ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
HGMOLFCO_00001 | 5.1e-136 | E | GDSL-like Lipase/Acylhydrolase family | |||
HGMOLFCO_00002 | 7.4e-123 | C | nitroreductase | |||
HGMOLFCO_00003 | 1.9e-175 | rihA | 3.2.2.1 | F | Inosine-uridine preferring nucleoside hydrolase | |
HGMOLFCO_00004 | 1.2e-11 | sucD | 6.2.1.5 | C | CoA-ligase | |
HGMOLFCO_00005 | 4.1e-203 | allD | 1.1.1.350 | C | Belongs to the LDH2 MDH2 oxidoreductase family | |
HGMOLFCO_00006 | 1.7e-98 | allC | 3.5.1.6, 3.5.1.87, 3.5.3.9 | E | Peptidase family M20/M25/M40 | |
HGMOLFCO_00007 | 8.3e-135 | allB | 3.5.2.5 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
HGMOLFCO_00008 | 2e-64 | pucR | QT | Purine catabolism regulatory protein-like family | ||
HGMOLFCO_00009 | 1.2e-21 | pucG | 2.6.1.112, 2.6.1.44, 2.6.1.45, 2.6.1.51 | E | Aminotransferase class-V | |
HGMOLFCO_00010 | 1.1e-59 | pucG | 2.6.1.112, 2.6.1.44, 2.6.1.45, 2.6.1.51 | E | Aminotransferase class-V | |
HGMOLFCO_00011 | 2.6e-26 | pucG | 2.6.1.112, 2.6.1.44, 2.6.1.45, 2.6.1.51 | E | Aminotransferase class-V | |
HGMOLFCO_00012 | 1.7e-179 | 1.1.1.26 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | ||
HGMOLFCO_00013 | 5.2e-102 | S | membrane transporter protein | |||
HGMOLFCO_00014 | 1.4e-89 | pgpA | 3.1.3.27 | I | Phosphatidylglycerophosphatase A | |
HGMOLFCO_00015 | 1.7e-193 | V | Beta-lactamase | |||
HGMOLFCO_00016 | 9.2e-228 | |||||
HGMOLFCO_00018 | 6.3e-154 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
HGMOLFCO_00019 | 0.0 | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | |||
HGMOLFCO_00020 | 6e-15 | S | ABC-type transport system involved in multi-copper enzyme maturation permease component | |||
HGMOLFCO_00021 | 5.1e-08 | S | ABC-2 family transporter protein | |||
HGMOLFCO_00022 | 7.8e-52 | T | Transcriptional regulatory protein, C terminal | |||
HGMOLFCO_00023 | 1.6e-63 | T | His Kinase A (phosphoacceptor) domain | |||
HGMOLFCO_00024 | 2.5e-54 | C | FMN binding | |||
HGMOLFCO_00025 | 3.4e-202 | 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 | |
HGMOLFCO_00026 | 9.1e-107 | ribE | 2.5.1.9, 3.5.4.25, 4.1.99.12 | H | Riboflavin synthase | |
HGMOLFCO_00027 | 9.2e-228 | ribBA | 3.5.4.25, 4.1.99.12 | H | Catalyzes the conversion of GTP to 2,5-diamino-6- ribosylamino-4(3H)-pyrimidinone 5'-phosphate (DARP), formate and pyrophosphate | |
HGMOLFCO_00028 | 1.9e-80 | 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 | |
HGMOLFCO_00029 | 2.1e-79 | K | 2 iron, 2 sulfur cluster binding | |||
HGMOLFCO_00030 | 7.1e-269 | K | COG COG0846 NAD-dependent protein deacetylases, SIR2 family | |||
HGMOLFCO_00031 | 5.3e-220 | serA | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
HGMOLFCO_00032 | 8.3e-204 | 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 | |
HGMOLFCO_00033 | 9.3e-112 | C | aldo keto reductase | |||
HGMOLFCO_00034 | 1.9e-112 | 3.1.3.73 | G | phosphoglycerate mutase | ||
HGMOLFCO_00035 | 3.3e-09 | |||||
HGMOLFCO_00036 | 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 | ||
HGMOLFCO_00037 | 1.5e-200 | hisC | 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
HGMOLFCO_00038 | 9.9e-52 | hisE | 3.5.4.19, 3.6.1.31, 5.3.1.16 | E | phosphoribosyl-ATP diphosphatase activity | |
HGMOLFCO_00039 | 9.7e-39 | ykuJ | S | Protein of unknown function (DUF1797) | ||
HGMOLFCO_00040 | 1.9e-181 | mprF | I | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms | ||
HGMOLFCO_00041 | 7.7e-199 | cpoA | GT4 | M | Glycosyltransferase, group 1 family protein | |
HGMOLFCO_00042 | 1.3e-229 | mgs | 2.4.1.337 | GT4 | M | Glycosyltransferase, group 1 family protein |
HGMOLFCO_00043 | 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) | |
HGMOLFCO_00044 | 1.4e-38 | ptsH | G | phosphocarrier protein HPR | ||
HGMOLFCO_00046 | 0.0 | clpE | O | Belongs to the ClpA ClpB family | ||
HGMOLFCO_00047 | 2.4e-127 | 3.6.1.13, 3.6.1.55 | F | NUDIX domain | ||
HGMOLFCO_00048 | 3.7e-110 | pncA | Q | Isochorismatase family | ||
HGMOLFCO_00049 | 6.6e-265 | 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 | |
HGMOLFCO_00050 | 1.7e-97 | S | Pfam:DUF3816 | |||
HGMOLFCO_00051 | 1e-141 | manA | 1.14.13.81, 5.3.1.8, 5.4.2.8 | G | MucBP domain | |
HGMOLFCO_00052 | 1.9e-136 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
HGMOLFCO_00053 | 6.5e-162 | EG | EamA-like transporter family | |||
HGMOLFCO_00054 | 6e-246 | yxbA | 6.3.1.12 | S | ATP-grasp enzyme | |
HGMOLFCO_00055 | 4.7e-61 | L | Transposase and inactivated derivatives, IS30 family DNA replication, recombination, and repair | |||
HGMOLFCO_00056 | 8.5e-21 | gshF | 6.3.2.2 | H | Belongs to the glutamate--cysteine ligase type 1 family | |
HGMOLFCO_00057 | 3.9e-226 | gshF | 6.3.2.2 | H | Belongs to the glutamate--cysteine ligase type 1 family | |
HGMOLFCO_00059 | 1.3e-36 | ywnB | S | NAD(P)H-binding | ||
HGMOLFCO_00060 | 7.2e-66 | yjcE | P | Sodium proton antiporter | ||
HGMOLFCO_00061 | 5.9e-76 | |||||
HGMOLFCO_00062 | 1.3e-184 | |||||
HGMOLFCO_00063 | 9e-127 | narI | 1.7.5.1 | C | Nitrate reductase | |
HGMOLFCO_00064 | 1.2e-101 | narJ | C | Nitrate reductase delta subunit | ||
HGMOLFCO_00065 | 0.0 | narH | 1.7.5.1 | C | Respiratory nitrate reductase beta C-terminal | |
HGMOLFCO_00066 | 0.0 | narG | 1.7.5.1 | C | Belongs to the prokaryotic molybdopterin-containing oxidoreductase family | |
HGMOLFCO_00067 | 1.4e-189 | moeB | 2.7.7.73, 2.7.7.80 | H | ThiF family | |
HGMOLFCO_00068 | 1.9e-86 | moaB | 2.7.7.75 | H | May be involved in the biosynthesis of molybdopterin | |
HGMOLFCO_00069 | 1.2e-230 | moeA | 2.10.1.1 | H | MoeA N-terminal region (domain I and II) | |
HGMOLFCO_00070 | 9.3e-85 | moaC | 4.6.1.17 | H | Catalyzes the conversion of (8S)-3',8-cyclo-7,8- dihydroguanosine 5'-triphosphate to cyclic pyranopterin monophosphate (cPMP) | |
HGMOLFCO_00071 | 1.1e-98 | mobA | 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 | |
HGMOLFCO_00072 | 4.2e-40 | |||||
HGMOLFCO_00073 | 1.4e-77 | nreA | T | GAF domain | ||
HGMOLFCO_00074 | 1.6e-183 | comP | 2.7.13.3 | F | Sensor histidine kinase | |
HGMOLFCO_00075 | 4e-116 | nreC | K | PFAM regulatory protein LuxR | ||
HGMOLFCO_00076 | 6e-39 | |||||
HGMOLFCO_00077 | 8.8e-184 | |||||
HGMOLFCO_00078 | 9.7e-169 | hepT | 2.5.1.30, 2.5.1.90 | H | geranyltranstransferase activity | |
HGMOLFCO_00080 | 6.7e-133 | menG | 2.1.1.163, 2.1.1.201 | H | Methyltransferase required for the conversion of demethylmenaquinol (DMKH2) to menaquinol (MKH2) | |
HGMOLFCO_00081 | 2.9e-162 | hipB | K | Helix-turn-helix | ||
HGMOLFCO_00082 | 1.5e-58 | yitW | S | Iron-sulfur cluster assembly protein | ||
HGMOLFCO_00083 | 3.6e-216 | narK | P | Major Facilitator Superfamily | ||
HGMOLFCO_00084 | 7.8e-196 | moaA | 4.1.99.22 | H | Catalyzes the cyclization of GTP to (8S)-3',8-cyclo-7,8- dihydroguanosine 5'-triphosphate | |
HGMOLFCO_00085 | 6.4e-35 | moaD | 2.8.1.12 | H | ThiS family | |
HGMOLFCO_00086 | 2.2e-72 | moaE | 2.8.1.12 | H | MoaE protein | |
HGMOLFCO_00087 | 1.5e-170 | fecD | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
HGMOLFCO_00088 | 1e-142 | fecE | 3.6.3.34 | HP | AAA domain, putative AbiEii toxin, Type IV TA system | |
HGMOLFCO_00089 | 4.2e-228 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
HGMOLFCO_00090 | 8e-54 | yitW | S | Iron-sulfur cluster assembly protein | ||
HGMOLFCO_00091 | 4.7e-19 | M1-755 | S | Domain of unknown function (DUF1858) | ||
HGMOLFCO_00092 | 9.5e-258 | XK27_04775 | S | PAS domain | ||
HGMOLFCO_00093 | 2.4e-142 | EG | EamA-like transporter family | |||
HGMOLFCO_00094 | 4e-68 | paiA | 2.3.1.57 | K | Acetyltransferase (GNAT) domain | |
HGMOLFCO_00095 | 4.2e-74 | O | OsmC-like protein | |||
HGMOLFCO_00096 | 1.6e-76 | K | Transcriptional regulator | |||
HGMOLFCO_00097 | 3e-162 | proX | M | ABC transporter, substrate-binding protein, QAT family | ||
HGMOLFCO_00098 | 1.8e-108 | proWZ | P | ABC transporter permease | ||
HGMOLFCO_00099 | 9.3e-141 | proV | E | ABC transporter, ATP-binding protein | ||
HGMOLFCO_00100 | 3.1e-102 | proW | P | ABC transporter, permease protein | ||
HGMOLFCO_00101 | 7.2e-183 | C | Zinc-binding dehydrogenase | |||
HGMOLFCO_00102 | 6.3e-196 | bdhA | 1.1.1.303, 1.1.1.4 | C | Zinc-binding dehydrogenase | |
HGMOLFCO_00103 | 2.1e-224 | 4.4.1.8 | E | Aminotransferase, class I | ||
HGMOLFCO_00104 | 3.6e-179 | pva3 | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
HGMOLFCO_00105 | 7.8e-202 | xerS | L | Belongs to the 'phage' integrase family | ||
HGMOLFCO_00106 | 9e-62 | ywkB | S | Membrane transport protein | ||
HGMOLFCO_00107 | 2.8e-235 | icd | 1.1.1.42 | C | Isocitrate/isopropylmalate dehydrogenase | |
HGMOLFCO_00108 | 1.7e-151 | pdxK | 2.7.1.35 | H | Phosphomethylpyrimidine kinase | |
HGMOLFCO_00109 | 2.6e-80 | hmpT | S | ECF-type riboflavin transporter, S component | ||
HGMOLFCO_00110 | 4.7e-165 | 1.1.1.346 | C | Aldo keto reductase | ||
HGMOLFCO_00111 | 7.5e-161 | S | DUF218 domain | |||
HGMOLFCO_00114 | 6.3e-96 | K | Acetyltransferase (GNAT) domain | |||
HGMOLFCO_00115 | 4.8e-162 | I | alpha/beta hydrolase fold | |||
HGMOLFCO_00116 | 2.2e-125 | S | Phage minor capsid protein 2 | |||
HGMOLFCO_00118 | 1.3e-148 | 2.6.1.1 | E | Aminotransferase | ||
HGMOLFCO_00119 | 5.3e-17 | mleP3 | S | Membrane transport protein | ||
HGMOLFCO_00121 | 2.6e-166 | 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 | |
HGMOLFCO_00122 | 2.5e-161 | glxR | 1.1.1.31, 1.1.1.60 | I | Dehydrogenase | |
HGMOLFCO_00123 | 2.5e-183 | fruR3 | K | Transcriptional regulator, LacI family | ||
HGMOLFCO_00124 | 1.1e-103 | wecD3 | K | Acetyltransferase (GNAT) family | ||
HGMOLFCO_00125 | 1.9e-68 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |||
HGMOLFCO_00126 | 2.2e-55 | crcB | D | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
HGMOLFCO_00127 | 2.9e-54 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
HGMOLFCO_00128 | 2.6e-280 | arlS | 2.7.13.3 | T | Histidine kinase | |
HGMOLFCO_00129 | 5.6e-121 | K | response regulator | |||
HGMOLFCO_00130 | 7.2e-28 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
HGMOLFCO_00131 | 3.5e-97 | yceD | S | Uncharacterized ACR, COG1399 | ||
HGMOLFCO_00132 | 6.4e-215 | ylbM | S | Belongs to the UPF0348 family | ||
HGMOLFCO_00133 | 5.4e-141 | yqeM | Q | Methyltransferase | ||
HGMOLFCO_00134 | 1.6e-58 | rsfS | J | Functions as a ribosomal silencing factor. Interacts with ribosomal protein L14 (rplN), blocking formation of intersubunit bridge B8. Prevents association of the 30S and 50S ribosomal subunits and the formation of functional ribosomes, thus repressing translation | ||
HGMOLFCO_00135 | 7.3e-112 | nadD | 2.7.6.3, 2.7.7.18 | H | Hydrolase, HD family | |
HGMOLFCO_00136 | 4.1e-94 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
HGMOLFCO_00137 | 1.3e-48 | yhbY | J | RNA-binding protein | ||
HGMOLFCO_00138 | 2.6e-216 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
HGMOLFCO_00139 | 2.2e-96 | yqeG | S | HAD phosphatase, family IIIA | ||
HGMOLFCO_00141 | 4.2e-19 | yoaK | S | Protein of unknown function (DUF1275) | ||
HGMOLFCO_00142 | 6.6e-57 | 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 | ||
HGMOLFCO_00143 | 1.5e-26 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
HGMOLFCO_00144 | 1.7e-85 | infC | J | IF-3 binds to the 30S ribosomal subunit and shifts the equilibrum between 70S ribosomes and their 50S and 30S subunits in favor of the free subunits, thus enhancing the availability of 30S subunits on which protein synthesis initiation begins | ||
HGMOLFCO_00145 | 2.5e-172 | dnaI | L | Primosomal protein DnaI | ||
HGMOLFCO_00146 | 3.6e-252 | dnaB | L | replication initiation and membrane attachment | ||
HGMOLFCO_00147 | 8.5e-81 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
HGMOLFCO_00148 | 3.5e-106 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
HGMOLFCO_00149 | 2.1e-162 | 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 | |
HGMOLFCO_00150 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
HGMOLFCO_00151 | 2.9e-139 | aroD | S | Serine hydrolase (FSH1) | ||
HGMOLFCO_00152 | 1.8e-114 | ybhL | S | Belongs to the BI1 family | ||
HGMOLFCO_00153 | 1.4e-250 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
HGMOLFCO_00154 | 2e-117 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
HGMOLFCO_00155 | 6.5e-56 | ytpP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
HGMOLFCO_00156 | 5.1e-59 | ytzB | S | Small secreted protein | ||
HGMOLFCO_00157 | 1.8e-124 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
HGMOLFCO_00158 | 1.3e-210 | ecsB | U | ABC transporter | ||
HGMOLFCO_00159 | 3e-133 | ecsA | V | ABC transporter, ATP-binding protein | ||
HGMOLFCO_00160 | 4.1e-77 | hit | FG | histidine triad | ||
HGMOLFCO_00162 | 3.1e-149 | prsA | 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
HGMOLFCO_00163 | 9.7e-180 | yhaM | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
HGMOLFCO_00164 | 9.8e-56 | yheA | S | Belongs to the UPF0342 family | ||
HGMOLFCO_00165 | 0.0 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
HGMOLFCO_00166 | 0.0 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
HGMOLFCO_00168 | 1.7e-36 | |||||
HGMOLFCO_00170 | 1.8e-201 | folP | 2.5.1.15 | H | dihydropteroate synthase | |
HGMOLFCO_00171 | 2.6e-106 | xtp | 2.5.1.15, 3.6.1.66 | F | Ham1 family | |
HGMOLFCO_00172 | 2.2e-243 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
HGMOLFCO_00173 | 3.1e-104 | folE | 2.7.6.3, 3.5.4.16 | F | GTP cyclohydrolase 1 | |
HGMOLFCO_00174 | 1.5e-94 | folK | 1.13.11.81, 2.5.1.15, 2.7.6.3, 3.5.4.16, 4.1.2.25, 5.1.99.8 | H | 7,8-dihydro-6-hydroxymethylpterin-pyrophosphokinase (HPPK) | |
HGMOLFCO_00175 | 1.9e-62 | folB | 1.13.11.81, 2.5.1.15, 2.7.6.3, 4.1.2.25, 5.1.99.8 | H | Catalyzes the conversion of 7,8-dihydroneopterin to 6- hydroxymethyl-7,8-dihydropterin | |
HGMOLFCO_00176 | 6.9e-119 | S | CAAX protease self-immunity | |||
HGMOLFCO_00177 | 9.9e-183 | rbsR | K | Periplasmic binding proteins and sugar binding domain of LacI family | ||
HGMOLFCO_00178 | 3.6e-111 | |||||
HGMOLFCO_00179 | 8.6e-116 | dck | 2.7.1.74 | F | deoxynucleoside kinase | |
HGMOLFCO_00180 | 9.7e-163 | 3.2.1.17 | NU | Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase | ||
HGMOLFCO_00181 | 4.2e-256 | S | Putative peptidoglycan binding domain | |||
HGMOLFCO_00182 | 3.3e-86 | uspA | T | Belongs to the universal stress protein A family | ||
HGMOLFCO_00183 | 2.9e-273 | pepV | 3.5.1.18 | E | dipeptidase PepV | |
HGMOLFCO_00184 | 9.8e-155 | nnrD | 4.2.1.136, 5.1.99.6 | H | Catalyzes the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. Together with NAD(P)HX epimerase, which catalyzes the epimerization of the S- and R-forms, the enzyme 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 | |
HGMOLFCO_00185 | 2.8e-61 | 3.2.1.23 | S | Domain of unknown function DUF302 | ||
HGMOLFCO_00186 | 1.4e-298 | ytgP | S | Polysaccharide biosynthesis protein | ||
HGMOLFCO_00187 | 2.6e-42 | |||||
HGMOLFCO_00188 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
HGMOLFCO_00189 | 1e-125 | 3.1.3.2, 3.1.3.27, 3.1.3.4, 3.1.3.81, 3.6.1.27 | I | Acid phosphatase homologues | ||
HGMOLFCO_00190 | 3.4e-225 | 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 | |
HGMOLFCO_00191 | 3.7e-140 | proB | 2.7.2.11 | F | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
HGMOLFCO_00192 | 1.1e-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 | |
HGMOLFCO_00193 | 8.5e-51 | |||||
HGMOLFCO_00194 | 6.8e-98 | tag | 3.2.2.20 | L | glycosylase | |
HGMOLFCO_00195 | 5.8e-253 | EGP | Major facilitator Superfamily | |||
HGMOLFCO_00196 | 2.8e-84 | perR | P | Belongs to the Fur family | ||
HGMOLFCO_00197 | 4.5e-247 | cycA | E | Amino acid permease | ||
HGMOLFCO_00198 | 4e-22 | |||||
HGMOLFCO_00200 | 6.3e-07 | tlpA2 | L | Transposase IS200 like | ||
HGMOLFCO_00201 | 4.6e-42 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
HGMOLFCO_00202 | 2.3e-35 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
HGMOLFCO_00203 | 1.8e-184 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
HGMOLFCO_00204 | 0.0 | comEC | S | Competence protein ComEC | ||
HGMOLFCO_00205 | 3.4e-88 | comEB | 3.5.4.12 | F | ComE operon protein 2 | |
HGMOLFCO_00206 | 3.8e-90 | comEA | L | Competence protein ComEA | ||
HGMOLFCO_00207 | 4.3e-197 | ylbL | T | Belongs to the peptidase S16 family | ||
HGMOLFCO_00208 | 9.6e-89 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
HGMOLFCO_00209 | 1.3e-99 | rsmD | 2.1.1.171 | L | RNA methyltransferase, RsmD family | |
HGMOLFCO_00210 | 1.4e-47 | ylbG | S | Uncharacterized protein conserved in bacteria (DUF2129) | ||
HGMOLFCO_00211 | 1.5e-214 | ftsW | D | Belongs to the SEDS family | ||
HGMOLFCO_00212 | 0.0 | typA | T | GTP-binding protein TypA | ||
HGMOLFCO_00213 | 1.1e-136 | suhB | 3.1.3.25 | G | Belongs to the inositol monophosphatase superfamily | |
HGMOLFCO_00214 | 2.4e-49 | yktA | S | Belongs to the UPF0223 family | ||
HGMOLFCO_00215 | 7.5e-103 | def | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions | |
HGMOLFCO_00216 | 1.2e-74 | |||||
HGMOLFCO_00217 | 2.2e-31 | ykzG | S | Belongs to the UPF0356 family | ||
HGMOLFCO_00218 | 5.8e-188 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic | |
