ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
GCKIAGNM_00001 | 1.1e-29 | L | PFAM Integrase catalytic | |||
GCKIAGNM_00002 | 8.5e-44 | yoeB | S | YoeB-like toxin of bacterial type II toxin-antitoxin system | ||
GCKIAGNM_00003 | 2.4e-32 | relB | L | RelB antitoxin | ||
GCKIAGNM_00004 | 1e-245 | argH | 4.3.2.1 | E | argininosuccinate lyase | |
GCKIAGNM_00005 | 1.2e-28 | thiS | 2.8.1.10 | H | ThiS family | |
GCKIAGNM_00006 | 4.8e-115 | thiG | 2.8.1.10 | H | Catalyzes the rearrangement of 1-deoxy-D-xylulose 5- phosphate (DXP) to produce the thiazole phosphate moiety of thiamine. Sulfur is provided by the thiocarboxylate moiety of the carrier protein ThiS. In vitro, sulfur can be provided by H(2)S | |
GCKIAGNM_00007 | 2e-25 | thiG | 2.8.1.10 | H | Catalyzes the rearrangement of 1-deoxy-D-xylulose 5- phosphate (DXP) to produce the thiazole phosphate moiety of thiamine. Sulfur is provided by the thiocarboxylate moiety of the carrier protein ThiS. In vitro, sulfur can be provided by H(2)S | |
GCKIAGNM_00008 | 1.2e-56 | moeB | 2.7.7.80 | H | ThiF family | |
GCKIAGNM_00009 | 8.4e-78 | moeB | 2.7.7.80 | H | ThiF family | |
GCKIAGNM_00010 | 3.1e-71 | M1-798 | P | Rhodanese Homology Domain | ||
GCKIAGNM_00011 | 1.7e-56 | 6.1.1.14 | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
GCKIAGNM_00012 | 2.8e-19 | 6.1.1.14 | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
GCKIAGNM_00013 | 7.4e-138 | S | Putative ABC-transporter type IV | |||
GCKIAGNM_00014 | 9.1e-82 | S | Protein of unknown function (DUF975) | |||
GCKIAGNM_00015 | 4.4e-42 | 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) | |
GCKIAGNM_00016 | 1.2e-92 | 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) | |
GCKIAGNM_00017 | 1.2e-153 | L | Tetratricopeptide repeat | |||
GCKIAGNM_00018 | 5.1e-198 | yutF | 3.1.3.41 | G | Haloacid dehalogenase-like hydrolase | |
GCKIAGNM_00020 | 6.7e-139 | tlyA | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
GCKIAGNM_00021 | 1.5e-42 | |||||
GCKIAGNM_00022 | 1.3e-49 | trkA | P | TrkA-N domain | ||
GCKIAGNM_00023 | 1.9e-41 | trkB | P | Cation transport protein | ||
GCKIAGNM_00024 | 4e-88 | nadK | 2.7.1.23 | H | Involved in the regulation of the intracellular balance of NAD and NADP, and is a key enzyme in the biosynthesis of NADP. Catalyzes specifically the phosphorylation on 2'-hydroxyl of the adenosine moiety of NAD to yield NADP | |
GCKIAGNM_00025 | 2.5e-67 | nadK | 2.7.1.23 | H | Involved in the regulation of the intracellular balance of NAD and NADP, and is a key enzyme in the biosynthesis of NADP. Catalyzes specifically the phosphorylation on 2'-hydroxyl of the adenosine moiety of NAD to yield NADP | |
GCKIAGNM_00026 | 5.1e-307 | recN | L | May be involved in recombinational repair of damaged DNA | ||
GCKIAGNM_00027 | 1.5e-94 | S | Haloacid dehalogenase-like hydrolase | |||
GCKIAGNM_00028 | 4.8e-56 | J | Acetyltransferase (GNAT) domain | |||
GCKIAGNM_00029 | 5.8e-22 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
GCKIAGNM_00030 | 2.2e-24 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
GCKIAGNM_00031 | 8.5e-173 | V | ATPases associated with a variety of cellular activities | |||
GCKIAGNM_00032 | 2.9e-120 | S | ABC-2 family transporter protein | |||
GCKIAGNM_00033 | 3.7e-107 | |||||
GCKIAGNM_00034 | 2.2e-09 | S | Psort location Cytoplasmic, score | |||
GCKIAGNM_00035 | 1.2e-154 | thrC | 4.2.3.1 | E | Threonine synthase N terminus | |
GCKIAGNM_00036 | 4.7e-112 | thrC | 4.2.3.1 | E | Threonine synthase N terminus | |
GCKIAGNM_00037 | 1.3e-58 | 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 | |
GCKIAGNM_00038 | 2.4e-96 | 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 | |
GCKIAGNM_00039 | 9.9e-28 | 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 | |
GCKIAGNM_00040 | 3e-96 | |||||
GCKIAGNM_00041 | 9.2e-138 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
GCKIAGNM_00042 | 5.2e-31 | ybbD | 3.2.1.52 | G | Glycosyl hydrolase family 3 N-terminal domain protein | |
GCKIAGNM_00044 | 5.1e-15 | ybbD | 3.2.1.52 | G | Glycosyl hydrolase family 3 N-terminal domain protein | |
GCKIAGNM_00045 | 2e-18 | ybbD | 3.2.1.52 | G | Glycosyl hydrolase family 3 N-terminal domain protein | |
GCKIAGNM_00046 | 3.8e-22 | ybbD | 3.2.1.52 | G | Glycosyl hydrolase family 3 N-terminal domain protein | |
GCKIAGNM_00047 | 4.9e-216 | S | Uncharacterised protein family (UPF0182) | |||
GCKIAGNM_00048 | 8.9e-104 | S | Uncharacterised protein family (UPF0182) | |||
GCKIAGNM_00049 | 2.5e-144 | S | Uncharacterised protein family (UPF0182) | |||
GCKIAGNM_00050 | 9.2e-12 | 2.3.1.183 | M | Acetyltransferase (GNAT) domain | ||
GCKIAGNM_00051 | 1.5e-114 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
GCKIAGNM_00052 | 7.7e-290 | 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 | ||
GCKIAGNM_00053 | 9.6e-305 | 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 | ||
GCKIAGNM_00054 | 6.2e-27 | 1.1.1.65 | C | Aldo/keto reductase family | ||
GCKIAGNM_00055 | 9.8e-82 | 1.1.1.65 | C | Aldo/keto reductase family | ||
GCKIAGNM_00056 | 6.9e-56 | 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 | |
GCKIAGNM_00057 | 2.3e-27 | 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 | |
GCKIAGNM_00058 | 1.6e-115 | 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 | |
GCKIAGNM_00059 | 8.1e-47 | divIC | D | Septum formation initiator | ||
GCKIAGNM_00060 | 1.6e-37 | ppx2 | 3.6.1.11, 3.6.1.40 | S | Protein of unknown function (DUF501) | |
GCKIAGNM_00061 | 1.4e-181 | ppx | 3.6.1.11, 3.6.1.40 | FP | Ppx/GppA phosphatase family | |
GCKIAGNM_00063 | 1.9e-19 | |||||
GCKIAGNM_00064 | 4.5e-62 | |||||
GCKIAGNM_00065 | 2.1e-151 | sdaA | 4.3.1.17 | E | Serine dehydratase alpha chain | |
GCKIAGNM_00066 | 9.9e-52 | sdaA | 4.3.1.17 | E | Serine dehydratase alpha chain | |
GCKIAGNM_00067 | 1.1e-56 | fkbP | 5.2.1.8 | G | Peptidyl-prolyl cis-trans | |
GCKIAGNM_00068 | 9.8e-80 | greA | K | Necessary for efficient RNA polymerase transcription elongation past template-encoded arresting sites. The arresting sites in DNA have the property of trapping a certain fraction of elongating RNA polymerases that pass through, resulting in locked ternary complexes. Cleavage of the nascent transcript by cleavage factors such as GreA or GreB allows the resumption of elongation from the new 3'terminus. GreA releases sequences of 2 to 3 nucleotides | ||
GCKIAGNM_00069 | 2e-38 | yplQ | S | Haemolysin-III related | ||
GCKIAGNM_00070 | 1.2e-79 | yplQ | S | Haemolysin-III related | ||
GCKIAGNM_00071 | 2.3e-08 | yplQ | S | Haemolysin-III related | ||
GCKIAGNM_00072 | 2.7e-43 | pdtaS | 2.7.13.3 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | |
GCKIAGNM_00073 | 2e-200 | pdtaS | 2.7.13.3 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | |
GCKIAGNM_00074 | 3.9e-10 | pdtaS | 2.7.13.3 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | |
GCKIAGNM_00075 | 4.9e-47 | whiB | K | Acts as a transcriptional regulator. Probably redox- responsive. The apo- but not holo-form probably binds DNA | ||
GCKIAGNM_00076 | 5.5e-245 | D | FtsK/SpoIIIE family | |||
GCKIAGNM_00077 | 2.5e-186 | K | Cell envelope-related transcriptional attenuator domain | |||
GCKIAGNM_00078 | 1.8e-55 | whiB | K | Acts as a transcriptional regulator. Probably redox- responsive. The apo- but not holo-form probably binds DNA | ||
GCKIAGNM_00079 | 3.4e-222 | S | Glycosyl transferase, family 2 | |||
GCKIAGNM_00080 | 8.8e-50 | S | Glycosyl transferase, family 2 | |||
GCKIAGNM_00081 | 3.2e-243 | S | Glycosyl transferase, family 2 | |||
GCKIAGNM_00082 | 1.5e-63 | |||||
GCKIAGNM_00083 | 7.1e-84 | |||||
GCKIAGNM_00084 | 1.6e-52 | |||||
GCKIAGNM_00085 | 6.3e-78 | MA20_43655 | 2.7.2.8 | S | Zincin-like metallopeptidase | |
GCKIAGNM_00086 | 5.5e-84 | cof | 5.2.1.8 | T | Eukaryotic phosphomannomutase | |
GCKIAGNM_00087 | 1.1e-19 | cof | 5.2.1.8 | T | Eukaryotic phosphomannomutase | |
GCKIAGNM_00088 | 5.8e-129 | ctsW | S | Phosphoribosyl transferase domain | ||
GCKIAGNM_00089 | 9.7e-191 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | |||
GCKIAGNM_00090 | 2.7e-273 | glgB | 2.4.1.18 | CBM48,GH13 | G | Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position |
GCKIAGNM_00091 | 3.4e-56 | glgB | 2.4.1.18 | CBM48,GH13 | G | Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position |
GCKIAGNM_00092 | 1.2e-29 | glgB | 2.4.1.18 | CBM48,GH13 | G | Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position |
GCKIAGNM_00093 | 1.9e-83 | carD | K | CarD-like/TRCF domain | ||
GCKIAGNM_00094 | 6.8e-57 | ispF | 2.1.1.228, 2.7.7.60, 4.6.1.12 | H | Involved in the biosynthesis of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP), two major building blocks of isoprenoid compounds. Catalyzes the conversion of 4- diphosphocytidyl-2-C-methyl-D-erythritol 2-phosphate (CDP-ME2P) to 2-C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-CPP) with a corresponding release of cytidine 5-monophosphate (CMP) | |
GCKIAGNM_00095 | 2.4e-120 | znuB | U | ABC 3 transport family | ||
GCKIAGNM_00096 | 3.8e-162 | znuC | P | ATPases associated with a variety of cellular activities | ||
GCKIAGNM_00097 | 3.7e-81 | P | Zinc-uptake complex component A periplasmic | |||
GCKIAGNM_00098 | 8.6e-32 | P | Zinc-uptake complex component A periplasmic | |||
GCKIAGNM_00099 | 1.5e-163 | 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 | |
GCKIAGNM_00100 | 4.7e-229 | rpsA | J | Ribosomal protein S1 | ||
GCKIAGNM_00101 | 1.8e-90 | coaE | 2.7.1.24 | H | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
GCKIAGNM_00102 | 1.3e-215 | 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 | ||
GCKIAGNM_00103 | 3.4e-152 | 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 | ||
GCKIAGNM_00104 | 2.1e-177 | terC | P | Integral membrane protein, TerC family | ||
GCKIAGNM_00105 | 3e-30 | pyk | 2.7.1.40 | G | Pyruvate kinase | |
GCKIAGNM_00106 | 1.3e-185 | pyk | 2.7.1.40 | G | Pyruvate kinase | |
GCKIAGNM_00107 | 1.1e-109 | aspA | 3.6.1.13 | L | NUDIX domain | |
GCKIAGNM_00109 | 2.8e-124 | pdtaR | T | Response regulator receiver domain protein | ||
GCKIAGNM_00110 | 1.7e-131 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
GCKIAGNM_00111 | 3.7e-288 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
GCKIAGNM_00112 | 4.6e-100 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
GCKIAGNM_00113 | 5.1e-178 | yqfO | 3.5.4.16 | L | NIF3 (NGG1p interacting factor 3) | |
GCKIAGNM_00114 | 1.2e-126 | 3.6.1.13 | L | NUDIX domain | ||
GCKIAGNM_00115 | 8.4e-66 | glgX | 3.2.1.68 | CBM48,GH13 | G | Belongs to the glycosyl hydrolase 13 family |
GCKIAGNM_00116 | 1.1e-179 | glgX | 3.2.1.68 | CBM48,GH13 | G | Belongs to the glycosyl hydrolase 13 family |
GCKIAGNM_00117 | 1.9e-118 | glgX | 3.2.1.68 | CBM48,GH13 | G | Belongs to the glycosyl hydrolase 13 family |
GCKIAGNM_00118 | 5.4e-25 | zntR | K | bacterial-type RNA polymerase transcription factor activity, metal ion regulated sequence-specific DNA binding | ||
GCKIAGNM_00119 | 1.1e-89 | K | Putative zinc ribbon domain | |||
GCKIAGNM_00120 | 9.4e-89 | S | GyrI-like small molecule binding domain | |||
GCKIAGNM_00121 | 3.3e-07 | S | GyrI-like small molecule binding domain | |||
GCKIAGNM_00123 | 2.1e-20 | tag | 3.2.2.20 | L | Methyladenine glycosylase | |
GCKIAGNM_00125 | 1.3e-122 | |||||
GCKIAGNM_00126 | 1.7e-213 | ykiI | ||||
GCKIAGNM_00127 | 3.5e-252 | aroA | 2.5.1.19 | E | Catalyzes the transfer of the enolpyruvyl moiety of phosphoenolpyruvate (PEP) to the 5-hydroxyl of shikimate-3- phosphate (S3P) to produce enolpyruvyl shikimate-3-phosphate and inorganic phosphate | |
GCKIAGNM_00128 | 8.1e-111 | ackA | 2.7.2.1, 2.7.2.15 | H | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
GCKIAGNM_00129 | 7.5e-83 | ackA | 2.7.2.1, 2.7.2.15 | H | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
GCKIAGNM_00130 | 4.3e-225 | pta | 1.1.1.40, 2.3.1.19, 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
GCKIAGNM_00131 | 5e-79 | pta | 1.1.1.40, 2.3.1.19, 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
GCKIAGNM_00133 | 9.1e-192 | 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) | |
GCKIAGNM_00134 | 0.0 | XK27_09800 | I | Psort location CytoplasmicMembrane, score 9.99 | ||
GCKIAGNM_00137 | 1.6e-28 | |||||
GCKIAGNM_00138 | 1.3e-19 | KL | Type III restriction enzyme res subunit | |||
GCKIAGNM_00139 | 7.2e-58 | KL | Type III restriction enzyme res subunit | |||
GCKIAGNM_00140 | 3.6e-41 | KL | Type III restriction enzyme res subunit | |||
GCKIAGNM_00141 | 1.9e-139 | 2.1.1.72, 3.1.21.3, 3.1.21.4 | V | T5orf172 | ||
GCKIAGNM_00142 | 8.4e-12 | 2.1.1.72, 3.1.21.3, 3.1.21.4 | V | T5orf172 | ||
GCKIAGNM_00143 | 4.3e-36 | 2.1.1.72, 3.1.21.4 | L | restriction endonuclease | ||
GCKIAGNM_00144 | 1.8e-40 | |||||
GCKIAGNM_00145 | 2.1e-172 | pip | S | YhgE Pip domain protein | ||
GCKIAGNM_00146 | 2.3e-19 | pip | S | YhgE Pip domain protein | ||
GCKIAGNM_00147 | 4.6e-38 | pip | S | YhgE Pip domain protein | ||
GCKIAGNM_00148 | 1.3e-214 | pip | S | YhgE Pip domain protein | ||
GCKIAGNM_00149 | 4.2e-67 | pip | S | YhgE Pip domain protein | ||
GCKIAGNM_00150 | 3e-122 | nfrA | 1.5.1.38, 1.5.1.39 | C | Nitroreductase family | |
GCKIAGNM_00151 | 4.4e-59 | S | Protein of unknown function (DUF4235) | |||
GCKIAGNM_00152 | 8.4e-136 | G | Phosphoglycerate mutase family | |||
GCKIAGNM_00153 | 6.4e-140 | amyE | G | Bacterial extracellular solute-binding protein | ||
GCKIAGNM_00154 | 1.2e-79 | amyE | G | Bacterial extracellular solute-binding protein | ||
GCKIAGNM_00155 | 1.4e-184 | K | Psort location Cytoplasmic, score | |||
GCKIAGNM_00156 | 1.4e-35 | malC | G | Binding-protein-dependent transport system inner membrane component | ||
GCKIAGNM_00157 | 1.4e-75 | msmF | G | Binding-protein-dependent transport system inner membrane component | ||
GCKIAGNM_00158 | 6.3e-74 | rafG | G | ABC transporter permease | ||
GCKIAGNM_00159 | 2.3e-66 | rafG | G | ABC transporter permease | ||
GCKIAGNM_00160 | 2e-81 | S | Protein of unknown function, DUF624 | |||
GCKIAGNM_00161 | 7.5e-15 | aroP | E | aromatic amino acid transport protein AroP K03293 | ||
GCKIAGNM_00162 | 1.3e-112 | aroP | E | aromatic amino acid transport protein AroP K03293 | ||
GCKIAGNM_00163 | 2.1e-12 | aroP | E | aromatic amino acid transport protein AroP K03293 | ||
GCKIAGNM_00164 | 3.3e-92 | aroP | E | aromatic amino acid transport protein AroP K03293 | ||
GCKIAGNM_00165 | 7.5e-129 | V | ABC transporter | |||
GCKIAGNM_00166 | 1.4e-178 | V | FtsX-like permease family | |||
GCKIAGNM_00168 | 3.9e-309 | V | FtsX-like permease family | |||
GCKIAGNM_00169 | 3.3e-155 | cycA | E | Amino acid permease | ||
GCKIAGNM_00170 | 7.5e-71 | cycA | E | Amino acid permease | ||
GCKIAGNM_00171 | 3.9e-90 | ydgJ | K | helix_turn_helix multiple antibiotic resistance protein | ||
GCKIAGNM_00172 | 0.0 | lmrA1 | V | ABC transporter, ATP-binding protein | ||
GCKIAGNM_00173 | 0.0 | lmrA2 | V | ABC transporter transmembrane region | ||
GCKIAGNM_00174 | 5.8e-29 | 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 | |
GCKIAGNM_00175 | 1.8e-120 | 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 | |
GCKIAGNM_00176 | 8.8e-33 | G | MFS/sugar transport protein | |||
GCKIAGNM_00177 | 9.9e-214 | G | MFS/sugar transport protein | |||
GCKIAGNM_00179 | 4.9e-148 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
GCKIAGNM_00180 | 2.3e-119 | |||||
GCKIAGNM_00181 | 6.4e-104 | metG | 6.1.1.10 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
GCKIAGNM_00182 | 1.6e-202 | metG | 6.1.1.10 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
GCKIAGNM_00183 | 2.4e-46 | |||||
GCKIAGNM_00184 | 4.1e-89 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
GCKIAGNM_00185 | 5.6e-42 | oppA | E | Bacterial extracellular solute-binding proteins, family 5 Middle | ||
GCKIAGNM_00186 | 2.6e-52 | oppA | E | Bacterial extracellular solute-binding proteins, family 5 Middle | ||
GCKIAGNM_00187 | 1.1e-42 | G | Glycosyl hydrolases family 43 | |||
GCKIAGNM_00188 | 3.9e-83 | S | Domain of unknown function (DUF4143) | |||
GCKIAGNM_00189 | 1.5e-129 | S | Domain of unknown function (DUF4143) | |||
GCKIAGNM_00190 | 2.3e-23 | S | ATPase domain predominantly from Archaea | |||
GCKIAGNM_00191 | 2.9e-200 | mdlA2 | V | ABC transporter | ||
GCKIAGNM_00192 | 5.5e-188 | yknV | V | ABC transporter | ||
GCKIAGNM_00193 | 3.2e-122 | yknV | V | ABC transporter | ||
GCKIAGNM_00194 | 9.1e-186 | tatD | L | TatD related DNase | ||
GCKIAGNM_00196 | 5.2e-66 | kup | P | Transport of potassium into the cell | ||
GCKIAGNM_00197 | 0.0 | kup | P | Transport of potassium into the cell | ||
GCKIAGNM_00198 | 5.5e-161 | S | Glutamine amidotransferase domain | |||
GCKIAGNM_00199 | 9.9e-143 | T | HD domain | |||
GCKIAGNM_00200 | 8.1e-184 | V | ABC transporter | |||
GCKIAGNM_00201 | 8.1e-47 | V | ABC transporter permease | |||
GCKIAGNM_00202 | 7.5e-195 | V | ABC transporter permease | |||
GCKIAGNM_00203 | 3.8e-225 | K | Cell envelope-related transcriptional attenuator domain | |||
GCKIAGNM_00204 | 6.7e-166 | lytC | 3.1.4.46, 3.2.1.17, 3.2.1.96 | M | Glycosyl hydrolases family 25 | |
GCKIAGNM_00205 | 5.2e-67 | M | L,D-transpeptidase catalytic domain | |||
GCKIAGNM_00206 | 4.8e-22 | M | nuclease | |||
GCKIAGNM_00207 | 8.5e-109 | rfbJ | M | Glycosyl transferase family 2 | ||
GCKIAGNM_00208 | 4e-153 | |||||
GCKIAGNM_00209 | 3.8e-45 | |||||
GCKIAGNM_00210 | 5e-154 | |||||
GCKIAGNM_00211 | 1.2e-86 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
GCKIAGNM_00212 | 8.6e-68 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
GCKIAGNM_00213 | 2.4e-286 | rmlC | 1.1.1.133, 5.1.3.13 | M | Catalyzes the reduction of dTDP-6-deoxy-L-lyxo-4- hexulose to yield dTDP-L-rhamnose | |
GCKIAGNM_00214 | 9.3e-158 | rfbA | 2.7.7.24 | H | Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis | |
GCKIAGNM_00215 | 4.7e-100 | rgpC | U | Transport permease protein | ||
GCKIAGNM_00216 | 1.1e-164 | rgpD | 3.6.3.38 | GM | ABC transporter, ATP-binding protein | |
GCKIAGNM_00217 | 1.2e-171 | GT2,GT4 | M | Glycosyl transferase family 2 | ||
GCKIAGNM_00218 | 0.0 | GT2,GT4 | M | Glycosyl transferase family 2 | ||
GCKIAGNM_00219 | 3.4e-100 | XK27_08315 | M | Psort location CytoplasmicMembrane, score 9.26 | ||
GCKIAGNM_00220 | 9.2e-53 | XK27_08315 | M | Psort location CytoplasmicMembrane, score 9.26 | ||
GCKIAGNM_00221 | 5.5e-144 | XK27_08315 | M | Psort location CytoplasmicMembrane, score 9.26 | ||
GCKIAGNM_00222 | 1.3e-100 | S | Predicted membrane protein (DUF2142) | |||
GCKIAGNM_00223 | 4.2e-27 | S | Predicted membrane protein (DUF2142) | |||
GCKIAGNM_00224 | 5.1e-181 | M | Glycosyltransferase like family 2 | |||
GCKIAGNM_00225 | 8.7e-37 | |||||
GCKIAGNM_00226 | 1.3e-40 | xylR | GK | ROK family | ||
GCKIAGNM_00227 | 2e-12 | xylR | GK | ROK family | ||
GCKIAGNM_00228 | 8.6e-167 | xylB | 1.1.1.57, 2.7.1.17 | G | Belongs to the FGGY kinase family | |
GCKIAGNM_00229 | 3e-61 | G | ABC-type sugar transport system periplasmic component | |||
GCKIAGNM_00230 | 1.3e-12 | araG_3 | 3.6.3.17 | G | Part of the ABC transporter complex RbsABC involved in ribose import. Responsible for energy coupling to the transport system | |
GCKIAGNM_00231 | 1.3e-100 | G | ATPases associated with a variety of cellular activities | |||
GCKIAGNM_00232 | 2.9e-73 | P | branched-chain amino acid ABC transporter, permease protein | |||
GCKIAGNM_00233 | 1.4e-59 | G | Branched-chain amino acid transport system / permease component | |||
GCKIAGNM_00234 | 3.6e-19 | 5.3.1.27 | G | sugar phosphate isomerase involved in capsule formation | ||
GCKIAGNM_00235 | 9.7e-213 | iscS1 | 2.8.1.7 | E | Aminotransferase class-V | |
GCKIAGNM_00236 | 5.9e-19 | naiP | U | Sugar (and other) transporter | ||
GCKIAGNM_00237 | 0.0 | V | FtsX-like permease family | |||
GCKIAGNM_00238 | 4.8e-137 | V | ATPases associated with a variety of cellular activities | |||
GCKIAGNM_00239 | 5.2e-102 | K | Virulence activator alpha C-term | |||
GCKIAGNM_00240 | 4.4e-189 | typA | T | Elongation factor G C-terminus | ||
GCKIAGNM_00241 | 1.2e-109 | typA | T | Elongation factor G C-terminus | ||
GCKIAGNM_00242 | 4e-46 | pheA | 1.3.1.12, 4.2.1.51, 5.4.99.5 | E | Prephenate dehydratase | |
GCKIAGNM_00243 | 1.4e-57 | pheA | 1.3.1.12, 4.2.1.51, 5.4.99.5 | E | Prephenate dehydratase | |
GCKIAGNM_00244 | 6.5e-190 | tyrA | 1.3.1.12, 1.3.1.43 | E | Prephenate dehydrogenase | |
GCKIAGNM_00245 | 2.8e-41 | |||||
GCKIAGNM_00246 | 7.3e-45 | MV | MacB-like periplasmic core domain | |||
GCKIAGNM_00247 | 1.9e-114 | MV | MacB-like periplasmic core domain | |||
GCKIAGNM_00248 | 2.8e-73 | MV | MacB-like periplasmic core domain | |||
GCKIAGNM_00249 | 2.6e-174 | MV | MacB-like periplasmic core domain | |||
GCKIAGNM_00250 | 8.2e-31 | V | ABC transporter, ATP-binding protein | |||
GCKIAGNM_00251 | 7.6e-101 | V | ABC transporter, ATP-binding protein | |||
GCKIAGNM_00252 | 5.4e-10 | xerC | D | Belongs to the 'phage' integrase family. XerC subfamily | ||
GCKIAGNM_00253 | 9.1e-128 | xerC | D | Belongs to the 'phage' integrase family. XerC subfamily | ||
GCKIAGNM_00254 | 9e-223 | E | ABC transporter, substrate-binding protein, family 5 | |||
GCKIAGNM_00255 | 1.4e-30 | E | ABC transporter, substrate-binding protein, family 5 | |||
GCKIAGNM_00256 | 2.6e-87 | dppB | EP | Binding-protein-dependent transport system inner membrane component | ||
GCKIAGNM_00257 | 3.2e-47 | dppB | EP | Binding-protein-dependent transport system inner membrane component | ||
GCKIAGNM_00259 | 3.4e-161 | dppC | EP | N-terminal TM domain of oligopeptide transport permease C | ||
GCKIAGNM_00260 | 5.9e-183 | dppD | EP | Oligopeptide/dipeptide transporter, C-terminal region | ||
GCKIAGNM_00261 | 3.1e-123 | dppD | EP | Oligopeptide/dipeptide transporter, C-terminal region | ||
GCKIAGNM_00262 | 1e-37 | dppD | EP | Oligopeptide/dipeptide transporter, C-terminal region | ||
GCKIAGNM_00263 | 3.3e-171 | exoA | 3.1.11.2 | L | Endonuclease/Exonuclease/phosphatase family | |
GCKIAGNM_00264 | 7.1e-150 | S | Protein of unknown function (DUF3710) | |||
GCKIAGNM_00265 | 3.8e-134 | S | Protein of unknown function (DUF3159) | |||
GCKIAGNM_00266 | 9e-242 | trmA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
GCKIAGNM_00267 | 2.2e-97 | |||||
GCKIAGNM_00268 | 1.2e-222 | ctpE | P | E1-E2 ATPase | ||
