ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
EOOGHDJN_00001 | 9.4e-137 | pre | D | Plasmid recombination enzyme | ||
EOOGHDJN_00004 | 4.4e-84 | L | Replication protein | |||
EOOGHDJN_00005 | 1.9e-83 | yoaA | 2.3.1.128 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | |
EOOGHDJN_00006 | 1.3e-262 | nox | C | NADH oxidase | ||
EOOGHDJN_00007 | 0.0 | XK27_00720 | S | Leucine-rich repeat (LRR) protein | ||
EOOGHDJN_00008 | 6.1e-164 | S | Cell surface protein | |||
EOOGHDJN_00009 | 1.5e-118 | S | WxL domain surface cell wall-binding | |||
EOOGHDJN_00010 | 2.3e-99 | S | WxL domain surface cell wall-binding | |||
EOOGHDJN_00011 | 3e-44 | |||||
EOOGHDJN_00012 | 5.4e-104 | K | Bacterial regulatory proteins, tetR family | |||
EOOGHDJN_00013 | 1.5e-49 | |||||
EOOGHDJN_00014 | 1.4e-248 | S | Putative metallopeptidase domain | |||
EOOGHDJN_00015 | 2.4e-220 | 3.1.3.1 | S | associated with various cellular activities | ||
EOOGHDJN_00016 | 1.8e-108 | aqpZ | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
EOOGHDJN_00017 | 0.0 | ubiB | S | ABC1 family | ||
EOOGHDJN_00018 | 1.3e-249 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
EOOGHDJN_00019 | 0.0 | lacS | G | Transporter | ||
EOOGHDJN_00020 | 0.0 | lacA | 3.2.1.23 | G | -beta-galactosidase | |
EOOGHDJN_00021 | 2.1e-188 | lacR | K | Transcriptional regulator | ||
EOOGHDJN_00022 | 0.0 | 3.2.1.40 | G | Bacterial alpha-L-rhamnosidase 6 hairpin glycosidase domain | ||
EOOGHDJN_00023 | 1.4e-229 | mdtH | P | Sugar (and other) transporter | ||
EOOGHDJN_00024 | 7.9e-304 | ram2 | 3.2.1.40 | G | Bacterial alpha-L-rhamnosidase 6 hairpin glycosidase domain | |
EOOGHDJN_00025 | 8.6e-232 | EGP | Major facilitator Superfamily | |||
EOOGHDJN_00026 | 7.4e-183 | rhaR | K | helix_turn_helix, arabinose operon control protein | ||
EOOGHDJN_00027 | 3.5e-111 | fic | D | Fic/DOC family | ||
EOOGHDJN_00028 | 1.6e-76 | K | Helix-turn-helix XRE-family like proteins | |||
EOOGHDJN_00029 | 2e-183 | galR | K | Transcriptional regulator | ||
EOOGHDJN_00030 | 1.3e-284 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
EOOGHDJN_00031 | 3.1e-192 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
EOOGHDJN_00032 | 7.8e-224 | galK | 2.7.1.6 | F | Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) | |
EOOGHDJN_00033 | 0.0 | lacL | 3.2.1.23 | G | Belongs to the glycosyl hydrolase 2 family | |
EOOGHDJN_00034 | 1.8e-186 | lacM | 3.2.1.23, 3.2.1.35, 3.2.1.51, 3.2.1.97 | GH101,GH29 | G | beta-galactosidase |
EOOGHDJN_00035 | 0.0 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
EOOGHDJN_00036 | 0.0 | lacS | G | Transporter | ||
EOOGHDJN_00037 | 1.3e-198 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
EOOGHDJN_00038 | 1.1e-173 | galR | K | Transcriptional regulator | ||
EOOGHDJN_00039 | 7.4e-194 | C | Aldo keto reductase family protein | |||
EOOGHDJN_00040 | 2.4e-65 | S | pyridoxamine 5-phosphate | |||
EOOGHDJN_00041 | 0.0 | 1.3.5.4 | C | FAD binding domain | ||
EOOGHDJN_00042 | 8.2e-179 | apbE | 2.7.1.180 | H | Flavin transferase that catalyzes the transfer of the FMN moiety of FAD and its covalent binding to the hydroxyl group of a threonine residue in a target flavoprotein | |
EOOGHDJN_00043 | 2.4e-133 | aroD | 1.1.1.25, 4.2.1.10 | E | Involved in the third step of the chorismate pathway, which leads to the biosynthesis of aromatic amino acids. Catalyzes the cis-dehydration of 3-dehydroquinate (DHQ) and introduces the first double bond of the aromatic ring to yield 3- dehydroshikimate | |
EOOGHDJN_00044 | 1.3e-165 | aroE | 1.1.1.25, 1.1.1.282, 1.3.5.4 | E | Involved in the biosynthesis of the chorismate, which leads to the biosynthesis of aromatic amino acids. Catalyzes the reversible NADPH linked reduction of 3-dehydroshikimate (DHSA) to yield shikimate (SA) | |
EOOGHDJN_00045 | 9.2e-175 | K | Transcriptional regulator, LysR family | |||
EOOGHDJN_00046 | 1.2e-219 | ydiN | EGP | Major Facilitator Superfamily | ||
EOOGHDJN_00047 | 1.9e-161 | aroE | 1.1.1.25 | E | Involved in the biosynthesis of the chorismate, which leads to the biosynthesis of aromatic amino acids. Catalyzes the reversible NADPH linked reduction of 3-dehydroshikimate (DHSA) to yield shikimate (SA) | |
EOOGHDJN_00048 | 2.7e-160 | aroE | 1.1.1.25 | E | Involved in the biosynthesis of the chorismate, which leads to the biosynthesis of aromatic amino acids. Catalyzes the reversible NADPH linked reduction of 3-dehydroshikimate (DHSA) to yield shikimate (SA) | |
EOOGHDJN_00049 | 1e-156 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
EOOGHDJN_00050 | 2.1e-165 | G | Xylose isomerase-like TIM barrel | |||
EOOGHDJN_00051 | 4.7e-168 | K | Transcriptional regulator, LysR family | |||
EOOGHDJN_00052 | 1.2e-201 | EGP | Major Facilitator Superfamily | |||
EOOGHDJN_00053 | 2.2e-63 | |||||
EOOGHDJN_00054 | 1.8e-155 | estA | S | Putative esterase | ||
EOOGHDJN_00055 | 8.1e-134 | K | UTRA domain | |||
EOOGHDJN_00056 | 3.6e-249 | pts29C | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
EOOGHDJN_00057 | 3e-165 | murQ | 4.2.1.126 | G | Specifically catalyzes the cleavage of the D-lactyl ether substituent of MurNAc 6-phosphate, producing GlcNAc 6- phosphate and D-lactate | |
EOOGHDJN_00058 | 1.9e-161 | 2.7.1.59 | G | BadF/BadG/BcrA/BcrD ATPase family | ||
EOOGHDJN_00059 | 1.7e-212 | S | Bacterial protein of unknown function (DUF871) | |||
EOOGHDJN_00060 | 1e-292 | bglH | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
EOOGHDJN_00061 | 0.0 | pts30BCA | 2.7.1.193, 2.7.1.211 | G | phosphotransferase system | |
EOOGHDJN_00062 | 1.3e-154 | licT | K | CAT RNA binding domain | ||
EOOGHDJN_00063 | 7.6e-293 | bglH | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
EOOGHDJN_00064 | 9.4e-291 | pbg10 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
EOOGHDJN_00065 | 0.0 | bglP | 2.7.1.193, 2.7.1.211 | G | phosphotransferase system | |
EOOGHDJN_00066 | 3.8e-159 | licT | K | CAT RNA binding domain | ||
EOOGHDJN_00067 | 0.0 | treP | 2.4.1.64 | GH65 | G | hydrolase, family 65, central catalytic |
EOOGHDJN_00068 | 2.1e-174 | K | Transcriptional regulator, LacI family | |||
EOOGHDJN_00069 | 1.5e-269 | G | Major Facilitator | |||
EOOGHDJN_00070 | 0.0 | malZ | 3.2.1.20 | GH31 | G | Belongs to the glycosyl hydrolase 31 family |
EOOGHDJN_00071 | 1.3e-187 | cbh | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
EOOGHDJN_00072 | 1.5e-144 | yxeH | S | hydrolase | ||
EOOGHDJN_00073 | 0.0 | tkt | 2.2.1.1 | H | Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate | |
EOOGHDJN_00074 | 7e-113 | tal | 2.2.1.2 | F | Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway | |
EOOGHDJN_00075 | 6.4e-241 | ulaA | 2.7.1.194 | S | PTS system sugar-specific permease component | |
EOOGHDJN_00076 | 6.3e-45 | ulaB | 2.7.1.194, 2.7.1.200 | G | Phosphotransferase system galactitol-specific IIB component | |
EOOGHDJN_00077 | 6.7e-78 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
EOOGHDJN_00078 | 0.0 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
EOOGHDJN_00079 | 1.3e-113 | gph | 3.1.3.18 | S | Haloacid dehalogenase-like hydrolase | |
EOOGHDJN_00080 | 8.6e-188 | gutB | 1.1.1.1, 1.1.1.14 | C | Zinc-binding dehydrogenase | |
EOOGHDJN_00081 | 1.1e-231 | gatC | G | PTS system sugar-specific permease component | ||
EOOGHDJN_00082 | 1.1e-44 | 2.7.1.194, 2.7.1.200 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
EOOGHDJN_00083 | 8.1e-79 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
EOOGHDJN_00084 | 5.2e-123 | K | DeoR C terminal sensor domain | |||
EOOGHDJN_00085 | 0.0 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
EOOGHDJN_00086 | 1.5e-49 | yueI | S | Protein of unknown function (DUF1694) | ||
EOOGHDJN_00087 | 8.1e-10 | yueI | S | Protein of unknown function (DUF1694) | ||
EOOGHDJN_00088 | 9.6e-103 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose O-acetyltransferase | |
EOOGHDJN_00089 | 1.3e-265 | araA | 5.3.1.4 | G | Catalyzes the conversion of L-arabinose to L-ribulose | |
EOOGHDJN_00090 | 1e-136 | araD | 4.1.2.17, 4.1.2.19, 5.1.3.4 | G | links the arabinose metabolic pathway to the pentose phosphate pathway and allows the bacteria to use arabinose as an energy source | |
EOOGHDJN_00091 | 9.5e-305 | araB | 2.7.1.12, 2.7.1.16, 2.7.1.5 | G | carbohydrate kinase FGGY | |
EOOGHDJN_00092 | 1.6e-255 | araP | U | Belongs to the major facilitator superfamily. Sugar transporter (TC 2.A.1.1) family | ||
EOOGHDJN_00093 | 3.1e-206 | araR | K | Transcriptional regulator | ||
EOOGHDJN_00094 | 1e-122 | nanE | 5.1.3.9 | G | Converts N-acetylmannosamine-6-phosphate (ManNAc-6-P) to N-acetylglucosamine-6-phosphate (GlcNAc-6-P) | |
EOOGHDJN_00095 | 1.3e-229 | 1.7.1.15 | S | Pyridine nucleotide-disulphide oxidoreductase | ||
EOOGHDJN_00096 | 4.2e-70 | S | Pyrimidine dimer DNA glycosylase | |||
EOOGHDJN_00097 | 1.6e-89 | folT | 2.7.13.3 | T | ECF transporter, substrate-specific component | |
EOOGHDJN_00098 | 3.6e-11 | |||||
EOOGHDJN_00099 | 9e-13 | ytgB | S | Transglycosylase associated protein | ||
EOOGHDJN_00100 | 3.2e-291 | katA | 1.11.1.6 | C | Belongs to the catalase family | |
EOOGHDJN_00101 | 4.9e-78 | yneH | 1.20.4.1 | K | ArsC family | |
EOOGHDJN_00102 | 5.7e-135 | K | LytTr DNA-binding domain | |||
EOOGHDJN_00103 | 3.2e-223 | 2.7.13.3 | T | GHKL domain | ||
EOOGHDJN_00104 | 5.7e-16 | |||||
EOOGHDJN_00105 | 8.5e-97 | agrB | KOT | May be involved in the proteolytic processing of a quorum sensing system signal molecule precursor | ||
EOOGHDJN_00106 | 0.0 | clpL | O | C-terminal, D2-small domain, of ClpB protein | ||
EOOGHDJN_00108 | 6.1e-202 | lctO | C | L-lactate dehydrogenase (FMN-dependent) and related alpha-hydroxy acid dehydrogenases | ||
EOOGHDJN_00109 | 0.0 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
EOOGHDJN_00110 | 8.7e-72 | K | Transcriptional regulator | |||
EOOGHDJN_00111 | 0.0 | spxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
EOOGHDJN_00112 | 4.2e-71 | yueI | S | Protein of unknown function (DUF1694) | ||
EOOGHDJN_00113 | 1e-125 | S | Membrane | |||
EOOGHDJN_00114 | 1.2e-165 | rhaD | 4.1.2.17, 4.1.2.19, 5.1.3.4 | H | Catalyzes the reversible cleavage of L-rhamnulose-1- phosphate to dihydroxyacetone phosphate (DHAP) and L-lactaldehyde | |
EOOGHDJN_00115 | 1.3e-256 | rhaA | 2.7.1.5, 5.3.1.14 | G | L-rhamnose isomerase (RhaA) | |
EOOGHDJN_00116 | 5e-56 | rhaM | 5.1.3.32 | G | Involved in the anomeric conversion of L-rhamnose | |
EOOGHDJN_00117 | 1.8e-286 | rhaB | 2.7.1.12, 2.7.1.16, 2.7.1.5, 5.3.1.14 | F | Involved in the catabolism of L-rhamnose (6-deoxy-L- mannose). Catalyzes the transfer of the gamma-phosphate group from ATP to the 1-hydroxyl group of L-rhamnulose to yield L-rhamnulose 1-phosphate | |
EOOGHDJN_00118 | 4.6e-244 | iolF | EGP | Major facilitator Superfamily | ||
EOOGHDJN_00119 | 3.8e-179 | rhaR | K | helix_turn_helix, arabinose operon control protein | ||
EOOGHDJN_00120 | 2.1e-140 | K | DeoR C terminal sensor domain | |||
EOOGHDJN_00121 | 4.2e-80 | pts36A | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
EOOGHDJN_00122 | 3.3e-52 | sgcB | 2.7.1.194, 2.7.1.200 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
EOOGHDJN_00123 | 1.1e-249 | pts36C | G | PTS system sugar-specific permease component | ||
EOOGHDJN_00125 | 1.5e-135 | araD | 4.1.2.17, 4.1.2.19, 5.1.3.4 | G | Class II Aldolase and Adducin N-terminal domain | |
EOOGHDJN_00126 | 2.8e-260 | iolT | EGP | Major facilitator Superfamily | ||
EOOGHDJN_00127 | 6.6e-198 | 1.1.1.18, 1.1.1.369 | S | Oxidoreductase family, C-terminal alpha/beta domain | ||
EOOGHDJN_00128 | 7.6e-202 | iolG | 1.1.1.18, 1.1.1.369 | C | Involved in the oxidation of myo-inositol (MI) and D- chiro-inositol (DCI) to 2-keto-myo-inositol (2KMI or 2-inosose) and 1-keto-D-chiro-inositol (1KDCI), respectively | |
EOOGHDJN_00129 | 5e-178 | iolE | 4.2.1.44 | G | Catalyzes the dehydration of inosose (2-keto-myo- inositol, 2KMI or 2,4,6 3,5-pentahydroxycyclohexanone) to 3D- (3,5 4)-trihydroxycyclohexane-1,2-dione (D-2,3-diketo-4-deoxy-epi- inositol) | |
EOOGHDJN_00130 | 4.2e-197 | iolG | 1.1.1.18, 1.1.1.369 | S | Oxidoreductase family, C-terminal alpha/beta domain | |
EOOGHDJN_00131 | 1.3e-268 | iolT | EGP | Major facilitator Superfamily | ||
EOOGHDJN_00132 | 1.2e-191 | iolG | 1.1.1.18, 1.1.1.369 | S | Oxidoreductase family, C-terminal alpha/beta domain | |
EOOGHDJN_00133 | 7.8e-82 | S | Haem-degrading | |||
EOOGHDJN_00134 | 2.1e-171 | 3.5.1.10 | C | Alcohol dehydrogenase GroES-like domain | ||
EOOGHDJN_00135 | 1.5e-177 | rihA | 3.2.2.1 | F | Inosine-uridine preferring nucleoside hydrolase | |
EOOGHDJN_00136 | 7.6e-118 | tal | 2.2.1.2 | H | Transaldolase/Fructose-6-phosphate aldolase | |
EOOGHDJN_00137 | 8.5e-63 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
EOOGHDJN_00138 | 6.5e-174 | srlE | 2.7.1.198 | G | Sorbitol phosphotransferase enzyme II N-terminus | |
EOOGHDJN_00139 | 6.3e-102 | srlA | G | PTS system enzyme II sorbitol-specific factor | ||
EOOGHDJN_00140 | 9.2e-92 | gutM | K | Glucitol operon activator protein (GutM) | ||
EOOGHDJN_00141 | 0.0 | srlM | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GKT | Mga helix-turn-helix domain | |
EOOGHDJN_00142 | 3.6e-144 | IQ | NAD dependent epimerase/dehydratase family | |||
EOOGHDJN_00143 | 5.9e-287 | bgl | 3.2.1.21, 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
EOOGHDJN_00144 | 7.9e-160 | ypbG | 2.7.1.2 | GK | ROK family | |
EOOGHDJN_00145 | 0.0 | mngB | 2.3.1.204, 3.2.1.170, 3.2.1.24 | GH38 | G | Glycosyl hydrolases family 38 N-terminal domain |
EOOGHDJN_00146 | 3.1e-253 | S | Metal-independent alpha-mannosidase (GH125) | |||
EOOGHDJN_00147 | 1e-193 | rliB | K | Transcriptional regulator | ||
EOOGHDJN_00148 | 0.0 | ypdD | G | Glycosyl hydrolase family 92 | ||
EOOGHDJN_00149 | 9.1e-217 | msmX | P | Belongs to the ABC transporter superfamily | ||
EOOGHDJN_00150 | 2.1e-165 | scrK | 2.7.1.2, 2.7.1.4 | GK | ROK family | |
EOOGHDJN_00151 | 6.3e-271 | yesN | K | helix_turn_helix, arabinose operon control protein | ||
EOOGHDJN_00152 | 0.0 | yesM | 2.7.13.3 | T | Histidine kinase | |
EOOGHDJN_00153 | 4.1e-107 | ypcB | S | integral membrane protein | ||
EOOGHDJN_00154 | 0.0 | dexB | 3.2.1.10, 3.2.1.70 | GH13 | G | Alpha amylase, catalytic domain protein |
EOOGHDJN_00155 | 9.8e-280 | G | Domain of unknown function (DUF3502) | |||
EOOGHDJN_00156 | 1.5e-161 | lplC | U | Binding-protein-dependent transport system inner membrane component | ||
EOOGHDJN_00157 | 5.2e-181 | U | Binding-protein-dependent transport system inner membrane component | |||
EOOGHDJN_00158 | 0.0 | 3.2.1.52 | GH20 | G | Glycosyl hydrolase family 20, catalytic domain | |
EOOGHDJN_00159 | 6e-94 | K | AraC-like ligand binding domain | |||
EOOGHDJN_00160 | 9.5e-38 | K | AraC-like ligand binding domain | |||
EOOGHDJN_00161 | 0.0 | mdlA2 | V | ABC transporter | ||
EOOGHDJN_00162 | 7.9e-308 | yknV | V | ABC transporter | ||
EOOGHDJN_00163 | 2.2e-193 | rliB | K | helix_turn_helix gluconate operon transcriptional repressor | ||
EOOGHDJN_00164 | 6.8e-156 | lrp | QT | PucR C-terminal helix-turn-helix domain | ||
EOOGHDJN_00165 | 8.6e-63 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
EOOGHDJN_00166 | 1e-174 | srlE | 2.7.1.198 | G | Sorbitol phosphotransferase enzyme II N-terminus | |
EOOGHDJN_00167 | 2e-100 | srlA | G | PTS system enzyme II sorbitol-specific factor | ||
EOOGHDJN_00168 | 1.1e-86 | gutM | K | Glucitol operon activator protein (GutM) | ||
EOOGHDJN_00169 | 0.0 | srlM | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GKT | Mga helix-turn-helix domain | |
EOOGHDJN_00170 | 1.5e-144 | IQ | NAD dependent epimerase/dehydratase family | |||
EOOGHDJN_00171 | 2.7e-160 | rbsU | U | ribose uptake protein RbsU | ||
EOOGHDJN_00172 | 1e-66 | rbsD | 5.4.99.62 | G | Catalyzes the interconversion of beta-pyran and beta- furan forms of D-ribose | |
EOOGHDJN_00173 | 2.3e-162 | 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 | |
EOOGHDJN_00174 | 5.9e-188 | rbsR | K | helix_turn _helix lactose operon repressor | ||
EOOGHDJN_00175 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
EOOGHDJN_00176 | 2.7e-79 | T | Universal stress protein family | |||
EOOGHDJN_00177 | 2.2e-99 | padR | K | Virulence activator alpha C-term | ||
EOOGHDJN_00178 | 1.7e-104 | padC | Q | Phenolic acid decarboxylase | ||
EOOGHDJN_00179 | 2.3e-142 | tesE | Q | hydratase | ||
EOOGHDJN_00180 | 2.2e-87 | yjaB_1 | K | Acetyltransferase (GNAT) domain | ||
EOOGHDJN_00181 | 1.2e-157 | degV | S | DegV family | ||
EOOGHDJN_00182 | 1.4e-58 | 2.6.1.2, 2.6.1.66 | K | Bacteriophage CI repressor helix-turn-helix domain | ||
EOOGHDJN_00183 | 1.5e-255 | pepC | 3.4.22.40 | E | aminopeptidase | |
EOOGHDJN_00185 | 3.6e-108 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
EOOGHDJN_00186 | 1.1e-302 | |||||
EOOGHDJN_00188 | 1.2e-159 | S | Bacterial protein of unknown function (DUF916) | |||
EOOGHDJN_00189 | 6.9e-93 | S | Cell surface protein | |||
EOOGHDJN_00190 | 0.0 | gidA | D | NAD-binding protein involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA-cmnm(5)s(2)U34 | ||
EOOGHDJN_00191 | 4.6e-255 | mnmE | S | Exhibits a very high intrinsic GTPase hydrolysis rate. Involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA- cmnm(5)s(2)U34 | ||
EOOGHDJN_00192 | 2.5e-130 | jag | S | R3H domain protein | ||
EOOGHDJN_00193 | 1.8e-105 | yidC | U | Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins | ||
EOOGHDJN_00194 | 6.4e-57 | 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 | |
EOOGHDJN_00195 | 9.1e-256 | 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 | ||
EOOGHDJN_00196 | 2e-208 | 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 | |
EOOGHDJN_00197 | 5e-37 | yaaA | S | S4 domain protein YaaA | ||
EOOGHDJN_00198 | 1.9e-206 | 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 | ||
EOOGHDJN_00199 | 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 | |
EOOGHDJN_00200 | 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 | |
EOOGHDJN_00201 | 1.5e-49 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
EOOGHDJN_00202 | 6.8e-62 | ssb | L | Plays an important role in DNA replication, recombination and repair. Binds to ssDNA and to an array of partner proteins to recruit them to their sites of action during DNA metabolism | ||
EOOGHDJN_00203 | 6.2e-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 | ||
EOOGHDJN_00204 | 0.0 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
EOOGHDJN_00205 | 1.4e-67 | rplI | J | Binds to the 23S rRNA | ||
EOOGHDJN_00206 | 7.8e-242 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
EOOGHDJN_00207 | 8.8e-226 | yttB | EGP | Major facilitator Superfamily | ||
EOOGHDJN_00208 | 3.6e-143 | proB | 2.7.2.11 | F | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
EOOGHDJN_00209 | 4.3e-228 | 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 | |
EOOGHDJN_00211 | 1.9e-276 | E | ABC transporter, substratebinding protein | |||
EOOGHDJN_00213 | 0.0 | glgB | 2.4.1.18, 3.2.1.141, 3.2.1.20 | CBM48,GH13,GH31 | G | Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position |
EOOGHDJN_00214 | 1.5e-214 | glgC | 2.7.7.27 | H | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
EOOGHDJN_00215 | 6.3e-197 | glgD | 2.4.1.21, 2.7.7.27 | GT5 | G | Nucleotidyl transferase |
EOOGHDJN_00216 | 2.2e-276 | glgA | 2.4.1.21 | GT5 | F | Synthesizes alpha-1,4-glucan chains using ADP-glucose |
EOOGHDJN_00217 | 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 |
EOOGHDJN_00218 | 0.0 | malQ | 2.4.1.25, 3.2.1.20, 3.2.1.41 | CBM48,GH13,GH31,GH77 | G | Belongs to the glycosyl hydrolase 13 family |
EOOGHDJN_00220 | 7.6e-143 | S | haloacid dehalogenase-like hydrolase | |||
EOOGHDJN_00221 | 1e-119 | pgmB | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | S | beta-phosphoglucomutase |
EOOGHDJN_00222 | 0.0 | trePP | 2.4.1.216, 2.4.1.8, 3.1.3.12, 3.2.1.28 | GH37,GH65 | G | Glycosyl hydrolase family 65 central catalytic domain |
EOOGHDJN_00223 | 1.5e-77 | S | Pyridoxamine 5'-phosphate oxidase | |||
EOOGHDJN_00224 | 1.6e-31 | cspA | K | Cold shock protein domain | ||
EOOGHDJN_00225 | 1.7e-37 | |||||
EOOGHDJN_00227 | 6.2e-131 | K | response regulator | |||
EOOGHDJN_00228 | 0.0 | vicK | 2.7.13.3 | T | Histidine kinase | |
EOOGHDJN_00229 | 1.2e-244 | yycH | S | YycH protein | ||
EOOGHDJN_00230 | 2.2e-151 | yycI | S | YycH protein | ||
EOOGHDJN_00231 | 8.9e-158 | vicX | 3.1.26.11 | S | domain protein | |
EOOGHDJN_00232 | 6.8e-173 | htrA | 3.4.21.107 | O | serine protease | |
EOOGHDJN_00233 | 1.2e-82 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
EOOGHDJN_00234 | 1.5e-95 | K | Bacterial regulatory proteins, tetR family | |||
EOOGHDJN_00235 | 7.5e-261 | calB | 1.2.1.68 | C | Belongs to the aldehyde dehydrogenase family | |
EOOGHDJN_00236 | 1.5e-167 | L | Cleaves both 3' and 5' ssDNA extremities of branched DNA structures | |||
EOOGHDJN_00237 | 6.8e-121 | ung2 | 3.2.2.27 | L | Uracil-DNA glycosylase | |
EOOGHDJN_00238 | 1.4e-121 | pnb | C | nitroreductase | ||
EOOGHDJN_00239 | 5.2e-65 | queD | 4.1.2.50, 4.2.3.12 | H | 6-pyruvoyl tetrahydropterin synthase | |
EOOGHDJN_00240 | 1.8e-116 | S | Elongation factor G-binding protein, N-terminal | |||
EOOGHDJN_00241 | 0.0 | nqr | 1.3.5.4, 1.5.1.36 | C | FMN_bind | |
EOOGHDJN_00242 | 1.6e-258 | P | Sodium:sulfate symporter transmembrane region | |||
EOOGHDJN_00243 | 5.7e-158 | K | LysR family | |||
EOOGHDJN_00244 | 1e-72 | C | FMN binding | |||
EOOGHDJN_00245 | 1.1e-74 | arsC | 1.20.4.1 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
EOOGHDJN_00246 | 1.5e-163 | ptlF | S | KR domain | ||
EOOGHDJN_00247 | 6.4e-159 | adc | 4.1.1.4 | Q | Acetoacetate decarboxylase (ADC) | |
EOOGHDJN_00248 | 1.3e-122 | drgA | C | Nitroreductase family | ||
EOOGHDJN_00249 | 1.3e-290 | QT | PucR C-terminal helix-turn-helix domain | |||
EOOGHDJN_00250 | 2.7e-120 | pgmB | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | S | beta-phosphoglucomutase |
EOOGHDJN_00251 | 5.1e-195 | pva1 | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
EOOGHDJN_00252 | 7.4e-250 | yjjP | S | Putative threonine/serine exporter | ||
EOOGHDJN_00253 | 5.7e-135 | wzb | 3.1.3.48 | T | Tyrosine phosphatase family | |
EOOGHDJN_00254 | 1.5e-253 | 1.14.14.9 | Q | 4-hydroxyphenylacetate | ||
EOOGHDJN_00255 | 2.9e-81 | 6.3.3.2 | S | ASCH | ||
EOOGHDJN_00256 | 5.5e-129 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
EOOGHDJN_00257 | 2.1e-171 | yobV1 | K | WYL domain | ||
EOOGHDJN_00258 | 1e-116 | azoR | C | Catalyzes the reductive cleavage of azo bond in aromatic azo compounds to the corresponding amines. Requires NADH, but not NADPH, as an electron donor for its activity | ||
EOOGHDJN_00259 | 0.0 | tetP | J | elongation factor G | ||
EOOGHDJN_00260 | 1.2e-126 | S | Protein of unknown function | |||
EOOGHDJN_00261 | 5e-154 | EG | EamA-like transporter family | |||
EOOGHDJN_00262 | 1.8e-92 | MA20_25245 | K | FR47-like protein | ||
EOOGHDJN_00263 | 2e-126 | hchA | S | DJ-1/PfpI family | ||
EOOGHDJN_00264 | 1.6e-185 | 1.1.1.1 | C | nadph quinone reductase | ||
EOOGHDJN_00265 | 9.3e-50 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
EOOGHDJN_00266 | 2.7e-236 | mepA | V | MATE efflux family protein | ||
EOOGHDJN_00267 | 0.0 | parE | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
EOOGHDJN_00268 | 0.0 | parC | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
EOOGHDJN_00269 | 1.2e-177 | K | Transcriptional regulator | |||
EOOGHDJN_00270 | 1.7e-168 | ppaC | 3.6.1.1 | C | inorganic pyrophosphatase | |
EOOGHDJN_00271 | 4e-80 | msrB | 1.8.4.11, 1.8.4.12 | O | peptide methionine sulfoxide reductase | |
EOOGHDJN_00272 | 1e-95 | msrA | 1.8.4.11, 1.8.4.12 | O | Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine | |
EOOGHDJN_00273 | 4.2e-32 | S | YozE SAM-like fold | |||
EOOGHDJN_00274 | 1.2e-157 | xerD | L | Phage integrase, N-terminal SAM-like domain | ||
EOOGHDJN_00275 | 1.2e-277 | GT89 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | ||
EOOGHDJN_00276 | 1.5e-244 | M | Glycosyl transferase family group 2 | |||
EOOGHDJN_00277 | 2.5e-65 | |||||
EOOGHDJN_00278 | 2.7e-252 | gshR1 | 1.8.1.7 | C | Glutathione reductase | |
EOOGHDJN_00279 | 7.8e-76 | mgrA | K | helix_turn_helix multiple antibiotic resistance protein | ||
EOOGHDJN_00280 | 5.3e-95 | paiA | 2.3.1.57 | K | Acetyltransferase (GNAT) domain | |
EOOGHDJN_00281 | 0.0 | tarL | 2.7.8.14, 2.7.8.47 | H | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | |
EOOGHDJN_00282 | 4.6e-197 | tarK | 2.7.8.14, 2.7.8.47 | H | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | |
EOOGHDJN_00283 | 4.1e-192 | tarJ | 1.1.1.137, 1.1.1.303, 1.1.1.4, 1.1.1.405 | E | Catalyzes the NADPH dependent reduction of D-ribulose 5- phosphate to D-ribitol 5-phosphate | |
EOOGHDJN_00284 | 3.7e-128 | ispD | 1.1.1.405, 2.7.7.40, 2.7.7.60, 4.6.1.12 | I | Catalyzes the transfer of the cytidylyl group of CTP to D-ribitol 5-phosphate | |
EOOGHDJN_00285 | 5.1e-227 | |||||
EOOGHDJN_00286 | 1.8e-279 | lldP | C | L-lactate permease | ||
EOOGHDJN_00287 | 4.1e-59 | |||||
EOOGHDJN_00288 | 4.4e-118 | |||||
EOOGHDJN_00289 | 1e-243 | cycA | E | Amino acid permease | ||
EOOGHDJN_00290 | 8e-133 | XK27_00890 | S | Domain of unknown function (DUF368) | ||
EOOGHDJN_00291 | 4.6e-129 | yejC | S | Protein of unknown function (DUF1003) | ||
EOOGHDJN_00292 | 6.2e-51 | XK27_08430 | S | Staphylococcal protein of unknown function (DUF960) | ||
EOOGHDJN_00293 | 4.6e-12 | |||||
EOOGHDJN_00294 | 1.2e-208 | pmrB | EGP | Major facilitator Superfamily | ||
EOOGHDJN_00295 | 1.4e-147 | 2.7.7.12 | C | Domain of unknown function (DUF4931) | ||
EOOGHDJN_00296 | 1.4e-49 | |||||
EOOGHDJN_00297 | 1.6e-09 | |||||
EOOGHDJN_00298 | 2.9e-131 | S | Protein of unknown function (DUF975) | |||
EOOGHDJN_00299 | 5.4e-77 | yjcF | 3.5.4.33, 4.4.1.8 | K | protein acetylation | |
EOOGHDJN_00300 | 2.1e-160 | degV | S | EDD domain protein, DegV family | ||
EOOGHDJN_00301 | 1.9e-66 | K | Transcriptional regulator | |||
EOOGHDJN_00302 | 3.3e-297 | FbpA | K | Fibronectin-binding protein | ||
EOOGHDJN_00303 | 1.3e-131 | S | ABC-2 family transporter protein | |||
EOOGHDJN_00304 | 1.6e-163 | V | ABC transporter, ATP-binding protein | |||
EOOGHDJN_00305 | 6.3e-90 | 3.6.1.55 | F | NUDIX domain | ||
EOOGHDJN_00307 | 2.9e-136 | S | Uncharacterized protein conserved in bacteria (DUF2087) | |||
EOOGHDJN_00308 | 3.5e-69 | S | LuxR family transcriptional regulator | |||
EOOGHDJN_00309 | 4.6e-128 | cat | 2.3.1.28 | V | Chloramphenicol acetyltransferase | |
EOOGHDJN_00311 | 5.8e-70 | frataxin | S | Domain of unknown function (DU1801) | ||
EOOGHDJN_00312 | 6.4e-113 | pgm5 | G | Phosphoglycerate mutase family | ||
EOOGHDJN_00313 | 4e-288 | S | Bacterial membrane protein, YfhO | |||
EOOGHDJN_00314 | 0.0 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
EOOGHDJN_00315 | 2.8e-207 | carA | 6.3.5.5 | F | Belongs to the CarA family | |
EOOGHDJN_00316 | 1.3e-88 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
EOOGHDJN_00317 | 2e-174 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
EOOGHDJN_00318 | 4.4e-74 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
EOOGHDJN_00319 | 4.1e-295 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
EOOGHDJN_00320 | 3.3e-62 | esbA | S | Family of unknown function (DUF5322) | ||
EOOGHDJN_00321 | 2.2e-66 | rnhA | 3.1.26.4 | L | Ribonuclease HI | |
EOOGHDJN_00322 | 1.1e-211 | yurR | 1.4.5.1 | E | FAD dependent oxidoreductase | |
EOOGHDJN_00323 | 1.5e-146 | S | hydrolase activity, acting on ester bonds | |||
EOOGHDJN_00324 | 2.1e-194 | |||||
EOOGHDJN_00325 | 6.6e-122 | 3.6.3.35 | P | ATPases associated with a variety of cellular activities | ||
EOOGHDJN_00326 | 9.2e-125 | |||||
EOOGHDJN_00327 | 4.7e-182 | mccF | 3.4.17.13 | V | LD-carboxypeptidase | |
EOOGHDJN_00328 | 6.9e-240 | M | hydrolase, family 25 | |||
EOOGHDJN_00329 | 1.4e-78 | K | Acetyltransferase (GNAT) domain | |||
EOOGHDJN_00330 | 5.1e-209 | mccF | V | LD-carboxypeptidase | ||
EOOGHDJN_00331 | 8.7e-243 | M | Glycosyltransferase, group 2 family protein | |||
EOOGHDJN_00332 | 1.2e-73 | S | SnoaL-like domain | |||
EOOGHDJN_00333 | 2.8e-145 | yjfP | S | COG1073 Hydrolases of the alpha beta superfamily | ||
EOOGHDJN_00334 | 6.8e-243 | P | Major Facilitator Superfamily | |||
EOOGHDJN_00335 | 1.2e-46 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
EOOGHDJN_00336 | 1.8e-223 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
EOOGHDJN_00338 | 3.2e-56 | gpsB | D | Divisome component that associates with the complex late in its assembly, after the Z-ring is formed, and is dependent on DivIC and PBP2B for its recruitment to the divisome. Together with EzrA, is a key component of the system that regulates PBP1 localization during cell cycle progression. Its main role could be the removal of PBP1 from the cell pole after pole maturation is completed. Also contributes to the recruitment of PBP1 to the division complex. Not essential for septum formation | ||
EOOGHDJN_00339 | 8.3e-110 | ypsA | S | Belongs to the UPF0398 family | ||
EOOGHDJN_00340 | 7.6e-117 | recU | L | Endonuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves mobile four-strand junctions by introducing symmetrical nicks in paired strands. Promotes annealing of linear ssDNA with homologous dsDNA. Required for DNA repair, homologous recombination and chromosome segregation | ||
EOOGHDJN_00341 | 0.0 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
EOOGHDJN_00342 | 7.4e-180 | phnT | 3.6.3.30 | P | ATPases associated with a variety of cellular activities | |
EOOGHDJN_00343 | 4.5e-183 | ftpB | P | Bacterial extracellular solute-binding protein | ||
EOOGHDJN_00344 | 1.9e-303 | ftpA | P | Binding-protein-dependent transport system inner membrane component | ||
EOOGHDJN_00345 | 7.6e-83 | uspA | T | Universal stress protein family | ||
EOOGHDJN_00346 | 2.7e-157 | metQ_4 | P | Belongs to the nlpA lipoprotein family | ||
EOOGHDJN_00347 | 7.7e-99 | metI | P | ABC transporter permease | ||
EOOGHDJN_00348 | 7e-187 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
EOOGHDJN_00350 | 2.9e-128 | dnaD | L | Replication initiation and membrane attachment | ||
EOOGHDJN_00351 | 5.4e-258 | asnS | 6.1.1.22 | J | Asparaginyl-tRNA synthetase | |
EOOGHDJN_00352 | 1.1e-225 | aspB | 2.6.1.1, 2.6.1.14 | E | Aminotransferase | |
EOOGHDJN_00353 | 2.1e-72 | ypmB | S | protein conserved in bacteria | ||
EOOGHDJN_00354 | 0.0 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
EOOGHDJN_00355 | 4e-170 | mvk | 1.1.1.88, 2.3.3.10, 2.7.1.36 | I | mevalonate kinase | |
EOOGHDJN_00356 | 7.4e-175 | mvaD | 4.1.1.33 | I | diphosphomevalonate decarboxylase | |
EOOGHDJN_00357 | 7.6e-205 | mvaK2 | 2.7.1.36, 2.7.1.43, 2.7.4.2 | I | phosphomevalonate kinase | |
EOOGHDJN_00358 | 3.6e-196 | fni | 1.1.1.88, 5.3.3.2 | C | Involved in the biosynthesis of isoprenoids. Catalyzes the 1,3-allylic rearrangement of the homoallylic substrate isopentenyl (IPP) to its allylic isomer, dimethylallyl diphosphate (DMAPP) | |
EOOGHDJN_00359 | 1.6e-193 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
EOOGHDJN_00360 | 0.0 | mapA | 2.4.1.8 | GH65 | G | hydrolase, family 65, central catalytic |
EOOGHDJN_00361 | 1.3e-249 | malT | G | Major Facilitator | ||
EOOGHDJN_00362 | 9.8e-78 | S | Domain of unknown function (DUF4767) | |||