HGMOLFCO_00219 | 4.2e-74 | spx4 | 1.20.4.1 | P | ArsC family | |
HGMOLFCO_00220 | 9.4e-178 | 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) | |
HGMOLFCO_00221 | 0.0 | recD | 3.1.11.5 | L | DNA-dependent ATPase and ATP-dependent 5'-3' DNA helicase. Has no activity on blunt DNA or DNA with 3'-overhangs, requires at least 10 bases of 5'-ssDNA for helicase activity | |
HGMOLFCO_00222 | 1.6e-123 | S | Repeat protein | |||
HGMOLFCO_00223 | 4.1e-121 | pgm6 | 5.4.2.11, 5.4.2.12 | G | phosphoglycerate mutase | |
HGMOLFCO_00224 | 4e-170 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
HGMOLFCO_00225 | 1.3e-306 | S | amidohydrolase | |||
HGMOLFCO_00226 | 5.8e-224 | 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 | |
HGMOLFCO_00227 | 3.4e-58 | XK27_04120 | S | Putative amino acid metabolism | ||
HGMOLFCO_00228 | 1.3e-125 | mtnN | 3.2.2.9 | E | 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 | |
HGMOLFCO_00230 | 3.8e-96 | nudF | 3.6.1.13 | L | ADP-ribose pyrophosphatase | |
HGMOLFCO_00231 | 1.2e-32 | cspB | K | Cold shock protein | ||
HGMOLFCO_00232 | 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) | |
HGMOLFCO_00234 | 4.8e-112 | divIVA | D | DivIVA domain protein | ||
HGMOLFCO_00235 | 1.9e-144 | ylmH | S | S4 domain protein | ||
HGMOLFCO_00236 | 6.8e-41 | yggT | S | YGGT family | ||
HGMOLFCO_00237 | 2.5e-75 | sepF | D | Cell division protein that is part of the divisome complex and is recruited early to the Z-ring. Probably stimulates Z-ring formation, perhaps through the cross-linking of FtsZ protofilaments. Its function overlaps with FtsA | ||
HGMOLFCO_00238 | 9e-221 | 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 | ||
HGMOLFCO_00239 | 3.2e-224 | 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 | ||
HGMOLFCO_00240 | 8.4e-151 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
HGMOLFCO_00241 | 2.8e-202 | murG | 2.4.1.227, 6.3.2.8 | 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) |
HGMOLFCO_00242 | 9.5e-261 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
HGMOLFCO_00243 | 9.1e-178 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
HGMOLFCO_00244 | 0.0 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
HGMOLFCO_00245 | 7e-09 | ftsL | D | Cell division protein FtsL | ||
HGMOLFCO_00246 | 1.1e-172 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
HGMOLFCO_00247 | 5.6e-79 | mraZ | K | Belongs to the MraZ family | ||
HGMOLFCO_00248 | 5.8e-58 | |||||
HGMOLFCO_00249 | 1.2e-07 | S | Protein of unknown function (DUF4044) | |||
HGMOLFCO_00250 | 0.0 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
HGMOLFCO_00251 | 1.5e-94 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
HGMOLFCO_00252 | 3.3e-163 | rrmA | 2.1.1.187 | H | Methyltransferase | |
HGMOLFCO_00253 | 1.5e-194 | pgl | 3.1.1.31 | G | Lactonase, 7-bladed beta-propeller | |
HGMOLFCO_00254 | 8.2e-173 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | G | Responsible for synthesis of pseudouridine from uracil | |
HGMOLFCO_00255 | 1e-153 | 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 | |
HGMOLFCO_00256 | 6e-123 | yjbM | 2.7.6.5 | S | RelA SpoT domain protein | |
HGMOLFCO_00257 | 1.8e-113 | yjbH | Q | Thioredoxin | ||
HGMOLFCO_00258 | 9.4e-205 | coiA | 3.6.4.12 | S | Competence protein | |
HGMOLFCO_00259 | 4.5e-113 | mecA | NOT | Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis | ||
HGMOLFCO_00260 | 1.7e-69 | spxA | 1.20.4.1 | K | Interferes with activator-stimulated transcription by interaction with the RNA polymerase alpha-CTD. May function to globally reduce transcription of genes involved in growth- and development-promoting processes and to increase transcription of genes involved in thiol homeostasis, during periods of extreme stress | |
HGMOLFCO_00261 | 2.8e-16 | traP | 1.14.99.57, 6.2.1.3 | S | enzyme involved in biosynthesis of extracellular polysaccharides | |
HGMOLFCO_00262 | 2.3e-157 | odh | 1.5.1.28 | C | NAD/NADP octopine/nopaline dehydrogenase, alpha-helical domain | |
HGMOLFCO_00263 | 1.2e-119 | 5.1.1.13 | M | racemase activity, acting on amino acids and derivatives | ||
HGMOLFCO_00264 | 7.8e-261 | arcD | E | Amino acid permease | ||
HGMOLFCO_00265 | 4.5e-199 | ilvE | 2.6.1.42 | E | Branched-chain amino acid aminotransferase | |
HGMOLFCO_00266 | 1.3e-55 | lacA | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
HGMOLFCO_00267 | 4.3e-36 | lacA | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
HGMOLFCO_00268 | 6.2e-77 | yncA | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
HGMOLFCO_00269 | 2.4e-84 | S | Fic/DOC family | |||
HGMOLFCO_00270 | 1.8e-96 | apt | 2.4.2.22, 2.4.2.7 | F | Phosphoribosyl transferase domain | |
HGMOLFCO_00271 | 1e-246 | EGP | Sugar (and other) transporter | |||
HGMOLFCO_00272 | 3.1e-69 | 1.4.1.1, 4.3.1.12 | E | Ornithine cyclodeaminase/mu-crystallin family | ||
HGMOLFCO_00273 | 1.1e-72 | 1.4.1.1, 4.3.1.12 | E | Ornithine cyclodeaminase/mu-crystallin family | ||
HGMOLFCO_00274 | 7.4e-77 | K | AsnC family | |||
HGMOLFCO_00275 | 1e-81 | uspA | T | universal stress protein | ||
HGMOLFCO_00276 | 2.3e-273 | 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 | |
HGMOLFCO_00277 | 2.6e-288 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
HGMOLFCO_00278 | 8.8e-207 | yeaN | P | Transporter, major facilitator family protein | ||
HGMOLFCO_00279 | 1.5e-74 | S | 3-demethylubiquinone-9 3-methyltransferase | |||
HGMOLFCO_00280 | 2.4e-83 | nrdI | F | Belongs to the NrdI family | ||
HGMOLFCO_00281 | 3.6e-252 | yhdP | S | Transporter associated domain | ||
HGMOLFCO_00282 | 5.2e-90 | GM | epimerase | |||
HGMOLFCO_00283 | 5.8e-86 | M1-874 | K | Domain of unknown function (DUF1836) | ||
HGMOLFCO_00284 | 8.3e-156 | 3.2.1.52 | GH20 | G | Xylose isomerase domain protein TIM barrel | |
HGMOLFCO_00285 | 1.6e-266 | pipD | E | Dipeptidase | ||
HGMOLFCO_00286 | 3.2e-130 | |||||
HGMOLFCO_00287 | 2.1e-88 | ybaK | J | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
HGMOLFCO_00288 | 6.4e-131 | gntR | K | UbiC transcription regulator-associated domain protein | ||
HGMOLFCO_00289 | 1.1e-149 | ybjI | 3.1.3.102, 3.1.3.104, 3.1.3.23 | S | haloacid dehalogenase-like hydrolase | |
HGMOLFCO_00290 | 0.0 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
HGMOLFCO_00291 | 2.9e-22 | S | Enoyl-(Acyl carrier protein) reductase | |||
HGMOLFCO_00292 | 1.9e-172 | K | Bacterial regulatory helix-turn-helix protein, lysR family | |||
HGMOLFCO_00293 | 1.7e-119 | cah | 4.2.1.1 | P | Eukaryotic-type carbonic anhydrase | |
HGMOLFCO_00294 | 0.0 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
HGMOLFCO_00295 | 6.9e-206 | carA | 6.3.5.5 | F | Belongs to the CarA family | |
HGMOLFCO_00296 | 7.6e-174 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
HGMOLFCO_00297 | 1.2e-73 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
HGMOLFCO_00298 | 1.4e-69 | esbA | S | Family of unknown function (DUF5322) | ||
HGMOLFCO_00299 | 3.1e-71 | rnhA | 3.1.26.4 | L | Ribonuclease HI | |
HGMOLFCO_00300 | 8.2e-108 | XK27_02070 | S | Nitroreductase family | ||
HGMOLFCO_00301 | 4e-156 | yckB | ET | Belongs to the bacterial solute-binding protein 3 family | ||
HGMOLFCO_00302 | 1.2e-118 | yecS | E | ABC transporter permease | ||
HGMOLFCO_00303 | 7.8e-36 | L | Integrase core domain | |||
HGMOLFCO_00304 | 5.8e-129 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
HGMOLFCO_00305 | 1.2e-16 | atpE | C | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
HGMOLFCO_00306 | 3.7e-53 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
HGMOLFCO_00307 | 7.4e-92 | 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 | ||
HGMOLFCO_00308 | 2.1e-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 | |
HGMOLFCO_00309 | 6.6e-165 | 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 | ||
HGMOLFCO_00310 | 4.4e-253 | 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 | |
HGMOLFCO_00311 | 4.4e-68 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
HGMOLFCO_00312 | 8.1e-29 | S | Protein of unknown function (DUF1146) | |||
HGMOLFCO_00313 | 2.7e-219 | murA | 2.5.1.7 | M | EPSP synthase (3-phosphoshikimate 1-carboxyvinyltransferase) | |
HGMOLFCO_00314 | 7.7e-183 | mbl | D | Cell shape determining protein MreB Mrl | ||
HGMOLFCO_00315 | 7.9e-32 | S | Protein of unknown function (DUF2969) | |||
HGMOLFCO_00316 | 2.2e-221 | rodA | D | Belongs to the SEDS family | ||
HGMOLFCO_00318 | 1.5e-180 | S | Protein of unknown function (DUF2785) | |||
HGMOLFCO_00319 | 7.7e-216 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
HGMOLFCO_00320 | 2.9e-151 | 2.3.1.19 | K | Helix-turn-helix XRE-family like proteins | ||
HGMOLFCO_00321 | 2.3e-81 | usp6 | T | universal stress protein | ||
HGMOLFCO_00323 | 1.3e-235 | rarA | L | recombination factor protein RarA | ||
HGMOLFCO_00324 | 1.5e-85 | yueI | S | Protein of unknown function (DUF1694) | ||
HGMOLFCO_00325 | 3.3e-76 | 4.4.1.5 | E | Glyoxalase | ||
HGMOLFCO_00326 | 5.3e-133 | S | Membrane | |||
HGMOLFCO_00327 | 4.6e-149 | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | |||
HGMOLFCO_00328 | 4.8e-269 | guaA | 2.3.1.128, 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
HGMOLFCO_00329 | 2e-114 | 2.7.6.5 | T | Region found in RelA / SpoT proteins | ||
HGMOLFCO_00330 | 1.8e-79 | K | response regulator | |||
HGMOLFCO_00331 | 1.9e-130 | sptS | 2.7.13.3 | T | Histidine kinase | |
HGMOLFCO_00332 | 2e-174 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
HGMOLFCO_00333 | 1.1e-103 | 2.3.1.128 | K | acetyltransferase | ||
HGMOLFCO_00334 | 3.4e-135 | IQ | Dehydrogenase reductase | |||
HGMOLFCO_00335 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
HGMOLFCO_00336 | 2.5e-161 | EG | EamA-like transporter family | |||
HGMOLFCO_00337 | 0.0 | helD | 3.6.4.12 | L | DNA helicase | |
HGMOLFCO_00338 | 4.3e-118 | dedA | S | SNARE associated Golgi protein | ||
HGMOLFCO_00339 | 4e-121 | pgm7 | 5.4.2.11, 5.4.2.12 | G | phosphoglycerate mutase | |
HGMOLFCO_00340 | 5e-232 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
HGMOLFCO_00341 | 1.4e-206 | menC | 4.2.1.113 | H | Converts 2-succinyl-6-hydroxy-2,4-cyclohexadiene-1- carboxylate (SHCHC) to 2-succinylbenzoate (OSB) | |
HGMOLFCO_00342 | 1.2e-134 | pnuC | H | nicotinamide mononucleotide transporter | ||
HGMOLFCO_00343 | 3.5e-299 | ybeC | E | amino acid | ||
HGMOLFCO_00344 | 1e-142 | aroA | 1.3.1.12, 1.3.1.43, 2.5.1.19 | E | Catalyzes the transfer of the enolpyruvyl moiety of phosphoenolpyruvate (PEP) to the 5-hydroxyl of shikimate-3- phosphate (S3P) to produce enolpyruvyl shikimate-3-phosphate and inorganic phosphate | |
HGMOLFCO_00345 | 2e-197 | tyrA | 1.3.1.12, 1.3.1.43 | E | prephenate dehydrogenase | |
HGMOLFCO_00346 | 2.5e-89 | aroK | 1.1.1.25, 2.7.1.71, 4.2.1.10, 4.2.3.4 | F | Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate | |
HGMOLFCO_00347 | 9.3e-217 | aspB | E | DegT/DnrJ/EryC1/StrS aminotransferase family | ||
HGMOLFCO_00348 | 2.5e-183 | 1.1.1.28 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | ||
HGMOLFCO_00349 | 1.6e-177 | hepT | 2.5.1.30, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
HGMOLFCO_00350 | 2.4e-156 | menA | 2.5.1.74 | H | 1,4-dihydroxy-2-naphthoate | |
HGMOLFCO_00351 | 6.7e-23 | S | Virus attachment protein p12 family | |||
HGMOLFCO_00352 | 0.0 | feoB | P | transporter of a GTP-driven Fe(2 ) uptake system | ||
HGMOLFCO_00353 | 1.4e-33 | feoA | P | FeoA domain | ||
HGMOLFCO_00354 | 8.5e-145 | sufC | O | FeS assembly ATPase SufC | ||
HGMOLFCO_00355 | 4.5e-244 | sufD | O | FeS assembly protein SufD | ||
HGMOLFCO_00356 | 1.8e-234 | sufS | 2.8.1.7, 4.4.1.16 | E | Catalyzes the removal of elemental sulfur and selenium atoms from L-cysteine, L-cystine, L-selenocysteine, and L- selenocystine to produce L-alanine | |
HGMOLFCO_00357 | 3.2e-83 | nifU | C | SUF system FeS assembly protein, NifU family | ||
HGMOLFCO_00358 | 4.2e-272 | sufB | O | assembly protein SufB | ||
HGMOLFCO_00359 | 6.1e-183 | fecB | P | Periplasmic binding protein | ||
HGMOLFCO_00360 | 1.2e-52 | yaaQ | S | Cyclic-di-AMP receptor | ||
HGMOLFCO_00361 | 6e-117 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
HGMOLFCO_00362 | 2.4e-21 | S | Protein of unknown function (DUF2508) | |||
HGMOLFCO_00363 | 1.1e-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 | ||
HGMOLFCO_00364 | 4.9e-40 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
HGMOLFCO_00365 | 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 | |
HGMOLFCO_00367 | 6.3e-80 | tadA | 3.5.4.33 | F | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
HGMOLFCO_00368 | 2e-35 | nrdH | O | Glutaredoxin | ||
HGMOLFCO_00369 | 0.0 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
HGMOLFCO_00370 | 1.9e-194 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
HGMOLFCO_00371 | 6e-247 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
HGMOLFCO_00372 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
HGMOLFCO_00373 | 0.0 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydC | ||
HGMOLFCO_00374 | 0.0 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydD | ||
HGMOLFCO_00375 | 1.5e-175 | cydB | 1.10.3.14 | C | Cytochrome d ubiquinol oxidase subunit II | |
HGMOLFCO_00376 | 1.1e-272 | cydA | 1.10.3.14 | C | ubiquinol oxidase | |
HGMOLFCO_00377 | 4.6e-53 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
HGMOLFCO_00378 | 8.4e-82 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
HGMOLFCO_00379 | 4.6e-244 | steT | E | amino acid | ||
HGMOLFCO_00380 | 2.2e-120 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
HGMOLFCO_00381 | 2.2e-51 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
HGMOLFCO_00382 | 5.9e-97 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
HGMOLFCO_00383 | 2.4e-23 | 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 | ||
HGMOLFCO_00384 | 7e-21 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
HGMOLFCO_00385 | 1.1e-104 | sigH | K | Belongs to the sigma-70 factor family | ||
HGMOLFCO_00386 | 2.6e-135 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
HGMOLFCO_00387 | 9.4e-71 | mrnC | J | Involved in correct processing of both the 5' and 3' ends of 23S rRNA precursor. Processes 30S rRNA precursor transcript even in absence of ribonuclease 3 (Rnc) | ||
HGMOLFCO_00388 | 6.5e-273 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
HGMOLFCO_00389 | 3.8e-99 | ywlG | S | Belongs to the UPF0340 family | ||
HGMOLFCO_00390 | 9.6e-291 | 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) | |
HGMOLFCO_00391 | 1.4e-204 | yacL | S | domain protein | ||
HGMOLFCO_00392 | 5.6e-253 | 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 | ||
HGMOLFCO_00393 | 1.4e-98 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | dUTP diphosphatase | |
HGMOLFCO_00394 | 4.2e-55 | HA62_12640 | S | GCN5-related N-acetyl-transferase | ||
HGMOLFCO_00395 | 4.3e-104 | rpiA | 2.7.1.12, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
HGMOLFCO_00396 | 1.1e-94 | maa | 2.3.1.18, 2.3.1.79 | S | Transferase hexapeptide repeat | |
HGMOLFCO_00397 | 4e-264 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
HGMOLFCO_00398 | 3e-167 | I | alpha/beta hydrolase fold | |||
HGMOLFCO_00399 | 5.2e-127 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
HGMOLFCO_00400 | 2.3e-168 | mleP2 | S | Sodium Bile acid symporter family | ||
HGMOLFCO_00401 | 1.8e-189 | lacM | 3.2.1.23, 3.2.1.35, 3.2.1.51, 3.2.1.97 | GH101,GH29 | G | beta-galactosidase |
HGMOLFCO_00402 | 0.0 | lacL | 3.2.1.23 | G | Belongs to the glycosyl hydrolase 2 family | |
HGMOLFCO_00404 | 1.1e-83 | ydcK | S | Belongs to the SprT family | ||
HGMOLFCO_00405 | 0.0 | yhgF | K | Tex-like protein N-terminal domain protein | ||
HGMOLFCO_00406 | 8.8e-153 | nadE | 6.3.1.5 | F | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
HGMOLFCO_00407 | 1.1e-283 | 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 | |
HGMOLFCO_00408 | 1.4e-127 | gntR1 | K | UbiC transcription regulator-associated domain protein | ||
HGMOLFCO_00409 | 4.3e-132 | racD | 5.1.1.13 | M | Belongs to the aspartate glutamate racemases family | |
HGMOLFCO_00410 | 3.3e-115 | |||||
HGMOLFCO_00413 | 4.6e-165 | yjjH | S | Calcineurin-like phosphoesterase | ||
HGMOLFCO_00414 | 1.9e-254 | dtpT | U | amino acid peptide transporter | ||
HGMOLFCO_00415 | 1.3e-163 | D | nuclear chromosome segregation | |||
HGMOLFCO_00416 | 9.7e-274 | rsmF | 2.1.1.176, 2.1.1.178 | J | NOL1 NOP2 sun family protein | |
HGMOLFCO_00417 | 1.3e-153 | yitU | 3.1.3.104 | S | hydrolase | |
HGMOLFCO_00418 | 1.4e-167 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
HGMOLFCO_00419 | 0.0 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
HGMOLFCO_00420 | 5.6e-208 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
HGMOLFCO_00421 | 1.5e-244 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
HGMOLFCO_00422 | 3.4e-180 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
HGMOLFCO_00423 | 1.3e-56 | ycsI | S | Protein of unknown function (DUF1445) | ||
HGMOLFCO_00425 | 0.0 | norZ | 1.7.2.5 | P | Cytochrome C and Quinol oxidase polypeptide I | |
HGMOLFCO_00426 | 4e-102 | norZ | 1.7.2.5 | P | Cytochrome C and Quinol oxidase polypeptide I | |
