidohydrolase | |
NECFGCCN_06909 | 3.8e-65 | S | integral membrane protein | |||
NECFGCCN_06910 | 4.8e-16 | K | regulation of DNA-templated transcription, elongation | |||
NECFGCCN_06911 | 8.9e-209 | P | periplasmic binding protein | |||
NECFGCCN_06912 | 8.5e-172 | irp6B | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
NECFGCCN_06913 | 9.7e-141 | fhuC_1 | 3.6.3.34 | HP | (ABC) transporter | |
NECFGCCN_06914 | 6.1e-205 | yiaV | V | secretion protein HlyD family | ||
NECFGCCN_06915 | 7.8e-55 | yiaW | S | Protein of unknown function (DUF3302) | ||
NECFGCCN_06916 | 5.5e-141 | K | Winged helix-turn-helix DNA binding | |||
NECFGCCN_06917 | 1.5e-169 | scrK | 2.7.1.4 | G | Belongs to the carbohydrate kinase PfkB family | |
NECFGCCN_06918 | 2.2e-258 | scrY | M | Maltoporin (phage lambda and maltose receptor) | ||
NECFGCCN_06919 | 2.1e-68 | MA20_06395 | K | transcriptional regulator | ||
NECFGCCN_06920 | 4e-148 | ghr | 1.1.1.31, 1.1.1.60, 1.1.1.79 | I | Dehydrogenase | |
NECFGCCN_06921 | 3.4e-203 | cdaR | KT | Putative sugar diacid recognition | ||
NECFGCCN_06922 | 1e-202 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
NECFGCCN_06923 | 2.9e-254 | G | Sugar (and other) transporter | |||
NECFGCCN_06924 | 5.4e-169 | 3.1.1.15 | G | gluconolactonase | ||
NECFGCCN_06925 | 1.6e-241 | G | Major Facilitator | |||
NECFGCCN_06926 | 9.6e-37 | lacI | K | binds specific sites in lac operon resulting in DNA looping between the operators | ||
NECFGCCN_06927 | 0.0 | lacZ | 3.2.1.23 | G | Belongs to the glycosyl hydrolase 2 family | |
NECFGCCN_06928 | 1.7e-216 | P | Major facilitator superfamily | |||
NECFGCCN_06929 | 3.5e-210 | S | AAA ATPase domain | |||
NECFGCCN_06930 | 9.2e-40 | |||||
NECFGCCN_06931 | 3.3e-29 | penP | 3.5.2.6 | V | Beta-lactamase | |
NECFGCCN_06932 | 9.7e-18 | |||||
NECFGCCN_06933 | 4.9e-103 | xerS | D | Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. Essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division | ||
NECFGCCN_06938 | 1e-148 | dmsC | S | Dimethyl sulfoxide reductase | ||
NECFGCCN_06939 | 8e-213 | ycaD | EGP | Major facilitator superfamily | ||
NECFGCCN_06940 | 4.9e-147 | pflA | 1.97.1.4 | C | Activation of pyruvate formate-lyase under anaerobic conditions by generation of an organic free radical, using S- adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine | |
NECFGCCN_06941 | 0.0 | pflB | 2.3.1.54 | C | formate C-acetyltransferase glycine radical | |
NECFGCCN_06942 | 2.3e-156 | focA | P | Formate nitrite | ||
NECFGCCN_06943 | 0.0 | ycaO | O | redox protein regulator of disulfide bond formation | ||
NECFGCCN_06944 | 3.9e-122 | ycaP | S | Membrane | ||
NECFGCCN_06945 | 5e-10 | |||||
NECFGCCN_06946 | 4.3e-208 | serC | 2.6.1.52 | E | Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine | |
NECFGCCN_06947 | 5.6e-239 | aroA | 2.5.1.19 | E | Catalyzes the transfer of the enolpyruvyl moiety of phosphoenolpyruvate (PEP) to the 5-hydroxyl of shikimate-3- phosphate (S3P) to produce enolpyruvyl shikimate-3-phosphate and inorganic phosphate | |
NECFGCCN_06948 | 2.2e-117 | cmk | 1.17.7.4, 2.5.1.19, 2.7.1.26, 2.7.4.25, 2.7.7.2, 6.3.2.1 | F | Belongs to the cytidylate kinase family. Type 1 subfamily | |
NECFGCCN_06949 | 0.0 | rpsA | 1.17.7.4 | J | thus facilitating recognition of the initiation point. It is needed to translate mRNA with a short Shine-Dalgarno (SD) purine-rich sequence | |
NECFGCCN_06950 | 4.3e-46 | himD | K | This protein is one of the two subunits of integration host factor, a specific DNA-binding protein that functions in genetic recombination as well as in transcriptional and translational control | ||
NECFGCCN_06951 | 0.0 | ycaI | S | DNA internalization-related competence protein ComEC Rec2 | ||
