ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
COCLMCBI_00001 | 1.1e-118 | L | COG4584 Transposase and inactivated derivatives | |||
COCLMCBI_00002 | 3e-134 | L | DNA replication protein | |||
COCLMCBI_00003 | 5.8e-19 | S | Protein of unknown function (DUF3054) | |||
COCLMCBI_00005 | 3e-287 | accD4 | 2.1.3.15, 6.4.1.3 | I | Acetyl-CoA carboxylase, carboxyltransferase component (subunits alpha and beta) | |
COCLMCBI_00006 | 0.0 | pks13 | Q | Polyketide synthase modules and related proteins | ||
COCLMCBI_00007 | 0.0 | fadD32 | IQ | Acyl-CoA synthetases (AMP-forming) AMP-acid ligases II | ||
COCLMCBI_00008 | 5.9e-158 | elrF | S | Cutinase | ||
COCLMCBI_00009 | 1.3e-28 | |||||
COCLMCBI_00010 | 0.0 | csp1 | M | Trehalose corynomycolyl transferase | ||
COCLMCBI_00011 | 3e-187 | cmtB | 2.3.1.122, 2.3.1.20 | S | esterase | |
COCLMCBI_00012 | 0.0 | aftB | GT89 | M | capsule polysaccharide biosynthetic process | |
COCLMCBI_00013 | 4.8e-174 | ubiA | 2.4.2.45 | H | Phosphoribose diphosphate decaprenyl-phosphate phosphoribosyltransferase | |
COCLMCBI_00014 | 1.1e-76 | 3.6.1.27 | I | Membrane-associated phospholipid phosphatase | ||
COCLMCBI_00015 | 0.0 | glfT | 2.4.1.288 | GT2 | S | Glycosyltransferases |
COCLMCBI_00016 | 8.9e-93 | V | HNH endonuclease | |||
COCLMCBI_00018 | 1.1e-180 | aftC | 2.4.2.47 | S | Glycosyltransferase family 87 | |
COCLMCBI_00019 | 3.7e-272 | P | NhaP-type Na H and K H antiporters | |||
COCLMCBI_00020 | 1.4e-169 | S | Domain of unknown function (DUF4143) | |||
COCLMCBI_00021 | 5.6e-34 | Z012_07300 | O | Glutaredoxin-related protein | ||
COCLMCBI_00022 | 2.1e-84 | K | BetI-type transcriptional repressor, C-terminal | |||
COCLMCBI_00023 | 1.2e-102 | O | Sap, sulfolipid-1-addressing protein | |||
COCLMCBI_00024 | 2.1e-235 | glf | 5.4.99.9 | M | UDP-galactopyranose mutase | |
COCLMCBI_00025 | 0.0 | lytC | M | protein potentially involved in peptidoglycan biosynthesis | ||
COCLMCBI_00026 | 1.2e-280 | 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 | |
COCLMCBI_00027 | 1.7e-162 | K | Psort location Cytoplasmic, score | |||
COCLMCBI_00028 | 1.8e-153 | yidA | S | hydrolases of the HAD superfamily | ||
COCLMCBI_00029 | 3.5e-157 | plsC1 | I | Phosphate acyltransferases | ||
COCLMCBI_00030 | 2.7e-146 | plsC1 | I | Acyltransferase | ||
COCLMCBI_00031 | 1.5e-214 | 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) | |
COCLMCBI_00032 | 8.2e-180 | S | Septum formation | |||
COCLMCBI_00033 | 1.3e-60 | S | protein conserved in bacteria | |||
COCLMCBI_00034 | 7.4e-115 | pgmB | 5.4.2.11 | G | Belongs to the phosphoglycerate mutase family | |
COCLMCBI_00035 | 1.7e-157 | pheA | 1.3.1.12, 4.2.1.51, 5.4.99.5 | E | Prephenate dehydratase | |
COCLMCBI_00036 | 7.3e-117 | S | metal-dependent membrane protease | |||
COCLMCBI_00037 | 2.5e-161 | lytR2 | K | function transcriptional attenuator common domain protein | ||
COCLMCBI_00038 | 1e-241 | proY | E | Gamma-aminobutyrate permease and related permeases | ||
COCLMCBI_00039 | 6.5e-160 | L | Phage integrase family | |||
COCLMCBI_00040 | 1.9e-19 | |||||
COCLMCBI_00042 | 2.2e-296 | |||||
COCLMCBI_00045 | 3.4e-64 | |||||
COCLMCBI_00046 | 5.6e-101 | 1.6.5.2 | S | NADPH-quinone reductase (modulator of drug activity B) | ||
COCLMCBI_00047 | 2.2e-38 | ydeP5 | K | transcriptional regulator | ||
COCLMCBI_00050 | 2.5e-161 | cotF | M | PFAM Coat F domain | ||
COCLMCBI_00051 | 6.7e-150 | glpQ | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
COCLMCBI_00052 | 0.0 | S | membrane | |||
COCLMCBI_00053 | 8.5e-136 | msrA | 1.8.4.11 | O | Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine | |
COCLMCBI_00054 | 1.4e-112 | sodA | 1.15.1.1 | C | Destroys radicals which are normally produced within the cells and which are toxic to biological systems | |
COCLMCBI_00055 | 1.5e-190 | 2.7.7.7 | L | Transposase and inactivated derivatives | ||
COCLMCBI_00056 | 4.8e-216 | ynfM | EGP | Major facilitator Superfamily | ||
COCLMCBI_00057 | 1.6e-274 | S | Nuclease, RecB family | |||
COCLMCBI_00058 | 3.7e-66 | |||||
COCLMCBI_00059 | 1.3e-106 | hrrA | T | helix_turn_helix, Lux Regulon | ||
COCLMCBI_00060 | 2.4e-170 | hrrS | T | Histidine kinase | ||
COCLMCBI_00061 | 1.1e-169 | E | GDSL-like Lipase/Acylhydrolase | |||
COCLMCBI_00062 | 7.4e-161 | yidC | U | inner membrane protein translocase component YidC | ||
COCLMCBI_00063 | 1.9e-91 | mcbR | K | Transcriptional regulator | ||
COCLMCBI_00064 | 4.1e-19 | ymgE | S | Transglycosylase associated protein | ||
COCLMCBI_00065 | 8.1e-152 | uspA1 | T | universal stress protein | ||
COCLMCBI_00066 | 1.4e-08 | |||||
COCLMCBI_00067 | 3.3e-162 | rluA | 5.4.99.28, 5.4.99.29 | J | Pseudouridylate synthases, 23S RNA-specific | |
COCLMCBI_00069 | 2.6e-149 | insK | L | Transposase and inactivated derivatives | ||
COCLMCBI_00070 | 1.4e-134 | L | DNA replication protein | |||
COCLMCBI_00071 | 2.4e-127 | L | COG4584 Transposase and inactivated derivatives | |||
COCLMCBI_00072 | 1.8e-33 | L | Helix-turn-helix domain | |||
COCLMCBI_00073 | 4.3e-13 | |||||
COCLMCBI_00074 | 6.7e-129 | |||||
COCLMCBI_00075 | 8.2e-127 | V | ABC-type multidrug transport system ATPase component | |||
COCLMCBI_00076 | 1.8e-60 | gntR1 | K | transcriptional | ||
COCLMCBI_00077 | 3.4e-190 | D | NYN domain | |||
COCLMCBI_00078 | 4.5e-107 | rsmP | KT | Phage shock protein A (IM30), suppresses sigma54-dependent transcription | ||
COCLMCBI_00079 | 3.3e-59 | trxA | 1.8.1.8, 1.8.1.9 | O | Belongs to the thioredoxin family | |
COCLMCBI_00080 | 6.5e-25 | copZ | P | mercury ion transmembrane transporter activity | ||
COCLMCBI_00081 | 4.9e-25 | copZ | P | mercury ion transmembrane transporter activity | ||
COCLMCBI_00082 | 0.0 | ctpA | 3.6.3.54 | P | cation transport ATPase | |
COCLMCBI_00083 | 9.1e-237 | naiP | EGP | Permeases of the major facilitator superfamily | ||
COCLMCBI_00084 | 6.4e-263 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
COCLMCBI_00085 | 4.4e-130 | |||||
COCLMCBI_00086 | 1.3e-76 | rplI | J | binds to the 23S rRNA | ||
COCLMCBI_00087 | 3.4e-71 | ssb | L | Single-stranded DNA-binding protein | ||
COCLMCBI_00088 | 1.2e-46 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
COCLMCBI_00089 | 5.2e-17 | |||||
COCLMCBI_00091 | 9.2e-281 | S | Integral membrane protein | |||
COCLMCBI_00092 | 0.0 | mrcB | 2.4.1.129, 3.4.16.4 | GT51 | M | Membrane carboxypeptidase (Penicillin-binding protein) |
COCLMCBI_00093 | 3.7e-76 | uspR | K | helix_turn_helix multiple antibiotic resistance protein | ||
COCLMCBI_00094 | 1.2e-169 | T | Universal stress protein UspA and related nucleotide-binding proteins | |||
COCLMCBI_00095 | 2.1e-85 | |||||
COCLMCBI_00096 | 4.4e-174 | yceA | S | Belongs to the UPF0176 family | ||
COCLMCBI_00097 | 9.6e-59 | K | helix_turn_helix, Lux Regulon | |||
COCLMCBI_00098 | 3.6e-49 | T | Histidine kinase | |||
COCLMCBI_00101 | 6.9e-90 | mutF | V | ABC transporter, ATP-binding protein | ||
COCLMCBI_00102 | 2.1e-277 | XK27_07020 | S | Belongs to the UPF0371 family | ||
COCLMCBI_00103 | 1.7e-28 | |||||
COCLMCBI_00104 | 1.9e-40 | XK27_10495 | DJ | ParE toxin of type II toxin-antitoxin system, parDE | ||
COCLMCBI_00105 | 0.0 | glcB | 2.3.3.9 | C | Involved in the glycolate utilization. Catalyzes the condensation and subsequent hydrolysis of acetyl-coenzyme A (acetyl-CoA) and glyoxylate to form malate and CoA | |
COCLMCBI_00106 | 3.5e-249 | aceA | 4.1.3.1 | C | Isocitrate lyase | |
COCLMCBI_00107 | 5.4e-85 | 2.3.1.82 | J | Acetyltransferase (GNAT) domain | ||
COCLMCBI_00108 | 3.9e-15 | |||||
COCLMCBI_00109 | 9.8e-44 | S | Toxic component of a toxin-antitoxin (TA) module. An RNase | |||
COCLMCBI_00110 | 3.5e-88 | rraA | H | Catalyzes the aldol cleavage of 4-hydroxy-4-methyl-2- oxoglutarate (HMG) into 2 molecules of pyruvate. Also contains a secondary oxaloacetate (OAA) decarboxylase activity due to the common pyruvate enolate transition state formed following C-C bond cleavage in the retro-aldol and decarboxylation reactions | ||
COCLMCBI_00111 | 1.1e-139 | nei1 | 3.2.2.23, 4.2.99.18 | L | Belongs to the FPG family | |
COCLMCBI_00112 | 2.5e-35 | |||||
COCLMCBI_00113 | 3.2e-77 | S | Toxic component of a toxin-antitoxin (TA) module. An RNase | |||
COCLMCBI_00114 | 9.4e-281 | nnrD | 4.2.1.136, 5.1.99.6 | G | Bifunctional enzyme that catalyzes the epimerization of the S- and R-forms of NAD(P)HX and the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. This allows the repair of both epimers of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration | |
COCLMCBI_00115 | 4.4e-143 | ywaF | S | Integral membrane protein (intg_mem_TP0381) | ||
COCLMCBI_00116 | 6.1e-184 | EGP | Major facilitator Superfamily | |||
COCLMCBI_00117 | 5.7e-98 | yhhW_2 | O | Belongs to the pirin family | ||
COCLMCBI_00118 | 5e-129 | S | Plasmid pRiA4b ORF-3-like protein | |||
COCLMCBI_00119 | 6.8e-48 | S | Domain of unknown function (DUF202) | |||
COCLMCBI_00120 | 3.1e-60 | yidH | S | membrane | ||
COCLMCBI_00121 | 2.2e-168 | adhT | C | Zinc-binding dehydrogenase | ||
COCLMCBI_00122 | 2.6e-126 | |||||
COCLMCBI_00123 | 1.7e-77 | V | Glycopeptide antibiotics resistance protein | |||
COCLMCBI_00124 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
COCLMCBI_00125 | 5.7e-291 | V | HNH endonuclease domain protein | |||
COCLMCBI_00126 | 4.5e-124 | |||||
COCLMCBI_00127 | 4.8e-122 | S | Psort location | |||
COCLMCBI_00128 | 3.3e-188 | sstT | U | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
COCLMCBI_00129 | 8e-57 | sdpI | S | Integral membrane protein | ||
COCLMCBI_00130 | 1.9e-113 | hipA_2 | 2.7.11.1 | S | TIGRFAM HipA N-terminal domain | |
COCLMCBI_00131 | 5.1e-11 | K | Helix-turn-helix XRE-family like proteins | |||
COCLMCBI_00132 | 2.8e-274 | trpE | 4.1.3.27 | E | Part of a heterotetrameric complex that catalyzes the two-step biosynthesis of anthranilate, an intermediate in the biosynthesis of L-tryptophan. In the first step, the glutamine- binding beta subunit (TrpG) of anthranilate synthase (AS) provides the glutamine amidotransferase activity which generates ammonia as a substrate that, along with chorismate, is used in the second step, catalyzed by the large alpha subunit of AS (TrpE) to produce anthranilate. In the absence of TrpG, TrpE can synthesize anthranilate directly from chorismate and high concentrations of ammonia | |
COCLMCBI_00133 | 3.1e-113 | trpG | 2.4.2.18, 2.6.1.85, 4.1.3.27 | EH | component II | |
COCLMCBI_00134 | 5.5e-189 | trpD | 2.4.2.18, 4.1.3.27 | F | Catalyzes the transfer of the phosphoribosyl group of 5- phosphorylribose-1-pyrophosphate (PRPP) to anthranilate to yield N-(5'-phosphoribosyl)-anthranilate (PRA) | |
COCLMCBI_00135 | 1.7e-268 | trpF | 4.1.1.48, 4.2.1.160, 4.2.1.20, 5.3.1.24 | E | Belongs to the TrpF family | |
COCLMCBI_00136 | 1.2e-230 | trpB | 4.2.1.20 | E | The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine | |
COCLMCBI_00137 | 1.9e-147 | trpA | 4.2.1.20 | E | The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate | |
COCLMCBI_00138 | 1.5e-62 | qcrA2 | 1.8.5.2 | P | domain protein | |
COCLMCBI_00139 | 1.2e-46 | |||||
COCLMCBI_00140 | 8.5e-215 | V | HNH endonuclease domain protein | |||
COCLMCBI_00141 | 1.9e-62 | |||||
COCLMCBI_00142 | 1.1e-46 | azlD | E | branched-chain amino acid | ||
COCLMCBI_00143 | 1.8e-116 | azlC | E | branched-chain amino acid permease (azaleucine resistance) | ||
COCLMCBI_00144 | 1.4e-110 | K | acr, cog1678 | |||
COCLMCBI_00145 | 1.3e-290 | cca | 2.7.7.19, 2.7.7.72 | J | tRNA nucleotidyltransferase poly(A) polymerase | |
COCLMCBI_00146 | 9.2e-90 | deoC | 3.6.1.13, 3.6.1.17, 3.6.1.55, 3.6.1.61 | L | NTP pyrophosphohydrolases including oxidative damage repair enzymes | |
COCLMCBI_00147 | 0.0 | NU | Tfp pilus assembly protein FimV | |||
COCLMCBI_00148 | 0.0 | murJ | S | Membrane | ||
COCLMCBI_00149 | 3.5e-92 | sigM | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
COCLMCBI_00150 | 2.4e-187 | trxB | 1.8.1.9, 4.3.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
COCLMCBI_00151 | 1.6e-41 | trxC | O | Belongs to the thioredoxin family | ||
COCLMCBI_00152 | 1e-210 | cwlM | 3.2.1.17, 3.5.1.28 | M | N-acetylmuramoyl-L-alanine amidase | |
COCLMCBI_00153 | 1.7e-126 | S | acetyltransferases and hydrolases with the alpha beta hydrolase fold | |||
COCLMCBI_00154 | 5.8e-104 | S | acetyltransferase | |||
COCLMCBI_00155 | 1.5e-178 | parB | K | Belongs to the ParB family | ||
COCLMCBI_00156 | 2.6e-164 | parA | D | ATPases involved in chromosome partitioning | ||
COCLMCBI_00157 | 1.2e-103 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
COCLMCBI_00158 | 6.6e-159 | yidC | U | Preprotein translocase subunit YidC | ||
COCLMCBI_00159 | 2.2e-52 | 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 | |
COCLMCBI_00160 | 2.1e-14 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
COCLMCBI_00161 | 2.3e-282 | 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 | ||
COCLMCBI_00162 | 1.3e-218 | 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 | |
COCLMCBI_00163 | 1.1e-209 | 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 | ||
COCLMCBI_00164 | 6.7e-110 | S | Zn-ribbon-containing, possibly RNA-binding protein and truncated derivatives | |||
COCLMCBI_00165 | 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 | |
COCLMCBI_00166 | 2.1e-169 | 1.1.3.6 | S | Alpha beta hydrolase | ||
COCLMCBI_00167 | 0.0 | surB | D | Lytic transglycosylase with a strong preference for naked glycan strands that lack stem peptides | ||
COCLMCBI_00168 | 6.9e-187 | P | ABC-type nitrate sulfonate bicarbonate transport systems periplasmic components | |||
COCLMCBI_00169 | 1.5e-130 | U | Binding-protein-dependent transport system inner membrane component | |||
COCLMCBI_00170 | 8.2e-134 | tauB | P | ATPases associated with a variety of cellular activities | ||
COCLMCBI_00171 | 9.4e-121 | tenA | 3.5.99.2 | K | Catalyzes an amino-pyrimidine hydrolysis reaction at the C5' of the pyrimidine moiety of thiamine compounds, a reaction that is part of a thiamine salvage pathway | |
COCLMCBI_00172 | 6.5e-122 | 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. Thus, catalyzes the conversion of 4-amino-5-aminomethyl-2-methylpyrimidine to 4-amino- 5-hydroxymethyl-2-methylpyrimidine (HMP) | ||
COCLMCBI_00173 | 1.3e-07 | |||||
COCLMCBI_00174 | 4.2e-64 | |||||
COCLMCBI_00175 | 3.1e-164 | |||||
COCLMCBI_00176 | 1.7e-36 | |||||
COCLMCBI_00177 | 1.8e-28 | |||||
COCLMCBI_00178 | 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 | |
COCLMCBI_00179 | 2.9e-49 | S | Transmembrane domain of unknown function (DUF3566) | |||
COCLMCBI_00182 | 2.8e-193 | K | Putative ATP-dependent DNA helicase recG C-terminal | |||
COCLMCBI_00183 | 5.6e-203 | CH | FAD binding domain | |||
COCLMCBI_00184 | 4.7e-125 | G | Polysaccharide deacetylase | |||
COCLMCBI_00185 | 9.7e-11 | S | CAAX protease self-immunity | |||
COCLMCBI_00186 | 6.8e-94 | T | Histidine kinase | |||
COCLMCBI_00187 | 2.4e-76 | K | Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | |||
COCLMCBI_00188 | 4.4e-191 | |||||
COCLMCBI_00190 | 2e-200 | G | PFAM glycoside hydrolase family 39 | |||
COCLMCBI_00192 | 3.1e-216 | S | Secretory lipase | |||
COCLMCBI_00193 | 5.4e-255 | yhgE | S | YhgE Pip domain protein | ||
COCLMCBI_00194 | 2.9e-104 | P | (ABC) transporter | |||
COCLMCBI_00195 | 1.4e-94 | kstR | K | transcriptional regulator | ||
COCLMCBI_00196 | 8.6e-14 | |||||
COCLMCBI_00197 | 2.6e-164 | metF | 1.5.1.20 | E | reductase | |
COCLMCBI_00198 | 0.0 | metE | 2.1.1.14 | H | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | |
COCLMCBI_00199 | 9.3e-108 | P | ABC transporter permease | |||
COCLMCBI_00200 | 4.2e-115 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
COCLMCBI_00201 | 1.7e-132 | P | ABC-type metal ion transport system, periplasmic component surface antigen | |||
COCLMCBI_00203 | 2.6e-94 | ppiA | 5.2.1.8 | O | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
COCLMCBI_00204 | 5.2e-82 | ybhB | 3.4.21.105 | S | membrane protein (homolog of Drosophila rhomboid) | |
COCLMCBI_00205 | 2.9e-249 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | NAD-dependent aldehyde dehydrogenases | |
COCLMCBI_00206 | 1.5e-43 | crgA | D | involved in cell division | ||
COCLMCBI_00207 | 2.2e-308 | pknB | 2.7.11.1 | KLT | serine threonine protein kinase | |
COCLMCBI_00208 | 4.3e-187 | KLT | serine threonine protein kinase | |||
COCLMCBI_00209 | 1.9e-251 | pbpA | M | Cell division protein FtsI penicillin-binding protein 2 | ||
COCLMCBI_00210 | 6.7e-219 | rodA | D | Belongs to the SEDS family | ||
COCLMCBI_00211 | 4e-214 | pstP | 3.1.3.16 | T | serine threonine protein phosphatase | |
COCLMCBI_00212 | 2.6e-58 | fhaB | T | FHA domain | ||
COCLMCBI_00213 | 6.5e-148 | fhaA | T | FHA domain | ||
COCLMCBI_00215 | 4.4e-35 | 2.7.7.7 | L | Transposase and inactivated derivatives | ||
COCLMCBI_00216 | 9.4e-153 | tnp7109-46 | L | Transposase and inactivated derivatives | ||
COCLMCBI_00217 | 9e-50 | L | Transposase and inactivated derivatives | |||
COCLMCBI_00218 | 2.6e-38 | S | MbtH-like protein | |||
COCLMCBI_00219 | 0.0 | V | ABC-type multidrug transport system, ATPase and permease components | |||
COCLMCBI_00220 | 7.4e-303 | V | ABC-type multidrug transport system, ATPase and permease components | |||
COCLMCBI_00221 | 8.5e-273 | 1.14.13.195, 1.14.13.196 | Q | L-lysine 6-monooxygenase (NADPH-requiring) | ||
COCLMCBI_00222 | 1.5e-40 | Q | Non-ribosomal peptide synthetase modules and related proteins | |||
COCLMCBI_00223 | 0.0 | Q | Non-ribosomal peptide synthetase modules and related proteins | |||
COCLMCBI_00224 | 1.7e-190 | fes | P | alpha/beta hydrolase fold | ||
COCLMCBI_00225 | 2.2e-156 | arnA | 1.1.1.305, 2.1.2.13, 2.1.2.9 | J | Formyl transferase, C-terminal domain | |
COCLMCBI_00226 | 1.6e-188 | P | ABC-type Fe3 -hydroxamate transport system, periplasmic component | |||
COCLMCBI_00227 | 1.5e-112 | dedA | S | Membrane-associated protein | ||
COCLMCBI_00228 | 1.5e-141 | 3.6.3.34 | HP | ATPases associated with a variety of cellular activities | ||
COCLMCBI_00229 | 3.2e-179 | fepG | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
COCLMCBI_00230 | 4.2e-190 | fepD | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
COCLMCBI_00231 | 1.3e-61 | 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 | ||
COCLMCBI_00232 | 2.5e-84 | 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 | ||
COCLMCBI_00233 | 3.9e-61 | 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 | ||
COCLMCBI_00234 | 1.9e-78 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
COCLMCBI_00235 | 3.2e-15 | rpmD | J | Ribosomal protein L30 | ||
COCLMCBI_00237 | 9e-50 | L | Transposase and inactivated derivatives | |||
COCLMCBI_00238 | 9.4e-153 | tnp7109-46 | L | Transposase and inactivated derivatives | ||
COCLMCBI_00239 | 6.3e-247 | L | Transposase and inactivated derivatives | |||
COCLMCBI_00241 | 2.9e-56 | repA | KT | Replicase family | ||
COCLMCBI_00242 | 1.1e-214 | 2.7.7.7 | L | Transposase and inactivated derivatives | ||
COCLMCBI_00243 | 2.9e-86 | |||||
COCLMCBI_00244 | 1e-125 | KT | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
COCLMCBI_00245 | 9.3e-196 | tcsS4 | 2.7.13.3 | T | Histidine kinase | |
COCLMCBI_00246 | 3.7e-31 | P | Heavy-metal-associated domain | |||
COCLMCBI_00247 | 0.0 | copB | 3.6.3.4 | P | cation transport ATPase | |
COCLMCBI_00248 | 4.4e-107 | glpF | U | water channel activity | ||
COCLMCBI_00249 | 1.6e-76 | S | Carboxymuconolactone decarboxylase family | |||
COCLMCBI_00250 | 6.6e-103 | 1.1.1.100, 1.1.1.401 | I | Belongs to the short-chain dehydrogenases reductases (SDR) family | ||
COCLMCBI_00251 | 0.0 | glsA | 3.5.1.2 | E | Belongs to the glutaminase family | |
COCLMCBI_00252 | 1.4e-38 | |||||
COCLMCBI_00253 | 1.7e-34 | K | Helix-turn-helix XRE-family like proteins | |||
COCLMCBI_00254 | 5.6e-45 | K | Transcriptional regulator | |||
COCLMCBI_00255 | 3.4e-217 | nplT | 3.2.1.1 | GH13 | G | Alpha amylase, catalytic domain protein |
COCLMCBI_00256 | 3.8e-96 | |||||
COCLMCBI_00257 | 2.4e-278 | gabD2 | 1.2.1.16, 1.2.1.20, 1.2.1.79, 1.2.99.10 | C | Belongs to the aldehyde dehydrogenase family | |
COCLMCBI_00258 | 6.4e-257 | E | COG0624 Acetylornithine deacetylase Succinyl-diaminopimelate desuccinylase and related deacylases | |||
COCLMCBI_00259 | 5.1e-108 | V | Beta-lactamase | |||
COCLMCBI_00260 | 2.7e-271 | amn | 3.2.2.4 | F | Catalyzes the hydrolysis of the N-glycosidic bond of AMP to form adenine and ribose 5-phosphate. Involved in regulation of AMP concentrations | |
COCLMCBI_00261 | 6.3e-171 | cobB | K | NAD-dependent protein deacetylase which modulates the activities of several enzymes which are inactive in their acetylated form | ||
COCLMCBI_00262 | 1.4e-208 | GT87 | S | Glycosyltransferase family 87 | ||
COCLMCBI_00263 | 1.7e-64 | gca | S | Carbonic anhydrases acetyltransferases, isoleucine patch superfamily | ||
COCLMCBI_00264 | 2.8e-183 | K | Transcriptional regulator sugar kinase | |||
COCLMCBI_00265 | 1.5e-133 | cobB | K | NAD-dependent lysine deacetylase and desuccinylase that specifically removes acetyl and succinyl groups on target proteins. Modulates the activities of several proteins which are inactive in their acylated form | ||
COCLMCBI_00266 | 1.4e-309 | S | protein conserved in bacteria | |||
COCLMCBI_00267 | 3.3e-162 | abrB | S | Ammonia monooxygenase | ||
COCLMCBI_00268 | 1.7e-118 | S | membrane transporter protein | |||
COCLMCBI_00270 | 1.7e-268 | lysI | E | L-lysine transport protein | ||
COCLMCBI_00271 | 0.0 | hrpB | 3.6.4.13 | L | ATP-dependent helicase | |
COCLMCBI_00272 | 3.3e-125 | |||||
COCLMCBI_00273 | 5.3e-104 | maa | 2.3.1.79 | S | acetyltransferase, isoleucine patch superfamily | |
COCLMCBI_00274 | 2.3e-122 | yusR | L | Belongs to the short-chain dehydrogenases reductases (SDR) family | ||
COCLMCBI_00275 | 3.7e-88 | rhtC | E | threonine efflux protein | ||
COCLMCBI_00276 | 2.6e-145 | dacB | 3.4.16.4 | M | Multidrug Resistance protein | |
COCLMCBI_00277 | 1.3e-48 | ybjQ | S | Belongs to the UPF0145 family | ||
COCLMCBI_00278 | 1.1e-32 | yaaA | S | S4 domain protein | ||
COCLMCBI_00279 | 1.8e-140 | cfp30B | S | enzyme related to lactoylglutathione lyase | ||
COCLMCBI_00280 | 1.3e-125 | dacB | 3.4.16.4 | M | Multidrug Resistance protein | |
COCLMCBI_00281 | 6.2e-202 | L | HNH endonuclease domain protein | |||
COCLMCBI_00282 | 3e-174 | I | esterase lipase | |||
COCLMCBI_00283 | 0.0 | pepO | 3.4.24.71 | O | Metalloendopeptidase | |
COCLMCBI_00284 | 0.0 | embC | M | Mycobacterial cell wall arabinan synthesis protein | ||
COCLMCBI_00285 | 0.0 | aftA | 2.4.2.46 | GT85 | S | Arabinofuranosyltransferase N terminal |
COCLMCBI_00286 | 1e-134 | dprE2 | 1.1.1.333 | S | Short chain dehydrogenase | |
COCLMCBI_00287 | 3.7e-276 | dprE1 | 1.1.98.3 | C | FAD FMN-containing dehydrogenases | |
COCLMCBI_00288 | 1.2e-29 | |||||
COCLMCBI_00289 | 7.4e-147 | |||||
COCLMCBI_00290 | 2.6e-77 | S | membrane | |||
COCLMCBI_00291 | 3.1e-167 | glfT1 | 2.4.1.287 | GT2 | S | Glycosyltransferase, group 2 family protein |
COCLMCBI_00292 | 1.3e-143 | |||||
COCLMCBI_00293 | 2.3e-145 | rfbE | 3.6.3.38 | GM | ABC-type polysaccharide polyol phosphate transport system ATPase component | |
COCLMCBI_00294 | 3.7e-171 | rfbD | GM | ABC-type polysaccharide polyol phosphate export systems permease component | ||
COCLMCBI_00295 | 1.6e-211 | csd | 2.8.1.7 | E | Selenocysteine lyase | |
COCLMCBI_00297 | 1e-58 | yvlD | S | membrane | ||
COCLMCBI_00298 | 2.5e-71 | |||||
COCLMCBI_00299 | 6.6e-182 | pat | 2.6.1.9 | E | May catalyze the transamination reaction in phenylalanine biosynthesis | |
COCLMCBI_00302 | 1.2e-199 | mgtE | P | Acts as a magnesium transporter | ||
COCLMCBI_00304 | 8.7e-174 | tyrA | 1.3.1.12, 1.3.1.43 | E | prephenate dehydrogenase | |
COCLMCBI_00305 | 7.1e-78 | S | tRNA adenosine | |||
COCLMCBI_00306 | 1.1e-75 | tadA | 3.5.4.1, 3.5.4.33, 3.8.1.5, 6.3.4.19 | FJ | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
COCLMCBI_00307 | 1.6e-15 | S | Belongs to the UPF0337 (CsbD) family | |||
COCLMCBI_00309 | 0.0 | mmpL2 | S | drug exporters of the RND superfamily | ||
COCLMCBI_00310 | 5.4e-231 | tgt | 2.4.2.29 | J | Catalyzes the base-exchange of a guanine (G) residue with the queuine precursor 7-aminomethyl-7-deazaguanine (PreQ1) at position 34 (anticodon wobble position) in tRNAs with GU(N) anticodons (tRNA-Asp, -Asn, -His and -Tyr). Catalysis occurs through a double-displacement mechanism. The nucleophile active site attacks the C1' of nucleotide 34 to detach the guanine base from the RNA, forming a covalent enzyme-RNA intermediate. The proton acceptor active site deprotonates the incoming PreQ1, allowing a nucleophilic attack on the C1' of the ribose to form the product. After dissociation, two additional enzymatic reactions on the tRNA convert PreQ1 to queuine (Q), resulting in the hypermodified nucleoside queuosine (7-(((4,5-cis-dihydroxy-2- cyclopenten-1-yl)amino)methyl)-7-deazaguanosine) | |