HGMOLFCO_00427 | 1.2e-290 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
HGMOLFCO_00428 | 1.9e-189 | dus | J | Catalyzes the synthesis of 5,6-dihydrouridine (D), a modified base found in the D-loop of most tRNAs, via the reduction of the C5-C6 double bond in target uridines | ||
HGMOLFCO_00429 | 2.6e-163 | hslO | O | Redox regulated molecular chaperone. Protects both thermally unfolding and oxidatively damaged proteins from irreversible aggregation. Plays an important role in the bacterial defense system toward oxidative stress | ||
HGMOLFCO_00430 | 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 | ||
HGMOLFCO_00431 | 4.1e-98 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
HGMOLFCO_00432 | 2.8e-257 | tilS | 2.4.2.8, 6.3.4.19 | J | 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 | |
HGMOLFCO_00433 | 3e-87 | yabR | J | RNA binding | ||
HGMOLFCO_00434 | 1.5e-56 | divIC | D | Septum formation initiator | ||
HGMOLFCO_00435 | 4.8e-39 | yabO | J | S4 domain protein | ||
HGMOLFCO_00436 | 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 | ||
HGMOLFCO_00437 | 9.6e-103 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
HGMOLFCO_00438 | 8.1e-114 | S | (CBS) domain | |||
HGMOLFCO_00439 | 8.6e-57 | L | Toxic component of a toxin-antitoxin (TA) module | |||
HGMOLFCO_00440 | 9.6e-211 | alr | 5.1.1.1 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
HGMOLFCO_00441 | 2.9e-60 | acpS | 2.7.6.3, 2.7.8.7, 5.1.1.1 | I | Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein | |
HGMOLFCO_00442 | 1.9e-254 | cshA | 3.6.4.13 | F | DEAD-box RNA helicase possibly involved in RNA degradation. Unwinds dsRNA in both 5'- and 3'-directions, has RNA- dependent ATPase activity | |
HGMOLFCO_00443 | 2.1e-260 | murF | 6.3.2.10, 6.3.2.13 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
HGMOLFCO_00444 | 2.9e-157 | htpX | O | Belongs to the peptidase M48B family | ||
HGMOLFCO_00445 | 2.5e-87 | lemA | S | LemA family | ||
HGMOLFCO_00446 | 4.8e-47 | ptpA | 3.1.3.48 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
HGMOLFCO_00447 | 4.7e-123 | srtA | 3.4.22.70 | M | sortase family | |
HGMOLFCO_00448 | 4.6e-117 | 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 | |
HGMOLFCO_00449 | 9.2e-231 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
HGMOLFCO_00450 | 8.5e-102 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
HGMOLFCO_00451 | 1.8e-96 | ymfM | S | Helix-turn-helix domain | ||
HGMOLFCO_00452 | 1.7e-251 | ymfH | S | Peptidase M16 | ||
HGMOLFCO_00453 | 3.3e-231 | ymfF | S | Peptidase M16 inactive domain protein | ||
HGMOLFCO_00454 | 2.4e-161 | aatB | ET | ABC transporter substrate-binding protein | ||
HGMOLFCO_00455 | 2.2e-114 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
HGMOLFCO_00456 | 1.4e-108 | glnP | P | ABC transporter permease | ||
HGMOLFCO_00457 | 4.3e-92 | mreD | M | rod shape-determining protein MreD | ||
HGMOLFCO_00458 | 3.7e-146 | mreC | M | Involved in formation and maintenance of cell shape | ||
HGMOLFCO_00459 | 1.9e-181 | mreB | D | cell shape determining protein MreB | ||
HGMOLFCO_00460 | 9.4e-115 | radC | L | DNA repair protein | ||
HGMOLFCO_00461 | 4.7e-249 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
HGMOLFCO_00462 | 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 | |
HGMOLFCO_00463 | 1.6e-88 | 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 | |
HGMOLFCO_00466 | 1.4e-204 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
HGMOLFCO_00467 | 2.9e-211 | EG | GntP family permease | |||
HGMOLFCO_00468 | 7.2e-228 | 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 | |
HGMOLFCO_00469 | 2.9e-215 | iscS2 | 2.8.1.7 | E | Aminotransferase class V | |
HGMOLFCO_00470 | 7e-306 | ezrA | D | modulates the frequency and position of FtsZ ring formation. Inhibits FtsZ ring formation at polar sites. Interacts either with FtsZ or with one of its binding partners to promote depolymerization | ||
HGMOLFCO_00471 | 1.7e-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 | ||
HGMOLFCO_00472 | 7.6e-188 | panE | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
HGMOLFCO_00473 | 2.9e-226 | mtnE | 2.6.1.83 | E | Aminotransferase | |
HGMOLFCO_00474 | 5.7e-146 | mtnU | 3.5.1.3 | S | Carbon-nitrogen hydrolase | |
HGMOLFCO_00475 | 2.1e-171 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
HGMOLFCO_00476 | 5.3e-184 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
HGMOLFCO_00477 | 9.6e-163 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
HGMOLFCO_00478 | 3.9e-176 | hprK | F | Catalyzes the ATP- as well as the pyrophosphate- dependent phosphorylation of a specific serine residue in HPr, a phosphocarrier protein of the phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS). HprK P also catalyzes the pyrophosphate-producing, inorganic phosphate-dependent dephosphorylation (phosphorolysis) of seryl-phosphorylated HPr (P- Ser-HPr). The two antagonistic activities of HprK P are regulated by several intracellular metabolites, which change their concentration in response to the absence or presence of rapidly metabolisable carbon sources (glucose, fructose, etc.) in the growth medium. Therefore, by controlling the phosphorylation state of HPr, HPrK P is a sensor enzyme that plays a major role in the regulation of carbon metabolism and sugar transport it mediates carbon catabolite repression (CCR), and regulates PTS-catalyzed carbohydrate uptake and inducer exclusion | ||
HGMOLFCO_00479 | 1.2e-47 | yvlD | S | Mycobacterial 4 TMS phage holin, superfamily IV | ||
HGMOLFCO_00480 | 4.1e-53 | KT | PspC domain protein | |||
HGMOLFCO_00481 | 4.5e-202 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
HGMOLFCO_00482 | 0.0 | secA | U | Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. Has a central role in coupling the hydrolysis of ATP to the transfer of proteins into and across the cell membrane, serving as an ATP-driven molecular motor driving the stepwise translocation of polypeptide chains across the membrane | ||
HGMOLFCO_00483 | 6.5e-96 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
HGMOLFCO_00484 | 6.1e-128 | comFC | S | Competence protein | ||
HGMOLFCO_00485 | 2e-252 | comFA | L | Helicase C-terminal domain protein | ||
HGMOLFCO_00486 | 9e-113 | yvyE | 3.4.13.9 | S | YigZ family | |
HGMOLFCO_00487 | 6.4e-38 | |||||
HGMOLFCO_00488 | 0.0 | ydaO | E | amino acid | ||
HGMOLFCO_00489 | 5.7e-289 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
HGMOLFCO_00490 | 7.4e-43 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
HGMOLFCO_00491 | 4.4e-115 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
HGMOLFCO_00492 | 0.0 | uup | S | ABC transporter, ATP-binding protein | ||
HGMOLFCO_00493 | 1.4e-173 | birA | 6.3.4.15 | H | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
HGMOLFCO_00494 | 9.7e-92 | bioY | S | BioY family | ||
HGMOLFCO_00495 | 1e-134 | fabI | 1.3.1.10, 1.3.1.9 | I | Enoyl- acyl-carrier-protein reductase NADH | |
HGMOLFCO_00496 | 1e-139 | accA | 2.1.3.15, 6.4.1.2 | I | alpha subunit | |
HGMOLFCO_00497 | 1.5e-160 | 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 | |
HGMOLFCO_00498 | 7.1e-264 | accC | 6.3.4.14, 6.4.1.2 | I | Acetyl-CoA carboxylase biotin carboxylase subunit | |
HGMOLFCO_00499 | 1.3e-75 | fabZ | 3.5.1.108, 4.2.1.59 | I | Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs | |
HGMOLFCO_00500 | 1.6e-63 | accB | 2.3.1.12, 4.1.1.3 | I | first, biotin carboxylase catalyzes the carboxylation of the carrier protein and then the transcarboxylase transfers the carboxyl group to form malonyl-CoA | |
HGMOLFCO_00501 | 1.7e-229 | 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 | |
HGMOLFCO_00502 | 2.7e-129 | IQ | reductase | |||
HGMOLFCO_00503 | 2.8e-171 | fabD | 2.3.1.39 | I | Malonyl CoA-acyl carrier protein transacylase | |
HGMOLFCO_00504 | 4.2e-34 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
HGMOLFCO_00505 | 4.4e-172 | 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 | |
HGMOLFCO_00506 | 1.4e-68 | marR | K | Transcriptional regulator, MarR family | ||
HGMOLFCO_00507 | 2.7e-76 | fabZ | 3.5.1.108, 4.2.1.59 | I | Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs | |
HGMOLFCO_00509 | 1.2e-194 | 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 | |
HGMOLFCO_00510 | 1.3e-110 | rimI | 2.3.1.128 | K | Ribosomal-protein-alanine acetyltransferase | |
HGMOLFCO_00511 | 8.4e-131 | yeaZ | 2.3.1.234 | O | Universal bacterial protein YeaZ | |
HGMOLFCO_00512 | 1.2e-114 | pyrE | 2.4.2.10, 4.1.1.23 | F | Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) | |
HGMOLFCO_00513 | 2.4e-130 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
HGMOLFCO_00514 | 1.9e-95 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
HGMOLFCO_00515 | 6.4e-257 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Belongs to the aldehyde dehydrogenase family | |
HGMOLFCO_00516 | 3e-248 | 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 | |
HGMOLFCO_00517 | 7.4e-167 | 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 | |
HGMOLFCO_00518 | 2.4e-93 | K | transcriptional regulator | |||
HGMOLFCO_00519 | 6.6e-128 | ybhF_2 | V | AAA domain, putative AbiEii toxin, Type IV TA system | ||
HGMOLFCO_00520 | 6e-189 | ybhR | V | ABC transporter | ||
HGMOLFCO_00521 | 1.7e-65 | arsC | 1.20.4.1 | P | Belongs to the ArsC family | |
HGMOLFCO_00522 | 2.2e-288 | glpQ | 3.1.4.46 | C | phosphodiesterase | |
HGMOLFCO_00523 | 6.8e-164 | yvgN | C | Aldo keto reductase | ||
HGMOLFCO_00524 | 0.0 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
HGMOLFCO_00525 | 0.0 | rexB | 3.1.21.3, 3.6.4.12 | L | The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination. This subunit has 5' - 3' nuclease activity | |
HGMOLFCO_00526 | 3.7e-279 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
HGMOLFCO_00527 | 0.0 | clpL | O | associated with various cellular activities | ||
HGMOLFCO_00528 | 2.7e-35 | |||||
HGMOLFCO_00529 | 1.2e-214 | patA | 2.6.1.1 | E | Aminotransferase | |
HGMOLFCO_00530 | 1.4e-183 | D | Alpha beta | |||
HGMOLFCO_00531 | 1.8e-189 | pacA | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
HGMOLFCO_00532 | 1.1e-110 | ysdA | CP | transmembrane transport | ||
HGMOLFCO_00533 | 1.4e-116 | pgmB | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | S | beta-phosphoglucomutase |
HGMOLFCO_00534 | 0.0 | mapA | 2.4.1.8 | GH65 | G | hydrolase, family 65, central catalytic |
HGMOLFCO_00535 | 7.4e-250 | malT | G | Major Facilitator | ||
HGMOLFCO_00536 | 3.7e-176 | malR | K | Transcriptional regulator, LacI family | ||
HGMOLFCO_00537 | 5.7e-71 | K | Transcriptional regulator | |||
HGMOLFCO_00538 | 3e-81 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
HGMOLFCO_00539 | 3e-208 | htrA | 3.4.21.107 | O | serine protease | |
HGMOLFCO_00540 | 6e-154 | vicX | 3.1.26.11 | S | domain protein | |
HGMOLFCO_00541 | 8e-143 | yycI | S | YycH protein | ||
HGMOLFCO_00542 | 1.1e-239 | yycH | S | YycH protein | ||
HGMOLFCO_00543 | 0.0 | vicK | 2.7.13.3 | T | Histidine kinase | |
HGMOLFCO_00544 | 6.8e-130 | K | response regulator | |||
HGMOLFCO_00547 | 1.3e-40 | rpmE2 | J | Ribosomal protein L31 | ||
HGMOLFCO_00548 | 2.3e-237 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
HGMOLFCO_00549 | 4.4e-311 | 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 | |
HGMOLFCO_00550 | 1.6e-47 | rpoE | K | Participates in both the initiation and recycling phases of transcription. In the presence of the delta subunit, RNAP displays an increased specificity of transcription, a decreased affinity for nucleic acids, and an increased efficiency of RNA synthesis because of enhanced recycling | ||
HGMOLFCO_00551 | 3.2e-74 | ywiB | S | Domain of unknown function (DUF1934) | ||
HGMOLFCO_00552 | 1.5e-266 | ywfO | S | HD domain protein | ||
HGMOLFCO_00553 | 6.4e-143 | yxeH | S | hydrolase | ||
HGMOLFCO_00554 | 4.5e-206 | V | domain protein | |||
HGMOLFCO_00555 | 1.9e-92 | K | Transcriptional regulator (TetR family) | |||
HGMOLFCO_00556 | 3.1e-187 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
HGMOLFCO_00557 | 2.2e-168 | |||||
HGMOLFCO_00559 | 4e-83 | zur | P | Belongs to the Fur family | ||
HGMOLFCO_00560 | 1.7e-105 | gmk2 | 2.7.4.8 | F | Guanylate kinase | |
HGMOLFCO_00561 | 1.3e-72 | apfA | 2.7.7.72, 3.6.1.61 | F | Nudix hydrolase | |
HGMOLFCO_00562 | 2.6e-205 | yfnA | E | Amino Acid | ||
HGMOLFCO_00563 | 0.0 | pepX | 3.4.14.11 | E | Removes N-terminal dipeptides sequentially from polypeptides having unsubstituted N-termini provided that the penultimate residue is proline | |
HGMOLFCO_00564 | 1.1e-243 | ganB | 3.2.1.89 | G | arabinogalactan | |
HGMOLFCO_00565 | 7.8e-64 | gntR1 | K | Transcriptional regulator, GntR family | ||
HGMOLFCO_00566 | 6.8e-156 | V | ABC transporter, ATP-binding protein | |||
HGMOLFCO_00567 | 1.2e-14 | |||||
HGMOLFCO_00568 | 2.8e-157 | 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 | ||
HGMOLFCO_00569 | 1e-202 | rny | S | Endoribonuclease that initiates mRNA decay | ||
HGMOLFCO_00570 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
HGMOLFCO_00571 | 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 | ||
HGMOLFCO_00572 | 1.1e-104 | 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 | |
HGMOLFCO_00573 | 1.1e-189 | 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 | |
HGMOLFCO_00574 | 2.9e-176 | 2.4.2.29 | F | queuine tRNA-ribosyltransferase activity | ||
HGMOLFCO_00575 | 5.5e-42 | yajC | U | Preprotein translocase | ||
HGMOLFCO_00576 | 6.8e-181 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
HGMOLFCO_00577 | 6.4e-233 | cshB | 3.6.4.13 | JKL | DEAD-box RNA helicase. May work in conjunction with the cold shock proteins to ensure proper initiation of transcription at low and optimal temperatures | |
HGMOLFCO_00578 | 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 | |
HGMOLFCO_00579 | 1.2e-42 | yrzL | S | Belongs to the UPF0297 family | ||
HGMOLFCO_00580 | 9.6e-74 | yqgF | J | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
HGMOLFCO_00581 | 1.6e-38 | yrzB | S | Belongs to the UPF0473 family | ||
HGMOLFCO_00582 | 4.6e-163 | rnhC | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
HGMOLFCO_00583 | 4.7e-91 | cvpA | S | Colicin V production protein | ||
HGMOLFCO_00584 | 0.0 | mutS2 | L | Endonuclease that is involved in the suppression of homologous recombination and may therefore have a key role in the control of bacterial genetic diversity | ||
HGMOLFCO_00585 | 8.5e-198 | ilvE | 2.6.1.42 | E | Branched-chain amino acid aminotransferase | |
HGMOLFCO_00586 | 6.2e-171 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
HGMOLFCO_00587 | 2.8e-137 | cof | S | haloacid dehalogenase-like hydrolase | ||
HGMOLFCO_00588 | 0.0 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase phosphomannomutase, alpha beta alpha domain | |
HGMOLFCO_00589 | 1.4e-113 | yfbR | S | HD containing hydrolase-like enzyme | ||
HGMOLFCO_00591 | 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 | ||
HGMOLFCO_00592 | 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 | ||
HGMOLFCO_00593 | 9.9e-205 | |||||
HGMOLFCO_00594 | 3.2e-161 | rapZ | S | Displays ATPase and GTPase activities | ||
HGMOLFCO_00595 | 1.7e-187 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
HGMOLFCO_00596 | 4.2e-167 | whiA | K | May be required for sporulation | ||
HGMOLFCO_00597 | 1.5e-120 | tenA | 3.5.99.2 | K | Catalyzes an amino-pyrimidine hydrolysis reaction at the C5' of the pyrimidine moiety of thiamine compounds, a reaction that is part of a thiamine salvage pathway | |
HGMOLFCO_00598 | 1.3e-102 | 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 | |
HGMOLFCO_00602 | 2.6e-91 | pstS | P | Phosphate | ||
HGMOLFCO_00603 | 1.2e-97 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
HGMOLFCO_00604 | 1.3e-103 | pstA | P | Phosphate transport system permease protein PstA | ||
HGMOLFCO_00605 | 2.8e-95 | pstB | 3.6.3.27 | L | Transposase and inactivated derivatives, IS30 family DNA replication, recombination, and repair | |
HGMOLFCO_00606 | 1.5e-205 | fni | 1.1.1.88, 5.3.3.2 | C | Involved in the biosynthesis of isoprenoids. Catalyzes the 1,3-allylic rearrangement of the homoallylic substrate isopentenyl (IPP) to its allylic isomer, dimethylallyl diphosphate (DMAPP) | |
HGMOLFCO_00607 | 1.5e-211 | mvaK2 | 2.7.1.36, 2.7.1.43, 2.7.4.2 | I | phosphomevalonate kinase | |
HGMOLFCO_00608 | 8.2e-182 | mvaD | 4.1.1.33 | I | diphosphomevalonate decarboxylase | |
HGMOLFCO_00609 | 5.4e-167 | mvk | 1.1.1.88, 2.3.3.10, 2.7.1.36 | I | mevalonate kinase | |
HGMOLFCO_00610 | 0.0 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
HGMOLFCO_00611 | 1.6e-88 | ypmB | S | Protein conserved in bacteria | ||
HGMOLFCO_00612 | 2.1e-257 | asnS | 6.1.1.22 | J | Asparaginyl-tRNA synthetase | |
HGMOLFCO_00613 | 4.7e-134 | dnaD | L | DnaD domain protein | ||
HGMOLFCO_00614 | 1.3e-121 | ypuA | S | Protein of unknown function (DUF1002) | ||
HGMOLFCO_00615 | 3.7e-193 | C | Aldo keto reductase family protein | |||
HGMOLFCO_00616 | 3.1e-159 | EG | EamA-like transporter family | |||
HGMOLFCO_00617 | 0.0 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