NECFGCCN_06952 | 7.5e-303 | msbA | V | Involved in lipid A export and possibly also in glycerophospholipid export and for biogenesis of the outer membrane. Transmembrane domains (TMD) form a pore in the inner membrane and the ATP-binding domain (NBD) is responsible for energy generation | ||
NECFGCCN_06953 | 1.3e-179 | lpxK | 2.7.1.130 | F | Transfers the gamma-phosphate of ATP to the 4'-position of a tetraacyldisaccharide 1-phosphate intermediate (termed DS-1- P) to form tetraacyldisaccharide 1,4'-bis-phosphate (lipid IVA) | |
NECFGCCN_06954 | 2.7e-235 | ycaQ | S | protein conserved in bacteria | ||
NECFGCCN_06955 | 6.9e-26 | ycaR | 2.7.1.130 | S | Belongs to the UPF0434 family | |
NECFGCCN_06956 | 6.3e-134 | kdsB | 2.7.7.38 | M | Activates KDO (a required 8-carbon sugar) for incorporation into bacterial lipopolysaccharide in Gram-negative bacteria | |
NECFGCCN_06957 | 7.2e-169 | ycbJ | S | Phosphotransferase enzyme family | ||
NECFGCCN_06958 | 7.8e-143 | ycbC | S | Gram-negative-bacterium-type cell wall biogenesis | ||
NECFGCCN_06959 | 7.4e-149 | cmoM | GT2,GT4 | J | Catalyzes the methylation of 5-carboxymethoxyuridine (cmo5U) to form 5-methoxycarbonylmethoxyuridine (mcmo5U) at position 34 in tRNAs | |
NECFGCCN_06960 | 1e-248 | mukF | D | Involved in chromosome condensation, segregation and cell cycle progression. May participate in facilitating chromosome segregation by condensation DNA from both sides of a centrally located replisome during cell division. Not required for mini-F plasmid partitioning. Probably acts via its interaction with MukB and MukE. Overexpression results in anucleate cells. It has a calcium binding activity | ||
NECFGCCN_06961 | 2.3e-125 | mukE | D | Involved in chromosome condensation, segregation and cell cycle progression. May participate in facilitating chromosome segregation by condensation DNA from both sides of a centrally located replisome during cell division. Probably acts via its interaction with MukB and MukF | ||
NECFGCCN_06962 | 0.0 | mukB | 3.5.4.40 | D | Plays a central role in chromosome condensation, segregation and cell cycle progression. Functions as a homodimer, which is essential for chromosome partition. Involved in negative DNA supercoiling in vivo, and by this means organize and compact chromosomes. May achieve or facilitate chromosome segregation by condensation DNA from both sides of a centrally located replisome during cell division | |
NECFGCCN_06963 | 0.0 | ycbB | M | protein conserved in bacteria | ||
NECFGCCN_06965 | 1.3e-100 | ycbK | S | protein conserved in bacteria | ||
NECFGCCN_06966 | 6.1e-125 | ycbL | 3.1.2.6 | P | COG0491 Zn-dependent hydrolases, including glyoxylases | |
NECFGCCN_06967 | 8.6e-226 | aspC | 2.6.1.1, 2.6.1.57 | E | aminotransferase | |
NECFGCCN_06968 | 1.8e-206 | ompF | M | Belongs to the Gram-negative porin family | ||
NECFGCCN_06969 | 3.5e-271 | asnS | 6.1.1.22 | J | Asparaginyl-tRNA synthetase | |
NECFGCCN_06970 | 8.3e-76 | K | Transcriptional | |||
NECFGCCN_06971 | 8.4e-221 | dpaL | 4.3.1.15, 4.3.1.19 | E | Diaminopropionate ammonia-lyase | |
NECFGCCN_06972 | 3.5e-225 | sdaC | E | Serine transporter | ||
NECFGCCN_06973 | 1.5e-209 | 3.5.1.6, 3.5.1.87, 3.5.3.9 | E | the allantoate amidohydrolase from Escherichia coli forms a dimer and binds zinc ions for catalytic activity and catalyzes the conversion of allantoate to (S)-ureidoglycolate and ammonia | ||
NECFGCCN_06974 | 9e-212 | 3.5.1.32 | S | amidohydrolase | ||
NECFGCCN_06975 | 4.6e-230 | pncB | 6.3.4.21 | F | Catalyzes the synthesis of beta-nicotinate D- ribonucleotide from nicotinate and 5-phospho-D-ribose 1-phosphate at the expense of ATP | |
NECFGCCN_06976 | 0.0 | pepN | 3.4.11.2 | E | aminopeptidase N | |
NECFGCCN_06977 | 1.8e-38 | ssuB | P | Part of the ABC transporter complex SsuABC involved in aliphatic sulfonates import. Responsible for energy coupling to the transport system | ||
NECFGCCN_06978 | 1.1e-158 | holB | 2.7.7.7 | L | dna polymerase iii | |
