ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
AIIGCJOP_00002 | 2.6e-18 | csgA | S | major curlin subunit | ||
AIIGCJOP_00003 | 2.7e-49 | csgC | O | Curli assembly protein | ||
AIIGCJOP_00004 | 3e-18 | |||||
AIIGCJOP_00005 | 6.9e-82 | 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 | ||
AIIGCJOP_00006 | 1.2e-242 | clsC | 2.7.8.8 | I | COG1502 Phosphatidylserine phosphatidylglycerophosphate cardiolipi n synthases and related enzymes | |
AIIGCJOP_00007 | 5.3e-204 | 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 | ||
AIIGCJOP_00008 | 5.2e-300 | mdoG | P | Involved in the biosynthesis of osmoregulated periplasmic glucans (OPGs) | ||
AIIGCJOP_00009 | 0.0 | mdoH | GT2 | M | Involved in the biosynthesis of osmoregulated periplasmic glucans (OPGs) | |
AIIGCJOP_00010 | 6.4e-37 | yceK | S | (Lipo)protein | ||
AIIGCJOP_00011 | 7e-65 | msyB | S | SecY secA suppressor protein | ||
AIIGCJOP_00012 | 5.4e-204 | mdtG | EGP | Major facilitator Superfamily | ||
AIIGCJOP_00013 | 1.6e-171 | 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) | |
AIIGCJOP_00014 | 7.1e-192 | yceA | S | Belongs to the UPF0176 family | ||
AIIGCJOP_00015 | 7.1e-101 | yceI | S | Belongs to the UPF0312 family | ||
AIIGCJOP_00016 | 7.6e-95 | yceJ | C | cytochrome b561 | ||
AIIGCJOP_00017 | 1.8e-07 | S | Protein of unknown function (DUF2770) | |||
AIIGCJOP_00018 | 2.2e-215 | solA | 1.5.3.1 | E | Belongs to the MSOX MTOX family. MTOX subfamily | |
AIIGCJOP_00019 | 4e-40 | 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 | ||
AIIGCJOP_00020 | 1.7e-35 | dinI | S | SOS response | ||
AIIGCJOP_00021 | 3.1e-195 | pyrC | 3.5.2.3 | F | Catalyzes the reversible cyclization of carbamoyl aspartate to dihydroorotate | |
AIIGCJOP_00022 | 9.7e-95 | yceB | S | Lipoprotein | ||
AIIGCJOP_00023 | 1.4e-215 | mdtH | U | Multidrug resistance protein mdtH | ||
AIIGCJOP_00024 | 9.1e-112 | rimJ | 2.3.1.128 | J | COG1670 Acetyltransferases, including N-acetylases of ribosomal proteins | |
AIIGCJOP_00025 | 5.3e-105 | yceH | S | Belongs to the UPF0502 family | ||
AIIGCJOP_00026 | 2.9e-165 | mviM | 1.1.1.18, 1.1.1.369 | S | oxidoreductase | |
AIIGCJOP_00027 | 9.2e-273 | murJ | S | Involved in peptidoglycan biosynthesis. Transports lipid-linked peptidoglycan precursors from the inner to the outer leaflet of the cytoplasmic membrane | ||
AIIGCJOP_00028 | 2.1e-62 | flgN | N | Flagellar biosynthesis protein | ||
AIIGCJOP_00029 | 5.4e-33 | flgM | KNU | Anti-sigma-28 factor FlgM | ||
AIIGCJOP_00030 | 1.2e-101 | flgA | N | Involved in the assembly process of the P-ring formation. It may associate with FlgF on the rod constituting a structure essential for the P-ring assembly or may act as a modulator protein for the P-ring assembly | ||
AIIGCJOP_00031 | 2.4e-66 | flgB | N | Structural component of flagellum, the bacterial motility apparatus. Part of the rod structure of flagellar basal body | ||
AIIGCJOP_00032 | 4.1e-63 | flgC | N | Belongs to the flagella basal body rod proteins family | ||
AIIGCJOP_00033 | 4.8e-99 | flgD | N | Required for flagellar hook formation. May act as a scaffolding protein | ||
AIIGCJOP_00034 | 6.3e-219 | flgE | N | Flagellar hook protein flgE | ||
AIIGCJOP_00035 | 1.2e-129 | flgF | N | flagellar basal body | ||
AIIGCJOP_00036 | 4e-139 | flgG | N | Belongs to the flagella basal body rod proteins family | ||
AIIGCJOP_00037 | 3e-122 | flgH | N | Assembles around the rod to form the L-ring and probably protects the motor basal body from shearing forces during rotation | ||
AIIGCJOP_00038 | 1.6e-186 | flgI | N | Assembles around the rod to form the L-ring and probably protects the motor basal body from shearing forces during rotation | ||
AIIGCJOP_00039 | 7e-170 | flgJ | 3.5.1.28 | N | Flagellar rod assembly protein muramidase FlgJ | |
AIIGCJOP_00040 | 2.4e-274 | flgK | N | flagellar hook-associated protein | ||
AIIGCJOP_00041 | 3.3e-151 | flgL | N | Belongs to the bacterial flagellin family | ||
AIIGCJOP_00042 | 1.3e-149 | ynfM_3 | EGP | Major facilitator Superfamily | ||
AIIGCJOP_00043 | 1.2e-158 | ttdR | K | transcriptional regulator | ||
AIIGCJOP_00044 | 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 | |
AIIGCJOP_00045 | 9.1e-167 | rluC | 5.4.99.24 | J | Responsible for synthesis of pseudouridine from uracil | |
AIIGCJOP_00046 | 4.8e-105 | maf | 1.1.1.25, 2.1.1.190 | D | Maf-like protein | |
AIIGCJOP_00047 | 3.9e-90 | yceD | S | metal-binding, possibly nucleic acid-binding protein | ||
AIIGCJOP_00048 | 2.8e-24 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
AIIGCJOP_00049 | 4.9e-137 | 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 | |
AIIGCJOP_00050 | 5.2e-173 | 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 | |
AIIGCJOP_00051 | 3e-165 | fabD | 2.3.1.39 | I | malonyl CoA-acyl carrier protein transacylase | |
AIIGCJOP_00052 | 7.6e-124 | IQ | reductase | |||
AIIGCJOP_00053 | 8.9e-34 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
AIIGCJOP_00054 | 4.3e-228 | 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 | |
AIIGCJOP_00055 | 1.8e-126 | pabC | 2.6.1.42, 4.1.3.38 | EH | 4-amino-4-deoxychorismate lyase | |
AIIGCJOP_00056 | 2.4e-184 | mltG | F | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
AIIGCJOP_00057 | 7.4e-107 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
AIIGCJOP_00058 | 7.8e-180 | holB | 2.7.7.7 | L | dna polymerase iii | |
AIIGCJOP_00059 | 2.8e-148 | ycfH | L | TatD family | ||
AIIGCJOP_00060 | 5.1e-265 | ptsG | 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | PTS system, glucose-specific IIBC subunit | |
AIIGCJOP_00061 | 0.0 | fhuE | P | receptor | ||
AIIGCJOP_00062 | 1.3e-60 | hinT | FG | COG0537 Diadenosine tetraphosphate (Ap4A) hydrolase and other HIT family hydrolases | ||
AIIGCJOP_00063 | 2.3e-38 | ycfL | S | cellular response to DNA damage stimulus | ||
AIIGCJOP_00064 | 3.2e-89 | lpoB | M | Regulator of peptidoglycan synthesis that is essential for the function of penicillin-binding protein 1B (PBP1b) | ||
AIIGCJOP_00065 | 2.6e-136 | thiK | 2.7.1.89 | M | Catalyzes the phosphorylation of thiamine to thiamine phosphate | |
AIIGCJOP_00066 | 9.4e-189 | 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 |
AIIGCJOP_00067 | 1.3e-104 | ycfP | S | Belongs to the UPF0227 family | ||
AIIGCJOP_00068 | 2.5e-239 | ndh | 1.6.99.3 | C | PFAM FAD-dependent pyridine nucleotide-disulphide oxidoreductase | |
AIIGCJOP_00069 | 5.3e-66 | ycfJ | S | Outer Membrane Lipoprotein | ||
AIIGCJOP_00070 | 1.7e-108 | ycfQ | K | Transcriptional regulator | ||
AIIGCJOP_00071 | 1.7e-33 | bhsA | S | Protein of unknown function (DUF1471) | ||
AIIGCJOP_00072 | 9.1e-170 | ycfS | M | ErfK YbiS YcfS YnhG family protein | ||
AIIGCJOP_00073 | 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 | ||
AIIGCJOP_00074 | 2.8e-191 | ycfT | S | Acyltransferase | ||
AIIGCJOP_00075 | 6e-192 | lolC | M | Lipoprotein releasing system transmembrane protein | ||
AIIGCJOP_00076 | 5e-125 | lolD | V | Part of the ABC transporter complex LolCDE involved in the translocation of | ||
AIIGCJOP_00077 | 1.3e-213 | lolE | M | Lipoprotein releasing system transmembrane protein | ||
AIIGCJOP_00078 | 4.6e-171 | 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 | |
AIIGCJOP_00079 | 1.6e-138 | 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 | ||
AIIGCJOP_00082 | 2.4e-192 | potD | P | Required for the activity of the bacterial periplasmic transport system of putrescine | ||
AIIGCJOP_00083 | 7.6e-130 | potC | P | ABC-type spermidine putrescine transport system, permease component II | ||
AIIGCJOP_00084 | 3.3e-147 | potB | P | ABC-type spermidine putrescine transport system, permease component I | ||
AIIGCJOP_00085 | 1.8e-209 | 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 | |
AIIGCJOP_00086 | 1.7e-229 | pepT | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
AIIGCJOP_00087 | 1.5e-216 | ycfD | 1.14.11.47 | S | Cupin 4 family protein | |
AIIGCJOP_00088 | 2.8e-255 | T | PhoQ Sensor | |||
AIIGCJOP_00089 | 5.5e-121 | K | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
AIIGCJOP_00090 | 4.2e-261 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
AIIGCJOP_00091 | 1.8e-105 | hflD | 4.3.2.2 | S | High frequency lysogenization protein hflD homolog | |
AIIGCJOP_00092 | 1.6e-213 | 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 | |
AIIGCJOP_00093 | 3.8e-84 | nudJ | L | Belongs to the Nudix hydrolase family. NudJ subfamily | ||
AIIGCJOP_00094 | 5.9e-107 | rluE | 5.4.99.19, 5.4.99.20, 5.4.99.22 | J | RNA pseudouridylate synthase | |
AIIGCJOP_00095 | 3.4e-241 | icd | 1.1.1.42 | C | Isocitrate dehydrogenase | |
AIIGCJOP_00096 | 1.2e-31 | |||||
AIIGCJOP_00098 | 5.3e-37 | yeaQ | S | transglycosylase associated protein | ||
AIIGCJOP_00099 | 1.7e-07 | yoaK | ||||
AIIGCJOP_00100 | 1.5e-47 | yeaP | 2.7.7.65 | T | Diguanylate cyclase | |
AIIGCJOP_00101 | 4.9e-86 | yeaP | 2.7.7.65 | T | Diguanylate cyclase with GAF sensor | |
AIIGCJOP_00102 | 9.7e-49 | |||||
AIIGCJOP_00103 | 2.2e-49 | yeaO | S | MarR family transcriptional regulator | ||
AIIGCJOP_00104 | 7.6e-121 | pyrG2 | 6.3.4.2 | F | CTP synthase | |
AIIGCJOP_00105 | 2.1e-200 | yeaN | P | Major facilitator superfamily | ||
AIIGCJOP_00106 | 4.6e-135 | yeaM | K | Transcriptional regulator | ||
AIIGCJOP_00107 | 6.6e-70 | yeaL | S | UPF0756 membrane protein | ||
AIIGCJOP_00108 | 0.0 | oprC | P | Receptor | ||
AIIGCJOP_00109 | 1.3e-225 | yhbH | S | Belongs to the UPF0229 family | ||
AIIGCJOP_00110 | 0.0 | prkA | T | Serine Protein Kinase | ||
AIIGCJOP_00111 | 5.3e-141 | mipA | M | MltA-interacting protein | ||
AIIGCJOP_00112 | 8.2e-146 | yeaE | 1.1.1.21 | S | Aldo keto | |
AIIGCJOP_00113 | 3.7e-165 | yeaD | 4.2.1.9, 5.1.3.15 | G | Belongs to the glucose-6-phosphate 1-epimerase family | |
AIIGCJOP_00114 | 2.1e-185 | gapA | 1.2.1.12, 1.2.1.72 | C | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
AIIGCJOP_00115 | 9.1e-74 | msrB | 1.8.4.12 | C | methionine sulfoxide reductase | |
AIIGCJOP_00116 | 6.8e-41 | yeaC | S | protein conserved in bacteria | ||
AIIGCJOP_00117 | 7.9e-222 | chiA1 | 3.2.1.14 | GH18 | M | Glyco_18 |
AIIGCJOP_00118 | 7.1e-118 | pncA | 2.7.11.1, 3.5.1.19 | Q | Nicotinamidase | |
AIIGCJOP_00119 | 1.9e-189 | ansA | 3.5.1.1 | EJ | COG0252 L-asparaginase archaeal Glu-tRNAGln amidotransferase subunit D | |
AIIGCJOP_00120 | 0.0 | sppA | OU | Signal peptide peptidase | ||
AIIGCJOP_00121 | 1e-96 | ydjA | C | Nitroreductase | ||
AIIGCJOP_00122 | 6.4e-193 | selD | 2.7.9.3 | F | Synthesizes selenophosphate from selenide and ATP | |
AIIGCJOP_00123 | 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 | |
AIIGCJOP_00124 | 2.1e-249 | gdhA | 1.4.1.4 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
AIIGCJOP_00125 | 3.5e-45 | ynjH | S | Protein of unknown function (DUF1496) | ||
AIIGCJOP_00126 | 4.3e-63 | nudG | 3.6.1.55, 3.6.1.65 | L | belongs to the nudix hydrolase family | |
AIIGCJOP_00127 | 3.1e-88 | 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 | ||
AIIGCJOP_00128 | 1.8e-105 | ynjF | 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
AIIGCJOP_00129 | 6.9e-237 | ynjE | 2.8.1.11 | M | sulfurtransferase | |
AIIGCJOP_00130 | 3.1e-97 | ynjD | S | ABC transporter | ||
AIIGCJOP_00131 | 3.9e-247 | ynjC | P | transport system permease component | ||
AIIGCJOP_00132 | 5.9e-211 | ynjB | S | transport system periplasmic component | ||
AIIGCJOP_00133 | 1.1e-100 | merA | M | Pfam SNARE associated Golgi protein | ||
AIIGCJOP_00134 | 2.5e-153 | xthA | 3.1.11.2 | L | Exodeoxyribonuclease III | |
AIIGCJOP_00135 | 2.2e-229 | argD | 2.6.1.11, 2.6.1.17, 2.6.1.81 | E | aminotransferase | |
AIIGCJOP_00136 | 2.9e-193 | astA | 1.2.1.71, 2.3.1.109 | E | arginine N-succinyltransferase | |
AIIGCJOP_00137 | 7.3e-275 | astD | 1.2.1.71 | C | Catalyzes the NAD-dependent reduction of succinylglutamate semialdehyde into succinylglutamate | |
AIIGCJOP_00138 | 4.6e-236 | astB | 3.5.3.23 | E | Catalyzes the hydrolysis of N(2)-succinylarginine into N(2)-succinylornithine, ammonia and CO(2) | |
AIIGCJOP_00139 | 3.1e-173 | astE | 3.5.1.96 | E | Belongs to the AspA AstE family. Succinylglutamate desuccinylase subfamily | |
AIIGCJOP_00140 | 1.1e-70 | spy | NPTU | Heavy-metal resistance | ||
AIIGCJOP_00141 | 1.5e-100 | ves | S | Belongs to the Ves family | ||
AIIGCJOP_00142 | 1.7e-162 | cho | 2.7.7.7 | L | Nuclease subunit of the excinuclease complex | |
AIIGCJOP_00143 | 2.2e-151 | nadE | 6.3.1.5 | F | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
AIIGCJOP_00144 | 1.4e-56 | osmE | J | activator of ntr-like gene protein | ||
AIIGCJOP_00145 | 7.7e-49 | 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 | |
AIIGCJOP_00146 | 7.5e-226 | 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 | ||
AIIGCJOP_00147 | 6e-50 | celC | 2.7.1.196, 2.7.1.205 | G | Phosphotransferase System | |
AIIGCJOP_00148 | 1.3e-151 | chbR | K | transcriptional regulator | ||
AIIGCJOP_00149 | 1.5e-258 | 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 |
AIIGCJOP_00150 | 2.4e-125 | 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 | |
AIIGCJOP_00151 | 0.0 | katE | 1.11.1.6 | C | serves to protect cells from the toxic effects of hydrogen peroxide | |
AIIGCJOP_00152 | 3.9e-37 | cedA | D | Activates the cell division inhibited by chromosomal DNA over-replication | ||
AIIGCJOP_00153 | 7.2e-216 | ydjN | U | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
AIIGCJOP_00154 | 3.7e-113 | ydjM | S | membrane-bound metal-dependent | ||
AIIGCJOP_00155 | 4.9e-134 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
AIIGCJOP_00156 | 1.7e-114 | yniC | 3.1.3.23 | S | HAD-superfamily hydrolase subfamily IA, variant 3 | |
AIIGCJOP_00157 | 3.9e-85 | yniB | S | Membrane | ||
AIIGCJOP_00158 | 1.5e-166 | yniA | G | Fructosamine kinase | ||
AIIGCJOP_00159 | 1.2e-40 | ydiZ | S | endoribonuclease activity | ||
AIIGCJOP_00160 | 1.7e-160 | pfkB | 2.7.1.11, 2.7.1.56 | H | belongs to the carbohydrate kinase PfkB family | |
AIIGCJOP_00161 | 1.9e-133 | ydiY | M | Protein of unknown function, DUF481 | ||
AIIGCJOP_00162 | 2.3e-29 | |||||
AIIGCJOP_00163 | 9.1e-10 | |||||
AIIGCJOP_00164 | 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) | |
AIIGCJOP_00165 | 3e-54 | 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 | ||
AIIGCJOP_00166 | 9.5e-29 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
AIIGCJOP_00167 | 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 | ||
AIIGCJOP_00168 | 5.1e-184 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
AIIGCJOP_00169 | 0.0 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
AIIGCJOP_00170 | 1.4e-47 | 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 | ||
AIIGCJOP_00171 | 3.5e-148 | btuC | H | Part of the ABC transporter complex BtuCDF involved in vitamin B12 import. Involved in the translocation of the substrate across the membrane | ||
AIIGCJOP_00172 | 8.7e-31 | S | membrane | |||
AIIGCJOP_00173 | 1.3e-149 | gtrB | GT2 | M | Bactoprenol glucosyl transferase | |
AIIGCJOP_00174 | 7.8e-89 | btuE | 1.11.1.9 | C | Non-specific peroxidase that can use thioredoxin or glutathione as a reducing agent | |
AIIGCJOP_00175 | 6.6e-115 | 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 | |
AIIGCJOP_00176 | 6.8e-78 | nlpC | 3.4.17.13 | M | NlpC/P60 family | |
AIIGCJOP_00177 | 8.2e-107 | ydiV | 3.1.4.52 | T | Diguanylate phosphodiesterase | |
AIIGCJOP_00178 | 1.9e-275 | ydiU | S | Belongs to the UPF0061 (SELO) family | ||
AIIGCJOP_00179 | 1e-22 | hemP | P | Hemin uptake protein | ||
AIIGCJOP_00180 | 9.6e-197 | 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) | |
AIIGCJOP_00181 | 2.7e-149 | 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 | |
AIIGCJOP_00182 | 0.0 | ppsA | 2.7.9.2 | H | Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate | |
AIIGCJOP_00183 | 8.5e-249 | G | Symporter | |||
AIIGCJOP_00184 | 0.0 | bxlA | 3.2.1.21 | GH3 | G | Fibronectin type III-like domain |
AIIGCJOP_00188 | 3.3e-179 | ydiK | S | ydiK promoter presents a PurR sequence, suggesting that its expression is purine-regulated | ||
AIIGCJOP_00189 | 0.0 | ydiJ | C | Fad linked oxidase | ||
AIIGCJOP_00190 | 1.5e-68 | 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) | |
AIIGCJOP_00192 | 2.3e-76 | arcR | T | Winged helix-turn-helix DNA binding | ||
AIIGCJOP_00193 | 4.6e-80 | arcR | T | Winged helix-turn-helix DNA binding | ||
AIIGCJOP_00194 | 2.1e-59 | sfaG | NU | Fimbrial protein | ||
AIIGCJOP_00195 | 1.6e-75 | M | Pili assembly chaperone PapD, C-terminal domain | |||
AIIGCJOP_00196 | 0.0 | NU | Usher protein | |||
AIIGCJOP_00197 | 1.2e-50 | NU | Fimbrial protein | |||
AIIGCJOP_00198 | 1.5e-46 | NU | Fimbrial protein | |||
AIIGCJOP_00199 | 9.1e-41 | rcsB_2 | K | LuxR family transcriptional regulator | ||
AIIGCJOP_00200 | 7.3e-59 | sufA | S | Iron-sulphur cluster biosynthesis | ||
AIIGCJOP_00201 | 6.6e-292 | sufB | O | FeS assembly protein SufB | ||
AIIGCJOP_00202 | 7.5e-135 | sufC | O | FeS assembly ATPase SufC | ||
AIIGCJOP_00203 | 1e-221 | sufD | O | FeS assembly protein SufD | ||
AIIGCJOP_00204 | 2.9e-221 | 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 | |
AIIGCJOP_00205 | 7.5e-68 | sufE | 2.8.1.7, 4.4.1.16 | S | Participates in cysteine desulfuration mediated by SufS. Cysteine desulfuration mobilizes sulfur from L-cysteine to yield L-alanine and constitutes an essential step in sulfur metabolism for biosynthesis of a variety of sulfur-containing biomolecules. Functions as a sulfur acceptor for SufS, by mediating the direct transfer of the sulfur atom from the S-sulfanylcysteine of SufS, an intermediate product of cysteine desulfuration process | |
AIIGCJOP_00206 | 1.1e-168 | ycfS | M | ErfK YbiS YcfS YnhG family protein | ||
AIIGCJOP_00207 | 2.2e-16 | lpp | M | major outer membrane lipoprotein | ||
AIIGCJOP_00208 | 3.5e-258 | pyk | 2.7.1.40, 2.7.7.4 | G | Pyruvate kinase | |
AIIGCJOP_00209 | 2.6e-183 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
AIIGCJOP_00210 | 9.7e-110 | metI | P | PFAM binding-protein-dependent transport systems inner membrane component | ||
AIIGCJOP_00211 | 2.6e-149 | metQ | P | Belongs to the NlpA lipoprotein family | ||
AIIGCJOP_00212 | 3.4e-29 | ydhZ | S | Protein of unknown function (DUF2767) | ||
AIIGCJOP_00213 | 5.9e-102 | glnP | P | PFAM binding-protein-dependent transport systems inner membrane component | ||
AIIGCJOP_00214 | 2.9e-110 | glnM | P | polar amino acid ABC transporter, inner membrane subunit | ||
AIIGCJOP_00215 | 2.7e-114 | glnQ | 3.6.3.21 | E | ABC transporter | |
AIIGCJOP_00216 | 9.3e-131 | fliY_2 | ET | belongs to the bacterial solute-binding protein 3 family | ||
AIIGCJOP_00217 | 4.4e-16 | |||||
AIIGCJOP_00218 | 5.4e-213 | fixL | 2.7.13.3 | T | Signal transduction histidine kinase | |
AIIGCJOP_00219 | 5.4e-99 | fixJ | K | response regulator | ||
AIIGCJOP_00220 | 1.1e-73 | S | Haem-degrading | |||
AIIGCJOP_00221 | 4.5e-17 | |||||
AIIGCJOP_00222 | 2.4e-131 | ymaE | S | Metallo-beta-lactamase superfamily | ||
AIIGCJOP_00223 | 2.3e-113 | cynT | 4.2.1.1 | P | Reversible hydration of carbon dioxide | |
AIIGCJOP_00224 | 4.5e-219 | G | 3-hydroxyanthranilate 3,4-dioxygenase activity | |||
AIIGCJOP_00225 | 3e-134 | garL | 4.1.2.20, 4.1.2.52 | G | Belongs to the HpcH HpaI aldolase family | |
AIIGCJOP_00226 | 2.4e-98 | 1.11.1.10, 3.1.1.24 | E | hydrolases or acyltransferases, alpha beta hydrolase superfamily | ||
AIIGCJOP_00227 | 6.9e-112 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
AIIGCJOP_00228 | 8.9e-240 | hisD2 | 1.1.1.308 | E | Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine | |
AIIGCJOP_00229 | 2.4e-210 | EGP | Major facilitator Superfamily | |||
AIIGCJOP_00230 | 2.1e-183 | K | transcriptional regulator | |||
AIIGCJOP_00231 | 9.3e-178 | S | SnoaL-like polyketide cyclase | |||
AIIGCJOP_00232 | 8.2e-226 | S | SnoaL-like polyketide cyclase | |||
AIIGCJOP_00233 | 2.8e-230 | hisD_3 | 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 | |
AIIGCJOP_00234 | 3.3e-178 | J | Belongs to the amidase family | |||
AIIGCJOP_00235 | 8.5e-253 | ydhS | S | FAD-NAD(P)-binding | ||
AIIGCJOP_00238 | 1.8e-232 | mdtK | P | Multidrug efflux pump that functions probably as a Na( ) drug antiporter | ||
AIIGCJOP_00239 | 1.5e-115 | ribE | 2.5.1.9 | H | Riboflavin synthase | |
AIIGCJOP_00240 | 5.9e-224 | cfa | 2.1.1.317, 2.1.1.79 | M | synthase | |
AIIGCJOP_00241 | 8.1e-200 | ydhC | EGP | Major facilitator Superfamily | ||
AIIGCJOP_00242 | 1.1e-175 | ydhB | K | Transcriptional regulator | ||
AIIGCJOP_00243 | 4.5e-191 | 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 | ||
AIIGCJOP_00245 | 2.2e-194 | ydhP | EGP | Major facilitator Superfamily | ||
AIIGCJOP_00246 | 4.1e-104 | 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 | |
AIIGCJOP_00247 | 1.1e-94 | ydhO | 3.2.1.14, 3.4.17.13 | GH18 | M | COG0791 Cell wall-associated hydrolases (invasion-associated proteins) |
AIIGCJOP_00248 | 1.3e-60 | grxD | C | Belongs to the glutaredoxin family. Monothiol subfamily | ||
AIIGCJOP_00249 | 4.5e-120 | 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 | ||
AIIGCJOP_00250 | 9.2e-71 | gloA | 4.4.1.5 | H | Catalyzes the conversion of hemimercaptal, formed from methylglyoxal and glutathione, to S-lactoylglutathione | |
AIIGCJOP_00251 | 1.6e-202 | nemA | C | nadh flavin | ||
AIIGCJOP_00252 | 1.2e-89 | nemR | K | transcriptional regulator | ||
AIIGCJOP_00253 | 1.4e-287 | eptA | 2.7.8.42, 2.7.8.43 | S | membrane-associated metal-dependent hydrolase | |
AIIGCJOP_00254 | 1.1e-161 | ydhF | S | Aldo Keto reductase | ||
AIIGCJOP_00255 | 1.1e-89 | sodC | 1.15.1.1 | P | Destroys radicals which are normally produced within the cells and which are toxic to biological systems | |
AIIGCJOP_00256 | 4.4e-150 | ydhK | S | Fusaric acid resistance protein | ||
AIIGCJOP_00257 | 9.1e-196 | ydhK | S | Fusaric acid resistance | ||
AIIGCJOP_00258 | 2.9e-129 | ydhJ | V | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | ||
AIIGCJOP_00259 | 6.4e-32 | ydhI | S | Protein of unknown function (DUF1656) | ||
AIIGCJOP_00260 | 3.2e-69 | slyA | K | Transcription regulator that can specifically activate or repress expression of target genes | ||
AIIGCJOP_00261 | 9.2e-192 | T | Diguanylate cyclase | |||
AIIGCJOP_00262 | 6e-50 | slyB | M | Outer Membrane Lipoprotein | ||
AIIGCJOP_00263 | 5.1e-212 | 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 | |
AIIGCJOP_00264 | 8.1e-54 | mliC | S | membrane-bound lysozyme inhibitor of c-type lysozyme | ||
AIIGCJOP_00265 | 4.1e-121 | 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) | |
AIIGCJOP_00266 | 7.2e-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) | |
AIIGCJOP_00267 | 7.2e-158 | 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 | |
AIIGCJOP_00268 | 4.8e-108 | gst | 2.5.1.18 | O | Belongs to the GST superfamily | |
AIIGCJOP_00269 | 6.9e-273 | dtpA | U | Proton-dependent permease that transports di- and tripeptides | ||
AIIGCJOP_00270 | 3e-116 | 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 | |
AIIGCJOP_00271 | 1.7e-101 | rnfE | 2.3.1.243, 4.2.99.18 | C | Part of a membrane complex involved in electron transport | |
AIIGCJOP_00272 | 2.4e-102 | rnfG | C | Part of a membrane complex involved in electron transport | ||
AIIGCJOP_00273 | 1.1e-192 | rnfD | 1.6.5.8 | C | Part of a membrane complex involved in electron transport | |
AIIGCJOP_00274 | 7.3e-263 | rnfC | C | Part of a membrane complex involved in electron transport | ||
AIIGCJOP_00275 | 6.9e-88 | rnfB | 1.12.98.1 | C | Part of a membrane complex involved in electron transport | |
AIIGCJOP_00276 | 1.3e-94 | rnfA | C | Part of a membrane complex involved in electron transport | ||
AIIGCJOP_00277 | 5.5e-69 | ydgK | S | Membrane | ||
AIIGCJOP_00278 | 2.6e-32 | cnu | S | expression modulating family protein | ||
AIIGCJOP_00279 | 7.1e-21 | blr | ||||
AIIGCJOP_00280 | 4.9e-201 | ydgJ | 1.1.1.371 | S | oxidoreductase | |
AIIGCJOP_00281 | 4.3e-178 | 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 | |
AIIGCJOP_00282 | 1.7e-210 | malY | 4.4.1.8 | E | Bifunctional PLP-dependent enzyme with beta-cystathionase and maltose regulon repressor activities | |
AIIGCJOP_00283 | 4.9e-293 | malX | 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | PTS system | |
AIIGCJOP_00284 | 2.8e-180 | malI | K | Periplasmic binding protein LacI transcriptional regulator | ||
AIIGCJOP_00285 | 1.5e-89 | K | LysR substrate binding domain | |||
AIIGCJOP_00286 | 1.2e-113 | ytnP | S | Metallo-beta-lactamase superfamily | ||
AIIGCJOP_00287 | 8.5e-143 | S | alpha/beta hydrolase fold | |||
AIIGCJOP_00288 | 8.5e-258 | ydgA | S | protein conserved in bacteria | ||
AIIGCJOP_00289 | 6.1e-208 | manA | 1.14.13.81, 5.3.1.8, 5.4.2.8 | G | Belongs to the mannose-6-phosphate isomerase type 1 family | |
AIIGCJOP_00290 | 0.0 | fumA | 4.2.1.2 | C | Catalyzes the reversible hydration of fumarate to (S)- malate | |
AIIGCJOP_00291 | 2.8e-260 | fumC | 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
AIIGCJOP_00292 | 1.1e-167 | 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 | ||
AIIGCJOP_00293 | 2.5e-234 | T | PhoQ Sensor | |||
AIIGCJOP_00294 | 7.7e-119 | 3.6.3.34 | HP | COG1120 ABC-type cobalamin Fe3 -siderophores transport systems, ATPase components | ||
AIIGCJOP_00295 | 1.7e-153 | U | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | |||
AIIGCJOP_00296 | 3e-163 | P | ABC transporter substrate-binding protein | |||
AIIGCJOP_00297 | 6.4e-126 | K | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
AIIGCJOP_00298 | 1.3e-49 | ydgC | S | GlpM family | ||
AIIGCJOP_00299 | 2.1e-126 | IQ | reductase | |||
AIIGCJOP_00300 | 1.4e-243 | ydgI | E | Arginine ornithine antiporter | ||
AIIGCJOP_00301 | 4.7e-158 | ydgH | S | Protein of unknown function (DUF1471) | ||
AIIGCJOP_00302 | 2.2e-266 | 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 | |
AIIGCJOP_00303 | 5.4e-248 | 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 | |
AIIGCJOP_00304 | 8.4e-191 | mscS | M | mechanosensitive ion channel | ||
AIIGCJOP_00305 | 3.7e-179 | uspE | T | universal stress protein | ||
AIIGCJOP_00306 | 1.9e-138 | fnr | K | COG0664 cAMP-binding proteins - catabolite gene activator and regulatory subunit of cAMP-dependent protein kinases | ||
AIIGCJOP_00307 | 4.4e-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 | |
AIIGCJOP_00308 | 2.7e-264 | abgT | H | AbgT putative transporter family | ||
AIIGCJOP_00309 | 4.3e-264 | abgB | 3.5.1.32 | S | amidohydrolase | |
AIIGCJOP_00310 | 2.3e-232 | abgA | 3.5.1.32 | S | Protein involved in hydrolase activity and metabolic process | |
AIIGCJOP_00311 | 5.5e-156 | abgR | K | transcriptional regulator | ||
AIIGCJOP_00312 | 1.2e-92 | ydaL | S | protein conserved in bacteria | ||
AIIGCJOP_00313 | 5.5e-143 | qor | 1.6.5.5 | C | alcohol dehydrogenase | |
AIIGCJOP_00314 | 3.3e-125 | tqsA | T | permease | ||
AIIGCJOP_00315 | 3.1e-46 | mdtJ | P | Catalyzes the excretion of spermidine | ||
AIIGCJOP_00316 | 9.5e-50 | mdtI | P | Catalyzes the excretion of spermidine | ||
AIIGCJOP_00317 | 0.0 | T | Diguanylate cyclase | |||
AIIGCJOP_00318 | 8.5e-140 | ydgD | M | Belongs to the peptidase S1B family | ||
AIIGCJOP_00320 | 1.6e-282 | 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 | |
AIIGCJOP_00321 | 3e-221 | ynfM | EGP | Major facilitator Superfamily | ||
AIIGCJOP_00322 | 3e-154 | ynfL | K | transcriptional regulator | ||
AIIGCJOP_00323 | 8.5e-221 | mlc | GK | Mlc, controls the expression of genes involved in the phosphotransferase and phosphoenolpyruvate systems, regulates genes involved in the uptake of sugars | ||
AIIGCJOP_00324 | 1.7e-120 | 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 | |
AIIGCJOP_00325 | 3.2e-218 | clcB | P | Voltage gated chloride channel | ||
AIIGCJOP_00326 | 1e-212 | opuCA | E | abc transporter atp-binding protein | ||
AIIGCJOP_00327 | 5.7e-107 | opuCB | P | Binding-protein-dependent transport system inner membrane component | ||
AIIGCJOP_00328 | 1.9e-161 | opuCC | M | Glycine betaine | ||
AIIGCJOP_00329 | 7.9e-118 | IV02_19100 | P | Binding-protein-dependent transport system inner membrane component | ||
AIIGCJOP_00330 | 5e-115 | S | Protein of unknown function (DUF1275) | |||
AIIGCJOP_00331 | 2.5e-115 | gst8 | 2.5.1.18 | O | Glutathione S-Transferase | |
AIIGCJOP_00332 | 2.1e-132 | K | DJ-1/PfpI family | |||
AIIGCJOP_00333 | 1.9e-102 | S | Phosphohydrolase | |||
AIIGCJOP_00334 | 1.4e-135 | K | Transcriptional regulator | |||
AIIGCJOP_00335 | 2.7e-147 | K | Transcriptional regulator | |||
AIIGCJOP_00336 | 1.6e-159 | S | Dienelactone hydrolase family | |||
AIIGCJOP_00337 | 5.5e-117 | IQ | oxidoreductase activity | |||
AIIGCJOP_00339 | 2.2e-26 | |||||
AIIGCJOP_00340 | 2.4e-213 | merA | 1.16.1.1, 1.8.1.7 | C | E3 component of pyruvate and 2-oxoglutarate dehydrogenase complex | |
AIIGCJOP_00341 | 5.9e-143 | tp53I3 | C | Alcohol dehydrogenase zinc-binding domain protein | ||
AIIGCJOP_00342 | 7.8e-159 | cinB | I | Alpha beta hydrolase | ||
AIIGCJOP_00343 | 5.1e-129 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
AIIGCJOP_00344 | 6.8e-149 | K | DJ-1/PfpI family | |||
AIIGCJOP_00345 | 2.8e-168 | opdE | EGP | Major facilitator superfamily | ||
AIIGCJOP_00346 | 1.2e-191 | S | X-Pro dipeptidyl-peptidase (S15 family) | |||
AIIGCJOP_00347 | 2e-150 | K | LysR substrate binding domain | |||
AIIGCJOP_00348 | 5.2e-54 | |||||
AIIGCJOP_00349 | 1.1e-64 | S | membrane | |||
AIIGCJOP_00350 | 2.4e-34 | msgA | S | DinI-like family | ||
AIIGCJOP_00351 | 1.4e-94 | 2.7.1.89 | M | Phosphotransferase enzyme family | ||
AIIGCJOP_00352 | 0.0 | iutA | H | Receptor | ||
AIIGCJOP_00353 | 1.9e-180 | EGP | Major facilitator Superfamily | |||
AIIGCJOP_00354 | 5.3e-128 | dltE | M | Belongs to the short-chain dehydrogenases reductases (SDR) family | ||
AIIGCJOP_00355 | 8.8e-08 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
AIIGCJOP_00356 | 1.8e-157 | K | DJ-1/PfpI family | |||
AIIGCJOP_00358 | 1.3e-163 | K | LysR family transcriptional regulator | |||
AIIGCJOP_00360 | 9.9e-81 | 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 | |||
AIIGCJOP_00361 | 4.2e-64 | S | Domain of unknown function (DUF4142) | |||
AIIGCJOP_00362 | 1.7e-188 | P | COG0715 ABC-type nitrate sulfonate bicarbonate transport systems, periplasmic components | |||
AIIGCJOP_00363 | 5.4e-139 | tauC | P | ABC-type nitrate sulfonate bicarbonate transport system permease component | ||
AIIGCJOP_00364 | 8.3e-137 | cysA_3 | P | ABC-type nitrate sulfonate bicarbonate transport system ATPase component | ||
AIIGCJOP_00365 | 2.1e-126 | IV02_09290 | P | Urea carboxylase-associated protein 2 | ||
AIIGCJOP_00366 | 1.7e-119 | ycgI | S | urea carboxylase-associated protein 1 | ||
AIIGCJOP_00367 | 0.0 | uca | 6.3.4.14, 6.3.4.6, 6.4.1.2 | EI | Biotin carboxylase | |
AIIGCJOP_00368 | 0.0 | atzF | 3.5.1.4, 3.5.1.54 | J | Allophanate hydrolase | |
AIIGCJOP_00369 | 9e-99 | 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 | ||
AIIGCJOP_00370 | 0.0 | ynfE | 1.8.5.3, 1.97.1.9 | C | Belongs to the prokaryotic molybdopterin-containing oxidoreductase family | |
AIIGCJOP_00371 | 3.6e-51 | ynfD | S | membrane | ||
AIIGCJOP_00372 | 1.8e-111 | ynfC | M | Uncharacterised protein family (UPF0257) | ||
AIIGCJOP_00373 | 2.3e-49 | ynfB | S | Belongs to the UPF0482 family | ||
AIIGCJOP_00374 | 1.7e-51 | ynfA | S | UPF0060 membrane protein | ||
AIIGCJOP_00375 | 1.7e-245 | rspA | 4.2.1.8 | M | Belongs to the mandelate racemase muconate lactonizing enzyme family | |
AIIGCJOP_00376 | 5.9e-175 | rspB | 1.1.1.380 | C | Dehydrogenase | |
AIIGCJOP_00377 | 8.9e-245 | L | Belongs to the 'phage' integrase family | |||
AIIGCJOP_00378 | 1.4e-40 | S | Putative excisionase (DUF1233) | |||
AIIGCJOP_00379 | 4.8e-35 | S | Protein involved in biological_process | |||
AIIGCJOP_00380 | 1.2e-21 | |||||
AIIGCJOP_00381 | 5.1e-38 | |||||
AIIGCJOP_00382 | 6.9e-201 | STY2074 | S | RecT family | ||
AIIGCJOP_00383 | 0.0 | 2.7.7.7 | L | Enterobacterial exodeoxyribonuclease VIII | ||
AIIGCJOP_00384 | 1.2e-18 | |||||
AIIGCJOP_00385 | 3.4e-29 | |||||
AIIGCJOP_00386 | 2.7e-17 | |||||
AIIGCJOP_00387 | 4.1e-14 | |||||
AIIGCJOP_00388 | 5.9e-65 | K | Helix-turn-helix | |||
AIIGCJOP_00389 | 4.1e-33 | S | Putative antitoxin of bacterial toxin-antitoxin system, YdaS/YdaT | |||
AIIGCJOP_00390 | 6e-84 | S | Putative bacterial toxin ydaT | |||
AIIGCJOP_00391 | 1.8e-125 | S | Protein involved in DNA replication initiation, regulation of DNA replication, viral process and DNA replication | |||
AIIGCJOP_00392 | 5.4e-125 | dnaC | L | DNA replication protein | ||
AIIGCJOP_00393 | 2.4e-40 | glpR | GK | Bacterial protein of unknown function (DUF977) | ||
AIIGCJOP_00394 | 2e-18 | |||||
AIIGCJOP_00396 | 2.2e-07 | Q | methyltransferase | |||
AIIGCJOP_00397 | 3.2e-64 | V | HNH endonuclease | |||
AIIGCJOP_00399 | 3.2e-15 | |||||
AIIGCJOP_00400 | 3.1e-99 | S | Protein of unknown function (DUF1367) | |||
AIIGCJOP_00401 | 7e-22 | |||||
AIIGCJOP_00402 | 2.4e-42 | |||||
AIIGCJOP_00403 | 5.3e-52 | J | Cold shock protein domain | |||
AIIGCJOP_00404 | 1.5e-15 | ylcG | ||||
AIIGCJOP_00405 | 1.3e-140 | O | Antitermination protein | |||
AIIGCJOP_00406 | 4.9e-27 | |||||
AIIGCJOP_00408 | 9.7e-30 | essD | S | Bacteriophage P21 holin S | ||
AIIGCJOP_00409 | 3.6e-81 | S | Phage lysozyme | |||
AIIGCJOP_00410 | 2.8e-48 | |||||
AIIGCJOP_00411 | 5.3e-23 | |||||
AIIGCJOP_00412 | 2.9e-94 | xtmA | L | terminase, small subunit | ||
AIIGCJOP_00413 | 0.0 | S | phage Terminase large subunit | |||
AIIGCJOP_00414 | 2.7e-263 | S | Domain of unknown function (DUF4055) | |||
AIIGCJOP_00415 | 4.1e-206 | S | Head morphogenesis protein | |||
AIIGCJOP_00417 | 8.9e-120 | |||||
AIIGCJOP_00418 | 3.2e-206 | S | P22 coat protein - gene protein 5 | |||
AIIGCJOP_00419 | 4.1e-15 | |||||
AIIGCJOP_00420 | 2.8e-82 | |||||
AIIGCJOP_00421 | 1.8e-54 | |||||
AIIGCJOP_00422 | 4.6e-103 | |||||
AIIGCJOP_00423 | 4.5e-74 | S | Bacteriophage related domain of unknown function | |||
AIIGCJOP_00424 | 1.5e-161 | BB2227 | N | Phage tail tube protein, TTP | ||
AIIGCJOP_00425 | 4e-51 | S | Phage tail assembly chaperone | |||
AIIGCJOP_00426 | 1.2e-45 | S | Phage related hypothetical protein (DUF1799) | |||
AIIGCJOP_00427 | 0.0 | sca1 | D | tail length tape measure | ||
AIIGCJOP_00429 | 2.2e-52 | S | minor tail family protein | |||
AIIGCJOP_00430 | 4.8e-137 | L | S | Phage minor tail protein L | ||
AIIGCJOP_00431 | 3.7e-139 | 3.5.1.28 | M | NLP P60 protein | ||
AIIGCJOP_00432 | 1.9e-96 | S | virus tail assembly | |||
AIIGCJOP_00433 | 0.0 | NT | Phage-related protein, tail component | |||
AIIGCJOP_00434 | 2.2e-57 | NT | transmembrane signaling receptor activity | |||
AIIGCJOP_00436 | 2.9e-41 | S | peptidoglycan catabolic process | |||
AIIGCJOP_00437 | 1.9e-23 | |||||
AIIGCJOP_00438 | 7.2e-47 | |||||
AIIGCJOP_00441 | 1.2e-217 | ydfJ | EGP | Major facilitator superfamily | ||
AIIGCJOP_00442 | 7.7e-243 | uxuT | G | MFS/sugar transport protein | ||
AIIGCJOP_00443 | 2.2e-252 | 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 | |
AIIGCJOP_00444 | 5.3e-119 | ydfH | K | transcriptional regulator | ||
AIIGCJOP_00445 | 1.8e-136 | ydfG | 1.1.1.381 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
AIIGCJOP_00446 | 0.0 | dcp | 3.4.15.5, 3.4.24.70 | E | PFAM peptidase M3A and M3B, thimet oligopeptidase F | |
AIIGCJOP_00447 | 1.1e-19 | L | Belongs to the 'phage' integrase family | |||
AIIGCJOP_00449 | 3.3e-47 | |||||
AIIGCJOP_00450 | 8e-210 | yxjG | 2.1.1.14 | E | methionine synthase | |
AIIGCJOP_00451 | 1.7e-240 | urtA | E | COG0683 ABC-type branched-chain amino acid transport systems, periplasmic component | ||
AIIGCJOP_00452 | 4.4e-262 | urtB | E | Belongs to the binding-protein-dependent transport system permease family | ||
AIIGCJOP_00453 | 1.7e-188 | urtC | E | Belongs to the binding-protein-dependent transport system permease family | ||
AIIGCJOP_00454 | 5e-137 | urtD | E | abc transporter atp-binding protein | ||
AIIGCJOP_00455 | 4e-122 | urtE | E | ABC transporter ATP-binding protein | ||
AIIGCJOP_00456 | 2.8e-114 | adcA | S | periplasmic or secreted protein | ||
AIIGCJOP_00457 | 2.6e-206 | ydeE | EGP | Major facilitator Superfamily | ||
AIIGCJOP_00458 | 3e-138 | eamA | EG | of the drug metabolite transporter (DMT) superfamily | ||
AIIGCJOP_00459 | 3e-28 | marB | S | Multiple antibiotic resistance | ||
AIIGCJOP_00460 | 7.6e-67 | marA | K | Transcriptional activator of genes involved in the multiple antibiotic resistance (Mar) phenotype | ||
AIIGCJOP_00461 | 1.8e-72 | marR | K | transcriptional regulator | ||
AIIGCJOP_00462 | 2.5e-102 | marC | U | UPF0056 membrane protein | ||
AIIGCJOP_00463 | 1.8e-191 | sotB | EGP | Major facilitator Superfamily | ||
AIIGCJOP_00464 | 9.9e-138 | S | Phenazine biosynthesis-like protein | |||
AIIGCJOP_00465 | 2.5e-144 | yddE | S | phenazine biosynthesis protein PhzF | ||
AIIGCJOP_00466 | 2.2e-96 | S | protein conserved in bacteria | |||
AIIGCJOP_00467 | 1.1e-105 | IQ | Short-chain dehydrogenase reductase Sdr | |||
AIIGCJOP_00468 | 1.1e-70 | yjgK | G | PFAM conserved | ||
AIIGCJOP_00469 | 9e-220 | 3.2.1.51 | GH29 | G | BNR repeat-like domain | |
AIIGCJOP_00470 | 5.7e-253 | E | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | |||
AIIGCJOP_00471 | 1.5e-150 | dapA_2 | 4.3.3.7 | EM | Belongs to the DapA family | |
AIIGCJOP_00472 | 9.7e-201 | dhaT | C | alcohol dehydrogenase | ||
AIIGCJOP_00473 | 1.2e-190 | ygbK | 2.7.1.219, 2.7.1.220 | G | type III effector | |
AIIGCJOP_00474 | 1.3e-179 | 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) | |
AIIGCJOP_00475 | 7.4e-130 | K | transcriptional regulator | |||
AIIGCJOP_00476 | 4.8e-171 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
AIIGCJOP_00477 | 6.2e-74 | ysnE | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
AIIGCJOP_00478 | 8.7e-159 | yneJ | K | Transcriptional regulator | ||
AIIGCJOP_00479 | 2.3e-246 | sad | 1.2.1.16, 1.2.1.20, 1.2.1.24, 1.2.1.79 | C | belongs to the aldehyde dehydrogenase family | |
AIIGCJOP_00480 | 7.8e-251 | cheD_2 | NT | Chemotaxis | ||
AIIGCJOP_00481 | 1.4e-162 | glsA | 3.5.1.2 | E | Belongs to the glutaminase family | |
AIIGCJOP_00482 | 1.3e-223 | yneF | T | Diguanylate cyclase | ||
AIIGCJOP_00483 | 2.2e-156 | yaiC | 2.7.7.65 | T | Diguanylate cyclase | |
AIIGCJOP_00484 | 1.4e-157 | T | Diguanylate cyclase | |||
AIIGCJOP_00485 | 4.2e-275 | 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 | |
AIIGCJOP_00486 | 2e-161 | yneE | S | Membrane | ||
AIIGCJOP_00487 | 7.5e-183 | S | Alpha beta hydrolase | |||
AIIGCJOP_00488 | 1.7e-131 | K | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
AIIGCJOP_00489 | 2.9e-219 | cpxA | 2.7.13.3 | T | phosphorelay sensor kinase activity and signal transduction | |
AIIGCJOP_00490 | 3e-16 | cpxA | 2.7.13.3 | T | phosphorelay sensor kinase activity and signal transduction | |
AIIGCJOP_00491 | 1.2e-200 | dipZ | CO | cytochrome c biogenesis protein | ||
AIIGCJOP_00492 | 1.7e-134 | tam | 2.1.1.144, 2.1.1.197 | S | Catalyzes the S-adenosylmethionine monomethyl esterification of trans-aconitate | |
AIIGCJOP_00493 | 2.4e-96 | nudK | 3.6.1.13 | L | Nudix-type nucleoside diphosphatase, YffH AdpP family | |
AIIGCJOP_00494 | 6.4e-118 | glcR | 3.6.4.12 | K | transcriptional regulator | |
AIIGCJOP_00495 | 3.7e-49 | |||||
AIIGCJOP_00496 | 2.1e-43 | bigR | K | transcriptional regulator | ||
AIIGCJOP_00497 | 1e-59 | E | transporter component | |||
AIIGCJOP_00498 | 5e-56 | S | Transporter Component | |||
AIIGCJOP_00499 | 1e-100 | grxB | O | Glutaredoxin 2 | ||
AIIGCJOP_00500 | 4.1e-42 | yebG | S | YebG family | ||
AIIGCJOP_00502 | 1e-103 | cat | 2.3.1.28 | V | This enzyme is an effector of chloramphenicol resistance in bacteria | |
AIIGCJOP_00503 | 1.5e-151 | T | Diguanylate cyclase | |||
AIIGCJOP_00504 | 9.7e-122 | I | Alpha/beta hydrolase family | |||
AIIGCJOP_00505 | 1.3e-153 | 1.11.1.10 | I | Serine aminopeptidase, S33 | ||
AIIGCJOP_00506 | 1.6e-50 | mgrA | K | transcription factor activity and regulation of transcription | ||
AIIGCJOP_00507 | 3.1e-43 | L | 2OG-Fe(II) oxygenase superfamily | |||
AIIGCJOP_00508 | 0.0 | uvrA1 | 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 | ||
AIIGCJOP_00509 | 4.8e-72 | K | transcriptional regulator | |||
AIIGCJOP_00510 | 8.3e-22 | ykkD | P | Multidrug Resistance protein | ||
AIIGCJOP_00511 | 5.6e-26 | ykkC | P | Multidrug Resistance protein | ||
AIIGCJOP_00512 | 1.5e-153 | nahR | K | transcriptional regulator | ||
AIIGCJOP_00513 | 2.1e-186 | EGP | Major facilitator superfamily | |||
AIIGCJOP_00514 | 1.2e-154 | cpo | 1.11.1.10 | I | Alpha beta hydrolase | |
AIIGCJOP_00515 | 1.6e-216 | lysN | EK | Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | ||
AIIGCJOP_00516 | 0.0 | P | Receptor | |||
AIIGCJOP_00517 | 6.6e-153 | S | amine dehydrogenase activity | |||
AIIGCJOP_00518 | 1.6e-09 | hipA | 2.7.11.1 | S | protein related to capsule biosynthesis enzymes | |
AIIGCJOP_00519 | 8.9e-32 | hipB | K | PFAM helix-turn-helix domain protein | ||
AIIGCJOP_00520 | 0.0 | tuaH | 5.4.99.9 | M | COG0438 Glycosyltransferase | |
AIIGCJOP_00521 | 2.6e-160 | L | AAA domain | |||
AIIGCJOP_00522 | 7.7e-202 | yddW | S | Lipoprotein | ||
AIIGCJOP_00523 | 6.7e-53 | 3.4.13.21 | S | ASCH | ||
AIIGCJOP_00524 | 6.3e-42 | IV02_09080 | S | conserved protein | ||
AIIGCJOP_00525 | 0.0 | glgX | 3.2.1.68 | CBM48,GH13 | G | Belongs to the glycosyl hydrolase 13 family |
AIIGCJOP_00526 | 0.0 | treY | 5.4.99.15 | GH13 | G | synthase |
AIIGCJOP_00527 | 1.4e-296 | treZ | 3.2.1.1, 3.2.1.141, 3.2.1.68 | CBM48,GH13 | G | 4-alpha-D-((1- 4)-alpha-D-glucano)trehalose trehalohydrolase |
AIIGCJOP_00528 | 9e-167 | tar | NT | methyl-accepting chemotaxis protein | ||
AIIGCJOP_00529 | 3.8e-200 | T | EAL domain | |||
AIIGCJOP_00530 | 2.1e-121 | IQ | Dehydrogenases with different specificities (Related to short-chain alcohol dehydrogenases) | |||
AIIGCJOP_00531 | 1.4e-148 | K | transcriptional regulator | |||
AIIGCJOP_00532 | 3e-72 | osmC | O | OsmC-like protein | ||
AIIGCJOP_00533 | 1.1e-27 | bdm | S | positive regulation of bacterial-type flagellum assembly | ||
AIIGCJOP_00534 | 8.4e-16 | sra | J | Although this protein associates with the 30S subunit of the ribosome it is not considered to be a bona fide ribosomal protein | ||
AIIGCJOP_00536 | 0.0 | maeA | 1.1.1.38 | C | Malic enzyme | |
AIIGCJOP_00537 | 4.4e-137 | S | Metallo-beta-lactamase superfamily | |||
AIIGCJOP_00538 | 2.2e-99 | K | helix_turn_helix, arabinose operon control protein | |||
AIIGCJOP_00539 | 2.5e-140 | 1.6.99.3 | C | Pyridine nucleotide-disulphide oxidoreductase | ||
AIIGCJOP_00540 | 5.1e-107 | IQ | KR domain | |||
AIIGCJOP_00541 | 7.2e-48 | K | helix_turn_helix, mercury resistance | |||
AIIGCJOP_00542 | 6.6e-157 | ynfM_2 | EGP | Major facilitator Superfamily | ||
AIIGCJOP_00543 | 5.6e-295 | tlrC | S | ABC transporter | ||
AIIGCJOP_00544 | 6.9e-107 | ppa | 3.6.1.1 | C | Catalyzes the hydrolysis of inorganic pyrophosphate (PPi) forming two phosphate ions | |
AIIGCJOP_00545 | 6.2e-185 | adhP | 1.1.1.1 | S | alcohol dehydrogenase | |
AIIGCJOP_00546 | 3.2e-292 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | |||
AIIGCJOP_00547 | 1.1e-148 | P | Binding-protein-dependent transport system inner membrane component | |||
AIIGCJOP_00548 | 6.8e-60 | P | Binding-protein-dependent transport system inner membrane component | |||
AIIGCJOP_00549 | 9.3e-260 | P | Belongs to the ABC transporter superfamily | |||
AIIGCJOP_00550 | 2.9e-158 | MA20_00170 | C | Luciferase-like monooxygenase | ||
AIIGCJOP_00551 | 2.3e-169 | 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 | |||
AIIGCJOP_00552 | 2.1e-88 | K | Bacterial regulatory proteins, tetR family | |||
AIIGCJOP_00553 | 5.7e-93 | kefF | 1.6.5.2 | S | NADPH-dependent FMN reductase | |
AIIGCJOP_00554 | 5.9e-187 | araJ | EGP | Major facilitator Superfamily | ||
AIIGCJOP_00555 | 1.9e-144 | ppk2 | 2.7.4.1 | H | polyphosphate kinase | |
AIIGCJOP_00556 | 3.1e-116 | fdnI | C | TIGRFAM Formate dehydrogenase, gamma subunit | ||
AIIGCJOP_00557 | 7.4e-174 | fdnH | C | formate dehydrogenase | ||
AIIGCJOP_00558 | 0.0 | fdnG | 1.17.1.9, 1.17.5.3 | C | Belongs to the prokaryotic molybdopterin-containing oxidoreductase family | |
AIIGCJOP_00559 | 1.7e-105 | fdnG | 1.17.1.9, 1.17.5.3 | C | Molybdopterin oxidoreductase Fe4S4 domain | |
AIIGCJOP_00560 | 1.1e-148 | yddG | EG | of the drug metabolite transporter (DMT) superfamily | ||
AIIGCJOP_00561 | 9.4e-167 | K | Transcriptional regulator | |||
AIIGCJOP_00562 | 1.1e-145 | livH | E | Belongs to the binding-protein-dependent transport system permease family | ||
AIIGCJOP_00563 | 8.6e-196 | livM | E | Belongs to the binding-protein-dependent transport system permease family | ||
AIIGCJOP_00564 | 6.7e-139 | livG | E | Part of the ABC transporter complexes LivFGHMJ and LivFGHMK involved in the high-affinity transport of branched-chain amino acids | ||
AIIGCJOP_00565 | 2.8e-123 | livF | P | Belongs to the ABC transporter superfamily | ||
AIIGCJOP_00566 | 9.9e-211 | livK | E | Extracellular ligand-binding receptor | ||
AIIGCJOP_00567 | 1.2e-85 | K | L-2-amino-thiazoline-4-carboxylic acid hydrolase | |||
AIIGCJOP_00568 | 2.1e-211 | amaB | 3.5.1.6, 3.5.1.87 | 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 | |
AIIGCJOP_00569 | 2.3e-137 | P | Binding-protein-dependent transport systems inner membrane component | |||
AIIGCJOP_00570 | 2.2e-111 | P | Binding-protein-dependent transport systems inner membrane component | |||
AIIGCJOP_00571 | 2.3e-191 | S | extracellular solute-binding protein, family 1 | |||