HGMOLFCO_00618 | 3.9e-116 | recU | L | Endonuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves mobile four-strand junctions by introducing symmetrical nicks in paired strands. Promotes annealing of linear ssDNA with homologous dsDNA. Required for DNA repair, homologous recombination and chromosome segregation | ||
HGMOLFCO_00619 | 1.7e-110 | ypsA | S | Belongs to the UPF0398 family | ||
HGMOLFCO_00620 | 4.6e-58 | gpsB | D | Divisome component that associates with the complex late in its assembly, after the Z-ring is formed, and is dependent on DivIC and PBP2B for its recruitment to the divisome. Together with EzrA, is a key component of the system that regulates PBP1 localization during cell cycle progression. Its main role could be the removal of PBP1 from the cell pole after pole maturation is completed. Also contributes to the recruitment of PBP1 to the division complex. Not essential for septum formation | ||
HGMOLFCO_00621 | 0.0 | tetP | J | elongation factor G | ||
HGMOLFCO_00622 | 4e-212 | S | Type IV secretion-system coupling protein DNA-binding domain | |||
HGMOLFCO_00623 | 8.9e-83 | F | Hydrolase, NUDIX family | |||
HGMOLFCO_00624 | 8.5e-215 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
HGMOLFCO_00625 | 1.3e-88 | arcD | S | C4-dicarboxylate anaerobic carrier | ||
HGMOLFCO_00626 | 5.9e-28 | arcD | S | C4-dicarboxylate anaerobic carrier | ||
HGMOLFCO_00627 | 1.2e-272 | nylA | 3.5.1.4 | J | Belongs to the amidase family | |
HGMOLFCO_00629 | 3.9e-276 | lacS | G | Transporter | ||
HGMOLFCO_00630 | 0.0 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
HGMOLFCO_00631 | 1.6e-180 | galR | K | Transcriptional regulator | ||
HGMOLFCO_00632 | 8.1e-287 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
HGMOLFCO_00633 | 1e-223 | galK | 2.7.1.6 | F | Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) | |
HGMOLFCO_00634 | 7.7e-185 | celE | 3.2.1.4 | GH5,GH9 | E | GDSL-like Lipase/Acylhydrolase family |
HGMOLFCO_00635 | 1.6e-143 | ptp3 | 3.1.3.48 | T | Tyrosine phosphatase family | |
HGMOLFCO_00636 | 2.7e-96 | yxkA | S | Phosphatidylethanolamine-binding protein | ||
HGMOLFCO_00637 | 2e-35 | |||||
HGMOLFCO_00638 | 6.6e-136 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
HGMOLFCO_00639 | 5.3e-119 | tcyB | U | Binding-protein-dependent transport system inner membrane component | ||
HGMOLFCO_00640 | 1.7e-140 | tcyA | ET | Belongs to the bacterial solute-binding protein 3 family | ||
HGMOLFCO_00641 | 2e-52 | |||||
HGMOLFCO_00642 | 9e-170 | MA20_03535 | 1.1.1.399, 1.1.1.95 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
HGMOLFCO_00643 | 1.7e-79 | 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 | ||
HGMOLFCO_00644 | 6.9e-147 | pnuC | H | nicotinamide mononucleotide transporter | ||
HGMOLFCO_00645 | 1.1e-92 | ymdB | S | Macro domain protein | ||
HGMOLFCO_00646 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
HGMOLFCO_00647 | 1.8e-229 | pbuG | S | permease | ||
HGMOLFCO_00648 | 2.1e-45 | |||||
HGMOLFCO_00649 | 1.4e-212 | S | Putative metallopeptidase domain | |||
HGMOLFCO_00650 | 2.6e-203 | 3.1.3.1 | S | associated with various cellular activities | ||
HGMOLFCO_00651 | 6.5e-116 | mpg | 3.2.2.21 | L | Belongs to the DNA glycosylase MPG family | |
HGMOLFCO_00652 | 6.8e-65 | yeaO | S | Protein of unknown function, DUF488 | ||
HGMOLFCO_00654 | 4.8e-125 | yrkL | S | Flavodoxin-like fold | ||
HGMOLFCO_00655 | 5.6e-55 | |||||
HGMOLFCO_00656 | 2.2e-108 | nnrD | 4.2.1.136, 5.1.99.6 | H | Catalyzes the epimerization of the S- and R-forms of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration. This is a prerequisite for the S- specific NAD(P)H-hydrate dehydratase to allow the repair of both epimers of NAD(P)HX | |
HGMOLFCO_00657 | 1e-96 | efp | J | Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase | ||
HGMOLFCO_00658 | 2.4e-102 | |||||
HGMOLFCO_00659 | 9.5e-26 | |||||
HGMOLFCO_00660 | 2.6e-127 | scrR | K | Transcriptional regulator, LacI family | ||
HGMOLFCO_00661 | 5.5e-172 | acm2 | 3.2.1.17 | NU | Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase | |
HGMOLFCO_00662 | 2.6e-46 | czrA | K | Transcriptional regulator, ArsR family | ||
HGMOLFCO_00663 | 1.9e-103 | |||||
HGMOLFCO_00664 | 1.3e-213 | 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 | |
HGMOLFCO_00665 | 7.6e-13 | pheA | 1.3.1.12, 2.3.1.79, 4.2.1.51, 5.4.99.5 | E | Chorismate mutase type II | |
HGMOLFCO_00666 | 1.2e-211 | ydiN | G | Major Facilitator Superfamily | ||
HGMOLFCO_00668 | 6.9e-249 | dtpT | U | amino acid peptide transporter | ||
HGMOLFCO_00671 | 1.5e-152 | S | Sucrose-6F-phosphate phosphohydrolase | |||
HGMOLFCO_00672 | 2.4e-44 | 1.6.5.2 | GM | NAD(P)H-binding | ||
HGMOLFCO_00673 | 1e-90 | 1.6.5.2 | GM | NAD(P)H-binding | ||
HGMOLFCO_00674 | 2.6e-42 | S | Alpha beta hydrolase | |||
HGMOLFCO_00675 | 1.5e-36 | S | Alpha beta hydrolase | |||
HGMOLFCO_00676 | 1.2e-34 | S | Alpha beta hydrolase | |||
HGMOLFCO_00677 | 1.5e-235 | lmrB | EGP | Major facilitator Superfamily | ||
HGMOLFCO_00679 | 0.0 | S | Bacterial membrane protein YfhO | |||
HGMOLFCO_00680 | 3.6e-41 | |||||
HGMOLFCO_00681 | 1e-120 | mleP3 | S | Membrane transport protein | ||
HGMOLFCO_00682 | 1.1e-52 | trxA | O | Belongs to the thioredoxin family | ||
HGMOLFCO_00683 | 1.7e-254 | gor | 1.8.1.7 | C | pyridine nucleotide-disulfide oxidoreductase | |
HGMOLFCO_00684 | 1.6e-208 | EGP | Major facilitator Superfamily | |||
HGMOLFCO_00685 | 4.6e-211 | ycsG | P | Natural resistance-associated macrophage protein | ||
HGMOLFCO_00686 | 1e-136 | ycsF | S | LamB/YcsF family | ||
HGMOLFCO_00687 | 7.6e-258 | accC | 6.3.4.14, 6.4.1.2 | I | Acetyl-CoA carboxylase biotin carboxylase subunit | |
HGMOLFCO_00688 | 3.2e-58 | accB | 2.3.1.12, 4.1.1.3 | I | first, biotin carboxylase catalyzes the carboxylation of the carrier protein and then the transcarboxylase transfers the carboxyl group to form malonyl-CoA | |
HGMOLFCO_00689 | 1.4e-189 | kipA | 6.3.4.6 | E | Allophanate hydrolase subunit 2 | |
HGMOLFCO_00690 | 7.9e-134 | ybgJ | 3.5.1.54 | E | Allophanate hydrolase subunit 1 | |
HGMOLFCO_00691 | 8.7e-72 | K | helix_turn_helix, mercury resistance | |||
HGMOLFCO_00692 | 5.9e-82 | S | Psort location Cytoplasmic, score | |||
HGMOLFCO_00693 | 1e-287 | dinB | 2.7.7.7 | L | impB/mucB/samB family C-terminal domain | |
HGMOLFCO_00694 | 1.1e-95 | wecD | K | Acetyltransferase (GNAT) family | ||
HGMOLFCO_00695 | 4.2e-104 | 3.2.1.17 | NU | mannosyl-glycoprotein | ||
HGMOLFCO_00696 | 9.1e-121 | asnA | 6.3.1.1 | F | aspartate--ammonia ligase | |
HGMOLFCO_00697 | 1.9e-08 | yjjG | 3.1.3.102, 3.1.3.104, 3.1.3.5, 3.8.1.2 | E | hydrolase | |
HGMOLFCO_00698 | 4.5e-208 | guaB | 1.1.1.205 | 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 | |
HGMOLFCO_00699 | 5.9e-135 | XK27_01040 | S | Protein of unknown function (DUF1129) | ||
HGMOLFCO_00700 | 4.4e-200 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
HGMOLFCO_00701 | 7.9e-31 | yyzM | S | Bacterial protein of unknown function (DUF951) | ||
HGMOLFCO_00702 | 3.3e-147 | spo0J | K | Belongs to the ParB family | ||
HGMOLFCO_00703 | 1.1e-156 | noc | K | Belongs to the ParB family | ||
HGMOLFCO_00704 | 9e-133 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
HGMOLFCO_00705 | 2.2e-144 | rihC | 3.2.2.1 | F | Nucleoside | |
HGMOLFCO_00706 | 1.9e-212 | nupG | F | Nucleoside transporter | ||
HGMOLFCO_00707 | 1.4e-251 | cycA | E | Amino acid permease | ||
HGMOLFCO_00708 | 2.2e-134 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
HGMOLFCO_00709 | 1.2e-226 | glnP | P | ABC transporter | ||
HGMOLFCO_00711 | 1e-187 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
HGMOLFCO_00713 | 1.2e-228 | serS | 6.1.1.11 | J | Catalyzes the attachment of serine to tRNA(Ser). Is also able to aminoacylate tRNA(Sec) with serine, to form the misacylated tRNA L-seryl-tRNA(Sec), which will be further converted into selenocysteinyl-tRNA(Sec) | |
HGMOLFCO_00714 | 0.0 | sbcC | L | Putative exonuclease SbcCD, C subunit | ||
HGMOLFCO_00715 | 1.5e-219 | 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 | ||
HGMOLFCO_00717 | 8.3e-298 | dltA | 6.1.1.13 | H | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
HGMOLFCO_00718 | 7e-239 | dltB | M | MBOAT, membrane-bound O-acyltransferase family | ||
HGMOLFCO_00719 | 1.2e-35 | dltC | 6.1.1.13 | J | Carrier protein involved in the D-alanylation of lipoteichoic acid (LTA). The loading of thioester-linked D-alanine onto DltC is catalyzed by D-alanine--D-alanyl carrier protein ligase DltA. The DltC-carried D-alanyl group is further transferred to cell membrane phosphatidylglycerol (PG) by forming an ester bond, probably catalyzed by DltD. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
HGMOLFCO_00720 | 7.1e-242 | dltD | M | Protein involved in D-alanine esterification of lipoteichoic acid and wall teichoic acid (D-alanine transfer protein) | ||
HGMOLFCO_00721 | 3.1e-122 | iolS | C | Aldo keto reductase | ||
HGMOLFCO_00722 | 7.3e-14 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
HGMOLFCO_00723 | 6.8e-87 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
HGMOLFCO_00724 | 9.9e-245 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
HGMOLFCO_00725 | 2.2e-218 | argE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
HGMOLFCO_00726 | 5.8e-97 | metI | P | ABC transporter permease | ||
HGMOLFCO_00727 | 1.6e-191 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
HGMOLFCO_00728 | 2.7e-149 | metQ1 | P | Belongs to the nlpA lipoprotein family | ||
HGMOLFCO_00729 | 1.6e-261 | tagE2 | 2.4.1.52 | GT4 | M | Poly(Glycerol-phosphate) alpha-glucosyltransferase |
HGMOLFCO_00730 | 3.2e-273 | tagE3 | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 |
HGMOLFCO_00731 | 6.9e-47 | |||||
HGMOLFCO_00732 | 7.9e-11 | gntT | EG | gluconate transmembrane transporter activity | ||
HGMOLFCO_00733 | 0.0 | kup | P | Transport of potassium into the cell | ||
HGMOLFCO_00735 | 3.9e-284 | 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 | |
HGMOLFCO_00736 | 5.4e-26 | dmpI | 5.3.2.6 | G | Belongs to the 4-oxalocrotonate tautomerase family | |
HGMOLFCO_00737 | 0.0 | yjbQ | P | TrkA C-terminal domain protein | ||
HGMOLFCO_00738 | 1.4e-275 | pipD | E | Dipeptidase | ||
HGMOLFCO_00739 | 3.4e-158 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
HGMOLFCO_00740 | 8.8e-240 | pts13C | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
HGMOLFCO_00741 | 5.4e-43 | 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 | ||
HGMOLFCO_00742 | 1.6e-168 | T | Calcineurin-like phosphoesterase superfamily domain | |||
HGMOLFCO_00743 | 9.5e-160 | EGP | Major facilitator Superfamily | |||
HGMOLFCO_00744 | 3.4e-201 | mdtG | EGP | Major facilitator Superfamily | ||
HGMOLFCO_00745 | 5.3e-251 | yhdP | S | Transporter associated domain | ||
HGMOLFCO_00746 | 3.3e-73 | K | LysR substrate binding domain protein | |||
HGMOLFCO_00747 | 4.4e-14 | K | LysR substrate binding domain protein | |||
HGMOLFCO_00748 | 3.4e-216 | E | GDSL-like Lipase/Acylhydrolase family | |||
HGMOLFCO_00749 | 2.3e-195 | lplA | 6.3.1.20 | H | Lipoate-protein ligase | |
HGMOLFCO_00750 | 6.9e-259 | lpdA | 1.8.1.4 | C | Dehydrogenase | |
HGMOLFCO_00751 | 1.5e-204 | pdhC | 2.3.1.12 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
HGMOLFCO_00752 | 5.8e-180 | pdhB | 1.2.4.1 | C | Transketolase, C-terminal domain protein | |
HGMOLFCO_00753 | 4.8e-183 | pdhA | 1.2.4.1, 1.2.4.4 | C | Dehydrogenase E1 component | |
HGMOLFCO_00754 | 2.4e-160 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
HGMOLFCO_00755 | 4.5e-127 | epsB | M | biosynthesis protein | ||
HGMOLFCO_00756 | 1.4e-112 | ywqD | 2.7.10.1 | D | Capsular exopolysaccharide family | |
HGMOLFCO_00757 | 5.1e-139 | ywqE | 3.1.3.48 | GM | PHP domain protein | |
HGMOLFCO_00758 | 4e-89 | capM | M | Bacterial sugar transferase | ||
HGMOLFCO_00759 | 3.6e-69 | M | Glycosyl transferase 4-like | |||
HGMOLFCO_00761 | 9.2e-86 | L | PFAM Integrase catalytic region | |||
HGMOLFCO_00762 | 3.4e-147 | ubiB | S | ABC1 family | ||
HGMOLFCO_00763 | 1e-130 | 1.14.12.17 | C | Oxidoreductase NAD-binding domain | ||
HGMOLFCO_00764 | 2.3e-170 | GK | ROK family | |||
HGMOLFCO_00765 | 3.9e-41 | |||||
HGMOLFCO_00766 | 4.2e-80 | copY | K | Copper transport repressor CopY TcrY | ||
HGMOLFCO_00768 | 1.6e-76 | 3.6.3.6 | P | ATPase, P-type transporting, HAD superfamily, subfamily IC | ||
HGMOLFCO_00769 | 4.1e-12 | traP | 1.14.99.57, 6.2.1.3 | S | enzyme involved in biosynthesis of extracellular polysaccharides | |
HGMOLFCO_00770 | 5.3e-170 | mutR | K | Transcriptional activator, Rgg GadR MutR family | ||
HGMOLFCO_00771 | 2e-288 | gntK | 2.7.1.12, 2.7.1.17 | G | Belongs to the FGGY kinase family | |
HGMOLFCO_00772 | 3.2e-229 | gntT | EG | Gluconate | ||
HGMOLFCO_00773 | 3.2e-181 | K | Transcriptional regulator, LacI family | |||
HGMOLFCO_00774 | 4.3e-61 | yneR | ||||
HGMOLFCO_00775 | 9.2e-220 | aspB | 2.6.1.1, 2.6.1.14 | E | Aminotransferase | |
HGMOLFCO_00776 | 2.2e-96 | V | VanZ like family | |||
HGMOLFCO_00777 | 7.3e-10 | gshF | 6.3.2.2 | H | Belongs to the glutamate--cysteine ligase type 1 family | |
HGMOLFCO_00778 | 1.9e-77 | XK27_08315 | M | Sulfatase | ||
HGMOLFCO_00779 | 3.8e-167 | map | 3.4.11.18 | E | Methionine Aminopeptidase | |
HGMOLFCO_00780 | 8.5e-78 | fld | C | Flavodoxin | ||
HGMOLFCO_00781 | 3e-75 | gtcA | S | Teichoic acid glycosylation protein | ||
HGMOLFCO_00783 | 2.6e-231 | yfmL | 3.6.4.13 | L | DEAD DEAH box helicase | |
HGMOLFCO_00784 | 1.3e-190 | mocA | S | Oxidoreductase | ||
HGMOLFCO_00785 | 4.9e-63 | S | Domain of unknown function (DUF4828) | |||
HGMOLFCO_00786 | 2e-103 | yvdD | 3.2.2.10 | S | Belongs to the LOG family | |
HGMOLFCO_00787 | 2.5e-161 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
HGMOLFCO_00788 | 5e-287 | gshF | 6.3.2.2 | H | Belongs to the glutamate--cysteine ligase type 1 family | |
HGMOLFCO_00789 | 8.9e-139 | S | NADPH-dependent FMN reductase | |||
HGMOLFCO_00790 | 3.9e-33 | yneR | S | Belongs to the HesB IscA family | ||
HGMOLFCO_00791 | 1.3e-304 | ybiT | S | ABC transporter, ATP-binding protein | ||
HGMOLFCO_00792 | 6.4e-84 | dps | P | Belongs to the Dps family | ||
HGMOLFCO_00793 | 1.6e-105 | |||||
HGMOLFCO_00794 | 4.3e-183 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
HGMOLFCO_00795 | 1.4e-101 | K | helix_turn_helix multiple antibiotic resistance protein | |||
HGMOLFCO_00796 | 6.6e-64 | fsr | EGP | Major Facilitator Superfamily | ||
HGMOLFCO_00797 | 2.8e-47 | fsr | EGP | Major Facilitator Superfamily | ||
HGMOLFCO_00798 | 2.1e-99 | ogt | 2.1.1.63, 3.2.2.20 | 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 | |
HGMOLFCO_00799 | 1.7e-102 | S | CAAX protease self-immunity | |||
HGMOLFCO_00801 | 4.1e-119 | Q | Methyltransferase domain | |||
HGMOLFCO_00802 | 1.2e-60 | 1.5.1.40 | S | NADP oxidoreductase coenzyme F420-dependent | ||
HGMOLFCO_00803 | 5.6e-20 | 1.5.1.40 | S | NADP oxidoreductase coenzyme F420-dependent | ||
HGMOLFCO_00804 | 1.4e-50 | K | 2 iron, 2 sulfur cluster binding | |||
HGMOLFCO_00805 | 0.0 | mco | Q | Multicopper oxidase | ||
HGMOLFCO_00806 | 7.1e-89 | S | Aminoacyl-tRNA editing domain | |||
HGMOLFCO_00807 | 3.1e-75 | ddaH | 3.5.3.18 | E | Amidinotransferase | |
HGMOLFCO_00809 | 1e-193 | nhaC | C | Na H antiporter NhaC | ||
HGMOLFCO_00810 | 2.1e-143 | S | Oxidoreductase family, NAD-binding Rossmann fold | |||
HGMOLFCO_00812 | 9.7e-179 | S | Phosphotransferase system, EIIC | |||
HGMOLFCO_00813 | 4.6e-23 | D | mRNA cleavage | |||
HGMOLFCO_00814 | 1.9e-21 | 2.3.1.15 | D | Antitoxin component of a toxin-antitoxin (TA) module | ||
HGMOLFCO_00815 | 3.6e-48 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
HGMOLFCO_00816 | 6.4e-91 | 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 | ||
HGMOLFCO_00817 | 2.1e-35 | rpsR | J | Binds as a heterodimer with protein S6 to the central domain of the 16S rRNA, where it helps stabilize the platform of the 30S subunit | ||
HGMOLFCO_00818 | 0.0 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
HGMOLFCO_00819 | 1.2e-74 | rplI | J | Binds to the 23S rRNA | ||
HGMOLFCO_00820 | 1.8e-243 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
HGMOLFCO_00821 | 6.7e-207 | lmrP | E | Major Facilitator Superfamily | ||
HGMOLFCO_00822 | 1.2e-48 | |||||
HGMOLFCO_00823 | 1.2e-166 | znuA | P | Belongs to the bacterial solute-binding protein 9 family | ||
HGMOLFCO_00824 | 5.4e-95 | fhuC | P | ABC transporter | ||
HGMOLFCO_00825 | 4.2e-128 | znuB | U | ABC 3 transport family | ||
HGMOLFCO_00826 | 7.5e-152 | purR | 2.4.2.22, 2.4.2.7 | F | pur operon repressor | |
HGMOLFCO_00827 | 7.3e-205 | 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 | |
HGMOLFCO_00828 | 1.4e-176 | prs | 2.7.6.1 | F | Involved in the biosynthesis of the central metabolite phospho-alpha-D-ribosyl-1-pyrophosphate (PRPP) via the transfer of pyrophosphoryl group from ATP to 1-hydroxyl of ribose-5-phosphate (Rib-5-P) | |
HGMOLFCO_00829 | 3e-32 | |||||
HGMOLFCO_00831 | 1.6e-85 | K | GNAT family | |||
HGMOLFCO_00832 | 5.2e-122 | XK27_08875 | O | PFAM peptidase M10A and M12B, matrixin and adamalysin | ||