NECFGCCN_06979 | 3.5e-109 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
NECFGCCN_06981 | 0.0 | tkt | 2.2.1.1 | G | Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate | |
NECFGCCN_06982 | 2.6e-135 | tpiA | 2.7.2.3, 5.3.1.1 | G | Involved in the gluconeogenesis. Catalyzes stereospecifically the conversion of dihydroxyacetone phosphate (DHAP) to D-glyceraldehyde-3-phosphate (G3P) | |
NECFGCCN_06983 | 1.6e-224 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
NECFGCCN_06984 | 6e-217 | ftsW | D | Belongs to the SEDS family | ||
NECFGCCN_06985 | 2.6e-68 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
NECFGCCN_06986 | 2.3e-262 | atpD | 3.6.3.14 | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The catalytic sites are hosted primarily by the beta subunits | |
NECFGCCN_06987 | 4.8e-157 | atpG | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The gamma chain is believed to be important in regulating ATPase activity and the flow of protons through the CF(0) complex | ||
NECFGCCN_06988 | 1e-279 | atpA | 3.6.3.14 | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit | |
NECFGCCN_06989 | 3.9e-85 | atpH | C | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
NECFGCCN_06990 | 9.5e-78 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
NECFGCCN_06991 | 1.8e-122 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
NECFGCCN_06992 | 2.4e-16 | atpE | C | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
NECFGCCN_06993 | 8.9e-183 | femA | 2.3.2.10, 2.3.2.16 | V | FemAB family | |
NECFGCCN_06994 | 0.0 | valS | 6.1.1.9 | J | amino acids such as threonine, to avoid such errors, it has a posttransfer editing activity that hydrolyzes mischarged Thr-tRNA(Val) in a tRNA-dependent manner | |
NECFGCCN_06995 | 8.9e-159 | |||||
NECFGCCN_06996 | 0.0 | S | Protein of unknown function (DUF1176) | |||
NECFGCCN_06997 | 8e-100 | yjdC | K | Transcriptional regulator | ||
NECFGCCN_06998 | 0.0 | dsbD | 1.8.1.8 | CO | Required to facilitate the formation of correct disulfide bonds in some periplasmic proteins and for the assembly of the periplasmic c-type cytochromes. Acts by transferring electrons from cytoplasmic thioredoxin to the periplasm. This transfer involves a cascade of disulfide bond formation and reduction steps | |
NECFGCCN_06999 | 2e-52 | cutA | 4.2.3.1 | P | Involved in resistance toward heavy metals | |
NECFGCCN_07000 | 5.5e-226 | dcuA | S | Responsible for the transport of C4-dicarboxylates from the periplasm across the inner membrane | ||
NECFGCCN_07001 | 9.5e-272 | aspA | 4.3.1.1 | E | Aspartate ammonia-lyase | |
NECFGCCN_07002 | 5.9e-61 | fxsA | S | protein affecting phage T7 exclusion by the F plasmid | ||
NECFGCCN_07003 | 4.8e-219 | yjeH | E | amino acid | ||
NECFGCCN_07004 | 9.1e-44 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
NECFGCCN_07005 | 9.9e-212 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
NECFGCCN_07007 | 1.6e-87 | alkD | L | Dna alkylation repair | ||
NECFGCCN_07008 | 1.1e-198 | asd | 1.2.1.11 | E | Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate | |
NECFGCCN_07013 | 8.2e-200 | S | the current gene model (or a revised gene model) may contain a frame shift | |||
NECFGCCN_07014 | 7.3e-231 | 2.7.13.3 | T | protein histidine kinase activity | ||
NECFGCCN_07015 | 4.5e-201 | hpk9 | 2.7.13.3 | T | protein histidine kinase activity | |
NECFGCCN_07016 | 1.6e-17 | hycB | C | Formate hydrogenlyase | ||
NECFGCCN_07017 | 0.0 | hycC | CP | formate hydrogenlyase subunit 3 | ||
NECFGCCN_07018 | 1.4e-159 | hycD | C | HycBCDEFG is part of the formate hydrogenlyase system which is involved in the cleaving of formate to dihydrogen and carbon dioxide | ||
NECFGCCN_07019 | 0.0 | hycE | C | HycBCDEFG is part of the formate hydrogenlyase system which is involved in the cleaving of formate to dihydrogen and carbon dioxide | ||