AIIGCJOP_00572 | 1.8e-149 | 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 | ||
AIIGCJOP_00573 | 1.6e-113 | MA20_22080 | S | of the beta-lactamase superfamily III | ||
AIIGCJOP_00574 | 2.1e-151 | K | Bacterial regulatory proteins, lacI family | |||
AIIGCJOP_00575 | 3.8e-223 | smvA | EGP | Major facilitator superfamily | ||
AIIGCJOP_00576 | 9.6e-90 | ybjK | K | transcriptional regulator | ||
AIIGCJOP_00577 | 5.3e-251 | narU | P | nitrate nitrite transporter | ||
AIIGCJOP_00578 | 0.0 | narG | 1.7.5.1 | C | Belongs to the prokaryotic molybdopterin-containing oxidoreductase family | |
AIIGCJOP_00579 | 7.3e-310 | narH | 1.7.5.1 | C | nitrate reductase beta subunit | |
AIIGCJOP_00580 | 2.7e-118 | narJ | 1.7.5.1 | C | nitrate reductase molybdenum cofactor assembly chaperone | |
AIIGCJOP_00581 | 1.1e-124 | narI | 1.7.5.1 | C | nitrate reductase, gamma subunit | |
AIIGCJOP_00582 | 5.3e-37 | chpR | K | Antitoxin component of a type II toxin-antitoxin (TA) system. Labile antitoxin that binds to the MazF endoribonuclease toxin and neutralizes its endoribonuclease activity. Is considered to be an 'addiction' molecule as the cell dies in its absence. Toxicity results when the levels of MazE decrease in the cell, leading to mRNA degradation. This effect can be rescued by expression of MazE, but after 6 hours in rich medium the overexpression of MazF leads to programmed cell death. Cell growth and viability are not affected when MazF and MazE are coexpressed. Both MazE and MazE-MazF bind to the promoter region of the mazE- mazF operon to inhibit their own transcription. There are 3 operators to which MazE binds. MazE has higher affinity for promoter DNA in the presence of MazF | ||
AIIGCJOP_00583 | 1.2e-52 | chpA | T | Transcriptional modulator of MazE toxin, MazF | ||
AIIGCJOP_00584 | 3.4e-152 | nhoA | 2.3.1.118, 2.3.1.5 | Q | Belongs to the arylamine N-acetyltransferase family | |
AIIGCJOP_00585 | 1.4e-266 | ftpA | P | ABC-type Fe3 transport system permease component | ||
AIIGCJOP_00586 | 2e-172 | ftpB | P | ABC transporter substrate-binding protein | ||
AIIGCJOP_00587 | 2.1e-115 | phnT | 3.6.3.30 | E | (ABC) transporter | |
AIIGCJOP_00588 | 9.8e-103 | yddH | S | Flavin reductase | ||
AIIGCJOP_00589 | 2.6e-101 | O | Trypsin-like serine proteases, typically periplasmic, contain C-terminal PDZ domain | |||
AIIGCJOP_00590 | 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 | ||
AIIGCJOP_00591 | 3.3e-159 | ttuD | 2.7.1.165 | G | Hydroxypyruvate reductase | |
AIIGCJOP_00592 | 7.8e-178 | ttuC | 1.1.1.83, 1.1.1.93, 4.1.1.73 | CE | Isocitrate/isopropylmalate dehydrogenase | |
AIIGCJOP_00593 | 3.2e-189 | G | Major facilitator superfamily | |||
AIIGCJOP_00594 | 1.1e-89 | K | LysR substrate binding domain | |||
AIIGCJOP_00595 | 1.8e-34 | pptA | 5.3.2.6 | S | Belongs to the 4-oxalocrotonate tautomerase family | |
AIIGCJOP_00596 | 1.7e-116 | yncG | 2.5.1.18 | O | Glutathione S-Transferase | |
AIIGCJOP_00597 | 7.2e-153 | fliY | ET | ABC transporter substrate-binding protein | ||
AIIGCJOP_00598 | 4.4e-138 | gluA | 3.6.3.21 | E | (ABC) transporter | |
AIIGCJOP_00599 | 2.9e-157 | P | amino acid ABC transporter | |||
AIIGCJOP_00600 | 1.6e-88 | K | N-acetyltransferase | |||
AIIGCJOP_00601 | 8.3e-168 | fliY_4 | ET | ABC transporter substrate-binding protein | ||
AIIGCJOP_00602 | 2.8e-246 | moxC | C | monooxygenase | ||
AIIGCJOP_00603 | 9.3e-198 | yxeP | 3.5.1.32 | S | amidohydrolase | |
AIIGCJOP_00604 | 7.3e-162 | ytmO | C | Luciferase Family | ||
AIIGCJOP_00605 | 8.4e-88 | adk | 2.7.4.3 | F | adenylate kinase | |
AIIGCJOP_00606 | 2.8e-189 | aer | T | Motif C-terminal to PAS motifs (likely to contribute to PAS structural domain) | ||
AIIGCJOP_00607 | 5.2e-149 | bacE | EGP | Major facilitator Superfamily | ||
AIIGCJOP_00608 | 2e-153 | T | MASE1 | |||
AIIGCJOP_00609 | 1.7e-219 | S | response to pH | |||
AIIGCJOP_00610 | 5.3e-71 | S | conserved protein, contains double-stranded beta-helix domain | |||
AIIGCJOP_00611 | 1.6e-147 | dmlR_3 | K | Transcriptional regulator | ||
AIIGCJOP_00613 | 2.2e-271 | ansP | E | Involved in the transporte of L-asparagine | ||
AIIGCJOP_00614 | 3e-66 | yjgH | J | endoribonuclease L-PSP | ||
AIIGCJOP_00615 | 2.9e-89 | K | transcriptional regulator | |||
AIIGCJOP_00616 | 7e-187 | yncE | S | DNA binding | ||
AIIGCJOP_00617 | 0.0 | yncD | P | receptor | ||
AIIGCJOP_00618 | 3.7e-112 | tar | NT | helical bimodular (HBM) domain | ||
AIIGCJOP_00619 | 8.6e-82 | mcbR | K | FCD | ||
AIIGCJOP_00620 | 2.1e-180 | yncB | S | nadp-dependent | ||
AIIGCJOP_00621 | 1.3e-97 | K | Helix-turn-helix domain | |||
AIIGCJOP_00622 | 5.6e-89 | yncA | 2.3.1.183 | M | N-acetyltransferase | |
AIIGCJOP_00623 | 1.8e-67 | ydcZ | S | membrane | ||
AIIGCJOP_00624 | 2.1e-27 | ydcY | S | Protein of unknown function (DUF2526) | ||
AIIGCJOP_00625 | 6.6e-306 | dppA | E | ABC-Type Dipeptide Transport System Periplasmic Component | ||
AIIGCJOP_00626 | 6.1e-180 | srfA | S | Virulence effector protein | ||
AIIGCJOP_00627 | 0.0 | srfB | S | PFAM virulence protein SrfB | ||
AIIGCJOP_00628 | 0.0 | srfC | S | Virulence | ||
AIIGCJOP_00630 | 3.4e-22 | ydcX | S | Toxin GhoT_OrtT | ||
AIIGCJOP_00631 | 6.4e-49 | yeaR | P | Domain of unknown function (DUF1971) | ||
AIIGCJOP_00632 | 3.9e-57 | P | Domain of unknown function (DUF1971) | |||
AIIGCJOP_00633 | 1.5e-25 | yoaG | S | Domain of unknown function (DUF1869) | ||
AIIGCJOP_00634 | 1.9e-227 | N | Flagellin is the subunit protein which polymerizes to form the filaments of bacterial flagella | |||
AIIGCJOP_00635 | 2.3e-265 | prr | 1.2.1.19, 1.2.1.3 | C | belongs to the aldehyde dehydrogenase family | |
AIIGCJOP_00636 | 3.4e-141 | ydcV | P | ABC transporter (permease) | ||
AIIGCJOP_00637 | 1.9e-167 | ydcU | P | ABC transporter (Permease | ||
AIIGCJOP_00638 | 5.3e-176 | 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 | |
AIIGCJOP_00639 | 1.2e-221 | ydcS | E | Spermidine putrescine ABC transporter substrate-binding protein | ||
AIIGCJOP_00640 | 9.4e-264 | ydcR | 2.7.7.65 | K | Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | |
AIIGCJOP_00641 | 1.9e-23 | |||||
AIIGCJOP_00642 | 1.6e-191 | luxA_2 | C | Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | ||
AIIGCJOP_00643 | 2.9e-27 | |||||
AIIGCJOP_00644 | 6.7e-262 | cioA | 1.10.3.14 | C | oxidase, subunit | |
AIIGCJOP_00645 | 3.9e-179 | cioB | 1.10.3.14 | C | oxidase subunit | |
AIIGCJOP_00646 | 1.1e-12 | S | Protein of unknown function (DUF2474) | |||
AIIGCJOP_00647 | 7.6e-30 | yncJ | S | Protein of unknown function (DUF2554) | ||
AIIGCJOP_00648 | 0.0 | ydcP | O | peptidase U32 | ||
AIIGCJOP_00649 | 1e-93 | ydcN | K | transcriptional regulator | ||
AIIGCJOP_00650 | 3.2e-193 | ydcO | Q | protein involved in benzoate metabolism | ||
AIIGCJOP_00651 | 6.6e-159 | K | AraC family transcriptional regulator | |||
AIIGCJOP_00652 | 2.6e-158 | BP3797 | EG | of the drug metabolite transporter (DMT) superfamily | ||
AIIGCJOP_00653 | 1.8e-119 | ydcL | S | Protein of unknown function (DUF3313) | ||
AIIGCJOP_00654 | 6.4e-301 | dppA | E | ABC-Type Dipeptide Transport System Periplasmic Component | ||
AIIGCJOP_00655 | 5e-229 | pepT | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
AIIGCJOP_00656 | 2.2e-105 | tehB | 2.1.1.265 | Q | Tellurite resistance protein TehB | |
AIIGCJOP_00657 | 2e-175 | tehA | P | PFAM C4-dicarboxylate transporter malic acid transport protein | ||
AIIGCJOP_00658 | 8e-137 | ydcK | M | Homologous to orf229 gp Streptococcus thermophilus bacteriophage Sfi19 gi 9632919 ref NP_049948.1 | ||
AIIGCJOP_00659 | 3e-93 | rimL | J | COG1670 Acetyltransferases, including N-acetylases of ribosomal proteins | ||
AIIGCJOP_00660 | 0.0 | mdoD | P | Involved in the biosynthesis of osmoregulated periplasmic glucans (OPGs) | ||
AIIGCJOP_00661 | 6.1e-140 | ET | belongs to the bacterial solute-binding protein 3 family | |||
AIIGCJOP_00662 | 5.1e-215 | ybdL | 2.6.1.17, 2.6.1.88 | E | aminotransferase | |
AIIGCJOP_00663 | 2.8e-146 | K | transcriptional regulator | |||
AIIGCJOP_00664 | 1.5e-264 | pnbA | CE10 | I | Belongs to the type-B carboxylesterase lipase family | |
AIIGCJOP_00665 | 1.6e-249 | ydcJ | S | protein conserved in bacteria | ||
AIIGCJOP_00666 | 0.0 | dmsA | 1.8.5.3 | C | Belongs to the prokaryotic molybdopterin-containing oxidoreductase family | |
AIIGCJOP_00667 | 5.7e-120 | C | reductase chain B | |||
AIIGCJOP_00668 | 2e-104 | S | anaerobic DMSO reductase chain C anchor subunit | |||
AIIGCJOP_00669 | 4.9e-69 | etfA | 1.12.98.1, 1.18.1.2, 1.19.1.1 | C | 4Fe-4S dicluster domain | |
AIIGCJOP_00670 | 8.8e-162 | pcaQ | K | transcriptional regulator | ||
AIIGCJOP_00671 | 0.0 | quiA | 1.1.5.8 | G | Dehydrogenase | |
AIIGCJOP_00672 | 2e-58 | M | Gram-negative bacterial TonB protein C-terminal | |||
AIIGCJOP_00673 | 4.5e-180 | trg | NT | chemotaxis, protein | ||
AIIGCJOP_00674 | 2.9e-215 | frmA | 1.1.1.1, 1.1.1.284 | C | Belongs to the zinc-containing alcohol dehydrogenase family. Class-III subfamily | |
AIIGCJOP_00675 | 2.7e-42 | frmR | S | protein conserved in bacteria | ||
AIIGCJOP_00676 | 5.3e-17 | ariR | K | Probably a connector protein for RcsB C regulation of biofilm and acid-resistance, providing additional signal input into the two-component signaling pathway. May serve to stimulate biofilm maturation, via the Rcs phosphorelay. Regulates expression of genes involved in acid-resistance and biofilm formation, including the RcsB C two-component system. May be a non-specific DNA-binding protein that binds genes and or intergenic regions via a geometric recognition. Also confers resistance to H(2)O(2). Overexpression at 28 and 16 degrees Celsius increases the production of colanic acid, an exopolysaccharide and matrix component, and reduces adhesive curli fimbriae expression. Both of these effects require RcsB | ||
AIIGCJOP_00677 | 5.3e-07 | |||||
AIIGCJOP_00678 | 3.2e-15 | ycgZ | S | Biofilm development protein YmgB/AriR | ||
AIIGCJOP_00679 | 1.7e-25 | |||||
AIIGCJOP_00680 | 1.8e-131 | |||||
AIIGCJOP_00681 | 3.4e-167 | S | Domain of unknown function (DUF1852) | |||
AIIGCJOP_00682 | 3.1e-192 | metE | 2.1.1.14 | E | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | |
AIIGCJOP_00683 | 5.4e-78 | 1.11.1.12, 1.11.1.9 | O | Belongs to the glutathione peroxidase family | ||
AIIGCJOP_00685 | 8.3e-125 | yedK | S | Belongs to the SOS response-associated peptidase family | ||
AIIGCJOP_00686 | 5e-200 | umuC | 2.7.7.7 | L | DNA polymerase | |
AIIGCJOP_00687 | 3.9e-131 | 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 | |
AIIGCJOP_00688 | 0.0 | dsbD | 1.8.1.8 | CO | Disulphide bond corrector protein DsbC | |
AIIGCJOP_00689 | 4.8e-14 | VPA1614 | ||||
AIIGCJOP_00690 | 2.3e-67 | pgaD | S | Poly-beta-1,6-N-acetyl-D-glucosamine biosynthesis protein PgaD | ||
AIIGCJOP_00691 | 7.3e-250 | pgaC | GT2 | M | Poly-beta-1,6-N-acetyl-D-glucosamine synthase | |
AIIGCJOP_00692 | 0.0 | pgaB | G | Polysaccharide deacetylase | ||
AIIGCJOP_00693 | 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 | |||
AIIGCJOP_00694 | 1.9e-264 | S | Protein of unknown function (DUF560) | |||
AIIGCJOP_00695 | 3.2e-08 | mrcB | 2.4.1.129, 3.4.16.4 | GT51 | M | Pfam:Lipoprotein_5 |
AIIGCJOP_00696 | 2.4e-21 | V | HNH endonuclease | |||
AIIGCJOP_00697 | 2.5e-83 | S | polyketide cyclase | |||
AIIGCJOP_00698 | 9.1e-114 | 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) | |||
AIIGCJOP_00699 | 8.1e-97 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
AIIGCJOP_00700 | 4.2e-111 | K | AraC family transcriptional regulator | |||
AIIGCJOP_00701 | 4.7e-122 | K | transcriptional | |||
AIIGCJOP_00702 | 1.8e-130 | GM | Nad-dependent epimerase dehydratase | |||
AIIGCJOP_00703 | 2e-126 | GM | NmrA-like family | |||
AIIGCJOP_00704 | 1.6e-112 | S | Beta-lactamase | |||
AIIGCJOP_00705 | 4.2e-135 | mexT | K | transcriptional regulator | ||
AIIGCJOP_00706 | 7.2e-121 | K | AraC-type transcriptional regulator N-terminus | |||
AIIGCJOP_00707 | 6.2e-121 | IQ | short-chain dehydrogenase | |||
AIIGCJOP_00708 | 3.2e-41 | yjgJ | K | tetR family | ||
AIIGCJOP_00709 | 1e-113 | S | Protein of unknown function (DUF1214) | |||
AIIGCJOP_00710 | 1.2e-45 | M | Glycosyltransferase sugar-binding region containing DXD motif | |||
AIIGCJOP_00711 | 1.1e-66 | umuD | KT | Belongs to the peptidase S24 family | ||
AIIGCJOP_00712 | 1.4e-173 | yhdH | C | Quinone oxidoreductase, YhdH YhfP family | ||
AIIGCJOP_00713 | 7.1e-113 | nemR | K | Bacterial transcriptional repressor C-terminal | ||
AIIGCJOP_00714 | 5.2e-122 | yjiJ | EGP | Major facilitator Superfamily | ||
AIIGCJOP_00716 | 6e-99 | gltR_2 | K | LysR substrate binding domain | ||
AIIGCJOP_00717 | 2.5e-128 | yrpB | 1.13.12.16 | S | Nitronate monooxygenase | |
AIIGCJOP_00718 | 8.6e-125 | K | Transcriptional regulator | |||
AIIGCJOP_00719 | 3.1e-98 | IQ | reductase | |||
AIIGCJOP_00720 | 6e-20 | dmpI | 5.3.2.6 | G | 4-oxalocrotonate tautomerase | |
AIIGCJOP_00722 | 9.3e-127 | GM | NmrA-like family | |||
AIIGCJOP_00723 | 2.5e-124 | K | Transcriptional regulator | |||
AIIGCJOP_00724 | 7.7e-96 | S | Phosphohydrolase | |||
AIIGCJOP_00725 | 1.3e-99 | K | transcriptional regulator | |||
AIIGCJOP_00726 | 1.8e-54 | S | Putative stress-induced transcription regulator | |||
AIIGCJOP_00727 | 6.9e-140 | S | Alpha/beta hydrolase family | |||
AIIGCJOP_00728 | 7.7e-254 | mscM | M | mechanosensitive ion channel | ||
AIIGCJOP_00729 | 3.1e-132 | dapA5 | 4.3.3.7 | EM | Belongs to the DapA family | |
AIIGCJOP_00732 | 1.1e-178 | EGP | Sugar (and other) transporter | |||
AIIGCJOP_00733 | 1.7e-93 | cybB | C | B-type di-heme cytochrome with a major alpha-absorption peak at 561 nm and a minor peak at 555 nm | ||
AIIGCJOP_00734 | 2.1e-180 | gap | 1.2.1.12, 1.2.1.72 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
AIIGCJOP_00735 | 2.1e-163 | xynB | I | esterase lipase | ||
AIIGCJOP_00736 | 2.5e-264 | aldA | 1.2.1.21, 1.2.1.22 | C | belongs to the aldehyde dehydrogenase family | |
AIIGCJOP_00737 | 3.5e-138 | ydcF | S | DUF218 domain | ||
AIIGCJOP_00738 | 6.4e-238 | proP | EGP | Major facilitator superfamily | ||
AIIGCJOP_00739 | 9.3e-271 | rmrB | EGP | Major facilitator superfamily | ||
AIIGCJOP_00740 | 5.7e-144 | hlyD | V | HlyD membrane-fusion protein of T1SS | ||
AIIGCJOP_00741 | 5.1e-230 | oprM | M | membrane | ||
AIIGCJOP_00742 | 2e-115 | mdmC | 2.1.1.104 | S | O-Methyltransferase | |
AIIGCJOP_00743 | 0.0 | hrpA | 3.6.4.13 | L | ATP-dependent helicase hrpA | |
AIIGCJOP_00744 | 3.2e-104 | 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 | ||
AIIGCJOP_00745 | 2.4e-194 | G | Major facilitator superfamily | |||
AIIGCJOP_00746 | 1.3e-83 | K | Transcriptional regulator | |||
AIIGCJOP_00747 | 4.3e-63 | ttr | K | Acetyltransferase (GNAT) domain | ||
AIIGCJOP_00748 | 1.9e-55 | 2.7.11.1 | T | Anti-sigma regulatory factor (Ser Thr protein kinase) | ||
AIIGCJOP_00749 | 8.8e-51 | rsbV | T | Belongs to the anti-sigma-factor antagonist family | ||
AIIGCJOP_00750 | 5.1e-202 | 3.1.3.3 | T | response regulator | ||
AIIGCJOP_00751 | 6.8e-167 | |||||
AIIGCJOP_00752 | 1.3e-216 | S | OpgC protein | |||
AIIGCJOP_00753 | 0.0 | 2.4.1.12 | GT2 | M | Cellulose synthase | |
AIIGCJOP_00754 | 3.9e-227 | NU | Protein of unknown function (DUF3131) | |||
AIIGCJOP_00755 | 5.6e-278 | G | Protein of unknown function (DUF3131) | |||
AIIGCJOP_00756 | 5.3e-251 | G | Protein of unknown function (DUF3131) | |||
AIIGCJOP_00757 | 3.2e-69 | VPA1107 | C | nitric oxide dioxygenase activity | ||
AIIGCJOP_00758 | 0.0 | T | PhoQ Sensor | |||
AIIGCJOP_00759 | 0.0 | 3.2.1.25 | G | Belongs to the glycosyl hydrolase 2 family | ||
AIIGCJOP_00760 | 3.5e-37 | S | RelE toxin of RelE / RelB toxin-antitoxin system | |||
AIIGCJOP_00761 | 5.7e-85 | paaY | S | Phenylacetic acid degradation protein PaaY | ||
AIIGCJOP_00762 | 1.8e-170 | paaX | K | phenylacetic acid degradation operon negative regulatory protein | ||
AIIGCJOP_00763 | 1.6e-247 | paaK | 6.2.1.30 | H | Catalyzes the activation of phenylacetic acid (PA) to phenylacetyl-CoA (PA-CoA) | |
AIIGCJOP_00764 | 5.3e-215 | 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 | |
AIIGCJOP_00765 | 2.1e-73 | paaI | Q | phenylacetic acid degradation protein | ||
AIIGCJOP_00766 | 1.7e-233 | paaH | 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 | |
AIIGCJOP_00767 | 2.5e-141 | paaG | 5.3.3.18 | I | Enoyl-CoA hydratase | |
AIIGCJOP_00768 | 3.3e-122 | paaF | 4.2.1.17 | I | Belongs to the enoyl-CoA hydratase isomerase family | |
AIIGCJOP_00769 | 2.3e-193 | paaE | C | COG1018 Flavodoxin reductases (ferredoxin-NADPH reductases) family 1 | ||
AIIGCJOP_00770 | 2.3e-87 | paaD | L | phenylacetate-CoA oxygenase, PaaJ subunit | ||
AIIGCJOP_00771 | 2.2e-131 | paaC | 1.14.13.149 | S | Phenylacetate-CoA oxygenase, PaaI subunit | |
AIIGCJOP_00772 | 3.1e-49 | paaB | Q | Phenylacetate-CoA oxygenase | ||
AIIGCJOP_00773 | 8e-179 | paaA | 1.14.13.149 | S | Phenylacetate-CoA oxygenase | |
AIIGCJOP_00774 | 0.0 | paaN | 1.2.1.91, 3.3.2.12 | CI | Aldehyde dehydrogenase | |
AIIGCJOP_00775 | 0.0 | tynA | 1.4.3.21 | Q | amine oxidase | |
AIIGCJOP_00776 | 0.0 | yjcS | Q | COG2015 Alkyl sulfatase and related hydrolases | ||
AIIGCJOP_00777 | 2.8e-114 | 2.7.7.65 | T | diguanylate cyclase | ||
AIIGCJOP_00778 | 2.7e-285 | feaB | 1.2.1.39 | C | belongs to the aldehyde dehydrogenase family | |
AIIGCJOP_00779 | 2.1e-163 | feaR | K | transcriptional regulator | ||
AIIGCJOP_00780 | 1.3e-43 | ydbL | S | protein conserved in bacteria | ||
AIIGCJOP_00781 | 1.6e-25 | ynbE | S | (Lipo)protein | ||
AIIGCJOP_00782 | 0.0 | ydbH | S | Dicarboxylate transport | ||
AIIGCJOP_00783 | 7.7e-180 | ldhA | 1.1.1.28 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
AIIGCJOP_00784 | 6.1e-62 | hslJ | O | Heat shock protein | ||
AIIGCJOP_00785 | 4.2e-40 | ydbJ | S | Domain of unknown function (DUF333) | ||
AIIGCJOP_00786 | 0.0 | nifJ | 1.2.7.1 | C | Oxidoreductase required for the transfer of electrons from pyruvate to flavodoxin | |
AIIGCJOP_00787 | 2.1e-189 | ompN | M | PFAM porin Gram-negative type | ||
AIIGCJOP_00788 | 3.3e-71 | S | Glutathione-dependent formaldehyde-activating | |||
AIIGCJOP_00789 | 7.7e-75 | |||||
AIIGCJOP_00790 | 2.9e-176 | 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 | |
AIIGCJOP_00791 | 1.1e-248 | 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 | |
AIIGCJOP_00794 | 1.8e-181 | zntB | P | Zinc transport protein zntB | ||
AIIGCJOP_00795 | 1.3e-130 | tse3 | NT | methyl-accepting chemotaxis protein | ||
AIIGCJOP_00797 | 2.6e-217 | ydaM | 2.7.7.65 | T | Diguanylate cyclase | |
AIIGCJOP_00798 | 2.3e-99 | pfpI | 3.5.1.124 | S | Intracellular protease | |
AIIGCJOP_00799 | 2.4e-57 | |||||
AIIGCJOP_00800 | 2.4e-128 | M | ImpA domain protein | |||
AIIGCJOP_00801 | 3.7e-76 | S | Gene 25-like lysozyme | |||
AIIGCJOP_00802 | 3.6e-86 | tssJ | S | Type VI secretion | ||
AIIGCJOP_00803 | 3.1e-198 | S | Type VI secretion, TssG | |||
AIIGCJOP_00804 | 0.0 | tssF | S | Type VI secretion | ||
AIIGCJOP_00805 | 1.6e-09 | S | Protein of unknown function (DUF1240) | |||
AIIGCJOP_00806 | 3.8e-45 | S | to Yersinia kristensenii ATCC 33638 | |||
AIIGCJOP_00807 | 6e-85 | S | to Yersinia kristensenii ATCC 33638 | |||
AIIGCJOP_00808 | 5.6e-25 | S | Type VI secretion, EvfE, EvfF, ImpA, BimE, VC_A0119, VasJ | |||
AIIGCJOP_00809 | 1.3e-101 | 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 | ||
AIIGCJOP_00810 | 0.0 | kefC | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
AIIGCJOP_00811 | 4.4e-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 | |
AIIGCJOP_00812 | 2.5e-163 | apaH | 3.6.1.41 | T | Hydrolyzes diadenosine 5',5'''-P1,P4-tetraphosphate to yield ADP | |
AIIGCJOP_00813 | 1.7e-63 | P | mitochondrion morphogenesis | |||
AIIGCJOP_00814 | 2.6e-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 | |
AIIGCJOP_00815 | 9.7e-183 | 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) | |
AIIGCJOP_00816 | 2e-228 | 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 | |
AIIGCJOP_00817 | 0.0 | lptD | M | Together with LptE, is involved in the assembly of lipopolysaccharide (LPS) at the surface of the outer membrane | ||
AIIGCJOP_00818 | 7.6e-133 | 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 | ||
AIIGCJOP_00819 | 5.8e-123 | rluA | 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
AIIGCJOP_00820 | 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 | ||
AIIGCJOP_00821 | 0.0 | polB | 2.7.7.7 | L | DNA polymerase | |
AIIGCJOP_00822 | 2.5e-132 | araD | 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 | |
AIIGCJOP_00823 | 1.9e-08 | araA | 5.3.1.4 | G | Catalyzes the conversion of L-arabinose to L-ribulose | |
AIIGCJOP_00824 | 0.0 | araB | 2.7.1.16 | C | Belongs to the ribulokinase family | |
AIIGCJOP_00825 | 6.6e-164 | araC | K | regulates the araBAD and araFGH operons and other genes involved in the transport and catabolism of L-arabinose | ||
AIIGCJOP_00826 | 1.5e-135 | yabI | 3.6.1.27 | I | membrane-associated protein | |
AIIGCJOP_00827 | 5.5e-116 | thiQ | P | Part of the ABC transporter complex ThiBPQ involved in thiamine import. Responsible for energy coupling to the transport system | ||
AIIGCJOP_00828 | 2e-286 | thiP | P | with TbpA and ThiQ functions in transport of thiamine and thiamine pyrophosphate into the cell | ||
AIIGCJOP_00829 | 3.8e-179 | tbpA | P | thiamine ABC transporter | ||
AIIGCJOP_00830 | 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 | ||
AIIGCJOP_00831 | 2.4e-16 | S | Inhibitor of glucose uptake transporter SgrT | |||
AIIGCJOP_00832 | 3.7e-197 | setA | EGP | Major facilitator Superfamily | ||
AIIGCJOP_00833 | 8.8e-110 | 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 | |
AIIGCJOP_00834 | 2.4e-259 | leuC | 4.2.1.33, 4.2.1.35 | H | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
AIIGCJOP_00835 | 9.3e-203 | 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 | |
AIIGCJOP_00836 | 5.9e-283 | 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) | |
AIIGCJOP_00837 | 4.9e-163 | leuO | K | transcriptional regulator | ||
AIIGCJOP_00838 | 0.0 | ilvI | 2.2.1.6 | H | acetolactate synthase | |
AIIGCJOP_00839 | 3.1e-81 | ilvH | 2.2.1.6 | E | acetolactate synthase | |
AIIGCJOP_00840 | 3e-187 | fruR | 3.2.1.26 | GH32 | K | Transcriptional |
AIIGCJOP_00841 | 7.2e-80 | 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 | ||
AIIGCJOP_00842 | 1.2e-169 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
AIIGCJOP_00843 | 3.3e-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 | ||
AIIGCJOP_00844 | 0.0 | ftsI | 3.4.16.4 | M | Catalyzes cross-linking of the peptidoglycan cell wall at the division septum | |
AIIGCJOP_00845 | 1.9e-275 | 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 | |
AIIGCJOP_00846 | 1.5e-237 | 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 | |
AIIGCJOP_00847 | 8.7e-201 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
AIIGCJOP_00848 | 5.7e-247 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
AIIGCJOP_00849 | 3.1e-226 | ftsW | 2.4.1.227 | GT28 | M | Peptidoglycan polymerase that is essential for cell division |
AIIGCJOP_00850 | 6.3e-196 | 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) |
AIIGCJOP_00851 | 8.6e-276 | murC | 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
AIIGCJOP_00852 | 1.9e-164 | ddl | 1.3.1.98, 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
AIIGCJOP_00853 | 5.4e-150 | 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 | |
AIIGCJOP_00854 | 3.7e-235 | 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 | ||
AIIGCJOP_00855 | 3e-207 | 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 | ||
AIIGCJOP_00856 | 7.2e-172 | 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 | |
AIIGCJOP_00857 | 8.6e-74 | secM | U | 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 | ||
AIIGCJOP_00858 | 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 | ||
AIIGCJOP_00859 | 7.2e-65 | mutT | 3.6.1.55, 3.6.1.65 | L | belongs to the nudix hydrolase family | |
AIIGCJOP_00860 | 1.1e-29 | 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 | |
AIIGCJOP_00861 | 1.7e-134 | 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 | ||
AIIGCJOP_00862 | 3.3e-96 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
AIIGCJOP_00863 | 1.7e-193 | 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 | |
AIIGCJOP_00864 | 3.2e-172 | hofC | U | type II secretion system | ||
AIIGCJOP_00865 | 5.4e-240 | hofB | NU | Type II secretory pathway, ATPase PulE Tfp pilus assembly pathway, ATPase PilB | ||
AIIGCJOP_00866 | 4.3e-69 | ppdD | NU | Belongs to the N-Me-Phe pilin family | ||
AIIGCJOP_00867 | 6.3e-157 | nadC | 2.4.2.19 | H | Belongs to the NadC ModD family | |
AIIGCJOP_00868 | 2e-103 | ampD | 3.5.1.28 | V | Negative regulator of beta-lactamase expression | |
AIIGCJOP_00869 | 2.9e-151 | ampE | 6.3.1.10 | V | regulatory protein AmpE | |
AIIGCJOP_00870 | 2.3e-189 | abf | G | Belongs to the glycosyl hydrolase 43 family | ||
AIIGCJOP_00871 | 3.6e-260 | yicJ | G | COG2211 Na melibiose symporter and related transporters | ||
AIIGCJOP_00872 | 1.5e-250 | aroP | E | amino acid | ||
AIIGCJOP_00873 | 1.6e-132 | pdhR | K | Regulatory protein GntR HTH | ||
AIIGCJOP_00874 | 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) | |
AIIGCJOP_00875 | 1.7e-284 | aceF | 2.3.1.12 | C | The pyruvate dehydrogenase complex catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2) | |
AIIGCJOP_00876 | 6.3e-268 | lpdA | 1.8.1.4 | F | Lipoamide dehydrogenase is a component of the glycine cleavage system as well as of the alpha-ketoacid dehydrogenase complexes | |
AIIGCJOP_00877 | 2e-125 | flgK | N | Protein of unknown function (DUF2950) | ||
AIIGCJOP_00878 | 2.8e-160 | yacH | M | Protein of unknown function (DUF3300) | ||
AIIGCJOP_00880 | 0.0 | acnB | 4.2.1.3, 4.2.1.99 | C | Belongs to the aconitase IPM isomerase family | |
AIIGCJOP_00881 | 2.6e-61 | yacL | S | Belongs to the UPF0231 family | ||
AIIGCJOP_00882 | 4.1e-147 | 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 | |
AIIGCJOP_00883 | 1.5e-163 | 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 | |
AIIGCJOP_00884 | 7.3e-52 | yacC | S | Type II secretion system pilotin lipoprotein (PulS_OutS) | ||
AIIGCJOP_00885 | 7.8e-275 | cueO | Q | Multi-copper | ||
AIIGCJOP_00886 | 0.0 | gcd | 1.1.5.2 | C | Dehydrogenase | |
AIIGCJOP_00887 | 1.5e-92 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
AIIGCJOP_00888 | 9.9e-123 | can | 4.2.1.1 | P | Reversible hydration of carbon dioxide | |
AIIGCJOP_00889 | 1.4e-162 | yadG | V | AAA domain, putative AbiEii toxin, Type IV TA system | ||
AIIGCJOP_00890 | 1.5e-135 | yadH | V | Transport Permease Protein | ||
AIIGCJOP_00891 | 8.2e-73 | yadI | G | IIa component | ||
AIIGCJOP_00892 | 2.5e-220 | yadE | 3.5.1.41 | G | Polysaccharide deacetylase | |
AIIGCJOP_00893 | 7.1e-65 | panD | 4.1.1.11 | H | Catalyzes the pyruvoyl-dependent decarboxylation of aspartate to produce beta-alanine | |
AIIGCJOP_00894 | 3.2e-142 | panC | 6.3.2.1 | H | Catalyzes the condensation of pantoate with beta-alanine in an ATP-dependent reaction via a pantoyl-adenylate intermediate | |
AIIGCJOP_00895 | 3.7e-140 | 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 | |
AIIGCJOP_00896 | 3e-81 | folK | 2.7.6.3, 4.1.2.25 | H | 2-amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase | |
AIIGCJOP_00897 | 1.3e-249 | 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 | |
AIIGCJOP_00898 | 8.8e-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 | ||
AIIGCJOP_00899 | 1.6e-79 | dksA | K | 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 | ||
AIIGCJOP_00900 | 1.7e-117 | sfsA | S | Belongs to the SfsA family | ||
AIIGCJOP_00901 | 3.3e-92 | ligT | 3.1.4.58, 3.5.1.42 | J | Hydrolyzes RNA 2',3'-cyclic phosphodiester to an RNA 2'- phosphomonoester | |
AIIGCJOP_00902 | 0.0 | hrpB | 3.6.4.13 | L | ATP-dependent helicase | |
AIIGCJOP_00903 | 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) |
AIIGCJOP_00904 | 0.0 | fhuA | P | TonB-dependent siderophore receptor | ||
AIIGCJOP_00905 | 6.3e-148 | fhuC | 3.6.3.34 | HP | ABC-type cobalamin Fe3 -siderophores transport systems, ATPase components | |
AIIGCJOP_00906 | 3e-159 | fhuD | P | ABC-type Fe3 -hydroxamate transport system, periplasmic component | ||
AIIGCJOP_00907 | 0.0 | fhuB | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
AIIGCJOP_00908 | 2.8e-238 | hemL | 5.4.3.8 | H | Glutamate-1-semialdehyde aminotransferase | |
AIIGCJOP_00909 | 9.5e-245 | 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 | ||
AIIGCJOP_00910 | 2e-58 | erpA | C | iron--sulfur cluster insertion protein erpA | ||
AIIGCJOP_00911 | 7.7e-109 | yadS | S | membrane | ||
AIIGCJOP_00912 | 1e-118 | 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 | ||
AIIGCJOP_00913 | 6.8e-122 | 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 | |
AIIGCJOP_00914 | 3.1e-281 | dgt | 3.1.5.1 | F | dGTPase preferentially hydrolyzes dGTP over the other canonical NTPs | |
AIIGCJOP_00915 | 9.9e-237 | degP | 1.3.1.74, 3.4.21.107 | M | Belongs to the peptidase S1C family | |
AIIGCJOP_00916 | 5.1e-215 | cdaR | KT | regulator | ||
AIIGCJOP_00917 | 7.7e-67 | yaeH | S | Belongs to the UPF0325 family | ||
AIIGCJOP_00918 | 9.4e-123 | dapD | 2.3.1.117, 2.3.1.89 | E | Belongs to the transferase hexapeptide repeat family | |
AIIGCJOP_00919 | 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 | |
AIIGCJOP_00920 | 1.6e-148 | map | 3.4.11.18 | E | Methionine aminopeptidase | |
AIIGCJOP_00921 | 4.4e-132 | rpsB | J | ribosomal protein | ||
AIIGCJOP_00922 | 1.3e-143 | 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 | ||
AIIGCJOP_00923 | 5.4e-130 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
AIIGCJOP_00924 | 1.2e-76 | 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 | ||
AIIGCJOP_00925 | 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) | |
AIIGCJOP_00926 | 7.3e-138 | 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 | |
AIIGCJOP_00927 | 2.2e-159 | cdsA | 2.7.7.41 | S | Belongs to the CDS family | |
AIIGCJOP_00928 | 1.2e-247 | rseP | 3.4.21.107 | M | zinc metalloprotease | |
AIIGCJOP_00929 | 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 | ||
AIIGCJOP_00930 | 8.3e-74 | skp | M | Belongs to the skp family | ||
AIIGCJOP_00931 | 1.6e-111 | 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 | |
AIIGCJOP_00932 | 4.9e-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 | |
AIIGCJOP_00933 | 3e-94 | |||||
AIIGCJOP_00934 | 3.3e-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 |
AIIGCJOP_00935 | 1.9e-104 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
AIIGCJOP_00936 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase | |
AIIGCJOP_00937 | 1e-176 | 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 | |
AIIGCJOP_00938 | 0.0 | ldcC | 4.1.1.17, 4.1.1.18, 4.1.1.19 | E | decarboxylase | |
AIIGCJOP_00939 | 4.4e-70 | yaeR | E | glyoxalase bleomycin resistance protein dioxygenase | ||
AIIGCJOP_00940 | 1.2e-217 | 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 | |
AIIGCJOP_00941 | 4.1e-40 | rof | K | Suppresses temperature-sensitive mutations in essential genes by modulating rho-dependent transcription termination | ||
AIIGCJOP_00942 | 3.6e-28 | yaeP | S | Belongs to the UPF0253 family | ||
AIIGCJOP_00943 | 1.9e-95 | yaeQ | S | protein conserved in bacteria | ||
AIIGCJOP_00944 | 4.2e-42 | yaeJ | J | chain release factor | ||
AIIGCJOP_00945 | 6.8e-114 | cutF | MP | Copper homeostasis | ||
AIIGCJOP_00946 | 5.2e-105 | yaeF | M | cysteine-type peptidase activity | ||
AIIGCJOP_00947 | 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 | |
AIIGCJOP_00948 | 5.6e-124 | yaeB | P | PFAM Uncharacterised protein family UPF0066 | ||
AIIGCJOP_00949 | 5.8e-65 | rcsF | M | colanic acid biosynthetic process | ||
AIIGCJOP_00950 | 4.6e-146 | metQ | P | Belongs to the NlpA lipoprotein family | ||
AIIGCJOP_00951 | 3.6e-77 | metI | P | ABC-type metal ion transport system permease component | ||
AIIGCJOP_00952 | 1.2e-180 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
AIIGCJOP_00953 | 5.2e-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 | |
AIIGCJOP_00955 | 9.7e-30 | yecF | S | Protein of unknown function (DUF2594) | ||
AIIGCJOP_00956 | 1.4e-117 | sdiA | K | Transcriptional regulator | ||
AIIGCJOP_00957 | 2.5e-130 | yecC | 3.6.3.21 | E | (ABC) transporter | |
AIIGCJOP_00958 | 4.7e-112 | yecS | P | amino acid ABC transporter | ||
AIIGCJOP_00959 | 2.1e-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 | |
AIIGCJOP_00960 | 1.3e-134 | fliY | ET | belongs to the bacterial solute-binding protein 3 family | ||
AIIGCJOP_00961 | 1.1e-95 | fliZ | N | biosynthesis protein FliZ | ||
AIIGCJOP_00962 | 2.7e-126 | fliA | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released. This sigma factor controls the expression of flagella-related genes | ||
AIIGCJOP_00963 | 2.1e-124 | flaA | N | Flagellin is the subunit protein which polymerizes to form the filaments of bacterial flagella | ||
AIIGCJOP_00964 | 1.3e-180 | fliD | N | Required for morphogenesis and for the elongation of the flagellar filament by facilitating polymerization of the flagellin monomers at the tip of growing filament. Forms a capping structure, which prevents flagellin subunits (transported through the central channel of the flagellum) from leaking out without polymerization at the distal end | ||
AIIGCJOP_00965 | 1e-61 | fliS | N | flagellar protein FliS | ||
AIIGCJOP_00966 | 1.3e-44 | fliT | N | Flagellar protein FliT | ||
AIIGCJOP_00967 | 3.1e-289 | amyA | 3.2.1.1 | GH13 | G | Cytoplasmic alpha-amylase |
AIIGCJOP_00968 | 3.7e-67 | yedD | S | (Lipo)protein | ||
AIIGCJOP_00969 | 2.6e-44 | fliE | N | Flagellar hook-basal body complex protein FliE | ||
AIIGCJOP_00970 | 5.9e-273 | fliF | N | The M ring may be actively involved in energy transduction | ||
AIIGCJOP_00971 | 3.2e-173 | fliG | N | FliG is one of three proteins (FliG, FliN, FliM) that forms the rotor-mounted switch complex (C ring), located at the base of the basal body. This complex interacts with the CheY and CheZ chemotaxis proteins, in addition to contacting components of the motor that determine the direction of flagellar rotation | ||
AIIGCJOP_00972 | 3.2e-79 | fliH | N | Flagellar assembly protein | ||
AIIGCJOP_00973 | 2.1e-252 | fliI | 3.6.3.14 | NU | Type III | |
AIIGCJOP_00974 | 2.3e-67 | fliJ | N | Flagellar protein that affects chemotactic events | ||
AIIGCJOP_00975 | 3.7e-144 | fliK | N | Flagellar hook-length control protein | ||
AIIGCJOP_00976 | 7.8e-74 | fliL | N | Controls the rotational direction of flagella during chemotaxis | ||
AIIGCJOP_00977 | 2.3e-187 | fliM | N | FliM is one of three proteins (FliG, FliN, FliM) that forms the rotor-mounted switch complex (C ring), located at the base of the basal body. This complex interacts with the CheY and CheZ chemotaxis proteins, in addition to contacting components of the motor that determine the direction of flagellar rotation | ||
AIIGCJOP_00978 | 8.2e-67 | fliN | N | FliN is one of three proteins (FliG, FliN, FliM) that form the rotor-mounted switch complex (C ring), located at the base of the basal body. This complex interacts with the CheY and CheZ chemotaxis proteins, in addition to contacting components of the motor that determine the direction of flagellar rotation | ||
AIIGCJOP_00979 | 1.5e-51 | fliO | N | flagellar | ||
AIIGCJOP_00980 | 4.6e-121 | fliP | N | Plays a role in the flagellum-specific transport system | ||
AIIGCJOP_00981 | 2.9e-36 | fliQ | N | Flagellar biosynthetic protein FliQ | ||
AIIGCJOP_00982 | 9.3e-112 | fliR | N | Role in flagellar biosynthesis | ||
AIIGCJOP_00983 | 4.6e-106 | rcsA | K | Component of the Rcs signaling system, which controls transcription of numerous genes. Binds to DNA to regulate expression of genes | ||
AIIGCJOP_00984 | 1.7e-27 | dsrB | S | Dextransucrase DSRB | ||
AIIGCJOP_00985 | 1.6e-32 | yodD | S | single-species biofilm formation on inanimate substrate | ||
AIIGCJOP_00986 | 6.9e-134 | yedP | 2.7.1.31, 3.1.3.70 | S | Mannosyl-3-phosphoglycerate phosphatase | |
AIIGCJOP_00987 | 2.3e-229 | yedQ | 2.7.7.65 | T | Protein involved in phosphorus-oxygen lyase activity, regulation of signal transduction, cyclic nucleotide biosynthetic process and intracellular signal transduction | |
AIIGCJOP_00988 | 3.1e-26 | yodC | S | Uncharacterized small protein (DUF2158) | ||
AIIGCJOP_00989 | 5.4e-127 | yedI | S | protein conserved in bacteria | ||
AIIGCJOP_00990 | 7.7e-150 | yedA | EG | of the drug metabolite transporter (DMT) superfamily | ||
AIIGCJOP_00991 | 2e-80 | vsr | L | May nick specific sequences that contain T G mispairs resulting from m5C-deamination | ||
AIIGCJOP_00992 | 7.2e-264 | dcm | 2.1.1.37 | H | Methyl-transferase | |
AIIGCJOP_00993 | 1.9e-108 | yedJ | S | Metal-dependent phosphohydrolase | ||
AIIGCJOP_00994 | 1.4e-30 | yedR | ||||
AIIGCJOP_00995 | 2.6e-181 | M | Gram-negative porin | |||
AIIGCJOP_00996 | 3.3e-273 | dcuS | 2.7.13.3 | T | signal transduction histidine kinase regulating citrate malate metabolism | |
AIIGCJOP_00997 | 6.4e-123 | dcuR | K | Transcriptional Regulatory protein | ||
AIIGCJOP_00999 | 5.3e-147 | mtfA | C | Belongs to the MtfA family | ||
AIIGCJOP_01001 | 2.3e-10 | L | Belongs to the 'phage' integrase family | |||
AIIGCJOP_01002 | 2.3e-12 | L | Belongs to the 'phage' integrase family | |||
AIIGCJOP_01003 | 1.5e-46 | proV | 3.6.3.32 | K | Helix-turn-helix domain | |
AIIGCJOP_01004 | 2.1e-55 | S | Phage derived protein Gp49-like (DUF891) | |||
AIIGCJOP_01005 | 1.5e-24 | nlp | K | transcriptional regulator | ||
AIIGCJOP_01006 | 2.5e-56 | |||||
AIIGCJOP_01007 | 1.1e-104 | T | Nacht domain | |||
AIIGCJOP_01008 | 1.5e-105 | T | Nacht domain | |||
AIIGCJOP_01009 | 0.0 | |||||
AIIGCJOP_01010 | 0.0 | |||||
AIIGCJOP_01011 | 6.1e-155 | |||||
AIIGCJOP_01012 | 8.8e-173 | cbl | K | transcriptional regulator | ||
AIIGCJOP_01013 | 8e-155 | nac | K | transcriptional regulator | ||
AIIGCJOP_01015 | 1.8e-157 | erfK | S | Catalyzes th removal of D-alanine and attachment of the murein lipoprotein to the peptidoglycan tetrapeptide chain | ||
AIIGCJOP_01016 | 5.7e-231 | shiA | EGP | Major facilitator superfamily | ||
AIIGCJOP_01017 | 8.4e-284 | 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 | |
AIIGCJOP_01018 | 0.0 | pepP | 3.4.11.9 | E | xaa-pro aminopeptidase | |
AIIGCJOP_01020 | 6e-258 | yeeO | V | Mate efflux family protein | ||
AIIGCJOP_01022 | 6.7e-51 | yeeX | S | Belongs to the UPF0265 family | ||
AIIGCJOP_01023 | 1e-190 | yeeA | S | Membrane | ||
AIIGCJOP_01024 | 2.7e-82 | 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 | ||
AIIGCJOP_01025 | 1.2e-219 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
AIIGCJOP_01026 | 1.8e-270 | sbcB | 3.1.11.1 | L | Exonucleolytic cleavage in the 3'- to 5'-direction to yield nucleoside 5'-phosphates | |
AIIGCJOP_01027 | 2.2e-249 | yeeF | E | PFAM amino acid permease-associated region | ||
AIIGCJOP_01028 | 2e-161 | yeeY | K | transcriptional regulator | ||
AIIGCJOP_01029 | 9.7e-152 | yeeZ | GM | COG0451 Nucleoside-diphosphate-sugar epimerases | ||
AIIGCJOP_01030 | 1e-162 | 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 | |
AIIGCJOP_01031 | 6.7e-224 | 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 | |
AIIGCJOP_01032 | 2e-189 | hisC | 1.1.1.23, 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
AIIGCJOP_01033 | 2.9e-201 | 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 | |
AIIGCJOP_01034 | 1e-107 | 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 | ||
AIIGCJOP_01035 | 1.7e-131 | hisA | 5.3.1.16 | E | 1-(5-phosphoribosyl)-5- (5-phosphoribosylamino)methylideneamino imidazole-4-carboxamide isomerase | |
AIIGCJOP_01036 | 2e-143 | 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 | |
AIIGCJOP_01037 | 3.4e-109 | 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 | |
AIIGCJOP_01038 | 2.3e-144 | wzzB | M | chain length | ||
AIIGCJOP_01039 | 2.1e-188 | capI | 5.1.3.6 | M | epimerase dehydratase | |
AIIGCJOP_01040 | 2.5e-206 | ugd | 1.1.1.22 | M | Belongs to the UDP-glucose GDP-mannose dehydrogenase family | |
AIIGCJOP_01041 | 5e-265 | 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 | |
AIIGCJOP_01042 | 6e-135 | galE | 5.1.3.2 | M | Polysaccharide biosynthesis protein | |
AIIGCJOP_01043 | 5e-143 | 2.4.1.52 | GT4 | M | to RfpB of Escherichia coli UniRef RepID B3I2Q7_ECOLX | |
AIIGCJOP_01044 | 6.9e-97 | wbpT | GT4 | M | Glycosyl transferase 4-like | |
AIIGCJOP_01045 | 1.1e-46 | cpsO | M | Glycosyltransferase like family 2 | ||
AIIGCJOP_01046 | 3.5e-46 | rgpB | GT2 | M | Glycosyl transferase family 2 | |
AIIGCJOP_01047 | 1.1e-18 | |||||
AIIGCJOP_01048 | 1.9e-111 | rfbE | S | Polysaccharide biosynthesis protein | ||
AIIGCJOP_01049 | 5e-154 | rfbA | 2.7.7.24 | H | Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis | |
AIIGCJOP_01050 | 5.2e-151 | rfbD | 1.1.1.133 | M | Catalyzes the reduction of dTDP-6-deoxy-L-lyxo-4- hexulose to yield dTDP-L-rhamnose | |
AIIGCJOP_01051 | 3.4e-208 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
AIIGCJOP_01052 | 2.1e-160 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
AIIGCJOP_01053 | 2.1e-244 | wcaM | S | Colanic acid biosynthesis protein | ||
AIIGCJOP_01054 | 6.3e-224 | wcaL | GT4 | M | Glycosyl Transferase | |
AIIGCJOP_01055 | 1.3e-240 | wcaK | S | biosynthesis protein | ||
AIIGCJOP_01056 | 6.4e-255 | wzxC | S | Membrane protein involved in the export of O-antigen and teichoic acid | ||
AIIGCJOP_01057 | 6.4e-265 | wcaJ | M | COG2148 Sugar transferases involved in lipopolysaccharide synthesis | ||
AIIGCJOP_01058 | 4.1e-264 | manB | 5.4.2.2, 5.4.2.8 | G | phosphomannomutase | |
AIIGCJOP_01059 | 1.9e-264 | cpsB | 2.7.7.13, 5.3.1.8 | GM | Belongs to the mannose-6-phosphate isomerase type 2 family | |
AIIGCJOP_01060 | 1.4e-215 | wcaI | GT4 | M | glycosyl transferase group 1 | |
AIIGCJOP_01061 | 2.1e-82 | gmm | 3.6.1.55 | F | Belongs to the Nudix hydrolase family | |
AIIGCJOP_01062 | 4.1e-178 | fcl | 1.1.1.271, 4.2.1.47 | GM | Catalyzes the two-step NADP-dependent conversion of GDP- 4-dehydro-6-deoxy-D-mannose to GDP-fucose, involving an epimerase and a reductase reaction | |
AIIGCJOP_01063 | 1.3e-210 | gmd | 4.2.1.47 | M | Catalyzes the conversion of GDP-D-mannose to GDP-4- dehydro-6-deoxy-D-mannose | |
AIIGCJOP_01064 | 5.7e-100 | wcaF | 2.3.1.79 | S | colanic acid biosynthesis acetyltransferase wcaF | |
AIIGCJOP_01065 | 6.5e-131 | wcaE | GT2 | M | Pfam Glycosyl transferase family 2 | |
AIIGCJOP_01066 | 2e-214 | wcaD | S | colanic acid is an exopolysaccharide produced under stress conditions that confers acid and heat tolerance | ||
AIIGCJOP_01067 | 2.3e-226 | wcaC | GT4 | M | Glycosyl Transferase | |
AIIGCJOP_01068 | 1.4e-76 | wcaB | 2.3.1.30 | E | Belongs to the transferase hexapeptide repeat family | |
AIIGCJOP_01069 | 2.7e-152 | wcaA | M | PFAM Glycosyl transferase, family 2 | ||
AIIGCJOP_01070 | 0.0 | wzc | D | protein involved in exopolysaccharide biosynthesis | ||
AIIGCJOP_01071 | 2.5e-77 | wzb | 3.1.3.48 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
AIIGCJOP_01072 | 1.5e-208 | wza | M | polysaccharide export | ||
AIIGCJOP_01073 | 3.5e-283 | yegH | P | membrane protein, terc | ||
AIIGCJOP_01074 | 5.1e-311 | asmA | M | Protein involved in outer membrane biogenesis | ||
AIIGCJOP_01075 | 1.9e-106 | dcd | 3.5.4.13 | F | Belongs to the dCTP deaminase family | |
AIIGCJOP_01076 | 4.3e-115 | udk | 2.7.1.48 | F | Cytidine monophosphokinase | |
AIIGCJOP_01077 | 0.0 | yegE | 2.1.1.80, 2.7.13.3, 2.7.7.65, 3.1.1.61 | T | MASE1 domain protein | |
AIIGCJOP_01078 | 2.9e-154 | alkA | 3.2.2.21 | L | 3-methyladenine DNA glycosylase 8-oxoguanine DNA glycosylase | |
AIIGCJOP_01079 | 6.7e-251 | yegD | O | Belongs to the heat shock protein 70 family | ||
AIIGCJOP_01080 | 2.9e-192 | mdtA | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | ||
AIIGCJOP_01081 | 0.0 | mdtB | V | Belongs to the resistance-nodulation-cell division (RND) (TC 2.A.6) family | ||
AIIGCJOP_01082 | 0.0 | mdtC | V | Belongs to the resistance-nodulation-cell division (RND) (TC 2.A.6) family | ||
AIIGCJOP_01083 | 1.2e-245 | mdtD | EGP | Major facilitator superfamily | ||
AIIGCJOP_01084 | 1.2e-263 | T | PhoQ Sensor | |||
AIIGCJOP_01085 | 3.4e-132 | K | response regulator | |||
AIIGCJOP_01086 | 1.7e-123 | ycgE | K | Transcriptional regulator | ||
AIIGCJOP_01087 | 3.1e-207 | ycgF | T | EAL domain | ||
AIIGCJOP_01088 | 3.8e-32 | ycgZ | S | Two-component-system connector protein YcgZ | ||
AIIGCJOP_01089 | 5.2e-37 | |||||
AIIGCJOP_01090 | 2.7e-31 | ariR | S | Two-component-system connector protein AriR | ||
AIIGCJOP_01091 | 1.1e-258 | yegQ | O | protease | ||
AIIGCJOP_01092 | 8.1e-152 | yegS | 2.7.1.107 | I | the in vivo substrate is | |
AIIGCJOP_01093 | 1.4e-136 | EP | (ABC) transporter | |||
AIIGCJOP_01094 | 4.9e-154 | oppD | EP | (ABC) transporter | ||
AIIGCJOP_01095 | 2.4e-156 | P | Binding-protein-dependent transport systems inner membrane component | |||
AIIGCJOP_01096 | 4.6e-183 | dppB_1 | P | PFAM binding-protein-dependent transport systems inner membrane component | ||
AIIGCJOP_01097 | 6e-307 | E | Extracellular solute-binding protein, family 5 | |||
AIIGCJOP_01098 | 3.1e-228 | M | Belongs to the mandelate racemase muconate lactonizing enzyme family | |||
AIIGCJOP_01099 | 8.7e-198 | fbaB | 4.1.2.13 | G | Catalyzes the formation of glycerone phosphate and D-glyceraldehyde 3-phosphate from D-fructose 1,6-bisphosphate | |
AIIGCJOP_01100 | 2e-138 | thiD | 2.7.1.49, 2.7.4.7 | H | phosphomethylpyrimidine kinase | |