COCLMCBI_00311 | 3.5e-17 | VY92_11025 | D | Antitoxin component of a toxin-antitoxin (TA) module | ||
COCLMCBI_00312 | 3.3e-34 | vapC | S | Toxic component of a toxin-antitoxin (TA) module. An RNase | ||
COCLMCBI_00313 | 1.7e-114 | yhhQ | S | Involved in the import of queuosine (Q) precursors, required for Q precursor salvage | ||
COCLMCBI_00314 | 1.8e-162 | gluQ | 6.1.1.17 | J | Catalyzes the tRNA-independent activation of glutamate in presence of ATP and the subsequent transfer of glutamate onto a tRNA(Asp). Glutamate is transferred on the 2-amino-5-(4,5- dihydroxy-2-cyclopenten-1-yl) moiety of the queuosine in the wobble position of the QUC anticodon | |
COCLMCBI_00315 | 1.4e-133 | 6.2.1.3 | H | Aldolase/RraA | ||
COCLMCBI_00317 | 1e-240 | aspT | EK | HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | ||
COCLMCBI_00318 | 7.9e-83 | S | Suppressor of fused protein (SUFU) | |||
COCLMCBI_00319 | 8.8e-108 | T | Response regulator receiver domain protein | |||
COCLMCBI_00320 | 8e-112 | T | Histidine kinase | |||
COCLMCBI_00321 | 1.3e-114 | V | ABC transporter, ATP-binding protein | |||
COCLMCBI_00322 | 1.8e-211 | V | Efflux ABC transporter, permease protein | |||
COCLMCBI_00323 | 9.1e-283 | 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 | |
COCLMCBI_00324 | 2.5e-43 | ybaB | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
COCLMCBI_00325 | 4.4e-115 | 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 | ||
COCLMCBI_00326 | 8.3e-115 | cobQ | S | glutamine amidotransferase | ||
COCLMCBI_00327 | 4e-213 | murD | 3.4.21.10, 6.3.2.13, 6.3.2.9 | M | UDP-N-acetylmuramyl tripeptide synthase | |
COCLMCBI_00328 | 7.2e-173 | dnaQ | 2.7.7.7 | L | DNA polymerase III, epsilon subunit and related 3'-5' exonucleases | |
COCLMCBI_00329 | 3e-63 | |||||
COCLMCBI_00330 | 0.0 | leuA | 2.3.3.13 | E | Catalyzes the condensation of the acetyl group of acetyl-CoA with 3-methyl-2-oxobutanoate (2-oxoisovalerate) to form 3-carboxy-3-hydroxy-4-methylpentanoate (2-isopropylmalate) | |
COCLMCBI_00331 | 7.9e-120 | EG | Permeases of the drug metabolite transporter (DMT) superfamily | |||
COCLMCBI_00332 | 5.1e-146 | fmdA | 3.5.1.4 | C | formamidase | |
COCLMCBI_00333 | 1.3e-219 | ask | 1.1.1.3, 2.7.2.4 | E | Belongs to the aspartokinase family | |
COCLMCBI_00334 | 8.3e-185 | 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 | |
COCLMCBI_00335 | 3.4e-92 | sigC | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
COCLMCBI_00336 | 0.0 | katA | 1.11.1.6 | C | Catalase | |
COCLMCBI_00337 | 1.7e-62 | mnhG | P | Multisubunit Na H antiporter MnhG subunit | ||
COCLMCBI_00338 | 2.2e-36 | mnhF | ||||
COCLMCBI_00339 | 3.3e-65 | mrpE | P | multisubunit Na H antiporter MnhE subunit | ||
COCLMCBI_00340 | 6.2e-277 | mnhD | CP | Formate hydrogenlyase subunit 3 Multisubunit Na H antiporter MnhD subunit | ||
COCLMCBI_00341 | 1.6e-59 | phaC | 1.6.5.3 | P | NADH-ubiquinone/plastoquinone oxidoreductase chain 4L | |
COCLMCBI_00342 | 0.0 | mrpA | 1.6.5.3 | CP | NADH ubiquinone oxidoreductase subunit 5 (Chain L) Multisubunit Na H antiporter, MnhA subunit | |
COCLMCBI_00343 | 1.4e-167 | yhgE | S | membrane | ||
COCLMCBI_00345 | 0.0 | phoA | 3.1.3.1, 3.1.3.39 | P | Belongs to the alkaline phosphatase family | |
COCLMCBI_00347 | 9.1e-164 | ykuE | S | Ser Thr phosphatase family protein | ||
COCLMCBI_00348 | 2.3e-67 | yqeY | S | Yqey-like protein | ||
COCLMCBI_00349 | 0.0 | pon1 | 2.4.1.129, 3.4.16.4 | GT51 | M | Membrane carboxypeptidase (Penicillin-binding protein) |
COCLMCBI_00350 | 4.1e-62 | whiB4 | K | Acts as a transcriptional regulator. Probably redox- responsive. The apo- but not holo-form probably binds DNA | ||
COCLMCBI_00351 | 3.5e-23 | S | Domain of unknown function (DUF4177) | |||
COCLMCBI_00352 | 5.1e-70 | yabJ | J | translation initiation inhibitor, yjgF family | ||
COCLMCBI_00353 | 8.2e-151 | MA20_07390 | 3.1.2.6 | S | Zn-dependent hydrolases including glyoxylases | |
COCLMCBI_00354 | 1.1e-121 | glxR | K | cAMP-binding proteins - catabolite gene activator and regulatory subunit of cAMP-dependent protein kinases | ||
COCLMCBI_00355 | 1.2e-149 | nth | 4.2.99.18 | L | DNA repair enzyme that has both DNA N-glycosylase activity and AP-lyase activity. The DNA N-glycosylase activity releases various damaged pyrimidines from DNA by cleaving the N- glycosidic bond, leaving an AP (apurinic apyrimidinic) site. The AP-lyase activity cleaves the phosphodiester bond 3' to the AP site by a beta-elimination, leaving a 3'-terminal unsaturated sugar and a product with a terminal 5'-phosphate | |
COCLMCBI_00356 | 4.7e-79 | resA_1 | CO | Thiol-disulfide isomerase and thioredoxins | ||
COCLMCBI_00357 | 2.1e-126 | nudL | L | NTP pyrophosphohydrolases including oxidative damage repair enzymes | ||
COCLMCBI_00358 | 1e-162 | cvpA | O | Trypsin-like serine proteases typically periplasmic contain C-terminal PDZ domain | ||
COCLMCBI_00359 | 2.5e-156 | ephE | S | hydrolases or acyltransferases (alpha beta hydrolase superfamily) | ||
COCLMCBI_00360 | 1.7e-83 | S | Putative Actinobacterial Holin-X, holin superfamily III | |||
COCLMCBI_00361 | 2.1e-132 | ssgB | E | phosphoserine phosphatase | ||
COCLMCBI_00362 | 1.2e-208 | 2.7.7.7 | L | Transposase and inactivated derivatives | ||
COCLMCBI_00363 | 1e-145 | cpaE | D | bacterial-type flagellum organization | ||
COCLMCBI_00364 | 2.3e-196 | cpaF | U | Flp pilus assembly protein, ATPase CpaF | ||
COCLMCBI_00365 | 2.4e-91 | U | Flp pilus assembly protein TadB | |||
COCLMCBI_00366 | 8.1e-80 | gspF | NU | Type II secretion system | ||
COCLMCBI_00367 | 1.8e-34 | S | Protein of unknown function (DUF4244) | |||
COCLMCBI_00368 | 1.3e-40 | |||||
COCLMCBI_00369 | 8.2e-28 | S | TIGRFAM helicase secretion neighborhood TadE-like protein | |||
COCLMCBI_00370 | 0.0 | yprA | L | Distinct helicase family with a unique C-terminal domain including a metal-binding cysteine cluster | ||
COCLMCBI_00371 | 2.3e-30 | cspA | K | Cold shock proteins | ||
COCLMCBI_00372 | 3.2e-110 | S | SNARE associated Golgi protein | |||
COCLMCBI_00373 | 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 | |
COCLMCBI_00374 | 2.2e-266 | cya | 4.6.1.1 | T | Adenylate cyclase, family 3 (some proteins contain HAMP domain) | |
COCLMCBI_00375 | 6.7e-218 | holB | 2.7.7.7 | L | DNA polymerase III | |
COCLMCBI_00377 | 9e-47 | sugE | P | Multidrug resistance protein | ||
COCLMCBI_00378 | 1.7e-32 | sugE | P | Multidrug resistance protein | ||
COCLMCBI_00379 | 6.6e-44 | guaD | 3.5.4.3, 3.5.4.33 | FJ | Cytidine and deoxycytidylate deaminase zinc-binding region | |
COCLMCBI_00380 | 1.1e-25 | Q | protein disulfide oxidoreductase activity | |||
COCLMCBI_00381 | 5.3e-29 | K | helix_turn_helix multiple antibiotic resistance protein | |||
COCLMCBI_00382 | 1e-83 | Q | Domain of unknown function (DUF4442) | |||
COCLMCBI_00383 | 1.4e-197 | fadD9 | IQ | Acyl-CoA synthetases (AMP-forming) AMP-acid ligases II | ||
COCLMCBI_00384 | 2.7e-157 | E | GDSL-like Lipase/Acylhydrolase family | |||
COCLMCBI_00385 | 3.7e-194 | adhC | 1.1.1.306 | C | Alcohol dehydrogenase GroES-like domain | |
COCLMCBI_00386 | 7.9e-114 | 3.1.2.6 | S | Zn-dependent hydrolases including glyoxylases | ||
COCLMCBI_00387 | 7.1e-135 | bdbD | O | DSBA-like thioredoxin domain | ||
COCLMCBI_00388 | 2.1e-59 | S | Uncharacterized conserved protein (DUF2304) | |||
COCLMCBI_00389 | 3.5e-126 | M | Glycosyltransferases involved in cell wall biogenesis | |||
COCLMCBI_00390 | 3.2e-134 | amsE | 2.4.1.303 | GT2 | M | involved in cell wall biogenesis |
COCLMCBI_00391 | 1.3e-165 | rfbA | 2.7.7.24 | H | Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis | |
COCLMCBI_00392 | 3.7e-261 | V | endonuclease | |||
COCLMCBI_00393 | 5.7e-250 | rmlC | 1.1.1.133, 5.1.3.13 | M | Catalyzes the reduction of dTDP-6-deoxy-L-lyxo-4- hexulose to yield dTDP-L-rhamnose | |
COCLMCBI_00394 | 8.6e-227 | EGP | Major facilitator Superfamily | |||
COCLMCBI_00395 | 1.2e-52 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
COCLMCBI_00396 | 6.5e-182 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
COCLMCBI_00397 | 5.4e-199 | S | polysaccharide biosynthetic process | |||
COCLMCBI_00398 | 3.6e-238 | 1.11.1.19 | P | Iron-dependent peroxidase | ||
COCLMCBI_00399 | 1.7e-76 | VY92_09940 | S | protein conserved in bacteria | ||
COCLMCBI_00400 | 0.0 | f1pep1 | 3.4.21.26 | E | Serine proteases of the peptidase family S9A | |
COCLMCBI_00401 | 7.5e-195 | cmtA | S | esterase | ||
COCLMCBI_00403 | 1.9e-211 | cmtA | S | esterase | ||
COCLMCBI_00404 | 4.1e-262 | lpd | 1.8.1.4 | C | Pyruvate 2-oxoglutarate dehydrogenase complex dihydrolipoamide dehydrogenase (E3) component and related enzymes | |
COCLMCBI_00405 | 2e-82 | S | Domain of unknown function (DUF4352) | |||
COCLMCBI_00406 | 1.2e-80 | S | Polyketide cyclase / dehydrase and lipid transport | |||
COCLMCBI_00407 | 2.6e-135 | sdhC | C | succinate dehydrogenase | ||
COCLMCBI_00408 | 0.0 | sdhA | 1.3.5.1, 1.3.5.4 | C | succinate dehydrogenase | |
COCLMCBI_00409 | 1.3e-142 | sdhB | 1.3.5.1, 1.3.5.4 | C | Succinate dehydrogenase fumarate reductase | |
COCLMCBI_00410 | 4.7e-61 | |||||
COCLMCBI_00411 | 8.4e-43 | L | Transposase and inactivated derivatives | |||
COCLMCBI_00412 | 2.5e-144 | insK | L | Transposase and inactivated derivatives | ||
COCLMCBI_00413 | 1.5e-239 | S | membrane | |||
COCLMCBI_00414 | 9.8e-88 | |||||
COCLMCBI_00415 | 2.3e-48 | S | Protein of unknown function (DUF2516) | |||
COCLMCBI_00416 | 1.3e-68 | deoC | 4.1.2.4 | F | deoxyribose-phosphate aldolase | |
COCLMCBI_00417 | 5.4e-118 | S | Protein of unknown function (DUF2993) | |||
COCLMCBI_00418 | 1e-153 | J | protein-(glutamine-N5) methyltransferase activity | |||
COCLMCBI_00419 | 2.6e-83 | S | Protein of unknown function (DUF2505) | |||
COCLMCBI_00420 | 7.8e-186 | murB | 1.3.1.98 | M | Cell wall formation | |
COCLMCBI_00421 | 0.0 | fadD7 | 6.2.1.3 | IQ | Acyl-CoA synthetases (AMP-forming) AMP-acid ligases II | |
COCLMCBI_00422 | 3.4e-181 | D | AAA domain | |||
COCLMCBI_00423 | 1.8e-221 | mshA | 2.4.1.250 | M | Catalyzes the transfer of a N-acetyl-glucosamine moiety to 1D-myo-inositol 3-phosphate to produce 1D-myo-inositol 2- acetamido-2-deoxy-glucopyranoside 3-phosphate in the mycothiol biosynthesis pathway | |
COCLMCBI_00424 | 2e-188 | |||||
COCLMCBI_00425 | 1e-139 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
COCLMCBI_00426 | 3.9e-202 | senX3 | 2.7.13.3 | T | Histidine kinase | |
COCLMCBI_00427 | 6.6e-125 | T | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
COCLMCBI_00428 | 1.7e-167 | |||||
COCLMCBI_00429 | 1e-165 | ppx | 3.6.1.11, 3.6.1.40 | FP | Exopolyphosphatase | |
COCLMCBI_00430 | 7.1e-65 | |||||
COCLMCBI_00431 | 1.5e-133 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
COCLMCBI_00432 | 1.8e-27 | xis | K | DNA binding domain, excisionase family | ||
COCLMCBI_00434 | 3.5e-132 | namA | C | NADH flavin oxidoreductase NADH oxidase | ||
COCLMCBI_00435 | 6.7e-162 | serB1 | E | phosphoserine phosphatase | ||
COCLMCBI_00436 | 1.7e-36 | O | Thiol-disulfide isomerase and thioredoxins | |||
COCLMCBI_00437 | 1.1e-219 | hemA | 1.2.1.70 | H | Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA) | |
COCLMCBI_00438 | 1.6e-147 | hemC | 2.1.1.107, 2.5.1.61, 4.2.1.75 | H | Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps | |
COCLMCBI_00439 | 8.4e-291 | hemD | 1.3.1.76, 2.1.1.107, 4.2.1.75, 4.99.1.4 | H | Uroporphyrinogen-III synthase | |
COCLMCBI_00440 | 1e-164 | hemB | 4.2.1.24 | H | Belongs to the ALAD family | |
COCLMCBI_00441 | 7.8e-55 | |||||
COCLMCBI_00442 | 7.8e-77 | |||||
COCLMCBI_00443 | 0.0 | ccoI | 3.6.3.4, 3.6.3.54 | P | cation transport ATPase | |
COCLMCBI_00444 | 3.7e-188 | hemE | 4.1.1.37 | H | Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III | |
COCLMCBI_00445 | 4.5e-261 | hemG | 1.3.3.15, 1.3.3.4 | H | Catalyzes the 6-electron oxidation of protoporphyrinogen-IX to form protoporphyrin-IX | |
COCLMCBI_00446 | 1.6e-137 | S | Pfam SNARE associated Golgi protein | |||
COCLMCBI_00447 | 3.4e-139 | S | UPF0126 domain | |||
COCLMCBI_00448 | 3.4e-148 | galM | 5.1.3.3 | G | Aldose 1-epimerase | |
COCLMCBI_00449 | 2.8e-196 | L | HNH endonuclease domain protein | |||
COCLMCBI_00450 | 5.6e-234 | hemL | 5.4.3.8 | H | Glutamate-1-semialdehyde aminotransferase | |
COCLMCBI_00451 | 1.5e-112 | 3.1.3.3, 3.1.3.73 | G | phosphoglycerate mutase | ||
COCLMCBI_00452 | 2.6e-98 | resA | CO | Thiol-disulfide isomerase and thioredoxins | ||
COCLMCBI_00453 | 5.1e-134 | ccdA | O | cytochrome c biogenesis protein | ||
COCLMCBI_00454 | 3.8e-309 | resB | O | ResB protein required for cytochrome c biosynthesis | ||
COCLMCBI_00455 | 8.3e-185 | ccsA | O | ABC-type transport system involved in cytochrome c biogenesis permease component | ||
COCLMCBI_00456 | 1.4e-37 | K | Helix-turn-helix domain | |||
COCLMCBI_00457 | 9.9e-26 | |||||
COCLMCBI_00458 | 6.1e-43 | S | Protein of unknown function (DUF4229) | |||
COCLMCBI_00459 | 1.9e-151 | mdcF | S | permeases | ||
COCLMCBI_00460 | 1.6e-166 | menA | 2.5.1.74 | H | Belongs to the MenA family. Type 1 subfamily | |
COCLMCBI_00461 | 6.6e-167 | M | transferase activity, transferring glycosyl groups | |||
COCLMCBI_00462 | 7.7e-208 | menE | 6.2.1.26 | IQ | O-succinylbenzoic acid--CoA ligase | |
COCLMCBI_00463 | 1.9e-185 | T | Histidine kinase | |||
COCLMCBI_00464 | 2.1e-112 | K | Response regulator receiver domain protein | |||
COCLMCBI_00465 | 2e-115 | V | ABC transporter, ATP-binding protein | |||
COCLMCBI_00466 | 1.5e-240 | mutE | S | ABC-2 family transporter protein | ||
COCLMCBI_00467 | 1e-173 | menB | 4.1.3.36 | H | Belongs to the enoyl-CoA hydratase isomerase family. MenB subfamily | |
COCLMCBI_00468 | 1.5e-08 | S | FeoA domain | |||
COCLMCBI_00469 | 4.4e-270 | feoB | P | transporter of a GTP-driven Fe(2 ) uptake system | ||
COCLMCBI_00470 | 6.6e-23 | S | FeoC like transcriptional regulator | |||
COCLMCBI_00472 | 7.1e-176 | menC | 4.2.1.113, 5.1.1.20, 5.1.1.3 | H | Converts 2-succinyl-6-hydroxy-2,4-cyclohexadiene-1- carboxylate (SHCHC) to 2-succinylbenzoate (OSB) | |
COCLMCBI_00473 | 1.1e-268 | sdcS | P | Transporter, DASS family | ||
COCLMCBI_00474 | 2e-48 | |||||
COCLMCBI_00475 | 7.1e-287 | menD | 2.2.1.9 | H | Catalyzes the thiamine diphosphate-dependent decarboxylation of 2-oxoglutarate and the subsequent addition of the resulting succinic semialdehyde-thiamine pyrophosphate anion to isochorismate to yield 2-succinyl-5-enolpyruvyl-6-hydroxy-3- cyclohexene-1-carboxylate (SEPHCHC) | |
COCLMCBI_00476 | 2.5e-69 | |||||
COCLMCBI_00477 | 6e-208 | mgtA | GT4 | M | Glycosyltransferase, group 1 family protein | |
COCLMCBI_00478 | 7.1e-124 | ubiE | 2.1.1.163, 2.1.1.201 | H | Methyltransferase required for the conversion of demethylmenaquinol (DMKH2) to menaquinol (MKH2) | |
COCLMCBI_00479 | 8.9e-221 | menJ | 1.3.99.38 | C | Dehydrogenases (flavoproteins) | |
COCLMCBI_00480 | 2.3e-171 | hepS | 2.5.1.30 | H | Belongs to the FPP GGPP synthase family | |
COCLMCBI_00482 | 7.2e-206 | 2.7.7.7 | L | Transposase and inactivated derivatives | ||
COCLMCBI_00483 | 8.1e-224 | S | Esterase-like activity of phytase | |||
COCLMCBI_00487 | 1.3e-46 | 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 | ||
COCLMCBI_00488 | 4.5e-122 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
COCLMCBI_00489 | 6.1e-73 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
COCLMCBI_00490 | 3.1e-122 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
COCLMCBI_00491 | 3.6e-135 | insK | L | Transposase and inactivated derivatives | ||
COCLMCBI_00492 | 7e-58 | L | Helix-turn-helix domain | |||
COCLMCBI_00493 | 3.9e-24 | V | Beta-lactamase class C and other penicillin binding proteins | |||
COCLMCBI_00494 | 3.7e-72 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
COCLMCBI_00495 | 1.3e-40 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
COCLMCBI_00496 | 4.5e-156 | S | Protein of unknown function (DUF3068) | |||
COCLMCBI_00497 | 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 | |
COCLMCBI_00498 | 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 | |
COCLMCBI_00499 | 7e-79 | 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 | ||
COCLMCBI_00500 | 3.5e-110 | casE | S | CRISPR_assoc | ||
COCLMCBI_00501 | 1.5e-111 | casD | S | CRISPR-associated protein (Cas_Cas5) | ||
COCLMCBI_00502 | 2.4e-172 | casC | L | CT1975-like protein | ||
COCLMCBI_00503 | 1.6e-93 | casB | S | CRISPR-associated protein Cse2 (CRISPR_cse2) | ||
COCLMCBI_00504 | 4.8e-222 | cas3 | L | CRISPR-associated protein Cse1 (CRISPR_cse1) | ||
COCLMCBI_00505 | 0.0 | cas3 | L | CRISPR-associated | ||
COCLMCBI_00506 | 2.3e-60 | 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 | ||
COCLMCBI_00507 | 5.1e-81 | rpsG | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the head domain of the 30S subunit. Is located at the subunit interface close to the decoding center, probably blocks exit of the E-site tRNA | ||
COCLMCBI_00508 | 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 | ||
COCLMCBI_00509 | 2.2e-221 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
COCLMCBI_00510 | 7.7e-102 | |||||
COCLMCBI_00511 | 2.2e-86 | |||||
COCLMCBI_00512 | 6.5e-92 | S | Protein conserved in bacteria | |||
COCLMCBI_00513 | 6.1e-79 | S | Asp23 family, cell envelope-related function | |||
COCLMCBI_00514 | 2.1e-15 | |||||
COCLMCBI_00515 | 1.1e-08 | S | Protein conserved in bacteria | |||
COCLMCBI_00516 | 1.2e-86 | S | protein conserved in bacteria | |||
COCLMCBI_00517 | 5.7e-49 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
COCLMCBI_00518 | 2.9e-106 | 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 | ||
COCLMCBI_00519 | 3.6e-117 | rplD | J | Forms part of the polypeptide exit tunnel | ||
COCLMCBI_00520 | 5.3e-47 | 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 | ||
COCLMCBI_00521 | 7e-158 | 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 | ||
COCLMCBI_00522 | 2.8e-47 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
COCLMCBI_00523 | 3.6e-55 | 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 | ||
COCLMCBI_00524 | 4.1e-109 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
COCLMCBI_00525 | 8.3e-75 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
COCLMCBI_00526 | 6.7e-34 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
COCLMCBI_00527 | 1.2e-49 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
COCLMCBI_00528 | 1.6e-62 | scrK | 2.7.1.20, 2.7.1.4 | G | pfkB family carbohydrate kinase | |
COCLMCBI_00529 | 5.1e-287 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 3.5.99.2 | H | Phosphomethylpyrimidine kinase | |
COCLMCBI_00530 | 9e-271 | PPA1638 | S | 50S ribosome-binding GTPase | ||
COCLMCBI_00531 | 0.0 | S | ABC transporter | |||
COCLMCBI_00532 | 4.8e-140 | fnt | P | Formate nitrite | ||
COCLMCBI_00533 | 5.1e-60 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
COCLMCBI_00534 | 3e-47 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
COCLMCBI_00535 | 2.3e-107 | 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 | ||
COCLMCBI_00536 | 6.9e-147 | P | Siderophore-interacting protein | |||
COCLMCBI_00537 | 1.5e-169 | fecS | P | ABC-type Fe3 -hydroxamate transport system, periplasmic component | ||
COCLMCBI_00538 | 4.9e-129 | fecB | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
COCLMCBI_00539 | 1.3e-174 | fecD | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
COCLMCBI_00540 | 8.6e-145 | 3.6.3.34 | HP | transport systems ATPase components | ||
COCLMCBI_00541 | 0.0 | alcC | Q | IucA / IucC family | ||
COCLMCBI_00542 | 7.4e-194 | alcA | 1.14.13.59 | Q | L-lysine 6-monooxygenase (NADPH-requiring) | |
COCLMCBI_00543 | 1.9e-174 | ddc | 4.1.1.86 | E | Pyridoxal-dependent decarboxylase conserved domain | |
COCLMCBI_00544 | 5.1e-60 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
COCLMCBI_00545 | 3e-47 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
COCLMCBI_00546 | 2.3e-107 | 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 | ||
COCLMCBI_00547 | 2.2e-208 | 3.1.3.1 | S | Esterase-like activity of phytase | ||
COCLMCBI_00548 | 8.2e-104 | |||||
COCLMCBI_00550 | 9.2e-181 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
COCLMCBI_00551 | 9.9e-80 | 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 | |||
COCLMCBI_00552 | 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 | ||
COCLMCBI_00553 | 5.4e-95 | 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 | ||
COCLMCBI_00554 | 2.8e-59 | 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 | ||
COCLMCBI_00555 | 4.4e-84 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
COCLMCBI_00556 | 7e-26 | rpmD | J | Ribosomal protein L30 | ||
COCLMCBI_00557 | 1.5e-95 | rplO | J | binds to the 23S rRNA | ||
COCLMCBI_00558 | 1.9e-229 | 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 | ||
COCLMCBI_00559 | 6.1e-94 | 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 | |
COCLMCBI_00560 | 1.4e-139 | map | 3.4.11.18 | E | Methionine aminopeptidase | |
COCLMCBI_00562 | 8.6e-110 | MA20_01915 | S | protein conserved in bacteria | ||
COCLMCBI_00563 | 8.3e-34 | 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 | ||
COCLMCBI_00564 | 1.7e-60 | 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 | ||
COCLMCBI_00565 | 1.5e-65 | 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 | ||
COCLMCBI_00566 | 2.2e-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 | ||
COCLMCBI_00567 | 4e-184 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
COCLMCBI_00568 | 2.1e-61 | rplQ | J | Ribosomal protein L17 | ||
COCLMCBI_00569 | 9.1e-151 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
COCLMCBI_00570 | 0.0 | S | Psort location CytoplasmicMembrane, score | |||
COCLMCBI_00571 | 2.7e-220 | eccB | S | type VII secretion protein EccB | ||
COCLMCBI_00574 | 4.7e-187 | mycP4 | M | Belongs to the peptidase S8 family | ||
COCLMCBI_00575 | 1.3e-179 | eccD | ||||
COCLMCBI_00576 | 0.0 | eccCa | D | DNA segregation ATPase FtsK SpoIIIE and related proteins | ||
COCLMCBI_00577 | 2.7e-130 | |||||
COCLMCBI_00578 | 5.4e-39 | esxU | S | Belongs to the WXG100 family | ||
COCLMCBI_00579 | 7.3e-38 | esxT | S | Belongs to the WXG100 family | ||
COCLMCBI_00580 | 9.1e-80 | 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 | ||
COCLMCBI_00581 | 9.8e-95 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
COCLMCBI_00582 | 1.4e-237 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
COCLMCBI_00583 | 2.5e-08 | |||||
COCLMCBI_00585 | 1.1e-34 | |||||
COCLMCBI_00586 | 7.9e-157 | 3.1.1.45 | Q | Dienelactone hydrolase | ||
COCLMCBI_00587 | 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 | |
COCLMCBI_00588 | 4.8e-109 | irp5 | ||||
COCLMCBI_00589 | 2.2e-191 | alr | 5.1.1.1 | M | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
COCLMCBI_00590 | 5.2e-81 | ydiB | 2.7.1.221, 5.1.1.1 | S | ATPase or kinase | |
COCLMCBI_00591 | 6.9e-74 | |||||
COCLMCBI_00592 | 2.8e-104 | yeaZ | 2.3.1.234 | O | Universal bacterial protein YeaZ | |
COCLMCBI_00593 | 1.7e-79 | rimI | 2.3.1.128, 2.3.1.234 | K | Acetyltransferase | |
COCLMCBI_00594 | 3.4e-181 | 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 | |
COCLMCBI_00595 | 5.2e-75 | |||||
COCLMCBI_00596 | 4.2e-62 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
COCLMCBI_00597 | 1.4e-287 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
COCLMCBI_00598 | 2.5e-55 | whiB3 | K | Acts as a transcriptional regulator. Probably redox- responsive. The apo- but not holo-form probably binds DNA | ||
COCLMCBI_00599 | 1.4e-99 | sigD | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
COCLMCBI_00600 | 8.2e-52 | |||||
COCLMCBI_00601 | 9.6e-64 | S | Family of unknown function (DUF5319) | |||
COCLMCBI_00602 | 2e-275 | guaB | 1.1.1.205 | F | Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate- limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth | |
COCLMCBI_00603 | 1.2e-206 | guaB | 1.1.1.205 | F | IMP dehydrogenase GMP reductase | |
COCLMCBI_00604 | 3.2e-135 | sitA | P | Belongs to the bacterial solute-binding protein 9 family | ||
COCLMCBI_00605 | 3.5e-111 | sitB | P | transport system, ATP-binding protein | ||
COCLMCBI_00606 | 1.9e-108 | mntB | P | ABC 3 transport family | ||
COCLMCBI_00607 | 1.4e-90 | sirR | K | Mn-dependent transcriptional regulator | ||
COCLMCBI_00608 | 6.7e-285 | guaA | 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
COCLMCBI_00609 | 2.9e-146 | pspC | KT | stress-responsive transcriptional regulator | ||
COCLMCBI_00610 | 5.1e-189 | tcsS3 | T | Signal transduction histidine kinase | ||
COCLMCBI_00611 | 3.2e-113 | degU | K | Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
COCLMCBI_00612 | 6.9e-259 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