HGMOLFCO_00833 | 4e-161 | ytbE | 1.1.1.346 | S | Aldo keto reductase | |
HGMOLFCO_00834 | 6.3e-145 | tpiA | 2.7.2.3, 5.3.1.1 | G | Involved in the gluconeogenesis. Catalyzes stereospecifically the conversion of dihydroxyacetone phosphate (DHAP) to D-glyceraldehyde-3-phosphate (G3P) | |
HGMOLFCO_00835 | 3.7e-131 | budA | 4.1.1.5 | H | Belongs to the alpha-acetolactate decarboxylase family | |
HGMOLFCO_00837 | 1e-56 | |||||
HGMOLFCO_00840 | 1.8e-78 | K | Winged helix DNA-binding domain | |||
HGMOLFCO_00841 | 0.0 | lmrA | V | ABC transporter, ATP-binding protein | ||
HGMOLFCO_00842 | 0.0 | yfiC | V | ABC transporter | ||
HGMOLFCO_00843 | 2.8e-193 | ampC | V | Beta-lactamase | ||
HGMOLFCO_00844 | 6.4e-287 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
HGMOLFCO_00845 | 2.8e-48 | |||||
HGMOLFCO_00846 | 3.4e-140 | cobQ | S | CobB/CobQ-like glutamine amidotransferase domain | ||
HGMOLFCO_00847 | 7.5e-263 | murF | 6.3.2.10, 6.3.2.13 | M | Domain of unknown function (DUF1727) | |
HGMOLFCO_00848 | 3.2e-109 | tdk | 2.7.1.21 | F | thymidine kinase | |
HGMOLFCO_00849 | 4.2e-155 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
HGMOLFCO_00850 | 1.6e-157 | prmB | 2.1.1.297, 2.1.1.298 | J | Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif | |
HGMOLFCO_00851 | 2.3e-195 | ywlC | 2.7.7.87, 3.1.3.48 | J | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine | |
HGMOLFCO_00852 | 4.6e-230 | 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 | |
HGMOLFCO_00853 | 1.2e-114 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
HGMOLFCO_00854 | 2.9e-183 | yibE | S | overlaps another CDS with the same product name | ||
HGMOLFCO_00855 | 1.5e-125 | yibF | S | overlaps another CDS with the same product name | ||
HGMOLFCO_00856 | 5.4e-218 | pyrP | F | Permease | ||
HGMOLFCO_00860 | 1.1e-09 | C | Aldo keto reductase | |||
HGMOLFCO_00861 | 7.3e-25 | C | Aldo keto reductase | |||
HGMOLFCO_00862 | 2.1e-07 | K | Bacterial regulatory helix-turn-helix protein, lysR family | |||
HGMOLFCO_00864 | 1.5e-45 | S | Alpha/beta hydrolase family | |||
HGMOLFCO_00865 | 6.4e-44 | S | Alpha/beta hydrolase family | |||
HGMOLFCO_00866 | 3e-119 | pnb | C | nitroreductase | ||
HGMOLFCO_00867 | 1.2e-32 | flpA | 4.1.99.16, 4.2.3.22, 4.2.3.75 | K | helix_turn_helix, cAMP Regulatory protein | |
HGMOLFCO_00868 | 2.4e-44 | S | Tautomerase enzyme | |||
HGMOLFCO_00869 | 3.6e-29 | S | Domain of unknown function (DUF4767) | |||
HGMOLFCO_00870 | 3.1e-178 | 3.4.11.5 | E | Releases the N-terminal proline from various substrates | ||
HGMOLFCO_00871 | 6.6e-116 | gph | 3.1.3.18 | S | HAD hydrolase, family IA, variant | |
HGMOLFCO_00872 | 1e-272 | S | Uncharacterized protein conserved in bacteria (DUF2325) | |||
HGMOLFCO_00873 | 1.2e-182 | 1.17.4.1 | F | Ribonucleotide reductase, small chain | ||
HGMOLFCO_00874 | 4.4e-169 | nrdF | 1.17.4.1 | F | Ribonucleotide reductase, small chain | |
HGMOLFCO_00875 | 0.0 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
HGMOLFCO_00876 | 1.4e-83 | nrdI | F | NrdI Flavodoxin like | ||
HGMOLFCO_00877 | 5.1e-110 | M | ErfK YbiS YcfS YnhG | |||
HGMOLFCO_00879 | 1.3e-204 | nrnB | S | DHHA1 domain | ||
HGMOLFCO_00880 | 3.4e-291 | S | ABC transporter, ATP-binding protein | |||
HGMOLFCO_00881 | 1.7e-179 | ABC-SBP | S | ABC transporter | ||
HGMOLFCO_00882 | 1e-138 | XK27_08840 | U | Belongs to the binding-protein-dependent transport system permease family | ||
HGMOLFCO_00883 | 1.4e-133 | XK27_08845 | S | ABC transporter, ATP-binding protein | ||
HGMOLFCO_00885 | 3.3e-225 | amtB | P | ammonium transporter | ||
HGMOLFCO_00886 | 4.3e-234 | mepA | V | MATE efflux family protein | ||
HGMOLFCO_00887 | 2.9e-170 | scrK | 2.7.1.2, 2.7.1.4 | GK | ROK family | |
HGMOLFCO_00888 | 5.2e-170 | cysK | 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
HGMOLFCO_00889 | 1.3e-153 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to | |
HGMOLFCO_00890 | 1.7e-131 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
HGMOLFCO_00891 | 1.5e-76 | yphH | S | Cupin domain | ||
HGMOLFCO_00892 | 1.8e-75 | argR | K | Regulates arginine biosynthesis genes | ||
HGMOLFCO_00893 | 5.5e-124 | devA | 3.6.3.25 | V | ABC transporter, ATP-binding protein | |
HGMOLFCO_00894 | 8.6e-158 | hrtB | V | ABC transporter permease | ||
HGMOLFCO_00895 | 1.1e-107 | ygfC | K | Bacterial regulatory proteins, tetR family | ||
HGMOLFCO_00896 | 2.4e-189 | tdh | 1.1.1.14 | E | Alcohol dehydrogenase GroES-like domain | |
HGMOLFCO_00897 | 1.4e-281 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
HGMOLFCO_00898 | 2.2e-22 | |||||
HGMOLFCO_00899 | 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) | |
HGMOLFCO_00900 | 1.2e-69 | L | nuclease | |||
HGMOLFCO_00901 | 8.4e-162 | F | DNA/RNA non-specific endonuclease | |||
HGMOLFCO_00902 | 6.6e-113 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
HGMOLFCO_00903 | 1.4e-292 | murE | 6.3.2.13, 6.3.2.7 | M | Catalyzes the addition of an amino acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
HGMOLFCO_00904 | 4.4e-291 | murE | 6.3.2.13, 6.3.2.7 | M | Catalyzes the addition of an amino acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
HGMOLFCO_00905 | 0.0 | asnB | 6.3.5.4 | E | Asparagine synthase | |
HGMOLFCO_00906 | 6.6e-220 | lysP | E | amino acid | ||
HGMOLFCO_00907 | 7e-49 | mscL | M | Channel that opens in response to stretch forces in the membrane lipid bilayer. May participate in the regulation of osmotic pressure changes within the cell | ||
HGMOLFCO_00908 | 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 | ||
HGMOLFCO_00909 | 1.1e-253 | mnmE | S | Exhibits a very high intrinsic GTPase hydrolysis rate. Involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA- cmnm(5)s(2)U34 | ||
HGMOLFCO_00910 | 1.2e-152 | jag | S | R3H domain protein | ||
HGMOLFCO_00911 | 3.4e-144 | 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 | ||
HGMOLFCO_00912 | 1.4e-56 | 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 | |
HGMOLFCO_00913 | 2.6e-14 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
HGMOLFCO_00914 | 1.4e-248 | 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 | ||
HGMOLFCO_00915 | 3.8e-207 | 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 | |
HGMOLFCO_00916 | 2.2e-34 | yaaA | S | S4 domain protein YaaA | ||
HGMOLFCO_00917 | 1.5e-203 | recF | L | it is required for DNA replication and normal SOS inducibility. RecF binds preferentially to single-stranded, linear DNA. It also seems to bind ATP | ||
HGMOLFCO_00918 | 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 | |
HGMOLFCO_00919 | 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 | |
HGMOLFCO_00920 | 2.9e-159 | 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 | |
HGMOLFCO_00921 | 1.2e-160 | 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 | |
HGMOLFCO_00922 | 5.6e-98 | rnmV | 3.1.26.8 | J | Required for correct processing of both the 5' and 3' ends of 5S rRNA precursor. Cleaves both sides of a double-stranded region yielding mature 5S rRNA in one step | |
HGMOLFCO_00923 | 1.8e-147 | tatD | L | hydrolase, TatD family | ||
HGMOLFCO_00924 | 0.0 | metG | 6.1.1.10 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
HGMOLFCO_00925 | 9.5e-163 | yunF | F | Protein of unknown function DUF72 | ||
HGMOLFCO_00926 | 5.3e-212 | norA | EGP | Major facilitator Superfamily | ||
HGMOLFCO_00927 | 4.4e-129 | cobB | K | SIR2 family | ||
HGMOLFCO_00928 | 2.2e-187 | |||||
HGMOLFCO_00929 | 6.8e-221 | mvaA | 1.1.1.34, 1.1.1.88, 2.3.1.9 | C | Belongs to the HMG-CoA reductase family | |
HGMOLFCO_00930 | 6.6e-173 | ppx | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
HGMOLFCO_00931 | 0.0 | helD | 3.6.4.12 | L | DNA helicase | |
HGMOLFCO_00932 | 1.2e-203 | napA | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
HGMOLFCO_00933 | 3.7e-154 | metQ_4 | P | Belongs to the nlpA lipoprotein family | ||
HGMOLFCO_00935 | 6e-140 | nfrA | 1.5.1.38, 1.5.1.39 | C | nitroreductase | |
HGMOLFCO_00936 | 3e-24 | phaG | GT1 | I | carboxylic ester hydrolase activity | |
HGMOLFCO_00937 | 1.8e-51 | K | Transcriptional regulator | |||
HGMOLFCO_00938 | 0.0 | pepN | 3.4.11.2 | E | aminopeptidase | |
HGMOLFCO_00939 | 8.1e-196 | 1.1.1.1, 1.1.1.14 | E | alcohol dehydrogenase | ||
HGMOLFCO_00940 | 2.1e-48 | S | Mazg nucleotide pyrophosphohydrolase | |||
HGMOLFCO_00941 | 9.9e-49 | 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 | ||
HGMOLFCO_00942 | 2.6e-86 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
HGMOLFCO_00943 | 6.5e-24 | rpmD | J | Ribosomal protein L30 | ||
HGMOLFCO_00944 | 5.6e-66 | rplO | J | Binds to the 23S rRNA | ||
HGMOLFCO_00945 | 2.6e-236 | 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 | ||
HGMOLFCO_00946 | 2.4e-121 | 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 | |
HGMOLFCO_00947 | 2e-32 | infA | J | One of the essential components for the initiation of protein synthesis. Stabilizes the binding of IF-2 and IF-3 on the 30S subunit to which N-formylmethionyl-tRNA(fMet) subsequently binds. Helps modulate mRNA selection, yielding the 30S pre- initiation complex (PIC). Upon addition of the 50S ribosomal subunit IF-1, IF-2 and IF-3 are released leaving the mature 70S translation initation complex | ||
HGMOLFCO_00948 | 1.1e-13 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
HGMOLFCO_00949 | 9.5e-59 | 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 | ||
HGMOLFCO_00950 | 1e-63 | rpsK | J | Located on the platform of the 30S subunit, it bridges several disparate RNA helices of the 16S rRNA. Forms part of the Shine-Dalgarno cleft in the 70S ribosome | ||
HGMOLFCO_00951 | 2e-169 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
HGMOLFCO_00952 | 2.8e-61 | rplQ | J | Ribosomal protein L17 | ||
HGMOLFCO_00953 | 4.6e-149 | cbiO | P | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
HGMOLFCO_00954 | 4.4e-155 | ecfA2 | 3.6.3.55 | P | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | |
HGMOLFCO_00955 | 4.1e-139 | ecfT | U | Transmembrane (T) component of an energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
HGMOLFCO_00956 | 2.2e-145 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
HGMOLFCO_00957 | 2.6e-79 | rplM | J | This protein is one of the early assembly proteins of the 50S ribosomal subunit, although it is not seen to bind rRNA by itself. It is important during the early stages of 50S assembly | ||
HGMOLFCO_00958 | 1.5e-65 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
HGMOLFCO_00959 | 3e-188 | S | interspecies interaction between organisms | |||
HGMOLFCO_00960 | 1.2e-138 | IQ | reductase | |||
HGMOLFCO_00961 | 5.8e-109 | acmC | 3.2.1.17, 3.2.1.96 | NU | mannosyl-glycoprotein | |
HGMOLFCO_00962 | 3.2e-101 | xpt | 2.4.2.22, 2.4.2.7 | F | Converts the preformed base xanthine, a product of nucleic acid breakdown, to xanthosine 5'-monophosphate (XMP), so it can be reused for RNA or DNA synthesis | |
HGMOLFCO_00963 | 1.4e-220 | purK2 | 6.3.4.18 | 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 | |
HGMOLFCO_00964 | 0.0 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
HGMOLFCO_00965 | 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 | |
HGMOLFCO_00966 | 2.2e-167 | camS | S | sex pheromone | ||
HGMOLFCO_00967 | 1e-48 | gatC | 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | |
HGMOLFCO_00968 | 3e-273 | gatA | 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Gln-tRNA(Gln) through the transamidation of misacylated Glu-tRNA(Gln) in organisms which lack glutaminyl-tRNA synthetase. The reaction takes place in the presence of glutamine and ATP through an activated gamma-phospho-Glu-tRNA(Gln) | |
HGMOLFCO_00969 | 5e-273 | gatB | 6.1.1.12, 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | |
HGMOLFCO_00970 | 1.9e-186 | yegS | 2.7.1.107 | G | Lipid kinase | |
HGMOLFCO_00971 | 6.3e-265 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
HGMOLFCO_00972 | 1.1e-49 | K | TRANSCRIPTIONal | |||
HGMOLFCO_00980 | 3e-07 | K | Bacterial regulatory proteins, tetR family | |||
HGMOLFCO_00982 | 3.8e-11 | qacC | P | COG2076 Membrane transporters of cations and cationic drugs | ||
HGMOLFCO_00983 | 9e-142 | ET | Bacterial periplasmic substrate-binding proteins | |||
HGMOLFCO_00984 | 2e-110 | XK27_05795 | P | ABC transporter permease | ||
HGMOLFCO_00985 | 0.0 | nrdD | 1.1.98.6 | F | Ribonucleoside-triphosphate reductase | |
HGMOLFCO_00986 | 2.4e-112 | 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 | |
HGMOLFCO_00987 | 5.4e-161 | sufD | O | Uncharacterized protein family (UPF0051) | ||
HGMOLFCO_00988 | 5.1e-235 | F | Permease | |||
HGMOLFCO_00989 | 1.1e-200 | adh | 1.1.1.1, 1.1.1.14 | C | Zinc-binding dehydrogenase | |
HGMOLFCO_00990 | 1.1e-62 | lytE | M | LysM domain protein | ||
HGMOLFCO_00991 | 4.8e-85 | ykhA | 3.1.2.20 | I | Thioesterase superfamily | |
HGMOLFCO_00992 | 1.4e-77 | hsp | O | Belongs to the small heat shock protein (HSP20) family | ||
HGMOLFCO_00993 | 0.0 | pacL | 3.6.3.8, 3.6.3.9 | P | Cation transporter/ATPase, N-terminus | |
HGMOLFCO_00995 | 3.1e-114 | |||||
HGMOLFCO_00996 | 4.7e-105 | S | Domain of unknown function (DUF4767) | |||
HGMOLFCO_00997 | 4.7e-54 | K | Helix-turn-helix domain | |||
HGMOLFCO_00998 | 1.8e-173 | 1.3.1.9 | S | Nitronate monooxygenase | ||
HGMOLFCO_01000 | 1.5e-76 | rocF | 3.5.3.1, 3.5.3.11 | E | Arginase family | |
HGMOLFCO_01001 | 1.4e-50 | ybjQ | S | Belongs to the UPF0145 family | ||
HGMOLFCO_01002 | 5.3e-281 | yjeM | E | Amino Acid | ||
HGMOLFCO_01003 | 4e-43 | K | helix_turn _helix lactose operon repressor | |||
HGMOLFCO_01004 | 3.1e-125 | K | helix_turn _helix lactose operon repressor | |||
HGMOLFCO_01005 | 9.8e-261 | G | PTS system Galactitol-specific IIC component | |||
HGMOLFCO_01006 | 9.3e-175 | 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 | |
HGMOLFCO_01007 | 1.5e-199 | S | Domain of unknown function (DUF4432) | |||
HGMOLFCO_01008 | 2.8e-114 | deoC | 4.1.2.4, 5.4.2.8 | F | Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate | |
HGMOLFCO_01009 | 3.7e-171 | deoR | K | sugar-binding domain protein | ||
HGMOLFCO_01010 | 2.2e-165 | 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 | |
HGMOLFCO_01011 | 2.1e-67 | rbsD | 5.4.99.62 | G | Catalyzes the interconversion of beta-pyran and beta- furan forms of D-ribose | |
HGMOLFCO_01012 | 2.7e-244 | fucP | G | Major Facilitator Superfamily | ||
HGMOLFCO_01013 | 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) | |
HGMOLFCO_01014 | 1e-11 | L | PFAM transposase, IS4 family protein | |||
HGMOLFCO_01015 | 3.3e-90 | L | PFAM transposase, IS4 family protein | |||
HGMOLFCO_01016 | 2.1e-123 | K | Crp-like helix-turn-helix domain | |||
HGMOLFCO_01017 | 6.8e-237 | larA | 5.1.2.1 | S | Domain of unknown function (DUF2088) | |
HGMOLFCO_01018 | 7.9e-132 | cpmA | S | AIR carboxylase | ||
HGMOLFCO_01019 | 7.3e-228 | larC | 4.99.1.12 | S | Involved in the biosynthesis of a nickel-pincer cofactor ((SCS)Ni(II) pincer complex). Binds Ni(2 ), and functions in nickel delivery to pyridinium-3,5-bisthiocarboxylic acid mononucleotide (P2TMN), to form the mature cofactor. Is thus probably required for the activation of nickel-pincer cofactor- dependent enzymes | |
HGMOLFCO_01020 | 3.3e-147 | larE | S | NAD synthase | ||
HGMOLFCO_01021 | 1.7e-122 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
HGMOLFCO_01022 | 4.1e-173 | hoxN | U | High-affinity nickel-transport protein | ||
HGMOLFCO_01023 | 0.0 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
HGMOLFCO_01024 | 4.1e-217 | argD | 2.6.1.11, 2.6.1.17 | E | acetylornithine | |
HGMOLFCO_01025 | 1e-136 | argB | 2.7.2.8 | F | Belongs to the acetylglutamate kinase family. ArgB subfamily | |
HGMOLFCO_01026 | 6.2e-208 | argJ | 2.3.1.1, 2.3.1.35, 2.7.2.8 | E | Catalyzes two activities which are involved in the cyclic version of arginine biosynthesis the synthesis of N- acetylglutamate from glutamate and acetyl-CoA as the acetyl donor, and of ornithine by transacetylation between N(2)-acetylornithine and glutamate | |
HGMOLFCO_01027 | 4.2e-197 | 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 | |
HGMOLFCO_01028 | 2.3e-206 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
HGMOLFCO_01029 | 0.0 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
HGMOLFCO_01030 | 3.3e-83 | rimP | J | Required for maturation of 30S ribosomal subunits | ||
HGMOLFCO_01031 | 8.3e-224 | nusA | K | Participates in both transcription termination and antitermination | ||
HGMOLFCO_01032 | 1.4e-47 | ylxR | K | Protein of unknown function (DUF448) | ||
HGMOLFCO_01033 | 9.3e-50 | ylxQ | J | ribosomal protein | ||
HGMOLFCO_01034 | 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 | ||
HGMOLFCO_01035 | 4.2e-59 | 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 | ||
HGMOLFCO_01036 | 5.7e-166 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
HGMOLFCO_01037 | 2.3e-184 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
HGMOLFCO_01038 | 9.3e-248 | EGP | Major facilitator Superfamily | |||
HGMOLFCO_01039 | 7.3e-141 | 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 | |
HGMOLFCO_01040 | 1.3e-128 | hisA | 5.3.1.16 | E | 1-(5-phosphoribosyl)-5- (5-phosphoribosylamino)methylideneamino imidazole-4-carboxamide isomerase | |