AIIGCJOP_01101 | 2.4e-128 | thiM | 2.7.1.50 | H | Catalyzes the phosphorylation of the hydroxyl group of 4-methyl-5-beta-hydroxyethylthiazole (THZ) | |
AIIGCJOP_01105 | 4.1e-125 | L | Reverse transcriptase (RNA-dependent DNA polymerase) | |||
AIIGCJOP_01106 | 6.3e-65 | L | Resolvase, N terminal domain | |||
AIIGCJOP_01107 | 2.1e-31 | |||||
AIIGCJOP_01108 | 1.6e-13 | |||||
AIIGCJOP_01109 | 1.1e-14 | |||||
AIIGCJOP_01110 | 1.7e-46 | |||||
AIIGCJOP_01111 | 7.6e-264 | NU | Usher protein | |||
AIIGCJOP_01112 | 4.4e-96 | NU | Fimbrial protein | |||
AIIGCJOP_01113 | 4.4e-36 | NU | Fimbrial protein | |||
AIIGCJOP_01114 | 8e-54 | K | LuxR family transcriptional regulator | |||
AIIGCJOP_01115 | 1.7e-45 | K | response regulator | |||
AIIGCJOP_01116 | 1.4e-261 | gor | 1.8.1.7 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
AIIGCJOP_01117 | 7.3e-155 | rlmJ | 2.1.1.266 | S | Specifically methylates the adenine in position 2030 of 23S rRNA | |
AIIGCJOP_01118 | 0.0 | prlC | 3.4.15.5, 3.4.24.70 | E | oligopeptidase | |
AIIGCJOP_01119 | 3.7e-134 | rsmJ | 2.1.1.242 | J | Specifically methylates the guanosine in position 1516 of 16S rRNA | |
AIIGCJOP_01120 | 2.3e-75 | uspA | T | Required for resistance to DNA-damaging agents | ||
AIIGCJOP_01121 | 2.4e-56 | uspB | S | Universal stress protein B | ||
AIIGCJOP_01122 | 2.5e-267 | pitA | P | phosphate transporter | ||
AIIGCJOP_01123 | 2.7e-225 | yhiN | S | HI0933 family | ||
AIIGCJOP_01124 | 9.4e-52 | P | Ion channel | |||
AIIGCJOP_01125 | 6.3e-185 | terC | P | membrane protein, terc | ||
AIIGCJOP_01126 | 1.1e-121 | cicA | 2.3.1.51, 3.1.3.27, 3.1.3.3 | E | Hydrolase | |
AIIGCJOP_01127 | 1.1e-133 | IQ | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
AIIGCJOP_01128 | 2.5e-126 | IV02_08490 | K | LysR substrate binding domain | ||
AIIGCJOP_01129 | 9e-92 | padC | Q | Phenolic acid decarboxylase (PAD) | ||
AIIGCJOP_01130 | 3.4e-95 | sfp | 2.7.8.7 | H | Belongs to the P-Pant transferase superfamily | |
AIIGCJOP_01131 | 5.9e-25 | fabF2 | 2.3.1.179 | H | Belongs to the beta-ketoacyl-ACP synthases family | |
AIIGCJOP_01132 | 4e-182 | yhhT | T | permease | ||
AIIGCJOP_01133 | 8.7e-202 | yhhS | EGP | MFS-type transporter | ||
AIIGCJOP_01134 | 2.6e-92 | dcrB | S | dcrb protein | ||
AIIGCJOP_01135 | 6.9e-116 | yhhQ | U | Involved in the import of queuosine (Q) precursors, required for Q precursor salvage | ||
AIIGCJOP_01136 | 1.4e-37 | tusA | J | 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 | ||
AIIGCJOP_01137 | 1.8e-173 | yiaO | G | Bacterial extracellular solute-binding protein, family 7 | ||
AIIGCJOP_01138 | 4.1e-84 | dctQ | G | Tripartite ATP-independent periplasmic transporter, DctQ | ||
AIIGCJOP_01139 | 2.4e-218 | dctM | G | TRAP-type C4-dicarboxylate transport system, large permease component | ||
AIIGCJOP_01140 | 0.0 | zntA | 3.6.3.3, 3.6.3.5 | P | P-type atpase | |
AIIGCJOP_01141 | 5e-108 | yhhN | S | YhhN family | ||
AIIGCJOP_01142 | 1.2e-21 | yhhM | S | Protein of unknown function (DUF2500) | ||
AIIGCJOP_01143 | 2.3e-44 | yhhL | S | Protein of unknown function (DUF1145) | ||
AIIGCJOP_01144 | 9.1e-107 | rsmD | 2.1.1.171 | L | Specifically methylates the guanine in position 966 of 16S rRNA in the assembled 30S particle | |
AIIGCJOP_01145 | 1.6e-165 | 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 | ||
AIIGCJOP_01146 | 4.2e-121 | ftsE | D | cell division ATP-binding protein FtsE | ||
AIIGCJOP_01147 | 1e-185 | ftsX | D | Part of the ABC transporter FtsEX involved in cellular division | ||
AIIGCJOP_01148 | 1.5e-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 | ||
AIIGCJOP_01149 | 3.9e-201 | livJ | E | With LivFGHM is involved in the high affinity leucine transport | ||
AIIGCJOP_01151 | 6.8e-200 | licB | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
AIIGCJOP_01152 | 3.5e-135 | yvaA | 1.1.1.371 | S | Oxidoreductase family, C-terminal alpha/beta domain | |
AIIGCJOP_01153 | 6.6e-79 | O | peptidase U32 | |||
AIIGCJOP_01154 | 1.3e-64 | K | Transcriptional regulator | |||
AIIGCJOP_01155 | 2.3e-58 | panZ | K | Controls both the activation and catalytic activity of PanD in a coenzyme A (CoA)-dependent fashion | ||
AIIGCJOP_01156 | 5.6e-203 | livK | E | With LivFGHM is involved in the high affinity leucine transport | ||
AIIGCJOP_01157 | 1.8e-146 | livH | P | Belongs to the binding-protein-dependent transport system permease family | ||
AIIGCJOP_01158 | 6.2e-214 | livM | E | Belongs to the binding-protein-dependent transport system permease family | ||
AIIGCJOP_01159 | 4.6e-140 | livG | E | Part of the ABC transporter complexes LivFGHMJ and LivFGHMK involved in the high-affinity transport of branched-chain amino acids | ||
AIIGCJOP_01160 | 1.2e-126 | livF | P | Branched-chain amino acid transport | ||
AIIGCJOP_01161 | 8.7e-31 | D | Antitoxin component of a toxin-antitoxin (TA) module | |||
AIIGCJOP_01162 | 4.4e-56 | doc | S | Death ON curing protein | ||
AIIGCJOP_01163 | 7.7e-252 | ugpB | G | Bacterial extracellular solute-binding protein | ||
AIIGCJOP_01164 | 3.3e-158 | ugpA | P | With UgpEC is involved in the uptake of glycerol-3-phosphate | ||
AIIGCJOP_01165 | 3.9e-148 | ugpE | P | probably responsible for the translocation of the substrate across the membrane | ||
AIIGCJOP_01166 | 1.1e-200 | ugpC | 3.6.3.20 | P | Part of the ABC transporter complex UgpABCE involved in sn-glycerol-3-phosphate import. Responsible for energy coupling to the transport system | |
AIIGCJOP_01167 | 1.4e-133 | ugpQ | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
AIIGCJOP_01168 | 7.7e-19 | yhhA | S | Protein of unknown function (DUF2756) | ||
AIIGCJOP_01169 | 0.0 | ggt | 2.3.2.2, 3.4.19.13 | M | Gamma-glutamyltransferase | |
AIIGCJOP_01170 | 1.2e-72 | speG_2 | K | PFAM GCN5-related N-acetyltransferase | ||
AIIGCJOP_01171 | 1.5e-54 | M | COG1664 Integral membrane protein CcmA involved in cell shape determination | |||
AIIGCJOP_01172 | 1.5e-194 | yhhX | 1.1.1.371 | S | oxidoreductase | |
AIIGCJOP_01173 | 1.6e-131 | yhhW | S | Belongs to the pirin family | ||
AIIGCJOP_01174 | 2e-183 | gntR | K | Periplasmic binding protein LacI transcriptional regulator | ||
AIIGCJOP_01175 | 1.1e-92 | gntK | 2.7.1.12 | F | Gluconokinase | |
AIIGCJOP_01176 | 1.3e-230 | gntU | EG | Gluconate | ||
AIIGCJOP_01177 | 7.1e-96 | yhgN | U | UPF0056 membrane protein | ||
AIIGCJOP_01178 | 4.7e-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 | |
AIIGCJOP_01179 | 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 |
AIIGCJOP_01180 | 0.0 | glgX | 3.2.1.196, 3.2.1.68 | CBM48,GH13 | G | Belongs to the glycosyl hydrolase 13 family |
AIIGCJOP_01181 | 6.2e-246 | glgC | 2.7.7.27 | H | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
AIIGCJOP_01182 | 1.6e-271 | glgA | 2.4.1.21 | GT5 | G | Synthesizes alpha-1,4-glucan chains using ADP-glucose |
AIIGCJOP_01183 | 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 |
AIIGCJOP_01184 | 2.9e-287 | glpD | 1.1.5.3 | C | Belongs to the FAD-dependent glycerol-3-phosphate dehydrogenase family | |
AIIGCJOP_01185 | 8e-57 | glpE | 2.8.1.1 | P | Catalyzes, although with low efficiency, the sulfur transfer reaction from thiosulfate to cyanide | |
AIIGCJOP_01186 | 2.2e-151 | glpG | S | Rhomboid-type serine protease that catalyzes intramembrane proteolysis | ||
AIIGCJOP_01187 | 7.6e-135 | glpR | K | transcriptional regulator | ||
AIIGCJOP_01188 | 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' | ||
AIIGCJOP_01189 | 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 |
AIIGCJOP_01190 | 0.0 | malQ | 2.4.1.25 | GH77 | G | 4-alpha-glucanotransferase |
AIIGCJOP_01191 | 3.5e-220 | gntT | EG | Gluconate | ||
AIIGCJOP_01192 | 1.8e-104 | 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 | ||
AIIGCJOP_01193 | 6.9e-103 | comF | S | Competence protein | ||
AIIGCJOP_01194 | 5.9e-127 | 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 | |
AIIGCJOP_01195 | 4.4e-37 | yahO | S | Protein of unknown function (DUF1471) | ||
AIIGCJOP_01196 | 2.6e-33 | feoC | K | metal cluster binding | ||
AIIGCJOP_01197 | 0.0 | feoB | P | Transporter of a GTP-driven Fe(2 ) uptake system | ||
AIIGCJOP_01198 | 2.8e-32 | feoA | P | FeoA domain | ||
AIIGCJOP_01199 | 0.0 | yhgF | K | accessory protein | ||
AIIGCJOP_01200 | 1.4e-83 | 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 | ||
AIIGCJOP_01201 | 5.7e-132 | K | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
AIIGCJOP_01202 | 1.4e-248 | T | PhoQ Sensor | |||
AIIGCJOP_01203 | 2.2e-311 | 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 | |
AIIGCJOP_01204 | 9e-164 | 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 | ||
AIIGCJOP_01205 | 1.8e-66 | hslR | J | Belongs to the HSP15 family | ||
AIIGCJOP_01206 | 1.2e-126 | yrfG | 3.1.3.5 | S | TIGRFAM HAD-superfamily hydrolase, subfamily IA, variant 3 | |
AIIGCJOP_01207 | 0.0 | yrfF | S | Intracellular growth attenuator | ||
AIIGCJOP_01208 | 1.9e-98 | nudE | L | Hydrolase | ||
AIIGCJOP_01209 | 0.0 | mrcA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
AIIGCJOP_01210 | 1.1e-125 | hofM | NU | Pilus assembly protein | ||
AIIGCJOP_01211 | 7e-58 | hofN | NU | carbon utilization | ||
AIIGCJOP_01212 | 1.3e-49 | hofO | S | carbon utilization | ||
AIIGCJOP_01213 | 1.1e-188 | pilQ | U | (Type IV) pilus | ||
AIIGCJOP_01214 | 3.3e-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 | |
AIIGCJOP_01215 | 2e-197 | 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) | |
AIIGCJOP_01216 | 8.3e-110 | damX | D | Cell division protein DamX | ||
AIIGCJOP_01217 | 2.8e-143 | dam | 2.1.1.72 | H | Site-specific DNA-methyltransferase (adenine-specific) | |
AIIGCJOP_01218 | 5.9e-123 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
AIIGCJOP_01219 | 1.2e-132 | gph | 3.1.3.18 | G | Phosphoglycolate phosphatase | |
AIIGCJOP_01220 | 3.9e-187 | trpS | 6.1.1.2 | J | Tryptophanyl-tRNA synthetase | |
AIIGCJOP_01221 | 1.6e-24 | yhfL | S | Protein of unknown function (DUF4223) | ||
AIIGCJOP_01222 | 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 | |
AIIGCJOP_01223 | 1.9e-147 | nirC | P | nitrite transporter | ||
AIIGCJOP_01224 | 1.8e-56 | nirD | 1.7.1.15 | P | Nitrite reductase | |
AIIGCJOP_01225 | 0.0 | nirB | 1.7.1.15 | C | Belongs to the nitrite and sulfite reductase 4Fe-4S domain family | |
AIIGCJOP_01226 | 1e-248 | codA | 3.5.4.1 | F | cytosine deaminase | |
AIIGCJOP_01227 | 6.6e-210 | tsgA | G | Protein tsgA homolog | ||
AIIGCJOP_01228 | 1.3e-94 | 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 | |
AIIGCJOP_01229 | 1.4e-107 | fic | D | cell filamentation protein Fic | ||
AIIGCJOP_01230 | 3.4e-100 | pabA | 2.4.2.18, 2.6.1.85, 4.1.3.27 | EH | anthranilate synthase | |
AIIGCJOP_01231 | 1.5e-230 | argD | 2.6.1.11, 2.6.1.17, 2.6.1.81 | E | aminotransferase | |
AIIGCJOP_01232 | 0.0 | yhfK | S | integral membrane protein, YccS YhfK family | ||
AIIGCJOP_01233 | 1.9e-115 | crp | K | COG0664 cAMP-binding proteins - catabolite gene activator and regulatory subunit of cAMP-dependent protein kinases | ||
AIIGCJOP_01234 | 2.1e-67 | yhfA | O | Redox protein regulator of disulfide bond formation | ||
AIIGCJOP_01235 | 8e-165 | prkB | 2.7.1.19 | G | Phosphoribulokinase | |
AIIGCJOP_01236 | 2.4e-33 | yheU | S | Belongs to the UPF0270 family | ||
AIIGCJOP_01237 | 3.3e-178 | yheT | S | PFAM Alpha beta hydrolase | ||
AIIGCJOP_01238 | 0.0 | mdcA | 2.3.1.187 | I | Malonate decarboxylase | |
AIIGCJOP_01239 | 8.3e-146 | 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 | |
AIIGCJOP_01240 | 1.4e-44 | 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 | ||
AIIGCJOP_01241 | 5.4e-150 | mdcD | 4.1.1.87 | I | Beta subunit | |
AIIGCJOP_01242 | 5.4e-139 | mdcE | 4.1.1.87 | I | Malonate decarboxylase gamma subunit | |
AIIGCJOP_01243 | 3e-160 | mdcF | S | auxin efflux carrier | ||
AIIGCJOP_01244 | 1e-89 | mdcG | 2.7.7.66 | H | Phosphoribosyl-dephospho-CoA transferase MdcG | |
AIIGCJOP_01245 | 3e-146 | mdcH | 2.3.1.39 | I | malonyl CoA-acyl carrier protein transacylase | |
AIIGCJOP_01246 | 3.5e-166 | mdcR | K | transcriptional regulator | ||
AIIGCJOP_01247 | 0.0 | yheS | S | ABC transporter | ||
AIIGCJOP_01248 | 7.5e-100 | kefG | S | Regulatory subunit of a potassium efflux system that confers protection against electrophiles. Required for full activity of KefB | ||
AIIGCJOP_01249 | 2.6e-306 | kefB | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
AIIGCJOP_01250 | 1.6e-31 | yheV | S | Probable metal-binding protein (DUF2387) | ||
AIIGCJOP_01251 | 5e-78 | slyD | 5.2.1.8 | G | Peptidyl-prolyl cis-trans | |
AIIGCJOP_01252 | 8.9e-28 | slyX | S | Belongs to the SlyX family | ||
AIIGCJOP_01253 | 1.6e-130 | fkpA | 5.2.1.8 | M | Peptidyl-prolyl cis-trans | |
AIIGCJOP_01254 | 1.8e-130 | yheO | S | protein conserved in bacteria | ||
AIIGCJOP_01255 | 1.4e-63 | 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 | ||
AIIGCJOP_01256 | 4.8e-47 | tusC | J | Part of a sulfur-relay system required for 2-thiolation of 5-methylaminomethyl-2-thiouridine (mnm(5)s(2)U) at tRNA wobble positions | ||
AIIGCJOP_01257 | 3.6e-37 | tusB | J | Part of a sulfur-relay system required for 2-thiolation of 5-methylaminomethyl-2-thiouridine (mnm(5)s(2)U) at tRNA wobble positions | ||
AIIGCJOP_01258 | 1.6e-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 | ||
AIIGCJOP_01259 | 6.2e-79 | 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 | ||
AIIGCJOP_01260 | 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 | ||
AIIGCJOP_01261 | 3e-92 | L | HTH-like domain | |||
AIIGCJOP_01262 | 0.0 | V | COG2274 ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | |||
AIIGCJOP_01263 | 2.2e-150 | M | Secretion Protein | |||
AIIGCJOP_01264 | 9.7e-167 | kamA | 5.4.3.2 | C | 4Fe-4S single cluster domain | |
AIIGCJOP_01265 | 7.5e-103 | 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 | ||
AIIGCJOP_01266 | 2.8e-08 | ecnA | S | Entericidin EcnA/B family | ||
AIIGCJOP_01267 | 1.9e-13 | ecnB | S | Entericidin | ||
AIIGCJOP_01268 | 1.1e-93 | ecnR | K | regulatory protein | ||
AIIGCJOP_01269 | 1.8e-45 | sugE | U | multidrug resistance protein | ||
AIIGCJOP_01270 | 3.3e-84 | blc | M | Outer Membrane Lipoprotein | ||
AIIGCJOP_01271 | 1.7e-60 | frdD | C | Seems to be involved in the anchoring of the catalytic components of the fumarate reductase complex to the cytoplasmic membrane | ||
AIIGCJOP_01272 | 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 | ||
AIIGCJOP_01273 | 8.1e-142 | frdB | 1.3.5.1, 1.3.5.4 | C | Belongs to the succinate dehydrogenase fumarate reductase iron-sulfur protein family | |
AIIGCJOP_01274 | 0.0 | frdA | 1.3.5.1, 1.3.5.4 | C | Belongs to the FAD-dependent oxidoreductase 2 family. FRD SDH subfamily | |
AIIGCJOP_01275 | 3e-184 | 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 | ||
AIIGCJOP_01276 | 0.0 | yjeP | M | mechanosensitive ion channel | ||
AIIGCJOP_01277 | 6.4e-179 | psd | 4.1.1.65 | I | Catalyzes the formation of phosphatidylethanolamine (PtdEtn) from phosphatidylserine (PtdSer) | |
AIIGCJOP_01278 | 4.6e-194 | 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 | |
AIIGCJOP_01279 | 9.7e-100 | orn | L | 3'-to-5' exoribonuclease specific for small oligoribonucleotides | ||
AIIGCJOP_01283 | 5.3e-217 | 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) | |
AIIGCJOP_01284 | 1.1e-222 | 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 | |
AIIGCJOP_01285 | 4e-78 | yjeE | S | ATPase or kinase | ||
AIIGCJOP_01286 | 6e-228 | amiB | 3.5.1.28 | M | N-acetylmuramoyl-L-alanine amidase | |
AIIGCJOP_01287 | 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 | ||
AIIGCJOP_01288 | 7.2e-167 | 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) | |
AIIGCJOP_01289 | 3.1e-34 | 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 | ||
AIIGCJOP_01290 | 2.4e-234 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
AIIGCJOP_01291 | 1.4e-165 | hflK | O | HflC and HflK could encode or regulate a protease | ||
AIIGCJOP_01292 | 7.9e-140 | hflC | O | HflC and HflK could regulate a protease | ||
AIIGCJOP_01293 | 5.1e-251 | 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 | |
AIIGCJOP_01294 | 1.3e-70 | nsrR | K | Nitric oxide-sensitive repressor of genes involved in protecting the cell against nitrosative stress. May require iron for activity | ||
AIIGCJOP_01295 | 0.0 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
AIIGCJOP_01296 | 1.3e-131 | rlmB | 2.1.1.185, 2.1.1.34 | J | Specifically methylates the ribose of guanosine 2251 in 23S rRNA | |
AIIGCJOP_01297 | 6.9e-221 | EGP | Major facilitator superfamily | |||
AIIGCJOP_01298 | 3.5e-307 | aidB | I | acyl-CoA dehydrogenase | ||
AIIGCJOP_01299 | 1.2e-64 | NT | Single cache domain 3 | |||
AIIGCJOP_01300 | 1.9e-223 | NT | chemotaxis, protein | |||
AIIGCJOP_01301 | 4.8e-39 | yjfN | S | Protein of unknown function (DUF1471) | ||
AIIGCJOP_01302 | 2.2e-18 | bsmA | CO | response to hydrogen peroxide | ||
AIIGCJOP_01303 | 4.3e-127 | yjfP | S | esterase activity towards palmitoyl-CoA and pNP-butyrate in vitro | ||
AIIGCJOP_01304 | 3.2e-133 | ulaR | K | transcriptional regulator | ||
AIIGCJOP_01305 | 1.1e-216 | 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 | ||
AIIGCJOP_01306 | 1.3e-254 | ulaA | 2.7.1.194 | S | PTS system sugar-specific permease component | |
AIIGCJOP_01307 | 2e-49 | ulaB | 2.7.1.194 | 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 | |
AIIGCJOP_01308 | 2.8e-79 | ulaC | 2.7.1.194, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
AIIGCJOP_01309 | 7.5e-115 | ulaD | 4.1.1.85, 4.1.2.43 | G | Orotidine 5'-phosphate decarboxylase / HUMPS family | |
AIIGCJOP_01310 | 2.6e-155 | ulaE | 5.1.3.22 | G | Xylose isomerase-like TIM barrel | |
AIIGCJOP_01311 | 1.3e-125 | ulaF | 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 | |
AIIGCJOP_01312 | 2e-40 | yjfY | S | Protein of unknown function (DUF1471) | ||
AIIGCJOP_01313 | 7.9e-67 | rpsF | 4.3.1.19 | J | Binds together with S18 to 16S ribosomal RNA | |
AIIGCJOP_01314 | 3.9e-53 | priB | L | Binds single-stranded DNA at the primosome assembly site (PAS) | ||
AIIGCJOP_01315 | 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 | ||
AIIGCJOP_01316 | 1.2e-71 | rplI | J | binds to the 23S rRNA | ||
AIIGCJOP_01317 | 3.9e-165 | CP_1064 | EG | transporter | ||
AIIGCJOP_01318 | 7.4e-107 | ytfB | M | Opacity-associated protein A | ||
AIIGCJOP_01319 | 3.8e-108 | fklB | 5.2.1.8 | O | Peptidyl-prolyl cis-trans | |
AIIGCJOP_01320 | 1.1e-253 | cycA | E | amino acid | ||
AIIGCJOP_01321 | 4.3e-118 | ytfE | D | Di-iron-containing protein involved in the repair of iron-sulfur clusters | ||
AIIGCJOP_01322 | 4.5e-148 | tar | NT | Methyl-accepting chemotaxis-like domains (chemotaxis sensory transducer). | ||
AIIGCJOP_01323 | 7.8e-169 | ytfF | EG | Permeases of the drug metabolite transporter (DMT) superfamily | ||
AIIGCJOP_01324 | 7.6e-157 | K | transcriptional regulator | |||
AIIGCJOP_01325 | 3e-140 | ytfG | 1.6.5.2 | GM | NmrA family | |
AIIGCJOP_01326 | 1.1e-62 | ytfH | K | transcriptional regulator | ||
AIIGCJOP_01327 | 0.0 | cpdB | 3.1.3.5, 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
AIIGCJOP_01328 | 7.4e-135 | cysQ | 3.1.3.7 | P | 3'(2'),5'-bisphosphate nucleotidase | |
AIIGCJOP_01329 | 1.1e-90 | ytfJ | S | transcriptional regulator | ||
AIIGCJOP_01330 | 5.2e-30 | ytfK | S | Protein of unknown function (DUF1107) | ||
AIIGCJOP_01331 | 5.5e-221 | ytfL | P | Hemolysins and related proteins containing CBS domains | ||
AIIGCJOP_01332 | 8.7e-116 | msrA | 1.8.4.11 | C | 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 | |
AIIGCJOP_01333 | 0.0 | ytfM | M | COG0729 Outer membrane protein | ||
AIIGCJOP_01334 | 0.0 | ytfN | M | protein conserved in bacteria | ||
AIIGCJOP_01335 | 1.1e-59 | ytfP | S | AIG2 family | ||
AIIGCJOP_01336 | 1.5e-97 | ppa | 3.6.1.1 | C | Catalyzes the hydrolysis of inorganic pyrophosphate (PPi) forming two phosphate ions | |
AIIGCJOP_01337 | 1.8e-165 | ytfQ | G | Periplasmic binding protein domain | ||
AIIGCJOP_01338 | 6.9e-273 | ytfR | 3.6.3.17 | P | import. Responsible for energy coupling to the transport system | |
AIIGCJOP_01339 | 1e-171 | ytfT | G | Belongs to the binding-protein-dependent transport system permease family | ||
AIIGCJOP_01340 | 6.6e-171 | yjfF | P | Belongs to the binding-protein-dependent transport system permease family | ||
AIIGCJOP_01341 | 4.4e-169 | tar | NT | chemotaxis, protein | ||
AIIGCJOP_01342 | 5.5e-32 | K | Bacterial regulatory helix-turn-helix protein, lysR family | |||
AIIGCJOP_01343 | 7e-189 | fbp | 3.1.3.11 | G | D-fructose-1,6-bisphosphate 1-phosphohydrolase class 1 | |
AIIGCJOP_01344 | 1.2e-263 | 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 | |
AIIGCJOP_01345 | 6.4e-91 | yjgA | S | Belongs to the UPF0307 family | ||
AIIGCJOP_01346 | 2.1e-244 | pmbA | S | Protease involved in proteolytic processing of the antibiotic Microcin B17 and in sensitivity to the DNA gyrase inhibitor LetD | ||
AIIGCJOP_01347 | 3e-55 | cybC | C | Cytochrome b(562) | ||
AIIGCJOP_01349 | 7.2e-53 | S | PRD domain protein | |||
AIIGCJOP_01350 | 2.6e-61 | S | Glycine-rich SFCGS | |||
AIIGCJOP_01351 | 7.6e-46 | S | Domain of unknown function (DUF4312) | |||
AIIGCJOP_01352 | 1.4e-139 | S | Domain of unknown function (DUF4311) | |||
AIIGCJOP_01353 | 6.5e-103 | S | Membrane | |||
AIIGCJOP_01354 | 1.6e-205 | dho | 3.5.2.3 | S | Catalyzes the reversible hydrolysis of the amide bond within dihydroorotate. This metabolic intermediate is required for the biosynthesis of pyrimidine nucleotides | |
AIIGCJOP_01355 | 2.9e-199 | selA | 2.9.1.1 | E | PFAM aromatic amino acid beta-eliminating lyase threonine aldolase | |
AIIGCJOP_01356 | 1.9e-130 | 4.1.2.14 | S | 2-dehydro-3-deoxyphosphooctonate aldolase | ||
AIIGCJOP_01357 | 7.5e-179 | ykgB | 3.1.1.31 | G | COG2706 3-carboxymuconate cyclase | |
AIIGCJOP_01358 | 0.0 | licR | 2.7.1.197 | GK | transcriptional antiterminator | |
AIIGCJOP_01359 | 4.1e-34 | relB | L | RelB antitoxin | ||
AIIGCJOP_01360 | 2.7e-37 | relE | DJ | ParE toxin of type II toxin-antitoxin system, parDE | ||
AIIGCJOP_01361 | 1.4e-86 | 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 | |
AIIGCJOP_01362 | 0.0 | nrdD | 1.1.98.6 | F | Ribonucleoside-triphosphate reductase | |
AIIGCJOP_01363 | 0.0 | treC | 3.2.1.93 | GH13 | G | COG0366 Glycosidases |
AIIGCJOP_01364 | 1.6e-258 | treB | 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | pts system | |
AIIGCJOP_01365 | 4.4e-164 | treR | K | trehalose | ||
AIIGCJOP_01366 | 0.0 | mgtA | 3.6.3.2 | P | ATPase, P-type (transporting), HAD superfamily, subfamily IC | |
AIIGCJOP_01367 | 0.0 | nahA | 3.2.1.52 | GH20 | G | PFAM Glycoside hydrolase, family 20 |
AIIGCJOP_01368 | 7.9e-258 | gbpA | AA10,CBM73 | E | Probably interacts with GlcNAc residues. May promote attachment to both epithelial cell surfaces and chitin | |
AIIGCJOP_01369 | 9.7e-62 | ridA | 3.5.99.10 | J | PFAM Endoribonuclease L-PSP | |
AIIGCJOP_01370 | 2.2e-81 | pyrI | 2.1.3.2 | F | Involved in allosteric regulation of aspartate carbamoyltransferase | |
AIIGCJOP_01371 | 2.2e-168 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
AIIGCJOP_01372 | 1.6e-76 | tabA | G | Toxin-antitoxin biofilm protein TabA | ||
AIIGCJOP_01373 | 1e-154 | yagE | 4.1.2.28, 4.1.3.3, 4.3.3.7 | EM | Belongs to the DapA family | |
AIIGCJOP_01374 | 0.0 | yagF | 4.2.1.82 | EG | Belongs to the IlvD Edd family | |
AIIGCJOP_01375 | 8.9e-251 | yagG | G | COG2211 Na melibiose symporter and related transporters | ||
AIIGCJOP_01376 | 0.0 | xynB | 3.2.1.37 | GH43 | G | Belongs to the glycosyl hydrolase 43 family |
AIIGCJOP_01377 | 3e-131 | yagI | K | transcriptional regulator | ||
AIIGCJOP_01378 | 1.2e-21 | iraM | S | Inhibits RpoS proteolysis by regulating RssB activity, thereby increasing the stability of the sigma stress factor RpoS during magnesium starvation | ||
AIIGCJOP_01379 | 6.6e-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 | |
AIIGCJOP_01380 | 2.7e-65 | 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 | ||
AIIGCJOP_01381 | 9.6e-138 | miaE | FJ | tRNA-(MS[2]IO[6]A)-hydroxylase (MiaE) | ||
AIIGCJOP_01382 | 1.1e-101 | |||||
AIIGCJOP_01384 | 1.5e-180 | metAS | 2.3.1.46 | E | Transfers a succinyl group from succinyl-CoA to L- homoserine, forming succinyl-L-homoserine | |
AIIGCJOP_01385 | 1.2e-307 | 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 | |
AIIGCJOP_01386 | 1e-243 | aceA | 4.1.3.1 | C | Isocitrate lyase | |
AIIGCJOP_01387 | 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 | |
AIIGCJOP_01388 | 1.9e-147 | iclR | K | transcriptional regulator | ||
AIIGCJOP_01389 | 0.0 | metH | 2.1.1.13 | E | methionine synthase | |
AIIGCJOP_01390 | 1.7e-277 | yjbB | P | Na Pi-Cotransporter | ||
AIIGCJOP_01391 | 1.6e-42 | K | Phage derived protein Gp49-like (DUF891) | |||
AIIGCJOP_01392 | 1.4e-35 | K | conserved small protein | |||
AIIGCJOP_01393 | 1.1e-158 | rluF | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
AIIGCJOP_01394 | 2.1e-39 | yjbD | S | YjbD family (DUF3811) | ||
AIIGCJOP_01395 | 2.6e-148 | yocS | S | Bile acid sodium symporter | ||
AIIGCJOP_01396 | 1.6e-231 | rtcR | K | regulates genes involved in forming a 2',3'-cyclic phosphodiester on RNA | ||
AIIGCJOP_01397 | 2.2e-27 | rtcR | K | regulates genes involved in forming a 2',3'-cyclic phosphodiester on RNA | ||
AIIGCJOP_01398 | 3.1e-231 | rtcB | 6.5.1.3 | S | Belongs to the RtcB family | |
AIIGCJOP_01399 | 2.5e-234 | lysC | 1.1.1.3, 2.7.2.4, 4.1.1.20 | E | Belongs to the aspartokinase family | |
AIIGCJOP_01400 | 0.0 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
AIIGCJOP_01401 | 8.4e-64 | psiE | S | Protein PsiE homolog | ||
AIIGCJOP_01402 | 1.4e-159 | malG | P | transport | ||
AIIGCJOP_01403 | 8.6e-287 | malF | P | transport | ||
AIIGCJOP_01404 | 5e-226 | malE | G | Functions in the MalKFGE ABC transporter complex to transport maltose into the cell by using ATP hydrolysis | ||
AIIGCJOP_01405 | 2.4e-206 | malK | P | Belongs to the ABC transporter superfamily | ||
AIIGCJOP_01406 | 5e-251 | lamB | M | involved in the transport of maltose and maltodextrins | ||
AIIGCJOP_01407 | 4.8e-142 | malM | S | maltose operon periplasmic | ||
AIIGCJOP_01408 | 2.8e-85 | 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 | |
AIIGCJOP_01409 | 2.1e-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 | |
AIIGCJOP_01410 | 0.0 | plsB | 2.3.1.15 | I | Belongs to the GPAT DAPAT family | |
AIIGCJOP_01411 | 1.6e-58 | dgkA | 2.7.1.107 | M | Recycling of diacylglycerol produced during the turnover of membrane phospholipid | |
AIIGCJOP_01412 | 1.1e-107 | lexA | 3.4.21.88 | K | Represses a number of genes involved in the response to DNA damage (SOS response), including recA and lexA. 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 | |
AIIGCJOP_01413 | 2.3e-219 | dinF | V | COG0534 Na -driven multidrug efflux pump | ||
AIIGCJOP_01414 | 3.1e-33 | yjbJ | S | Belongs to the UPF0337 (CsbD) family | ||
AIIGCJOP_01415 | 4.3e-89 | zur | P | belongs to the Fur family | ||
AIIGCJOP_01416 | 6e-93 | manC | S | Cupin domain | ||
AIIGCJOP_01417 | 6.8e-192 | traF | S | transfer protein | ||
AIIGCJOP_01418 | 3.5e-188 | 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 | ||
AIIGCJOP_01419 | 2.3e-29 | pspG | S | Phage Shock Protein G | ||
AIIGCJOP_01420 | 8.5e-179 | qor | 1.6.5.5 | C | COG0604 NADPH quinone reductase and related Zn-dependent oxidoreductases | |
AIIGCJOP_01421 | 3.6e-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 | |
AIIGCJOP_01422 | 1.1e-198 | alr | 5.1.1.1 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
AIIGCJOP_01424 | 5.6e-225 | tyrB | 2.6.1.1, 2.6.1.57 | E | aminotransferase | |
AIIGCJOP_01425 | 5.3e-74 | yjbQ | S | Secondary thiamine-phosphate synthase enzyme | ||
AIIGCJOP_01426 | 5.4e-59 | yjbR | S | protein conserved in bacteria | ||
AIIGCJOP_01427 | 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 | ||
AIIGCJOP_01428 | 1.6e-59 | 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 | ||
AIIGCJOP_01429 | 2.8e-42 | yjcB | S | membrane | ||
AIIGCJOP_01430 | 4.1e-219 | T | Diguanylate cyclase | |||
AIIGCJOP_01431 | 4.4e-270 | yjcC | 3.1.4.52 | T | signal transduction protein containing sensor and EAL | |
AIIGCJOP_01432 | 1.4e-53 | soxS | K | transcriptional regulator | ||
AIIGCJOP_01433 | 1.8e-78 | soxR | K | redox-sensitive transcriptional activator SoxR | ||
AIIGCJOP_01434 | 9.4e-113 | gstA | 2.5.1.18 | O | Belongs to the GST superfamily | |
AIIGCJOP_01435 | 6.1e-228 | yjcD | S | permease | ||
AIIGCJOP_01436 | 2.2e-288 | yjcE | P | NhaP-type Na H and K H antiporters | ||
AIIGCJOP_01437 | 1.8e-164 | ywbI | K | transcriptional regulator | ||
AIIGCJOP_01438 | 4.5e-65 | cidA | S | LrgA family | ||
AIIGCJOP_01439 | 1.3e-117 | ywbG | M | effector of murein hydrolase | ||
AIIGCJOP_01440 | 5.9e-233 | G | ABC transporter substrate-binding protein | |||
AIIGCJOP_01441 | 1.4e-242 | yteT | S | oxidoreductase | ||
AIIGCJOP_01442 | 8.5e-290 | 3.2.1.139 | G | Belongs to the glycosyl hydrolase 67 family | ||
AIIGCJOP_01443 | 7.3e-292 | actP | P | Cation acetate symporter ActP | ||
AIIGCJOP_01444 | 4.5e-49 | yjcH | S | Protein of unknown function, DUF485 | ||
AIIGCJOP_01445 | 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 | |
AIIGCJOP_01446 | 1.3e-227 | gltP | U | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
AIIGCJOP_01447 | 5.2e-79 | yjcO | S | Sel1 repeat | ||
AIIGCJOP_01448 | 4.7e-311 | fdhF | 1.17.1.10, 1.17.1.9, 1.17.99.7 | C | Belongs to the prokaryotic molybdopterin-containing oxidoreductase family | |
AIIGCJOP_01449 | 1.3e-67 | fdhF | 1.17.1.10, 1.17.1.9, 1.17.99.7 | C | Belongs to the prokaryotic molybdopterin-containing oxidoreductase family | |
AIIGCJOP_01450 | 4.2e-122 | K | response regulator | |||
AIIGCJOP_01451 | 1.1e-178 | 2.7.1.15, 2.7.1.4 | G | PfkB domain protein | ||
AIIGCJOP_01452 | 2.7e-152 | 4.1.2.13 | G | Aldolase | ||
AIIGCJOP_01453 | 7.3e-129 | 5.3.1.15 | S | D-lyxose isomerase | ||
AIIGCJOP_01454 | 1.3e-165 | rbsB | G | PFAM Periplasmic binding protein LacI transcriptional regulator | ||
AIIGCJOP_01455 | 5.8e-167 | MA20_14255 | U | Belongs to the binding-protein-dependent transport system permease family | ||
AIIGCJOP_01456 | 1e-276 | rbsA | 3.6.3.17 | P | import. Responsible for energy coupling to the transport system | |
AIIGCJOP_01457 | 0.0 | virA | T | Histidine kinase | ||
AIIGCJOP_01458 | 5e-100 | |||||
AIIGCJOP_01459 | 1.6e-09 | |||||
AIIGCJOP_01460 | 8.9e-144 | phnP | 3.1.4.55 | S | Carbon-phosphorus lyase complex accessory protein | |
AIIGCJOP_01461 | 1.6e-73 | phnO | K | Escherichia coli uses a different mechanism of phosphonate catabolism where PhnO is not essential and seems to play a regulatory role | ||
AIIGCJOP_01462 | 2.7e-89 | phnN | 2.7.4.23 | F | Catalyzes the phosphorylation of ribose 1,5-bisphosphate to 5-phospho-D-ribosyl alpha-1-diphosphate (PRPP) | |
AIIGCJOP_01463 | 1.5e-203 | phnM | 3.6.1.63 | P | phosphonate metabolism protein PhnM | |
AIIGCJOP_01464 | 1.5e-121 | phnL | 2.7.8.37 | P | phosphonate C-P lyase system protein PhnL | |
AIIGCJOP_01465 | 1.5e-135 | phnK | 4.7.1.1 | P | Phosphonate C-P lyase | |
AIIGCJOP_01466 | 5.8e-160 | 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 | |
AIIGCJOP_01467 | 5e-185 | phnI | 2.7.8.37 | P | Phosphonate | |
AIIGCJOP_01468 | 4.7e-100 | phnH | 2.7.8.37 | P | phosphonate C-P lyase system protein PhnH | |
AIIGCJOP_01469 | 1.2e-71 | phnG | 2.7.8.37 | P | Phosphonate C-P lyase system protein PhnG | |
AIIGCJOP_01470 | 8.3e-131 | phnF | K | Transcriptional regulator | ||
AIIGCJOP_01471 | 2.8e-140 | phnE | 3.6.1.63 | P | Phosphonate ABC transporter | |
AIIGCJOP_01472 | 7.9e-180 | phnD | P | Phosphonate ABC transporter | ||
AIIGCJOP_01473 | 2.6e-138 | 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 | |
AIIGCJOP_01474 | 2.8e-57 | phnA | P | Alkylphosphonate utilization operon protein PhnA | ||
AIIGCJOP_01475 | 0.0 | yjdA | S | chromosome segregation | ||
AIIGCJOP_01476 | 3.1e-148 | yjcZ | S | YjcZ-like protein | ||
AIIGCJOP_01477 | 2.1e-148 | kdgT | 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 | ||
AIIGCJOP_01478 | 3.4e-272 | proP | EGP | transporter | ||
AIIGCJOP_01479 | 7.3e-224 | wcaJ | M | COG2148 Sugar transferases involved in lipopolysaccharide synthesis | ||
AIIGCJOP_01480 | 1.2e-244 | S | Putative beta-barrel porin 2 | |||
AIIGCJOP_01481 | 9e-93 | M | COG1596 Periplasmic protein involved in polysaccharide export | |||
AIIGCJOP_01482 | 1.7e-293 | ywqD | 2.7.10.1, 2.7.10.2 | D | protein involved in exopolysaccharide biosynthesis | |
AIIGCJOP_01483 | 2.6e-198 | wzx | S | polysaccharide biosynthetic process | ||
AIIGCJOP_01484 | 9.9e-218 | |||||
AIIGCJOP_01485 | 8.9e-176 | M | PFAM Glycosyl transferase family 2 | |||
AIIGCJOP_01486 | 5.1e-210 | M | glycosyl transferase group 1 | |||
AIIGCJOP_01487 | 5.6e-195 | M | PFAM Glycosyl transferase, group 1 | |||
AIIGCJOP_01488 | 7.1e-63 | |||||
AIIGCJOP_01489 | 9.5e-156 | 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 | |
AIIGCJOP_01490 | 1.5e-245 | G | Domain of unknown function (DUF4832) | |||
AIIGCJOP_01491 | 4.3e-147 | murI | 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
AIIGCJOP_01492 | 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 | ||
AIIGCJOP_01493 | 4.1e-206 | 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) | |
AIIGCJOP_01494 | 2.7e-58 | yijD | S | membrane | ||
AIIGCJOP_01495 | 1.5e-107 | 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 | ||
AIIGCJOP_01496 | 2.1e-271 | 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 | |
AIIGCJOP_01497 | 2.8e-168 | oxyR | K | Transcriptional regulator | ||
AIIGCJOP_01498 | 1e-254 | argH | 2.3.1.1, 4.3.2.1 | E | argininosuccinate lyase | |
AIIGCJOP_01499 | 1.5e-138 | argB | 2.3.1.1, 2.7.2.8 | E | Catalyzes the ATP-dependent phosphorylation of N-acetyl- L-glutamate | |
AIIGCJOP_01500 | 9.2e-189 | 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 | |
AIIGCJOP_01501 | 2e-227 | argE | 3.5.1.16 | E | Belongs to the peptidase M20A family. ArgE subfamily | |
AIIGCJOP_01502 | 0.0 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
AIIGCJOP_01503 | 1.8e-99 | yijO | K | Transcriptional regulator | ||
AIIGCJOP_01504 | 1.1e-102 | tal | 2.2.1.2 | H | Catalyzes the reversible formation of fructose 6- phosphate from dihydroxyacetone and D-glyceraldehyde 3-phosphate via an aldolization reaction | |
AIIGCJOP_01505 | 1.8e-198 | gldA | 1.1.1.6 | C | glycerol dehydrogenase | |
AIIGCJOP_01506 | 0.0 | katG | 1.11.1.21 | P | Bifunctional enzyme with both catalase and broad- spectrum peroxidase activity | |
AIIGCJOP_01507 | 2.2e-170 | metF | 1.5.1.20 | E | Methylenetetrahydrofolate reductase | |
AIIGCJOP_01508 | 0.0 | metL | 1.1.1.3, 2.7.2.4 | E | belongs to the aspartokinase family | |
AIIGCJOP_01509 | 2.9e-218 | metB | 2.5.1.48, 4.4.1.8 | E | Catalyzes the formation of L-homocysteine from O- succinyl-L-homoserine (OSHS) and hydrogen sulfide | |
AIIGCJOP_01510 | 1e-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 | ||
AIIGCJOP_01511 | 1.9e-35 | rpmE | J | Binds the 23S rRNA | ||
AIIGCJOP_01512 | 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 | ||
AIIGCJOP_01513 | 7.1e-175 | cytR | K | transcriptional | ||
AIIGCJOP_01514 | 8.2e-101 | 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 | ||
AIIGCJOP_01515 | 5.5e-92 | hslV | 3.4.25.2 | O | Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery | |
AIIGCJOP_01516 | 3e-243 | 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 | ||
AIIGCJOP_01517 | 1.6e-158 | menA | 2.5.1.74 | H | Belongs to the MenA family. Type 1 subfamily | |
AIIGCJOP_01518 | 3.2e-86 | 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 | ||
AIIGCJOP_01520 | 6.5e-32 | 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 | |
AIIGCJOP_01521 | 2.2e-146 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
AIIGCJOP_01522 | 4.9e-295 | 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 | |
AIIGCJOP_01523 | 2.1e-180 | glpX | 2.2.1.1, 3.1.3.11, 3.1.3.37 | G | Fructose-1,6-bisphosphatase | |
AIIGCJOP_01524 | 5.4e-117 | fpr | 1.18.1.2, 1.19.1.1 | C | COG1018 Flavodoxin reductases (ferredoxin-NADPH reductases) family 1 | |
AIIGCJOP_01525 | 3.3e-71 | yiiR | S | Membrane | ||
AIIGCJOP_01526 | 1.2e-82 | yiiQ | S | Protein of unknown function (DUF1454) | ||
AIIGCJOP_01527 | 9e-136 | tpiA | 5.3.1.1 | G | Involved in the gluconeogenesis. Catalyzes stereospecifically the conversion of dihydroxyacetone phosphate (DHAP) to D-glyceraldehyde-3-phosphate (G3P) | |
AIIGCJOP_01528 | 6.3e-230 | P | Citrate transporter | |||
AIIGCJOP_01529 | 6.6e-123 | cdh | 3.6.1.26 | I | CDP-diacylglycerol pyrophosphatase | |
AIIGCJOP_01530 | 5.2e-184 | sbp | P | sulfate ABC transporter | ||
AIIGCJOP_01531 | 1.8e-181 | 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 | |
AIIGCJOP_01532 | 4.8e-160 | fieF | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
AIIGCJOP_01533 | 1.8e-76 | cpxP | NPTU | Repressor of the Cpx envelope stress response pathway which occurs via periplasmic interactions with CpxA | ||
AIIGCJOP_01534 | 1.1e-124 | K | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
AIIGCJOP_01535 | 6.4e-249 | T | PhoQ Sensor | |||
AIIGCJOP_01536 | 6.9e-119 | yiiM | S | MOSC domain containing protein | ||
AIIGCJOP_01537 | 3.8e-116 | sodA | 1.15.1.1 | C | Destroys radicals which are normally produced within the cells and which are toxic to biological systems | |
AIIGCJOP_01538 | 1.5e-152 | rhaR | K | Activates expression of the rhaSR operon in response to L-rhamnose | ||
AIIGCJOP_01539 | 4.1e-158 | rhaS | K | Activates expression of the rhaBAD and rhaT operons | ||
AIIGCJOP_01540 | 1.7e-271 | 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 | |
AIIGCJOP_01541 | 5.8e-241 | rhaA | 2.7.1.5, 5.3.1.14 | G | L-rhamnose isomerase | |
AIIGCJOP_01542 | 1.3e-156 | rhaD | 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 | |
AIIGCJOP_01543 | 5.3e-173 | rhaS | G | (ABC) transporter | ||
AIIGCJOP_01544 | 1.9e-275 | rbsA | 3.6.3.17 | P | import. Responsible for energy coupling to the transport system | |
AIIGCJOP_01545 | 1.5e-170 | rhaP | U | Belongs to the binding-protein-dependent transport system permease family | ||
AIIGCJOP_01546 | 2.4e-165 | rhaQ | U | Belongs to the binding-protein-dependent transport system permease family | ||
AIIGCJOP_01547 | 2.2e-202 | fucO | 1.1.1.1 | C | alcohol dehydrogenase | |
AIIGCJOP_01548 | 2.3e-53 | rhaM | 5.1.3.32 | G | Involved in the anomeric conversion of L-rhamnose | |
AIIGCJOP_01549 | 8.6e-232 | lacY | G | Major facilitator superfamily | ||
AIIGCJOP_01550 | 0.0 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
AIIGCJOP_01551 | 2.9e-174 | aglR | K | PFAM Periplasmic binding protein LacI transcriptional regulator | ||
AIIGCJOP_01552 | 2.3e-93 | sinR | K | Transcriptional regulator | ||
AIIGCJOP_01553 | 2.7e-112 | azlC | E | branched-chain amino acid | ||
AIIGCJOP_01554 | 3.8e-43 | S | Branched-chain amino acid transport protein (AzlD) | |||
AIIGCJOP_01555 | 1.4e-25 | S | Protein of unknown function (DUF1471) | |||
AIIGCJOP_01556 | 3e-132 | 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 | ||
AIIGCJOP_01557 | 8e-108 | fdoG | 1.17.1.9, 1.17.5.3 | C | PFAM Molybdopterin oxidoreductase Fe4S4 region | |
AIIGCJOP_01558 | 0.0 | fdoG | 1.17.1.9, 1.17.5.3 | C | Belongs to the prokaryotic molybdopterin-containing oxidoreductase family | |
AIIGCJOP_01559 | 5.8e-182 | fdoH | C | TIGRFAM formate dehydrogenase, beta subunit | ||
AIIGCJOP_01560 | 1.7e-116 | fdoI | C | formate dehydrogenase | ||
AIIGCJOP_01561 | 2e-174 | fdhE | O | Necessary for formate dehydrogenase activity | ||
AIIGCJOP_01562 | 2.8e-07 | pagC | M | Membrane | ||
AIIGCJOP_01563 | 3.2e-186 | yiiD | K | Putative thioesterase (yiiD_Cterm) | ||
AIIGCJOP_01564 | 1.9e-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 | ||
AIIGCJOP_01565 | 1.4e-120 | rbn | K | UPF0761 membrane protein | ||
AIIGCJOP_01566 | 3.8e-105 | yihX | 3.1.3.10 | S | TIGRFAM HAD-superfamily hydrolase, subfamily IA, variant 3 | |
AIIGCJOP_01567 | 9.1e-139 | yihW | K | Transcriptional regulator | ||
AIIGCJOP_01568 | 2.5e-153 | yihV | 2.7.1.15, 2.7.1.184 | G | Phosphorylates 6-deoxy-6-sulfo-D-fructose (SF) to 6- deoxy-6-sulfo-D-fructose 1-phosphate (SFP) | |
AIIGCJOP_01569 | 1.4e-156 | yihU | 1.1.1.373, 1.1.1.411, 1.1.1.61 | C | Reduces 3-sulfolactaldehyde (SLA) to 2,3- dihydroxypropane 1-sulfonate (DHPS) | |
AIIGCJOP_01570 | 1.5e-155 | lacD | 4.1.2.40, 4.1.2.57 | G | Cleaves 6-deoxy-6-sulfo-D-fructose 1-phosphate (SFP) to form dihydroxyacetone phosphate (DHAP) and 3-sulfolactaldehyde (SLA) | |
AIIGCJOP_01571 | 4.1e-255 | yihS | 5.1.3.11, 5.3.1.31 | G | Catalyzes the isomerization of sulfoquinovose (SQ) to 6- deoxy-6-sulfo-D-fructose (SF) | |
AIIGCJOP_01572 | 0.0 | yihQ | 3.2.1.177, 3.2.1.199 | GH31 | G | Belongs to the glycosyl hydrolase 31 family |
AIIGCJOP_01573 | 2.7e-263 | yihP | G | transporter | ||
AIIGCJOP_01574 | 2.8e-263 | yihO | G | transporter | ||
AIIGCJOP_01575 | 9.3e-100 | lptD | M | Outer membrane channel protein that allows an efficient diffusion of low-molecular-weight solutes such as small sugars and tetraglycine. However, the specific substrate recognized by the OmpL channel is | ||
AIIGCJOP_01576 | 0.0 | typA | T | GTP-binding protein | ||
AIIGCJOP_01577 | 1.8e-275 | glnA | 5.4.4.3, 6.3.1.2 | E | glutamine synthetase | |
AIIGCJOP_01578 | 7.6e-194 | glnL | 2.7.13.3 | T | Signal transduction histidine kinase, nitrogen specific | |
AIIGCJOP_01579 | 8.8e-270 | glnG | T | COG2204 Response regulator containing CheY-like receiver, AAA-type ATPase, and DNA-binding domains | ||
AIIGCJOP_01580 | 2.8e-260 | hemN | 1.3.98.3 | H | Belongs to the anaerobic coproporphyrinogen-III oxidase family | |
AIIGCJOP_01581 | 2.7e-43 | yihI | S | A GTPase-activating protein (GAP) that modifies Der EngA GTPase function. May play a role in ribosome biogenesis | ||
AIIGCJOP_01582 | 9.4e-107 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
AIIGCJOP_01583 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
AIIGCJOP_01584 | 2.5e-153 | yihG | I | Acyltransferase | ||
AIIGCJOP_01585 | 1.3e-111 | dsbA | O | Thiol disulfide interchange protein | ||
AIIGCJOP_01586 | 8.8e-184 | 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 | ||
AIIGCJOP_01587 | 1.7e-41 | yihD | S | protein conserved in bacteria | ||
AIIGCJOP_01588 | 6.1e-76 | 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 | |
AIIGCJOP_01589 | 7.9e-72 | mobB | 2.10.1.1, 2.7.7.77 | H | molybdopterin-guanine dinucleotide biosynthesis protein | |
AIIGCJOP_01590 | 3.5e-37 | IQ | Phosphopantetheine attachment site | |||
AIIGCJOP_01591 | 3.6e-80 | fabZ | 4.2.1.59 | I | FabA-like domain | |
AIIGCJOP_01592 | 8.7e-107 | IQ | 3-oxoacyl- acyl-carrier-protein reductase | |||
AIIGCJOP_01593 | 7.6e-40 | acpS | 2.7.8.7, 4.2.1.136 | I | Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein | |
AIIGCJOP_01594 | 6.6e-205 | U | hemolysin activation secretion protein | |||
AIIGCJOP_01595 | 7e-176 | U | haemagglutination activity domain | |||
AIIGCJOP_01596 | 3.5e-125 | S | alpha beta | |||
AIIGCJOP_01597 | 0.0 | S | TIGRFAM outer membrane autotransporter barrel | |||
AIIGCJOP_01598 | 3.6e-165 | yghU | O | Belongs to the GST superfamily | ||
AIIGCJOP_01600 | 3.9e-176 | T | Diguanylate cyclase | |||
AIIGCJOP_01601 | 1.6e-126 | fucR | K | transcriptional regulator | ||
AIIGCJOP_01602 | 7.5e-198 | tar | NT | chemotaxis, protein | ||
AIIGCJOP_01603 | 0.0 | S | Autotransporter beta-domain | |||
AIIGCJOP_01604 | 1.1e-161 | yghX | 3.1.1.45 | Q | dienelactone hydrolase | |
AIIGCJOP_01605 | 1e-198 | yghZ | C | reductase | ||
AIIGCJOP_01606 | 1.2e-80 | yqhA | S | UPF0114 protein | ||
AIIGCJOP_01607 | 8.1e-85 | |||||
AIIGCJOP_01608 | 6.1e-67 | |||||
AIIGCJOP_01609 | 5.7e-66 | |||||
AIIGCJOP_01610 | 3.7e-157 | IQ | Dehydrogenases with different specificities (Related to short-chain alcohol dehydrogenases) | |||
AIIGCJOP_01611 | 6.9e-61 | exbD | U | Biopolymer transport protein, ExbD | ||
AIIGCJOP_01612 | 2.1e-118 | exbB | U | tonB-system energizer ExbB | ||
AIIGCJOP_01613 | 7e-220 | metC | 2.5.1.48, 4.4.1.11, 4.4.1.8 | E | cystathionine beta-lyase | |
AIIGCJOP_01614 | 8.9e-116 | yghB | S | Pfam SNARE associated Golgi protein | ||
AIIGCJOP_01615 | 3.3e-153 | yqhC | K | transcriptional regulator | ||
AIIGCJOP_01616 | 5.4e-217 | yqhD | C | alcohol dehydrogenase | ||
AIIGCJOP_01617 | 5e-156 | dkgA | 1.1.1.346 | S | reductase | |
AIIGCJOP_01618 | 0.0 | ygiQ | C | UPF0313 protein | ||
AIIGCJOP_01619 | 1.4e-238 | trkH | P | Low-affinity potassium transport system. Interacts with Trk system potassium uptake protein TrkA | ||
AIIGCJOP_01620 | 2e-269 | 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 | ||
AIIGCJOP_01621 | 1.9e-127 | plsC | 2.3.1.51, 3.1.3.3 | I | Belongs to the 1-acyl-sn-glycerol-3-phosphate acyltransferase family | |
AIIGCJOP_01622 | 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 | |
AIIGCJOP_01623 | 2e-62 | ygiW | S | PFAM conserved | ||
AIIGCJOP_01624 | 1e-111 | K | response regulator | |||
AIIGCJOP_01625 | 1.7e-209 | qseC | 2.7.13.3 | T | Integral membrane sensor signal transduction histidine kinase | |
AIIGCJOP_01626 | 3.4e-111 | mdaB | S | modulator of drug activity B | ||
AIIGCJOP_01627 | 8.8e-53 | ygiN | S | monooxygenase | ||
AIIGCJOP_01628 | 2.3e-75 | ygaU | S | peptidoglycan-binding protein | ||
AIIGCJOP_01629 | 9.4e-92 | |||||
AIIGCJOP_01630 | 4e-231 | ugl | 3.2.1.180 | GH88 | S | Hydrolase |
AIIGCJOP_01631 | 6.9e-226 | lacY | P | Major facilitator superfamily | ||
AIIGCJOP_01632 | 0.0 | S | protein conserved in bacteria | |||