COCLMCBI_00613 | 9.2e-109 | imuA | S | Component of the SOS system and an inhibitor of cell division. Accumulation of SulA causes rapid cessation of cell division and the appearance of long, non-septate filaments. In the presence of GTP, binds a polymerization-competent form of FtsZ in a 1 1 ratio, thus inhibiting FtsZ polymerization and therefore preventing it from participating in the assembly of the Z ring. This mechanism prevents the premature segregation of damaged DNA to daughter cells during cell division | ||
COCLMCBI_00614 | 9.7e-278 | dinB_2 | L | DNA polymerase involved in DNA repair | ||
COCLMCBI_00615 | 2e-169 | O | protein conserved in bacteria containing thioredoxin-like domain | |||
COCLMCBI_00616 | 1.2e-115 | metI | P | ABC-type metal ion transport system permease component | ||
COCLMCBI_00617 | 1.3e-188 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
COCLMCBI_00618 | 2e-150 | metQ | P | ABC-type metal ion transport system, periplasmic component surface antigen | ||
COCLMCBI_00619 | 0.0 | dnaE2 | 2.7.7.6, 2.7.7.7 | L | DNA polymerase involved in damage-induced mutagenesis and translesion synthesis (TLS). It is not the major replicative DNA polymerase | |
COCLMCBI_00620 | 1.3e-165 | C | Thiosulfate reductase cytochrome B subunit (membrane anchoring protein) | |||
COCLMCBI_00621 | 2.1e-94 | S | Bacterial PH domain | |||
COCLMCBI_00622 | 1.2e-239 | S | membrane | |||
COCLMCBI_00623 | 4.8e-84 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
COCLMCBI_00624 | 1.7e-159 | folD | 1.5.1.5, 3.5.4.9 | F | Catalyzes the oxidation of 5,10- methylenetetrahydrofolate to 5,10-methenyltetrahydrofolate and then the hydrolysis of 5,10-methenyltetrahydrofolate to 10- formyltetrahydrofolate | |
COCLMCBI_00625 | 1.5e-34 | S | Protein of unknown function (DUF3017) | |||
COCLMCBI_00626 | 3.5e-90 | Q | Methyltransferase domain | |||
COCLMCBI_00627 | 1e-24 | K | SpoVT / AbrB like domain | |||
COCLMCBI_00628 | 3e-29 | vapC | S | Toxic component of a toxin-antitoxin (TA) module. An RNase | ||
COCLMCBI_00629 | 2.4e-225 | metXA | 2.3.1.31 | E | Transfers an acetyl group from acetyl-CoA to L- homoserine, forming acetyl-L-homoserine | |
COCLMCBI_00630 | 1.9e-242 | metY | 2.5.1.49 | E | O-acetylhomoserine | |
COCLMCBI_00631 | 6.3e-256 | |||||
COCLMCBI_00632 | 0.0 | mtsE | S | VWA domain containing CoxE-like protein | ||
COCLMCBI_00633 | 6.3e-199 | S | ATPase family associated with various cellular activities (AAA) | |||
COCLMCBI_00634 | 0.0 | |||||
COCLMCBI_00635 | 0.0 | |||||
COCLMCBI_00636 | 2e-158 | C | Domain of unknown function (DUF4132) | |||
COCLMCBI_00637 | 1.7e-07 | S | Protein of unknown function (DUF2510) | |||
COCLMCBI_00638 | 0.0 | icd | 1.1.1.42 | C | Isocitrate dehydrogenase | |
COCLMCBI_00639 | 6.6e-170 | exoA | 3.1.11.2 | L | exodeoxyribonuclease III | |
COCLMCBI_00640 | 5.4e-75 | S | protein with SCP PR1 domains | |||
COCLMCBI_00641 | 9.6e-176 | bioB | 2.8.1.6 | H | Catalyzes the conversion of dethiobiotin (DTB) to biotin by the insertion of a sulfur atom into dethiobiotin via a radical- based mechanism | |
COCLMCBI_00642 | 5.5e-24 | |||||
COCLMCBI_00643 | 5.5e-95 | |||||
COCLMCBI_00644 | 5.6e-130 | V | (ABC) transporter | |||
COCLMCBI_00645 | 1.5e-56 | K | transcriptional | |||
COCLMCBI_00646 | 1.1e-192 | trpS | 6.1.1.2 | J | Tryptophanyl-tRNA synthetase | |
COCLMCBI_00647 | 2e-152 | yhjD | S | membrane | ||
COCLMCBI_00648 | 2.5e-202 | dac | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
COCLMCBI_00649 | 5.4e-101 | S | membrane | |||
COCLMCBI_00650 | 2.9e-216 | |||||
COCLMCBI_00651 | 8.3e-113 | M | NlpC P60 family protein | |||
COCLMCBI_00653 | 1.3e-111 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
COCLMCBI_00654 | 9.6e-68 | K | Helix-turn-helix XRE-family like proteins | |||
COCLMCBI_00655 | 4.6e-227 | amiA | S | amidohydrolase | ||
COCLMCBI_00656 | 2.3e-254 | lpdA | 1.8.1.4 | C | Pyruvate 2-oxoglutarate dehydrogenase complex, dihydrolipoamide dehydrogenase (E3) component, and related enzymes | |
COCLMCBI_00657 | 4.2e-26 | prpC | 2.3.3.1, 2.3.3.5 | C | Belongs to the citrate synthase family | |
COCLMCBI_00658 | 6.7e-204 | S | ATPase (AAA superfamily) | |||
COCLMCBI_00659 | 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 | |
COCLMCBI_00660 | 1.7e-97 | chrA | K | COG2197 Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
COCLMCBI_00661 | 2.4e-172 | chrS | T | Histidine kinase | ||
COCLMCBI_00662 | 8.6e-139 | hrtB | V | ABC-type antimicrobial peptide transport system, permease component | ||
COCLMCBI_00663 | 1.6e-109 | hrtA | V | ABC-type antimicrobial peptide transport system, ATPase component | ||
COCLMCBI_00664 | 9.4e-83 | K | Acetyltransferase | |||
COCLMCBI_00665 | 1.8e-293 | bccA | 6.3.4.14, 6.4.1.2, 6.4.1.3 | I | Acetyl propionyl-CoA carboxylase alpha subunit | |
COCLMCBI_00666 | 1.6e-173 | sseA | 2.8.1.1, 2.8.1.2 | P | Sulfurtransferase | |
COCLMCBI_00667 | 1.3e-204 | HJ | ligase activity | |||
COCLMCBI_00668 | 2.5e-29 | K | Domain of unknown function (DUF4282) | |||
COCLMCBI_00669 | 3.2e-68 | S | Protein of unknown function (DUF3151) | |||
COCLMCBI_00670 | 9.9e-36 | S | Protein of unknown function (DUF3253) | |||
COCLMCBI_00671 | 1.9e-30 | S | membrane | |||
COCLMCBI_00672 | 3.6e-94 | maf | 1.1.1.25, 2.1.1.190 | D | Maf-like protein | |
COCLMCBI_00673 | 2e-11 | S | Acyl-CoA carboxylase epsilon subunit | |||
COCLMCBI_00674 | 6.1e-269 | accD2 | 2.1.3.15, 6.4.1.3 | I | Acetyl-CoA carboxylase, carboxyltransferase component (subunits alpha and beta) | |
COCLMCBI_00675 | 7.5e-60 | |||||
COCLMCBI_00676 | 3.1e-90 | K | Belongs to the sigma-70 factor family. ECF subfamily | |||
COCLMCBI_00678 | 2.9e-292 | hscA | O | Belongs to the heat shock protein 70 family | ||
COCLMCBI_00679 | 1.9e-203 | |||||
COCLMCBI_00680 | 8.3e-305 | S | Dynamin family | |||
COCLMCBI_00681 | 1.3e-268 | S | Dynamin family | |||
COCLMCBI_00682 | 0.0 | 2.7.7.7 | L | DNA polymerase III, epsilon subunit | ||
COCLMCBI_00684 | 1.4e-161 | S | Type I phosphodiesterase / nucleotide pyrophosphatase | |||
COCLMCBI_00685 | 2.6e-203 | 3.6.3.30 | P | Part of the ABC transporter complex CysAWTP involved in sulfate thiosulfate import. Responsible for energy coupling to the transport system | ||
COCLMCBI_00686 | 2.7e-136 | P | Binding-protein-dependent transport system inner membrane component | |||
COCLMCBI_00687 | 2.5e-167 | P | Binding-protein-dependent transport systems inner membrane component | |||
COCLMCBI_00688 | 3.1e-193 | P | Bacterial extracellular solute-binding protein | |||
COCLMCBI_00689 | 4.2e-97 | pgmB | 3.1.3.18, 5.4.2.6 | S | HAD hydrolase, family IA, variant 3 | |
COCLMCBI_00690 | 1.9e-107 | 2.7.7.7 | L | DNA polymerase III, epsilon subunit | ||
COCLMCBI_00691 | 3.9e-245 | yfjM | K | Protein of unknown function DUF262 | ||
COCLMCBI_00692 | 0.0 | 3.6.4.13 | L | Restriction endonuclease | ||
COCLMCBI_00695 | 9.4e-153 | tnp7109-46 | L | Transposase and inactivated derivatives | ||
COCLMCBI_00696 | 9e-50 | L | Transposase and inactivated derivatives | |||
COCLMCBI_00697 | 3.2e-115 | L | Transposase and inactivated derivatives | |||
COCLMCBI_00700 | 2.5e-247 | |||||
COCLMCBI_00701 | 4e-43 | arsR | K | transcriptional | ||
COCLMCBI_00702 | 2.5e-190 | arsB | P | Arsenite efflux pump ACR3 and related permeases | ||
COCLMCBI_00703 | 4.3e-71 | arsC | 1.20.4.1, 2.8.4.2 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
COCLMCBI_00704 | 8.6e-76 | S | Protein of unknown function, DUF488 | |||
COCLMCBI_00705 | 2.7e-138 | birA | 2.7.1.33, 6.3.4.15 | H | Biotin-(Acetyl-CoA carboxylase) ligase | |
COCLMCBI_00706 | 3.9e-67 | S | Bacterial PH domain | |||
COCLMCBI_00707 | 2e-138 | budA | 4.1.1.5 | Q | Belongs to the alpha-acetolactate decarboxylase family | |
COCLMCBI_00708 | 3.5e-208 | 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) | |
COCLMCBI_00709 | 1.4e-76 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
COCLMCBI_00710 | 6.7e-76 | sanA | S | DUF218 domain | ||
COCLMCBI_00711 | 1.1e-124 | IQ | COG0365 Acyl-coenzyme A synthetases AMP-(fatty) acid ligases | |||
COCLMCBI_00712 | 1.3e-256 | lytR2 | K | transcriptional | ||
COCLMCBI_00713 | 3.4e-155 | wbbL | 2.4.1.289 | S | Glycosyltransferases | |
COCLMCBI_00714 | 4.7e-170 | manC | 2.7.7.13, 5.4.2.8 | JM | Nucleoside-diphosphate-sugar pyrophosphorylase involved in lipopolysaccharide biosynthesis translation initiation factor 2B gamma epsilon subunits | |
COCLMCBI_00715 | 5.4e-51 | whiB2 | K | Acts as a transcriptional regulator. Probably redox- responsive. The apo- but not holo-form probably binds DNA | ||
COCLMCBI_00716 | 8.2e-61 | MA20_43655 | 2.7.2.8 | S | Zincin-like metallopeptidase | |
COCLMCBI_00717 | 5e-69 | S | Protein of unknown function (DUF3499) | |||
COCLMCBI_00718 | 1.3e-35 | VY92_11025 | D | Antitoxin component of a toxin-antitoxin (TA) module | ||
COCLMCBI_00719 | 1.7e-67 | vapC | S | Toxic component of a toxin-antitoxin (TA) module. An RNase | ||
COCLMCBI_00720 | 2.1e-247 | manB | 5.4.2.2, 5.4.2.8 | G | the resulting product is then converted to GDP-mannose by ManC which is then used in the synthesis of mannose-containing glycoconjugates that are important for mediating entry into host cells | |
COCLMCBI_00721 | 4.9e-158 | 5.3.1.8, 5.3.1.9 | K | Transcriptional regulator | ||
COCLMCBI_00722 | 3.2e-199 | manA | 1.14.13.81, 5.3.1.8, 5.4.2.8 | G | isomerase | |
COCLMCBI_00724 | 2.7e-53 | |||||
COCLMCBI_00725 | 1.6e-274 | ahcY | 3.3.1.1 | H | May play a key role in the regulation of the intracellular concentration of adenosylhomocysteine | |
COCLMCBI_00726 | 9.7e-64 | tmk | 2.1.1.45, 2.7.4.9, 4.1.1.19 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
COCLMCBI_00727 | 9.8e-118 | T | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
COCLMCBI_00728 | 1.5e-270 | mtrB | 2.7.13.3 | T | Histidine kinase | |
COCLMCBI_00729 | 2.7e-308 | lpqB | S | Lipoprotein LpqB | ||
COCLMCBI_00730 | 9.1e-102 | ctsW | S | phosphoribosyltransferase | ||
COCLMCBI_00731 | 4.9e-101 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
COCLMCBI_00732 | 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 | ||
COCLMCBI_00733 | 7e-57 | |||||
COCLMCBI_00734 | 1.6e-70 | 3.1.3.10, 3.1.3.102, 3.1.3.104 | S | hydrolase | ||
COCLMCBI_00735 | 1.1e-81 | |||||
COCLMCBI_00736 | 6.3e-247 | L | Transposase and inactivated derivatives | |||
COCLMCBI_00737 | 9.6e-184 | 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 | |
COCLMCBI_00738 | 2.8e-230 | aroA | 2.5.1.19 | E | Catalyzes the transfer of the enolpyruvyl moiety of phosphoenolpyruvate (PEP) to the 5-hydroxyl of shikimate-3- phosphate (S3P) to produce enolpyruvyl shikimate-3-phosphate and inorganic phosphate | |
COCLMCBI_00739 | 1.3e-93 | yedK | S | Belongs to the SOS response-associated peptidase family | ||
COCLMCBI_00740 | 1e-73 | ybaK | S | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
COCLMCBI_00741 | 6.1e-100 | sigH | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
COCLMCBI_00742 | 6.6e-15 | |||||
COCLMCBI_00743 | 6.7e-43 | whiB | K | Acts as a transcriptional regulator. Probably redox- responsive. The apo- but not holo-form probably binds DNA | ||
COCLMCBI_00744 | 2.4e-73 | |||||
COCLMCBI_00745 | 2.3e-210 | S | ErfK ybiS ycfS ynhG family protein | |||
COCLMCBI_00746 | 9.9e-215 | deaD | 3.6.4.13 | L | Belongs to the DEAD box helicase family | |
COCLMCBI_00747 | 3.8e-18 | S | Protein of unknown function (DUF3107) | |||
COCLMCBI_00748 | 2.7e-160 | M | Protein of unknown function (DUF3152) | |||
COCLMCBI_00749 | 2.1e-126 | S | Aminoglycoside phosphotransferase | |||
COCLMCBI_00750 | 0.0 | uvrD | 3.6.4.12 | L | Belongs to the helicase family. UvrD subfamily | |
COCLMCBI_00751 | 0.0 | uvrD2 | 3.6.4.12 | L | Belongs to the helicase family. UvrD subfamily | |
COCLMCBI_00752 | 3.5e-197 | kch | 3.6.1.22 | P | Kef-type K transport systems | |
COCLMCBI_00753 | 0.0 | uvrD2 | 3.6.4.12 | L | DNA helicase | |
COCLMCBI_00754 | 9e-50 | L | Transposase and inactivated derivatives | |||
COCLMCBI_00755 | 9.4e-153 | tnp7109-46 | L | Transposase and inactivated derivatives | ||
COCLMCBI_00756 | 4.7e-106 | |||||
COCLMCBI_00757 | 1.2e-83 | S | Metal-dependent hydrolase | |||
COCLMCBI_00758 | 8.7e-228 | S | hydrolase | |||
COCLMCBI_00759 | 5.5e-179 | lon | T | Belongs to the peptidase S16 family | ||
COCLMCBI_00760 | 6.4e-72 | |||||
COCLMCBI_00761 | 4.9e-85 | |||||
COCLMCBI_00762 | 0.0 | S | UPF0182 protein | |||
COCLMCBI_00764 | 3.9e-187 | S | Domain of unknown function (DUF4192) | |||
COCLMCBI_00765 | 4.9e-19 | |||||
COCLMCBI_00766 | 1.9e-66 | L | single-stranded DNA binding | |||
COCLMCBI_00767 | 6e-123 | sirR | K | Mn-dependent transcriptional regulator | ||
COCLMCBI_00768 | 3.7e-75 | nrdI | F | Probably involved in ribonucleotide reductase function | ||
COCLMCBI_00769 | 0.0 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
COCLMCBI_00770 | 1.7e-190 | nrdF | 1.17.4.1 | F | reductase beta subunit | |
COCLMCBI_00771 | 5.1e-107 | yieF | S | NADPH-dependent FMN reductase | ||
COCLMCBI_00772 | 7.9e-124 | |||||
COCLMCBI_00773 | 3.6e-138 | insK | L | Transposase and inactivated derivatives | ||
COCLMCBI_00774 | 4.9e-43 | L | Transposase and inactivated derivatives | |||
COCLMCBI_00775 | 3.4e-21 | |||||
COCLMCBI_00776 | 0.0 | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | ||
COCLMCBI_00777 | 1.6e-08 | S | Helix-turn-helix domain | |||
COCLMCBI_00779 | 3.7e-139 | L | Phage integrase family | |||
COCLMCBI_00780 | 2.7e-11 | |||||
COCLMCBI_00782 | 4.6e-16 | |||||
COCLMCBI_00783 | 5e-100 | S | Psort location Cytoplasmic, score 7.50 | |||
COCLMCBI_00785 | 5.3e-104 | S | Pfam PF00149 | |||
COCLMCBI_00787 | 7.8e-169 | chr | P | COG2059 Chromate transport protein ChrA | ||
COCLMCBI_00788 | 1.6e-188 | C | Coenzyme F420-dependent N5N10-methylene tetrahydromethanopterin reductase and related | |||
COCLMCBI_00789 | 3.6e-197 | agxT | 2.6.1.44, 2.6.1.45, 2.6.1.51 | E | Serine-pyruvate aminotransferase archaeal aspartate aminotransferase | |
COCLMCBI_00790 | 2.4e-20 | |||||
COCLMCBI_00791 | 2.1e-199 | thiF | 2.7.7.80, 2.8.1.11 | H | Dinucleotide-utilizing enzymes involved in molybdopterin and thiamine biosynthesis family 2 | |
COCLMCBI_00792 | 6.4e-241 | ectP | M | Belongs to the BCCT transporter (TC 2.A.15) family | ||
COCLMCBI_00793 | 1.2e-158 | fieF | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
COCLMCBI_00794 | 2e-138 | thiG | 2.8.1.10 | H | Catalyzes the rearrangement of 1-deoxy-D-xylulose 5- phosphate (DXP) to produce the thiazole phosphate moiety of thiamine. Sulfur is provided by the thiocarboxylate moiety of the carrier protein ThiS. In vitro, sulfur can be provided by H(2)S | |
COCLMCBI_00795 | 4.8e-12 | thiS | H | ThiS family | ||
COCLMCBI_00796 | 5.5e-203 | thiO | 1.4.3.19 | E | Glycine D-amino acid oxidases (deaminating) | |
COCLMCBI_00797 | 2.5e-101 | tcsR2 | K | Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
COCLMCBI_00798 | 1.3e-166 | 2.7.13.3 | T | Histidine kinase | ||
COCLMCBI_00799 | 5.7e-130 | V | ABC-type multidrug transport system, permease component | |||
COCLMCBI_00800 | 5.5e-139 | V | ATP-binding protein | |||
COCLMCBI_00801 | 1.5e-67 | ectC | 4.2.1.108 | G | Ectoine synthase | |
COCLMCBI_00802 | 5.1e-97 | P | Cation efflux family | |||
COCLMCBI_00803 | 1e-232 | V | HNH endonuclease | |||
COCLMCBI_00804 | 3.3e-204 | mntH | P | Mn2 and Fe2 transporters of the NRAMP family | ||
COCLMCBI_00805 | 4.5e-200 | scoB | 2.8.3.5, 2.8.3.8, 2.8.3.9 | I | Acyl CoA acetate 3-ketoacid CoA transferase beta subunit | |
COCLMCBI_00806 | 8.4e-148 | atoE | I | Short chain fatty acid transporter | ||
COCLMCBI_00807 | 1e-108 | thiE | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | 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) | |
COCLMCBI_00808 | 1.1e-149 | S | Protein of unknown function (DUF418) | |||
COCLMCBI_00809 | 3.4e-138 | hisN | 3.1.3.15 | G | Archaeal fructose-16-bisphosphatase and related enzymes of inositol monophosphatase family | |
COCLMCBI_00810 | 1.2e-125 | 3.1.3.25 | G | Archaeal fructose-16-bisphosphatase and related enzymes of inositol monophosphatase family | ||
COCLMCBI_00811 | 2.6e-192 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
COCLMCBI_00812 | 9.7e-50 | QT | PucR C-terminal helix-turn-helix domain | |||
COCLMCBI_00813 | 4.5e-181 | Q | Flavin containing amine oxidoreductase | |||
COCLMCBI_00814 | 2.4e-174 | S | Transmembrane protein of unknown function (DUF3556) | |||
COCLMCBI_00815 | 1.1e-281 | 6.2.1.3 | IQ | AMP-binding enzyme C-terminal domain | ||
COCLMCBI_00816 | 4.1e-121 | ftsE | D | cell division ATP-binding protein | ||
COCLMCBI_00817 | 2.4e-151 | ftsX | D | Part of the ABC transporter FtsEX involved in cellular division | ||
COCLMCBI_00818 | 1.2e-85 | smpB | O | the 2 termini fold to resemble tRNA(Ala) and it encodes a tag peptide , a short internal open reading frame. During trans-translation Ala- aminoacylated tmRNA acts like a tRNA, entering the A-site of stalled ribosomes, displacing the stalled mRNA. The ribosome then switches to translate the ORF on the tmRNA | ||
COCLMCBI_00819 | 7.5e-115 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
COCLMCBI_00821 | 1.3e-149 | fatB | P | Periplasmic binding protein | ||
COCLMCBI_00822 | 2.4e-163 | fatB | P | ABC-type enterochelin transport system periplasmic component | ||
COCLMCBI_00823 | 1.3e-166 | feuB | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
COCLMCBI_00824 | 3.7e-177 | fatC | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
COCLMCBI_00825 | 3.5e-132 | yclP | 3.6.3.34 | P | ABC transporter, ATP-binding protein | |
COCLMCBI_00826 | 1.9e-13 | |||||
COCLMCBI_00827 | 1.4e-110 | S | membrane transporter protein | |||
COCLMCBI_00828 | 0.0 | ppe1 | S | Pfam PF00149 | ||
COCLMCBI_00829 | 2.2e-162 | ugpC | 3.6.3.20 | P | Belongs to the ABC transporter superfamily | |
COCLMCBI_00830 | 7.9e-196 | ugpB | G | Bacterial extracellular solute-binding protein | ||
COCLMCBI_00831 | 3.7e-150 | ugpE | P | ABC transporter permease | ||
COCLMCBI_00832 | 2.6e-156 | ugpA | P | ABC transporter permease | ||
COCLMCBI_00833 | 1.4e-82 | ugpQ_1 | 3.1.4.46 | C | Glycerophosphoryl diester phosphodiesterase family | |
COCLMCBI_00834 | 2.4e-113 | S | Protein of unknown function (DUF3239) | |||
COCLMCBI_00835 | 3.7e-304 | ercc3 | 3.6.4.12 | L | DNA or RNA helicases of superfamily II | |
COCLMCBI_00836 | 1.7e-26 | parD1 | K | Bacterial antitoxin of ParD toxin-antitoxin type II system and RHH | ||
COCLMCBI_00837 | 1.1e-124 | CP | ABC-type Na efflux pump, permease component | |||
COCLMCBI_00838 | 8.5e-138 | S | ABC transporter, ATP-binding protein | |||
COCLMCBI_00839 | 5.4e-76 | |||||
COCLMCBI_00840 | 4.5e-35 | K | Helix-turn-helix XRE-family like proteins | |||
COCLMCBI_00841 | 7.6e-238 | M1-1077 | K | Helicase conserved C-terminal domain | ||
COCLMCBI_00842 | 3e-25 | |||||
COCLMCBI_00843 | 1.8e-87 | rpfA | GH23 | M | Protein of unknown function (DUF3235) | |
COCLMCBI_00844 | 1.3e-60 | cspB | K | Cold shock proteins | ||
COCLMCBI_00845 | 6e-69 | S | Protein of unknown function (DUF2771) | |||
COCLMCBI_00846 | 3.5e-122 | 2.3.2.5 | M | Glutamine cyclotransferase | ||
COCLMCBI_00847 | 2.4e-122 | S | Protein of unknown function (DUF3027) | |||
COCLMCBI_00848 | 9.2e-257 | yjcD | S | permeases | ||
COCLMCBI_00849 | 1.2e-146 | spoU2 | 2.1.1.185 | J | rRNA methylases | |
COCLMCBI_00850 | 3.6e-125 | |||||
COCLMCBI_00851 | 2e-153 | S | Protein of unknown function (DUF3071) | |||
COCLMCBI_00852 | 1.1e-209 | serC | 2.6.1.52 | E | Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine | |
COCLMCBI_00853 | 7.8e-249 | gltA | 2.3.3.1 | C | Belongs to the citrate synthase family | |
COCLMCBI_00854 | 6.3e-63 | fkb | 5.2.1.8 | O | Peptidyl-prolyl cis-trans | |
COCLMCBI_00855 | 1.7e-151 | dkgA | 1.1.1.346 | S | Aldo keto reductases, related to diketogulonate reductase | |
COCLMCBI_00856 | 1.7e-54 | yjcH | S | membrane | ||
COCLMCBI_00857 | 1.9e-284 | actP | S | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
COCLMCBI_00858 | 1.2e-151 | M | Tat pathway signal sequence domain protein | |||
COCLMCBI_00859 | 1.7e-08 | |||||
COCLMCBI_00860 | 1.9e-25 | glpQ | 3.1.4.46 | C | Glycerophosphoryl diester phosphodiesterase family | |
COCLMCBI_00861 | 1.5e-75 | K | Bacterial regulatory proteins, tetR family | |||
COCLMCBI_00862 | 3.7e-175 | J | Acetyltransferase (GNAT) domain | |||
COCLMCBI_00864 | 7.4e-10 | K | Winged helix DNA-binding domain | |||
COCLMCBI_00865 | 3.4e-35 | grxA | 1.20.4.3 | O | Glutaredoxin | |
COCLMCBI_00866 | 6.1e-67 | folA | 1.5.1.3 | H | dihydrofolate reductase | |
COCLMCBI_00867 | 8.5e-148 | 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 | |
COCLMCBI_00868 | 4.1e-144 | cysQ | 3.1.3.7 | P | Inositol monophosphatase | |
COCLMCBI_00869 | 2.5e-264 | 3.6.4.12 | K | transcriptional regulator containing an HTH domain and an | ||
COCLMCBI_00870 | 0.0 | lhr | L | Lhr-like helicases | ||
COCLMCBI_00871 | 2.1e-24 | |||||
COCLMCBI_00872 | 2e-149 | nei | 4.2.99.18 | L | formamidopyrimidine-DNA glycosylase | |
COCLMCBI_00873 | 1e-113 | apl | 3.1.3.1 | S | membrane-associated protein | |
COCLMCBI_00874 | 4.6e-285 | ybdK_1 | S | glutamate--cysteine ligase | ||
COCLMCBI_00875 | 9.4e-308 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
COCLMCBI_00876 | 9.2e-53 | 1.14.99.57 | S | Antibiotic biosynthesis monooxygenase | ||
COCLMCBI_00877 | 8.7e-110 | |||||
COCLMCBI_00878 | 1.5e-46 | tyrA | 1.3.1.12, 5.4.99.5 | E | chorismate mutase | |
COCLMCBI_00879 | 0.0 | pcrA | 3.6.4.12 | L | Superfamily I DNA and RNA helicases | |
COCLMCBI_00880 | 4.5e-123 | M | Peptidase, M23 | |||
COCLMCBI_00881 | 1.2e-208 | 2.7.7.7 | L | Transposase and inactivated derivatives | ||
COCLMCBI_00882 | 3.3e-116 | mepA | M | Membrane proteins related to metalloendopeptidases | ||
COCLMCBI_00883 | 2.2e-164 | |||||
COCLMCBI_00884 | 1e-83 | purN | 2.1.2.2, 2.1.2.3, 3.5.4.10 | 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 | |
COCLMCBI_00885 | 9e-260 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
COCLMCBI_00886 | 2.2e-66 | KLT | serine threonine protein kinase | |||
COCLMCBI_00887 | 1.4e-113 | V | Beta-lactamase | |||
COCLMCBI_00888 | 2.2e-114 | amtR | K | Transcriptional regulator | ||
COCLMCBI_00889 | 1.9e-156 | V | Beta-lactamase | |||
COCLMCBI_00890 | 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 | ||
COCLMCBI_00891 | 1.8e-47 | 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 | ||
COCLMCBI_00892 | 3.8e-23 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
COCLMCBI_00893 | 1.2e-35 | rpmB | J | Belongs to the bacterial ribosomal protein bL28 family | ||
COCLMCBI_00894 | 5.8e-19 | arsB | P | COG1055 Na H antiporter NhaD and related arsenite permeases | ||
COCLMCBI_00895 | 1.1e-136 | S | Protein of unknown function (DUF418) | |||
COCLMCBI_00896 | 6.2e-47 | rpmE2 | J | Ribosomal protein L31 | ||
COCLMCBI_00897 | 1.1e-23 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
COCLMCBI_00898 | 2.2e-120 | KT | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
COCLMCBI_00899 | 1.7e-231 | T | PhoQ Sensor | |||
COCLMCBI_00900 | 2.8e-179 | pepD | O | Trypsin-like serine proteases typically periplasmic contain C-terminal PDZ domain | ||
COCLMCBI_00901 | 4.1e-93 | moaB | 4.2.1.96 | H | Molybdenum cofactor biosynthesis protein | |
COCLMCBI_00903 | 6.9e-61 | 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 | ||
COCLMCBI_00904 | 3.6e-42 | cpaB | U | SAF | ||
COCLMCBI_00905 | 1.2e-82 | fthC | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
COCLMCBI_00906 | 1.2e-169 | galU | 2.7.7.9 | M | UDP-glucose pyrophosphorylase | |
COCLMCBI_00907 | 2e-220 | moeA | 2.10.1.1 | H | Molybdenum cofactor synthesis | |
COCLMCBI_00908 | 2.6e-126 | rimJ | 2.3.1.128 | J | Acetyltransferases including N-acetylases of ribosomal proteins | |
COCLMCBI_00909 | 4.3e-94 | |||||
COCLMCBI_00910 | 2.6e-97 | Q | Domain of unknown function (DUF4442) | |||
COCLMCBI_00911 | 6.5e-309 | ilvG | 2.2.1.6 | EH | Belongs to the TPP enzyme family | |
COCLMCBI_00912 | 1.1e-133 | tag | 3.2.2.20 | L | 3-methyladenine DNA glycosylase | |
COCLMCBI_00913 | 1.3e-61 | catD | S | membrane | ||
COCLMCBI_00914 | 8.3e-106 | sigC | S | integral membrane protein | ||
COCLMCBI_00915 | 2.3e-295 | pmt | 2.4.1.109 | GT39 | O | Dolichyl-phosphate-mannose--protein |
COCLMCBI_00916 | 8.4e-127 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
COCLMCBI_00917 | 6e-258 | betP | M | Belongs to the BCCT transporter (TC 2.A.15) family | ||
COCLMCBI_00918 | 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 | |
COCLMCBI_00919 | 2.3e-66 | S | Domain of unknown function (DUF3806) | |||
COCLMCBI_00920 | 1.7e-146 | tatD | L | Mg-dependent DNase | ||
COCLMCBI_00921 | 3.3e-190 | yabE | S | protein conserved in bacteria | ||