NECFGCCN_07020 | 3.4e-89 | hycF | C | the formate hydrogenlyase complex comprises of a formate dehydrogenase, unidentified electron carriers and hydrogenase-3 | ||
NECFGCCN_07021 | 5.1e-147 | hycG | C | NADH ubiquinone oxidoreductase, 20 | ||
NECFGCCN_07022 | 9.3e-71 | hycH | E | Formate hydrogen-lyase | ||
NECFGCCN_07023 | 2.1e-82 | hycI | 3.4.23.51 | C | hydrogenase 3 maturation protease | |
NECFGCCN_07024 | 5.4e-47 | S | Toxin SymE, type I toxin-antitoxin system | |||
NECFGCCN_07025 | 1.1e-288 | ascB | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
NECFGCCN_07026 | 1.8e-254 | ascF | 2.7.1.192, 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | Phosphotransferase System | |
NECFGCCN_07027 | 1.2e-183 | ascG | K | Transcriptional regulator | ||
NECFGCCN_07028 | 1.3e-101 | hydN | C | electron transport | ||
NECFGCCN_07029 | 0.0 | hypF | O | Along with HypE, it catalyzes the synthesis of the CN ligands of the active site iron of NiFe -hydrogenases using carbamoylphosphate as a substrate. It functions as a carbamoyl transferase using carbamoylphosphate as a substrate and transferring the carboxamido moiety in an ATP-dependent reaction to the thiolate of the C-terminal cysteine of HypE yielding a protein-S-carboxamide | ||
NECFGCCN_07030 | 7.9e-172 | hoxN | S | rRNA processing | ||
NECFGCCN_07031 | 1.3e-202 | norW | 1.7.1.15 | C | One of at least two accessory proteins for anaerobic nitric oxide (NO) reductase. Reduces the rubredoxin moiety of NO reductase | |
NECFGCCN_07032 | 1.3e-49 | norV | 1.6.3.4 | C | uses NADH to detoxify nitric oxide (NO), protecting several 4Fe-4S NO-sensitive enzymes. Has at least 2 reductase partners, only one of which (NorW, flavorubredoxin reductase) has been identified. NO probably binds to the di-iron center | |
NECFGCCN_07033 | 6e-155 | XK27_03015 | S | permease | ||
NECFGCCN_07035 | 0.0 | yhgF | K | Transcriptional accessory protein | ||
NECFGCCN_07036 | 2.2e-145 | moaF | S | MoaF C-terminal domain | ||
NECFGCCN_07037 | 2.4e-136 | 1.1.1.100, 1.1.1.304, 1.1.1.76 | S | KR domain | ||
NECFGCCN_07038 | 0.0 | atsA | 3.1.6.1 | P | COG3119 Arylsulfatase A and related enzymes | |
NECFGCCN_07039 | 1.1e-214 | atsB | C | Radical SAM domain protein | ||
NECFGCCN_07040 | 5.6e-121 | moaR | K | transcriptional regulator | ||
NECFGCCN_07041 | 2.3e-131 | EGP | Major facilitator Superfamily | |||
NECFGCCN_07042 | 7.5e-178 | ddpB | P | Binding-protein-dependent transport systems inner membrane component | ||
NECFGCCN_07043 | 7.7e-299 | ddpA | E | Extracellular solute-binding protein, family 5 | ||
NECFGCCN_07044 | 5.1e-130 | rimL | J | Acetyltransferases including N-acetylases of ribosomal proteins | ||
NECFGCCN_07045 | 0.0 | betA | 1.1.99.1 | E | Involved in the biosynthesis of the osmoprotectant glycine betaine. Catalyzes the oxidation of choline to betaine aldehyde and betaine aldehyde to glycine betaine at the same rate | |
NECFGCCN_07046 | 1e-276 | betB | 1.2.1.8 | C | belongs to the aldehyde dehydrogenase family | |
NECFGCCN_07047 | 3.1e-104 | betI | K | Repressor involved in choline regulation of the bet genes | ||
NECFGCCN_07048 | 0.0 | betT | M | Belongs to the BCCT transporter (TC 2.A.15) family | ||
NECFGCCN_07049 | 8e-76 | ivy | S | Inhibitor of vertebrate lysozyme | ||
NECFGCCN_07050 | 3.5e-230 | ybdG | M | Mechanosensitive Ion channel | ||
NECFGCCN_07051 | 7.2e-161 | K | LysR substrate binding domain | |||
NECFGCCN_07052 | 4.7e-103 | gstN | 2.5.1.18 | O | Glutathione S-transferase | |
NECFGCCN_07053 | 3.3e-141 | IQ | Dehydrogenases with different specificities (Related to short-chain alcohol dehydrogenases) | |||
NECFGCCN_07054 | 1e-150 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
NECFGCCN_07055 | 1.1e-187 | G | Belongs to the binding-protein-dependent transport system permease family | |||