AIIGCJOP_01633 | 2.3e-156 | K | AraC family transcriptional regulator | |||
AIIGCJOP_01634 | 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 | |
AIIGCJOP_01635 | 3.9e-107 | yqiA | S | esterase | ||
AIIGCJOP_01636 | 1.6e-154 | 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 | |
AIIGCJOP_01637 | 1.2e-76 | yqiB | S | Protein of unknown function (DUF1249) | ||
AIIGCJOP_01638 | 2.7e-109 | nudF | 3.6.1.13 | L | COG0494 NTP pyrophosphohydrolases including oxidative damage repair enzymes | |
AIIGCJOP_01639 | 1.5e-213 | tolC | MU | type I secretion outer membrane protein, TolC | ||
AIIGCJOP_01640 | 6.3e-101 | ygiB | S | Belongs to the UPF0441 family | ||
AIIGCJOP_01641 | 1e-223 | ygiC | E | Glutathionylspermidine synthase | ||
AIIGCJOP_01642 | 2.8e-148 | ygiD | 1.13.11.8 | C | PFAM Extradiol ring-cleavage dioxygenase, class III | |
AIIGCJOP_01643 | 1.1e-117 | zupT | P | Mediates zinc uptake. May also transport other divalent cations | ||
AIIGCJOP_01644 | 5.9e-112 | 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 | |
AIIGCJOP_01645 | 7.3e-41 | yqiC | S | protein conserved in bacteria | ||
AIIGCJOP_01646 | 3.9e-265 | 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 | |
AIIGCJOP_01647 | 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 | |
AIIGCJOP_01648 | 8.8e-224 | ygiF | 3.6.1.25 | S | Adenylate cyclase | |
AIIGCJOP_01649 | 1.3e-107 | ygiM | T | sh3 domain protein | ||
AIIGCJOP_01650 | 1.6e-230 | 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 | |
AIIGCJOP_01651 | 9.6e-144 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
AIIGCJOP_01652 | 5.3e-57 | 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 | |
AIIGCJOP_01653 | 9.9e-109 | 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 | |
AIIGCJOP_01654 | 4.2e-147 | ureD | O | Required for maturation of urease via the functional incorporation of the urease nickel metallocenter | ||
AIIGCJOP_01655 | 2e-46 | ureA | 3.5.1.5 | E | Belongs to the urease gamma subunit family | |
AIIGCJOP_01656 | 1.1e-47 | ureB | 3.5.1.5 | E | Belongs to the urease beta subunit family | |
AIIGCJOP_01657 | 0.0 | ureC | 3.5.1.5 | E | Belongs to the metallo-dependent hydrolases superfamily. Urease alpha subunit family | |
AIIGCJOP_01658 | 4.9e-68 | ureE | O | Involved in urease metallocenter assembly. Binds nickel. Probably functions as a nickel donor during metallocenter assembly | ||
AIIGCJOP_01659 | 4.6e-86 | ureJ | O | urease accessory protein | ||
AIIGCJOP_01660 | 3.8e-114 | ureF | O | Required for maturation of urease via the functional incorporation of the urease nickel metallocenter | ||
AIIGCJOP_01661 | 8.1e-111 | ureG | H | Facilitates the functional incorporation of the urease nickel metallocenter. This process requires GTP hydrolysis, probably effectuated by UreG | ||
AIIGCJOP_01662 | 7.4e-233 | chiA | 3.2.1.14, 3.2.1.17 | AA10,CBM15,CBM73,GH18 | O | Subtilase family |
AIIGCJOP_01663 | 1.3e-66 | K | helix_turn_helix, Lux Regulon | |||
AIIGCJOP_01664 | 8.7e-187 | 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 | |
AIIGCJOP_01665 | 1.6e-29 | rpsU | J | Belongs to the bacterial ribosomal protein bS21 family | ||
AIIGCJOP_01666 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
AIIGCJOP_01667 | 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 | ||
AIIGCJOP_01668 | 2.9e-90 | 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 | |
AIIGCJOP_01671 | 1.1e-40 | K | DNA-templated transcription, initiation | |||
AIIGCJOP_01673 | 1.4e-67 | S | Putative inner membrane protein (DUF1819) | |||
AIIGCJOP_01674 | 5.7e-85 | S | Domain of unknown function (DUF1788) | |||
AIIGCJOP_01675 | 0.0 | L | DNA recombination | |||
AIIGCJOP_01676 | 0.0 | V | COG1002 Type II restriction enzyme, methylase subunits | |||
AIIGCJOP_01677 | 7.3e-102 | S | AAA domain, putative AbiEii toxin, Type IV TA system | |||
AIIGCJOP_01678 | 4.2e-37 | |||||
AIIGCJOP_01679 | 0.0 | S | PglZ domain | |||
AIIGCJOP_01680 | 0.0 | 3.4.21.53 | O | ATP-dependent Lon-type protease | ||
AIIGCJOP_01683 | 3.5e-146 | hdfR | K | Negatively regulates the transcription of the flagellar master operon flhDC by binding to the upstream region of the operon | ||
AIIGCJOP_01684 | 5.4e-48 | yifE | S | Protein of unknown function, DUF | ||
AIIGCJOP_01685 | 8.3e-258 | comM | O | ATPase with chaperone activity | ||
AIIGCJOP_01686 | 1.3e-309 | ilvG | 2.2.1.6 | H | acetolactate synthase | |
AIIGCJOP_01687 | 4.7e-39 | ilvM | 2.2.1.6 | S | acetolactate synthase | |
AIIGCJOP_01688 | 3.4e-177 | ilvE | 2.6.1.21, 2.6.1.42 | E | Belongs to the class-IV pyridoxal-phosphate-dependent aminotransferase family | |
AIIGCJOP_01689 | 0.0 | ilvD | 4.2.1.9 | H | Belongs to the IlvD Edd family | |
AIIGCJOP_01690 | 8.9e-292 | 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 | |
AIIGCJOP_01691 | 3.7e-165 | ilvY | K | transcriptional regulator | ||
AIIGCJOP_01692 | 2e-280 | 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 | |
AIIGCJOP_01693 | 4.9e-47 | ppiC | 5.2.1.8 | O | PPIC-type PPIASE domain | |
AIIGCJOP_01694 | 6.7e-44 | ppiC | 5.2.1.8 | G | PPIC-type PPIASE domain | |
AIIGCJOP_01695 | 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 | |
AIIGCJOP_01696 | 6.4e-263 | 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 | |
AIIGCJOP_01697 | 1.1e-239 | rhlB | 3.6.4.13 | JKL | DEAD-box RNA helicase involved in RNA degradation. Has RNA-dependent ATPase activity and unwinds double-stranded RNA | |
AIIGCJOP_01698 | 4.7e-57 | trxA | O | Belongs to the thioredoxin family | ||
AIIGCJOP_01699 | 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 | ||
AIIGCJOP_01700 | 5.8e-184 | 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) | |
AIIGCJOP_01701 | 5.4e-192 | wzzE | M | Modulates the polysaccharide chain length of enterobacterial common antigen (ECA) | ||
AIIGCJOP_01702 | 1.5e-200 | 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 | |
AIIGCJOP_01703 | 4.8e-235 | wecC | 1.1.1.336 | M | Belongs to the UDP-glucose GDP-mannose dehydrogenase family | |
AIIGCJOP_01704 | 2.3e-111 | 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) | |
AIIGCJOP_01705 | 1.2e-200 | 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 | |
AIIGCJOP_01706 | 1.5e-217 | 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) | ||
AIIGCJOP_01707 | 7.8e-202 | rffT | 2.4.1.325 | GT56 | CG | Catalyzes the synthesis of Und-PP-GlcNAc-ManNAcA-Fuc4NAc (Lipid III), the third lipid-linked intermediate involved in ECA synthesis |
AIIGCJOP_01708 | 2.1e-244 | wzyE | S | Probably involved in the polymerization of enterobacterial common antigen (ECA) trisaccharide repeat units | ||
AIIGCJOP_01709 | 7.9e-129 | 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 |
AIIGCJOP_01710 | 1.6e-247 | yifK | E | 'involved in the transport across the cytoplasmic membrane of D-alanine, D-serine and glycine' | ||
AIIGCJOP_01714 | 1.7e-07 | |||||
AIIGCJOP_01715 | 9.4e-180 | S | Protein involved in biological_process | |||
AIIGCJOP_01716 | 4.7e-216 | hemY | H | enzyme of heme biosynthesis | ||
AIIGCJOP_01717 | 2.1e-160 | hemX | 2.1.1.107, 4.2.1.75 | H | HemX, putative uroporphyrinogen-III C-methyltransferase | |
AIIGCJOP_01718 | 1.9e-122 | hemD | 2.1.1.107, 2.5.1.61, 4.2.1.75 | H | Uroporphyrinogen-III synthase | |
AIIGCJOP_01719 | 1.5e-144 | 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 | |
AIIGCJOP_01720 | 0.0 | cyaA | 4.6.1.1 | F | Adenylate cyclase | |
AIIGCJOP_01721 | 6.6e-56 | cyaY | 1.16.3.1 | P | Belongs to the frataxin family | |
AIIGCJOP_01722 | 7e-27 | yifL | N | Prokaryotic lipoprotein-attachment site | ||
AIIGCJOP_01723 | 8.5e-156 | 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 | |
AIIGCJOP_01724 | 9e-122 | yigA | S | protein conserved in bacteria | ||
AIIGCJOP_01725 | 1.3e-165 | xerC | D | Belongs to the 'phage' integrase family. XerC subfamily | ||
AIIGCJOP_01726 | 2.7e-126 | yigB | 3.1.3.10, 3.1.3.102, 3.1.3.104 | S | Hydrolase | |
AIIGCJOP_01727 | 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 | |
AIIGCJOP_01728 | 6.1e-174 | corA | P | Mediates influx of magnesium ions | ||
AIIGCJOP_01729 | 2.6e-158 | rarD | S | TIGRFAM RarD protein | ||
AIIGCJOP_01730 | 1.6e-79 | yigI | Q | Thioesterase-like superfamily | ||
AIIGCJOP_01731 | 8e-157 | pldA | 3.1.1.32, 3.1.1.4 | M | Phospholipase | |
AIIGCJOP_01732 | 0.0 | recQ | 3.6.4.12 | L | DNA helicase | |
AIIGCJOP_01733 | 7.9e-106 | rhtC | E | threonine efflux protein | ||
AIIGCJOP_01734 | 8.7e-105 | rhtB | E | efflux protein | ||
AIIGCJOP_01735 | 4.7e-193 | pldB | 3.1.1.5 | I | PFAM Alpha beta hydrolase | |
AIIGCJOP_01736 | 1.9e-152 | yigL | S | Hydrolase | ||
AIIGCJOP_01737 | 4.6e-163 | yigM | EG | COG0697 Permeases of the drug metabolite transporter (DMT) superfamily | ||
AIIGCJOP_01738 | 8.5e-176 | metR | K | transcriptional regulator | ||
AIIGCJOP_01739 | 0.0 | metE | 2.1.1.14 | E | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | |
AIIGCJOP_01740 | 4.1e-32 | |||||
AIIGCJOP_01741 | 2.5e-35 | S | Protein of unknown function (DUF2778) | |||
AIIGCJOP_01742 | 4.6e-52 | S | Type VI secretion system effector | |||
AIIGCJOP_01743 | 1.2e-148 | ysgA | 3.1.1.45 | Q | Dienelactone hydrolase | |
AIIGCJOP_01744 | 2e-135 | 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 | |
AIIGCJOP_01745 | 1.9e-219 | rmuC | V | DNA Recombination protein RmuC | ||
AIIGCJOP_01746 | 7e-141 | 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) | |
AIIGCJOP_01747 | 2.9e-105 | yigP | S | protein conserved in bacteria | ||
AIIGCJOP_01748 | 0.0 | ubiB | S | Is probably a protein kinase regulator of UbiI activity which is involved in aerobic coenzyme Q (ubiquinone) biosynthesis | ||
AIIGCJOP_01749 | 7.4e-34 | 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 | ||
AIIGCJOP_01750 | 4.4e-65 | 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 | ||
AIIGCJOP_01751 | 1e-123 | 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 | ||
AIIGCJOP_01752 | 5.6e-141 | 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 | ||
AIIGCJOP_01753 | 4.7e-85 | 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 | ||
AIIGCJOP_01754 | 2.7e-293 | 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 | |
AIIGCJOP_01755 | 4.4e-129 | fre | 1.16.1.3, 1.17.1.1, 1.5.1.41 | C | COG0543 2-polyprenylphenol hydroxylase and related flavodoxin oxidoreductases | |
AIIGCJOP_01756 | 2.7e-216 | 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 | |
AIIGCJOP_01757 | 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 | |
AIIGCJOP_01758 | 8.3e-262 | pepQ | 3.4.11.9, 3.4.13.9 | E | Splits dipeptides with a prolyl residue in the C- terminal position | |
AIIGCJOP_01759 | 3e-105 | yigZ | 2.1.1.45, 3.4.13.9 | S | YigZ family | |
AIIGCJOP_01760 | 1.2e-269 | trkH | P | Low-affinity potassium transport system. Interacts with trk system potassium uptake protein TrkA | ||
AIIGCJOP_01761 | 4.2e-95 | hemG | 1.3.5.3 | CH | Protoporphyrinogen oxidase | |
AIIGCJOP_01762 | 1.8e-187 | murB | 1.3.1.98 | M | cell wall formation | |
AIIGCJOP_01763 | 1.6e-169 | 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 | |
AIIGCJOP_01764 | 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 | ||
AIIGCJOP_01765 | 2.7e-225 | dctA | U | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
AIIGCJOP_01766 | 6.8e-262 | yhjJ | S | Peptidase, M16 | ||
AIIGCJOP_01767 | 1.5e-161 | kdgK | 2.7.1.45 | G | COG0524 Sugar kinases, ribokinase family | |
AIIGCJOP_01768 | 1.2e-135 | yhjH | 3.1.4.52 | T | In Escherichia coli this protein is involved in flagellar function | |
AIIGCJOP_01769 | 0.0 | yhjG | M | protein involved in outer membrane biogenesis | ||
AIIGCJOP_01770 | 5.9e-236 | yhjE | EGP | Major facilitator superfamily | ||
AIIGCJOP_01771 | 6.7e-182 | yhjD | S | Membrane | ||
AIIGCJOP_01772 | 1.5e-161 | yhjC | K | transcriptional regulator | ||
AIIGCJOP_01773 | 1e-123 | IQ | short-chain dehydrogenase | |||
AIIGCJOP_01774 | 1.6e-91 | J | Acetyltransferases, including N-acetylases of ribosomal proteins | |||
AIIGCJOP_01775 | 6e-259 | |||||
AIIGCJOP_01776 | 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 |
AIIGCJOP_01777 | 4.1e-08 | S | Domain of unknown function (DUF4762) | |||
AIIGCJOP_01778 | 1.1e-68 | dsbA_1 | O | Thiol disulfide interchange protein | ||
AIIGCJOP_01779 | 5.1e-96 | htrB | 2.3.1.241 | M | (ABC) transporter | |
AIIGCJOP_01780 | 2.2e-272 | lagD | V | COG2274 ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
AIIGCJOP_01781 | 1.6e-118 | macA | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | ||
AIIGCJOP_01782 | 1.4e-278 | 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 | ||
AIIGCJOP_01783 | 3e-145 | cusC | MU | outer_NodT efflux transporter, outer membrane factor (OMF) lipo, NodT family protein | ||
AIIGCJOP_01784 | 8.6e-192 | fabF_1 | 2.3.1.179 | IQ | Belongs to the beta-ketoacyl-ACP synthases family | |
AIIGCJOP_01785 | 1.3e-52 | I | MaoC like domain | |||
AIIGCJOP_01786 | 2.6e-23 | IQ | acyl carrier protein | |||
AIIGCJOP_01787 | 4.5e-84 | IQ | 3-oxoacyl- acyl-carrier protein reductase | |||
AIIGCJOP_01788 | 1.9e-09 | |||||
AIIGCJOP_01789 | 6.1e-52 | |||||
AIIGCJOP_01790 | 1.6e-77 | cre | L | Phage integrase family | ||
AIIGCJOP_01793 | 2.7e-168 | 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 | |||
AIIGCJOP_01795 | 1.4e-33 | yegD | O | StbA protein | ||
AIIGCJOP_01799 | 4.9e-42 | K | Helix-turn-helix XRE-family like proteins | |||
AIIGCJOP_01800 | 1.9e-27 | DJ | Addiction module toxin, RelE StbE family | |||
AIIGCJOP_01802 | 6.5e-20 | |||||
AIIGCJOP_01808 | 3e-31 | S | VRR-NUC domain | |||
AIIGCJOP_01809 | 4.6e-28 | |||||
AIIGCJOP_01810 | 3.1e-18 | |||||
AIIGCJOP_01811 | 1.3e-43 | higA | K | transcriptional regulator | ||
AIIGCJOP_01812 | 1.5e-18 | higB | S | HigB_toxin, RelE-like toxic component of a toxin-antitoxin system | ||
AIIGCJOP_01813 | 2.5e-43 | L | Transposase and inactivated derivatives | |||
AIIGCJOP_01816 | 2.2e-100 | parA | D | Cobyrinic acid a,c-diamide synthase | ||
AIIGCJOP_01817 | 2.7e-22 | S | ParG | |||
AIIGCJOP_01818 | 1.4e-156 | S | RePlication protein | |||
AIIGCJOP_01819 | 2.2e-105 | L | Phage integrase family protein | |||
AIIGCJOP_01821 | 6.1e-48 | L | IS1 transposase | |||
AIIGCJOP_01822 | 2.6e-45 | L | transposition, DNA-mediated | |||
AIIGCJOP_01826 | 3.6e-15 | |||||
AIIGCJOP_01828 | 4.8e-46 | G | 4-amino-4-deoxy-alpha-L-arabinopyranosyl undecaprenyl phosphate biosynthetic process | |||
AIIGCJOP_01829 | 7.3e-186 | ISPlu13C | L | Transposase | ||
AIIGCJOP_01830 | 3.3e-110 | E | LysE type translocator | |||
AIIGCJOP_01831 | 1.6e-98 | arcR | T | Winged helix-turn-helix DNA binding | ||
AIIGCJOP_01832 | 1.2e-146 | amiD | 3.5.1.28 | V | N-acetylmuramoyl-L-alanine amidase | |
AIIGCJOP_01833 | 1.9e-50 | ybjQ | S | Belongs to the UPF0145 family | ||
AIIGCJOP_01834 | 3.1e-87 | ybjP | M | Induced during stationary phase and by acivicin (a glutamine analog) | ||
AIIGCJOP_01835 | 3.2e-130 | artP | E | Arginine ABC transporter, ATP-binding protein | ||
AIIGCJOP_01836 | 4.4e-132 | artI | ET | belongs to the bacterial solute-binding protein 3 family | ||
AIIGCJOP_01837 | 2.5e-124 | artQ | P | arginine transporter permease subunit ArtQ | ||
AIIGCJOP_01838 | 9.4e-105 | artM | P | (ABC) transporter | ||
AIIGCJOP_01839 | 3.6e-134 | artJ | ET | belongs to the bacterial solute-binding protein 3 family | ||
AIIGCJOP_01840 | 6.5e-252 | T | PhoQ Sensor | |||
AIIGCJOP_01841 | 2.4e-119 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
AIIGCJOP_01842 | 5.5e-206 | rumB | 2.1.1.189, 2.1.1.190 | J | Catalyzes the formation of 5-methyl-uridine at position 747 (m5U747) in 23S rRNA | |
AIIGCJOP_01843 | 1.5e-80 | ybjO | S | Membrane | ||
AIIGCJOP_01844 | 2.8e-146 | potI | P | ABC-type spermidine putrescine transport system, permease component II | ||
AIIGCJOP_01845 | 4.8e-171 | potH | P | ABC-type spermidine putrescine transport system, permease component I | ||
AIIGCJOP_01846 | 1.3e-207 | potG | P | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | ||
AIIGCJOP_01847 | 2.1e-210 | potF | P | Required for the activity of the bacterial periplasmic transport system of putrescine | ||
AIIGCJOP_01848 | 1.3e-79 | ybjN | S | sensory transduction regulator | ||
AIIGCJOP_01849 | 4.3e-161 | rimK | 6.3.1.17, 6.3.2.32, 6.3.2.41 | F | Belongs to the RimK family | |
AIIGCJOP_01850 | 7.5e-132 | nfsA | 1.5.1.38, 1.5.1.39 | C | Nitroreductase | |
AIIGCJOP_01851 | 4.1e-43 | grxA | 1.17.4.1 | O | Glutaredoxin | |
AIIGCJOP_01852 | 1.2e-43 | ybjM | S | Putative inner membrane protein of Enterobacteriaceae | ||
AIIGCJOP_01853 | 7e-311 | ybjL | P | transport protein | ||
AIIGCJOP_01854 | 6.4e-88 | crtZ | 1.14.15.24 | I | Fatty acid hydroxylase superfamily | |
AIIGCJOP_01855 | 2.3e-157 | crtB | 2.5.1.32, 2.5.1.99 | I | Phytoene squalene synthetase | |
AIIGCJOP_01856 | 1.6e-282 | crtI | 1.3.99.26, 1.3.99.28, 1.3.99.29, 1.3.99.31 | Q | COG1233 Phytoene dehydrogenase and related proteins | |
AIIGCJOP_01857 | 2e-190 | crtL | 5.5.1.19 | CH | lycopene cyclase | |
AIIGCJOP_01858 | 1.4e-171 | fni | 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) | |
AIIGCJOP_01859 | 6.5e-157 | 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 | |
AIIGCJOP_01860 | 3.9e-83 | S | Uncharacterized protein conserved in bacteria (DUF2239) | |||
AIIGCJOP_01861 | 6.1e-94 | ybjK | K | transcriptional regulator | ||
AIIGCJOP_01862 | 4.1e-207 | ybjJ | G | Major facilitator superfamily | ||
AIIGCJOP_01863 | 6.8e-142 | ybjI | 3.1.3.102, 3.1.3.104, 3.1.3.23 | C | Hydrolase | |
AIIGCJOP_01864 | 2.3e-218 | mdfA | EGP | multi-drug | ||
AIIGCJOP_01865 | 8.4e-107 | S | PAP2 superfamily | |||
AIIGCJOP_01866 | 5.4e-105 | ybjG | 3.6.1.27 | I | Phosphatase | |
AIIGCJOP_01867 | 2.8e-137 | deoR | K | transcriptional | ||
AIIGCJOP_01868 | 1.5e-222 | dacC | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
AIIGCJOP_01869 | 1.8e-110 | yliJ | 2.5.1.18 | O | Glutathione S-Transferase | |
AIIGCJOP_01870 | 3e-204 | yliI | G | glucose sorbosone | ||
AIIGCJOP_01871 | 4.7e-193 | mdoB | 2.7.8.20 | M | PFAM Sulfatase | |
AIIGCJOP_01872 | 1.1e-65 | bssR | S | Biofilm formation protein (YliH/bssR) | ||
AIIGCJOP_01873 | 1.9e-258 | rimO | 2.8.4.4 | J | Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein S12 | |
AIIGCJOP_01874 | 1.9e-186 | agaS | M | Glucosamine--fructose-6-phosphate aminotransferase | ||
AIIGCJOP_01875 | 8.3e-180 | M | glucosamine--fructose-6-phosphate aminotransferase | |||
AIIGCJOP_01876 | 4.9e-151 | G | PTS mannose transporter subunit IID | |||
AIIGCJOP_01877 | 2.7e-111 | G | PTS system | |||
AIIGCJOP_01878 | 4.8e-79 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | ||
AIIGCJOP_01879 | 2.8e-62 | G | PTS sugar transporter | |||
AIIGCJOP_01880 | 0.0 | K | transcriptional regulator | |||
AIIGCJOP_01881 | 8.9e-48 | |||||
AIIGCJOP_01882 | 1.2e-11 | |||||
AIIGCJOP_01883 | 3.1e-72 | K | Acetyltransferase | |||
AIIGCJOP_01884 | 2.7e-115 | 3.5.1.124 | F | intracellular protease amidase | ||
AIIGCJOP_01885 | 1.3e-134 | nfrA2 | 1.5.1.39 | C | nitroreductase | |
AIIGCJOP_01886 | 1.4e-148 | gsiD | P | transport | ||
AIIGCJOP_01887 | 8e-163 | gsiC | P | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
AIIGCJOP_01888 | 9.8e-291 | gsiB | E | Extracellular solute-binding protein, family 5 | ||
AIIGCJOP_01889 | 0.0 | gsiA | P | ATPase activity | ||
AIIGCJOP_01890 | 6.7e-165 | iaaA | 3.4.19.5, 3.5.1.1 | E | asparaginase | |
AIIGCJOP_01891 | 1.2e-225 | moeA | 2.10.1.1 | H | molybdopterin | |
AIIGCJOP_01892 | 1.2e-127 | moeB | 2.7.7.73, 2.7.7.80 | H | COG0476 Dinucleotide-utilizing enzymes involved in molybdopterin and thiamine biosynthesis family 2 | |
AIIGCJOP_01893 | 1.2e-107 | tal | 2.2.1.2 | H | Belongs to the transaldolase family. Type | |
AIIGCJOP_01894 | 3.6e-168 | ybiY | 1.97.1.4 | O | Pyruvate formate lyase-activating protein | |
AIIGCJOP_01895 | 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 | |
AIIGCJOP_01896 | 1.2e-146 | supH | 3.1.3.102, 3.1.3.104, 3.1.3.23 | C | Hydrolase | |
AIIGCJOP_01897 | 8.4e-248 | ybiU | S | Protein of unknown function (DUF1479) | ||
AIIGCJOP_01898 | 8.1e-296 | ybiT | S | ABC transporter | ||
AIIGCJOP_01899 | 1.4e-172 | ybiS | M | ErfK YbiS YcfS YnhG family protein | ||
AIIGCJOP_01900 | 1.9e-278 | nodT | M | RND efflux system, outer membrane lipoprotein | ||
AIIGCJOP_01901 | 1.2e-288 | emrb1 | EGP | Major facilitator Superfamily | ||
AIIGCJOP_01902 | 2.7e-77 | emrK | V | multidrug resistance | ||
AIIGCJOP_01903 | 4.1e-190 | ybiR | P | Citrate transporter | ||
AIIGCJOP_01904 | 1.3e-79 | mntR | K | transcriptional regulator | ||
AIIGCJOP_01905 | 5.8e-16 | |||||
AIIGCJOP_01906 | 2.5e-297 | ybiP | 2.7.8.42, 2.7.8.43 | S | membrane-associated metal-dependent hydrolase | |
AIIGCJOP_01907 | 2.2e-85 | ompX | M | PFAM virulence-related outer membrane protein | ||
AIIGCJOP_01908 | 1.7e-146 | rhtA | S | EamA-like transporter family | ||
AIIGCJOP_01909 | 1.5e-86 | 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 | ||
AIIGCJOP_01910 | 7e-133 | glnH | ET | belongs to the bacterial solute-binding protein 3 family | ||
AIIGCJOP_01911 | 7.8e-112 | glnP | P | (ABC) transporter | ||
AIIGCJOP_01912 | 1e-128 | glnQ | E | (ABC) transporter | ||
AIIGCJOP_01913 | 0.0 | ybiO | M | mechanosensitive ion channel | ||
AIIGCJOP_01914 | 3.1e-167 | rlmF | 2.1.1.181 | J | Specifically methylates the adenine in position 1618 of 23S rRNA | |
AIIGCJOP_01915 | 2.1e-36 | mcbA | S | colanic acid metabolic process | ||
AIIGCJOP_01916 | 0.0 | fiu | P | receptor | ||
AIIGCJOP_01917 | 2.1e-120 | ybiX | S | PkhD-type hydroxylase | ||
AIIGCJOP_01918 | 1.7e-41 | ybiI | T | DnaK suppressor protein | ||
AIIGCJOP_01920 | 7.8e-169 | ybiB | 2.4.2.18 | E | Glycosyl transferase | |
AIIGCJOP_01921 | 2.1e-62 | NU | Fimbrial protein | |||
AIIGCJOP_01922 | 8.1e-88 | M | PFAM pili assembly chaperone | |||
AIIGCJOP_01923 | 0.0 | NU | COG3188 P pilus assembly protein, porin PapC | |||
AIIGCJOP_01924 | 1.6e-84 | NU | Fimbrial protein | |||
AIIGCJOP_01925 | 1.1e-57 | NU | Fimbrial protein | |||
AIIGCJOP_01926 | 0.0 | dinG | 3.6.4.12 | KL | helicase | |
AIIGCJOP_01927 | 3.5e-215 | rhlE | 3.6.4.13 | JKL | DEAD-box RNA helicase involved in | |
AIIGCJOP_01928 | 7e-116 | ybiH | K | Transcriptional regulator | ||
AIIGCJOP_01929 | 3.3e-130 | ybhG | M | PFAM secretion protein HlyD | ||
AIIGCJOP_01930 | 0.0 | ybhF | V | (ABC) transporter | ||
AIIGCJOP_01931 | 3.7e-194 | ybhS | V | ABC-type multidrug transport system, permease component | ||
AIIGCJOP_01932 | 1.2e-197 | ybhR | V | Transport Permease Protein | ||
AIIGCJOP_01933 | 4.5e-65 | ybhQ | S | inner membrane protein YbhQ | ||
AIIGCJOP_01934 | 5.8e-143 | ybhP | L | Endonuclease Exonuclease Phosphatase | ||
AIIGCJOP_01935 | 2.8e-235 | clsB | 2.7.8.8 | I | Catalyzes the phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | |
AIIGCJOP_01936 | 9.5e-167 | mprF | 2.3.2.3 | S | Membrane | |
AIIGCJOP_01937 | 2.4e-119 | ybhL | S | Belongs to the BI1 family | ||
AIIGCJOP_01938 | 1.3e-78 | moaE | 2.8.1.12 | H | Molybdopterin converting factor, large subunit | |
AIIGCJOP_01939 | 1.9e-31 | moaD | 2.7.7.77, 2.8.1.12 | H | Involved in sulfur transfer in the conversion of molybdopterin precursor Z to molybdopterin | |
AIIGCJOP_01940 | 2.4e-81 | moaC | 4.6.1.17 | H | Catalyzes the conversion of (8S)-3',8-cyclo-7,8- dihydroguanosine 5'-triphosphate to cyclic pyranopterin monophosphate (cPMP) | |
AIIGCJOP_01941 | 4.5e-91 | moaB | 2.7.7.75 | H | May be involved in the biosynthesis of molybdopterin | |
AIIGCJOP_01942 | 1.9e-186 | moaA | 4.1.99.22 | H | Catalyzes the cyclization of GTP to (8S)-3',8-cyclo-7,8- dihydroguanosine 5'-triphosphate | |
AIIGCJOP_01943 | 1.4e-156 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
AIIGCJOP_01944 | 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 | ||
AIIGCJOP_01945 | 1.1e-114 | urtE | E | ABC transporter ATP-binding protein | ||
AIIGCJOP_01946 | 1.1e-114 | 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 | |
AIIGCJOP_01947 | 1.7e-118 | 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 | |
AIIGCJOP_01948 | 6.7e-191 | 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 | |
AIIGCJOP_01949 | 2.6e-194 | 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 | |
AIIGCJOP_01950 | 1.5e-250 | 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 | |
AIIGCJOP_01951 | 7e-86 | ybhB | S | PFAM PEBP family protein | ||
AIIGCJOP_01952 | 1.7e-271 | hutH | 3.5.2.7, 4.3.1.3 | E | histidine ammonia-lyase | |
AIIGCJOP_01953 | 0.0 | hutU | 4.2.1.49 | E | Catalyzes the conversion of urocanate to 4-imidazolone- 5-propionate | |
AIIGCJOP_01954 | 3.5e-129 | hutC | K | histidine utilization repressor | ||
AIIGCJOP_01955 | 3.5e-158 | hutG | 3.5.3.8 | E | Catalyzes the conversion of N-formimidoyl-L-glutamate to L-glutamate and formamide | |
AIIGCJOP_01956 | 1.2e-217 | hutI | 3.5.2.7 | Q | 'catalyzing the hydrolysis of 4-imidazolone-5-propionate to N-formimidoyl-L-glutamate, the third step in the histidine degradation pathway' | |
AIIGCJOP_01957 | 1.2e-238 | ybhC | 3.1.1.11, 4.2.2.2 | G | Pectinesterase | |
AIIGCJOP_01959 | 1.5e-191 | pgl | 3.1.1.31 | G | Catalyzes the hydrolysis of 6-phosphogluconolactone to 6-phosphogluconate | |
AIIGCJOP_01960 | 3.1e-142 | ybhA | S | hydrolases of the HAD superfamily | ||
AIIGCJOP_01961 | 6.3e-196 | 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 | |
AIIGCJOP_01962 | 2.7e-115 | modB | 3.6.3.29 | P | PFAM binding-protein-dependent transport systems inner membrane component | |
AIIGCJOP_01963 | 8e-124 | modA | P | TIGRFAM molybdenum ABC transporter, periplasmic | ||
AIIGCJOP_01964 | 5.3e-16 | acrZ | U | drug transmembrane transporter activity | ||
AIIGCJOP_01965 | 1.2e-130 | modE | H | Transcriptional regulator | ||
AIIGCJOP_01966 | 2e-264 | modF | 3.6.3.21, 3.6.3.34 | P | ABC-type molybdenum transport system ATPase component photorepair protein PhrA | |
AIIGCJOP_01967 | 7.1e-197 | galE | 5.1.3.2 | M | udp-glucose 4-epimerase | |
AIIGCJOP_01968 | 1.4e-203 | galT | 2.7.7.12 | H | galactose-1-phosphate uridylyltransferase | |
AIIGCJOP_01969 | 2.9e-210 | 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) | |
AIIGCJOP_01970 | 1.7e-193 | galM | 2.7.1.6, 5.1.3.3 | G | converts alpha-aldose to the beta-anomer | |
AIIGCJOP_01971 | 1.5e-143 | gpmA | 5.4.2.11 | G | Belongs to the phosphoglycerate mutase family. BPG- dependent PGAM subfamily | |
AIIGCJOP_01972 | 2.7e-199 | 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) | |
AIIGCJOP_01973 | 2.9e-08 | ybgS | S | YbgS-like protein | ||
AIIGCJOP_01974 | 2.1e-166 | zitB | P | cation diffusion facilitator family transporter | ||
AIIGCJOP_01975 | 3.6e-126 | pnuC | H | nicotinamide mononucleotide transporter | ||
AIIGCJOP_01976 | 2e-194 | nadA | 2.5.1.72 | H | Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate | |
AIIGCJOP_01982 | 5.5e-80 | cpoB | 3.5.1.28 | D | Mediates coordination of peptidoglycan synthesis and outer membrane constriction during cell division | |
AIIGCJOP_01983 | 1.4e-60 | pal | M | Belongs to the ompA family | ||
AIIGCJOP_01984 | 3.6e-153 | tolB | U | involved in the tonB-independent uptake of proteins | ||
AIIGCJOP_01985 | 1.7e-49 | tolA | M | Required for outer membrane integrity, uptake of group A colicins, role in translocation of filamenous phage DNA to cytoplasm, role in surface expression of O-antigen | ||
AIIGCJOP_01986 | 7e-69 | tolR | U | biopolymer transport protein | ||
AIIGCJOP_01987 | 1.3e-117 | tolQ | U | PFAM MotA TolQ ExbB proton channel | ||
AIIGCJOP_01988 | 2.8e-67 | ybgC | S | Acyl-CoA thioesterase | ||
AIIGCJOP_01989 | 3e-44 | ybgE | S | cyd operon protein YbgE | ||
AIIGCJOP_01990 | 3.5e-12 | ybgT | 1.10.3.14 | S | oxidoreductase activity, acting on diphenols and related substances as donors | |
AIIGCJOP_01991 | 3.8e-207 | cydB | 1.10.3.14 | C | cytochrome d ubiquinol oxidase, subunit | |
AIIGCJOP_01992 | 4e-287 | cydA | 1.10.3.14 | C | oxidase, subunit | |
AIIGCJOP_01993 | 4.6e-160 | 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 | |
AIIGCJOP_01994 | 3.5e-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 | |
AIIGCJOP_01995 | 1.6e-203 | sucB | 2.3.1.61 | C | The 2-oxoglutarate dehydrogenase complex catalyzes the overall conversion of 2-oxoglutarate to succinyl-CoA and CO(2) | |
AIIGCJOP_01996 | 0.0 | sucA | 1.2.4.2, 4.1.1.71 | C | Dehydrogenase E1 component | |
AIIGCJOP_01997 | 5.3e-138 | sdhB | 1.3.5.1, 1.3.5.4 | C | Belongs to the succinate dehydrogenase fumarate reductase iron-sulfur protein family | |
AIIGCJOP_01998 | 0.0 | sdhA | 1.3.5.1, 1.3.5.4 | C | Belongs to the FAD-dependent oxidoreductase 2 family. FRD SDH subfamily | |
AIIGCJOP_01999 | 5.7e-29 | sdhD | C | Membrane-anchoring subunit of succinate dehydrogenase (SDH) | ||
AIIGCJOP_02000 | 1.9e-83 | sdhC | C | succinate dehydrogenase | ||
AIIGCJOP_02001 | 5e-248 | gltA | 2.3.3.1 | C | Belongs to the citrate synthase family | |
AIIGCJOP_02002 | 1.5e-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 | |
AIIGCJOP_02003 | 2.1e-109 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
AIIGCJOP_02004 | 2.3e-176 | S | Membrane | |||
AIIGCJOP_02005 | 1.6e-123 | S | Membrane | |||
AIIGCJOP_02006 | 2.3e-128 | ybgL | E | Belongs to the UPF0271 (lamB) family | ||
AIIGCJOP_02007 | 6.6e-173 | ybgK | 3.5.1.54, 6.3.4.6 | E | Allophanate hydrolase subunit 2 | |
AIIGCJOP_02008 | 2.9e-114 | kipI | 3.5.1.54 | E | Allophanate hydrolase subunit 1 | |
AIIGCJOP_02009 | 2.1e-137 | ybgI | 3.5.4.16 | S | metal-binding protein | |
AIIGCJOP_02010 | 1.6e-263 | phrB | 4.1.99.3 | L | Belongs to the DNA photolyase family | |
AIIGCJOP_02011 | 9.7e-32 | ybfA | S | Membrane | ||
AIIGCJOP_02012 | 1e-296 | 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 | |
AIIGCJOP_02013 | 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 | |
AIIGCJOP_02014 | 2e-87 | 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 | |
AIIGCJOP_02015 | 0.0 | T | PhoQ Sensor | |||
AIIGCJOP_02016 | 3.3e-121 | K | response regulator | |||
AIIGCJOP_02017 | 1.6e-310 | pgm | 5.4.2.2 | G | Phosphoglucomutase | |
AIIGCJOP_02018 | 2e-89 | 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 | ||
AIIGCJOP_02019 | 1.4e-139 | ybfF | S | Alpha beta hydrolase | ||
AIIGCJOP_02020 | 1.7e-42 | ybfE | S | CopG domain protein DNA-binding domain protein | ||
AIIGCJOP_02021 | 4.7e-99 | fldA | C | Low-potential electron donor to a number of redox enzymes | ||
AIIGCJOP_02022 | 1.5e-82 | fur | K | Belongs to the Fur family | ||
AIIGCJOP_02023 | 6.9e-48 | ybfN | S | YbfN-like lipoprotein | ||
AIIGCJOP_02024 | 1.2e-274 | chiP | S | Outer membrane porin | ||
AIIGCJOP_02025 | 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 | |
AIIGCJOP_02026 | 0.0 | nagE | 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | Phosphotransferase System | |
AIIGCJOP_02027 | 1.1e-149 | 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 | |
AIIGCJOP_02028 | 7e-217 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
AIIGCJOP_02029 | 7.4e-225 | 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 | |
AIIGCJOP_02030 | 1.9e-138 | nagD | G | HAD-superfamily hydrolase, subfamily IIA | ||
AIIGCJOP_02031 | 0.0 | asnB | 6.3.5.4 | E | Asparagine synthase, glutamine-hydrolyzing | |
AIIGCJOP_02033 | 1.3e-08 | |||||
AIIGCJOP_02034 | 1.7e-07 | |||||
AIIGCJOP_02035 | 1.7e-07 | |||||
AIIGCJOP_02039 | 4.7e-208 | ubiF | CH | ubiquinone biosynthesis hydroxylase, UbiH UbiF VisC COQ6 | ||
AIIGCJOP_02040 | 4.7e-271 | 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 | |
AIIGCJOP_02041 | 6.5e-185 | ybeZ | T | phosphate starvation-inducible protein PhoH | ||
AIIGCJOP_02042 | 9.2e-83 | 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 | |
AIIGCJOP_02043 | 6e-160 | corC | P | Mg2 and Co2 transporter CorC | ||
AIIGCJOP_02044 | 1.6e-277 | lnt | GT2 | M | Transfers the fatty acyl group on membrane lipoproteins | |
AIIGCJOP_02045 | 3.1e-167 | gltI | ET | ABC-type amino acid transport signal transduction systems periplasmic component domain | ||
AIIGCJOP_02046 | 2.2e-126 | gltJ | P | amino acid ABC transporter | ||
AIIGCJOP_02047 | 6.8e-111 | gltK | P | With GltJLPS and GadC for glutamate and GltJLP, DctA and DcuAB for aspartate is involved in the transport of glutamate and aspartate | ||
AIIGCJOP_02048 | 2.6e-124 | gltL | 3.6.3.21 | P | Part of the ABC transporter complex GltIJKL involved in glutamate and aspartate uptake. Probably responsible for energy coupling to the transport system | |
AIIGCJOP_02049 | 1.3e-163 | rihA | G | Belongs to the IUNH family | ||
AIIGCJOP_02050 | 3.1e-81 | ybeL | 1.17.4.1, 4.6.1.1 | J | Zinc-ribbon containing domain | |
AIIGCJOP_02051 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
AIIGCJOP_02052 | 3.4e-95 | 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 | ||
AIIGCJOP_02053 | 1.1e-184 | holA | 2.7.7.7 | L | dna polymerase III delta subunit | |
AIIGCJOP_02054 | 7e-113 | 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) | |
AIIGCJOP_02055 | 1.3e-51 | 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 | |
AIIGCJOP_02056 | 2e-79 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
AIIGCJOP_02057 | 0.0 | mrdA | 3.4.16.4 | M | Catalyzes cross-linking of the peptidoglycan cell wall | |
AIIGCJOP_02058 | 3.2e-198 | mrdB | M | Peptidoglycan polymerase that is essential for cell wall elongation | ||
AIIGCJOP_02059 | 1.2e-176 | rlpA | M | Lytic transglycosylase with a strong preference for naked glycan strands that lack stem peptides | ||
AIIGCJOP_02060 | 2.2e-229 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
AIIGCJOP_02061 | 3.8e-41 | ybeD | S | Protein of unknown function (DUF493) | ||
AIIGCJOP_02062 | 1e-116 | 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 | |
AIIGCJOP_02063 | 4.5e-153 | ybeF | K | transcriptional regulator | ||
AIIGCJOP_02064 | 1.7e-184 | 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 | |
AIIGCJOP_02065 | 2.5e-24 | 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 | ||
AIIGCJOP_02066 | 4.5e-130 | ybeM | 3.5.1.3 | S | Nitrilase cyanide hydratase and apolipoprotein N-acyltransferase | |
AIIGCJOP_02067 | 1.9e-62 | crcB | D | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
AIIGCJOP_02068 | 4.3e-32 | cspE | K | SMART Cold shock protein | ||
AIIGCJOP_02069 | 1.8e-46 | 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 | |
AIIGCJOP_02070 | 1.4e-232 | dcuC | C | C4-dicarboxylate | ||
AIIGCJOP_02071 | 4.1e-147 | rna | 3.1.27.1, 3.1.27.6 | J | Belongs to the RNase T2 family | |
AIIGCJOP_02072 | 7.4e-112 | IV02_24660 | S | Conserved protein domain typically associated with flavoprotein oxygenases DIM6 NTAB family | ||
AIIGCJOP_02073 | 6.2e-67 | rnk | K | regulator of nucleoside diphosphate kinase | ||
AIIGCJOP_02074 | 5.2e-234 | ybdR | 1.1.1.14 | E | COG1063 Threonine dehydrogenase and related Zn-dependent dehydrogenases | |
AIIGCJOP_02075 | 1.1e-66 | uspG | T | Belongs to the universal stress protein A family | ||
AIIGCJOP_02076 | 9e-292 | ahpF | O | alkyl hydroperoxide reductase | ||
AIIGCJOP_02077 | 3.9e-104 | ahpC | 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 | |
AIIGCJOP_02079 | 1.2e-115 | ybdO | K | LysR substrate binding domain | ||
AIIGCJOP_02080 | 2.8e-213 | ybdL | 2.6.1.17, 2.6.1.88 | E | aminotransferase | |
AIIGCJOP_02081 | 2.6e-109 | mtnB | 3.1.3.87, 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) | |
AIIGCJOP_02082 | 7.4e-121 | 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) | |
AIIGCJOP_02083 | 6.3e-99 | 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 | |
AIIGCJOP_02084 | 4.3e-173 | mtnA | 4.2.1.109, 5.3.1.23 | J | Catalyzes the interconversion of methylthioribose-1- phosphate (MTR-1-P) into methylthioribulose-1-phosphate (MTRu-1- P) | |
AIIGCJOP_02085 | 6e-222 | mtnK | 2.7.1.100 | F | Catalyzes the phosphorylation of methylthioribose into methylthioribose-1-phosphate | |
AIIGCJOP_02086 | 1.3e-245 | S | LVIVD repeat | |||
AIIGCJOP_02087 | 5.9e-194 | G | Sugar ABC Transporter | |||
AIIGCJOP_02088 | 2.4e-165 | rbsC_3 | G | Belongs to the binding-protein-dependent transport system permease family | ||
AIIGCJOP_02089 | 3.1e-273 | mglA_3 | 3.6.3.17 | G | (ABC) transporter | |
AIIGCJOP_02090 | 2.2e-188 | gldA | 1.1.1.1, 1.1.1.6 | C | Iron-containing alcohol dehydrogenase | |
AIIGCJOP_02091 | 4e-120 | IQ | KR domain | |||
AIIGCJOP_02092 | 6.8e-31 | relE | DJ | nuclease activity | ||
AIIGCJOP_02093 | 2.5e-60 | K | transcriptional regulator | |||
AIIGCJOP_02094 | 1.8e-32 | ybdD | S | Pfam:DUF466 | ||
AIIGCJOP_02095 | 0.0 | cstA | T | Carbon starvation protein | ||
AIIGCJOP_02096 | 1.3e-23 | J | SmpA / OmlA family | |||
AIIGCJOP_02097 | 6.5e-61 | |||||
AIIGCJOP_02098 | 4.2e-71 | 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 | |
AIIGCJOP_02099 | 6.1e-121 | IQ | involved in the biosynthesis of siderophores, enterobactin, bacillibactin or vibriobactin | |||
AIIGCJOP_02100 | 3.7e-162 | entB | 3.3.2.1, 6.3.2.14 | Q | Isochorismatase | |
AIIGCJOP_02101 | 5.4e-292 | entE | 2.7.7.58, 6.3.2.14 | Q | 2,3-dihydroxybenzoate-AMP ligase | |
AIIGCJOP_02102 | 2.8e-205 | entC | 5.4.4.2 | HQ | Isochorismate synthase | |
AIIGCJOP_02103 | 4.3e-159 | fepB | P | Periplasmic binding protein | ||
AIIGCJOP_02104 | 3.4e-209 | entS | EGP | Exports the siderophore enterobactin out of the cell | ||
AIIGCJOP_02105 | 1.4e-160 | fepD | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
AIIGCJOP_02106 | 1.5e-154 | fepG | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
AIIGCJOP_02107 | 8.2e-140 | fepC | 3.6.3.34 | HP | (ABC) transporter | |
AIIGCJOP_02108 | 1.2e-195 | |||||
AIIGCJOP_02109 | 5.5e-16 | L | Resolvase | |||
AIIGCJOP_02110 | 0.0 | entF | 6.3.2.14 | Q | amino acid activation for nonribosomal peptide biosynthetic process | |
AIIGCJOP_02111 | 3.4e-32 | ybdZ | P | PFAM MbtH domain protein | ||
AIIGCJOP_02112 | 9e-215 | fes | P | esterase | ||
AIIGCJOP_02113 | 0.0 | fepA | P | Receptor | ||
AIIGCJOP_02115 | 0.0 | fdhF | 1.17.1.10, 1.17.1.9, 1.17.99.7 | C | Belongs to the prokaryotic molybdopterin-containing oxidoreductase family | |
AIIGCJOP_02116 | 1.2e-73 | fdhF | 1.17.1.10, 1.17.1.9, 1.17.99.7 | C | Belongs to the prokaryotic molybdopterin-containing oxidoreductase family | |
AIIGCJOP_02117 | 1.1e-181 | hoxN | S | rRNA processing | ||
AIIGCJOP_02118 | 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 | ||
AIIGCJOP_02119 | 0.0 | fdhF | 1.17.1.10, 1.17.1.9, 1.17.99.7 | C | Belongs to the prokaryotic molybdopterin-containing oxidoreductase family | |
AIIGCJOP_02120 | 5.1e-101 | hydN | C | electron transport | ||
AIIGCJOP_02121 | 3.8e-84 | S | Type VI secretion system effector | |||
AIIGCJOP_02122 | 5.5e-76 | S | Protein involved in biological_process | |||
AIIGCJOP_02123 | 1.8e-265 | iphP | 3.1.3.48 | T | Tyrosine phosphatase family | |
AIIGCJOP_02124 | 1.1e-53 | |||||
AIIGCJOP_02125 | 2.4e-14 | S | Domain of unknown function (DUF4440) | |||
AIIGCJOP_02126 | 6e-125 | S | Dienelactone hydrolase | |||
AIIGCJOP_02127 | 6.5e-105 | K | transcriptional regulator | |||
AIIGCJOP_02128 | 1.2e-69 | E | LysE type translocator | |||
AIIGCJOP_02129 | 1.9e-49 | tolA | M | TolA C-terminal | ||
AIIGCJOP_02130 | 1e-35 | S | Protein of unknown function (DUF1493) | |||
AIIGCJOP_02131 | 4.1e-78 | S | Type VI secretion system effector | |||
AIIGCJOP_02132 | 3.8e-81 | hycI | 3.4.23.51 | C | hydrogenase 3 maturation protease | |
AIIGCJOP_02133 | 8.2e-67 | hycH | E | Formate hydrogen-lyase | ||
AIIGCJOP_02134 | 3.3e-130 | hyfI | C | NADH ubiquinone oxidoreductase, 20 | ||
AIIGCJOP_02135 | 2.8e-83 | hycF | C | the formate hydrogenlyase complex comprises of a formate dehydrogenase, unidentified electron carriers and hydrogenase-3 | ||
AIIGCJOP_02136 | 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 | ||
AIIGCJOP_02137 | 3.7e-152 | hycD | C | HycBCDEFG is part of the formate hydrogenlyase system which is involved in the cleaving of formate to dihydrogen and carbon dioxide | ||
AIIGCJOP_02138 | 4e-299 | hycC | CP | formate hydrogenlyase subunit 3 | ||
AIIGCJOP_02139 | 1.6e-106 | hycB | C | Formate hydrogenlyase | ||
AIIGCJOP_02140 | 1.7e-68 | hycA | E | seems to prevent binding of FhlA transcriptional activator to the activator sequence of hyc operon | ||
AIIGCJOP_02141 | 1.3e-57 | hypA | S | Probably plays a role in a hydrogenase nickel cofactor insertion step | ||
AIIGCJOP_02142 | 1.1e-142 | hypB | KO | Hydrogenase accessory protein HypB | ||
AIIGCJOP_02143 | 1.2e-40 | hypC | O | Hydrogenase assembly chaperone hypC hupF | ||
AIIGCJOP_02144 | 3.8e-199 | hypD | O | Belongs to the HypD family | ||
AIIGCJOP_02145 | 5.7e-170 | hypE | O | hydrogenase expression formation protein HypE | ||
AIIGCJOP_02146 | 0.0 | fhlA | KT | transcriptional regulator | ||
AIIGCJOP_02147 | 3.8e-95 | entD | 6.3.2.14 | Q | Belongs to the P-Pant transferase superfamily | |
AIIGCJOP_02148 | 2.6e-169 | rbsB_1 | G | Periplasmic binding protein LacI transcriptional regulator | ||
AIIGCJOP_02149 | 3.4e-101 | S | Lipoprotein | |||
AIIGCJOP_02150 | 8.9e-276 | rbsA_1 | 3.6.3.17 | P | import. Responsible for energy coupling to the transport system | |
AIIGCJOP_02151 | 7.4e-184 | G | Belongs to the binding-protein-dependent transport system permease family | |||
AIIGCJOP_02152 | 1.7e-168 | deoR_1 | K | transcriptional regulator | ||
AIIGCJOP_02153 | 3.9e-63 | S | Type VI secretion system effector, Hcp | |||
AIIGCJOP_02154 | 3.6e-07 | |||||
AIIGCJOP_02155 | 7e-58 | |||||
AIIGCJOP_02156 | 9.4e-155 | tktB | 2.2.1.1 | G | Transketolase | |
AIIGCJOP_02157 | 5.3e-170 | tktA | 2.2.1.1 | G | Transketolase | |
AIIGCJOP_02158 | 1e-270 | G | L-fucose isomerase | |||
AIIGCJOP_02159 | 9.6e-267 | glpK3 | 2.7.1.30 | G | Belongs to the FGGY kinase family | |
AIIGCJOP_02160 | 3.2e-90 | csy4 | S | crispr-associated protein, csy4 | ||
AIIGCJOP_02161 | 1.5e-178 | csy3 | S | crispr-associated protein | ||
AIIGCJOP_02162 | 7e-167 | csy2 | S | crispr-associated protein | ||
AIIGCJOP_02163 | 9.2e-213 | csy1 | S | crispr-associated protein | ||
AIIGCJOP_02164 | 0.0 | cas3 | L | CRISPR-associated helicase, Cas3 | ||
AIIGCJOP_02165 | 4.6e-169 | cas1 | L | CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Acts as a dsDNA endonuclease. Involved in the integration of spacer DNA into the CRISPR cassette | ||
AIIGCJOP_02166 | 6e-15 | hokE | S | Hok/gef family | ||
AIIGCJOP_02167 | 1.5e-11 | |||||
AIIGCJOP_02169 | 2.7e-126 | rimL | J | Acetyltransferases including N-acetylases of ribosomal proteins | ||
AIIGCJOP_02170 | 1.4e-78 | csp | K | Cold-Shock Protein | ||
AIIGCJOP_02171 | 5.4e-34 | ymjA | S | Protein of unknown function (DUF2543) | ||
AIIGCJOP_02172 | 7.9e-205 | ybdK | H | ATP-dependent carboxylate-amine ligase which exhibits weak glutamate--cysteine ligase activity | ||
AIIGCJOP_02173 | 0.0 | ctpF | P | ATPase, P-type (transporting), HAD superfamily, subfamily IC | ||
AIIGCJOP_02174 | 1.9e-08 | |||||
AIIGCJOP_02175 | 5.8e-28 | ybdJ | S | Protein of unknown function (DUF1158) | ||
AIIGCJOP_02176 | 1.7e-57 | ramA | K | Transcriptional regulator | ||
AIIGCJOP_02177 | 3.6e-210 | romA | S | Zn-dependent hydrolases of the beta-lactamase fold | ||
AIIGCJOP_02178 | 8.6e-102 | K | transcriptional regulator | |||
AIIGCJOP_02179 | 2.4e-65 | ybdF | S | YjbR | ||
AIIGCJOP_02180 | 2.1e-117 | nfnB | 1.5.1.34 | C | Nitroreductase | |
AIIGCJOP_02181 | 4.6e-40 | K | sequence-specific DNA binding | |||
AIIGCJOP_02182 | 5.8e-47 | S | Phage-related protein | |||
AIIGCJOP_02183 | 1.4e-164 | K | transcriptional | |||
AIIGCJOP_02184 | 3e-249 | EGP | Major facilitator superfamily | |||
AIIGCJOP_02185 | 1.2e-222 | ybdG | M | Mechanosensitive Ion channel | ||
AIIGCJOP_02186 | 4.8e-166 | cytR | 5.1.1.1 | K | Periplasmic binding protein LacI transcriptional regulator | |
AIIGCJOP_02187 | 7.5e-211 | S | oxidoreductase | |||
AIIGCJOP_02188 | 7.5e-194 | iolE | G | AP endonuclease | ||
AIIGCJOP_02189 | 2.7e-214 | yegT | G | Nucleoside H+ symporter | ||
AIIGCJOP_02190 | 3.8e-52 | S | protein conserved in bacteria | |||
AIIGCJOP_02191 | 2.3e-42 | proV | 3.6.3.32 | K | transcriptional regulator | |
AIIGCJOP_02192 | 1.2e-247 | pheP | E | amino acid | ||
AIIGCJOP_02193 | 0.0 | S | Phosphatase | |||
AIIGCJOP_02194 | 0.0 | fcuA | P | receptor | ||
AIIGCJOP_02195 | 3.2e-187 | S | amine dehydrogenase activity | |||
AIIGCJOP_02196 | 1.9e-86 | VP1566 | ||||
AIIGCJOP_02197 | 2.7e-63 | yajD | 2.1.1.148 | L | HNH endonuclease | |
AIIGCJOP_02199 | 9.8e-155 | 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 | |
AIIGCJOP_02200 | 4.9e-31 | yaaA | S | S4 domain | ||
AIIGCJOP_02201 | 1.9e-275 | ptsG | 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | PTS system | |
AIIGCJOP_02202 | 3.7e-177 | K | Protein involved in sequence-specific DNA binding transcription factor activity, DNA binding and regulation of transcription, DNA-templated | |||
AIIGCJOP_02203 | 4.5e-94 | ybcI | S | LexA-binding, inner membrane-associated putative hydrolase | ||
AIIGCJOP_02204 | 1.1e-267 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
AIIGCJOP_02205 | 1.4e-89 | ppiB | 2.7.11.1, 5.2.1.8 | O | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
AIIGCJOP_02206 | 2.9e-128 | 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 | |
AIIGCJOP_02207 | 7.4e-24 | S | Protein of unknown function (DUF1471) | |||
AIIGCJOP_02208 | 7.7e-20 | |||||
AIIGCJOP_02209 | 5.7e-86 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
AIIGCJOP_02210 | 4.5e-202 | 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) | |
AIIGCJOP_02211 | 1.9e-187 | selU | H | Catalyzes the transfer of selenium from selenophosphate for conversion of 2-thiouridine to 2-selenouridine at the wobble position in tRNA | ||