GCKIAGNM_00269 | 5.5e-220 | ctpE | P | E1-E2 ATPase | ||
GCKIAGNM_00270 | 5.3e-129 | acnA | 4.2.1.3 | C | Catalyzes the isomerization of citrate to isocitrate via cis-aconitate | |
GCKIAGNM_00271 | 3.4e-56 | acnA | 4.2.1.3 | C | Catalyzes the isomerization of citrate to isocitrate via cis-aconitate | |
GCKIAGNM_00272 | 1.6e-107 | acnA | 4.2.1.3 | C | Catalyzes the isomerization of citrate to isocitrate via cis-aconitate | |
GCKIAGNM_00273 | 2.2e-140 | acnA | 4.2.1.3 | C | Catalyzes the isomerization of citrate to isocitrate via cis-aconitate | |
GCKIAGNM_00274 | 9.5e-103 | E | Psort location Cytoplasmic, score 8.87 | |||
GCKIAGNM_00275 | 1.6e-111 | K | helix_turn_helix, Lux Regulon | |||
GCKIAGNM_00276 | 1.5e-136 | ybhL | S | Belongs to the BI1 family | ||
GCKIAGNM_00277 | 2.1e-166 | ydeD | EG | EamA-like transporter family | ||
GCKIAGNM_00278 | 1.9e-121 | relA2 | 2.7.6.5 | S | Region found in RelA / SpoT proteins | |
GCKIAGNM_00279 | 2.5e-59 | miaB | 2.8.4.3 | H | Catalyzes the methylthiolation of N6- (dimethylallyl)adenosine (i(6)A), leading to the formation of 2- methylthio-N6-(dimethylallyl)adenosine (ms(2)i(6)A) at position 37 in tRNAs that read codons beginning with uridine | |
GCKIAGNM_00280 | 4.8e-210 | miaB | 2.8.4.3 | H | Catalyzes the methylthiolation of N6- (dimethylallyl)adenosine (i(6)A), leading to the formation of 2- methylthio-N6-(dimethylallyl)adenosine (ms(2)i(6)A) at position 37 in tRNAs that read codons beginning with uridine | |
GCKIAGNM_00281 | 1.5e-50 | 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) | |
GCKIAGNM_00282 | 3.3e-61 | 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) | |
GCKIAGNM_00283 | 2.1e-150 | fic | D | Fic/DOC family | ||
GCKIAGNM_00284 | 1.9e-72 | ftsK | D | FtsK SpoIIIE family protein | ||
GCKIAGNM_00285 | 9.8e-72 | ftsK | D | FtsK SpoIIIE family protein | ||
GCKIAGNM_00286 | 1.1e-292 | ftsK | D | FtsK SpoIIIE family protein | ||
GCKIAGNM_00287 | 2.1e-117 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
GCKIAGNM_00288 | 1.5e-48 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
GCKIAGNM_00289 | 8.4e-23 | K | Helix-turn-helix XRE-family like proteins | |||
GCKIAGNM_00290 | 6.2e-36 | K | Helix-turn-helix XRE-family like proteins | |||
GCKIAGNM_00291 | 7e-39 | S | Protein of unknown function (DUF3046) | |||
GCKIAGNM_00292 | 2.4e-168 | 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 | ||
GCKIAGNM_00293 | 8.7e-102 | recX | S | Modulates RecA activity | ||
GCKIAGNM_00294 | 2.4e-113 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
GCKIAGNM_00295 | 1.4e-47 | 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 | ||
GCKIAGNM_00297 | 7e-207 | 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 | ||
GCKIAGNM_00298 | 8.8e-218 | 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 | ||
GCKIAGNM_00299 | 1.1e-22 | 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) | |
GCKIAGNM_00300 | 1.1e-156 | 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) | |
GCKIAGNM_00301 | 1.9e-22 | |||||
GCKIAGNM_00302 | 1.2e-83 | |||||
GCKIAGNM_00303 | 1e-125 | plsC2 | 2.3.1.51 | I | Phosphate acyltransferases | |
GCKIAGNM_00304 | 1.8e-72 | pknL | 2.7.11.1 | KLT | PASTA | |
GCKIAGNM_00305 | 7.7e-245 | pknL | 2.7.11.1 | KLT | PASTA | |
GCKIAGNM_00306 | 1.5e-44 | pknL | 2.7.11.1 | KLT | PASTA | |
GCKIAGNM_00307 | 4.2e-101 | crtE | 2.5.1.1, 2.5.1.10, 2.5.1.29 | H | Belongs to the FPP GGPP synthase family | |
GCKIAGNM_00308 | 8.4e-82 | crtE | 2.5.1.1, 2.5.1.10, 2.5.1.29 | H | Belongs to the FPP GGPP synthase family | |
GCKIAGNM_00309 | 2.4e-40 | |||||
GCKIAGNM_00310 | 8.9e-56 | |||||
GCKIAGNM_00311 | 8.2e-191 | 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 | ||
GCKIAGNM_00312 | 3.7e-137 | gyrB2 | 5.99.1.3 | L | DNA topoisomerase (ATP-hydrolyzing) | |
GCKIAGNM_00313 | 7.5e-269 | gyrB2 | 5.99.1.3 | L | DNA topoisomerase (ATP-hydrolyzing) | |
GCKIAGNM_00314 | 1.2e-144 | G | Major Facilitator Superfamily | |||
GCKIAGNM_00315 | 6e-55 | G | Major Facilitator Superfamily | |||
GCKIAGNM_00316 | 1.7e-171 | 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 | |
GCKIAGNM_00317 | 8.7e-74 | lhr | L | DEAD DEAH box helicase | ||
GCKIAGNM_00318 | 3.5e-68 | lhr | L | DEAD DEAH box helicase | ||
GCKIAGNM_00319 | 1.9e-143 | lhr | L | DEAD DEAH box helicase | ||
GCKIAGNM_00320 | 2.7e-106 | lhr | L | DEAD DEAH box helicase | ||
GCKIAGNM_00321 | 2.7e-35 | lhr | L | DEAD DEAH box helicase | ||
GCKIAGNM_00322 | 6.3e-260 | lhr | L | DEAD DEAH box helicase | ||
GCKIAGNM_00323 | 1.2e-48 | K | Psort location Cytoplasmic, score | |||
GCKIAGNM_00324 | 5.2e-43 | K | Psort location Cytoplasmic, score | |||
GCKIAGNM_00326 | 6.3e-128 | gyrA | 5.99.1.3 | L | DNA topoisomerase (ATP-hydrolyzing) | |
GCKIAGNM_00327 | 2.6e-35 | gyrA | 5.99.1.3 | L | DNA topoisomerase (ATP-hydrolyzing) | |
GCKIAGNM_00328 | 1.3e-71 | gyrA | 5.99.1.3 | L | DNA topoisomerase (ATP-hydrolyzing) | |
GCKIAGNM_00329 | 4.7e-79 | gyrA | 5.99.1.3 | L | DNA topoisomerase (ATP-hydrolyzing) | |
GCKIAGNM_00330 | 2.4e-116 | gyrA | 5.99.1.3 | L | DNA topoisomerase (ATP-hydrolyzing) | |
GCKIAGNM_00331 | 1.2e-18 | S | Type I phosphodiesterase / nucleotide pyrophosphatase | |||
GCKIAGNM_00332 | 4.9e-34 | S | Type I phosphodiesterase / nucleotide pyrophosphatase | |||
GCKIAGNM_00333 | 2e-140 | S | Type I phosphodiesterase / nucleotide pyrophosphatase | |||
GCKIAGNM_00334 | 2.9e-98 | S | Protein of unknown function (DUF3071) | |||
GCKIAGNM_00336 | 1.4e-47 | S | Domain of unknown function (DUF4193) | |||
GCKIAGNM_00337 | 3e-72 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | This enzyme is involved in nucleotide metabolism it produces dUMP, the immediate precursor of thymidine nucleotides and it decreases the intracellular concentration of dUTP so that uracil cannot be incorporated into DNA | |
GCKIAGNM_00338 | 0.0 | relA | 2.7.6.5, 3.1.7.2 | KT | In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance | |
GCKIAGNM_00339 | 2.8e-99 | ppiA | 5.2.1.8 | G | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
GCKIAGNM_00341 | 4.8e-97 | mntP | P | Probably functions as a manganese efflux pump | ||
GCKIAGNM_00342 | 2.8e-90 | ppa | 3.6.1.1 | C | Catalyzes the hydrolysis of inorganic pyrophosphate (PPi) forming two phosphate ions | |
GCKIAGNM_00343 | 1.4e-62 | glgE | 2.4.99.16 | GH13 | G | Maltosyltransferase that uses maltose 1-phosphate (M1P) as the sugar donor to elongate linear or branched alpha-(1- 4)- glucans. Is involved in a branched alpha-glucan biosynthetic pathway from trehalose, together with TreS, Mak and GlgB |
GCKIAGNM_00344 | 0.0 | glgE | 2.4.99.16 | GH13 | G | Maltosyltransferase that uses maltose 1-phosphate (M1P) as the sugar donor to elongate linear or branched alpha-(1- 4)- glucans. Is involved in a branched alpha-glucan biosynthetic pathway from trehalose, together with TreS, Mak and GlgB |
GCKIAGNM_00345 | 0.0 | K | RNA polymerase II activating transcription factor binding | |||
GCKIAGNM_00347 | 4.1e-88 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to L- homoserine, forming acetyl-L-homoserine | |
GCKIAGNM_00348 | 8.6e-72 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to L- homoserine, forming acetyl-L-homoserine | |
GCKIAGNM_00349 | 1.4e-09 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
GCKIAGNM_00350 | 2.5e-121 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
GCKIAGNM_00351 | 3.6e-29 | 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 | ||
GCKIAGNM_00352 | 1e-36 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
GCKIAGNM_00353 | 2.4e-150 | 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 | ||
GCKIAGNM_00354 | 4.3e-09 | 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 | |
GCKIAGNM_00355 | 8.3e-279 | atpA | 3.6.3.14 | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit | |
GCKIAGNM_00356 | 5.5e-164 | 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 | ||
GCKIAGNM_00357 | 6.1e-282 | 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 | |
GCKIAGNM_00358 | 1.7e-44 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
GCKIAGNM_00359 | 1.9e-11 | nucS | L | Cleaves both 3' and 5' ssDNA extremities of branched DNA structures | ||
GCKIAGNM_00360 | 6.2e-102 | nucS | L | Cleaves both 3' and 5' ssDNA extremities of branched DNA structures | ||
GCKIAGNM_00361 | 3.6e-158 | fkbB | 5.2.1.8 | M | FKBP-type peptidyl-prolyl cis-trans isomerase | |
GCKIAGNM_00362 | 1.7e-12 | |||||
GCKIAGNM_00363 | 1.3e-92 | |||||
GCKIAGNM_00364 | 1.7e-15 | |||||
GCKIAGNM_00365 | 3.4e-138 | |||||
GCKIAGNM_00366 | 5.6e-101 | trxA2 | O | Tetratricopeptide repeat | ||
GCKIAGNM_00367 | 3.4e-117 | cyaA | 4.6.1.1 | S | CYTH | |
GCKIAGNM_00370 | 3.6e-64 | psp1 | 3.5.99.10 | J | Endoribonuclease L-PSP | |
GCKIAGNM_00371 | 2.5e-188 | plsC2 | 2.3.1.51 | I | Phosphate acyltransferases | |
GCKIAGNM_00372 | 6.3e-114 | gpsA | 1.1.1.94 | I | NAD-dependent glycerol-3-phosphate dehydrogenase C-terminus | |
GCKIAGNM_00373 | 3.2e-157 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
GCKIAGNM_00374 | 1.6e-31 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
GCKIAGNM_00375 | 8.5e-23 | P | Bacterial extracellular solute-binding protein | |||
GCKIAGNM_00376 | 1e-18 | P | Bacterial extracellular solute-binding protein | |||
GCKIAGNM_00377 | 2.1e-111 | P | Bacterial extracellular solute-binding protein | |||
GCKIAGNM_00378 | 1.8e-148 | U | Binding-protein-dependent transport system inner membrane component | |||
GCKIAGNM_00379 | 2.4e-151 | U | Binding-protein-dependent transport system inner membrane component | |||
GCKIAGNM_00380 | 5.7e-239 | 3.6.3.30 | E | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | ||
GCKIAGNM_00381 | 3.7e-185 | S | CAAX protease self-immunity | |||
GCKIAGNM_00382 | 3.9e-24 | M | Mechanosensitive ion channel | |||
GCKIAGNM_00383 | 5.5e-100 | M | Mechanosensitive ion channel | |||
GCKIAGNM_00384 | 6.2e-108 | aspA | 4.3.1.1 | E | Fumarase C C-terminus | |
GCKIAGNM_00385 | 2.4e-124 | aspA | 4.3.1.1 | E | Fumarase C C-terminus | |
GCKIAGNM_00386 | 5e-11 | L | Transposase DDE domain | |||
GCKIAGNM_00387 | 2.9e-25 | S | Sulfite exporter TauE/SafE | |||
GCKIAGNM_00388 | 5.4e-57 | S | Sulfite exporter TauE/SafE | |||
GCKIAGNM_00389 | 2.5e-35 | aslB | C | Iron-sulfur cluster-binding domain | ||
GCKIAGNM_00390 | 6.6e-143 | aslB | C | Iron-sulfur cluster-binding domain | ||
GCKIAGNM_00391 | 3.5e-194 | K | helix_turn _helix lactose operon repressor | |||
GCKIAGNM_00392 | 4.7e-306 | Z012_09690 | P | Domain of unknown function (DUF4976) | ||
GCKIAGNM_00393 | 1.6e-29 | G | Bacterial extracellular solute-binding protein | |||
GCKIAGNM_00394 | 7.3e-49 | G | Bacterial extracellular solute-binding protein | |||
GCKIAGNM_00395 | 7.7e-85 | G | Bacterial extracellular solute-binding protein | |||
GCKIAGNM_00396 | 2.9e-165 | malC | P | Binding-protein-dependent transport system inner membrane component | ||
GCKIAGNM_00397 | 1.6e-177 | P | Binding-protein-dependent transport system inner membrane component | |||
GCKIAGNM_00398 | 2.2e-237 | S | AAA domain | |||
GCKIAGNM_00399 | 2.2e-27 | L | Transposase, Mutator family | |||
GCKIAGNM_00400 | 1.3e-106 | K | Bacterial regulatory proteins, tetR family | |||
GCKIAGNM_00401 | 1.3e-209 | MA20_36090 | S | Psort location Cytoplasmic, score 8.87 | ||
GCKIAGNM_00402 | 9.2e-46 | ogt | 2.1.1.63, 3.2.2.20 | L | Involved in the cellular defense against the biological effects of O6-methylguanine (O6-MeG) and O4-methylthymine (O4-MeT) in DNA. Repairs the methylated nucleobase in DNA by stoichiometrically transferring the methyl group to a cysteine residue in the enzyme. This is a suicide reaction the enzyme is irreversibly inactivated | |
GCKIAGNM_00403 | 8.3e-54 | acpS | 2.7.8.7, 3.2.1.52 | I | Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein | |
GCKIAGNM_00404 | 1.3e-70 | ams | 2.4.1.4, 3.2.1.1, 5.4.99.16 | GH13 | G | Alpha amylase, catalytic domain |
GCKIAGNM_00405 | 4.4e-17 | P | Sodium/hydrogen exchanger family | |||
GCKIAGNM_00407 | 1e-80 | |||||
GCKIAGNM_00408 | 1.1e-08 | Q | von Willebrand factor (vWF) type A domain | |||
GCKIAGNM_00409 | 0.0 | Q | von Willebrand factor (vWF) type A domain | |||
GCKIAGNM_00410 | 6.6e-38 | M | LPXTG cell wall anchor motif | |||
GCKIAGNM_00411 | 8.8e-38 | M | LPXTG cell wall anchor motif | |||
GCKIAGNM_00412 | 1.9e-44 | M | LPXTG cell wall anchor motif | |||
GCKIAGNM_00413 | 1.3e-39 | M | LPXTG cell wall anchor motif | |||
GCKIAGNM_00414 | 2e-15 | M | LPXTG cell wall anchor motif | |||
GCKIAGNM_00416 | 1.7e-27 | |||||
GCKIAGNM_00417 | 3.8e-18 | |||||
GCKIAGNM_00418 | 1.7e-109 | |||||
GCKIAGNM_00419 | 5.4e-26 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
GCKIAGNM_00420 | 4.3e-214 | pnp | 2.7.7.8 | J | Involved in mRNA degradation. Catalyzes the phosphorolysis of single-stranded polyribonucleotides processively in the 3'- to 5'-direction | |
GCKIAGNM_00421 | 1.1e-188 | pnp | 2.7.7.8 | J | Involved in mRNA degradation. Catalyzes the phosphorolysis of single-stranded polyribonucleotides processively in the 3'- to 5'-direction | |
GCKIAGNM_00422 | 1.8e-14 | V | ABC transporter, ATP-binding protein | |||
GCKIAGNM_00423 | 4.9e-30 | V | ABC transporter, ATP-binding protein | |||
GCKIAGNM_00424 | 2.7e-35 | V | ABC transporter, ATP-binding protein | |||
GCKIAGNM_00425 | 2e-33 | macB_7 | V | FtsX-like permease family | ||
GCKIAGNM_00426 | 2.4e-88 | lemA | S | LemA family | ||
GCKIAGNM_00427 | 1.7e-116 | S | Predicted membrane protein (DUF2207) | |||
GCKIAGNM_00428 | 6.2e-114 | S | Predicted membrane protein (DUF2207) | |||
GCKIAGNM_00429 | 1.3e-87 | S | Predicted membrane protein (DUF2207) | |||
GCKIAGNM_00430 | 2.1e-09 | S | Predicted membrane protein (DUF2207) | |||
GCKIAGNM_00431 | 2.6e-175 | S | Predicted membrane protein (DUF2207) | |||
GCKIAGNM_00432 | 2.5e-13 | |||||
GCKIAGNM_00433 | 2.4e-169 | 1.1.1.65 | C | Oxidoreductase, aldo keto reductase family protein | ||
GCKIAGNM_00434 | 8.7e-73 | iunH1 | 3.2.2.1 | F | Inosine-uridine preferring nucleoside hydrolase | |
GCKIAGNM_00435 | 5.7e-103 | iunH1 | 3.2.2.1 | F | Inosine-uridine preferring nucleoside hydrolase | |
GCKIAGNM_00436 | 1e-79 | 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 | ||
GCKIAGNM_00437 | 1e-34 | CP_0960 | S | Belongs to the UPF0109 family | ||
GCKIAGNM_00438 | 4.9e-31 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
GCKIAGNM_00439 | 4.8e-102 | S | Endonuclease/Exonuclease/phosphatase family | |||
GCKIAGNM_00440 | 3.7e-170 | 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 | |
GCKIAGNM_00441 | 2.3e-94 | bgl2 | 3.2.1.21 | GH3 | G | Fibronectin type III-like domain |
GCKIAGNM_00443 | 1.2e-45 | S | Nucleotidyltransferase domain | |||
GCKIAGNM_00444 | 2.6e-70 | S | Nucleotidyltransferase substrate binding protein like | |||
GCKIAGNM_00445 | 5e-211 | 3.2.1.58 | G | Belongs to the glycosyl hydrolase 5 (cellulase A) family | ||
GCKIAGNM_00446 | 1.5e-85 | K | Bacterial regulatory proteins, tetR family | |||
GCKIAGNM_00447 | 2.3e-186 | bglB | 3.2.1.21 | GH3 | G | Glycosyl hydrolase family 3 N-terminal domain protein |
GCKIAGNM_00448 | 1.1e-172 | bglB | 3.2.1.21 | GH3 | G | Glycosyl hydrolase family 3 N-terminal domain protein |
GCKIAGNM_00449 | 1.5e-35 | K | MarR family | |||
GCKIAGNM_00450 | 7.4e-43 | K | MarR family | |||
GCKIAGNM_00451 | 0.0 | V | ABC transporter, ATP-binding protein | |||
GCKIAGNM_00452 | 2.2e-188 | V | ABC transporter transmembrane region | |||
GCKIAGNM_00453 | 3.2e-175 | V | ABC transporter transmembrane region | |||
GCKIAGNM_00454 | 4.7e-47 | rbsR | K | helix_turn _helix lactose operon repressor | ||
GCKIAGNM_00455 | 5e-20 | rbsR | K | helix_turn _helix lactose operon repressor | ||
GCKIAGNM_00456 | 2.4e-43 | K | acetyltransferase | |||
GCKIAGNM_00457 | 2.6e-105 | rihB | 3.2.2.1 | F | Inosine-uridine preferring nucleoside hydrolase | |
GCKIAGNM_00458 | 2.3e-161 | dcuD | C | C4-dicarboxylate anaerobic carrier | ||
GCKIAGNM_00459 | 1.3e-152 | rbsK | 2.7.1.15 | H | Catalyzes the phosphorylation of ribose at O-5 in a reaction requiring ATP and magnesium. The resulting D-ribose-5- phosphate can then be used either for sythesis of nucleotides, histidine, and tryptophan, or as a component of the pentose phosphate pathway | |
GCKIAGNM_00460 | 4.9e-238 | 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) | |
GCKIAGNM_00461 | 1.1e-127 | 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) | |
GCKIAGNM_00462 | 1.4e-98 | 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) | |
GCKIAGNM_00463 | 4.8e-107 | 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) | |
GCKIAGNM_00464 | 2.1e-22 | 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) | |
GCKIAGNM_00465 | 1.3e-199 | P | Bacterial extracellular solute-binding protein | |||
GCKIAGNM_00466 | 7.2e-140 | U | Binding-protein-dependent transport system inner membrane component | |||
GCKIAGNM_00467 | 2.2e-160 | U | Binding-protein-dependent transport system inner membrane component | |||
GCKIAGNM_00468 | 2.1e-89 | 3.6.3.30 | E | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | ||
GCKIAGNM_00469 | 1.4e-101 | 3.6.3.30 | E | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | ||
GCKIAGNM_00470 | 1.4e-158 | I | type I phosphodiesterase nucleotide pyrophosphatase | |||
GCKIAGNM_00472 | 0.0 | hsdR | 3.1.21.3 | L | Subunit R is required for both nuclease and ATPase activities, but not for modification | |
GCKIAGNM_00473 | 2.5e-156 | hsdM | 2.1.1.72 | V | HsdM N-terminal domain | |
GCKIAGNM_00474 | 7.8e-76 | hsdM | 2.1.1.72 | V | HsdM N-terminal domain | |
GCKIAGNM_00475 | 1.1e-44 | hsdS | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | |
GCKIAGNM_00477 | 2.6e-49 | 3.1.21.3 | V | restriction modification system DNA specificity | ||
GCKIAGNM_00478 | 1.7e-94 | L | Belongs to the 'phage' integrase family | |||
GCKIAGNM_00480 | 3.9e-57 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | ||
GCKIAGNM_00481 | 2.9e-96 | 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 | |
GCKIAGNM_00482 | 3.8e-120 | 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 | |
GCKIAGNM_00483 | 4.2e-46 | rpoZ | 2.7.7.6 | K | Promotes RNA polymerase assembly. Latches the N- and C- terminal regions of the beta' subunit thereby facilitating its interaction with the beta and alpha subunits | |
GCKIAGNM_00484 | 0.0 | ilvD | 4.2.1.9 | H | Belongs to the IlvD Edd family | |
GCKIAGNM_00485 | 1.1e-136 | fmt | 2.1.1.176, 2.1.2.9 | J | Attaches a formyl group to the free amino group of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by promoting its recognition by IF2 and preventing the misappropriation of this tRNA by the elongation apparatus | |
GCKIAGNM_00486 | 3.1e-07 | fmt | 2.1.1.176, 2.1.2.9 | J | Attaches a formyl group to the free amino group of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by promoting its recognition by IF2 and preventing the misappropriation of this tRNA by the elongation apparatus | |
GCKIAGNM_00487 | 2e-58 | 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | ||
GCKIAGNM_00488 | 1.9e-63 | 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | ||
GCKIAGNM_00489 | 2e-102 | 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 | ||
GCKIAGNM_00490 | 5.2e-229 | 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 | ||
GCKIAGNM_00491 | 8.2e-38 | 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 | ||
GCKIAGNM_00492 | 6.6e-120 | serB | 3.1.3.3 | E | haloacid dehalogenase-like hydrolase | |
GCKIAGNM_00493 | 1.1e-98 | apl | 3.1.3.1 | S | SNARE associated Golgi protein | |
GCKIAGNM_00494 | 7e-284 | arc | O | AAA ATPase forming ring-shaped complexes | ||
GCKIAGNM_00495 | 5.8e-17 | 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | ||
GCKIAGNM_00496 | 3.7e-108 | 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | ||
GCKIAGNM_00497 | 4.3e-145 | manR | K | PRD domain | ||
GCKIAGNM_00498 | 7.1e-104 | manR | K | PRD domain | ||
GCKIAGNM_00499 | 3e-72 | H | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |||
GCKIAGNM_00500 | 1.1e-78 | 2.7.1.194, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
GCKIAGNM_00501 | 2.1e-46 | fruA | 2.7.1.202 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
GCKIAGNM_00502 | 1.3e-37 | G | Phosphotransferase System | |||
GCKIAGNM_00503 | 1.7e-14 | G | Phosphotransferase System | |||
GCKIAGNM_00504 | 8.1e-39 | G | Phosphotransferase System | |||
GCKIAGNM_00505 | 1.6e-15 | G | Phosphotransferase System | |||
GCKIAGNM_00506 | 3.9e-12 | G | Phosphotransferase System | |||
GCKIAGNM_00507 | 2.1e-134 | alsE | 5.1.3.1 | G | Ribulose-phosphate 3 epimerase family | |
GCKIAGNM_00508 | 0.0 | dop | 3.5.1.119, 6.3.1.19 | S | Pup-ligase protein | |
GCKIAGNM_00509 | 8.9e-175 | hisN | 3.1.3.25 | G | Inositol monophosphatase family | |
GCKIAGNM_00511 | 1.6e-134 | pafA | 6.3.1.19 | O | Catalyzes the covalent attachment of the prokaryotic ubiquitin-like protein modifier Pup to the proteasomal substrate proteins, thereby targeting them for proteasomal degradation. This tagging system is termed pupylation. The ligation reaction involves the side-chain carboxylate of the C-terminal glutamate of Pup and the side-chain amino group of a substrate lysine | |
GCKIAGNM_00512 | 2.9e-24 | pafA | 6.3.1.19 | O | Catalyzes the covalent attachment of the prokaryotic ubiquitin-like protein modifier Pup to the proteasomal substrate proteins, thereby targeting them for proteasomal degradation. This tagging system is termed pupylation. The ligation reaction involves the side-chain carboxylate of the C-terminal glutamate of Pup and the side-chain amino group of a substrate lysine | |
GCKIAGNM_00513 | 6e-30 | pafA | 6.3.1.19 | O | Catalyzes the covalent attachment of the prokaryotic ubiquitin-like protein modifier Pup to the proteasomal substrate proteins, thereby targeting them for proteasomal degradation. This tagging system is termed pupylation. The ligation reaction involves the side-chain carboxylate of the C-terminal glutamate of Pup and the side-chain amino group of a substrate lysine | |
GCKIAGNM_00514 | 1.4e-56 | pafA | 6.3.1.19 | O | Catalyzes the covalent attachment of the prokaryotic ubiquitin-like protein modifier Pup to the proteasomal substrate proteins, thereby targeting them for proteasomal degradation. This tagging system is termed pupylation. The ligation reaction involves the side-chain carboxylate of the C-terminal glutamate of Pup and the side-chain amino group of a substrate lysine | |