COCLMCBI_00922 | 1.5e-153 | ksgA | 2.1.1.182 | J | Specifically dimethylates two adjacent adenosines (A1518 and A1519) in the loop of a conserved hairpin near the 3'-end of 16S rRNA in the 30S particle. May play a critical role in biogenesis of 30S subunits | |
COCLMCBI_00923 | 1.4e-157 | ispE | 2.1.1.182, 2.7.1.148 | I | Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol | |
COCLMCBI_00924 | 0.0 | yjjK | S | ATPase components of ABC transporters with duplicated ATPase domains | ||
COCLMCBI_00925 | 8.6e-234 | 3.5.1.23 | S | Neutral/alkaline non-lysosomal ceramidase, N-terminal | ||
COCLMCBI_00926 | 1.4e-53 | S | Antibiotic biosynthesis monooxygenase | |||
COCLMCBI_00927 | 1.6e-160 | ppk2 | 2.7.4.1 | S | polyphosphate kinase | |
COCLMCBI_00928 | 7.1e-98 | mpg | 3.2.2.21 | L | Belongs to the DNA glycosylase MPG family | |
COCLMCBI_00929 | 2.8e-135 | supH | S | hydrolases of the HAD superfamily | ||
COCLMCBI_00930 | 1.8e-176 | echA3 | 4.2.1.17 | I | Enoyl-CoA hydratase carnithine racemase | |
COCLMCBI_00931 | 1.9e-275 | gapA | 1.2.1.12, 4.1.1.32 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
COCLMCBI_00932 | 1.7e-219 | manA | 1.14.13.81, 5.3.1.8, 5.4.2.8 | G | isomerase | |
COCLMCBI_00934 | 8e-205 | sqdX | M | Glycosyltransferase | ||
COCLMCBI_00935 | 9.8e-230 | sqdB | 3.13.1.1 | GM | Sulfolipid biosynthesis protein | |
COCLMCBI_00936 | 0.0 | MA20_22130 | S | FAD-binding dehydrogenase | ||
COCLMCBI_00938 | 6.5e-216 | dsdA | 4.3.1.18 | E | Belongs to the serine threonine dehydratase family. DsdA subfamily | |
COCLMCBI_00939 | 9.2e-218 | EGP | Permeases of the major facilitator superfamily | |||
COCLMCBI_00940 | 5.9e-130 | V | antibiotic catabolic process | |||
COCLMCBI_00941 | 4.8e-64 | |||||
COCLMCBI_00943 | 5.6e-201 | rbn | S | membrane | ||
COCLMCBI_00944 | 1e-159 | IQ | Dehydrogenases with different specificities (Related to short-chain alcohol dehydrogenases) | |||
COCLMCBI_00945 | 6.6e-159 | S | esterase of the alpha-beta hydrolase superfamily | |||
COCLMCBI_00946 | 6e-160 | S | esterase of the alpha-beta hydrolase superfamily | |||
COCLMCBI_00947 | 3.9e-253 | V | endonuclease | |||
COCLMCBI_00948 | 9.2e-250 | ybhI | P | Sodium:sulfate symporter transmembrane region | ||
COCLMCBI_00949 | 7.7e-310 | prfC | J | Increases the formation of ribosomal termination complexes and stimulates activities of RF-1 and RF-2. It binds guanine nucleotides and has strong preference for UGA stop codons. It may interact directly with the ribosome. The stimulation of RF- 1 and RF-2 is significantly reduced by GTP and GDP, but not by GMP | ||
COCLMCBI_00951 | 7e-98 | S | reductase | |||
COCLMCBI_00952 | 2.8e-109 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
COCLMCBI_00955 | 9.8e-164 | ycf23 | 1.1.1.205, 1.13.12.16 | S | 2-nitropropane dioxygenase | |
COCLMCBI_00956 | 8e-49 | |||||
COCLMCBI_00957 | 8e-97 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
COCLMCBI_00958 | 4.6e-99 | ctc | J | This is one of the proteins that binds to the 5S RNA in the ribosome where it forms part of the central protuberance | ||
COCLMCBI_00959 | 1.1e-166 | EGP | Permeases of the major facilitator superfamily | |||
COCLMCBI_00960 | 9.5e-267 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Belongs to the aldehyde dehydrogenase family | |
COCLMCBI_00961 | 3.1e-125 | aroP | E | Gamma-aminobutyrate permease and related permeases | ||
COCLMCBI_00962 | 1.5e-80 | aroP | E | Gamma-aminobutyrate permease and related permeases | ||
COCLMCBI_00963 | 1.8e-184 | 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) | |
COCLMCBI_00964 | 8.4e-247 | 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 | |
COCLMCBI_00966 | 8.8e-189 | EGP | Major facilitator Superfamily | |||
COCLMCBI_00967 | 2.4e-268 | Q | Tat pathway signal sequence domain protein | |||
COCLMCBI_00968 | 7.3e-10 | 3.6.4.13 | M | Cell wall-binding repeat protein | ||
COCLMCBI_00971 | 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 | ||
COCLMCBI_00972 | 8.9e-162 | proX | M | Periplasmic glycine betaine choline-binding (lipo)protein of an ABC-type transport system (osmoprotectant binding protein) | ||
COCLMCBI_00973 | 2.7e-115 | proZ | P | ABC transporter permease | ||
COCLMCBI_00974 | 7.1e-94 | proW | P | ABC-type proline glycine betaine transport systems, permease component | ||
COCLMCBI_00975 | 1.1e-139 | proV | E | COG1125 ABC-type proline glycine betaine transport systems, ATPase components | ||
COCLMCBI_00976 | 1.2e-101 | S | Abortive infection protein | |||
COCLMCBI_00977 | 1.7e-232 | ybjT | GM | NmrA-like family | ||
COCLMCBI_00979 | 9.9e-178 | btrU | S | Suppressor of fused protein (SUFU) | ||
COCLMCBI_00980 | 6.9e-135 | S | membrane | |||
COCLMCBI_00981 | 6.3e-247 | L | Transposase and inactivated derivatives | |||
COCLMCBI_00982 | 5.2e-69 | |||||
COCLMCBI_00983 | 3.4e-86 | 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 | ||
COCLMCBI_00984 | 4.4e-61 | S | Domain of unknown function (DUF4307) | |||
COCLMCBI_00985 | 5e-170 | mca | 3.5.1.115 | S | A mycothiol (MSH, N-acetylcysteinyl-glucosaminyl- inositol) S-conjugate amidase, it recycles conjugated MSH to the N-acetyl cysteine conjugate (AcCys S-conjugate, a mercapturic acid) and the MSH precursor. Involved in MSH-dependent detoxification of a number of alkylating agents and antibiotics | |
COCLMCBI_00986 | 2.8e-45 | |||||
COCLMCBI_00987 | 1.2e-135 | uppS1 | 2.5.1.31, 2.5.1.68 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
COCLMCBI_00988 | 8.6e-173 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
COCLMCBI_00989 | 3.6e-246 | 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 | |
COCLMCBI_00990 | 5.9e-35 | |||||
COCLMCBI_00991 | 2.7e-91 | K | Transcriptional regulator | |||
COCLMCBI_00992 | 1.9e-64 | M | protein potentially involved in peptidoglycan biosynthesis | |||
COCLMCBI_00993 | 2.1e-252 | phoH | T | ATPase related to phosphate starvation-inducible protein PhoH | ||
COCLMCBI_00994 | 7.8e-105 | ywnH | 2.3.1.183 | M | Sortase and related acyltransferases | |
COCLMCBI_00995 | 3.2e-265 | bmr3 | EGP | Major facilitator Superfamily | ||
COCLMCBI_00996 | 1.1e-256 | fumC | 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
COCLMCBI_00997 | 1.8e-179 | glpX | 3.1.3.11, 3.1.3.37 | G | fructose-1,6-bisphosphatase | |
COCLMCBI_00998 | 2.9e-85 | S | Protein of unknown function (DUF4245) | |||
COCLMCBI_00999 | 1e-38 | 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 | |
COCLMCBI_01000 | 1.1e-223 | 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 | |
COCLMCBI_01001 | 3.2e-146 | ispH | 1.17.7.4, 2.7.4.25 | IM | Catalyzes the conversion of 1-hydroxy-2-methyl-2-(E)- butenyl 4-diphosphate (HMBPP) into a mixture of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP). Acts in the terminal step of the DOXP MEP pathway for isoprenoid precursor biosynthesis | |
COCLMCBI_01002 | 9.9e-52 | E | amino acid transport | |||
COCLMCBI_01003 | 3.5e-165 | rmuC | S | DNA recombination protein | ||
COCLMCBI_01004 | 1.2e-238 | S | permease | |||
COCLMCBI_01005 | 2.6e-254 | S | Pfam PF00149 | |||
COCLMCBI_01006 | 1.5e-192 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
COCLMCBI_01007 | 1.5e-25 | |||||
COCLMCBI_01008 | 8.9e-262 | merA | 1.16.1.1 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
COCLMCBI_01009 | 2.4e-68 | K | Transcriptional regulator | |||
COCLMCBI_01010 | 9.5e-14 | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | |||
COCLMCBI_01011 | 3.5e-89 | 1.3.1.45 | GM | epimerase dehydratase | ||
COCLMCBI_01012 | 6.7e-44 | S | Bacteriocin (Lactococcin_972) | |||
COCLMCBI_01013 | 0.0 | |||||
COCLMCBI_01014 | 4.2e-130 | V | ABC transporter, ATP-binding protein | |||
COCLMCBI_01015 | 1.6e-42 | higB | S | Plasmid maintenance system killer protein | ||
COCLMCBI_01016 | 1.6e-46 | higA | K | Plasmid maintenance system antidote protein | ||
COCLMCBI_01017 | 1.7e-70 | S | Putative glycolipid-binding | |||
COCLMCBI_01019 | 1.2e-129 | irp6C | 3.6.3.34 | HP | ATP-binding protein | |
COCLMCBI_01020 | 1e-172 | irp6B | U | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
COCLMCBI_01021 | 1e-208 | irp6A | P | Periplasmic binding protein | ||
COCLMCBI_01022 | 3.7e-49 | prfA | J | Peptide chain release factor I | ||
COCLMCBI_01023 | 1.5e-56 | phnB2 | S | protein conserved in bacteria | ||
COCLMCBI_01024 | 8.5e-46 | chr | P | COG2059 Chromate transport protein ChrA | ||
COCLMCBI_01025 | 3.6e-135 | insK | L | Transposase and inactivated derivatives | ||
COCLMCBI_01026 | 7e-58 | L | Helix-turn-helix domain | |||
COCLMCBI_01027 | 3.9e-62 | cskE | S | Anti-sigma-K factor rskA | ||
COCLMCBI_01028 | 1.1e-85 | sigK | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
COCLMCBI_01030 | 2.8e-243 | dipZ | CO | Cytochrome C biogenesis protein transmembrane region | ||
COCLMCBI_01031 | 3.3e-37 | higA | K | Plasmid maintenance system antidote protein | ||
COCLMCBI_01032 | 1.7e-53 | prfA | J | Peptide chain release factor I | ||
COCLMCBI_01033 | 9.5e-101 | S | Putative glycolipid-binding | |||
COCLMCBI_01034 | 4.7e-29 | XK27_10495 | DJ | ParE toxin of type II toxin-antitoxin system, parDE | ||
COCLMCBI_01035 | 2.3e-20 | |||||
COCLMCBI_01036 | 1.3e-11 | S | Domain of unknown function (DUF1707) | |||
COCLMCBI_01037 | 1.1e-133 | tipA | K | transcriptional regulators | ||
COCLMCBI_01038 | 2.1e-33 | |||||
COCLMCBI_01039 | 2.1e-253 | S | protein with a von Willebrand factor type A (vWA) domain | |||
COCLMCBI_01040 | 6.7e-238 | chlI | 6.6.1.1 | H | COG1239 Mg-chelatase subunit ChlI | |
COCLMCBI_01041 | 3.9e-88 | 3.1.3.3, 3.1.3.73, 5.4.2.12 | G | COG0406 Fructose-2,6-bisphosphatase | ||
COCLMCBI_01042 | 1e-120 | BDLTU | Phosphatidylinositol | |||
COCLMCBI_01043 | 9.1e-90 | C | Protein of unknown function, DUF488 | |||
COCLMCBI_01044 | 1.6e-115 | arsO | P | flavoprotein involved in K transport | ||
COCLMCBI_01045 | 0.0 | cadA | P | E1-E2 ATPase | ||
COCLMCBI_01046 | 9.3e-59 | cmtR | K | transcriptional | ||
COCLMCBI_01047 | 5.7e-10 | C | Coenzyme F420-dependent N5N10-methylene tetrahydromethanopterin reductase and related | |||
COCLMCBI_01048 | 2.1e-77 | S | Protein of unknown function DUF2625 | |||
COCLMCBI_01049 | 1.3e-46 | prfA | J | Peptide chain release factor I | ||
COCLMCBI_01050 | 3.7e-99 | C | Protein of unknown function, DUF488 | |||
COCLMCBI_01051 | 7.8e-67 | E | glyoxalase | |||
COCLMCBI_01052 | 3.3e-31 | S | Ribbon-helix-helix protein, copG family | |||
COCLMCBI_01053 | 3.4e-82 | |||||
COCLMCBI_01054 | 7.6e-10 | |||||
COCLMCBI_01055 | 3.1e-86 | S | Putative glycolipid-binding | |||
COCLMCBI_01057 | 1.1e-79 | S | Domain of unknown function (DUF1707) | |||
COCLMCBI_01058 | 1.6e-79 | S | membrane | |||
COCLMCBI_01059 | 6e-142 | S | CAAX amino terminal protease family protein | |||
COCLMCBI_01060 | 5.3e-170 | tcsS5 | T | Histidine kinase | ||
COCLMCBI_01061 | 2.2e-101 | T | cheY-homologous receiver domain | |||
COCLMCBI_01062 | 1e-196 | yhaZ | L | DNA alkylation repair | ||
COCLMCBI_01065 | 7.6e-104 | ku | L | Ku70/Ku80 beta-barrel domain | ||
COCLMCBI_01066 | 1.8e-283 | ligD | 6.5.1.1, 6.5.1.6, 6.5.1.7 | L | DNA polymerase LigD polymerase domain | |
COCLMCBI_01067 | 3.4e-273 | yhgE | S | YhgE Pip domain protein | ||
COCLMCBI_01068 | 1.7e-125 | yplQ | S | protein, hemolysin III | ||
COCLMCBI_01069 | 2.9e-71 | speE | 2.5.1.16 | E | spermidine synthase | |
COCLMCBI_01070 | 5e-159 | IQ | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
COCLMCBI_01071 | 1.3e-233 | EGP | the major facilitator superfamily | |||
COCLMCBI_01072 | 8.7e-303 | F | Belongs to the 5'-nucleotidase family | |||
COCLMCBI_01073 | 0.0 | S | protein with a von Willebrand factor type A (vWA) domain | |||
COCLMCBI_01074 | 2.4e-259 | chlI | 6.6.1.1 | H | COG1239 Mg-chelatase subunit ChlI | |
COCLMCBI_01075 | 1.6e-100 | 3.1.3.3, 3.1.3.73, 5.4.2.12 | G | COG0406 Fructose-2,6-bisphosphatase | ||
COCLMCBI_01076 | 8.5e-139 | BDLTU | Phosphatidylinositol | |||
COCLMCBI_01077 | 6.8e-77 | tcmJ | G | Cupin domain | ||
COCLMCBI_01078 | 1.4e-47 | S | Domain of unknown function (DUF4298) | |||
COCLMCBI_01079 | 2e-12 | S | Domain of unknown function (DUF4298) | |||
COCLMCBI_01080 | 2.4e-128 | M | translation initiation factor activity | |||
COCLMCBI_01081 | 9.8e-137 | yedI | S | protein conserved in bacteria | ||
COCLMCBI_01082 | 1.4e-56 | S | Uncharacterized protein conserved in bacteria (DUF2218) | |||
COCLMCBI_01083 | 3.4e-98 | S | Protein of unknown function (DUF402) | |||
COCLMCBI_01084 | 3.7e-92 | |||||
COCLMCBI_01085 | 0.0 | typA | T | GTP-binding protein | ||
COCLMCBI_01086 | 4e-256 | lpqW | E | ABC transporter, substrate-binding protein, family 5 | ||
COCLMCBI_01087 | 1.8e-162 | mshB | 3.5.1.103 | S | Catalyzes the deacetylation of 1D-myo-inositol 2- acetamido-2-deoxy-alpha-D-glucopyranoside (GlcNAc-Ins) in the mycothiol biosynthesis pathway | |
COCLMCBI_01088 | 1.8e-12 | |||||
COCLMCBI_01089 | 1.7e-59 | fdxA | C | ferredoxin | ||
COCLMCBI_01090 | 6.5e-196 | dapC | E | Aspartate tyrosine aromatic aminotransferase | ||
COCLMCBI_01091 | 4.5e-103 | MA20_09515 | 2.4.1.83 | GT2 | S | GtrA-like protein |
COCLMCBI_01092 | 4.7e-194 | L | HNH endonuclease domain protein | |||
COCLMCBI_01093 | 1.8e-173 | dapD | 2.3.1.117 | E | Catalyzes the conversion of the cyclic tetrahydrodipicolinate (THDP) into the acyclic N-succinyl-L-2- amino-6-oxopimelate using succinyl-CoA | |
COCLMCBI_01094 | 1.6e-239 | aroP | E | amino acid | ||
COCLMCBI_01095 | 1.5e-240 | aroP | E | amino acid | ||
COCLMCBI_01096 | 7.4e-172 | dapD | 2.3.1.117 | E | Catalyzes the conversion of the cyclic tetrahydrodipicolinate (THDP) into the acyclic N-succinyl-L-2- amino-6-oxopimelate using succinyl-CoA | |
COCLMCBI_01097 | 1.5e-200 | dapE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
COCLMCBI_01098 | 2e-154 | fmt2 | 3.2.2.10 | S | Belongs to the LOG family | |
COCLMCBI_01099 | 3.8e-151 | folP2 | 2.5.1.15 | H | Catalyzes the condensation of para-aminobenzoate (pABA) with 6-hydroxymethyl-7,8-dihydropterin diphosphate (DHPt-PP) to form 7,8-dihydropteroate (H2Pte), the immediate precursor of folate derivatives | |
COCLMCBI_01100 | 1.1e-122 | gpgS | 2.4.1.266, 2.4.1.268 | GT81 | M | Glycosyltransferases involved in cell wall biogenesis |
COCLMCBI_01101 | 2.3e-49 | |||||
COCLMCBI_01102 | 1.7e-18 | S | Protein of unknown function (DUF3117) | |||
COCLMCBI_01103 | 6e-152 | rrmA | 2.1.1.187 | Q | SAM-dependent | |
COCLMCBI_01104 | 5.4e-264 | scrB | 3.2.1.26 | GH32 | G | Belongs to the glycosyl hydrolase 32 family |
COCLMCBI_01105 | 5.8e-219 | glgA | 2.4.1.342 | GT4 | G | Glycogen synthase, Corynebacterium family |
COCLMCBI_01106 | 1.8e-202 | glgC | 2.7.7.27 | H | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
COCLMCBI_01107 | 1.5e-97 | safC | S | O-methyltransferase | ||
COCLMCBI_01108 | 2.1e-106 | sigE | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
COCLMCBI_01109 | 6.2e-48 | cseE | 2.1.1.63 | K | AntiSigma factor | |
COCLMCBI_01110 | 1.9e-54 | tatB | U | Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. Together with TatC, TatB is part of a receptor directly interacting with Tat signal peptides. TatB may form an oligomeric binding site that transiently accommodates folded Tat precursor proteins before their translocation | ||
COCLMCBI_01111 | 4.4e-203 | mrp | D | Binds and transfers iron-sulfur (Fe-S) clusters to target apoproteins. Can hydrolyze ATP | ||
COCLMCBI_01112 | 5.1e-64 | |||||
COCLMCBI_01113 | 3e-44 | |||||
COCLMCBI_01114 | 0.0 | sucA | 1.2.4.2, 4.1.1.71 | C | 2-oxoglutarate dehydrogenase complex dehydrogenase (E1) component and related enzymes | |
COCLMCBI_01115 | 0.0 | V | ABC-type multidrug transport system, ATPase and permease components | |||
COCLMCBI_01116 | 4.5e-164 | S | 5-oxoprolinase (ATP-hydrolyzing) activity | |||
COCLMCBI_01117 | 4.9e-306 | lipT | CE10 | I | Belongs to the type-B carboxylesterase lipase family | |
COCLMCBI_01118 | 1.1e-126 | |||||
COCLMCBI_01119 | 8.3e-79 | |||||
COCLMCBI_01120 | 1.5e-199 | blt | EGP | Major facilitator Superfamily | ||
COCLMCBI_01121 | 9.1e-189 | iunH | 3.2.2.1 | F | inosine-uridine preferring nucleoside hydrolase | |
COCLMCBI_01123 | 5.1e-56 | V | HNH endonuclease | |||
COCLMCBI_01124 | 1.8e-174 | dcm | 2.1.1.37 | L | DNA restriction-modification system | |
COCLMCBI_01125 | 1.7e-53 | nudG | 3.6.1.55, 3.6.1.65 | L | NTP pyrophosphohydrolases including oxidative damage repair enzymes | |
COCLMCBI_01126 | 9.4e-153 | tnp7109-46 | L | Transposase and inactivated derivatives | ||
COCLMCBI_01127 | 9e-50 | L | Transposase and inactivated derivatives | |||
COCLMCBI_01128 | 2e-141 | 2.7.7.7 | L | Transposase and inactivated derivatives | ||
COCLMCBI_01129 | 9.4e-153 | tnp7109-46 | L | Transposase and inactivated derivatives | ||
COCLMCBI_01130 | 9e-50 | L | Transposase and inactivated derivatives | |||
COCLMCBI_01131 | 4.1e-88 | repB | EP | Plasmid replication protein | ||
COCLMCBI_01137 | 3.4e-115 | orn | L | 3'-to-5' exoribonuclease specific for small oligoribonucleotides | ||
COCLMCBI_01138 | 1.2e-143 | cmrA | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | ||
COCLMCBI_01139 | 1.1e-28 | yozG | K | Cro/C1-type HTH DNA-binding domain | ||
COCLMCBI_01140 | 8.4e-102 | |||||
COCLMCBI_01144 | 0.0 | P | CytoChrome c oxidase Caa3 assembly factor | |||
COCLMCBI_01145 | 6.5e-89 | L | Single-stranded DNA-binding protein | |||
COCLMCBI_01146 | 0.0 | yjjK | S | ATPase components of ABC transporters with duplicated ATPase domains | ||
COCLMCBI_01147 | 5.4e-66 | S | Thioesterase | |||
COCLMCBI_01148 | 1.4e-83 | |||||
COCLMCBI_01149 | 2.2e-217 | gulO | 1.1.3.8 | C | FAD FMN-containing dehydrogenases | |
COCLMCBI_01150 | 7.1e-196 | E | Alanine racemase, N-terminal domain | |||
COCLMCBI_01151 | 3.9e-74 | glbO | S | Hemoglobin-like protein | ||
COCLMCBI_01152 | 5.7e-222 | metB | 2.5.1.48, 4.4.1.1, 4.4.1.8 | E | Cystathionine beta-lyases cystathionine | |
COCLMCBI_01153 | 0.0 | pepN | 3.4.11.2 | E | aminopeptidase | |
COCLMCBI_01154 | 9.2e-115 | yjbH | Q | DSBA oxidoreductase | ||
COCLMCBI_01155 | 1e-84 | rpiB | 5.3.1.6 | G | Ribose 5-phosphate isomerase | |
COCLMCBI_01156 | 8.7e-65 | K | Psort location Cytoplasmic, score | |||
COCLMCBI_01157 | 8.9e-57 | S | Domain of unknown function (DUF4440) | |||
COCLMCBI_01158 | 5.7e-33 | |||||
COCLMCBI_01159 | 1.2e-12 | |||||
COCLMCBI_01160 | 9.6e-164 | S | N-terminal domain of galactosyltransferase | |||
COCLMCBI_01161 | 1.2e-155 | S | Glycosyl transferase, family 2 | |||
COCLMCBI_01162 | 5e-159 | |||||
COCLMCBI_01163 | 6.6e-168 | S | Glycosyl transferase, family 2 | |||
COCLMCBI_01164 | 1.9e-211 | M | Glycosyltransferase Family 4 | |||
COCLMCBI_01165 | 4.9e-171 | S | Glycosyl transferase, family 2 | |||
COCLMCBI_01166 | 7.7e-135 | S | Glycosyl transferase, family 2 | |||
COCLMCBI_01167 | 6.7e-176 | ycdO | P | periplasmic lipoprotein involved in iron transport | ||
COCLMCBI_01168 | 1.4e-131 | 4.2.1.17, 5.3.3.18 | I | Enoyl-CoA hydratase/isomerase | ||
COCLMCBI_01169 | 3.1e-181 | MA20_15180 | 1.13.12.16 | S | Nitronate monooxygenase | |
COCLMCBI_01170 | 1.6e-97 | |||||
COCLMCBI_01173 | 6.4e-236 | 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 | ||
COCLMCBI_01174 | 1.2e-103 | 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 | |
COCLMCBI_01175 | 7.1e-107 | 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 | |
COCLMCBI_01176 | 1.4e-47 | |||||
COCLMCBI_01177 | 6.3e-53 | |||||
COCLMCBI_01178 | 2.7e-140 | pcaD | 3.1.1.24, 3.4.11.5, 4.1.1.44 | S | hydrolases or acyltransferases (alpha beta hydrolase superfamily) | |
COCLMCBI_01179 | 2.3e-232 | 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 | ||
COCLMCBI_01180 | 3.4e-141 | ytfA | K | Transcriptional regulator | ||
COCLMCBI_01181 | 9.7e-183 | mdh | 1.1.1.37 | C | Catalyzes the reversible oxidation of malate to oxaloacetate | |
COCLMCBI_01182 | 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 | |
COCLMCBI_01183 | 8.5e-260 | folC | 6.3.2.12, 6.3.2.17 | H | Folylpolyglutamate synthase | |
COCLMCBI_01184 | 1.5e-77 | S | Protein of unknown function (DUF4233) | |||
COCLMCBI_01185 | 4e-212 | thlA | 2.3.1.9 | I | Belongs to the thiolase family | |
COCLMCBI_01186 | 0.0 | fadB | 1.1.1.35, 4.2.1.17, 5.1.2.3 | I | 3-hydroxyacyl-CoA dehydrogenase | |
COCLMCBI_01187 | 4.7e-46 | J | Acetyltransferases including N-acetylases of ribosomal proteins | |||
COCLMCBI_01188 | 1.6e-147 | S | Uncharacterized protein conserved in bacteria (DUF2262) | |||
COCLMCBI_01189 | 5.1e-226 | 1.3.8.6 | I | Acyl-CoA dehydrogenases | ||
COCLMCBI_01190 | 4.7e-224 | 1.3.8.6 | I | Acyl-CoA dehydrogenases | ||
COCLMCBI_01191 | 2.1e-280 | fadD7 | IQ | Acyl-CoA synthetases (AMP-forming) AMP-acid ligases II | ||
COCLMCBI_01192 | 2.2e-40 | |||||
COCLMCBI_01193 | 8.4e-72 | ndk | 2.7.4.6 | F | Major role in the synthesis of nucleoside triphosphates other than ATP. The ATP gamma phosphate is transferred to the NDP beta phosphate via a ping-pong mechanism, using a phosphorylated active-site intermediate | |
COCLMCBI_01194 | 4.3e-294 | phoD | 3.1.3.1 | P | Alkaline phosphatase D | |
COCLMCBI_01195 | 5.6e-301 | rne | 3.1.26.12 | J | Ribonucleases G and E | |
COCLMCBI_01196 | 8.3e-49 | |||||
COCLMCBI_01197 | 0.0 | S | Dynamin family | |||
COCLMCBI_01198 | 1.1e-259 | S | Dynamin family | |||
COCLMCBI_01199 | 3.3e-134 | hscA | O | Belongs to the heat shock protein 70 family | ||
COCLMCBI_01200 | 2.1e-198 | hscA | O | Belongs to the heat shock protein 70 family | ||
COCLMCBI_01201 | 2.5e-43 | hscA | O | Belongs to the heat shock protein 70 family | ||
COCLMCBI_01202 | 8.1e-91 | K | Belongs to the sigma-70 factor family. ECF subfamily | |||
COCLMCBI_01204 | 1.2e-46 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
COCLMCBI_01205 | 5.2e-54 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
COCLMCBI_01206 | 1.1e-278 | 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 | ||
COCLMCBI_01207 | 1.4e-193 | proB | 2.7.2.11 | E | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
COCLMCBI_01208 | 2e-137 | pdxB | 1.1.1.399, 1.1.1.95 | EH | Phosphoglycerate dehydrogenase and related dehydrogenases | |
COCLMCBI_01210 | 5.5e-210 | 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 | |
COCLMCBI_01211 | 5.3e-98 | |||||
COCLMCBI_01213 | 3.9e-122 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
COCLMCBI_01214 | 1.7e-76 | rsfS | 2.7.7.18 | J | Functions as a ribosomal silencing factor. Interacts with ribosomal protein L14 (rplN), blocking formation of intersubunit bridge B8. Prevents association of the 30S and 50S ribosomal subunits and the formation of functional ribosomes, thus repressing translation | |
COCLMCBI_01215 | 3.7e-109 | gpmB | 3.1.3.73, 3.1.3.85 | G | Belongs to the phosphoglycerate mutase family | |
COCLMCBI_01216 | 1.9e-128 | S | protein conserved in bacteria | |||
COCLMCBI_01217 | 5.7e-89 | comEA | L | DNA uptake protein and related DNA-binding proteins | ||
COCLMCBI_01218 | 2.5e-228 | comE | L | membrane metal-binding protein | ||
COCLMCBI_01219 | 4.5e-169 | holA | 2.7.7.7 | L | DNA polymerase III, delta' subunit | |
COCLMCBI_01220 | 8.8e-53 | S | ankyrin repeat | |||
COCLMCBI_01221 | 1.6e-93 | rhtC | E | threonine efflux protein | ||
COCLMCBI_01222 | 6.3e-123 | CE1 | Q | Poly(3-hydroxybutyrate) depolymerase | ||
COCLMCBI_01223 | 2.8e-36 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
COCLMCBI_01224 | 5.2e-93 | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
COCLMCBI_01225 | 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 | ||
COCLMCBI_01226 | 4.7e-91 | ligT | 3.1.4.58 | J | Hydrolyzes RNA 2',3'-cyclic phosphodiester to an RNA 2'- phosphomonoester | |
COCLMCBI_01227 | 1.7e-119 | S | CAAX protease self-immunity | |||
COCLMCBI_01228 | 0.0 | betP2 | M | Belongs to the BCCT transporter (TC 2.A.15) family | ||
COCLMCBI_01229 | 6.6e-248 | pip | 3.4.11.5 | S | hydrolases or acyltransferases (alpha beta hydrolase superfamily) | |
COCLMCBI_01231 | 1.9e-137 | 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 | |
COCLMCBI_01232 | 1.3e-238 | phoC | I | Membrane-associated phospholipid phosphatase | ||
COCLMCBI_01233 | 1.1e-245 | oppDF2 | P | Belongs to the ABC transporter superfamily | ||
COCLMCBI_01234 | 7e-139 | oppC4 | P | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
COCLMCBI_01235 | 4.9e-152 | oppB4 | P | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
COCLMCBI_01236 | 1.3e-255 | E | ABC-type dipeptide transport system periplasmic component | |||
COCLMCBI_01237 | 2.3e-126 | K | transcriptional | |||
COCLMCBI_01238 | 2.4e-176 | yvbT | C | Coenzyme F420-dependent N5N10-methylene tetrahydromethanopterin reductase and related | ||
COCLMCBI_01239 | 1.1e-80 | K | transcriptional | |||
COCLMCBI_01240 | 1.3e-135 | E | Glycine D-amino acid oxidases (deaminating) | |||
COCLMCBI_01241 | 7.6e-108 | phnD | P | ABC transporter, phosphonate, periplasmic substrate-binding protein | ||