EOOGHDJN_00363 | 9.4e-269 | rsmF | 2.1.1.176, 2.1.1.178 | J | NOL1 NOP2 sun family protein | |
EOOGHDJN_00364 | 1.2e-149 | yitU | 3.1.3.104 | S | hydrolase | |
EOOGHDJN_00365 | 1.4e-265 | yfnA | E | Amino Acid | ||
EOOGHDJN_00366 | 8.7e-259 | gabT | 2.6.1.19, 5.1.1.21 | E | Belongs to the class-III pyridoxal-phosphate-dependent aminotransferase family | |
EOOGHDJN_00367 | 2.4e-43 | |||||
EOOGHDJN_00368 | 1.9e-49 | |||||
EOOGHDJN_00369 | 1.4e-136 | potC | 2.1.1.172, 2.1.1.80, 3.1.1.61 | U | Ion channel | |
EOOGHDJN_00370 | 1e-170 | 2.5.1.74 | H | UbiA prenyltransferase family | ||
EOOGHDJN_00371 | 5.7e-255 | lysA | 4.1.1.19, 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
EOOGHDJN_00372 | 5.1e-27 | dmpI | 5.3.2.6 | G | Belongs to the 4-oxalocrotonate tautomerase family | |
EOOGHDJN_00373 | 2.5e-280 | pipD | E | Dipeptidase | ||
EOOGHDJN_00374 | 9.4e-40 | |||||
EOOGHDJN_00375 | 4.8e-29 | S | CsbD-like | |||
EOOGHDJN_00376 | 6.5e-41 | S | transglycosylase associated protein | |||
EOOGHDJN_00377 | 3.1e-14 | |||||
EOOGHDJN_00378 | 3.5e-36 | |||||
EOOGHDJN_00379 | 4.1e-164 | yegS | 2.7.1.107 | I | Diacylglycerol kinase catalytic domain | |
EOOGHDJN_00380 | 8e-66 | S | Protein of unknown function (DUF805) | |||
EOOGHDJN_00381 | 6.3e-76 | uspA | T | Belongs to the universal stress protein A family | ||
EOOGHDJN_00382 | 1.9e-67 | tspO | T | TspO/MBR family | ||
EOOGHDJN_00383 | 7.9e-41 | |||||
EOOGHDJN_00384 | 4.2e-46 | ycnE | 3.1.1.29 | S | Antibiotic biosynthesis monooxygenase | |
EOOGHDJN_00385 | 4.5e-114 | 1.14.99.53 | AA10 | S | Lytic polysaccharide mono-oxygenase, cellulose-degrading | |
EOOGHDJN_00386 | 2.7e-208 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
EOOGHDJN_00387 | 3.6e-28 | |||||
EOOGHDJN_00388 | 8.5e-54 | |||||
EOOGHDJN_00389 | 1.2e-139 | f42a | O | Band 7 protein | ||
EOOGHDJN_00390 | 5e-304 | norB | EGP | Major Facilitator | ||
EOOGHDJN_00391 | 6.2e-94 | K | transcriptional regulator | |||
EOOGHDJN_00392 | 6.5e-193 | 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 | |
EOOGHDJN_00393 | 4.6e-88 | ykhA | 3.1.2.20 | I | Thioesterase superfamily | |
EOOGHDJN_00394 | 3.6e-160 | K | LysR substrate binding domain | |||
EOOGHDJN_00395 | 1.3e-123 | S | Protein of unknown function (DUF554) | |||
EOOGHDJN_00396 | 4.9e-99 | 2.7.8.7 | H | Belongs to the P-Pant transferase superfamily | ||
EOOGHDJN_00397 | 1.5e-135 | fabI | 1.3.1.10, 1.3.1.9 | I | Enoyl- acyl-carrier-protein reductase NADH | |
EOOGHDJN_00398 | 3e-139 | accA | 2.1.3.15, 6.4.1.2 | I | alpha subunit | |
EOOGHDJN_00399 | 1.6e-157 | accD | 2.1.3.15, 6.4.1.2 | I | Component of the acetyl coenzyme A carboxylase (ACC) complex. Biotin carboxylase (BC) catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the transcarboxylase to acetyl-CoA to form malonyl- CoA | |
EOOGHDJN_00400 | 1.2e-260 | accC | 6.3.4.14, 6.4.1.2 | I | Acetyl-CoA carboxylase biotin carboxylase subunit | |
EOOGHDJN_00401 | 6.1e-70 | fabZ | 3.5.1.108, 4.2.1.59 | I | FabA-like domain | |
EOOGHDJN_00402 | 2.3e-73 | accB | 2.3.1.12, 4.1.1.3 | I | first, biotin carboxylase catalyzes the carboxylation of the carrier protein and then the transcarboxylase transfers the carboxyl group to form malonyl-CoA | |
EOOGHDJN_00403 | 1.6e-227 | fabF | 2.3.1.179 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP | |
EOOGHDJN_00404 | 1.2e-126 | IQ | reductase | |||
EOOGHDJN_00405 | 2e-169 | fabD | 2.3.1.39 | I | Malonyl CoA-acyl carrier protein transacylase | |
EOOGHDJN_00406 | 1.3e-35 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
EOOGHDJN_00407 | 1e-179 | fabH | 2.3.1.180 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids | |
EOOGHDJN_00408 | 2.3e-75 | fabZ | 3.5.1.108, 4.2.1.59 | I | Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs | |
EOOGHDJN_00409 | 1.1e-178 | yneE | K | Transcriptional regulator | ||
EOOGHDJN_00410 | 4.3e-144 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
EOOGHDJN_00412 | 2.1e-58 | S | Protein of unknown function (DUF1648) | |||
EOOGHDJN_00413 | 1.9e-197 | adhB | 1.1.1.1, 1.1.1.14 | E | alcohol dehydrogenase | |
EOOGHDJN_00414 | 1.4e-178 | 1.6.5.5 | C | Zinc-binding dehydrogenase | ||
EOOGHDJN_00415 | 5.3e-98 | entB | 3.5.1.19 | Q | Isochorismatase family | |
EOOGHDJN_00416 | 3.9e-142 | trpA | 4.2.1.20 | E | The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate | |
EOOGHDJN_00417 | 2.3e-226 | trpB | 4.2.1.20 | E | The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine | |
EOOGHDJN_00418 | 5e-108 | trpF | 4.1.1.48, 4.2.1.160, 4.2.1.20, 5.3.1.24 | E | Belongs to the TrpF family | |
EOOGHDJN_00419 | 2.4e-123 | trpC | 4.1.1.48, 5.3.1.24 | E | Belongs to the TrpC family | |
EOOGHDJN_00420 | 1.2e-167 | 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) | |
EOOGHDJN_00421 | 4.2e-104 | trpG | 2.4.2.18, 2.6.1.85, 4.1.3.27 | EH | Peptidase C26 | |
EOOGHDJN_00422 | 2.9e-268 | trpE | 4.1.3.27 | EH | Anthranilate synthase component I, N terminal region | |
EOOGHDJN_00424 | 6e-283 | XK27_00765 | ||||
EOOGHDJN_00425 | 2.3e-139 | ecsA_2 | V | AAA domain, putative AbiEii toxin, Type IV TA system | ||
EOOGHDJN_00426 | 2e-85 | |||||
EOOGHDJN_00427 | 0.0 | pelX | UW | LPXTG-motif cell wall anchor domain protein | ||
EOOGHDJN_00428 | 1.4e-50 | |||||
EOOGHDJN_00429 | 1.9e-59 | 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 | ||
EOOGHDJN_00430 | 2.9e-139 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
EOOGHDJN_00431 | 8.2e-96 | 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 | ||
EOOGHDJN_00432 | 2.6e-39 | ylqC | S | Belongs to the UPF0109 family | ||
EOOGHDJN_00433 | 2.9e-44 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
EOOGHDJN_00434 | 1.1e-219 | 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 | |
EOOGHDJN_00435 | 2.6e-58 | ylxM | S | Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY ffh. May be a regulatory protein | ||
EOOGHDJN_00436 | 5.6e-169 | 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) | ||
EOOGHDJN_00437 | 0.0 | smc | D | Required for chromosome condensation and partitioning | ||
EOOGHDJN_00438 | 5.7e-129 | 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 | |
EOOGHDJN_00439 | 1.7e-35 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
EOOGHDJN_00440 | 2.3e-190 | plsX | 2.3.1.15 | I | Catalyzes the reversible formation of acyl-phosphate (acyl-PO(4)) from acyl- acyl-carrier-protein (acyl-ACP). This enzyme utilizes acyl-ACP as fatty acyl donor, but not acyl-CoA | |
EOOGHDJN_00441 | 0.0 | recG | 3.6.4.12 | L | Critical role in recombination and DNA repair. Helps process Holliday junction intermediates to mature products by catalyzing branch migration. Has a DNA unwinding activity characteristic of a DNA helicase with a 3'- to 5'- polarity. Unwinds branched duplex DNA (Y-DNA) | |
EOOGHDJN_00442 | 0.0 | yloV | S | DAK2 domain fusion protein YloV | ||
EOOGHDJN_00443 | 1.8e-57 | asp | S | Asp23 family, cell envelope-related function | ||
EOOGHDJN_00444 | 4.9e-27 | rpmB | J | Belongs to the bacterial ribosomal protein bL28 family | ||
EOOGHDJN_00445 | 3.4e-123 | thiN | 2.7.6.2 | H | thiamine pyrophosphokinase | |
EOOGHDJN_00446 | 3.3e-118 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
EOOGHDJN_00447 | 3.2e-164 | rsgA | 3.1.3.100 | S | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Helps release RbfA from mature subunits. May play a role in the assembly of ribosomal proteins into the subunit. Circularly permuted GTPase that catalyzes slow GTP hydrolysis, GTPase activity is stimulated by the 30S ribosomal subunit | |
EOOGHDJN_00448 | 0.0 | prkC | 2.7.11.1 | KLT | serine threonine protein kinase | |
EOOGHDJN_00449 | 1.7e-134 | stp | 3.1.3.16 | T | phosphatase | |
EOOGHDJN_00450 | 3e-251 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
EOOGHDJN_00451 | 4.2e-175 | fmt | 2.1.2.9 | J | Attaches a formyl group to the free amino group of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by promoting its recognition by IF2 and preventing the misappropriation of this tRNA by the elongation apparatus | |
EOOGHDJN_00452 | 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 | ||
EOOGHDJN_00453 | 2e-217 | 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 | |
EOOGHDJN_00454 | 2.4e-30 | 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 | |
EOOGHDJN_00455 | 3.3e-112 | gmk | 2.7.4.8 | F | Essential for recycling GMP and indirectly, cGMP | |
EOOGHDJN_00456 | 4.5e-55 | |||||
EOOGHDJN_00457 | 6.4e-106 | opuCD | P | Binding-protein-dependent transport system inner membrane component | ||
EOOGHDJN_00458 | 6e-174 | opuCC | M | Periplasmic glycine betaine choline-binding (lipo)protein of an ABC-type transport system (osmoprotectant binding protein) | ||
EOOGHDJN_00459 | 1.2e-104 | opuCB | E | ABC transporter permease | ||
EOOGHDJN_00460 | 5.7e-222 | opuCA | 3.6.3.32 | E | ABC transporter, ATP-binding protein | |
EOOGHDJN_00461 | 4.4e-308 | recN | L | May be involved in recombinational repair of damaged DNA | ||
EOOGHDJN_00462 | 7.4e-77 | argR | K | Regulates arginine biosynthesis genes | ||
EOOGHDJN_00463 | 4e-150 | rrmJ | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
EOOGHDJN_00464 | 8.3e-157 | ispA | 2.5.1.1, 2.5.1.10, 2.5.1.29, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
EOOGHDJN_00465 | 4.3e-33 | 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 | |
EOOGHDJN_00466 | 9.3e-245 | 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 | |
EOOGHDJN_00467 | 1.5e-150 | 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 | |
EOOGHDJN_00468 | 5.8e-68 | nusB | K | Involved in transcription antitermination. Required for transcription of ribosomal RNA (rRNA) genes. Binds specifically to the boxA antiterminator sequence of the ribosomal RNA (rrn) operons | ||
EOOGHDJN_00469 | 3.5e-74 | yqhY | S | Asp23 family, cell envelope-related function | ||
EOOGHDJN_00470 | 2.2e-99 | 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 | ||
EOOGHDJN_00471 | 1.6e-194 | pepP | 3.4.11.9, 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
EOOGHDJN_00472 | 5.4e-46 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
EOOGHDJN_00473 | 3.2e-53 | ysxB | J | Cysteine protease Prp | ||
EOOGHDJN_00474 | 7.5e-49 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
EOOGHDJN_00475 | 5.2e-89 | K | Transcriptional regulator | |||
EOOGHDJN_00476 | 5.4e-19 | |||||
EOOGHDJN_00479 | 1.7e-30 | |||||
EOOGHDJN_00480 | 5.3e-56 | |||||
EOOGHDJN_00481 | 6.2e-99 | dut | S | Protein conserved in bacteria | ||
EOOGHDJN_00482 | 4e-181 | |||||
EOOGHDJN_00483 | 2.5e-161 | |||||
EOOGHDJN_00484 | 6.2e-265 | glnA | 6.3.1.2 | E | glutamine synthetase | |
EOOGHDJN_00485 | 4.6e-64 | glnR | K | Transcriptional regulator | ||
EOOGHDJN_00486 | 2.4e-175 | miaA | 2.5.1.75 | F | Catalyzes the transfer of a dimethylallyl group onto the adenine at position 37 in tRNAs that read codons beginning with uridine, leading to the formation of N6-(dimethylallyl)adenosine (i(6)A) | |
EOOGHDJN_00487 | 1.7e-139 | glpQ | 3.1.4.46 | C | phosphodiesterase | |
EOOGHDJN_00488 | 6.9e-23 | WQ51_02665 | S | Protein of unknown function (DUF3042) | ||
EOOGHDJN_00489 | 4.4e-68 | yqhL | P | Rhodanese-like protein | ||
EOOGHDJN_00490 | 2.1e-109 | pepE | 3.4.13.21 | E | Belongs to the peptidase S51 family | |
EOOGHDJN_00491 | 5.7e-180 | glk | 2.7.1.2 | G | Glucokinase | |
EOOGHDJN_00492 | 1.4e-33 | yqgQ | S | Bacterial protein of unknown function (DUF910) | ||
EOOGHDJN_00493 | 1.3e-114 | gluP | 3.4.21.105 | S | Peptidase, S54 family | |
EOOGHDJN_00494 | 6.3e-102 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
EOOGHDJN_00495 | 1.4e-21 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
EOOGHDJN_00496 | 0.0 | pbp2b | 3.4.16.4 | M | Penicillin-binding Protein | |
EOOGHDJN_00497 | 0.0 | S | membrane | |||
EOOGHDJN_00498 | 1.5e-54 | yneR | S | Belongs to the HesB IscA family | ||
EOOGHDJN_00499 | 3.4e-74 | XK27_02470 | K | LytTr DNA-binding domain | ||
EOOGHDJN_00500 | 9.5e-95 | liaI | S | membrane | ||
EOOGHDJN_00501 | 6.8e-81 | greA | K | Necessary for efficient RNA polymerase transcription elongation past template-encoded arresting sites. The arresting sites in DNA have the property of trapping a certain fraction of elongating RNA polymerases that pass through, resulting in locked ternary complexes. Cleavage of the nascent transcript by cleavage factors such as GreA or GreB allows the resumption of elongation from the new 3'terminus. GreA releases sequences of 2 to 3 nucleotides | ||
EOOGHDJN_00502 | 2.6e-112 | udk | 2.7.1.48 | F | Cytidine monophosphokinase | |
EOOGHDJN_00503 | 6.6e-186 | mltG | S | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
EOOGHDJN_00504 | 0.0 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
EOOGHDJN_00505 | 4.9e-201 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
EOOGHDJN_00506 | 7.4e-64 | yodB | K | Transcriptional regulator, HxlR family | ||
EOOGHDJN_00507 | 1.3e-93 | XK27_09705 | 6.1.1.14 | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | |
EOOGHDJN_00508 | 7.9e-140 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
EOOGHDJN_00509 | 6.4e-44 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
EOOGHDJN_00510 | 6.8e-162 | yidC | U | Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins | ||
EOOGHDJN_00511 | 3.9e-99 | S | SdpI/YhfL protein family | |||
EOOGHDJN_00512 | 4.5e-227 | sbcD | L | SbcCD cleaves DNA hairpin structures. These structures can inhibit DNA replication and are intermediates in certain DNA recombination reactions. The complex acts as a 3'- 5' double strand exonuclease that can open hairpins. It also has a 5' single-strand endonuclease activity | ||
EOOGHDJN_00513 | 0.0 | sbcC | L | Putative exonuclease SbcCD, C subunit | ||
EOOGHDJN_00514 | 5.8e-172 | 2.5.1.74 | H | 1,4-dihydroxy-2-naphthoate | ||
EOOGHDJN_00515 | 5.2e-306 | arlS | 2.7.13.3 | T | Histidine kinase | |
EOOGHDJN_00516 | 4.3e-121 | K | response regulator | |||
EOOGHDJN_00517 | 4.2e-245 | rarA | L | recombination factor protein RarA | ||
EOOGHDJN_00518 | 3e-273 | gnd | 1.1.1.343, 1.1.1.44 | H | Catalyzes the oxidative decarboxylation of 6- phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NADP to NADPH | |
EOOGHDJN_00519 | 1e-168 | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | |||
EOOGHDJN_00520 | 2.2e-89 | S | Peptidase propeptide and YPEB domain | |||
EOOGHDJN_00521 | 1.6e-97 | yceD | S | Uncharacterized ACR, COG1399 | ||
EOOGHDJN_00522 | 6.4e-218 | ylbM | S | Belongs to the UPF0348 family | ||
EOOGHDJN_00523 | 5.8e-140 | yqeM | Q | Methyltransferase | ||
EOOGHDJN_00524 | 2.1e-58 | rsfS | J | Functions as a ribosomal silencing factor. Interacts with ribosomal protein L14 (rplN), blocking formation of intersubunit bridge B8. Prevents association of the 30S and 50S ribosomal subunits and the formation of functional ribosomes, thus repressing translation | ||
EOOGHDJN_00525 | 9.3e-115 | nadD | 2.7.6.3, 2.7.7.18 | H | Hydrolase, HD family | |
EOOGHDJN_00526 | 1.4e-118 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
EOOGHDJN_00527 | 1.1e-50 | yhbY | J | RNA-binding protein | ||
EOOGHDJN_00528 | 4.5e-216 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
EOOGHDJN_00529 | 3e-98 | yqeG | S | HAD phosphatase, family IIIA | ||
EOOGHDJN_00530 | 1.3e-79 | |||||
EOOGHDJN_00531 | 3.8e-251 | pgaC | GT2 | M | Glycosyl transferase | |
EOOGHDJN_00532 | 3.3e-92 | racD | 5.1.1.13 | G | Belongs to the aspartate glutamate racemases family | |
EOOGHDJN_00533 | 1e-62 | hxlR | K | Transcriptional regulator, HxlR family | ||
EOOGHDJN_00534 | 7.2e-197 | qor | 1.1.1.1, 1.6.5.5 | C | Belongs to the zinc-containing alcohol dehydrogenase family. Quinone oxidoreductase subfamily | |
EOOGHDJN_00535 | 9.4e-239 | yrvN | L | AAA C-terminal domain | ||
EOOGHDJN_00536 | 9.9e-57 | |||||
EOOGHDJN_00537 | 7.3e-56 | rplT | J | Binds directly to 23S ribosomal RNA and is necessary for the in vitro assembly process of the 50S ribosomal subunit. It is not involved in the protein synthesizing functions of that subunit | ||
EOOGHDJN_00538 | 1.9e-26 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
EOOGHDJN_00539 | 1.8e-84 | infC | J | IF-3 binds to the 30S ribosomal subunit and shifts the equilibrum between 70S ribosomes and their 50S and 30S subunits in favor of the free subunits, thus enhancing the availability of 30S subunits on which protein synthesis initiation begins | ||
EOOGHDJN_00540 | 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) | |
EOOGHDJN_00541 | 3.3e-172 | dnaI | L | Primosomal protein DnaI | ||
EOOGHDJN_00542 | 1.1e-248 | dnaB | L | replication initiation and membrane attachment | ||
EOOGHDJN_00543 | 4.6e-91 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
EOOGHDJN_00544 | 2.7e-103 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
EOOGHDJN_00545 | 7.6e-157 | 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 | |
EOOGHDJN_00546 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
EOOGHDJN_00547 | 4.5e-121 | ybhL | S | Belongs to the BI1 family | ||
EOOGHDJN_00548 | 3.1e-111 | hipB | K | Helix-turn-helix | ||
EOOGHDJN_00549 | 5.5e-45 | yitW | S | Iron-sulfur cluster assembly protein | ||
EOOGHDJN_00550 | 2.5e-272 | sufB | O | assembly protein SufB | ||
EOOGHDJN_00551 | 7.1e-83 | nifU | C | SUF system FeS assembly protein, NifU family | ||
EOOGHDJN_00552 | 1.2e-233 | 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 | |
EOOGHDJN_00553 | 1.3e-243 | sufD | O | FeS assembly protein SufD | ||
EOOGHDJN_00554 | 4.2e-144 | sufC | O | FeS assembly ATPase SufC | ||
EOOGHDJN_00555 | 1.3e-34 | feoA | P | FeoA domain | ||
EOOGHDJN_00556 | 0.0 | feoB | P | transporter of a GTP-driven Fe(2 ) uptake system | ||
EOOGHDJN_00557 | 7.9e-21 | S | Virus attachment protein p12 family | |||
EOOGHDJN_00558 | 1.1e-253 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
EOOGHDJN_00559 | 2.4e-310 | sftA | D | Belongs to the FtsK SpoIIIE SftA family | ||
EOOGHDJN_00560 | 2e-169 | znuA | P | Belongs to the bacterial solute-binding protein 9 family | ||
EOOGHDJN_00561 | 4.7e-83 | cvpA | S | Colicin V production protein | ||
EOOGHDJN_00562 | 2.2e-63 | folB | 1.13.11.81, 2.5.1.15, 2.7.6.3, 4.1.2.25, 5.1.99.8 | H | Catalyzes the conversion of 7,8-dihydroneopterin to 6- hydroxymethyl-7,8-dihydropterin | |
EOOGHDJN_00563 | 2.8e-93 | folK | 1.13.11.81, 2.5.1.15, 2.7.6.3, 3.5.4.16, 4.1.2.25, 5.1.99.8 | H | 7,8-dihydro-6-hydroxymethylpterin-pyrophosphokinase (HPPK) | |
EOOGHDJN_00564 | 4.4e-103 | folE | 2.7.6.3, 3.5.4.16 | F | GTP cyclohydrolase 1 | |
EOOGHDJN_00565 | 1.8e-248 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
EOOGHDJN_00566 | 1.9e-101 | xtp | 2.5.1.15, 3.6.1.66 | F | Ham1 family | |
EOOGHDJN_00567 | 1.4e-204 | folP | 2.5.1.15 | H | dihydropteroate synthase | |
EOOGHDJN_00568 | 3.6e-94 | tag | 3.2.2.20 | L | glycosylase | |
EOOGHDJN_00569 | 3.3e-84 | 1.6.5.5 | C | nadph quinone reductase | ||
EOOGHDJN_00571 | 8.4e-71 | ribA | 3.5.4.25, 4.1.99.12 | H | belongs to the DHBP synthase family | |
EOOGHDJN_00572 | 2.6e-57 | cmk | 2.3.1.51 | I | Acyltransferase | |
EOOGHDJN_00573 | 8.2e-38 | IQ | reductase | |||
EOOGHDJN_00574 | 9.4e-69 | fabH | 2.3.1.180 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids | |
EOOGHDJN_00576 | 3.5e-60 | fabK | 1.3.1.9 | S | 2-Nitropropane dioxygenase | |
EOOGHDJN_00577 | 7.2e-31 | fabD | 2.3.1.39 | I | Malonyl CoA-acyl carrier protein transacylase | |
EOOGHDJN_00578 | 5.5e-87 | fabF | 2.3.1.179 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP | |
EOOGHDJN_00579 | 9.1e-10 | accB | 2.3.1.12, 4.1.1.3 | I | first, biotin carboxylase catalyzes the carboxylation of the carrier protein and then the transcarboxylase transfers the carboxyl group to form malonyl-CoA | |
EOOGHDJN_00580 | 5.3e-16 | fabZ | 3.5.1.108, 4.2.1.59 | I | 3-hydroxyoctanoyl-[acyl-carrier-protein] dehydratase activity | |
EOOGHDJN_00581 | 1.3e-126 | accC | 6.3.4.14, 6.4.1.2 | I | acetyl-CoA carboxylase, biotin carboxylase | |
EOOGHDJN_00582 | 4.4e-56 | accD | 2.1.3.15, 6.4.1.2 | I | Component of the acetyl coenzyme A carboxylase (ACC) complex. Biotin carboxylase (BC) catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the transcarboxylase to acetyl-CoA to form malonyl- CoA | |
EOOGHDJN_00583 | 4.1e-42 | accA | 2.1.3.15, 6.4.1.2 | I | Acetyl co-enzyme A carboxylase carboxyltransferase alpha subunit | |
EOOGHDJN_00584 | 3.1e-76 | K | Helix-turn-helix | |||
EOOGHDJN_00585 | 2.3e-24 | birA | 6.3.4.15 | H | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
EOOGHDJN_00586 | 1.5e-16 | |||||
EOOGHDJN_00587 | 4.7e-160 | czcD | P | cation diffusion facilitator family transporter | ||
EOOGHDJN_00588 | 7.3e-53 | nmtR | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
EOOGHDJN_00589 | 3e-116 | hly | S | protein, hemolysin III | ||
EOOGHDJN_00590 | 1.1e-44 | qacH | U | Small Multidrug Resistance protein | ||
EOOGHDJN_00591 | 4.4e-59 | qacC | P | Small Multidrug Resistance protein | ||
EOOGHDJN_00592 | 1.7e-215 | yxjG | 2.1.1.14 | E | methionine synthase, vitamin-B12 independent | |
EOOGHDJN_00593 | 3.1e-179 | K | AI-2E family transporter | |||
EOOGHDJN_00594 | 1e-165 | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | |||
EOOGHDJN_00595 | 0.0 | kup | P | Transport of potassium into the cell | ||
EOOGHDJN_00597 | 2.3e-257 | yhdG | E | C-terminus of AA_permease | ||
EOOGHDJN_00598 | 6.2e-82 | |||||
EOOGHDJN_00600 | 1.1e-278 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
EOOGHDJN_00601 | 1.7e-145 | ptp2 | 3.1.3.48 | T | Tyrosine phosphatase family | |
EOOGHDJN_00602 | 1.8e-184 | guaC | 1.1.1.205, 1.7.1.7 | F | Catalyzes the irreversible NADPH-dependent deamination of GMP to IMP. It functions in the conversion of nucleobase, nucleoside and nucleotide derivatives of G to A nucleotides, and in maintaining the intracellular balance of A and G nucleotides | |
EOOGHDJN_00603 | 1.4e-253 | 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 | |
EOOGHDJN_00604 | 7.4e-247 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
EOOGHDJN_00605 | 3.4e-55 | S | Enterocin A Immunity | |||
EOOGHDJN_00606 | 5.2e-256 | gor | 1.8.1.7 | C | Glutathione reductase | |
EOOGHDJN_00607 | 9.2e-198 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
EOOGHDJN_00608 | 1.7e-184 | D | Alpha beta | |||
EOOGHDJN_00609 | 7.4e-166 | crtB | 2.5.1.21, 2.5.1.32, 2.5.1.99 | I | Squalene/phytoene synthase | |
EOOGHDJN_00610 | 2.9e-295 | crtI | 1.3.99.26, 1.3.99.28, 1.3.99.29, 1.3.99.31 | Q | Flavin containing amine oxidoreductase | |
EOOGHDJN_00611 | 7.5e-54 | L | Belongs to the 'phage' integrase family | |||
EOOGHDJN_00616 | 2e-22 | |||||
EOOGHDJN_00617 | 3.7e-16 | tcdC | ||||
EOOGHDJN_00619 | 8e-80 | K | Peptidase S24-like | |||
EOOGHDJN_00620 | 4.3e-17 | |||||
EOOGHDJN_00621 | 1e-59 | S | ORF6C domain | |||
EOOGHDJN_00632 | 1.3e-124 | L | DnaD domain protein | |||
EOOGHDJN_00633 | 2.7e-160 | dnaC | L | IstB-like ATP binding protein | ||
EOOGHDJN_00635 | 2.7e-46 | |||||
EOOGHDJN_00636 | 7.4e-16 | |||||
EOOGHDJN_00639 | 1.8e-15 | |||||
EOOGHDJN_00640 | 1.2e-63 | S | Transcriptional regulator, RinA family | |||
EOOGHDJN_00641 | 1.6e-42 | |||||
EOOGHDJN_00642 | 8.2e-13 | V | HNH nucleases | |||
EOOGHDJN_00643 | 2.1e-88 | L | HNH nucleases | |||
EOOGHDJN_00644 | 2.3e-46 | L | Phage terminase, small subunit | |||
EOOGHDJN_00645 | 7.4e-179 | S | Phage Terminase | |||
EOOGHDJN_00646 | 1.2e-23 | S | Protein of unknown function (DUF1056) | |||
EOOGHDJN_00647 | 4.9e-205 | S | Phage portal protein | |||
EOOGHDJN_00648 | 3e-120 | S | Clp protease | |||
EOOGHDJN_00649 | 3.3e-212 | S | Phage capsid family | |||
EOOGHDJN_00650 | 4e-51 | S | Phage gp6-like head-tail connector protein | |||
EOOGHDJN_00651 | 6.8e-25 | S | Phage head-tail joining protein | |||
EOOGHDJN_00652 | 3.1e-40 | |||||
EOOGHDJN_00653 | 4.5e-27 | |||||
EOOGHDJN_00654 | 1.9e-70 | S | Phage tail tube protein | |||
EOOGHDJN_00657 | 0.0 | S | peptidoglycan catabolic process | |||
EOOGHDJN_00658 | 2.3e-230 | S | Phage tail protein | |||
EOOGHDJN_00659 | 6.1e-295 | S | Phage minor structural protein | |||
EOOGHDJN_00660 | 1e-268 | |||||
EOOGHDJN_00663 | 8.2e-55 | |||||
EOOGHDJN_00664 | 7.4e-178 | 3.5.1.28 | M | Glycosyl hydrolases family 25 | ||
EOOGHDJN_00665 | 3.3e-37 | S | Haemolysin XhlA | |||
EOOGHDJN_00667 | 3.5e-118 | yugP | S | Putative neutral zinc metallopeptidase | ||
EOOGHDJN_00668 | 4.1e-25 | |||||
EOOGHDJN_00669 | 2.5e-145 | DegV | S | EDD domain protein, DegV family | ||
EOOGHDJN_00670 | 7.3e-127 | lrgB | M | LrgB-like family | ||
EOOGHDJN_00671 | 5.1e-64 | lrgA | S | LrgA family | ||
EOOGHDJN_00672 | 3.8e-104 | J | Acetyltransferase (GNAT) domain | |||
EOOGHDJN_00673 | 1.8e-169 | cpdA | 2.1.2.2, 3.1.4.17, 3.1.4.53 | S | Calcineurin-like phosphoesterase | |
EOOGHDJN_00674 | 5.4e-36 | S | Phospholipase_D-nuclease N-terminal | |||
EOOGHDJN_00675 | 7.1e-59 | S | Enterocin A Immunity | |||
EOOGHDJN_00676 | 3.7e-87 | perR | P | Belongs to the Fur family | ||
EOOGHDJN_00677 | 4.2e-104 | |||||
EOOGHDJN_00678 | 7.9e-238 | S | module of peptide synthetase | |||
EOOGHDJN_00679 | 2e-100 | S | NADPH-dependent FMN reductase | |||
EOOGHDJN_00680 | 1.4e-08 | |||||
EOOGHDJN_00681 | 3.9e-127 | magIII | L | Base excision DNA repair protein, HhH-GPD family | ||
EOOGHDJN_00682 | 5.8e-225 | treB | 2.7.1.193, 2.7.1.211 | G | phosphotransferase system | |
EOOGHDJN_00683 | 2.7e-121 | treB | 2.7.1.193, 2.7.1.211 | G | phosphotransferase system | |
EOOGHDJN_00684 | 7.7e-155 | 1.6.5.2 | GM | NmrA-like family | ||
EOOGHDJN_00685 | 2e-77 | merR | K | MerR family regulatory protein | ||
EOOGHDJN_00686 | 2.2e-90 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GKT | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
EOOGHDJN_00687 | 1.7e-20 | fryA | 2.7.1.202 | G | COG1762 Phosphotransferase system mannitol fructose-specific IIA domain (Ntr-type) | |
EOOGHDJN_00688 | 2.4e-26 | mngA | 2.7.1.195, 2.7.1.202 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
EOOGHDJN_00689 | 2.8e-122 | mngA | 2.7.1.195, 2.7.1.202 | U | Phosphotransferase system, EIIC | |
EOOGHDJN_00690 | 3e-308 | mngB | 3.2.1.170, 3.2.1.24 | GH38 | G | Glycosyl hydrolases family 38 N-terminal domain |
EOOGHDJN_00691 | 1.1e-92 | scrK | 2.7.1.2, 2.7.1.4 | GK | ROK family | |
EOOGHDJN_00692 | 1.7e-148 | cof | S | haloacid dehalogenase-like hydrolase | ||
EOOGHDJN_00693 | 1.5e-152 | qorB | 1.6.5.2 | GM | NmrA-like family | |
EOOGHDJN_00694 | 4e-164 | K | LysR substrate binding domain | |||
EOOGHDJN_00695 | 1.2e-233 | |||||
EOOGHDJN_00696 | 6.8e-242 | S | Neutral/alkaline non-lysosomal ceramidase, N-terminal | |||
EOOGHDJN_00697 | 0.0 | 2.7.1.193, 2.7.1.211 | G | phosphotransferase system | ||
EOOGHDJN_00698 | 3.9e-206 | 4.1.1.45 | E | amidohydrolase | ||
EOOGHDJN_00699 | 9.4e-77 | |||||
EOOGHDJN_00700 | 4.2e-275 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
EOOGHDJN_00701 | 9.4e-118 | ybbL | S | ABC transporter, ATP-binding protein | ||
EOOGHDJN_00702 | 2e-127 | ybbM | S | Uncharacterised protein family (UPF0014) | ||
EOOGHDJN_00703 | 1.3e-204 | S | DUF218 domain | |||
EOOGHDJN_00704 | 1.3e-182 | 5.1.1.1 | K | Periplasmic binding proteins and sugar binding domain of LacI family | ||
EOOGHDJN_00705 | 0.0 | malA | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain protein |
EOOGHDJN_00706 | 0.0 | scrA | 2.7.1.193, 2.7.1.211 | G | phosphotransferase system | |
EOOGHDJN_00707 | 1.7e-128 | S | Putative adhesin | |||
EOOGHDJN_00708 | 4.5e-88 | XK27_06920 | S | Protein of unknown function (DUF1700) | ||
EOOGHDJN_00709 | 6.8e-53 | K | Transcriptional regulator | |||
EOOGHDJN_00710 | 5.8e-79 | KT | response to antibiotic | |||
EOOGHDJN_00711 | 9.7e-120 | tcyA | ET | Belongs to the bacterial solute-binding protein 3 family | ||
EOOGHDJN_00712 | 3.6e-137 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
EOOGHDJN_00713 | 8.1e-123 | tcyB | E | ABC transporter | ||
EOOGHDJN_00714 | 2.3e-126 | tcyA | ET | Belongs to the bacterial solute-binding protein 3 family | ||
EOOGHDJN_00715 | 1.9e-236 | EK | Aminotransferase, class I | |||
EOOGHDJN_00716 | 4.7e-168 | K | LysR substrate binding domain | |||
EOOGHDJN_00717 | 1.5e-147 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
EOOGHDJN_00718 | 0.0 | S | Bacterial membrane protein YfhO | |||
EOOGHDJN_00719 | 4.1e-226 | nupG | F | Nucleoside | ||
EOOGHDJN_00720 | 1.9e-130 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
EOOGHDJN_00721 | 2.7e-149 | noc | K | Belongs to the ParB family | ||
EOOGHDJN_00722 | 1.8e-136 | soj | D | Sporulation initiation inhibitor | ||
EOOGHDJN_00723 | 4.8e-157 | spo0J | K | Belongs to the ParB family | ||
EOOGHDJN_00724 | 9.8e-31 | yyzM | S | Bacterial protein of unknown function (DUF951) | ||
EOOGHDJN_00725 | 2e-200 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
EOOGHDJN_00726 | 5.2e-125 | XK27_01040 | S | Protein of unknown function (DUF1129) | ||
EOOGHDJN_00727 | 2.3e-212 | guaB | 1.1.1.205 | F | Catalyzes the irreversible NADPH-dependent deamination of GMP to IMP. It functions in the conversion of nucleobase, nucleoside and nucleotide derivatives of G to A nucleotides, and in maintaining the intracellular balance of A and G nucleotides | |
EOOGHDJN_00728 | 5.8e-161 | prsA | 3.1.3.16, 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
EOOGHDJN_00729 | 5.5e-124 | yoaK | S | Protein of unknown function (DUF1275) | ||
EOOGHDJN_00730 | 3.2e-124 | K | response regulator | |||
EOOGHDJN_00731 | 1.3e-213 | hpk31 | 2.7.13.3 | T | Histidine kinase | |
EOOGHDJN_00732 | 4.9e-238 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
EOOGHDJN_00733 | 1.3e-90 | ywnH | 2.3.1.183 | M | Acetyltransferase (GNAT) domain | |
EOOGHDJN_00734 | 5.1e-131 | azlC | E | branched-chain amino acid | ||
EOOGHDJN_00735 | 2.3e-54 | azlD | S | branched-chain amino acid | ||
EOOGHDJN_00736 | 3.6e-110 | S | membrane transporter protein | |||
EOOGHDJN_00738 | 4.8e-55 | |||||
EOOGHDJN_00739 | 1.9e-74 | S | Psort location Cytoplasmic, score | |||
EOOGHDJN_00740 | 6e-97 | S | Domain of unknown function (DUF4352) | |||
EOOGHDJN_00741 | 2.9e-23 | S | Protein of unknown function (DUF4064) | |||
EOOGHDJN_00742 | 4.5e-202 | KLT | Protein tyrosine kinase | |||
EOOGHDJN_00743 | 3.6e-163 | |||||
EOOGHDJN_00744 | 4.7e-232 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
EOOGHDJN_00745 | 1e-81 | |||||
EOOGHDJN_00746 | 8.3e-210 | xylR | GK | ROK family | ||
EOOGHDJN_00747 | 1.9e-171 | K | AI-2E family transporter | |||
EOOGHDJN_00748 | 7.9e-131 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
EOOGHDJN_00749 | 8.8e-40 | |||||
EOOGHDJN_00750 | 6.8e-33 | L | transposase activity | |||
EOOGHDJN_00752 | 2.4e-104 | K | Bacterial regulatory proteins, tetR family | |||
EOOGHDJN_00753 | 9.2e-65 | S | Domain of unknown function (DUF4440) | |||
EOOGHDJN_00754 | 1.2e-258 | qacA | EGP | Fungal trichothecene efflux pump (TRI12) | ||
EOOGHDJN_00755 | 3.2e-77 | 3.5.4.1 | GM | SnoaL-like domain | ||
EOOGHDJN_00756 | 3.7e-108 | GM | NAD(P)H-binding | |||
EOOGHDJN_00757 | 5.9e-112 | akr5f | 1.1.1.346 | S | reductase | |
EOOGHDJN_00758 | 8.8e-22 | M | ErfK YbiS YcfS YnhG | |||
EOOGHDJN_00759 | 2.5e-36 | 3.2.1.17, 3.4.17.14, 3.5.1.28 | NU | Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase | ||