NECFGCCN_07056 | 1.1e-289 | rbsA_4 | P | import. Responsible for energy coupling to the transport system | ||
NECFGCCN_07057 | 7.4e-112 | S | (Lipo)protein | |||
NECFGCCN_07058 | 5.4e-167 | G | Periplasmic binding protein LacI transcriptional regulator | |||
NECFGCCN_07059 | 1.9e-294 | glpK3 | 2.7.1.30 | G | Belongs to the FGGY kinase family | |
NECFGCCN_07060 | 3.3e-172 | deoR_1 | K | transcriptional regulator | ||
NECFGCCN_07061 | 2.6e-157 | tktB | 2.2.1.1 | G | Transketolase | |
NECFGCCN_07062 | 4.2e-167 | tktA | 2.2.1.1 | G | Transketolase | |
NECFGCCN_07063 | 5.4e-110 | entD | 6.3.2.14 | Q | Belongs to the P-Pant transferase superfamily | |
NECFGCCN_07064 | 0.0 | fepA | P | Receptor | ||
NECFGCCN_07066 | 5.1e-22 | K | Transcriptional | |||
NECFGCCN_07067 | 5.1e-98 | slsA | Q | COG1335 Amidases related to nicotinamidase | ||
NECFGCCN_07068 | 1.1e-161 | yhhW_1 | S | Belongs to the pirin family | ||
NECFGCCN_07069 | 2e-166 | K | transcriptional regulator | |||
NECFGCCN_07070 | 4.1e-206 | livJ | E | With LivFGHM is involved in the high affinity leucine transport | ||
NECFGCCN_07071 | 1.5e-225 | E | Amino acid permease | |||
NECFGCCN_07072 | 1.8e-237 | gabT | 2.6.1.19, 2.6.1.22 | E | Belongs to the class-III pyridoxal-phosphate-dependent aminotransferase family | |
NECFGCCN_07073 | 5.3e-289 | gabR_1 | K | Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | ||
NECFGCCN_07074 | 5.7e-155 | rpoH | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released. This sigma factor is involved in regulation of expression of heat shock genes | ||
NECFGCCN_07075 | 2.2e-185 | ftsX | D | Part of the ABC transporter FtsEX involved in cellular division | ||
NECFGCCN_07076 | 3.2e-121 | ftsE | D | cell division ATP-binding protein FtsE | ||
NECFGCCN_07077 | 1.3e-173 | ftsY | D | Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Acts as a receptor for the complex formed by the signal recognition particle (SRP) and the ribosome-nascent chain (RNC). Interaction with SRP-RNC leads to the transfer of the RNC complex to the Sec translocase for insertion into the membrane, the hydrolysis of GTP by both Ffh and FtsY, and the dissociation of the SRP-FtsY complex into the individual components | ||
NECFGCCN_07078 | 3e-110 | rsmD | 2.1.1.171 | L | Specifically methylates the guanine in position 966 of 16S rRNA in the assembled 30S particle | |
NECFGCCN_07079 | 4.7e-42 | yhhL | S | Membrane | ||
NECFGCCN_07080 | 3.7e-39 | yhhM | S | Protein of unknown function (DUF2500) | ||
NECFGCCN_07081 | 2.4e-110 | yhhN | S | membrane | ||
NECFGCCN_07082 | 0.0 | zntA | 3.6.3.3, 3.6.3.5 | P | P-type atpase | |
NECFGCCN_07083 | 1.6e-38 | tusA | O | Sulfur carrier protein involved in sulfur trafficking in the cell. Part of a sulfur-relay system required for 2-thiolation during synthesis of 2-thiouridine of the modified wobble base 5- methylaminomethyl-2-thiouridine (mnm(5)s(2)U) in tRNA. Interacts with IscS and stimulates its cysteine desulfurase activity. Accepts an activated sulfur from IscS, which is then transferred to TusD, and thus determines the direction of sulfur flow from IscS to 2-thiouridine formation. Also appears to be involved in sulfur transfer for the biosynthesis of molybdopterin | ||
NECFGCCN_07084 | 9.6e-118 | yhhQ | U | Involved in the import of queuosine (Q) precursors, required for Q precursor salvage | ||
NECFGCCN_07085 | 4.5e-92 | dcrB | S | dcrb protein | ||
NECFGCCN_07086 | 3.1e-215 | yhhS | EGP | MFS-type transporter | ||
NECFGCCN_07087 | 6.7e-166 | yhhT | T | permease | ||
NECFGCCN_07088 | 3.9e-63 | arnF | U | Translocates 4-amino-4-deoxy-L-arabinose- phosphoundecaprenol (alpha-L-Ara4N-phosphoundecaprenol) from the cytoplasmic to the periplasmic side of the inner membrane | ||
NECFGCCN_07089 | 1.1e-56 | arnE | U | Translocates 4-amino-4-deoxy-L-arabinose- phosphoundecaprenol (alpha-L-Ara4N-phosphoundecaprenol) from the cytoplasmic to the periplasmic side of the inner membrane | ||