HGMOLFCO_01041 | 1.2e-111 | 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 | ||
HGMOLFCO_01042 | 1.3e-102 | hisB | 1.1.1.23, 2.6.1.9, 3.1.3.15, 4.2.1.19 | E | imidazoleglycerol-phosphate dehydratase | |
HGMOLFCO_01043 | 2.6e-228 | 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 | |
HGMOLFCO_01044 | 5.8e-109 | 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 | |
HGMOLFCO_01045 | 3.8e-218 | hisZ | 2.4.2.17, 6.1.1.21 | E | Required for the first step of histidine biosynthesis. May allow the feedback regulation of ATP phosphoribosyltransferase activity by histidine | |
HGMOLFCO_01046 | 1.3e-167 | hisK | 3.1.3.15 | E | Histidinol phosphate phosphatase, HisJ | |
HGMOLFCO_01047 | 8.5e-51 | 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 | |
HGMOLFCO_01048 | 1.6e-08 | 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 | |
HGMOLFCO_01049 | 2.8e-50 | 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 | ||
HGMOLFCO_01050 | 7.2e-177 | 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 | ||
HGMOLFCO_01051 | 0.0 | dnaK | O | Heat shock 70 kDa protein | ||
HGMOLFCO_01052 | 5.6e-61 | 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 | ||
HGMOLFCO_01053 | 2.2e-193 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
HGMOLFCO_01054 | 1.1e-62 | |||||
HGMOLFCO_01055 | 5e-56 | arsC | 1.20.4.1 | T | Low molecular weight phosphotyrosine protein phosphatase | |
HGMOLFCO_01057 | 9.2e-217 | argE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
HGMOLFCO_01058 | 3.9e-259 | guaD | 3.5.4.3 | F | Amidohydrolase family | |
HGMOLFCO_01059 | 7.7e-175 | tdh | 1.1.1.14 | C | Zinc-binding dehydrogenase | |
HGMOLFCO_01060 | 1.1e-30 | S | Sugar efflux transporter for intercellular exchange | |||
HGMOLFCO_01061 | 8e-32 | higA | K | Helix-turn-helix XRE-family like proteins | ||
HGMOLFCO_01062 | 9.8e-136 | E | Amino acid permease | |||
HGMOLFCO_01063 | 1e-238 | gadB | 4.1.1.15 | E | Belongs to the group II decarboxylase family | |
HGMOLFCO_01064 | 8.3e-16 | |||||
HGMOLFCO_01065 | 2.9e-103 | dedA | S | SNARE-like domain protein | ||
HGMOLFCO_01066 | 5.7e-25 | S | Protein of unknown function (DUF1461) | |||
HGMOLFCO_01067 | 6.6e-142 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
HGMOLFCO_01068 | 1.2e-97 | yutD | S | Protein of unknown function (DUF1027) | ||
HGMOLFCO_01069 | 5.3e-110 | S | Calcineurin-like phosphoesterase | |||
HGMOLFCO_01070 | 2.1e-224 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
HGMOLFCO_01071 | 3.9e-159 | ytxK | 2.1.1.72 | L | N-6 DNA Methylase | |
HGMOLFCO_01073 | 1.7e-14 | |||||
HGMOLFCO_01075 | 2.3e-15 | NU | general secretion pathway protein | |||
HGMOLFCO_01076 | 1.1e-47 | comGC | U | competence protein ComGC | ||
HGMOLFCO_01077 | 1e-158 | comGB | NU | type II secretion system | ||
HGMOLFCO_01078 | 7e-178 | comGA | NU | Type II IV secretion system protein | ||
HGMOLFCO_01079 | 0.0 | ykcB | M | Dolichyl-phosphate-mannose-protein mannosyltransferase | ||
HGMOLFCO_01080 | 8.3e-84 | mltD | CBM50 | M | PFAM NLP P60 protein | |
HGMOLFCO_01081 | 3.7e-134 | yebC | K | Transcriptional regulatory protein | ||
HGMOLFCO_01082 | 3.6e-85 | |||||
HGMOLFCO_01083 | 7.4e-186 | ccpA | K | catabolite control protein A | ||
HGMOLFCO_01084 | 9.1e-214 | pepQ | 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
HGMOLFCO_01085 | 8.5e-70 | |||||
HGMOLFCO_01086 | 9.2e-26 | WQ51_05790 | S | protein containing a divergent version of the methyl-accepting chemotaxis-like domain | ||
HGMOLFCO_01087 | 6.2e-157 | ykuT | M | mechanosensitive ion channel | ||
HGMOLFCO_01088 | 3.8e-151 | 3.1.3.102, 3.1.3.104, 3.1.3.23 | S | haloacid dehalogenase-like hydrolase | ||
HGMOLFCO_01089 | 1.4e-95 | S | Phosphoesterase | |||
HGMOLFCO_01090 | 3.6e-108 | 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 | |
HGMOLFCO_01091 | 5.4e-147 | murI | 3.6.1.66, 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
HGMOLFCO_01092 | 1.3e-91 | yslB | S | Protein of unknown function (DUF2507) | ||
HGMOLFCO_01093 | 1e-224 | clcA_2 | P | Chloride transporter, ClC family | ||
HGMOLFCO_01094 | 1.4e-53 | trxA | O | Belongs to the thioredoxin family | ||
HGMOLFCO_01095 | 3e-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 | |
HGMOLFCO_01096 | 1e-165 | arcC | 2.7.2.2 | E | Belongs to the carbamate kinase family | |
HGMOLFCO_01097 | 9.1e-239 | arcA | 3.5.3.6 | E | Arginine | |
HGMOLFCO_01098 | 3.5e-258 | E | Arginine ornithine antiporter | |||
HGMOLFCO_01099 | 2.7e-221 | yxjG | 2.1.1.14 | E | methionine synthase, vitamin-B12 independent | |
HGMOLFCO_01100 | 8.7e-215 | arcT | 2.6.1.1 | E | Aminotransferase | |
HGMOLFCO_01101 | 1.1e-169 | 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 | |
HGMOLFCO_01102 | 1.8e-179 | 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 | |
HGMOLFCO_01103 | 7.7e-263 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
HGMOLFCO_01104 | 2.4e-253 | lysA | 4.1.1.19, 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
HGMOLFCO_01105 | 2.9e-72 | dapD | 2.3.1.117, 2.3.1.89 | E | Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate | |
HGMOLFCO_01106 | 1.8e-220 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
HGMOLFCO_01107 | 9.2e-175 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
HGMOLFCO_01108 | 2.8e-140 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
HGMOLFCO_01109 | 6.5e-218 | patA | 2.6.1.1 | E | Aminotransferase | |
HGMOLFCO_01110 | 1.5e-197 | 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 | |
HGMOLFCO_01111 | 3e-227 | ktrB | P | Potassium uptake protein | ||
HGMOLFCO_01112 | 7.5e-118 | ktrA | P | domain protein | ||
HGMOLFCO_01113 | 1.7e-125 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
HGMOLFCO_01114 | 1.7e-156 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
HGMOLFCO_01115 | 6.6e-237 | pepT | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
HGMOLFCO_01117 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase | |
HGMOLFCO_01118 | 8.3e-268 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
HGMOLFCO_01119 | 1.6e-168 | cvfB | S | S1 domain | ||
HGMOLFCO_01120 | 6e-160 | xerD | D | recombinase XerD | ||
HGMOLFCO_01121 | 3.1e-93 | P | Cadmium resistance transporter | |||
HGMOLFCO_01122 | 4.6e-32 | ydzE | EG | spore germination | ||
HGMOLFCO_01123 | 6.5e-54 | 4.1.1.44 | 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 | ||
HGMOLFCO_01124 | 4.9e-46 | |||||
HGMOLFCO_01125 | 2.1e-255 | isdH | M | Iron Transport-associated domain | ||
HGMOLFCO_01126 | 1e-94 | M | Iron Transport-associated domain | |||
HGMOLFCO_01127 | 2.8e-149 | isdE | P | Periplasmic binding protein | ||
HGMOLFCO_01128 | 7.5e-153 | isdF | U | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
HGMOLFCO_01129 | 4.2e-141 | fhuC | 3.6.3.34 | HP | ABC transporter, ATP-binding protein | |
HGMOLFCO_01130 | 2.2e-235 | kgtP | EGP | Sugar (and other) transporter | ||
HGMOLFCO_01131 | 2.2e-57 | |||||
HGMOLFCO_01132 | 4.9e-159 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
HGMOLFCO_01133 | 4.3e-172 | L | PFAM Integrase, catalytic core | |||
HGMOLFCO_01134 | 1.2e-219 | iscS | 2.8.1.7 | E | Aminotransferase class V | |
HGMOLFCO_01136 | 1.2e-71 | tkt | 2.2.1.1 | H | 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 | |
HGMOLFCO_01137 | 2.6e-18 | tkt | 2.2.1.1 | H | 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 | |
HGMOLFCO_01138 | 1.4e-12 | tkt | 2.2.1.1 | H | 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 | |
HGMOLFCO_01139 | 1.7e-125 | rpiA | 2.7.1.12, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
HGMOLFCO_01140 | 2.3e-136 | tal | 2.2.1.2 | H | Transaldolase/Fructose-6-phosphate aldolase | |
HGMOLFCO_01141 | 0.0 | tkt | 2.2.1.1 | H | 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 | |
HGMOLFCO_01142 | 5.5e-245 | glpT | G | Major Facilitator Superfamily | ||
HGMOLFCO_01143 | 2.4e-128 | qmcA | O | prohibitin homologues | ||
HGMOLFCO_01145 | 3.1e-75 | uspA | T | universal stress protein | ||
HGMOLFCO_01146 | 2.1e-59 | |||||
HGMOLFCO_01147 | 6.6e-20 | |||||
HGMOLFCO_01148 | 1.7e-159 | |||||
HGMOLFCO_01149 | 8.4e-75 | K | Transcriptional regulator | |||
HGMOLFCO_01150 | 1.1e-186 | D | Alpha beta | |||
HGMOLFCO_01151 | 1.6e-73 | O | OsmC-like protein | |||
HGMOLFCO_01152 | 3.4e-191 | lplA2 | 6.3.1.20 | H | Bacterial lipoate protein ligase C-terminus | |
HGMOLFCO_01153 | 0.0 | yjcE | P | Sodium proton antiporter | ||
HGMOLFCO_01154 | 1.2e-16 | yvlA | ||||
HGMOLFCO_01155 | 1.4e-113 | P | Cobalt transport protein | |||
HGMOLFCO_01156 | 3.7e-257 | cbiO1 | S | ABC transporter, ATP-binding protein | ||
HGMOLFCO_01157 | 1.6e-100 | S | ABC-type cobalt transport system, permease component | |||
HGMOLFCO_01158 | 2e-180 | iunH2 | 3.2.2.1 | F | nucleoside hydrolase | |
HGMOLFCO_01159 | 4.4e-183 | yumC | 1.18.1.2, 1.19.1.1, 1.8.1.9 | C | Ferredoxin--NADP reductase | |
HGMOLFCO_01160 | 0.0 | cadA | 3.6.3.3, 3.6.3.5 | P | P-type ATPase | |
HGMOLFCO_01161 | 2.8e-32 | copZ | P | Heavy-metal-associated domain | ||
HGMOLFCO_01162 | 3.4e-100 | dps | P | Belongs to the Dps family | ||
HGMOLFCO_01163 | 1.8e-108 | rcfA | 4.1.99.16, 4.2.3.22, 4.2.3.75 | K | helix_turn_helix, cAMP Regulatory protein | |
HGMOLFCO_01164 | 2e-85 | |||||
HGMOLFCO_01165 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
HGMOLFCO_01166 | 2.5e-126 | pgm3 | G | phosphoglycerate mutase family | ||
HGMOLFCO_01167 | 1.9e-150 | qorB | 1.6.5.2 | GM | NmrA-like family | |
HGMOLFCO_01168 | 9.3e-229 | pbuX | F | xanthine permease | ||
HGMOLFCO_01169 | 1e-170 | corA | P | CorA-like Mg2+ transporter protein | ||
HGMOLFCO_01170 | 9.3e-169 | rluA | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
HGMOLFCO_01171 | 2.3e-142 | terC | P | membrane | ||
HGMOLFCO_01172 | 1e-56 | trxA1 | O | Belongs to the thioredoxin family | ||
HGMOLFCO_01173 | 9.1e-164 | fadB4 | 1.1.1.157 | I | 3-hydroxyacyl-CoA dehydrogenase | |
HGMOLFCO_01174 | 2.6e-163 | endA | F | DNA RNA non-specific endonuclease | ||
HGMOLFCO_01175 | 4e-267 | pipD | E | Dipeptidase | ||
HGMOLFCO_01177 | 7.8e-255 | yifK | E | Amino acid permease | ||
HGMOLFCO_01179 | 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) | |
HGMOLFCO_01180 | 2.7e-238 | N | Uncharacterized conserved protein (DUF2075) | |||
HGMOLFCO_01181 | 1.6e-12 | S | SNARE associated Golgi protein | |||
HGMOLFCO_01182 | 2.7e-24 | S | SNARE associated Golgi protein | |||
HGMOLFCO_01183 | 2.2e-78 | ndk | 2.7.4.6 | F | Belongs to the NDK family | |
HGMOLFCO_01184 | 1.8e-68 | padR | K | Virulence activator alpha C-term | ||
HGMOLFCO_01186 | 4.4e-216 | I | transferase activity, transferring acyl groups other than amino-acyl groups | |||
HGMOLFCO_01188 | 1.6e-131 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
HGMOLFCO_01189 | 1.8e-223 | patA | 2.6.1.1, 2.6.1.57 | E | Aminotransferase | |
HGMOLFCO_01190 | 1.9e-178 | |||||
HGMOLFCO_01191 | 4.2e-46 | silP | 1.9.3.1, 3.6.3.54 | S | Cupredoxin-like domain | |
HGMOLFCO_01192 | 3.3e-52 | silP | 1.9.3.1, 3.6.3.54 | S | Cupredoxin-like domain | |
HGMOLFCO_01193 | 0.0 | copA | 3.6.3.54 | P | P-type ATPase | |
HGMOLFCO_01194 | 3.4e-18 | EGP | Major facilitator Superfamily | |||
HGMOLFCO_01195 | 3.9e-89 | 2.4.2.6 | F | nucleoside 2-deoxyribosyltransferase | ||
HGMOLFCO_01196 | 2.5e-147 | KT | YcbB domain | |||
HGMOLFCO_01197 | 1e-192 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
HGMOLFCO_01198 | 2.3e-173 | ppx | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
HGMOLFCO_01199 | 0.0 | ppk | 2.7.4.1 | P | Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) | |
HGMOLFCO_01200 | 1.9e-283 | ppx3 | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
HGMOLFCO_01201 | 7.3e-146 | fat | 3.1.2.21 | I | Acyl-ACP thioesterase | |
HGMOLFCO_01202 | 1.2e-157 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
HGMOLFCO_01203 | 1.5e-55 | yabA | L | Involved in initiation control of chromosome replication | ||
HGMOLFCO_01204 | 6.2e-70 | holB | 2.7.7.7 | L | DNA polymerase III | |
HGMOLFCO_01205 | 5.6e-36 | gshF | 6.3.2.2 | H | Belongs to the glutamate--cysteine ligase type 1 family | |
HGMOLFCO_01206 | 0.0 | rnjB | J | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
HGMOLFCO_01207 | 3.5e-163 | S | Tetratricopeptide repeat | |||
HGMOLFCO_01208 | 4.3e-225 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
HGMOLFCO_01209 | 5.7e-215 | 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 | ||
HGMOLFCO_01210 | 1.5e-233 | 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 | ||
HGMOLFCO_01211 | 2.3e-107 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
HGMOLFCO_01212 | 8.3e-53 | MA20_27270 | S | mazG nucleotide pyrophosphohydrolase | ||
HGMOLFCO_01214 | 3.3e-135 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
HGMOLFCO_01215 | 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 | ||
HGMOLFCO_01216 | 6.7e-248 | obg | S | An essential GTPase which binds GTP, GDP and possibly (p)ppGpp with moderate affinity, with high nucleotide exchange rates and a fairly low GTP hydrolysis rate. Plays a role in control of the cell cycle, stress response, ribosome biogenesis and in those bacteria that undergo differentiation, in morphogenesis control | ||
HGMOLFCO_01217 | 3.2e-175 | rnz | 3.1.26.11 | J | Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA | |
HGMOLFCO_01218 | 1.9e-155 | XK27_05435 | 1.1.1.100 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
HGMOLFCO_01219 | 0.0 | recJ | L | Single-stranded-DNA-specific exonuclease RecJ | ||
HGMOLFCO_01220 | 2.4e-95 | apt | 2.4.2.22, 2.4.2.7 | F | Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis | |
HGMOLFCO_01221 | 9.3e-59 | S | Domain of unknown function (DUF4440) | |||
HGMOLFCO_01222 | 8.2e-100 | P | Cadmium resistance transporter | |||
HGMOLFCO_01223 | 3.2e-116 | S | Protein of unknown function (DUF554) | |||
HGMOLFCO_01224 | 8.4e-104 | msrA | 1.8.4.11, 1.8.4.12 | O | Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine | |
HGMOLFCO_01225 | 5.5e-158 | P | Belongs to the nlpA lipoprotein family | |||
HGMOLFCO_01226 | 3.9e-98 | msrA | 1.8.4.11, 1.8.4.12 | O | Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine | |
HGMOLFCO_01227 | 6.4e-38 | V | CAAX protease self-immunity | |||
HGMOLFCO_01228 | 2.3e-67 | psiE | S | Phosphate-starvation-inducible E | ||
HGMOLFCO_01229 | 1.5e-149 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
HGMOLFCO_01230 | 1.7e-111 | thiE | 2.5.1.3 | 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) | |
HGMOLFCO_01231 | 7.2e-144 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
HGMOLFCO_01232 | 8.7e-139 | thiM | 2.7.1.50 | H | Catalyzes the phosphorylation of the hydroxyl group of 4-methyl-5-beta-hydroxyethylthiazole (THZ) | |
HGMOLFCO_01233 | 0.0 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
HGMOLFCO_01234 | 0.0 | cas9 | 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). In type II CRISPR systems correct processing of pre-crRNA requires a trans-encoded small RNA (tracrRNA), endogenous ribonuclease 3 (rnc) and this protein. The tracrRNA serves as a guide for ribonuclease 3-aided processing of pre-crRNA. Subsequently Cas9 crRNA tracrRNA endonucleolytically cleaves linear or circular dsDNA target complementary to the spacer | ||
HGMOLFCO_01235 | 2.5e-92 | 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 | ||
HGMOLFCO_01236 | 3.2e-34 | cas2 | 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 sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Functions as a ssRNA-specific endoribonuclease. Involved in the integration of spacer DNA into the CRISPR cassette | ||
HGMOLFCO_01237 | 1.9e-36 | S | CRISPR-associated protein (Cas_Csn2) | |||
HGMOLFCO_01239 | 2.1e-33 | aes | I | Hydrolase, alpha beta domain protein | ||
HGMOLFCO_01240 | 6e-35 | aes | I | Carboxylesterase family | ||
HGMOLFCO_01242 | 7.1e-97 | S | integral membrane protein | |||
HGMOLFCO_01243 | 1.5e-172 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
HGMOLFCO_01245 | 1.2e-54 | |||||
HGMOLFCO_01246 | 4.9e-176 | prmA | J | Ribosomal protein L11 methyltransferase | ||
HGMOLFCO_01247 | 2e-135 | 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 | |
HGMOLFCO_01248 | 4.4e-58 | |||||
HGMOLFCO_01249 | 0.0 | relA | 2.7.6.5 | KT | In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance | |
HGMOLFCO_01250 | 2.4e-77 | 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 | ||
HGMOLFCO_01251 | 3.5e-85 | slyA | K | Transcriptional regulator | ||
HGMOLFCO_01252 | 2.3e-218 | metC1 | 2.5.1.48, 4.4.1.8 | E | cystathionine | |
HGMOLFCO_01253 | 3.3e-211 | metB | 2.5.1.48, 4.4.1.8 | E | Cys/Met metabolism PLP-dependent enzyme | |
HGMOLFCO_01255 | 3.1e-67 | yxeM | ET | Bacterial periplasmic substrate-binding proteins | ||
HGMOLFCO_01256 | 9.2e-47 | yxeL | K | acetyltransferase | ||
HGMOLFCO_01257 | 2.2e-70 | yxeN | U | ABC transporter, permease protein | ||
HGMOLFCO_01258 | 1.2e-78 | yxeO | 3.6.3.21 | E | ATPases associated with a variety of cellular activities | |
HGMOLFCO_01259 | 1.7e-146 | 3.5.1.47 | E | Peptidase dimerisation domain | ||