EOOGHDJN_00760 | 3.2e-203 | mdh | 1.1.1.350 | C | Belongs to the LDH2 MDH2 oxidoreductase family | |
EOOGHDJN_00761 | 2.3e-51 | K | Helix-turn-helix domain | |||
EOOGHDJN_00762 | 1.7e-64 | V | ABC transporter | |||
EOOGHDJN_00763 | 1.3e-65 | |||||
EOOGHDJN_00764 | 8.3e-41 | K | HxlR-like helix-turn-helix | |||
EOOGHDJN_00765 | 4e-107 | ydeA | S | intracellular protease amidase | ||
EOOGHDJN_00766 | 1.9e-43 | S | Protein of unknown function (DUF3781) | |||
EOOGHDJN_00767 | 1.5e-207 | S | Membrane | |||
EOOGHDJN_00768 | 7.6e-64 | S | Protein of unknown function (DUF1093) | |||
EOOGHDJN_00769 | 1.3e-23 | rmeD | K | helix_turn_helix, mercury resistance | ||
EOOGHDJN_00770 | 9.4e-41 | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | ||
EOOGHDJN_00771 | 1.5e-11 | |||||
EOOGHDJN_00772 | 4.1e-65 | |||||
EOOGHDJN_00773 | 1.7e-234 | celD | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
EOOGHDJN_00774 | 4.4e-269 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
EOOGHDJN_00775 | 2.2e-115 | K | UTRA | |||
EOOGHDJN_00776 | 1.7e-84 | dps | P | Belongs to the Dps family | ||
EOOGHDJN_00777 | 0.0 | 3.2.1.4, 3.2.1.78, 3.2.1.8 | GH26,GH5,GH9 | S | MucBP domain | |
EOOGHDJN_00778 | 1.7e-284 | 1.3.5.4 | C | FAD binding domain | ||
EOOGHDJN_00779 | 7.9e-163 | K | LysR substrate binding domain | |||
EOOGHDJN_00780 | 1.5e-152 | nudC | 1.3.7.1, 3.6.1.22 | L | NADH pyrophosphatase zinc ribbon domain | |
EOOGHDJN_00781 | 2.7e-291 | yjcE | P | Sodium proton antiporter | ||
EOOGHDJN_00782 | 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 | ||
EOOGHDJN_00783 | 2.1e-117 | K | Bacterial regulatory proteins, tetR family | |||
EOOGHDJN_00784 | 5.4e-189 | NU | Mycoplasma protein of unknown function, DUF285 | |||
EOOGHDJN_00785 | 2.1e-89 | S | WxL domain surface cell wall-binding | |||
EOOGHDJN_00786 | 3e-174 | S | Bacterial protein of unknown function (DUF916) | |||
EOOGHDJN_00787 | 0.0 | pelX | UW | LPXTG-motif cell wall anchor domain protein | ||
EOOGHDJN_00788 | 1.6e-64 | K | helix_turn_helix, mercury resistance | |||
EOOGHDJN_00789 | 3.4e-152 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
EOOGHDJN_00790 | 1.3e-68 | maa | S | transferase hexapeptide repeat | ||
EOOGHDJN_00791 | 2.5e-130 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
EOOGHDJN_00792 | 2.7e-15 | GM | NmrA-like family | |||
EOOGHDJN_00793 | 1.3e-134 | GM | NmrA-like family | |||
EOOGHDJN_00794 | 5.4e-92 | K | Bacterial regulatory proteins, tetR family | |||
EOOGHDJN_00795 | 8.6e-171 | fhuG | U | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
EOOGHDJN_00796 | 9.5e-178 | sirB | U | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
EOOGHDJN_00797 | 5.5e-144 | fhuC | 3.6.3.34 | HP | ABC transporter | |
EOOGHDJN_00798 | 3.7e-168 | fhuD | P | Periplasmic binding protein | ||
EOOGHDJN_00799 | 7.4e-109 | K | Bacterial regulatory proteins, tetR family | |||
EOOGHDJN_00800 | 7.8e-253 | yfjF | U | Sugar (and other) transporter | ||
EOOGHDJN_00801 | 1.5e-180 | S | Aldo keto reductase | |||
EOOGHDJN_00802 | 4.1e-101 | S | Protein of unknown function (DUF1211) | |||
EOOGHDJN_00803 | 3.5e-191 | 1.1.1.219 | GM | Male sterility protein | ||
EOOGHDJN_00804 | 3.2e-98 | K | Bacterial regulatory proteins, tetR family | |||
EOOGHDJN_00805 | 9.8e-132 | ydfG | S | KR domain | ||
EOOGHDJN_00806 | 3.7e-63 | hxlR | K | HxlR-like helix-turn-helix | ||
EOOGHDJN_00807 | 1e-47 | S | Domain of unknown function (DUF1905) | |||
EOOGHDJN_00808 | 0.0 | M | Glycosyl hydrolases family 25 | |||
EOOGHDJN_00809 | 9.1e-267 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Belongs to the aldehyde dehydrogenase family | |
EOOGHDJN_00810 | 2.8e-168 | GM | NmrA-like family | |||
EOOGHDJN_00811 | 7.9e-100 | fadR | K | Bacterial regulatory proteins, tetR family | ||
EOOGHDJN_00812 | 3e-205 | 2.7.13.3 | T | GHKL domain | ||
EOOGHDJN_00813 | 5.7e-135 | K | LytTr DNA-binding domain | |||
EOOGHDJN_00814 | 0.0 | asnB | 6.3.5.4 | E | Asparagine synthase | |
EOOGHDJN_00815 | 1.4e-94 | M | ErfK YbiS YcfS YnhG | |||
EOOGHDJN_00816 | 1.4e-212 | ytbD | EGP | Major facilitator Superfamily | ||
EOOGHDJN_00817 | 2e-61 | K | Transcriptional regulator, HxlR family | |||
EOOGHDJN_00818 | 3e-116 | S | Haloacid dehalogenase-like hydrolase | |||
EOOGHDJN_00819 | 2.3e-116 | |||||
EOOGHDJN_00820 | 6.7e-213 | NU | Mycoplasma protein of unknown function, DUF285 | |||
EOOGHDJN_00821 | 1.1e-62 | |||||
EOOGHDJN_00822 | 7.5e-101 | S | WxL domain surface cell wall-binding | |||
EOOGHDJN_00823 | 1.4e-187 | S | Cell surface protein | |||
EOOGHDJN_00824 | 2.5e-115 | S | GyrI-like small molecule binding domain | |||
EOOGHDJN_00825 | 3.8e-69 | S | Iron-sulphur cluster biosynthesis | |||
EOOGHDJN_00826 | 1e-176 | 1.6.5.5 | C | Alcohol dehydrogenase GroES-like domain | ||
EOOGHDJN_00827 | 1.6e-91 | S | WxL domain surface cell wall-binding | |||
EOOGHDJN_00828 | 5.6e-184 | S | Cell surface protein | |||
EOOGHDJN_00829 | 1.3e-75 | |||||
EOOGHDJN_00830 | 8.4e-263 | |||||
EOOGHDJN_00831 | 3.5e-228 | hpk9 | 2.7.13.3 | T | GHKL domain | |
EOOGHDJN_00832 | 2.9e-38 | S | TfoX C-terminal domain | |||
EOOGHDJN_00833 | 6e-140 | K | Helix-turn-helix domain | |||
EOOGHDJN_00834 | 2.4e-65 | silP | 1.9.3.1, 3.6.3.54 | S | Cupredoxin-like domain | |
EOOGHDJN_00835 | 2.4e-43 | silP | 1.9.3.1, 3.6.3.54 | S | Cupredoxin-like domain | |
EOOGHDJN_00836 | 0.0 | ctpA | 3.6.3.54 | P | P-type ATPase | |
EOOGHDJN_00837 | 5.2e-72 | adhC | 1.1.1.90 | C | Zn-dependent alcohol dehydrogenases, class III | |
EOOGHDJN_00838 | 5.7e-106 | adhC | 1.1.1.90 | C | Zn-dependent alcohol dehydrogenases, class III | |
EOOGHDJN_00839 | 4.2e-225 | mtnE | 2.6.1.83 | E | Aminotransferase | |
EOOGHDJN_00840 | 2.9e-147 | panE | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
EOOGHDJN_00841 | 3.7e-85 | metI | U | Binding-protein-dependent transport system inner membrane component | ||
EOOGHDJN_00842 | 1.5e-125 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
EOOGHDJN_00843 | 1.1e-110 | metQ | P | NLPA lipoprotein | ||
EOOGHDJN_00844 | 2.8e-60 | S | CHY zinc finger | |||
EOOGHDJN_00845 | 1.4e-178 | birA | 6.3.4.15 | H | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
EOOGHDJN_00846 | 6.8e-96 | bioY | S | BioY family | ||
EOOGHDJN_00847 | 3e-40 | |||||
EOOGHDJN_00848 | 1.7e-281 | pipD | E | Dipeptidase | ||
EOOGHDJN_00849 | 3e-30 | |||||
EOOGHDJN_00850 | 3e-122 | qmcA | O | prohibitin homologues | ||
EOOGHDJN_00851 | 2.3e-240 | xylP1 | G | MFS/sugar transport protein | ||
EOOGHDJN_00853 | 2.8e-162 | fba | 4.1.2.13, 4.1.2.29 | G | Fructose-1,6-bisphosphate aldolase, class II | |
EOOGHDJN_00854 | 1.1e-256 | adhE | 1.1.1.1, 1.2.1.10 | C | Aldehyde dehydrogenase family | |
EOOGHDJN_00855 | 1.9e-189 | |||||
EOOGHDJN_00856 | 2e-163 | ytrB | V | ABC transporter | ||
EOOGHDJN_00857 | 1.4e-59 | ytrA | K | helix_turn_helix gluconate operon transcriptional repressor | ||
EOOGHDJN_00858 | 8.1e-22 | |||||
EOOGHDJN_00859 | 3e-90 | K | acetyltransferase | |||
EOOGHDJN_00860 | 1e-84 | K | GNAT family | |||
EOOGHDJN_00861 | 1.1e-83 | 6.3.3.2 | S | ASCH | ||
EOOGHDJN_00862 | 5e-96 | puuR | K | Cupin domain | ||
EOOGHDJN_00863 | 3.5e-205 | potA | 3.6.3.30, 3.6.3.31 | P | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | |
EOOGHDJN_00864 | 1e-148 | potB | P | ABC transporter permease | ||
EOOGHDJN_00865 | 2.9e-140 | potC | P | ABC transporter permease | ||
EOOGHDJN_00866 | 1.5e-205 | potD | P | ABC transporter | ||
EOOGHDJN_00867 | 7.1e-21 | U | Preprotein translocase subunit SecB | |||
EOOGHDJN_00868 | 1.7e-30 | |||||
EOOGHDJN_00869 | 1.2e-07 | S | Motility quorum-sensing regulator, toxin of MqsA | |||
EOOGHDJN_00870 | 6.2e-39 | |||||
EOOGHDJN_00871 | 3e-226 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
EOOGHDJN_00872 | 1.7e-75 | K | Transcriptional regulator | |||
EOOGHDJN_00873 | 5e-78 | elaA | S | GNAT family | ||
EOOGHDJN_00874 | 8.9e-223 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
EOOGHDJN_00875 | 6.8e-57 | |||||
EOOGHDJN_00876 | 0.0 | dinG | 3.1.12.1, 3.6.4.12 | KL | DEAD_2 | |
EOOGHDJN_00877 | 3.7e-131 | |||||
EOOGHDJN_00878 | 5.7e-177 | sepS16B | ||||
EOOGHDJN_00879 | 2.2e-66 | gcvH | E | Glycine cleavage H-protein | ||
EOOGHDJN_00880 | 6.5e-39 | lytE | M | LysM domain protein | ||
EOOGHDJN_00881 | 2.3e-49 | M | Lysin motif | |||
EOOGHDJN_00882 | 2.9e-120 | S | CAAX protease self-immunity | |||
EOOGHDJN_00883 | 2.5e-114 | V | CAAX protease self-immunity | |||
EOOGHDJN_00884 | 2.7e-120 | yclH | V | ABC transporter | ||
EOOGHDJN_00885 | 3e-188 | yclI | V | MacB-like periplasmic core domain | ||
EOOGHDJN_00886 | 0.0 | XK27_00720 | S | Leucine-rich repeat (LRR) protein | ||
EOOGHDJN_00887 | 1e-107 | tag | 3.2.2.20 | L | glycosylase | |
EOOGHDJN_00888 | 0.0 | ydgH | S | MMPL family | ||
EOOGHDJN_00889 | 3.1e-104 | K | transcriptional regulator | |||
EOOGHDJN_00890 | 2.7e-123 | 2.7.6.5 | S | RelA SpoT domain protein | ||
EOOGHDJN_00891 | 1.3e-47 | |||||
EOOGHDJN_00892 | 2e-258 | loxD | 1.1.3.15 | C | FAD linked oxidases, C-terminal domain | |
EOOGHDJN_00893 | 1.4e-184 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
EOOGHDJN_00894 | 2.1e-41 | |||||
EOOGHDJN_00895 | 9.9e-57 | |||||
EOOGHDJN_00896 | 1e-243 | celB | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
EOOGHDJN_00897 | 2.1e-129 | yidA | K | Helix-turn-helix domain, rpiR family | ||
EOOGHDJN_00898 | 1.8e-49 | |||||
EOOGHDJN_00899 | 8.3e-128 | K | Transcriptional regulatory protein, C terminal | |||
EOOGHDJN_00900 | 4.9e-249 | T | PhoQ Sensor | |||
EOOGHDJN_00901 | 2.1e-64 | K | helix_turn_helix, mercury resistance | |||
EOOGHDJN_00902 | 9.7e-253 | ydiC1 | EGP | Major facilitator Superfamily | ||
EOOGHDJN_00903 | 1e-40 | |||||
EOOGHDJN_00904 | 9.4e-20 | |||||
EOOGHDJN_00905 | 5.5e-118 | |||||
EOOGHDJN_00906 | 8.5e-233 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
EOOGHDJN_00907 | 4.3e-121 | K | Bacterial regulatory proteins, tetR family | |||
EOOGHDJN_00908 | 1.8e-72 | K | Transcriptional regulator | |||
EOOGHDJN_00909 | 4.6e-70 | |||||
EOOGHDJN_00910 | 1.1e-99 | ubiX | 2.5.1.129 | H | Flavin prenyltransferase that catalyzes the synthesis of the prenylated FMN cofactor (prenyl-FMN) for 4-hydroxy-3- polyprenylbenzoic acid decarboxylase UbiD. The prenyltransferase is metal-independent and links a dimethylallyl moiety from dimethylallyl monophosphate (DMAP) to the flavin N5 and C6 atoms of FMN | |
EOOGHDJN_00911 | 9.2e-144 | |||||
EOOGHDJN_00912 | 0.0 | pts4ABC | 2.7.1.193, 2.7.1.211 | G | phosphotransferase system, EIIB | |
EOOGHDJN_00913 | 0.0 | treB | 2.7.1.193, 2.7.1.211 | G | phosphotransferase system | |
EOOGHDJN_00914 | 0.0 | treC | 3.2.1.93 | GH13 | G | Alpha amylase, catalytic domain protein |
EOOGHDJN_00915 | 3.5e-129 | treR | K | UTRA | ||
EOOGHDJN_00916 | 1.6e-39 | |||||
EOOGHDJN_00917 | 7.3e-43 | S | Protein of unknown function (DUF2089) | |||
EOOGHDJN_00918 | 4.3e-141 | pnuC | H | nicotinamide mononucleotide transporter | ||
EOOGHDJN_00919 | 7.8e-159 | map | 3.4.11.18 | E | Methionine Aminopeptidase | |
EOOGHDJN_00920 | 4.5e-166 | mccA | 2.5.1.134, 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
EOOGHDJN_00921 | 9.8e-211 | metC | 2.5.1.48, 4.4.1.1, 4.4.1.2, 4.4.1.8 | E | cystathionine | |
EOOGHDJN_00922 | 5.1e-93 | cysE | 2.3.1.30 | E | Bacterial transferase hexapeptide (six repeats) | |
EOOGHDJN_00923 | 2.2e-190 | kdgK | 2.7.1.45 | G | pfkB family carbohydrate kinase | |
EOOGHDJN_00924 | 4.6e-129 | 4.1.2.14 | S | KDGP aldolase | ||
EOOGHDJN_00925 | 8e-202 | selA | 2.9.1.1 | H | L-seryl-tRNA selenium transferase | |
EOOGHDJN_00926 | 2.3e-212 | dho | 3.5.2.3 | S | Amidohydrolase family | |
EOOGHDJN_00927 | 7.2e-211 | S | Bacterial protein of unknown function (DUF871) | |||
EOOGHDJN_00928 | 4.7e-39 | |||||
EOOGHDJN_00929 | 1.5e-228 | pts3C | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
EOOGHDJN_00930 | 3.6e-123 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
EOOGHDJN_00931 | 5.4e-98 | yieF | S | NADPH-dependent FMN reductase | ||
EOOGHDJN_00932 | 2.4e-253 | S | Uncharacterized protein conserved in bacteria (DUF2252) | |||
EOOGHDJN_00933 | 5e-81 | ndk | 2.7.4.6 | F | Belongs to the NDK family | |
EOOGHDJN_00934 | 2e-62 | |||||
EOOGHDJN_00935 | 6.6e-96 | |||||
EOOGHDJN_00936 | 2.2e-51 | |||||
EOOGHDJN_00937 | 6.2e-57 | trxA1 | O | Belongs to the thioredoxin family | ||
EOOGHDJN_00938 | 2.1e-73 | |||||
EOOGHDJN_00939 | 4.3e-222 | mtlD | 1.1.1.17 | C | mannitol-1-phosphate 5-dehydrogenase activity | |
EOOGHDJN_00940 | 1.7e-78 | mtlF | 2.7.1.197 | G | catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | |
EOOGHDJN_00941 | 0.0 | mtlR | K | Mga helix-turn-helix domain | ||
EOOGHDJN_00942 | 0.0 | mtlA | 2.7.1.197 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
EOOGHDJN_00943 | 6.7e-278 | pipD | E | Dipeptidase | ||
EOOGHDJN_00944 | 4.8e-99 | K | Helix-turn-helix domain | |||
EOOGHDJN_00945 | 3.5e-224 | 1.3.5.4 | C | FAD dependent oxidoreductase | ||
EOOGHDJN_00946 | 7.7e-174 | P | Major Facilitator Superfamily | |||
EOOGHDJN_00947 | 7.4e-132 | nagB | 3.1.1.31, 3.5.99.6 | G | Catalyzes the reversible isomerization-deamination of glucosamine 6-phosphate (GlcN6P) to form fructose 6-phosphate (Fru6P) and ammonium ion | |
EOOGHDJN_00948 | 1e-69 | |||||
EOOGHDJN_00949 | 1.4e-78 | 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 | ||
EOOGHDJN_00950 | 2.4e-158 | dkgB | S | reductase | ||
EOOGHDJN_00951 | 1.4e-89 | btuE | 1.11.1.9 | O | Belongs to the glutathione peroxidase family | |
EOOGHDJN_00952 | 9.2e-101 | S | ABC transporter permease | |||
EOOGHDJN_00953 | 1.5e-258 | P | ABC transporter | |||
EOOGHDJN_00954 | 8.9e-116 | P | cobalt transport | |||
EOOGHDJN_00955 | 2.3e-260 | S | ATPases associated with a variety of cellular activities | |||
EOOGHDJN_00956 | 8.5e-50 | crcB | D | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
EOOGHDJN_00957 | 3.5e-58 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
EOOGHDJN_00959 | 4.5e-219 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
EOOGHDJN_00960 | 4e-164 | FbpA | K | Domain of unknown function (DUF814) | ||
EOOGHDJN_00961 | 1.3e-60 | S | Domain of unknown function (DU1801) | |||
EOOGHDJN_00962 | 4.9e-34 | |||||
EOOGHDJN_00963 | 1e-179 | yghZ | C | Aldo keto reductase family protein | ||
EOOGHDJN_00964 | 3e-113 | pgm1 | G | phosphoglycerate mutase | ||
EOOGHDJN_00965 | 7e-203 | 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 | |
EOOGHDJN_00966 | 2.3e-215 | serA | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
EOOGHDJN_00967 | 1.7e-78 | yiaC | K | Acetyltransferase (GNAT) domain | ||
EOOGHDJN_00968 | 3.5e-310 | oppA | E | ABC transporter, substratebinding protein | ||
EOOGHDJN_00969 | 0.0 | oppA | E | ABC transporter, substratebinding protein | ||
EOOGHDJN_00970 | 3e-156 | hipB | K | Helix-turn-helix | ||
EOOGHDJN_00972 | 1.3e-42 | 3.6.4.13 | M | domain protein | ||
EOOGHDJN_00973 | 1.7e-165 | mleR | K | LysR substrate binding domain | ||
EOOGHDJN_00974 | 0.0 | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain protein | |
EOOGHDJN_00975 | 1.1e-217 | nhaC | C | Na H antiporter NhaC | ||
EOOGHDJN_00976 | 1.3e-165 | 3.5.1.10 | C | nadph quinone reductase | ||
EOOGHDJN_00977 | 0.0 | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain protein | |
EOOGHDJN_00978 | 9.1e-173 | scrR | K | Transcriptional regulator, LacI family | ||
EOOGHDJN_00979 | 3.4e-304 | scrB | 3.2.1.26 | GH32 | G | invertase |
EOOGHDJN_00980 | 0.0 | scrA | 2.7.1.193, 2.7.1.211, 5.3.1.1 | G | phosphotransferase system | |
EOOGHDJN_00981 | 0.0 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
EOOGHDJN_00982 | 1.8e-169 | scrK | 2.7.1.2, 2.7.1.4 | GK | ROK family | |
EOOGHDJN_00983 | 1.5e-45 | ygbF | S | Sugar efflux transporter for intercellular exchange | ||
EOOGHDJN_00984 | 0.0 | 3.2.1.96 | G | Glycosyl hydrolase family 85 | ||
EOOGHDJN_00985 | 0.0 | mapA | 2.4.1.8 | GH65 | G | hydrolase, family 65, central catalytic |
EOOGHDJN_00986 | 4e-209 | msmK | P | Belongs to the ABC transporter superfamily | ||
EOOGHDJN_00987 | 2.2e-259 | malS | 3.2.1.1 | GH13 | G | Glycogen debranching enzyme, glucanotransferase domain |
EOOGHDJN_00988 | 5.3e-150 | malA | S | maltodextrose utilization protein MalA | ||
EOOGHDJN_00989 | 1.4e-161 | malD | P | ABC transporter permease | ||
EOOGHDJN_00990 | 2.2e-227 | malC | P | Binding-protein-dependent transport system inner membrane component | ||
EOOGHDJN_00991 | 4.2e-231 | mdxE | G | Bacterial extracellular solute-binding protein | ||
EOOGHDJN_00992 | 0.0 | malL | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain |
EOOGHDJN_00993 | 2e-180 | yvdE | K | helix_turn _helix lactose operon repressor | ||
EOOGHDJN_00994 | 5e-190 | malR | K | Transcriptional regulator, LacI family | ||
EOOGHDJN_00995 | 8.6e-133 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
EOOGHDJN_00996 | 9e-57 | dhaM | 2.7.1.121 | S | PTS system fructose IIA component | |
EOOGHDJN_00997 | 1.2e-100 | dhaL | 2.7.1.121 | S | Dak2 | |
EOOGHDJN_00998 | 1.9e-186 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dak1 domain | |
EOOGHDJN_00999 | 2.2e-190 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dak1 domain | |
EOOGHDJN_01000 | 1.1e-92 | K | Bacterial regulatory proteins, tetR family | |||
EOOGHDJN_01002 | 8.6e-74 | folT | 2.7.13.3 | T | ECF transporter, substrate-specific component | |
EOOGHDJN_01003 | 2.1e-277 | C | Electron transfer flavoprotein FAD-binding domain | |||
EOOGHDJN_01004 | 1.6e-117 | K | Transcriptional regulator | |||
EOOGHDJN_01005 | 4.3e-297 | M | Exporter of polyketide antibiotics | |||
EOOGHDJN_01006 | 3.3e-169 | yjjC | V | ABC transporter | ||
EOOGHDJN_01007 | 1.2e-143 | IQ | Oxidoreductase, short chain dehydrogenase reductase family protein | |||
EOOGHDJN_01008 | 9.1e-89 | |||||
EOOGHDJN_01009 | 4.7e-151 | |||||
EOOGHDJN_01010 | 1.4e-144 | |||||
EOOGHDJN_01011 | 3.2e-53 | K | Transcriptional regulator PadR-like family | |||
EOOGHDJN_01012 | 1.6e-129 | K | UbiC transcription regulator-associated domain protein | |||
EOOGHDJN_01014 | 2.5e-98 | S | UPF0397 protein | |||
EOOGHDJN_01015 | 0.0 | ykoD | P | ABC transporter, ATP-binding protein | ||
EOOGHDJN_01016 | 7.1e-150 | cbiQ | P | cobalt transport | ||
EOOGHDJN_01017 | 7e-206 | C | Oxidoreductase | |||
EOOGHDJN_01018 | 2.2e-258 | |||||
EOOGHDJN_01019 | 5e-52 | |||||
EOOGHDJN_01020 | 0.0 | lai | 4.2.1.53 | S | Myosin-crossreactive antigen | |
EOOGHDJN_01021 | 1.3e-81 | 2.4.2.6 | F | Nucleoside 2-deoxyribosyltransferase like | ||
EOOGHDJN_01022 | 6.2e-165 | 1.1.1.65 | C | Aldo keto reductase | ||
EOOGHDJN_01023 | 1.5e-155 | S | reductase | |||
EOOGHDJN_01025 | 8.1e-216 | yeaN | P | Transporter, major facilitator family protein | ||
EOOGHDJN_01026 | 5e-51 | cadC1 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
EOOGHDJN_01027 | 4.7e-227 | mdtG | EGP | Major facilitator Superfamily | ||
EOOGHDJN_01028 | 6.1e-67 | K | LytTr DNA-binding domain | |||
EOOGHDJN_01029 | 8.7e-30 | S | Protein of unknown function (DUF3021) | |||
EOOGHDJN_01030 | 1.7e-72 | hsp1 | O | Belongs to the small heat shock protein (HSP20) family | ||
EOOGHDJN_01031 | 1.9e-75 | papX3 | K | Transcriptional regulator | ||
EOOGHDJN_01032 | 7.2e-112 | S | NADPH-dependent FMN reductase | |||
EOOGHDJN_01033 | 1.6e-28 | KT | PspC domain | |||
EOOGHDJN_01034 | 0.0 | pacL1 | P | P-type ATPase | ||
EOOGHDJN_01035 | 1.1e-149 | ydjP | I | Alpha/beta hydrolase family | ||
EOOGHDJN_01036 | 5.6e-124 | |||||
EOOGHDJN_01037 | 2.6e-250 | yifK | E | Amino acid permease | ||
EOOGHDJN_01038 | 3.4e-85 | F | NUDIX domain | |||
EOOGHDJN_01039 | 2.5e-305 | L | HIRAN domain | |||
EOOGHDJN_01040 | 1.6e-137 | S | peptidase C26 | |||
EOOGHDJN_01041 | 3.8e-205 | cytX | U | Belongs to the purine-cytosine permease (2.A.39) family | ||
EOOGHDJN_01042 | 2.5e-110 | thiE | 2.5.1.3 | H | Condenses 4-methyl-5-(beta-hydroxyethyl)thiazole monophosphate (THZ-P) and 2-methyl-4-amino-5-hydroxymethyl pyrimidine pyrophosphate (HMP-PP) to form thiamine monophosphate (TMP) | |
EOOGHDJN_01043 | 9.1e-150 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
EOOGHDJN_01044 | 1.3e-137 | thiM | 2.7.1.50 | H | Catalyzes the phosphorylation of the hydroxyl group of 4-methyl-5-beta-hydroxyethylthiazole (THZ) | |
EOOGHDJN_01045 | 1.9e-178 | 1.6.5.5 | C | Zinc-binding dehydrogenase | ||
EOOGHDJN_01046 | 6.3e-151 | larE | S | NAD synthase | ||
EOOGHDJN_01047 | 1.5e-132 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
EOOGHDJN_01048 | 5e-75 | larC | 4.99.1.12 | S | Protein of unknown function DUF111 | |
EOOGHDJN_01049 | 6.3e-132 | larC | 4.99.1.12 | S | Involved in the biosynthesis of a nickel-pincer cofactor ((SCS)Ni(II) pincer complex). Binds Ni(2 ), and functions in nickel delivery to pyridinium-3,5-bisthiocarboxylic acid mononucleotide (P2TMN), to form the mature cofactor. Is thus probably required for the activation of nickel-pincer cofactor- dependent enzymes | |
EOOGHDJN_01050 | 2.4e-125 | larB | S | AIR carboxylase | ||
EOOGHDJN_01051 | 1e-240 | larA | 5.1.2.1 | S | Domain of unknown function (DUF2088) | |
EOOGHDJN_01052 | 4.2e-121 | K | Crp-like helix-turn-helix domain | |||
EOOGHDJN_01053 | 4.8e-182 | nikMN | P | PDGLE domain | ||
EOOGHDJN_01054 | 5.8e-149 | P | Cobalt transport protein | |||
EOOGHDJN_01055 | 3.9e-128 | cbiO | P | ABC transporter | ||
EOOGHDJN_01056 | 4.8e-40 | |||||
EOOGHDJN_01057 | 3.6e-140 | 2.7.7.47 | H | Mediates bacterial resistance to the antibiotics streptomycin and spectomycin | ||
EOOGHDJN_01059 | 2.4e-141 | |||||
EOOGHDJN_01060 | 0.0 | oppA | E | Bacterial extracellular solute-binding proteins, family 5 Middle | ||
EOOGHDJN_01061 | 6e-76 | |||||
EOOGHDJN_01062 | 1.6e-140 | S | Belongs to the UPF0246 family | |||
EOOGHDJN_01063 | 2.9e-170 | pepI | 3.4.11.5, 3.5.1.101 | E | Releases the N-terminal proline from various substrates | |
EOOGHDJN_01064 | 2.1e-19 | G | Transmembrane secretion effector | |||
EOOGHDJN_01065 | 9.2e-139 | EGP | Transmembrane secretion effector | |||
EOOGHDJN_01066 | 3e-131 | 1.5.1.39 | C | nitroreductase | ||
EOOGHDJN_01067 | 3e-72 | |||||
EOOGHDJN_01068 | 1.5e-52 | |||||
EOOGHDJN_01069 | 1.3e-206 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
EOOGHDJN_01070 | 1.1e-104 | K | Bacterial regulatory proteins, tetR family | |||
EOOGHDJN_01071 | 1.3e-148 | 3.1.3.23 | S | Sucrose-6F-phosphate phosphohydrolase | ||
EOOGHDJN_01072 | 1.3e-122 | yliE | T | EAL domain | ||
EOOGHDJN_01073 | 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 | |
EOOGHDJN_01074 | 1.6e-252 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
EOOGHDJN_01075 | 1.6e-129 | ybbR | S | YbbR-like protein | ||
EOOGHDJN_01076 | 4.6e-149 | dacA | 2.7.7.85 | S | Catalyzes the condensation of 2 ATP molecules into cyclic di-AMP (c-di-AMP), a second messenger used to regulate differing processes in different bacteria | |
EOOGHDJN_01077 | 7.1e-121 | S | Protein of unknown function (DUF1361) | |||
EOOGHDJN_01078 | 1.3e-90 | K | helix_turn_helix multiple antibiotic resistance protein | |||
EOOGHDJN_01079 | 0.0 | yjcE | P | Sodium proton antiporter | ||
EOOGHDJN_01080 | 6.2e-168 | murB | 1.3.1.98 | M | Cell wall formation | |
EOOGHDJN_01081 | 1.2e-158 | yceM | 1.1.1.18, 1.1.1.369 | S | Oxidoreductase family, NAD-binding Rossmann fold | |
EOOGHDJN_01082 | 1.6e-153 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
EOOGHDJN_01083 | 5.6e-100 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
EOOGHDJN_01084 | 3.1e-87 | 2.3.1.128, 2.3.1.178 | J | Acetyltransferase (GNAT) domain | ||
EOOGHDJN_01085 | 5e-81 | ydiB | 2.7.1.221, 5.1.1.1 | O | Hydrolase, P-loop family | |
EOOGHDJN_01086 | 1.4e-178 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
EOOGHDJN_01087 | 1.6e-136 | ung | 3.2.2.27 | L | Excises uracil residues from the DNA which can arise as a result of misincorporation of dUMP residues by DNA polymerase or due to deamination of cytosine | |
EOOGHDJN_01088 | 4.4e-155 | ycsE | S | Sucrose-6F-phosphate phosphohydrolase | ||
EOOGHDJN_01089 | 5.1e-104 | yxjI | ||||
EOOGHDJN_01090 | 1.2e-132 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
EOOGHDJN_01091 | 1.5e-256 | glnP | P | ABC transporter | ||
EOOGHDJN_01092 | 0.0 | 3.4.21.72 | M | Bacterial Ig-like domain (group 3) | ||
EOOGHDJN_01093 | 9.3e-83 | smpB | J | the 2 termini fold to resemble tRNA(Ala) and it encodes a tag peptide , a short internal open reading frame. During trans-translation Ala- aminoacylated tmRNA acts like a tRNA, entering the A-site of stalled ribosomes, displacing the stalled mRNA. The ribosome then switches to translate the ORF on the tmRNA | ||
EOOGHDJN_01094 | 0.0 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
EOOGHDJN_01095 | 1.3e-139 | est | 3.1.1.1 | S | Serine aminopeptidase, S33 | |
EOOGHDJN_01096 | 1.2e-30 | secG | U | Preprotein translocase | ||
EOOGHDJN_01097 | 6.6e-295 | clcA | P | chloride | ||
EOOGHDJN_01098 | 1.3e-133 | |||||
EOOGHDJN_01099 | 1.6e-249 | 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 | |
EOOGHDJN_01100 | 1.2e-137 | 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) | |
EOOGHDJN_01101 | 8.1e-224 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
EOOGHDJN_01102 | 2.6e-191 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
EOOGHDJN_01103 | 7.3e-189 | cggR | K | Putative sugar-binding domain | ||
EOOGHDJN_01104 | 4.2e-245 | rpoN | K | Sigma-54 factor, core binding domain | ||
EOOGHDJN_01106 | 3e-102 | clpP | 3.4.21.92 | O | Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins | |
EOOGHDJN_01107 | 1e-176 | 1.1.1.26 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | ||
EOOGHDJN_01108 | 4.4e-305 | oppA | E | ABC transporter, substratebinding protein | ||
EOOGHDJN_01109 | 3.7e-168 | whiA | K | May be required for sporulation | ||
EOOGHDJN_01110 | 2.9e-190 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
EOOGHDJN_01111 | 1.1e-161 | rapZ | S | Displays ATPase and GTPase activities | ||
EOOGHDJN_01112 | 9.3e-87 | S | Short repeat of unknown function (DUF308) | |||
EOOGHDJN_01113 | 7.2e-264 | argH | 4.3.2.1 | E | argininosuccinate lyase | |
EOOGHDJN_01114 | 1.8e-231 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
EOOGHDJN_01115 | 6.7e-89 | luxS | 4.4.1.21 | H | Involved in the synthesis of autoinducer 2 (AI-2) which is secreted by bacteria and is used to communicate both the cell density and the metabolic potential of the environment. The regulation of gene expression in response to changes in cell density is called quorum sensing. Catalyzes the transformation of S-ribosylhomocysteine (RHC) to homocysteine (HC) and 4,5- dihydroxy-2,3-pentadione (DPD) | |
EOOGHDJN_01116 | 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 | ||
EOOGHDJN_01117 | 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 | ||
EOOGHDJN_01118 | 1.2e-117 | yfbR | S | HD containing hydrolase-like enzyme | ||
EOOGHDJN_01119 | 9.2e-212 | norA | EGP | Major facilitator Superfamily | ||
EOOGHDJN_01120 | 5.6e-103 | ddpX | 3.4.13.22 | E | Catalyzes hydrolysis of the D-alanyl-D-alanine dipeptide | |
EOOGHDJN_01121 | 1.4e-259 | nox | S | Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain | ||
EOOGHDJN_01122 | 3.3e-132 | yliE | T | Putative diguanylate phosphodiesterase | ||
EOOGHDJN_01123 | 0.0 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase phosphomannomutase, alpha beta alpha domain | |
EOOGHDJN_01124 | 1.1e-61 | S | Protein of unknown function (DUF3290) | |||
EOOGHDJN_01125 | 2e-109 | yviA | S | Protein of unknown function (DUF421) | ||
EOOGHDJN_01126 | 1.7e-176 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
EOOGHDJN_01127 | 1e-132 | 2.7.7.65 | T | diguanylate cyclase activity | ||
EOOGHDJN_01128 | 0.0 | ydaN | S | Bacterial cellulose synthase subunit | ||
EOOGHDJN_01129 | 6.8e-218 | ydaM | M | Glycosyl transferase family group 2 | ||
EOOGHDJN_01130 | 3.8e-205 | S | Protein conserved in bacteria | |||
EOOGHDJN_01131 | 1.2e-245 | |||||
EOOGHDJN_01132 | 4.3e-163 | G | Belongs to the glycosyl hydrolase 8 (cellulase D) family | |||
EOOGHDJN_01133 | 3.9e-270 | nox | C | NADH oxidase | ||
EOOGHDJN_01134 | 1.9e-124 | yliE | T | Putative diguanylate phosphodiesterase | ||
EOOGHDJN_01135 | 2.1e-171 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
EOOGHDJN_01136 | 3.2e-181 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
EOOGHDJN_01137 | 1.9e-163 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
EOOGHDJN_01138 | 1.4e-176 | hprK | F | Catalyzes the ATP- as well as the pyrophosphate- dependent phosphorylation of a specific serine residue in HPr, a phosphocarrier protein of the phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS). HprK P also catalyzes the pyrophosphate-producing, inorganic phosphate-dependent dephosphorylation (phosphorolysis) of seryl-phosphorylated HPr (P- Ser-HPr). The two antagonistic activities of HprK P are regulated by several intracellular metabolites, which change their concentration in response to the absence or presence of rapidly metabolisable carbon sources (glucose, fructose, etc.) in the growth medium. Therefore, by controlling the phosphorylation state of HPr, HPrK P is a sensor enzyme that plays a major role in the regulation of carbon metabolism and sugar transport it mediates carbon catabolite repression (CCR), and regulates PTS-catalyzed carbohydrate uptake and inducer exclusion | ||
EOOGHDJN_01139 | 9.2e-54 | yvlD | S | Mycobacterial 4 TMS phage holin, superfamily IV | ||
EOOGHDJN_01140 | 2e-49 | pspC | KT | positive regulation of macromolecule biosynthetic process | ||
EOOGHDJN_01141 | 8.3e-117 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
EOOGHDJN_01142 | 1e-139 | pstB | 3.6.3.27 | P | Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system | |
EOOGHDJN_01143 | 1.1e-147 | 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 | |
EOOGHDJN_01144 | 1.5e-155 | pstA | P | Phosphate transport system permease protein PstA | ||
EOOGHDJN_01145 | 6.8e-162 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
EOOGHDJN_01146 | 1.1e-150 | pstS | P | Phosphate | ||
EOOGHDJN_01147 | 3.5e-250 | phoR | 2.7.13.3 | T | Histidine kinase | |
EOOGHDJN_01148 | 1.5e-132 | K | response regulator | |||
EOOGHDJN_01149 | 1.2e-216 | minJ | O | Domain present in PSD-95, Dlg, and ZO-1/2. | ||
EOOGHDJN_01150 | 1.2e-202 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
EOOGHDJN_01151 | 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 | ||
EOOGHDJN_01152 | 3.5e-100 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
EOOGHDJN_01153 | 7.5e-126 | comFC | S | Competence protein | ||
EOOGHDJN_01154 | 2.8e-257 | comFA | L | Helicase C-terminal domain protein | ||
EOOGHDJN_01155 | 1.7e-114 | yvyE | 3.4.13.9 | S | YigZ family | |
EOOGHDJN_01156 | 4.3e-145 | pstS | P | Phosphate | ||
EOOGHDJN_01157 | 2.7e-181 | tagO | 2.7.8.33, 2.7.8.35 | M | transferase | |
EOOGHDJN_01158 | 0.0 | ydaO | E | amino acid | ||
EOOGHDJN_01159 | 8.5e-293 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
EOOGHDJN_01160 | 1e-31 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
EOOGHDJN_01161 | 6.1e-109 | ydiL | S | CAAX protease self-immunity | ||
EOOGHDJN_01162 | 1.4e-119 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
EOOGHDJN_01163 | 7.4e-307 | uup | S | ABC transporter, ATP-binding protein | ||