NECFGCCN_07090 | 2.9e-304 | arnT | 2.4.2.43 | M | Catalyzes the transfer of the L-Ara4N moiety of the glycolipid undecaprenyl phosphate-alpha-L-Ara4N to lipid A. The modified arabinose is attached to lipid A and is required for resistance to polymyxin and cationic antimicrobial peptides | |
NECFGCCN_07091 | 2e-174 | arnD | G | Catalyzes the deformylation of 4-deoxy-4-formamido-L- arabinose-phosphoundecaprenol to 4-amino-4-deoxy-L-arabinose- phosphoundecaprenol. The modified arabinose is attached to lipid A and is required for resistance to polymyxin and cationic antimicrobial peptides | ||
NECFGCCN_07092 | 0.0 | arnA | 1.1.1.305, 2.1.2.13, 2.1.2.9, 5.1.3.2 | GJM | Bifunctional enzyme that catalyzes the oxidative decarboxylation of UDP-glucuronic acid (UDP-GlcUA) to UDP-4-keto- arabinose (UDP-Ara4O) and the addition of a formyl group to UDP-4- amino-4-deoxy-L-arabinose (UDP-L-Ara4N) to form UDP-L-4-formamido- arabinose (UDP-L-Ara4FN). The modified arabinose is attached to lipid A and is required for resistance to polymyxin and cationic antimicrobial peptides | |
NECFGCCN_07093 | 6.5e-179 | arnC | 2.4.2.53 | GT2 | M | Catalyzes the transfer of 4-deoxy-4-formamido-L- arabinose from UDP to undecaprenyl phosphate. The modified arabinose is attached to lipid A and is required for resistance to polymyxin and cationic antimicrobial peptides |
NECFGCCN_07094 | 1.6e-216 | arnB | 2.6.1.87 | E | Belongs to the DegT DnrJ EryC1 family | |
NECFGCCN_07095 | 3.8e-98 | padC | Q | Phenolic acid decarboxylase | ||
NECFGCCN_07096 | 5.4e-153 | IV02_08490 | K | transcriptional regulator | ||
NECFGCCN_07097 | 2e-286 | nikA | E | nickel ABC transporter | ||
NECFGCCN_07098 | 4.2e-159 | nikB | P | transport | ||
NECFGCCN_07099 | 1.4e-150 | nikC | 3.6.3.24 | P | transport | |
NECFGCCN_07100 | 8.4e-134 | nikD | 3.6.3.24 | P | Part of the ABC transporter complex NikABCDE involved in nickel import. Responsible for energy coupling to the transport system | |
NECFGCCN_07101 | 6.5e-137 | nikE | 3.6.3.24 | P | Part of the ABC transporter complex NikABCDE involved in nickel import. Responsible for energy coupling to the transport system | |
NECFGCCN_07102 | 2.7e-67 | nikR | K | Transcriptional repressor of the nikABCDE operon. Is active in the presence of excessive concentrations of intracellular nickel | ||
NECFGCCN_07103 | 2.2e-177 | mgtE | 3.6.1.1 | P | Acts as a magnesium transporter | |
NECFGCCN_07104 | 1.6e-227 | yhiN | S | HI0933 family | ||
NECFGCCN_07105 | 4.6e-269 | pitA | P | phosphate transporter | ||
NECFGCCN_07106 | 2.8e-57 | uspB | S | ppGpp-dependent, membrane associated, stress protein produced under conditions of nutrient deprivation, osmotic shock and oxidative stress | ||
NECFGCCN_07107 | 6e-76 | uspA | T | Required for resistance to DNA-damaging agents | ||
NECFGCCN_07108 | 4.4e-111 | dtpB | U | Proton-dependent permease that transports di- and tripeptides | ||
NECFGCCN_07109 | 2e-71 | S | Region found in RelA / SpoT proteins | |||
NECFGCCN_07110 | 5.6e-17 | |||||
NECFGCCN_07111 | 6.3e-36 | comGA | NU | Type II secretory pathway, ATPase PulE Tfp pilus assembly pathway, ATPase PilB | ||
NECFGCCN_07112 | 2.4e-12 | S | PcfK-like protein | |||
NECFGCCN_07113 | 4.4e-177 | ghrA | 1.1.1.79, 1.1.1.81 | EH | D-isomer specific 2-hydroxyacid dehydrogenase | |
NECFGCCN_07114 | 3.8e-139 | ycdX | E | Belongs to the PHP family | ||
NECFGCCN_07115 | 9.5e-103 | ycdY | S | chaperone | ||
NECFGCCN_07116 | 4e-81 | ycdZ | S | Protein of unknown function (DUF1097) | ||
NECFGCCN_07117 | 8.8e-90 | ymdB | S | Deacetylates O-acetyl-ADP ribose. Down-regulates ribonuclease 3 (RNase III) activity. Acts by interacting directly with the region of the ribonuclease that is required for dimerization activation | ||