GCKIAGNM_00515 | 3.3e-22 | hup | L | Belongs to the bacterial histone-like protein family | ||
GCKIAGNM_00517 | 0.0 | S | Lysylphosphatidylglycerol synthase TM region | |||
GCKIAGNM_00518 | 1.1e-127 | purB | 4.3.2.2 | F | Adenylosuccinate lyase C-terminal | |
GCKIAGNM_00519 | 2.3e-105 | purB | 4.3.2.2 | F | Adenylosuccinate lyase C-terminal | |
GCKIAGNM_00520 | 1.3e-111 | ykoE | S | ABC-type cobalt transport system, permease component | ||
GCKIAGNM_00521 | 1.7e-81 | S | PGAP1-like protein | |||
GCKIAGNM_00522 | 8.8e-148 | S | PGAP1-like protein | |||
GCKIAGNM_00525 | 2.1e-52 | |||||
GCKIAGNM_00526 | 9.1e-96 | S | von Willebrand factor (vWF) type A domain | |||
GCKIAGNM_00527 | 7.8e-27 | S | von Willebrand factor (vWF) type A domain | |||
GCKIAGNM_00528 | 3.3e-189 | S | von Willebrand factor (vWF) type A domain | |||
GCKIAGNM_00529 | 1.1e-84 | |||||
GCKIAGNM_00530 | 1.3e-163 | S | Protein of unknown function DUF58 | |||
GCKIAGNM_00531 | 1.1e-44 | moxR | S | ATPase family associated with various cellular activities (AAA) | ||
GCKIAGNM_00532 | 3.9e-84 | moxR | S | ATPase family associated with various cellular activities (AAA) | ||
GCKIAGNM_00533 | 6.9e-43 | drrC | L | ABC transporter | ||
GCKIAGNM_00534 | 1.3e-202 | drrC | L | ABC transporter | ||
GCKIAGNM_00535 | 7.9e-140 | drrC | L | ABC transporter | ||
GCKIAGNM_00536 | 5.1e-105 | V | MatE | |||
GCKIAGNM_00537 | 5.1e-46 | V | MatE | |||
GCKIAGNM_00538 | 3.5e-44 | V | MatE | |||
GCKIAGNM_00539 | 1.2e-28 | S | rRNA binding | |||
GCKIAGNM_00540 | 1.1e-58 | K | Arac family | |||
GCKIAGNM_00541 | 2.8e-46 | K | Arac family | |||
GCKIAGNM_00542 | 2.9e-21 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
GCKIAGNM_00543 | 2.1e-159 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
GCKIAGNM_00544 | 6.7e-111 | papP | E | Binding-protein-dependent transport system inner membrane component | ||
GCKIAGNM_00545 | 1e-65 | E | Binding-protein-dependent transport system inner membrane component | |||
GCKIAGNM_00546 | 5.1e-41 | E | Binding-protein-dependent transport system inner membrane component | |||
GCKIAGNM_00547 | 2.6e-138 | glnQ | 3.6.3.21 | E | ATP binding protein of ABC transporter for glutamate aspartate K02028 | |
GCKIAGNM_00548 | 8.1e-154 | cjaA | ET | Bacterial periplasmic substrate-binding proteins | ||
GCKIAGNM_00549 | 1.4e-147 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
GCKIAGNM_00550 | 2.4e-268 | pip | 3.4.11.5 | S | alpha/beta hydrolase fold | |
GCKIAGNM_00551 | 2.9e-278 | tcsS2 | T | Histidine kinase | ||
GCKIAGNM_00552 | 7.2e-136 | tcsS2 | T | Histidine kinase | ||
GCKIAGNM_00553 | 3.2e-139 | K | helix_turn_helix, Lux Regulon | |||
GCKIAGNM_00554 | 3.5e-265 | MV | MacB-like periplasmic core domain | |||
GCKIAGNM_00555 | 1.6e-60 | MV | MacB-like periplasmic core domain | |||
GCKIAGNM_00556 | 4e-92 | MV | MacB-like periplasmic core domain | |||
GCKIAGNM_00557 | 1.5e-135 | V | ABC transporter, ATP-binding protein | |||
GCKIAGNM_00558 | 4e-195 | metY | 2.5.1.49 | E | Aminotransferase class-V | |
GCKIAGNM_00559 | 8e-134 | pdxK | 2.7.1.35 | H | Phosphomethylpyrimidine kinase | |
GCKIAGNM_00560 | 1.6e-23 | L | Transposase and inactivated derivatives IS30 family | |||
GCKIAGNM_00561 | 2.2e-75 | yraN | L | Belongs to the UPF0102 family | ||
GCKIAGNM_00562 | 2.2e-128 | comM | O | Magnesium chelatase, subunit ChlI C-terminal | ||
GCKIAGNM_00563 | 7.3e-132 | dprA | 5.99.1.2 | LU | DNA recombination-mediator protein A | |
GCKIAGNM_00564 | 2.5e-158 | dprA | 5.99.1.2 | LU | DNA recombination-mediator protein A | |
GCKIAGNM_00565 | 0.0 | sdhA | 1.3.5.1, 1.3.5.4 | C | Succinate dehydrogenase flavoprotein subunit | |
GCKIAGNM_00566 | 1.2e-90 | sdhB | 1.3.5.1, 1.3.5.4 | C | 4Fe-4S dicluster domain | |
GCKIAGNM_00567 | 4.6e-27 | sdhB | 1.3.5.1, 1.3.5.4 | C | 4Fe-4S dicluster domain | |
GCKIAGNM_00568 | 1.9e-113 | safC | S | O-methyltransferase | ||
GCKIAGNM_00569 | 4.2e-164 | fmt2 | 3.2.2.10 | S | Belongs to the LOG family | |
GCKIAGNM_00570 | 5.3e-40 | nhaA | P | Na( ) H( ) antiporter that extrudes sodium in exchange for external protons | ||
GCKIAGNM_00571 | 4.9e-188 | nhaA | P | Na( ) H( ) antiporter that extrudes sodium in exchange for external protons | ||
GCKIAGNM_00572 | 5e-178 | patB | 4.4.1.8 | E | Aminotransferase, class I II | |
GCKIAGNM_00573 | 2.6e-48 | patB | 4.4.1.8 | E | Aminotransferase, class I II | |
GCKIAGNM_00576 | 3e-162 | 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 | ||
GCKIAGNM_00577 | 1.8e-65 | 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 | ||
GCKIAGNM_00578 | 7.3e-121 | 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 | |
GCKIAGNM_00579 | 6.4e-38 | 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 | |
GCKIAGNM_00580 | 1.7e-39 | 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 | |
GCKIAGNM_00581 | 2e-59 | |||||
GCKIAGNM_00582 | 3.7e-19 | clcA_2 | P | Voltage gated chloride channel | ||
GCKIAGNM_00583 | 3.9e-110 | clcA_2 | P | Voltage gated chloride channel | ||
GCKIAGNM_00584 | 4.4e-234 | 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 | ||
GCKIAGNM_00585 | 1.3e-207 | rnd | 3.1.13.5 | J | 3'-5' exonuclease | |
GCKIAGNM_00586 | 7.4e-97 | S | Protein of unknown function (DUF3000) | |||
GCKIAGNM_00587 | 3.8e-33 | 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 | |
GCKIAGNM_00588 | 4.5e-113 | 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 | |
GCKIAGNM_00589 | 2.3e-184 | pflB | 2.3.1.54 | C | Pyruvate formate lyase-like | |
GCKIAGNM_00590 | 4.5e-96 | pflB | 2.3.1.54 | C | Pyruvate formate lyase-like | |
GCKIAGNM_00591 | 7.2e-22 | pflB | 2.3.1.54 | C | Pyruvate formate lyase-like | |
GCKIAGNM_00592 | 2e-20 | |||||
GCKIAGNM_00593 | 1.4e-146 | nadE | 6.3.1.5, 6.3.5.1 | H | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses L-glutamine as a nitrogen source | |
GCKIAGNM_00594 | 1.7e-117 | nadE | 6.3.1.5, 6.3.5.1 | H | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses L-glutamine as a nitrogen source | |
GCKIAGNM_00595 | 2.8e-119 | S | Peptidase dimerisation domain | |||
GCKIAGNM_00596 | 3.6e-83 | S | Peptidase dimerisation domain | |||
GCKIAGNM_00597 | 1.3e-10 | metI | P | Binding-protein-dependent transport system inner membrane component | ||
GCKIAGNM_00598 | 7.8e-82 | metI | P | Binding-protein-dependent transport system inner membrane component | ||
GCKIAGNM_00599 | 1.4e-44 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
GCKIAGNM_00600 | 2.8e-160 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
GCKIAGNM_00601 | 1.8e-176 | metQ | P | NLPA lipoprotein | ||
GCKIAGNM_00604 | 1.5e-24 | 3.1.3.85 | G | Phosphoglycerate mutase family | ||
GCKIAGNM_00605 | 2.5e-65 | rsfS | 2.7.7.18 | J | Functions as a ribosomal silencing factor. Interacts with ribosomal protein L14 (rplN), blocking formation of intersubunit bridge B8. Prevents association of the 30S and 50S ribosomal subunits and the formation of functional ribosomes, thus repressing translation | |
GCKIAGNM_00606 | 4.6e-57 | 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 | |
GCKIAGNM_00607 | 2.5e-192 | 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 | |
GCKIAGNM_00608 | 5.8e-64 | xfp | 4.1.2.22, 4.1.2.9 | G | D-xylulose 5-phosphate/D-fructose 6-phosphate phosphoketolase | |
GCKIAGNM_00609 | 5.6e-163 | xfp | 4.1.2.22, 4.1.2.9 | G | D-xylulose 5-phosphate/D-fructose 6-phosphate phosphoketolase | |
GCKIAGNM_00610 | 9.1e-38 | xfp | 4.1.2.22, 4.1.2.9 | G | D-xylulose 5-phosphate/D-fructose 6-phosphate phosphoketolase | |
GCKIAGNM_00611 | 4.1e-69 | xfp | 4.1.2.22, 4.1.2.9 | G | D-xylulose 5-phosphate/D-fructose 6-phosphate phosphoketolase | |
GCKIAGNM_00612 | 1.3e-21 | xfp | 4.1.2.22, 4.1.2.9 | G | D-xylulose 5-phosphate/D-fructose 6-phosphate phosphoketolase | |
GCKIAGNM_00613 | 1.3e-301 | guaA | 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
GCKIAGNM_00614 | 1.9e-47 | K | Helix-turn-helix XRE-family like proteins | |||
GCKIAGNM_00615 | 2.5e-63 | yqgF | L | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
GCKIAGNM_00616 | 1.7e-194 | mltG | S | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
GCKIAGNM_00617 | 5.3e-70 | 3.4.23.43 | S | Type IV leader peptidase family | ||
GCKIAGNM_00618 | 1e-193 | 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 | |
GCKIAGNM_00619 | 2.3e-14 | 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 | |
GCKIAGNM_00620 | 9.9e-258 | aroK | 2.7.1.71, 4.2.3.4 | H | Catalyzes the conversion of 3-deoxy-D-arabino- heptulosonate 7-phosphate (DAHP) to dehydroquinate (DHQ) | |
GCKIAGNM_00621 | 1.8e-34 | aroK | 2.7.1.71, 4.2.3.4 | H | Catalyzes the conversion of 3-deoxy-D-arabino- heptulosonate 7-phosphate (DAHP) to dehydroquinate (DHQ) | |
GCKIAGNM_00622 | 7e-44 | aroQ | 4.2.1.10 | E | Catalyzes a trans-dehydration via an enolate intermediate | |
GCKIAGNM_00623 | 1.3e-24 | aroQ | 4.2.1.10 | E | Catalyzes a trans-dehydration via an enolate intermediate | |
GCKIAGNM_00624 | 2.7e-118 | 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 | |
GCKIAGNM_00625 | 2.5e-194 | 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 | |
GCKIAGNM_00626 | 8.4e-19 | S | L,D-transpeptidase catalytic domain | |||
GCKIAGNM_00627 | 5.1e-93 | S | L,D-transpeptidase catalytic domain | |||
GCKIAGNM_00628 | 1.7e-176 | S | L,D-transpeptidase catalytic domain | |||
GCKIAGNM_00629 | 1.3e-290 | sufB | O | FeS assembly protein SufB | ||
GCKIAGNM_00630 | 4.3e-236 | sufD | O | FeS assembly protein SufD | ||
GCKIAGNM_00631 | 5.8e-14 | sufC | O | FeS assembly ATPase SufC | ||
GCKIAGNM_00632 | 5.9e-91 | sufC | O | FeS assembly ATPase SufC | ||
GCKIAGNM_00633 | 3.1e-173 | 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 | |
GCKIAGNM_00634 | 8.3e-35 | 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 | |
GCKIAGNM_00635 | 2.8e-94 | iscU | C | SUF system FeS assembly protein, NifU family | ||
GCKIAGNM_00636 | 3.2e-109 | yitW | S | Iron-sulfur cluster assembly protein | ||
GCKIAGNM_00637 | 4.4e-82 | glgC | 2.7.7.27 | H | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
GCKIAGNM_00638 | 3.7e-143 | glgC | 2.7.7.27 | H | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
GCKIAGNM_00639 | 1.1e-135 | spoU | 2.1.1.185 | J | SpoU rRNA Methylase family | |
GCKIAGNM_00641 | 4.5e-58 | 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 | |
GCKIAGNM_00642 | 2.4e-62 | 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 | |
GCKIAGNM_00643 | 2.6e-45 | hinT | 2.1.1.226, 2.1.1.227 | FG | Scavenger mRNA decapping enzyme C-term binding | |
GCKIAGNM_00644 | 2.7e-176 | phoH | T | PhoH-like protein | ||
GCKIAGNM_00645 | 3.7e-29 | 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 | |
GCKIAGNM_00646 | 4e-26 | 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 | |
GCKIAGNM_00647 | 5.6e-248 | corC | S | CBS domain | ||
GCKIAGNM_00648 | 6e-97 | 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 | ||
GCKIAGNM_00649 | 8.4e-75 | 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 | ||
GCKIAGNM_00650 | 1e-16 | fadD | 6.2.1.3 | I | AMP-binding enzyme | |
GCKIAGNM_00651 | 1.8e-128 | fadD | 6.2.1.3 | I | AMP-binding enzyme | |
GCKIAGNM_00652 | 5.3e-93 | fadD | 6.2.1.3 | I | AMP-binding enzyme | |
GCKIAGNM_00653 | 2.6e-37 | fadD | 6.2.1.3 | I | AMP-binding enzyme | |
GCKIAGNM_00654 | 2.8e-45 | pntA | 1.6.1.2 | C | NAD(P) transhydrogenase subunit alpha part 1 K00324 | |
GCKIAGNM_00655 | 2.1e-149 | pntA | 1.6.1.2 | C | NAD(P) transhydrogenase subunit alpha part 1 K00324 | |
GCKIAGNM_00656 | 2.1e-43 | pntAA | 1.6.1.2 | C | 4TM region of pyridine nucleotide transhydrogenase, mitoch | |
GCKIAGNM_00657 | 2.8e-89 | pntB | 1.6.1.2 | C | The transhydrogenation between NADH and NADP is coupled to respiration and ATP hydrolysis and functions as a proton pump across the membrane | |
GCKIAGNM_00658 | 2e-109 | pntB | 1.6.1.2 | C | The transhydrogenation between NADH and NADP is coupled to respiration and ATP hydrolysis and functions as a proton pump across the membrane | |
GCKIAGNM_00659 | 2.9e-45 | yhjX | EGP | Major facilitator Superfamily | ||
GCKIAGNM_00660 | 3e-176 | yhjX | EGP | Major facilitator Superfamily | ||
GCKIAGNM_00661 | 2.2e-70 | ctc | J | This is one of the proteins that binds to the 5S RNA in the ribosome where it forms part of the central protuberance | ||
GCKIAGNM_00662 | 6e-168 | ilvE | 2.6.1.42 | E | Amino-transferase class IV | |
GCKIAGNM_00663 | 8.8e-143 | mazG | 3.6.1.66 | S | Psort location Cytoplasmic, score 8.87 | |
GCKIAGNM_00664 | 7.1e-33 | S | UPF0126 domain | |||
GCKIAGNM_00665 | 1.2e-67 | S | UPF0126 domain | |||
GCKIAGNM_00666 | 5.8e-34 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
GCKIAGNM_00667 | 1.2e-46 | 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 | ||
GCKIAGNM_00668 | 7.4e-123 | 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 | ||
GCKIAGNM_00669 | 5.8e-132 | 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 | ||
GCKIAGNM_00670 | 2.1e-171 | hemN | H | Involved in the biosynthesis of porphyrin-containing compound | ||
GCKIAGNM_00672 | 4.7e-134 | K | helix_turn _helix lactose operon repressor | |||
GCKIAGNM_00673 | 1.7e-49 | K | helix_turn _helix lactose operon repressor | |||
GCKIAGNM_00674 | 3.4e-27 | gltB | 1.4.1.13, 1.4.1.14, 1.4.7.1 | E | glutamate synthase NADPH large subunit | |
GCKIAGNM_00675 | 2.3e-99 | gltB | 1.4.1.13, 1.4.1.14, 1.4.7.1 | E | glutamate synthase NADPH large subunit | |
GCKIAGNM_00676 | 7.8e-83 | gltB | 1.4.1.13, 1.4.1.14, 1.4.7.1 | E | glutamate synthase NADPH large subunit | |
GCKIAGNM_00677 | 0.0 | gltB | 1.4.1.13, 1.4.1.14, 1.4.7.1 | E | glutamate synthase NADPH large subunit | |
GCKIAGNM_00678 | 1.9e-176 | gltD | 1.4.1.13, 1.4.1.14 | C | Dihydroprymidine dehydrogenase domain II, 4Fe-4S cluster | |
GCKIAGNM_00679 | 3.5e-80 | gltD | 1.4.1.13, 1.4.1.14 | C | Dihydroprymidine dehydrogenase domain II, 4Fe-4S cluster | |
GCKIAGNM_00680 | 3.1e-158 | E | ABC transporter, substrate-binding protein, family 5 | |||
GCKIAGNM_00681 | 2.5e-103 | E | ABC transporter, substrate-binding protein, family 5 | |||
GCKIAGNM_00682 | 0.0 | S | Glycosyl hydrolases related to GH101 family, GH129 | |||
GCKIAGNM_00683 | 6.6e-81 | |||||
GCKIAGNM_00684 | 2.2e-19 | glgA | 2.4.1.342 | GT4 | G | Starch synthase catalytic domain |
GCKIAGNM_00685 | 2.5e-194 | glgA | 2.4.1.342 | GT4 | G | Starch synthase catalytic domain |
GCKIAGNM_00686 | 7.2e-42 | modF | 3.6.3.21, 3.6.3.34 | P | ATPases associated with a variety of cellular activities | |
GCKIAGNM_00687 | 2.6e-97 | modF | 3.6.3.21, 3.6.3.34 | P | ATPases associated with a variety of cellular activities | |
GCKIAGNM_00688 | 9.3e-158 | S | Sucrose-6F-phosphate phosphohydrolase | |||
GCKIAGNM_00689 | 6.3e-91 | bcp | 1.11.1.15 | O | Redoxin | |
GCKIAGNM_00690 | 3.2e-139 | |||||
GCKIAGNM_00691 | 6.1e-27 | ssb1 | L | Single-strand binding protein family | ||
GCKIAGNM_00693 | 6.4e-47 | recT | L | RecT family | ||
GCKIAGNM_00695 | 6.3e-86 | yqaJ | L | YqaJ-like viral recombinase domain | ||
GCKIAGNM_00699 | 4.6e-17 | K | BRO family, N-terminal domain | |||
GCKIAGNM_00700 | 1.6e-75 | K | BRO family, N-terminal domain | |||
GCKIAGNM_00701 | 2.5e-83 | 2.1.1.37 | L | C-5 cytosine-specific DNA methylase | ||
GCKIAGNM_00702 | 2.6e-08 | |||||
GCKIAGNM_00703 | 2.9e-50 | Q | methyltransferase | |||
GCKIAGNM_00705 | 1.2e-07 | |||||
GCKIAGNM_00708 | 9.4e-09 | |||||
GCKIAGNM_00710 | 3.5e-64 | |||||
GCKIAGNM_00711 | 1.4e-12 | |||||
GCKIAGNM_00712 | 2.1e-172 | ftsQ | 6.3.2.4 | D | Cell division protein FtsQ | |
GCKIAGNM_00713 | 1.5e-29 | murC | 6.3.2.8 | M | Belongs to the MurCDEF family | |
GCKIAGNM_00714 | 2.3e-196 | murC | 6.3.2.8 | M | Belongs to the MurCDEF family | |
GCKIAGNM_00715 | 1.2e-219 | 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) |
GCKIAGNM_00716 | 1.1e-107 | ftsW | 2.4.1.227 | GT28 | D | Belongs to the SEDS family |
GCKIAGNM_00717 | 3.9e-53 | ftsW | 2.4.1.227 | GT28 | D | Belongs to the SEDS family |
GCKIAGNM_00718 | 2.5e-29 | ftsW | 2.4.1.227 | GT28 | D | Belongs to the SEDS family |
GCKIAGNM_00719 | 5.1e-273 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
GCKIAGNM_00720 | 1.2e-157 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
GCKIAGNM_00721 | 8.9e-44 | murF | 6.3.2.10 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
GCKIAGNM_00722 | 4.3e-77 | murF | 6.3.2.10 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
GCKIAGNM_00723 | 8.8e-82 | murF | 6.3.2.10 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
GCKIAGNM_00724 | 2e-155 | yqeC | 6.3.2.10, 6.3.2.13 | M | Catalyzes the addition of meso-diaminopimelic acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
GCKIAGNM_00725 | 0.0 | ftsI | 3.4.16.4 | M | Penicillin-binding protein, transpeptidase domain protein | |
GCKIAGNM_00726 | 6.9e-67 | ftsL | D | Essential cell division protein. May link together the upstream cell division proteins, which are predominantly cytoplasmic, with the downstream cell division proteins, which are predominantly periplasmic | ||
GCKIAGNM_00727 | 2.3e-148 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
GCKIAGNM_00728 | 3e-53 | mraZ | K | Belongs to the MraZ family | ||
GCKIAGNM_00729 | 5.7e-49 | L | DNA helicase | |||
GCKIAGNM_00730 | 3.7e-222 | L | DNA helicase | |||
GCKIAGNM_00731 | 1.6e-91 | L | DNA helicase | |||
GCKIAGNM_00732 | 7.5e-230 | serA | 1.1.1.399, 1.1.1.95 | EH | D-isomer specific 2-hydroxyacid dehydrogenase, catalytic domain | |
GCKIAGNM_00733 | 8.4e-78 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
GCKIAGNM_00734 | 1.1e-30 | M | Lysin motif | |||
GCKIAGNM_00735 | 5e-10 | 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 | |
GCKIAGNM_00736 | 1.3e-89 | 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 | |
GCKIAGNM_00737 | 1.4e-162 | czcD | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
GCKIAGNM_00738 | 2.9e-63 | ldh | 1.1.1.27, 1.1.1.37 | C | Belongs to the LDH MDH superfamily. LDH family | |
GCKIAGNM_00739 | 3.2e-84 | ldh | 1.1.1.27, 1.1.1.37 | C | Belongs to the LDH MDH superfamily. LDH family | |
GCKIAGNM_00740 | 4.6e-208 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
GCKIAGNM_00741 | 1.2e-14 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
GCKIAGNM_00742 | 1.4e-93 | hrpA | 3.6.4.13 | L | Helicase associated domain (HA2) Add an annotation | |
GCKIAGNM_00743 | 6.9e-201 | hrpA | 3.6.4.13 | L | Helicase associated domain (HA2) Add an annotation | |
GCKIAGNM_00744 | 3.7e-76 | hrpA | 3.6.4.13 | L | Helicase associated domain (HA2) Add an annotation | |
GCKIAGNM_00745 | 0.0 | hrpA | 3.6.4.13 | L | Helicase associated domain (HA2) Add an annotation | |
GCKIAGNM_00746 | 4.5e-169 | EGP | Major facilitator Superfamily | |||
GCKIAGNM_00747 | 9.1e-24 | EGP | Major facilitator Superfamily | |||
GCKIAGNM_00748 | 5.7e-71 | glnA2 | 6.3.1.2 | E | glutamine synthetase | |
GCKIAGNM_00749 | 4.1e-118 | glnA2 | 6.3.1.2 | E | glutamine synthetase | |
GCKIAGNM_00750 | 3.7e-73 | S | Uncharacterized protein conserved in bacteria (DUF2252) | |||
GCKIAGNM_00751 | 4.9e-118 | S | Uncharacterized protein conserved in bacteria (DUF2252) | |||
GCKIAGNM_00752 | 9.2e-29 | S | Uncharacterized protein conserved in bacteria (DUF2252) | |||
GCKIAGNM_00753 | 1.4e-130 | hisA | 5.3.1.16, 5.3.1.24 | E | Histidine biosynthesis protein | |
GCKIAGNM_00754 | 5.2e-43 | 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 | ||
GCKIAGNM_00755 | 3.7e-27 | 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 | ||
GCKIAGNM_00756 | 5e-99 | |||||
GCKIAGNM_00757 | 1.9e-47 | hisB | 1.1.1.23, 2.6.1.9, 3.1.3.15, 4.2.1.19 | E | Imidazoleglycerol-phosphate dehydratase | |
GCKIAGNM_00758 | 1.3e-37 | hisB | 1.1.1.23, 2.6.1.9, 3.1.3.15, 4.2.1.19 | E | Imidazoleglycerol-phosphate dehydratase | |
GCKIAGNM_00759 | 1.8e-220 | hisC | 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
GCKIAGNM_00760 | 1.9e-253 | 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 | |
GCKIAGNM_00761 | 1.1e-53 | acyP | 3.6.1.7 | C | Acylphosphatase | |
GCKIAGNM_00762 | 7.7e-157 | yvgN | 1.1.1.346 | S | Aldo/keto reductase family | |
GCKIAGNM_00763 | 4.2e-233 | 2.4.1.230, 3.2.1.51 | GH65,GH95 | G | Glycosyl hydrolase family 65, N-terminal domain | |
GCKIAGNM_00764 | 6.2e-186 | 2.4.1.230, 3.2.1.51 | GH65,GH95 | G | Glycosyl hydrolase family 65, N-terminal domain | |
GCKIAGNM_00765 | 7.5e-166 | dapA | 4.1.2.28, 4.3.3.7 | EM | Dihydrodipicolinate synthetase family | |
GCKIAGNM_00766 | 6.9e-37 | S | Amidohydrolase | |||
GCKIAGNM_00767 | 8.4e-91 | S | Amidohydrolase | |||
GCKIAGNM_00768 | 1.1e-62 | IQ | KR domain | |||
GCKIAGNM_00769 | 9e-167 | 4.2.1.68 | M | Enolase C-terminal domain-like | ||
GCKIAGNM_00770 | 6.6e-122 | pstS | P | Part of the ABC transporter complex PstSACB involved in phosphate import | ||
GCKIAGNM_00771 | 1.7e-115 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
GCKIAGNM_00772 | 2.1e-25 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
GCKIAGNM_00773 | 9e-54 | pstA | P | Phosphate transport system permease | ||
GCKIAGNM_00774 | 6.3e-77 | pstA | P | Phosphate transport system permease | ||
GCKIAGNM_00775 | 2.1e-148 | 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 | |
GCKIAGNM_00776 | 3.3e-167 | pbuO | S | Permease family | ||
GCKIAGNM_00777 | 1.4e-72 | pbuO | S | Permease family | ||
GCKIAGNM_00778 | 2e-146 | 3.2.1.8 | S | alpha beta | ||
GCKIAGNM_00779 | 2.4e-87 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
GCKIAGNM_00780 | 9.3e-49 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
GCKIAGNM_00781 | 8.6e-174 | T | Forkhead associated domain | |||
GCKIAGNM_00782 | 5.2e-97 | L | Superfamily I DNA and RNA helicases and helicase subunits | |||
GCKIAGNM_00783 | 0.0 | L | Superfamily I DNA and RNA helicases and helicase subunits | |||
GCKIAGNM_00784 | 2.9e-72 | L | Superfamily I DNA and RNA helicases and helicase subunits | |||
GCKIAGNM_00785 | 4.5e-42 | L | Superfamily I DNA and RNA helicases and helicase subunits | |||
GCKIAGNM_00786 | 4.8e-28 | L | Superfamily I DNA and RNA helicases and helicase subunits | |||
GCKIAGNM_00787 | 6.2e-106 | flgA | NO | SAF | ||
GCKIAGNM_00788 | 1.2e-32 | fmdB | S | Putative regulatory protein | ||