EOOGHDJN_01164 | 6.6e-258 | cshA | 3.6.4.13 | F | DEAD-box RNA helicase possibly involved in RNA degradation. Unwinds dsRNA in both 5'- and 3'-directions, has RNA- dependent ATPase activity | |
EOOGHDJN_01165 | 5.6e-261 | murF | 6.3.2.10, 6.3.2.13 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
EOOGHDJN_01166 | 2e-146 | |||||
EOOGHDJN_01167 | 1e-138 | htpX | O | Belongs to the peptidase M48B family | ||
EOOGHDJN_01168 | 1.7e-91 | lemA | S | LemA family | ||
EOOGHDJN_01169 | 9.2e-127 | srtA | 3.4.22.70 | M | sortase family | |
EOOGHDJN_01170 | 9.4e-214 | J | translation release factor activity | |||
EOOGHDJN_01171 | 7.8e-41 | rpmE2 | J | Ribosomal protein L31 | ||
EOOGHDJN_01172 | 4.3e-239 | 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 | ||
EOOGHDJN_01173 | 3.6e-238 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
EOOGHDJN_01174 | 5.1e-27 | |||||
EOOGHDJN_01175 | 2.9e-131 | S | YheO-like PAS domain | |||
EOOGHDJN_01176 | 7.6e-158 | sdaAA | 4.3.1.17 | E | L-serine dehydratase, iron-sulfur-dependent, alpha subunit | |
EOOGHDJN_01177 | 9.8e-123 | sdaAB | 4.3.1.17 | E | Serine dehydratase beta chain | |
EOOGHDJN_01178 | 3.1e-229 | tdcC | E | amino acid | ||
EOOGHDJN_01179 | 4.7e-246 | 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) | |
EOOGHDJN_01180 | 3.4e-310 | pyrG | 6.3.4.2 | F | Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen. Regulates intracellular CTP levels through interactions with the four ribonucleotide triphosphates | |
EOOGHDJN_01181 | 4e-46 | rpoE | K | Participates in both the initiation and recycling phases of transcription. In the presence of the delta subunit, RNAP displays an increased specificity of transcription, a decreased affinity for nucleic acids, and an increased efficiency of RNA synthesis because of enhanced recycling | ||
EOOGHDJN_01182 | 3.8e-78 | ywiB | S | Domain of unknown function (DUF1934) | ||
EOOGHDJN_01183 | 9.7e-155 | lipL | 2.3.1.200, 2.3.1.204 | H | biotin lipoate A B protein ligase | |
EOOGHDJN_01184 | 9e-264 | ywfO | S | HD domain protein | ||
EOOGHDJN_01185 | 1.7e-148 | yxeH | S | hydrolase | ||
EOOGHDJN_01186 | 2.2e-126 | |||||
EOOGHDJN_01187 | 1.2e-183 | S | DUF218 domain | |||
EOOGHDJN_01188 | 1.2e-177 | 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) | |
EOOGHDJN_01189 | 3.1e-150 | bla1 | 3.5.2.6 | V | Beta-lactamase enzyme family | |
EOOGHDJN_01190 | 1.2e-207 | 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 | |
EOOGHDJN_01191 | 6.6e-148 | purR | 2.4.2.22, 2.4.2.7 | F | pur operon repressor | |
EOOGHDJN_01192 | 5.9e-130 | znuB | U | ABC 3 transport family | ||
EOOGHDJN_01193 | 9.8e-129 | fhuC | 3.6.3.35 | P | ABC transporter | |
EOOGHDJN_01194 | 1.5e-180 | S | Prolyl oligopeptidase family | |||
EOOGHDJN_01195 | 1.5e-163 | ispE | 2.1.1.182, 2.7.1.148 | F | Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol | |
EOOGHDJN_01196 | 3.2e-37 | veg | S | Biofilm formation stimulator VEG | ||
EOOGHDJN_01197 | 8e-160 | ksgA | 2.1.1.182 | J | Specifically dimethylates two adjacent adenosines (A1518 and A1519) in the loop of a conserved hairpin near the 3'-end of 16S rRNA in the 30S particle. May play a critical role in biogenesis of 30S subunits | |
EOOGHDJN_01198 | 4.7e-97 | rnmV | 3.1.26.8 | J | Required for correct processing of both the 5' and 3' ends of 5S rRNA precursor. Cleaves both sides of a double-stranded region yielding mature 5S rRNA in one step | |
EOOGHDJN_01199 | 5.7e-146 | tatD | L | hydrolase, TatD family | ||
EOOGHDJN_01200 | 2e-214 | bcr1 | EGP | Major facilitator Superfamily | ||
EOOGHDJN_01201 | 0.0 | metG | 6.1.1.10, 6.1.1.20 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
EOOGHDJN_01202 | 4e-71 | mutT | 3.6.1.55 | F | DNA mismatch repair protein MutT | |
EOOGHDJN_01203 | 2e-160 | yunF | F | Protein of unknown function DUF72 | ||
EOOGHDJN_01204 | 3.9e-133 | cobB | K | SIR2 family | ||
EOOGHDJN_01205 | 3.1e-178 | |||||
EOOGHDJN_01206 | 6.8e-229 | mvaA | 1.1.1.34, 1.1.1.88, 2.3.1.9 | C | Belongs to the HMG-CoA reductase family | |
EOOGHDJN_01207 | 8.2e-168 | ppx | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
EOOGHDJN_01208 | 3.5e-151 | S | Psort location Cytoplasmic, score | |||
EOOGHDJN_01209 | 1.1e-206 | |||||
EOOGHDJN_01210 | 2.8e-191 | 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 | ||
EOOGHDJN_01211 | 4.1e-133 | K | Helix-turn-helix domain, rpiR family | |||
EOOGHDJN_01212 | 1e-162 | GK | ROK family | |||
EOOGHDJN_01213 | 7.3e-296 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
EOOGHDJN_01214 | 2.6e-250 | chbC | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
EOOGHDJN_01215 | 2.6e-76 | S | Domain of unknown function (DUF3284) | |||
EOOGHDJN_01216 | 3.9e-24 | |||||
EOOGHDJN_01217 | 1.9e-253 | celB | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
EOOGHDJN_01218 | 9e-130 | K | UbiC transcription regulator-associated domain protein | |||
EOOGHDJN_01219 | 2.6e-191 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
EOOGHDJN_01220 | 1e-142 | mtnU | 3.5.1.3 | S | Carbon-nitrogen hydrolase | |
EOOGHDJN_01221 | 0.0 | helD | 3.6.4.12 | L | DNA helicase | |
EOOGHDJN_01222 | 2.6e-29 | |||||
EOOGHDJN_01223 | 6.7e-114 | S | CAAX protease self-immunity | |||
EOOGHDJN_01224 | 1.4e-108 | V | CAAX protease self-immunity | |||
EOOGHDJN_01225 | 9.7e-118 | ypbD | S | CAAX protease self-immunity | ||
EOOGHDJN_01226 | 1.2e-107 | S | CAAX protease self-immunity | |||
EOOGHDJN_01227 | 9e-90 | mesE | M | Transport protein ComB | ||
EOOGHDJN_01228 | 1.3e-132 | mesE | M | Transport protein ComB | ||
EOOGHDJN_01229 | 0.0 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
EOOGHDJN_01230 | 6.7e-23 | |||||
EOOGHDJN_01231 | 2.4e-22 | plnF | ||||
EOOGHDJN_01232 | 2.2e-129 | S | CAAX protease self-immunity | |||
EOOGHDJN_01233 | 2e-132 | plnD | K | LytTr DNA-binding domain | ||
EOOGHDJN_01234 | 5.5e-130 | plnC | K | LytTr DNA-binding domain | ||
EOOGHDJN_01235 | 7.8e-228 | plnB | 2.7.13.3 | T | GHKL domain | |
EOOGHDJN_01236 | 4.3e-18 | plnA | ||||
EOOGHDJN_01237 | 8.4e-27 | |||||
EOOGHDJN_01238 | 7e-117 | plnP | S | CAAX protease self-immunity | ||
EOOGHDJN_01239 | 3.9e-226 | M | Glycosyl transferase family 2 | |||
EOOGHDJN_01241 | 2.8e-28 | |||||
EOOGHDJN_01242 | 3.5e-24 | plnJ | ||||
EOOGHDJN_01243 | 5.2e-23 | plnK | ||||
EOOGHDJN_01244 | 1.7e-117 | |||||
EOOGHDJN_01245 | 2.9e-17 | plnR | ||||
EOOGHDJN_01246 | 7.2e-32 | |||||
EOOGHDJN_01247 | 2.1e-208 | napA | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
EOOGHDJN_01248 | 3.2e-256 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
EOOGHDJN_01249 | 1.4e-150 | S | hydrolase | |||
EOOGHDJN_01250 | 3.3e-166 | K | Transcriptional regulator | |||
EOOGHDJN_01251 | 6.9e-147 | 3.1.3.102, 3.1.3.104 | G | Sucrose-6F-phosphate phosphohydrolase | ||
EOOGHDJN_01252 | 2e-195 | uhpT | EGP | Major facilitator Superfamily | ||
EOOGHDJN_01253 | 9.6e-120 | lacA | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
EOOGHDJN_01254 | 6.1e-19 | S | Barstar (barnase inhibitor) | |||
EOOGHDJN_01255 | 1.4e-61 | |||||
EOOGHDJN_01256 | 7.1e-29 | |||||
EOOGHDJN_01258 | 1.2e-34 | |||||
EOOGHDJN_01259 | 1.9e-114 | L | Transposase and inactivated derivatives, IS30 family | |||
EOOGHDJN_01262 | 2.4e-51 | |||||
EOOGHDJN_01263 | 4.8e-61 | 1.1.98.6, 3.6.3.14, 3.6.3.15, 4.1.1.35 | L | Participates in initiation and elongation during chromosome replication | ||
EOOGHDJN_01264 | 0.0 | M | domain protein | |||
EOOGHDJN_01265 | 4.7e-134 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
EOOGHDJN_01266 | 0.0 | glpD | 1.1.3.21, 1.1.5.3 | C | C-terminal domain of alpha-glycerophosphate oxidase | |
EOOGHDJN_01267 | 1.3e-300 | 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 | |
EOOGHDJN_01268 | 6.4e-254 | gshR | 1.8.1.7 | C | Glutathione reductase | |
EOOGHDJN_01269 | 2.9e-179 | proV | E | ABC transporter, ATP-binding protein | ||
EOOGHDJN_01270 | 1.8e-276 | proWX | EM | Periplasmic glycine betaine choline-binding (lipo)protein of an ABC-type transport system (osmoprotectant binding protein) | ||
EOOGHDJN_01271 | 2.2e-78 | 3.1.26.4 | L | RNA-DNA hybrid ribonuclease activity | ||
EOOGHDJN_01272 | 1e-106 | |||||
EOOGHDJN_01273 | 1.4e-117 | S | Domain of unknown function (DUF4811) | |||
EOOGHDJN_01274 | 7e-270 | lmrB | EGP | Major facilitator Superfamily | ||
EOOGHDJN_01275 | 8.3e-84 | merR | K | MerR HTH family regulatory protein | ||
EOOGHDJN_01276 | 5.8e-58 | |||||
EOOGHDJN_01277 | 2e-120 | sirR | K | iron dependent repressor | ||
EOOGHDJN_01278 | 6e-31 | cspC | K | Cold shock protein | ||
EOOGHDJN_01279 | 1.5e-130 | thrE | S | Putative threonine/serine exporter | ||
EOOGHDJN_01280 | 2.2e-76 | S | Threonine/Serine exporter, ThrE | |||
EOOGHDJN_01281 | 1.5e-189 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
EOOGHDJN_01282 | 3.9e-119 | lssY | 3.6.1.27 | I | phosphatase | |
EOOGHDJN_01283 | 2e-154 | I | alpha/beta hydrolase fold | |||
EOOGHDJN_01284 | 2.8e-99 | 2.3.1.128 | J | Acetyltransferase (GNAT) domain | ||
EOOGHDJN_01285 | 4.2e-92 | K | Transcriptional regulator | |||
EOOGHDJN_01286 | 0.0 | alsS | 2.2.1.6 | EH | Belongs to the TPP enzyme family | |
EOOGHDJN_01287 | 1.5e-264 | lysP | E | amino acid | ||
EOOGHDJN_01288 | 2.5e-114 | vanY | 3.4.17.14 | M | D-alanyl-D-alanine carboxypeptidase | |
EOOGHDJN_01289 | 2.5e-115 | dak | 2.7.1.74, 2.7.1.76 | F | deoxynucleoside kinase | |
EOOGHDJN_01290 | 4.1e-218 | 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) | |
EOOGHDJN_01298 | 6.9e-78 | ctsR | K | Belongs to the CtsR family | ||
EOOGHDJN_01299 | 0.0 | clpC | O | Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE | ||
EOOGHDJN_01300 | 1.5e-109 | K | Bacterial regulatory proteins, tetR family | |||
EOOGHDJN_01301 | 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 | |
EOOGHDJN_01302 | 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 | |
EOOGHDJN_01303 | 7.8e-115 | pilD | 3.4.23.43 | NOU | Bacterial Peptidase A24 N-terminal domain | |
EOOGHDJN_01304 | 3.6e-70 | 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 | ||
EOOGHDJN_01305 | 5.5e-83 | rpsG | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the head domain of the 30S subunit. Is located at the subunit interface close to the decoding center, probably blocks exit of the E-site tRNA | ||
EOOGHDJN_01306 | 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 | ||
EOOGHDJN_01307 | 2.6e-49 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
EOOGHDJN_01308 | 4.4e-112 | 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 | ||
EOOGHDJN_01309 | 5.5e-107 | rplD | J | Forms part of the polypeptide exit tunnel | ||
EOOGHDJN_01310 | 1.8e-44 | rplW | J | One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome | ||
EOOGHDJN_01311 | 8.1e-146 | 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 | ||
EOOGHDJN_01312 | 8.2e-47 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
EOOGHDJN_01313 | 2.8e-52 | rplV | J | The globular domain of the protein is located near the polypeptide exit tunnel on the outside of the subunit, while an extended beta-hairpin is found that lines the wall of the exit tunnel in the center of the 70S ribosome | ||
EOOGHDJN_01314 | 2.1e-117 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
EOOGHDJN_01315 | 9.2e-77 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
EOOGHDJN_01316 | 1.4e-24 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
EOOGHDJN_01317 | 2.5e-40 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
EOOGHDJN_01318 | 4.3e-59 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
EOOGHDJN_01319 | 2.4e-50 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
EOOGHDJN_01320 | 3.2e-95 | rplE | J | This is 1 of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance. In the 70S ribosome it contacts protein S13 of the 30S subunit (bridge B1b), connecting the 2 subunits | ||
EOOGHDJN_01321 | 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 | ||
EOOGHDJN_01322 | 3.5e-94 | 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 | ||
EOOGHDJN_01323 | 3.3e-56 | 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 | ||
EOOGHDJN_01324 | 6.8e-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 | ||
EOOGHDJN_01325 | 2.2e-24 | rpmD | J | Ribosomal protein L30 | ||
EOOGHDJN_01326 | 6.3e-70 | rplO | J | Binds to the 23S rRNA | ||
EOOGHDJN_01327 | 1.5e-236 | secY | U | The central subunit of the protein translocation channel SecYEG. Consists of two halves formed by TMs 1-5 and 6-10. These two domains form a lateral gate at the front which open onto the bilayer between TMs 2 and 7, and are clamped together by SecE at the back. The channel is closed by both a pore ring composed of hydrophobic SecY resides and a short helix (helix 2A) on the extracellular side of the membrane which forms a plug. The plug probably moves laterally to allow the channel to open. The ring and the pore may move independently | ||
EOOGHDJN_01328 | 2.1e-125 | 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 | |
EOOGHDJN_01329 | 3.1e-33 | infA | J | One of the essential components for the initiation of protein synthesis. Stabilizes the binding of IF-2 and IF-3 on the 30S subunit to which N-formylmethionyl-tRNA(fMet) subsequently binds. Helps modulate mRNA selection, yielding the 30S pre- initiation complex (PIC). Upon addition of the 50S ribosomal subunit IF-1, IF-2 and IF-3 are released leaving the mature 70S translation initation complex | ||
EOOGHDJN_01330 | 1.1e-59 | rpsM | J | Located at the top of the head of the 30S subunit, it contacts several helices of the 16S rRNA. In the 70S ribosome it contacts the 23S rRNA (bridge B1a) and protein L5 of the 50S subunit (bridge B1b), connecting the 2 subunits | ||
EOOGHDJN_01331 | 3.4e-62 | 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 | ||
EOOGHDJN_01332 | 5.7e-172 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
EOOGHDJN_01333 | 2.1e-61 | rplQ | J | Ribosomal protein L17 | ||
EOOGHDJN_01334 | 1.4e-181 | hepT | 2.5.1.30, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
EOOGHDJN_01335 | 1.7e-94 | gerCA | 2.5.1.30 | S | Heptaprenyl diphosphate synthase component I | |
EOOGHDJN_01336 | 1.4e-86 | ynhH | S | NusG domain II | ||
EOOGHDJN_01337 | 0.0 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
EOOGHDJN_01338 | 3.5e-142 | cad | S | FMN_bind | ||
EOOGHDJN_01339 | 1.5e-208 | apbE | 2.7.1.180 | H | Flavin transferase that catalyzes the transfer of the FMN moiety of FAD and its covalent binding to the hydroxyl group of a threonine residue in a target flavoprotein | |
EOOGHDJN_01340 | 1.4e-153 | ecfA1 | P | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
EOOGHDJN_01341 | 2.2e-165 | ecfA2 | 3.6.3.55 | P | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | |
EOOGHDJN_01342 | 8e-143 | ecfT | U | Transmembrane (T) component of an energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
EOOGHDJN_01343 | 3.9e-150 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
EOOGHDJN_01344 | 1.3e-78 | 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 | ||
EOOGHDJN_01345 | 1.9e-65 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
EOOGHDJN_01346 | 2e-163 | degV | S | Uncharacterised protein, DegV family COG1307 | ||
EOOGHDJN_01347 | 1.5e-184 | ywhK | S | Membrane | ||
EOOGHDJN_01348 | 7.6e-205 | mdh | 1.1.1.350 | C | Belongs to the LDH2 MDH2 oxidoreductase family | |
EOOGHDJN_01349 | 0.0 | tkt | 2.2.1.1 | H | Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate | |
EOOGHDJN_01350 | 5.7e-166 | aroE | 1.1.1.25 | E | Involved in the biosynthesis of the chorismate, which leads to the biosynthesis of aromatic amino acids. Catalyzes the reversible NADPH linked reduction of 3-dehydroshikimate (DHSA) to yield shikimate (SA) | |
EOOGHDJN_01351 | 1.8e-184 | aroF | 2.5.1.54 | E | DAHP synthetase I family | |
EOOGHDJN_01352 | 1.4e-198 | 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) | |
EOOGHDJN_01353 | 1.2e-263 | P | Sodium:sulfate symporter transmembrane region | |||
EOOGHDJN_01354 | 4.1e-115 | ttdB | 4.2.1.2, 4.2.1.32 | C | Catalyzes the reversible hydration of fumarate to (S)- malate | |
EOOGHDJN_01355 | 4.4e-177 | ttdA | 4.2.1.32 | C | Fumarate hydratase (Fumerase) | |
EOOGHDJN_01356 | 1.9e-197 | K | Helix-turn-helix domain | |||
EOOGHDJN_01357 | 1.4e-153 | citG | 2.4.2.52, 2.7.7.61 | H | 2-(5''-triphosphoribosyl)-3'-dephosphocoenzyme-A synthase | |
EOOGHDJN_01358 | 4.5e-132 | mntB | 3.6.3.35 | P | ABC transporter | |
EOOGHDJN_01359 | 1.8e-140 | mtsB | U | ABC 3 transport family | ||
EOOGHDJN_01360 | 1.2e-174 | sitA | P | Belongs to the bacterial solute-binding protein 9 family | ||
EOOGHDJN_01361 | 3.1e-50 | |||||
EOOGHDJN_01362 | 4.6e-166 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
EOOGHDJN_01363 | 1.7e-260 | citP | P | Sodium:sulfate symporter transmembrane region | ||
EOOGHDJN_01364 | 2.9e-179 | citR | K | sugar-binding domain protein | ||
EOOGHDJN_01365 | 6.6e-207 | mez_1 | 1.1.1.38 | C | Malic enzyme, NAD binding domain | |
EOOGHDJN_01366 | 5.7e-189 | citC | 6.2.1.22 | H | Acetylation of prosthetic group (2-(5''-phosphoribosyl)- 3'-dephosphocoenzyme-A) of the gamma subunit of citrate lyase | |
EOOGHDJN_01367 | 9e-44 | citD | C | Covalent carrier of the coenzyme of citrate lyase | ||
EOOGHDJN_01368 | 6.7e-162 | citE | 4.1.3.25, 4.1.3.34 | G | Belongs to the HpcH HpaI aldolase family | |
EOOGHDJN_01369 | 4.6e-288 | citF | 2.8.3.10 | H | Citrate (pro-3S)-lyase alpha chain | |
EOOGHDJN_01370 | 3e-179 | L | PFAM Integrase, catalytic core | |||
EOOGHDJN_01371 | 7e-26 | K | sequence-specific DNA binding | |||
EOOGHDJN_01373 | 4.6e-165 | yniA | G | Fructosamine kinase | ||
EOOGHDJN_01374 | 1.9e-155 | lytH | 3.5.1.28 | M | N-acetylmuramoyl-L-alanine amidase | |
EOOGHDJN_01375 | 2.2e-243 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
EOOGHDJN_01376 | 0.0 | aspS | 6.1.1.12 | J | Catalyzes the attachment of L-aspartate to tRNA(Asp) in a two-step reaction L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp) | |
EOOGHDJN_01377 | 3.2e-100 | msrA | 1.8.4.11, 1.8.4.12 | O | Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine | |
EOOGHDJN_01378 | 1.7e-159 | yitT | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
EOOGHDJN_01379 | 8.6e-223 | tagB | 2.7.8.14, 2.7.8.44, 2.7.8.47 | M | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | |
EOOGHDJN_01380 | 1.1e-169 | nfo | 3.1.21.2 | L | Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin | |
EOOGHDJN_01381 | 3.8e-128 | C | Enoyl-(Acyl carrier protein) reductase | |||
EOOGHDJN_01382 | 2.1e-151 | yqfL | 2.7.11.33, 2.7.4.28 | F | Bifunctional serine threonine kinase and phosphorylase involved in the regulation of the pyruvate, phosphate dikinase (PPDK) by catalyzing its phosphorylation dephosphorylation | |
EOOGHDJN_01383 | 9.7e-23 | rpsU | J | Belongs to the bacterial ribosomal protein bS21 family | ||
EOOGHDJN_01384 | 2.6e-71 | yqeY | S | YqeY-like protein | ||
EOOGHDJN_01385 | 3.4e-180 | phoH | T | phosphate starvation-inducible protein PhoH | ||
EOOGHDJN_01386 | 6.6e-84 | 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 | |
EOOGHDJN_01387 | 4.5e-73 | dgkA | 2.7.1.107, 2.7.1.66 | M | Diacylglycerol kinase | |
EOOGHDJN_01388 | 1.5e-169 | 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 | ||
EOOGHDJN_01389 | 3.1e-147 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
EOOGHDJN_01390 | 6.8e-175 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
EOOGHDJN_01391 | 1.3e-66 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
EOOGHDJN_01392 | 0.0 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
EOOGHDJN_01393 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
EOOGHDJN_01394 | 4.6e-197 | 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 | ||
EOOGHDJN_01395 | 3.6e-64 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
EOOGHDJN_01396 | 4.8e-165 | ytrB | V | ABC transporter, ATP-binding protein | ||
EOOGHDJN_01397 | 1.8e-203 | |||||
EOOGHDJN_01398 | 3.6e-199 | |||||
EOOGHDJN_01399 | 2.3e-128 | S | ABC-2 family transporter protein | |||
EOOGHDJN_01400 | 3.9e-162 | V | ABC transporter, ATP-binding protein | |||
EOOGHDJN_01401 | 3.8e-114 | S | Psort location CytoplasmicMembrane, score | |||
EOOGHDJN_01402 | 2.1e-73 | K | MarR family | |||
EOOGHDJN_01403 | 6e-82 | K | Acetyltransferase (GNAT) domain | |||
EOOGHDJN_01405 | 2.6e-158 | yvfR | V | ABC transporter | ||
EOOGHDJN_01406 | 1.3e-134 | yvfS | V | ABC-2 type transporter | ||
EOOGHDJN_01407 | 1.5e-203 | desK | 2.7.13.3 | T | Histidine kinase | |
EOOGHDJN_01408 | 1.2e-103 | desR | K | helix_turn_helix, Lux Regulon | ||
EOOGHDJN_01409 | 9.3e-272 | nox | C | Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain | ||
EOOGHDJN_01410 | 2.8e-14 | S | Alpha beta hydrolase | |||
EOOGHDJN_01411 | 1.3e-173 | C | nadph quinone reductase | |||
EOOGHDJN_01412 | 6.5e-162 | K | Transcriptional regulator | |||
EOOGHDJN_01413 | 9.8e-79 | S | Uncharacterized protein conserved in bacteria (DUF2255) | |||
EOOGHDJN_01414 | 2e-112 | GM | NmrA-like family | |||
EOOGHDJN_01415 | 1.2e-160 | S | Alpha beta hydrolase | |||
EOOGHDJN_01416 | 6.5e-128 | K | Helix-turn-helix domain, rpiR family | |||
EOOGHDJN_01417 | 3.7e-76 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose O-acetyltransferase | |
EOOGHDJN_01418 | 1.3e-117 | ppaX_1 | 3.1.3.18, 3.6.1.1 | S | haloacid dehalogenase-like hydrolase | |
EOOGHDJN_01419 | 0.0 | CP_1020 | S | Zinc finger, swim domain protein | ||
EOOGHDJN_01420 | 2.3e-113 | GM | epimerase | |||
EOOGHDJN_01421 | 1.4e-68 | S | Protein of unknown function (DUF1722) | |||
EOOGHDJN_01422 | 9.1e-71 | yneH | 1.20.4.1 | P | ArsC family | |
EOOGHDJN_01423 | 1.7e-108 | yjhB | 3.6.1.13, 3.6.1.55 | F | NUDIX domain | |
EOOGHDJN_01424 | 2.8e-137 | K | DeoR C terminal sensor domain | |||
EOOGHDJN_01425 | 0.0 | naoX | P | Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain | ||
EOOGHDJN_01426 | 3e-212 | dapE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
EOOGHDJN_01427 | 4.3e-77 | K | Transcriptional regulator | |||
EOOGHDJN_01428 | 1.3e-241 | EGP | Major facilitator Superfamily | |||
EOOGHDJN_01429 | 6.8e-245 | 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 | |
EOOGHDJN_01430 | 0.0 | 3.6.3.6 | P | Cation transporter/ATPase, N-terminus | ||
EOOGHDJN_01431 | 2e-180 | C | Zinc-binding dehydrogenase | |||
EOOGHDJN_01432 | 1.4e-217 | I | transferase activity, transferring acyl groups other than amino-acyl groups | |||
EOOGHDJN_01433 | 3.5e-208 | |||||
EOOGHDJN_01434 | 2.1e-91 | yetL | K | helix_turn_helix multiple antibiotic resistance protein | ||
EOOGHDJN_01435 | 1.9e-62 | P | Rhodanese Homology Domain | |||
EOOGHDJN_01436 | 0.0 | ppsA | 2.7.9.2 | H | Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate | |
EOOGHDJN_01437 | 3.1e-84 | K | helix_turn_helix multiple antibiotic resistance protein | |||
EOOGHDJN_01438 | 3.2e-167 | drrA | V | ABC transporter | ||
EOOGHDJN_01439 | 4.5e-119 | drrB | U | ABC-2 type transporter | ||
EOOGHDJN_01440 | 6.9e-223 | M | O-Antigen ligase | |||
EOOGHDJN_01441 | 1e-125 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
EOOGHDJN_01442 | 3.8e-198 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
EOOGHDJN_01443 | 6.8e-234 | pepT | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
EOOGHDJN_01444 | 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 | ||
EOOGHDJN_01446 | 5.6e-29 | S | Protein of unknown function (DUF2929) | |||
EOOGHDJN_01447 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase | |
EOOGHDJN_01448 | 1.5e-180 | pfkA | 2.7.1.11 | F | Catalyzes the phosphorylation of D-fructose 6-phosphate to fructose 1,6-bisphosphate by ATP, the first committing step of glycolysis | |
EOOGHDJN_01449 | 0.0 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
EOOGHDJN_01450 | 5.2e-167 | natA | S | ABC transporter, ATP-binding protein | ||
EOOGHDJN_01451 | 4.7e-211 | natB | CP | ABC-2 family transporter protein | ||
EOOGHDJN_01452 | 1e-128 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
EOOGHDJN_01453 | 2.5e-55 | yphJ | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | |
EOOGHDJN_01454 | 3.5e-75 | yphH | S | Cupin domain | ||
EOOGHDJN_01455 | 4.4e-79 | K | transcriptional regulator, MerR family | |||
EOOGHDJN_01456 | 4.3e-236 | dapE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
EOOGHDJN_01457 | 0.0 | ylbB | V | ABC transporter permease | ||
EOOGHDJN_01458 | 7.5e-121 | macB | V | ABC transporter, ATP-binding protein | ||
EOOGHDJN_01460 | 8e-117 | nth | 4.2.99.18 | L | DNA repair enzyme that has both DNA N-glycosylase activity and AP-lyase activity. The DNA N-glycosylase activity releases various damaged pyrimidines from DNA by cleaving the N- glycosidic bond, leaving an AP (apurinic apyrimidinic) site. The AP-lyase activity cleaves the phosphodiester bond 3' to the AP site by a beta-elimination, leaving a 3'-terminal unsaturated sugar and a product with a terminal 5'-phosphate | |
EOOGHDJN_01461 | 2.2e-100 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
EOOGHDJN_01462 | 8.4e-116 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
EOOGHDJN_01463 | 1.3e-113 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
EOOGHDJN_01464 | 2.2e-84 | |||||
EOOGHDJN_01465 | 5e-87 | yvbK | 3.1.3.25 | K | GNAT family | |
EOOGHDJN_01466 | 3.2e-37 | |||||
EOOGHDJN_01467 | 8.2e-48 | |||||
EOOGHDJN_01468 | 1.2e-112 | pgm8 | G | Histidine phosphatase superfamily (branch 1) | ||
EOOGHDJN_01469 | 2.9e-63 | S | Domain of unknown function (DUF4440) | |||
EOOGHDJN_01470 | 2.8e-157 | K | LysR substrate binding domain | |||
EOOGHDJN_01471 | 9.6e-101 | GM | NAD(P)H-binding | |||
EOOGHDJN_01472 | 9.9e-194 | adh | 1.1.1.1, 1.1.1.14 | E | alcohol dehydrogenase | |
EOOGHDJN_01473 | 1.6e-149 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
EOOGHDJN_01474 | 3.4e-35 | |||||
EOOGHDJN_01475 | 6.1e-76 | T | Belongs to the universal stress protein A family | |||
EOOGHDJN_01476 | 5.8e-95 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose O-acetyltransferase | |
EOOGHDJN_01477 | 2.4e-127 | yjjG | 3.1.3.102, 3.1.3.104, 3.1.3.5, 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | |
EOOGHDJN_01478 | 1.2e-62 | |||||
EOOGHDJN_01479 | 1e-102 | 1.5.1.40 | S | NADP oxidoreductase coenzyme F420-dependent | ||
EOOGHDJN_01480 | 4.8e-221 | patB | 4.4.1.8 | E | Aminotransferase, class I | |
EOOGHDJN_01481 | 1.9e-102 | M | Protein of unknown function (DUF3737) | |||
EOOGHDJN_01482 | 9.8e-194 | C | Aldo/keto reductase family | |||
EOOGHDJN_01484 | 0.0 | mdlB | V | ABC transporter | ||
EOOGHDJN_01485 | 0.0 | mdlA | V | ABC transporter | ||
EOOGHDJN_01486 | 5.7e-245 | EGP | Major facilitator Superfamily | |||
EOOGHDJN_01488 | 6.6e-131 | yhgE | V | domain protein | ||
EOOGHDJN_01489 | 8.1e-111 | K | Transcriptional regulator (TetR family) | |||
EOOGHDJN_01490 | 1.4e-53 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
EOOGHDJN_01491 | 8.2e-139 | endA | F | DNA RNA non-specific endonuclease | ||
EOOGHDJN_01492 | 3.2e-103 | speG | J | Acetyltransferase (GNAT) domain | ||
EOOGHDJN_01493 | 2.8e-96 | 2.3.1.128 | J | Acetyltransferase (GNAT) domain | ||
EOOGHDJN_01494 | 1e-132 | 2.7.1.89 | M | Phosphotransferase enzyme family | ||
EOOGHDJN_01495 | 7.3e-225 | S | CAAX protease self-immunity | |||
EOOGHDJN_01496 | 5.5e-308 | ybiT | S | ABC transporter, ATP-binding protein | ||
EOOGHDJN_01497 | 2.4e-147 | 3.1.3.102, 3.1.3.104 | S | hydrolase | ||
EOOGHDJN_01498 | 0.0 | S | Predicted membrane protein (DUF2207) | |||
EOOGHDJN_01499 | 0.0 | uvrA3 | L | excinuclease ABC | ||
EOOGHDJN_01500 | 1.7e-208 | EGP | Major facilitator Superfamily | |||
EOOGHDJN_01501 | 7.1e-172 | ropB | K | Helix-turn-helix XRE-family like proteins | ||
EOOGHDJN_01502 | 1.7e-233 | yxiO | S | Vacuole effluxer Atg22 like | ||
EOOGHDJN_01503 | 3.9e-256 | npp | S | type I phosphodiesterase nucleotide pyrophosphatase | ||
EOOGHDJN_01504 | 2.4e-158 | I | alpha/beta hydrolase fold | |||
EOOGHDJN_01505 | 2e-129 | treR | K | UTRA | ||
EOOGHDJN_01506 | 1.6e-237 | |||||
EOOGHDJN_01507 | 5.6e-39 | S | Cytochrome B5 | |||
EOOGHDJN_01508 | 7.5e-89 | pts21A | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | ||
EOOGHDJN_01509 | 6.2e-218 | 2.7.7.65 | T | Diguanylate cyclase, GGDEF domain | ||
EOOGHDJN_01510 | 3.1e-127 | yliE | T | EAL domain | ||
EOOGHDJN_01511 | 2.2e-104 | nrdG | 1.97.1.4 | O | Activation of anaerobic ribonucleoside-triphosphate reductase under anaerobic conditions by generation of an organic free radical, using S-adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine | |
EOOGHDJN_01512 | 0.0 | nrdD | 1.1.98.6 | F | Ribonucleoside-triphosphate reductase | |
EOOGHDJN_01513 | 2e-80 | |||||
EOOGHDJN_01514 | 4.5e-73 | def2 | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins | |
EOOGHDJN_01515 | 1.5e-191 | apbE | 2.7.1.180 | H | Flavin transferase that catalyzes the transfer of the FMN moiety of FAD and its covalent binding to the hydroxyl group of a threonine residue in a target flavoprotein | |
EOOGHDJN_01516 | 5.8e-191 | 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 | ||
EOOGHDJN_01517 | 4.9e-22 | |||||
EOOGHDJN_01518 | 4.9e-78 | |||||
EOOGHDJN_01519 | 2.2e-165 | K | LysR substrate binding domain | |||
EOOGHDJN_01520 | 2.4e-243 | P | Sodium:sulfate symporter transmembrane region | |||
EOOGHDJN_01521 | 1.1e-286 | ubiD | 4.1.1.98 | H | 3-octaprenyl-4-hydroxybenzoate carboxy-lyase | |
EOOGHDJN_01522 | 2.2e-167 | S | Cysteine-rich secretory protein family | |||
EOOGHDJN_01523 | 3.5e-233 | EGP | Major facilitator Superfamily | |||
EOOGHDJN_01524 | 3.8e-57 | hxlR | K | HxlR-like helix-turn-helix | ||
EOOGHDJN_01525 | 1.1e-116 | XK27_07075 | V | CAAX protease self-immunity | ||
EOOGHDJN_01526 | 0.0 | L | AAA domain | |||
EOOGHDJN_01527 | 1.7e-63 | K | Helix-turn-helix XRE-family like proteins | |||
EOOGHDJN_01528 | 6.2e-50 | |||||
EOOGHDJN_01529 | 2.5e-302 | guaA | 2.3.1.128, 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
EOOGHDJN_01530 | 5.7e-177 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
EOOGHDJN_01531 | 1.7e-165 | fabK | 1.3.1.9 | S | Nitronate monooxygenase | |
EOOGHDJN_01532 | 0.0 | helD | 3.6.4.12 | L | DNA helicase | |
EOOGHDJN_01533 | 7.7e-112 | dedA | S | SNARE associated Golgi protein | ||
EOOGHDJN_01534 | 3.1e-178 | yqkA | 3.6.1.55 | F | Belongs to the Nudix hydrolase family | |
EOOGHDJN_01535 | 0.0 | yjbQ | P | TrkA C-terminal domain protein | ||
EOOGHDJN_01536 | 4.7e-125 | pgm3 | G | Phosphoglycerate mutase family | ||
EOOGHDJN_01537 | 4.7e-128 | pgm3 | G | Phosphoglycerate mutase family | ||
EOOGHDJN_01538 | 1.2e-26 | |||||
EOOGHDJN_01539 | 1.3e-48 | sugE | U | Multidrug resistance protein | ||
EOOGHDJN_01540 | 6.4e-78 | 3.6.1.55 | F | NUDIX domain | ||
EOOGHDJN_01541 | 8.7e-232 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
EOOGHDJN_01542 | 7.1e-98 | K | Bacterial regulatory proteins, tetR family | |||
EOOGHDJN_01543 | 3.8e-85 | S | membrane transporter protein | |||
EOOGHDJN_01544 | 8.3e-210 | EGP | Major facilitator Superfamily | |||
EOOGHDJN_01545 | 2e-71 | K | MarR family | |||
EOOGHDJN_01546 | 3.7e-149 | XK27_00825 | S | Sulfite exporter TauE/SafE | ||
EOOGHDJN_01547 | 4.8e-73 | mgrA | K | helix_turn_helix multiple antibiotic resistance protein | ||
EOOGHDJN_01548 | 2.4e-245 | steT | E | amino acid | ||