NECFGCCN_07118 | 1.2e-95 | K | transcriptional regulator | |||
NECFGCCN_07119 | 4.6e-216 | mdoC | I | Necessary for the succinyl substitution of periplasmic glucans. Could catalyze the transfer of succinyl residues from the cytoplasmic side of the membrane to the nascent glucan backbones on the periplasmic side of the membrane | ||
NECFGCCN_07120 | 1.3e-306 | mdoG | P | Involved in the biosynthesis of osmoregulated periplasmic glucans (OPGs) | ||
NECFGCCN_07121 | 0.0 | mdoH | GT2 | M | Involved in the biosynthesis of osmoregulated periplasmic glucans (OPGs) | |
NECFGCCN_07122 | 5.4e-36 | yceK | S | (Lipo)protein | ||
NECFGCCN_07123 | 2.2e-66 | msyB | S | SecY secA suppressor protein | ||
NECFGCCN_07124 | 3.8e-213 | mdtG | EGP | Major facilitator Superfamily | ||
NECFGCCN_07125 | 2e-182 | lpxL | 2.3.1.241, 2.3.1.242, 2.3.1.243 | M | Catalyzes the transfer of laurate from lauroyl-acyl carrier protein (ACP) to Kdo(2)-lipid IV(A) to form Kdo(2)- (lauroyl)-lipid IV(A) | |
NECFGCCN_07126 | 4.7e-207 | yceA | S | Belongs to the UPF0176 family | ||
NECFGCCN_07127 | 6.3e-09 | yceO | S | Protein of unknown function (DUF2770) | ||
NECFGCCN_07128 | 3.9e-212 | solA | 1.5.3.1 | E | Belongs to the MSOX MTOX family. MTOX subfamily | |
NECFGCCN_07129 | 2.8e-41 | bssS | S | disruption of this gene in Escherichia coli led to effects on biofilm formation, alteration in expression of a number of genes and mutations in bssS led to defects in indole transport and autoinducer-2 uptake and processing | ||
NECFGCCN_07130 | 1.3e-38 | dinI | S | SOS response | ||
NECFGCCN_07131 | 2.4e-200 | pyrC | 3.5.2.3 | F | Catalyzes the reversible cyclization of carbamoyl aspartate to dihydroorotate | |
NECFGCCN_07132 | 1.9e-95 | yceB | S | Lipoprotein | ||
NECFGCCN_07133 | 2.6e-222 | mdtH | U | Multidrug resistance protein mdtH | ||
NECFGCCN_07134 | 1.6e-111 | rimJ | 2.3.1.128 | J | COG1670 Acetyltransferases, including N-acetylases of ribosomal proteins | |
NECFGCCN_07135 | 9.8e-115 | yceH | S | Belongs to the UPF0502 family | ||
NECFGCCN_07136 | 1.4e-170 | mviM | 1.1.1.18, 1.1.1.369 | S | oxidoreductase | |
NECFGCCN_07137 | 5.1e-271 | murJ | S | Involved in peptidoglycan biosynthesis. Transports lipid-linked peptidoglycan precursors from the inner to the outer leaflet of the cytoplasmic membrane | ||
NECFGCCN_07138 | 1.9e-164 | ynfM_3 | EGP | Major facilitator Superfamily | ||
NECFGCCN_07139 | 6.2e-171 | ttdR | K | transcriptional regulator | ||
NECFGCCN_07140 | 0.0 | rne | 3.1.26.12 | J | Endoribonuclease that plays a central role in RNA processing and decay. Required for the maturation of 5S and 16S rRNAs and the majority of tRNAs. Also involved in the degradation of most mRNAs | |
NECFGCCN_07141 | 2.6e-183 | rluC | 5.4.99.24 | J | Responsible for synthesis of pseudouridine from uracil | |
NECFGCCN_07142 | 2.6e-103 | maf | 1.1.1.25, 2.1.1.190 | D | Maf-like protein | |
NECFGCCN_07143 | 9.3e-92 | yceD | S | metal-binding, possibly nucleic acid-binding protein | ||
NECFGCCN_07144 | 3.6e-24 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
NECFGCCN_07145 | 4.6e-208 | plsX | 2.3.1.15 | I | Catalyzes the reversible formation of acyl-phosphate (acyl-PO(4)) from acyl- acyl-carrier-protein (acyl-ACP). This enzyme utilizes acyl-ACP as fatty acyl donor, but not acyl-CoA | |
NECFGCCN_07146 | 4.7e-174 | fabH | 2.3.1.180 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids | |
NECFGCCN_07147 | 2.5e-164 | fabD | 2.3.1.39 | I | malonyl CoA-acyl carrier protein transacylase | |
NECFGCCN_07148 | 3.6e-126 | IQ | reductase | |||
NECFGCCN_07149 | 8.9e-34 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
NECFGCCN_07150 | 1.9e-231 | fabF | 2.3.1.179 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP | |
NECFGCCN_07151 | 1.4e-150 | pabC | 2.6.1.42, 4.1.3.38 | EH | 4-amino-4-deoxychorismate lyase | |