HGMOLFCO_01260 | 1.1e-171 | pcaB | 4.3.2.2 | F | Adenylosuccinate lyase C-terminus | |
HGMOLFCO_01261 | 3.9e-91 | yxeQ | S | MmgE/PrpD family | ||
HGMOLFCO_01263 | 4.2e-113 | papP | P | ABC transporter, permease protein | ||
HGMOLFCO_01264 | 2e-115 | P | ABC transporter permease | |||
HGMOLFCO_01265 | 3.9e-136 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
HGMOLFCO_01266 | 3.1e-153 | cjaA | ET | ABC transporter substrate-binding protein | ||
HGMOLFCO_01267 | 6.1e-137 | IQ | KR domain | |||
HGMOLFCO_01268 | 4e-212 | hom1 | 1.1.1.3 | E | Homoserine dehydrogenase | |
HGMOLFCO_01269 | 2.4e-158 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to | |
HGMOLFCO_01270 | 3.6e-54 | yphJ | 4.1.1.44 | S | decarboxylase | |
HGMOLFCO_01271 | 2.8e-54 | azlD | E | Branched-chain amino acid transport | ||
HGMOLFCO_01272 | 9.8e-121 | azlC | E | azaleucine resistance protein AzlC | ||
HGMOLFCO_01273 | 1.9e-286 | thrC | 4.2.3.1 | E | Threonine synthase | |
HGMOLFCO_01274 | 3.5e-233 | hom | 1.1.1.3, 2.7.2.4 | E | homoserine dehydrogenase | |
HGMOLFCO_01275 | 8e-157 | thrB | 2.7.1.39 | F | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
HGMOLFCO_01276 | 3.5e-99 | K | Acetyltransferase (GNAT) domain | |||
HGMOLFCO_01277 | 5.3e-113 | ylbE | GM | NAD(P)H-binding | ||
HGMOLFCO_01278 | 1.5e-118 | ypgQ | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
HGMOLFCO_01279 | 1.8e-133 | S | Belongs to the UPF0246 family | |||
HGMOLFCO_01280 | 1.3e-97 | |||||
HGMOLFCO_01281 | 5.5e-161 | degV | S | EDD domain protein, DegV family | ||
HGMOLFCO_01282 | 0.0 | FbpA | K | Fibronectin-binding protein | ||
HGMOLFCO_01284 | 5.1e-89 | |||||
HGMOLFCO_01285 | 1.3e-78 | F | Nucleoside 2-deoxyribosyltransferase | |||
HGMOLFCO_01286 | 6.7e-184 | scrR3 | K | Transcriptional regulator, LacI family | ||
HGMOLFCO_01287 | 2.8e-12 | |||||
HGMOLFCO_01288 | 2.4e-16 | hbd2 | 1.1.1.157 | I | 3-hydroxyacyl-CoA dehydrogenase | |
HGMOLFCO_01289 | 1.1e-06 | M | domain protein | |||
HGMOLFCO_01291 | 4.1e-12 | S | CHY zinc finger | |||
HGMOLFCO_01293 | 0.0 | asnB | 6.3.5.4 | E | Aluminium induced protein | |
HGMOLFCO_01295 | 1.4e-190 | EGP | Major facilitator Superfamily | |||
HGMOLFCO_01298 | 1.1e-103 | S | Bacterial transferase hexapeptide (six repeats) | |||
HGMOLFCO_01299 | 6e-120 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
HGMOLFCO_01300 | 3.7e-199 | gldA | 1.1.1.6 | C | dehydrogenase | |
HGMOLFCO_01301 | 2.3e-11 | xre | K | Helix-turn-helix domain | ||
HGMOLFCO_01302 | 2.1e-51 | S | Sugar efflux transporter for intercellular exchange | |||
HGMOLFCO_01303 | 1.1e-179 | S | AI-2E family transporter | |||
HGMOLFCO_01304 | 8.8e-215 | phbA | 2.3.1.9 | I | Belongs to the thiolase family | |
HGMOLFCO_01305 | 3.5e-160 | rssA | S | Phospholipase, patatin family | ||
HGMOLFCO_01306 | 7.5e-169 | K | LysR substrate binding domain | |||
HGMOLFCO_01307 | 0.0 | 1.3.5.4 | C | FAD binding domain | ||
HGMOLFCO_01308 | 1.3e-73 | S | Domain of unknown function (DUF4352) | |||
HGMOLFCO_01309 | 6.8e-114 | yicL | EG | EamA-like transporter family | ||
HGMOLFCO_01310 | 6.3e-63 | |||||
HGMOLFCO_01313 | 1.7e-35 | |||||
HGMOLFCO_01314 | 4.1e-68 | S | pyridoxamine 5-phosphate | |||
HGMOLFCO_01315 | 2.8e-179 | yobV1 | K | WYL domain | ||
HGMOLFCO_01316 | 7.9e-244 | XK27_08635 | S | UPF0210 protein | ||
HGMOLFCO_01317 | 2.5e-40 | gcvR | T | Belongs to the UPF0237 family | ||
HGMOLFCO_01318 | 1.3e-168 | mccA | 2.5.1.134, 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
HGMOLFCO_01319 | 7.5e-211 | metC | 2.5.1.48, 4.4.1.1, 4.4.1.2, 4.4.1.8 | E | cystathionine | |
HGMOLFCO_01320 | 1.9e-208 | adh | 1.1.1.1, 1.1.1.14 | C | Zinc-binding dehydrogenase | |
HGMOLFCO_01321 | 1.7e-218 | G | Transporter, major facilitator family protein | |||
HGMOLFCO_01322 | 3.4e-277 | menE | 6.2.1.26 | H | Belongs to the ATP-dependent AMP-binding enzyme family. MenE subfamily | |
HGMOLFCO_01323 | 5.3e-158 | menB | 4.1.3.36 | H | Converts o-succinylbenzoyl-CoA (OSB-CoA) to 1,4- dihydroxy-2-naphthoyl-CoA (DHNA-CoA) | |
HGMOLFCO_01324 | 2.7e-56 | ydiI | Q | Thioesterase superfamily | ||
HGMOLFCO_01325 | 5.5e-61 | birA | 6.3.4.15 | H | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
HGMOLFCO_01326 | 0.0 | pyc | 6.4.1.1 | C | Catalyzes a 2-step reaction, involving the ATP-dependent carboxylation of the covalently attached biotin in the first step and the transfer of the carboxyl group to pyruvate in the second | |
HGMOLFCO_01327 | 1.4e-162 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
HGMOLFCO_01329 | 2.6e-184 | adhC | 1.1.1.90 | C | Zn-dependent alcohol dehydrogenases, class III | |
HGMOLFCO_01330 | 4.3e-91 | citR | K | sugar-binding domain protein | ||
HGMOLFCO_01331 | 4.8e-138 | citG | 2.4.2.52, 2.7.7.61 | H | 2-(5''-triphosphoribosyl)-3'-dephosphocoenzyme-A synthase | |
HGMOLFCO_01332 | 3.2e-42 | ydjP | I | Alpha/beta hydrolase family | ||
HGMOLFCO_01333 | 2.3e-107 | L | Integrase | |||
HGMOLFCO_01334 | 3.3e-45 | K | transcriptional regulator | |||
HGMOLFCO_01335 | 2.7e-109 | GM | NmrA-like family | |||
HGMOLFCO_01336 | 1.1e-24 | C | Flavodoxin | |||
HGMOLFCO_01337 | 9.9e-241 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
HGMOLFCO_01338 | 3.8e-295 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
HGMOLFCO_01339 | 2.3e-107 | 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 | |
HGMOLFCO_01340 | 1.1e-197 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
HGMOLFCO_01341 | 2.6e-280 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
HGMOLFCO_01342 | 0.0 | purL | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
HGMOLFCO_01343 | 8e-128 | purQ | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
HGMOLFCO_01344 | 6.8e-37 | purS | 6.3.2.6, 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
HGMOLFCO_01345 | 6.5e-136 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
HGMOLFCO_01346 | 2.1e-13 | nagZ | 3.2.1.52 | G | Glycosyl hydrolase family 3 N terminal domain | |
HGMOLFCO_01347 | 6.3e-237 | S | response to antibiotic | |||
HGMOLFCO_01348 | 2.1e-172 | hrpQ | 4.6.1.1 | T | histone H2A K63-linked ubiquitination | |
HGMOLFCO_01349 | 1.2e-254 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
HGMOLFCO_01350 | 7.7e-216 | 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) | |
HGMOLFCO_01351 | 4e-81 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
HGMOLFCO_01352 | 0.0 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
HGMOLFCO_01353 | 4.8e-164 | K | AI-2E family transporter | |||
HGMOLFCO_01354 | 3.1e-10 | K | transcriptional regulator | |||
HGMOLFCO_01355 | 7.5e-39 | S | Sugar efflux transporter for intercellular exchange | |||
HGMOLFCO_01356 | 4.1e-113 | flp | 4.1.99.16, 4.2.3.22, 4.2.3.75 | K | Transcriptional regulator, Crp Fnr family | |
HGMOLFCO_01357 | 5.4e-46 | D | Di-iron-containing protein involved in the repair of iron-sulfur clusters | |||
HGMOLFCO_01358 | 5.6e-33 | copZ | P | Heavy-metal-associated domain | ||
HGMOLFCO_01359 | 0.0 | cadA | 3.6.3.3, 3.6.3.5 | P | E1-E2 ATPase | |
HGMOLFCO_01360 | 9.8e-82 | |||||
HGMOLFCO_01361 | 0.0 | alsS | 2.2.1.6 | EH | Belongs to the TPP enzyme family | |
HGMOLFCO_01362 | 0.0 | N | Uncharacterized conserved protein (DUF2075) | |||
HGMOLFCO_01364 | 6.9e-101 | K | DNA-templated transcription, initiation | |||
HGMOLFCO_01365 | 1.1e-56 | arsD | S | Arsenical resistance operon trans-acting repressor ArsD | ||
HGMOLFCO_01366 | 2.7e-233 | arsB | U | Involved in arsenical resistance. Thought to form the channel of an arsenite pump | ||
HGMOLFCO_01367 | 2.2e-216 | S | CAAX protease self-immunity | |||
HGMOLFCO_01368 | 0.0 | rnjA | J | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
HGMOLFCO_01369 | 2e-58 | |||||
HGMOLFCO_01370 | 1.9e-74 | merR | K | MerR HTH family regulatory protein | ||
HGMOLFCO_01371 | 6.6e-268 | lmrB | EGP | Major facilitator Superfamily | ||
HGMOLFCO_01372 | 2.4e-114 | S | Domain of unknown function (DUF4811) | |||
HGMOLFCO_01373 | 8.5e-150 | araA | 5.3.1.4 | G | Catalyzes the conversion of L-arabinose to L-ribulose | |
HGMOLFCO_01374 | 2.3e-93 | L | Helix-turn-helix domain | |||
HGMOLFCO_01375 | 1.9e-115 | L | PFAM Integrase catalytic region | |||
HGMOLFCO_01376 | 1.7e-170 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
HGMOLFCO_01378 | 0.0 | mprF | 2.3.2.3 | S | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms | |
HGMOLFCO_01379 | 2.7e-108 | thiJ | 2.7.11.1, 3.5.1.124 | S | DJ-1/PfpI family | |
HGMOLFCO_01380 | 2.4e-189 | I | Alpha beta | |||
HGMOLFCO_01381 | 2.5e-121 | ung2 | 3.2.2.27 | L | Uracil-DNA glycosylase | |
HGMOLFCO_01382 | 1.9e-253 | yjjP | S | Putative threonine/serine exporter | ||
HGMOLFCO_01383 | 3.8e-162 | mleR | K | LysR family transcriptional regulator | ||
HGMOLFCO_01384 | 1.9e-224 | yflS | P | Sodium:sulfate symporter transmembrane region | ||
HGMOLFCO_01385 | 8e-215 | frdC | 1.3.5.4 | C | FAD binding domain | |
HGMOLFCO_01386 | 6.1e-223 | fumC | 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
HGMOLFCO_01387 | 1.9e-91 | XK27_09620 | S | NADPH-dependent FMN reductase | ||
HGMOLFCO_01388 | 1.9e-181 | XK27_09615 | S | reductase | ||
HGMOLFCO_01389 | 1.4e-229 | sfcA | 1.1.1.38, 4.1.1.101 | C | Malic enzyme | |
HGMOLFCO_01390 | 1.1e-79 | mleR | K | LysR family | ||
HGMOLFCO_01391 | 1.3e-52 | nlhH_1 | I | Carboxylesterase family | ||
HGMOLFCO_01392 | 1e-107 | ppiB | 5.2.1.8 | G | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
HGMOLFCO_01393 | 0.0 | scrA | 2.7.1.211, 5.3.1.1 | G | phosphotransferase system | |
HGMOLFCO_01394 | 1e-195 | adhA | 1.1.1.1 | C | Zinc-binding alcohol dehydrogenase family protein | |
HGMOLFCO_01395 | 4.5e-301 | scrB | 3.2.1.26 | GH32 | G | invertase |
HGMOLFCO_01396 | 7.3e-261 | S | Uncharacterized protein conserved in bacteria (DUF2252) | |||
HGMOLFCO_01397 | 3.2e-164 | K | LysR substrate binding domain | |||
HGMOLFCO_01398 | 6.8e-164 | S | Polyphosphate nucleotide phosphotransferase, PPK2 family | |||
HGMOLFCO_01399 | 5.5e-112 | |||||
HGMOLFCO_01401 | 9e-265 | yjeM | E | Amino Acid | ||
HGMOLFCO_01402 | 2.2e-148 | ponA | V | Beta-lactamase enzyme family | ||
HGMOLFCO_01403 | 1.7e-224 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
HGMOLFCO_01404 | 1.3e-96 | |||||
HGMOLFCO_01405 | 5.9e-199 | pgl | 3.1.1.31 | G | Lactonase, 7-bladed beta-propeller | |
HGMOLFCO_01406 | 4.7e-108 | lssY | 3.6.1.27 | I | Acid phosphatase homologues | |
HGMOLFCO_01407 | 1.6e-54 | S | MazG-like family | |||
HGMOLFCO_01408 | 0.0 | L | Helicase C-terminal domain protein | |||
HGMOLFCO_01409 | 2.2e-72 | nudG | 3.6.1.55, 3.6.1.65 | L | NUDIX domain | |
HGMOLFCO_01410 | 7.7e-97 | K | transcriptional regulator | |||
HGMOLFCO_01411 | 5.9e-137 | lmrB | EGP | Major facilitator Superfamily | ||
HGMOLFCO_01413 | 4.4e-12 | yfjR | K | Psort location Cytoplasmic, score | ||
HGMOLFCO_01414 | 1e-37 | S | Cytochrome B5 | |||
HGMOLFCO_01415 | 3e-89 | 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) | |
HGMOLFCO_01416 | 6.4e-215 | 2.1.1.14 | E | methionine synthase, vitamin-B12 independent | ||
HGMOLFCO_01417 | 8.1e-33 | elaA | S | GNAT family | ||
HGMOLFCO_01418 | 4.5e-85 | usp1 | T | Belongs to the universal stress protein A family | ||
HGMOLFCO_01419 | 2.2e-109 | S | VIT family | |||
HGMOLFCO_01420 | 7.2e-116 | S | membrane | |||
HGMOLFCO_01421 | 1.6e-163 | czcD | P | cation diffusion facilitator family transporter | ||
HGMOLFCO_01422 | 4.4e-123 | sirR | K | iron dependent repressor | ||
HGMOLFCO_01423 | 8.7e-30 | cspA | K | Cold shock protein | ||
HGMOLFCO_01424 | 6.3e-126 | thrE | S | Putative threonine/serine exporter | ||
HGMOLFCO_01425 | 2.8e-82 | S | Threonine/Serine exporter, ThrE | |||
HGMOLFCO_01426 | 1.3e-114 | lssY | 3.6.1.27 | I | phosphatase | |
HGMOLFCO_01427 | 1.3e-156 | I | alpha/beta hydrolase fold | |||
HGMOLFCO_01429 | 3.9e-268 | lysP | E | amino acid | ||
HGMOLFCO_01430 | 7.9e-117 | dak | 2.7.1.74, 2.7.1.76 | F | deoxynucleoside kinase | |
HGMOLFCO_01436 | 2e-11 | IQ | Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
HGMOLFCO_01437 | 1.3e-45 | IQ | reductase | |||
HGMOLFCO_01438 | 9.4e-147 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
HGMOLFCO_01439 | 3.7e-42 | S | ABC-type cobalt transport system, permease component | |||
HGMOLFCO_01441 | 2.7e-120 | J | 2'-5' RNA ligase superfamily | |||
HGMOLFCO_01442 | 4.3e-132 | XK27_07210 | 6.1.1.6 | S | B3 4 domain | |
HGMOLFCO_01443 | 9.7e-194 | adhP | 1.1.1.1 | C | alcohol dehydrogenase | |
HGMOLFCO_01444 | 4.8e-79 | ctsR | K | Belongs to the CtsR family | ||
HGMOLFCO_01445 | 0.0 | clpC | 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 | ||
HGMOLFCO_01446 | 5.8e-106 | K | Bacterial regulatory proteins, tetR family | |||
HGMOLFCO_01447 | 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 | |
HGMOLFCO_01448 | 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 | |
HGMOLFCO_01449 | 5.6e-135 | puuD | S | peptidase C26 | ||
HGMOLFCO_01450 | 2.2e-213 | ykiI | ||||
HGMOLFCO_01451 | 1.6e-32 | pilD | 3.4.23.43 | NOU | aspartic-type endopeptidase activity | |
HGMOLFCO_01452 | 3.2e-71 | 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 | ||
HGMOLFCO_01453 | 7.1e-83 | rpsG | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the head domain of the 30S subunit. Is located at the subunit interface close to the decoding center, probably blocks exit of the E-site tRNA | ||
HGMOLFCO_01454 | 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 | ||
HGMOLFCO_01455 | 2.6e-49 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
HGMOLFCO_01456 | 8.7e-119 | 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 | ||
HGMOLFCO_01457 | 8.8e-105 | rplD | J | Forms part of the polypeptide exit tunnel | ||
HGMOLFCO_01458 | 4.8e-45 | rplW | J | One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome | ||
HGMOLFCO_01459 | 3.2e-150 | 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 | ||
HGMOLFCO_01460 | 8.4e-47 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
HGMOLFCO_01461 | 2.2e-52 | 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 | ||
HGMOLFCO_01462 | 6.2e-117 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
HGMOLFCO_01463 | 6e-76 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
HGMOLFCO_01464 | 1.1e-27 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
HGMOLFCO_01465 | 6.5e-41 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
HGMOLFCO_01466 | 6.6e-60 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
HGMOLFCO_01467 | 5.2e-50 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
HGMOLFCO_01468 | 4.2e-95 | 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 | ||
HGMOLFCO_01469 | 5.2e-29 | 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 | ||
HGMOLFCO_01470 | 1e-66 | 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 | ||
HGMOLFCO_01471 | 3e-93 | rplF | J | This protein binds to the 23S rRNA, and is important in its secondary structure. It is located near the subunit interface in the base of the L7 L12 stalk, and near the tRNA binding site of the peptidyltransferase center | ||
HGMOLFCO_01472 | 1.1e-141 | scpA | D | Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpB that pull DNA away from mid-cell into both cell halves | ||
HGMOLFCO_01473 | 5e-102 | scpB | D | Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpA that pull DNA away from mid-cell into both cell halves | ||
HGMOLFCO_01474 | 1.1e-130 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
HGMOLFCO_01475 | 3.7e-81 | U | Mediates riboflavin uptake, may also transport FMN and roseoflavin. Probably a riboflavin-binding protein that interacts with the energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates. The substrates themselves are bound by transmembrane, not extracytoplasmic soluble proteins | |||
HGMOLFCO_01476 | 5e-198 | ypbB | 5.1.3.1 | S | Helix-turn-helix domain | |
HGMOLFCO_01477 | 3.1e-278 | recQ1 | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
HGMOLFCO_01478 | 9.7e-31 | M | Lysin motif | |||
HGMOLFCO_01479 | 5.8e-118 | 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 | |
HGMOLFCO_01480 | 5.8e-209 | rpsA | 1.17.7.4 | J | Ribosomal protein S1 | |
HGMOLFCO_01481 | 7.4e-247 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
HGMOLFCO_01482 | 4.4e-40 | hup | L | Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions | ||
HGMOLFCO_01483 | 1.8e-234 | S | Tetratricopeptide repeat protein | |||
HGMOLFCO_01484 | 4.7e-165 | xerD | L | Phage integrase, N-terminal SAM-like domain | ||
HGMOLFCO_01485 | 2.6e-222 | cca | 2.7.7.19, 2.7.7.72 | J | Catalyzes the addition and repair of the essential 3'- terminal CCA sequence in tRNAs without using a nucleic acid template. Adds these three nucleotides in the order of C, C, and A to the tRNA nucleotide-73, using CTP and ATP as substrates and producing inorganic pyrophosphate | |
HGMOLFCO_01486 | 0.0 | yfmR | S | ABC transporter, ATP-binding protein | ||
HGMOLFCO_01487 | 2.1e-190 | 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 | |
HGMOLFCO_01488 | 3.3e-94 | 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 | |
HGMOLFCO_01489 | 1.2e-109 | hlyIII | S | protein, hemolysin III | ||