COCLMCBI_01242 | 1.2e-98 | phnC | 3.6.3.28 | P | Part of the ABC transporter complex PhnCDE involved in phosphonates import. Responsible for energy coupling to the transport system | |
COCLMCBI_01243 | 1.6e-180 | phnE_2 | 3.6.1.63 | P | Binding-protein-dependent transport system inner membrane component | |
COCLMCBI_01244 | 5.2e-79 | S | HAD-hyrolase-like | |||
COCLMCBI_01245 | 5.8e-98 | 1.1.1.1 | E | COG1063 Threonine dehydrogenase and related Zn-dependent dehydrogenases | ||
COCLMCBI_01246 | 7.6e-253 | brnQ | E | Component of the transport system for branched-chain amino acids | ||
COCLMCBI_01247 | 1.8e-177 | treS | 2.4.1.18, 2.7.1.175, 3.2.1.1, 5.4.99.16 | CBM48,GH13 | G | protein, probably involved in trehalose biosynthesis |
COCLMCBI_01248 | 0.0 | treS | 3.2.1.1, 5.4.99.16 | GH13 | G | Trehalose synthase |
COCLMCBI_01249 | 6.1e-211 | aecD | 4.4.1.8 | E | Bifunctional PLP-dependent enzyme with beta-cystathionase and maltose regulon repressor activities | |
COCLMCBI_01251 | 0.0 | exsA | V | ABC-type multidrug transport system, ATPase and permease components | ||
COCLMCBI_01252 | 4.9e-88 | |||||
COCLMCBI_01253 | 9.5e-90 | idi | 5.3.3.2 | I | Catalyzes the 1,3-allylic rearrangement of the homoallylic substrate isopentenyl (IPP) to its highly electrophilic allylic isomer, dimethylallyl diphosphate (DMAPP) | |
COCLMCBI_01254 | 4.8e-235 | estC | CE10 | I | Belongs to the type-B carboxylesterase lipase family | |
COCLMCBI_01256 | 3.8e-16 | |||||
COCLMCBI_01257 | 0.0 | malQ | 2.4.1.18, 2.4.1.25, 3.2.1.196, 5.4.99.15 | CBM48,GH13,GH77 | G | 4-alpha-glucanotransferase |
COCLMCBI_01258 | 0.0 | acsbg2 | 6.2.1.3 | I | Long-chain acyl-CoA synthetases (AMP-forming) | |
COCLMCBI_01259 | 0.0 | acsbg2 | 6.2.1.3 | I | Long-chain acyl-CoA synthetases (AMP-forming) | |
COCLMCBI_01260 | 1.2e-94 | |||||
COCLMCBI_01261 | 1.5e-217 | hemN | H | Involved in the biosynthesis of porphyrin-containing compound | ||
COCLMCBI_01262 | 4.6e-172 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
COCLMCBI_01263 | 2e-192 | 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 | ||
COCLMCBI_01264 | 2.8e-118 | 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 | |
COCLMCBI_01265 | 1.5e-168 | phoH | T | Phosphate starvation-inducible protein PhoH | ||
COCLMCBI_01266 | 8e-108 | 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 | |
COCLMCBI_01267 | 4.3e-251 | corC | S | Hemolysins and related proteins containing CBS domains | ||
COCLMCBI_01268 | 4e-156 | pdxY | 2.7.1.35 | H | Belongs to the pyridoxine kinase family | |
COCLMCBI_01269 | 3.6e-191 | 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 | ||
COCLMCBI_01270 | 9.9e-132 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
COCLMCBI_01271 | 2.9e-134 | uppS | 2.5.1.31, 2.5.1.86, 2.5.1.88 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
COCLMCBI_01272 | 5.1e-72 | zur | P | Belongs to the Fur family | ||
COCLMCBI_01273 | 5.7e-72 | znr | K | transcriptional | ||
COCLMCBI_01274 | 2.3e-275 | glyQS | 6.1.1.14 | J | Catalyzes the attachment of glycine to tRNA(Gly) | |
COCLMCBI_01275 | 1.4e-88 | |||||
COCLMCBI_01276 | 3.8e-09 | |||||
COCLMCBI_01277 | 5e-266 | U | TPM domain | |||
COCLMCBI_01278 | 5.2e-237 | dgt | 3.1.5.1 | F | Belongs to the dGTPase family. Type 2 subfamily | |
COCLMCBI_01279 | 7.7e-15 | K | Psort location Cytoplasmic, score | |||
COCLMCBI_01280 | 2.5e-23 | rnaSA | 3.1.27.3 | F | Guanyl-specific ribonuclease Sa | |
COCLMCBI_01281 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
COCLMCBI_01282 | 1.9e-102 | 3.6.1.66 | S | MazG nucleotide pyrophosphohydrolase domain protein | ||
COCLMCBI_01283 | 1e-27 | S | Alpha helical Porin B | |||
COCLMCBI_01284 | 5.8e-131 | lpqU | M | Membrane-bound lytic murein transglycosylase B | ||
COCLMCBI_01285 | 2.3e-08 | |||||
COCLMCBI_01287 | 3.7e-235 | 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 | |
COCLMCBI_01288 | 3.7e-45 | divIC | D | septum formation initiator | ||
COCLMCBI_01289 | 7.6e-97 | ppx2 | 3.6.1.11, 3.6.1.40 | S | Septum formation initiator family protein | |
COCLMCBI_01290 | 4.7e-158 | ppx | 3.6.1.11, 3.6.1.40 | FP | Exopolyphosphatase | |
COCLMCBI_01291 | 5.5e-40 | |||||
COCLMCBI_01294 | 2.7e-91 | |||||
COCLMCBI_01295 | 1.2e-219 | MA20_32325 | 3.4.17.11 | E | Peptidase dimerisation domain | |
COCLMCBI_01296 | 6.1e-151 | bla | V | Beta-lactamase class C and other penicillin binding proteins | ||
COCLMCBI_01297 | 1.5e-142 | S | membrane | |||
COCLMCBI_01299 | 2.1e-14 | IQ | acyl carrier protein | |||
COCLMCBI_01300 | 3.5e-172 | S | hydrolases or acyltransferases alpha beta hydrolase superfamily | |||
COCLMCBI_01301 | 1e-292 | ethA | 1.14.13.22 | P | flavoprotein involved in K transport | |
COCLMCBI_01303 | 6e-18 | L | Excalibur calcium-binding domain | |||
COCLMCBI_01308 | 0.0 | aceE | 1.2.4.1 | C | component of the pyruvate dehydrogenase (PDH) complex, that catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2) | |
COCLMCBI_01309 | 1.1e-68 | S | Protein of unknown function (DUF3052) | |||
COCLMCBI_01312 | 3e-144 | surf1 | S | SURF1-like protein | ||
COCLMCBI_01313 | 9.5e-80 | ptpA | 3.1.3.48 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
COCLMCBI_01314 | 8.8e-116 | pgp | 3.1.3.18 | S | HAD hydrolase, family IA, variant 1 | |
COCLMCBI_01315 | 8.5e-215 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
COCLMCBI_01316 | 7.1e-113 | CP_0228 | 3.5.4.16 | S | Zn-ribbon protein | |
COCLMCBI_01317 | 1.6e-197 | rnhA | 3.1.26.4, 3.1.3.3, 3.1.3.73, 3.1.3.85, 5.4.2.12 | GL | Ribonuclease HI | |
COCLMCBI_01318 | 6e-256 | rnr | K | Exoribonuclease R | ||
COCLMCBI_01319 | 3.3e-193 | galK | 2.7.1.157, 2.7.1.6 | G | Belongs to the GHMP kinase family | |
COCLMCBI_01320 | 7.3e-32 | |||||
COCLMCBI_01321 | 5.2e-93 | K | Psort location Cytoplasmic, score | |||
COCLMCBI_01322 | 2.4e-277 | S | CHAD domain protein | |||
COCLMCBI_01323 | 3.7e-254 | glnA2 | 6.3.1.2 | E | glutamine synthetase | |
COCLMCBI_01324 | 0.0 | glnE | 2.7.7.42, 2.7.7.89 | H | Involved in the regulation of glutamine synthetase GlnA, a key enzyme in the process to assimilate ammonia. When cellular nitrogen levels are high, the C-terminal adenylyl transferase (AT) inactivates GlnA by covalent transfer of an adenylyl group from ATP to specific tyrosine residue of GlnA, thus reducing its activity. Conversely, when nitrogen levels are low, the N-terminal adenylyl removase (AR) activates GlnA by removing the adenylyl group by phosphorolysis, increasing its activity. The regulatory region of GlnE binds the signal transduction protein PII (GlnB) which indicates the nitrogen status of the cell | |
COCLMCBI_01325 | 8.3e-48 | |||||
COCLMCBI_01326 | 2.6e-272 | thrC | 4.2.3.1 | E | Threonine synthase | |
COCLMCBI_01327 | 5.2e-24 | |||||
COCLMCBI_01328 | 5.1e-171 | O | Trypsin | |||
COCLMCBI_01329 | 1.4e-107 | |||||
COCLMCBI_01330 | 1.2e-91 | 3.6.1.55 | L | NTP pyrophosphohydrolases including oxidative damage repair enzymes | ||
COCLMCBI_01331 | 3.6e-103 | M | Glycosyl hydrolases family 25 | |||
COCLMCBI_01332 | 3.4e-50 | |||||
COCLMCBI_01333 | 7.6e-161 | mae1 | P | Tellurite resistance protein and related permeases | ||
COCLMCBI_01335 | 2e-45 | S | CAAX protease self-immunity | |||
COCLMCBI_01336 | 9.2e-283 | glnA | 6.3.1.2 | E | glutamine synthetase | |
COCLMCBI_01337 | 4.3e-80 | S | RDD family | |||
COCLMCBI_01339 | 1.1e-134 | S | Domain of unknown function (DUF4191) | |||
COCLMCBI_01340 | 3.4e-175 | I | MaoC like domain | |||
COCLMCBI_01341 | 5.4e-245 | IQ | Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
COCLMCBI_01342 | 3.1e-237 | fadI | 2.3.1.9 | I | Catalyzes the synthesis of acetoacetyl coenzyme A from two molecules of acetyl coenzyme A. It can also act as a thiolase, catalyzing the reverse reaction and generating two-carbon units from the four-carbon product of fatty acid oxidation | |
COCLMCBI_01343 | 0.0 | acx | 1.3.3.6 | I | Acyl-CoA dehydrogenases | |
COCLMCBI_01344 | 7.7e-205 | lipA | 2.8.1.8 | H | Catalyzes the radical-mediated insertion of two sulfur atoms into the C-6 and C-8 positions of the octanoyl moiety bound to the lipoyl domains of lipoate-dependent enzymes, thereby converting the octanoylated domains into lipoylated derivatives | |
COCLMCBI_01345 | 3.4e-132 | lipB | 2.3.1.181 | H | Catalyzes the transfer of endogenously produced octanoic acid from octanoyl-acyl-carrier-protein onto the lipoyl domains of lipoate-dependent enzymes. Lipoyl-ACP can also act as a substrate although octanoyl-ACP is likely to be the physiological substrate | |
COCLMCBI_01346 | 4.3e-65 | gcvH | E | The glycine cleavage system catalyzes the degradation of glycine. The H protein shuttles the methylamine group of glycine from the P protein to the T protein | ||
COCLMCBI_01347 | 1.3e-201 | gcvT | 2.1.2.10 | E | The glycine cleavage system catalyzes the degradation of glycine | |
COCLMCBI_01348 | 0.0 | gcvP | 1.4.4.2 | E | Belongs to the GcvP family | |
COCLMCBI_01349 | 1.2e-310 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dak1 domain | |
COCLMCBI_01350 | 1.1e-258 | sucB | 2.3.1.61 | C | Pyruvate 2-oxoglutarate dehydrogenase complex dihydrolipoamide acyltransferase (E2) component and related enzymes | |
COCLMCBI_01351 | 1e-64 | |||||
COCLMCBI_01352 | 1.5e-278 | pepA | 3.4.11.1 | E | Presumably involved in the processing and regular turnover of intracellular proteins. Catalyzes the removal of unsubstituted N-terminal amino acids from various peptides | |
COCLMCBI_01353 | 4.3e-203 | ilvE | 2.6.1.42 | EH | Branched-chain amino acid aminotransferase | |
COCLMCBI_01354 | 2.3e-166 | cobT | 2.4.2.21 | H | the synthesis of alpha-ribazole-5'-phosphate from nicotinate mononucleotide (NAMN) and 5,6- dimethylbenzimidazole (DMB) | |
COCLMCBI_01355 | 2.4e-101 | S | Protein of unknown function (DUF3043) | |||
COCLMCBI_01356 | 2.6e-58 | erpA | S | Belongs to the HesB IscA family | ||
COCLMCBI_01357 | 0.0 | asnB | 6.3.5.4 | E | Asparagine synthase | |
COCLMCBI_01358 | 7.3e-155 | ctaC | 1.9.3.1 | C | Heme copper-type cytochrome quinol oxidases subunit 2 | |
COCLMCBI_01359 | 3.8e-75 | ctaF | C | Belongs to the cytochrome c oxidase bacterial subunit CtaF family | ||
COCLMCBI_01360 | 1.9e-100 | ctaE | 1.9.3.1 | C | Heme copper-type cytochrome quinol oxidase subunit 3 | |
COCLMCBI_01361 | 3e-156 | qcrC | C | cytochrome C | ||
COCLMCBI_01362 | 1.1e-239 | qcrA | C | C reductase | ||
COCLMCBI_01363 | 2.3e-311 | petD | C | cytochrome b subunit | ||
COCLMCBI_01364 | 3.8e-86 | M | NlpC/P60 family | |||
COCLMCBI_01365 | 1.1e-136 | M | Cell wall-associated hydrolases | |||
COCLMCBI_01366 | 2.2e-175 | pimB | 2.4.1.346, 3.2.1.8 | GT4 | M | Glycosyltransferase, group 1 family protein |
COCLMCBI_01367 | 2.4e-170 | glk | 2.7.1.2 | G | Transcriptional regulator sugar kinase | |
COCLMCBI_01368 | 2.5e-146 | plsC | 2.3.1.51 | I | Acyltransferase | |
COCLMCBI_01369 | 2e-94 | L | Exonuclease that cleaves single-stranded 3' overhangs of double-stranded RNA | |||
COCLMCBI_01370 | 3.4e-266 | aroG | 2.5.1.54 | E | Belongs to the class-II DAHP synthase family | |
COCLMCBI_01371 | 6.1e-177 | KLT | serine threonine protein kinase | |||
COCLMCBI_01372 | 4.1e-57 | S | transcriptional regulator | |||
COCLMCBI_01373 | 1.1e-245 | mptA | S | Carotene biosynthesis associated membrane protein | ||
COCLMCBI_01374 | 2.9e-191 | crtE | 2.5.1.1, 2.5.1.10, 2.5.1.29 | H | Belongs to the FPP GGPP synthase family | |
COCLMCBI_01375 | 5.4e-96 | K | GNAT family | |||
COCLMCBI_01376 | 5.6e-58 | |||||
COCLMCBI_01377 | 6.8e-55 | S | Protein of unknown function (DUF3040) | |||
COCLMCBI_01378 | 1.5e-74 | mraZ | K | Belongs to the MraZ family | ||
COCLMCBI_01379 | 6.6e-171 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
COCLMCBI_01380 | 8.6e-64 | ftsL | D | Essential cell division protein. May link together the upstream cell division proteins, which are predominantly cytoplasmic, with the downstream cell division proteins, which are predominantly periplasmic | ||
COCLMCBI_01381 | 0.0 | ftsI | 3.4.16.4 | M | Cell division protein FtsI penicillin-binding protein | |
COCLMCBI_01382 | 1.7e-250 | murE | 6.3.2.10, 6.3.2.13 | M | Catalyzes the addition of meso-diaminopimelic acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
COCLMCBI_01383 | 4.7e-253 | murF | 6.3.2.10 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
COCLMCBI_01384 | 4.1e-198 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
COCLMCBI_01385 | 1.3e-239 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
COCLMCBI_01386 | 6.7e-238 | ftsW | 2.4.1.227 | GT28 | D | Belongs to the SEDS family |
COCLMCBI_01387 | 5.3e-177 | 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) |
COCLMCBI_01388 | 1.8e-246 | murC | 6.3.2.8 | M | Belongs to the MurCDEF family | |
COCLMCBI_01389 | 4.6e-96 | ftsQ | 6.3.2.4 | D | Cell division protein FtsQ | |
COCLMCBI_01390 | 3.5e-207 | ftsZ | D | Essential cell division protein that forms a contractile ring structure (Z ring) at the future cell division site. The regulation of the ring assembly controls the timing and the location of cell division. One of the functions of the FtsZ ring is to recruit other cell division proteins to the septum to produce a new cell wall between the dividing cells. Binds GTP and shows GTPase activity | ||
COCLMCBI_01391 | 1e-114 | yfiH | S | Belongs to the multicopper oxidase YfiH RL5 family | ||
COCLMCBI_01392 | 6.4e-120 | yggS | S | Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis | ||
COCLMCBI_01393 | 2.5e-55 | 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 | ||
COCLMCBI_01394 | 2.3e-39 | yggT | S | Integral membrane protein | ||
COCLMCBI_01395 | 7.1e-31 | ag84 | D | Cell division initiation protein | ||
COCLMCBI_01396 | 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) | |
COCLMCBI_01397 | 1.9e-131 | |||||
COCLMCBI_01398 | 1.8e-230 | dinB | 2.7.7.7 | L | Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII | |
COCLMCBI_01399 | 6.3e-117 | ansA | 3.5.1.1 | EJ | L-asparaginase archaeal Glu-tRNAGln amidotransferase subunit D | |
COCLMCBI_01400 | 1.9e-79 | |||||
COCLMCBI_01401 | 1.2e-302 | yheS_2 | S | ATPase components of ABC transporters with duplicated ATPase domains | ||
COCLMCBI_01402 | 5.8e-125 | |||||
COCLMCBI_01403 | 1.1e-90 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
COCLMCBI_01404 | 1.2e-171 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
COCLMCBI_01405 | 1.4e-63 | |||||
COCLMCBI_01406 | 9.1e-156 | macA | M | Barrel-sandwich domain of CusB or HlyD membrane-fusion | ||
COCLMCBI_01407 | 1.6e-137 | macB | V | ABC transporter, ATP-binding protein | ||
COCLMCBI_01408 | 9.1e-189 | yknZ | V | Efflux ABC transporter, permease protein | ||
COCLMCBI_01409 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase | |
COCLMCBI_01410 | 2.4e-28 | |||||
COCLMCBI_01411 | 1.5e-236 | ilvA | 4.3.1.19 | E | Catalyzes the anaerobic formation of alpha-ketobutyrate and ammonia from threonine in a two-step reaction. The first step involved a dehydration of threonine and a production of enamine intermediates (aminocrotonate), which tautomerizes to its imine form (iminobutyrate). Both intermediates are unstable and short- lived. The second step is the nonenzymatic hydrolysis of the enamine imine intermediates to form 2-ketobutyrate and free ammonia. In the low water environment of the cell, the second step is accelerated by RidA | |
COCLMCBI_01412 | 0.0 | treZ | 3.2.1.141 | CBM48,GH13 | G | 4-alpha-D-((1- 4)-alpha-D-glucano)trehalose trehalohydrolase |
COCLMCBI_01413 | 1.6e-101 | yigZ | 2.1.1.45, 3.4.13.9 | S | Uncharacterized protein family UPF0029 | |
COCLMCBI_01414 | 9.8e-33 | |||||
COCLMCBI_01415 | 2.3e-60 | hslR | 5.4.99.23, 5.4.99.24 | J | Ribosome-associated heat shock protein implicated in the recycling of the 50S subunit (S4 paralog) | |
COCLMCBI_01416 | 2.2e-151 | S | Protein of unknown function (DUF1266) | |||
COCLMCBI_01417 | 7.7e-14 | |||||
COCLMCBI_01419 | 0.0 | treY | 2.4.1.25, 5.4.99.15 | GH13,GH77 | G | Maltooligosyl trehalose synthase |
COCLMCBI_01420 | 1.4e-97 | S | Protein of unknown function (DUF1266) | |||
COCLMCBI_01421 | 1.9e-12 | |||||
COCLMCBI_01423 | 5.2e-85 | |||||
COCLMCBI_01424 | 4.1e-188 | ligA | 2.7.7.7, 6.5.1.2 | L | COG0847 DNA polymerase III, epsilon subunit and related 3'-5' exonucleases | |
COCLMCBI_01425 | 0.0 | glgX | 3.2.1.68 | CBM48,GH13 | G | Belongs to the glycosyl hydrolase 13 family |
COCLMCBI_01426 | 6.7e-80 | tetR | K | Transcriptional regulator | ||
COCLMCBI_01427 | 1.3e-96 | |||||
COCLMCBI_01428 | 1.7e-29 | |||||
COCLMCBI_01429 | 1.4e-213 | 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 | |
COCLMCBI_01430 | 3e-193 | hisC | 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
COCLMCBI_01431 | 1.1e-109 | hisB | 1.1.1.23, 2.6.1.9, 3.1.3.15, 4.2.1.19 | E | imidazoleglycerol-phosphate dehydratase | |
COCLMCBI_01432 | 2.4e-07 | |||||
COCLMCBI_01433 | 8.4e-197 | EGP | Major facilitator Superfamily | |||
COCLMCBI_01434 | 1.2e-117 | 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 | ||
COCLMCBI_01435 | 3.6e-129 | hisA | 5.3.1.16, 5.3.1.24 | E | 1-(5-phosphoribosyl)-5- (5-phosphoribosylamino)methylideneamino imidazole-4-carboxamide isomerase | |
COCLMCBI_01436 | 2.5e-141 | impA | 3.1.3.25 | G | Archaeal fructose-16-bisphosphatase and related enzymes of inositol monophosphatase family | |
COCLMCBI_01437 | 3.4e-138 | hisF | 4.1.3.27 | 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 | |
COCLMCBI_01438 | 6.1e-61 | hisI | 3.5.4.19, 3.6.1.31 | E | Catalyzes the hydrolysis of the adenine ring of phosphoribosyl-AMP | |
COCLMCBI_01439 | 9.9e-107 | S | Trp region conserved | |||
COCLMCBI_01440 | 2.7e-146 | trpC | 4.1.1.48 | E | Indole-3-glycerol phosphate synthase | |
COCLMCBI_01441 | 6.3e-168 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
COCLMCBI_01442 | 1.5e-264 | pyk | 2.7.1.40 | G | Belongs to the pyruvate kinase family | |
COCLMCBI_01443 | 0.0 | uvrA2 | L | Excinuclease ATPase subunit | ||
COCLMCBI_01444 | 1.8e-125 | styA | 2.6.1.42, 3.2.1.21 | GH3 | EH | Amino-transferase class IV |
COCLMCBI_01445 | 0.0 | pabB | 2.6.1.85, 4.1.3.38, 5.4.4.2 | HQ | Anthranilate synthase component I, N terminal region | |
COCLMCBI_01446 | 2.4e-11 | ydaH | H | Transporter | ||
COCLMCBI_01447 | 1.5e-118 | S | Suppressor of fused protein (SUFU) | |||
COCLMCBI_01448 | 0.0 | glgP | 2.4.1.1 | GT35 | G | Phosphorylase is an important allosteric enzyme in carbohydrate metabolism. Enzymes from different sources differ in their regulatory mechanisms and in their natural substrates. However, all known phosphorylases share catalytic and structural properties |
COCLMCBI_01449 | 5.1e-256 | C | uridylyltransferase | |||
COCLMCBI_01450 | 1.5e-62 | |||||
COCLMCBI_01451 | 2.9e-205 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
COCLMCBI_01452 | 3.8e-262 | gdhA | 1.4.1.3, 1.4.1.4 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
COCLMCBI_01453 | 2.6e-21 | D | Cell division initiation protein | |||
COCLMCBI_01454 | 1.9e-95 | yceD | S | metal-binding, possibly nucleic acid-binding protein | ||
COCLMCBI_01455 | 1.9e-133 | 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 | |
COCLMCBI_01456 | 9.2e-150 | 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 | |
COCLMCBI_01457 | 3.4e-278 | agcS | E | alanine symporter | ||
COCLMCBI_01458 | 2.2e-42 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
COCLMCBI_01459 | 0.0 | smc | D | Required for chromosome condensation and partitioning | ||
COCLMCBI_01461 | 3.7e-179 | 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) | ||
COCLMCBI_01462 | 3.3e-184 | amt | P | ammonium transporter | ||
COCLMCBI_01463 | 5.4e-40 | glnK | K | nitrogen regulatory protein P-II | ||
COCLMCBI_01464 | 3.2e-237 | 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 | |
COCLMCBI_01465 | 0.0 | wbpC | I | acyltransferases | ||
COCLMCBI_01466 | 6.5e-64 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
COCLMCBI_01467 | 2.3e-219 | K | Transcriptional regulator | |||
COCLMCBI_01468 | 6.6e-163 | |||||
COCLMCBI_01469 | 4e-269 | |||||
COCLMCBI_01470 | 1.1e-86 | 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 | ||
COCLMCBI_01471 | 4.3e-225 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
COCLMCBI_01472 | 2e-58 | 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 | ||
COCLMCBI_01473 | 7.4e-146 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
COCLMCBI_01474 | 1.7e-106 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
COCLMCBI_01475 | 1.8e-50 | S | Protein of unknown function (DUF2469) | |||
COCLMCBI_01476 | 1.4e-65 | yraN | L | Belongs to the UPF0102 family | ||
COCLMCBI_01477 | 4.1e-281 | comM | O | ATPase with chaperone activity | ||
COCLMCBI_01478 | 5.6e-217 | dprA | 5.99.1.2 | LU | Rossmann fold nucleotide-binding protein involved in DNA uptake | |
COCLMCBI_01481 | 2.6e-155 | xerC | D | Belongs to the 'phage' integrase family. XerC subfamily | ||
COCLMCBI_01482 | 1.3e-88 | M | Membrane proteins related to metalloendopeptidases | |||
COCLMCBI_01483 | 5.7e-143 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
COCLMCBI_01484 | 1.3e-137 | 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 | ||
COCLMCBI_01485 | 4.3e-135 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
COCLMCBI_01486 | 3.6e-139 | ydcZ | S | protein conserved in bacteria | ||
COCLMCBI_01487 | 1.6e-178 | 3.5.1.4 | J | Belongs to the amidase family | ||
COCLMCBI_01488 | 3.4e-92 | 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 | ||
COCLMCBI_01489 | 1.2e-158 | cdsA | 2.7.7.41, 2.7.7.67 | I | Belongs to the CDS family | |
COCLMCBI_01490 | 6.6e-212 | rlmN | 2.1.1.192 | J | Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs | |
COCLMCBI_01491 | 8.6e-55 | S | NADH-flavin reductase | |||
COCLMCBI_01492 | 5.5e-73 | pecM | EG | Permeases of the drug metabolite transporter DMT superfamily | ||
COCLMCBI_01493 | 1.4e-92 | K | Transcriptional regulator | |||
COCLMCBI_01494 | 2e-89 | S | Protein of unknown function (DUF2631) | |||
COCLMCBI_01495 | 1.6e-197 | dxr | 1.1.1.267 | I | Catalyzes the NADP-dependent rearrangement and reduction of 1-deoxy-D-xylulose-5-phosphate (DXP) to 2-C-methyl-D-erythritol 4-phosphate (MEP) | |
COCLMCBI_01496 | 1.5e-214 | rseP | M | membrane-associated Zn-dependent proteases 1 | ||
COCLMCBI_01497 | 8.7e-215 | ispG | 1.17.7.1, 1.17.7.3 | I | Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate | |
COCLMCBI_01498 | 0.0 | pbp2B | 3.4.16.4 | M | Cell division protein FtsI penicillin-binding protein 2 | |
COCLMCBI_01499 | 1e-162 | map | 3.4.11.18 | E | Methionine aminopeptidase | |
COCLMCBI_01500 | 8.8e-21 | |||||
COCLMCBI_01501 | 7.8e-13 | |||||
COCLMCBI_01502 | 1.7e-10 | mtr | 1.8.1.15, 1.8.1.4 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
COCLMCBI_01503 | 1.7e-265 | mtr | 1.8.1.15, 1.8.1.4 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
COCLMCBI_01504 | 7.1e-197 | I | Lysophospholipase | |||
COCLMCBI_01505 | 4.6e-299 | mqo | 1.1.5.4 | C | malate quinone oxidoreductase | |
COCLMCBI_01506 | 2e-214 | ydiU | S | Uncharacterized ACR, YdiU/UPF0061 family | ||
COCLMCBI_01507 | 1.9e-127 | cysG | 1.13.11.79, 1.3.1.76, 2.1.1.107, 4.99.1.4 | H | Uroporphyrinogen-III | |
COCLMCBI_01508 | 7.5e-159 | rlmG | 2.1.1.172, 2.1.1.174 | J | Methyltransferase small domain | |
COCLMCBI_01509 | 4.3e-81 | 3.1.31.1 | L | Staphylococcal nuclease homologues | ||
COCLMCBI_01510 | 3.3e-124 | |||||
COCLMCBI_01511 | 3.5e-158 | K | Psort location Cytoplasmic, score | |||
COCLMCBI_01512 | 0.0 | proS | 6.1.1.15 | J | Catalyzes the attachment of proline to tRNA(Pro) in a two-step reaction proline is first activated by ATP to form Pro- AMP and then transferred to the acceptor end of tRNA(Pro). As ProRS can inadvertently accommodate and process non-cognate amino acids such as alanine and cysteine, to avoid such errors it has two additional distinct editing activities against alanine. One activity is designated as 'pretransfer' editing and involves the tRNA(Pro)-independent hydrolysis of activated Ala-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Ala-tRNA(Pro). The misacylated Cys- tRNA(Pro) is not edited by ProRS | |
COCLMCBI_01513 | 4e-112 | yaaA | S | Belongs to the UPF0246 family | ||
COCLMCBI_01514 | 5.1e-113 | |||||
COCLMCBI_01515 | 5e-94 | rimP | S | Required for maturation of 30S ribosomal subunits | ||
COCLMCBI_01516 | 8.8e-179 | nusA | K | Participates in both transcription termination and antitermination | ||
COCLMCBI_01517 | 1.7e-28 | ylxR | K | nucleic-acid-binding protein implicated in transcription termination | ||
COCLMCBI_01518 | 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 | ||
COCLMCBI_01519 | 3e-67 | 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 | ||
COCLMCBI_01520 | 3.4e-135 | nrnA | 2.7.7.72, 3.1.13.3, 3.1.3.7 | S | Exopolyphosphatase-related proteins | |