AIIGCJOP_02212 | 3.1e-225 | omp | M | Membrane | ||
AIIGCJOP_02213 | 0.0 | ybbP | Q | ABC-type transport system involved in lysophospholipase L1 biosynthesis permease component | ||
AIIGCJOP_02214 | 9.9e-118 | ybbA | Q | (ABC) transporter | ||
AIIGCJOP_02215 | 1.9e-101 | tesA | 3.1.1.5 | E | COG2755 Lysophospholipase L1 and related esterases | |
AIIGCJOP_02216 | 1.8e-139 | ybbO | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | ||
AIIGCJOP_02217 | 9.7e-147 | ybbN | O | Thioredoxin | ||
AIIGCJOP_02218 | 6.1e-133 | |||||
AIIGCJOP_02219 | 7e-119 | qmcA | O | COG0330 Membrane protease subunits stomatin prohibitin homologs | ||
AIIGCJOP_02220 | 5.9e-74 | ybbJ | OU | Membrane protein implicated in regulation of membrane protease activity | ||
AIIGCJOP_02221 | 0.0 | S | Mediates coordination of peptidoglycan synthesis and outer membrane constriction during cell division | |||
AIIGCJOP_02222 | 1.1e-119 | S | Protein of unknown function (DUF3142) | |||
AIIGCJOP_02223 | 5.6e-68 | cueR | K | Transcriptional regulator | ||
AIIGCJOP_02224 | 0.0 | copA | 3.6.3.54 | P | P-type atpase | |
AIIGCJOP_02225 | 4.5e-138 | ybaP | S | protein conserved in bacteria | ||
AIIGCJOP_02226 | 9.8e-80 | ybaK | S | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
AIIGCJOP_02227 | 0.0 | ushA | 3.1.3.5, 3.6.1.45 | F | Belongs to the 5'-nucleotidase family | |
AIIGCJOP_02228 | 2.9e-213 | fsr | P | fosmidomycin resistance protein | ||
AIIGCJOP_02229 | 4.5e-281 | ybaL | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
AIIGCJOP_02230 | 1.5e-252 | gsk | 2.7.1.20, 2.7.1.73, 2.7.1.92 | G | COG0524 Sugar kinases, ribokinase family | |
AIIGCJOP_02231 | 6.6e-176 | hemH | 4.99.1.1, 4.99.1.9 | H | Catalyzes the ferrous insertion into protoporphyrin IX | |
AIIGCJOP_02232 | 3.3e-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 | |
AIIGCJOP_02233 | 0.0 | htpG | O | Molecular chaperone. Has ATPase activity | ||
AIIGCJOP_02234 | 3.3e-109 | 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 | ||
AIIGCJOP_02235 | 2.5e-42 | |||||
AIIGCJOP_02236 | 0.0 | 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 | |
AIIGCJOP_02237 | 6e-97 | 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 | |
AIIGCJOP_02238 | 1e-60 | ybaN | S | membrane | ||
AIIGCJOP_02239 | 1.8e-79 | priC | L | primosomal replication protein | ||
AIIGCJOP_02240 | 3.7e-15 | ybaM | S | cellular response to cell envelope stress | ||
AIIGCJOP_02241 | 0.0 | kefA | M | mechanosensitive ion channel | ||
AIIGCJOP_02242 | 6.2e-49 | acrR | K | transcriptional regulator | ||
AIIGCJOP_02243 | 8.4e-197 | acrA | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | ||
AIIGCJOP_02244 | 0.0 | acrB | V | Belongs to the resistance-nodulation-cell division (RND) (TC 2.A.6) family | ||
AIIGCJOP_02245 | 1.3e-69 | tomB | S | Biofilm formation regulator YbaJ | ||
AIIGCJOP_02246 | 1.8e-33 | hha | S | non-specific DNA-binding protein which affects the production of multiple proteins | ||
AIIGCJOP_02247 | 3.4e-77 | ylaC | S | Membrane | ||
AIIGCJOP_02248 | 7e-18 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
AIIGCJOP_02249 | 5.9e-259 | ylaB | 3.1.4.52 | T | signal transduction protein containing sensor and EAL | |
AIIGCJOP_02250 | 1.1e-59 | ybaA | S | RNA signal recognition particle 4.5S RNA | ||
AIIGCJOP_02251 | 0.0 | lacZ | 3.2.1.23 | G | Belongs to the glycosyl hydrolase 2 family | |
AIIGCJOP_02252 | 4.3e-176 | lacI | K | binds specific sites in lac operon resulting in DNA looping between the operators | ||
AIIGCJOP_02253 | 1.6e-98 | S | Membrane | |||
AIIGCJOP_02254 | 3.8e-252 | K | Transcriptional regulator | |||
AIIGCJOP_02255 | 2e-35 | |||||
AIIGCJOP_02256 | 1e-35 | |||||
AIIGCJOP_02257 | 5.8e-49 | ybaZ | 2.1.1.63 | L | PFAM Methylated-DNA- protein -cysteine S-methyltransferase | |
AIIGCJOP_02258 | 4.1e-93 | ybaY | S | protein conserved in bacteria | ||
AIIGCJOP_02259 | 1.2e-160 | tesB | I | Acyl-CoA thioesterase | ||
AIIGCJOP_02260 | 2.3e-208 | amtB | P | Ammonium transporter | ||
AIIGCJOP_02261 | 8.5e-54 | glnK | K | Belongs to the P(II) protein family | ||
AIIGCJOP_02262 | 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 | ||
AIIGCJOP_02263 | 0.0 | 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 | ||
AIIGCJOP_02264 | 3.6e-79 | ybaO | K | transcriptional regulator | ||
AIIGCJOP_02265 | 1.6e-199 | cysK_2 | 2.5.1.47 | E | cysteine synthase | |
AIIGCJOP_02266 | 1.2e-154 | 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) | ||
AIIGCJOP_02267 | 0.0 | ybaE | S | ABC transporter substrate-binding protein | ||
AIIGCJOP_02268 | 3.9e-130 | queC | 6.3.4.20 | F | Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) | |
AIIGCJOP_02269 | 1.3e-64 | tesC | S | Thioesterase | ||
AIIGCJOP_02270 | 1.5e-33 | ybaV | 3.1.26.11 | L | TIGRFAM competence protein ComEA helix-hairpin-helix | |
AIIGCJOP_02271 | 7.7e-298 | ppiD | 5.2.1.8 | O | peptidylprolyl isomerase | |
AIIGCJOP_02272 | 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 | ||
AIIGCJOP_02273 | 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 | |
AIIGCJOP_02274 | 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 | ||
AIIGCJOP_02275 | 1.6e-114 | clpP | 3.4.21.92 | O | 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 | |
AIIGCJOP_02276 | 1.1e-231 | 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 | ||
AIIGCJOP_02278 | 8.8e-53 | bolA | T | Belongs to the BolA IbaG family | ||
AIIGCJOP_02279 | 9e-96 | yajG | M | lipoprotein | ||
AIIGCJOP_02280 | 2.4e-254 | ampG | P | Major facilitator superfamily | ||
AIIGCJOP_02281 | 1.1e-172 | cyoA | 1.10.3.10, 1.10.3.12 | C | ubiquinol oxidase subunit | |
AIIGCJOP_02282 | 0.0 | cyoB | 1.10.3.10, 1.10.3.12, 1.9.3.1 | C | Belongs to the heme-copper respiratory oxidase family | |
AIIGCJOP_02283 | 2.5e-112 | cyoC | C | PFAM cytochrome c oxidase, subunit III | ||
AIIGCJOP_02284 | 7e-53 | cyoD | C | cytochrome o ubiquinol oxidase | ||
AIIGCJOP_02285 | 2.6e-158 | 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 | |
AIIGCJOP_02287 | 1.1e-237 | yajR | EGP | Major facilitator Superfamily | ||
AIIGCJOP_02288 | 3.7e-82 | yajQ | S | Belongs to the UPF0234 family | ||
AIIGCJOP_02289 | 8.7e-162 | panE | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
AIIGCJOP_02290 | 3e-102 | thiJ | 2.7.11.1, 3.5.1.124 | S | TIGRFAM DJ-1 family protein | |
AIIGCJOP_02291 | 9.6e-272 | 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 | |
AIIGCJOP_02292 | 6.4e-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 | |
AIIGCJOP_02293 | 1.4e-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 | |
AIIGCJOP_02294 | 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) | |
AIIGCJOP_02295 | 6.2e-182 | yajO | 1.1.1.91 | C | Aldo keto reductase | |
AIIGCJOP_02296 | 5.2e-181 | 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 | |
AIIGCJOP_02297 | 1.1e-69 | 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 | ||
AIIGCJOP_02298 | 4.5e-77 | 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 | |
AIIGCJOP_02299 | 1.7e-204 | 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 | |
AIIGCJOP_02300 | 1.5e-77 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
AIIGCJOP_02301 | 4.5e-89 | yajI | M | Lipoprotein | ||
AIIGCJOP_02302 | 4.2e-177 | tsx | M | nucleoside-specific channel-forming protein | ||
AIIGCJOP_02303 | 9.8e-36 | |||||
AIIGCJOP_02304 | 1.3e-166 | 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 | ||
AIIGCJOP_02305 | 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 | ||
AIIGCJOP_02306 | 6e-52 | yajC | U | Preprotein translocase | ||
AIIGCJOP_02307 | 2.6e-224 | tgt | 2.4.2.29 | J | 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) | |
AIIGCJOP_02308 | 8.9e-198 | 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) | |
AIIGCJOP_02309 | 1.9e-106 | acpH | 3.1.4.14 | S | Converts holo-ACP to apo-ACP by hydrolytic cleavage of the phosphopantetheine prosthetic group from ACP | |
AIIGCJOP_02310 | 1.1e-112 | ahpC | 1.11.1.15 | O | PFAM alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen | |
AIIGCJOP_02311 | 2.4e-171 | S | Protein of unknown function (DUF3999) | |||
AIIGCJOP_02312 | 0.0 | S | Predicted membrane protein (DUF2339) | |||
AIIGCJOP_02313 | 0.0 | malZ | 3.2.1.20 | GH31 | G | Belongs to the glycosyl hydrolase 13 family |
AIIGCJOP_02314 | 5.2e-251 | proY | E | Cryptic permease that may be involved in the transport of proline across the inner membrane | ||
AIIGCJOP_02315 | 7.8e-228 | brnQ | P | Component of the transport system for branched-chain amino acids | ||
AIIGCJOP_02316 | 3.5e-241 | phoR | 2.7.13.3 | T | Histidine kinase | |
AIIGCJOP_02317 | 7.4e-129 | K | phosphate regulon transcriptional regulatory protein PhoB | |||
AIIGCJOP_02318 | 2.2e-213 | 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 | ||
AIIGCJOP_02319 | 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 | ||
AIIGCJOP_02320 | 1.7e-157 | mak | 2.7.1.4, 2.7.1.59 | GK | ROK family | |
AIIGCJOP_02321 | 4.1e-165 | rdgC | L | May be involved in recombination | ||
AIIGCJOP_02322 | 3.2e-46 | 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 | |
AIIGCJOP_02323 | 4.7e-104 | aroM | E | AroM protein | ||
AIIGCJOP_02324 | 1e-27 | yaiA | S | YaiA protein | ||
AIIGCJOP_02325 | 1.1e-87 | 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 | |
AIIGCJOP_02326 | 4.8e-76 | yaiI | S | Belongs to the UPF0178 family | ||
AIIGCJOP_02327 | 3.2e-139 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
AIIGCJOP_02328 | 4.1e-174 | adrA | 2.7.7.65 | T | Diguanylate cyclase | |
AIIGCJOP_02329 | 5.3e-21 | psiF | S | Phosphate starvation-inducible protein, PSIF | ||
AIIGCJOP_02330 | 1.9e-29 | 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 | ||
AIIGCJOP_02331 | 5e-205 | pmrA | EGP | Major facilitator Superfamily | ||
AIIGCJOP_02332 | 1.4e-122 | S | extensin | |||
AIIGCJOP_02333 | 2.2e-199 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
AIIGCJOP_02334 | 3.7e-34 | yaiZ | S | Protein of unknown function (DUF2754) | ||
AIIGCJOP_02335 | 4.5e-46 | yaiY | S | Protein of unknown function (DUF2755) | ||
AIIGCJOP_02336 | 8.3e-199 | yaiW | S | Lipoprotein | ||
AIIGCJOP_02337 | 1.6e-222 | sbmA | I | In Escherichia coli SbmA is involved in uptake of microcin J25 | ||
AIIGCJOP_02338 | 1.5e-206 | ampH | 3.4.16.4 | V | This protein has no known enzymatic function | |
AIIGCJOP_02339 | 1.1e-94 | iprA | T | Involved in oxidative stress resistance | ||
AIIGCJOP_02340 | 0.0 | MU | outer membrane autotransporter barrel | |||
AIIGCJOP_02341 | 7.4e-175 | hemB | 4.2.1.24 | H | Belongs to the ALAD family | |
AIIGCJOP_02342 | 0.0 | I | Acyltransferase | |||
AIIGCJOP_02343 | 3.4e-160 | tauD | 1.14.11.17 | Q | taurine catabolism dioxygenase | |
AIIGCJOP_02344 | 4.1e-126 | tauC | P | ABC-type nitrate sulfonate bicarbonate transport system permease component | ||
AIIGCJOP_02345 | 5.1e-131 | 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 | |
AIIGCJOP_02346 | 5.4e-170 | tauA | P | taurine ABC transporter | ||
AIIGCJOP_02347 | 7.7e-109 | uhpA | K | response regulator | ||
AIIGCJOP_02348 | 1.7e-271 | uhpB | 2.7.13.3 | T | Histidine kinase | |
AIIGCJOP_02349 | 2.5e-247 | uhpC | G | transporter | ||
AIIGCJOP_02350 | 1.3e-193 | afuA | P | ABC-type Fe3 transport system, periplasmic component | ||
AIIGCJOP_02351 | 0.0 | afuB | P | Binding-protein-dependent transport system inner membrane component | ||
AIIGCJOP_02352 | 1.8e-187 | 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 | |
AIIGCJOP_02353 | 9.9e-169 | mmuM | 1.5.1.20, 2.1.1.10 | H | homocysteine | |
AIIGCJOP_02354 | 1.6e-255 | mmuP | E | amino acid | ||
AIIGCJOP_02356 | 5.2e-193 | ydiK_1 | S | permease | ||
AIIGCJOP_02357 | 4.8e-297 | 2.7.13.3 | T | (GGDEF) domain | ||
AIIGCJOP_02358 | 1.3e-134 | yfjM | S | Protein of unknown function DUF262 | ||
AIIGCJOP_02359 | 4.7e-44 | ysdA | K | Membrane | ||
AIIGCJOP_02360 | 2e-258 | wcoR | G | Glucoamylase and related glycosyl hydrolases | ||
AIIGCJOP_02361 | 3e-09 | hicB | S | HicB family | ||
AIIGCJOP_02362 | 3.3e-105 | yagT | 1.3.99.16 | C | Aerobic-type carbon monoxide dehydrogenase small subunit CoxS | |
AIIGCJOP_02363 | 6.8e-165 | yagS | 1.17.1.4 | C | Aerobic-type carbon monoxide dehydrogenase, middle subunit CoxM | |
AIIGCJOP_02364 | 0.0 | yagR | 1.17.1.4 | C | Xanthine dehydrogenase | |
AIIGCJOP_02365 | 2e-110 | yagQ | O | Xanthine and CO dehydrogenases maturation factor XdhC CoxF family | ||
AIIGCJOP_02366 | 1.7e-180 | gntR | K | Bacterial regulatory proteins, lacI family | ||
AIIGCJOP_02367 | 3.7e-131 | yafS | Q | Methyl-transferase | ||
AIIGCJOP_02368 | 1.6e-87 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
AIIGCJOP_02369 | 6.3e-134 | 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 | |
AIIGCJOP_02371 | 1.7e-72 | C | Prokaryotic cytochrome b561 | |||
AIIGCJOP_02372 | 2.8e-145 | yafV | 3.5.1.3 | S | Hydrolase | |
AIIGCJOP_02373 | 0.0 | fadE | I | acyl-CoA dehydrogenase | ||
AIIGCJOP_02374 | 3.4e-103 | gmhA | 5.3.1.28 | G | Catalyzes the isomerization of sedoheptulose 7-phosphate in D-glycero-D-manno-heptose 7-phosphate | |
AIIGCJOP_02375 | 1e-150 | yafJ | S | glutamine amidotransferase | ||
AIIGCJOP_02376 | 3.3e-135 | yafK | S | ErfK YbiS YcfS YnhG family protein | ||
AIIGCJOP_02377 | 1e-232 | 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 | |
AIIGCJOP_02378 | 7e-231 | 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 | |
AIIGCJOP_02379 | 3.4e-138 | 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 | |
AIIGCJOP_02380 | 4.8e-106 | 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 | |
AIIGCJOP_02381 | 1.1e-99 | 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 | |
AIIGCJOP_02382 | 2.4e-231 | 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 | |
AIIGCJOP_02383 | 6e-29 | Z012_07620 | 2.7.1.180 | S | protein conserved in bacteria | |
AIIGCJOP_02384 | 2.1e-141 | ugpQ_1 | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
AIIGCJOP_02385 | 1e-190 | 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 | |
AIIGCJOP_02386 | 1.9e-275 | pepD | E | aminoacyl-histidine dipeptidase | ||
AIIGCJOP_02387 | 4.8e-84 | gpt | 2.4.2.22 | F | Acts on guanine, xanthine and to a lesser extent hypoxanthine | |
AIIGCJOP_02388 | 2.4e-239 | frsA | S | Belongs to the UPF0255 family | ||
AIIGCJOP_02389 | 6.3e-64 | 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 | ||
AIIGCJOP_02390 | 3.7e-196 | phoE | M | Belongs to the Gram-negative porin family | ||
AIIGCJOP_02391 | 3.6e-202 | proB | 2.7.2.11 | E | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
AIIGCJOP_02392 | 1.4e-223 | 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 | |
AIIGCJOP_02393 | 0.0 | gmr_2 | T | Diguanylate cyclase | ||
AIIGCJOP_02398 | 8e-296 | purH | 2.1.2.3, 3.5.4.10 | F | bifunctional purine biosynthesis protein purh | |
AIIGCJOP_02399 | 1e-240 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
AIIGCJOP_02400 | 1.3e-109 | yjaH | S | Protein of unknown function (DUF1481) | ||
AIIGCJOP_02401 | 5.6e-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 | ||
AIIGCJOP_02402 | 1.3e-105 | yjaG | S | protein conserved in bacteria | ||
AIIGCJOP_02403 | 1.1e-124 | 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 | |
AIIGCJOP_02404 | 3.7e-204 | hemE | 4.1.1.37 | H | Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III | |
AIIGCJOP_02405 | 7.4e-146 | nudC | 1.3.7.1, 3.6.1.22 | L | nadh pyrophosphatase | |
AIIGCJOP_02406 | 4.7e-85 | 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 | ||
AIIGCJOP_02407 | 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 | |
AIIGCJOP_02408 | 2.8e-106 | 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) | |
AIIGCJOP_02409 | 1e-123 | thiF | 2.7.7.73, 2.7.7.80 | H | COG0476 Dinucleotide-utilizing enzymes involved in molybdopterin and thiamine biosynthesis family 2 | |
AIIGCJOP_02410 | 3.8e-25 | thiS | 2.8.1.10 | H | ThiS family | |
AIIGCJOP_02411 | 1.5e-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 | |
AIIGCJOP_02412 | 6.7e-212 | thiH | 4.1.99.19 | C | In Escherichia coli this enzyme functions in thiamine biosynthesis along with thiFSGI and iscS | |
AIIGCJOP_02413 | 1.9e-37 | chbB | 2.7.1.196, 2.7.1.205 | G | Phosphotransferase System | |
AIIGCJOP_02414 | 3.3e-47 | celC | 2.7.1.196, 2.7.1.205 | G | Phosphotransferase System | |
AIIGCJOP_02415 | 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 | |
AIIGCJOP_02416 | 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 | |
AIIGCJOP_02417 | 2.7e-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 | ||
AIIGCJOP_02418 | 3.5e-80 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
AIIGCJOP_02419 | 5.4e-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 | ||
AIIGCJOP_02420 | 2.8e-70 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
AIIGCJOP_02421 | 9.7e-100 | nusG | K | Participates in transcription elongation, termination and antitermination. In the absence of Rho, increases the rate of transcription elongation by the RNA polymerase (RNAP), probably by partially suppressing pausing. In the presence of Rho, modulates most Rho-dependent termination events by interacting with the RNAP to render the complex more susceptible to the termination activity of Rho. May be required to overcome a kinetic limitation of Rho to function at certain terminators. Also involved in ribosomal RNA transcriptional antitermination | ||
AIIGCJOP_02422 | 1.1e-57 | 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 | ||
AIIGCJOP_02423 | 1.1e-29 | bfd | P | could be a general redox and or regulatory component participating in the iron storage mobilization functions of BFR. Could participate in the release or the delivery of iron from to bacterioferritin (or other iron complexes) | ||
AIIGCJOP_02424 | 2.3e-81 | 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 | |
AIIGCJOP_02425 | 2e-70 | hopD | 3.4.23.43 | NOU | Cleaves type-4 fimbrial leader sequence and methylates the N-terminal (generally Phe) residue | |
AIIGCJOP_02426 | 2e-49 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
AIIGCJOP_02427 | 6.3e-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 | ||
AIIGCJOP_02428 | 1.8e-102 | rplD | J | Forms part of the polypeptide exit tunnel | ||
AIIGCJOP_02429 | 1.9e-49 | |||||
AIIGCJOP_02430 | 4.6e-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 | ||
AIIGCJOP_02431 | 1.9e-46 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
AIIGCJOP_02432 | 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 | ||
AIIGCJOP_02433 | 1.7e-125 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
AIIGCJOP_02434 | 2.1e-70 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
AIIGCJOP_02435 | 8.9e-24 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
AIIGCJOP_02436 | 1.2e-39 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
AIIGCJOP_02437 | 9.3e-62 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
AIIGCJOP_02438 | 1.2e-49 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
AIIGCJOP_02439 | 2.9e-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 | ||
AIIGCJOP_02440 | 3.7e-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 | ||
AIIGCJOP_02441 | 2.8e-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 | ||
AIIGCJOP_02442 | 2.6e-89 | rplF | J | 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 | ||
AIIGCJOP_02443 | 2.3e-54 | rplR | J | This is one 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 | ||
AIIGCJOP_02444 | 1.6e-85 | |||||
AIIGCJOP_02445 | 1.7e-24 | rpmD | J | Ribosomal protein L30 | ||
AIIGCJOP_02446 | 3.9e-59 | rplO | J | binds to the 23S rRNA | ||
AIIGCJOP_02447 | 1.2e-241 | 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 | ||
AIIGCJOP_02448 | 9.6e-56 | 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 | ||
AIIGCJOP_02449 | 2.9e-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 | ||
AIIGCJOP_02450 | 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 | |
AIIGCJOP_02451 | 5.6e-62 | rplQ | J | Ribosomal protein L17 | ||
AIIGCJOP_02452 | 7.4e-51 | yhdN | S | PFAM DnaJ homologue, subfamily C, member 28, conserved domain | ||
AIIGCJOP_02453 | 3.9e-72 | zntR | K | transcriptional regulator | ||
AIIGCJOP_02454 | 1e-22 | arfA | S | protein conserved in bacteria | ||
AIIGCJOP_02455 | 1.9e-55 | 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 | ||
AIIGCJOP_02456 | 1.4e-251 | trkA | P | found to be peripherally associated with the inner membrane in Escherichia coli | ||
AIIGCJOP_02457 | 1.7e-243 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
AIIGCJOP_02458 | 3.1e-170 | 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 | |
AIIGCJOP_02459 | 1.5e-86 | 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 | |
AIIGCJOP_02460 | 8.5e-191 | dprA | LU | Rossmann fold nucleotide-binding protein involved in DNA uptake | ||
AIIGCJOP_02461 | 7.2e-83 | smg | S | Belongs to the Smg family | ||
AIIGCJOP_02462 | 8.5e-72 | yrdD | L | dNA topoisomerase | ||
AIIGCJOP_02463 | 3.1e-96 | 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 | |
AIIGCJOP_02464 | 2.5e-136 | 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) | |
AIIGCJOP_02465 | 5.9e-36 | yrdB | S | Protein of unknown function (DUF1488) | ||
AIIGCJOP_02466 | 4.4e-84 | yrdA | S | COG0663 Carbonic anhydrases acetyltransferases, isoleucine patch superfamily | ||
AIIGCJOP_02468 | 7.9e-35 | vagC | S | Virulence-associated protein | ||
AIIGCJOP_02469 | 1.5e-65 | vapC | S | PIN domain | ||
AIIGCJOP_02470 | 1.7e-224 | L | ATP-dependent endonuclease | |||
AIIGCJOP_02471 | 2e-160 | penP | 3.5.2.6 | V | Beta-lactamase | |
AIIGCJOP_02472 | 3.1e-93 | tnpR | L | Resolvase, N terminal domain | ||
AIIGCJOP_02473 | 0.0 | L | Transposase | |||
AIIGCJOP_02474 | 5.5e-57 | L | ATP-dependent endonuclease | |||
AIIGCJOP_02475 | 1.9e-189 | 3.6.4.12 | L | DNA helicase | ||
AIIGCJOP_02476 | 3.4e-143 | mcrA | L | HNH endonuclease | ||
AIIGCJOP_02477 | 1.6e-55 | S | Domain of unknown function (DUF305) | |||
AIIGCJOP_02478 | 1e-35 | |||||
AIIGCJOP_02479 | 3.2e-270 | cusS | 2.7.13.3 | T | Member of a two-component regulatory system | |
AIIGCJOP_02480 | 6.6e-122 | KT | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
AIIGCJOP_02481 | 4.7e-252 | cusC | MU | Outer membrane efflux protein | ||
AIIGCJOP_02482 | 4.6e-58 | cusF | S | Copper binding periplasmic protein CusF | ||
AIIGCJOP_02483 | 4.9e-243 | cusB | M | Long alpha hairpin domain of cation efflux system protein, CusB | ||
AIIGCJOP_02484 | 0.0 | cusA | P | AcrB/AcrD/AcrF family | ||
AIIGCJOP_02485 | 4.3e-74 | copG | S | Protein of unknown function, DUF | ||
AIIGCJOP_02486 | 0.0 | pacS | 3.6.3.4, 3.6.3.54 | P | P-type atpase | |
AIIGCJOP_02488 | 1.8e-133 | 2.7.1.50 | M | Peptidase family M23 | ||
AIIGCJOP_02489 | 1.2e-20 | 3.1.2.12 | CE1 | S | Serine hydrolase involved in the detoxification of formaldehyde | |
AIIGCJOP_02490 | 1.5e-60 | L | Resolvase, N terminal domain | |||
AIIGCJOP_02492 | 4.2e-64 | S | Protein of unknown function (DUF2787) | |||
AIIGCJOP_02493 | 9.4e-74 | radC | L | RadC-like JAB domain | ||
AIIGCJOP_02494 | 8.1e-242 | 3.6.4.12 | L | D5 N terminal like | ||
AIIGCJOP_02496 | 0.0 | L | Phage integrase family | |||
AIIGCJOP_02498 | 1.3e-156 | K | AraC-like ligand binding domain | |||
AIIGCJOP_02499 | 7.3e-93 | E | Lysine exporter protein (LYSE YGGA) | |||
AIIGCJOP_02500 | 9.9e-103 | yjdC | K | Transcriptional regulator | ||
AIIGCJOP_02501 | 1.7e-296 | 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 | |
AIIGCJOP_02502 | 5.8e-52 | cutA | 4.2.3.1 | P | Involved in resistance toward heavy metals | |
AIIGCJOP_02503 | 1.7e-222 | dcuA | S | Responsible for the transport of C4-dicarboxylates from the periplasm across the inner membrane | ||
AIIGCJOP_02504 | 1.4e-270 | aspA | 4.3.1.1 | E | Aspartate ammonia-lyase | |
AIIGCJOP_02505 | 2.8e-71 | fxsA | S | protein affecting phage T7 exclusion by the F plasmid | ||
AIIGCJOP_02506 | 3.6e-219 | yjeH | E | amino acid | ||
AIIGCJOP_02507 | 3.1e-44 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
AIIGCJOP_02508 | 7.3e-284 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
AIIGCJOP_02509 | 5.2e-54 | yjeI | S | Membrane | ||
AIIGCJOP_02510 | 2.3e-47 | yjeJ | S | YjeJ-like | ||
AIIGCJOP_02512 | 2.2e-140 | dkgB | 1.1.1.346 | S | reductase | |
AIIGCJOP_02513 | 1.2e-160 | yafC | K | Transcriptional regulator | ||
AIIGCJOP_02514 | 6.8e-199 | ytbD | EGP | Major facilitator Superfamily | ||
AIIGCJOP_02515 | 5.7e-149 | yafD | S | Endonuclease Exonuclease Phosphatase | ||
AIIGCJOP_02516 | 8.8e-131 | yafE | Q | methyltransferase | ||
AIIGCJOP_02517 | 1.5e-211 | mltD | M | COG0741 Soluble lytic murein transglycosylase and related regulatory proteins (some contain LysM invasin domains) | ||
AIIGCJOP_02518 | 2.5e-59 | gloB | 3.1.2.6 | S | Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid | |
AIIGCJOP_02519 | 6.2e-85 | ISPlu13C | L | Transposase | ||
AIIGCJOP_02520 | 7.9e-11 | uvrD-2 | 3.6.4.12 | L | DNA helicase | |
AIIGCJOP_02521 | 4.3e-144 | 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 | |
AIIGCJOP_02522 | 2.7e-51 | glmM | 5.4.2.10 | G | Phosphoglucomutase/phosphomannomutase, alpha/beta/alpha domain I | |
AIIGCJOP_02523 | 2.5e-291 | M | Putative transposase | |||
AIIGCJOP_02524 | 9.1e-36 | |||||
AIIGCJOP_02525 | 1.2e-121 | parA | L | Resolvase, N terminal domain | ||
AIIGCJOP_02526 | 3.2e-41 | S | MbeB-like, N-term conserved region | |||
AIIGCJOP_02527 | 7.9e-21 | S | Relaxase/Mobilisation nuclease domain | |||
AIIGCJOP_02530 | 3.3e-15 | |||||
AIIGCJOP_02531 | 2.9e-36 | ybaQ | K | addiction module antidote protein, HigA family | ||
AIIGCJOP_02532 | 1.9e-47 | S | Bacterial mobilisation protein (MobC) | |||
AIIGCJOP_02533 | 5.2e-145 | csgG | M | Curli production assembly/transport component CsgG | ||
AIIGCJOP_02534 | 3.7e-82 | ycdZ | S | Protein of unknown function (DUF1097) | ||
AIIGCJOP_02535 | 2.9e-99 | ycdY | S | chaperone | ||
AIIGCJOP_02536 | 4.6e-129 | ycdX | E | Belongs to the PHP family | ||
AIIGCJOP_02537 | 3.9e-173 | ghrA | 1.1.1.79, 1.1.1.81 | EH | D-isomer specific 2-hydroxyacid dehydrogenase | |
AIIGCJOP_02539 | 1.6e-163 | V | HNH endonuclease | |||
AIIGCJOP_02540 | 3.8e-280 | O | heat shock protein binding | |||
AIIGCJOP_02541 | 2.5e-50 | symE | J | endoribonuclease activity | ||
AIIGCJOP_02542 | 1.6e-29 | S | PAAR repeat-containing protein | |||
AIIGCJOP_02543 | 7.1e-276 | S | type VI secretion-associated protein | |||
AIIGCJOP_02544 | 0.0 | S | Intracellular multiplication and human macrophage-killing | |||
AIIGCJOP_02547 | 4.1e-18 | S | Domain of unknown function (DUF4123) | |||
AIIGCJOP_02549 | 5.6e-127 | L | transposition, DNA-mediated | |||
AIIGCJOP_02550 | 0.0 | 1.1.1.169, 1.3.1.12, 4.2.1.51, 5.4.99.5 | E | Prephenate dehydrogenase | ||
AIIGCJOP_02551 | 6.7e-38 | S | PAAR motif | |||
AIIGCJOP_02552 | 0.0 | S | Uncharacterized protein conserved in bacteria (DUF2345) | |||
AIIGCJOP_02553 | 0.0 | clpV | O | C-terminal, D2-small domain, of ClpB protein | ||
AIIGCJOP_02554 | 4.1e-89 | hcp | S | Type VI secretion system effector | ||
AIIGCJOP_02555 | 3e-272 | M | Belongs to the ompA family | |||
AIIGCJOP_02556 | 5.1e-122 | S | Type VI secretion system protein DotU | |||
AIIGCJOP_02557 | 2.1e-244 | S | type VI secretion protein | |||
AIIGCJOP_02558 | 2.9e-96 | S | Type VI secretion protein, EvpB/VC_A0108, tail sheath | |||
AIIGCJOP_02559 | 3.1e-122 | S | type VI secretion protein | |||
AIIGCJOP_02560 | 3.7e-50 | S | type VI secretion protein | |||
AIIGCJOP_02561 | 7.5e-75 | tssB | S | Type VI secretion system, VipA, VC_A0107 or Hcp2 | ||
AIIGCJOP_02562 | 3.8e-309 | mppA | E | ABC transporter substrate-binding protein | ||
AIIGCJOP_02563 | 1.3e-136 | mpaA | E | Murein peptide amidase A | ||
AIIGCJOP_02564 | 4.9e-163 | ycjG | 5.1.1.20 | M | Belongs to the mandelate racemase muconate lactonizing enzyme family | |
AIIGCJOP_02565 | 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 | |
AIIGCJOP_02566 | 1.1e-119 | xylR | 5.3.1.12 | K | Transcriptional regulator | |
AIIGCJOP_02567 | 1.9e-196 | G | Protein of unknown function (DUF1593) | |||
AIIGCJOP_02568 | 9.2e-289 | tyrR | K | Transcriptional regulator of aromatic amino acids metabolism | ||
AIIGCJOP_02569 | 7e-163 | ycjF | S | UPF0283 membrane protein | ||
AIIGCJOP_02570 | 7.4e-269 | ycjX | S | COG3106 Predicted ATPase | ||
AIIGCJOP_02571 | 8.2e-169 | ycjW | K | helix_turn _helix lactose operon repressor | ||
AIIGCJOP_02572 | 3.1e-175 | ompG | M | Outer membrane protein G (OmpG) | ||
AIIGCJOP_02573 | 3.5e-194 | msmK | P | Belongs to the ABC transporter superfamily | ||
AIIGCJOP_02574 | 9.8e-102 | pgmB | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | G | beta-phosphoglucomutase |
AIIGCJOP_02575 | 0.0 | ycjT | 2.4.1.230 | GH65 | G | hydrolase family 65, central catalytic |
AIIGCJOP_02576 | 1.2e-183 | ycjS | S | Oxidoreductase family, C-terminal alpha/beta domain | ||
AIIGCJOP_02577 | 6.9e-147 | ycjR | G | isomerase activity | ||
AIIGCJOP_02578 | 3.5e-199 | 1.1.1.2 | E | L-arabinose catabolic process | ||
AIIGCJOP_02579 | 3.6e-146 | ycjP | P | ABC transporter (permease) | ||
AIIGCJOP_02580 | 8.2e-157 | ycjO | P | Binding-protein-dependent transport system inner membrane component | ||
AIIGCJOP_02581 | 1.9e-223 | ycjN | G | Sugar ABC transporter substrate-binding protein | ||
AIIGCJOP_02582 | 1.7e-291 | ycjM | 2.4.1.7 | GH13 | G | Alpha amylase catalytic |
AIIGCJOP_02583 | 1.6e-29 | pspD | S | Phage Shock Protein | ||
AIIGCJOP_02584 | 3.8e-52 | pspC | KT | phage shock protein C | ||
AIIGCJOP_02585 | 3e-31 | pspB | S | Phage shock protein B | ||
AIIGCJOP_02586 | 1.8e-103 | pspA | KT | Phage shock protein A | ||
AIIGCJOP_02587 | 5.1e-168 | pspF | K | transcriptional activator | ||
AIIGCJOP_02588 | 1.6e-302 | sapA | E | ABC transporter substrate-binding protein | ||
AIIGCJOP_02589 | 2.1e-169 | sapB | P | peptide transport system, permease | ||
AIIGCJOP_02590 | 1.2e-142 | sapC | V | peptide transport system, permease | ||
AIIGCJOP_02591 | 1.8e-189 | sapD | P | ATPase activity | ||
AIIGCJOP_02592 | 2e-141 | sapF | P | ATPase activity | ||
AIIGCJOP_02593 | 2.8e-140 | fabI | 1.3.1.10, 1.3.1.9 | I | Enoyl- acyl-carrier-protein reductase NADH | |
AIIGCJOP_02594 | 1.2e-164 | yciW | S | protein conserved in bacteria | ||
AIIGCJOP_02595 | 0.0 | rnb | 3.1.13.1 | J | Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3' to 5' direction | |
AIIGCJOP_02596 | 0.0 | gmr | 3.1.4.52 | T | Diguanylate cyclase | |
AIIGCJOP_02597 | 4e-164 | rpfF | I | Enoyl-CoA hydratase | ||
AIIGCJOP_02598 | 2.4e-18 | yciZ | S | Belongs to the UPF0509 family | ||
AIIGCJOP_02599 | 5.8e-124 | yciT | K | transcriptional regulator | ||
AIIGCJOP_02600 | 1.3e-23 | osmB | M | Lipoprotein | ||
AIIGCJOP_02601 | 3.6e-49 | yciH | J | Translation Initiation Factor | ||
AIIGCJOP_02602 | 9e-125 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
AIIGCJOP_02603 | 2.2e-213 | 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 | ||
AIIGCJOP_02604 | 4.3e-44 | lapA | S | Involved in the assembly of lipopolysaccharide (LPS) | ||
AIIGCJOP_02605 | 1.7e-142 | pgpB | 3.1.3.27, 3.1.3.4, 3.1.3.81, 3.6.1.27 | I | phosphatidylglycerophosphatase | |
AIIGCJOP_02606 | 1.2e-106 | 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 | |
AIIGCJOP_02607 | 0.0 | acnA | 4.2.1.3 | C | Catalyzes the isomerization of citrate to isocitrate via cis-aconitate | |
AIIGCJOP_02608 | 9.6e-183 | cysB | K | transcriptional regulator | ||
AIIGCJOP_02609 | 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 | |
AIIGCJOP_02610 | 1.9e-37 | yciN | S | Protein of unknown function (DUF2498) | ||
AIIGCJOP_02611 | 8.8e-166 | sohB | OU | peptidase | ||
AIIGCJOP_02612 | 4.5e-135 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
AIIGCJOP_02613 | 4.6e-103 | 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 | |
AIIGCJOP_02614 | 5.6e-158 | rluB | 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
AIIGCJOP_02615 | 1.4e-86 | S | Type VI secretion system effector | |||
AIIGCJOP_02616 | 4.5e-78 | S | Protein of unknown function (DUF2778) | |||
AIIGCJOP_02617 | 2.1e-114 | yciO | 2.7.7.87 | J | Belongs to the SUA5 family | |
AIIGCJOP_02618 | 1.5e-155 | trpH | 3.1.3.97 | S | Metal-dependent phosphoesterases (PHP family) | |
AIIGCJOP_02619 | 1.2e-275 | trpE | 4.1.3.27 | H | Anthranilate synthase component | |
AIIGCJOP_02620 | 7.3e-297 | 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) | |
AIIGCJOP_02621 | 1.7e-241 | trpF | 4.1.1.48, 4.2.1.160, 4.2.1.20, 5.3.1.24 | E | Belongs to the TrpC family | |
AIIGCJOP_02622 | 1.3e-226 | trpB | 4.2.1.20 | E | The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine | |
AIIGCJOP_02623 | 2.2e-140 | trpA | 4.2.1.20 | E | The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate | |
AIIGCJOP_02624 | 1.5e-225 | yedE | S | transporter component | ||
AIIGCJOP_02625 | 2.2e-37 | yedF | O | Sulfurtransferase TusA | ||
AIIGCJOP_02626 | 8.1e-39 | S | Bacterial protein of unknown function (DUF883) | |||
AIIGCJOP_02628 | 2.8e-46 | |||||
AIIGCJOP_02629 | 1.4e-21 | |||||
AIIGCJOP_02630 | 6.4e-41 | S | peptidoglycan catabolic process | |||
AIIGCJOP_02632 | 4.2e-61 | NT | transmembrane signaling receptor activity | |||
AIIGCJOP_02633 | 0.0 | NT | Phage-related protein, tail component | |||
AIIGCJOP_02634 | 7.1e-75 | S | Corresponds to locus_tag | |||
AIIGCJOP_02635 | 3.9e-107 | S | peptidoglycan catabolic process | |||
AIIGCJOP_02636 | 4.2e-122 | L | S | TIGRFAM phage minor tail protein L | ||
AIIGCJOP_02637 | 4e-51 | S | Phage minor tail protein | |||
AIIGCJOP_02638 | 0.0 | sca1 | D | Lambda phage tail tape-measure protein (Tape_meas_lam_C) | ||
AIIGCJOP_02639 | 2.1e-37 | GJ12_01675 | S | phage tail assembly protein T | ||
AIIGCJOP_02640 | 5.2e-45 | S | Bacteriophage lambda tail assembly chaperone, TAC, protein G | |||
AIIGCJOP_02641 | 2.9e-115 | S | peptidase activity | |||
AIIGCJOP_02642 | 8.8e-50 | S | Phage minor tail protein U | |||
AIIGCJOP_02643 | 8.1e-70 | JD73_18875 | S | prophage | ||
AIIGCJOP_02644 | 5e-28 | S | ATP-binding sugar transporter from pro-phage | |||
AIIGCJOP_02645 | 3.8e-35 | S | Uncharacterized conserved protein (DUF2190) | |||
AIIGCJOP_02646 | 0.0 | clpP | 3.4.21.92 | E | Clp protease | |
AIIGCJOP_02647 | 7.5e-227 | S | portal protein | |||
AIIGCJOP_02648 | 3e-23 | |||||
AIIGCJOP_02649 | 0.0 | S | Phage terminase large subunit (GpA) | |||
AIIGCJOP_02650 | 2.5e-70 | S | Protein of unknown function (DUF1441) | |||
AIIGCJOP_02651 | 6e-15 | S | Uncharacterized conserved protein (DUF2190) | |||
AIIGCJOP_02652 | 4.6e-09 | gvpU | S | gas vesicle protein | ||
AIIGCJOP_02653 | 5.2e-49 | |||||
AIIGCJOP_02654 | 2.6e-91 | rrrD | 3.2.1.17 | G | lysozyme | |
AIIGCJOP_02655 | 4.3e-36 | essD | S | Bacteriophage P21 holin S | ||
AIIGCJOP_02656 | 3.1e-84 | sppA | OU | Serine dehydrogenase proteinase | ||
AIIGCJOP_02657 | 1.4e-102 | |||||
AIIGCJOP_02658 | 5.3e-168 | ydfU | V | Protein of unknown function (DUF968) | ||
AIIGCJOP_02659 | 8.4e-60 | L | endodeoxyribonuclease RusA | |||
AIIGCJOP_02660 | 1e-14 | |||||
AIIGCJOP_02661 | 1e-34 | dinI | S | SOS response | ||
AIIGCJOP_02662 | 7.5e-46 | |||||
AIIGCJOP_02663 | 6.5e-115 | yhdJ | 2.1.1.72 | L | DNA methylase | |
AIIGCJOP_02664 | 8.6e-20 | |||||
AIIGCJOP_02665 | 1.3e-41 | glpR | GK | Bacterial protein of unknown function (DUF977) | ||
AIIGCJOP_02666 | 3.4e-68 | K | PerC transcriptional activator | |||
AIIGCJOP_02667 | 1.2e-78 | S | Replication protein P | |||
AIIGCJOP_02668 | 7.1e-82 | S | Putative bacterial toxin ydaT | |||
AIIGCJOP_02669 | 3.4e-16 | K | Helix-turn-helix XRE-family like proteins | |||
AIIGCJOP_02670 | 2.2e-07 | |||||
AIIGCJOP_02672 | 2.4e-48 | iscR | 2.8.1.7 | K | Transcriptional regulator | |
AIIGCJOP_02673 | 0.0 | 2.7.7.7 | L | 3' exoribonuclease, RNase T-like | ||
AIIGCJOP_02674 | 7.3e-150 | L | Belongs to the 'phage' integrase family | |||
AIIGCJOP_02675 | 3.3e-115 | ompW | M | outer membrane protein W | ||
AIIGCJOP_02676 | 2.9e-115 | yciC | S | UPF0259 membrane protein | ||
AIIGCJOP_02677 | 1.1e-92 | ispZ | D | probably involved in intracellular septation | ||
AIIGCJOP_02678 | 9.3e-68 | yciA | I | Thioesterase superfamily | ||
AIIGCJOP_02679 | 1.8e-69 | tonB | M | 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 | ||
AIIGCJOP_02680 | 6.8e-47 | yciI | T | YciI from Haemophilus influenzae presents crystal structure similarity to a muconolactone isomerase, but does not seem to catalyze any of the | ||
AIIGCJOP_02681 | 1.6e-104 | leuE | E | Efflux Protein | ||
AIIGCJOP_02682 | 1.2e-19 | |||||
AIIGCJOP_02683 | 1e-276 | 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 | |
AIIGCJOP_02684 | 2.8e-57 | yciU | S | Belongs to the UPF0263 family | ||
AIIGCJOP_02685 | 1.1e-189 | oppF | P | Belongs to the ABC transporter superfamily | ||
AIIGCJOP_02686 | 1.7e-182 | oppD | P | Belongs to the ABC transporter superfamily | ||
AIIGCJOP_02687 | 1.3e-144 | oppC | P | COG1173 ABC-type dipeptide oligopeptide nickel transport systems permease components | ||
AIIGCJOP_02688 | 6.7e-162 | oppB | P | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
AIIGCJOP_02689 | 0.0 | oppA | E | ABC transporter substrate-binding protein | ||
AIIGCJOP_02691 | 2.3e-108 | ychE | U | UPF0056 membrane protein | ||
AIIGCJOP_02692 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
AIIGCJOP_02693 | 1.5e-101 | tdk | 2.7.1.21 | F | thymidine kinase | |
AIIGCJOP_02694 | 5.2e-61 | hns | K | Belongs to the histone-like protein H-NS family | ||
AIIGCJOP_02695 | 2.4e-164 | galU | 2.7.7.9 | M | Utp--glucose-1-phosphate uridylyltransferase | |
AIIGCJOP_02696 | 1.6e-177 | KT | 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 | |||
AIIGCJOP_02697 | 3.1e-151 | rssA | S | Patatin-like phospholipase | ||
AIIGCJOP_02698 | 1.1e-158 | purU | 2.7.7.72, 3.5.1.10 | F | Catalyzes the hydrolysis of 10-formyltetrahydrofolate (formyl-FH4) to formate and tetrahydrofolate (FH4) | |
AIIGCJOP_02701 | 5.9e-71 | lrpC | K | AsnC family transcriptional regulator | ||
AIIGCJOP_02702 | 4.1e-140 | yxxF | EG | EamA-like transporter family | ||
AIIGCJOP_02703 | 2.3e-122 | narI | 1.7.5.1 | C | nitrate reductase, gamma subunit | |
AIIGCJOP_02704 | 2.6e-121 | narJ | 1.7.5.1 | C | nitrate reductase molybdenum cofactor assembly chaperone | |
AIIGCJOP_02705 | 1.1e-310 | narH | 1.7.5.1 | C | nitrate reductase beta subunit | |
AIIGCJOP_02706 | 0.0 | narG | 1.7.5.1 | C | Belongs to the prokaryotic molybdopterin-containing oxidoreductase family | |
AIIGCJOP_02707 | 2e-258 | narK | P | nitrate nitrite transporter | ||
AIIGCJOP_02708 | 3.9e-291 | narX | 2.7.13.3 | T | Histidine kinase | |
AIIGCJOP_02709 | 1.3e-111 | narL | K | response regulator | ||
AIIGCJOP_02710 | 2.7e-234 | ychO | 3.2.1.14 | GH18 | M | entry into host |
AIIGCJOP_02711 | 0.0 | nasA | 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 | |
AIIGCJOP_02712 | 0.0 | nirB | 1.7.1.15 | C | Belongs to the nitrite and sulfite reductase 4Fe-4S domain family | |
AIIGCJOP_02713 | 7.9e-143 | nasD | 3.6.3.36 | P | (ABC) transporter | |
AIIGCJOP_02714 | 1.9e-153 | nasE | P | ABC-type nitrate sulfonate bicarbonate transport system permease component | ||
AIIGCJOP_02715 | 2.4e-234 | nasF | P | COG0715 ABC-type nitrate sulfonate bicarbonate transport systems periplasmic components | ||
AIIGCJOP_02716 | 7.3e-145 | nasR | K | ANTAR | ||
AIIGCJOP_02717 | 1.9e-56 | ychN | P | conserved protein involved in intracellular sulfur reduction | ||
AIIGCJOP_02718 | 2.3e-251 | cheD2 | NT | chemotaxis, protein | ||
AIIGCJOP_02719 | 4.7e-38 | S | Protein involved in biological_process | |||
AIIGCJOP_02720 | 4.1e-127 | 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 | ||
AIIGCJOP_02721 | 4.6e-35 | chaB | K | Might be a regulator of the sodium-potassium proton antiporter ChaA | ||
AIIGCJOP_02722 | 2.6e-184 | chaA | P | Calcium Proton | ||
AIIGCJOP_02723 | 1.4e-156 | M | 2-dehydro-3-deoxyphosphooctonate aldolase | |||
AIIGCJOP_02724 | 2.5e-152 | ychA | S | Transglutaminase-like superfamily | ||
AIIGCJOP_02725 | 1.8e-63 | sirB2 | S | Invasion gene expression up-regulator SirB | ||
AIIGCJOP_02726 | 2.2e-135 | 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 | |
AIIGCJOP_02727 | 1.4e-195 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
AIIGCJOP_02728 | 2.5e-223 | hemA | 1.2.1.70 | H | Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA) | |
AIIGCJOP_02729 | 3.7e-108 | lolB | M | Plays a critical role in the incorporation of lipoproteins in the outer membrane after they are released by the LolA protein | ||
AIIGCJOP_02730 | 4e-156 | 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 | |
AIIGCJOP_02731 | 3.3e-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) | |
AIIGCJOP_02732 | 1.2e-270 | sulP | P | COG0659 Sulfate permease and related transporters (MFS superfamily) | ||
AIIGCJOP_02733 | 1.4e-147 | nolA | K | helix_turn_helix, mercury resistance | ||
AIIGCJOP_02734 | 1.5e-43 | ychH | S | Protein of unknown function (DUF2583) | ||
AIIGCJOP_02735 | 3e-107 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
AIIGCJOP_02736 | 3.2e-203 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
AIIGCJOP_02737 | 1.1e-165 | ftrA | K | Transcriptional regulator containing an amidase domain and an AraC-type DNA-binding HTH domain | ||
AIIGCJOP_02738 | 6.6e-66 | XK27_05625 | P | Rhodanese | ||
AIIGCJOP_02739 | 3.1e-246 | fcy21 | U | Belongs to the purine-cytosine permease (2.A.39) family | ||
AIIGCJOP_02740 | 0.0 | cbbbC | C | Belongs to the prokaryotic molybdopterin-containing oxidoreductase family | ||
AIIGCJOP_02741 | 6.5e-61 | yybH | S | SnoaL-like domain | ||
AIIGCJOP_02742 | 7.1e-69 | |||||
AIIGCJOP_02743 | 2.3e-40 | azlD | S | branched-chain amino acid | ||
AIIGCJOP_02744 | 5.7e-103 | azlC | E | branched-chain amino acid | ||
AIIGCJOP_02745 | 1.1e-43 | S | Fusaric acid resistance protein-like | |||
AIIGCJOP_02746 | 2.8e-171 | catA | 1.13.11.1 | Q | catechol 1,2-dioxygenase | |
AIIGCJOP_02747 | 3e-44 | catC | 5.3.3.4 | Q | muconolactone delta-isomerase | |
AIIGCJOP_02748 | 2.4e-193 | catB | 5.5.1.1 | M | Belongs to the mandelate racemase muconate lactonizing enzyme family | |
AIIGCJOP_02749 | 1.8e-115 | pcaD | 3.1.1.24, 4.1.1.44 | I | 3-oxoadipate enol-lactonase | |
AIIGCJOP_02750 | 2.5e-118 | pcaJ | 2.8.3.6 | I | COG2057 Acyl CoA acetate 3-ketoacid CoA transferase, beta subunit | |
AIIGCJOP_02751 | 1.8e-119 | pcaI | 2.8.3.6 | I | COG1788 Acyl CoA acetate 3-ketoacid CoA transferase, alpha subunit | |
AIIGCJOP_02752 | 1e-232 | EGP | Major facilitator superfamily | |||
AIIGCJOP_02753 | 4.7e-85 | hpaC | 1.5.1.36 | S | Flavin reductase | |
AIIGCJOP_02754 | 1.5e-137 | C | Flavodoxin reductases (Ferredoxin-NADPH reductases) family 1 | |||
AIIGCJOP_02755 | 1.3e-118 | IQ | reductase | |||
AIIGCJOP_02756 | 1.2e-82 | hcaA2 | Q | Aromatic-ring-hydroxylating dioxygenase | ||
AIIGCJOP_02757 | 2.1e-249 | antA | P | Phenylpropionate dioxygenase and related ring-hydroxylating dioxygenases large terminal subunit | ||
AIIGCJOP_02758 | 1.2e-83 | S | SnoaL-like domain | |||
AIIGCJOP_02759 | 1.2e-61 | |||||
AIIGCJOP_02760 | 1.3e-204 | 1.14.13.235 | I | acyl-CoA dehydrogenase | ||
AIIGCJOP_02761 | 1.1e-169 | gatA | 3.5.1.4, 6.3.5.6, 6.3.5.7 | J | Belongs to the amidase family | |
AIIGCJOP_02762 | 7.3e-72 | K | transcriptional regulator | |||
AIIGCJOP_02763 | 5.6e-237 | G | Major facilitator superfamily | |||
AIIGCJOP_02764 | 8.3e-15 | |||||
AIIGCJOP_02765 | 9.2e-125 | S | phage-encoded protein | |||
AIIGCJOP_02766 | 1.6e-154 | S | Zn-dependent hydrolases, including glyoxylases | |||
AIIGCJOP_02767 | 1.4e-139 | S | Protein of unknown function (DUF1264) | |||
AIIGCJOP_02768 | 3.7e-209 | rafY | S | Porin-like glycoporin RafY | ||
AIIGCJOP_02769 | 4e-219 | G | COG2211 Na melibiose symporter and related transporters | |||
AIIGCJOP_02771 | 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 |
AIIGCJOP_02772 | 3e-35 | ymgE | S | transglycosylase associated protein | ||
AIIGCJOP_02773 | 2.8e-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 | ||
AIIGCJOP_02774 | 8.6e-113 | 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 | |
AIIGCJOP_02775 | 1.5e-158 | ldcA | 3.4.17.13 | V | proteins, homologs of microcin C7 resistance protein MccF | |
AIIGCJOP_02776 | 2.4e-311 | nhaP2 | P | K( ) H( ) antiporter that extrudes potassium in exchange for external protons and maintains the internal concentration of potassium under toxic levels | ||
AIIGCJOP_02777 | 1.7e-196 | alr | 5.1.1.1 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
AIIGCJOP_02778 | 1.4e-250 | dadA | 1.4.5.1 | E | Oxidative deamination of D-amino acids | |
AIIGCJOP_02779 | 7.7e-304 | spoVR | S | SpoVR family | ||
AIIGCJOP_02780 | 2e-132 | fadR | K | Multifunctional regulator of fatty acid metabolism | ||
AIIGCJOP_02781 | 9e-236 | nhaB | P | Na( ) H( ) antiporter that extrudes sodium in exchange for external protons | ||
AIIGCJOP_02782 | 1.1e-95 | dsbB | O | Required for disulfide bond formation in some periplasmic proteins. Acts by oxidizing the DsbA protein | ||
AIIGCJOP_02783 | 7.9e-84 | ycgN | S | Belongs to the UPF0260 family | ||
AIIGCJOP_02784 | 7.8e-120 | ycgM | Q | COG0179 2-keto-4-pentenoate hydratase 2-oxohepta-3-ene-1,7-dioic acid hydratase (catechol pathway) | ||
AIIGCJOP_02785 | 3.6e-42 | ycgL | S | YcgL domain-containing protein | ||
AIIGCJOP_02786 | 2.2e-112 | 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 | ||
AIIGCJOP_02787 | 3.3e-144 | minD | D | Belongs to the ParA family | ||
AIIGCJOP_02788 | 2.5e-40 | 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 | ||