GCKIAGNM_00789 | 4.1e-55 | fthC | 6.3.3.2 | H | 5-formyltetrahydrofolate cyclo-ligase family | |
GCKIAGNM_00790 | 2.2e-114 | rimJ | 2.3.1.128 | J | Acetyltransferase (GNAT) domain | |
GCKIAGNM_00791 | 1.1e-135 | |||||
GCKIAGNM_00792 | 1.5e-46 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
GCKIAGNM_00796 | 4.1e-25 | rpmG | J | Ribosomal protein L33 | ||
GCKIAGNM_00797 | 1.1e-46 | murB | 1.3.1.98 | M | Cell wall formation | |
GCKIAGNM_00798 | 1.3e-96 | murB | 1.3.1.98 | M | Cell wall formation | |
GCKIAGNM_00799 | 8.1e-32 | E | aromatic amino acid transport protein AroP K03293 | |||
GCKIAGNM_00800 | 1.9e-223 | E | aromatic amino acid transport protein AroP K03293 | |||
GCKIAGNM_00801 | 2.9e-59 | fdxA | C | 4Fe-4S binding domain | ||
GCKIAGNM_00802 | 1.8e-223 | dapC | E | Aminotransferase class I and II | ||
GCKIAGNM_00803 | 2.6e-49 | 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 | |
GCKIAGNM_00804 | 1.7e-72 | 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 | |
GCKIAGNM_00805 | 4.6e-41 | 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 | |
GCKIAGNM_00806 | 8.7e-21 | S | EamA-like transporter family | |||
GCKIAGNM_00807 | 3.5e-103 | L | Resolvase, N terminal domain | |||
GCKIAGNM_00808 | 1.5e-186 | L | Helix-turn-helix domain | |||
GCKIAGNM_00809 | 8.5e-17 | S | EamA-like transporter family | |||
GCKIAGNM_00810 | 9.2e-09 | S | EamA-like transporter family | |||
GCKIAGNM_00812 | 5.2e-22 | |||||
GCKIAGNM_00813 | 2e-191 | rbsR | K | helix_turn _helix lactose operon repressor | ||
GCKIAGNM_00814 | 5.2e-153 | malE | G | Bacterial extracellular solute-binding protein | ||
GCKIAGNM_00815 | 1.5e-53 | malC | U | Binding-protein-dependent transport system inner membrane component | ||
GCKIAGNM_00816 | 5.8e-17 | malC | U | Binding-protein-dependent transport system inner membrane component | ||
GCKIAGNM_00817 | 8e-64 | malC | U | Binding-protein-dependent transport system inner membrane component | ||
GCKIAGNM_00818 | 6.1e-160 | U | Binding-protein-dependent transport system inner membrane component | |||
GCKIAGNM_00819 | 1.2e-152 | bglA | 3.2.1.21 | G | Glycosyl hydrolase family 1 | |
GCKIAGNM_00820 | 4.5e-75 | bglA | 3.2.1.21 | G | Glycosyl hydrolase family 1 | |
GCKIAGNM_00821 | 1.1e-72 | M | Bacterial capsule synthesis protein PGA_cap | |||
GCKIAGNM_00822 | 1.3e-15 | M | Bacterial capsule synthesis protein PGA_cap | |||
GCKIAGNM_00823 | 5.1e-21 | MA20_16500 | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
GCKIAGNM_00824 | 3.8e-156 | MA20_16500 | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
GCKIAGNM_00825 | 7.3e-62 | yigZ | 2.1.1.45, 3.4.13.9 | S | Uncharacterized protein family UPF0029 | |
GCKIAGNM_00826 | 2.5e-40 | yigZ | 2.1.1.45, 3.4.13.9 | S | Uncharacterized protein family UPF0029 | |
GCKIAGNM_00827 | 8.4e-117 | |||||
GCKIAGNM_00828 | 0.0 | malQ | 2.4.1.18, 2.4.1.25, 3.2.1.196, 5.4.99.15 | CBM48,GH13,GH77 | G | 4-alpha-glucanotransferase |
GCKIAGNM_00829 | 3.9e-36 | malQ | 2.4.1.18, 2.4.1.25, 3.2.1.196, 5.4.99.15 | CBM48,GH13,GH77 | G | 4-alpha-glucanotransferase |
GCKIAGNM_00830 | 1.5e-46 | 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 | ||
GCKIAGNM_00831 | 8.7e-33 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
GCKIAGNM_00832 | 4.8e-17 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
GCKIAGNM_00833 | 4.1e-305 | glgX | 3.2.1.196, 3.2.1.68 | CBM48,GH13 | G | Belongs to the glycosyl hydrolase 13 family |
GCKIAGNM_00834 | 3e-100 | glgX | 3.2.1.196, 3.2.1.68 | CBM48,GH13 | G | Belongs to the glycosyl hydrolase 13 family |
GCKIAGNM_00835 | 1.3e-58 | glgX | 3.2.1.196, 3.2.1.68 | CBM48,GH13 | G | Belongs to the glycosyl hydrolase 13 family |
GCKIAGNM_00836 | 3.1e-151 | tdh | 1.1.1.14 | C | Zinc-binding dehydrogenase | |
GCKIAGNM_00837 | 1.1e-10 | tdh | 1.1.1.14 | C | Zinc-binding dehydrogenase | |
GCKIAGNM_00838 | 2e-28 | EGP | Major facilitator Superfamily | |||
GCKIAGNM_00839 | 3.3e-51 | EGP | Major facilitator Superfamily | |||
GCKIAGNM_00840 | 2.1e-130 | EGP | Major facilitator Superfamily | |||
GCKIAGNM_00841 | 6e-75 | 4.4.1.5 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | ||
GCKIAGNM_00842 | 2.4e-89 | 2.7.1.2 | GK | transcriptional repressor of nag (N-acetylglucosamine) operon K02565 | ||
GCKIAGNM_00843 | 4.6e-40 | 2.7.1.2 | GK | transcriptional repressor of nag (N-acetylglucosamine) operon K02565 | ||
GCKIAGNM_00844 | 7.2e-21 | 2.7.1.2 | GK | transcriptional repressor of nag (N-acetylglucosamine) operon K02565 | ||
GCKIAGNM_00845 | 2.7e-196 | EGP | Major facilitator Superfamily | |||
GCKIAGNM_00846 | 2.9e-187 | Z012_01000 | 1.1.1.14, 1.1.1.9 | C | Zinc-binding dehydrogenase | |
GCKIAGNM_00847 | 1.7e-47 | rhaR_1 | K | helix_turn_helix, arabinose operon control protein | ||
GCKIAGNM_00848 | 5.2e-288 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
GCKIAGNM_00849 | 2.3e-66 | trxB2 | 1.8.1.9 | C | Thioredoxin domain | |
GCKIAGNM_00850 | 1.3e-21 | trxB2 | 1.8.1.9 | C | Thioredoxin domain | |
GCKIAGNM_00851 | 1e-107 | ahpC | 1.11.1.15 | O | C-terminal domain of 1-Cys peroxiredoxin | |
GCKIAGNM_00852 | 7.1e-53 | cah | 4.2.1.1 | P | Reversible hydration of carbon dioxide | |
GCKIAGNM_00853 | 4.9e-38 | cah | 4.2.1.1 | P | Reversible hydration of carbon dioxide | |
GCKIAGNM_00854 | 9.7e-211 | S | AAA ATPase domain | |||
GCKIAGNM_00855 | 2.2e-32 | ytfL | P | Transporter associated domain | ||
GCKIAGNM_00856 | 1.2e-44 | ytfL | P | Transporter associated domain | ||
GCKIAGNM_00857 | 6.4e-125 | ytfL | P | Transporter associated domain | ||
GCKIAGNM_00858 | 2.1e-82 | dps | P | Belongs to the Dps family | ||
GCKIAGNM_00859 | 2.7e-225 | S | Domain of unknown function (DUF4143) | |||
GCKIAGNM_00861 | 3.8e-122 | S | Protein of unknown function DUF45 | |||
GCKIAGNM_00864 | 2.4e-174 | S | Psort location CytoplasmicMembrane, score | |||
GCKIAGNM_00865 | 7.6e-82 | gdhA | 1.4.1.4 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
GCKIAGNM_00866 | 7e-36 | gdhA | 1.4.1.4 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
GCKIAGNM_00867 | 1.8e-119 | gdhA | 1.4.1.4 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
GCKIAGNM_00868 | 3.5e-206 | V | VanZ like family | |||
GCKIAGNM_00869 | 2.1e-141 | lacL | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
GCKIAGNM_00870 | 0.0 | lacL | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
GCKIAGNM_00871 | 2.3e-13 | lacS | G | Psort location CytoplasmicMembrane, score 10.00 | ||
GCKIAGNM_00872 | 4.9e-138 | lacR | K | Transcriptional regulator, LacI family | ||
GCKIAGNM_00873 | 2.4e-50 | S | Transmembrane domain of unknown function (DUF3566) | |||
GCKIAGNM_00874 | 8.8e-99 | 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 | |
GCKIAGNM_00875 | 1.5e-55 | 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 | |
GCKIAGNM_00876 | 4e-83 | 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 | |
GCKIAGNM_00877 | 1.8e-24 | 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 | |
GCKIAGNM_00878 | 3.8e-151 | 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 | |
GCKIAGNM_00879 | 1e-20 | 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 | |
GCKIAGNM_00880 | 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 | |
GCKIAGNM_00881 | 4.2e-83 | S | Protein of unknown function (DUF721) | |||
GCKIAGNM_00882 | 8.7e-164 | 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 | ||
GCKIAGNM_00883 | 1.3e-57 | 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 | |
GCKIAGNM_00884 | 6.6e-78 | 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 | |
GCKIAGNM_00885 | 1.4e-38 | 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 | |
GCKIAGNM_00887 | 3e-30 | 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 | ||
GCKIAGNM_00888 | 5.6e-60 | 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 | ||
GCKIAGNM_00889 | 1.6e-64 | 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 | ||
GCKIAGNM_00890 | 6.3e-73 | 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 | ||
GCKIAGNM_00891 | 2.6e-14 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
GCKIAGNM_00892 | 1.6e-55 | 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 | |
GCKIAGNM_00893 | 2e-57 | yidD | S | Could be involved in insertion of integral membrane proteins into the membrane | ||
GCKIAGNM_00894 | 5.8e-19 | yidC | U | Membrane protein insertase, YidC Oxa1 family | ||
GCKIAGNM_00895 | 1.7e-148 | yidC | U | Membrane protein insertase, YidC Oxa1 family | ||
GCKIAGNM_00896 | 6.6e-93 | jag | S | Putative single-stranded nucleic acids-binding domain | ||
GCKIAGNM_00897 | 1.2e-123 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
GCKIAGNM_00898 | 9.6e-175 | parA | D | CobQ CobB MinD ParA nucleotide binding domain protein | ||
GCKIAGNM_00899 | 2.7e-153 | parB | K | Belongs to the ParB family | ||
GCKIAGNM_00900 | 2.5e-59 | parB | K | Belongs to the ParB family | ||
GCKIAGNM_00901 | 7e-176 | trxB | 1.8.1.9, 4.3.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
GCKIAGNM_00902 | 6.4e-82 | murJ | KLT | MviN-like protein | ||
GCKIAGNM_00903 | 1.6e-220 | murJ | KLT | MviN-like protein | ||
GCKIAGNM_00904 | 2.5e-282 | murJ | KLT | MviN-like protein | ||
GCKIAGNM_00905 | 1.6e-55 | |||||
GCKIAGNM_00906 | 3e-137 | |||||
GCKIAGNM_00907 | 8.7e-87 | |||||
GCKIAGNM_00908 | 1.1e-74 | |||||
GCKIAGNM_00909 | 1.5e-137 | deoC | 3.6.1.13, 3.6.1.17, 3.6.1.55, 3.6.1.61 | L | Belongs to the Nudix hydrolase family | |
GCKIAGNM_00910 | 9.2e-283 | cca | 2.7.7.19, 2.7.7.72 | J | Probable RNA and SrmB- binding site of polymerase A | |
GCKIAGNM_00911 | 8.3e-111 | S | LytR cell envelope-related transcriptional attenuator | |||
GCKIAGNM_00912 | 1e-113 | 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 | |
GCKIAGNM_00913 | 5.4e-43 | 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 | |
GCKIAGNM_00914 | 1.2e-123 | ksgA | 2.1.1.182, 2.1.1.184 | 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 | |
GCKIAGNM_00915 | 5.2e-47 | S | G5 | |||
GCKIAGNM_00916 | 1.9e-65 | S | G5 | |||
GCKIAGNM_00918 | 1e-137 | O | Thioredoxin | |||
GCKIAGNM_00919 | 7.9e-260 | G | Bacterial extracellular solute-binding protein | |||
GCKIAGNM_00920 | 1.1e-47 | cydD | V | ABC transporter transmembrane region | ||
GCKIAGNM_00921 | 1.6e-115 | cydD | V | ABC transporter transmembrane region | ||
GCKIAGNM_00922 | 1.2e-152 | cydD | V | ABC transporter transmembrane region | ||
GCKIAGNM_00923 | 0.0 | cydD | V | ABC transporter transmembrane region | ||
GCKIAGNM_00925 | 1.7e-20 | araE | EGP | Major facilitator Superfamily | ||
GCKIAGNM_00926 | 4.5e-39 | araE | EGP | Major facilitator Superfamily | ||
GCKIAGNM_00927 | 3.9e-106 | fadD | 6.2.1.3 | I | AMP-binding enzyme | |
GCKIAGNM_00928 | 4.6e-227 | fadD | 6.2.1.3 | I | AMP-binding enzyme | |
GCKIAGNM_00929 | 6.8e-12 | araD | 4.1.2.17, 5.1.3.4 | G | Class II Aldolase and Adducin N-terminal domain | |
GCKIAGNM_00930 | 9e-36 | K | helix_turn _helix lactose operon repressor | |||
GCKIAGNM_00931 | 4.4e-120 | K | helix_turn _helix lactose operon repressor | |||
GCKIAGNM_00932 | 5.3e-71 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
GCKIAGNM_00933 | 1.5e-164 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
GCKIAGNM_00934 | 8.1e-60 | 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 | ||
GCKIAGNM_00936 | 0.0 | opuAB | P | Binding-protein-dependent transport system inner membrane component | ||
GCKIAGNM_00937 | 7.3e-99 | abcT3 | P | ATPases associated with a variety of cellular activities | ||
GCKIAGNM_00938 | 3.1e-153 | abcT3 | P | ATPases associated with a variety of cellular activities | ||
GCKIAGNM_00939 | 1.2e-24 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
GCKIAGNM_00940 | 1.2e-240 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
GCKIAGNM_00943 | 6e-65 | S | Auxin Efflux Carrier | |||
GCKIAGNM_00944 | 5.4e-16 | S | Auxin Efflux Carrier | |||
GCKIAGNM_00945 | 2.1e-15 | S | Auxin Efflux Carrier | |||
GCKIAGNM_00946 | 6.6e-42 | 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 | |
GCKIAGNM_00947 | 3e-96 | rph | 2.7.7.56, 3.6.1.66 | J | Phosphorolytic exoribonuclease that removes nucleotide residues following the -CCA terminus of tRNA and adds nucleotides to the ends of RNA molecules by using nucleoside diphosphates as substrates | |
GCKIAGNM_00948 | 2.2e-15 | rph | 2.7.7.56, 3.6.1.66 | J | Phosphorolytic exoribonuclease that removes nucleotide residues following the -CCA terminus of tRNA and adds nucleotides to the ends of RNA molecules by using nucleoside diphosphates as substrates | |
GCKIAGNM_00949 | 8.9e-237 | 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 | |
GCKIAGNM_00950 | 5.9e-114 | |||||
GCKIAGNM_00951 | 1.1e-77 | soxR | K | MerR, DNA binding | ||
GCKIAGNM_00952 | 1.6e-196 | yghZ | C | Aldo/keto reductase family | ||
GCKIAGNM_00953 | 2.4e-49 | S | Protein of unknown function (DUF3039) | |||
GCKIAGNM_00954 | 6e-88 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
GCKIAGNM_00955 | 6.9e-62 | |||||
GCKIAGNM_00956 | 1.5e-115 | yceD | S | Uncharacterized ACR, COG1399 | ||
GCKIAGNM_00957 | 2.4e-133 | rnc | 3.1.26.3 | J | Digests double-stranded RNA. Involved in the processing of primary rRNA transcript to yield the immediate precursors to the large and small rRNAs (23S and 16S). Processes some mRNAs, and tRNAs when they are encoded in the rRNA operon. Processes pre- crRNA and tracrRNA of type II CRISPR loci if present in the organism | |
GCKIAGNM_00958 | 1.1e-70 | ilvB | 2.2.1.6 | H | Thiamine pyrophosphate enzyme, central domain | |
GCKIAGNM_00959 | 1.5e-62 | ilvB | 2.2.1.6 | H | Thiamine pyrophosphate enzyme, central domain | |
GCKIAGNM_00960 | 4.9e-212 | ilvB | 2.2.1.6 | H | Thiamine pyrophosphate enzyme, central domain | |
GCKIAGNM_00961 | 9e-93 | ilvN | 2.2.1.6 | E | ACT domain | |
GCKIAGNM_00962 | 7e-27 | stbC | S | Plasmid stability protein | ||
GCKIAGNM_00963 | 3.9e-72 | vapC | S | Toxic component of a toxin-antitoxin (TA) module. An RNase | ||
GCKIAGNM_00964 | 0.0 | yjjK | S | ABC transporter | ||
GCKIAGNM_00965 | 1.8e-112 | |||||
GCKIAGNM_00966 | 1.3e-136 | guaA1 | 6.3.5.2 | F | Peptidase C26 | |
GCKIAGNM_00967 | 1.9e-51 | cysS | 6.1.1.16 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
GCKIAGNM_00968 | 1e-71 | cysS | 6.1.1.16 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
GCKIAGNM_00969 | 5.2e-123 | cysS | 6.1.1.16 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
GCKIAGNM_00970 | 2.3e-162 | P | Cation efflux family | |||
GCKIAGNM_00971 | 2.9e-69 | 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 | |
GCKIAGNM_00972 | 5.7e-64 | 2.7.11.1 | NU | Tfp pilus assembly protein FimV | ||
GCKIAGNM_00973 | 2.9e-221 | dxr | 1.1.1.267 | I | Catalyzes the NADP-dependent rearrangement and reduction of 1-deoxy-D-xylulose-5-phosphate (DXP) to 2-C-methyl-D-erythritol 4-phosphate (MEP) | |
GCKIAGNM_00974 | 3.5e-171 | ispG | 1.17.7.1, 1.17.7.3 | I | Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate | |
GCKIAGNM_00975 | 6.8e-22 | ispG | 1.17.7.1, 1.17.7.3 | I | Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate | |
GCKIAGNM_00976 | 6.3e-16 | ispG | 1.17.7.1, 1.17.7.3 | I | Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate | |
GCKIAGNM_00977 | 2e-28 | I | acetylesterase activity | |||
GCKIAGNM_00978 | 3.3e-228 | I | acetylesterase activity | |||
GCKIAGNM_00979 | 1.7e-41 | I | acetylesterase activity | |||
GCKIAGNM_00980 | 2.1e-123 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
GCKIAGNM_00982 | 1e-103 | uppS | 2.5.1.31, 2.5.1.86, 2.5.1.88 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
GCKIAGNM_00983 | 7.4e-22 | ytlD1 | 2.7.1.50 | P | Binding-protein-dependent transport system inner membrane component | |
GCKIAGNM_00984 | 6.1e-95 | ytlD1 | 2.7.1.50 | P | Binding-protein-dependent transport system inner membrane component | |
GCKIAGNM_00985 | 1.5e-189 | P | NMT1/THI5 like | |||
GCKIAGNM_00986 | 3.3e-115 | E | Aminotransferase class I and II | |||
GCKIAGNM_00987 | 5.1e-99 | E | Aminotransferase class I and II | |||
GCKIAGNM_00988 | 4.3e-52 | bioM | P | ATPases associated with a variety of cellular activities | ||
GCKIAGNM_00989 | 1.3e-27 | bioM | P | ATPases associated with a variety of cellular activities | ||
GCKIAGNM_00991 | 3.8e-113 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
GCKIAGNM_00992 | 2.1e-127 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
GCKIAGNM_00993 | 7.5e-166 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
GCKIAGNM_00994 | 0.0 | S | Tetratricopeptide repeat | |||
GCKIAGNM_00995 | 7.2e-37 | S | Tetratricopeptide repeat | |||
GCKIAGNM_00996 | 4.7e-120 | S | Tetratricopeptide repeat | |||
GCKIAGNM_00997 | 6.1e-296 | 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 | |
GCKIAGNM_00998 | 2.3e-182 | 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 | |
GCKIAGNM_00999 | 1.8e-173 | mrp | D | Binds and transfers iron-sulfur (Fe-S) clusters to target apoproteins. Can hydrolyze ATP | ||
GCKIAGNM_01000 | 7.4e-08 | mrp | D | Binds and transfers iron-sulfur (Fe-S) clusters to target apoproteins. Can hydrolyze ATP | ||
GCKIAGNM_01001 | 2.6e-241 | glnA | 6.3.1.2 | E | glutamine synthetase | |
GCKIAGNM_01002 | 5.2e-25 | glnA | 6.3.1.2 | E | glutamine synthetase | |
GCKIAGNM_01003 | 9.2e-144 | S | Domain of unknown function (DUF4191) | |||
GCKIAGNM_01004 | 6.6e-23 | lpdA | 1.16.1.1, 1.8.1.4 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
GCKIAGNM_01005 | 1.4e-184 | lpdA | 1.16.1.1, 1.8.1.4 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
GCKIAGNM_01006 | 5.6e-33 | lpdA | 1.16.1.1, 1.8.1.4 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
GCKIAGNM_01007 | 6.9e-102 | S | Protein of unknown function (DUF3043) | |||
GCKIAGNM_01008 | 8.7e-56 | argE | E | Peptidase dimerisation domain | ||
GCKIAGNM_01009 | 1.1e-116 | argE | E | Peptidase dimerisation domain | ||
GCKIAGNM_01010 | 2.2e-15 | argE | E | Peptidase dimerisation domain | ||
GCKIAGNM_01011 | 1.1e-14 | argE | E | Peptidase dimerisation domain | ||
GCKIAGNM_01012 | 2.9e-26 | ykoE | S | ABC-type cobalt transport system, permease component | ||
GCKIAGNM_01013 | 3e-16 | ykoE | S | ABC-type cobalt transport system, permease component | ||
GCKIAGNM_01014 | 6.5e-276 | ykoD | P | ATPases associated with a variety of cellular activities | ||
GCKIAGNM_01015 | 2.1e-163 | cbiQ | P | Cobalt transport protein | ||
GCKIAGNM_01016 | 2.1e-29 | IV02_28330 | 2.1.1.185, 2.1.1.34 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
GCKIAGNM_01017 | 7.1e-98 | IV02_28330 | 2.1.1.185, 2.1.1.34 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
GCKIAGNM_01018 | 9.9e-194 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
GCKIAGNM_01019 | 0.0 | pheT | 6.1.1.20 | J | Phenylalanyl-tRNA synthetase beta | |
GCKIAGNM_01020 | 4.6e-109 | pheT | 6.1.1.20 | J | Phenylalanyl-tRNA synthetase beta | |
GCKIAGNM_01021 | 1.9e-89 | |||||
GCKIAGNM_01022 | 1.1e-54 | 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 | |
GCKIAGNM_01023 | 8.8e-84 | 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 | |
GCKIAGNM_01024 | 2.4e-212 | 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 | |
GCKIAGNM_01025 | 3.9e-22 | argB | 2.7.2.8 | E | Belongs to the acetylglutamate kinase family. ArgB subfamily | |
GCKIAGNM_01026 | 8.3e-148 | argB | 2.7.2.8 | E | Belongs to the acetylglutamate kinase family. ArgB subfamily | |
GCKIAGNM_01027 | 5.5e-33 | argD | 2.6.1.11, 2.6.1.17 | E | Aminotransferase class-III | |
GCKIAGNM_01028 | 8.2e-36 | argD | 2.6.1.11, 2.6.1.17 | E | Aminotransferase class-III | |
GCKIAGNM_01029 | 4.9e-159 | argD | 2.6.1.11, 2.6.1.17 | E | Aminotransferase class-III | |
GCKIAGNM_01030 | 3.9e-184 | 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 | |
GCKIAGNM_01031 | 5.9e-83 | argR | K | Regulates arginine biosynthesis genes | ||
GCKIAGNM_01032 | 1.2e-238 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
GCKIAGNM_01033 | 1.7e-206 | purL | 6.3.5.3 | F | CobB/CobQ-like glutamine amidotransferase domain | |
GCKIAGNM_01034 | 7.8e-158 | purL | 6.3.5.3 | F | CobB/CobQ-like glutamine amidotransferase domain | |
GCKIAGNM_01035 | 1.4e-41 | purL | 6.3.5.3 | F | CobB/CobQ-like glutamine amidotransferase domain | |
GCKIAGNM_01036 | 8.7e-51 | purL | 6.3.5.3 | F | CobB/CobQ-like glutamine amidotransferase domain | |
GCKIAGNM_01037 | 1.7e-60 | purL | 6.3.5.3 | F | CobB/CobQ-like glutamine amidotransferase domain | |
GCKIAGNM_01038 | 4.8e-222 | I | alpha/beta hydrolase fold | |||
GCKIAGNM_01039 | 5.4e-128 | Q | D-alanine [D-alanyl carrier protein] ligase activity | |||
GCKIAGNM_01040 | 2e-46 | Q | D-alanine [D-alanyl carrier protein] ligase activity | |||
GCKIAGNM_01041 | 6.6e-111 | Q | D-alanine [D-alanyl carrier protein] ligase activity | |||
GCKIAGNM_01042 | 3.6e-101 | |||||
GCKIAGNM_01045 | 2.4e-08 | S | Protein of unknown function (DUF4230) | |||
GCKIAGNM_01046 | 1.7e-85 | mug | 3.2.2.28 | L | Uracil DNA glycosylase superfamily | |
GCKIAGNM_01047 | 1.7e-12 | C | Aldo/keto reductase family | |||
GCKIAGNM_01048 | 3.4e-21 | |||||
GCKIAGNM_01049 | 2.3e-298 | umuC | 2.7.7.7 | L | DNA-damage repair protein (DNA polymerase IV) K00961 | |
GCKIAGNM_01050 | 3.5e-293 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
GCKIAGNM_01051 | 9.2e-184 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
GCKIAGNM_01052 | 1.1e-44 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
GCKIAGNM_01053 | 2.6e-177 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
GCKIAGNM_01054 | 6.4e-105 | aldH | 1.2.1.3, 1.2.1.5 | C | Aldehyde dehydrogenase family | |
GCKIAGNM_01055 | 2.3e-139 | aldH | 1.2.1.3, 1.2.1.5 | C | Aldehyde dehydrogenase family | |
GCKIAGNM_01056 | 8.3e-19 | aldH | 1.2.1.3, 1.2.1.5 | C | Aldehyde dehydrogenase family | |
GCKIAGNM_01057 | 8.2e-15 | XK27_08315 | M | Psort location CytoplasmicMembrane, score 9.26 | ||
GCKIAGNM_01058 | 7.5e-248 | XK27_08315 | M | Psort location CytoplasmicMembrane, score 9.26 | ||
GCKIAGNM_01059 | 5.9e-68 | XK27_08315 | M | Psort location CytoplasmicMembrane, score 9.26 | ||
GCKIAGNM_01060 | 1.4e-99 | P | Zinc-uptake complex component A periplasmic | |||
GCKIAGNM_01061 | 4.2e-17 | 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 | ||
GCKIAGNM_01063 | 6.1e-181 | ycgR | S | Predicted permease | ||
GCKIAGNM_01064 | 1.9e-101 | S | TIGRFAM TIGR03943 family protein | |||