EOOGHDJN_01549 | 4.6e-140 | G | YdjC-like protein | |||
EOOGHDJN_01550 | 1e-257 | 2.7.1.193, 2.7.1.211 | G | phosphotransferase system, EIIB | ||
EOOGHDJN_01551 | 4.7e-154 | K | CAT RNA binding domain | |||
EOOGHDJN_01552 | 2.6e-83 | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | |||
EOOGHDJN_01553 | 4e-108 | glnP | P | ABC transporter permease | ||
EOOGHDJN_01554 | 1.3e-108 | gluC | P | ABC transporter permease | ||
EOOGHDJN_01555 | 7.8e-149 | glnH | ET | ABC transporter substrate-binding protein | ||
EOOGHDJN_01556 | 9e-133 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
EOOGHDJN_01558 | 8e-41 | |||||
EOOGHDJN_01559 | 3.3e-170 | ldhD | 1.1.1.28 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
EOOGHDJN_01560 | 3e-210 | patA | 2.6.1.1, 2.6.1.57 | E | Aminotransferase | |
EOOGHDJN_01561 | 3.3e-112 | gph | 3.1.3.18 | S | HAD hydrolase, family IA, variant | |
EOOGHDJN_01562 | 6.4e-148 | |||||
EOOGHDJN_01563 | 7e-12 | 3.2.1.14 | GH18 | |||
EOOGHDJN_01564 | 1.3e-81 | zur | P | Belongs to the Fur family | ||
EOOGHDJN_01565 | 6.3e-105 | gmk2 | 2.7.4.8 | F | Guanylate kinase | |
EOOGHDJN_01566 | 1.8e-19 | |||||
EOOGHDJN_01567 | 4.6e-73 | apfA | 2.7.7.72, 3.6.1.61 | F | Nudix hydrolase | |
EOOGHDJN_01568 | 9.9e-149 | pdxK | 2.7.1.35 | H | Phosphomethylpyrimidine kinase | |
EOOGHDJN_01569 | 2.5e-88 | |||||
EOOGHDJN_01570 | 8.2e-252 | yfnA | E | Amino Acid | ||
EOOGHDJN_01571 | 5.1e-47 | |||||
EOOGHDJN_01572 | 5e-69 | O | OsmC-like protein | |||
EOOGHDJN_01573 | 0.0 | pepX | 3.4.14.11 | E | Removes N-terminal dipeptides sequentially from polypeptides having unsubstituted N-termini provided that the penultimate residue is proline | |
EOOGHDJN_01574 | 0.0 | oatA | I | Acyltransferase | ||
EOOGHDJN_01575 | 2.7e-180 | birA | 6.3.4.15 | H | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
EOOGHDJN_01576 | 5.4e-180 | pip | 3.4.11.5 | E | Releases the N-terminal proline from various substrates | |
EOOGHDJN_01577 | 0.0 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
EOOGHDJN_01578 | 1.8e-153 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
EOOGHDJN_01579 | 0.0 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
EOOGHDJN_01580 | 1.2e-225 | pbuG | S | permease | ||
EOOGHDJN_01581 | 1.5e-19 | |||||
EOOGHDJN_01582 | 1.3e-82 | K | Transcriptional regulator | |||
EOOGHDJN_01583 | 5e-153 | licD | M | LicD family | ||
EOOGHDJN_01584 | 1.8e-289 | ppx3 | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
EOOGHDJN_01585 | 0.0 | ppk | 2.7.4.1 | P | Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) | |
EOOGHDJN_01586 | 3.2e-175 | ppx | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
EOOGHDJN_01587 | 8.7e-241 | EGP | Major facilitator Superfamily | |||
EOOGHDJN_01588 | 1.2e-88 | V | VanZ like family | |||
EOOGHDJN_01589 | 1.5e-33 | |||||
EOOGHDJN_01590 | 1.9e-71 | spxA | 1.20.4.1 | P | ArsC family | |
EOOGHDJN_01592 | 2.5e-141 | |||||
EOOGHDJN_01593 | 7.5e-299 | 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 | |
EOOGHDJN_01594 | 9.1e-197 | |||||
EOOGHDJN_01595 | 0.0 | typA | T | GTP-binding protein TypA | ||
EOOGHDJN_01596 | 6.3e-137 | suhB | 3.1.3.25 | G | Belongs to the inositol monophosphatase superfamily | |
EOOGHDJN_01597 | 3.3e-46 | yktA | S | Belongs to the UPF0223 family | ||
EOOGHDJN_01598 | 4.7e-163 | 1.1.1.27 | C | L-malate dehydrogenase activity | ||
EOOGHDJN_01599 | 2.6e-266 | lpdA | 1.8.1.4 | C | Dehydrogenase | |
EOOGHDJN_01600 | 1.8e-208 | pdhC | 2.3.1.12 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
EOOGHDJN_01601 | 4.5e-180 | pdhB | 1.2.4.1 | C | Transketolase, C-terminal domain protein | |
EOOGHDJN_01602 | 1.6e-210 | pdhA | 1.2.4.1, 1.2.4.4 | C | Dehydrogenase E1 component | |
EOOGHDJN_01603 | 3.1e-101 | def | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions | |
EOOGHDJN_01604 | 1.6e-85 | |||||
EOOGHDJN_01605 | 3.1e-33 | ykzG | S | Belongs to the UPF0356 family | ||
EOOGHDJN_01606 | 0.0 | rnjA | J | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
EOOGHDJN_01607 | 5.7e-188 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic domain | |
EOOGHDJN_01608 | 1.7e-28 | |||||
EOOGHDJN_01609 | 4.1e-108 | mltD | CBM50 | M | NlpC P60 family protein | |
EOOGHDJN_01610 | 4e-173 | 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) | |
EOOGHDJN_01611 | 0.0 | recD2 | 3.1.11.5 | L | DNA-dependent ATPase and ATP-dependent 5'-3' DNA helicase. Has no activity on blunt DNA or DNA with 3'-overhangs, requires at least 10 bases of 5'-ssDNA for helicase activity | |
EOOGHDJN_01612 | 1.6e-120 | S | Repeat protein | |||
EOOGHDJN_01613 | 1.6e-120 | pgm6 | 5.4.2.11, 5.4.2.12 | G | phosphoglycerate mutase | |
EOOGHDJN_01614 | 1.1e-267 | N | domain, Protein | |||
EOOGHDJN_01615 | 1.7e-193 | S | Bacterial protein of unknown function (DUF916) | |||
EOOGHDJN_01616 | 2.3e-120 | N | WxL domain surface cell wall-binding | |||
EOOGHDJN_01617 | 2.6e-115 | ktrA | P | domain protein | ||
EOOGHDJN_01618 | 1.3e-241 | ktrB | P | Potassium uptake protein | ||
EOOGHDJN_01619 | 9e-225 | 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 | |
EOOGHDJN_01620 | 4.9e-57 | XK27_04120 | S | Putative amino acid metabolism | ||
EOOGHDJN_01621 | 1.2e-216 | iscS | 2.8.1.7 | E | Aminotransferase class V | |
EOOGHDJN_01622 | 1.8e-122 | mtnN | 3.2.2.9 | E | Catalyzes the irreversible cleavage of the glycosidic bond in both 5'-methylthioadenosine (MTA) and S- adenosylhomocysteine (SAH AdoHcy) to adenine and the corresponding thioribose, 5'-methylthioribose and S-ribosylhomocysteine, respectively | |
EOOGHDJN_01623 | 4.6e-28 | |||||
EOOGHDJN_01624 | 1.9e-95 | nudF | 3.6.1.13 | L | ADP-ribose pyrophosphatase | |
EOOGHDJN_01625 | 3.2e-189 | 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 | |
EOOGHDJN_01626 | 9e-18 | S | Protein of unknown function (DUF3021) | |||
EOOGHDJN_01627 | 2.9e-36 | K | LytTr DNA-binding domain | |||
EOOGHDJN_01628 | 4.7e-80 | cylB | U | ABC-2 type transporter | ||
EOOGHDJN_01629 | 3.5e-49 | cylA | V | abc transporter atp-binding protein | ||
EOOGHDJN_01630 | 1.1e-23 | cylA | V | AAA domain, putative AbiEii toxin, Type IV TA system | ||
EOOGHDJN_01631 | 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) | |
EOOGHDJN_01632 | 1.2e-86 | divIVA | D | DivIVA domain protein | ||
EOOGHDJN_01633 | 9.9e-146 | ylmH | S | S4 domain protein | ||
EOOGHDJN_01634 | 1.2e-36 | yggT | S | YGGT family | ||
EOOGHDJN_01635 | 3.3e-71 | 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 | ||
EOOGHDJN_01636 | 1.4e-229 | 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 | ||
EOOGHDJN_01637 | 5.5e-245 | ftsA | D | Cell division protein that is involved in the assembly of the Z ring. May serve as a membrane anchor for the Z ring | ||
EOOGHDJN_01638 | 5.8e-163 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
EOOGHDJN_01639 | 1.5e-197 | 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) |
EOOGHDJN_01640 | 8e-260 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
EOOGHDJN_01641 | 8.3e-179 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
EOOGHDJN_01642 | 0.0 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
EOOGHDJN_01643 | 2.7e-24 | ftsL | D | Cell division protein FtsL | ||
EOOGHDJN_01645 | 1.9e-175 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
EOOGHDJN_01646 | 1.9e-77 | mraZ | K | Belongs to the MraZ family | ||
EOOGHDJN_01647 | 4.2e-62 | S | Protein of unknown function (DUF3397) | |||
EOOGHDJN_01648 | 1.2e-174 | corA | P | CorA-like Mg2+ transporter protein | ||
EOOGHDJN_01649 | 0.0 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
EOOGHDJN_01650 | 5.2e-95 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
EOOGHDJN_01651 | 1.8e-113 | ywnB | S | NAD(P)H-binding | ||
EOOGHDJN_01652 | 3.8e-198 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
EOOGHDJN_01654 | 1.1e-161 | rrmA | 2.1.1.187 | H | Methyltransferase | |
EOOGHDJN_01655 | 1.7e-41 | 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 | ||
EOOGHDJN_01656 | 4.3e-206 | XK27_05220 | S | AI-2E family transporter | ||
EOOGHDJN_01657 | 3.9e-57 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
EOOGHDJN_01658 | 1.6e-193 | pgl | 3.1.1.31 | G | Lactonase, 7-bladed beta-propeller | |
EOOGHDJN_01659 | 5.1e-116 | cutC | P | Participates in the control of copper homeostasis | ||
EOOGHDJN_01660 | 8.9e-175 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | G | Responsible for synthesis of pseudouridine from uracil | |
EOOGHDJN_01661 | 4.7e-151 | nadK | 2.7.1.23 | F | Involved in the regulation of the intracellular balance of NAD and NADP, and is a key enzyme in the biosynthesis of NADP. Catalyzes specifically the phosphorylation on 2'-hydroxyl of the adenosine moiety of NAD to yield NADP | |
EOOGHDJN_01662 | 2.7e-120 | yjbM | 2.7.6.5 | S | RelA SpoT domain protein | |
EOOGHDJN_01663 | 3.6e-114 | yjbH | Q | Thioredoxin | ||
EOOGHDJN_01664 | 0.0 | pepF | E | oligoendopeptidase F | ||
EOOGHDJN_01665 | 8.4e-204 | coiA | 3.6.4.12 | S | Competence protein | |
EOOGHDJN_01666 | 2.2e-131 | mecA | NOT | Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis | ||
EOOGHDJN_01667 | 2.7e-67 | spxA | 1.20.4.1 | K | Interferes with activator-stimulated transcription by interaction with the RNA polymerase alpha-CTD. May function to globally reduce transcription of genes involved in growth- and development-promoting processes and to increase transcription of genes involved in thiol homeostasis, during periods of extreme stress | |
EOOGHDJN_01668 | 2.2e-139 | yhfI | S | Metallo-beta-lactamase superfamily | ||
EOOGHDJN_01669 | 1.3e-90 | traP | 1.14.99.57, 6.2.1.3 | S | enzyme involved in biosynthesis of extracellular polysaccharides | |
EOOGHDJN_01675 | 2.1e-88 | niaR | S | 3H domain | ||
EOOGHDJN_01676 | 5.2e-224 | EGP | Major facilitator Superfamily | |||
EOOGHDJN_01677 | 2.1e-232 | S | Sterol carrier protein domain | |||
EOOGHDJN_01678 | 3.8e-212 | S | Bacterial protein of unknown function (DUF871) | |||
EOOGHDJN_01679 | 1.8e-36 | XK27_01315 | S | Protein of unknown function (DUF2829) | ||
EOOGHDJN_01680 | 7.5e-135 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
EOOGHDJN_01681 | 7.8e-69 | FG | Scavenger mRNA decapping enzyme C-term binding | |||
EOOGHDJN_01682 | 3.1e-101 | 3.6.1.13 | L | Belongs to the Nudix hydrolase family | ||
EOOGHDJN_01683 | 1.7e-111 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
EOOGHDJN_01684 | 9.8e-11 | mcbG | S | Pentapeptide repeats (8 copies) | ||
EOOGHDJN_01685 | 8.5e-145 | XK27_02985 | S | Sucrose-6F-phosphate phosphohydrolase | ||
EOOGHDJN_01686 | 1.5e-280 | thrC | 4.2.3.1 | E | Threonine synthase | |
EOOGHDJN_01687 | 0.0 | nplT | 3.2.1.133, 3.2.1.135, 3.2.1.54 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
EOOGHDJN_01689 | 1.5e-52 | |||||
EOOGHDJN_01690 | 5.4e-118 | |||||
EOOGHDJN_01691 | 7.3e-86 | 2.7.7.1, 3.6.1.55 | F | belongs to the nudix hydrolase family | ||
EOOGHDJN_01692 | 1.7e-234 | malY | 4.4.1.8 | E | Aminotransferase, class I | |
EOOGHDJN_01694 | 2.1e-49 | |||||
EOOGHDJN_01695 | 4.3e-88 | |||||
EOOGHDJN_01696 | 4.2e-71 | gtcA | S | Teichoic acid glycosylation protein | ||
EOOGHDJN_01697 | 1.2e-35 | |||||
EOOGHDJN_01698 | 6.7e-81 | uspA | T | universal stress protein | ||
EOOGHDJN_01699 | 2.9e-148 | |||||
EOOGHDJN_01700 | 6.9e-164 | V | ABC transporter, ATP-binding protein | |||
EOOGHDJN_01701 | 7.9e-61 | gntR1 | K | Transcriptional regulator, GntR family | ||
EOOGHDJN_01702 | 8e-42 | |||||
EOOGHDJN_01703 | 0.0 | V | FtsX-like permease family | |||
EOOGHDJN_01704 | 1.7e-139 | cysA | V | ABC transporter, ATP-binding protein | ||
EOOGHDJN_01705 | 1.5e-180 | ansA | 3.5.1.1 | EJ | Asparaginase | |
EOOGHDJN_01706 | 7.5e-149 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
EOOGHDJN_01707 | 9.2e-118 | cah | 4.2.1.1 | P | Eukaryotic-type carbonic anhydrase | |
EOOGHDJN_01708 | 1.4e-147 | ptp3 | 3.1.3.48 | T | Tyrosine phosphatase family | |
EOOGHDJN_01709 | 3.2e-189 | lplA2 | 6.3.1.20 | H | Bacterial lipoate protein ligase C-terminus | |
EOOGHDJN_01710 | 1.8e-110 | XK27_09620 | 1.3.5.4 | S | NADPH-dependent FMN reductase | |
EOOGHDJN_01711 | 1.5e-223 | XK27_09615 | 1.3.5.4 | S | reductase | |
EOOGHDJN_01712 | 1.7e-79 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
EOOGHDJN_01713 | 3.9e-212 | 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) | |
EOOGHDJN_01714 | 2.9e-131 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
EOOGHDJN_01715 | 3.6e-41 | 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 | |
EOOGHDJN_01716 | 2e-126 | 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 | |
EOOGHDJN_01717 | 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 | |
EOOGHDJN_01718 | 1.1e-280 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
EOOGHDJN_01719 | 7.7e-191 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
EOOGHDJN_01720 | 9.9e-103 | purN | 2.1.2.2 | F | Catalyzes the transfer of a formyl group from 10- formyltetrahydrofolate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR) and tetrahydrofolate | |
EOOGHDJN_01721 | 2.3e-287 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
EOOGHDJN_01722 | 6.4e-216 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
EOOGHDJN_01723 | 2e-123 | 2.1.1.14 | E | Methionine synthase | ||
EOOGHDJN_01724 | 9.2e-253 | pgaC | GT2 | M | Glycosyl transferase | |
EOOGHDJN_01725 | 2.6e-94 | |||||
EOOGHDJN_01726 | 6.5e-156 | T | EAL domain | |||
EOOGHDJN_01727 | 1.5e-161 | GM | NmrA-like family | |||
EOOGHDJN_01728 | 4e-221 | pbuG | S | Permease family | ||
EOOGHDJN_01729 | 3.5e-236 | pbuX | F | xanthine permease | ||
EOOGHDJN_01730 | 1e-298 | pucR | QT | Purine catabolism regulatory protein-like family | ||
EOOGHDJN_01731 | 1.1e-95 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
EOOGHDJN_01732 | 5.6e-172 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
EOOGHDJN_01733 | 4.9e-243 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
EOOGHDJN_01734 | 1.2e-213 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
EOOGHDJN_01735 | 0.0 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
EOOGHDJN_01736 | 3.7e-168 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
EOOGHDJN_01737 | 1.8e-125 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
EOOGHDJN_01738 | 1.4e-113 | pyrE | 2.4.2.10, 4.1.1.23 | F | Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) | |
EOOGHDJN_01739 | 4.6e-169 | ydcZ | S | Putative inner membrane exporter, YdcZ | ||
EOOGHDJN_01740 | 0.0 | rexB | 3.1.21.3, 3.6.4.12 | L | The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination. This subunit has 5' - 3' nuclease activity | |
EOOGHDJN_01741 | 0.0 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
EOOGHDJN_01742 | 7.9e-114 | 3.1.3.18 | J | HAD-hyrolase-like | ||
EOOGHDJN_01743 | 8.5e-78 | 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 | ||
EOOGHDJN_01744 | 0.0 | relA | 2.7.6.5 | KT | In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance | |
EOOGHDJN_01745 | 9.6e-58 | |||||
EOOGHDJN_01746 | 2.9e-134 | 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 | |
EOOGHDJN_01747 | 4.5e-177 | prmA | J | Ribosomal protein L11 methyltransferase | ||
EOOGHDJN_01748 | 3.6e-114 | mpg | 3.2.2.21 | L | Belongs to the DNA glycosylase MPG family | |
EOOGHDJN_01749 | 1.4e-49 | |||||
EOOGHDJN_01750 | 1.4e-49 | |||||
EOOGHDJN_01751 | 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 | ||
EOOGHDJN_01752 | 6.1e-246 | dltD | M | Protein involved in D-alanine esterification of lipoteichoic acid and wall teichoic acid (D-alanine transfer protein) | ||
EOOGHDJN_01753 | 4e-34 | dltC | 6.1.1.13 | J | Carrier protein involved in the D-alanylation of lipoteichoic acid (LTA). The loading of thioester-linked D-alanine onto DltC is catalyzed by D-alanine--D-alanyl carrier protein ligase DltA. The DltC-carried D-alanyl group is further transferred to cell membrane phosphatidylglycerol (PG) by forming an ester bond, probably catalyzed by DltD. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
EOOGHDJN_01754 | 1.1e-233 | dltB | M | MBOAT, membrane-bound O-acyltransferase family | ||
EOOGHDJN_01755 | 7e-297 | dltA | 6.1.1.13 | H | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
EOOGHDJN_01756 | 8.8e-19 | dltX | S | D-Ala-teichoic acid biosynthesis protein | ||
EOOGHDJN_01757 | 4.4e-198 | pbpX2 | V | Beta-lactamase | ||
EOOGHDJN_01758 | 1.2e-184 | 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 | ||
EOOGHDJN_01759 | 0.0 | dnaK | O | Heat shock 70 kDa protein | ||
EOOGHDJN_01760 | 3e-81 | 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 | ||
EOOGHDJN_01761 | 2.4e-195 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
EOOGHDJN_01762 | 7.3e-132 | budA | 4.1.1.5 | Q | Alpha-acetolactate decarboxylase | |
EOOGHDJN_01763 | 1.2e-188 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
EOOGHDJN_01764 | 9.4e-172 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
EOOGHDJN_01765 | 2.4e-87 | aroK | 1.1.1.25, 2.7.1.71, 4.2.1.10, 4.2.3.4 | F | Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate | |
EOOGHDJN_01766 | 7.7e-197 | tyrA | 1.3.1.12, 1.3.1.43 | E | prephenate dehydrogenase | |
EOOGHDJN_01767 | 1.5e-236 | aroA | 1.3.1.12, 1.3.1.43, 2.5.1.19 | E | Catalyzes the transfer of the enolpyruvyl moiety of phosphoenolpyruvate (PEP) to the 5-hydroxyl of shikimate-3- phosphate (S3P) to produce enolpyruvyl shikimate-3-phosphate and inorganic phosphate | |
EOOGHDJN_01768 | 1e-93 | |||||
EOOGHDJN_01769 | 9.3e-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 | |
EOOGHDJN_01770 | 2.1e-266 | ydiN | 5.4.99.5 | G | Major Facilitator | |
EOOGHDJN_01771 | 4.6e-50 | 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 | ||
EOOGHDJN_01772 | 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 | ||
EOOGHDJN_01773 | 1.1e-47 | ylxQ | J | ribosomal protein | ||
EOOGHDJN_01774 | 9.5e-49 | ylxR | K | Protein of unknown function (DUF448) | ||
EOOGHDJN_01775 | 1.1e-217 | nusA | K | Participates in both transcription termination and antitermination | ||
EOOGHDJN_01776 | 4.2e-83 | rimP | J | Required for maturation of 30S ribosomal subunits | ||
EOOGHDJN_01777 | 0.0 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
EOOGHDJN_01778 | 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 | |
EOOGHDJN_01779 | 1e-229 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
EOOGHDJN_01780 | 8.4e-137 | cdsA | 2.7.7.41 | I | Belongs to the CDS family | |
EOOGHDJN_01781 | 1.8e-147 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
EOOGHDJN_01782 | 2.5e-82 | 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 | ||
EOOGHDJN_01783 | 2.2e-128 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
EOOGHDJN_01784 | 1.3e-151 | 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 | ||
EOOGHDJN_01785 | 6.5e-145 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
EOOGHDJN_01786 | 4.7e-134 | S | Haloacid dehalogenase-like hydrolase | |||
EOOGHDJN_01787 | 2.3e-187 | ldhA | 1.1.1.28 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
EOOGHDJN_01788 | 2e-49 | yazA | L | GIY-YIG catalytic domain protein | ||
EOOGHDJN_01789 | 2.8e-137 | yabB | 2.1.1.223 | L | Methyltransferase small domain | |
EOOGHDJN_01790 | 6.4e-119 | plsC | 2.3.1.51 | I | Acyltransferase | |
EOOGHDJN_01791 | 4.3e-33 | yneF | S | Uncharacterised protein family (UPF0154) | ||
EOOGHDJN_01792 | 2.9e-36 | ynzC | S | UPF0291 protein | ||
EOOGHDJN_01793 | 5.6e-115 | lexA | 3.4.21.88 | K | Represses a number of genes involved in the response to DNA damage (SOS response), including recA and lexA. In the presence of single-stranded DNA, RecA interacts with LexA causing an autocatalytic cleavage which disrupts the DNA-binding part of LexA, leading to derepression of the SOS regulon and eventually DNA repair | |
EOOGHDJN_01794 | 7e-86 | |||||
EOOGHDJN_01795 | 7.9e-216 | mvaS | 2.3.3.10 | I | Hydroxymethylglutaryl-CoA synthase | |
EOOGHDJN_01796 | 3.7e-74 | |||||
EOOGHDJN_01797 | 1.3e-66 | |||||
EOOGHDJN_01798 | 3.4e-177 | csbB | 2.4.1.83 | GT2 | M | Glycosyltransferase like family 2 |
EOOGHDJN_01799 | 2.1e-100 | L | Helix-turn-helix domain | |||
EOOGHDJN_01800 | 2.1e-221 | lytR5 | K | Cell envelope-related transcriptional attenuator domain | ||
EOOGHDJN_01801 | 2.3e-142 | P | ATPases associated with a variety of cellular activities | |||
EOOGHDJN_01802 | 0.0 | opuAB | P | Binding-protein-dependent transport system inner membrane component | ||
EOOGHDJN_01803 | 5.8e-230 | rodA | D | Cell cycle protein | ||
EOOGHDJN_01805 | 1.6e-31 | |||||
EOOGHDJN_01806 | 4.9e-142 | Q | Methyltransferase | |||
EOOGHDJN_01807 | 8.5e-57 | ybjQ | S | Belongs to the UPF0145 family | ||
EOOGHDJN_01808 | 7.2e-212 | EGP | Major facilitator Superfamily | |||
EOOGHDJN_01809 | 4.5e-103 | K | Helix-turn-helix domain | |||
EOOGHDJN_01810 | 6.9e-308 | 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 | ||
EOOGHDJN_01811 | 3.4e-255 | gor | 1.8.1.7 | C | Glutathione reductase | |
EOOGHDJN_01812 | 1.7e-170 | gnd | 1.1.1.343, 1.1.1.44 | G | Dehydrogenase | |
EOOGHDJN_01813 | 4.6e-293 | gntK | 2.7.1.12, 2.7.1.16, 2.7.1.17, 2.7.1.5 | G | Belongs to the FGGY kinase family | |
EOOGHDJN_01814 | 9.5e-213 | gntP | EG | Gluconate | ||
EOOGHDJN_01815 | 3.7e-72 | tagD | 2.7.7.15, 2.7.7.39 | IM | Glycerol-3-phosphate cytidylyltransferase | |
EOOGHDJN_01816 | 1.3e-186 | yueF | S | AI-2E family transporter | ||
EOOGHDJN_01817 | 3.4e-169 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
EOOGHDJN_01818 | 1.7e-148 | pbpX | V | Beta-lactamase | ||
EOOGHDJN_01819 | 1.3e-27 | S | Antitoxin component of a toxin-antitoxin (TA) module | |||
EOOGHDJN_01820 | 7.8e-48 | K | sequence-specific DNA binding | |||
EOOGHDJN_01821 | 1.5e-133 | cwlO | M | NlpC/P60 family | ||
EOOGHDJN_01822 | 4.1e-106 | ygaC | J | Belongs to the UPF0374 family | ||
EOOGHDJN_01823 | 2.2e-140 | recX | 2.4.1.337 | GT4 | S | Regulatory protein RecX |
EOOGHDJN_01824 | 3.9e-125 | |||||
EOOGHDJN_01825 | 2.6e-100 | K | DNA-templated transcription, initiation | |||
EOOGHDJN_01826 | 1.5e-26 | |||||
EOOGHDJN_01827 | 7e-30 | |||||
EOOGHDJN_01828 | 7.3e-33 | S | Protein of unknown function (DUF2922) | |||
EOOGHDJN_01829 | 3.8e-53 | |||||
EOOGHDJN_01830 | 3.2e-121 | rfbP | M | Bacterial sugar transferase | ||
EOOGHDJN_01831 | 1.1e-259 | rfbX | S | Membrane protein involved in the export of O-antigen and teichoic acid | ||
EOOGHDJN_01832 | 9.6e-74 | K | helix_turn_helix multiple antibiotic resistance protein | |||
EOOGHDJN_01833 | 4.7e-137 | K | helix_turn_helix, arabinose operon control protein | |||
EOOGHDJN_01834 | 4.7e-148 | cps1D | M | Domain of unknown function (DUF4422) | ||
EOOGHDJN_01835 | 1.9e-200 | cps3I | G | Acyltransferase family | ||
EOOGHDJN_01836 | 8e-202 | cps3H | ||||
EOOGHDJN_01837 | 1.6e-163 | cps3F | ||||
EOOGHDJN_01838 | 4.8e-111 | cps3E | ||||
EOOGHDJN_01839 | 3.5e-202 | cps3D | ||||
EOOGHDJN_01840 | 1.2e-221 | glf | 5.4.99.9 | M | UDP-galactopyranose mutase | |
EOOGHDJN_01841 | 2.8e-179 | cps3B | S | Glycosyltransferase like family 2 | ||
EOOGHDJN_01842 | 6.5e-133 | cps3A | S | Glycosyltransferase like family 2 | ||
EOOGHDJN_01843 | 9e-19 | relB | L | bacterial-type proximal promoter sequence-specific DNA binding | ||
EOOGHDJN_01844 | 1.1e-92 | S | Acyltransferase family | |||
EOOGHDJN_01845 | 7.3e-241 | cps2I | S | Psort location CytoplasmicMembrane, score | ||
EOOGHDJN_01846 | 3.5e-132 | sacB | GT2,GT4 | M | Stealth protein CR2, conserved region 2 | |
EOOGHDJN_01847 | 2.7e-127 | waaB | GT4 | M | Glycosyl transferases group 1 | |
EOOGHDJN_01849 | 7.8e-151 | sacB | GT2,GT4 | M | Stealth protein CR2, conserved region 2 | |
EOOGHDJN_01850 | 1.3e-46 | wceM | M | Glycosyltransferase like family 2 | ||
EOOGHDJN_01851 | 1.4e-124 | tuaA | M | Bacterial sugar transferase | ||
EOOGHDJN_01852 | 4.6e-174 | cps2D | 5.1.3.2 | M | RmlD substrate binding domain | |
EOOGHDJN_01853 | 3e-139 | ywqE | 3.1.3.48 | GM | PHP domain protein | |
EOOGHDJN_01854 | 1.3e-128 | ywqD | 2.7.10.1 | D | Capsular exopolysaccharide family | |
EOOGHDJN_01855 | 3.9e-131 | epsB | M | biosynthesis protein | ||
EOOGHDJN_01856 | 3.4e-103 | L | Integrase | |||
EOOGHDJN_01857 | 1.6e-157 | rfbD | 1.1.1.133, 5.1.3.13 | M | Catalyzes the reduction of dTDP-6-deoxy-L-lyxo-4- hexulose to yield dTDP-L-rhamnose | |
EOOGHDJN_01858 | 1.9e-205 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
EOOGHDJN_01859 | 1e-107 | rfbC | 5.1.3.13 | M | Catalyzes the epimerization of the C3' and C5'positions of dTDP-6-deoxy-D-xylo-4-hexulose, forming dTDP-6-deoxy-L-lyxo-4- hexulose | |
EOOGHDJN_01860 | 1.4e-148 | rfbA | 2.7.7.24 | H | Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis | |
EOOGHDJN_01861 | 2.3e-146 | cps2I | S | Psort location CytoplasmicMembrane, score | ||
EOOGHDJN_01862 | 5.1e-26 | V | Beta-lactamase | |||
EOOGHDJN_01863 | 4e-30 | D | protein tyrosine kinase activity | |||
EOOGHDJN_01864 | 3.2e-28 | wcoI | 2.7.10.1, 2.7.10.2 | M | biosynthesis protein | |
EOOGHDJN_01866 | 2.1e-53 | cps1B | GT2,GT4 | M | Glycosyl transferases group 1 | |
EOOGHDJN_01867 | 1.2e-46 | GT2 | S | Glycosyl transferase family 2 | ||
EOOGHDJN_01868 | 1e-20 | V | Glycosyl transferase, family 2 | |||
EOOGHDJN_01869 | 5.4e-61 | sacB | GT2,GT4 | M | Stealth protein CR2, conserved region 2 | |
EOOGHDJN_01870 | 8e-47 | wbbL | M | PFAM Glycosyl transferase family 2 | ||
EOOGHDJN_01871 | 4.4e-97 | M | Parallel beta-helix repeats | |||
EOOGHDJN_01872 | 1.6e-83 | GT2,GT4 | G | Glycosyltransferase Family 4 | ||
EOOGHDJN_01873 | 9.7e-132 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
EOOGHDJN_01874 | 1.1e-156 | yihY | S | Belongs to the UPF0761 family | ||
EOOGHDJN_01875 | 6.8e-209 | mnaA | 5.1.3.14 | G | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
EOOGHDJN_01876 | 2.6e-219 | pbpX1 | V | Beta-lactamase | ||
EOOGHDJN_01877 | 4e-256 | gdhA | 1.4.1.4 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
EOOGHDJN_01878 | 5e-107 | |||||
EOOGHDJN_01879 | 1.3e-73 | |||||
EOOGHDJN_01881 | 1.8e-164 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
EOOGHDJN_01882 | 1.4e-245 | pts14C | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
EOOGHDJN_01883 | 2.3e-75 | T | Universal stress protein family | |||
EOOGHDJN_01885 | 2.6e-239 | yfmL | 3.6.4.13 | L | DEAD DEAH box helicase | |
EOOGHDJN_01886 | 2.4e-189 | mocA | S | Oxidoreductase | ||
EOOGHDJN_01887 | 2.7e-31 | cspA | K | 'Cold-shock' DNA-binding domain | ||
EOOGHDJN_01888 | 1.1e-62 | S | Domain of unknown function (DUF4828) | |||
EOOGHDJN_01889 | 9.1e-144 | lys | M | Glycosyl hydrolases family 25 | ||
EOOGHDJN_01890 | 2.3e-151 | gntR | K | rpiR family | ||
EOOGHDJN_01891 | 1.1e-115 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
EOOGHDJN_01892 | 9.1e-34 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
EOOGHDJN_01893 | 4e-240 | pts13C | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
EOOGHDJN_01894 | 0.0 | yfgQ | P | E1-E2 ATPase | ||
EOOGHDJN_01895 | 2.1e-100 | yobS | K | Bacterial regulatory proteins, tetR family | ||
EOOGHDJN_01896 | 4e-259 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
EOOGHDJN_01897 | 1e-190 | yegS | 2.7.1.107 | G | Lipid kinase | |
EOOGHDJN_01898 | 7.7e-274 | gatB | 6.1.1.12, 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | |
EOOGHDJN_01899 | 2.5e-275 | 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) | |
EOOGHDJN_01900 | 3.2e-50 | 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) | |
EOOGHDJN_01901 | 2.6e-198 | camS | S | sex pheromone | ||
EOOGHDJN_01902 | 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 | |
EOOGHDJN_01903 | 0.0 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
EOOGHDJN_01904 | 1.3e-218 | purK2 | 6.3.4.18 | F | Involved in the de novo purine biosynthesis. Catalyzes the transfer of formate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR). Formate is provided by PurU via hydrolysis of 10-formyl-tetrahydrofolate | |
EOOGHDJN_01905 | 1e-93 | S | UPF0316 protein | |||
EOOGHDJN_01906 | 9.1e-104 | xpt | 2.4.2.22, 2.4.2.7 | F | Converts the preformed base xanthine, a product of nucleic acid breakdown, to xanthosine 5'-monophosphate (XMP), so it can be reused for RNA or DNA synthesis | |
EOOGHDJN_01907 | 2.6e-112 | acmA | 3.2.1.17 | NU | mannosyl-glycoprotein | |
EOOGHDJN_01908 | 3.3e-183 | S | Oxidoreductase family, NAD-binding Rossmann fold | |||
EOOGHDJN_01909 | 2.9e-165 | menA | 2.5.1.74 | H | 1,4-dihydroxy-2-naphthoate | |
EOOGHDJN_01910 | 2.3e-182 | hepT | 2.5.1.30, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
EOOGHDJN_01911 | 1.5e-156 | ddpX | 3.4.13.22 | S | L,D-transpeptidase catalytic domain | |
EOOGHDJN_01912 | 0.0 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydC | ||
EOOGHDJN_01913 | 0.0 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydD | ||
EOOGHDJN_01914 | 2.6e-183 | cydB | 1.10.3.14 | C | Cytochrome d ubiquinol oxidase subunit II | |
EOOGHDJN_01915 | 5.4e-275 | cydA | 1.10.3.14 | C | ubiquinol oxidase | |
EOOGHDJN_01916 | 0.0 | S | Alpha beta | |||
EOOGHDJN_01917 | 1.8e-23 | |||||
EOOGHDJN_01918 | 3e-99 | S | ECF transporter, substrate-specific component | |||
EOOGHDJN_01919 | 5.8e-253 | yfnA | E | Amino Acid | ||
EOOGHDJN_01920 | 4.8e-166 | mleP | S | Sodium Bile acid symporter family | ||
EOOGHDJN_01921 | 4.2e-308 | sfcA | 1.1.1.38, 4.1.1.101 | C | Malic enzyme | |
EOOGHDJN_01922 | 1.8e-167 | mleR | K | LysR family | ||
EOOGHDJN_01923 | 1.4e-161 | mleR | K | LysR family transcriptional regulator | ||
EOOGHDJN_01924 | 1.2e-94 | citX | 2.4.2.52, 2.7.7.61 | HI | Apo-citrate lyase phosphoribosyl-dephospho-CoA transferase | |
EOOGHDJN_01925 | 3.9e-262 | frdC | 1.3.5.4 | C | FAD binding domain | |
EOOGHDJN_01926 | 6.4e-257 | fumC | 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
EOOGHDJN_01927 | 2.4e-16 | ltrA_1 | L | PFAM RNA-directed DNA polymerase (Reverse transcriptase) | ||
EOOGHDJN_01928 | 8e-137 | M | domain protein | |||
EOOGHDJN_01929 | 7.6e-61 | M | domain protein | |||
EOOGHDJN_01930 | 1.6e-76 | 2.4.2.6 | F | Nucleoside 2-deoxyribosyltransferase | ||
EOOGHDJN_01931 | 2.6e-100 | |||||
EOOGHDJN_01932 | 0.0 | 1.3.5.4 | C | FAD binding domain | ||
EOOGHDJN_01933 | 6.2e-111 | 1.3.5.4 | S | NADPH-dependent FMN reductase | ||
EOOGHDJN_01934 | 1.2e-177 | K | LysR substrate binding domain | |||
EOOGHDJN_01935 | 5.6e-183 | 3.4.21.102 | M | Peptidase family S41 | ||
EOOGHDJN_01936 | 5.1e-215 | |||||
EOOGHDJN_01937 | 2.9e-187 | yhaM | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
EOOGHDJN_01938 | 0.0 | L | AAA domain | |||
EOOGHDJN_01939 | 9.1e-231 | yhaO | L | Ser Thr phosphatase family protein | ||
EOOGHDJN_01940 | 1e-54 | yheA | S | Belongs to the UPF0342 family | ||
EOOGHDJN_01941 | 0.0 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
EOOGHDJN_01942 | 2.9e-12 | |||||
EOOGHDJN_01943 | 4.4e-77 | argR | K | Regulates arginine biosynthesis genes | ||
EOOGHDJN_01944 | 7.1e-214 | arcT | 2.6.1.1 | E | Aminotransferase | |
EOOGHDJN_01945 | 1.4e-102 | argO | S | LysE type translocator | ||
EOOGHDJN_01946 | 2.1e-282 | ydfD | K | Alanine-glyoxylate amino-transferase | ||
EOOGHDJN_01947 | 4e-34 | dltC | 6.1.1.13 | J | Carrier protein involved in the D-alanylation of lipoteichoic acid (LTA). The loading of thioester-linked D-alanine onto DltC is catalyzed by D-alanine--D-alanyl carrier protein ligase DltA. The DltC-carried D-alanyl group is further transferred to cell membrane phosphatidylglycerol (PG) by forming an ester bond, probably catalyzed by DltD. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