AIIGCJOP_02789 | 2.5e-209 | 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 | |
AIIGCJOP_02790 | 0.0 | fadD | 6.2.1.3 | IQ | AMP-binding enzyme C-terminal domain | |
AIIGCJOP_02791 | 9.8e-74 | yeaY | M | Outer Membrane Lipoprotein | ||
AIIGCJOP_02792 | 3.6e-115 | yeaZ | 2.3.1.234 | O | PFAM Peptidase M22, glycoprotease | |
AIIGCJOP_02793 | 0.0 | dinG | 3.6.4.12 | KL | helicase | |
AIIGCJOP_02794 | 5.4e-56 | yoaB | J | Translation Initiation Inhibitor YjgF Family | ||
AIIGCJOP_02795 | 2.7e-22 | yoaH | S | Belongs to the UPF0181 family | ||
AIIGCJOP_02796 | 1.6e-241 | 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 | |
AIIGCJOP_02797 | 3.3e-98 | nudL | L | NUDIX hydrolase | ||
AIIGCJOP_02798 | 2.9e-254 | sdaA | 4.3.1.17 | E | PFAM Serine dehydratase alpha chain | |
AIIGCJOP_02799 | 3.5e-270 | adrB | 3.1.4.52 | T | EAL domain | |
AIIGCJOP_02800 | 1.8e-279 | yoaE | P | membrane protein, terc | ||
AIIGCJOP_02801 | 2e-151 | manX | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
AIIGCJOP_02802 | 8.2e-132 | manY | G | pts system | ||
AIIGCJOP_02803 | 2.5e-155 | manZ | G | PTS system mannose fructose sorbose family IID component | ||
AIIGCJOP_02804 | 4.5e-66 | yobD | S | UPF0266 membrane protein | ||
AIIGCJOP_02805 | 5.5e-104 | mntP | P | Probably functions as a manganese efflux pump | ||
AIIGCJOP_02806 | 4e-142 | rrmA | 2.1.1.187 | Q | Methyl-transferase | |
AIIGCJOP_02807 | 0.0 | ftsI | 3.4.16.4 | M | Catalyzes cross-linking of the peptidoglycan cell wall at the division septum | |
AIIGCJOP_02808 | 1.1e-32 | cspC | K | Cold shock | ||
AIIGCJOP_02809 | 8e-177 | 3.1.4.54 | S | Zn-dependent hydrolases of the beta-lactamase fold | ||
AIIGCJOP_02810 | 4e-36 | yebO | S | YebO-like protein | ||
AIIGCJOP_02811 | 5.3e-34 | yobH | S | YobH-like protein | ||
AIIGCJOP_02812 | 5.6e-141 | kdgR | K | transcriptional regulator | ||
AIIGCJOP_02813 | 1.1e-232 | yebQ | EGP | Major facilitator Superfamily | ||
AIIGCJOP_02814 | 1.5e-150 | htpX | O | Belongs to the peptidase M48B family | ||
AIIGCJOP_02815 | 0.0 | prc | 3.4.21.102 | M | Belongs to the peptidase S41A family | |
AIIGCJOP_02816 | 7.7e-78 | proQ | T | RNA chaperone with significant RNA binding, RNA strand exchange and RNA duplexing activities | ||
AIIGCJOP_02817 | 6.4e-82 | yebR | 1.8.4.14 | T | Domain present in phytochromes and cGMP-specific phosphodiesterases. | |
AIIGCJOP_02818 | 4e-221 | yebS | S | paraquat-inducible protein A | ||
AIIGCJOP_02819 | 0.0 | yebT | Q | paraquat-inducible protein b | ||
AIIGCJOP_02820 | 3.5e-255 | rsmF | 2.1.1.176, 2.1.1.178 | J | Specifically methylates the cytosine at position 1407 (m5C1407) of 16S rRNA | |
AIIGCJOP_02821 | 1.1e-38 | yebV | S | Protein of unknown function (DUF1480) | ||
AIIGCJOP_02822 | 1.1e-29 | yebW | S | Protein of unknown function (DUF1482) | ||
AIIGCJOP_02823 | 7.4e-107 | pphA | 3.1.3.16 | T | Serine Threonine protein | |
AIIGCJOP_02824 | 1.4e-149 | virK | S | protein conserved in bacteria | ||
AIIGCJOP_02825 | 1e-54 | yebY | S | Protein of unknown function (DUF2511) | ||
AIIGCJOP_02826 | 5.6e-134 | yebZ | P | copper resistance protein | ||
AIIGCJOP_02827 | 6.4e-47 | yobA | S | Resistance protein | ||
AIIGCJOP_02828 | 2.5e-33 | holE | 2.7.7.7 | L | DNA polymerase III | |
AIIGCJOP_02829 | 2.4e-95 | yobB | 6.3.5.1 | S | Protein involved in hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds and nitrogen compound metabolic process | |
AIIGCJOP_02830 | 3.9e-127 | exoX | L | 3'-5' exonuclease activity on single or double-strand DNA | ||
AIIGCJOP_02831 | 0.0 | ptrB | 3.4.21.83 | E | Protease II | |
AIIGCJOP_02832 | 1.9e-102 | yebE | S | protein conserved in bacteria | ||
AIIGCJOP_02833 | 3.8e-49 | yebF | S | YebF-like protein | ||
AIIGCJOP_02834 | 1e-202 | 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 | |
AIIGCJOP_02835 | 4.8e-114 | eda | 4.1.2.14, 4.1.3.42 | G | Aldolase | |
AIIGCJOP_02836 | 0.0 | edd | 4.2.1.12 | EG | Belongs to the IlvD Edd family | |
AIIGCJOP_02837 | 4.2e-283 | zwf | 1.1.1.363, 1.1.1.49 | H | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
AIIGCJOP_02838 | 1.5e-150 | hexR | K | transcriptional regulator | ||
AIIGCJOP_02839 | 6.9e-262 | pyk | 2.7.1.40 | G | Belongs to the pyruvate kinase family | |
AIIGCJOP_02840 | 5.6e-183 | 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 | |
AIIGCJOP_02841 | 6.1e-241 | yebA | M | COG0739 Membrane proteins related to metalloendopeptidases | ||
AIIGCJOP_02842 | 2.9e-158 | znuA | P | Zinc-uptake complex component A periplasmic | ||
AIIGCJOP_02843 | 2.1e-137 | znuC | P | Part of the ABC transporter complex ZnuABC involved in zinc import. Responsible for energy coupling to the transport system | ||
AIIGCJOP_02844 | 1.3e-110 | znuB | P | COG1108 ABC-type Mn2 Zn2 transport systems permease components | ||
AIIGCJOP_02845 | 1.1e-184 | 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 | |
AIIGCJOP_02846 | 4.7e-103 | 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 | |
AIIGCJOP_02847 | 2.8e-88 | 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 | |
AIIGCJOP_02848 | 3.1e-125 | yebC | K | transcriptional regulatory protein | ||
AIIGCJOP_02849 | 2e-74 | nudB | 2.3.1.181, 3.6.1.13, 3.6.1.55, 3.6.1.67 | L | NUDIX domain | |
AIIGCJOP_02850 | 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) | |
AIIGCJOP_02851 | 2.6e-95 | yecD | Q | Isochorismatase family | ||
AIIGCJOP_02852 | 8.6e-13 | yecE | S | Protein of unknown function DUF72 | ||
AIIGCJOP_02853 | 1e-32 | S | DinI-like family | |||
AIIGCJOP_02855 | 1.8e-64 | S | N-acetylmuramoyl-L-alanine amidase activity | |||
AIIGCJOP_02857 | 2.1e-60 | NT | transmembrane signaling receptor activity | |||
AIIGCJOP_02858 | 0.0 | NT | Phage-related protein, tail component | |||
AIIGCJOP_02861 | 4.7e-76 | S | virus tail assembly | |||
AIIGCJOP_02862 | 1.4e-135 | 3.5.1.28 | M | JAB/MPN domain | ||
AIIGCJOP_02863 | 4.4e-135 | S | Phage minor tail protein L | |||
AIIGCJOP_02864 | 2e-55 | S | Phage minor tail protein | |||
AIIGCJOP_02865 | 2.7e-150 | M | tape measure protein | |||
AIIGCJOP_02867 | 3.4e-21 | S | Protein of unknown function (DUF4035) | |||
AIIGCJOP_02868 | 1.5e-33 | S | Phage tail assembly chaperone | |||
AIIGCJOP_02869 | 3.6e-55 | |||||
AIIGCJOP_02870 | 1e-51 | S | Protein of unknown function (DUF3168) | |||
AIIGCJOP_02871 | 1.5e-74 | S | Bacteriophage HK97-gp10, putative tail-component | |||
AIIGCJOP_02872 | 2.8e-36 | S | Phage head-tail joining protein | |||
AIIGCJOP_02873 | 1.1e-47 | S | Phage gp6-like head-tail connector protein | |||
AIIGCJOP_02874 | 3.3e-07 | |||||
AIIGCJOP_02875 | 1.5e-212 | xkdG | S | capsid protein | ||
AIIGCJOP_02876 | 4.1e-137 | clpP | 3.4.21.92 | OU | ATP-dependent Clp protease proteolytic subunit | |
AIIGCJOP_02877 | 2.7e-233 | S | Phage portal protein, HK97 family | |||
AIIGCJOP_02878 | 4.6e-289 | S | Phage Terminase | |||
AIIGCJOP_02879 | 4.1e-70 | S | Phage terminase, small subunit | |||
AIIGCJOP_02880 | 2e-31 | L | NUMOD4 domain protein | |||
AIIGCJOP_02881 | 6.2e-55 | L | Endonuclease | |||
AIIGCJOP_02883 | 6.2e-78 | S | Phage regulatory protein Rha (Phage_pRha) | |||
AIIGCJOP_02884 | 1e-20 | |||||
AIIGCJOP_02885 | 9e-98 | S | secretion activating protein | |||
AIIGCJOP_02886 | 9.1e-17 | S | Putative 3TM holin, Phage_holin_3 | |||
AIIGCJOP_02887 | 1.3e-08 | S | Putative phage holin | |||
AIIGCJOP_02888 | 7.1e-40 | L | COG2801 Transposase and inactivated derivatives | |||
AIIGCJOP_02889 | 2.2e-156 | L | Transposase and inactivated derivatives | |||
AIIGCJOP_02890 | 7e-26 | |||||
AIIGCJOP_02892 | 3.5e-106 | rlfA | S | Protein of unknown function (DUF3800) | ||
AIIGCJOP_02893 | 8.4e-100 | O | Antitermination protein | |||
AIIGCJOP_02894 | 9.2e-49 | S | sequence-specific DNA binding transcription factor activity | |||
AIIGCJOP_02895 | 6.5e-155 | S | Zinc-binding domain of primase-helicase | |||
AIIGCJOP_02896 | 1.1e-273 | res | L | helicase | ||
AIIGCJOP_02897 | 1.2e-14 | croE | S | protein conserved in bacteria, prophage-related | ||
AIIGCJOP_02898 | 3.7e-23 | KT | Peptidase S24-like | |||
AIIGCJOP_02902 | 1.1e-41 | |||||
AIIGCJOP_02903 | 8.3e-27 | |||||
AIIGCJOP_02904 | 5e-15 | |||||
AIIGCJOP_02905 | 1.3e-37 | |||||
AIIGCJOP_02906 | 4.3e-142 | S | ORF6N domain | |||
AIIGCJOP_02907 | 9.4e-10 | |||||
AIIGCJOP_02908 | 2.7e-33 | S | Putative excisionase (DUF1233) | |||
AIIGCJOP_02909 | 3.6e-241 | intR | L | Pfam:DUF3596 | ||
AIIGCJOP_02910 | 4.7e-134 | yecE | S | Protein of unknown function DUF72 | ||
AIIGCJOP_02911 | 6e-67 | yecN | S | relative of glutathione S-transferase, MAPEG superfamily | ||
AIIGCJOP_02912 | 4.6e-137 | cmoA | Q | Catalyzes the conversion of S-adenosyl-L-methionine (SAM) to carboxy-S-adenosyl-L-methionine (Cx-SAM) | ||
AIIGCJOP_02913 | 1.2e-182 | 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 | ||
AIIGCJOP_02914 | 2.8e-126 | cutC | P | Participates in the control of copper homeostasis | ||
AIIGCJOP_02915 | 8.2e-102 | yecM | S | protein conserved in bacteria | ||
AIIGCJOP_02916 | 0.0 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
AIIGCJOP_02917 | 1.7e-223 | yesR | 3.2.1.172 | GH105 | S | Glycosyl Hydrolase Family 88 |
AIIGCJOP_02918 | 4.9e-293 | G | Major Facilitator | |||
AIIGCJOP_02919 | 1.3e-29 | yhaI | S | Protein of unknown function (DUF805) | ||
AIIGCJOP_02920 | 8.2e-12 | |||||
AIIGCJOP_02921 | 1.3e-61 | flhE | N | Flagellar protein flhE | ||
AIIGCJOP_02922 | 0.0 | flhA | N | Required for formation of the rod structure of the flagellar apparatus. Together with FliI and FliH, may constitute the export apparatus of flagellin | ||
AIIGCJOP_02923 | 4.6e-208 | flhB | N | Required for formation of the rod structure in the basal body of the flagellar apparatus. Together with FliI and FliH, may constitute the export apparatus of flagellin | ||
AIIGCJOP_02924 | 1.2e-109 | cheZ | NT | Plays an important role in bacterial chemotaxis signal transduction pathway by accelerating the dephosphorylation of phosphorylated CheY (CheY-P) | ||
AIIGCJOP_02925 | 6.1e-64 | KT | Chemotaxis regulator that, when phosphorylated, interacts with the flagellar motor causing the flagella to spin clockwise which causes the cell to tumble | |||
AIIGCJOP_02926 | 3.9e-190 | cheB | 3.1.1.61, 3.5.1.44 | NT | catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR | |
AIIGCJOP_02927 | 6.6e-159 | cheR | 2.1.1.80 | NT | Methylation of the membrane-bound methyl-accepting chemotaxis proteins (MCP) to form gamma-glutamyl methyl ester residues in MCP | |
AIIGCJOP_02928 | 1.2e-150 | tap | NT | chemotaxis | ||
AIIGCJOP_02929 | 4.6e-193 | tar | NT | chemotaxis, protein | ||
AIIGCJOP_02930 | 3.5e-145 | csuE | S | spore coat U domain protein | ||
AIIGCJOP_02931 | 0.0 | csuD | M | Fimbrial biogenesis outer membrane usher protein | ||
AIIGCJOP_02932 | 1.7e-110 | csuC | M | chaperone | ||
AIIGCJOP_02933 | 1.8e-69 | csuB | S | Spore Coat Protein U domain | ||
AIIGCJOP_02934 | 2.4e-85 | csuA | S | spore coat U domain protein | ||
AIIGCJOP_02935 | 4.8e-85 | cheW | NT | chemotaxis signal transduction protein | ||
AIIGCJOP_02936 | 0.0 | cheA | 2.7.13.3 | T | COG0643 Chemotaxis protein histidine kinase and related kinases | |
AIIGCJOP_02937 | 2.9e-168 | motB | N | Flagellar Motor Protein | ||
AIIGCJOP_02938 | 5.5e-153 | motA | N | With MotB forms the ion channels that couple flagellar rotation to proton sodium motive force across the membrane and forms the stator elements of the rotary flagellar machine | ||
AIIGCJOP_02939 | 1.8e-104 | flhC | K | Functions in complex with FlhD as a master transcriptional regulator that regulates transcription of several flagellar and non-flagellar operons by binding to their promoter region. Activates expression of class 2 flagellar genes, including fliA, which is a flagellum-specific sigma factor that turns on the class 3 genes. Also regulates genes whose products function in a variety of physiological pathways | ||
AIIGCJOP_02940 | 6.8e-54 | flhD | K | Functions in complex with FlhC as a master transcriptional regulator that regulates transcription of several flagellar and non-flagellar operons by binding to their promoter region. Activates expression of class 2 flagellar genes, including fliA, which is a flagellum-specific sigma factor that turns on the class 3 genes. Also regulates genes whose products function in a variety of physiological pathways | ||
AIIGCJOP_02941 | 1.4e-64 | uspC | T | Required for resistance to DNA-damaging agents | ||
AIIGCJOP_02942 | 2.4e-267 | 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 |
AIIGCJOP_02943 | 6.4e-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 |
AIIGCJOP_02944 | 2.6e-156 | araH | G | Belongs to the binding-protein-dependent transport system permease family | ||
AIIGCJOP_02945 | 6.7e-284 | 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 | |
AIIGCJOP_02946 | 3.3e-183 | araF | G | l-arabinose-binding periplasmic protein | ||
AIIGCJOP_02947 | 5.8e-92 | thiJ | 2.7.11.1, 3.5.1.124 | S | Thij pfpi | |
AIIGCJOP_02948 | 9.6e-78 | ftnA | 1.16.3.2 | P | Iron-storage protein | |
AIIGCJOP_02949 | 2.3e-35 | yecJ | S | Protein of unknown function (DUF2766) | ||
AIIGCJOP_02950 | 2.7e-242 | EGP | Major facilitator Superfamily | |||
AIIGCJOP_02951 | 7.8e-117 | YPO1991 | 5.3.1.26, 5.3.1.6 | G | isomerase | |
AIIGCJOP_02952 | 2.9e-41 | yecR | S | YecR-like lipoprotein | ||
AIIGCJOP_02953 | 4.3e-86 | ftnA | 1.16.3.2 | P | Iron-storage protein | |
AIIGCJOP_02954 | 3.8e-32 | yecH | S | Protein of unknown function (DUF2492) | ||
AIIGCJOP_02955 | 3e-54 | |||||
AIIGCJOP_02956 | 5.7e-209 | tyrP | E | amino acid | ||
AIIGCJOP_02957 | 2.5e-126 | yecA | C | Belongs to the UPF0149 family | ||
AIIGCJOP_02958 | 5.3e-209 | livJ | E | With LivFGHM is involved in the high affinity leucine transport | ||
AIIGCJOP_02959 | 1.3e-160 | livH | E | Belongs to the binding-protein-dependent transport system permease family | ||
AIIGCJOP_02960 | 1.5e-220 | livM | U | Belongs to the binding-protein-dependent transport system permease family | ||
AIIGCJOP_02961 | 9.3e-161 | livG | E | Part of the ABC transporter complexes LivFGHMJ and LivFGHMK involved in the high-affinity transport of branched-chain amino acids | ||
AIIGCJOP_02962 | 5.7e-124 | livF | P | Branched-chain amino acid transport | ||
AIIGCJOP_02963 | 4.7e-272 | 2.7.8.42, 2.7.8.43 | S | membrane-associated metal-dependent hydrolase | ||
AIIGCJOP_02964 | 4.2e-38 | copZ | P | Heavy-metal-associated domain | ||
AIIGCJOP_02965 | 3.5e-50 | S | mercuric transport protein | |||
AIIGCJOP_02966 | 6.5e-215 | E | Transglutaminase-like enzymes | |||
AIIGCJOP_02967 | 8.2e-174 | lsrB_2 | G | (ABC) transporter | ||
AIIGCJOP_02968 | 1.1e-249 | 3.6.3.17 | G | ABC transporter | ||
AIIGCJOP_02969 | 8.8e-160 | U | Belongs to the binding-protein-dependent transport system permease family | |||
AIIGCJOP_02970 | 4.3e-151 | G | Belongs to the binding-protein-dependent transport system permease family | |||
AIIGCJOP_02975 | 9.1e-98 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
AIIGCJOP_02976 | 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 | ||
AIIGCJOP_02977 | 2.2e-82 | uvrY | K | response regulator | ||
AIIGCJOP_02978 | 2.1e-155 | K | transcriptional regulator | |||
AIIGCJOP_02979 | 3.1e-153 | yhhW_1 | S | Pirin C-terminal cupin domain | ||
AIIGCJOP_02980 | 4.9e-101 | Q | COG1335 Amidases related to nicotinamidase | |||
AIIGCJOP_02982 | 8e-139 | L | Transposase IS66 family | |||
AIIGCJOP_02983 | 6.1e-48 | L | IS1 transposase | |||
AIIGCJOP_02984 | 2.1e-48 | L | cog cog1662 | |||
AIIGCJOP_02985 | 3.3e-112 | L | Transposase and inactivated derivatives | |||
AIIGCJOP_02986 | 1.9e-40 | L | Transposase | |||
AIIGCJOP_02987 | 7.2e-64 | S | Domain of unknown function (DUF4385) | |||
AIIGCJOP_02988 | 2.7e-233 | kgtP | EGP | transporter | ||
AIIGCJOP_02989 | 9e-53 | yfiM | S | Required for high salt suppression of motility | ||
AIIGCJOP_02990 | 1.6e-257 | 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 | |
AIIGCJOP_02991 | 0.0 | yfiQ | C | Acyl-CoA synthetase (NDP forming) | ||
AIIGCJOP_02992 | 1.3e-117 | yfiP | S | DTW domain containing protein | ||
AIIGCJOP_02993 | 1.5e-76 | trxC | 1.8.1.8 | O | Thioredoxin | |
AIIGCJOP_02994 | 1.3e-183 | yfiF | 2.1.1.185, 2.1.1.34 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
AIIGCJOP_02995 | 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 | |
AIIGCJOP_02996 | 3.9e-63 | grcA | 1.14.13.236 | S | Acts as a radical domain for damaged PFL and possibly other radical proteins | |
AIIGCJOP_02997 | 4.3e-210 | srmB | 3.6.4.13 | F | 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 | |
AIIGCJOP_02998 | 1.5e-127 | yfiC | 2.1.1.223, 2.1.1.72 | J | Specifically methylates the adenine in position 37 of tRNA(1)(Val) (anticodon cmo5UAC) | |
AIIGCJOP_02999 | 7.9e-307 | nadB | 1.3.5.4, 1.4.3.16 | H | Catalyzes the oxidation of L-aspartate to iminoaspartate | |
AIIGCJOP_03000 | 3.5e-100 | rpoE | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
AIIGCJOP_03001 | 3.5e-88 | 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 | ||
AIIGCJOP_03002 | 1.4e-165 | rseB | T | Negative regulator of sigma E activity | ||
AIIGCJOP_03003 | 8e-74 | rseC | T | Positive regulator of | ||
AIIGCJOP_03004 | 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 | ||
AIIGCJOP_03005 | 3e-184 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
AIIGCJOP_03006 | 7.8e-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 | |
AIIGCJOP_03007 | 2.5e-169 | era | J | 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 | ||
AIIGCJOP_03008 | 4.4e-115 | recO | 2.6.99.2 | L | Involved in DNA repair and RecF pathway recombination | |
AIIGCJOP_03009 | 6.2e-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 | |
AIIGCJOP_03010 | 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 | |
AIIGCJOP_03011 | 1.9e-45 | yfhL | C | Ferredoxin | ||
AIIGCJOP_03012 | 2.9e-143 | yfhH | K | Transcriptional regulator | ||
AIIGCJOP_03013 | 4.4e-150 | 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. 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 | |
AIIGCJOP_03014 | 3.8e-230 | ybbF | 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 | |
AIIGCJOP_03015 | 1.9e-118 | yfhB | 3.1.3.27 | E | HAD superfamily (Subfamily IF) hydrolase, YfhB | |
AIIGCJOP_03016 | 4.2e-87 | tadA | 3.4.17.13, 3.5.4.1, 3.5.4.3, 3.5.4.33, 3.8.1.5 | F | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
AIIGCJOP_03017 | 4.5e-275 | 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 | ||
AIIGCJOP_03018 | 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 | |
AIIGCJOP_03019 | 1.3e-228 | T | PhoQ Sensor | |||
AIIGCJOP_03020 | 5.8e-122 | yfhG | NU | YfhG lipoprotein | ||
AIIGCJOP_03021 | 2.4e-245 | yfhA | T | COG2204 Response regulator containing CheY-like receiver, AAA-type ATPase, and DNA-binding domains | ||
AIIGCJOP_03022 | 2e-55 | glnB | K | nitrogen regulatory protein P-II | ||
AIIGCJOP_03023 | 6.8e-215 | 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 | |
AIIGCJOP_03024 | 2.3e-237 | 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 | |
AIIGCJOP_03025 | 4.9e-67 | yphA | S | SURF4 family | ||
AIIGCJOP_03026 | 9.3e-188 | yphH | 2.7.1.2 | GK | ROK family | |
AIIGCJOP_03027 | 0.0 | S | Domain of unknown function (DUF5107) | |||
AIIGCJOP_03028 | 6.1e-234 | EGP | Major facilitator Superfamily | |||
AIIGCJOP_03029 | 2.8e-106 | yphB | 5.1.3.3 | G | Aldose 1-epimerase | |
AIIGCJOP_03030 | 1.5e-203 | hcaT | 1.5.1.2 | EGP | Major facilitator Superfamily | |
AIIGCJOP_03031 | 6.8e-229 | csiE | K | Stationary phase inducible protein CsiE | ||
AIIGCJOP_03032 | 3.3e-107 | MA20_06510 | 2.7.4.1 | S | transport system periplasmic component | |
AIIGCJOP_03033 | 3.4e-164 | yohM | P | Belongs to the NiCoT transporter (TC 2.A.52) family | ||
AIIGCJOP_03035 | 2e-146 | suhB | 3.1.3.25 | G | Inositol monophosphatase | |
AIIGCJOP_03036 | 2.3e-128 | 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 | |
AIIGCJOP_03037 | 6.1e-85 | 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 | |
AIIGCJOP_03038 | 9e-231 | 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 | |
AIIGCJOP_03039 | 8.5e-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 | ||
AIIGCJOP_03040 | 2.4e-53 | iscA | C | iron-sulfur cluster assembly protein | ||
AIIGCJOP_03041 | 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 | ||
AIIGCJOP_03042 | 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 | ||
AIIGCJOP_03043 | 6.7e-59 | fdx | C | Ferredoxin, 2Fe-2S type, ISC system | ||
AIIGCJOP_03044 | 4.9e-33 | iscX | S | Fe-S assembly protein IscX | ||
AIIGCJOP_03045 | 1.1e-239 | pepB | 3.4.11.1, 3.4.11.23 | E | Probably plays an important role in intracellular peptide degradation | |
AIIGCJOP_03046 | 1.6e-140 | sseB | S | enhanced serine sensitivity protein SseB | ||
AIIGCJOP_03047 | 4.4e-130 | K | Transcriptional regulator | |||
AIIGCJOP_03048 | 6.9e-161 | sseA | 2.8.1.1, 2.8.1.2 | P | sulfurtransferase | |
AIIGCJOP_03049 | 8.5e-262 | malH | 3.2.1.122, 3.2.1.86 | GH4,GT4 | G | 6-phospho-alpha-glucosidase |
AIIGCJOP_03050 | 2.6e-275 | 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | PTS system | ||
AIIGCJOP_03051 | 0.0 | yfhM | P | Large extracellular alpha-helical protein | ||
AIIGCJOP_03052 | 0.0 | pbpC | 2.4.1.129 | GT51 | M | penicillin-binding protein 1C |
AIIGCJOP_03053 | 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 | |
AIIGCJOP_03054 | 6.2e-221 | rlmN | 2.1.1.192 | J | Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs | |
AIIGCJOP_03055 | 3.4e-122 | rodZ | S | Cytoskeletal protein that is involved in cell-shape control through regulation of the length of the long axis | ||
AIIGCJOP_03056 | 1.1e-203 | 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 | |
AIIGCJOP_03057 | 5.9e-241 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
AIIGCJOP_03058 | 9.3e-99 | yfgM | S | Tetratricopeptide repeat-like domain | ||
AIIGCJOP_03059 | 8.1e-168 | 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 | ||
AIIGCJOP_03060 | 1.8e-265 | der | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | ||
AIIGCJOP_03061 | 7.6e-283 | dtpT | U | Proton-dependent permease that transports di- and tripeptides | ||
AIIGCJOP_03062 | 3.5e-159 | S | Protein involved in oxidoreductase activity | |||
AIIGCJOP_03063 | 1.1e-33 | yfgJ | S | zinc-ribbons | ||
AIIGCJOP_03064 | 1.7e-49 | |||||
AIIGCJOP_03065 | 2.2e-185 | prt1 | E | Zinc metalloprotease (Elastase) | ||
AIIGCJOP_03066 | 1.2e-147 | EGP | Major facilitator Superfamily | |||
AIIGCJOP_03067 | 5.3e-195 | 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 | |
AIIGCJOP_03068 | 1.2e-266 | 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 | |
AIIGCJOP_03069 | 1.3e-309 | guaA | 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
AIIGCJOP_03070 | 8.3e-118 | S | Alpha/beta hydrolase family | |||
AIIGCJOP_03071 | 2.9e-30 | S | Protein of unknown function (DUF1471) | |||
AIIGCJOP_03072 | 2.5e-80 | |||||
AIIGCJOP_03073 | 3.4e-116 | IQ | reductase | |||
AIIGCJOP_03074 | 1.3e-186 | P | Major facilitator superfamily | |||
AIIGCJOP_03075 | 3.6e-136 | cysL_1 | K | transcriptional regulator | ||
AIIGCJOP_03076 | 0.0 | yfgF | T | phosphodiesterase | ||
AIIGCJOP_03077 | 5.6e-270 | ppx | 3.6.1.11, 3.6.1.40 | FP | Belongs to the GppA Ppx family | |
AIIGCJOP_03078 | 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) | |
AIIGCJOP_03079 | 3.4e-112 | 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 | |
AIIGCJOP_03080 | 4.1e-192 | purM | 6.3.3.1, 6.3.4.13 | F | AIR synthase related protein, N-terminal domain | |
AIIGCJOP_03081 | 1.9e-288 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AIIGCJOP_03082 | 1.4e-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 | |
AIIGCJOP_03083 | 2.4e-226 | uraA | F | Xanthine uracil | ||
AIIGCJOP_03084 | 2e-126 | 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 | ||
AIIGCJOP_03085 | 3.2e-51 | arsC | 1.20.4.1 | P | arsenate reductase | |
AIIGCJOP_03086 | 4.5e-261 | 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 | ||
AIIGCJOP_03087 | 3.7e-172 | perM | S | permease | ||
AIIGCJOP_03088 | 1.5e-85 | bcp | 1.11.1.15 | O | PFAM alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen | |
AIIGCJOP_03089 | 3.8e-99 | gcvR | E | glycine cleavage system | ||
AIIGCJOP_03090 | 5.8e-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) | |
AIIGCJOP_03091 | 4.7e-180 | 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 | ||
AIIGCJOP_03092 | 7.4e-132 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
AIIGCJOP_03093 | 9.5e-142 | ypfJ | S | Putative neutral zinc metallopeptidase | ||
AIIGCJOP_03094 | 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) | |
AIIGCJOP_03095 | 4.8e-120 | ypfH | S | Phospholipase Carboxylesterase | ||
AIIGCJOP_03096 | 2.3e-30 | ypfN | S | Uncharacterised protein family (UPF0370) | ||
AIIGCJOP_03097 | 9.6e-219 | 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 | |
AIIGCJOP_03098 | 9.9e-61 | yffB | 1.20.4.1 | P | Belongs to the ArsC family | |
AIIGCJOP_03099 | 0.0 | acrD | V | Belongs to the resistance-nodulation-cell division (RND) (TC 2.A.6) family | ||
AIIGCJOP_03100 | 1.8e-269 | narQ | 2.7.13.3 | T | Histidine kinase | |
AIIGCJOP_03101 | 0.0 | gltD | 1.4.1.13, 1.4.1.14 | C | Glutamate synthase | |
AIIGCJOP_03102 | 1.1e-96 | nudK | 3.6.1.13 | L | GDP-mannose pyrophosphatase | |
AIIGCJOP_03103 | 4.2e-184 | ypfG | S | Protein of unknown function (DUF1176) | ||
AIIGCJOP_03104 | 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 | |
AIIGCJOP_03105 | 5.9e-169 | tal | 2.2.1.2 | G | Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway | |
AIIGCJOP_03106 | 0.0 | maeB | 1.1.1.38, 1.1.1.40, 2.3.1.8 | C | Malic enzyme | |
AIIGCJOP_03107 | 1.7e-170 | 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 | |
AIIGCJOP_03108 | 1.7e-154 | amiA | 3.5.1.28 | M | N-acetylmuramoyl-L-alanine amidase | |
AIIGCJOP_03109 | 6.9e-77 | ypeA | K | Belongs to the acetyltransferase family. YpeA subfamily | ||
AIIGCJOP_03110 | 2.9e-73 | yfeZ | S | Protein of unknown function (DUF2919) | ||
AIIGCJOP_03111 | 1.5e-95 | yfeY | S | Protein of unknown function (DUF1131) | ||
AIIGCJOP_03112 | 1.8e-167 | yfeX | P | peroxidase | ||
AIIGCJOP_03113 | 7.2e-189 | cysP | P | Thiosulfate transporter subunit | ||
AIIGCJOP_03114 | 1.4e-145 | cysT | P | sulfate ABC transporter | ||
AIIGCJOP_03115 | 6.2e-157 | cysW | P | (ABC) transporter | ||
AIIGCJOP_03116 | 3.1e-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 | |
AIIGCJOP_03117 | 1.2e-163 | cysM | 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
AIIGCJOP_03118 | 3.7e-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 | |
AIIGCJOP_03119 | 4.3e-86 | crr | G | pts system | ||
AIIGCJOP_03120 | 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) | |
AIIGCJOP_03121 | 1.1e-37 | ptsH | 2.7.1.121, 2.7.1.202 | G | PTS HPr component phosphorylation site | |
AIIGCJOP_03122 | 5.1e-176 | cysK | 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
AIIGCJOP_03123 | 2e-143 | cysZ | U | High affinity, high specificity proton-dependent sulfate transporter, which mediates sulfate uptake. Provides the sulfur source for the cysteine synthesis pathway | ||
AIIGCJOP_03124 | 1e-110 | 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 | ||
AIIGCJOP_03125 | 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 | |
AIIGCJOP_03126 | 6.9e-33 | ypeB | 2.7.7.7 | S | protein conserved in bacteria | |
AIIGCJOP_03127 | 9.5e-170 | yfeH | S | Bile acid sodium symporter | ||
AIIGCJOP_03128 | 4.5e-153 | yfeR | K | transcriptional regulator | ||
AIIGCJOP_03134 | 7.2e-280 | 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) | |
AIIGCJOP_03135 | 1.2e-51 | yfeD | L | Putative transcription regulator (DUF1323) | ||
AIIGCJOP_03136 | 4.2e-51 | yfeC | L | Negative Regulator | ||
AIIGCJOP_03139 | 0.0 | yfeA | T | cyclic-guanylate-specific phosphodiesterase activity | ||
AIIGCJOP_03140 | 1.4e-196 | nupC | P | Belongs to the concentrative nucleoside transporter (CNT) (TC 2.A.41) family | ||
AIIGCJOP_03141 | 3.8e-208 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
AIIGCJOP_03142 | 1.5e-24 | ypeC | S | Protein of unknown function (DUF2502) | ||
AIIGCJOP_03143 | 2e-180 | yghZ | C | reductase | ||
AIIGCJOP_03144 | 1.5e-308 | ipdC | 4.1.1.74 | GH | Belongs to the TPP enzyme family | |
AIIGCJOP_03145 | 1.2e-201 | yfeO | P | ion-transport protein | ||
AIIGCJOP_03146 | 2.1e-182 | glk | 2.7.1.2 | F | Belongs to the bacterial glucokinase family | |
AIIGCJOP_03147 | 1.9e-127 | ypdB | K | response regulator | ||
AIIGCJOP_03148 | 1.1e-303 | ypdA | 2.7.13.3 | T | Histidine kinase | |
AIIGCJOP_03149 | 9.2e-239 | yfdZ | 2.6.1.83 | E | aminotransferase | |
AIIGCJOP_03150 | 1.3e-157 | 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) | |
AIIGCJOP_03151 | 2.7e-221 | |||||
AIIGCJOP_03153 | 0.0 | murF | 3.4.16.4, 6.3.2.10, 6.3.2.29, 6.3.2.30 | M | Bacterial capsule synthesis protein PGA_cap | |
AIIGCJOP_03154 | 1.6e-134 | S | alpha beta | |||
AIIGCJOP_03155 | 1.8e-306 | M | Pfam Methyltransferase | |||
AIIGCJOP_03156 | 6.7e-114 | S | Periplasmic Protein | |||
AIIGCJOP_03157 | 0.0 | lapD | T | GGDEF domain | ||
AIIGCJOP_03158 | 4.7e-52 | S | Tryptophan synthase subunit beta | |||
AIIGCJOP_03160 | 7.3e-191 | 3.4.21.10 | Q | calcium- and calmodulin-responsive adenylate cyclase activity | ||
AIIGCJOP_03161 | 1.5e-234 | aggA | MU | type I secretion outer membrane protein, TolC | ||
AIIGCJOP_03162 | 0.0 | lapB | V | COG2274 ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
AIIGCJOP_03163 | 1.7e-206 | lapC | M | Type I secretion membrane fusion protein, HlyD | ||
AIIGCJOP_03164 | 4.6e-70 | yaiL | S | Uncharacterized protein conserved in bacteria (DUF2058) | ||
AIIGCJOP_03165 | 1.8e-69 | 3.5.1.19 | Q | Isochorismatase family | ||
AIIGCJOP_03166 | 5.7e-155 | fliC1 | N | Flagellin is the subunit protein which polymerizes to form the filaments of bacterial flagella | ||
AIIGCJOP_03169 | 2.5e-151 | yfdC | P | Formate nitrite | ||
AIIGCJOP_03170 | 1.5e-143 | vacJ | M | Lipoprotein | ||
AIIGCJOP_03171 | 3e-256 | fadL | I | long-chain fatty acid transport protein | ||
AIIGCJOP_03172 | 2e-40 | yfcZ | S | protein conserved in bacteria | ||
AIIGCJOP_03173 | 5e-235 | 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 | |
AIIGCJOP_03174 | 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 | |
AIIGCJOP_03175 | 7.9e-64 | sixA | T | phosphohistidine phosphatase | ||
AIIGCJOP_03176 | 2.4e-98 | yfcN | S | Belongs to the UPF0115 family | ||
AIIGCJOP_03177 | 5.9e-182 | prmB | 2.1.1.297, 2.1.1.298 | J | Specifically methylates the 50S ribosomal protein L3 on a specific glutamine residue | |
AIIGCJOP_03178 | 3.9e-201 | 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 | |
AIIGCJOP_03179 | 8.8e-153 | 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 | ||
AIIGCJOP_03180 | 5.1e-134 | yfcA | S | membrane transporter protein | ||
AIIGCJOP_03181 | 7.7e-105 | yfcM | S | protein conserved in bacteria | ||
AIIGCJOP_03182 | 3.1e-41 | yfcL | S | YfcL protein | ||
AIIGCJOP_03183 | 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 | |
AIIGCJOP_03184 | 5.3e-223 | fabB | 2.3.1.41 | H | Belongs to the beta-ketoacyl-ACP synthases family | |
AIIGCJOP_03185 | 3.1e-204 | yfcJ | EGP | Major facilitator Superfamily | ||
AIIGCJOP_03186 | 9.9e-167 | 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 | ||
AIIGCJOP_03187 | 5e-207 | pdxB | 1.1.1.290 | H | Catalyzes the oxidation of erythronate-4-phosphate to 3- hydroxy-2-oxo-4-phosphonooxybutanoate | |
AIIGCJOP_03188 | 1.7e-174 | 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 | |
AIIGCJOP_03189 | 3.9e-153 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
AIIGCJOP_03190 | 1.7e-114 | dedA | I | Pfam SNARE associated Golgi protein | ||
AIIGCJOP_03191 | 9.9e-166 | 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 | |
AIIGCJOP_03192 | 1e-229 | 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 | |
AIIGCJOP_03193 | 5.1e-93 | dedD | D | Non-essential cell division protein that could be required for efficient cell constriction | ||
AIIGCJOP_03194 | 9.7e-83 | cvpA | S | Colicin v production | ||
AIIGCJOP_03195 | 9.7e-291 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
AIIGCJOP_03196 | 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 | |
AIIGCJOP_03197 | 3.1e-139 | argT | ET | belongs to the bacterial solute-binding protein 3 family | ||
AIIGCJOP_03198 | 1.2e-140 | hisJ | ET | belongs to the bacterial solute-binding protein 3 family | ||
AIIGCJOP_03199 | 3.5e-115 | hisQ | P | (ABC) transporter | ||
AIIGCJOP_03200 | 2.8e-123 | hisM | P | polar amino acid ABC transporter, inner membrane subunit | ||
AIIGCJOP_03201 | 1.8e-136 | hisP | 3.6.3.21 | E | abc transporter atp-binding protein | |
AIIGCJOP_03202 | 2.5e-81 | J | PFAM GCN5-related N-acetyltransferase | |||
AIIGCJOP_03203 | 1.3e-162 | yfcH | CH | epimerase | ||
AIIGCJOP_03204 | 3.4e-56 | folX | 1.13.11.81, 4.1.2.25, 5.1.99.7, 5.1.99.8 | H | Dihydroneopterin aldolase | |
AIIGCJOP_03205 | 1.6e-101 | yfcG | O | Belongs to the GST superfamily | ||
AIIGCJOP_03206 | 1.7e-106 | yfcF | 2.5.1.18 | O | Glutathione S-transferase | |
AIIGCJOP_03207 | 9.2e-98 | yfcE | S | Phosphoesterase | ||
AIIGCJOP_03208 | 1.3e-91 | yfcD | L | Nudix hydrolase | ||
AIIGCJOP_03209 | 0.0 | pta | 1.1.1.40, 2.3.1.8 | C | belongs to the CobB CobQ family | |
AIIGCJOP_03210 | 8.7e-226 | 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 | |
AIIGCJOP_03211 | 1.9e-80 | yfbV | S | UPF0208 membrane protein | ||
AIIGCJOP_03212 | 1.4e-89 | yfbU | S | Belongs to the UPF0304 family | ||
AIIGCJOP_03213 | 9e-108 | yfbT | 3.1.3.23 | S | Phosphatase | |
AIIGCJOP_03214 | 0.0 | yfbS | P | COG0471 Di- and tricarboxylate transporters | ||
AIIGCJOP_03215 | 6e-103 | yfbR | 3.1.3.89 | S | Catalyzes the strictly specific dephosphorylation of 2'- deoxyribonucleoside 5'-monophosphates | |
AIIGCJOP_03216 | 1.1e-236 | 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' | |
AIIGCJOP_03217 | 1.1e-162 | lrhA | K | Transcriptional regulator | ||
AIIGCJOP_03218 | 1.5e-74 | 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 | |
AIIGCJOP_03219 | 4.2e-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 | |
AIIGCJOP_03220 | 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 | |
AIIGCJOP_03221 | 6.2e-93 | nuoE | 1.6.5.3 | C | PFAM NADH dehydrogenase (ubiquinone) 24 kDa subunit | |
AIIGCJOP_03222 | 1.3e-267 | 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 | |
AIIGCJOP_03223 | 0.0 | nuoG | 1.6.5.3 | C | NADH-quinone oxidoreductase | |
AIIGCJOP_03224 | 6.2e-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 | |
AIIGCJOP_03225 | 6.5e-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 | |
AIIGCJOP_03226 | 6.6e-88 | nuoJ | 1.6.5.3 | C | Belongs to the complex I subunit 6 family | |
AIIGCJOP_03227 | 2.5e-28 | 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 | |
AIIGCJOP_03228 | 0.0 | nuoL | 1.6.5.3 | CP | NADH ubiquinone | |
AIIGCJOP_03229 | 1e-284 | nuoM | 1.6.5.3 | C | NADH ubiquinone oxidoreductase subunit | |
AIIGCJOP_03230 | 7.7e-261 | 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 | |
AIIGCJOP_03231 | 1.5e-175 | cheV | 2.7.13.3 | T | Two component signalling adaptor domain | |
AIIGCJOP_03232 | 1.4e-162 | 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 | |
AIIGCJOP_03233 | 5.2e-78 | elaA | S | Acyltransferase | ||
AIIGCJOP_03234 | 7.7e-46 | elaB | S | ribosome binding | ||
AIIGCJOP_03235 | 1.9e-210 | menF | 5.4.4.2 | H | Catalyzes the conversion of chorismate to isochorismate | |
AIIGCJOP_03236 | 5.6e-308 | 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) | |
AIIGCJOP_03237 | 1.9e-109 | 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) | |
AIIGCJOP_03238 | 9.4e-166 | menB | 4.1.3.36 | H | Converts o-succinylbenzoyl-CoA (OSB-CoA) to 1,4- dihydroxy-2-naphthoyl-CoA (DHNA-CoA) | |
AIIGCJOP_03239 | 4.6e-177 | menC | 4.2.1.113 | H | Converts 2-succinyl-6-hydroxy-2,4-cyclohexadiene-1- carboxylate (SHCHC) to 2-succinylbenzoate (OSB) | |
AIIGCJOP_03240 | 2.6e-263 | menE | 4.2.1.113, 6.2.1.26 | IQ | TIGRFAM O-succinylbenzoate-CoA ligase | |
AIIGCJOP_03241 | 3.8e-247 | tctA | S | Tripartite tricarboxylate transporter TctA | ||
AIIGCJOP_03242 | 7e-77 | tctB | S | Tripartite tricarboxylate transporter TctB family | ||
AIIGCJOP_03243 | 5.7e-183 | tctC | S | Tripartite tricarboxylate transporter family receptor | ||
AIIGCJOP_03244 | 1.7e-122 | T | Transcriptional | |||
AIIGCJOP_03245 | 3.5e-242 | tctE | 2.7.13.3 | T | Two-component sensor kinase N-terminal | |
AIIGCJOP_03246 | 1.2e-94 | yfaZ | S | YfaZ precursor | ||
AIIGCJOP_03247 | 1.7e-205 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
AIIGCJOP_03248 | 3.6e-232 | glpC | 1.1.5.3 | C | Dehydrogenase | |
AIIGCJOP_03249 | 9.4e-220 | glpB | 1.1.5.3 | C | Conversion of glycerol 3-phosphate to dihydroxyacetone. Uses fumarate or nitrate as electron acceptor | |
AIIGCJOP_03250 | 4.5e-311 | glpA | 1.1.5.3 | C | Belongs to the FAD-dependent glycerol-3-phosphate dehydrogenase family | |
AIIGCJOP_03251 | 2.5e-258 | glpT | G | transporter | ||
AIIGCJOP_03252 | 3.2e-200 | glpQ | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
AIIGCJOP_03253 | 5.6e-42 | yfaE | C | Ferredoxin | ||
AIIGCJOP_03254 | 8.4e-215 | nrdB | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
AIIGCJOP_03255 | 0.0 | nrdA | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
AIIGCJOP_03256 | 3.4e-132 | ubiG | 2.1.1.222, 2.1.1.64 | H | O-methyltransferase that catalyzes the 2 O-methylation steps in the ubiquinone biosynthetic pathway | |
AIIGCJOP_03257 | 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 | |
AIIGCJOP_03258 | 0.0 | rcsC | 2.7.13.3 | T | PhoQ Sensor | |
AIIGCJOP_03259 | 4.8e-114 | 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 | ||
AIIGCJOP_03260 | 0.0 | rcsD | 2.7.13.3, 4.6.1.1 | T | PhoQ Sensor | |
AIIGCJOP_03261 | 3.2e-198 | ompC | M | Belongs to the Gram-negative porin family | ||
AIIGCJOP_03262 | 4.5e-186 | 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 | |
AIIGCJOP_03263 | 7e-179 | 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 | |
AIIGCJOP_03264 | 8.3e-114 | alkB | 1.14.11.33 | L | Alkylated DNA repair protein | |
AIIGCJOP_03265 | 3.8e-301 | yojI | PQ | Cyclic peptide transporter | ||
AIIGCJOP_03266 | 6.7e-249 | mgtE | P | Acts as a magnesium transporter | ||
AIIGCJOP_03267 | 1.6e-192 | P | COG0659 Sulfate permease and related transporters (MFS superfamily) | |||
AIIGCJOP_03268 | 6e-286 | mqo | 1.1.5.4 | C | malate quinone oxidoreductase | |
AIIGCJOP_03269 | 6.1e-77 | eco | M | General inhibitor of pancreatic serine proteases inhibits chymotrypsin, trypsin, elastases, factor X, kallikrein as well as a variety of other proteases | ||
AIIGCJOP_03270 | 1.2e-36 | ynaJ | S | Protein of unknown function (DUF2534) | ||
AIIGCJOP_03271 | 3.3e-201 | yajR_1 | EGP | Major facilitator Superfamily | ||
AIIGCJOP_03272 | 1.2e-255 | S | Domain of unknown function (DUF1996) | |||
AIIGCJOP_03273 | 1.4e-66 | 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) | |||
AIIGCJOP_03274 | 1e-168 | 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) | |||
AIIGCJOP_03275 | 0.0 | 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) | |||
AIIGCJOP_03276 | 5.4e-84 | matC | 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) | ||
AIIGCJOP_03277 | 2e-66 | 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 | ||
AIIGCJOP_03279 | 0.0 | yejM | S | Hydrolase of alkaline phosphatase superfamily | ||
AIIGCJOP_03280 | 6.2e-32 | yejL | S | Belongs to the UPF0352 family | ||
AIIGCJOP_03281 | 7.1e-181 | ndpA | S | Nucleoid-associated protein | ||
AIIGCJOP_03282 | 1.8e-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 | ||
AIIGCJOP_03283 | 0.0 | yejH | L | Type III restriction protein res subunit | ||
AIIGCJOP_03284 | 1.5e-129 | rsuA | 5.4.99.19, 5.4.99.20, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
AIIGCJOP_03285 | 2e-206 | bcr | EGP | Major facilitator Superfamily | ||
AIIGCJOP_03286 | 6.6e-54 | yejG | S | YejG-like protein | ||
AIIGCJOP_03287 | 1.8e-279 | yejF | P | ATPase activity | ||
AIIGCJOP_03288 | 3.1e-163 | yejE | P | ABC transporter (Permease | ||
AIIGCJOP_03289 | 1.4e-198 | yejB | P | ABC transporter (permease) | ||
AIIGCJOP_03290 | 0.0 | yejA | E | ABC-type oligopeptide transport system, periplasmic component | ||
AIIGCJOP_03291 | 7.6e-262 | rtn | T | Involved in resistance to the phages N4 and lambda | ||
AIIGCJOP_03292 | 4.6e-92 | spr | 3.4.17.13 | M | NlpC/P60 family | |
AIIGCJOP_03293 | 8.1e-118 | 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) | |
AIIGCJOP_03294 | 6.5e-179 | yeiR | S | cobalamin synthesis protein, P47K | ||
AIIGCJOP_03295 | 2e-272 | 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 | |
AIIGCJOP_03296 | 7.7e-227 | uxuA | 4.2.1.8 | G | Catalyzes the dehydration of D-mannonate | |
AIIGCJOP_03297 | 2.9e-102 | efp | J | Elongation factor P | ||
AIIGCJOP_03298 | 7.8e-31 | yeiW | S | Putative zinc- or iron-chelating domain | ||
AIIGCJOP_03299 | 3.5e-203 | setB | EGP | Major facilitator Superfamily | ||
AIIGCJOP_03300 | 1.4e-196 | fruB | 2.7.1.121, 2.7.1.202, 2.7.3.9 | G | Bifunctional PTS system fructose-specific transporter subunit IIA HPr protein | |
AIIGCJOP_03301 | 2.4e-175 | fruK | 2.7.1.11, 2.7.1.56 | H | belongs to the carbohydrate kinase PfkB family | |
AIIGCJOP_03302 | 3.1e-269 | fruA | 2.7.1.202 | G | protein-phosphocysteine-D-fructose-phosphotransferase system transporter activity | |
AIIGCJOP_03303 | 1.1e-132 | psuK | 2.7.1.15, 2.7.1.45, 2.7.1.83 | G | pseudouridine kinase activity | |
AIIGCJOP_03304 | 4.8e-147 | psuG | 4.2.1.70 | Q | Catalyzes the reversible cleavage of pseudouridine 5'- phosphate (PsiMP) to ribose 5-phosphate and uracil. Functions biologically in the cleavage direction, as part of a pseudouridine degradation pathway | |
AIIGCJOP_03305 | 4e-189 | yeiM | F | Belongs to the concentrative nucleoside transporter (CNT) (TC 2.A.41) family | ||
AIIGCJOP_03306 | 1.5e-152 | yeiI | 2.7.1.15, 2.7.1.45, 2.7.1.83 | G | PfkB domain protein | |
AIIGCJOP_03307 | 2.2e-151 | 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 | |
AIIGCJOP_03308 | 1.1e-176 | yeiH | S | Belongs to the UPF0324 family | ||
AIIGCJOP_03309 | 1.4e-156 | yeiE | K | transcriptional regulator | ||
AIIGCJOP_03310 | 1.3e-271 | lysP | E | amino acid | ||
AIIGCJOP_03311 | 0.0 | cirA | P | receptor | ||
AIIGCJOP_03312 | 6.6e-156 | yeiG | 3.1.2.12 | CE1 | S | Serine hydrolase involved in the detoxification of formaldehyde |
AIIGCJOP_03313 | 2.5e-198 | yjiJ | EGP | Major facilitator Superfamily | ||
AIIGCJOP_03314 | 1.7e-114 | folE | 2.7.6.3, 3.5.4.16 | F | GTP cyclohydrolase | |
AIIGCJOP_03315 | 5.4e-209 | yeiB | S | Membrane | ||
AIIGCJOP_03316 | 1.7e-182 | galS | K | transcriptional regulator | ||
AIIGCJOP_03317 | 3.7e-182 | mglB | G | Wtih MglAC is involved in the transport of beta-methylgalactoside | ||
AIIGCJOP_03318 | 1.1e-286 | mglA | 3.6.3.17 | P | import. Responsible for energy coupling to the transport system | |
AIIGCJOP_03319 | 2.1e-172 | mglC | P | Belongs to the binding-protein-dependent transport system permease family | ||
AIIGCJOP_03320 | 5.5e-127 | sanA | S | Vancomycin high temperature exclusion protein | ||
AIIGCJOP_03321 | 2.4e-156 | cdd | 3.5.4.5 | F | This enzyme scavenges exogenous and endogenous cytidine and 2'-deoxycytidine for UMP synthesis | |
AIIGCJOP_03322 | 1.2e-113 | yohK | M | effector of murein hydrolase | ||
AIIGCJOP_03323 | 1.5e-44 | lrgA | S | UPF0299 membrane protein | ||
AIIGCJOP_03324 | 1.7e-168 | 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 | ||
AIIGCJOP_03325 | 1.1e-222 | mdtQ | MU | RND efflux system, outer membrane lipoprotein | ||
AIIGCJOP_03326 | 1.5e-138 | IQ | oxidoreductase | |||
AIIGCJOP_03327 | 1.3e-94 | yohD | S | Membrane | ||
AIIGCJOP_03328 | 1.2e-15 | |||||
AIIGCJOP_03329 | 8.3e-105 | yohC | S | Membrane | ||
AIIGCJOP_03330 | 4.8e-160 | pbpG | 3.4.16.4, 6.3.2.10 | M | Belongs to the peptidase S11 family | |
AIIGCJOP_03331 | 4.1e-98 | pat | 2.3.1.183 | M | N-acetyltransferase | |
AIIGCJOP_03332 | 0.0 | dld | 1.1.5.12 | C | Catalyzes the oxidation of D-lactate to pyruvate | |
AIIGCJOP_03333 | 0.0 | bglX | 3.2.1.21 | GH3 | G | Belongs to the glycosyl hydrolase 3 family |
AIIGCJOP_03334 | 1.3e-190 | G | Belongs to the glycosyl hydrolase 28 family | |||
AIIGCJOP_03335 | 1.6e-264 | G | MFS/sugar transport protein | |||
AIIGCJOP_03336 | 2.3e-205 | csbX | EGP | Major facilitator superfamily | ||
AIIGCJOP_03337 | 2.5e-164 | yehZ | M | Periplasmic glycine betaine choline-binding (lipo)protein of an ABC-type transport system (osmoprotectant binding protein) | ||
AIIGCJOP_03338 | 1.8e-167 | yehY | P | permease | ||
AIIGCJOP_03339 | 7.8e-158 | yehX | E | abc transporter atp-binding protein | ||
AIIGCJOP_03340 | 7.2e-114 | yehW | P | permease | ||
AIIGCJOP_03341 | 6.3e-09 | yohO | S | UPF0387 membrane protein YohO | ||
AIIGCJOP_03342 | 7.3e-135 | mlrA | K | Transcriptional regulator | ||
AIIGCJOP_03343 | 2.7e-286 | yehU | 2.7.13.3 | T | Histidine kinase | |
AIIGCJOP_03344 | 7.4e-124 | yehT | KT | Response regulator of the LytR AlgR family | ||
AIIGCJOP_03345 | 3e-81 | yehS | S | Protein of unknown function (DUF1456) | ||
AIIGCJOP_03346 | 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 | |
AIIGCJOP_03347 | 3.3e-203 | mrp | D | Binds and transfers iron-sulfur (Fe-S) clusters to target apoproteins. Can hydrolyze ATP | ||
AIIGCJOP_03348 | 9.9e-55 | yohN | D | response to cobalt ion | ||
AIIGCJOP_03349 | 1.6e-149 | comEA | M | polysaccharide export | ||