GCKIAGNM_01065 | 1.1e-29 | zur | P | Ferric uptake regulator family | ||
GCKIAGNM_01066 | 7.1e-64 | |||||
GCKIAGNM_01067 | 6.5e-45 | tetR | K | Transcriptional regulator C-terminal region | ||
GCKIAGNM_01068 | 1.7e-43 | XK27_06785 | V | ABC transporter | ||
GCKIAGNM_01069 | 1.5e-14 | XK27_06785 | V | ABC transporter | ||
GCKIAGNM_01070 | 6e-28 | ylbB | V | FtsX-like permease family | ||
GCKIAGNM_01071 | 3e-12 | ylbB | V | FtsX-like permease family | ||
GCKIAGNM_01072 | 1.7e-59 | ylbB | V | FtsX-like permease family | ||
GCKIAGNM_01073 | 2.4e-82 | 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) | |
GCKIAGNM_01074 | 1.1e-82 | 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) | |
GCKIAGNM_01075 | 9.6e-86 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
GCKIAGNM_01076 | 1.3e-148 | adh3 | C | Zinc-binding dehydrogenase | ||
GCKIAGNM_01077 | 8.3e-12 | adh3 | C | Zinc-binding dehydrogenase | ||
GCKIAGNM_01078 | 4.4e-161 | 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) | |
GCKIAGNM_01079 | 2.2e-55 | 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) | |
GCKIAGNM_01080 | 7.9e-106 | macB_8 | V | MacB-like periplasmic core domain | ||
GCKIAGNM_01081 | 2.5e-159 | macB_8 | V | MacB-like periplasmic core domain | ||
GCKIAGNM_01082 | 1.3e-181 | M | Conserved repeat domain | |||
GCKIAGNM_01083 | 5.3e-134 | V | ATPases associated with a variety of cellular activities | |||
GCKIAGNM_01084 | 2.1e-85 | msrA | 1.8.4.11, 1.8.4.12 | O | peptide-methionine (S)-S-oxide reductase activity | |
GCKIAGNM_01085 | 1.1e-86 | E | ABC transporter, substrate-binding protein, family 5 | |||
GCKIAGNM_01086 | 1.6e-163 | E | ABC transporter, substrate-binding protein, family 5 | |||
GCKIAGNM_01087 | 4.5e-13 | L | Psort location Cytoplasmic, score 8.87 | |||
GCKIAGNM_01088 | 2.1e-186 | 3.2.1.10 | GH13 | G | Alpha amylase, catalytic domain protein | |
GCKIAGNM_01089 | 1.3e-37 | glkA | 2.7.1.2 | G | ROK family | |
GCKIAGNM_01091 | 6.7e-52 | EGP | Major Facilitator Superfamily | |||
GCKIAGNM_01092 | 3.7e-21 | EGP | Major Facilitator Superfamily | |||
GCKIAGNM_01093 | 2.6e-133 | EGP | Major Facilitator Superfamily | |||
GCKIAGNM_01094 | 2.6e-22 | EGP | Major Facilitator Superfamily | |||
GCKIAGNM_01096 | 1.4e-142 | yjjK | S | ATP-binding cassette protein, ChvD family | ||
GCKIAGNM_01097 | 1.6e-22 | yjjK | S | ATP-binding cassette protein, ChvD family | ||
GCKIAGNM_01098 | 6.3e-43 | yjjK | S | ATP-binding cassette protein, ChvD family | ||
GCKIAGNM_01099 | 8.2e-72 | yjjK | S | ATP-binding cassette protein, ChvD family | ||
GCKIAGNM_01100 | 4e-48 | tesB | I | Thioesterase-like superfamily | ||
GCKIAGNM_01101 | 1.5e-42 | tesB | I | Thioesterase-like superfamily | ||
GCKIAGNM_01102 | 5e-47 | tesB | I | Thioesterase-like superfamily | ||
GCKIAGNM_01103 | 4.4e-13 | S | Protein of unknown function (DUF3180) | |||
GCKIAGNM_01104 | 6.1e-54 | S | Protein of unknown function (DUF3180) | |||
GCKIAGNM_01105 | 6.5e-226 | folK | 1.13.11.81, 2.5.1.15, 2.7.6.3, 3.5.4.16, 3.5.4.39, 4.1.2.25, 5.1.99.8 | H | Catalyzes the conversion of 7,8-dihydroneopterin to 6- hydroxymethyl-7,8-dihydropterin | |
GCKIAGNM_01106 | 2e-123 | folP | 1.13.11.81, 2.5.1.15, 2.7.6.3, 4.1.2.25, 5.1.99.8 | H | Catalyzes the condensation of para-aminobenzoate (pABA) with 6-hydroxymethyl-7,8-dihydropterin diphosphate (DHPt-PP) to form 7,8-dihydropteroate (H2Pte), the immediate precursor of folate derivatives | |
GCKIAGNM_01107 | 8.5e-19 | folP | 1.13.11.81, 2.5.1.15, 2.7.6.3, 4.1.2.25, 5.1.99.8 | H | Catalyzes the condensation of para-aminobenzoate (pABA) with 6-hydroxymethyl-7,8-dihydropterin diphosphate (DHPt-PP) to form 7,8-dihydropteroate (H2Pte), the immediate precursor of folate derivatives | |
GCKIAGNM_01108 | 2.8e-117 | folE | 2.7.6.3, 3.5.4.16 | H | GTP cyclohydrolase | |
GCKIAGNM_01109 | 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 | ||
GCKIAGNM_01110 | 1.1e-72 | hpt | 2.4.2.8, 6.3.4.19 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
GCKIAGNM_01111 | 1.3e-148 | 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 | |
GCKIAGNM_01112 | 2.8e-39 | 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 | |
GCKIAGNM_01113 | 4.7e-150 | dacB | 3.4.16.4 | M | D-Ala-D-Ala carboxypeptidase 3 (S13) family | |
GCKIAGNM_01114 | 5.8e-56 | |||||
GCKIAGNM_01115 | 2.6e-150 | |||||
GCKIAGNM_01116 | 1.6e-46 | |||||
GCKIAGNM_01117 | 1.9e-98 | natA | V | ATPases associated with a variety of cellular activities | ||
GCKIAGNM_01118 | 4.7e-235 | epsG | M | Glycosyl transferase family 21 | ||
GCKIAGNM_01119 | 2.2e-101 | S | AI-2E family transporter | |||
GCKIAGNM_01120 | 1.9e-102 | S | AI-2E family transporter | |||
GCKIAGNM_01121 | 2.9e-41 | S | AI-2E family transporter | |||
GCKIAGNM_01122 | 1.7e-156 | 3.4.14.13 | M | Glycosyltransferase like family 2 | ||
GCKIAGNM_01123 | 5.2e-204 | fucO | 1.1.1.1, 1.1.1.77, 1.1.99.37, 1.2.98.1 | C | Iron-containing alcohol dehydrogenase | |
GCKIAGNM_01124 | 2.1e-122 | cma | 2.1.1.79 | M | Mycolic acid cyclopropane synthetase | |
GCKIAGNM_01125 | 7.7e-84 | cma | 2.1.1.79 | M | Mycolic acid cyclopropane synthetase | |
GCKIAGNM_01126 | 2.2e-16 | cma | 2.1.1.79 | M | Mycolic acid cyclopropane synthetase | |
GCKIAGNM_01129 | 1.4e-92 | trmB | 2.1.1.297, 2.1.1.33, 2.4.99.12, 2.4.99.13, 2.4.99.14, 2.4.99.15 | GT30 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA |
GCKIAGNM_01131 | 1.2e-15 | L | Phage integrase family | |||
GCKIAGNM_01132 | 6.2e-29 | lacS | G | Psort location CytoplasmicMembrane, score 10.00 | ||
GCKIAGNM_01133 | 3.9e-179 | lacS | G | Psort location CytoplasmicMembrane, score 10.00 | ||
GCKIAGNM_01134 | 2.4e-167 | lacL | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
GCKIAGNM_01135 | 3.3e-183 | lacL | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
GCKIAGNM_01136 | 9.5e-47 | lacL | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
GCKIAGNM_01137 | 4.8e-185 | lacR | K | Transcriptional regulator, LacI family | ||
GCKIAGNM_01138 | 1.4e-21 | L | Helix-turn-helix domain | |||
GCKIAGNM_01139 | 1.5e-132 | G | Bacterial extracellular solute-binding protein | |||
GCKIAGNM_01140 | 3.1e-105 | G | Bacterial extracellular solute-binding protein | |||
GCKIAGNM_01141 | 3.8e-138 | GK | ROK family | |||
GCKIAGNM_01142 | 2.3e-50 | GK | ROK family | |||
GCKIAGNM_01143 | 1.4e-20 | U | Binding-protein-dependent transport system inner membrane component | |||
GCKIAGNM_01144 | 9.2e-221 | G | Glycosyl hydrolase family 20, domain 2 | |||
GCKIAGNM_01145 | 4.7e-64 | G | Glycosyl hydrolase family 20, domain 2 | |||
GCKIAGNM_01146 | 6.7e-08 | L | HTH-like domain | |||
GCKIAGNM_01147 | 2.3e-219 | vex3 | V | ABC transporter permease | ||
GCKIAGNM_01148 | 1.4e-81 | vex1 | V | Efflux ABC transporter, permease protein | ||
GCKIAGNM_01149 | 1.7e-25 | vex1 | V | Efflux ABC transporter, permease protein | ||
GCKIAGNM_01150 | 3.6e-36 | guaB | 1.1.1.205 | F | Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate- limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth | |
GCKIAGNM_01151 | 1.9e-59 | guaB | 1.1.1.205 | F | Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate- limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth | |
GCKIAGNM_01152 | 6.3e-56 | orn | L | 3'-to-5' exoribonuclease specific for small oligoribonucleotides | ||
GCKIAGNM_01153 | 2.9e-241 | recD2 | 3.6.4.12 | L | PIF1-like helicase | |
GCKIAGNM_01154 | 3.5e-120 | pflA | 1.97.1.4 | O | Radical SAM superfamily | |
GCKIAGNM_01155 | 7.9e-293 | 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 | |
GCKIAGNM_01156 | 1e-48 | 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 | |
GCKIAGNM_01157 | 1.1e-59 | L | Single-strand binding protein family | |||
GCKIAGNM_01158 | 5.4e-243 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
GCKIAGNM_01159 | 3e-136 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
GCKIAGNM_01160 | 1.3e-16 | S | Short repeat of unknown function (DUF308) | |||
GCKIAGNM_01161 | 1.1e-49 | S | Short repeat of unknown function (DUF308) | |||
GCKIAGNM_01162 | 2.6e-114 | map | 3.4.11.18 | E | Methionine aminopeptidase | |
GCKIAGNM_01163 | 3.6e-247 | gltA | 2.3.3.1 | C | Citrate synthase, C-terminal domain | |
GCKIAGNM_01164 | 1.4e-13 | dapD | 2.3.1.117 | E | Catalyzes the conversion of the cyclic tetrahydrodipicolinate (THDP) into the acyclic N-succinyl-L-2- amino-6-oxopimelate using succinyl-CoA | |
GCKIAGNM_01165 | 2.4e-96 | dapD | 2.3.1.117 | E | Catalyzes the conversion of the cyclic tetrahydrodipicolinate (THDP) into the acyclic N-succinyl-L-2- amino-6-oxopimelate using succinyl-CoA | |
GCKIAGNM_01166 | 7.3e-12 | snf | 2.7.11.1 | KL | Psort location Cytoplasmic, score 8.87 | |
GCKIAGNM_01167 | 5.3e-301 | snf | 2.7.11.1 | KL | Psort location Cytoplasmic, score 8.87 | |
GCKIAGNM_01168 | 2.7e-189 | snf | 2.7.11.1 | KL | Psort location Cytoplasmic, score 8.87 | |
GCKIAGNM_01169 | 3.2e-218 | snf | 2.7.11.1 | KL | Psort location Cytoplasmic, score 8.87 | |
GCKIAGNM_01170 | 1.2e-100 | XK27_03610 | K | Acetyltransferase (GNAT) domain | ||
GCKIAGNM_01171 | 2.4e-56 | vsr | L | May nick specific sequences that contain T G mispairs resulting from m5C-deamination | ||
GCKIAGNM_01172 | 9.7e-127 | afr_2 | S | Oxidoreductase family, NAD-binding Rossmann fold | ||
GCKIAGNM_01173 | 1.1e-31 | afr_2 | S | Oxidoreductase family, NAD-binding Rossmann fold | ||
GCKIAGNM_01174 | 3e-234 | aspB | E | Aminotransferase class-V | ||
GCKIAGNM_01175 | 2.9e-179 | ppx | 3.6.1.11, 3.6.1.40 | FP | Ppx/GppA phosphatase family | |
GCKIAGNM_01176 | 1.6e-192 | S | Endonuclease/Exonuclease/phosphatase family | |||
GCKIAGNM_01178 | 7.9e-34 | F | Nucleoside 2-deoxyribosyltransferase | |||
GCKIAGNM_01179 | 3.2e-65 | 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 | ||
GCKIAGNM_01180 | 1.3e-29 | fadD | 6.2.1.3 | I | AMP-binding enzyme | |
GCKIAGNM_01181 | 6.2e-40 | fadD | 6.2.1.3 | I | AMP-binding enzyme | |
GCKIAGNM_01182 | 1.2e-115 | fadD | 6.2.1.3 | I | AMP-binding enzyme | |
GCKIAGNM_01183 | 7.5e-28 | fadD | 6.2.1.3 | I | AMP-binding enzyme | |
GCKIAGNM_01184 | 3.9e-60 | fadD | 6.2.1.3 | I | AMP-binding enzyme | |
GCKIAGNM_01185 | 2.2e-42 | ywrO | 1.6.5.2 | S | Flavodoxin-like fold | |
GCKIAGNM_01186 | 1.6e-20 | ywrO | 1.6.5.2 | S | Flavodoxin-like fold | |
GCKIAGNM_01187 | 2.4e-41 | 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 | |
GCKIAGNM_01188 | 8.3e-257 | xseA | 3.1.11.6 | L | Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides | |
GCKIAGNM_01189 | 2.6e-60 | nrdD | 1.1.98.6 | F | Anaerobic ribonucleoside-triphosphate reductase | |
GCKIAGNM_01190 | 6.1e-100 | nrdD | 1.1.98.6 | F | Anaerobic ribonucleoside-triphosphate reductase | |
GCKIAGNM_01191 | 4.5e-204 | nrdD | 1.1.98.6 | F | Anaerobic ribonucleoside-triphosphate reductase | |
GCKIAGNM_01192 | 6.5e-136 | 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 | |
GCKIAGNM_01193 | 8.3e-89 | hgdC | I | CoA enzyme activase uncharacterised domain (DUF2229) | ||
GCKIAGNM_01194 | 4e-69 | hgdC | I | CoA enzyme activase uncharacterised domain (DUF2229) | ||
GCKIAGNM_01195 | 0.0 | hgdC | I | CoA enzyme activase uncharacterised domain (DUF2229) | ||
GCKIAGNM_01196 | 1.5e-186 | hgdC | I | CoA enzyme activase uncharacterised domain (DUF2229) | ||
GCKIAGNM_01197 | 5.5e-255 | gshA | 6.3.2.2 | H | Glutamate-cysteine ligase family 2(GCS2) | |
GCKIAGNM_01198 | 9.2e-132 | K | Bacterial regulatory proteins, tetR family | |||
GCKIAGNM_01199 | 6.3e-23 | bgl2 | 3.2.1.21 | GH3 | G | Fibronectin type III-like domain |
GCKIAGNM_01200 | 8.4e-170 | bgl2 | 3.2.1.21 | GH3 | G | Fibronectin type III-like domain |
GCKIAGNM_01201 | 8.6e-30 | hisS | 6.1.1.21 | J | Histidyl-tRNA synthetase | |
GCKIAGNM_01202 | 8.8e-150 | hisS | 6.1.1.21 | J | Histidyl-tRNA synthetase | |
GCKIAGNM_01203 | 2.2e-91 | aspS | 6.1.1.12 | J | Aspartyl-tRNA synthetase with relaxed tRNA specificity since it is able to aspartylate not only its cognate tRNA(Asp) but also tRNA(Asn). Reaction proceeds in two steps L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp Asn) | |
GCKIAGNM_01204 | 6.1e-102 | S | Aminoacyl-tRNA editing domain | |||
GCKIAGNM_01205 | 3.5e-152 | gluA | 3.6.3.21 | E | ATP-binding protein of ABC transporter for glutamate K02028 | |
GCKIAGNM_01206 | 2.3e-22 | gluB | ET | Belongs to the bacterial solute-binding protein 3 family | ||
GCKIAGNM_01207 | 1.9e-15 | gluB | ET | Belongs to the bacterial solute-binding protein 3 family | ||
GCKIAGNM_01208 | 1.2e-44 | gluB | ET | Belongs to the bacterial solute-binding protein 3 family | ||
GCKIAGNM_01209 | 1.2e-110 | gluC | E | Binding-protein-dependent transport system inner membrane component | ||
GCKIAGNM_01210 | 1e-193 | gluD | E | Binding-protein-dependent transport system inner membrane component | ||
GCKIAGNM_01211 | 8.5e-184 | phoN | I | PAP2 superfamily | ||
GCKIAGNM_01212 | 2.2e-92 | argO | S | LysE type translocator | ||
GCKIAGNM_01213 | 6.3e-287 | ydfD | EK | Alanine-glyoxylate amino-transferase | ||
GCKIAGNM_01214 | 6e-49 | 2.7.4.1 | S | Polyphosphate kinase 2 (PPK2) | ||
GCKIAGNM_01215 | 6.1e-81 | 2.7.4.1 | S | Polyphosphate kinase 2 (PPK2) | ||
GCKIAGNM_01216 | 3.4e-194 | helY | L | DEAD DEAH box helicase | ||
GCKIAGNM_01217 | 1.4e-76 | helY | L | DEAD DEAH box helicase | ||
GCKIAGNM_01218 | 2.7e-91 | helY | L | DEAD DEAH box helicase | ||
GCKIAGNM_01219 | 2e-48 | rarA | L | Recombination factor protein RarA | ||
GCKIAGNM_01220 | 3.7e-48 | rarA | L | Recombination factor protein RarA | ||
GCKIAGNM_01221 | 8.6e-46 | rarA | L | Recombination factor protein RarA | ||
GCKIAGNM_01222 | 6.9e-11 | KT | Transcriptional regulatory protein, C terminal | |||
GCKIAGNM_01223 | 2.3e-33 | mtrB | 2.7.13.3 | T | HAMP (Histidine kinases, Adenylyl cyclases, Methyl binding proteins, Phosphatases) domain | |
GCKIAGNM_01224 | 9.3e-187 | EGP | Major facilitator Superfamily | |||
GCKIAGNM_01225 | 6.3e-50 | EGP | Major facilitator Superfamily | |||
GCKIAGNM_01226 | 3.8e-187 | ghrA | EH | D-isomer specific 2-hydroxyacid dehydrogenase, NAD binding domain | ||
GCKIAGNM_01227 | 5.1e-56 | |||||
GCKIAGNM_01228 | 1.4e-54 | yvlD | S | Mycobacterial 4 TMS phage holin, superfamily IV | ||
GCKIAGNM_01229 | 3.1e-47 | yhbY | J | CRS1_YhbY | ||
GCKIAGNM_01230 | 6.5e-97 | ecfA | GP | ABC transporter, ATP-binding protein | ||
GCKIAGNM_01231 | 2.6e-107 | ecfA | GP | ABC transporter, ATP-binding protein | ||
GCKIAGNM_01232 | 1.8e-126 | ecfA | GP | ABC transporter, ATP-binding protein | ||
GCKIAGNM_01233 | 1.3e-93 | ribU | U | Mediates riboflavin uptake, may also transport FMN and roseoflavin. Probably a riboflavin-binding protein that interacts with the energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates. The substrates themselves are bound by transmembrane, not extracytoplasmic soluble proteins | ||
GCKIAGNM_01234 | 7.1e-198 | S | Glycosyltransferase, group 2 family protein | |||
GCKIAGNM_01235 | 1.6e-30 | C | Putative TM nitroreductase | |||
GCKIAGNM_01236 | 1.3e-53 | C | Putative TM nitroreductase | |||
GCKIAGNM_01237 | 1.2e-39 | ppgK | 2.7.1.2, 2.7.1.63 | GK | ROK family | |
GCKIAGNM_01238 | 1.9e-86 | ppgK | 2.7.1.2, 2.7.1.63 | GK | ROK family | |
GCKIAGNM_01239 | 3.3e-280 | cscA | 3.2.1.26 | GH32 | G | Belongs to the glycosyl hydrolase 32 family |
GCKIAGNM_01240 | 6.2e-241 | lacY | P | LacY proton/sugar symporter | ||
GCKIAGNM_01241 | 2.8e-87 | K | helix_turn _helix lactose operon repressor | |||
GCKIAGNM_01242 | 5.5e-74 | K | helix_turn _helix lactose operon repressor | |||
GCKIAGNM_01243 | 1.3e-257 | O | SERine Proteinase INhibitors | |||
GCKIAGNM_01244 | 4.5e-191 | |||||
GCKIAGNM_01245 | 8.2e-70 | K | helix_turn_helix, Lux Regulon | |||
GCKIAGNM_01246 | 1.8e-214 | 2.7.13.3 | T | Histidine kinase | ||
GCKIAGNM_01247 | 3e-85 | ydjK | G | Sugar (and other) transporter | ||
GCKIAGNM_01248 | 2.4e-125 | ydjK | G | Sugar (and other) transporter | ||
GCKIAGNM_01249 | 3.1e-37 | S | Thiamine-binding protein | |||
GCKIAGNM_01250 | 1.4e-11 | S | Thiamine-binding protein | |||
GCKIAGNM_01251 | 4.1e-193 | O | AAA domain (Cdc48 subfamily) | |||
GCKIAGNM_01252 | 3.1e-45 | |||||
GCKIAGNM_01253 | 4.5e-65 | int8 | L | Phage integrase family | ||
GCKIAGNM_01254 | 7.4e-19 | int8 | L | Phage integrase family | ||
GCKIAGNM_01255 | 1.9e-53 | 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 | ||
GCKIAGNM_01256 | 7.2e-71 | G | Major Facilitator Superfamily | |||
GCKIAGNM_01257 | 6.4e-43 | G | Major Facilitator Superfamily | |||
GCKIAGNM_01258 | 4e-119 | 2.7.1.4 | G | pfkB family carbohydrate kinase | ||
GCKIAGNM_01259 | 3e-19 | 2.7.1.4 | G | pfkB family carbohydrate kinase | ||
GCKIAGNM_01261 | 5.9e-174 | GK | ROK family | |||
GCKIAGNM_01262 | 4.7e-27 | GK | ROK family | |||
GCKIAGNM_01263 | 1.1e-83 | 2.7.1.2 | GK | ROK family | ||
GCKIAGNM_01264 | 2.6e-31 | 2.7.1.2 | GK | ROK family | ||
GCKIAGNM_01265 | 1.1e-208 | GK | ROK family | |||
GCKIAGNM_01266 | 6.2e-151 | 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 | |
GCKIAGNM_01267 | 6.5e-248 | nagA | 3.5.1.25 | G | Amidohydrolase family | |
GCKIAGNM_01268 | 6.9e-21 | 3.6.1.55 | F | NUDIX domain | ||
GCKIAGNM_01269 | 1.7e-51 | 3.6.1.55 | F | NUDIX domain | ||
GCKIAGNM_01270 | 2.8e-162 | pepP | 3.4.11.9 | E | Aminopeptidase P, N-terminal domain | |
GCKIAGNM_01271 | 6.8e-29 | pepP | 3.4.11.9 | E | Aminopeptidase P, N-terminal domain | |
GCKIAGNM_01272 | 8.7e-33 | folC | 6.3.2.12, 6.3.2.17 | H | Mur ligase middle domain | |
GCKIAGNM_01273 | 1.4e-192 | folC | 6.3.2.12, 6.3.2.17 | H | Mur ligase middle domain | |
GCKIAGNM_01274 | 1.4e-126 | smc | D | Required for chromosome condensation and partitioning | ||
GCKIAGNM_01275 | 0.0 | smc | D | Required for chromosome condensation and partitioning | ||
GCKIAGNM_01276 | 1.2e-24 | V | Acetyltransferase (GNAT) domain | |||
GCKIAGNM_01277 | 2.7e-15 | V | Acetyltransferase (GNAT) domain | |||
GCKIAGNM_01278 | 1.9e-85 | V | Acetyltransferase (GNAT) domain | |||
GCKIAGNM_01279 | 1.5e-79 | V | Acetyltransferase (GNAT) domain | |||
GCKIAGNM_01280 | 7.1e-297 | murE | 6.3.2.13, 6.3.2.7 | M | Catalyzes the addition of an amino acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
GCKIAGNM_01281 | 3.9e-142 | sigH | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
GCKIAGNM_01282 | 3.3e-52 | |||||
GCKIAGNM_01283 | 9.6e-120 | galM | 5.1.3.3 | G | Aldose 1-epimerase | |
GCKIAGNM_01284 | 4.2e-50 | galM | 5.1.3.3 | G | Aldose 1-epimerase | |
GCKIAGNM_01285 | 1.7e-66 | galM | 5.1.3.3 | G | Aldose 1-epimerase | |
GCKIAGNM_01286 | 6.7e-91 | galM | 5.1.3.3 | G | Aldose 1-epimerase | |
GCKIAGNM_01287 | 1.6e-40 | ispH | 1.17.7.4, 2.7.4.25 | IM | Catalyzes the conversion of 1-hydroxy-2-methyl-2-(E)- butenyl 4-diphosphate (HMBPP) into a mixture of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP). Acts in the terminal step of the DOXP MEP pathway for isoprenoid precursor biosynthesis | |
GCKIAGNM_01288 | 1.3e-75 | ispH | 1.17.7.4, 2.7.4.25 | IM | Catalyzes the conversion of 1-hydroxy-2-methyl-2-(E)- butenyl 4-diphosphate (HMBPP) into a mixture of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP). Acts in the terminal step of the DOXP MEP pathway for isoprenoid precursor biosynthesis | |
GCKIAGNM_01289 | 8.3e-20 | ispH | 1.17.7.4, 2.7.4.25 | IM | Catalyzes the conversion of 1-hydroxy-2-methyl-2-(E)- butenyl 4-diphosphate (HMBPP) into a mixture of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP). Acts in the terminal step of the DOXP MEP pathway for isoprenoid precursor biosynthesis | |
GCKIAGNM_01290 | 4.2e-89 | ybaK | J | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
GCKIAGNM_01291 | 7e-18 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
GCKIAGNM_01292 | 4.7e-158 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
GCKIAGNM_01293 | 4.2e-135 | 2.7.6.2 | H | Thiamin pyrophosphokinase, vitamin B1 binding domain | ||
GCKIAGNM_01294 | 2e-55 | S | Spermine/spermidine synthase domain | |||
GCKIAGNM_01295 | 3e-110 | 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 | ||
GCKIAGNM_01296 | 6.2e-25 | rpmI | J | Ribosomal protein L35 | ||
GCKIAGNM_01297 | 1.8e-60 | 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 | ||
GCKIAGNM_01298 | 1.9e-59 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
GCKIAGNM_01299 | 6e-143 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
GCKIAGNM_01300 | 6.2e-34 | xerD | D | recombinase XerD | ||
GCKIAGNM_01301 | 1.9e-110 | xerD | D | recombinase XerD | ||
GCKIAGNM_01302 | 1.4e-151 | soj | D | CobQ CobB MinD ParA nucleotide binding domain protein | ||
GCKIAGNM_01303 | 7.2e-76 | 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 | ||
GCKIAGNM_01304 | 2.3e-60 | 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 | ||
GCKIAGNM_01305 | 6.2e-82 | 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 | ||
GCKIAGNM_01306 | 1.8e-66 | nrtR | 3.6.1.55 | F | NUDIX hydrolase | |
GCKIAGNM_01307 | 7.8e-35 | nrtR | 3.6.1.55 | F | NUDIX hydrolase | |
GCKIAGNM_01308 | 1.2e-71 | nadA | 2.5.1.72 | H | Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate | |
GCKIAGNM_01309 | 1.8e-89 | nadA | 2.5.1.72 | H | Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate | |
GCKIAGNM_01310 | 1.1e-68 | nadB | 1.3.5.4, 1.4.3.16, 2.4.2.19 | H | Catalyzes the oxidation of L-aspartate to iminoaspartate | |
GCKIAGNM_01311 | 5.2e-65 | nadB | 1.3.5.4, 1.4.3.16, 2.4.2.19 | H | Catalyzes the oxidation of L-aspartate to iminoaspartate | |
GCKIAGNM_01312 | 1.2e-14 | nadB | 1.3.5.4, 1.4.3.16, 2.4.2.19 | H | Catalyzes the oxidation of L-aspartate to iminoaspartate | |
GCKIAGNM_01313 | 1.7e-208 | malL | 3.2.1.1, 5.4.99.16 | GH13 | G | Alpha-amylase domain |
GCKIAGNM_01314 | 1.3e-59 | malE | G | Bacterial extracellular solute-binding protein | ||
GCKIAGNM_01315 | 7.9e-90 | malE | G | Bacterial extracellular solute-binding protein | ||
GCKIAGNM_01316 | 2.8e-38 | malE | G | Bacterial extracellular solute-binding protein | ||
GCKIAGNM_01317 | 7.5e-83 | malF | G | Binding-protein-dependent transport system inner membrane component | ||
GCKIAGNM_01318 | 2.9e-75 | malF | G | Binding-protein-dependent transport system inner membrane component | ||
GCKIAGNM_01319 | 8.5e-165 | malG | G | Binding-protein-dependent transport system inner membrane component | ||
GCKIAGNM_01320 | 1.9e-144 | traX | S | TraX protein | ||