EOOGHDJN_01948 | 2.8e-85 | M | ErfK YbiS YcfS YnhG | |||
EOOGHDJN_01949 | 6.6e-210 | EGP | Major facilitator Superfamily | |||
EOOGHDJN_01950 | 5.2e-289 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family | |
EOOGHDJN_01951 | 1.2e-218 | pts15C | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
EOOGHDJN_01952 | 1.1e-47 | pts15B | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
EOOGHDJN_01953 | 1.4e-51 | chbA | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIA subunit | |
EOOGHDJN_01954 | 2.4e-62 | S | Domain of unknown function (DUF3284) | |||
EOOGHDJN_01955 | 0.0 | K | PRD domain | |||
EOOGHDJN_01956 | 7.6e-107 | |||||
EOOGHDJN_01957 | 0.0 | yhcA | V | MacB-like periplasmic core domain | ||
EOOGHDJN_01958 | 2.7e-82 | |||||
EOOGHDJN_01959 | 0.0 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
EOOGHDJN_01960 | 2.7e-79 | elaA | S | Acetyltransferase (GNAT) domain | ||
EOOGHDJN_01963 | 1.9e-31 | |||||
EOOGHDJN_01964 | 2.1e-244 | dinF | V | MatE | ||
EOOGHDJN_01965 | 0.0 | yfbS | P | Sodium:sulfate symporter transmembrane region | ||
EOOGHDJN_01966 | 2.1e-305 | astA | 2.8.2.22 | M | Arylsulfotransferase Ig-like domain | |
EOOGHDJN_01967 | 2.9e-176 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain | |
EOOGHDJN_01968 | 7.4e-112 | cysC | 2.7.1.25, 2.7.7.4 | F | Catalyzes the synthesis of activated sulfate | |
EOOGHDJN_01969 | 3.3e-230 | sat | 2.7.7.4 | H | the enzyme from Thermus thermophilus is dimeric and binds a zinc ion that is coordinated by cysteine and histidine residues that are not found in all related proteins but is found in some thermophilic organisms | |
EOOGHDJN_01970 | 2.3e-306 | S | Protein conserved in bacteria | |||
EOOGHDJN_01971 | 0.0 | metE | 2.1.1.14 | E | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | |
EOOGHDJN_01972 | 0.0 | yitJ | 1.5.1.20, 2.1.1.10, 2.1.1.13 | E | catalyzes the formation of 5,10-methylenetetrahydrofolate from 5-methyltetrahydrofolate and S-adenosyl-L-homocysteine and methionine from S-adenosyl-L-methionine and L-homocysteine | |
EOOGHDJN_01973 | 3.6e-58 | S | Protein of unknown function (DUF1516) | |||
EOOGHDJN_01974 | 1.9e-89 | gtcA | S | Teichoic acid glycosylation protein | ||
EOOGHDJN_01975 | 7.9e-180 | |||||
EOOGHDJN_01976 | 3.5e-10 | |||||
EOOGHDJN_01977 | 7.4e-55 | |||||
EOOGHDJN_01979 | 2.9e-93 | apt | 2.4.2.22, 2.4.2.7 | F | Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis | |
EOOGHDJN_01980 | 0.0 | recJ | L | Single-stranded-DNA-specific exonuclease RecJ | ||
EOOGHDJN_01981 | 2e-50 | yrvD | S | Lipopolysaccharide assembly protein A domain | ||
EOOGHDJN_01982 | 5.6e-141 | XK27_05435 | 1.1.1.100 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
EOOGHDJN_01983 | 2.3e-178 | rnz | 3.1.26.11 | J | Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA | |
EOOGHDJN_01984 | 3.2e-46 | |||||
EOOGHDJN_01985 | 2.4e-245 | 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 | ||
EOOGHDJN_01986 | 1.5e-135 | fruR | K | DeoR C terminal sensor domain | ||
EOOGHDJN_01987 | 1.8e-170 | pfkB | 2.7.1.11, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
EOOGHDJN_01988 | 6.7e-292 | fruA | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GT | Phosphotransferase System | |
EOOGHDJN_01989 | 1e-251 | cpdA | S | Calcineurin-like phosphoesterase | ||
EOOGHDJN_01990 | 3.1e-262 | cps4J | S | Polysaccharide biosynthesis protein | ||
EOOGHDJN_01991 | 6e-177 | cps4I | M | Glycosyltransferase like family 2 | ||
EOOGHDJN_01992 | 6.4e-227 | |||||
EOOGHDJN_01993 | 2.4e-184 | cps4G | M | Glycosyltransferase Family 4 | ||
EOOGHDJN_01994 | 1.2e-202 | cps4F | 2.4.1.21, 2.4.1.306 | GT4,GT5 | M | Glycosyl transferases group 1 |
EOOGHDJN_01995 | 1.8e-127 | tuaA | M | Bacterial sugar transferase | ||
EOOGHDJN_01996 | 4.8e-179 | cps4D | 5.1.3.2 | M | RmlD substrate binding domain | |
EOOGHDJN_01997 | 1.2e-146 | ywqE | 3.1.3.48 | GM | PHP domain protein | |
EOOGHDJN_01998 | 4.3e-124 | ywqD | 2.7.10.1 | D | Capsular exopolysaccharide family | |
EOOGHDJN_01999 | 9e-128 | epsB | M | biosynthesis protein | ||
EOOGHDJN_02000 | 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 | ||
EOOGHDJN_02001 | 1.3e-134 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
EOOGHDJN_02002 | 9.2e-270 | glnPH2 | P | ABC transporter permease | ||
EOOGHDJN_02003 | 7.4e-22 | |||||
EOOGHDJN_02004 | 9.9e-73 | S | Iron-sulphur cluster biosynthesis | |||
EOOGHDJN_02005 | 2.2e-49 | MA20_27270 | S | mazG nucleotide pyrophosphohydrolase | ||
EOOGHDJN_02006 | 5.1e-110 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
EOOGHDJN_02007 | 3.3e-236 | 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 | ||
EOOGHDJN_02008 | 4.1e-213 | 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 | ||
EOOGHDJN_02009 | 6.1e-224 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
EOOGHDJN_02010 | 3.1e-159 | S | Tetratricopeptide repeat | |||
EOOGHDJN_02011 | 0.0 | rnjB | J | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
EOOGHDJN_02012 | 6.2e-157 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
EOOGHDJN_02013 | 4.8e-192 | mdtG | EGP | Major Facilitator Superfamily | ||
EOOGHDJN_02014 | 6e-42 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
EOOGHDJN_02015 | 1.5e-34 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
EOOGHDJN_02016 | 5.9e-186 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
EOOGHDJN_02017 | 0.0 | comEC | S | Competence protein ComEC | ||
EOOGHDJN_02018 | 6.4e-79 | comEB | 3.5.4.12 | F | ComE operon protein 2 | |
EOOGHDJN_02019 | 2e-121 | comEA | L | Competence protein ComEA | ||
EOOGHDJN_02020 | 1.6e-196 | ylbL | T | Belongs to the peptidase S16 family | ||
EOOGHDJN_02021 | 1.4e-84 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
EOOGHDJN_02022 | 5.3e-101 | rsmD | 2.1.1.171 | L | RNA methyltransferase, RsmD family | |
EOOGHDJN_02023 | 1.5e-49 | ylbG | S | Uncharacterized protein conserved in bacteria (DUF2129) | ||
EOOGHDJN_02024 | 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 | |
EOOGHDJN_02025 | 1.6e-205 | ftsW | D | Belongs to the SEDS family | ||
EOOGHDJN_02026 | 1.4e-292 | |||||
EOOGHDJN_02027 | 5.1e-259 | ica2 | GT2 | M | Glycosyl transferase family group 2 | |
EOOGHDJN_02028 | 1.2e-103 | |||||
EOOGHDJN_02029 | 2.7e-157 | glxR | 1.1.1.31, 1.1.1.60 | I | Dehydrogenase | |
EOOGHDJN_02030 | 4.8e-137 | terC | P | membrane | ||
EOOGHDJN_02031 | 2.9e-83 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
EOOGHDJN_02032 | 5.8e-197 | hisC | 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
EOOGHDJN_02033 | 2.2e-51 | hisE | 3.5.4.19, 3.6.1.31, 5.3.1.16 | E | phosphoribosyl-ATP diphosphatase activity | |
EOOGHDJN_02034 | 2.5e-58 | hisI | 3.5.4.19, 3.5.4.25, 3.6.1.31, 5.3.1.16 | E | Catalyzes the hydrolysis of the adenine ring of phosphoribosyl-AMP | |
EOOGHDJN_02035 | 7.6e-135 | hisF | 3.5.4.19, 3.6.1.31 | E | IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisF subunit catalyzes the cyclization activity that produces IGP and AICAR from PRFAR using the ammonia provided by the HisH subunit | |
EOOGHDJN_02036 | 3.5e-129 | hisA | 5.3.1.16 | E | 1-(5-phosphoribosyl)-5- (5-phosphoribosylamino)methylideneamino imidazole-4-carboxamide isomerase | |
EOOGHDJN_02037 | 1.8e-110 | hisH | E | IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisH subunit provides the glutamine amidotransferase activity that produces the ammonia necessary to HisF for the synthesis of IGP and AICAR | ||
EOOGHDJN_02038 | 5.1e-107 | hisB | 1.1.1.23, 2.6.1.9, 3.1.3.15, 4.2.1.19 | E | imidazoleglycerol-phosphate dehydratase | |
EOOGHDJN_02039 | 1.2e-233 | 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 | |
EOOGHDJN_02040 | 4.3e-118 | hisG | 2.4.2.17 | F | Catalyzes the condensation of ATP and 5-phosphoribose 1- diphosphate to form N'-(5'-phosphoribosyl)-ATP (PR-ATP). Has a crucial role in the pathway because the rate of histidine biosynthesis seems to be controlled primarily by regulation of HisG enzymatic activity | |
EOOGHDJN_02041 | 8.6e-215 | hisZ | 2.4.2.17, 6.1.1.21 | E | Required for the first step of histidine biosynthesis. May allow the feedback regulation of ATP phosphoribosyltransferase activity by histidine | |
EOOGHDJN_02042 | 1.7e-164 | hisK | 3.1.3.15 | E | Histidinol phosphate phosphatase, HisJ | |
EOOGHDJN_02043 | 4.6e-216 | ysaA | V | RDD family | ||
EOOGHDJN_02044 | 7.6e-166 | corA | P | CorA-like Mg2+ transporter protein | ||
EOOGHDJN_02045 | 3.4e-50 | S | Domain of unknown function (DU1801) | |||
EOOGHDJN_02046 | 3.5e-13 | rmeB | K | transcriptional regulator, MerR family | ||
EOOGHDJN_02047 | 8e-199 | 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 | |
EOOGHDJN_02048 | 2.2e-184 | pva3 | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
EOOGHDJN_02049 | 3.7e-34 | |||||
EOOGHDJN_02050 | 3.2e-112 | S | Protein of unknown function (DUF1211) | |||
EOOGHDJN_02051 | 0.0 | ydgH | S | MMPL family | ||
EOOGHDJN_02052 | 1.1e-74 | yjcF | S | Acetyltransferase (GNAT) domain | ||
EOOGHDJN_02053 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
EOOGHDJN_02054 | 0.0 | glpQ | 3.1.4.46 | C | phosphodiesterase | |
EOOGHDJN_02055 | 2.3e-184 | trxB1 | 1.18.1.2, 1.19.1.1 | C | Ferredoxin--NADP reductase | |
EOOGHDJN_02056 | 4.4e-143 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
EOOGHDJN_02057 | 2.6e-182 | 3.6.4.13 | S | domain, Protein | ||
EOOGHDJN_02058 | 3.6e-168 | S | Polyphosphate kinase 2 (PPK2) | |||
EOOGHDJN_02059 | 2.5e-98 | drgA | C | Nitroreductase family | ||
EOOGHDJN_02060 | 3.1e-178 | iunH2 | 3.2.2.1 | F | nucleoside hydrolase | |
EOOGHDJN_02061 | 1.7e-146 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
EOOGHDJN_02062 | 8.8e-123 | S | Sucrose-6F-phosphate phosphohydrolase | |||
EOOGHDJN_02063 | 2.3e-157 | ccpB | 5.1.1.1 | K | lacI family | |
EOOGHDJN_02064 | 2.4e-116 | K | Helix-turn-helix domain, rpiR family | |||
EOOGHDJN_02065 | 3.9e-176 | S | Oxidoreductase family, NAD-binding Rossmann fold | |||
EOOGHDJN_02066 | 1.1e-197 | yhhX | 1.1.1.371 | S | Oxidoreductase family, C-terminal alpha/beta domain | |
EOOGHDJN_02067 | 0.0 | yjcE | P | Sodium proton antiporter | ||
EOOGHDJN_02068 | 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) | |
EOOGHDJN_02069 | 3.7e-107 | pncA | Q | Isochorismatase family | ||
EOOGHDJN_02070 | 1e-131 | |||||
EOOGHDJN_02071 | 5.1e-125 | skfE | V | ABC transporter | ||
EOOGHDJN_02072 | 9.5e-65 | yvoA_1 | K | Transcriptional regulator, GntR family | ||
EOOGHDJN_02073 | 1.2e-45 | S | Enterocin A Immunity | |||
EOOGHDJN_02074 | 0.0 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
EOOGHDJN_02075 | 2.1e-67 | |||||
EOOGHDJN_02076 | 2.4e-144 | yjfP | S | Dienelactone hydrolase family | ||
EOOGHDJN_02077 | 2.3e-56 | dsbJ | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
EOOGHDJN_02078 | 9.3e-206 | metB | 2.5.1.48, 4.4.1.8 | E | Cys/Met metabolism PLP-dependent enzyme | |
EOOGHDJN_02079 | 5.2e-47 | |||||
EOOGHDJN_02080 | 6.3e-45 | |||||
EOOGHDJN_02081 | 5e-82 | yybC | S | Protein of unknown function (DUF2798) | ||
EOOGHDJN_02082 | 1.7e-73 | |||||
EOOGHDJN_02083 | 4e-60 | |||||
EOOGHDJN_02084 | 5.1e-195 | lplA | 6.3.1.20 | H | Lipoate-protein ligase | |
EOOGHDJN_02085 | 0.0 | acm2 | 3.2.1.17 | NU | Bacterial SH3 domain | |
EOOGHDJN_02086 | 4.7e-79 | uspA | T | universal stress protein | ||
EOOGHDJN_02087 | 1.1e-153 | rluA | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
EOOGHDJN_02088 | 5.7e-20 | |||||
EOOGHDJN_02089 | 4.2e-44 | S | zinc-ribbon domain | |||
EOOGHDJN_02090 | 3.7e-69 | S | response to antibiotic | |||
EOOGHDJN_02091 | 1.7e-48 | K | Cro/C1-type HTH DNA-binding domain | |||
EOOGHDJN_02092 | 5.6e-21 | S | Protein of unknown function (DUF2929) | |||
EOOGHDJN_02093 | 1.2e-224 | lsgC | M | Glycosyl transferases group 1 | ||
EOOGHDJN_02094 | 0.0 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
EOOGHDJN_02095 | 3.1e-161 | S | Putative esterase | |||
EOOGHDJN_02096 | 2.4e-130 | gntR2 | K | Transcriptional regulator | ||
EOOGHDJN_02097 | 5.8e-91 | ybaK | S | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
EOOGHDJN_02098 | 5.8e-138 | |||||
EOOGHDJN_02099 | 3.1e-116 | ypgQ | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
EOOGHDJN_02100 | 5.5e-138 | rrp8 | K | LytTr DNA-binding domain | ||
EOOGHDJN_02101 | 4.2e-92 | M1-874 | K | Domain of unknown function (DUF1836) | ||
EOOGHDJN_02102 | 7.7e-61 | |||||
EOOGHDJN_02103 | 4.1e-74 | hspX | O | Belongs to the small heat shock protein (HSP20) family | ||
EOOGHDJN_02104 | 4.4e-58 | |||||
EOOGHDJN_02105 | 1.2e-239 | yhdP | S | Transporter associated domain | ||
EOOGHDJN_02106 | 4.9e-87 | nrdI | F | Belongs to the NrdI family | ||
EOOGHDJN_02107 | 2.6e-270 | yjcE | P | Sodium proton antiporter | ||
EOOGHDJN_02108 | 1.5e-211 | yttB | EGP | Major facilitator Superfamily | ||
EOOGHDJN_02109 | 2.5e-62 | K | helix_turn_helix, mercury resistance | |||
EOOGHDJN_02110 | 1.8e-173 | C | Zinc-binding dehydrogenase | |||
EOOGHDJN_02111 | 8.5e-57 | S | SdpI/YhfL protein family | |||
EOOGHDJN_02112 | 6.3e-295 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
EOOGHDJN_02113 | 5.5e-261 | gabR | K | Bacterial regulatory proteins, gntR family | ||
EOOGHDJN_02114 | 1.4e-217 | patA | 2.6.1.1 | E | Aminotransferase | |
EOOGHDJN_02115 | 7.8e-160 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
EOOGHDJN_02116 | 3e-18 | |||||
EOOGHDJN_02117 | 1.7e-126 | S | membrane transporter protein | |||
EOOGHDJN_02118 | 1.9e-161 | mleR | K | LysR family | ||
EOOGHDJN_02119 | 5.6e-115 | ylbE | GM | NAD(P)H-binding | ||
EOOGHDJN_02120 | 8.2e-96 | wecD | K | Acetyltransferase (GNAT) family | ||
EOOGHDJN_02121 | 4.3e-219 | int | L | Belongs to the 'phage' integrase family | ||
EOOGHDJN_02122 | 1.8e-29 | |||||
EOOGHDJN_02123 | 1.9e-83 | S | Protein of unknown function DUF262 | |||
EOOGHDJN_02124 | 3e-158 | dcm | 2.1.1.37 | L | Belongs to the class I-like SAM-binding methyltransferase superfamily. C5-methyltransferase family | |
EOOGHDJN_02129 | 3.3e-35 | ycnE | 3.1.1.29 | S | Antibiotic biosynthesis monooxygenase | |
EOOGHDJN_02130 | 3.2e-27 | |||||
EOOGHDJN_02131 | 3.5e-24 | 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 | ||
EOOGHDJN_02135 | 5.9e-53 | |||||
EOOGHDJN_02137 | 2.1e-58 | |||||
EOOGHDJN_02138 | 1.1e-76 | E | IrrE N-terminal-like domain | |||
EOOGHDJN_02139 | 4.5e-61 | yvaO | K | Helix-turn-helix domain | ||
EOOGHDJN_02140 | 1.3e-37 | K | Helix-turn-helix | |||
EOOGHDJN_02143 | 8.9e-07 | |||||
EOOGHDJN_02144 | 1.5e-17 | K | Cro/C1-type HTH DNA-binding domain | |||
EOOGHDJN_02148 | 2.2e-53 | |||||
EOOGHDJN_02149 | 2.1e-80 | |||||
EOOGHDJN_02151 | 5.4e-55 | S | Bacteriophage Mu Gam like protein | |||
EOOGHDJN_02152 | 2.6e-63 | |||||
EOOGHDJN_02153 | 1.4e-156 | L | DnaD domain protein | |||
EOOGHDJN_02154 | 7e-49 | |||||
EOOGHDJN_02155 | 1.6e-94 | |||||
EOOGHDJN_02156 | 6.2e-64 | |||||
EOOGHDJN_02157 | 1.6e-64 | rusA | 3.1.22.4 | L | Endonuclease that resolves Holliday junction intermediates made during homologous genetic recombination and DNA repair. Exhibits sequence and structure-selective cleavage of four-way DNA junctions, where it introduces symmetrical nicks in two strands of the same polarity at the 5' side of dinucleotides. Corrects the defects in genetic recombination and DNA repair associated with inactivation of ruvAB or ruvC | |
EOOGHDJN_02159 | 1.7e-81 | arpU | S | Phage transcriptional regulator, ArpU family | ||
EOOGHDJN_02164 | 1.8e-24 | S | Protein of unknown function (DUF2829) | |||
EOOGHDJN_02165 | 7.8e-62 | ps333 | L | Terminase small subunit | ||
EOOGHDJN_02166 | 1.8e-239 | ps334 | S | Terminase-like family | ||
EOOGHDJN_02167 | 8.8e-268 | S | Phage portal protein, SPP1 Gp6-like | |||
EOOGHDJN_02168 | 9.4e-295 | S | Phage Mu protein F like protein | |||
EOOGHDJN_02169 | 2.4e-30 | |||||
EOOGHDJN_02171 | 3.1e-15 | S | Domain of unknown function (DUF4355) | |||
EOOGHDJN_02172 | 4.2e-48 | |||||
EOOGHDJN_02173 | 6.5e-174 | S | Phage major capsid protein E | |||
EOOGHDJN_02175 | 1.3e-51 | |||||
EOOGHDJN_02176 | 1.5e-50 | |||||
EOOGHDJN_02177 | 3e-88 | |||||
EOOGHDJN_02178 | 1.4e-54 | |||||
EOOGHDJN_02179 | 6.9e-78 | S | Phage tail tube protein, TTP | |||
EOOGHDJN_02180 | 6.3e-64 | |||||
EOOGHDJN_02181 | 0.0 | D | NLP P60 protein | |||
EOOGHDJN_02182 | 5e-60 | |||||
EOOGHDJN_02183 | 0.0 | sidC | GT2,GT4 | LM | DNA recombination | |
EOOGHDJN_02184 | 2.7e-47 | S | Protein of unknown function (DUF1617) | |||
EOOGHDJN_02186 | 1.8e-180 | M | hydrolase, family 25 | |||
EOOGHDJN_02187 | 1.2e-46 | |||||
EOOGHDJN_02188 | 1.5e-30 | hol | S | Bacteriophage holin | ||
EOOGHDJN_02189 | 4.6e-117 | S | Protein of unknown function (DUF1461) | |||
EOOGHDJN_02190 | 1.5e-146 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
EOOGHDJN_02191 | 1.5e-80 | yutD | S | Protein of unknown function (DUF1027) | ||
EOOGHDJN_02192 | 1.3e-270 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
EOOGHDJN_02193 | 4.4e-117 | S | Calcineurin-like phosphoesterase | |||
EOOGHDJN_02194 | 5.6e-253 | cycA | E | Amino acid permease | ||
EOOGHDJN_02195 | 7e-220 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
EOOGHDJN_02196 | 3.6e-186 | ytxK | 2.1.1.72 | L | N-6 DNA Methylase | |
EOOGHDJN_02198 | 4.5e-88 | S | Prokaryotic N-terminal methylation motif | |||
EOOGHDJN_02199 | 8.6e-20 | |||||
EOOGHDJN_02200 | 3.2e-83 | gspG | NU | general secretion pathway protein | ||
EOOGHDJN_02201 | 2.1e-42 | comGC | U | competence protein ComGC | ||
EOOGHDJN_02202 | 1.9e-189 | comGB | NU | type II secretion system | ||
EOOGHDJN_02203 | 4.8e-174 | comGA | NU | Type II IV secretion system protein | ||
EOOGHDJN_02204 | 4.8e-160 | 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 | |
EOOGHDJN_02205 | 8.3e-131 | yebC | K | Transcriptional regulatory protein | ||
EOOGHDJN_02206 | 5.4e-50 | S | DsrE/DsrF-like family | |||
EOOGHDJN_02207 | 5.2e-164 | 3.2.1.52 | GH20 | G | Xylose isomerase domain protein TIM barrel | |
EOOGHDJN_02208 | 1.9e-181 | ccpA | K | catabolite control protein A | ||
EOOGHDJN_02209 | 1.7e-215 | pepQ | 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
EOOGHDJN_02210 | 1.1e-80 | K | helix_turn_helix, mercury resistance | |||
EOOGHDJN_02211 | 1.8e-52 | |||||
EOOGHDJN_02212 | 1.9e-23 | WQ51_05790 | S | protein containing a divergent version of the methyl-accepting chemotaxis-like domain | ||
EOOGHDJN_02213 | 2.6e-158 | ykuT | M | mechanosensitive ion channel | ||
EOOGHDJN_02214 | 1.7e-226 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
EOOGHDJN_02215 | 2.6e-76 | dapD | 2.3.1.117, 2.3.1.89 | E | Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate | |
EOOGHDJN_02216 | 6.5e-87 | ykuL | S | (CBS) domain | ||
EOOGHDJN_02217 | 9.5e-97 | S | Phosphoesterase | |||
EOOGHDJN_02218 | 1e-110 | 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 | |
EOOGHDJN_02219 | 4.1e-150 | murI | 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
EOOGHDJN_02220 | 7.6e-126 | yslB | S | Protein of unknown function (DUF2507) | ||
EOOGHDJN_02221 | 3.3e-52 | trxA | O | Belongs to the thioredoxin family | ||
EOOGHDJN_02222 | 0.0 | mutS2 | L | Endonuclease that is involved in the suppression of homologous recombination and may therefore have a key role in the control of bacterial genetic diversity | ||
EOOGHDJN_02223 | 2.7e-36 | zapA | D | Activator of cell division through the inhibition of FtsZ GTPase activity, therefore promoting FtsZ assembly into bundles of protofilaments necessary for the formation of the division Z ring. It is recruited early at mid-cell but it is not essential for cell division | ||
EOOGHDJN_02224 | 1.6e-48 | yrzB | S | Belongs to the UPF0473 family | ||
EOOGHDJN_02225 | 7.3e-74 | yqgF | J | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
EOOGHDJN_02226 | 2.4e-43 | yrzL | S | Belongs to the UPF0297 family | ||
EOOGHDJN_02227 | 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 | |
EOOGHDJN_02228 | 4.6e-244 | cshB | 3.6.4.13 | JKL | DEAD-box RNA helicase. May work in conjunction with the cold shock proteins to ensure proper initiation of transcription at low and optimal temperatures | |
EOOGHDJN_02229 | 7e-178 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
EOOGHDJN_02230 | 5.3e-217 | 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 | |
EOOGHDJN_02231 | 2.8e-29 | yajC | U | Preprotein translocase | ||
EOOGHDJN_02232 | 3.3e-227 | tgt | 2.4.2.29 | F | Catalyzes the base-exchange of a guanine (G) residue with the queuine precursor 7-aminomethyl-7-deazaguanine (PreQ1) at position 34 (anticodon wobble position) in tRNAs with GU(N) anticodons (tRNA-Asp, -Asn, -His and -Tyr). Catalysis occurs through a double-displacement mechanism. The nucleophile active site attacks the C1' of nucleotide 34 to detach the guanine base from the RNA, forming a covalent enzyme-RNA intermediate. The proton acceptor active site deprotonates the incoming PreQ1, allowing a nucleophilic attack on the C1' of the ribose to form the product. After dissociation, two additional enzymatic reactions on the tRNA convert PreQ1 to queuine (Q), resulting in the hypermodified nucleoside queuosine (7-(((4,5-cis-dihydroxy-2- cyclopenten-1-yl)amino)methyl)-7-deazaguanosine) | |
EOOGHDJN_02233 | 6.3e-201 | queA | 2.4.99.17 | J | Transfers and isomerizes the ribose moiety from AdoMet to the 7-aminomethyl group of 7-deazaguanine (preQ1-tRNA) to give epoxyqueuosine (oQ-tRNA) | |
EOOGHDJN_02234 | 2.1e-188 | 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 | |
EOOGHDJN_02235 | 4.6e-106 | 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 | |
EOOGHDJN_02236 | 1.3e-90 | |||||
EOOGHDJN_02237 | 0.0 | S | Bacterial membrane protein YfhO | |||
EOOGHDJN_02238 | 1.3e-72 | |||||
EOOGHDJN_02239 | 2.1e-99 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | dUTP diphosphatase | |
EOOGHDJN_02240 | 1.2e-51 | HA62_12640 | S | GCN5-related N-acetyl-transferase | ||
EOOGHDJN_02241 | 3.5e-123 | rpiA | 2.7.1.12, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
EOOGHDJN_02242 | 7.3e-258 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
EOOGHDJN_02243 | 8.8e-113 | zmp2 | O | Zinc-dependent metalloprotease | ||
EOOGHDJN_02244 | 2.5e-129 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
EOOGHDJN_02245 | 1.7e-177 | EG | EamA-like transporter family | |||
EOOGHDJN_02246 | 3.3e-167 | mleP2 | S | Transporter, auxin efflux carrier (AEC) family protein | ||
EOOGHDJN_02247 | 4.8e-168 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
EOOGHDJN_02248 | 1.8e-136 | accA | 2.1.3.15, 6.4.1.2 | I | Acetyl co-enzyme A carboxylase carboxyltransferase alpha subunit | |
EOOGHDJN_02249 | 9.8e-141 | accD | 2.1.3.15, 6.4.1.2 | I | Component of the acetyl coenzyme A carboxylase (ACC) complex. Biotin carboxylase (BC) catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the transcarboxylase to acetyl-CoA to form malonyl- CoA | |
EOOGHDJN_02250 | 3.4e-247 | accC2 | 6.3.4.14, 6.4.1.2 | I | Biotin carboxylase C-terminal domain | |
EOOGHDJN_02251 | 9.7e-65 | accB | 2.3.1.12 | I | Biotin-requiring enzyme | |
EOOGHDJN_02252 | 5.4e-178 | fabH | 2.3.1.180 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids | |
EOOGHDJN_02253 | 3.1e-87 | pts10B | 2.7.1.191, 2.7.1.202 | G | PTS system sorbose subfamily IIB component | |
EOOGHDJN_02254 | 8.6e-72 | pts10A | 2.7.1.191 | G | PTS system fructose IIA component | |
EOOGHDJN_02255 | 0.0 | levR | K | Sigma-54 interaction domain | ||
EOOGHDJN_02256 | 4.7e-64 | S | Domain of unknown function (DUF956) | |||
EOOGHDJN_02257 | 3.6e-171 | manN | G | system, mannose fructose sorbose family IID component | ||
EOOGHDJN_02258 | 3.4e-133 | manY | G | PTS system | ||
EOOGHDJN_02259 | 1.3e-168 | manL | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
EOOGHDJN_02260 | 6.4e-156 | G | Peptidase_C39 like family | |||
EOOGHDJN_02262 | 3.1e-156 | thrB | 2.7.1.39 | F | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
EOOGHDJN_02263 | 4e-237 | hom | 1.1.1.3, 2.7.2.4 | E | homoserine dehydrogenase | |
EOOGHDJN_02264 | 6.3e-81 | ydcK | S | Belongs to the SprT family | ||
EOOGHDJN_02265 | 0.0 | yhgF | K | Tex-like protein N-terminal domain protein | ||
EOOGHDJN_02266 | 8.9e-72 | |||||
EOOGHDJN_02267 | 0.0 | pacL | 3.6.3.8 | P | P-type ATPase | |
EOOGHDJN_02268 | 4.7e-154 | nadE | 6.3.1.5 | F | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
EOOGHDJN_02269 | 5.2e-289 | pncB | 6.3.4.21 | F | Catalyzes the synthesis of beta-nicotinate D- ribonucleotide from nicotinate and 5-phospho-D-ribose 1-phosphate at the expense of ATP | |
EOOGHDJN_02270 | 1.2e-137 | tagA | 2.4.1.187 | GT26 | F | Catalyzes the conversion of GlcNAc-PP-undecaprenol into ManNAc-GlcNAc-PP-undecaprenol, the first committed lipid intermediate in the de novo synthesis of teichoic acid |
EOOGHDJN_02271 | 1.6e-123 | gntR1 | K | UbiC transcription regulator-associated domain protein | ||
EOOGHDJN_02272 | 6.1e-221 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
EOOGHDJN_02273 | 2.9e-137 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
EOOGHDJN_02274 | 1.6e-151 | pnuC | H | nicotinamide mononucleotide transporter | ||
EOOGHDJN_02275 | 5.8e-192 | ybiR | P | Citrate transporter | ||
EOOGHDJN_02276 | 1.1e-166 | pphA | 3.1.3.16 | T | Calcineurin-like phosphoesterase | |
EOOGHDJN_02277 | 2.7e-43 | S | Cupin domain | |||
EOOGHDJN_02278 | 1.2e-49 | 5.3.3.19 | S | Cupin 2, conserved barrel domain protein | ||
EOOGHDJN_02282 | 2e-151 | yjjH | S | Calcineurin-like phosphoesterase | ||
EOOGHDJN_02283 | 3e-252 | dtpT | U | amino acid peptide transporter | ||
EOOGHDJN_02286 | 0.0 | yhcA | V | ABC transporter, ATP-binding protein | ||
EOOGHDJN_02287 | 2.3e-24 | P | Concanavalin A-like lectin/glucanases superfamily | |||
EOOGHDJN_02288 | 7.4e-64 | |||||
EOOGHDJN_02289 | 7.5e-160 | T | Calcineurin-like phosphoesterase superfamily domain | |||
EOOGHDJN_02290 | 1.6e-54 | |||||
EOOGHDJN_02291 | 5.3e-150 | dicA | K | Helix-turn-helix domain | ||
EOOGHDJN_02292 | 6.8e-75 | pts23A | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | ||
EOOGHDJN_02293 | 7e-53 | ptcB | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
EOOGHDJN_02294 | 3.5e-269 | pts23C | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
EOOGHDJN_02295 | 1.3e-278 | pbg6 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
EOOGHDJN_02296 | 1.7e-185 | 1.1.1.219 | GM | Male sterility protein | ||
EOOGHDJN_02297 | 5.1e-75 | K | helix_turn_helix, mercury resistance | |||
EOOGHDJN_02298 | 2.3e-65 | M | LysM domain | |||
EOOGHDJN_02299 | 2.3e-95 | M | Lysin motif | |||
EOOGHDJN_02300 | 4e-107 | S | SdpI/YhfL protein family | |||
EOOGHDJN_02301 | 1.8e-54 | nudA | S | ASCH | ||
EOOGHDJN_02302 | 9.1e-164 | psaA | P | Belongs to the bacterial solute-binding protein 9 family | ||
EOOGHDJN_02303 | 9.4e-92 | |||||
EOOGHDJN_02304 | 2.6e-120 | tag | 3.2.2.20 | L | Methyladenine glycosylase | |
EOOGHDJN_02305 | 3.3e-219 | T | diguanylate cyclase | |||
EOOGHDJN_02306 | 1.2e-73 | S | Psort location Cytoplasmic, score | |||
EOOGHDJN_02307 | 2e-283 | dinB | 2.7.7.7 | L | impB/mucB/samB family C-terminal domain | |
EOOGHDJN_02308 | 2.6e-166 | K | Bacterial regulatory helix-turn-helix protein, lysR family | |||
EOOGHDJN_02309 | 6e-73 | |||||
EOOGHDJN_02310 | 3.8e-131 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
EOOGHDJN_02311 | 4.3e-176 | C | C4-dicarboxylate transmembrane transporter activity | |||
EOOGHDJN_02312 | 1.7e-116 | GM | NAD(P)H-binding | |||
EOOGHDJN_02313 | 4.7e-93 | S | Phosphatidylethanolamine-binding protein | |||
EOOGHDJN_02314 | 2.7e-78 | yphH | S | Cupin domain | ||
EOOGHDJN_02315 | 3.7e-60 | I | sulfurtransferase activity | |||
EOOGHDJN_02316 | 1.9e-138 | IQ | reductase | |||
EOOGHDJN_02317 | 1.1e-116 | GM | NAD(P)H-binding | |||
EOOGHDJN_02318 | 8.6e-218 | ykiI | ||||
EOOGHDJN_02319 | 0.0 | V | ABC transporter | |||
EOOGHDJN_02320 | 4.8e-311 | XK27_09600 | V | ABC transporter, ATP-binding protein | ||
EOOGHDJN_02321 | 1e-175 | O | protein import | |||
EOOGHDJN_02322 | 2.4e-228 | amd | 3.5.1.47 | E | Peptidase family M20/M25/M40 | |
EOOGHDJN_02323 | 5e-162 | IQ | KR domain | |||
EOOGHDJN_02325 | 1.4e-69 | |||||
EOOGHDJN_02326 | 1.9e-144 | K | Helix-turn-helix XRE-family like proteins | |||
EOOGHDJN_02327 | 3.6e-266 | yjeM | E | Amino Acid | ||
EOOGHDJN_02328 | 3.9e-66 | lysM | M | LysM domain | ||
EOOGHDJN_02329 | 1.3e-223 | dhaT | 1.1.1.1, 1.1.1.202 | C | Dehydrogenase | |
EOOGHDJN_02330 | 1.5e-74 | yeaL | S | Protein of unknown function (DUF441) | ||
EOOGHDJN_02331 | 6.5e-170 | cvfB | S | S1 domain | ||
EOOGHDJN_02332 | 5.5e-164 | xerD | D | recombinase XerD | ||
EOOGHDJN_02333 | 4.8e-69 | ribT | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
EOOGHDJN_02334 | 8.2e-129 | 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 | ||
EOOGHDJN_02335 | 7.9e-103 | 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 | ||
EOOGHDJN_02336 | 1.1e-130 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
EOOGHDJN_02337 | 1.1e-96 | U | Mediates riboflavin uptake, may also transport FMN and roseoflavin. Probably a riboflavin-binding protein that interacts with the energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates. The substrates themselves are bound by transmembrane, not extracytoplasmic soluble proteins | |||
EOOGHDJN_02338 | 3.6e-196 | ypbB | 5.1.3.1 | S | Helix-turn-helix domain | |
EOOGHDJN_02339 | 6.2e-271 | recQ1 | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
EOOGHDJN_02340 | 2e-19 | M | Lysin motif | |||
EOOGHDJN_02341 | 3.8e-117 | cmk | 1.17.7.4, 2.5.1.19, 2.7.1.26, 2.7.4.25, 2.7.7.2, 6.3.2.1 | F | Belongs to the cytidylate kinase family. Type 1 subfamily | |
EOOGHDJN_02342 | 1.8e-213 | rpsA | 1.17.7.4 | J | Ribosomal protein S1 | |
EOOGHDJN_02343 | 2.7e-249 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
EOOGHDJN_02344 | 1.1e-40 | hup | L | Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions | ||
EOOGHDJN_02345 | 1.6e-214 | S | Tetratricopeptide repeat protein | |||
EOOGHDJN_02346 | 3.3e-149 | 3.1.3.102, 3.1.3.104 | S | hydrolase | ||
EOOGHDJN_02347 | 5.4e-144 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
EOOGHDJN_02348 | 2.5e-228 | cca | 2.7.7.19, 2.7.7.72 | J | Catalyzes the addition and repair of the essential 3'- terminal CCA sequence in tRNAs without using a nucleic acid template. Adds these three nucleotides in the order of C, C, and A to the tRNA nucleotide-73, using CTP and ATP as substrates and producing inorganic pyrophosphate | |
EOOGHDJN_02349 | 9.6e-85 | |||||
EOOGHDJN_02350 | 0.0 | yfmR | S | ABC transporter, ATP-binding protein | ||
EOOGHDJN_02351 | 1.1e-188 | 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 | |
EOOGHDJN_02352 | 5.1e-92 | folA | 1.5.1.3 | H | Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis | |
EOOGHDJN_02353 | 5.1e-148 | DegV | S | EDD domain protein, DegV family | ||
EOOGHDJN_02354 | 6.1e-150 | ypmR | E | GDSL-like Lipase/Acylhydrolase | ||
EOOGHDJN_02355 | 3.1e-113 | ypmS | S | Uncharacterized protein conserved in bacteria (DUF2140) | ||
EOOGHDJN_02356 | 3.4e-35 | yozE | S | Belongs to the UPF0346 family | ||