AIIGCJOP_03350 | 4.9e-68 | etp | 3.1.3.48 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
AIIGCJOP_03351 | 6.7e-301 | wzc | D | protein involved in exopolysaccharide biosynthesis | ||
AIIGCJOP_03352 | 4.2e-267 | ddc | 2.6.1.76, 4.1.1.86 | E | decarboxylase | |
AIIGCJOP_03353 | 7e-264 | dat | 2.6.1.76 | E | Belongs to the class-III pyridoxal-phosphate-dependent aminotransferase family | |
AIIGCJOP_03354 | 5.8e-45 | |||||
AIIGCJOP_03355 | 1e-169 | S | PAAR repeat-containing protein | |||
AIIGCJOP_03356 | 3.6e-58 | S | PAAR repeat-containing protein | |||
AIIGCJOP_03357 | 0.0 | IQ | Belongs to the beta-ketoacyl-ACP synthases family | |||
AIIGCJOP_03358 | 5.8e-161 | 2.3.1.179 | H | Belongs to the beta-ketoacyl-ACP synthases family | ||
AIIGCJOP_03359 | 3.2e-122 | |||||
AIIGCJOP_03360 | 1.6e-107 | V | ATPases associated with a variety of cellular activities | |||
AIIGCJOP_03361 | 3.5e-56 | |||||
AIIGCJOP_03362 | 4.6e-196 | lolE_2 | M | MacB-like periplasmic core domain | ||
AIIGCJOP_03363 | 7.4e-117 | M | Outer membrane lipoprotein-sorting protein | |||
AIIGCJOP_03364 | 7.8e-162 | |||||
AIIGCJOP_03365 | 1.7e-128 | fabD | 2.3.1.39 | I | Acyl transferase domain | |
AIIGCJOP_03366 | 1.5e-91 | ycdU | ||||
AIIGCJOP_03368 | 5.5e-111 | yqgA | S | Membrane | ||
AIIGCJOP_03369 | 0.0 | speC | 4.1.1.17, 4.1.1.18, 4.1.1.19 | E | decarboxylase | |
AIIGCJOP_03370 | 1.4e-226 | nupG | G | Broad-specificity transporter of purine and pyrimidine nucleosides. Driven by a proton motive force | ||
AIIGCJOP_03371 | 1.3e-199 | mltC | GH23 | M | Murein-degrading enzyme. May play a role in recycling of muropeptides during cell elongation and or cell division | |
AIIGCJOP_03372 | 7.6e-45 | yggX | CO | 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 | ||
AIIGCJOP_03373 | 6.2e-204 | mutY | L | a g-specific adenine glycosylase | ||
AIIGCJOP_03374 | 5.9e-137 | 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 |
AIIGCJOP_03375 | 2.2e-54 | yggL | S | protein conserved in bacteria | ||
AIIGCJOP_03376 | 3.3e-124 | yggN | S | Protein of unknown function (DUF2884) | ||
AIIGCJOP_03377 | 6.3e-206 | G | Tripartite ATP-independent periplasmic transporter, DctM component | |||
AIIGCJOP_03378 | 1.5e-59 | G | TRAP-type C4-dicarboxylate transport system small permease component | |||
AIIGCJOP_03379 | 3.4e-151 | G | Bacterial extracellular solute-binding protein, family 7 | |||
AIIGCJOP_03380 | 5.5e-214 | hemN | H | Involved in the biosynthesis of porphyrin-containing compound | ||
AIIGCJOP_03381 | 1.3e-102 | 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 | |
AIIGCJOP_03382 | 1.2e-46 | yggU | S | Belongs to the UPF0235 family | ||
AIIGCJOP_03383 | 2.9e-91 | yggT | S | integral membrane protein | ||
AIIGCJOP_03384 | 2.2e-120 | yggS | E | Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis | ||
AIIGCJOP_03385 | 1.8e-149 | yggR | NU | PFAM Type II secretion system protein E | ||
AIIGCJOP_03386 | 1.6e-118 | K | Transcriptional regulator | |||
AIIGCJOP_03387 | 1.1e-71 | yqgF | L | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
AIIGCJOP_03388 | 5.5e-98 | yqgE | K | Belongs to the UPF0301 (AlgH) family | ||
AIIGCJOP_03389 | 1.3e-179 | gshB | 6.3.2.2, 6.3.2.3 | H | Belongs to the prokaryotic GSH synthase family | |
AIIGCJOP_03390 | 3.5e-129 | 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 | |
AIIGCJOP_03391 | 3.4e-121 | endA | 3.1.21.1 | L | endonuclease I | |
AIIGCJOP_03392 | 1e-81 | sprT | S | Belongs to the SprT family | ||
AIIGCJOP_03393 | 7.4e-253 | galP | EGP | Major facilitator Superfamily | ||
AIIGCJOP_03394 | 1.4e-209 | 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 | |
AIIGCJOP_03395 | 0.0 | speA | 4.1.1.19 | H | Catalyzes the biosynthesis of agmatine from arginine | |
AIIGCJOP_03397 | 1.1e-217 | 3.2.1.139 | G | Belongs to the glycosyl hydrolase 67 family | ||
AIIGCJOP_03398 | 8.5e-218 | 4.2.2.6 | U | Oligogalacturonate lyase | ||
AIIGCJOP_03399 | 1.5e-223 | G | ABC transporter substrate-binding protein | |||
AIIGCJOP_03400 | 1.7e-124 | G | isomerase activity | |||
AIIGCJOP_03401 | 8.8e-178 | speB | 3.5.3.11 | F | Catalyzes the formation of putrescine from agmatine | |
AIIGCJOP_03402 | 4.5e-206 | EGP | Major Facilitator Superfamily | |||
AIIGCJOP_03403 | 3.8e-59 | ndoA | 1.7.1.15 | C | Rieske [2Fe-2S] domain | |
AIIGCJOP_03404 | 2.3e-50 | |||||
AIIGCJOP_03405 | 4.2e-205 | carAa | P | Rieske [2Fe-2S] domain | ||
AIIGCJOP_03406 | 1.5e-130 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
AIIGCJOP_03407 | 6e-143 | K | helix_turn_helix isocitrate lyase regulation | |||
AIIGCJOP_03408 | 3.4e-177 | todE | C | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | ||
AIIGCJOP_03409 | 3.5e-211 | andAa | 1.18.1.3, 1.7.1.15 | P | Pyridine nucleotide-disulphide oxidoreductase | |
AIIGCJOP_03410 | 7.4e-228 | sauU | G | Major Facilitator Superfamily | ||
AIIGCJOP_03411 | 8e-99 | G | WxcM-like, C-terminal | |||
AIIGCJOP_03412 | 1.9e-133 | I | Alpha/beta hydrolase family | |||
AIIGCJOP_03413 | 1.6e-140 | IQ | KR domain | |||
AIIGCJOP_03414 | 1.3e-126 | nadX | 1.4.1.21 | H | Specifically catalyzes the NAD or NADP-dependent dehydrogenation of L-aspartate to iminoaspartate | |
AIIGCJOP_03415 | 2.7e-269 | aldA | 1.2.1.3, 1.2.1.8 | C | Aldehyde dehydrogenase family | |
AIIGCJOP_03416 | 3.8e-293 | 2.2.1.6, 4.1.1.75 | C | Thiamine pyrophosphate enzyme, central domain | ||
AIIGCJOP_03417 | 3.4e-127 | yggG | O | metalloprotease | ||
AIIGCJOP_03418 | 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 | |
AIIGCJOP_03419 | 1.7e-190 | epd | 1.2.1.12, 1.2.1.72 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
AIIGCJOP_03420 | 8.4e-210 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
AIIGCJOP_03421 | 4.7e-207 | fbaA | 4.1.2.13 | G | Aldolase | |
AIIGCJOP_03422 | 2e-128 | mscS | M | Mechanosensitive Ion channel | ||
AIIGCJOP_03423 | 5.1e-108 | argO | S | Involved in the export of arginine. Important to control the intracellular level of arginine and the correct balance between arginine and lysine | ||
AIIGCJOP_03424 | 1.8e-118 | yggE | S | Oxidative stress defense protein | ||
AIIGCJOP_03425 | 2.6e-166 | argP | K | Controls the transcription of genes involved in arginine and lysine metabolism | ||
AIIGCJOP_03426 | 3e-122 | rpiA | 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
AIIGCJOP_03427 | 9.5e-228 | serA | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
AIIGCJOP_03428 | 9e-86 | fthC | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
AIIGCJOP_03429 | 8.6e-43 | 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 | ||
AIIGCJOP_03430 | 1.8e-104 | ygfB | S | Belongs to the UPF0149 family | ||
AIIGCJOP_03431 | 5e-243 | pepP | 3.4.11.9 | E | aminopeptidase | |
AIIGCJOP_03432 | 4.4e-214 | ubiH | CH | hydroxylase | ||
AIIGCJOP_03433 | 4e-223 | visC | CH | ubiquinone biosynthesis hydroxylase, UbiH UbiF VisC COQ6 | ||
AIIGCJOP_03434 | 1.2e-202 | gcvT | 2.1.2.10 | H | The glycine cleavage system catalyzes the degradation of glycine | |
AIIGCJOP_03435 | 5.2e-63 | 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 | ||
AIIGCJOP_03436 | 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 | |
AIIGCJOP_03437 | 6.3e-126 | IQ | Dehydrogenases with different specificities (Related to short-chain alcohol dehydrogenases) | |||
AIIGCJOP_03438 | 5.7e-293 | bglA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AIIGCJOP_03439 | 1.9e-130 | ybbH_1 | K | transcriptional regulator | ||
AIIGCJOP_03440 | 1.1e-47 | yqfB | S | Belongs to the UPF0267 family | ||
AIIGCJOP_03441 | 1.2e-112 | yqfA | S | hemolysin iii | ||
AIIGCJOP_03442 | 1.6e-177 | 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 | ||
AIIGCJOP_03443 | 1.6e-42 | sdhE | 1.3.5.1, 1.3.5.4 | S | Flavinator of succinate dehydrogenase | |
AIIGCJOP_03444 | 3.8e-64 | ygfX | S | Membrane | ||
AIIGCJOP_03445 | 2.5e-97 | fldB | C | Low-potential electron donor to a number of redox enzymes | ||
AIIGCJOP_03446 | 2.5e-161 | xerD | D | recombinase XerD | ||
AIIGCJOP_03447 | 4.9e-128 | 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 | |
AIIGCJOP_03448 | 0.0 | recJ | L | Single-stranded-DNA-specific exonuclease | ||
AIIGCJOP_03449 | 1.6e-160 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
AIIGCJOP_03450 | 1.9e-286 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
AIIGCJOP_03451 | 3e-88 | 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) | |
AIIGCJOP_03453 | 8.3e-111 | nlpD | DM | COG0739 Membrane proteins related to metalloendopeptidases | ||
AIIGCJOP_03455 | 8.6e-84 | arcR | T | Winged helix-turn-helix DNA binding | ||
AIIGCJOP_03456 | 3.6e-151 | ompA | M | OmpA-like transmembrane domain | ||
AIIGCJOP_03457 | 2e-25 | |||||
AIIGCJOP_03458 | 4.8e-40 | yjdI | 1.6.3.4 | S | Divergent 4Fe-4S mono-cluster | |
AIIGCJOP_03459 | 1.1e-43 | yjdJ | S | GCN5-related N-acetyl-transferase | ||
AIIGCJOP_03460 | 2.9e-208 | yqeG | E | transporter | ||
AIIGCJOP_03461 | 3.6e-71 | YPO2978 | S | PFAM transmembrane pair domain protein | ||
AIIGCJOP_03462 | 5.1e-151 | allS_3 | K | Transcriptional regulator | ||
AIIGCJOP_03463 | 5e-82 | S | protein containing double-stranded beta helix domain | |||
AIIGCJOP_03464 | 1.9e-209 | 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 | |
AIIGCJOP_03465 | 3.8e-125 | lptD | M | oligogalacturonate-specific porin | ||
AIIGCJOP_03466 | 1.3e-239 | ogl | 4.2.2.6 | U | oligogalacturonate lyase | |
AIIGCJOP_03467 | 1.5e-160 | kduI | 5.3.1.17 | G | Catalyzes the isomerization of 5-dehydro-4-deoxy-D- glucuronate to 3-deoxy-D-glycero-2,5-hexodiulosonate | |
AIIGCJOP_03468 | 3.3e-138 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
AIIGCJOP_03469 | 1.5e-242 | araE | EGP | Major facilitator Superfamily | ||
AIIGCJOP_03470 | 9.3e-222 | ogl | 4.2.2.6 | U | Oligogalacturonate lyase | |
AIIGCJOP_03471 | 6.6e-248 | yesO | G | ABC transporter substrate-binding protein | ||
AIIGCJOP_03472 | 4e-209 | ugpC | P | Belongs to the ABC transporter superfamily | ||
AIIGCJOP_03473 | 8.4e-165 | togN | P | PFAM binding-protein-dependent transport systems inner membrane component | ||
AIIGCJOP_03474 | 7.7e-163 | ycjO | P | PFAM binding-protein-dependent transport systems inner membrane component | ||
AIIGCJOP_03475 | 1e-56 | kdgF | S | PFAM Cupin 2, conserved barrel domain protein | ||
AIIGCJOP_03476 | 1.5e-121 | ygeA | 5.1.1.13 | M | Belongs to the aspartate glutamate racemases family | |
AIIGCJOP_03477 | 2.1e-163 | lysR | K | transcriptional regulator | ||
AIIGCJOP_03478 | 6.9e-234 | lysA | 2.7.2.4, 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
AIIGCJOP_03479 | 4.4e-186 | ascG | K | Transcriptional regulator | ||
AIIGCJOP_03480 | 4e-240 | 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 | ||
AIIGCJOP_03481 | 4.4e-285 | celH | 3.2.1.21, 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AIIGCJOP_03482 | 2.4e-136 | uxuR | K | FCD | ||
AIIGCJOP_03483 | 8.5e-84 | mshD | 2.3.1.189 | S | PFAM GCN5-related N-acetyltransferase | |
AIIGCJOP_03484 | 1.8e-187 | galR | K | transcriptional regulator | ||
AIIGCJOP_03485 | 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 | |
AIIGCJOP_03486 | 7.4e-185 | 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 | |
AIIGCJOP_03487 | 5.8e-194 | tas | C | Aldo keto reductase | ||
AIIGCJOP_03488 | 7.7e-32 | ygdR | S | (Lipo)protein | ||
AIIGCJOP_03489 | 6.5e-125 | mutH | L | Sequence-specific endonuclease that cleaves unmethylated GATC sequences. It is involved in DNA mismatch repair | ||
AIIGCJOP_03490 | 6.2e-69 | 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 | ||
AIIGCJOP_03491 | 0.0 | ptsP | 2.7.3.9 | T | Belongs to the PEP-utilizing enzyme family | |
AIIGCJOP_03492 | 3e-167 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
AIIGCJOP_03493 | 6e-159 | 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 | |
AIIGCJOP_03494 | 3.4e-77 | ppdA | NU | prepilin peptidase dependent protein A | ||
AIIGCJOP_03495 | 8.3e-78 | ppdB | U | prepilin peptidase dependent protein | ||
AIIGCJOP_03496 | 6.1e-48 | ygdB | S | Protein of unknown function (DUF2509) | ||
AIIGCJOP_03497 | 2.2e-43 | ppdC | NU | Prepilin peptidase dependent protein c | ||
AIIGCJOP_03498 | 0.0 | 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 | |
AIIGCJOP_03499 | 0.0 | ptrA | 3.4.24.55, 3.4.24.56 | O | Belongs to the peptidase M16 family | |
AIIGCJOP_03500 | 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 | |
AIIGCJOP_03501 | 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 | |
AIIGCJOP_03502 | 1.6e-241 | argA | 2.3.1.1, 2.7.2.8 | E | Belongs to the acetyltransferase family. ArgA subfamily | |
AIIGCJOP_03503 | 5.4e-212 | amiC | 3.5.1.28 | M | N-acetylmuramoyl-L-alanine amidase | |
AIIGCJOP_03504 | 5.9e-08 | |||||
AIIGCJOP_03505 | 5.9e-08 | |||||
AIIGCJOP_03506 | 5.9e-08 | |||||
AIIGCJOP_03507 | 7.5e-200 | mltA | GH102 | M | Murein-degrading enzyme. May play a role in recycling of muropeptides during cell elongation and or cell division | |
AIIGCJOP_03508 | 5.9e-146 | ygdL | 2.7.7.73, 2.7.7.80 | H | Dinucleotide-utilizing enzymes involved in molybdopterin and thiamine biosynthesis family 1 | |
AIIGCJOP_03509 | 1.4e-69 | csdE | 2.8.1.7, 4.4.1.16 | S | cysteine desulfurase, sulfur acceptor subunit CsdE | |
AIIGCJOP_03510 | 9e-215 | 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 | |
AIIGCJOP_03511 | 3e-34 | ygdI | S | Lipoprotein | ||
AIIGCJOP_03512 | 6.9e-167 | gcvA | K | transcriptional regulator | ||
AIIGCJOP_03513 | 6.6e-66 | ygdD | S | Small membrane protein | ||
AIIGCJOP_03514 | 2.5e-211 | rlmM | 2.1.1.186 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA methyltransferase RlmE family. RlmM subfamily | |
AIIGCJOP_03515 | 2.8e-137 | 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 | |
AIIGCJOP_03516 | 7.7e-255 | sdaB | 4.3.1.17 | E | l-serine dehydratase | |
AIIGCJOP_03517 | 7.9e-225 | sdaC | E | serine transporter | ||
AIIGCJOP_03518 | 3.7e-257 | ygdH | 3.2.2.10 | S | Rossmann fold nucleotide-binding protein | |
AIIGCJOP_03519 | 9.9e-160 | queF | 1.7.1.13 | K | Catalyzes the NADPH-dependent reduction of 7-cyano-7- deazaguanine (preQ0) to 7-aminomethyl-7-deazaguanine (preQ1) | |
AIIGCJOP_03520 | 2.9e-88 | syd | S | regulation of protein complex assembly | ||
AIIGCJOP_03521 | 1.4e-53 | yqcC | 3.5.1.28, 5.1.3.13, 5.4.99.26 | S | protein conserved in bacteria | |
AIIGCJOP_03522 | 1.1e-139 | truC | 5.4.99.26 | J | Pseudouridine synthase | |
AIIGCJOP_03523 | 2.7e-79 | yqcA | C | flavodoxin binds one FMN molecule, which serves as a redox-active prosthetic group | ||
AIIGCJOP_03524 | 1.9e-250 | gudP | G | transporter | ||
AIIGCJOP_03525 | 6.6e-267 | gudD | 4.2.1.40 | M | Belongs to the mandelate racemase muconate lactonizing enzyme family | |
AIIGCJOP_03526 | 7.1e-261 | gudD | 4.2.1.40 | M | Belongs to the mandelate racemase muconate lactonizing enzyme family | |
AIIGCJOP_03527 | 2e-200 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
AIIGCJOP_03528 | 0.0 | barA | 2.7.13.3 | T | PhoQ Sensor | |
AIIGCJOP_03529 | 4.5e-244 | rlmD | 2.1.1.190 | J | Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA | |
AIIGCJOP_03530 | 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 | |
AIIGCJOP_03531 | 1.2e-143 | mazG | 3.6.1.66, 3.6.1.9 | C | nucleoside triphosphate pyrophosphohydrolase | |
AIIGCJOP_03532 | 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 | |
AIIGCJOP_03533 | 9.9e-236 | 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 | |
AIIGCJOP_03534 | 5.5e-212 | crtX | 2.4.1.276 | GT1 | CG | Belongs to the UDP-glycosyltransferase family |
AIIGCJOP_03535 | 7.4e-126 | 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 | |
AIIGCJOP_03536 | 4.5e-202 | norB | G | Quinolone resistance protein | ||
AIIGCJOP_03537 | 5.5e-209 | 3.5.1.32 | S | amidohydrolase | ||
AIIGCJOP_03538 | 0.0 | K | helix_turn_helix, arabinose operon control protein | |||
AIIGCJOP_03539 | 5.5e-67 | queD | 4.1.2.50, 4.2.3.12 | H | 6-pyruvoyl tetrahydropterin synthase | |
AIIGCJOP_03540 | 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 | |
AIIGCJOP_03541 | 0.0 | cysI | 1.7.7.1, 1.8.1.2, 1.8.7.1 | H | 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 | |
AIIGCJOP_03542 | 2.3e-136 | cysH | 1.8.4.10, 1.8.4.8 | EH | Reduction of activated sulfate into sulfite | |
AIIGCJOP_03543 | 6e-183 | iap | N | Catalyzes the sequential removal of 2 amino-terminal arginines from alkaline phosphatase isozyme 1 to form isozymes 2 and 3 | ||
AIIGCJOP_03545 | 1.8e-175 | cysD | 1.8.4.10, 1.8.4.8, 2.7.7.4 | H | Sulfate adenylyltransferase subunit 2 | |
AIIGCJOP_03546 | 1.7e-260 | 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 | |
AIIGCJOP_03547 | 1.7e-105 | cysC | 2.7.1.25 | F | Catalyzes the synthesis of activated sulfate | |
AIIGCJOP_03548 | 1.9e-47 | ygbE | S | membrane | ||
AIIGCJOP_03549 | 1.8e-50 | 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 | ||
AIIGCJOP_03550 | 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) | |
AIIGCJOP_03551 | 7e-86 | ispF | 2.1.1.228, 2.7.7.60, 4.6.1.12 | H | 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) | |
AIIGCJOP_03552 | 2.3e-190 | truD | 5.4.99.27 | J | Responsible for synthesis of pseudouridine from uracil- 13 in transfer RNAs | |
AIIGCJOP_03553 | 1.1e-128 | surE | 3.1.3.5 | S | Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates | |
AIIGCJOP_03554 | 2.2e-111 | 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 | |
AIIGCJOP_03555 | 2.6e-148 | nlpD | M | Lysin motif | ||
AIIGCJOP_03556 | 2.8e-177 | rpoS | K | RNA polymerase sigma | ||
AIIGCJOP_03557 | 1.5e-54 | S | protein conserved in bacteria | |||
AIIGCJOP_03558 | 7.4e-193 | EGP | Major Facilitator Superfamily | |||
AIIGCJOP_03559 | 9.4e-145 | ptxR | K | LysR substrate binding domain | ||
AIIGCJOP_03560 | 6.4e-64 | hosA | K | helix_turn_helix multiple antibiotic resistance protein | ||
AIIGCJOP_03561 | 4.4e-101 | ubiX | 2.5.1.129 | H | Flavin prenyltransferase that catalyzes the synthesis of the prenylated FMN cofactor (prenyl-FMN) for phenolic acid decarboxylase C. Involved in the decarboxylation and detoxification of phenolic derivatives under both aerobic and anaerobic conditions | |
AIIGCJOP_03562 | 1.5e-277 | 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 | |
AIIGCJOP_03563 | 2.5e-39 | bsdD | 4.1.1.61 | S | 4-hydroxybenzoate decarboxylase | |
AIIGCJOP_03564 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
AIIGCJOP_03565 | 9e-31 | S | Toxin SymE, type I toxin-antitoxin system | |||
AIIGCJOP_03566 | 2.4e-59 | ygbA | S | Nitrous oxide-stimulated promoter | ||
AIIGCJOP_03567 | 1.4e-67 | G | COG2513 PEP phosphonomutase and related enzymes | |||
AIIGCJOP_03568 | 1.1e-142 | ada | 2.1.1.63, 3.2.2.21 | 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 | |
AIIGCJOP_03569 | 1.9e-215 | yceL | EGP | Major facilitator Superfamily | ||
AIIGCJOP_03570 | 6.4e-134 | 3.6.3.34 | HP | COG1120 ABC-type cobalamin Fe3 -siderophores transport systems, ATPase components | ||
AIIGCJOP_03571 | 9.3e-160 | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | |||
AIIGCJOP_03572 | 3.9e-179 | P | ABC transporter substrate-binding protein | |||
AIIGCJOP_03574 | 6.5e-281 | ascB | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AIIGCJOP_03575 | 1.4e-254 | ascF | 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | Phosphotransferase System | |
AIIGCJOP_03576 | 1.1e-178 | ascG | K | Transcriptional regulator | ||
AIIGCJOP_03577 | 9.9e-297 | S | bacterial-type RNA polymerase regulatory region sequence-specific DNA binding | |||
AIIGCJOP_03578 | 4.8e-12 | |||||
AIIGCJOP_03579 | 1.5e-200 | 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 | |
AIIGCJOP_03580 | 5.1e-273 | 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 | |
AIIGCJOP_03581 | 5e-271 | norR | KT | transcriptional regulator | ||
AIIGCJOP_03582 | 9.9e-164 | gutQ | 5.3.1.13 | M | Arabinose 5-phosphate isomerase | |
AIIGCJOP_03583 | 7.5e-138 | srlR | K | DeoR C terminal sensor domain | ||
AIIGCJOP_03584 | 7.7e-53 | gutM | K | Glucitol operon activator | ||
AIIGCJOP_03585 | 6.4e-137 | IQ | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
AIIGCJOP_03586 | 1e-60 | srlB | 2.7.1.198 | G | system, glucitol sorbitol-specific | |
AIIGCJOP_03587 | 4e-157 | srlE | 2.7.1.198 | G | PTS system, glucitol sorbitol-specific, IIBC subunit | |
AIIGCJOP_03588 | 1.1e-98 | srlA | G | PTS system glucitol sorbitol-specific | ||
AIIGCJOP_03589 | 1.5e-208 | mltB | GH103 | M | Lytic murein transglycosylase | |
AIIGCJOP_03590 | 6.2e-85 | ygaD | 3.5.1.42 | J | Belongs to the CinA family | |
AIIGCJOP_03591 | 9.7e-189 | 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 | ||
AIIGCJOP_03592 | 1.2e-80 | recX | 2.4.1.337 | GT4 | S | Modulates RecA activity |
AIIGCJOP_03593 | 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 | |
AIIGCJOP_03594 | 1.5e-23 | csrA | J | Could accelerate the degradation of some genes transcripts potentially through selective RNA binding | ||
AIIGCJOP_03602 | 3.1e-101 | yqaB | S | HAD-superfamily hydrolase, subfamily IA, variant 3 | ||
AIIGCJOP_03603 | 3.5e-55 | yqaA | S | SNARE associated Golgi protein | ||
AIIGCJOP_03604 | 1.5e-291 | gshA | 6.3.2.2 | H | Belongs to the glutamate--cysteine ligase type 1 family. Type 1 subfamily | |
AIIGCJOP_03605 | 4.9e-93 | 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) | |
AIIGCJOP_03606 | 1.4e-14 | |||||
AIIGCJOP_03607 | 1.5e-47 | D | Domain amino terminal to FKBP-type peptidyl-prolyl isomerase | |||
AIIGCJOP_03608 | 1.4e-281 | emrB | EGP | Major facilitator Superfamily | ||
AIIGCJOP_03609 | 1.5e-190 | emrA | V | multidrug resistance efflux pump | ||
AIIGCJOP_03610 | 3.8e-93 | mprA | K | Transcriptional | ||
AIIGCJOP_03611 | 7.3e-177 | ygaY | EGP | Major facilitator Superfamily | ||
AIIGCJOP_03612 | 7e-189 | proX | E | glycine, betaine | ||
AIIGCJOP_03613 | 1.5e-160 | proW | P | PFAM binding-protein-dependent transport systems inner membrane component | ||
AIIGCJOP_03614 | 1.3e-218 | proV | 3.6.3.32 | E | glycine, betaine | |
AIIGCJOP_03615 | 2.1e-174 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
AIIGCJOP_03616 | 0.0 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
AIIGCJOP_03617 | 4.6e-70 | nrdI | F | Probably involved in ribonucleotide reductase function | ||
AIIGCJOP_03618 | 6.2e-30 | nrdH | O | Glutaredoxin-like protein NrdH | ||
AIIGCJOP_03619 | 5.2e-16 | ygaM | S | ribosome binding | ||
AIIGCJOP_03620 | 1.4e-59 | ygaC | S | Protein of unknown function (DUF2002) | ||
AIIGCJOP_03621 | 1.1e-75 | alaE | U | L-alanine exporter AlaE | ||
AIIGCJOP_03622 | 6.2e-51 | stpA | S | Belongs to the histone-like protein H-NS family | ||
AIIGCJOP_03623 | 3.2e-23 | |||||
AIIGCJOP_03624 | 3.4e-21 | yqaE | S | Proteolipid membrane potential modulator | ||
AIIGCJOP_03625 | 8.6e-173 | yahB | K | Transcriptional regulator | ||
AIIGCJOP_03626 | 2.2e-105 | yahD | L | ankyrin repeat | ||
AIIGCJOP_03627 | 2.9e-274 | sucD | 6.2.1.5 | C | CoA-ligase | |
AIIGCJOP_03628 | 6.5e-265 | yahG | C | Protein of unknown function (DUF1116) | ||
AIIGCJOP_03629 | 3.8e-282 | Z012_07875 | F | Psort location CytoplasmicMembrane, score 10.00 | ||
AIIGCJOP_03630 | 5.3e-170 | yahI | 2.7.2.2 | E | Belongs to the carbamate kinase family | |
AIIGCJOP_03631 | 1.5e-250 | yahJ | F | Amidohydrolase family | ||
AIIGCJOP_03632 | 4.2e-164 | K | LysR substrate binding domain | |||
AIIGCJOP_03633 | 3.2e-237 | G | Major Facilitator Superfamily | |||
AIIGCJOP_03634 | 2.8e-126 | IQ | KR domain | |||
AIIGCJOP_03635 | 7.1e-158 | tktB | 2.2.1.1 | G | Transketolase, thiamine diphosphate binding domain | |
AIIGCJOP_03636 | 3.3e-178 | 2.2.1.1 | G | Transketolase | ||
AIIGCJOP_03637 | 1.6e-103 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
AIIGCJOP_03638 | 2.7e-160 | K | transcriptional regulator | |||
AIIGCJOP_03639 | 3.9e-96 | pagC | M | Membrane | ||
AIIGCJOP_03640 | 5.8e-42 | |||||
AIIGCJOP_03641 | 8.9e-20 | |||||
AIIGCJOP_03642 | 2.9e-28 | |||||
AIIGCJOP_03643 | 1.2e-68 | S | Immunity protein 63 | |||
AIIGCJOP_03644 | 2.8e-49 | |||||
AIIGCJOP_03645 | 5.2e-56 | |||||
AIIGCJOP_03646 | 1.1e-58 | |||||
AIIGCJOP_03648 | 1.9e-45 | U | domain, Protein | |||
AIIGCJOP_03649 | 3e-48 | S | Cell wall assembly protein | |||
AIIGCJOP_03650 | 2e-28 | |||||
AIIGCJOP_03651 | 6.2e-49 | |||||
AIIGCJOP_03652 | 3.5e-45 | |||||
AIIGCJOP_03653 | 1.4e-87 | S | Uncharacterized protein conserved in bacteria (DUF2247) | |||
AIIGCJOP_03654 | 0.0 | U | Large exoproteins involved in heme utilization or adhesion | |||
AIIGCJOP_03655 | 4.8e-99 | hlyC | O | RTX toxin acyltransferase | ||
AIIGCJOP_03656 | 0.0 | fhaC | U | hemolysin activation secretion protein | ||
AIIGCJOP_03657 | 1.9e-44 | ydeI | S | single-species biofilm formation on inanimate substrate | ||
AIIGCJOP_03658 | 4.4e-70 | |||||
AIIGCJOP_03659 | 1.3e-65 | S | Protein of unknown function (DUF421) | |||
AIIGCJOP_03660 | 9.8e-89 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
AIIGCJOP_03661 | 1.8e-136 | yxnA | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | ||
AIIGCJOP_03662 | 2.6e-183 | cioB | 1.10.3.14 | C | oxidase subunit | |
AIIGCJOP_03663 | 2.2e-265 | cioA | 1.10.3.14 | C | oxidase, subunit | |
AIIGCJOP_03664 | 2.6e-155 | katN | P | Mn-containing catalase | ||
AIIGCJOP_03665 | 1.8e-84 | yciE | S | protein conserved in bacteria | ||
AIIGCJOP_03666 | 1e-79 | yciF | S | protein conserved in bacteria | ||
AIIGCJOP_03668 | 1.5e-73 | |||||
AIIGCJOP_03669 | 6.1e-48 | yycE | 3.4.21.26, 5.3.1.24 | E | PFAM Glyoxalase bleomycin resistance protein dioxygenase | |
AIIGCJOP_03670 | 3.9e-114 | rluA | 5.4.99.28, 5.4.99.29 | J | Pseudouridine synthase | |
AIIGCJOP_03671 | 1.1e-183 | tetV | EGP | Major facilitator Superfamily | ||
AIIGCJOP_03672 | 1.5e-64 | S | protein conserved in bacteria | |||
AIIGCJOP_03673 | 1.1e-66 | S | protein conserved in bacteria | |||
AIIGCJOP_03674 | 3.1e-162 | K | transcriptional regulator | |||
AIIGCJOP_03675 | 9.8e-90 | |||||
AIIGCJOP_03677 | 4e-90 | K | transcriptional Regulator, LysR family | |||
AIIGCJOP_03678 | 5e-161 | hpaX | G | Major facilitator Superfamily | ||
AIIGCJOP_03679 | 7.7e-106 | 4.1.2.17 | G | Class II aldolase adducin family protein | ||
AIIGCJOP_03680 | 1e-210 | M | Type I secretion membrane fusion protein, HlyD | |||
AIIGCJOP_03681 | 0.0 | V | COG2274 ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | |||
AIIGCJOP_03682 | 2.1e-247 | MU | type I secretion outer membrane protein, TolC | |||
AIIGCJOP_03683 | 0.0 | bipA | U | Bacterial Ig-like domain (group 3) | ||
AIIGCJOP_03684 | 0.0 | bipA | NU | TIGRFAM Outer membrane protein | ||
AIIGCJOP_03685 | 4.8e-78 | yceI | S | Belongs to the UPF0312 family | ||
AIIGCJOP_03686 | 7.2e-108 | 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) | |
AIIGCJOP_03687 | 6e-172 | C | Belongs to the zinc-containing alcohol dehydrogenase family. Quinone oxidoreductase subfamily | |||
AIIGCJOP_03688 | 2.2e-45 | S | Antibiotic biosynthesis monooxygenase | |||
AIIGCJOP_03689 | 2.8e-10 | |||||
AIIGCJOP_03690 | 1.1e-86 | 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 | ||
AIIGCJOP_03691 | 4.3e-74 | ratA | I | oligoketide cyclase lipid transport protein | ||
AIIGCJOP_03692 | 1.5e-38 | rnfH | S | Belongs to the UPF0125 (RnfH) family | ||
AIIGCJOP_03693 | 9.2e-56 | 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 | ||
AIIGCJOP_03694 | 1.1e-300 | recN | L | May be involved in recombinational repair of damaged DNA | ||
AIIGCJOP_03695 | 2e-163 | 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 | |
AIIGCJOP_03696 | 2.1e-95 | 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 | ||
AIIGCJOP_03697 | 1.3e-213 | yfjD | P | Mg2 and Co2 transporter CorB | ||
AIIGCJOP_03698 | 1.3e-143 | ypjD | S | Cytochrome c assembly protein | ||
AIIGCJOP_03699 | 4.4e-234 | 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 | |
AIIGCJOP_03700 | 2.2e-38 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
AIIGCJOP_03701 | 1.8e-98 | 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 | ||
AIIGCJOP_03702 | 1.2e-143 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
AIIGCJOP_03703 | 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 | ||
AIIGCJOP_03704 | 2.9e-61 | copB | P | Protein of unknown function (DUF2946) | ||
AIIGCJOP_03705 | 1.4e-235 | S | Iron-regulated membrane protein | |||
AIIGCJOP_03706 | 5.8e-177 | yfiN | 2.7.7.65 | T | Diguanylate cyclase | |
AIIGCJOP_03707 | 1.5e-68 | yfiR | S | bacterial-type flagellum-dependent swarming motility | ||
AIIGCJOP_03708 | 1.8e-57 | yfiL | S | Protein of unknown function (DUF2799) | ||
AIIGCJOP_03709 | 2.9e-201 | 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) | |
AIIGCJOP_03710 | 3.5e-205 | tyrA | 1.3.1.12, 1.3.1.13, 1.3.1.43, 5.4.99.5 | E | T-protein | |
AIIGCJOP_03711 | 3.6e-173 | yvrE | 3.1.1.15 | G | gluconolactonase | |
AIIGCJOP_03712 | 1.6e-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 | |
AIIGCJOP_03713 | 1.1e-56 | hpf | J | Sigma 54 modulation protein ribosomal protein S30EA | ||
AIIGCJOP_03714 | 1.6e-134 | 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 | |
AIIGCJOP_03715 | 1.4e-181 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
AIIGCJOP_03716 | 1.1e-130 | yfiH | S | Belongs to the multicopper oxidase YfiH RL5 family | ||
AIIGCJOP_03717 | 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 | ||
AIIGCJOP_03718 | 7.2e-116 | yieP | K | transcriptional regulator | ||
AIIGCJOP_03719 | 3.1e-246 | hsrA | EGP | Major facilitator Superfamily | ||
AIIGCJOP_03720 | 4.5e-180 | 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 | ||
AIIGCJOP_03721 | 2.2e-152 | 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 | |
AIIGCJOP_03722 | 1.3e-154 | rbsB | G | Periplasmic | ||
AIIGCJOP_03723 | 4.8e-150 | rbsC | G | Belongs to the binding-protein-dependent transport system permease family | ||
AIIGCJOP_03724 | 3.2e-278 | rbsA | 3.6.3.17 | P | import. Responsible for energy coupling to the transport system | |
AIIGCJOP_03725 | 5.8e-68 | rbsD | 5.4.99.62 | G | Catalyzes the interconversion of beta-pyran and beta- furan forms of D-ribose | |
AIIGCJOP_03726 | 0.0 | kup | P | transport of potassium into the cell | ||
AIIGCJOP_03727 | 1.5e-272 | ravA | S | Functions as an ATPase. May play a role in metal insertion (metal-chelatase) or as a chaperone | ||
AIIGCJOP_03728 | 3.9e-265 | viaA | S | VWA domain protein interacting with AAA ATPase | ||
AIIGCJOP_03729 | 1.9e-186 | asnA | 6.3.1.1 | E | aspartate--ammonia ligase | |
AIIGCJOP_03730 | 6.1e-79 | asnC | K | transcriptional | ||
AIIGCJOP_03731 | 1.6e-79 | mioC | C | flavodoxin binds one FMN molecule, which serves as a redox-active prosthetic group | ||
AIIGCJOP_03732 | 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 | ||
AIIGCJOP_03733 | 1.1e-107 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of guanine in position 527 of 16S rRNA | |
AIIGCJOP_03734 | 1e-55 | 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 | ||
AIIGCJOP_03735 | 9.9e-149 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
AIIGCJOP_03736 | 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 | ||
AIIGCJOP_03737 | 2.8e-55 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
AIIGCJOP_03738 | 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 | ||
AIIGCJOP_03739 | 3.6e-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 | |
AIIGCJOP_03740 | 1.7e-151 | 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 | ||
AIIGCJOP_03741 | 6.8e-259 | 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 | |
AIIGCJOP_03742 | 1.5e-68 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
AIIGCJOP_03743 | 0.0 | pelX | 4.2.2.9 | M | Parallel beta-helix repeats | |
AIIGCJOP_03744 | 1.5e-250 | 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 | |
AIIGCJOP_03745 | 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 | |
AIIGCJOP_03746 | 1.7e-193 | pstS | P | Part of the ABC transporter complex PstSACB involved in phosphate import | ||
AIIGCJOP_03747 | 2.7e-169 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
AIIGCJOP_03748 | 3.8e-154 | pstA | P | phosphate transport system permease | ||
AIIGCJOP_03749 | 5.3e-144 | 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 | |
AIIGCJOP_03750 | 1.2e-129 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
AIIGCJOP_03751 | 3.2e-180 | yieL | P | Belongs to the glycosyl hydrolase 13 family | ||
AIIGCJOP_03752 | 3.6e-123 | yieH | S | HAD-superfamily hydrolase subfamily IA, variant 3 | ||
AIIGCJOP_03753 | 1.8e-227 | yieG | S | PFAM Xanthine uracil vitamin C permease | ||
AIIGCJOP_03754 | 3.6e-97 | yieF | S | NAD(P)H-dependent FMN reductase | ||
AIIGCJOP_03755 | 5.7e-119 | yieE | 2.7.8.7 | H | Phosphopantetheinyl transferase | |
AIIGCJOP_03756 | 3.3e-183 | yidZ | K | Involved in anaerobic NO protection | ||
AIIGCJOP_03757 | 7.9e-187 | mdtL | EGP | Major facilitator superfamily MFS_1 | ||
AIIGCJOP_03758 | 3.2e-215 | tnaB | E | amino acid | ||
AIIGCJOP_03759 | 3.2e-272 | tnaA | 4.1.99.1 | E | Belongs to the beta-eliminating lyase family | |
AIIGCJOP_03760 | 8.3e-249 | 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 | ||
AIIGCJOP_03761 | 8.6e-293 | 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 | ||
AIIGCJOP_03762 | 1.3e-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 | |
AIIGCJOP_03763 | 5e-257 | 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 | ||
AIIGCJOP_03764 | 5.9e-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 | |
AIIGCJOP_03765 | 4.7e-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 | ||
AIIGCJOP_03766 | 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 | |
AIIGCJOP_03767 | 7.6e-141 | yidA | S | HAD-superfamily hydrolase, subfamily IIB | ||
AIIGCJOP_03768 | 3.9e-122 | dgoR | K | FCD domain | ||
AIIGCJOP_03769 | 2.6e-155 | dgoK | 2.7.1.58 | G | 2-keto-3-deoxy-galactonokinase | |
AIIGCJOP_03770 | 2.7e-106 | dgoA | 4.1.2.14, 4.1.2.21, 4.1.3.42 | G | KDPG and KHG aldolase | |
AIIGCJOP_03771 | 7.7e-224 | dgoD | 4.2.1.6 | H | Catalyzes the dehydration of D-galactonate to 2-keto-3- deoxy-D-galactonate | |
AIIGCJOP_03772 | 3.4e-244 | dgoT | G | Major facilitator superfamily | ||
AIIGCJOP_03773 | 8.3e-224 | yidR | U | Biopolymer transporter Tol | ||
AIIGCJOP_03774 | 2.9e-46 | yidQ | S | Protein of unknown function (DUF1375) | ||
AIIGCJOP_03775 | 4.2e-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 | ||
AIIGCJOP_03776 | 5.5e-74 | 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 | ||
AIIGCJOP_03777 | 3.9e-293 | yidE | U | transport protein | ||
AIIGCJOP_03778 | 8.4e-263 | P | Sulfatase | |||
AIIGCJOP_03779 | 1.9e-47 | 2.7.1.194, 2.7.1.200 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
AIIGCJOP_03780 | 1.1e-232 | S | PTS system sugar-specific permease component | |||
AIIGCJOP_03781 | 3.1e-198 | 2.8.2.22 | S | Arylsulfotransferase Ig-like domain | ||
AIIGCJOP_03782 | 8.8e-54 | yidH | S | Membrane | ||
AIIGCJOP_03783 | 3.7e-55 | yidG | S | Membrane | ||
AIIGCJOP_03784 | 5.3e-166 | yidF | C | Anaerobic sulfatase maturase | ||
AIIGCJOP_03785 | 2.2e-227 | dsdA | 4.3.1.18 | E | Belongs to the serine threonine dehydratase family. DsdA subfamily | |
AIIGCJOP_03786 | 5.2e-199 | emrD | EGP | Major facilitator Superfamily | ||
AIIGCJOP_03787 | 4.7e-76 | K | Acetyltransferase (GNAT) domain | |||
AIIGCJOP_03790 | 0.0 | ilvB | 2.2.1.6 | H | acetolactate synthase | |
AIIGCJOP_03791 | 2.9e-47 | ilvN | 2.2.1.6 | E | acetolactate synthase | |
AIIGCJOP_03792 | 3.3e-101 | uhpA | K | Two component transcriptional regulator, LuxR family | ||
AIIGCJOP_03793 | 2.4e-273 | uhpB | 2.7.13.3 | T | Signal transduction histidine kinase | |
AIIGCJOP_03794 | 3.5e-244 | uhpC | G | PFAM Major facilitator superfamily | ||
AIIGCJOP_03795 | 2.5e-253 | uhpT | G | PFAM Major facilitator superfamily | ||
AIIGCJOP_03796 | 8.9e-192 | mhpC | 3.4.11.5 | I | Alpha beta hydrolase | |
AIIGCJOP_03797 | 1.1e-75 | yicN | S | Protein of unknown function (DUF1198) | ||
AIIGCJOP_03798 | 1.6e-200 | nepI | EGP | Major facilitator Superfamily | ||
AIIGCJOP_03799 | 2.8e-152 | yicL | EG | transporter | ||
AIIGCJOP_03800 | 7.5e-266 | lamB | G | Maltoporin (phage lambda and maltose receptor) | ||
AIIGCJOP_03801 | 6.9e-47 | celC | 2.7.1.196, 2.7.1.205 | G | PTS system, cellobiose-specific IIA component | |
AIIGCJOP_03802 | 6.4e-281 | gmuD | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AIIGCJOP_03803 | 2.4e-237 | 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 | ||
AIIGCJOP_03804 | 3.1e-50 | celA | 2.7.1.196, 2.7.1.205 | G | Phosphotransferase system, lactose cellobiose-specific IIB subunit | |
AIIGCJOP_03805 | 8.2e-171 | ascG_1 | K | transcriptional regulator | ||
AIIGCJOP_03806 | 3.4e-46 | |||||
AIIGCJOP_03807 | 1.7e-67 | S | Acetyltransferase (GNAT) domain | |||
AIIGCJOP_03808 | 2.8e-109 | K | Transcriptional regulator | |||
AIIGCJOP_03809 | 2.1e-266 | bmr3 | EGP | Major facilitator Superfamily | ||
AIIGCJOP_03810 | 1.7e-137 | metQ | M | Belongs to the nlpA lipoprotein family | ||
AIIGCJOP_03811 | 3.1e-123 | yddR | S | Beta-lactamase superfamily domain | ||
AIIGCJOP_03812 | 1.4e-154 | adpA | K | DJ-1/PfpI family | ||
AIIGCJOP_03813 | 6.9e-198 | S | AAA ATPase domain | |||
AIIGCJOP_03814 | 7e-178 | ybgA | S | Conserved Protein | ||
AIIGCJOP_03815 | 8.2e-67 | hiuH | 3.5.2.17, 4.1.1.97 | S | Belongs to the transthyretin family. 5-hydroxyisourate hydrolase subfamily | |
AIIGCJOP_03816 | 1.1e-127 | K | helix_turn_helix, mercury resistance | |||
AIIGCJOP_03817 | 8.5e-93 | blc | M | Outer Membrane Lipoprotein | ||
AIIGCJOP_03818 | 8.6e-171 | |||||
AIIGCJOP_03819 | 3.2e-42 | |||||
AIIGCJOP_03820 | 6.6e-20 | proV | 3.6.3.32 | K | sequence-specific DNA binding | |
AIIGCJOP_03821 | 2.4e-69 | yjaB | K | Acetyltransferase (GNAT) domain | ||
AIIGCJOP_03822 | 2.8e-142 | ydeC | K | AraC-like ligand binding domain | ||
AIIGCJOP_03823 | 0.0 | bglB | 3.2.1.21 | GH3 | G | Belongs to the glycosyl hydrolase 3 family |
AIIGCJOP_03824 | 2.7e-215 | G | transporter | |||
AIIGCJOP_03825 | 6.8e-44 | S | Toxin SymE, type I toxin-antitoxin system | |||
AIIGCJOP_03826 | 1e-24 | S | protein encoded in hypervariable junctions of pilus gene clusters | |||
AIIGCJOP_03829 | 2.6e-28 | immA | E | IrrE N-terminal-like domain | ||
AIIGCJOP_03830 | 1.5e-43 | S | Beta protein | |||
AIIGCJOP_03831 | 1.4e-14 | |||||
AIIGCJOP_03833 | 1.1e-256 | yicJ | G | COG2211 Na melibiose symporter and related transporters | ||
AIIGCJOP_03834 | 0.0 | yicI | 3.2.1.177 | GH31 | G | Belongs to the glycosyl hydrolase 31 family |
AIIGCJOP_03835 | 0.0 | yicH | M | AsmA Family | ||
AIIGCJOP_03836 | 1.8e-243 | xanP | F | xanthine | ||
AIIGCJOP_03837 | 8.2e-200 | gltS | P | Catalyzes the sodium-dependent transport of glutamate | ||
AIIGCJOP_03838 | 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) | |
AIIGCJOP_03839 | 8.9e-116 | trmH | 2.1.1.185, 2.1.1.34 | J | Catalyzes the 2'-O methylation of guanosine at position 18 in tRNA | |
AIIGCJOP_03840 | 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 | |
AIIGCJOP_03841 | 6.1e-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 | |
AIIGCJOP_03842 | 2.4e-110 | F | Guanylate kinase | |||
AIIGCJOP_03843 | 4.1e-266 | 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 | |
AIIGCJOP_03844 | 1.4e-99 | yicG | S | Membrane | ||
AIIGCJOP_03845 | 2.6e-115 | I | Acyltransferase family | |||
AIIGCJOP_03846 | 9.5e-150 | yicC | S | Stress-induced protein | ||
AIIGCJOP_03847 | 1e-125 | 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 | |
AIIGCJOP_03848 | 2e-112 | 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) | |
AIIGCJOP_03849 | 2.1e-100 | 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 | ||
AIIGCJOP_03850 | 6.1e-79 | 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 | |
AIIGCJOP_03851 | 4.8e-216 | 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 | |
AIIGCJOP_03852 | 1.4e-105 | radC | E | Belongs to the UPF0758 family | ||
AIIGCJOP_03853 | 6.6e-37 | rpmB | J | Belongs to the bacterial ribosomal protein bL28 family | ||
AIIGCJOP_03854 | 1.9e-22 | rpmG | J | there are paralogous genes in several bacterial genomes, and a CXXC motif for zinc binding and an upstream regulation region of the paralog lacking this motif that are regulated by zinc | ||
AIIGCJOP_03855 | 4.3e-152 | 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 | |
AIIGCJOP_03856 | 1.8e-81 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
AIIGCJOP_03857 | 1.5e-133 | waaE | GT2 | S | PFAM Glycosyl transferase, family 2 | |
AIIGCJOP_03858 | 6.3e-235 | kdtA | 2.4.99.12, 2.4.99.13, 2.4.99.14, 2.4.99.15 | GT30 | M | glycosyl transferase group 1 |
AIIGCJOP_03859 | 2.2e-293 | Z012_09105 | 2.7.8.42, 2.7.8.43 | S | Sulfatase | |
AIIGCJOP_03860 | 3.8e-187 | M | transferase activity, transferring glycosyl groups | |||
AIIGCJOP_03861 | 2.3e-184 | wgaB | 2.4.2.53 | GT2 | M | Glycosyl transferase, family 2 |
AIIGCJOP_03862 | 5.7e-227 | S | O-Antigen ligase | |||
AIIGCJOP_03863 | 7.3e-195 | walR | GT4 | M | glycosyl transferase group 1 | |
AIIGCJOP_03864 | 8e-202 | rfaG | GT4 | M | Catalyzes the addition of the first glucose residue to the LPS core | |
AIIGCJOP_03865 | 5.2e-209 | rfaQ | GT9 | M | heptosyltransferase | |
AIIGCJOP_03866 | 6.5e-179 | rfaC | GT9 | M | PFAM glycosyl transferase family 9 | |
AIIGCJOP_03867 | 2.1e-199 | rfaF | GT9 | M | heptosyltransferase | |
AIIGCJOP_03868 | 1.8e-178 | 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 | |
AIIGCJOP_03869 | 8.9e-223 | 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 | |
AIIGCJOP_03870 | 1.5e-199 | tdh | 1.1.1.103 | C | Catalyzes the NAD( )-dependent oxidation of L-threonine to 2-amino-3-ketobutyrate | |
AIIGCJOP_03871 | 1.2e-141 | M | COG0463 Glycosyltransferases involved in cell wall biogenesis | |||
AIIGCJOP_03872 | 7.3e-164 | yibQ | S | protein conserved in bacteria | ||
AIIGCJOP_03873 | 2.9e-139 | envC | D | Peptidase family M23 | ||
AIIGCJOP_03874 | 3.5e-288 | gpmI | 5.4.2.12 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
AIIGCJOP_03875 | 3.4e-71 | yibN | 2.8.1.1, 2.8.1.2 | P | rhodanese-related sulfurtransferase | |
AIIGCJOP_03876 | 7.3e-42 | grxC | O | Has a glutathione-disulfide oxidoreductase activity in the presence of NADPH and glutathione reductase. Reduces low molecular weight disulfides and proteins | ||
AIIGCJOP_03877 | 3.8e-84 | 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 | ||
AIIGCJOP_03878 | 2.8e-185 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
AIIGCJOP_03879 | 1.1e-150 | cysE | 2.3.1.30 | E | serine acetyltransferase | |
AIIGCJOP_03880 | 4.2e-83 | 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 | |
AIIGCJOP_03881 | 3.7e-221 | lldD | 1.1.2.3 | C | Catalyzes the conversion of L-lactate to pyruvate. Is coupled to the respiratory chain | |
AIIGCJOP_03882 | 8.2e-129 | lldR | K | FCD | ||
AIIGCJOP_03883 | 3e-301 | lldP | C | L-lactate permease | ||
AIIGCJOP_03884 | 2.9e-52 | yibL | S | Protein of unknown function (DUF2810) | ||
AIIGCJOP_03885 | 3.3e-101 | mtlR | K | Mannitol repressor | ||
AIIGCJOP_03886 | 6.2e-205 | mtlD | 1.1.1.17 | C | Mannitol-1-Phosphate 5-Dehydrogenase | |
AIIGCJOP_03887 | 0.0 | mtlA | 2.7.1.197, 2.7.1.202 | G | PTS system mannitol-specific | |
AIIGCJOP_03888 | 1.2e-58 | yibI | S | Protein of unknown function (DUF3302) | ||
AIIGCJOP_03889 | 7.2e-198 | yibH | V | secretion protein HlyD family | ||
AIIGCJOP_03890 | 3.3e-104 | yibF | 2.5.1.18 | O | Glutathione S-Transferase | |
AIIGCJOP_03891 | 8.2e-228 | selA | 2.9.1.1 | J | Converts seryl-tRNA(Sec) to selenocysteinyl-tRNA(Sec) required for selenoprotein biosynthesis | |
AIIGCJOP_03892 | 0.0 | selB | J | Translation elongation factor | ||
AIIGCJOP_03893 | 1.2e-152 | GK | ROK family | |||
AIIGCJOP_03894 | 8.3e-298 | aldB | C | belongs to the aldehyde dehydrogenase family | ||
AIIGCJOP_03895 | 1.5e-156 | yiaU | K | Transcriptional regulator | ||
AIIGCJOP_03896 | 2.6e-116 | yiaT | M | MltA-interacting protein | ||
AIIGCJOP_03897 | 0.0 | 3.2.1.185 | GH127 | S | protein conserved in bacteria | |
AIIGCJOP_03898 | 2.6e-258 | G | COG2211 Na melibiose symporter and related transporters | |||
AIIGCJOP_03899 | 2.5e-139 | yisR | K | transcriptional regulator | ||
AIIGCJOP_03900 | 3.8e-76 | ysaA | C | Electron transport protein | ||
AIIGCJOP_03901 | 5.4e-247 | avtA | 2.6.1.66 | E | Valine--pyruvate aminotransferase | |
AIIGCJOP_03902 | 0.0 | malS | 3.2.1.1 | GH13 | G | alpha-amylase |
AIIGCJOP_03903 | 1.1e-101 | bax | GH73 | S | FlgJ-related protein | |
AIIGCJOP_03904 | 4.8e-221 | xylR | 5.3.1.12 | K | transcriptional regulator | |
AIIGCJOP_03905 | 8.3e-189 | xylH | G | Belongs to the binding-protein-dependent transport system permease family | ||
AIIGCJOP_03906 | 2.1e-280 | xylG | 3.6.3.17 | P | import. Responsible for energy coupling to the transport system | |
AIIGCJOP_03907 | 5e-179 | xylF | G | D-xylose ABC transporter periplasmic substrate-binding protein | ||
AIIGCJOP_03908 | 3e-264 | xylA | 5.3.1.5 | G | Belongs to the xylose isomerase family | |
AIIGCJOP_03909 | 2.7e-274 | xylB | 2.7.1.17, 2.7.1.189, 2.7.1.5 | G | xylulose kinase | |
AIIGCJOP_03910 | 3.5e-68 | yiaA | S | Membrane | ||
AIIGCJOP_03911 | 2.3e-176 | wecH | S | Responsible for the incorporation of O-acetyl groups into the enterobacterial common antigen (ECA) trisaccharide repeat units | ||
AIIGCJOP_03912 | 6.7e-42 | ysaB | S | YsaB-like lipoprotein | ||
AIIGCJOP_03913 | 1.3e-178 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
AIIGCJOP_03914 | 0.0 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
AIIGCJOP_03915 | 6.3e-272 | yheS_2 | S | ATPase components of ABC transporters with duplicated ATPase domains | ||