COCLMCBI_01521 | 1.8e-197 | dinF | V | Na -driven multidrug efflux pump | ||
COCLMCBI_01522 | 1e-142 | S | serine threonine protein phosphatase | |||
COCLMCBI_01523 | 6e-115 | pptA | Q | Belongs to the P-Pant transferase superfamily | ||
COCLMCBI_01524 | 4.5e-13 | |||||
COCLMCBI_01525 | 0.0 | |||||
COCLMCBI_01526 | 1.5e-142 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
COCLMCBI_01527 | 3.4e-156 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
COCLMCBI_01528 | 2.5e-167 | iunH2 | 3.2.2.1 | F | nucleoside | |
COCLMCBI_01529 | 5e-41 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
COCLMCBI_01530 | 0.0 | pnp | 2.7.7.8 | J | Involved in mRNA degradation. Catalyzes the phosphorolysis of single-stranded polyribonucleotides processively in the 3'- to 5'-direction | |
COCLMCBI_01531 | 3.3e-97 | S | PFAM Sporulation and spore germination | |||
COCLMCBI_01532 | 2.9e-115 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
COCLMCBI_01533 | 2.5e-130 | thyX | 2.1.1.148 | 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 NADPH and FADH(2) as the reductant | |
COCLMCBI_01534 | 1.9e-153 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
COCLMCBI_01535 | 0.0 | rnj | S | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
COCLMCBI_01536 | 2.9e-17 | |||||
COCLMCBI_01537 | 9.8e-112 | 1.17.1.9, 1.7.7.2 | C | molybdopterin cofactor binding | ||
COCLMCBI_01538 | 0.0 | ftsK | D | DNA segregation ATPase FtsK SpoIIIE and related proteins | ||
COCLMCBI_01539 | 2.6e-211 | terC | P | Membrane protein TerC, possibly involved in tellurium resistance | ||
COCLMCBI_01540 | 1.6e-39 | S | protein conserved in bacteria | |||
COCLMCBI_01541 | 1.7e-94 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
COCLMCBI_01542 | 1.3e-100 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
COCLMCBI_01543 | 2.9e-52 | clgR | K | transcriptional regulators | ||
COCLMCBI_01544 | 4.8e-141 | pspA | KT | Phage shock protein A (IM30), suppresses sigma54-dependent transcription | ||
COCLMCBI_01545 | 2.5e-104 | bioN | P | Cobalt transport protein | ||
COCLMCBI_01546 | 2.6e-118 | bioM | P | ABC transporter, ATP-binding protein | ||
COCLMCBI_01547 | 1e-44 | bioY | S | BioY family | ||
COCLMCBI_01548 | 9.4e-155 | L | HNH endonuclease domain protein | |||
COCLMCBI_01549 | 7e-34 | S | Protein of unknown function (DUF3046) | |||
COCLMCBI_01550 | 3.4e-214 | 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 | ||
COCLMCBI_01551 | 2.4e-99 | recX | S | Modulates RecA activity | ||
COCLMCBI_01552 | 1.9e-150 | gluB | ET | ABC-type amino acid transport signal transduction systems periplasmic component domain | ||
COCLMCBI_01553 | 3.6e-280 | miaB | 2.8.4.3 | J | Catalyzes the methylthiolation of N6- (dimethylallyl)adenosine (i(6)A), leading to the formation of 2- methylthio-N6-(dimethylallyl)adenosine (ms(2)i(6)A) at position 37 in tRNAs that read codons beginning with uridine | |
COCLMCBI_01554 | 3.8e-95 | |||||
COCLMCBI_01556 | 3.1e-300 | glt | E | Belongs to the glutamate synthase family | ||
COCLMCBI_01557 | 8.3e-172 | 2.3.1.178, 2.3.1.57, 2.3.1.82 | J | Histone acetyltransferase HPA2 and related acetyltransferases | ||
COCLMCBI_01558 | 1.5e-160 | D | Domain of Unknown Function (DUF349) | |||
COCLMCBI_01559 | 1.7e-94 | 2.8.4.3 | S | ferrous iron binding | ||
COCLMCBI_01560 | 5.2e-154 | miaA | 2.5.1.75 | J | 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) | |
COCLMCBI_01561 | 5.4e-151 | 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 | |
COCLMCBI_01562 | 5.9e-186 | afuA | P | ABC transporter, solute-binding protein | ||
COCLMCBI_01563 | 2.2e-191 | 3.6.3.29, 3.6.3.30 | E | ATPases associated with a variety of cellular activities | ||
COCLMCBI_01564 | 9.6e-281 | afuB2 | P | ABC transporter permease | ||
COCLMCBI_01565 | 1.3e-85 | |||||
COCLMCBI_01566 | 5.1e-123 | |||||
COCLMCBI_01567 | 6.8e-268 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
COCLMCBI_01568 | 1.2e-62 | sugR | K | Transcriptional regulators of sugar metabolism | ||
COCLMCBI_01569 | 3.6e-120 | 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 | |
COCLMCBI_01571 | 3.9e-73 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
COCLMCBI_01572 | 0.0 | hrpA | 3.6.4.13 | L | ATP-dependent helicase | |
COCLMCBI_01573 | 1.3e-144 | oxyR | K | Transcriptional regulator | ||
COCLMCBI_01574 | 0.0 | L | DEAD DEAH box helicase | |||
COCLMCBI_01575 | 1.7e-185 | pac | S | PAC2 family | ||
COCLMCBI_01576 | 2.4e-188 | S | Domain of unknown function (DUF4192) | |||
COCLMCBI_01577 | 7.4e-175 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
COCLMCBI_01578 | 7.9e-115 | ideR | K | repressor | ||
COCLMCBI_01579 | 2.5e-178 | sigA | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
COCLMCBI_01580 | 6.6e-67 | 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 | ||
COCLMCBI_01581 | 1.2e-275 | prmC_2 | J | Methylase of polypeptide chain release factors | ||
COCLMCBI_01582 | 2.5e-69 | S | Protein of unknown function (DUF3099) | |||
COCLMCBI_01583 | 3.1e-43 | S | Protein of unknown function (DUF3039) | |||
COCLMCBI_01584 | 2.2e-310 | sdrA | L | DNA or RNA helicases of superfamily II | ||
COCLMCBI_01586 | 3.1e-178 | 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 | ||
COCLMCBI_01587 | 3.7e-137 | ppgK | 2.7.1.2, 2.7.1.63 | GK | polyphosphate glucokinase | |
COCLMCBI_01588 | 1.5e-134 | suhB | 3.1.3.25 | G | Archaeal fructose-16-bisphosphatase and related enzymes of inositol monophosphatase family | |
COCLMCBI_01589 | 6.1e-48 | S | Domain of unknown function (DUF4193) | |||
COCLMCBI_01590 | 4.1e-93 | S | Protein of unknown function (DUF3093) | |||
COCLMCBI_01591 | 8.2e-76 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | This enzyme is involved in nucleotide metabolism it produces dUMP, the immediate precursor of thymidine nucleotides and it decreases the intracellular concentration of dUTP so that uracil cannot be incorporated into DNA | |
COCLMCBI_01592 | 1.4e-108 | S | Protein of unknown function (DUF3710) | |||
COCLMCBI_01593 | 1.2e-214 | trmA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
COCLMCBI_01594 | 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) | |
COCLMCBI_01595 | 2.9e-205 | rnd | 3.1.13.5 | J | Ribonuclease D | |
COCLMCBI_01596 | 1.3e-108 | S | Protein of unknown function (DUF3000) | |||
COCLMCBI_01597 | 1e-133 | hemH | 4.99.1.1, 4.99.1.9 | S | Chlorite | |
COCLMCBI_01598 | 1.6e-230 | aftC | 2.4.2.47 | S | Glycosyltransferase family 87 | |
COCLMCBI_01599 | 4.1e-102 | ribD | 1.1.1.193, 3.5.4.26 | H | Riboflavin biosynthesis | |
COCLMCBI_01607 | 1e-249 | EGP | Permeases of the major facilitator superfamily | |||
COCLMCBI_01608 | 1.7e-110 | copC | S | protein homolog of Cu resistance protein CopC | ||
COCLMCBI_01609 | 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) | |
COCLMCBI_01610 | 7.3e-98 | hit | 2.7.7.53 | FG | Diadenosine tetraphosphate (Ap4A) hydrolase and other HIT family hydrolases | |
COCLMCBI_01611 | 5.3e-100 | pgsA1 | 2.7.8.11, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
COCLMCBI_01612 | 2.6e-169 | htrB | 2.3.1.241, 2.3.1.265 | M | Lauroyl myristoyl acyltransferase | |
COCLMCBI_01613 | 3.5e-189 | pimA | 2.4.1.345 | GT4 | M | Glycosyltransferase |
COCLMCBI_01614 | 5.7e-64 | S | LemA family | |||
COCLMCBI_01615 | 9.6e-163 | tesB | I | Acyl-CoA thioesterase | ||
COCLMCBI_01616 | 1.9e-130 | yebC | K | Transcriptional regulatory protein | ||
COCLMCBI_01617 | 1.1e-95 | ruvC | 3.1.22.4 | L | Nuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves the cruciform structure in supercoiled DNA by nicking to strands with the same polarity at sites symmetrically opposed at the junction in the homologous arms and leaves a 5'-terminal phosphate and a 3'-terminal hydroxyl group | |
COCLMCBI_01618 | 1e-100 | 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 | |
COCLMCBI_01619 | 4.4e-197 | 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 | |
COCLMCBI_01620 | 1.8e-36 | yajC | U | Preprotein translocase subunit YajC | ||
COCLMCBI_01621 | 0.0 | secD | U | Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. SecDF uses the proton motive force (PMF) to complete protein translocation after the ATP-dependent function of SecA | ||
COCLMCBI_01622 | 6.4e-184 | secF | U | Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. SecDF uses the proton motive force (PMF) to complete protein translocation after the ATP-dependent function of SecA | ||
COCLMCBI_01623 | 2.5e-303 | dciAE | E | ABC-type dipeptide transport system periplasmic component | ||
COCLMCBI_01624 | 1.5e-101 | apt | 2.4.2.7 | F | Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis | |
COCLMCBI_01625 | 0.0 | relA | 2.7.6.5, 3.1.7.2 | KT | In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance | |
COCLMCBI_01626 | 5.7e-18 | |||||
COCLMCBI_01627 | 1.9e-119 | ppiB | 5.2.1.8 | O | Peptidyl-prolyl cis-trans isomerase | |
COCLMCBI_01628 | 1e-79 | 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 | |
COCLMCBI_01629 | 3.8e-114 | ycbL | 3.1.2.6 | S | Metallo-beta-lactamase domain protein | |
COCLMCBI_01630 | 4.9e-246 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
COCLMCBI_01631 | 6.7e-61 | S | 5-oxoprolinase (ATP-hydrolyzing) activity | |||
COCLMCBI_01632 | 5.4e-206 | ugpC | P | Belongs to the ABC transporter superfamily | ||
COCLMCBI_01633 | 8.6e-240 | inaA | T | Domain of unknown function (DUF4032) | ||
COCLMCBI_01634 | 9.3e-253 | amyE | G | ABC transporter | ||
COCLMCBI_01635 | 1.3e-146 | msmF | G | permease | ||
COCLMCBI_01636 | 6.9e-162 | rafG | G | ABC transporter permease | ||
COCLMCBI_01637 | 3.4e-96 | S | Psort location CytoplasmicMembrane, score | |||
COCLMCBI_01638 | 3.7e-131 | XK27_07850 | S | CBS domain | ||
COCLMCBI_01639 | 9.6e-140 | ypfJ | S | Metalloprotease | ||
COCLMCBI_01640 | 0.0 | aspS | 6.1.1.12 | J | Aspartyl-tRNA synthetase with relaxed tRNA specificity since it is able to aspartylate not only its cognate tRNA(Asp) but also tRNA(Asn). Reaction proceeds in two steps L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp Asn) | |
COCLMCBI_01641 | 1.7e-221 | 2.7.1.39 | S | A protein kinase that phosphorylates Ser and Thr residues. Probably acts to suppress the effects of stress linked to accumulation of reactive oxygen species. Probably involved in the extracytoplasmic stress response | ||
COCLMCBI_01642 | 5.5e-237 | rarA | L | ATPase related to the helicase subunit of the Holliday junction resolvase | ||
COCLMCBI_01643 | 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 | |
COCLMCBI_01644 | 5.8e-83 | yqgF | J | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
COCLMCBI_01645 | 2.8e-197 | mltG | S | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
COCLMCBI_01646 | 4.7e-152 | aroE | 1.1.1.25 | E | Shikimate | |
COCLMCBI_01647 | 1.2e-47 | pppA | 3.4.23.43 | NOU | aspartic-type endopeptidase activity | |
COCLMCBI_01648 | 2e-217 | aroC | 4.2.3.5 | E | Catalyzes the anti-1,4-elimination of the C-3 phosphate and the C-6 proR hydrogen from 5-enolpyruvylshikimate-3-phosphate (EPSP) to yield chorismate, which is the branch point compound that serves as the starting substrate for the three terminal pathways of aromatic amino acid biosynthesis. This reaction introduces a second double bond into the aromatic ring system | |
COCLMCBI_01649 | 6.1e-109 | aroK | 2.7.1.71, 4.2.3.4 | F | Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate | |
COCLMCBI_01650 | 3.6e-191 | aroB | 2.7.1.71, 4.2.3.4 | E | Catalyzes the conversion of 3-deoxy-D-arabino- heptulosonate 7-phosphate (DAHP) to dehydroquinate (DHQ) | |
COCLMCBI_01651 | 1.7e-70 | aroQ | 4.2.1.10 | E | Catalyzes a trans-dehydration via an enolate intermediate | |
COCLMCBI_01652 | 5e-196 | pepQ | 3.4.11.9, 3.4.13.9 | E | Belongs to the peptidase M24B family | |
COCLMCBI_01653 | 2.4e-101 | 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 | ||
COCLMCBI_01654 | 4.9e-95 | 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 | ||
COCLMCBI_01655 | 6e-157 | 2.7.4.1 | S | Polyphosphate kinase 2 (PPK2) | ||
COCLMCBI_01657 | 3.2e-62 | S | Putative bacterial sensory transduction regulator | |||
COCLMCBI_01658 | 4.9e-74 | S | Putative bacterial sensory transduction regulator | |||
COCLMCBI_01659 | 2.4e-240 | S | nucleoside-diphosphate sugar epimerase | |||
COCLMCBI_01660 | 5.4e-90 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
COCLMCBI_01661 | 3.9e-165 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
COCLMCBI_01662 | 5e-232 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
COCLMCBI_01663 | 1.4e-215 | carA | 6.3.5.5 | F | Belongs to the CarA family | |
COCLMCBI_01664 | 0.0 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthetase ammonia chain | |
COCLMCBI_01665 | 1.9e-136 | pyrF | 2.4.2.10, 4.1.1.23 | F | Belongs to the OMP decarboxylase family. Type 2 subfamily | |
COCLMCBI_01666 | 8.1e-46 | mihF | 2.7.4.8 | J | integration host factor | |
COCLMCBI_01667 | 8.9e-99 | gmk | 2.7.4.8, 4.1.1.23 | F | Essential for recycling GMP and indirectly, cGMP | |
COCLMCBI_01668 | 5.1e-47 | 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 | |
COCLMCBI_01669 | 2.4e-177 | L | HNH endonuclease domain protein | |||
COCLMCBI_01670 | 1e-65 | S | Protein of unknown function (DUF3558) | |||
COCLMCBI_01671 | 3.9e-17 | esxH | S | Belongs to the WXG100 family | ||
COCLMCBI_01672 | 3e-216 | coaBC | 4.1.1.36, 6.3.2.5 | H | Catalyzes two steps in the biosynthesis of coenzyme A. In the first step cysteine is conjugated to 4'-phosphopantothenate to form 4-phosphopantothenoylcysteine, in the latter compound is decarboxylated to form 4'-phosphopantotheine | |
COCLMCBI_01673 | 1.9e-220 | 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 | |
COCLMCBI_01675 | 4.5e-117 | 3.5.1.104 | G | Polysaccharide deacetylase | ||
COCLMCBI_01676 | 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 | ||
COCLMCBI_01677 | 3.7e-88 | def | 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions | |
COCLMCBI_01678 | 7.4e-172 | fmt | 2.1.1.176, 2.1.2.9 | J | Attaches a formyl group to the free amino group of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by promoting its recognition by IF2 and preventing the misappropriation of this tRNA by the elongation apparatus | |
COCLMCBI_01679 | 7e-238 | sun | 2.1.1.176 | JK | Belongs to the class I-like SAM-binding methyltransferase superfamily. RsmB NOP family | |
COCLMCBI_01680 | 3.7e-114 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
COCLMCBI_01681 | 5.9e-125 | 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 | |
COCLMCBI_01682 | 4e-83 | ribE | 2.5.1.9, 3.5.4.25, 4.1.99.12 | H | Riboflavin synthase | |
COCLMCBI_01683 | 1.4e-215 | ribBA | 3.5.4.25, 4.1.99.12 | H | Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate | |
COCLMCBI_01684 | 1.4e-76 | 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 | |
COCLMCBI_01685 | 3.6e-97 | S | Bacterial PH domain | |||
COCLMCBI_01686 | 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 | ||
COCLMCBI_01687 | 1.9e-158 | rapZ | S | Displays ATPase and GTPase activities | ||
COCLMCBI_01688 | 1.1e-176 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
COCLMCBI_01689 | 1.7e-147 | whiA | K | May be required for sporulation | ||
COCLMCBI_01690 | 2.7e-188 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
COCLMCBI_01691 | 1e-226 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
COCLMCBI_01692 | 2.5e-141 | 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) | |
COCLMCBI_01693 | 6e-30 | secG | U | Preprotein translocase subunit SecG | ||
COCLMCBI_01694 | 4.6e-129 | pgl | 3.1.1.31 | G | 6-phosphogluconolactonase | |
COCLMCBI_01695 | 6.2e-171 | opcA | G | Glucose-6-P dehydrogenase subunit | ||
COCLMCBI_01696 | 1.9e-294 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
COCLMCBI_01697 | 3e-193 | tal | 2.2.1.2 | H | Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway | |
COCLMCBI_01698 | 0.0 | tkt | 2.2.1.1 | G | Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate | |
COCLMCBI_01699 | 1.8e-180 | capA | M | Bacterial capsule synthesis protein PGA_cap | ||
COCLMCBI_01700 | 9.8e-161 | ctaB | 2.5.1.141 | O | Converts heme B (protoheme IX) to heme O by substitution of the vinyl group on carbon 2 of heme B porphyrin ring with a hydroxyethyl farnesyl side group | |
COCLMCBI_01701 | 2.9e-171 | qor | 1.6.5.5 | C | NADPH quinone reductase | |
COCLMCBI_01702 | 5e-177 | ctaA | O | cytochrome oxidase assembly | ||
COCLMCBI_01703 | 3.2e-125 | V | ABC-type multidrug transport system, permease component | |||
COCLMCBI_01704 | 1.2e-142 | drrA_2 | V | ABC transporter, ATP-binding protein | ||
COCLMCBI_01705 | 3.7e-262 | mptB | S | Carotene biosynthesis associated membrane protein | ||
COCLMCBI_01706 | 3.3e-116 | sufR | K | Transcriptional regulator | ||
COCLMCBI_01707 | 1.1e-272 | sufB | O | ABC-type transport system involved in Fe-S cluster assembly, permease component | ||
COCLMCBI_01708 | 1.4e-220 | sufD | O | ABC-type transport system involved in Fe-S cluster assembly, permease component | ||
COCLMCBI_01709 | 3e-139 | sufC | O | ABC-type transport system involved in Fe-S cluster assembly ATPase component | ||
COCLMCBI_01710 | 4.6e-238 | sufS | 2.8.1.7, 4.4.1.16 | E | Catalyzes the removal of elemental sulfur and selenium atoms from L-cysteine, L-cystine, L-selenocysteine, and L- selenocystine to produce L-alanine | |
COCLMCBI_01711 | 6e-79 | iscU | C | NifU homolog involved in Fe-S cluster formation | ||
COCLMCBI_01712 | 4.1e-81 | yitW | S | metal-sulfur cluster biosynthetic enzyme | ||
COCLMCBI_01713 | 4.9e-272 | yheS_1 | S | ATPase components of ABC transporters with duplicated ATPase domains | ||
COCLMCBI_01715 | 1.3e-08 | yheS_1 | S | ATPase components of ABC transporters with duplicated ATPase domains | ||
COCLMCBI_01716 | 2.5e-47 | S | InterPro IPR014922 | |||
COCLMCBI_01718 | 1.3e-118 | insK | L | Integrase core domain | ||
COCLMCBI_01719 | 2.1e-41 | L | Transposase and inactivated derivatives | |||
COCLMCBI_01720 | 3.8e-99 | 6.3.5.2 | F | glutamine amidotransferase | ||
COCLMCBI_01721 | 1.5e-36 | |||||
COCLMCBI_01722 | 8.6e-246 | XK27_08635 | S | UPF0210 protein | ||
COCLMCBI_01723 | 8.6e-41 | 1.1.1.3 | T | Belongs to the UPF0237 family | ||
COCLMCBI_01724 | 3e-114 | GM | Nucleoside-diphosphate-sugar epimerases | |||
COCLMCBI_01725 | 2.7e-133 | 6.3.5.2 | F | glutamine amidotransferase | ||
COCLMCBI_01726 | 0.0 | acnA | 4.2.1.3 | C | Catalyzes the isomerization of citrate to isocitrate via cis-aconitate | |
COCLMCBI_01727 | 1.6e-56 | |||||
COCLMCBI_01728 | 1.4e-179 | rpfI | 3.1.3.48 | DM | NlpC/P60 family | |
COCLMCBI_01729 | 2.3e-198 | hemH | 4.99.1.1, 4.99.1.9 | H | Catalyzes the ferrous insertion into protoporphyrin IX | |
COCLMCBI_01730 | 4.4e-130 | |||||
COCLMCBI_01731 | 6e-157 | trpH | 3.1.3.97 | S | Protein of unknown function (DUF3097) | |
COCLMCBI_01732 | 2.4e-69 | nfeD | OU | Membrane protein implicated in regulation of membrane protease activity | ||
COCLMCBI_01733 | 1.6e-172 | qmcA | O | Membrane protease subunits, stomatin prohibitin homologs | ||
COCLMCBI_01734 | 2.6e-79 | O | sequence-specific DNA binding | |||
COCLMCBI_01735 | 8.7e-103 | ydjZ | S | SNARE-like domain protein | ||
COCLMCBI_01737 | 4.5e-102 | ybhB | S | Phospholipid-binding protein | ||
COCLMCBI_01738 | 1.3e-41 | |||||
COCLMCBI_01739 | 5.2e-190 | pyrD | 1.3.1.14, 1.3.5.2, 1.3.98.1 | F | Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor | |
COCLMCBI_01740 | 1.7e-193 | lppL | S | amine dehydrogenase activity | ||
COCLMCBI_01741 | 2.6e-149 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
COCLMCBI_01742 | 1.5e-228 | cysS | 6.1.1.16, 6.3.1.13 | J | Catalyzes the ATP-dependent condensation of GlcN-Ins and L-cysteine to form L-Cys-GlcN-Ins | |
COCLMCBI_01743 | 1e-63 | |||||
COCLMCBI_01744 | 9.6e-115 | yniC | 3.1.3.23 | E | phosphatase phosphohexomutase | |
COCLMCBI_01745 | 5.7e-41 | hisE | 3.5.4.19, 3.6.1.31, 5.3.1.16 | E | Phosphoribosyl-ATP | |
COCLMCBI_01746 | 3e-148 | hisG | 2.4.2.17 | F | ATP phosphoribosyltransferase | |
COCLMCBI_01747 | 4.5e-266 | aspA | 4.3.1.1 | E | Aspartate ammonia-lyase | |
COCLMCBI_01748 | 2.4e-213 | dcuB | S | C4-dicarboxylate | ||
COCLMCBI_01749 | 6.7e-309 | fhs | 6.3.4.3 | H | Belongs to the formate--tetrahydrofolate ligase family | |
COCLMCBI_01750 | 3.4e-157 | recB | L | RecB family exonuclease | ||
COCLMCBI_01751 | 9e-220 | apeB | 3.4.11.21 | E | M18 family aminopeptidase | |
COCLMCBI_01752 | 4.2e-163 | trmI | 2.1.1.219, 2.1.1.220 | J | Catalyzes the S-adenosyl-L-methionine-dependent formation of N(1)-methyladenine at position 58 (m1A58) in tRNA | |
COCLMCBI_01753 | 9.9e-272 | arc | O | AAA ATPase forming ring-shaped complexes | ||
COCLMCBI_01754 | 2.1e-20 | mazF3 | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | ||
COCLMCBI_01756 | 7.4e-229 | pdxR | K | HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | ||
COCLMCBI_01757 | 4.6e-158 | pdxS | 4.3.3.6 | H | Catalyzes the formation of pyridoxal 5'-phosphate from ribose 5-phosphate (RBP), glyceraldehyde 3-phosphate (G3P) and ammonia. The ammonia is provided by the PdxT subunit. Can also use ribulose 5-phosphate and dihydroxyacetone phosphate as substrates, resulting from enzyme-catalyzed isomerization of RBP and G3P, respectively | |
COCLMCBI_01758 | 4.9e-279 | dop | 3.5.1.119, 6.3.1.19 | S | accessory factor | |
COCLMCBI_01759 | 1.7e-24 | pup | O | Pup-like protein | ||
COCLMCBI_01760 | 4e-262 | pafA | 6.3.1.19 | H | Catalyzes the covalent attachment of the prokaryotic ubiquitin-like protein modifier Pup to the proteasomal substrate proteins, thereby targeting them for proteasomal degradation. This tagging system is termed pupylation. The ligation reaction involves the side-chain carboxylate of the C-terminal glutamate of Pup and the side-chain amino group of a substrate lysine | |
COCLMCBI_01761 | 5.3e-170 | K | Transcriptional regulator | |||
COCLMCBI_01762 | 1.3e-165 | pafC | K | Transcriptional regulator | ||
COCLMCBI_01763 | 2.7e-32 | tatA | U | Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. TatA could form the protein-conducting channel of the Tat system | ||
COCLMCBI_01764 | 2.7e-153 | tatC | U | Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. Together with TatB, TatC is part of a receptor directly interacting with Tat signal peptides | ||
COCLMCBI_01765 | 0.0 | helY | L | DEAD DEAH box helicase | ||
COCLMCBI_01766 | 5.7e-71 | O | Trypsin-like serine proteases, typically periplasmic, contain C-terminal PDZ domain | |||
COCLMCBI_01767 | 1.8e-204 | pepE | 3.4.13.9 | E | Peptidase M24 | |
COCLMCBI_01768 | 2.2e-123 | MA20_24385 | S | Dehydrogenases with different specificities (Related to short-chain alcohol dehydrogenases) | ||
COCLMCBI_01769 | 4.5e-252 | 3.1.1.3 | S | Secretory lipase | ||
COCLMCBI_01770 | 3.9e-82 | fxsA | 2.3.3.13 | S | Protein affecting phage T7 exclusion by the F plasmid | |
COCLMCBI_01771 | 2.3e-295 | lnt | GT2 | M | Transfers the fatty acyl group on membrane lipoproteins | |
COCLMCBI_01772 | 3.3e-170 | ppm1 | 2.4.1.83 | GT2 | M | Glycosyltransferases involved in cell wall biogenesis |
COCLMCBI_01773 | 1.4e-47 | rbpA | K | Binds to RNA polymerase (RNAP), stimulating transcription from principal, but not alternative sigma factor promoters | ||
COCLMCBI_01774 | 8.3e-46 | |||||
COCLMCBI_01775 | 2.2e-117 | S | Belongs to the UPF0312 family | |||
COCLMCBI_01776 | 3.7e-197 | cfa | 2.1.1.317, 2.1.1.79 | M | Cyclopropane fatty acid synthase and related methyltransferases | |
COCLMCBI_01777 | 1.1e-261 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
COCLMCBI_01778 | 2.6e-189 | corA | P | Magnesium transport protein CorA | ||
COCLMCBI_01779 | 3.1e-72 | ydiI | Q | protein possibly involved in aromatic compounds catabolism | ||
COCLMCBI_01780 | 5.2e-273 | gnd | 1.1.1.343, 1.1.1.44 | G | Catalyzes the oxidative decarboxylation of 6- phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NADP to NADPH | |
COCLMCBI_01781 | 1e-218 | deaD | 3.6.4.13 | L | Superfamily II DNA and RNA helicases | |
COCLMCBI_01782 | 9.6e-229 | tlyC | S | Hemolysins and related proteins containing CBS domains | ||
COCLMCBI_01783 | 5.1e-182 | ytfL | S | Hemolysins and related proteins containing CBS domains | ||
COCLMCBI_01784 | 6.8e-148 | S | 3-methyladenine DNA glycosylase | |||
COCLMCBI_01785 | 4.4e-189 | S | von Willebrand factor (vWF) type A domain | |||
COCLMCBI_01786 | 7.3e-98 | merR2 | K | transcriptional | ||
COCLMCBI_01787 | 3.3e-101 | S | Bifunctional nuclease | |||
COCLMCBI_01788 | 2.3e-103 | merR1 | K | transcriptional | ||
COCLMCBI_01789 | 2.8e-70 | odhI | T | Oxoglutarate dehydrogenase inhibitor | ||
COCLMCBI_01790 | 0.0 | secA2 | U | Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. Has a central role in coupling the hydrolysis of ATP to the transfer of proteins into and across the cell membrane, serving as an ATP-driven molecular motor driving the stepwise translocation of polypeptide chains across the membrane | ||