EOOGHDJN_02357 | 1.2e-261 | ctpA | 3.4.21.102 | M | Belongs to the peptidase S41A family | |
EOOGHDJN_02358 | 3.3e-251 | emrY | EGP | Major facilitator Superfamily | ||
EOOGHDJN_02359 | 1.5e-197 | XK27_00915 | C | Luciferase-like monooxygenase | ||
EOOGHDJN_02360 | 1.2e-123 | 1.5.1.40 | S | NADP oxidoreductase coenzyme F420-dependent | ||
EOOGHDJN_02361 | 2.5e-172 | L | restriction endonuclease | |||
EOOGHDJN_02362 | 2.3e-170 | cpsY | K | Transcriptional regulator, LysR family | ||
EOOGHDJN_02363 | 1.4e-228 | XK27_05470 | E | Methionine synthase | ||
EOOGHDJN_02365 | 4.8e-162 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
EOOGHDJN_02366 | 3.1e-136 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
EOOGHDJN_02367 | 3.3e-158 | dprA | LU | DNA protecting protein DprA | ||
EOOGHDJN_02368 | 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 | |
EOOGHDJN_02369 | 6.8e-248 | trmFO | 2.1.1.74 | J | Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs | |
EOOGHDJN_02370 | 1.5e-177 | xerC | D | Belongs to the 'phage' integrase family. XerC subfamily | ||
EOOGHDJN_02371 | 6.7e-93 | hslV | 3.4.25.2 | O | Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery | |
EOOGHDJN_02372 | 2.3e-257 | hslU | O | this subunit has chaperone activity. The binding of ATP and its subsequent hydrolysis by HslU are essential for unfolding of protein substrates subsequently hydrolyzed by HslV. HslU recognizes the N-terminal part of its protein substrates and unfolds these before they are guided to HslV for hydrolysis | ||
EOOGHDJN_02373 | 6.4e-170 | lacX | 5.1.3.3 | G | Aldose 1-epimerase | |
EOOGHDJN_02374 | 2.3e-232 | pyrP | F | Permease | ||
EOOGHDJN_02375 | 6.5e-128 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
EOOGHDJN_02376 | 2.5e-27 | 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 | ||
EOOGHDJN_02377 | 6e-51 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
EOOGHDJN_02378 | 1.8e-90 | 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 | ||
EOOGHDJN_02379 | 2.7e-280 | 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 | |
EOOGHDJN_02380 | 2.3e-165 | atpG | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The gamma chain is believed to be important in regulating ATPase activity and the flow of protons through the CF(0) complex | ||
EOOGHDJN_02381 | 2.1e-263 | 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 | |
EOOGHDJN_02382 | 1.1e-50 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
EOOGHDJN_02383 | 4.4e-247 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
EOOGHDJN_02384 | 2.1e-102 | J | Acetyltransferase (GNAT) domain | |||
EOOGHDJN_02385 | 2.7e-180 | mbl | D | Cell shape determining protein MreB Mrl | ||
EOOGHDJN_02386 | 2.3e-43 | yidD | S | Could be involved in insertion of integral membrane proteins into the membrane | ||
EOOGHDJN_02387 | 3.3e-33 | S | Protein of unknown function (DUF2969) | |||
EOOGHDJN_02388 | 9.3e-220 | rodA | D | Belongs to the SEDS family | ||
EOOGHDJN_02389 | 3.6e-48 | gcsH2 | E | glycine cleavage | ||
EOOGHDJN_02390 | 4e-187 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
EOOGHDJN_02391 | 1.4e-111 | metI | U | ABC transporter permease | ||
EOOGHDJN_02392 | 2.2e-148 | metQ | M | Belongs to the nlpA lipoprotein family | ||
EOOGHDJN_02393 | 2.8e-168 | hicD1 | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
EOOGHDJN_02394 | 3.5e-177 | S | Protein of unknown function (DUF2785) | |||
EOOGHDJN_02395 | 4.7e-188 | qor | 1.1.1.1, 1.6.5.5 | C | Belongs to the zinc-containing alcohol dehydrogenase family. Quinone oxidoreductase subfamily | |
EOOGHDJN_02396 | 5.4e-214 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
EOOGHDJN_02397 | 7.1e-297 | glpQ3 | 3.1.4.46 | C | Glycerophosphoryl diester phosphodiesterase family | |
EOOGHDJN_02398 | 3.3e-161 | 2.3.1.19 | K | Helix-turn-helix XRE-family like proteins | ||
EOOGHDJN_02399 | 6.1e-205 | bla2 | 3.5.2.6 | V | Beta-lactamase enzyme family | |
EOOGHDJN_02400 | 6.2e-82 | usp6 | T | universal stress protein | ||
EOOGHDJN_02401 | 1.5e-38 | |||||
EOOGHDJN_02402 | 8e-238 | rarA | L | recombination factor protein RarA | ||
EOOGHDJN_02403 | 0.0 | gshF | 6.3.2.2 | H | Belongs to the glutamate--cysteine ligase type 1 family | |
EOOGHDJN_02404 | 5.9e-95 | cytR | 5.1.1.1 | K | Periplasmic binding proteins and sugar binding domain of LacI family | |
EOOGHDJN_02405 | 6e-66 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | ||
EOOGHDJN_02406 | 3.6e-103 | G | PTS system sorbose-specific iic component | |||
EOOGHDJN_02407 | 2.7e-104 | G | PTS system mannose fructose sorbose family IID component | |||
EOOGHDJN_02408 | 9.2e-42 | 2.7.1.191 | G | PTS system fructose IIA component | ||
EOOGHDJN_02409 | 5.7e-231 | malL | 3.2.1.10 | GH13 | G | COG0366 Glycosidases |
EOOGHDJN_02410 | 1.7e-44 | czrA | K | Helix-turn-helix domain | ||
EOOGHDJN_02411 | 3.1e-110 | S | Protein of unknown function (DUF1648) | |||
EOOGHDJN_02412 | 7.3e-80 | yueI | S | Protein of unknown function (DUF1694) | ||
EOOGHDJN_02413 | 5.2e-113 | yktB | S | Belongs to the UPF0637 family | ||
EOOGHDJN_02414 | 3.1e-107 | 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 | ||
EOOGHDJN_02415 | 5e-81 | ytsP | 1.8.4.14 | T | GAF domain-containing protein | |
EOOGHDJN_02416 | 0.0 | ezrA | D | modulates the frequency and position of FtsZ ring formation. Inhibits FtsZ ring formation at polar sites. Interacts either with FtsZ or with one of its binding partners to promote depolymerization | ||
EOOGHDJN_02417 | 1.7e-218 | iscS2 | 2.8.1.7 | E | Aminotransferase class V | |
EOOGHDJN_02418 | 1.9e-228 | thiI | 2.8.1.4 | H | Catalyzes the ATP-dependent transfer of a sulfur to tRNA to produce 4-thiouridine in position 8 of tRNAs, which functions as a near-UV photosensor. Also catalyzes the transfer of sulfur to the sulfur carrier protein ThiS, forming ThiS-thiocarboxylate. This is a step in the synthesis of thiazole, in the thiamine biosynthesis pathway. The sulfur is donated as persulfide by IscS | |
EOOGHDJN_02421 | 0.0 | S | Pfam Methyltransferase | |||
EOOGHDJN_02422 | 4.4e-267 | tagE2 | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 |
EOOGHDJN_02423 | 7.5e-299 | tagE3 | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 |
EOOGHDJN_02424 | 4.2e-29 | |||||
EOOGHDJN_02425 | 2e-106 | ytqB | 2.1.1.176 | J | Putative rRNA methylase | |
EOOGHDJN_02426 | 1e-124 | 3.6.1.27 | I | Acid phosphatase homologues | ||
EOOGHDJN_02427 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
EOOGHDJN_02428 | 6.7e-301 | ytgP | S | Polysaccharide biosynthesis protein | ||
EOOGHDJN_02429 | 1.8e-136 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
EOOGHDJN_02430 | 1.7e-151 | nnrD | 4.2.1.136, 5.1.99.6 | H | Catalyzes the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. Together with NAD(P)HX epimerase, which catalyzes the epimerization of the S- and R-forms, the enzyme allows the repair of both epimers of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration | |
EOOGHDJN_02431 | 1.5e-272 | pepV | 3.5.1.18 | E | dipeptidase PepV | |
EOOGHDJN_02432 | 4.1e-84 | uspA | T | Belongs to the universal stress protein A family | ||
EOOGHDJN_02433 | 6.1e-202 | ugpC | 3.6.3.20 | E | Belongs to the ABC transporter superfamily | |
EOOGHDJN_02434 | 2e-172 | ugpA | U | Binding-protein-dependent transport system inner membrane component | ||
EOOGHDJN_02435 | 1.1e-150 | ugpE | G | ABC transporter permease | ||
EOOGHDJN_02436 | 4.2e-261 | ugpB | G | Bacterial extracellular solute-binding protein | ||
EOOGHDJN_02437 | 4.9e-125 | glpQ1 | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
EOOGHDJN_02438 | 3.8e-119 | dck | 2.7.1.74 | F | deoxynucleoside kinase | |
EOOGHDJN_02439 | 5.5e-41 | 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 | ||
EOOGHDJN_02440 | 4.6e-180 | XK27_06930 | V | domain protein | ||
EOOGHDJN_02442 | 4.8e-126 | V | Transport permease protein | |||
EOOGHDJN_02443 | 1.5e-155 | V | ABC transporter | |||
EOOGHDJN_02444 | 5.7e-175 | K | LytTr DNA-binding domain | |||
EOOGHDJN_02446 | 7.7e-154 | msrA | 1.8.4.11, 1.8.4.12 | O | Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine | |
EOOGHDJN_02447 | 3.6e-64 | K | helix_turn_helix, mercury resistance | |||
EOOGHDJN_02448 | 5.1e-116 | GM | NAD(P)H-binding | |||
EOOGHDJN_02449 | 1e-157 | ypaH | EG | COG0697 Permeases of the drug metabolite transporter (DMT) superfamily | ||
EOOGHDJN_02450 | 6.5e-148 | S | Sucrose-6F-phosphate phosphohydrolase | |||
EOOGHDJN_02451 | 1.7e-108 | |||||
EOOGHDJN_02452 | 2.2e-224 | pltK | 2.7.13.3 | T | GHKL domain | |
EOOGHDJN_02453 | 1.6e-137 | pltR | K | LytTr DNA-binding domain | ||
EOOGHDJN_02454 | 4.5e-55 | |||||
EOOGHDJN_02455 | 2.5e-59 | |||||
EOOGHDJN_02456 | 5.1e-114 | S | CAAX protease self-immunity | |||
EOOGHDJN_02457 | 1.6e-85 | ohrR | K | helix_turn_helix multiple antibiotic resistance protein | ||
EOOGHDJN_02458 | 1e-90 | |||||
EOOGHDJN_02459 | 2.5e-46 | |||||
EOOGHDJN_02460 | 0.0 | uvrA2 | L | ABC transporter | ||
EOOGHDJN_02462 | 1.3e-257 | 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 | ||
EOOGHDJN_02463 | 3.7e-205 | yacL | S | domain protein | ||
EOOGHDJN_02464 | 8.9e-289 | gltX | 6.1.1.17, 6.1.1.24 | J | Catalyzes the attachment of glutamate to tRNA(Glu) in a two-step reaction glutamate is first activated by ATP to form Glu-AMP and then transferred to the acceptor end of tRNA(Glu) | |
EOOGHDJN_02465 | 6.7e-270 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
EOOGHDJN_02466 | 3.5e-70 | mrnC | J | Involved in correct processing of both the 5' and 3' ends of 23S rRNA precursor. Processes 30S rRNA precursor transcript even in absence of ribonuclease 3 (Rnc) | ||
EOOGHDJN_02467 | 3.3e-138 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
EOOGHDJN_02468 | 5.3e-98 | yacP | S | YacP-like NYN domain | ||
EOOGHDJN_02469 | 9.1e-101 | sigH | K | Sigma-70 region 2 | ||
EOOGHDJN_02470 | 6.5e-22 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
EOOGHDJN_02471 | 6.8e-29 | 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 | ||
EOOGHDJN_02472 | 3.7e-99 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
EOOGHDJN_02473 | 3e-159 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
EOOGHDJN_02474 | 2.4e-69 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
EOOGHDJN_02475 | 5.1e-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 | ||
EOOGHDJN_02476 | 4.6e-80 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
EOOGHDJN_02477 | 9.9e-56 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
EOOGHDJN_02478 | 1.2e-177 | F | DNA/RNA non-specific endonuclease | |||
EOOGHDJN_02479 | 9e-39 | L | nuclease | |||
EOOGHDJN_02480 | 0.0 | mprF | 2.3.2.3 | S | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms | |
EOOGHDJN_02481 | 2.1e-108 | yvdD | 3.2.2.10 | S | Belongs to the LOG family | |
EOOGHDJN_02482 | 2.2e-198 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
EOOGHDJN_02483 | 0.0 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
EOOGHDJN_02484 | 5.5e-36 | nrdH | O | Glutaredoxin | ||
EOOGHDJN_02485 | 5.7e-109 | rsmC | 2.1.1.172 | J | Methyltransferase | |
EOOGHDJN_02486 | 5.9e-91 | tadA | 3.5.4.33 | F | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
EOOGHDJN_02487 | 0.0 | dnaX | 2.7.7.7 | L | DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
EOOGHDJN_02488 | 5.8e-41 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
EOOGHDJN_02489 | 7.4e-109 | recR | L | May play a role in DNA repair. It seems to be involved in an RecBC-independent recombinational process of DNA repair. It may act with RecF and RecO | ||
EOOGHDJN_02490 | 2.2e-38 | yaaL | S | Protein of unknown function (DUF2508) | ||
EOOGHDJN_02491 | 3.3e-118 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
EOOGHDJN_02492 | 2.4e-53 | yaaQ | S | Cyclic-di-AMP receptor | ||
EOOGHDJN_02493 | 3.3e-186 | holB | 2.7.7.7 | L | DNA polymerase III | |
EOOGHDJN_02494 | 1e-57 | yabA | L | Involved in initiation control of chromosome replication | ||
EOOGHDJN_02495 | 5.4e-164 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
EOOGHDJN_02496 | 2.1e-148 | fat | 3.1.2.21 | I | Acyl-ACP thioesterase | |
EOOGHDJN_02497 | 2e-191 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
EOOGHDJN_02498 | 1.5e-211 | phnW | 2.5.1.49, 2.6.1.37, 3.11.1.1 | E | Belongs to the class-V pyridoxal-phosphate-dependent aminotransferase family. PhnW subfamily | |
EOOGHDJN_02499 | 2.1e-143 | phnX | 2.6.1.37, 3.1.3.18, 3.11.1.1 | E | Belongs to the HAD-like hydrolase superfamily. PhnX family | |
EOOGHDJN_02500 | 2.6e-144 | phnE1 | 3.6.1.63 | U | ABC transporter permease | |
EOOGHDJN_02501 | 7.7e-138 | phnE | 3.6.1.63 | U | Phosphonate ABC transporter permease | |
EOOGHDJN_02502 | 9.7e-138 | phnC | 3.6.3.28 | P | Part of the ABC transporter complex PhnCDE involved in phosphonates import. Responsible for energy coupling to the transport system | |
EOOGHDJN_02503 | 5.1e-190 | phnD | P | Phosphonate ABC transporter | ||
EOOGHDJN_02504 | 1.7e-128 | yeaZ | 2.3.1.234 | O | Universal bacterial protein YeaZ | |
EOOGHDJN_02505 | 6.7e-101 | rimI | 2.3.1.128 | K | Ribosomal-protein-alanine acetyltransferase | |
EOOGHDJN_02506 | 1e-81 | rimI | 2.3.1.128 | K | This enzyme acetylates the N-terminal alanine of ribosomal protein S18 | |
EOOGHDJN_02507 | 1.5e-194 | tsaD | 2.3.1.234 | J | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaE and TsaB. TsaD likely plays a direct catalytic role in this reaction | |
EOOGHDJN_02508 | 2.1e-263 | S | response to antibiotic | |||
EOOGHDJN_02509 | 2.8e-134 | S | zinc-ribbon domain | |||
EOOGHDJN_02511 | 1.2e-36 | |||||
EOOGHDJN_02512 | 8.2e-134 | aroD | S | Alpha/beta hydrolase family | ||
EOOGHDJN_02513 | 5.2e-177 | S | Phosphotransferase system, EIIC | |||
EOOGHDJN_02514 | 2.5e-269 | I | acetylesterase activity | |||
EOOGHDJN_02515 | 4.1e-58 | sdrF | M | Collagen binding domain | ||
EOOGHDJN_02516 | 2.4e-159 | yicL | EG | EamA-like transporter family | ||
EOOGHDJN_02517 | 4.4e-129 | E | lipolytic protein G-D-S-L family | |||
EOOGHDJN_02518 | 3e-178 | 4.1.1.52 | S | Amidohydrolase | ||
EOOGHDJN_02519 | 2.1e-111 | K | Transcriptional regulator C-terminal region | |||
EOOGHDJN_02520 | 1.4e-47 | 3.6.4.12 | K | HxlR-like helix-turn-helix | ||
EOOGHDJN_02521 | 1.7e-162 | ypbG | 2.7.1.2 | GK | ROK family | |
EOOGHDJN_02522 | 0.0 | lmrA | 3.6.3.44 | V | ABC transporter | |
EOOGHDJN_02523 | 1.1e-95 | rmaB | K | Transcriptional regulator, MarR family | ||
EOOGHDJN_02524 | 1.5e-118 | drgA | C | Nitroreductase family | ||
EOOGHDJN_02525 | 0.0 | nagE | 2.7.1.193, 2.7.1.199, 2.7.1.211 | G | phosphotransferase system, EIIB | |
EOOGHDJN_02526 | 2.4e-116 | cmpC | S | ATPases associated with a variety of cellular activities | ||
EOOGHDJN_02527 | 1.9e-154 | WQ51_06230 | U | Belongs to the binding-protein-dependent transport system permease family | ||
EOOGHDJN_02528 | 5.1e-168 | XK27_00670 | S | ABC transporter | ||
EOOGHDJN_02529 | 4.4e-259 | |||||
EOOGHDJN_02530 | 8.6e-63 | |||||
EOOGHDJN_02531 | 2.5e-189 | S | Cell surface protein | |||
EOOGHDJN_02532 | 2.3e-91 | S | WxL domain surface cell wall-binding | |||
EOOGHDJN_02533 | 1.8e-97 | acuB | S | Domain in cystathionine beta-synthase and other proteins. | ||
EOOGHDJN_02534 | 3.3e-124 | livF | E | ABC transporter | ||
EOOGHDJN_02535 | 1.8e-139 | livG | E | Branched-chain amino acid ATP-binding cassette transporter | ||
EOOGHDJN_02536 | 1.2e-140 | livM | E | Branched-chain amino acid transport system / permease component | ||
EOOGHDJN_02537 | 6.5e-154 | livH | U | Branched-chain amino acid transport system / permease component | ||
EOOGHDJN_02538 | 5.4e-212 | livJ | E | Receptor family ligand binding region | ||
EOOGHDJN_02540 | 7e-33 | |||||
EOOGHDJN_02541 | 3.5e-114 | zmp3 | O | Zinc-dependent metalloprotease | ||
EOOGHDJN_02542 | 1.4e-81 | gtrA | S | GtrA-like protein | ||
EOOGHDJN_02543 | 1.6e-122 | K | Helix-turn-helix XRE-family like proteins | |||
EOOGHDJN_02544 | 4.1e-284 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
EOOGHDJN_02545 | 6.8e-72 | T | Belongs to the universal stress protein A family | |||
EOOGHDJN_02546 | 1.1e-46 | |||||
EOOGHDJN_02547 | 1.9e-116 | S | SNARE associated Golgi protein | |||
EOOGHDJN_02548 | 2e-49 | K | Transcriptional regulator, ArsR family | |||
EOOGHDJN_02549 | 1.2e-95 | cadD | P | Cadmium resistance transporter | ||
EOOGHDJN_02550 | 4.9e-30 | K | transcriptional regulator | |||
EOOGHDJN_02551 | 6.5e-50 | S | Protein of unknown function with HXXEE motif | |||
EOOGHDJN_02552 | 3e-106 | ps461 | M | Glycosyl hydrolases family 25 | ||
EOOGHDJN_02557 | 1.6e-21 | S | Protein of unknown function (DUF1617) | |||
EOOGHDJN_02558 | 6.3e-18 | sidC | GT2,GT4 | LM | DNA recombination | |
EOOGHDJN_02559 | 1.1e-92 | GT2,GT4 | M | cellulase activity | ||
EOOGHDJN_02560 | 1.6e-34 | S | Phage tail protein | |||
EOOGHDJN_02561 | 1.3e-136 | M | Phage tail tape measure protein TP901 | |||
EOOGHDJN_02564 | 6.9e-38 | S | Phage tail tube protein | |||
EOOGHDJN_02565 | 4.1e-21 | |||||
EOOGHDJN_02566 | 4.5e-33 | |||||
EOOGHDJN_02567 | 1.2e-24 | |||||
EOOGHDJN_02568 | 2e-17 | |||||
EOOGHDJN_02569 | 2e-113 | S | Phage capsid family | |||
EOOGHDJN_02570 | 8.2e-57 | clpP | 3.4.21.92 | OU | Clp protease | |
EOOGHDJN_02571 | 2.1e-104 | S | Phage portal protein | |||
EOOGHDJN_02572 | 2.4e-181 | S | Phage Terminase | |||
EOOGHDJN_02573 | 2.5e-14 | S | Phage terminase, small subunit | |||
EOOGHDJN_02576 | 2.9e-25 | V | HNH nucleases | |||
EOOGHDJN_02579 | 6.4e-22 | |||||
EOOGHDJN_02580 | 1.2e-35 | S | Domain of unknown function (DUF4393) | |||
EOOGHDJN_02586 | 1.2e-36 | S | hydrolase activity, acting on ester bonds | |||
EOOGHDJN_02587 | 2.4e-133 | S | Virulence-associated protein E | |||
EOOGHDJN_02588 | 9.9e-77 | S | Bifunctional DNA primase/polymerase, N-terminal | |||
EOOGHDJN_02589 | 2.4e-27 | |||||
EOOGHDJN_02590 | 1.2e-73 | L | AAA domain | |||
EOOGHDJN_02591 | 1.3e-10 | K | Helix-turn-helix XRE-family like proteins | |||
EOOGHDJN_02592 | 7.2e-176 | S | helicase activity | |||
EOOGHDJN_02593 | 3.1e-41 | S | Siphovirus Gp157 | |||
EOOGHDJN_02595 | 6e-25 | |||||
EOOGHDJN_02601 | 2.3e-27 | S | Domain of unknown function (DUF771) | |||
EOOGHDJN_02605 | 2.5e-19 | |||||
EOOGHDJN_02606 | 9.8e-62 | |||||
EOOGHDJN_02608 | 7.7e-26 | ps115 | K | Helix-turn-helix XRE-family like proteins | ||
EOOGHDJN_02609 | 1.8e-28 | S | Pfam:DUF955 | |||
EOOGHDJN_02611 | 1e-47 | |||||
EOOGHDJN_02612 | 7.9e-96 | L | Belongs to the 'phage' integrase family | |||
EOOGHDJN_02613 | 5e-304 | U | Belongs to the BCCT transporter (TC 2.A.15) family | |||
EOOGHDJN_02614 | 0.0 | cadA | P | P-type ATPase | ||
EOOGHDJN_02616 | 2.7e-64 | yyaQ | S | YjbR | ||
EOOGHDJN_02617 | 7.9e-25 | S | Uncharacterized protein conserved in bacteria (DUF2325) | |||
EOOGHDJN_02618 | 1.4e-59 | S | Uncharacterized protein conserved in bacteria (DUF2325) | |||
EOOGHDJN_02619 | 0.0 | ade | 3.5.4.2 | F | Belongs to the metallo-dependent hydrolases superfamily. Adenine deaminase family | |
EOOGHDJN_02620 | 1.3e-199 | frlB | M | SIS domain | ||
EOOGHDJN_02621 | 1.2e-25 | 3.2.2.10 | S | Belongs to the LOG family | ||
EOOGHDJN_02622 | 1.5e-253 | nhaC | C | Na H antiporter NhaC | ||
EOOGHDJN_02623 | 1.8e-251 | cycA | E | Amino acid permease | ||
EOOGHDJN_02624 | 3e-167 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
EOOGHDJN_02625 | 7.3e-86 | pgpA | 3.1.3.27 | I | Phosphatidylglycerophosphatase A | |
EOOGHDJN_02626 | 9.7e-163 | azoB | GM | NmrA-like family | ||
EOOGHDJN_02627 | 5.8e-68 | K | Winged helix DNA-binding domain | |||
EOOGHDJN_02628 | 7e-71 | spx4 | 1.20.4.1 | P | ArsC family | |
EOOGHDJN_02629 | 1.7e-66 | yeaO | S | Protein of unknown function, DUF488 | ||
EOOGHDJN_02630 | 4e-53 | |||||
EOOGHDJN_02631 | 7e-214 | mutY | L | A G-specific adenine glycosylase | ||
EOOGHDJN_02632 | 1.9e-62 | |||||
EOOGHDJN_02633 | 1.3e-85 | |||||
EOOGHDJN_02634 | 2e-79 | hsp3 | O | Belongs to the small heat shock protein (HSP20) family | ||
EOOGHDJN_02635 | 3.5e-11 | |||||
EOOGHDJN_02636 | 2.1e-14 | |||||
EOOGHDJN_02637 | 4.3e-115 | GM | NmrA-like family | |||
EOOGHDJN_02638 | 1.3e-81 | elaA | S | GNAT family | ||
EOOGHDJN_02639 | 1.6e-158 | EG | EamA-like transporter family | |||
EOOGHDJN_02640 | 2.4e-119 | S | membrane | |||
EOOGHDJN_02641 | 1.4e-111 | S | VIT family | |||
EOOGHDJN_02642 | 1.1e-189 | pva2 | 3.5.1.24 | M | Linear amide C-N hydrolases, choloylglycine hydrolase family | |
EOOGHDJN_02643 | 0.0 | copB | 3.6.3.4 | P | P-type ATPase | |
EOOGHDJN_02644 | 4.7e-73 | copR | K | Copper transport repressor CopY TcrY | ||
EOOGHDJN_02645 | 7.4e-40 | |||||
EOOGHDJN_02646 | 7.7e-73 | S | COG NOG18757 non supervised orthologous group | |||
EOOGHDJN_02647 | 2.5e-248 | lmrB | EGP | Major facilitator Superfamily | ||
EOOGHDJN_02648 | 3.4e-25 | |||||
EOOGHDJN_02649 | 4.2e-49 | |||||
EOOGHDJN_02650 | 7.1e-65 | ycgX | S | Protein of unknown function (DUF1398) | ||
EOOGHDJN_02651 | 5.2e-251 | U | Belongs to the purine-cytosine permease (2.A.39) family | |||
EOOGHDJN_02652 | 5.9e-214 | mdtG | EGP | Major facilitator Superfamily | ||
EOOGHDJN_02653 | 1.8e-181 | D | Alpha beta | |||
EOOGHDJN_02654 | 1e-76 | M1-874 | K | Domain of unknown function (DUF1836) | ||
EOOGHDJN_02655 | 4.4e-35 | yyaN | K | MerR HTH family regulatory protein | ||
EOOGHDJN_02656 | 1.3e-120 | azlC | E | branched-chain amino acid | ||
EOOGHDJN_02657 | 7.2e-50 | azlD | S | Branched-chain amino acid transport protein (AzlD) | ||
EOOGHDJN_02658 | 0.0 | asnB | 6.3.5.4 | E | Asparagine synthase | |
EOOGHDJN_02659 | 1.6e-219 | dapG | 1.1.1.3, 2.7.2.4 | E | Amino acid kinase family | |
EOOGHDJN_02660 | 8e-282 | murE | 6.3.2.10, 6.3.2.13, 6.3.2.7 | M | Catalyzes the addition of an amino acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
EOOGHDJN_02661 | 1.5e-253 | xylP2 | G | symporter | ||
EOOGHDJN_02662 | 1e-190 | nlhH_1 | I | alpha/beta hydrolase fold | ||
EOOGHDJN_02663 | 5.6e-49 | |||||
EOOGHDJN_02664 | 5.9e-123 | pgm6 | 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | |
EOOGHDJN_02665 | 2.6e-103 | 3.2.2.20 | K | FR47-like protein | ||
EOOGHDJN_02666 | 1.3e-126 | yibF | S | overlaps another CDS with the same product name | ||
EOOGHDJN_02667 | 1.4e-218 | yibE | S | overlaps another CDS with the same product name | ||
EOOGHDJN_02668 | 3.9e-179 | |||||
EOOGHDJN_02669 | 1.3e-137 | S | NADPH-dependent FMN reductase | |||
EOOGHDJN_02670 | 1.5e-50 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
EOOGHDJN_02671 | 2.9e-162 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
EOOGHDJN_02672 | 0.0 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
EOOGHDJN_02673 | 4.1e-32 | L | leucine-zipper of insertion element IS481 | |||
EOOGHDJN_02674 | 8.5e-41 | |||||
EOOGHDJN_02675 | 1.5e-220 | 2.7.7.7, 3.6.4.12 | L | DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. The epsilon subunit contain the editing function and is a proofreading 3'-5' exonuclease | ||
EOOGHDJN_02676 | 4.8e-276 | pipD | E | Dipeptidase | ||
EOOGHDJN_02677 | 9.9e-199 | asnA | 6.3.1.1 | F | aspartate--ammonia ligase | |
EOOGHDJN_02678 | 3.4e-252 | asnS | 6.1.1.22 | J | Asparaginyl-tRNA synthetase | |
EOOGHDJN_02679 | 4.2e-115 | azoR | I | Catalyzes the reductive cleavage of azo bond in aromatic azo compounds to the corresponding amines. Requires NADH, but not NADPH, as an electron donor for its activity | ||
EOOGHDJN_02680 | 2.3e-81 | rmaD | K | Transcriptional regulator | ||
EOOGHDJN_02682 | 0.0 | 1.3.5.4 | C | FMN_bind | ||
EOOGHDJN_02683 | 9.5e-172 | K | Transcriptional regulator | |||
EOOGHDJN_02684 | 7.8e-97 | K | Helix-turn-helix domain | |||
EOOGHDJN_02685 | 4.5e-140 | K | sequence-specific DNA binding | |||
EOOGHDJN_02686 | 3.5e-88 | S | AAA domain | |||
EOOGHDJN_02688 | 0.0 | nagH | 2.7.13.3, 3.2.1.4, 3.2.1.52, 3.2.1.78, 3.2.1.8 | GH20,GH26,GH5,GH9 | M | MucBP domain |
EOOGHDJN_02689 | 1.8e-23 | XK27_09665 | 5.4.2.11 | G | Phosphoglycerate mutase family | |
EOOGHDJN_02690 | 1.8e-53 | XK27_09665 | 5.4.2.11 | G | Phosphoglycerate mutase family | |
EOOGHDJN_02691 | 1e-17 | |||||
EOOGHDJN_02692 | 3e-292 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
EOOGHDJN_02693 | 1.2e-188 | 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 | ||
EOOGHDJN_02694 | 1.2e-163 | hslO | O | Redox regulated molecular chaperone. Protects both thermally unfolding and oxidatively damaged proteins from irreversible aggregation. Plays an important role in the bacterial defense system toward oxidative stress | ||
EOOGHDJN_02695 | 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 | ||
EOOGHDJN_02696 | 1.7e-96 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
EOOGHDJN_02697 | 1e-251 | 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 | |
EOOGHDJN_02698 | 3.1e-74 | yabR | J | RNA binding | ||
EOOGHDJN_02699 | 1.1e-63 | divIC | D | Septum formation initiator | ||
EOOGHDJN_02701 | 2.2e-42 | yabO | J | S4 domain protein | ||
EOOGHDJN_02702 | 3.3e-289 | yabM | S | Polysaccharide biosynthesis protein | ||
EOOGHDJN_02703 | 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 | ||
EOOGHDJN_02704 | 1.5e-100 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
EOOGHDJN_02705 | 3.5e-177 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
EOOGHDJN_02706 | 1.4e-264 | S | Putative peptidoglycan binding domain | |||
EOOGHDJN_02707 | 2.1e-114 | S | (CBS) domain | |||
EOOGHDJN_02708 | 4.1e-84 | S | QueT transporter | |||
EOOGHDJN_02709 | 9.4e-189 | 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 | |
EOOGHDJN_02710 | 1e-215 | argD | 2.6.1.11, 2.6.1.17 | E | acetylornithine | |
EOOGHDJN_02711 | 9.4e-130 | argB | 2.7.2.8 | F | Belongs to the acetylglutamate kinase family. ArgB subfamily | |
EOOGHDJN_02712 | 2e-230 | 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 | |
EOOGHDJN_02713 | 6.1e-188 | 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 | |
EOOGHDJN_02714 | 7e-203 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
EOOGHDJN_02715 | 0.0 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
EOOGHDJN_02716 | 5e-134 | P | ATPases associated with a variety of cellular activities | |||
EOOGHDJN_02717 | 2.2e-129 | ssuC2 | U | Binding-protein-dependent transport system inner membrane component | ||
EOOGHDJN_02718 | 2.9e-193 | P | ABC transporter, substratebinding protein | |||
EOOGHDJN_02719 | 0.0 | kup | P | Transport of potassium into the cell | ||
EOOGHDJN_02720 | 2.3e-63 | ndoA | L | Toxic component of a toxin-antitoxin (TA) module | ||
EOOGHDJN_02721 | 4.9e-215 | alr | 5.1.1.1 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
EOOGHDJN_02722 | 1e-60 | acpS | 2.7.6.3, 2.7.8.7, 5.1.1.1 | I | Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein | |
EOOGHDJN_02723 | 2e-106 | 3.2.2.20 | K | acetyltransferase | ||
EOOGHDJN_02724 | 7.8e-296 | S | ABC transporter, ATP-binding protein | |||
EOOGHDJN_02725 | 8.6e-218 | 2.7.7.65 | T | diguanylate cyclase | ||
EOOGHDJN_02726 | 5.1e-34 | |||||
EOOGHDJN_02727 | 2e-35 | |||||
EOOGHDJN_02728 | 6.6e-81 | K | AsnC family | |||
EOOGHDJN_02729 | 2.8e-173 | ykfC | 3.4.14.13 | M | NlpC/P60 family | |
EOOGHDJN_02730 | 5.5e-158 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
EOOGHDJN_02732 | 3.8e-23 | |||||
EOOGHDJN_02733 | 9.4e-138 | 3.6.1.13, 3.6.1.55 | F | NUDIX domain | ||
EOOGHDJN_02734 | 9.8e-214 | yceI | EGP | Major facilitator Superfamily | ||
EOOGHDJN_02735 | 1.1e-47 | |||||
EOOGHDJN_02736 | 7.7e-92 | S | ECF-type riboflavin transporter, S component | |||
EOOGHDJN_02738 | 1.5e-169 | EG | EamA-like transporter family | |||
EOOGHDJN_02739 | 8.9e-38 | gcvR | T | Belongs to the UPF0237 family | ||
EOOGHDJN_02740 | 3e-243 | XK27_08635 | S | UPF0210 protein | ||
EOOGHDJN_02741 | 1.6e-134 | K | response regulator | |||
EOOGHDJN_02742 | 2.9e-287 | yclK | 2.7.13.3 | T | Histidine kinase | |
EOOGHDJN_02743 | 4.7e-216 | ywbD | 2.1.1.191 | J | S-adenosylmethionine-dependent methyltransferase | |
EOOGHDJN_02744 | 9.7e-155 | glcU | U | sugar transport | ||
EOOGHDJN_02745 | 3.9e-259 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
EOOGHDJN_02746 | 6.8e-24 | |||||
EOOGHDJN_02747 | 0.0 | macB3 | V | ABC transporter, ATP-binding protein | ||
EOOGHDJN_02748 | 2.9e-274 | tagE | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 |
EOOGHDJN_02749 | 0.0 | msbA2 | 3.6.3.44 | P | ABC transporter transmembrane region | |
EOOGHDJN_02750 | 1.6e-16 | |||||
EOOGHDJN_02751 | 1.9e-18 | |||||
EOOGHDJN_02752 | 1.6e-16 | |||||
EOOGHDJN_02753 | 1.6e-16 | |||||
EOOGHDJN_02754 | 1.6e-16 | |||||
EOOGHDJN_02755 | 1.1e-18 | |||||
EOOGHDJN_02756 | 5.2e-15 | |||||
EOOGHDJN_02757 | 7.2e-17 | |||||
EOOGHDJN_02758 | 2.7e-16 | |||||
EOOGHDJN_02759 | 0.0 | M | MucBP domain | |||
EOOGHDJN_02760 | 0.0 | bztC | D | nuclear chromosome segregation | ||
EOOGHDJN_02761 | 7.3e-83 | K | MarR family | |||
EOOGHDJN_02762 | 1.4e-43 | |||||
EOOGHDJN_02763 | 2e-38 | |||||
EOOGHDJN_02765 | 8.9e-30 | |||||
EOOGHDJN_02767 | 3.3e-115 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
EOOGHDJN_02768 | 1.6e-54 | ytzB | S | Peptidase propeptide and YPEB domain | ||
EOOGHDJN_02769 | 9e-121 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
EOOGHDJN_02770 | 3.2e-152 | ytmP | 2.7.1.89 | M | Choline/ethanolamine kinase | |
EOOGHDJN_02771 | 5.6e-225 | ecsB | U | ABC transporter | ||
EOOGHDJN_02772 | 1.6e-134 | ecsA | V | ABC transporter, ATP-binding protein | ||
EOOGHDJN_02773 | 9.9e-82 | hit | FG | histidine triad | ||
EOOGHDJN_02774 | 2e-42 | |||||
EOOGHDJN_02775 | 3.3e-129 | prsA | 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
EOOGHDJN_02776 | 3.5e-78 | S | WxL domain surface cell wall-binding | |||
EOOGHDJN_02777 | 2.4e-103 | S | WxL domain surface cell wall-binding | |||
EOOGHDJN_02778 | 1.4e-192 | S | Fn3-like domain | |||
EOOGHDJN_02779 | 2.7e-61 | |||||
EOOGHDJN_02780 | 0.0 | |||||
EOOGHDJN_02781 | 9.4e-242 | npr | 1.11.1.1 | C | NADH oxidase | |
EOOGHDJN_02782 | 3.3e-112 | K | Bacterial regulatory proteins, tetR family | |||
EOOGHDJN_02783 | 7.9e-117 | flpA | 4.1.99.16, 4.2.3.22, 4.2.3.75 | K | helix_turn_helix, cAMP Regulatory protein | |
EOOGHDJN_02784 | 1.4e-106 | |||||
EOOGHDJN_02785 | 4.6e-105 | GBS0088 | S | Nucleotidyltransferase | ||
EOOGHDJN_02786 | 2.1e-82 | 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 | |
EOOGHDJN_02787 | 2.5e-225 | ribBA | 3.5.4.25, 4.1.99.12 | H | Catalyzes the conversion of GTP to 2,5-diamino-6- ribosylamino-4(3H)-pyrimidinone 5'-phosphate (DARP), formate and pyrophosphate | |
EOOGHDJN_02788 | 1.8e-86 | ribE | 2.5.1.9, 3.5.4.25, 4.1.99.12 | H | Riboflavin synthase | |
EOOGHDJN_02789 | 1.2e-170 | 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 | |
EOOGHDJN_02790 | 0.0 | S | membrane | |||
EOOGHDJN_02791 | 2.6e-68 | S | NUDIX domain | |||
EOOGHDJN_02792 | 0.0 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
EOOGHDJN_02793 | 6.1e-185 | ykoT | GT2 | M | Glycosyl transferase family 2 | |
EOOGHDJN_02794 | 1e-268 | mutS | L | MutS domain V | ||
EOOGHDJN_02795 | 1e-271 | mutS | L | ATPase domain of DNA mismatch repair MUTS family | ||
EOOGHDJN_02796 | 1e-200 | 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 | |
EOOGHDJN_02797 | 0.0 | 3.6.3.6 | P | Cation transporter/ATPase, N-terminus | ||
EOOGHDJN_02798 | 5.6e-183 | celE | 3.2.1.4 | GH5,GH9 | E | GDSL-like Lipase/Acylhydrolase family |