AIIGCJOP_03916 | 1.8e-44 | yiaG | K | transcriptional regulator | ||
AIIGCJOP_03917 | 1.6e-123 | yiaF | S | exported protein | ||
AIIGCJOP_03918 | 4e-33 | cspA | K | Cold shock | ||
AIIGCJOP_03919 | 1.6e-174 | 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 | |
AIIGCJOP_03920 | 5.4e-242 | G | Major facilitator superfamily | |||
AIIGCJOP_03921 | 2.9e-160 | kdgK | 2.7.1.13, 2.7.1.45 | G | 2-dehydro-3-deoxygluconokinase | |
AIIGCJOP_03922 | 1.5e-122 | kguE | 2.7.1.45 | G | Xylose isomerase domain protein TIM barrel | |
AIIGCJOP_03923 | 1.7e-182 | ptxS | K | transcriptional regulator | ||
AIIGCJOP_03924 | 3.4e-83 | yiaD | M | Belongs to the ompA family | ||
AIIGCJOP_03925 | 0.0 | bisC | 1.7.2.3, 1.8.5.3 | C | Belongs to the prokaryotic molybdopterin-containing oxidoreductase family | |
AIIGCJOP_03926 | 7.2e-77 | yiaC | 2.3.1.1, 2.3.1.210 | K | acetyltransferase | |
AIIGCJOP_03927 | 7.4e-106 | tag | 3.2.2.20 | L | glycosylase | |
AIIGCJOP_03928 | 2.9e-120 | yhjY | N | outer membrane autotransporter | ||
AIIGCJOP_03930 | 3.4e-182 | yhjX | P | Major facilitator superfamily | ||
AIIGCJOP_03931 | 0.0 | eptB | 2.7.8.42, 2.7.8.43 | S | membrane-associated metal-dependent hydrolase | |
AIIGCJOP_03932 | 1.7e-07 | |||||
AIIGCJOP_03933 | 0.0 | dppA | E | Bacterial extracellular solute-binding proteins, family 5 Middle | ||
AIIGCJOP_03934 | 3.7e-185 | dppB | P | Binding-protein-dependent transport system inner membrane component | ||
AIIGCJOP_03935 | 1.2e-123 | dppC | P | N-terminal TM domain of oligopeptide transport permease C | ||
AIIGCJOP_03936 | 3.6e-177 | dppD | P | Belongs to the ABC transporter superfamily | ||
AIIGCJOP_03937 | 1.1e-189 | dppF | P | Belongs to the ABC transporter superfamily | ||
AIIGCJOP_03938 | 2.5e-172 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
AIIGCJOP_03945 | 3.7e-142 | yhdZ | 3.6.3.21 | E | (ABC) transporter | |
AIIGCJOP_03946 | 1.6e-202 | yhdY | P | amino acid ABC transporter | ||
AIIGCJOP_03947 | 3.1e-204 | yhdX | P | amino acid ABC transporter | ||
AIIGCJOP_03948 | 1.3e-190 | aapJ | ET | Belongs to the bacterial solute-binding protein 3 family | ||
AIIGCJOP_03949 | 6e-32 | yhdV | S | Protein involved in biological_process | ||
AIIGCJOP_03950 | 0.0 | acrF | V | Hydrophobe amphiphile efflux-1 HAE1 | ||
AIIGCJOP_03951 | 9.2e-193 | acrE | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | ||
AIIGCJOP_03952 | 2.9e-87 | ttgR | K | acrEF envCD operon | ||
AIIGCJOP_03953 | 0.0 | gmr | 2.7.7.65 | T | MHYT domain | |
AIIGCJOP_03954 | 5.5e-22 | yhdU | S | Protein of unknown function (DUF2556) | ||
AIIGCJOP_03955 | 4.4e-46 | fis | K | Activates ribosomal RNA transcription. Plays a direct role in upstream activation of rRNA promoters | ||
AIIGCJOP_03956 | 1.4e-161 | dusB | H | 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 | ||
AIIGCJOP_03957 | 9.1e-109 | cah | 4.2.1.1 | P | Eukaryotic-type carbonic anhydrase | |
AIIGCJOP_03958 | 2.4e-164 | prmA | J | Ribosomal protein L11 methyltransferase | ||
AIIGCJOP_03959 | 2.7e-237 | panF | H | Sodium:solute symporter family | ||
AIIGCJOP_03960 | 1.3e-38 | yhdT | S | Membrane | ||
AIIGCJOP_03961 | 1.4e-256 | accC | 6.3.4.14, 6.4.1.2 | I | Biotin carboxylase | |
AIIGCJOP_03962 | 1.4e-62 | accB | 2.3.1.12 | I | first, biotin carboxylase catalyzes the carboxylation of the carrier protein and then the transcarboxylase transfers the carboxyl group to form malonyl-CoA | |
AIIGCJOP_03963 | 4.3e-77 | aroQ | 3.4.13.9, 4.2.1.10 | E | Catalyzes a trans-dehydration via an enolate intermediate | |
AIIGCJOP_03964 | 6e-103 | 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 | ||
AIIGCJOP_03965 | 8e-193 | 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 | ||
AIIGCJOP_03966 | 2.7e-177 | yhdH | C | COG0604 NADPH quinone reductase and related Zn-dependent oxidoreductases | ||
AIIGCJOP_03967 | 0.0 | csrD | T | GGDEF domain | ||
AIIGCJOP_03968 | 1.3e-190 | mreB | D | rod shape-determining protein MreB | ||
AIIGCJOP_03969 | 2.2e-177 | mreC | M | Involved in formation and maintenance of cell shape | ||
AIIGCJOP_03970 | 1.6e-82 | mreD | M | Involved in formation of the rod shape of the cell. May also contribute to regulation of formation of penicillin-binding proteins | ||
AIIGCJOP_03971 | 1.2e-100 | maf | 2.1.1.190 | D | Maf-like protein | |
AIIGCJOP_03972 | 3.6e-274 | rng | J | Involved in the processing of the 5'-end of 16S rRNA | ||
AIIGCJOP_03973 | 0.0 | yhdP | D | Membrane | ||
AIIGCJOP_03974 | 4.2e-267 | 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 | ||
AIIGCJOP_03975 | 8.5e-165 | aaeR | K | Transcriptional regulator | ||
AIIGCJOP_03976 | 2e-29 | aaeX | S | Protein of unknown function (DUF1656) | ||
AIIGCJOP_03977 | 1.2e-161 | aaeA | V | P-hydroxybenzoic acid efflux pump subunit AaeA | ||
AIIGCJOP_03978 | 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 | ||
AIIGCJOP_03979 | 3e-257 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Belongs to the aldehyde dehydrogenase family | |
AIIGCJOP_03980 | 7.3e-40 | yhcO | K | inhibitor | ||
AIIGCJOP_03981 | 7.1e-32 | bhsA_1 | S | Protein of unknown function (DUF1471) | ||
AIIGCJOP_03982 | 6.1e-15 | yhcN | S | Protein of unknown function (DUF1471) | ||
AIIGCJOP_03983 | 1.5e-77 | argR | K | Regulates arginine biosynthesis genes | ||
AIIGCJOP_03984 | 7.1e-167 | mdh | 1.1.1.37 | C | Catalyzes the reversible oxidation of malate to oxaloacetate | |
AIIGCJOP_03985 | 2.3e-193 | degS | 3.4.21.107 | O | Periplasmic serine protease DegS | |
AIIGCJOP_03986 | 3.5e-215 | degQ | 1.3.1.74, 3.4.21.107 | M | Belongs to the peptidase S1C family | |
AIIGCJOP_03987 | 1.4e-63 | yhcB | S | Cytochrome D ubiquinol oxidase, subunit | ||
AIIGCJOP_03988 | 1.1e-201 | zapE | D | Reduces the stability of FtsZ polymers in the presence of ATP | ||
AIIGCJOP_03989 | 3.1e-77 | 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 | ||
AIIGCJOP_03990 | 8.1e-64 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
AIIGCJOP_03991 | 1e-116 | sspA | O | Belongs to the GST superfamily | ||
AIIGCJOP_03992 | 9e-81 | sspB | S | stringent starvation protein b | ||
AIIGCJOP_03993 | 1.5e-277 | gltD | 1.4.1.13, 1.4.1.14 | C | Glutamate synthase | |
AIIGCJOP_03994 | 0.0 | gltB | 1.4.1.13, 1.4.1.14, 1.4.7.1 | E | GXGXG motif | |
AIIGCJOP_03995 | 4.1e-170 | yhcC | S | radical SAM protein | ||
AIIGCJOP_03996 | 8.5e-263 | yjgR | S | Domain of unknown function DUF87 | ||
AIIGCJOP_03997 | 1.7e-277 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dihydroxyacetone kinase | |
AIIGCJOP_03998 | 5.1e-195 | yjgB | 1.1.1.1 | S | alcohol dehydrogenase | |
AIIGCJOP_03999 | 1.1e-78 | yjgM | K | Acetyltransferase | ||
AIIGCJOP_04000 | 4.4e-65 | yjgN | S | Bacterial protein of unknown function (DUF898) | ||
AIIGCJOP_04001 | 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 | |
AIIGCJOP_04002 | 9.6e-79 | holC | 2.7.7.7 | L | DNA polymerase III chi subunit | |
AIIGCJOP_04003 | 3.1e-289 | 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 | |
AIIGCJOP_04004 | 1.4e-187 | lptF | S | Permease | ||
AIIGCJOP_04005 | 1.1e-190 | lptG | S | permease | ||
AIIGCJOP_04006 | 0.0 | arcB | 2.7.13.3 | T | PhoQ Sensor | |
AIIGCJOP_04007 | 5.4e-105 | elbB | Q | Displays glyoxalase activity, catalyzing the conversion of glyoxal to glycolate | ||
AIIGCJOP_04008 | 6.1e-126 | mtgA | 2.4.1.129, 3.4.16.4 | GT51 | M | Peptidoglycan polymerase that catalyzes glycan chain elongation from lipid-linked precursors |
AIIGCJOP_04009 | 3e-41 | ptsO | 2.7.1.121, 2.7.1.202, 2.7.3.9 | G | Phosphotransferase System | |
AIIGCJOP_04010 | 1.2e-157 | 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 | ||
AIIGCJOP_04011 | 1.6e-80 | ptsN | 2.7.1.194, 2.7.1.195, 2.7.1.202, 2.7.3.9 | G | PTS IIA-like nitrogen-regulatory protein PtsN | |
AIIGCJOP_04012 | 4.7e-45 | hpf | J | sigma (54) modulation protein | ||
AIIGCJOP_04013 | 1.5e-245 | rpoN | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
AIIGCJOP_04014 | 2.4e-130 | lptB | S | abc transporter atp-binding protein | ||
AIIGCJOP_04015 | 2.4e-90 | 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 | ||
AIIGCJOP_04016 | 7.3e-98 | 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 | ||
AIIGCJOP_04017 | 8.5e-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 | |
AIIGCJOP_04018 | 1e-176 | kdsD | 5.3.1.13 | M | Arabinose 5-phosphate isomerase | |
AIIGCJOP_04019 | 2.6e-164 | yrbG | P | antiporter | ||
AIIGCJOP_04020 | 1.6e-143 | mlaF | Q | (ABC) transporter | ||
AIIGCJOP_04021 | 6.6e-134 | mlaE | Q | COG0767 ABC-type transport system involved in resistance to organic solvents, permease component | ||
AIIGCJOP_04022 | 6.3e-94 | mlaD | Q | ABC-type transport system involved in resistance to organic solvents periplasmic component | ||
AIIGCJOP_04023 | 2.4e-110 | mlaC | Q | ABC-type transport system involved in resistance to organic solvents auxiliary component | ||
AIIGCJOP_04024 | 6.7e-31 | mlaB | S | NTP binding protein (Contains STAS domain) | ||
AIIGCJOP_04025 | 3.1e-40 | yrbA | K | Belongs to the BolA IbaG family | ||
AIIGCJOP_04026 | 7.7e-233 | murA | 2.5.1.7 | M | Belongs to the EPSP synthase family. MurA subfamily | |
AIIGCJOP_04027 | 1.8e-44 | sfsB | K | transcriptional regulator | ||
AIIGCJOP_04028 | 6.2e-174 | ispB | 2.5.1.30, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
AIIGCJOP_04029 | 8.1e-51 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
AIIGCJOP_04030 | 3.7e-41 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
AIIGCJOP_04031 | 2.1e-169 | yhbE | EG | EamA-like transporter family | ||
AIIGCJOP_04032 | 1e-199 | 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 | ||
AIIGCJOP_04033 | 2.1e-172 | T | PhoQ Sensor | |||
AIIGCJOP_04034 | 4.5e-115 | T | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
AIIGCJOP_04035 | 4e-254 | dacB | 3.4.16.4 | M | D-alanyl-D-alanine carboxypeptidase | |
AIIGCJOP_04036 | 7.5e-80 | 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 | ||
AIIGCJOP_04037 | 9.3e-53 | yhbY | J | RNA-binding protein containing KH domain possibly ribosomal protein | ||
AIIGCJOP_04038 | 2e-112 | 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 | |
AIIGCJOP_04039 | 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 | ||
AIIGCJOP_04040 | 5.5e-150 | 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 | |
AIIGCJOP_04041 | 1.1e-248 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
AIIGCJOP_04042 | 1.3e-46 | secG | U | Preprotein translocase, subunit SecG | ||
AIIGCJOP_04044 | 4.4e-263 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type | |
AIIGCJOP_04045 | 5.9e-08 | |||||
AIIGCJOP_04046 | 1.4e-81 | rimP | J | Required for maturation of 30S ribosomal subunits | ||
AIIGCJOP_04047 | 2.4e-270 | nusA | K | Participates in both transcription termination and antitermination | ||
AIIGCJOP_04048 | 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 | ||
AIIGCJOP_04049 | 1.2e-62 | 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 | ||
AIIGCJOP_04050 | 1.8e-170 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
AIIGCJOP_04051 | 1.9e-40 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
AIIGCJOP_04053 | 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 | |
AIIGCJOP_04054 | 1.3e-162 | nlpI | S | May be involved in cell division | ||
AIIGCJOP_04055 | 3.9e-281 | 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 | |
AIIGCJOP_04056 | 3.4e-225 | mtr | E | amino acid | ||
AIIGCJOP_04057 | 2.4e-189 | yhbW | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | ||
AIIGCJOP_04058 | 5.8e-163 | yhbV | O | protease | ||
AIIGCJOP_04059 | 8.9e-184 | yhbU | O | Peptidase U32 | ||
AIIGCJOP_04060 | 6.3e-88 | yhbT | I | lipid carrier protein | ||
AIIGCJOP_04061 | 1.5e-86 | yhbS | S | N-acetyltransferase | ||
AIIGCJOP_04062 | 9.7e-79 | yhbP | S | Belongs to the UPF0306 family | ||
AIIGCJOP_04063 | 5.8e-86 | yfkM | 3.5.1.124 | S | intracellular protease | |
AIIGCJOP_04064 | 3.8e-111 | yraR | GM | Nucleoside-diphosphate-sugar epimerases | ||
AIIGCJOP_04065 | 1.6e-84 | yraP | S | bacterial OsmY and nodulation domain | ||
AIIGCJOP_04066 | 3.2e-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 | |
AIIGCJOP_04067 | 4e-63 | yraN | L | Belongs to the UPF0102 family | ||
AIIGCJOP_04068 | 0.0 | lpoA | M | Regulator of peptidoglycan synthesis that is essential for the function of penicillin-binding protein 1A (PBP1a) | ||
AIIGCJOP_04069 | 1.4e-156 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
AIIGCJOP_04070 | 4.8e-142 | K | filamentation induced by cAMP | |||
AIIGCJOP_04071 | 1.8e-276 | garD | 4.2.1.42, 4.2.1.7 | G | Catalyzes the dehydration of galactarate to form 5- dehydro-4-deoxy-D-glucarate | |
AIIGCJOP_04072 | 1.6e-244 | garP | G | transporter | ||
AIIGCJOP_04073 | 1.1e-141 | garL | 4.1.2.20, 4.1.2.52 | G | Belongs to the HpcH HpaI aldolase family | |
AIIGCJOP_04074 | 3.7e-157 | garR | 1.1.1.60 | I | Catalyzes the reduction of tatronate semialdehyde to D- glycerate | |
AIIGCJOP_04075 | 2e-203 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
AIIGCJOP_04076 | 3.4e-231 | yhaO | E | Serine transporter | ||
AIIGCJOP_04077 | 2e-207 | yhaM | S | Belongs to the UPF0597 family | ||
AIIGCJOP_04078 | 4.5e-126 | yhaK | S | Belongs to the pirin family | ||
AIIGCJOP_04079 | 2.1e-160 | yhaJ | K | transcriptional regulator | ||
AIIGCJOP_04080 | 4.4e-64 | yhaH | S | Membrane | ||
AIIGCJOP_04081 | 1.1e-197 | yqjG | 1.8.5.7, 2.5.1.18 | O | Glutathione S-Transferase | |
AIIGCJOP_04082 | 1.2e-64 | yqjF | S | membrane | ||
AIIGCJOP_04083 | 3.7e-35 | yqjK | S | YqjK-like protein | ||
AIIGCJOP_04084 | 3.1e-48 | yqjE | S | Membrane | ||
AIIGCJOP_04085 | 5.7e-25 | yqjD | S | Membrane protein YqjD | ||
AIIGCJOP_04086 | 8.7e-28 | yqjC | S | Protein of unknown function (DUF1090) | ||
AIIGCJOP_04087 | 2.1e-54 | mzrA | S | SecD export protein N-terminal TM region | ||
AIIGCJOP_04088 | 2.8e-117 | yqjA | S | Inner membrane protein yqjA | ||
AIIGCJOP_04089 | 1.5e-141 | exuR | K | Transcriptional | ||
AIIGCJOP_04090 | 1.7e-235 | exuT | G | Major facilitator superfamily | ||
AIIGCJOP_04091 | 2.2e-276 | uxaC | 5.3.1.12 | G | glucuronate isomerase | |
AIIGCJOP_04092 | 2.1e-282 | uxaA | 4.2.1.7 | G | Catalyzes the dehydration of galactarate to form 5- dehydro-4-deoxy-D-glucarate | |
AIIGCJOP_04093 | 7.1e-207 | sstT | E | Involved in the import of serine and threonine into the cell, with the concomitant import of sodium (symport system) | ||
AIIGCJOP_04094 | 7.3e-167 | alx | P | membrane protein, terc | ||
AIIGCJOP_04095 | 3.9e-179 | ygjR | S | oxidoreductase | ||
AIIGCJOP_04096 | 4.2e-89 | ygjP | S | WLM domain | ||
AIIGCJOP_04097 | 1.1e-211 | rlmG | 2.1.1.172, 2.1.1.174 | J | Specifically methylates the guanine in position 1835 (m2G1835) of 23S rRNA | |
AIIGCJOP_04098 | 0.0 | fadH | 1.3.1.34 | C | PFAM NADH flavin oxidoreductase NADH oxidase | |
AIIGCJOP_04099 | 1.1e-297 | 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 | |
AIIGCJOP_04100 | 1.6e-166 | lsrR | K | transcriptional regulator | ||
AIIGCJOP_04101 | 4.2e-270 | 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 | |
AIIGCJOP_04102 | 1.1e-173 | lsrC | U | Belongs to the binding-protein-dependent transport system permease family | ||
AIIGCJOP_04103 | 9.4e-162 | lsrD | U | Belongs to the binding-protein-dependent transport system permease family | ||
AIIGCJOP_04104 | 1.9e-181 | lsrB | G | Part of the ABC transporter complex LsrABCD involved in autoinducer 2 (AI-2) import. Binds AI-2 and delivers it to the LsrC and LsrD permeases | ||
AIIGCJOP_04105 | 9.1e-164 | lsrF | 2.3.1.245, 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 | |
AIIGCJOP_04106 | 5.7e-46 | 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) | |
AIIGCJOP_04107 | 9.8e-258 | 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 | |
AIIGCJOP_04108 | 1.2e-184 | aer | T | Motif C-terminal to PAS motifs (likely to contribute to PAS structural domain) | ||
AIIGCJOP_04109 | 8.4e-173 | cheM | NT | Four helix bundle sensory module for signal transduction | ||
AIIGCJOP_04110 | 3.7e-75 | yqjI | K | transcriptional regulator | ||
AIIGCJOP_04111 | 2.5e-138 | yqjH | 1.16.1.9 | P | Siderophore-interacting protein | |
AIIGCJOP_04112 | 1.7e-197 | I | Heat shock protein | |||
AIIGCJOP_04113 | 3.4e-55 | S | Cellulose biosynthesis protein BcsO | |||
AIIGCJOP_04114 | 1.2e-146 | yhjQ | D | cellulose synthase operon protein YhjQ | ||
AIIGCJOP_04115 | 0.0 | bcsA | 2.4.1.12 | GT2 | M | Cellulose synthase |
AIIGCJOP_04116 | 0.0 | bcsB | NU | cellulose synthase | ||
AIIGCJOP_04117 | 0.0 | bcsC | 1.8.1.9, 2.7.11.1 | O | Cellulose synthase operon protein C C-terminus (BCSC_C) | |
AIIGCJOP_04118 | 3.6e-79 | bcsD | S | cellulose synthase | ||
AIIGCJOP_04119 | 5.9e-188 | celC | 3.2.1.4 | GH8 | G | Belongs to the glycosyl hydrolase 8 (cellulase D) family |
AIIGCJOP_04120 | 6.7e-38 | |||||
AIIGCJOP_04122 | 8.9e-48 | L | Phage integrase family | |||
AIIGCJOP_04123 | 5.6e-35 | L | Transposase and inactivated derivatives | |||
AIIGCJOP_04124 | 1e-21 | L | Homeodomain-like domain | |||
AIIGCJOP_04126 | 1.9e-195 | VP0380 | L | Arm DNA-binding domain | ||
AIIGCJOP_04127 | 3.4e-256 | alsT | E | alanine symporter | ||
AIIGCJOP_04128 | 4.6e-162 | phoH | T | PhoH-like protein | ||
AIIGCJOP_04129 | 6.6e-240 | efeB | P | peroxidase | ||
AIIGCJOP_04130 | 4.8e-202 | efeO | P | periplasmic lipoprotein involved in iron transport | ||
AIIGCJOP_04131 | 6.1e-146 | efeU | P | PFAM Iron permease FTR1 | ||
AIIGCJOP_04132 | 1.2e-200 | nupC | F | Belongs to the concentrative nucleoside transporter (CNT) (TC 2.A.41) family | ||
AIIGCJOP_04133 | 3.3e-71 | J | Protein of unknown function (DUF3574) | |||
AIIGCJOP_04134 | 3.6e-269 | putP | E | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
AIIGCJOP_04135 | 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 | |
AIIGCJOP_04136 | 4e-55 | S | Lysozyme inhibitor LprI | |||
AIIGCJOP_04137 | 2.1e-109 | rutR | K | transcriptional regulator | ||
AIIGCJOP_04138 | 1.5e-205 | 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 | |
AIIGCJOP_04139 | 3.2e-124 | 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 | |
AIIGCJOP_04140 | 3.4e-67 | rutC | 3.5.99.10 | J | May reduce aminoacrylate peracid to aminoacrylate. Required to remove a toxic intermediate produce by the pyrimidine nitrogen degradation | |
AIIGCJOP_04141 | 2.8e-135 | rutD | F | May increase the rate of spontaneous hydrolysis of aminoacrylate to malonic semialdehyde. Required to remove a toxic intermediate produce in the pyrimidine nitrogen degradation | ||
AIIGCJOP_04142 | 1.2e-106 | rutE | C | May reduce toxic product malonic semialdehyde to 3- hydroxypropionic acid, which is excreted | ||
AIIGCJOP_04143 | 6.5e-87 | 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 | |
AIIGCJOP_04144 | 2e-223 | rutG | F | Xanthine uracil | ||
AIIGCJOP_04145 | 2.6e-145 | yedA | EG | of the drug metabolite transporter (DMT) superfamily | ||
AIIGCJOP_04146 | 4.6e-103 | wrbA | 1.6.5.2 | S | Belongs to the WrbA family | |
AIIGCJOP_04147 | 9.5e-33 | yccJ | S | YccJ-like protein | ||
AIIGCJOP_04148 | 4.3e-228 | agp | 3.1.3.10 | S | Acid phosphatase | |
AIIGCJOP_04149 | 5.1e-70 | K | transcriptional regulator | |||
AIIGCJOP_04150 | 7.4e-88 | S | 50S ribosomal protein L21 | |||
AIIGCJOP_04152 | 1e-96 | K | transcriptional regulator | |||
AIIGCJOP_04153 | 3.9e-71 | S | Domain of unknown function (DUF4865) | |||
AIIGCJOP_04154 | 1.6e-56 | 5.3.2.6 | S | tautomerase | ||
AIIGCJOP_04155 | 2.5e-45 | yphJ | 4.1.1.44 | I | decarboxylase | |
AIIGCJOP_04156 | 5e-130 | dgdR | K | transcriptional regulator | ||
AIIGCJOP_04157 | 1.5e-308 | 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) | |
AIIGCJOP_04158 | 3.9e-126 | MA20_10370 | 2.1.1.63, 3.2.2.21 | K | AraC family transcriptional regulator | |
AIIGCJOP_04159 | 6.6e-78 | S | YcxB-like protein | |||
AIIGCJOP_04161 | 7.2e-89 | S | HTH domain | |||
AIIGCJOP_04162 | 3.5e-114 | yddE | S | phenazine biosynthesis protein PhzF | ||
AIIGCJOP_04163 | 1.2e-12 | emrE | P | Small multidrug resistance protein | ||
AIIGCJOP_04164 | 9.7e-15 | emrE | P | Multidrug Resistance protein | ||
AIIGCJOP_04165 | 0.0 | cutC | 4.3.99.4 | C | Glycine radical enzyme that catalyzes the cleavage of a C-N bond in choline, producing trimethylamine (TMA) and acetaldehyde | |
AIIGCJOP_04166 | 5.2e-80 | 1.97.1.4 | C | Catalyzes activation of the choline trimethylamine-lyase CutC under anaerobic conditions by generation of an organic free radical on a glycine residue, via an homolytic cleavage of S- adenosyl-L-methionine (SAM) | ||
AIIGCJOP_04168 | 3.4e-27 | ygdR | S | (Lipo)protein | ||
AIIGCJOP_04170 | 6.9e-156 | IQ | Dehydrogenases with different specificities (Related to short-chain alcohol dehydrogenases) | |||
AIIGCJOP_04171 | 7.1e-80 | D | Membrane | |||
AIIGCJOP_04172 | 5.5e-307 | T | Diguanylate cyclase | |||
AIIGCJOP_04173 | 1.8e-76 | S | Oxidoreductase molybdopterin binding domain | |||
AIIGCJOP_04174 | 7.9e-80 | EG | COG0697 Permeases of the drug metabolite transporter (DMT) superfamily | |||
AIIGCJOP_04175 | 7e-115 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
AIIGCJOP_04176 | 1e-67 | mocA | 1.1.1.328, 2.7.7.76 | S | Mo(VI)-molybdopterin cytosine dinucleotide biosynthetic process | |
AIIGCJOP_04177 | 1.1e-26 | MA20_39405 | S | Protein of unknown function (DUF1272) | ||
AIIGCJOP_04178 | 1.1e-229 | yndD | E | xaa-pro aminopeptidase | ||
AIIGCJOP_04179 | 4.1e-185 | ampC | 3.5.2.6 | V | Beta-lactamase | |
AIIGCJOP_04180 | 9.1e-102 | NU | Fimbrial protein | |||
AIIGCJOP_04181 | 0.0 | fimD_3 | NU | PapC N-terminal domain | ||
AIIGCJOP_04182 | 3.8e-90 | NU | Pili assembly chaperone PapD, C-terminal domain | |||
AIIGCJOP_04183 | 7.5e-47 | NU | Fimbrial protein | |||
AIIGCJOP_04184 | 1.3e-196 | namA | 1.6.99.1 | C | COG1902 NADH flavin oxidoreductases, Old Yellow Enzyme family | |
AIIGCJOP_04185 | 7e-248 | G | Major facilitator superfamily | |||
AIIGCJOP_04186 | 1e-254 | 1.1.1.3 | E | homoserine dehydrogenase | ||
AIIGCJOP_04187 | 5.5e-137 | glxR | 1.1.1.60 | I | COG2084 3-hydroxyisobutyrate dehydrogenase and related beta-hydroxyacid dehydrogenases | |
AIIGCJOP_04188 | 9.9e-167 | 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 | |||
AIIGCJOP_04191 | 1.5e-134 | S | Serine aminopeptidase, S33 | |||
AIIGCJOP_04192 | 0.0 | 1.1.5.2 | G | Dehydrogenase | ||
AIIGCJOP_04193 | 5.2e-33 | |||||
AIIGCJOP_04194 | 0.0 | betT | U | BCCT, betaine/carnitine/choline family transporter | ||
AIIGCJOP_04196 | 1.4e-300 | oppA-1 | E | ABC transporter substrate-binding protein | ||
AIIGCJOP_04197 | 5.3e-108 | yccA | S | Belongs to the BI1 family | ||
AIIGCJOP_04198 | 3.7e-57 | tusE | P | part of a sulfur-relay system | ||
AIIGCJOP_04199 | 2.5e-43 | acyP | 3.6.1.7 | C | Acylphosphate phosphohydrolase | |
AIIGCJOP_04200 | 3.9e-118 | ybcM | K | helix_turn_helix, arabinose operon control protein | ||
AIIGCJOP_04201 | 6.5e-75 | ybcL | S | Phosphatidylethanolamine-binding protein | ||
AIIGCJOP_04202 | 2.5e-225 | rlmI | 2.1.1.191 | J | Specifically methylates the cytosine at position 1962 (m5C1962) of 23S rRNA | |
AIIGCJOP_04203 | 9.1e-50 | hspQ | S | Involved in the degradation of certain denaturated proteins, including DnaA, during heat shock stress | ||
AIIGCJOP_04204 | 1.3e-67 | yccU | 2.5.1.49 | S | CoA-binding protein | |
AIIGCJOP_04205 | 4.5e-115 | yccT | S | Belongs to the UPF0319 family | ||
AIIGCJOP_04206 | 6.1e-79 | mgsA | 4.2.3.3 | G | Methylglyoxal synthase | |
AIIGCJOP_04207 | 0.0 | helD | 3.6.4.12 | L | DNA helicase | |
AIIGCJOP_04208 | 5.9e-71 | yccF | S | Membrane | ||
AIIGCJOP_04209 | 0.0 | yccS | S | Membrane | ||
AIIGCJOP_04210 | 3.7e-87 | sxy | K | regulator of competence-specific genes | ||
AIIGCJOP_04211 | 6.5e-78 | 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 | ||
AIIGCJOP_04212 | 5.3e-195 | ompA | M | Belongs to the ompA family | ||
AIIGCJOP_04213 | 1.5e-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 | ||
AIIGCJOP_04214 | 0.0 | ycbZ | O | Belongs to the peptidase S16 family | ||
AIIGCJOP_04215 | 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 | |
AIIGCJOP_04216 | 4.2e-98 | ymbA | S | protein conserved in bacteria | ||
AIIGCJOP_04217 | 1.1e-282 | pqiB | Q | paraquat-inducible protein b | ||
AIIGCJOP_04218 | 3.7e-211 | pqiA | S | paraquat-inducible protein A | ||
AIIGCJOP_04219 | 0.0 | uup | S | COG0488 ATPase components of ABC transporters with duplicated ATPase domains | ||
AIIGCJOP_04220 | 0.0 | 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 | |
AIIGCJOP_04221 | 6.2e-202 | ycbX | 1.17.1.1 | C | Mosc domain protein beta barrel domain protein | |
AIIGCJOP_04222 | 4.9e-96 | 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 | ||
AIIGCJOP_04223 | 5.1e-187 | pyrD | 1.3.1.14, 1.3.5.2 | F | Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor | |
AIIGCJOP_04224 | 1.2e-100 | ssuE | 1.5.1.38 | S | fmn reductase | |
AIIGCJOP_04225 | 2.1e-166 | ssuA | P | ABC transporter | ||
AIIGCJOP_04226 | 2.2e-210 | ssuD | 1.14.14.5 | C | Catalyzes the desulfonation of aliphatic sulfonates | |
AIIGCJOP_04227 | 6.3e-132 | ssuC | 1.14.14.5 | P | ABC-type nitrate sulfonate bicarbonate transport system permease component | |
AIIGCJOP_04228 | 3e-131 | ssuB | P | Part of the ABC transporter complex SsuABC involved in aliphatic sulfonates import. Responsible for energy coupling to the transport system | ||
AIIGCJOP_04229 | 0.0 | pepN | 3.4.11.2 | E | aminopeptidase N | |
AIIGCJOP_04230 | 2.1e-224 | 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 | |
AIIGCJOP_04231 | 5.3e-267 | asnS | 6.1.1.22 | J | Asparaginyl-tRNA synthetase | |
AIIGCJOP_04232 | 7.1e-195 | M | Belongs to the Gram-negative porin family | |||
AIIGCJOP_04233 | 4.7e-224 | aspC | 2.6.1.1, 2.6.1.57 | E | aminotransferase | |
AIIGCJOP_04234 | 1.8e-124 | ycbL | 3.1.2.6 | P | COG0491 Zn-dependent hydrolases, including glyoxylases | |
AIIGCJOP_04235 | 3.7e-99 | ycbK | S | protein conserved in bacteria | ||
AIIGCJOP_04236 | 0.0 | ycbB | M | protein conserved in bacteria | ||
AIIGCJOP_04237 | 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 | |
AIIGCJOP_04238 | 2.1e-126 | 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 | ||
AIIGCJOP_04239 | 1.4e-245 | 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 | ||
AIIGCJOP_04240 | 7.3e-141 | cmoM | GT2,GT4 | J | Catalyzes the methylation of 5-carboxymethoxyuridine (cmo5U) to form 5-methoxycarbonylmethoxyuridine (mcmo5U) at position 34 in tRNAs | |
AIIGCJOP_04241 | 8.3e-129 | ycbC | S | Gram-negative-bacterium-type cell wall biogenesis | ||
AIIGCJOP_04242 | 5.5e-169 | ycbJ | S | Phosphotransferase enzyme family | ||
AIIGCJOP_04243 | 1.6e-132 | kdsB | 2.7.7.38 | M | Activates KDO (a required 8-carbon sugar) for incorporation into bacterial lipopolysaccharide in Gram-negative bacteria | |
AIIGCJOP_04244 | 1.2e-25 | ycaR | 2.7.1.130 | S | Belongs to the UPF0434 family | |
AIIGCJOP_04245 | 1.8e-223 | ycaQ | S | protein conserved in bacteria | ||
AIIGCJOP_04246 | 4.4e-175 | 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) | |
AIIGCJOP_04247 | 0.0 | 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 | ||
AIIGCJOP_04248 | 0.0 | ycaI | S | DNA internalization-related competence protein ComEC Rec2 | ||
AIIGCJOP_04249 | 1.9e-46 | L | Bacterial DNA-binding protein | |||
AIIGCJOP_04250 | 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 | |
AIIGCJOP_04251 | 5.4e-116 | 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 | |
AIIGCJOP_04252 | 1.5e-236 | 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 | |
AIIGCJOP_04253 | 3.9e-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 | |
AIIGCJOP_04254 | 3e-122 | ycaP | S | Membrane | ||
AIIGCJOP_04255 | 0.0 | ycaO | O | redox protein regulator of disulfide bond formation | ||
AIIGCJOP_04256 | 1.3e-145 | focA | P | Formate nitrite | ||
AIIGCJOP_04257 | 0.0 | pflB | 2.3.1.54 | C | formate C-acetyltransferase glycine radical | |
AIIGCJOP_04258 | 1.2e-145 | 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 | |
AIIGCJOP_04259 | 5.9e-38 | cigR | S | response to cobalt ion | ||
AIIGCJOP_04260 | 1.2e-208 | ycaD | EGP | Major facilitator superfamily | ||
AIIGCJOP_04261 | 3e-143 | dmsC | S | PFAM DMSO reductase anchor subunit (DmsC) | ||
AIIGCJOP_04262 | 1.6e-122 | dmsB | C | reductase, chain B | ||
AIIGCJOP_04263 | 0.0 | dmsA | 1.8.5.3, 1.97.1.9 | C | Belongs to the prokaryotic molybdopterin-containing oxidoreductase family | |
AIIGCJOP_04264 | 1.4e-242 | 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) | |
AIIGCJOP_04265 | 2.1e-252 | rarA | L | MgsA AAA+ ATPase C terminal | ||
AIIGCJOP_04266 | 8.9e-110 | 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) | ||
AIIGCJOP_04267 | 0.0 | ftsK | D | PFAM cell divisionFtsK SpoIIIE | ||
AIIGCJOP_04268 | 8.5e-87 | lrp | K | Transcriptional regulator | ||
AIIGCJOP_04269 | 9.5e-183 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
AIIGCJOP_04270 | 0.0 | cydD | V | (ABC) transporter | ||
AIIGCJOP_04271 | 1.9e-295 | cydC | V | (ABC) transporter | ||
AIIGCJOP_04272 | 7.8e-126 | 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 | |
AIIGCJOP_04273 | 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 | ||
AIIGCJOP_04274 | 1.1e-42 | |||||
AIIGCJOP_04275 | 0.0 | clpA | O | Belongs to the ClpA ClpB family | ||
AIIGCJOP_04276 | 1.2e-54 | clpS | S | Involved in the modulation of the specificity of the ClpAP-mediated ATP-dependent protein degradation | ||
AIIGCJOP_04277 | 1.1e-36 | cspD | K | Cold shock | ||
AIIGCJOP_04278 | 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 | ||
AIIGCJOP_04279 | 5.8e-192 | macA | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | ||
AIIGCJOP_04280 | 8e-166 | ybjX | S | protein conserved in bacteria | ||
AIIGCJOP_04281 | 0.0 | ybjD | L | ATP-dependent endonuclease of the OLD family | ||
AIIGCJOP_04282 | 3.7e-120 | 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 | ||
AIIGCJOP_04283 | 1.7e-149 | ybjE | S | membrane | ||
AIIGCJOP_04284 | 0.0 | hcp | 1.7.99.1 | C | hydroxylamine reductase activity | |
AIIGCJOP_04285 | 1.1e-178 | hcr | C | oxidoreductase | ||
AIIGCJOP_04286 | 0.0 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
AIIGCJOP_04287 | 2.4e-181 | ltaE | 4.1.2.48 | E | PFAM aromatic amino acid beta-eliminating lyase threonine aldolase | |
AIIGCJOP_04288 | 2.6e-261 | ybjT | GM | Epimerase dehydratase | ||
AIIGCJOP_04289 | 1.6e-193 | ybjS | 1.1.1.133, 5.1.3.13 | M | 3-beta hydroxysteroid dehydrogenase | |
AIIGCJOP_04290 | 0.0 | MU | Chitinase class I | |||
AIIGCJOP_04291 | 1e-70 | iagB | M | invasion protein IagB | ||
AIIGCJOP_04292 | 0.0 | chiA | 3.2.1.14 | GH18 | G | chitinase |
AIIGCJOP_04293 | 2e-117 | 3.4.23.43 | NOU | Cleaves type-4 fimbrial leader sequence and methylates the N-terminal (generally Phe) residue | ||
AIIGCJOP_04294 | 3.9e-68 | gspM | U | Involved in a type II secretion system (T2SS, formerly general secretion pathway, GSP) for the export of proteins | ||
AIIGCJOP_04295 | 2.6e-171 | gspL | U | Involved in a type II secretion system (T2SS, formerly general secretion pathway, GSP) for the export of proteins | ||
AIIGCJOP_04296 | 2.7e-140 | gspK | U | COG3156 Type II secretory pathway component PulK | ||
AIIGCJOP_04297 | 6.4e-98 | gspJ | U | General secretion pathway protein J | ||
AIIGCJOP_04298 | 1.1e-48 | gspI | NU | general secretion pathway protein | ||
AIIGCJOP_04299 | 1.1e-75 | gspH | NU | general secretion pathway protein | ||
AIIGCJOP_04300 | 1.9e-77 | gspG | U | General Secretion Pathway protein | ||
AIIGCJOP_04301 | 2.9e-256 | MU | Autotransporter beta-domain | |||
AIIGCJOP_04302 | 4.2e-28 | ygdi3 | S | Bacterial protein of unknown function (DUF903) | ||
AIIGCJOP_04303 | 0.0 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthetase ammonia chain | |
AIIGCJOP_04304 | 1.2e-216 | carA | 6.3.5.5 | F | Belongs to the CarA family | |
AIIGCJOP_04305 | 6.9e-142 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
AIIGCJOP_04306 | 5e-95 | alaS_2 | 6.1.1.7 | S | Alanyl-tRNA synthetase | |
AIIGCJOP_04307 | 1.7e-157 | K | transcriptional regulator | |||
AIIGCJOP_04308 | 5.1e-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 | |
AIIGCJOP_04309 | 2.8e-76 | fkpB | 5.2.1.8 | G | Peptidyl-prolyl cis-trans | |
AIIGCJOP_04310 | 6.6e-87 | lspA | 3.4.23.36 | M | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
AIIGCJOP_04311 | 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) | |
AIIGCJOP_04312 | 7.3e-172 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
AIIGCJOP_04313 | 3.3e-37 | rpsT | J | 30S ribosomal protein S20 | ||
AIIGCJOP_04314 | 4.4e-166 | nhaR | K | Transcriptional regulator | ||
AIIGCJOP_04315 | 1e-178 | nhaA | P | Na( ) H( ) antiporter that extrudes sodium in exchange for external protons | ||
AIIGCJOP_04316 | 7.7e-176 | 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 | ||
AIIGCJOP_04317 | 0.0 | dnaK | O | Heat shock 70 kDa protein | ||
AIIGCJOP_04318 | 4.7e-97 | yaaH | S | GPR1 FUN34 yaaH family protein | ||
AIIGCJOP_04319 | 1.1e-213 | tphA | EGP | Major facilitator superfamily | ||
AIIGCJOP_04320 | 5e-102 | mog | 2.7.7.75, 2.8.1.12 | H | Molybdenum cofactor | |
AIIGCJOP_04321 | 5.2e-173 | tal | 2.2.1.2 | H | Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway | |
AIIGCJOP_04322 | 1.9e-235 | yaaJ | E | alanine symporter | ||
AIIGCJOP_04323 | 2.7e-135 | yaaA | S | Belongs to the UPF0246 family | ||
AIIGCJOP_04324 | 7.3e-14 | yaaX | S | Protein of unknown function (DUF2502) | ||
AIIGCJOP_04325 | 1.7e-243 | thrC | 4.2.3.1 | E | Threonine synthase | |
AIIGCJOP_04326 | 8e-171 | thrB | 2.7.1.39 | E | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
AIIGCJOP_04327 | 0.0 | thrA | 1.1.1.3, 2.7.2.4 | E | belongs to the aspartokinase family | |
AIIGCJOP_04329 | 1.3e-114 | 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 | |
AIIGCJOP_04330 | 1.1e-132 | K | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
AIIGCJOP_04331 | 5.7e-218 | creD | V | Inner membrane protein CreD | ||
AIIGCJOP_04332 | 3.1e-230 | T | PhoQ Sensor | |||
AIIGCJOP_04333 | 1.1e-119 | K | Transcriptional regulatory protein, C terminal | |||
AIIGCJOP_04334 | 1.2e-77 | creA | S | protein conserved in bacteria | ||
AIIGCJOP_04335 | 3.6e-165 | rob | K | Binds to the right arm of the replication origin oriC | ||
AIIGCJOP_04336 | 2e-115 | gpmB | 5.4.2.12 | G | Belongs to the phosphoglycerate mutase family | |
AIIGCJOP_04337 | 2.6e-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 | ||
AIIGCJOP_04338 | 3.8e-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 | ||
AIIGCJOP_04339 | 0.0 | slt | GH23 | M | Soluble lytic murein transglycosylase and related regulatory proteins (some contain LysM invasin domains) | |
AIIGCJOP_04340 | 0.0 | yjjK | 3.6.3.25 | S | A translation factor that gates the progression of the 70S ribosomal initiation complex (IC, containing tRNA(fMet) in the P site) into the translation elongation cycle by using a mechanism sensitive to the ATP ADP ratio. Binds to the 70S ribosome E site where it modulates the state of the translating ribosome during subunit translocation | |
AIIGCJOP_04341 | 7.5e-241 | nadR | 2.7.1.22, 2.7.7.1 | H | transcriptional regulator | |
AIIGCJOP_04342 | 3.5e-255 | 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 | ||
AIIGCJOP_04343 | 1.1e-175 | serB | 3.1.3.3 | E | phosphoserine phosphatase | |
AIIGCJOP_04344 | 2.2e-106 | smp | 2.4.1.15, 2.4.1.347, 2.7.13.3, 6.3.1.20 | GT20 | S | membrane protein affecting hemolysin expression |
AIIGCJOP_04345 | 6.9e-192 | 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 | |
AIIGCJOP_04346 | 4.8e-131 | deoD | 2.4.2.1, 2.4.2.28 | F | Purine nucleoside phosphorylase | |
AIIGCJOP_04347 | 2.8e-240 | deoB | 5.4.2.7 | G | Phosphotransfer between the C1 and C5 carbon atoms of pentose | |
AIIGCJOP_04348 | 1.2e-239 | 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 | |
AIIGCJOP_04349 | 1.4e-136 | 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 | |
AIIGCJOP_04350 | 9.6e-278 | yjjI | F | anaerobic respiration | ||
AIIGCJOP_04351 | 2.3e-127 | yjjW | 1.97.1.4 | O | 4Fe-4S single cluster domain | |
AIIGCJOP_04352 | 7.1e-128 | yjjV | L | Deoxyribonuclease | ||
AIIGCJOP_04353 | 9.8e-197 | yjjU | I | esterase of the alpha-beta hydrolase superfamily | ||
AIIGCJOP_04354 | 1.6e-18 | ytjA | S | UPF0391 membrane protein | ||
AIIGCJOP_04355 | 9e-94 | osmY | S | Periplasmic or secreted lipoprotein | ||
AIIGCJOP_04356 | 1.1e-305 | 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 | ||
AIIGCJOP_04357 | 1.4e-119 | yjjG | 3.1.3.102, 3.1.3.104, 3.1.3.5, 3.8.1.2 | S | hydrolase | |
AIIGCJOP_04358 | 5.1e-75 | rimI | 2.3.1.128, 2.3.1.234 | K | This enzyme acetylates the N-terminal alanine of ribosomal protein S18 | |
AIIGCJOP_04359 | 1e-64 | 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 | |
AIIGCJOP_04360 | 2.2e-193 | rsmC | 2.1.1.172, 2.1.1.174 | J | Specifically methylates the guanine in position 1207 of 16S rRNA in the 30S particle | |
AIIGCJOP_04364 | 2.4e-23 | yjjZ | S | Protein of unknown function (DUF1435) | ||
AIIGCJOP_04365 | 2.9e-137 | fhuF | S | Iron reductase | ||
AIIGCJOP_04366 | 4.5e-247 | 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 | ||
AIIGCJOP_04367 | 2.3e-76 | ywhH | S | Prolyl-tRNA synthetase | ||
AIIGCJOP_04368 | 6.3e-88 | bglJ | K | transcriptional | ||
AIIGCJOP_04369 | 4.8e-94 | yjjQ | K | regulator | ||
AIIGCJOP_04370 | 2.9e-134 | yjjP | S | Membrane | ||
AIIGCJOP_04371 | 1.8e-78 | yjjB | S | UPF0442 protein | ||
AIIGCJOP_04372 | 4.6e-109 | nicS | K | transcriptional regulator | ||
AIIGCJOP_04373 | 2.1e-73 | ohr | O | Organic Hydroperoxide Resistance Protein | ||
AIIGCJOP_04374 | 1.8e-93 | 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' | ||
AIIGCJOP_04375 | 5.5e-130 | dnaC | L | DNA replication protein | ||
AIIGCJOP_04376 | 1.9e-44 | yjjA | S | Glycoprotein Receptor | ||
AIIGCJOP_04377 | 0.0 | mdoB | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
AIIGCJOP_04378 | 2.1e-190 | tsr | NT | chemotaxis, protein | ||
AIIGCJOP_04379 | 1.2e-60 | hpaR | K | Homoprotocatechuate degradative operon repressor | ||
AIIGCJOP_04380 | 1e-224 | hpaG | 4.1.1.68 | Q | 4-hydroxyphenylacetate degradation bifunctional isomerase | |
AIIGCJOP_04381 | 5.2e-281 | hpaE | 1.2.1.60 | C | belongs to the aldehyde dehydrogenase family | |
AIIGCJOP_04382 | 3.7e-162 | hpaD | 1.13.11.15 | S | 3,4-dihydroxyphenylacetate 2,3-dioxygenase | |
AIIGCJOP_04383 | 4.6e-64 | hpcD | 4.1.1.68, 5.3.3.10 | E | 5-carboxymethyl-2-hydroxymuconate isomerase | |
AIIGCJOP_04384 | 3e-150 | hpaH | Q | hydratase | ||
AIIGCJOP_04385 | 3.2e-136 | hpaI | 4.1.2.20, 4.1.2.52 | G | HpcH/HpaI aldolase/citrate lyase family | |
AIIGCJOP_04386 | 1.7e-241 | hpaX | G | Major facilitator superfamily | ||
AIIGCJOP_04387 | 2.4e-164 | hpaA | K | AraC-like ligand binding domain | ||
AIIGCJOP_04388 | 1.2e-111 | K | Transcriptional regulator, AbiEi antitoxin N-terminal domain | |||
AIIGCJOP_04389 | 2.8e-152 | S | Nucleotidyl transferase AbiEii toxin, Type IV TA system | |||
AIIGCJOP_04390 | 2.2e-311 | hpaB | 1.14.14.9 | Q | 4-hydroxyphenylacetate 3-monooxygenase oxygenase component | |
AIIGCJOP_04391 | 1.3e-85 | hpaC | 1.5.1.36 | S | 4-hydroxyphenylacetate 3-monooxygenase, reductase component | |
AIIGCJOP_04392 | 5.7e-43 | |||||
AIIGCJOP_04393 | 4.9e-288 | kpsD | M | polysaccharide export | ||
AIIGCJOP_04394 | 2.4e-131 | kpsM | GM | Transport Permease Protein | ||
AIIGCJOP_04395 | 1.1e-66 | kpsT | 3.6.3.38 | GM | ABC transporter | |
AIIGCJOP_04396 | 2e-187 | kpsE | M | COG3524 Capsule polysaccharide export protein | ||
AIIGCJOP_04397 | 3.9e-84 | GT2,GT4 | S | Glycosyltransferase like family 2 | ||
AIIGCJOP_04398 | 2.3e-117 | wgeG | M | Glycosyl transferase 4-like domain | ||
AIIGCJOP_04402 | 8.8e-149 | M | Glycosyltransferase family 92 | |||
AIIGCJOP_04403 | 4e-253 | GT2,GT4 | G | Glycosyl transferase, family 2 | ||
AIIGCJOP_04404 | 1.2e-172 | rgpF | GT2,GT4 | M | transferase activity, transferring glycosyl groups | |
AIIGCJOP_04405 | 4.8e-199 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
AIIGCJOP_04406 | 2.5e-161 | rfbD | 1.1.1.133 | M | Catalyzes the reduction of dTDP-6-deoxy-L-lyxo-4- hexulose to yield dTDP-L-rhamnose | |
AIIGCJOP_04407 | 2.1e-157 | rfbA | 2.7.7.24 | M | Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis | |
AIIGCJOP_04408 | 1.5e-95 | rfbC | 5.1.3.13 | M | Catalyzes the epimerization of the C3' and C5'positions of dTDP-6-deoxy-D-xylo-4-hexulose, forming dTDP-6-deoxy-L-lyxo-4- hexulose | |
AIIGCJOP_04409 | 0.0 | kpsC | M | Capsule polysaccharide biosynthesis protein | ||
AIIGCJOP_04410 | 1.9e-223 | kpsS | M | capsule polysaccharide | ||
AIIGCJOP_04411 | 6e-185 | insH5 | L | COG3039 Transposase and inactivated derivatives IS5 family | ||
AIIGCJOP_04412 | 5.5e-145 | K | transcriptional regulator | |||
AIIGCJOP_04413 | 0.0 | cstA | T | Carbon starvation protein | ||
AIIGCJOP_04414 | 5.9e-34 | yjiX | S | small protein | ||
AIIGCJOP_04415 | 2.9e-176 | yjiA | S | cobalamin synthesis protein | ||
AIIGCJOP_04416 | 1.6e-94 | S | YfaZ precursor | |||
AIIGCJOP_04417 | 1.2e-250 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.24, 1.2.1.79 | C | belongs to the aldehyde dehydrogenase family | |
AIIGCJOP_04418 | 4.6e-77 | S | Type VI secretion system effector | |||
AIIGCJOP_04419 | 1.2e-12 | |||||
AIIGCJOP_04420 | 1.7e-104 | |||||
AIIGCJOP_04421 | 2.1e-35 | S | BrnA antitoxin of type II toxin-antitoxin system | |||
AIIGCJOP_04422 | 3.1e-117 | ybfI | K | transcriptional regulator | ||
AIIGCJOP_04423 | 6.5e-90 | rhtC | E | PFAM Lysine exporter protein (LYSE YGGA) | ||
AIIGCJOP_04424 | 8.1e-230 | yjiN | S | Membrane | ||
AIIGCJOP_04425 | 1.3e-185 | 3.2.1.172 | GH105 | S | PFAM glycosyl hydrolase family 88 | |
AIIGCJOP_04426 | 2.8e-98 | |||||
AIIGCJOP_04427 | 8.2e-283 | 3.2.1.139 | G | Belongs to the glycosyl hydrolase 67 family | ||
AIIGCJOP_04428 | 3.4e-189 | S | Protein of unknown function (DUF2955) | |||
AIIGCJOP_04429 | 3.5e-186 | yiaV | V | Secretion Protein | ||
AIIGCJOP_04430 | 2.9e-76 | slyA | K | Transcriptional regulator | ||
AIIGCJOP_04432 | 9.2e-35 | S | Protein of unknown function (DUF1778) | |||
AIIGCJOP_04433 | 1.4e-71 | Z012_05445 | 2.3.1.189 | K | acetyltransferase | |
AIIGCJOP_04434 | 2.5e-108 | ydfF | K | transcriptional regulator | ||
AIIGCJOP_04435 | 3e-58 | 1.3.1.12 | S | ACT domain protein | ||
AIIGCJOP_04436 | 5.5e-50 | yqjZ | C | Antibiotic biosynthesis monooxygenase | ||
AIIGCJOP_04437 | 1.5e-240 | 1.2.1.3 | C | belongs to the aldehyde dehydrogenase family | ||
AIIGCJOP_04438 | 2.8e-152 | K | transcriptional regulator | |||
AIIGCJOP_04439 | 2.4e-78 | 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 | |||
AIIGCJOP_04440 | 1.1e-251 | K | Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | |||
AIIGCJOP_04441 | 4.7e-18 | yjiS | S | Domain of unknown function (DUF1127) | ||
AIIGCJOP_04442 | 1.2e-234 | yjiR | K | Transcriptional regulator | ||
AIIGCJOP_04443 | 0.0 | foxA | P | Receptor | ||
AIIGCJOP_04444 | 9.1e-165 | K | Transcriptional regulator | |||
AIIGCJOP_04445 | 1e-26 | S | Uncharacterized protein conserved in bacteria (DUF2171) | |||
AIIGCJOP_04446 | 1.2e-22 | |||||
AIIGCJOP_04447 | 4.9e-215 | ycfD | 1.14.11.47 | S | Cupin 4 family protein | |
AIIGCJOP_04448 | 1.2e-32 | |||||
AIIGCJOP_04449 | 4.2e-125 | glpR_5 | K | Transcriptional Regulator, DeoR family | ||
AIIGCJOP_04451 | 1.1e-180 | ybjJ | EGP | Major facilitator Superfamily | ||
AIIGCJOP_04452 | 2.2e-61 | yyaH | 4.4.1.5 | E | bleomycin resistance protein | |
AIIGCJOP_04453 | 0.0 | mcrB | TV | AAA domain (dynein-related subfamily) | ||
AIIGCJOP_04454 | 6.8e-184 | mcrC | V | McrBC 5-methylcytosine restriction system component | ||
AIIGCJOP_04455 | 1.4e-94 | K | response regulator | |||
AIIGCJOP_04456 | 0.0 | fixL | T | Histidine kinase | ||
AIIGCJOP_04457 | 6.4e-55 | T | response regulator | |||
AIIGCJOP_04458 | 7e-40 | S | ABC transporter substrate-binding protein | |||
AIIGCJOP_04459 | 1.4e-27 | S | Protein of unknown function (DUF1427) | |||
AIIGCJOP_04460 | 8.4e-126 | ycaC | Q | Hydrolase | ||
AIIGCJOP_04461 | 0.0 | S | metal-dependent hydrolase with the TIM-barrel fold | |||
AIIGCJOP_04462 | 3.4e-65 | 1.6.99.3, 1.8.5.2 | S | LysR family transcriptional regulator | ||
AIIGCJOP_04463 | 1.3e-293 | EGP | permeases of the major facilitator superfamily | |||
AIIGCJOP_04464 | 1.4e-155 | cpo | 1.11.1.10 | I | Alpha beta hydrolase | |
AIIGCJOP_04465 | 1.6e-73 | fosB | 2.5.1.18 | E | Glutathione transferase | |
AIIGCJOP_04466 | 6.6e-10 | |||||
AIIGCJOP_04467 | 2.2e-268 | prr | 1.2.1.19, 1.2.1.3 | C | belongs to the aldehyde dehydrogenase family | |
AIIGCJOP_04468 | 4e-265 | E | amino acid | |||
AIIGCJOP_04469 | 2.5e-178 | csiD | C | May be involved in the control of utilization of gamma- aminobutyric acid | ||
AIIGCJOP_04470 | 9.4e-223 | lhgO | S | L-2-hydroxyglutarate oxidase LhgO | ||
AIIGCJOP_04471 | 4.5e-269 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | belongs to the aldehyde dehydrogenase family | |
AIIGCJOP_04472 | 8.9e-237 | gabT | 2.6.1.19, 2.6.1.22, 2.6.1.48 | E | Belongs to the class-III pyridoxal-phosphate-dependent aminotransferase family | |
AIIGCJOP_04473 | 2.4e-116 | csiR | K | Transcriptional | ||
AIIGCJOP_04474 | 9.6e-191 | 2.7.11.1 | S | protein related to capsule biosynthesis enzymes | ||
AIIGCJOP_04475 | 3.4e-42 | K | Helix-turn-helix XRE-family like proteins | |||
AIIGCJOP_04476 | 1.1e-29 | S | acyl carrier protein |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)