COCLMCBI_01792 | 2e-195 | ybdR | 1.1.1.14 | E | COG1063 Threonine dehydrogenase and related Zn-dependent dehydrogenases | |
COCLMCBI_01793 | 5.7e-56 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |||
COCLMCBI_01794 | 9e-154 | CE1 | Q | Poly(3-hydroxybutyrate) depolymerase | ||
COCLMCBI_01795 | 2.8e-132 | Q | SAM-dependent | |||
COCLMCBI_01796 | 2e-278 | V | HNH endonuclease domain protein | |||
COCLMCBI_01797 | 2e-93 | CE1 | Q | xylan catabolic process | ||
COCLMCBI_01798 | 9.8e-132 | CE1 | Q | Phospholipase/Carboxylesterase | ||
COCLMCBI_01799 | 1.6e-258 | der | 1.1.1.399, 1.1.1.95 | F | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
COCLMCBI_01800 | 1.2e-115 | 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 | |
COCLMCBI_01801 | 3.3e-159 | rluB | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
COCLMCBI_01802 | 1.6e-86 | 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 | ||
COCLMCBI_01803 | 5.1e-145 | 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 | ||
COCLMCBI_01804 | 4.3e-158 | soj | D | ATPases involved in chromosome partitioning | ||
COCLMCBI_01805 | 8.1e-152 | xerD | D | recombinase XerD | ||
COCLMCBI_01806 | 2.2e-106 | nudF | 3.6.1.13 | L | NTP pyrophosphohydrolases including oxidative damage repair enzymes | |
COCLMCBI_01807 | 3.1e-133 | mctB | S | Copper transport outer membrane protein, MctB | ||
COCLMCBI_01808 | 6.3e-208 | S | membrane-anchored protein conserved in bacteria | |||
COCLMCBI_01809 | 4.8e-233 | recN | L | May be involved in recombinational repair of damaged DNA | ||
COCLMCBI_01810 | 1.5e-175 | nadK | 2.7.1.23 | H | Involved in the regulation of the intracellular balance of NAD and NADP, and is a key enzyme in the biosynthesis of NADP. Catalyzes specifically the phosphorylation on 2'-hydroxyl of the adenosine moiety of NAD to yield NADP | |
COCLMCBI_01811 | 5e-148 | tlyA | 2.1.1.226, 2.1.1.227 | J | ribosomal RNA large subunit methyltransferase J | |
COCLMCBI_01813 | 3e-171 | yutF | 3.1.3.41 | G | sugar phosphatases of the HAD superfamily | |
COCLMCBI_01814 | 3.3e-136 | J | pseudouridine synthase activity | |||
COCLMCBI_01815 | 3.7e-235 | tyrS | 6.1.1.1 | J | Catalyzes the attachment of tyrosine to tRNA(Tyr) in a two-step reaction tyrosine is first activated by ATP to form Tyr- AMP and then transferred to the acceptor end of tRNA(Tyr) | |
COCLMCBI_01816 | 6.6e-30 | S | Trm112p-like protein | |||
COCLMCBI_01817 | 3.1e-100 | |||||
COCLMCBI_01818 | 9.2e-268 | P | protein containing a von Willebrand factor type A (vWA) domain | |||
COCLMCBI_01819 | 4.9e-210 | P | Sulfate ABC transporter periplasmic sulfate-binding protein | |||
COCLMCBI_01820 | 1.6e-255 | argH | 4.3.2.1 | E | argininosuccinate lyase | |
COCLMCBI_01821 | 1.4e-226 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
COCLMCBI_01822 | 5.9e-83 | argR | K | Regulates arginine biosynthesis genes | ||
COCLMCBI_01823 | 2.4e-162 | 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 | |
COCLMCBI_01824 | 1.6e-203 | argD | 2.6.1.11, 2.6.1.17 | E | acetylornithine aminotransferase | |
COCLMCBI_01825 | 1e-173 | argB | 2.7.2.8 | E | Belongs to the acetylglutamate kinase family. ArgB subfamily | |
COCLMCBI_01826 | 1.8e-199 | 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 | |
COCLMCBI_01827 | 3.9e-204 | 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 | |
COCLMCBI_01828 | 0.0 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
COCLMCBI_01829 | 1.2e-197 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
COCLMCBI_01830 | 2.2e-132 | tsnR | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
COCLMCBI_01831 | 2.4e-193 | |||||
COCLMCBI_01832 | 1e-168 | 2.7.7.7 | L | Transposase and inactivated derivatives | ||
COCLMCBI_01833 | 6.3e-61 | 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 | ||
COCLMCBI_01834 | 8.2e-25 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
COCLMCBI_01835 | 1.7e-54 | infC | J | 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 | ||
COCLMCBI_01836 | 1.2e-178 | S | Predicted membrane protein (DUF2339) | |||
COCLMCBI_01837 | 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 | ||
COCLMCBI_01838 | 1.3e-110 | S | Zn-dependent hydrolases including glyoxylases | |||
COCLMCBI_01839 | 1.8e-84 | doxX | S | DoxX family | ||
COCLMCBI_01840 | 0.0 | helD | L | Superfamily I DNA and RNA helicases | ||
COCLMCBI_01841 | 4.5e-71 | uspA3 | T | universal stress protein | ||
COCLMCBI_01842 | 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 | ||
COCLMCBI_01843 | 4.8e-93 | S | SBF-like CPA transporter family (DUF4137) | |||
COCLMCBI_01844 | 2.8e-101 | K | BetI-type transcriptional repressor, C-terminal | |||
COCLMCBI_01845 | 5e-258 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | |||
COCLMCBI_01846 | 4.1e-154 | P | ABC transporter permease | |||
COCLMCBI_01847 | 9e-126 | P | ABC-type dipeptide oligopeptide nickel transport systems, permease components | |||
COCLMCBI_01848 | 1.8e-264 | P | Belongs to the ABC transporter superfamily | |||
COCLMCBI_01849 | 1.1e-237 | 2.3.1.21, 2.3.1.7 | S | Choline/Carnitine o-acyltransferase | ||
COCLMCBI_01850 | 1.8e-51 | S | Domain of unknown function (DUF4259) | |||
COCLMCBI_01851 | 1.5e-69 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
COCLMCBI_01852 | 1.7e-223 | rpsA | J | Ribosomal protein S1 | ||
COCLMCBI_01853 | 7.7e-95 | Q | SAM-dependent methyltransferases | |||
COCLMCBI_01854 | 2.8e-166 | S | Membrane | |||
COCLMCBI_01855 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
COCLMCBI_01858 | 1.4e-53 | |||||
COCLMCBI_01859 | 2.2e-130 | S | EamA-like transporter family | |||
COCLMCBI_01860 | 1.2e-77 | M | Protein of unknown function (DUF1541) | |||
COCLMCBI_01861 | 5.3e-184 | G | transmembrane transporter activity | |||
COCLMCBI_01862 | 5.4e-228 | S | Metal-dependent amidase aminoacylase carboxypeptidase | |||
COCLMCBI_01863 | 3.4e-283 | alsT | E | Amino acid carrier protein | ||
COCLMCBI_01864 | 1.6e-96 | E | GDSL-like Lipase/Acylhydrolase family | |||
COCLMCBI_01865 | 7.7e-69 | |||||
COCLMCBI_01866 | 1.9e-119 | phr | 4.1.99.3 | L | Belongs to the DNA photolyase family | |
COCLMCBI_01867 | 1.6e-146 | 3.1.1.74 | S | Cutinase | ||
COCLMCBI_01868 | 6.9e-30 | |||||
COCLMCBI_01869 | 3e-162 | pknD | ET | ABC-type amino acid transport signal transduction systems periplasmic component domain | ||
COCLMCBI_01870 | 4.8e-152 | yecS | P | ABC-type amino acid transport system permease component | ||
COCLMCBI_01871 | 1.1e-133 | atrC | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
COCLMCBI_01872 | 9e-50 | L | Transposase and inactivated derivatives | |||
COCLMCBI_01873 | 9.4e-153 | tnp7109-46 | L | Transposase and inactivated derivatives | ||
COCLMCBI_01875 | 5.9e-69 | L | Integrase core domain | |||
COCLMCBI_01876 | 9.9e-88 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
COCLMCBI_01877 | 3.2e-101 | rsmD | 2.1.1.171 | L | DNA methylase | |
COCLMCBI_01878 | 0.0 | recG | 3.6.4.12 | L | ATP-dependent DNA helicase | |
COCLMCBI_01879 | 5.7e-238 | dak3 | 2.7.1.28, 2.7.1.29, 4.6.1.15 | S | kinase related to dihydroxyacetone kinase | |
COCLMCBI_01880 | 9.3e-118 | 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 | |
COCLMCBI_01881 | 2.3e-160 | thiL | 2.7.4.16 | H | Catalyzes the ATP-dependent phosphorylation of thiamine- monophosphate (TMP) to form thiamine-pyrophosphate (TPP), the active form of vitamin B1 | |
COCLMCBI_01882 | 2.3e-130 | S | Protein of unknown function (DUF3515) | |||
COCLMCBI_01883 | 1.3e-193 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
COCLMCBI_01884 | 6.4e-174 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
COCLMCBI_01885 | 4.2e-189 | mutT | 3.6.1.55, 5.4.2.12 | FG | Belongs to the Nudix hydrolase family | |
COCLMCBI_01886 | 9.5e-109 | leuD | 4.2.1.33, 4.2.1.35 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
COCLMCBI_01887 | 3.3e-272 | leuC | 4.2.1.33, 4.2.1.35 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
COCLMCBI_01888 | 2.4e-111 | ltbR | K | Transcriptional regulator | ||
COCLMCBI_01889 | 0.0 | 4.1.1.20 | E | Diaminopimelate decarboxylase | ||
COCLMCBI_01890 | 2.9e-168 | cysM | 2.5.1.140 | E | Cysteine synthase | |
COCLMCBI_01891 | 3.4e-65 | pcaC | 4.1.1.44 | S | homolog of gamma-carboxymuconolactone decarboxylase subunit | |
COCLMCBI_01892 | 6e-94 | S | response to pH | |||
COCLMCBI_01893 | 3.4e-80 | S | response to pH | |||
COCLMCBI_01894 | 5.4e-93 | |||||
COCLMCBI_01895 | 7e-58 | L | Helix-turn-helix domain | |||
COCLMCBI_01896 | 1.4e-134 | insK | L | Transposase and inactivated derivatives | ||
COCLMCBI_01898 | 1e-168 | 2.7.7.7 | L | Transposase and inactivated derivatives | ||
COCLMCBI_01902 | 1.2e-208 | 2.7.7.7 | L | Transposase and inactivated derivatives | ||
COCLMCBI_01903 | 3.6e-178 | 2.7.7.7 | L | Transposase and inactivated derivatives | ||
COCLMCBI_01904 | 9.4e-153 | tnp7109-46 | L | Transposase and inactivated derivatives | ||
COCLMCBI_01905 | 9e-50 | L | Transposase and inactivated derivatives | |||
COCLMCBI_01906 | 4.3e-118 | L | COG4584 Transposase and inactivated derivatives | |||
COCLMCBI_01907 | 1.4e-134 | L | DNA replication protein | |||
COCLMCBI_01910 | 1.8e-262 | gltX | 6.1.1.17 | 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) | |
COCLMCBI_01911 | 3e-105 | lpqC | CE1 | Q | Poly(3-hydroxybutyrate) depolymerase | |
COCLMCBI_01912 | 1.7e-218 | menF | 5.4.4.2 | HQ | Isochorismate synthase | |
COCLMCBI_01913 | 7.7e-138 | odx | Q | 2-keto-4-pentenoate hydratase 2-oxohepta-3-ene-17-dioic acid hydratase (catechol pathway) | ||
COCLMCBI_01914 | 9.7e-98 | dnaQ3 | 2.7.7.7 | L | DNA polymerase III | |
COCLMCBI_01915 | 0.0 | VP1725 | T | signal-transduction protein containing cAMP-binding and CBS domains | ||
COCLMCBI_01916 | 4.5e-232 | 2.8.1.7, 4.4.1.16 | S | domain, Protein | ||
COCLMCBI_01917 | 2.3e-171 | leuB | 1.1.1.85 | CE | Catalyzes the oxidation of 3-carboxy-2-hydroxy-4- methylpentanoate (3-isopropylmalate) to 3-carboxy-4-methyl-2- oxopentanoate. The product decarboxylates to 4-methyl-2 oxopentanoate | |
COCLMCBI_01918 | 3.8e-94 | nrp | GM | NAD(P)H-binding | ||
COCLMCBI_01919 | 8.1e-272 | serA | 1.1.1.399, 1.1.1.95 | E | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
COCLMCBI_01920 | 1.1e-135 | |||||
COCLMCBI_01921 | 0.0 | S | Protein of unknown function DUF262 | |||
COCLMCBI_01922 | 3.1e-132 | czcD | P | Co Zn Cd efflux system component | ||
COCLMCBI_01924 | 4.3e-200 | L | Transposase and inactivated derivatives IS30 family | |||
COCLMCBI_01926 | 2.2e-190 | ilvC | 1.1.1.86 | EH | Involved in the biosynthesis of branched-chain amino acids (BCAA). Catalyzes an alkyl-migration followed by a ketol- acid reduction of (S)-2-acetolactate (S2AL) to yield (R)-2,3- dihydroxy-isovalerate. In the isomerase reaction, S2AL is rearranged via a Mg-dependent methyl migration to produce 3- hydroxy-3-methyl-2-ketobutyrate (HMKB). In the reductase reaction, this 2-ketoacid undergoes a metal-dependent reduction by NADPH to yield (R)-2,3-dihydroxy-isovalerate | |
COCLMCBI_01927 | 1.9e-84 | ilvN | 2.2.1.6 | E | Acetolactate synthase small | |
COCLMCBI_01928 | 0.0 | ilvB | 2.2.1.6 | H | Thiamine pyrophosphate-requiring enzymes acetolactate synthase pyruvate dehydrogenase (cytochrome) glyoxylate carboligase phosphonopyruvate decarboxylase | |
COCLMCBI_01929 | 8.5e-215 | mscS | M | Transporter, small conductance mechanosensitive ion channel MscS family protein | ||
COCLMCBI_01930 | 1.1e-81 | cfp6 | S | Bacterial PH domain | ||
COCLMCBI_01931 | 0.0 | ilvD | 4.2.1.9 | EG | Belongs to the IlvD Edd family | |
COCLMCBI_01932 | 3.5e-217 | GT87 | S | Pfam:DUF2029 | ||
COCLMCBI_01933 | 9e-57 | mhqP | S | membrane | ||
COCLMCBI_01934 | 2.4e-187 | yghZ | C | oxidoreductases (related to | ||
COCLMCBI_01935 | 8e-239 | S | Membrane | |||
COCLMCBI_01936 | 3.7e-274 | gatB | 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) | |
COCLMCBI_01937 | 8.8e-128 | yocS | S | Na -dependent transporter | ||
COCLMCBI_01938 | 2e-115 | nadC | 2.4.2.19 | H | Belongs to the NadC ModD family | |
COCLMCBI_01939 | 3.9e-83 | J | Acetyltransferases, including N-acetylases of ribosomal proteins | |||
COCLMCBI_01940 | 3.4e-121 | galE1 | 4.2.1.46, 5.1.3.2 | M | 4-epimerase | |
COCLMCBI_01941 | 8.3e-185 | pfkA | 2.7.1.11, 2.7.1.90 | F | Catalyzes the phosphorylation of D-fructose 6-phosphate to fructose 1,6-bisphosphate by ATP, the first committing step of glycolysis | |
COCLMCBI_01942 | 4.5e-212 | emrB | EGP | the major facilitator superfamily | ||
COCLMCBI_01943 | 1.7e-263 | 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) | |
COCLMCBI_01944 | 3.5e-43 | 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) | |
COCLMCBI_01945 | 3.1e-116 | 2.7.6.5, 3.1.7.2 | KT | ACT domain protein | ||
COCLMCBI_01947 | 2.3e-147 | V | Beta-lactamase class C and other penicillin binding proteins | |||
COCLMCBI_01948 | 2.3e-53 | K | Helix-turn-helix domain | |||
COCLMCBI_01950 | 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 | |
COCLMCBI_01951 | 2.7e-132 | tipA | K | transcriptional regulators | ||
COCLMCBI_01952 | 5e-122 | dnaQ2 | 2.7.7.7 | L | DNA polymerase III | |
COCLMCBI_01954 | 1.4e-153 | 2.1.1.14 | E | Methionine synthase | ||
COCLMCBI_01956 | 6e-202 | 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 | |
COCLMCBI_01957 | 3e-180 | T | Histidine kinase | |||
COCLMCBI_01958 | 8.7e-114 | K | Response regulator receiver domain protein | |||
COCLMCBI_01959 | 4.4e-107 | clvF | V | ABC transporter, ATP-binding protein | ||
COCLMCBI_01960 | 9e-50 | L | Transposase and inactivated derivatives | |||
COCLMCBI_01961 | 9.4e-153 | tnp7109-46 | L | Transposase and inactivated derivatives | ||
COCLMCBI_01962 | 5.2e-42 | clvF | V | ABC transporter, ATP-binding protein | ||
COCLMCBI_01963 | 5.4e-109 | S | ABC-2 family transporter protein | |||
COCLMCBI_01964 | 1.5e-119 | S | ABC-2 family transporter protein | |||
COCLMCBI_01965 | 9.6e-149 | speE | 2.5.1.16 | E | Spermidine synthase | |
COCLMCBI_01966 | 2.5e-200 | acm_1 | M | Lyzozyme M1 (1,4-beta-N-acetylmuramidase) | ||
COCLMCBI_01967 | 4.1e-171 | iscS | 2.8.1.7 | E | Cysteine sulfinate desulfinase cysteine desulfurase and related enzymes | |
COCLMCBI_01968 | 4.1e-162 | etfA | C | Electron transfer flavoprotein | ||
COCLMCBI_01969 | 4.4e-130 | etfB | 1.3.1.108 | C | Electron transfer flavoprotein | |
COCLMCBI_01970 | 1.3e-197 | J | SAM-dependent methyltransferases | |||
COCLMCBI_01971 | 3.4e-157 | MA20_36340 | L | NTP pyrophosphohydrolases including oxidative damage repair enzymes | ||
COCLMCBI_01972 | 9.7e-155 | modF | 3.6.3.21, 3.6.3.34 | P | ABC-type molybdenum transport system ATPase component photorepair protein PhrA | |
COCLMCBI_01973 | 0.0 | glgE | 2.4.99.16 | GH13 | G | Maltosyltransferase that uses maltose 1-phosphate (M1P) as the sugar donor to elongate linear or branched alpha-(1- 4)- glucans. Is involved in a branched alpha-glucan biosynthetic pathway from trehalose, together with TreS, Mak and GlgB |
COCLMCBI_01974 | 0.0 | glgB | 2.4.1.18 | CBM48,GH13 | G | Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position |
COCLMCBI_01975 | 3e-46 | S | Thiamine-binding protein | |||
COCLMCBI_01976 | 6.3e-128 | nucS | L | Cleaves both 3' and 5' ssDNA extremities of branched DNA structures | ||
COCLMCBI_01977 | 7.2e-72 | S | Protein of unknown function (DUF2550) | |||
COCLMCBI_01978 | 4.8e-55 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
COCLMCBI_01979 | 3.5e-280 | 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 | |
COCLMCBI_01980 | 2e-156 | 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 | ||
COCLMCBI_01981 | 2.3e-301 | 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 | |
COCLMCBI_01982 | 4.3e-139 | 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 | ||
COCLMCBI_01983 | 1e-62 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
COCLMCBI_01984 | 2.6e-33 | 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 | ||
COCLMCBI_01985 | 8.2e-132 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
COCLMCBI_01986 | 3.1e-67 | atpI | ||||
COCLMCBI_01987 | 7.8e-88 | |||||
COCLMCBI_01988 | 2.3e-201 | S | Membrane | |||
COCLMCBI_01989 | 0.0 | Q | Non-ribosomal peptide synthetase modules and related proteins | |||
COCLMCBI_01990 | 4.6e-192 | tagO | 2.7.8.33, 2.7.8.35 | M | UDP-N-acetylmuramyl pentapeptide phosphotransferase UDP-N-acetylglucosamine-1-phosphate transferase | |
COCLMCBI_01991 | 7.1e-121 | ywlC | 2.7.7.87 | J | Belongs to the SUA5 family | |
COCLMCBI_01992 | 6e-158 | prmC | 2.1.1.297, 2.6.1.85 | J | Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif | |
COCLMCBI_01993 | 2.1e-162 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
COCLMCBI_01994 | 2.6e-216 | rho | K | Facilitates transcription termination by a mechanism that involves Rho binding to the nascent RNA, activation of Rho's RNA-dependent ATPase activity, and release of the mRNA from the DNA template | ||
COCLMCBI_01995 | 0.0 | fadD4 | IQ | Acyl-CoA synthetases (AMP-forming) AMP-acid ligases II | ||
COCLMCBI_01996 | 2.2e-210 | gldA | 1.1.1.6 | C | Iron-containing alcohol dehydrogenase | |
COCLMCBI_01997 | 3.5e-166 | thrB | 2.7.1.39 | E | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
COCLMCBI_01998 | 1.7e-238 | hom | 1.1.1.3 | E | homoserine dehydrogenase | |
COCLMCBI_01999 | 6.9e-259 | lysA | 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
COCLMCBI_02000 | 1.9e-308 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
COCLMCBI_02001 | 3.9e-299 | lldT | C | permease | ||
COCLMCBI_02002 | 1.5e-146 | lutA | C | Fe-S oxidoreductase | ||
COCLMCBI_02003 | 3.6e-296 | lutB | C | conserved protein containing a ferredoxin-like domain | ||
COCLMCBI_02004 | 1.4e-100 | lutC | S | conserved protein containing a ferredoxin-like domain | ||
COCLMCBI_02005 | 2e-278 | S | hydrolases or acyltransferases (alpha beta hydrolase superfamily) | |||
COCLMCBI_02006 | 1.3e-122 | S | DJ-1/PfpI family | |||
COCLMCBI_02007 | 3.3e-106 | |||||
COCLMCBI_02008 | 7.1e-95 | S | CAAX amino terminal protease | |||
COCLMCBI_02009 | 1.7e-12 | |||||
COCLMCBI_02010 | 2.6e-89 | yceI | S | Belongs to the UPF0312 family | ||
COCLMCBI_02012 | 8.5e-60 | cmtR | K | transcriptional | ||
COCLMCBI_02013 | 9.7e-85 | cadD | P | Pfam PF03596 | ||
COCLMCBI_02014 | 6.7e-66 | |||||
COCLMCBI_02016 | 5.8e-61 | |||||
COCLMCBI_02017 | 1.3e-163 | S | Endonuclease/Exonuclease/phosphatase family | |||
COCLMCBI_02018 | 3.6e-29 | pspC | KT | PspC domain protein | ||
COCLMCBI_02019 | 9.4e-73 | rosR | K | Transcriptional regulator, MarR family | ||
COCLMCBI_02020 | 0.0 | sbcC | L | DNA repair | ||
COCLMCBI_02021 | 1.4e-207 | sbcD | L | DNA repair exonuclease | ||
COCLMCBI_02022 | 1.6e-149 | S | zinc finger | |||
COCLMCBI_02023 | 0.0 | helZ | 2.7.11.1 | L | SNF2 family | |
COCLMCBI_02024 | 3.4e-278 | putP | E | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
COCLMCBI_02025 | 1.4e-121 | L | HNH endonuclease | |||
COCLMCBI_02026 | 2.1e-77 | |||||
COCLMCBI_02027 | 2.9e-290 | deaD | 3.6.4.13 | JKL | DEAD-box RNA helicase involved in various cellular processes at low temperature, including ribosome biogenesis, mRNA degradation and translation initiation | |
COCLMCBI_02028 | 2.9e-84 | 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 | |||
COCLMCBI_02029 | 8.4e-106 | rhtC | E | threonine efflux protein | ||
COCLMCBI_02031 | 3.3e-55 | |||||
COCLMCBI_02033 | 3.2e-08 | |||||
COCLMCBI_02034 | 9e-50 | L | Transposase and inactivated derivatives | |||
COCLMCBI_02035 | 9.4e-153 | tnp7109-46 | L | Transposase and inactivated derivatives | ||
COCLMCBI_02036 | 6.3e-247 | L | Transposase and inactivated derivatives | |||
COCLMCBI_02038 | 1.8e-86 | L | Phage integrase family | |||
COCLMCBI_02039 | 7.6e-13 | 6.3.5.2 | F | glutamine amidotransferase | ||
COCLMCBI_02040 | 3.9e-89 | mae1 | P | Tellurite resistance protein and related permeases | ||
COCLMCBI_02041 | 2.6e-86 | K | LysR substrate binding domain | |||
COCLMCBI_02042 | 1.8e-199 | lppS | S | protein conserved in bacteria | ||
COCLMCBI_02044 | 1.1e-90 | pncA | 2.7.11.1, 3.5.1.19 | Q | Amidases related to nicotinamidase | |
COCLMCBI_02045 | 2.4e-25 | S | Protein of unknown function (DUF3618) | |||
COCLMCBI_02046 | 8.8e-81 | bcp | 1.11.1.15 | O | bacterioferritin comigratory protein | |
COCLMCBI_02048 | 6e-60 | lprD | V | PFAM secretion protein HlyD family protein | ||
COCLMCBI_02049 | 4e-55 | S | Domain of unknown function (DUF3817) | |||
COCLMCBI_02050 | 3.6e-61 | |||||
COCLMCBI_02051 | 1.6e-95 | 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 | |
COCLMCBI_02052 | 3.7e-131 | rph | 2.7.7.56, 3.6.1.66 | J | Phosphorolytic exoribonuclease that removes nucleotide residues following the -CCA terminus of tRNA and adds nucleotides to the ends of RNA molecules by using nucleoside diphosphates as substrates | |
COCLMCBI_02053 | 9.1e-144 | yhfI | S | Metal-dependent hydrolases of the beta-lactamase superfamily III | ||
COCLMCBI_02054 | 3.9e-148 | murI | 3.6.1.66, 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
COCLMCBI_02055 | 9.2e-87 | K | transcriptional | |||
COCLMCBI_02056 | 2.5e-109 | SEN0012 | S | membrane protein (homolog of Drosophila rhomboid) | ||
COCLMCBI_02057 | 1.3e-155 | dmpA | 3.4.11.19 | EQ | L-aminopeptidase D-esterase | |
COCLMCBI_02058 | 2.5e-92 | S | Domain of unknown function (DUF2017) | |||
COCLMCBI_02059 | 1.8e-56 | clpS | S | Involved in the modulation of the specificity of the ClpAP-mediated ATP-dependent protein degradation | ||
COCLMCBI_02060 | 1.6e-241 | pncB | 6.3.4.21 | H | Catalyzes the synthesis of beta-nicotinate D- ribonucleotide from nicotinate and 5-phospho-D-ribose 1-phosphate at the expense of ATP | |
COCLMCBI_02061 | 0.0 | dinG | 2.7.7.7, 3.6.4.12 | L | Rad3-related DNA helicases | |
COCLMCBI_02062 | 1.7e-121 | pth_2 | 3.1.1.29 | S | peptidyl-tRNA hydrolase, PTH2 | |
COCLMCBI_02063 | 6.5e-208 | serB | 3.1.3.3 | ET | phosphoserine phosphatase | |
COCLMCBI_02064 | 0.0 | ctaD | 1.9.3.1 | C | Cytochrome c oxidase is the component of the respiratory chain that catalyzes the reduction of oxygen to water. Subunits 1- 3 form the functional core of the enzyme complex. CO I is the catalytic subunit of the enzyme. Electrons originating in cytochrome c are transferred via the copper A center of subunit 2 and heme A of subunit 1 to the bimetallic center formed by heme A3 and copper B | |
COCLMCBI_02065 | 4.7e-193 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
COCLMCBI_02066 | 0.0 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
COCLMCBI_02067 | 8.3e-88 | nrdI | F | Probably involved in ribonucleotide reductase function | ||
COCLMCBI_02068 | 1.6e-35 | nrdH | O | Glutaredoxin | ||
COCLMCBI_02069 | 9.1e-14 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
COCLMCBI_02070 | 3.1e-227 | EGP | Major facilitator Superfamily | |||
COCLMCBI_02071 | 5.9e-152 | nadE | 6.3.1.5 | H | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
COCLMCBI_02072 | 1.2e-25 | |||||
COCLMCBI_02073 | 2.2e-55 | S | Antitoxin component of a toxin-antitoxin (TA) module | |||
COCLMCBI_02074 | 8.2e-137 | G | Fructosamine kinase | |||
COCLMCBI_02075 | 4.2e-67 | ogt | 2.1.1.63 | L | Involved in the cellular defense against the biological effects of O6-methylguanine (O6-MeG) and O4-methylthymine (O4-MeT) in DNA. Repairs the methylated nucleobase in DNA by stoichiometrically transferring the methyl group to a cysteine residue in the enzyme. This is a suicide reaction the enzyme is irreversibly inactivated | |
COCLMCBI_02076 | 1e-185 | 3.6.3.29, 3.6.3.30 | E | ATPases associated with a variety of cellular activities | ||
COCLMCBI_02077 | 2e-278 | afuB2 | P | ABC transporter permease | ||
COCLMCBI_02078 | 4.3e-181 | afuA | P | ABC transporter, solute-binding protein | ||
COCLMCBI_02081 | 3e-78 | pknE | 2.7.11.1 | O | Protein-disulfide isomerase | |
COCLMCBI_02082 | 9.1e-52 | S | DoxX family | |||
COCLMCBI_02083 | 1.4e-146 | S | AAA ATPase domain | |||
COCLMCBI_02084 | 0.0 | pgm | 5.4.2.2 | G | Phosphoglucomutase | |
COCLMCBI_02085 | 2.4e-51 | crcB | D | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
COCLMCBI_02086 | 5.7e-71 | crcB | D | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
COCLMCBI_02087 | 0.0 | Q | ABC-type antimicrobial peptide transport system, permease component | |||
COCLMCBI_02088 | 1.4e-139 | V | ABC-type antimicrobial peptide transport system, ATPase component | |||
COCLMCBI_02090 | 9.6e-13 | |||||
COCLMCBI_02091 | 1.5e-198 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
COCLMCBI_02092 | 6.2e-146 | ramA | K | transcriptional regulator (LuxR family) | ||
COCLMCBI_02093 | 1.4e-167 | cysK | 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
COCLMCBI_02094 | 2.4e-75 | cysE | 2.3.1.30 | E | serine acetyltransferase | |