GCKIAGNM_01321 | 1.1e-194 | K | Psort location Cytoplasmic, score | |||
GCKIAGNM_01322 | 9.8e-40 | pulA | 3.2.1.1, 3.2.1.41 | CBM48,GH13 | M | Aamy_C |
GCKIAGNM_01323 | 1.6e-142 | pulA | 3.2.1.1, 3.2.1.41 | CBM48,GH13 | M | Aamy_C |
GCKIAGNM_01324 | 2.3e-181 | pulA | 3.2.1.1, 3.2.1.41 | CBM48,GH13 | M | Aamy_C |
GCKIAGNM_01325 | 4.6e-57 | pulA | 3.2.1.1, 3.2.1.41 | CBM48,GH13 | M | Aamy_C |
GCKIAGNM_01326 | 4.8e-146 | pulA | 3.2.1.1, 3.2.1.41 | CBM48,GH13 | M | Aamy_C |
GCKIAGNM_01327 | 2.7e-298 | pulA | 3.2.1.1, 3.2.1.41 | CBM48,GH13 | M | Aamy_C |
GCKIAGNM_01328 | 6.2e-180 | dnaK | O | Heat shock 70 kDa protein | ||
GCKIAGNM_01329 | 9.2e-72 | dnaK | O | Heat shock 70 kDa protein | ||
GCKIAGNM_01330 | 6.9e-51 | dnaK | O | Heat shock 70 kDa protein | ||
GCKIAGNM_01332 | 4.8e-44 | 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 | ||
GCKIAGNM_01333 | 7.2e-124 | dnaJ1 | O | DnaJ molecular chaperone homology domain | ||
GCKIAGNM_01334 | 3.8e-19 | dnaJ1 | O | DnaJ molecular chaperone homology domain | ||
GCKIAGNM_01335 | 3.3e-52 | hspR | K | transcriptional regulator, MerR family | ||
GCKIAGNM_01336 | 1.4e-33 | hspR | K | transcriptional regulator, MerR family | ||
GCKIAGNM_01337 | 3.1e-17 | F | Psort location CytoplasmicMembrane, score 10.00 | |||
GCKIAGNM_01338 | 1.6e-93 | luxC | 1.2.1.50 | C | Acyl-CoA reductase (LuxC) | |
GCKIAGNM_01339 | 2.6e-98 | IQ | Oxidoreductase, short chain dehydrogenase reductase family protein | |||
GCKIAGNM_01340 | 4.5e-111 | S | HAD hydrolase, family IA, variant 3 | |||
GCKIAGNM_01341 | 1.8e-110 | dedA | S | SNARE associated Golgi protein | ||
GCKIAGNM_01342 | 6.1e-18 | dedA | S | SNARE associated Golgi protein | ||
GCKIAGNM_01343 | 2.4e-123 | cpaE | D | bacterial-type flagellum organization | ||
GCKIAGNM_01344 | 2.9e-174 | cpaF | U | Type II IV secretion system protein | ||
GCKIAGNM_01345 | 1.3e-94 | U | Type ii secretion system | |||
GCKIAGNM_01346 | 5.3e-32 | gspF | NU | Type II secretion system (T2SS), protein F | ||
GCKIAGNM_01347 | 1.4e-40 | gspF | NU | Type II secretion system (T2SS), protein F | ||
GCKIAGNM_01348 | 1.3e-18 | S | Protein of unknown function (DUF4244) | |||
GCKIAGNM_01349 | 1.4e-57 | U | TadE-like protein | |||
GCKIAGNM_01350 | 6.5e-54 | S | TIGRFAM helicase secretion neighborhood TadE-like protein | |||
GCKIAGNM_01351 | 8.2e-131 | dagK | 2.7.1.107 | I | Diacylglycerol kinase catalytic domain protein | |
GCKIAGNM_01352 | 4.8e-66 | dagK | 2.7.1.107 | I | Diacylglycerol kinase catalytic domain protein | |
GCKIAGNM_01353 | 6.5e-97 | K | Bacterial regulatory proteins, tetR family | |||
GCKIAGNM_01354 | 5.6e-237 | dnaX | 2.7.7.7 | L | DNA polymerase III subunit gamma tau | |
GCKIAGNM_01355 | 5.7e-23 | dnaX | 2.7.7.7 | L | DNA polymerase III subunit gamma tau | |
GCKIAGNM_01356 | 8.7e-110 | recR | L | May play a role in DNA repair. It seems to be involved in an RecBC-independent recombinational process of DNA repair. It may act with RecF and RecO | ||
GCKIAGNM_01357 | 3.4e-36 | S | ATPase domain predominantly from Archaea | |||
GCKIAGNM_01358 | 3.3e-196 | 3.4.22.70 | M | Sortase family | ||
GCKIAGNM_01359 | 3.7e-168 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
GCKIAGNM_01360 | 2.1e-121 | ask | 1.1.1.3, 2.7.2.4 | E | Amino acid kinase family | |
GCKIAGNM_01361 | 9.4e-98 | askB | 1.1.1.3, 2.7.2.4 | E | ACT domain | |
GCKIAGNM_01362 | 9.4e-21 | asd | 1.2.1.11, 1.2.1.12 | E | Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate | |
GCKIAGNM_01363 | 4.4e-167 | asd | 1.2.1.11, 1.2.1.12 | E | Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate | |
GCKIAGNM_01364 | 1.4e-93 | |||||
GCKIAGNM_01365 | 3.2e-43 | gcvR | T | Belongs to the UPF0237 family | ||
GCKIAGNM_01366 | 2.6e-142 | S | UPF0210 protein | |||
GCKIAGNM_01367 | 4.8e-67 | S | UPF0210 protein | |||
GCKIAGNM_01368 | 2.4e-12 | S | UPF0210 protein | |||
GCKIAGNM_01370 | 7.6e-115 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
GCKIAGNM_01371 | 2.9e-127 | mutY | 2.1.1.37, 2.1.3.15, 6.4.1.2 | L | FES | |
GCKIAGNM_01372 | 3e-127 | |||||
GCKIAGNM_01373 | 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 | |
GCKIAGNM_01374 | 3.5e-138 | rpoB | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
GCKIAGNM_01375 | 7.9e-17 | rpoC | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
GCKIAGNM_01376 | 4.2e-53 | rpoC | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
GCKIAGNM_01377 | 1.4e-100 | rpoC | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
GCKIAGNM_01378 | 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 | |
GCKIAGNM_01379 | 2.5e-74 | E | Transglutaminase-like superfamily | |||
GCKIAGNM_01380 | 5.7e-144 | E | Transglutaminase-like superfamily | |||
GCKIAGNM_01381 | 6.2e-177 | E | Transglutaminase-like superfamily | |||
GCKIAGNM_01382 | 1.9e-240 | S | Protein of unknown function DUF58 | |||
GCKIAGNM_01383 | 6.1e-161 | S | Fibronectin type 3 domain | |||
GCKIAGNM_01384 | 1.1e-163 | S | Fibronectin type 3 domain | |||
GCKIAGNM_01385 | 3.8e-257 | S | Fibronectin type 3 domain | |||
GCKIAGNM_01386 | 6.9e-174 | S | Fibronectin type 3 domain | |||
GCKIAGNM_01387 | 4.6e-54 | S | Fibronectin type 3 domain | |||
GCKIAGNM_01388 | 4.6e-29 | KLT | Protein tyrosine kinase | |||
GCKIAGNM_01389 | 7.6e-115 | KLT | Protein tyrosine kinase | |||
GCKIAGNM_01390 | 0.0 | uvrD | 3.6.4.12 | L | PD-(D/E)XK nuclease superfamily | |
GCKIAGNM_01391 | 6.2e-199 | uvrD | 3.6.4.12 | L | PD-(D/E)XK nuclease superfamily | |
GCKIAGNM_01392 | 1.4e-47 | uvrD | 3.6.4.12 | L | PD-(D/E)XK nuclease superfamily | |
GCKIAGNM_01393 | 2.1e-151 | uvrD | 3.6.4.12 | L | PD-(D/E)XK nuclease superfamily | |
GCKIAGNM_01394 | 1.1e-87 | uvrD2 | 3.6.4.12 | L | Belongs to the helicase family. UvrD subfamily | |
GCKIAGNM_01395 | 1.8e-310 | uvrD2 | 3.6.4.12 | L | Belongs to the helicase family. UvrD subfamily | |
GCKIAGNM_01396 | 5.3e-195 | uvrD2 | 3.6.4.12 | L | Belongs to the helicase family. UvrD subfamily | |
GCKIAGNM_01397 | 3.4e-113 | G | Major Facilitator Superfamily | |||
GCKIAGNM_01398 | 3.1e-93 | G | Major Facilitator Superfamily | |||
GCKIAGNM_01399 | 1e-18 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
GCKIAGNM_01400 | 1.1e-176 | K | helix_turn _helix lactose operon repressor | |||
GCKIAGNM_01401 | 1.5e-20 | G | Bacterial extracellular solute-binding protein | |||
GCKIAGNM_01402 | 6.9e-139 | G | Bacterial extracellular solute-binding protein | |||
GCKIAGNM_01405 | 4.2e-08 | K | Helix-turn-helix domain, rpiR family | |||
GCKIAGNM_01406 | 5.9e-60 | K | Helix-turn-helix domain, rpiR family | |||
GCKIAGNM_01407 | 8.9e-54 | K | Helix-turn-helix domain, rpiR family | |||
GCKIAGNM_01408 | 7e-43 | G | Alpha-L-arabinofuranosidase C-terminal domain | |||
GCKIAGNM_01409 | 3.3e-30 | |||||
GCKIAGNM_01410 | 3.3e-164 | ybiR | P | Citrate transporter | ||
GCKIAGNM_01411 | 6.2e-36 | ybiR | P | Citrate transporter | ||
GCKIAGNM_01412 | 3.7e-276 | EK | Alanine-glyoxylate amino-transferase | |||
GCKIAGNM_01413 | 2.6e-08 | EK | Alanine-glyoxylate amino-transferase | |||
GCKIAGNM_01414 | 1.1e-115 | pdxT | 4.3.3.6 | H | Catalyzes the hydrolysis of glutamine to glutamate and ammonia as part of the biosynthesis of pyridoxal 5'-phosphate. The resulting ammonia molecule is channeled to the active site of PdxS | |
GCKIAGNM_01415 | 3.6e-123 | pdxS | 4.3.3.6 | H | Catalyzes the formation of pyridoxal 5'-phosphate from ribose 5-phosphate (RBP), glyceraldehyde 3-phosphate (G3P) and ammonia. The ammonia is provided by the PdxT subunit. Can also use ribulose 5-phosphate and dihydroxyacetone phosphate as substrates, resulting from enzyme-catalyzed isomerization of RBP and G3P, respectively | |
GCKIAGNM_01416 | 5.1e-34 | |||||
GCKIAGNM_01417 | 7.4e-08 | S | PIN domain | |||
GCKIAGNM_01418 | 5.8e-46 | S | PIN domain | |||
GCKIAGNM_01419 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
GCKIAGNM_01420 | 3.9e-78 | dgt | 3.1.5.1 | F | Phosphohydrolase-associated domain | |
GCKIAGNM_01421 | 2.5e-76 | dgt | 3.1.5.1 | F | Phosphohydrolase-associated domain | |
GCKIAGNM_01422 | 1.9e-31 | alr | 5.1.1.1 | M | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
GCKIAGNM_01423 | 9e-16 | alr | 5.1.1.1 | M | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
GCKIAGNM_01424 | 2.7e-85 | alr | 5.1.1.1 | M | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
GCKIAGNM_01425 | 8.5e-268 | yhdG | E | aromatic amino acid transport protein AroP K03293 | ||
GCKIAGNM_01426 | 1.7e-104 | cysE | 2.3.1.178 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | |
GCKIAGNM_01427 | 8e-93 | luxS | 4.4.1.21 | H | Involved in the synthesis of autoinducer 2 (AI-2) which is secreted by bacteria and is used to communicate both the cell density and the metabolic potential of the environment. The regulation of gene expression in response to changes in cell density is called quorum sensing. Catalyzes the transformation of S-ribosylhomocysteine (RHC) to homocysteine (HC) and 4,5- dihydroxy-2,3-pentadione (DPD) | |
GCKIAGNM_01428 | 0.0 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
GCKIAGNM_01429 | 1.2e-219 | metB | 2.5.1.48, 4.4.1.1, 4.4.1.8 | E | Cys/Met metabolism PLP-dependent enzyme | |
GCKIAGNM_01430 | 4e-56 | cbs | 2.5.1.47, 4.2.1.22 | E | Pyridoxal-phosphate dependent enzyme | |
GCKIAGNM_01431 | 4.7e-100 | cbs | 2.5.1.47, 4.2.1.22 | E | Pyridoxal-phosphate dependent enzyme | |
GCKIAGNM_01432 | 1.5e-124 | sapF | E | ATPases associated with a variety of cellular activities | ||
GCKIAGNM_01433 | 6.5e-137 | oppD | EP | oligopeptide transport protein of the ABC superfamily, ATP-binding component | ||
GCKIAGNM_01434 | 1.8e-48 | EP | Binding-protein-dependent transport system inner membrane component | |||
GCKIAGNM_01435 | 1e-31 | EP | Binding-protein-dependent transport system inner membrane component | |||
GCKIAGNM_01436 | 1.6e-29 | P | Binding-protein-dependent transport system inner membrane component | |||
GCKIAGNM_01437 | 1.3e-48 | P | Binding-protein-dependent transport system inner membrane component | |||
GCKIAGNM_01438 | 2.2e-65 | P | Binding-protein-dependent transport system inner membrane component | |||
GCKIAGNM_01439 | 1.7e-63 | E | ABC transporter, substrate-binding protein, family 5 | |||
GCKIAGNM_01440 | 8.5e-12 | E | ABC transporter, substrate-binding protein, family 5 | |||
GCKIAGNM_01441 | 4.1e-188 | E | ABC transporter, substrate-binding protein, family 5 | |||
GCKIAGNM_01442 | 4.5e-143 | coaX | 2.7.1.33 | H | Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis | |
GCKIAGNM_01443 | 6.2e-44 | G | Bacterial extracellular solute-binding protein | |||
GCKIAGNM_01444 | 6.3e-100 | G | Bacterial extracellular solute-binding protein | |||
GCKIAGNM_01445 | 6.7e-107 | G | Bacterial extracellular solute-binding protein | |||
GCKIAGNM_01446 | 8.7e-181 | G | Bacterial extracellular solute-binding protein | |||
GCKIAGNM_01447 | 2.5e-83 | lacZ5 | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
GCKIAGNM_01448 | 2.4e-181 | lacZ5 | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
GCKIAGNM_01449 | 1.3e-39 | lacZ5 | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
GCKIAGNM_01450 | 3.8e-142 | KT | Transcriptional regulatory protein, C terminal | |||
GCKIAGNM_01451 | 1e-208 | senX3 | 2.7.13.3 | T | His Kinase A (phosphoacceptor) domain | |
GCKIAGNM_01452 | 1.9e-224 | EGP | Sugar (and other) transporter | |||
GCKIAGNM_01453 | 5.7e-124 | 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 | |
GCKIAGNM_01454 | 3.4e-88 | aroG | 2.5.1.54 | E | Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) | |
GCKIAGNM_01455 | 6.6e-131 | aroG | 2.5.1.54 | E | Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) | |
GCKIAGNM_01456 | 6.8e-144 | aroG | 2.5.1.54 | E | Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) | |
GCKIAGNM_01457 | 2.7e-64 | aroG | 2.5.1.54 | E | Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) | |
GCKIAGNM_01458 | 7.9e-93 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
GCKIAGNM_01459 | 1.6e-163 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
GCKIAGNM_01460 | 2.4e-34 | D | nuclear chromosome segregation | |||
GCKIAGNM_01461 | 9.2e-35 | D | nuclear chromosome segregation | |||
GCKIAGNM_01462 | 6.3e-72 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
GCKIAGNM_01463 | 3.7e-39 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
GCKIAGNM_01464 | 1.2e-100 | ispD | 1.1.1.405, 2.7.7.40, 2.7.7.60, 4.6.1.12 | I | Catalyzes the formation of 4-diphosphocytidyl-2-C- methyl-D-erythritol from CTP and 2-C-methyl-D-erythritol 4- phosphate (MEP) | |
GCKIAGNM_01465 | 3.1e-24 | ispD | 1.1.1.405, 2.7.7.40, 2.7.7.60, 4.6.1.12 | I | Catalyzes the formation of 4-diphosphocytidyl-2-C- methyl-D-erythritol from CTP and 2-C-methyl-D-erythritol 4- phosphate (MEP) | |
GCKIAGNM_01466 | 1.8e-113 | yfiH | Q | Multi-copper polyphenol oxidoreductase laccase | ||
GCKIAGNM_01467 | 5.8e-43 | yfiH | Q | Multi-copper polyphenol oxidoreductase laccase | ||
GCKIAGNM_01468 | 1.2e-17 | yfiH | Q | Multi-copper polyphenol oxidoreductase laccase | ||
GCKIAGNM_01469 | 9.9e-263 | yegQ | O | Peptidase family U32 C-terminal domain | ||
GCKIAGNM_01470 | 7.8e-25 | yegQ | O | Peptidase family U32 C-terminal domain | ||
GCKIAGNM_01471 | 3e-139 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
GCKIAGNM_01472 | 5e-102 | rsmD | 2.1.1.171 | L | Conserved hypothetical protein 95 | |
GCKIAGNM_01473 | 0.0 | recG | 3.6.4.12 | L | helicase superfamily c-terminal domain | |
GCKIAGNM_01474 | 6.7e-26 | rpmB | J | Ribosomal L28 family | ||
GCKIAGNM_01475 | 3.4e-88 | yegV | G | pfkB family carbohydrate kinase | ||
GCKIAGNM_01476 | 6.4e-81 | yegV | G | pfkB family carbohydrate kinase | ||
GCKIAGNM_01477 | 6e-115 | yxiO | S | Vacuole effluxer Atg22 like | ||
GCKIAGNM_01478 | 3.2e-110 | yxiO | S | Vacuole effluxer Atg22 like | ||
GCKIAGNM_01479 | 2.6e-95 | K | helix_turn_helix, mercury resistance | |||
GCKIAGNM_01480 | 2.2e-69 | T | Toxic component of a toxin-antitoxin (TA) module | |||
GCKIAGNM_01481 | 3.6e-20 | relB | L | RelB antitoxin | ||
GCKIAGNM_01482 | 6.1e-25 | yxiO | G | Major facilitator Superfamily | ||
GCKIAGNM_01483 | 8.9e-182 | K | Helix-turn-helix XRE-family like proteins | |||
GCKIAGNM_01484 | 8.9e-21 | |||||
GCKIAGNM_01486 | 9.5e-115 | S | Alpha/beta hydrolase family | |||
GCKIAGNM_01490 | 1.9e-17 | EGP | Major facilitator Superfamily | |||
GCKIAGNM_01491 | 5e-24 | XK27_04590 | S | NADPH-dependent FMN reductase | ||
GCKIAGNM_01492 | 1.1e-121 | fas | 2.3.1.179 | I | Beta-ketoacyl synthase, C-terminal domain | |
GCKIAGNM_01493 | 3e-88 | fas | 2.3.1.179 | I | Beta-ketoacyl synthase, C-terminal domain | |
GCKIAGNM_01494 | 1.6e-128 | fas | 2.3.1.179 | I | Beta-ketoacyl synthase, C-terminal domain | |
GCKIAGNM_01495 | 8.6e-123 | fas | 2.3.1.179 | I | Beta-ketoacyl synthase, C-terminal domain | |
GCKIAGNM_01496 | 8.5e-61 | fas | 2.3.1.179 | I | Beta-ketoacyl synthase, C-terminal domain | |
GCKIAGNM_01499 | 5.3e-145 | yplQ | S | Haemolysin-III related | ||
GCKIAGNM_01500 | 1.2e-52 | ybjQ | S | Putative heavy-metal-binding | ||
GCKIAGNM_01501 | 2.8e-60 | nudG | 3.6.1.55, 3.6.1.65 | L | NUDIX domain | |
GCKIAGNM_01502 | 0.0 | KL | Domain of unknown function (DUF3427) | |||
GCKIAGNM_01503 | 1e-50 | KL | Domain of unknown function (DUF3427) | |||
GCKIAGNM_01504 | 2.7e-111 | KL | Domain of unknown function (DUF3427) | |||
GCKIAGNM_01505 | 1.5e-100 | M | Glycosyltransferase like family 2 | |||
GCKIAGNM_01506 | 4.3e-158 | S | Fic/DOC family | |||
GCKIAGNM_01507 | 4.4e-132 | S | Pyridoxamine 5'-phosphate oxidase | |||
GCKIAGNM_01508 | 4.8e-201 | 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 | |
GCKIAGNM_01509 | 3.5e-140 | lysX | S | Uncharacterised conserved protein (DUF2156) | ||
GCKIAGNM_01510 | 8e-155 | lysX | S | Uncharacterised conserved protein (DUF2156) | ||
GCKIAGNM_01511 | 3.5e-56 | lysX | S | Uncharacterised conserved protein (DUF2156) | ||
GCKIAGNM_01512 | 1.2e-255 | S | Putative esterase | |||
GCKIAGNM_01513 | 1.3e-23 | |||||
GCKIAGNM_01514 | 3.1e-53 | yddG | EG | EamA-like transporter family | ||
GCKIAGNM_01515 | 2.7e-112 | yddG | EG | EamA-like transporter family | ||
GCKIAGNM_01516 | 3.1e-75 | hsp20 | O | Hsp20/alpha crystallin family | ||
GCKIAGNM_01517 | 7.5e-213 | pldB | 3.1.1.5 | I | Serine aminopeptidase, S33 | |
GCKIAGNM_01518 | 2.3e-176 | dpp4 | 3.4.14.5 | E | Dipeptidyl peptidase IV (DPP IV) N-terminal region | |
GCKIAGNM_01519 | 1.2e-271 | dpp4 | 3.4.14.5 | E | Dipeptidyl peptidase IV (DPP IV) N-terminal region | |
GCKIAGNM_01520 | 2e-129 | fhaA | T | Protein of unknown function (DUF2662) | ||
GCKIAGNM_01521 | 1e-74 | fhaB | T | Inner membrane component of T3SS, cytoplasmic domain | ||
GCKIAGNM_01522 | 1.2e-160 | pstP | 3.1.3.16 | T | Sigma factor PP2C-like phosphatases | |
GCKIAGNM_01523 | 2.2e-56 | pstP | 3.1.3.16 | T | Sigma factor PP2C-like phosphatases | |
GCKIAGNM_01524 | 1.2e-19 | rodA | D | Belongs to the SEDS family | ||
GCKIAGNM_01525 | 2.7e-161 | rodA | D | Belongs to the SEDS family | ||
GCKIAGNM_01526 | 4.2e-138 | pbpA | M | penicillin-binding protein | ||
GCKIAGNM_01527 | 1.3e-27 | pbpA | M | penicillin-binding protein | ||
GCKIAGNM_01528 | 1e-173 | T | Protein tyrosine kinase | |||
GCKIAGNM_01529 | 7.8e-180 | pknB | 2.7.11.1 | KLT | Protein tyrosine kinase | |
GCKIAGNM_01530 | 1.3e-144 | pknB | 2.7.11.1 | KLT | Protein tyrosine kinase | |
GCKIAGNM_01531 | 2e-120 | trpG | 2.6.1.85 | EH | para-aminobenzoate synthase glutamine amidotransferase component II | |
GCKIAGNM_01532 | 2.8e-162 | srtA | 3.4.22.70 | M | Sortase family | |
GCKIAGNM_01534 | 7.4e-49 | S | Protein of unknown function (DUF2089) | |||
GCKIAGNM_01535 | 1.3e-52 | |||||
GCKIAGNM_01536 | 9.3e-66 | K | Transcriptional regulator | |||
GCKIAGNM_01537 | 3.2e-110 | |||||
GCKIAGNM_01538 | 3.7e-45 | K | sequence-specific DNA binding | |||
GCKIAGNM_01539 | 8.3e-34 | hipA | 2.7.11.1 | S | kinase activity | |
GCKIAGNM_01540 | 4.4e-42 | 2.6.1.76 | EGP | Major Facilitator Superfamily | ||
GCKIAGNM_01541 | 7e-19 | 2.6.1.76 | EGP | Major Facilitator Superfamily | ||
GCKIAGNM_01542 | 1.6e-253 | mmuP | E | amino acid | ||
GCKIAGNM_01543 | 1.8e-22 | mmuP | E | amino acid | ||
GCKIAGNM_01545 | 1.7e-64 | yeaO | K | Protein of unknown function, DUF488 | ||
GCKIAGNM_01546 | 1.3e-75 | |||||
GCKIAGNM_01547 | 5e-174 | 3.6.4.12 | ||||
GCKIAGNM_01548 | 1.2e-62 | yijF | S | Domain of unknown function (DUF1287) | ||
GCKIAGNM_01549 | 5.4e-20 | yijF | S | Domain of unknown function (DUF1287) | ||
GCKIAGNM_01550 | 1.9e-203 | trpE | 4.1.3.27 | E | Part of a heterotetrameric complex that catalyzes the two-step biosynthesis of anthranilate, an intermediate in the biosynthesis of L-tryptophan. In the first step, the glutamine- binding beta subunit (TrpG) of anthranilate synthase (AS) provides the glutamine amidotransferase activity which generates ammonia as a substrate that, along with chorismate, is used in the second step, catalyzed by the large alpha subunit of AS (TrpE) to produce anthranilate. In the absence of TrpG, TrpE can synthesize anthranilate directly from chorismate and high concentrations of ammonia | |
GCKIAGNM_01551 | 9.6e-72 | trpE | 4.1.3.27 | E | Part of a heterotetrameric complex that catalyzes the two-step biosynthesis of anthranilate, an intermediate in the biosynthesis of L-tryptophan. In the first step, the glutamine- binding beta subunit (TrpG) of anthranilate synthase (AS) provides the glutamine amidotransferase activity which generates ammonia as a substrate that, along with chorismate, is used in the second step, catalyzed by the large alpha subunit of AS (TrpE) to produce anthranilate. In the absence of TrpG, TrpE can synthesize anthranilate directly from chorismate and high concentrations of ammonia | |
GCKIAGNM_01552 | 5.3e-71 | hisI | 3.5.4.19, 3.6.1.31 | E | Catalyzes the hydrolysis of the adenine ring of phosphoribosyl-AMP | |
GCKIAGNM_01553 | 6.1e-140 | hisF | 4.1.3.27 | E | IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisF subunit catalyzes the cyclization activity that produces IGP and AICAR from PRFAR using the ammonia provided by the HisH subunit | |
GCKIAGNM_01554 | 2.1e-36 | 3.5.1.124 | S | DJ-1/PfpI family | ||
GCKIAGNM_01555 | 2.7e-224 | rlmN | 2.1.1.192 | J | Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs | |
GCKIAGNM_01556 | 1.1e-159 | cdsA | 2.7.7.41, 2.7.7.67 | I | Cytidylyltransferase family | |
GCKIAGNM_01557 | 1.6e-35 | 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 | ||
GCKIAGNM_01558 | 1e-42 | 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 | ||
GCKIAGNM_01559 | 1.4e-59 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
GCKIAGNM_01560 | 4.8e-61 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
GCKIAGNM_01561 | 1.8e-57 | 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 | ||
GCKIAGNM_01562 | 1.3e-53 | 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 | ||
GCKIAGNM_01565 | 9.4e-118 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
GCKIAGNM_01566 | 2.2e-87 | def | 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions | |
GCKIAGNM_01567 | 2.5e-149 | fadD3 | 6.2.1.3 | I | long-chain-fatty acid CoA ligase | |
GCKIAGNM_01568 | 5.8e-157 | fadD3 | 6.2.1.3 | I | long-chain-fatty acid CoA ligase | |
GCKIAGNM_01569 | 5.5e-80 | |||||
GCKIAGNM_01570 | 4.6e-73 | guaB | 1.1.1.205 | F | IMP dehydrogenase family protein | |
GCKIAGNM_01571 | 2.3e-49 | guaB | 1.1.1.205 | F | IMP dehydrogenase family protein | |
GCKIAGNM_01572 | 1.9e-195 | icd | 1.1.1.42 | C | Belongs to the isocitrate and isopropylmalate dehydrogenases family | |
GCKIAGNM_01573 | 1.5e-12 | icd | 1.1.1.42 | C | Belongs to the isocitrate and isopropylmalate dehydrogenases family | |
GCKIAGNM_01574 | 8.1e-103 | G | ABC transporter substrate-binding protein | |||
GCKIAGNM_01575 | 2e-145 | G | ABC transporter substrate-binding protein | |||
GCKIAGNM_01576 | 2.9e-93 | M | Peptidase family M23 | |||
GCKIAGNM_01578 | 5.4e-34 | xerH | L | Phage integrase family | ||
GCKIAGNM_01579 | 3.4e-20 | 2.7.11.1 | S | HipA-like C-terminal domain | ||
GCKIAGNM_01581 | 4.5e-123 | S | Fic/DOC family | |||
GCKIAGNM_01582 | 1.6e-62 | L | PFAM Relaxase mobilization nuclease family protein | |||
GCKIAGNM_01583 | 1.7e-56 | L | PFAM Relaxase mobilization nuclease family protein | |||