HGMOLFCO_01490 | 2.4e-153 | DegV | S | EDD domain protein, DegV family | ||
HGMOLFCO_01491 | 2.9e-218 | 1.1.1.399, 1.1.1.95 | EH | D-isomer specific 2-hydroxyacid dehydrogenase | ||
HGMOLFCO_01492 | 1.1e-107 | cat | S | Bacterial transferase hexapeptide (six repeats) | ||
HGMOLFCO_01493 | 1.1e-167 | ypmR | E | lipolytic protein G-D-S-L family | ||
HGMOLFCO_01494 | 7.1e-104 | ypmS | S | Uncharacterized protein conserved in bacteria (DUF2140) | ||
HGMOLFCO_01495 | 3.1e-36 | yozE | S | Belongs to the UPF0346 family | ||
HGMOLFCO_01496 | 8.4e-162 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
HGMOLFCO_01497 | 3.9e-139 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
HGMOLFCO_01498 | 3.6e-165 | dprA | LU | DNA protecting protein DprA | ||
HGMOLFCO_01499 | 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 | |
HGMOLFCO_01500 | 2.6e-152 | D | DNA integration | |||
HGMOLFCO_01501 | 5.3e-172 | lacX | 5.1.3.3 | G | Aldose 1-epimerase | |
HGMOLFCO_01502 | 1.1e-102 | plsY | 2.3.1.15, 3.5.1.104 | I | Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP | |
HGMOLFCO_01503 | 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 | |
HGMOLFCO_01504 | 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 | |
HGMOLFCO_01505 | 5.2e-95 | S | Protein of unknown function (DUF1440) | |||
HGMOLFCO_01506 | 7.3e-172 | ppaC | 3.6.1.1 | C | inorganic pyrophosphatase | |
HGMOLFCO_01507 | 2.3e-71 | yqkB | S | Belongs to the HesB IscA family | ||
HGMOLFCO_01508 | 3.4e-76 | msrB | 1.8.4.11, 1.8.4.12 | O | peptide methionine sulfoxide reductase | |
HGMOLFCO_01509 | 8.2e-93 | ywnH | 2.3.1.183 | M | Acetyltransferase (GNAT) domain | |
HGMOLFCO_01510 | 1.7e-81 | yebR | 1.8.4.14 | T | GAF domain-containing protein | |
HGMOLFCO_01511 | 4.7e-244 | U | Belongs to the purine-cytosine permease (2.A.39) family | |||
HGMOLFCO_01512 | 8e-243 | codA | 3.5.4.1 | F | cytosine deaminase | |
HGMOLFCO_01513 | 0.0 | oppD | EP | Psort location Cytoplasmic, score | ||
HGMOLFCO_01515 | 1.8e-256 | rarA | L | recombination factor protein RarA | ||
HGMOLFCO_01516 | 4.7e-120 | S | Protein of unknown function (DUF554) | |||
HGMOLFCO_01517 | 2.3e-243 | yhjX | P | Major Facilitator Superfamily | ||
HGMOLFCO_01519 | 2.5e-17 | lmrB | EGP | Major facilitator Superfamily | ||
HGMOLFCO_01520 | 2.6e-20 | clcA | P | chloride | ||
HGMOLFCO_01521 | 7.7e-30 | clcA | P | chloride | ||
HGMOLFCO_01522 | 1e-15 | |||||
HGMOLFCO_01523 | 4.5e-191 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
HGMOLFCO_01524 | 6.6e-226 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
HGMOLFCO_01525 | 3.1e-144 | tpiA | 2.7.2.3, 5.3.1.1 | G | Involved in the gluconeogenesis. Catalyzes stereospecifically the conversion of dihydroxyacetone phosphate (DHAP) to D-glyceraldehyde-3-phosphate (G3P) | |
HGMOLFCO_01526 | 1e-248 | 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 | |
HGMOLFCO_01527 | 3.3e-253 | yifK | E | Amino acid permease | ||
HGMOLFCO_01528 | 2.2e-290 | clcA | P | chloride | ||
HGMOLFCO_01529 | 4.5e-33 | secG | U | Preprotein translocase | ||
HGMOLFCO_01530 | 0.0 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
HGMOLFCO_01531 | 2.9e-84 | smpB | J | the 2 termini fold to resemble tRNA(Ala) and it encodes a tag peptide , a short internal open reading frame. During trans-translation Ala- aminoacylated tmRNA acts like a tRNA, entering the A-site of stalled ribosomes, displacing the stalled mRNA. The ribosome then switches to translate the ORF on the tmRNA | ||
HGMOLFCO_01532 | 5.5e-109 | yxjI | ||||
HGMOLFCO_01533 | 2.8e-136 | 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 | |
HGMOLFCO_01534 | 7.1e-178 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
HGMOLFCO_01535 | 2.9e-81 | ydiB | 2.7.1.221, 5.1.1.1 | O | Hydrolase, P-loop family | |
HGMOLFCO_01536 | 7.3e-89 | K | Acetyltransferase (GNAT) domain | |||
HGMOLFCO_01537 | 1.3e-101 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
HGMOLFCO_01538 | 5.7e-166 | murB | 1.3.1.98 | M | Cell wall formation | |
HGMOLFCO_01539 | 7.8e-149 | dacA | 2.7.7.85 | S | Catalyzes the condensation of 2 ATP molecules into cyclic di-AMP (c-di-AMP), a second messenger used to regulate differing processes in different bacteria | |
HGMOLFCO_01540 | 3.5e-115 | ybbR | S | YbbR-like protein | ||
HGMOLFCO_01541 | 3.2e-253 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
HGMOLFCO_01542 | 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 | |
HGMOLFCO_01543 | 3.3e-52 | |||||
HGMOLFCO_01544 | 5.4e-211 | oatA | I | Acyltransferase | ||
HGMOLFCO_01545 | 4e-150 | XK27_02985 | S | Sucrose-6F-phosphate phosphohydrolase | ||
HGMOLFCO_01546 | 2.6e-69 | lytE | M | Lysin motif | ||
HGMOLFCO_01547 | 2.3e-158 | MA20_14895 | S | Conserved hypothetical protein 698 | ||
HGMOLFCO_01548 | 9.6e-169 | K | LysR substrate binding domain | |||
HGMOLFCO_01549 | 1.9e-130 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
HGMOLFCO_01550 | 5.1e-148 | yitS | S | EDD domain protein, DegV family | ||
HGMOLFCO_01551 | 6.5e-90 | racA | K | Domain of unknown function (DUF1836) | ||
HGMOLFCO_01552 | 2.3e-181 | yfeX | P | Peroxidase | ||
HGMOLFCO_01553 | 5.3e-181 | manL | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
HGMOLFCO_01554 | 3.5e-114 | manY | G | PTS system | ||
HGMOLFCO_01555 | 3e-170 | manN | G | system, mannose fructose sorbose family IID component | ||
HGMOLFCO_01556 | 1.6e-57 | S | Domain of unknown function (DUF956) | |||
HGMOLFCO_01558 | 1.5e-133 | L | PFAM transposase, IS4 family protein | |||
HGMOLFCO_01559 | 4.8e-131 | K | response regulator | |||
HGMOLFCO_01560 | 1.3e-250 | yclK | 2.7.13.3 | T | Histidine kinase | |
HGMOLFCO_01561 | 5.9e-152 | glcU | U | sugar transport | ||
HGMOLFCO_01562 | 3.5e-216 | xylR | GK | ROK family | ||
HGMOLFCO_01563 | 2.1e-252 | xylT | EGP | Major facilitator Superfamily | ||
HGMOLFCO_01564 | 6.4e-270 | xylA | 5.3.1.5 | G | Belongs to the xylose isomerase family | |
HGMOLFCO_01565 | 1.8e-297 | xylB | 2.7.1.12, 2.7.1.17 | G | Xylulose kinase | |
HGMOLFCO_01566 | 2.3e-84 | 3.2.1.37 | GH43 | K | helix_turn_helix, arabinose operon control protein | |
HGMOLFCO_01567 | 0.0 | 3.2.1.37 | GH43 | G | Belongs to the glycosyl hydrolase 43 family | |
HGMOLFCO_01568 | 3.9e-221 | G | Major Facilitator | |||
HGMOLFCO_01569 | 6.1e-105 | ahpC | 1.11.1.15 | O | Peroxiredoxin | |
HGMOLFCO_01570 | 0.0 | trxB2 | 1.8.1.9 | C | Thioredoxin domain | |
HGMOLFCO_01571 | 9.7e-29 | L | Transposase | |||
HGMOLFCO_01572 | 3.1e-124 | S | Membrane | |||
HGMOLFCO_01573 | 3.2e-234 | gltP | U | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
HGMOLFCO_01574 | 0.0 | pepF | E | oligoendopeptidase F | ||
HGMOLFCO_01575 | 5.1e-179 | K | helix_turn _helix lactose operon repressor | |||
HGMOLFCO_01576 | 7.2e-141 | IQ | Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
HGMOLFCO_01577 | 1.2e-233 | V | MatE | |||
HGMOLFCO_01578 | 6.7e-69 | def_1 | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins | |
HGMOLFCO_01579 | 1e-141 | 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 | ||
HGMOLFCO_01580 | 4.1e-46 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
HGMOLFCO_01581 | 1.2e-141 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
HGMOLFCO_01582 | 7.8e-91 | XK27_09705 | 6.1.1.14 | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | |
HGMOLFCO_01583 | 7.8e-60 | yodB | K | Transcriptional regulator, HxlR family | ||
HGMOLFCO_01584 | 5.1e-198 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
HGMOLFCO_01585 | 0.0 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
HGMOLFCO_01586 | 3e-116 | udk | 2.7.1.48 | F | Cytidine monophosphokinase | |
HGMOLFCO_01587 | 2.2e-79 | 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 | ||
HGMOLFCO_01588 | 0.0 | S | membrane | |||
HGMOLFCO_01589 | 0.0 | pbp2b | 3.4.16.4 | M | Penicillin-binding Protein | |
HGMOLFCO_01590 | 3.2e-21 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
HGMOLFCO_01591 | 2.4e-98 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
HGMOLFCO_01592 | 1.1e-116 | gluP | 3.4.21.105 | S | Peptidase, S54 family | |
HGMOLFCO_01593 | 9.6e-36 | yqgQ | S | Bacterial protein of unknown function (DUF910) | ||
HGMOLFCO_01594 | 3.7e-179 | glk | 2.7.1.2 | G | Glucokinase | |
HGMOLFCO_01595 | 1.5e-71 | yqhL | P | Rhodanese-like protein | ||
HGMOLFCO_01596 | 4.8e-24 | WQ51_02665 | S | Protein of unknown function (DUF3042) | ||
HGMOLFCO_01597 | 1.2e-171 | 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) | |
HGMOLFCO_01598 | 1.4e-261 | glnA | 6.3.1.2 | E | glutamine synthetase | |
HGMOLFCO_01599 | 4.7e-13 | |||||
HGMOLFCO_01600 | 2.2e-149 | |||||
HGMOLFCO_01601 | 3.9e-176 | |||||
HGMOLFCO_01602 | 1.9e-92 | dut | S | Protein conserved in bacteria | ||
HGMOLFCO_01604 | 1.3e-114 | K | Transcriptional regulator | |||
HGMOLFCO_01605 | 5.2e-50 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
HGMOLFCO_01606 | 9e-53 | ysxB | J | Cysteine protease Prp | ||
HGMOLFCO_01607 | 7.1e-46 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
HGMOLFCO_01608 | 8.9e-206 | pepP | 3.4.11.9, 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
HGMOLFCO_01609 | 4.1e-72 | yqhY | S | Asp23 family, cell envelope-related function | ||
HGMOLFCO_01610 | 2e-68 | 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 | ||
HGMOLFCO_01611 | 2.6e-160 | 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 | |
HGMOLFCO_01612 | 2.3e-257 | 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 | |
HGMOLFCO_01613 | 1e-18 | 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 | |
HGMOLFCO_01614 | 2.1e-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 | |
HGMOLFCO_01615 | 3.2e-147 | rrmJ | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
HGMOLFCO_01616 | 2.3e-75 | argR | K | Regulates arginine biosynthesis genes | ||
HGMOLFCO_01617 | 1.3e-307 | recN | L | May be involved in recombinational repair of damaged DNA | ||
HGMOLFCO_01618 | 2.5e-15 | |||||
HGMOLFCO_01619 | 3.9e-113 | gmk | 2.7.4.8 | F | Essential for recycling GMP and indirectly, cGMP | |
HGMOLFCO_01620 | 9.4e-46 | 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 | |
HGMOLFCO_01621 | 2.3e-221 | 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 | |
HGMOLFCO_01622 | 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 | ||
HGMOLFCO_01623 | 2.7e-174 | 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 | |
HGMOLFCO_01624 | 2e-247 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
HGMOLFCO_01625 | 2.2e-131 | stp | 3.1.3.16 | T | phosphatase | |
HGMOLFCO_01626 | 0.0 | KLT | serine threonine protein kinase | |||
HGMOLFCO_01627 | 4.1e-164 | 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 | |
HGMOLFCO_01628 | 1.1e-118 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
HGMOLFCO_01629 | 4e-124 | thiN | 2.7.6.2 | H | thiamine pyrophosphokinase | |
HGMOLFCO_01630 | 1.4e-26 | rpmB | J | Belongs to the bacterial ribosomal protein bL28 family | ||
HGMOLFCO_01631 | 3.6e-58 | asp | S | Asp23 family, cell envelope-related function | ||
HGMOLFCO_01632 | 5.8e-297 | yloV | S | DAK2 domain fusion protein YloV | ||
HGMOLFCO_01633 | 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) | |
HGMOLFCO_01634 | 3.1e-163 | 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 | |
HGMOLFCO_01635 | 4.5e-36 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
HGMOLFCO_01636 | 4e-130 | 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 | |
HGMOLFCO_01637 | 0.0 | smc | D | Required for chromosome condensation and partitioning | ||
HGMOLFCO_01638 | 1.5e-198 | ftsY | U | Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Acts as a receptor for the complex formed by the signal recognition particle (SRP) and the ribosome-nascent chain (RNC) | ||
HGMOLFCO_01639 | 3.7e-57 | ylxM | S | Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY ffh. May be a regulatory protein | ||
HGMOLFCO_01640 | 7.6e-245 | 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 | |
HGMOLFCO_01642 | 4.3e-93 | |||||
HGMOLFCO_01643 | 2.6e-129 | K | Transcriptional regulatory protein, C-terminal domain protein | |||
HGMOLFCO_01644 | 5.1e-159 | pstS | P | Phosphate | ||
HGMOLFCO_01645 | 4.7e-152 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
HGMOLFCO_01646 | 1.6e-152 | pstA | P | Phosphate transport system permease protein PstA | ||
HGMOLFCO_01647 | 6.8e-136 | 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 | |
HGMOLFCO_01648 | 1.1e-122 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
HGMOLFCO_01649 | 2.9e-44 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
HGMOLFCO_01650 | 5.4e-40 | ylqC | S | Belongs to the UPF0109 family | ||
HGMOLFCO_01651 | 2.1e-88 | 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 | ||
HGMOLFCO_01652 | 2.9e-142 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
HGMOLFCO_01653 | 4.9e-260 | yfnA | E | Amino Acid | ||
HGMOLFCO_01654 | 1.3e-57 | 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 | ||
HGMOLFCO_01655 | 2.7e-291 | cas3 | L | CRISPR-associated helicase cas3 | ||
HGMOLFCO_01656 | 5.9e-156 | casA | L | the current gene model (or a revised gene model) may contain a frame shift | ||
HGMOLFCO_01657 | 5.4e-40 | casB | S | CRISPR-associated protein Cse2 (CRISPR_cse2) | ||
HGMOLFCO_01658 | 9e-129 | casC | L | CT1975-like protein | ||
HGMOLFCO_01659 | 1.4e-66 | casD | S | CRISPR-associated protein (Cas_Cas5) | ||
HGMOLFCO_01660 | 2.6e-32 | casE | S | CRISPR_assoc | ||
HGMOLFCO_01661 | 3.2e-127 | 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 | ||
HGMOLFCO_01662 | 1.4e-79 | cas2 | 2.7.7.7 | L | CRISPR-associated protein (Cas_Cas2CT1978) | |
HGMOLFCO_01663 | 3.4e-17 | lutA | C | Cysteine-rich domain | ||
HGMOLFCO_01664 | 7.1e-217 | mvaS | 2.3.3.10 | I | Hydroxymethylglutaryl-CoA synthase | |
HGMOLFCO_01665 | 4.2e-115 | 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 | |
HGMOLFCO_01666 | 2.4e-37 | ynzC | S | UPF0291 protein | ||
HGMOLFCO_01667 | 2.7e-27 | yneF | S | Uncharacterised protein family (UPF0154) | ||
HGMOLFCO_01668 | 2.1e-114 | plsC | 2.3.1.51 | I | Acyltransferase | |
HGMOLFCO_01669 | 8e-137 | yabB | 2.1.1.223 | L | Methyltransferase small domain | |
HGMOLFCO_01670 | 2.3e-47 | yazA | L | GIY-YIG catalytic domain protein | ||
HGMOLFCO_01671 | 5e-142 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
HGMOLFCO_01672 | 4.9e-154 | 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 | ||
HGMOLFCO_01673 | 7e-130 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
HGMOLFCO_01674 | 4.1e-93 | 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 | ||
HGMOLFCO_01675 | 2.9e-142 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
HGMOLFCO_01676 | 2.3e-134 | cdsA | 2.7.7.41 | I | Belongs to the CDS family | |
HGMOLFCO_01677 | 1e-232 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
HGMOLFCO_01678 | 1.3e-11 | |||||
HGMOLFCO_01679 | 2.7e-19 | |||||
HGMOLFCO_01680 | 1.1e-197 | S | Psort location Cytoplasmic, score | |||
HGMOLFCO_01681 | 3.9e-106 | S | RloB-like protein | |||
HGMOLFCO_01682 | 3.8e-207 | sigA | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released. This sigma factor is the primary sigma factor during exponential growth | ||
HGMOLFCO_01683 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
HGMOLFCO_01684 | 0.0 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
HGMOLFCO_01685 | 4.9e-187 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
HGMOLFCO_01686 | 3.2e-155 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
HGMOLFCO_01687 | 8.7e-170 | era | S | An essential GTPase that binds both GDP and GTP, with rapid nucleotide exchange. Plays a role in 16S rRNA processing and 30S ribosomal subunit biogenesis and possibly also in cell cycle regulation and energy metabolism | ||
HGMOLFCO_01688 | 3.9e-66 | dgkA | 2.7.1.107, 2.7.1.66 | M | Diacylglycerol kinase | |
HGMOLFCO_01689 | 2.5e-80 | ybeY | 2.6.99.2, 3.5.4.5 | S | Single strand-specific metallo-endoribonuclease involved in late-stage 70S ribosome quality control and in maturation of the 3' terminus of the 16S rRNA | |
HGMOLFCO_01690 | 1.1e-178 | phoH | T | phosphate starvation-inducible protein PhoH | ||
HGMOLFCO_01691 | 4.6e-71 | yqeY | S | YqeY-like protein | ||
HGMOLFCO_01692 | 5.7e-23 | rpsU | J | Belongs to the bacterial ribosomal protein bS21 family | ||
HGMOLFCO_01693 | 5.1e-130 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
HGMOLFCO_01694 | 0.0 | aspS | 6.1.1.12 | J | Catalyzes the attachment of L-aspartate to tRNA(Asp) in a two-step reaction L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp) | |
HGMOLFCO_01695 | 1e-248 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
HGMOLFCO_01696 | 1e-195 | 6.3.1.20 | H | Lipoate-protein ligase | ||
HGMOLFCO_01697 | 1.6e-174 | lytH | 3.5.1.28 | M | Ami_3 | |
HGMOLFCO_01698 | 1.4e-169 | yniA | G | Phosphotransferase enzyme family | ||
HGMOLFCO_01699 | 5e-173 | mmuM | 1.5.1.20, 2.1.1.10 | H | homocysteine S-methyltransferase | |
HGMOLFCO_01700 | 1.4e-246 | mmuP | E | amino acid | ||
HGMOLFCO_01701 | 2.3e-83 | lacR | K | Transcriptional regulator | ||
HGMOLFCO_01702 | 4.1e-217 | lacS | G | Transporter |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)