COCLMCBI_02095 | 2.9e-42 | S | acetyltransferase | |||
COCLMCBI_02100 | 2.9e-60 | S | Protein of unknown function (DUF1345) | |||
COCLMCBI_02101 | 5.4e-66 | yccF | S | membrane | ||
COCLMCBI_02102 | 2.5e-125 | zupT | P | Mediates zinc uptake. May also transport other divalent cations | ||
COCLMCBI_02103 | 4.8e-105 | G | Trehalose synthase | |||
COCLMCBI_02104 | 0.0 | fadD7 | 6.2.1.3 | IQ | Acyl-CoA synthetases (AMP-forming) AMP-acid ligases II | |
COCLMCBI_02105 | 1.3e-101 | ubiA | 2.5.1.133, 2.5.1.62 | H | COG0382 4-hydroxybenzoate polyprenyltransferase and related prenyltransferases | |
COCLMCBI_02106 | 1.1e-40 | crtYf | H | lycopene cyclase domain | ||
COCLMCBI_02107 | 1.6e-48 | crtYe | S | lycopene cyclase | ||
COCLMCBI_02108 | 7.8e-288 | crtI | 1.3.99.26, 1.3.99.28, 1.3.99.29, 1.3.99.31, 1.3.99.37 | Q | Phytoene dehydrogenase and related proteins | |
COCLMCBI_02109 | 1.6e-149 | crtB | 2.5.1.21, 2.5.1.32, 2.5.1.96, 2.5.1.99 | I | phytoene squalene synthetase | |
COCLMCBI_02110 | 4.8e-110 | M | COG0463 Glycosyltransferases involved in cell wall biogenesis | |||
COCLMCBI_02112 | 2.8e-282 | scpC | 2.8.3.18, 3.1.2.1 | C | succinate CoA transferase | |
COCLMCBI_02113 | 5.5e-217 | 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 | ||
COCLMCBI_02114 | 4e-128 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
COCLMCBI_02115 | 2.6e-143 | 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 | |
COCLMCBI_02116 | 1.7e-153 | pstA | P | phosphate transport system permease | ||
COCLMCBI_02117 | 1e-177 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
COCLMCBI_02118 | 1.1e-174 | pstS | P | Part of the ABC transporter complex PstSACB involved in phosphate import | ||
COCLMCBI_02119 | 4.5e-153 | mshD | 2.3.1.189, 2.7.4.1 | K | Catalyzes the transfer of acetyl from acetyl-CoA to desacetylmycothiol (Cys-GlcN-Ins) to form mycothiol | |
COCLMCBI_02120 | 2.8e-124 | S | Protein of unknown function (DUF2993) | |||
COCLMCBI_02121 | 1.1e-124 | S | May play a role in the intracellular transport of hydrophobic ligands | |||
COCLMCBI_02122 | 5.7e-161 | pabC | 2.6.1.42, 4.1.3.38 | EH | 4-amino-4-deoxychorismate lyase | |
COCLMCBI_02123 | 2.7e-200 | ygfZ | 2.1.2.10 | S | Belongs to the GcvT family | |
COCLMCBI_02124 | 1e-31 | S | Protein of unknown function (DUF3073) | |||
COCLMCBI_02125 | 2.1e-199 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
COCLMCBI_02126 | 2.3e-284 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
COCLMCBI_02127 | 4e-60 | I | Sterol carrier protein | |||
COCLMCBI_02128 | 5.4e-189 | 3.1.2.20, 3.1.2.23 | I | Acyl-CoA hydrolase | ||
COCLMCBI_02130 | 1.2e-80 | S | Region found in RelA / SpoT proteins | |||
COCLMCBI_02131 | 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 | |
COCLMCBI_02132 | 2.9e-125 | 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 | |
COCLMCBI_02133 | 1.1e-31 | 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 | |
COCLMCBI_02134 | 1.7e-111 | P | ABC-type metal ion transport system periplasmic component surface adhesin | |||
COCLMCBI_02135 | 6e-107 | fhuC | P | ATP-binding protein | ||
COCLMCBI_02136 | 6e-117 | znuB | P | ABC-type Mn2 Zn2 transport systems permease components | ||
COCLMCBI_02137 | 9.3e-124 | S | deacetylase | |||
COCLMCBI_02138 | 0.0 | ptrB | 3.4.21.83 | E | Peptidase, S9A B C family, catalytic domain protein | |
COCLMCBI_02139 | 9.9e-163 | purC | 6.3.2.6, 6.3.4.13 | F | Belongs to the SAICAR synthetase family | |
COCLMCBI_02140 | 2.5e-16 | |||||
COCLMCBI_02141 | 3.7e-263 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
COCLMCBI_02142 | 3e-210 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
COCLMCBI_02143 | 1.5e-69 | hit | FG | Diadenosine tetraphosphate (Ap4A) hydrolase and other HIT family hydrolases | ||
COCLMCBI_02144 | 3.7e-247 | phoR | 2.7.13.3 | T | Histidine kinase | |
COCLMCBI_02145 | 1.2e-129 | KT | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
COCLMCBI_02146 | 3.4e-200 | L | HNH endonuclease domain protein | |||
COCLMCBI_02148 | 3.2e-255 | thrE | S | Amino acid export carrier protein | ||
COCLMCBI_02149 | 1.3e-28 | |||||
COCLMCBI_02150 | 5.2e-248 | otsA | 2.4.1.15, 2.4.1.347, 3.1.3.12 | GT20 | G | synthase |
COCLMCBI_02151 | 4.5e-66 | O | response to heat | |||
COCLMCBI_02152 | 6.9e-126 | otsB | 2.4.1.15, 2.4.1.347, 3.1.3.12 | GT20 | G | Removes the phosphate from trehalose 6-phosphate to produce free trehalose |
COCLMCBI_02153 | 6.2e-186 | lacI | K | Transcriptional regulator, LacI family | ||
COCLMCBI_02154 | 2e-158 | CE1 | Q | depolymerase | ||
COCLMCBI_02155 | 2.3e-173 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
COCLMCBI_02156 | 1.4e-270 | cysS | 6.1.1.16 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
COCLMCBI_02157 | 1.4e-81 | ispF | 2.1.1.228, 2.7.7.60, 4.6.1.12 | I | Involved in the biosynthesis of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP), two major building blocks of isoprenoid compounds. Catalyzes the conversion of 4- diphosphocytidyl-2-C-methyl-D-erythritol 2-phosphate (CDP-ME2P) to 2-C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-CPP) with a corresponding release of cytidine 5-monophosphate (CMP) | |
COCLMCBI_02158 | 1.2e-124 | ispD | 1.1.1.405, 2.7.7.40, 2.7.7.60, 4.6.1.12 | I | Catalyzes the formation of 4-diphosphocytidyl-2-C- methyl-D-erythritol from CTP and 2-C-methyl-D-erythritol 4- phosphate (MEP) | |
COCLMCBI_02159 | 5.4e-96 | carD | K | to M. xanthus CarD | ||
COCLMCBI_02160 | 4.1e-80 | lpqE | S | Copper chaperone PCu(A)C | ||
COCLMCBI_02161 | 2.3e-254 | 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 | ||
COCLMCBI_02162 | 9.3e-184 | disA | 2.7.7.85 | L | DNA integrity scanning protein DisA | |
COCLMCBI_02163 | 6.1e-86 | |||||
COCLMCBI_02164 | 9.3e-99 | cah | 4.2.1.1 | P | Reversible hydration of carbon dioxide | |
COCLMCBI_02165 | 2.6e-155 | mutY | L | A G-specific | ||
COCLMCBI_02166 | 0.0 | |||||
COCLMCBI_02167 | 1.8e-23 | S | Protein of unknown function (DUF4236) | |||
COCLMCBI_02168 | 0.0 | clpC | O | ATPases with chaperone activity, ATP-binding subunit | ||
COCLMCBI_02169 | 1.9e-36 | |||||
COCLMCBI_02171 | 7.8e-41 | T | ATPase activity | |||
COCLMCBI_02172 | 1.7e-95 | KLT | serine threonine protein kinase | |||
COCLMCBI_02173 | 1.1e-65 | S | Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane | |||
COCLMCBI_02174 | 3e-40 | |||||
COCLMCBI_02175 | 3.9e-52 | S | TM2 domain protein | |||
COCLMCBI_02176 | 8.2e-19 | J | TM2 domain | |||
COCLMCBI_02177 | 3.5e-79 | |||||
COCLMCBI_02178 | 8.5e-287 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
COCLMCBI_02179 | 1e-127 | S | Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane | |||
COCLMCBI_02180 | 3.1e-131 | panC | 6.3.2.1 | H | Catalyzes the condensation of pantoate with beta-alanine in an ATP-dependent reaction via a pantoyl-adenylate intermediate | |
COCLMCBI_02181 | 2.2e-120 | S | nadp oxidoreductase, coenzyme f420-dependent | |||
COCLMCBI_02182 | 1.3e-70 | |||||
COCLMCBI_02183 | 2.4e-75 | S | Protein of unknown function (DUF3180) | |||
COCLMCBI_02184 | 1.4e-75 | folK | 1.13.11.81, 2.5.1.15, 2.7.6.3, 3.5.4.16, 3.5.4.39, 4.1.2.25, 5.1.99.8 | H | 2-amino-4-hydroxy-6-hydroxymethyldihydropteridine | |
COCLMCBI_02185 | 2.1e-68 | folB | 1.13.11.81, 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 | |
COCLMCBI_02186 | 6.8e-159 | folP | 2.5.1.15 | H | Catalyzes the condensation of para-aminobenzoate (pABA) with 6-hydroxymethyl-7,8-dihydropterin diphosphate (DHPt-PP) to form 7,8-dihydropteroate (H2Pte), the immediate precursor of folate derivatives | |
COCLMCBI_02187 | 2.1e-115 | folE | 2.7.6.3, 3.5.4.16 | H | GTP cyclohydrolase | |
COCLMCBI_02188 | 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 | ||
COCLMCBI_02189 | 8.2e-114 | hpt | 2.4.2.8, 6.3.4.19 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
COCLMCBI_02193 | 1e-128 | 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 | |
COCLMCBI_02194 | 2.7e-217 | dacB | 3.4.16.4 | M | D-alanyl-D-alanine carboxypeptidase | |
COCLMCBI_02195 | 5e-115 | M | isomerase activity | |||
COCLMCBI_02196 | 8.2e-87 | ppa | 3.6.1.1 | C | Catalyzes the hydrolysis of inorganic pyrophosphate (PPi) forming two phosphate ions | |
COCLMCBI_02197 | 1.3e-85 | |||||
COCLMCBI_02198 | 3.7e-112 | ylcC | 3.4.22.70 | M | Sortase (surface protein transpeptidase) | |
COCLMCBI_02199 | 1.3e-42 | glpE | P | Sulfurtransferase | ||
COCLMCBI_02200 | 4.1e-73 | marR1 | K | transcriptional | ||
COCLMCBI_02201 | 6e-111 | echA6 | 4.2.1.17 | I | Belongs to the enoyl-CoA hydratase isomerase family | |
COCLMCBI_02202 | 1.6e-182 | ppk2 | 2.7.4.1 | S | polyphosphate kinase | |
COCLMCBI_02205 | 1.2e-286 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
COCLMCBI_02206 | 1.1e-266 | V | endonuclease | |||
COCLMCBI_02207 | 4e-252 | tpdA | E | desuccinylase and related deacylases | ||
COCLMCBI_02208 | 1e-90 | E | Belongs to the alpha-IPM synthase homocitrate synthase family | |||
COCLMCBI_02209 | 0.0 | mrpA | 1.6.5.3 | CP | NADH ubiquinone oxidoreductase subunit 5 (Chain L) Multisubunit Na H antiporter, MnhA subunit | |
COCLMCBI_02210 | 1.7e-79 | phaC | 1.6.5.3 | P | H antiporter | |
COCLMCBI_02211 | 0.0 | mrpD | CP | Formate hydrogenlyase subunit 3 Multisubunit Na H antiporter, MnhD subunit | ||
COCLMCBI_02212 | 7.1e-84 | mrpE | P | H antiporter | ||
COCLMCBI_02213 | 4.7e-42 | mrpF | P | monovalent cation H antiporter subunit F | ||
COCLMCBI_02214 | 1.2e-58 | mrpG | P | Subunit G of antiporter complex involved in resistance to high concentrations of Na , K , Li and or alkali | ||
COCLMCBI_02215 | 5.8e-153 | D | Protein of unknown function (DUF3375) | |||
COCLMCBI_02216 | 1.2e-80 | S | Domain of unknown function (DUF4194) | |||
COCLMCBI_02217 | 0.0 | S | Putative exonuclease SbcCD, C subunit | |||
COCLMCBI_02218 | 9.6e-110 | S | Uncharacterized protein conserved in bacteria N-term (DUF3322) | |||
COCLMCBI_02219 | 1.1e-222 | ybdK | H | ATP-dependent carboxylate-amine ligase which exhibits weak glutamate--cysteine ligase activity | ||
COCLMCBI_02220 | 3.2e-55 | S | LytR cell envelope-related transcriptional attenuator | |||
COCLMCBI_02221 | 1e-28 | S | Protein of unknown function (DUF3263) | |||
COCLMCBI_02222 | 2.3e-110 | def | 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions | |
COCLMCBI_02223 | 4.2e-173 | yobR | 2.3.1.1 | K | Acetyltransferase | |
COCLMCBI_02224 | 1.2e-146 | xthA | 3.1.11.2, 6.5.1.1 | L | exodeoxyribonuclease III | |
COCLMCBI_02225 | 0.0 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
COCLMCBI_02226 | 5.6e-39 | K | Psort location Cytoplasmic, score | |||
COCLMCBI_02227 | 2.8e-121 | sagI | S | ABC-2 family transporter protein | ||
COCLMCBI_02228 | 8.6e-155 | drrA_3 | V | ABC transporter, ATP-binding protein | ||
COCLMCBI_02229 | 5.9e-82 | mutT3 | 3.6.1.13, 3.6.1.55 | L | NUDIX domain | |
COCLMCBI_02230 | 1.5e-227 | 4.6.1.1 | T | phosphoserine phosphatase activity | ||
COCLMCBI_02231 | 2.7e-156 | glnH | ET | ABC-type amino acid transport signal transduction systems periplasmic component domain | ||
COCLMCBI_02232 | 0.0 | KLT | serine threonine protein kinase | |||
COCLMCBI_02233 | 8.6e-81 | |||||
COCLMCBI_02234 | 2.3e-100 | spoIVA | S | Conserved hypothetical ATP binding protein | ||
COCLMCBI_02235 | 7.5e-59 | T | response regulator | |||
COCLMCBI_02236 | 4.2e-212 | ackA | 2.7.2.1, 2.7.2.15 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
COCLMCBI_02237 | 4e-235 | pta | 1.1.1.40, 2.3.1.19, 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
COCLMCBI_02238 | 1.2e-263 | fprA | 1.18.1.2, 1.19.1.1 | E | NADPH-dependent glutamate synthase beta chain and related oxidoreductases | |
COCLMCBI_02239 | 3.8e-51 | |||||
COCLMCBI_02240 | 1.6e-49 | fprA | 1.18.1.2, 1.19.1.1 | E | NADPH-dependent glutamate synthase beta chain and related oxidoreductases | |
COCLMCBI_02241 | 3.5e-28 | fprA | 1.18.1.2, 1.19.1.1 | E | NADPH-dependent glutamate synthase beta chain and related oxidoreductases | |
COCLMCBI_02242 | 2.6e-26 | K | Helix-turn-helix domain | |||
COCLMCBI_02243 | 5.8e-34 | |||||
COCLMCBI_02244 | 3.6e-152 | |||||
COCLMCBI_02245 | 5.4e-14 | K | cell wall organization | |||
COCLMCBI_02247 | 4.7e-119 | ylcC | 3.4.22.70 | M | Sortase family | |
COCLMCBI_02248 | 1.6e-82 | D | CobQ CobB MinD ParA nucleotide binding domain | |||
COCLMCBI_02250 | 6.3e-18 | 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 | |
COCLMCBI_02252 | 5.6e-247 | purA | 6.3.4.4 | F | Plays an important role in the de novo pathway of purine nucleotide biosynthesis. Catalyzes the first committed step in the biosynthesis of AMP from IMP | |
COCLMCBI_02253 | 1.2e-136 | I | lipid kinase activity | |||
COCLMCBI_02254 | 2.3e-111 | puhA | S | protein conserved in bacteria | ||
COCLMCBI_02255 | 7.8e-220 | S | membrane | |||
COCLMCBI_02256 | 1.2e-191 | fbaA | 4.1.2.13 | G | aldolase | |
COCLMCBI_02257 | 3.4e-219 | G | hydrolase | |||
COCLMCBI_02258 | 3.5e-113 | spoU | 2.1.1.185 | J | RNA methyltransferase | |
COCLMCBI_02259 | 3.6e-106 | pyrE | 2.4.2.10 | F | Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) | |
COCLMCBI_02260 | 2.1e-109 | |||||
COCLMCBI_02261 | 4.3e-155 | sseB | 2.8.1.1, 2.8.1.2 | P | Rhodanese-related sulfurtransferase | |
COCLMCBI_02262 | 4e-66 | S | Domain of unknown function (DUF4265) | |||
COCLMCBI_02263 | 1.6e-38 | K | Psort location Cytoplasmic, score | |||
COCLMCBI_02264 | 0.0 | clpB | O | Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE | ||
COCLMCBI_02265 | 3e-68 | yobV3 | K | regulation of single-species biofilm formation | ||
COCLMCBI_02266 | 1.9e-248 | gltT | E | glutamate symporter | ||
COCLMCBI_02267 | 2.8e-128 | 1.16.1.3, 1.5.1.41 | C | 2 iron, 2 sulfur cluster binding | ||
COCLMCBI_02268 | 7.4e-141 | S | amidohydrolase | |||
COCLMCBI_02270 | 2.4e-180 | S | Alpha/beta hydrolase | |||
COCLMCBI_02271 | 0.0 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
COCLMCBI_02272 | 2.5e-46 | D | nuclear chromosome segregation | |||
COCLMCBI_02273 | 1.1e-63 | hspR | K | transcriptional | ||
COCLMCBI_02274 | 8.8e-170 | 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 | ||
COCLMCBI_02275 | 5.1e-96 | grpE | O | Participates actively in the response to hyperosmotic and heat shock by preventing the aggregation of stress-denatured proteins, in association with DnaK and GrpE. It is the nucleotide exchange factor for DnaK and may function as a thermosensor. Unfolded proteins bind initially to DnaJ | ||
COCLMCBI_02276 | 0.0 | dnaK | O | Heat shock 70 kDa protein | ||
COCLMCBI_02278 | 1.8e-87 | pfpI | 3.5.1.124 | S | Intracellular protease | |
COCLMCBI_02279 | 2.3e-190 | lplA | 6.3.1.20 | H | lipoate-protein ligase A | |
COCLMCBI_02280 | 1.5e-113 | S | Golgi phosphoprotein 3 (GPP34) | |||
COCLMCBI_02281 | 1.1e-78 | slyA | K | Winged helix DNA-binding domain | ||
COCLMCBI_02282 | 1e-48 | |||||
COCLMCBI_02283 | 2e-119 | ribB | 3.5.4.25, 4.1.99.12 | H | Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate | |
COCLMCBI_02284 | 2.6e-173 | 2.3.1.51 | I | Phosphate acyltransferases | ||
COCLMCBI_02285 | 0.0 | S | MMPL family | |||
COCLMCBI_02286 | 8.8e-98 | S | Golgi phosphoprotein 3 (GPP34) | |||
COCLMCBI_02287 | 1.3e-155 | ytnM | S | membrane transporter protein | ||
COCLMCBI_02288 | 2.1e-110 | cbiX | S | sirohydrochlorin cobaltochelatase | ||
COCLMCBI_02289 | 1.4e-221 | cysN | 2.7.1.25, 2.7.7.4 | H | Belongs to the TRAFAC class translation factor GTPase superfamily. Classic translation factor GTPase family. CysN NodQ subfamily | |
COCLMCBI_02290 | 1e-170 | cysD | 1.8.4.10, 1.8.4.8, 2.7.7.4 | H | 3'-phosphoadenosine 5'-phosphosulfate sulfotransferase (PAPS reductase) FAD synthetase and related enzymes | |
COCLMCBI_02291 | 2.9e-134 | cysH | 1.8.4.10, 1.8.4.8 | EH | Reduction of activated sulfate into sulfite | |
COCLMCBI_02292 | 1.4e-45 | |||||
COCLMCBI_02293 | 2e-308 | sir | 1.7.7.1, 1.8.7.1 | C | Belongs to the nitrite and sulfite reductase 4Fe-4S domain family | |
COCLMCBI_02294 | 7.8e-80 | 1.18.1.2, 1.19.1.1 | E | 'glutamate synthase | ||
COCLMCBI_02295 | 5.9e-70 | vapC | S | ribonuclease activity | ||
COCLMCBI_02297 | 3.5e-289 | ycfI | V | ABC-type multidrug transport system, ATPase and permease components | ||
COCLMCBI_02298 | 0.0 | V | ABC-type multidrug transport system, ATPase and permease components | |||
COCLMCBI_02299 | 4e-179 | nptA | P | phosphate symporter | ||
COCLMCBI_02300 | 2.6e-218 | nptA | P | phosphate symporter | ||
COCLMCBI_02301 | 4.7e-37 | |||||
COCLMCBI_02302 | 1.8e-160 | P | PBP superfamily domain | |||
COCLMCBI_02304 | 2.1e-09 | |||||
COCLMCBI_02305 | 7.7e-96 | S | Domain of unknown function (DUF1707) | |||
COCLMCBI_02306 | 1.2e-241 | alaA | 2.6.1.2, 2.6.1.66 | E | Aspartate tyrosine aromatic aminotransferase | |
COCLMCBI_02307 | 0.0 | crpB | M | Large extracellular alpha-helical protein | ||
COCLMCBI_02308 | 2.8e-241 | ugd | 1.1.1.22 | M | Belongs to the UDP-glucose GDP-mannose dehydrogenase family | |
COCLMCBI_02310 | 1.4e-98 | dcd | 3.5.4.13 | F | Belongs to the dCTP deaminase family | |
COCLMCBI_02312 | 8e-55 | S | acetyltransferases and hydrolases with the alpha beta hydrolase fold | |||
COCLMCBI_02313 | 6.5e-128 | S | acetyltransferases and hydrolases with the alpha beta hydrolase fold | |||
COCLMCBI_02314 | 6.5e-285 | vanW | V | vancomycin resistance protein | ||
COCLMCBI_02315 | 3.5e-179 | lpqI | 3.2.1.52 | G | Beta-glucosidase-related glycosidases | |
COCLMCBI_02316 | 9.7e-27 | S | Protein of unknown function (DUF2613) | |||
COCLMCBI_02317 | 0.0 | aftD | I | Domain of unknown function (DUF3367) | ||
COCLMCBI_02318 | 1.7e-173 | I | Acyltransferase | |||
COCLMCBI_02319 | 6.1e-86 | S | Protein of unknown function (DUF3068) | |||
COCLMCBI_02320 | 6.5e-242 | |||||
COCLMCBI_02321 | 2.6e-181 | M | Glycosyltransferase, group 1 family protein | |||
COCLMCBI_02322 | 1.4e-136 | bioC | 2.1.1.197 | Q | (SAM)-dependent | |
COCLMCBI_02323 | 0.0 | pckG | 4.1.1.32, 4.1.1.49 | H | Catalyzes the conversion of oxaloacetate (OAA) to phosphoenolpyruvate (PEP), the rate-limiting step in the metabolic pathway that produces glucose from lactate and other precursors derived from the citric acid cycle | |
COCLMCBI_02324 | 2.9e-134 | trmB | 2.1.1.297, 2.1.1.33, 2.4.99.12, 2.4.99.13, 2.4.99.14, 2.4.99.15 | GT30 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA |
COCLMCBI_02325 | 2e-126 | S | NYN domain | |||
COCLMCBI_02326 | 0.0 | mmpL3 | S | drug exporters of the RND superfamily | ||
COCLMCBI_02327 | 1.6e-164 | S | integral membrane protein | |||
COCLMCBI_02328 | 2.5e-101 | M | LPXTG-motif cell wall anchor domain protein | |||
COCLMCBI_02329 | 2.3e-11 | M | LPXTG-motif cell wall anchor domain protein | |||
COCLMCBI_02330 | 4.5e-17 | S | integral membrane protein | |||
COCLMCBI_02331 | 2.5e-271 | 1.3.1.72 | C | FAD FMN-containing dehydrogenases | ||
COCLMCBI_02332 | 5.7e-263 | cma | 2.1.1.79 | M | Cyclopropane fatty acid synthase and related methyltransferases | |
COCLMCBI_02333 | 1.2e-59 | S | Protein of unknown function (DUF3054) | |||
COCLMCBI_02335 | 3.7e-72 | M | LPXTG-motif cell wall anchor domain protein | |||
COCLMCBI_02336 | 1.5e-33 | S | Type I phosphodiesterase / nucleotide pyrophosphatase | |||
COCLMCBI_02337 | 2.4e-108 | S | Type I phosphodiesterase / nucleotide pyrophosphatase | |||
COCLMCBI_02338 | 1.9e-107 | 3.6.3.30 | P | Part of the ABC transporter complex CysAWTP involved in sulfate thiosulfate import. Responsible for energy coupling to the transport system | ||
COCLMCBI_02339 | 1.1e-102 | P | Binding-protein-dependent transport system inner membrane component | |||
COCLMCBI_02340 | 6e-20 | P | Binding-protein-dependent transport systems inner membrane component | |||
COCLMCBI_02341 | 3e-31 | P | Binding-protein-dependent transport systems inner membrane component | |||
COCLMCBI_02342 | 1.4e-32 | P | Bacterial extracellular solute-binding protein | |||
COCLMCBI_02343 | 6.7e-52 | P | Bacterial extracellular solute-binding protein | |||
COCLMCBI_02344 | 4.2e-97 | pgmB | 3.1.3.18, 5.4.2.6 | S | HAD hydrolase, family IA, variant 3 | |
COCLMCBI_02345 | 1.9e-107 | 2.7.7.7 | L | DNA polymerase III, epsilon subunit | ||
COCLMCBI_02346 | 3.9e-245 | yfjM | K | Protein of unknown function DUF262 | ||
COCLMCBI_02347 | 1.9e-88 | 3.6.4.13 | L | Restriction endonuclease | ||
COCLMCBI_02348 | 2.7e-28 | 3.6.4.13 | L | Restriction endonuclease | ||
COCLMCBI_02349 | 2.9e-25 | 3.6.4.13 | L | Restriction endonuclease | ||
COCLMCBI_02350 | 0.0 | 3.6.4.13 | L | Restriction endonuclease | ||
COCLMCBI_02352 | 2.3e-08 | D | Domain of Unknown Function (DUF349) | |||
COCLMCBI_02353 | 1.1e-12 | tnp3521a1 | L | Transposase and inactivated derivatives | ||
COCLMCBI_02354 | 6.9e-109 | L | Transposase and inactivated derivatives | |||
COCLMCBI_02355 | 9.4e-153 | tnp7109-46 | L | Transposase and inactivated derivatives | ||
COCLMCBI_02356 | 9e-50 | L | Transposase and inactivated derivatives | |||
COCLMCBI_02357 | 3.2e-115 | L | Transposase and inactivated derivatives | |||
COCLMCBI_02360 | 3.1e-205 | |||||
COCLMCBI_02361 | 4e-43 | arsR | K | transcriptional | ||
COCLMCBI_02362 | 3.8e-47 | sbcC | L | DNA repair | ||
COCLMCBI_02363 | 4.8e-43 | sbcC | L | DNA repair | ||
COCLMCBI_02364 | 1e-19 | sbcC | L | DNA repair | ||
COCLMCBI_02365 | 2.2e-31 | sbcD | L | DNA repair exonuclease | ||
COCLMCBI_02366 | 1.9e-20 | sbcD | L | DNA repair exonuclease | ||
COCLMCBI_02367 | 1.7e-31 | helZ | 2.7.11.1 | L | SNF2 family | |
COCLMCBI_02368 | 1.6e-77 | helZ | 2.7.11.1 | L | SNF2 family | |
COCLMCBI_02369 | 6.5e-49 | helZ | 2.7.11.1 | L | SNF2 family | |
COCLMCBI_02370 | 4.3e-91 | helZ | 2.7.11.1 | L | SNF2 family | |
COCLMCBI_02371 | 4.1e-61 | helZ | 2.7.11.1 | L | SNF2 family | |
COCLMCBI_02372 | 5.9e-35 | helZ | 2.7.11.1 | L | SNF2 family | |
COCLMCBI_02373 | 3.4e-278 | putP | E | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
COCLMCBI_02374 | 1.4e-121 | L | HNH endonuclease | |||
COCLMCBI_02375 | 2.1e-77 | |||||
COCLMCBI_02376 | 2.9e-290 | deaD | 3.6.4.13 | JKL | DEAD-box RNA helicase involved in various cellular processes at low temperature, including ribosome biogenesis, mRNA degradation and translation initiation | |
COCLMCBI_02377 | 2.9e-84 | 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 | |||
COCLMCBI_02378 | 8.4e-106 | rhtC | E | threonine efflux protein | ||
COCLMCBI_02380 | 3.3e-55 | |||||
COCLMCBI_02382 | 3.2e-08 | |||||
COCLMCBI_02383 | 1.9e-53 | nudG | 3.6.1.55, 3.6.1.65 | L | NTP pyrophosphohydrolases including oxidative damage repair enzymes | |
COCLMCBI_02384 | 1.8e-174 | dcm | 2.1.1.37 | L | DNA restriction-modification system | |
COCLMCBI_02385 | 4.2e-17 | V | endonuclease activity | |||
COCLMCBI_02386 | 2.4e-10 | V | endonuclease activity | |||
COCLMCBI_02388 | 2.2e-111 | iunH | 3.2.2.1 | F | inosine-uridine preferring nucleoside hydrolase | |
COCLMCBI_02389 | 5.7e-67 | iunH | 3.2.2.1 | F | inosine-uridine preferring nucleoside hydrolase | |
COCLMCBI_02390 | 2.1e-153 | blt | EGP | Major facilitator Superfamily | ||
COCLMCBI_02391 | 7.8e-29 | |||||
COCLMCBI_02393 | 3.8e-69 | |||||
COCLMCBI_02394 | 9.7e-171 | lipT | CE10 | I | Belongs to the type-B carboxylesterase lipase family | |
COCLMCBI_02395 | 1.1e-126 | |||||
COCLMCBI_02396 | 5.4e-78 | |||||
COCLMCBI_02397 | 3.6e-30 | blt | EGP | Major facilitator Superfamily | ||
COCLMCBI_02398 | 6e-41 | iunH | 3.2.2.1 | F | inosine-uridine preferring nucleoside hydrolase | |
COCLMCBI_02399 | 6.4e-125 | iunH | 3.2.2.1 | F | inosine-uridine preferring nucleoside hydrolase | |
COCLMCBI_02401 | 5.1e-56 | V | HNH endonuclease | |||
COCLMCBI_02402 | 1.8e-174 | dcm | 2.1.1.37 | L | DNA restriction-modification system | |
COCLMCBI_02403 | 1.7e-53 | nudG | 3.6.1.55, 3.6.1.65 | L | NTP pyrophosphohydrolases including oxidative damage repair enzymes | |
COCLMCBI_02404 | 9.4e-153 | tnp7109-46 | L | Transposase and inactivated derivatives | ||
COCLMCBI_02405 | 9e-50 | L | Transposase and inactivated derivatives | |||
COCLMCBI_02406 | 3.1e-59 | L | Transposase and inactivated derivatives | |||
COCLMCBI_02409 | 2.5e-247 | |||||
COCLMCBI_02410 | 4e-43 | arsR | K | transcriptional | ||
COCLMCBI_02411 | 2.5e-190 | arsB | P | Arsenite efflux pump ACR3 and related permeases | ||
COCLMCBI_02412 | 4.3e-71 | arsC | 1.20.4.1, 2.8.4.2 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
COCLMCBI_02413 | 8.6e-76 | S | Protein of unknown function, DUF488 | |||
COCLMCBI_02414 | 1.2e-43 | birA | 2.7.1.33, 6.3.4.15 | H | Biotin-(Acetyl-CoA carboxylase) ligase | |
COCLMCBI_02415 | 4.2e-56 | birA | 2.7.1.33, 6.3.4.15 | H | Biotin-(Acetyl-CoA carboxylase) ligase | |
COCLMCBI_02416 | 3.9e-67 | S | Bacterial PH domain | |||
COCLMCBI_02417 | 2e-138 | budA | 4.1.1.5 | Q | Belongs to the alpha-acetolactate decarboxylase family |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)