GCKIAGNM_01584 | 4.2e-38 | V | AAA domain, putative AbiEii toxin, Type IV TA system | |||
GCKIAGNM_01585 | 3.3e-30 | V | AAA domain, putative AbiEii toxin, Type IV TA system | |||
GCKIAGNM_01586 | 1.2e-13 | V | ATPases associated with a variety of cellular activities | |||
GCKIAGNM_01587 | 5.3e-143 | V | Efflux ABC transporter, permease protein | |||
GCKIAGNM_01588 | 6.3e-71 | V | Efflux ABC transporter, permease protein | |||
GCKIAGNM_01589 | 2.4e-15 | V | Efflux ABC transporter, permease protein | |||
GCKIAGNM_01590 | 4.1e-192 | K | Bacterial regulatory proteins, lacI family | |||
GCKIAGNM_01591 | 3.2e-134 | 4.2.1.68 | M | Enolase C-terminal domain-like | ||
GCKIAGNM_01592 | 3.1e-80 | 4.2.1.68 | M | Enolase C-terminal domain-like | ||
GCKIAGNM_01593 | 2.8e-148 | IQ | KR domain | |||
GCKIAGNM_01594 | 2e-202 | fucP | G | Major Facilitator Superfamily | ||
GCKIAGNM_01595 | 1.3e-37 | S | Amidohydrolase | |||
GCKIAGNM_01596 | 1.7e-41 | S | Amidohydrolase | |||
GCKIAGNM_01597 | 3.2e-39 | S | Amidohydrolase | |||
GCKIAGNM_01598 | 5.7e-166 | dapA | 4.1.2.28, 4.3.3.7 | EM | Dihydrodipicolinate synthetase family | |
GCKIAGNM_01599 | 1.9e-167 | mdcF | S | Transporter, auxin efflux carrier (AEC) family protein | ||
GCKIAGNM_01600 | 1.4e-12 | dapE | 3.5.1.18 | E | Peptidase dimerisation domain | |
GCKIAGNM_01601 | 1.2e-103 | dapE | 3.5.1.18 | E | Peptidase dimerisation domain | |
GCKIAGNM_01602 | 2.7e-10 | dapE | 3.5.1.18 | E | Peptidase dimerisation domain | |
GCKIAGNM_01603 | 2.4e-18 | dapE | 3.5.1.18 | E | Peptidase dimerisation domain | |
GCKIAGNM_01604 | 1.9e-10 | rne | 3.1.26.12 | J | Ribonuclease E/G family | |
GCKIAGNM_01605 | 9e-92 | rne | 3.1.26.12 | J | Ribonuclease E/G family | |
GCKIAGNM_01606 | 5.6e-200 | rne | 3.1.26.12 | J | Ribonuclease E/G family | |
GCKIAGNM_01607 | 1.5e-27 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
GCKIAGNM_01608 | 3.4e-21 | rpmA | J | Ribosomal L27 protein | ||
GCKIAGNM_01609 | 2.9e-55 | 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 | ||
GCKIAGNM_01610 | 8.2e-210 | 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 | ||
GCKIAGNM_01611 | 8.3e-199 | proB | 2.7.2.11 | E | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
GCKIAGNM_01612 | 1.3e-208 | G | polysaccharide deacetylase | |||
GCKIAGNM_01613 | 1.2e-50 | aspC | E | DegT/DnrJ/EryC1/StrS aminotransferase family | ||
GCKIAGNM_01614 | 5.9e-94 | aspC | E | DegT/DnrJ/EryC1/StrS aminotransferase family | ||
GCKIAGNM_01616 | 1.8e-31 | 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 | ||
GCKIAGNM_01617 | 3.8e-65 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
GCKIAGNM_01618 | 4.5e-21 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
GCKIAGNM_01619 | 2.3e-19 | K | Psort location Cytoplasmic, score | |||
GCKIAGNM_01620 | 5.4e-112 | K | Psort location Cytoplasmic, score | |||
GCKIAGNM_01621 | 1e-72 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
GCKIAGNM_01622 | 4.6e-103 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
GCKIAGNM_01623 | 5.1e-66 | QT | PucR C-terminal helix-turn-helix domain | |||
GCKIAGNM_01624 | 6.9e-48 | QT | PucR C-terminal helix-turn-helix domain | |||
GCKIAGNM_01625 | 1.7e-119 | |||||
GCKIAGNM_01626 | 2.8e-75 | |||||
GCKIAGNM_01627 | 1.4e-138 | |||||
GCKIAGNM_01628 | 5.3e-55 | birA | 2.7.1.33, 6.3.4.15 | H | Biotin/lipoate A/B protein ligase family | |
GCKIAGNM_01629 | 4.7e-79 | birA | 2.7.1.33, 6.3.4.15 | H | Biotin/lipoate A/B protein ligase family | |
GCKIAGNM_01630 | 9e-14 | bioY | S | BioY family | ||
GCKIAGNM_01631 | 9.8e-42 | bioY | S | BioY family | ||
GCKIAGNM_01632 | 4e-195 | accA | 6.3.4.14, 6.4.1.2, 6.4.1.3 | I | Carbamoyl-phosphate synthase L chain, ATP binding domain protein | |
GCKIAGNM_01633 | 2.3e-84 | accA | 6.3.4.14, 6.4.1.2, 6.4.1.3 | I | Carbamoyl-phosphate synthase L chain, ATP binding domain protein | |
GCKIAGNM_01634 | 3.2e-27 | accA | 6.3.4.14, 6.4.1.2, 6.4.1.3 | I | Carbamoyl-phosphate synthase L chain, ATP binding domain protein | |
GCKIAGNM_01635 | 1.6e-10 | L | Transposase | |||
GCKIAGNM_01636 | 3.4e-50 | |||||
GCKIAGNM_01637 | 3e-45 | |||||
GCKIAGNM_01638 | 4.9e-34 | V | ABC transporter | |||
GCKIAGNM_01639 | 1.6e-66 | V | ABC transporter | |||
GCKIAGNM_01640 | 8.3e-112 | K | COG2197 Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | |||
GCKIAGNM_01641 | 2.8e-191 | 2.7.13.3 | T | Histidine kinase | ||
GCKIAGNM_01642 | 2.7e-20 | L | Transposase | |||
GCKIAGNM_01643 | 1e-75 | EGP | Major Facilitator Superfamily | |||
GCKIAGNM_01644 | 1.3e-49 | EGP | Major Facilitator Superfamily | |||
GCKIAGNM_01645 | 1.4e-40 | EGP | Major Facilitator Superfamily | |||
GCKIAGNM_01646 | 6.2e-43 | |||||
GCKIAGNM_01647 | 4.6e-43 | |||||
GCKIAGNM_01648 | 6.2e-47 | xerH | L | Belongs to the 'phage' integrase family | ||
GCKIAGNM_01649 | 1.6e-67 | xerH | L | Belongs to the 'phage' integrase family | ||
GCKIAGNM_01650 | 1e-128 | gla | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
GCKIAGNM_01651 | 0.0 | pacS | 1.9.3.1, 3.6.3.54 | P | E1-E2 ATPase | |
GCKIAGNM_01652 | 1.2e-40 | pacS | 1.9.3.1, 3.6.3.54 | P | E1-E2 ATPase | |
GCKIAGNM_01653 | 1.3e-42 | csoR | S | Metal-sensitive transcriptional repressor | ||
GCKIAGNM_01654 | 1.6e-210 | rmuC | S | RmuC family | ||
GCKIAGNM_01655 | 7e-60 | pyrE | 2.4.2.10 | F | Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) | |
GCKIAGNM_01656 | 2.6e-36 | pyrE | 2.4.2.10 | F | Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) | |
GCKIAGNM_01657 | 2.6e-78 | spoU | 2.1.1.185 | J | RNA methyltransferase TrmH family | |
GCKIAGNM_01658 | 6.2e-28 | spoU | 2.1.1.185 | J | RNA methyltransferase TrmH family | |
GCKIAGNM_01659 | 1.1e-14 | V | ABC transporter | |||
GCKIAGNM_01660 | 1.3e-161 | |||||
GCKIAGNM_01661 | 7.9e-117 | K | Psort location Cytoplasmic, score | |||
GCKIAGNM_01662 | 2.7e-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) | |
GCKIAGNM_01663 | 1.8e-96 | gatA | 6.3.5.6, 6.3.5.7 | F | 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) | |
GCKIAGNM_01664 | 5.4e-12 | gatA | 6.3.5.6, 6.3.5.7 | F | 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) | |
GCKIAGNM_01665 | 3.7e-88 | gatA | 6.3.5.6, 6.3.5.7 | F | 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) | |
GCKIAGNM_01666 | 2.6e-42 | gatA | 6.3.5.6, 6.3.5.7 | F | 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) | |
GCKIAGNM_01667 | 3.5e-199 | gatB | 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | |
GCKIAGNM_01668 | 1.1e-54 | gatB | 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | |
GCKIAGNM_01669 | 2.2e-148 | 2.3.1.57 | J | Acetyltransferase (GNAT) domain | ||
GCKIAGNM_01670 | 3.3e-52 | S | Protein of unknown function (DUF2469) | |||
GCKIAGNM_01671 | 1.2e-159 | 5.4.99.9 | H | Flavin containing amine oxidoreductase | ||
GCKIAGNM_01672 | 1.6e-119 | 5.4.99.9 | H | Flavin containing amine oxidoreductase | ||
GCKIAGNM_01673 | 2.7e-293 | 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 | ||
GCKIAGNM_01675 | 1.9e-37 | pabC | 2.6.1.42, 4.1.3.38 | EH | Amino-transferase class IV | |
GCKIAGNM_01676 | 2.1e-126 | L | Transposase | |||
GCKIAGNM_01677 | 6.5e-59 | gnpA | 2.4.1.211 | S | Lacto-N-biose phosphorylase C-terminal domain | |
GCKIAGNM_01678 | 2e-178 | mdsC | 2.7.1.162, 2.7.1.39 | S | Phosphotransferase enzyme family | |
GCKIAGNM_01679 | 4.1e-168 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
GCKIAGNM_01680 | 1.5e-50 | degU | K | helix_turn_helix, Lux Regulon | ||
GCKIAGNM_01681 | 1.5e-56 | degU | K | helix_turn_helix, Lux Regulon | ||
GCKIAGNM_01682 | 4.5e-171 | tcsS3 | KT | PspC domain | ||
GCKIAGNM_01683 | 4.4e-47 | pspC | KT | PspC domain | ||
GCKIAGNM_01684 | 3.5e-201 | pspC | KT | PspC domain | ||
GCKIAGNM_01685 | 2.9e-24 | |||||
GCKIAGNM_01686 | 1.6e-22 | |||||
GCKIAGNM_01687 | 0.0 | S | alpha beta | |||
GCKIAGNM_01688 | 1.5e-115 | S | Protein of unknown function (DUF4125) | |||
GCKIAGNM_01689 | 6.3e-193 | S | Domain of unknown function (DUF4037) | |||
GCKIAGNM_01690 | 1.6e-174 | S | Domain of unknown function (DUF4037) | |||
GCKIAGNM_01691 | 1.3e-201 | araJ | EGP | Major facilitator Superfamily | ||
GCKIAGNM_01693 | 1.9e-38 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
GCKIAGNM_01694 | 1.3e-66 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
GCKIAGNM_01695 | 9.5e-78 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
GCKIAGNM_01696 | 7.3e-175 | menA | 2.5.1.74 | H | Belongs to the MenA family. Type 1 subfamily | |
GCKIAGNM_01697 | 2.4e-131 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
GCKIAGNM_01698 | 1.1e-95 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
GCKIAGNM_01699 | 1.5e-172 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | |||
GCKIAGNM_01700 | 1.8e-32 | |||||
GCKIAGNM_01701 | 5e-215 | 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 | |
GCKIAGNM_01702 | 3.7e-113 | usp | 3.5.1.28 | CBM50 | S | CHAP domain |
GCKIAGNM_01703 | 4.2e-32 | M | NlpC/P60 family | |||
GCKIAGNM_01704 | 6.3e-64 | M | NlpC/P60 family | |||
GCKIAGNM_01705 | 3.2e-101 | M | NlpC/P60 family | |||
GCKIAGNM_01706 | 1.6e-10 | M | NlpC/P60 family | |||
GCKIAGNM_01707 | 1.7e-181 | T | Universal stress protein family | |||
GCKIAGNM_01708 | 3.4e-73 | attW | O | OsmC-like protein | ||
GCKIAGNM_01709 | 2.9e-54 | 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 | |
GCKIAGNM_01710 | 2.7e-67 | 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 | |
GCKIAGNM_01711 | 8.2e-28 | folA | 1.5.1.3 | H | dihydrofolate reductase | |
GCKIAGNM_01712 | 6.3e-69 | folA | 1.5.1.3 | H | dihydrofolate reductase | |
GCKIAGNM_01713 | 3e-92 | ptpA | 3.1.3.48 | T | low molecular weight | |
GCKIAGNM_01714 | 1.4e-11 | azlC | E | AzlC protein | ||
GCKIAGNM_01715 | 9.8e-14 | vex2 | V | ABC transporter, ATP-binding protein | ||
GCKIAGNM_01716 | 3.4e-62 | |||||
GCKIAGNM_01717 | 1e-50 | |||||
GCKIAGNM_01722 | 9.2e-43 | D | DNA N-6-adenine-methyltransferase (Dam) | |||
GCKIAGNM_01723 | 4.2e-75 | |||||
GCKIAGNM_01724 | 9.8e-09 | |||||
GCKIAGNM_01728 | 4.3e-15 | |||||
GCKIAGNM_01729 | 8e-121 | |||||
GCKIAGNM_01730 | 7e-28 | L | HNH nucleases | |||
GCKIAGNM_01732 | 7.4e-38 | |||||
GCKIAGNM_01733 | 7.7e-50 | S | Terminase | |||
GCKIAGNM_01734 | 7.1e-75 | S | Terminase | |||
GCKIAGNM_01735 | 5e-117 | S | Terminase | |||
GCKIAGNM_01736 | 9.8e-09 | S | Phage portal protein | |||
GCKIAGNM_01737 | 2.8e-52 | S | Phage portal protein | |||
GCKIAGNM_01738 | 3.7e-33 | xkdG | S | Phage capsid family | ||
GCKIAGNM_01739 | 2.7e-110 | xkdG | S | Phage capsid family | ||
GCKIAGNM_01740 | 1.6e-19 | |||||
GCKIAGNM_01741 | 2.2e-09 | |||||
GCKIAGNM_01742 | 1.3e-11 | |||||
GCKIAGNM_01743 | 5.4e-25 | |||||
GCKIAGNM_01744 | 5.8e-31 | |||||
GCKIAGNM_01745 | 1.4e-43 | |||||
GCKIAGNM_01747 | 1.7e-23 | |||||
GCKIAGNM_01750 | 3.9e-68 | NT | phage tail tape measure protein | |||
GCKIAGNM_01751 | 8.5e-09 | NT | phage tail tape measure protein | |||
GCKIAGNM_01752 | 4.6e-21 | S | phage tail tape measure protein | |||
GCKIAGNM_01755 | 2.2e-232 | ebh | 2.1.1.80, 3.1.1.61 | S | cellulase activity | |
GCKIAGNM_01756 | 1.2e-58 | ebh | 2.1.1.80, 3.1.1.61 | S | cellulase activity | |
GCKIAGNM_01757 | 5.6e-60 | ebh | 2.1.1.80, 3.1.1.61 | S | cellulase activity | |
GCKIAGNM_01760 | 2.3e-37 | |||||
GCKIAGNM_01768 | 2.4e-57 | V | Ami_2 | |||
GCKIAGNM_01769 | 3e-12 | M | peptidoglycan receptor activity | |||
GCKIAGNM_01770 | 2.6e-11 | |||||
GCKIAGNM_01771 | 2.7e-48 | |||||
GCKIAGNM_01772 | 4.2e-39 | S | Protein of unknown function (DUF805) | |||
GCKIAGNM_01774 | 2.1e-221 | gltX | 6.1.1.17 | J | Catalyzes the attachment of glutamate to tRNA(Glu) in a two-step reaction glutamate is first activated by ATP to form Glu-AMP and then transferred to the acceptor end of tRNA(Glu) | |
GCKIAGNM_01778 | 3.3e-48 | efeU_1 | P | Iron permease FTR1 family | ||
GCKIAGNM_01779 | 1.2e-192 | efeU_1 | P | Iron permease FTR1 family | ||
GCKIAGNM_01781 | 6.9e-57 | tpd | P | Fe2+ transport protein | ||
GCKIAGNM_01782 | 9.2e-15 | tpd | P | Fe2+ transport protein | ||
GCKIAGNM_01783 | 5.1e-123 | S | Predicted membrane protein (DUF2318) | |||
GCKIAGNM_01784 | 4.8e-99 | S | Predicted membrane protein (DUF2318) | |||
GCKIAGNM_01785 | 7e-221 | macB_2 | V | ABC transporter permease | ||
GCKIAGNM_01786 | 6.1e-199 | Z012_06715 | V | FtsX-like permease family | ||
GCKIAGNM_01787 | 1.7e-145 | macB | V | ABC transporter, ATP-binding protein | ||
GCKIAGNM_01788 | 2.4e-53 | S | FMN_bind | |||
GCKIAGNM_01789 | 6.4e-105 | K | Psort location Cytoplasmic, score 8.87 | |||
GCKIAGNM_01790 | 4.7e-134 | pip | S | YhgE Pip domain protein | ||
GCKIAGNM_01791 | 3e-97 | pip | S | YhgE Pip domain protein | ||
GCKIAGNM_01792 | 8.2e-28 | pip | S | YhgE Pip domain protein | ||
GCKIAGNM_01793 | 3.2e-150 | pip | S | YhgE Pip domain protein | ||
GCKIAGNM_01794 | 1.9e-129 | pip | S | YhgE Pip domain protein | ||
GCKIAGNM_01795 | 2.7e-31 | pip | S | YhgE Pip domain protein | ||
GCKIAGNM_01796 | 2.5e-253 | S | Putative ABC-transporter type IV | |||
GCKIAGNM_01797 | 3.9e-21 | S | Putative ABC-transporter type IV | |||
GCKIAGNM_01798 | 1.5e-63 | 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 | |
GCKIAGNM_01799 | 1.2e-191 | 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 | |
GCKIAGNM_01800 | 1.3e-140 | pgl | 3.1.1.31, 3.5.99.6 | G | Glucosamine-6-phosphate isomerases/6-phosphogluconolactonase | |
GCKIAGNM_01801 | 2.8e-51 | opcA | G | Glucose-6-phosphate dehydrogenase subunit | ||
GCKIAGNM_01802 | 2.8e-63 | opcA | G | Glucose-6-phosphate dehydrogenase subunit | ||
GCKIAGNM_01803 | 2e-47 | opcA | G | Glucose-6-phosphate dehydrogenase subunit | ||
GCKIAGNM_01804 | 4.7e-127 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
GCKIAGNM_01805 | 3.2e-51 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
GCKIAGNM_01806 | 2.6e-197 | 3.5.2.6 | V | Beta-lactamase enzyme family | ||
GCKIAGNM_01807 | 3.8e-44 | 3.5.2.6 | V | Beta-lactamase enzyme family | ||
GCKIAGNM_01809 | 2.2e-57 | pepD | E | Peptidase family C69 | ||
GCKIAGNM_01810 | 1.5e-50 | |||||
GCKIAGNM_01811 | 5.6e-65 | S | Acetyltransferase (GNAT) domain | |||
GCKIAGNM_01812 | 5.7e-24 | cefD | 5.1.1.17 | E | Aminotransferase class-V | |
GCKIAGNM_01813 | 1.3e-14 | cefD | 5.1.1.17 | E | Aminotransferase, class V | |
GCKIAGNM_01814 | 3.8e-134 | V | VanZ like family | |||
GCKIAGNM_01815 | 2e-19 | EGP | Major facilitator Superfamily | |||
GCKIAGNM_01817 | 7.7e-103 | mmuP | E | amino acid | ||
GCKIAGNM_01818 | 4.3e-141 | mmuP | E | amino acid | ||
GCKIAGNM_01819 | 6.3e-130 | 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 | |
GCKIAGNM_01820 | 1.6e-131 | S | SOS response associated peptidase (SRAP) | |||
GCKIAGNM_01821 | 6.7e-44 | trpB | 4.1.1.48, 4.2.1.20 | E | The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine | |
GCKIAGNM_01822 | 4.3e-294 | trpB | 4.1.1.48, 4.2.1.20 | E | The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine | |
GCKIAGNM_01823 | 7.7e-126 | trpA | 4.2.1.20 | E | The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate | |
GCKIAGNM_01824 | 9.1e-186 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
GCKIAGNM_01825 | 7.9e-112 | rpe | 5.1.3.1 | G | Ribulose-phosphate 3-epimerase | |
GCKIAGNM_01826 | 3.9e-24 | hisE | 3.5.4.19, 3.6.1.31, 5.3.1.16 | E | Phosphoribosyl-ATP pyrophosphohydrolase | |
GCKIAGNM_01827 | 8.2e-80 | hisG | 2.4.2.17 | F | ATP phosphoribosyltransferase | |
GCKIAGNM_01828 | 2.1e-64 | hisG | 2.4.2.17 | F | ATP phosphoribosyltransferase | |
GCKIAGNM_01829 | 1.4e-47 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
GCKIAGNM_01830 | 2.9e-154 | S | Bacterial protein of unknown function (DUF881) | |||
GCKIAGNM_01831 | 3.9e-35 | sbp | S | Protein of unknown function (DUF1290) | ||
GCKIAGNM_01832 | 2e-29 | S | Bacterial protein of unknown function (DUF881) | |||
GCKIAGNM_01833 | 7.6e-101 | S | Bacterial protein of unknown function (DUF881) | |||
GCKIAGNM_01834 | 7e-40 | garA | T | Inner membrane component of T3SS, cytoplasmic domain | ||
GCKIAGNM_01835 | 6.3e-11 | garA | T | Inner membrane component of T3SS, cytoplasmic domain | ||
GCKIAGNM_01836 | 2.6e-112 | K | helix_turn_helix, mercury resistance | |||
GCKIAGNM_01837 | 2.4e-63 | |||||
GCKIAGNM_01838 | 2e-35 | |||||
GCKIAGNM_01839 | 5.7e-140 | pgp | 3.1.3.18 | S | HAD-hyrolase-like | |
GCKIAGNM_01840 | 5.1e-62 | rbpA | K | Binds to RNA polymerase (RNAP), stimulating transcription from principal, but not alternative sigma factor promoters | ||
GCKIAGNM_01841 | 0.0 | helY | L | DEAD DEAH box helicase | ||
GCKIAGNM_01842 | 3.4e-47 | helY | L | DEAD DEAH box helicase | ||
GCKIAGNM_01843 | 1.4e-47 | |||||
GCKIAGNM_01844 | 1.4e-147 | pafB | K | WYL domain | ||
GCKIAGNM_01845 | 2.1e-115 | pafB | K | WYL domain | ||
GCKIAGNM_01846 | 1.1e-42 | pafB | K | WYL domain | ||
GCKIAGNM_01847 | 8.8e-13 | ugpA | 2.7.7.9 | G | UTP-glucose-1-phosphate uridylyltransferase | |
GCKIAGNM_01848 | 2.7e-263 | ugpA | 2.7.7.9 | G | UTP-glucose-1-phosphate uridylyltransferase | |
GCKIAGNM_01849 | 2.3e-74 | supH | S | Sucrose-6F-phosphate phosphohydrolase | ||
GCKIAGNM_01850 | 3.9e-66 | supH | S | Sucrose-6F-phosphate phosphohydrolase | ||
GCKIAGNM_01852 | 8.9e-213 | 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 | ||
GCKIAGNM_01853 | 6.1e-73 | 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 | ||
GCKIAGNM_01854 | 4.8e-82 | 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 | ||
GCKIAGNM_01855 | 2.5e-40 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
GCKIAGNM_01856 | 1.9e-153 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
GCKIAGNM_01857 | 7.1e-86 | ribF | 2.7.1.26, 2.7.7.2 | H | riboflavin kinase | |
GCKIAGNM_01858 | 3.1e-98 | ribF | 2.7.1.26, 2.7.7.2 | H | riboflavin kinase | |
GCKIAGNM_01859 | 1.6e-137 | 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 | ||
GCKIAGNM_01860 | 8.7e-109 | 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 | ||
GCKIAGNM_01861 | 1.6e-98 | |||||
GCKIAGNM_01862 | 2.4e-83 | rpiA | 2.7.1.12, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
GCKIAGNM_01863 | 1.2e-25 | rpiA | 2.7.1.12, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
GCKIAGNM_01864 | 1.1e-166 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
GCKIAGNM_01865 | 2.7e-277 | merA | 1.16.1.1, 1.8.1.7 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
GCKIAGNM_01866 | 1.6e-54 | K | Transcriptional regulator | |||
GCKIAGNM_01867 | 4.6e-26 | gmk | 1.1.1.23, 2.7.4.8 | S | Protein conserved in bacteria | |
GCKIAGNM_01868 | 7.4e-152 | gmk | 1.1.1.23, 2.7.4.8 | S | Protein conserved in bacteria | |
GCKIAGNM_01869 | 1.3e-122 | pgm | 5.4.2.2 | G | Phosphoglucomutase/phosphomannomutase, alpha/beta/alpha domain II | |
GCKIAGNM_01870 | 4.7e-169 | pgm | 5.4.2.2 | G | Phosphoglucomutase/phosphomannomutase, alpha/beta/alpha domain II | |
GCKIAGNM_01871 | 5.2e-115 | crr | 2.7.1.193 | G | pts system, glucose-specific IIABC component | |
GCKIAGNM_01872 | 2.2e-51 | crr | 2.7.1.193 | G | pts system, glucose-specific IIABC component | |
GCKIAGNM_01873 | 1.8e-81 | crr | 2.7.1.193 | G | pts system, glucose-specific IIABC component | |
GCKIAGNM_01874 | 6e-29 | crr | 2.7.1.193 | G | pts system, glucose-specific IIABC component | |
GCKIAGNM_01875 | 1.3e-162 | arbG | K | CAT RNA binding domain | ||
GCKIAGNM_01876 | 2.5e-138 | I | Diacylglycerol kinase catalytic domain | |||
GCKIAGNM_01877 | 1.4e-39 | I | Diacylglycerol kinase catalytic domain | |||
GCKIAGNM_01878 | 6.6e-108 | 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) | |
GCKIAGNM_01879 | 1.1e-43 | 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) | |
GCKIAGNM_01881 | 2.5e-231 | G | Bacterial extracellular solute-binding protein | |||
GCKIAGNM_01882 | 6.9e-173 | malC | G | Binding-protein-dependent transport system inner membrane component | ||
GCKIAGNM_01883 | 1.8e-25 | G | ABC transporter permease | |||
GCKIAGNM_01884 | 1.2e-77 | G | ABC transporter permease | |||
GCKIAGNM_01885 | 1.9e-09 | G | ABC transporter permease | |||
GCKIAGNM_01886 | 7.7e-158 | gnpA | 2.4.1.211 | S | Lacto-N-biose phosphorylase C-terminal domain | |
GCKIAGNM_01888 | 7.8e-21 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
GCKIAGNM_01889 | 1.9e-86 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
GCKIAGNM_01890 | 1.5e-212 | purT | 2.1.2.2 | F | Involved in the de novo purine biosynthesis. Catalyzes the transfer of formate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR). Formate is provided by PurU via hydrolysis of 10-formyl-tetrahydrofolate | |
GCKIAGNM_01891 | 2.1e-230 | mtnE | 2.6.1.83 | E | Aminotransferase class I and II | |
GCKIAGNM_01892 | 1.1e-180 | M | Glycosyl transferase 4-like domain | |||
GCKIAGNM_01893 | 4.2e-197 | ltaE | 4.1.2.48 | E | Beta-eliminating lyase | |
GCKIAGNM_01895 | 1.8e-67 | yocS | S | SBF-like CPA transporter family (DUF4137) | ||
GCKIAGNM_01896 | 9.3e-62 | 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 | ||
GCKIAGNM_01897 | 2.4e-62 | 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 | ||
GCKIAGNM_01898 | 4e-168 | 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 | ||
GCKIAGNM_01899 | 1.2e-148 | 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 | ||
GCKIAGNM_01900 | 6.2e-232 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
GCKIAGNM_01901 | 3.4e-80 | tmp1 | S | Domain of unknown function (DUF4391) | ||
GCKIAGNM_01902 | 1.3e-35 | tmp1 | S | Domain of unknown function (DUF4391) | ||
GCKIAGNM_01903 | 7.1e-147 | rlrG | K | Bacterial regulatory helix-turn-helix protein, lysR family | ||
GCKIAGNM_01904 | 5.6e-31 | MA20_14895 | S | Conserved hypothetical protein 698 | ||
GCKIAGNM_01905 | 1.3e-27 | MA20_14895 | S | Conserved hypothetical protein 698 | ||
GCKIAGNM_01906 | 9.7e-59 | MA20_14895 | S | Conserved hypothetical protein 698 | ||
GCKIAGNM_01907 | 8.2e-21 | S | Psort location CytoplasmicMembrane, score | |||
GCKIAGNM_01908 | 1.2e-28 | S | polysaccharide biosynthetic process | |||
GCKIAGNM_01909 | 1.3e-60 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
GCKIAGNM_01910 | 9.3e-85 | D | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | |||
GCKIAGNM_01911 | 5.2e-75 | K | MerR family regulatory protein | |||
GCKIAGNM_01912 | 8.1e-148 | 1.1.1.1, 1.1.1.14 | C | Zinc-binding dehydrogenase | ||
GCKIAGNM_01913 | 8.8e-259 | S | Domain of unknown function (DUF4143) | |||