EOOGHDJN_02799 | 2.4e-127 | ydcF | S | Gram-negative-bacterium-type cell wall biogenesis | ||
EOOGHDJN_02800 | 1.3e-136 | menG | 2.1.1.163, 2.1.1.201 | H | Methyltransferase required for the conversion of demethylmenaquinol (DMKH2) to menaquinol (MKH2) | |
EOOGHDJN_02801 | 1.2e-182 | yfeX | P | Peroxidase | ||
EOOGHDJN_02802 | 6.7e-99 | K | transcriptional regulator | |||
EOOGHDJN_02803 | 5.3e-160 | 4.1.1.46 | S | Amidohydrolase | ||
EOOGHDJN_02804 | 2.5e-52 | S | Uncharacterized protein conserved in bacteria (DUF2316) | |||
EOOGHDJN_02805 | 3e-40 | |||||
EOOGHDJN_02806 | 6.8e-53 | |||||
EOOGHDJN_02808 | 4.2e-62 | |||||
EOOGHDJN_02809 | 2.5e-53 | |||||
EOOGHDJN_02810 | 1.5e-75 | mltD | CBM50 | M | PFAM NLP P60 protein | |
EOOGHDJN_02811 | 2.1e-284 | gadB | 4.1.1.15 | E | Belongs to the group II decarboxylase family | |
EOOGHDJN_02812 | 1.8e-27 | |||||
EOOGHDJN_02813 | 0.0 | pckA | 4.1.1.49 | H | Phosphoenolpyruvate carboxykinase | |
EOOGHDJN_02814 | 2.4e-116 | luxT | K | Bacterial regulatory proteins, tetR family | ||
EOOGHDJN_02815 | 3.5e-88 | K | Winged helix DNA-binding domain | |||
EOOGHDJN_02816 | 1.5e-135 | T | Response regulator containing CheY-like receiver domain and AraC-type DNA-binding domain | |||
EOOGHDJN_02817 | 1.7e-129 | S | WxL domain surface cell wall-binding | |||
EOOGHDJN_02818 | 5.8e-186 | S | Bacterial protein of unknown function (DUF916) | |||
EOOGHDJN_02819 | 0.0 | |||||
EOOGHDJN_02820 | 1e-160 | ypuA | S | Protein of unknown function (DUF1002) | ||
EOOGHDJN_02821 | 5.5e-50 | yvlA | ||||
EOOGHDJN_02822 | 4.4e-95 | K | transcriptional regulator | |||
EOOGHDJN_02823 | 2.7e-91 | ymdB | S | Macro domain protein | ||
EOOGHDJN_02824 | 1.5e-147 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
EOOGHDJN_02825 | 2.3e-43 | S | Protein of unknown function (DUF1093) | |||
EOOGHDJN_02826 | 2e-77 | S | Threonine/Serine exporter, ThrE | |||
EOOGHDJN_02827 | 5e-131 | thrE | S | Putative threonine/serine exporter | ||
EOOGHDJN_02828 | 5.2e-164 | yvgN | C | Aldo keto reductase | ||
EOOGHDJN_02829 | 3.8e-152 | ywkB | S | Membrane transport protein | ||
EOOGHDJN_02830 | 2.1e-311 | cpdB | 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
EOOGHDJN_02831 | 0.0 | pacL3 | 3.6.3.8 | P | Cation transporter/ATPase, N-terminus | |
EOOGHDJN_02832 | 5.9e-85 | 2.4.2.6 | F | Nucleoside 2-deoxyribosyltransferase | ||
EOOGHDJN_02833 | 1.1e-245 | dsdA | 4.3.1.18 | E | Belongs to the serine threonine dehydratase family. DsdA subfamily | |
EOOGHDJN_02834 | 5.2e-294 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
EOOGHDJN_02835 | 3.3e-296 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
EOOGHDJN_02836 | 1.8e-54 | chbA | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose Cellobiose specific IIA subunit | |
EOOGHDJN_02837 | 2.3e-48 | pts20B | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
EOOGHDJN_02838 | 2e-129 | gntR | K | UTRA | ||
EOOGHDJN_02839 | 6.8e-141 | epsV | 2.7.8.12 | S | glycosyl transferase family 2 | |
EOOGHDJN_02840 | 6.5e-122 | pgm7 | 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | |
EOOGHDJN_02841 | 1.8e-81 | |||||
EOOGHDJN_02842 | 9.8e-152 | S | hydrolase | |||
EOOGHDJN_02843 | 6.5e-182 | panE | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
EOOGHDJN_02844 | 8.3e-152 | EG | EamA-like transporter family | |||
EOOGHDJN_02845 | 1.3e-176 | pdxB | 1.1.1.399, 1.1.1.95 | EH | D-isomer specific 2-hydroxyacid dehydrogenase, NAD binding domain | |
EOOGHDJN_02846 | 1.2e-100 | 1.5.1.40 | S | NADP oxidoreductase coenzyme F420-dependent | ||
EOOGHDJN_02847 | 4.5e-233 | |||||
EOOGHDJN_02848 | 1.1e-77 | fld | C | Flavodoxin | ||
EOOGHDJN_02849 | 0.0 | M | Bacterial Ig-like domain (group 3) | |||
EOOGHDJN_02850 | 1.1e-58 | M | Bacterial Ig-like domain (group 3) | |||
EOOGHDJN_02851 | 0.0 | M | Bacterial surface protein 26-residue PARCEL repeat (3 repeats) | |||
EOOGHDJN_02852 | 2.7e-32 | |||||
EOOGHDJN_02853 | 3.5e-127 | aroD | 1.1.1.25, 4.2.1.10 | E | Type I 3-dehydroquinase | |
EOOGHDJN_02854 | 2.2e-268 | ycaM | E | amino acid | ||
EOOGHDJN_02855 | 3.9e-78 | K | Winged helix DNA-binding domain | |||
EOOGHDJN_02856 | 7.3e-166 | S | Oxidoreductase, aldo keto reductase family protein | |||
EOOGHDJN_02857 | 5.7e-163 | akr5f | 1.1.1.346 | S | reductase | |
EOOGHDJN_02858 | 4.6e-163 | K | Transcriptional regulator | |||
EOOGHDJN_02860 | 5.5e-68 | |||||
EOOGHDJN_02861 | 1.4e-195 | |||||
EOOGHDJN_02862 | 6.5e-198 | M | MucBP domain | |||
EOOGHDJN_02863 | 7.1e-161 | lysR5 | K | LysR substrate binding domain | ||
EOOGHDJN_02864 | 5.5e-126 | yxaA | S | membrane transporter protein | ||
EOOGHDJN_02865 | 3.2e-57 | ywjH | S | Protein of unknown function (DUF1634) | ||
EOOGHDJN_02866 | 1.5e-308 | oppA | E | ABC transporter, substratebinding protein | ||
EOOGHDJN_02867 | 2.3e-165 | oppB | P | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
EOOGHDJN_02868 | 1.1e-189 | oppC | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
EOOGHDJN_02869 | 9.2e-203 | oppD | P | Belongs to the ABC transporter superfamily | ||
EOOGHDJN_02870 | 1.8e-181 | oppF | P | Belongs to the ABC transporter superfamily | ||
EOOGHDJN_02871 | 1e-63 | K | Winged helix DNA-binding domain | |||
EOOGHDJN_02872 | 1.6e-102 | L | Integrase | |||
EOOGHDJN_02873 | 0.0 | clpE | O | Belongs to the ClpA ClpB family | ||
EOOGHDJN_02874 | 6.5e-30 | |||||
EOOGHDJN_02875 | 2.7e-39 | ptsH | G | phosphocarrier protein HPR | ||
EOOGHDJN_02876 | 0.0 | ptsI | 2.7.3.9 | G | General (non sugar-specific) component of the phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS). This major carbohydrate active-transport system catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. Enzyme I transfers the phosphoryl group from phosphoenolpyruvate (PEP) to the phosphoryl carrier protein (HPr) | |
EOOGHDJN_02877 | 1.5e-222 | mgs | 2.4.1.337 | GT4 | M | Glycosyltransferase, group 1 family protein |
EOOGHDJN_02878 | 6.9e-200 | cpoA | GT4 | M | Glycosyltransferase, group 1 family protein | |
EOOGHDJN_02879 | 1.7e-188 | mprF | I | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms | ||
EOOGHDJN_02880 | 4.3e-228 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
EOOGHDJN_02881 | 1.8e-228 | patA | 2.6.1.1 | E | Aminotransferase | |
EOOGHDJN_02882 | 4e-34 | ykuJ | S | Protein of unknown function (DUF1797) | ||
EOOGHDJN_02883 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
EOOGHDJN_02884 | 1.6e-49 | N | Uncharacterized conserved protein (DUF2075) | |||
EOOGHDJN_02886 | 0.0 | pepN | 3.4.11.2 | E | aminopeptidase | |
EOOGHDJN_02887 | 8.4e-231 | S | PglZ domain | |||
EOOGHDJN_02888 | 6e-200 | V | site-specific DNA-methyltransferase (adenine-specific) activity | |||
EOOGHDJN_02889 | 1.7e-148 | L | Belongs to the 'phage' integrase family | |||
EOOGHDJN_02890 | 0.0 | 2.1.1.72 | LV | Eco57I restriction-modification methylase | ||
EOOGHDJN_02891 | 0.0 | FbpA | 3.1.21.3, 3.2.1.170 | GH38 | K | RNA-binding protein homologous to eukaryotic snRNP |
EOOGHDJN_02892 | 4.1e-72 | S | Domain of unknown function (DUF1788) | |||
EOOGHDJN_02893 | 3.8e-65 | S | Putative inner membrane protein (DUF1819) | |||
EOOGHDJN_02894 | 8.7e-149 | ram2 | 3.2.1.40 | G | Bacterial alpha-L-rhamnosidase 6 hairpin glycosidase domain | |
EOOGHDJN_02895 | 3.4e-47 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIA subunit | ||
EOOGHDJN_02896 | 6.3e-161 | yjdB | S | Domain of unknown function (DUF4767) | ||
EOOGHDJN_02897 | 3.5e-146 | Q | Fumarylacetoacetate (FAA) hydrolase family | |||
EOOGHDJN_02898 | 5.3e-72 | asp2 | S | Asp23 family, cell envelope-related function | ||
EOOGHDJN_02899 | 8.7e-72 | asp | S | Asp23 family, cell envelope-related function | ||
EOOGHDJN_02900 | 7.2e-23 | |||||
EOOGHDJN_02901 | 2.8e-83 | |||||
EOOGHDJN_02902 | 7.1e-37 | S | Transglycosylase associated protein | |||
EOOGHDJN_02903 | 8.3e-255 | fbp | 3.1.3.11 | G | phosphatase activity | |
EOOGHDJN_02905 | 1.2e-50 | L | Transposase and inactivated derivatives, IS30 family | |||
EOOGHDJN_02906 | 1.5e-84 | L | Integrase core domain | |||
EOOGHDJN_02907 | 8.9e-105 | L | Resolvase, N terminal domain | |||
EOOGHDJN_02908 | 5.2e-159 | ypjC | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
EOOGHDJN_02909 | 2.7e-103 | |||||
EOOGHDJN_02910 | 5.2e-122 | psaA | P | Belongs to the bacterial solute-binding protein 9 family | ||
EOOGHDJN_02911 | 1.5e-78 | lytH | 3.5.1.28 | M | N-acetylmuramoyl-L-alanine amidase | |
EOOGHDJN_02913 | 2.1e-31 | 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 | ||
EOOGHDJN_02914 | 2.3e-11 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
EOOGHDJN_02916 | 3.9e-160 | cycA | E | Amino acid permease | ||
EOOGHDJN_02917 | 4.6e-70 | cycA | E | Amino acid permease | ||
EOOGHDJN_02919 | 2.3e-56 | T | Belongs to the universal stress protein A family | |||
EOOGHDJN_02920 | 1.1e-249 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
EOOGHDJN_02921 | 3.9e-47 | sirR | K | Helix-turn-helix diphteria tox regulatory element | ||
EOOGHDJN_02923 | 6.9e-17 | |||||
EOOGHDJN_02924 | 1.1e-293 | norB | EGP | Major Facilitator | ||
EOOGHDJN_02925 | 5.6e-98 | K | Bacterial regulatory proteins, tetR family | |||
EOOGHDJN_02926 | 6e-52 | L | Helix-turn-helix domain of Hin and related proteins, a family of DNA-binding domains unique to bacteria and represented by the Hin protein of Salmonella. The basic HTH domain is a simple fold comprised of three core helices that form a right-handed | |||
EOOGHDJN_02930 | 1.4e-90 | apt | 2.4.2.22, 2.4.2.7 | F | Phosphoribosyl transferase domain | |
EOOGHDJN_02931 | 8.9e-182 | P | secondary active sulfate transmembrane transporter activity | |||
EOOGHDJN_02932 | 5.8e-94 | |||||
EOOGHDJN_02933 | 2e-94 | K | Acetyltransferase (GNAT) domain | |||
EOOGHDJN_02934 | 1.3e-156 | T | Calcineurin-like phosphoesterase superfamily domain | |||
EOOGHDJN_02937 | 9.8e-231 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
EOOGHDJN_02938 | 5.8e-188 | hemH | 4.99.1.1, 4.99.1.9 | H | Catalyzes the ferrous insertion into protoporphyrin IX | |
EOOGHDJN_02939 | 4.3e-253 | mmuP | E | amino acid | ||
EOOGHDJN_02940 | 8.3e-168 | mmuM | 1.5.1.20, 2.1.1.10 | H | homocysteine S-methyltransferase | |
EOOGHDJN_02941 | 1.9e-291 | tagE1 | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 |
EOOGHDJN_02942 | 1.6e-121 | |||||
EOOGHDJN_02943 | 4.1e-212 | 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 | |
EOOGHDJN_02944 | 1.4e-278 | bmr3 | EGP | Major facilitator Superfamily | ||
EOOGHDJN_02946 | 9.8e-71 | |||||
EOOGHDJN_02947 | 6.7e-99 | |||||
EOOGHDJN_02951 | 2.9e-35 | osmC | O | OsmC-like protein | ||
EOOGHDJN_02952 | 8.2e-41 | osmC | O | OsmC-like protein | ||
EOOGHDJN_02953 | 1.1e-66 | slyA | K | helix_turn_helix multiple antibiotic resistance protein | ||
EOOGHDJN_02955 | 4e-163 | gor | 1.8.1.7 | C | Pyridine nucleotide-disulphide oxidoreductase | |
EOOGHDJN_02956 | 5.1e-45 | trxA | O | Belongs to the thioredoxin family | ||
EOOGHDJN_02958 | 5.7e-99 | frnE | Q | dithiol-disulfide isomerase involved in polyketide biosynthesis | ||
EOOGHDJN_02959 | 4.4e-137 | trxB | 1.8.1.9 | O | Glucose inhibited division protein A | |
EOOGHDJN_02960 | 1e-20 | CO | cell redox homeostasis | |||
EOOGHDJN_02961 | 4.8e-75 | M1-798 | K | Rhodanese Homology Domain | ||
EOOGHDJN_02962 | 2.7e-242 | G | Glycosyl hydrolases family 32 | |||
EOOGHDJN_02963 | 1.7e-38 | |||||
EOOGHDJN_02964 | 1.4e-134 | levD | G | PTS system mannose/fructose/sorbose family IID component | ||
EOOGHDJN_02965 | 1.4e-137 | M | PTS system sorbose-specific iic component | |||
EOOGHDJN_02966 | 6.6e-79 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | ||
EOOGHDJN_02967 | 9.6e-42 | levA | G | PTS system fructose IIA component | ||
EOOGHDJN_02968 | 7.7e-301 | K | Sigma-54 interaction domain | |||
EOOGHDJN_02970 | 2.2e-218 | |||||
EOOGHDJN_02971 | 3.5e-154 | tagG | U | Transport permease protein | ||
EOOGHDJN_02972 | 1e-201 | tagH | 3.6.3.38, 3.6.3.40 | GM | Part of the ABC transporter complex TagGH involved in teichoic acids export. Responsible for energy coupling to the transport system | |
EOOGHDJN_02973 | 3.8e-44 | |||||
EOOGHDJN_02974 | 1.6e-91 | K | Transcriptional regulator PadR-like family | |||
EOOGHDJN_02975 | 2.1e-258 | P | Major Facilitator Superfamily | |||
EOOGHDJN_02976 | 4.7e-241 | amtB | P | ammonium transporter | ||
EOOGHDJN_02977 | 4.8e-179 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
EOOGHDJN_02978 | 3.7e-44 | |||||
EOOGHDJN_02979 | 1.8e-101 | zmp1 | O | Zinc-dependent metalloprotease | ||
EOOGHDJN_02980 | 2.7e-120 | rpiA | 5.3.1.6 | G | Ribose 5-phosphate isomerase A (phosphoriboisomerase A) | |
EOOGHDJN_02981 | 3.1e-310 | mco | Q | Multicopper oxidase | ||
EOOGHDJN_02982 | 3.2e-54 | ypaA | S | Protein of unknown function (DUF1304) | ||
EOOGHDJN_02983 | 8.8e-95 | yxkA | S | Phosphatidylethanolamine-binding protein | ||
EOOGHDJN_02984 | 1.1e-231 | flhF | N | Uncharacterized conserved protein (DUF2075) | ||
EOOGHDJN_02985 | 9.3e-83 | ywnA | K | Winged helix-turn-helix transcription repressor, HrcA DNA-binding | ||
EOOGHDJN_02986 | 9.3e-80 | |||||
EOOGHDJN_02987 | 5.4e-69 | accB | 2.3.1.12 | I | first, biotin carboxylase catalyzes the carboxylation of the carrier protein and then the transcarboxylase transfers the carboxyl group to form malonyl-CoA | |
EOOGHDJN_02988 | 3.8e-173 | rihC | 3.2.2.1 | F | Nucleoside | |
EOOGHDJN_02989 | 1.1e-161 | vdlC | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | ||
EOOGHDJN_02990 | 4.7e-114 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
EOOGHDJN_02991 | 2.4e-231 | 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 | |
EOOGHDJN_02992 | 5.9e-191 | ywlC | 2.7.7.87, 3.1.3.48 | J | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine | |
EOOGHDJN_02993 | 1.9e-158 | prmB | 2.1.1.297, 2.1.1.298 | J | Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif | |
EOOGHDJN_02994 | 1.2e-197 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
EOOGHDJN_02995 | 9.3e-109 | tdk | 2.7.1.21 | F | thymidine kinase | |
EOOGHDJN_02996 | 1.5e-263 | murF | 6.3.2.10, 6.3.2.13 | M | Domain of unknown function (DUF1727) | |
EOOGHDJN_02997 | 5.9e-137 | cobQ | S | glutamine amidotransferase | ||
EOOGHDJN_02998 | 9.8e-196 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
EOOGHDJN_02999 | 6.9e-192 | ampC | V | Beta-lactamase | ||
EOOGHDJN_03000 | 1.2e-28 | |||||
EOOGHDJN_03001 | 1.2e-202 | ilvE | 2.6.1.42 | E | Branched-chain amino acid aminotransferase | |
EOOGHDJN_03002 | 1.9e-58 | |||||
EOOGHDJN_03003 | 6.3e-126 | |||||
EOOGHDJN_03004 | 0.0 | yfiC | V | ABC transporter | ||
EOOGHDJN_03005 | 0.0 | ycfI | V | ABC transporter, ATP-binding protein | ||
EOOGHDJN_03006 | 1.6e-67 | S | Protein of unknown function (DUF1093) | |||
EOOGHDJN_03007 | 3.8e-135 | yxkH | G | Polysaccharide deacetylase | ||
EOOGHDJN_03009 | 0.0 | mutL | L | This protein is involved in the repair of mismatches in DNA. It is required for dam-dependent methyl-directed DNA mismatch repair. May act as a molecular matchmaker , a protein that promotes the formation of a stable complex between two or more DNA-binding proteins in an ATP-dependent manner without itself being part of a final effector complex | ||
EOOGHDJN_03010 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
EOOGHDJN_03011 | 2.7e-154 | ymdB | S | YmdB-like protein | ||
EOOGHDJN_03012 | 2.1e-216 | rny | S | Endoribonuclease that initiates mRNA decay | ||
EOOGHDJN_03013 | 3.3e-190 | 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 | ||
EOOGHDJN_03014 | 1.9e-231 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
EOOGHDJN_03015 | 3.7e-97 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
EOOGHDJN_03016 | 5.7e-110 | ymfM | S | Helix-turn-helix domain | ||
EOOGHDJN_03017 | 2.9e-251 | ymfH | S | Peptidase M16 | ||
EOOGHDJN_03018 | 4.2e-231 | ymfF | S | Peptidase M16 inactive domain protein | ||
EOOGHDJN_03019 | 3.8e-254 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
EOOGHDJN_03020 | 2.6e-31 | L | Transposase and inactivated derivatives, IS30 family | |||
EOOGHDJN_03021 | 5e-217 | yifK | E | Amino acid permease | ||
EOOGHDJN_03022 | 1.9e-27 | |||||
EOOGHDJN_03023 | 4.8e-80 | L | Integrase | |||
EOOGHDJN_03024 | 2.5e-56 | S | Phage derived protein Gp49-like (DUF891) | |||
EOOGHDJN_03025 | 3.8e-39 | K | Helix-turn-helix domain | |||
EOOGHDJN_03026 | 7.2e-90 | |||||
EOOGHDJN_03027 | 6.2e-22 | S | Small integral membrane protein (DUF2273) | |||
EOOGHDJN_03028 | 7.7e-73 | S | Asp23 family, cell envelope-related function | |||
EOOGHDJN_03029 | 1.3e-11 | S | Transglycosylase associated protein | |||
EOOGHDJN_03030 | 3.8e-16 | |||||
EOOGHDJN_03031 | 3e-248 | uvrX | 2.7.7.7 | L | Belongs to the DNA polymerase type-Y family | |
EOOGHDJN_03032 | 1.8e-53 | |||||
EOOGHDJN_03033 | 2.3e-63 | |||||
EOOGHDJN_03034 | 1.8e-170 | hprA | 1.1.1.29 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
EOOGHDJN_03035 | 5.3e-193 | L | Psort location Cytoplasmic, score | |||
EOOGHDJN_03036 | 3.4e-32 | |||||
EOOGHDJN_03037 | 4.7e-66 | M | ErfK YbiS YcfS YnhG | |||
EOOGHDJN_03038 | 1e-95 | acmD | 3.2.1.17 | NU | Bacterial SH3 domain | |
EOOGHDJN_03039 | 2.4e-136 | K | Helix-turn-helix domain | |||
EOOGHDJN_03040 | 7.8e-17 | K | Helix-turn-helix domain | |||
EOOGHDJN_03042 | 2.4e-58 | S | Protein of unknown function (DUF2992) | |||
EOOGHDJN_03043 | 3.2e-53 | K | Helix-turn-helix XRE-family like proteins | |||
EOOGHDJN_03044 | 0.0 | uvrA2 | L | ABC transporter | ||
EOOGHDJN_03045 | 8.6e-43 | papX3 | K | Transcriptional regulator | ||
EOOGHDJN_03046 | 1.1e-56 | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
EOOGHDJN_03047 | 1.4e-40 | K | prlF antitoxin for toxin YhaV_toxin | |||
EOOGHDJN_03048 | 3.6e-108 | L | Integrase | |||
EOOGHDJN_03049 | 2.2e-112 | |||||
EOOGHDJN_03050 | 4.2e-161 | S | MobA/MobL family | |||
EOOGHDJN_03053 | 9.4e-16 | |||||
EOOGHDJN_03054 | 6.8e-234 | gshF | 6.3.2.2 | H | Belongs to the glutamate--cysteine ligase type 1 family | |
EOOGHDJN_03055 | 3e-89 | 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 | |
EOOGHDJN_03056 | 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 | |
EOOGHDJN_03057 | 4.7e-249 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
EOOGHDJN_03058 | 6.6e-116 | radC | L | DNA repair protein | ||
EOOGHDJN_03059 | 2.8e-161 | mreB | D | cell shape determining protein MreB | ||
EOOGHDJN_03060 | 9.9e-144 | mreC | M | Involved in formation and maintenance of cell shape | ||
EOOGHDJN_03061 | 1.2e-88 | mreD | M | rod shape-determining protein MreD | ||
EOOGHDJN_03062 | 1.1e-116 | minC | D | Cell division inhibitor that blocks the formation of polar Z ring septums. Rapidly oscillates between the poles of the cell to destabilize FtsZ filaments that have formed before they mature into polar Z rings. Prevents FtsZ polymerization | ||
EOOGHDJN_03063 | 1e-145 | minD | D | Belongs to the ParA family | ||
EOOGHDJN_03064 | 4.6e-109 | glnP | P | ABC transporter permease | ||
EOOGHDJN_03065 | 2.5e-115 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
EOOGHDJN_03066 | 1.5e-155 | aatB | ET | ABC transporter substrate-binding protein | ||
EOOGHDJN_03067 | 1.6e-115 | S | Protein of unknown function (DUF554) | |||
EOOGHDJN_03068 | 6.4e-148 | KT | helix_turn_helix, mercury resistance | |||
EOOGHDJN_03069 | 1.7e-227 | gltP | U | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
EOOGHDJN_03070 | 6.6e-95 | S | Protein of unknown function (DUF1440) | |||
EOOGHDJN_03071 | 1.9e-171 | hrtB | V | ABC transporter permease | ||
EOOGHDJN_03072 | 5.6e-121 | devA | 3.6.3.25 | V | ABC transporter, ATP-binding protein | |
EOOGHDJN_03073 | 3.7e-91 | 2.7.7.65 | T | phosphorelay sensor kinase activity | ||
EOOGHDJN_03074 | 4.2e-186 | iunH | 3.2.2.1 | F | Inosine-uridine preferring nucleoside hydrolase | |
EOOGHDJN_03075 | 1.1e-98 | 1.5.1.3 | H | RibD C-terminal domain | ||
EOOGHDJN_03076 | 5.9e-187 | napA | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
EOOGHDJN_03077 | 7.5e-110 | S | Membrane | |||
EOOGHDJN_03078 | 1.2e-155 | mleP3 | S | Membrane transport protein | ||
EOOGHDJN_03079 | 1.7e-257 | aspA | 4.2.1.2, 4.3.1.1 | E | Fumarase C C-terminus | |
EOOGHDJN_03080 | 1.8e-92 | ogt | 2.1.1.63 | L | Methyltransferase | |
EOOGHDJN_03081 | 7e-54 | lytE | M | LysM domain | ||
EOOGHDJN_03082 | 7.3e-36 | lytE | M | LysM domain protein | ||
EOOGHDJN_03083 | 1.8e-268 | tagE6 | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 |
EOOGHDJN_03084 | 2.4e-297 | tagE5 | 2.4.1.52 | GT4 | M | Poly(Glycerol-phosphate) alpha-glucosyltransferase |
EOOGHDJN_03085 | 3.7e-151 | rlrG | K | Transcriptional regulator | ||
EOOGHDJN_03086 | 9.3e-173 | S | Conserved hypothetical protein 698 | |||
EOOGHDJN_03087 | 2.1e-102 | rimL | J | Acetyltransferase (GNAT) domain | ||
EOOGHDJN_03088 | 1.4e-76 | S | Domain of unknown function (DUF4811) | |||
EOOGHDJN_03089 | 1.1e-270 | lmrB | EGP | Major facilitator Superfamily | ||
EOOGHDJN_03090 | 1.9e-126 | hadL | 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | |
EOOGHDJN_03091 | 4.4e-182 | ynfM | EGP | Major facilitator Superfamily | ||
EOOGHDJN_03092 | 1.5e-49 | |||||
EOOGHDJN_03093 | 6.6e-105 | |||||
EOOGHDJN_03094 | 7.4e-50 | S | Cag pathogenicity island, type IV secretory system | |||
EOOGHDJN_03095 | 2.5e-35 | |||||
EOOGHDJN_03096 | 3.4e-115 | |||||
EOOGHDJN_03097 | 0.0 | traE | U | type IV secretory pathway VirB4 | ||
EOOGHDJN_03098 | 1.1e-232 | polC | 2.4.1.129, 2.7.7.7, 3.4.16.4 | GT51 | S | WXG100 protein secretion system (Wss), protein YukC |
EOOGHDJN_03099 | 9.2e-209 | M | CHAP domain | |||
EOOGHDJN_03100 | 3.7e-87 | |||||
EOOGHDJN_03101 | 1.4e-54 | CO | COG0526, thiol-disulfide isomerase and thioredoxins | |||
EOOGHDJN_03102 | 5.6e-80 | |||||
EOOGHDJN_03103 | 1e-268 | traK | U | TraM recognition site of TraD and TraG | ||
EOOGHDJN_03104 | 5.7e-62 | |||||
EOOGHDJN_03105 | 3.5e-149 | |||||
EOOGHDJN_03106 | 3.7e-67 | |||||
EOOGHDJN_03107 | 7.1e-59 | yafQ | S | Bacterial toxin of type II toxin-antitoxin system, YafQ | ||
EOOGHDJN_03108 | 1.7e-44 | yefM | 2.3.1.15 | D | Antitoxin component of a toxin-antitoxin (TA) module | |
EOOGHDJN_03109 | 3.4e-106 | L | Integrase | |||
EOOGHDJN_03110 | 1.2e-55 | |||||
EOOGHDJN_03112 | 0.0 | cadA | 3.6.3.3, 3.6.3.5 | P | P-type ATPase | |
EOOGHDJN_03113 | 1.4e-141 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
EOOGHDJN_03114 | 6e-08 | S | Enterocin A Immunity | |||
EOOGHDJN_03115 | 2.1e-54 | txlA | O | Thioredoxin-like domain | ||
EOOGHDJN_03116 | 1.1e-38 | yrkD | S | Metal-sensitive transcriptional repressor | ||
EOOGHDJN_03117 | 3.8e-17 | |||||
EOOGHDJN_03118 | 2.8e-94 | dps | P | Belongs to the Dps family | ||
EOOGHDJN_03119 | 1.6e-32 | copZ | P | Heavy-metal-associated domain | ||
EOOGHDJN_03120 | 3.3e-118 | 4.1.99.16, 4.2.3.22, 4.2.3.75 | K | Transcriptional regulator, Crp Fnr family | ||
EOOGHDJN_03121 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
EOOGHDJN_03123 | 2.3e-16 | |||||
EOOGHDJN_03124 | 4.1e-15 | L | Phage-associated protein | |||
EOOGHDJN_03125 | 1.6e-31 | S | Phage terminase, small subunit | |||
EOOGHDJN_03126 | 4.9e-251 | terL | S | overlaps another CDS with the same product name | ||
EOOGHDJN_03128 | 9.5e-112 | S | Phage portal protein | |||
EOOGHDJN_03129 | 9.6e-182 | S | Phage capsid family | |||
EOOGHDJN_03131 | 5.1e-07 | |||||
EOOGHDJN_03132 | 1.4e-95 | V | VanZ like family | |||
EOOGHDJN_03133 | 5e-195 | blaA6 | V | Beta-lactamase | ||
EOOGHDJN_03134 | 0.0 | pflB | 2.3.1.54 | C | Pyruvate formate lyase-like | |
EOOGHDJN_03135 | 6.7e-161 | pflA | 1.97.1.4 | C | Activation of pyruvate formate-lyase under anaerobic conditions by generation of an organic free radical, using S- adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine | |
EOOGHDJN_03136 | 5.1e-53 | yitW | S | Pfam:DUF59 | ||
EOOGHDJN_03137 | 7.7e-174 | S | Aldo keto reductase | |||
EOOGHDJN_03138 | 3.3e-97 | FG | HIT domain | |||
EOOGHDJN_03139 | 2e-36 | S | Bacteriocin-protection, YdeI or OmpD-Associated | |||
EOOGHDJN_03140 | 1.4e-77 | |||||
EOOGHDJN_03141 | 6.2e-122 | E | GDSL-like Lipase/Acylhydrolase family | |||
EOOGHDJN_03142 | 1.2e-85 | L | HTH-like domain | |||
EOOGHDJN_03143 | 1.6e-157 | scrK | 2.7.1.2, 2.7.1.4 | GK | ROK family | |
EOOGHDJN_03144 | 7.8e-108 | scrR3 | K | Transcriptional regulator, LacI family | ||
EOOGHDJN_03145 | 3.9e-189 | rafB | P | LacY proton/sugar symporter | ||
EOOGHDJN_03146 | 3.4e-181 | cscA | 3.2.1.26 | GH32 | G | invertase |
EOOGHDJN_03147 | 4.4e-291 | L | Transposase IS66 family | |||
EOOGHDJN_03148 | 1.3e-57 | XK27_01125 | L | PFAM IS66 Orf2 family protein | ||
EOOGHDJN_03149 | 9e-26 | |||||
EOOGHDJN_03150 | 4.9e-57 | pemK | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | ||
EOOGHDJN_03151 | 4.8e-44 | T | Antidote-toxin recognition MazE, bacterial antitoxin | |||
EOOGHDJN_03152 | 4.4e-106 | L | Integrase | |||
EOOGHDJN_03153 | 2.2e-81 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |||
EOOGHDJN_03154 | 2.7e-39 | |||||
EOOGHDJN_03155 | 0.0 | nagE | 2.7.1.193, 2.7.1.199, 2.7.1.211 | G | phosphotransferase system, EIIB | |
EOOGHDJN_03156 | 9.6e-191 | panE1 | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
EOOGHDJN_03157 | 1.3e-162 | degV | S | Uncharacterised protein, DegV family COG1307 | ||
EOOGHDJN_03158 | 7.3e-231 | hom1 | 1.1.1.3 | E | Homoserine dehydrogenase | |
EOOGHDJN_03159 | 2.6e-244 | metY | 2.5.1.49 | E | Catalyzes the formation of L-methionine and acetate from O-acetyl-L-homoserine and methanethiol | |
EOOGHDJN_03160 | 4.8e-165 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to | |
EOOGHDJN_03161 | 1.1e-92 | yueI | S | Protein of unknown function (DUF1694) | ||
EOOGHDJN_03162 | 5.9e-143 | yvpB | S | Peptidase_C39 like family | ||
EOOGHDJN_03163 | 2.8e-161 | M | Glycosyl hydrolases family 25 | |||
EOOGHDJN_03164 | 1e-111 | |||||
EOOGHDJN_03165 | 1.5e-241 | 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) | |
EOOGHDJN_03166 | 1.8e-84 | hmpT | S | Pfam:DUF3816 | ||
EOOGHDJN_03167 | 2.8e-32 | |||||
EOOGHDJN_03168 | 1.6e-181 | L | Psort location Cytoplasmic, score | |||
EOOGHDJN_03169 | 8.7e-145 | cdr | P | Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain | ||
EOOGHDJN_03170 | 2.5e-32 | arsR | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
EOOGHDJN_03171 | 1.5e-178 | arsB | U | Involved in arsenical resistance. Thought to form the channel of an arsenite pump | ||
EOOGHDJN_03174 | 1.4e-176 | XK27_08835 | S | ABC transporter | ||
EOOGHDJN_03175 | 1.9e-153 | XK27_08840 | U | Belongs to the binding-protein-dependent transport system permease family | ||
EOOGHDJN_03176 | 6.4e-137 | XK27_08845 | S | ABC transporter, ATP-binding protein | ||
EOOGHDJN_03177 | 7.4e-258 | npr | 1.11.1.1 | C | NADH oxidase | |
EOOGHDJN_03178 | 1.9e-46 | L | Transposase | |||
EOOGHDJN_03179 | 1.4e-169 | L | Integrase core domain | |||
EOOGHDJN_03180 | 4.8e-132 | D | CobQ CobB MinD ParA nucleotide binding domain protein | |||
EOOGHDJN_03182 | 1e-78 | repA | S | Replication initiator protein A | ||
EOOGHDJN_03183 | 6.2e-42 | relB | L | Addiction module antitoxin, RelB DinJ family | ||
EOOGHDJN_03184 | 5.9e-28 | |||||
EOOGHDJN_03185 | 5.5e-46 | |||||
EOOGHDJN_03186 | 6e-58 | |||||
EOOGHDJN_03187 | 2.5e-163 | |||||
EOOGHDJN_03188 | 1.3e-72 | K | Transcriptional regulator | |||
EOOGHDJN_03189 | 0.0 | pepF2 | E | Oligopeptidase F | ||
EOOGHDJN_03190 | 7e-175 | D | Alpha beta | |||
EOOGHDJN_03191 | 3.8e-31 | copZ | P | Heavy-metal-associated domain | ||
EOOGHDJN_03192 | 2.7e-171 | L | Transposase and inactivated derivatives, IS30 family DNA replication, recombination, and repair | |||
EOOGHDJN_03193 | 3.7e-301 | ybeC | E | amino acid | ||
EOOGHDJN_03194 | 1.5e-194 | L | Transposase and inactivated derivatives, IS30 family | |||
EOOGHDJN_03195 | 8.9e-50 | tnpR | L | Resolvase, N terminal domain | ||
EOOGHDJN_03196 | 0.0 | cadA | 3.6.3.3, 3.6.3.5 | P | P-type ATPase | |
EOOGHDJN_03197 | 6.3e-142 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
EOOGHDJN_03198 | 1.5e-55 | txlA | O | Thioredoxin-like domain | ||
EOOGHDJN_03199 | 4.3e-40 | yrkD | S | Metal-sensitive transcriptional repressor | ||
EOOGHDJN_03200 | 1.2e-18 | |||||
EOOGHDJN_03201 | 1.7e-72 | |||||
EOOGHDJN_03202 | 2.2e-210 | M | Glycosyl transferase family 2 | |||
EOOGHDJN_03203 | 5.8e-63 | K | helix_turn_helix multiple antibiotic resistance protein | |||
EOOGHDJN_03205 | 1.8e-162 | L | Replication protein | |||
EOOGHDJN_03206 | 2.7e-29 | pre | D | Plasmid recombination enzyme | ||
EOOGHDJN_03207 | 1.5e-42 | S | COG NOG38524 non supervised orthologous group | |||
EOOGHDJN_03208 | 1.3e-38 | |||||
EOOGHDJN_03210 | 1.3e-249 | EGP | Major facilitator Superfamily | |||
EOOGHDJN_03211 | 3.5e-64 | |||||
EOOGHDJN_03212 | 1.6e-75 | yugI | 5.3.1.9 | J | general stress protein | |
EOOGHDJN_03213 | 2.7e-108 | ppiB | 5.2.1.8 | G | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
EOOGHDJN_03214 | 3e-119 | dedA | S | SNARE-like domain protein | ||
EOOGHDJN_03215 | 3e-70 | V | ABC transporter | |||
EOOGHDJN_03216 | 3.1e-116 | K | Transcriptional regulator | |||
EOOGHDJN_03217 | 3.4e-95 | pncB | 6.3.4.21 | F | Catalyzes the synthesis of beta-nicotinate D- ribonucleotide from nicotinate and 5-phospho-D-ribose 1-phosphate at the expense of ATP | |
EOOGHDJN_03218 | 1.2e-23 | S | Family of unknown function (DUF5388) | |||
EOOGHDJN_03219 | 1.6e-143 | soj | D | CobQ CobB MinD ParA nucleotide binding domain protein | ||
EOOGHDJN_03221 | 7.1e-121 | S | Plasmid replication protein | |||
EOOGHDJN_03222 | 2.4e-37 | L | Transposase | |||
EOOGHDJN_03223 | 6.1e-85 | tnp2PF3 | L | Transposase | ||
EOOGHDJN_03224 | 2.7e-143 | D | CobQ CobB MinD ParA nucleotide binding domain protein | |||
EOOGHDJN_03227 | 3.2e-124 | tnp | L | DDE domain | ||
EOOGHDJN_03228 | 1.2e-27 | S | Protein of unknown function (DUF1093) | |||
EOOGHDJN_03229 | 5.3e-133 | V | AAA domain, putative AbiEii toxin, Type IV TA system | |||
EOOGHDJN_03238 | 3.2e-36 | 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 | |
EOOGHDJN_03239 | 3.4e-53 | eda | 4.1.2.14, 4.1.3.42 | G | KDPG and KHG aldolase | |
EOOGHDJN_03240 | 5.2e-24 | S | Polysaccharide biosynthesis protein | |||
EOOGHDJN_03242 | 4.1e-27 | S | Protein of unknown function (DUF2969) | |||
EOOGHDJN_03244 | 3.6e-16 | bcr1 | EGP | Sugar (and other) transporter | ||
EOOGHDJN_03245 | 1.8e-42 | comEC | S | Competence protein | ||
EOOGHDJN_03246 | 4.7e-35 | XK27_10405 | S | Bacterial membrane protein YfhO | ||
EOOGHDJN_03247 | 2.5e-27 | |||||
EOOGHDJN_03248 | 3.1e-41 | |||||
EOOGHDJN_03249 | 2.8e-28 | cspD | K | 'Cold-shock' DNA-binding domain | ||
EOOGHDJN_03250 | 1.9e-74 | fabZ | 3.5.1.108, 4.2.1.59 | I | Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs | |
EOOGHDJN_03251 | 1.1e-29 | glnP | P | Bacterial periplasmic substrate-binding proteins | ||
EOOGHDJN_03252 | 4.6e-16 | U | Relaxase/Mobilisation nuclease domain | |||
EOOGHDJN_03253 | 9.8e-39 | licD | M | LicD family | ||
EOOGHDJN_03254 | 2e-56 | traI | 5.99.1.2 | L | This gene contains a nucleotide ambiguity which may be the result of a sequencing error | |
EOOGHDJN_03255 | 1.9e-56 | tcyN | 3.6.3.21 | E | abc transporter atp-binding protein | |
EOOGHDJN_03256 | 5.9e-36 | S | Protein of unknown function (DUF3021) |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)