NECFGCCN_07152 | 1.1e-189 | mltG | F | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
NECFGCCN_07153 | 3.4e-112 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
NECFGCCN_07154 | 1.5e-186 | holB | 2.7.7.7 | L | dna polymerase iii | |
NECFGCCN_07155 | 1.3e-148 | ycfH | L | TatD family | ||
NECFGCCN_07156 | 1.3e-265 | ptsG | 2.7.1.192, 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | Phosphotransferase System | |
NECFGCCN_07157 | 1.3e-60 | hinT | FG | COG0537 Diadenosine tetraphosphate (Ap4A) hydrolase and other HIT family hydrolases | ||
NECFGCCN_07158 | 1e-60 | ycfL | S | cellular response to DNA damage stimulus | ||
NECFGCCN_07159 | 5.5e-94 | lpoB | M | Regulator of peptidoglycan synthesis that is essential for the function of penicillin-binding protein 1B (PBP1b) | ||
NECFGCCN_07160 | 5e-148 | thiK | 2.7.1.89 | M | Catalyzes the phosphorylation of thiamine to thiamine phosphate | |
NECFGCCN_07161 | 1.7e-190 | nagZ | 2.7.8.7, 3.2.1.21, 3.2.1.52 | GH3 | G | Plays a role in peptidoglycan recycling by cleaving the terminal beta-1,4-linked N-acetylglucosamine (GlcNAc) from peptide-linked peptidoglycan fragments, giving rise to free GlcNAc, anhydro-N-acetylmuramic acid and anhydro-N-acetylmuramic acid-linked peptides |
NECFGCCN_07162 | 2.2e-104 | ycfP | S | Belongs to the UPF0227 family | ||
NECFGCCN_07163 | 1e-248 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
NECFGCCN_07164 | 3.4e-73 | ycfJ | S | Outer Membrane Lipoprotein | ||
NECFGCCN_07165 | 0.0 | iutA | H | Receptor | ||
NECFGCCN_07166 | 1.9e-110 | ycfQ | K | Transcriptional regulator | ||
NECFGCCN_07167 | 4.7e-36 | bhsA | S | Multiple stress resistance protein BhsA | ||
NECFGCCN_07168 | 1.8e-178 | ycfS | M | ErfK YbiS YcfS YnhG family protein | ||
NECFGCCN_07169 | 0.0 | mfd | L | Couples transcription and DNA repair by recognizing RNA polymerase (RNAP) stalled at DNA lesions. Mediates ATP-dependent release of RNAP and its truncated transcript from the DNA, and recruitment of nucleotide excision repair machinery to the damaged site | ||
NECFGCCN_07170 | 4.6e-203 | lolC | M | Lipoprotein releasing system transmembrane protein | ||
NECFGCCN_07171 | 5.9e-126 | lolD | V | Part of the ABC transporter complex LolCDE involved in the translocation of | ||
NECFGCCN_07172 | 5.6e-228 | lolE | M | Lipoprotein releasing system transmembrane protein | ||
NECFGCCN_07173 | 1.2e-174 | nagK | 2.7.1.4, 2.7.1.59 | F | Catalyzes the phosphorylation of N-acetyl-D-glucosamine (GlcNAc) derived from cell-wall degradation, yielding GlcNAc-6-P | |
NECFGCCN_07174 | 5.5e-155 | cobB | K | NAD-dependent lysine deacetylase and desuccinylase that specifically removes acetyl and succinyl groups on target proteins. Modulates the activities of several proteins which are inactive in their acylated form | ||
NECFGCCN_07176 | 3.3e-175 | lsrR | K | Transcriptional regulator | ||
NECFGCCN_07177 | 3.7e-148 | tpiA | 2.7.2.3, 5.1.3.39, 5.3.1.1, 5.3.1.33 | G | triose-phosphate isomerase | |
NECFGCCN_07178 | 1.9e-194 | pdxA | 1.1.1.262, 1.1.1.408, 1.1.1.409 | H | Catalyzes the NAD(P)-dependent oxidation of 4- (phosphohydroxy)-L-threonine (HTP) into 2-amino-3-oxo-4- (phosphohydroxy)butyric acid which spontaneously decarboxylates to form 3-amino-2-oxopropyl phosphate (AHAP) | |
NECFGCCN_07179 | 0.0 | 2.7.1.198, 2.7.1.219, 2.7.1.220 | G | PTS system glucitol sorbitol-specific | ||
NECFGCCN_07180 | 3.6e-172 | kdgT4 | U | The 2-keto-3-deoxygluconate permease transports the degraded pectin products into the bacterial cell, where they serve as carbon and energy sources. This is a hydrogen coupled transport system | ||
NECFGCCN_07181 | 1.1e-62 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
NECFGCCN_07182 | 2.7e-79 | rpiB | 5.3.1.6 | G | Ribose 5-phosphate isomerase | |
NECFGCCN_07183 | 6.9e-178 | tal | 2.2.1.2 | G | Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)