GCKIAGNM_01914 | 3.4e-109 | P | Protein of unknown function DUF47 | |||
GCKIAGNM_01915 | 6.4e-170 | ugpQ | 3.1.4.46 | C | Domain of unknown function | |
GCKIAGNM_01916 | 5.3e-11 | ugpB | G | Bacterial extracellular solute-binding protein | ||
GCKIAGNM_01917 | 1.2e-54 | ugpB | G | Bacterial extracellular solute-binding protein | ||
GCKIAGNM_01918 | 3.1e-131 | ugpB | G | Bacterial extracellular solute-binding protein | ||
GCKIAGNM_01919 | 4e-142 | ugpE | G | Binding-protein-dependent transport system inner membrane component | ||
GCKIAGNM_01920 | 3.6e-59 | ugpA | P | Binding-protein-dependent transport system inner membrane component | ||
GCKIAGNM_01921 | 5.1e-86 | ugpA | P | Binding-protein-dependent transport system inner membrane component | ||
GCKIAGNM_01922 | 5.5e-65 | KLT | Protein tyrosine kinase | |||
GCKIAGNM_01923 | 7e-199 | KLT | Protein tyrosine kinase | |||
GCKIAGNM_01924 | 8.2e-08 | KLT | Protein tyrosine kinase | |||
GCKIAGNM_01925 | 3.5e-26 | 3.2.1.21 | GH3 | G | Fibronectin type III-like domain | |
GCKIAGNM_01926 | 1.7e-246 | 3.2.1.21 | GH3 | G | Fibronectin type III-like domain | |
GCKIAGNM_01927 | 1.7e-204 | 3.2.1.21 | GH3 | G | Fibronectin type III-like domain | |
GCKIAGNM_01928 | 1.2e-79 | kcsA | U | Ion channel | ||
GCKIAGNM_01929 | 2.6e-126 | S | Protein of unknown function (DUF3990) | |||
GCKIAGNM_01930 | 5.3e-121 | K | Helix-turn-helix XRE-family like proteins | |||
GCKIAGNM_01931 | 1.9e-22 | 3.2.1.21 | GH3 | G | Glycosyl hydrolase family 3 N-terminal domain protein | |
GCKIAGNM_01932 | 7.9e-300 | 3.2.1.21 | GH3 | G | Glycosyl hydrolase family 3 N-terminal domain protein | |
GCKIAGNM_01933 | 1.2e-17 | 3.2.1.21 | GH3 | G | Glycosyl hydrolase family 3 N-terminal domain protein | |
GCKIAGNM_01934 | 9.8e-123 | S | Psort location CytoplasmicMembrane, score | |||
GCKIAGNM_01935 | 1.5e-29 | nrdH | O | Glutaredoxin | ||
GCKIAGNM_01936 | 2.1e-88 | nrdI | F | Probably involved in ribonucleotide reductase function | ||
GCKIAGNM_01937 | 0.0 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
GCKIAGNM_01939 | 5e-41 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
GCKIAGNM_01940 | 6.9e-92 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
GCKIAGNM_01941 | 2.7e-79 | T | GHKL domain | |||
GCKIAGNM_01942 | 4.1e-31 | T | GHKL domain | |||
GCKIAGNM_01943 | 8.5e-69 | T | GHKL domain | |||
GCKIAGNM_01944 | 5.1e-142 | K | LytTr DNA-binding domain | |||
GCKIAGNM_01945 | 1e-123 | 2.4.1.166 | GT2 | M | Glycosyltransferase like family 2 | |
GCKIAGNM_01946 | 1.3e-33 | 2.4.1.166 | GT2 | M | Glycosyltransferase like family 2 | |
GCKIAGNM_01947 | 2.1e-73 | 2.7.1.194, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
GCKIAGNM_01948 | 3.7e-45 | ulaB | 2.7.1.194 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
GCKIAGNM_01949 | 5.6e-176 | ulaA | 2.7.1.194 | S | PTS system sugar-specific permease component | |
GCKIAGNM_01950 | 2.5e-47 | ulaA | 2.7.1.194 | S | PTS system sugar-specific permease component | |
GCKIAGNM_01951 | 4.2e-58 | K | UTRA domain | |||
GCKIAGNM_01952 | 9.3e-55 | K | UTRA domain | |||
GCKIAGNM_01953 | 6.1e-172 | ugpC | E | Belongs to the ABC transporter superfamily | ||
GCKIAGNM_01954 | 5.8e-17 | ugpC | E | Belongs to the ABC transporter superfamily | ||
GCKIAGNM_01955 | 6.2e-48 | S | LPXTG-motif cell wall anchor domain protein | |||
GCKIAGNM_01957 | 1.6e-197 | 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 | ||
GCKIAGNM_01958 | 8.9e-81 | aroE | 1.1.1.25 | E | Shikimate dehydrogenase substrate binding domain | |
GCKIAGNM_01959 | 6.4e-90 | aroE | 1.1.1.25 | E | Shikimate dehydrogenase substrate binding domain | |
GCKIAGNM_01960 | 5.1e-21 | rapZ | S | Displays ATPase and GTPase activities | ||
GCKIAGNM_01961 | 1.2e-52 | rapZ | S | Displays ATPase and GTPase activities | ||
GCKIAGNM_01962 | 3.5e-38 | rapZ | S | Displays ATPase and GTPase activities | ||
GCKIAGNM_01963 | 2.5e-115 | whiA | K | May be required for sporulation | ||
GCKIAGNM_01964 | 4.4e-84 | pgk | 2.7.2.3, 5.3.1.1 | F | Phosphoglycerate kinase | |
GCKIAGNM_01965 | 9.4e-71 | pgk | 2.7.2.3, 5.3.1.1 | F | Phosphoglycerate kinase | |
GCKIAGNM_01966 | 3.5e-146 | 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) | |
GCKIAGNM_01967 | 2.5e-34 | secG | U | Preprotein translocase SecG subunit | ||
GCKIAGNM_01968 | 8.5e-176 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
GCKIAGNM_01969 | 2.6e-79 | S | Sucrose-6F-phosphate phosphohydrolase | |||
GCKIAGNM_01970 | 1.9e-39 | S | Sucrose-6F-phosphate phosphohydrolase | |||
GCKIAGNM_01971 | 1.3e-204 | alaA | 2.6.1.2, 2.6.1.66 | E | Aminotransferase, class I II | |
GCKIAGNM_01972 | 5.8e-190 | |||||
GCKIAGNM_01973 | 6.8e-99 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
GCKIAGNM_01974 | 8e-82 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
GCKIAGNM_01975 | 5.8e-13 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
GCKIAGNM_01976 | 3.8e-55 | tal | 2.2.1.2 | H | Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway | |
GCKIAGNM_01977 | 2.1e-78 | tal | 2.2.1.2 | H | Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway | |
GCKIAGNM_01978 | 5.9e-60 | tkt | 2.2.1.1 | H | Belongs to the transketolase family | |
GCKIAGNM_01979 | 8.5e-44 | tkt | 2.2.1.1 | H | Belongs to the transketolase family | |
GCKIAGNM_01980 | 4e-133 | tkt | 2.2.1.1 | H | Belongs to the transketolase family | |
GCKIAGNM_01981 | 1.3e-124 | tkt | 2.2.1.1 | H | Belongs to the transketolase family | |
GCKIAGNM_01982 | 3.1e-186 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
GCKIAGNM_01983 | 6.2e-185 | 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 | ||
GCKIAGNM_01984 | 1.8e-49 | G | Fructosamine kinase | |||
GCKIAGNM_01985 | 3.3e-81 | G | Fructosamine kinase | |||
GCKIAGNM_01986 | 1.4e-125 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
GCKIAGNM_01987 | 7.4e-44 | S | PAC2 family | |||
GCKIAGNM_01988 | 6.9e-82 | S | PAC2 family | |||
GCKIAGNM_01994 | 4.9e-76 | 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) | |
GCKIAGNM_01995 | 1e-50 | 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) | |
GCKIAGNM_01996 | 1.8e-162 | menD | 2.2.1.9 | H | Thiamine pyrophosphate enzyme, N-terminal TPP binding domain | |
GCKIAGNM_01997 | 1.3e-46 | M | Glycosyltransferase like family 2 | |||
GCKIAGNM_01998 | 3.2e-110 | S | Psort location CytoplasmicMembrane, score 9.99 | |||
GCKIAGNM_01999 | 1.5e-31 | C | Polysaccharide pyruvyl transferase | |||
GCKIAGNM_02000 | 4.8e-09 | |||||
GCKIAGNM_02001 | 1.7e-52 | GT4 | M | Psort location Cytoplasmic, score 8.87 | ||
GCKIAGNM_02002 | 3.3e-125 | M | Psort location Cytoplasmic, score 8.87 | |||
GCKIAGNM_02003 | 3.4e-18 | L | Transposase and inactivated derivatives IS30 family | |||
GCKIAGNM_02004 | 8.6e-46 | L | Transposase and inactivated derivatives IS30 family | |||
GCKIAGNM_02005 | 2e-92 | L | Transposase and inactivated derivatives IS30 family | |||
GCKIAGNM_02007 | 2e-17 | S | Psort location CytoplasmicMembrane, score 9.99 | |||
GCKIAGNM_02008 | 1.5e-85 | S | Psort location CytoplasmicMembrane, score 9.99 | |||
GCKIAGNM_02009 | 6.3e-108 | 3.1.3.48 | T | Low molecular weight phosphatase family | ||
GCKIAGNM_02010 | 6.6e-235 | rfbP | 2.7.8.6 | M | Exopolysaccharide biosynthesis polyprenyl glycosylphosphotransferase | |
GCKIAGNM_02011 | 7.7e-311 | 2.1.1.107, 2.1.1.294, 2.7.1.181, 2.7.11.1 | H | Protein of unknown function (DUF4012) | ||
GCKIAGNM_02012 | 2.7e-283 | EGP | Major facilitator Superfamily | |||
GCKIAGNM_02013 | 2.7e-236 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
GCKIAGNM_02014 | 4.9e-142 | L | Protein of unknown function (DUF1524) | |||
GCKIAGNM_02015 | 2.6e-28 | dkgA | 1.1.1.346 | S | Oxidoreductase, aldo keto reductase family protein | |
GCKIAGNM_02016 | 3.8e-31 | dkgA | 1.1.1.346 | S | Oxidoreductase, aldo keto reductase family protein | |
GCKIAGNM_02017 | 2.4e-37 | K | helix_turn _helix lactose operon repressor | |||
GCKIAGNM_02018 | 5.3e-110 | K | helix_turn _helix lactose operon repressor | |||
GCKIAGNM_02019 | 1.4e-08 | K | helix_turn _helix lactose operon repressor | |||
GCKIAGNM_02020 | 0.0 | bga1 | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
GCKIAGNM_02021 | 1.6e-98 | tnp3503b | 2.7.7.7 | L | Transposase and inactivated derivatives | |
GCKIAGNM_02022 | 3e-13 | tnp3503b | 2.7.7.7 | L | Transposase and inactivated derivatives | |
GCKIAGNM_02025 | 8.3e-30 | rplI | J | Binds to the 23S rRNA | ||
GCKIAGNM_02026 | 2e-36 | 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 | ||
GCKIAGNM_02027 | 3e-26 | ssb1 | L | Single-stranded DNA-binding protein | ||
GCKIAGNM_02028 | 2e-39 | ssb1 | L | Single-stranded DNA-binding protein | ||
GCKIAGNM_02029 | 2.6e-08 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
GCKIAGNM_02030 | 9e-16 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
GCKIAGNM_02031 | 4.3e-172 | prs | 2.7.6.1 | F | Involved in the biosynthesis of the central metabolite phospho-alpha-D-ribosyl-1-pyrophosphate (PRPP) via the transfer of pyrophosphoryl group from ATP to 1-hydroxyl of ribose-5-phosphate (Rib-5-P) | |
GCKIAGNM_02032 | 3.1e-09 | yggS | S | Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis | ||
GCKIAGNM_02033 | 4.3e-120 | yggS | S | Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis | ||
GCKIAGNM_02034 | 7.9e-137 | 3.2.1.185 | GH127 | S | Beta-L-arabinofuranosidase, GH127 | |
GCKIAGNM_02035 | 9.1e-112 | 3.2.1.185 | GH127 | S | Beta-L-arabinofuranosidase, GH127 | |
GCKIAGNM_02036 | 3.2e-07 | K | Periplasmic binding protein domain | |||
GCKIAGNM_02037 | 0.0 | ubiB | S | ABC1 family | ||
GCKIAGNM_02038 | 4.6e-37 | S | granule-associated protein | |||
GCKIAGNM_02039 | 3.7e-142 | cobQ | S | CobB/CobQ-like glutamine amidotransferase domain | ||
GCKIAGNM_02040 | 5.1e-119 | murD | 3.4.21.10, 6.3.2.13, 6.3.2.9 | M | Domain of unknown function (DUF1727) | |
GCKIAGNM_02041 | 3.9e-123 | murD | 3.4.21.10, 6.3.2.13, 6.3.2.9 | M | Domain of unknown function (DUF1727) | |
GCKIAGNM_02042 | 5.3e-130 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
GCKIAGNM_02044 | 2.8e-25 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
GCKIAGNM_02045 | 8.4e-49 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
GCKIAGNM_02046 | 1.8e-240 | dinF | V | MatE | ||
GCKIAGNM_02047 | 5.3e-134 | 2.7.7.19, 2.7.7.59 | O | Nucleotidyltransferase domain | ||
GCKIAGNM_02048 | 2.7e-144 | 2.7.7.19, 2.7.7.59 | O | Nucleotidyltransferase domain | ||
GCKIAGNM_02049 | 1e-54 | glnB | K | Nitrogen regulatory protein P-II | ||
GCKIAGNM_02050 | 1e-227 | amt | U | Ammonium Transporter Family | ||
GCKIAGNM_02051 | 4.9e-171 | 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) | ||
GCKIAGNM_02052 | 1e-151 | icaR | K | Bacterial regulatory proteins, tetR family | ||
GCKIAGNM_02053 | 1.1e-197 | XK27_01805 | M | Glycosyltransferase like family 2 | ||
GCKIAGNM_02054 | 6.2e-172 | pepD | E | Peptidase family C69 | ||
GCKIAGNM_02055 | 4.3e-186 | K | Periplasmic binding protein domain | |||
GCKIAGNM_02056 | 3e-157 | rluA | 5.4.99.28, 5.4.99.29 | J | RNA pseudouridylate synthase | |
GCKIAGNM_02057 | 2.8e-185 | 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 | |
GCKIAGNM_02058 | 6.8e-55 | 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 | |
GCKIAGNM_02059 | 1.4e-150 | tcyC | 3.6.3.21 | E | ATPases associated with a variety of cellular activities | |
GCKIAGNM_02060 | 1.1e-41 | yecS | E | Binding-protein-dependent transport system inner membrane component | ||
GCKIAGNM_02061 | 2.2e-13 | yecS | E | Binding-protein-dependent transport system inner membrane component | ||
GCKIAGNM_02062 | 2e-43 | yecS | E | Binding-protein-dependent transport system inner membrane component | ||
GCKIAGNM_02063 | 8.2e-124 | pknD | ET | ABC transporter, substrate-binding protein, family 3 | ||
GCKIAGNM_02064 | 3e-126 | pknD | ET | ABC transporter, substrate-binding protein, family 3 | ||
GCKIAGNM_02065 | 1.3e-75 | 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 | ||
GCKIAGNM_02067 | 3.3e-135 | usp | 3.5.1.28 | CBM50 | D | CHAP domain protein |
GCKIAGNM_02068 | 3.6e-106 | ftsX | D | Part of the ABC transporter FtsEX involved in cellular division | ||
GCKIAGNM_02069 | 1.6e-25 | ftsX | D | Part of the ABC transporter FtsEX involved in cellular division | ||
GCKIAGNM_02070 | 1.3e-205 | ftsE | D | Cell division ATP-binding protein FtsE | ||
GCKIAGNM_02071 | 2.1e-70 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
GCKIAGNM_02072 | 4.6e-108 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
GCKIAGNM_02073 | 2.2e-84 | recE | 2.7.7.7, 3.6.4.12 | L | Psort location Cytoplasmic, score | |
GCKIAGNM_02074 | 1.3e-94 | recE | 2.7.7.7, 3.6.4.12 | L | Psort location Cytoplasmic, score | |
GCKIAGNM_02075 | 1.5e-54 | def | 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions | |
GCKIAGNM_02076 | 3.1e-19 | def | 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions | |
GCKIAGNM_02077 | 9.6e-77 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
GCKIAGNM_02078 | 1e-113 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
GCKIAGNM_02079 | 4.4e-17 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
GCKIAGNM_02080 | 4.3e-42 | pepN | 3.4.11.2 | E | Peptidase family M1 domain | |
GCKIAGNM_02081 | 4.9e-18 | pepN | 3.4.11.2 | E | Peptidase family M1 domain | |
GCKIAGNM_02082 | 0.0 | pepN | 3.4.11.2 | E | Peptidase family M1 domain | |
GCKIAGNM_02083 | 2.8e-307 | rnj | 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 | ||
GCKIAGNM_02084 | 2.6e-161 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
GCKIAGNM_02085 | 6.3e-41 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
GCKIAGNM_02086 | 8.3e-143 | 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 | |
GCKIAGNM_02087 | 6.1e-35 | 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 | |
GCKIAGNM_02088 | 1.5e-209 | 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 | |
GCKIAGNM_02089 | 1.6e-35 | |||||
GCKIAGNM_02090 | 1e-48 | WQ51_05790 | S | Bacterial protein of unknown function (DUF948) | ||
GCKIAGNM_02091 | 1.6e-128 | pgm3 | G | Phosphoglycerate mutase family | ||
GCKIAGNM_02092 | 1.2e-48 | relB | L | RelB antitoxin | ||
GCKIAGNM_02093 | 1.6e-16 | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
GCKIAGNM_02094 | 1.8e-40 | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
GCKIAGNM_02095 | 1.2e-111 | E | Transglutaminase-like superfamily | |||
GCKIAGNM_02096 | 3.1e-46 | sdpI | S | SdpI/YhfL protein family | ||
GCKIAGNM_02097 | 2.5e-91 | 3.5.4.5 | F | cytidine deaminase activity | ||
GCKIAGNM_02098 | 1.3e-79 | S | Peptidase C26 | |||
GCKIAGNM_02099 | 1.7e-108 | rpsD | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the body of the 30S subunit | ||
GCKIAGNM_02100 | 2.5e-161 | lolD | V | ABC transporter | ||
GCKIAGNM_02101 | 3.4e-189 | V | FtsX-like permease family | |||
GCKIAGNM_02102 | 9.5e-18 | S | Domain of unknown function (DUF4418) | |||
GCKIAGNM_02103 | 2.9e-33 | S | Domain of unknown function (DUF4418) | |||
GCKIAGNM_02104 | 2.7e-47 | pcrA | 3.6.4.12 | L | DNA helicase | |
GCKIAGNM_02105 | 8.4e-165 | pcrA | 3.6.4.12 | L | DNA helicase | |
GCKIAGNM_02106 | 7.2e-149 | pcrA | 3.6.4.12 | L | DNA helicase | |
GCKIAGNM_02107 | 9.7e-106 | 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 | |
GCKIAGNM_02108 | 2.8e-55 | pbuX | F | Permease family | ||
GCKIAGNM_02109 | 1.1e-176 | pbuX | F | Permease family | ||
GCKIAGNM_02110 | 2.8e-31 | yozG | K | Cro/C1-type HTH DNA-binding domain | ||
GCKIAGNM_02111 | 1.1e-40 | S | Protein of unknown function (DUF2975) | |||
GCKIAGNM_02112 | 4.8e-159 | I | Serine aminopeptidase, S33 | |||
GCKIAGNM_02113 | 2.1e-163 | M | pfam nlp p60 | |||
GCKIAGNM_02114 | 5.1e-110 | 3.4.13.21 | E | Peptidase family S51 | ||
GCKIAGNM_02115 | 7.1e-183 | |||||
GCKIAGNM_02116 | 4.9e-213 | 3.1.26.12, 3.2.1.8 | S | Domain of Unknown Function (DUF349) | ||
GCKIAGNM_02117 | 2.9e-125 | 3.1.3.5 | F | 5'-nucleotidase, C-terminal domain | ||
GCKIAGNM_02118 | 1.3e-114 | 3.1.3.5 | F | 5'-nucleotidase, C-terminal domain | ||
GCKIAGNM_02119 | 6.3e-21 | 3.1.3.5 | F | 5'-nucleotidase, C-terminal domain | ||
GCKIAGNM_02120 | 6.4e-142 | 3.5.2.10 | S | Creatinine amidohydrolase | ||
GCKIAGNM_02121 | 3.7e-91 | proP | EGP | Sugar (and other) transporter | ||
GCKIAGNM_02122 | 1.4e-129 | proP | EGP | Sugar (and other) transporter | ||
GCKIAGNM_02124 | 5.3e-167 | purR | QT | Purine catabolism regulatory protein-like family | ||
GCKIAGNM_02125 | 2.3e-73 | purR | QT | Purine catabolism regulatory protein-like family | ||
GCKIAGNM_02126 | 1.8e-256 | codA | 3.5.4.1, 3.5.4.21 | F | Amidohydrolase family | |
GCKIAGNM_02127 | 0.0 | clpC | O | ATPase family associated with various cellular activities (AAA) | ||
GCKIAGNM_02128 | 1.3e-17 | clpC | O | ATPase family associated with various cellular activities (AAA) | ||
GCKIAGNM_02129 | 3.3e-78 | uspA | T | Belongs to the universal stress protein A family | ||
GCKIAGNM_02130 | 6e-34 | uspA | T | Belongs to the universal stress protein A family | ||
GCKIAGNM_02131 | 1.2e-49 | S | Protein of unknown function (DUF3027) | |||
GCKIAGNM_02132 | 8.6e-116 | S | Protein of unknown function (DUF3027) | |||
GCKIAGNM_02133 | 3.4e-36 | cspB | K | 'Cold-shock' DNA-binding domain | ||
GCKIAGNM_02134 | 5.8e-12 | cspB | K | 'Cold-shock' DNA-binding domain | ||
GCKIAGNM_02135 | 1.6e-24 | 2.7.13.3 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | ||
GCKIAGNM_02136 | 1.5e-137 | 2.7.13.3 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | ||
GCKIAGNM_02137 | 6.7e-117 | 2.7.13.3 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | ||
GCKIAGNM_02138 | 2e-132 | KT | Response regulator receiver domain protein | |||
GCKIAGNM_02139 | 4.3e-99 | |||||
GCKIAGNM_02140 | 4.2e-33 | S | Proteins of 100 residues with WXG | |||
GCKIAGNM_02142 | 9.9e-10 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
GCKIAGNM_02143 | 1.6e-177 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
GCKIAGNM_02144 | 6.1e-38 | K | 'Cold-shock' DNA-binding domain | |||
GCKIAGNM_02145 | 3.6e-59 | S | LytR cell envelope-related transcriptional attenuator | |||
GCKIAGNM_02146 | 4.3e-110 | 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 | |
GCKIAGNM_02148 | 1e-50 | K | Helix-turn-helix domain | |||
GCKIAGNM_02150 | 1.5e-214 | glf | 5.4.99.9 | M | UDP-galactopyranose mutase | |
GCKIAGNM_02151 | 1.3e-149 | |||||
GCKIAGNM_02152 | 1.2e-116 | S | Domain of unknown function (DUF4190) | |||
GCKIAGNM_02153 | 1.3e-24 | fahA | Q | Fumarylacetoacetate (FAA) hydrolase family | ||
GCKIAGNM_02154 | 7.1e-114 | fahA | Q | Fumarylacetoacetate (FAA) hydrolase family | ||
GCKIAGNM_02155 | 2.2e-91 | S | Auxin Efflux Carrier | |||
GCKIAGNM_02156 | 1.4e-55 | S | Auxin Efflux Carrier | |||
GCKIAGNM_02157 | 2.2e-180 | 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 | ||
GCKIAGNM_02158 | 7.9e-142 | 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 | ||
GCKIAGNM_02159 | 2.3e-136 | 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 | ||
GCKIAGNM_02160 | 4.4e-146 | gluQ | 6.1.1.17 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
GCKIAGNM_02161 | 1.5e-146 | ugpQ | 3.1.4.46 | C | Glycerophosphoryl diester phosphodiesterase family | |
GCKIAGNM_02162 | 1.6e-47 | ugpQ | 3.1.4.46 | C | Glycerophosphoryl diester phosphodiesterase family | |
GCKIAGNM_02163 | 2.8e-82 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
GCKIAGNM_02164 | 3.4e-116 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
GCKIAGNM_02165 | 7.2e-128 | K | helix_turn _helix lactose operon repressor | |||
GCKIAGNM_02166 | 2.5e-58 | G | Bacterial extracellular solute-binding protein | |||
GCKIAGNM_02167 | 4.1e-64 | G | Bacterial extracellular solute-binding protein | |||
GCKIAGNM_02168 | 2.2e-35 | G | Bacterial extracellular solute-binding protein | |||
GCKIAGNM_02169 | 2e-11 | U | Binding-protein-dependent transport system inner membrane component | |||
GCKIAGNM_02170 | 8.5e-188 | U | Binding-protein-dependent transport system inner membrane component | |||
GCKIAGNM_02171 | 9.1e-140 | P | Binding-protein-dependent transport system inner membrane component | |||
GCKIAGNM_02172 | 4e-57 | G | N-terminal domain of (some) glycogen debranching enzymes | |||
GCKIAGNM_02173 | 8.4e-280 | G | N-terminal domain of (some) glycogen debranching enzymes | |||
GCKIAGNM_02174 | 2.6e-83 | |||||
GCKIAGNM_02175 | 2e-274 | thiC | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Catalyzes the synthesis of the hydroxymethylpyrimidine phosphate (HMP-P) moiety of thiamine from aminoimidazole ribotide (AIR) in a radical S-adenosyl-L-methionine (SAM)-dependent reaction | |
GCKIAGNM_02176 | 5.5e-208 | thiC | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Catalyzes the synthesis of the hydroxymethylpyrimidine phosphate (HMP-P) moiety of thiamine from aminoimidazole ribotide (AIR) in a radical S-adenosyl-L-methionine (SAM)-dependent reaction | |
GCKIAGNM_02177 | 2.6e-33 | thiM | 2.7.1.50 | H | Catalyzes the phosphorylation of the hydroxyl group of 4-methyl-5-beta-hydroxyethylthiazole (THZ) | |
GCKIAGNM_02178 | 3.3e-52 | thiM | 2.7.1.50 | H | Catalyzes the phosphorylation of the hydroxyl group of 4-methyl-5-beta-hydroxyethylthiazole (THZ) | |
GCKIAGNM_02179 | 5.7e-296 | glyQS | 6.1.1.14 | J | Catalyzes the attachment of glycine to tRNA(Gly) | |
GCKIAGNM_02180 | 1.6e-39 | 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 | ||
GCKIAGNM_02181 | 1.9e-85 | 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 | ||
GCKIAGNM_02182 | 3.1e-29 | 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 | ||
GCKIAGNM_02183 | 5.8e-49 | 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 | ||
GCKIAGNM_02184 | 5.3e-102 | 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 | ||
GCKIAGNM_02185 | 5.9e-69 | 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 | ||
GCKIAGNM_02186 | 4.9e-45 | yggT | S | YGGT family | ||
GCKIAGNM_02187 | 5.2e-22 | tccB2 | V | DivIVA protein | ||
GCKIAGNM_02188 | 1.3e-60 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
GCKIAGNM_02189 | 9e-178 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
GCKIAGNM_02190 | 6.4e-170 | K | WYL domain | |||
GCKIAGNM_02191 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase III alpha subunit | |
GCKIAGNM_02192 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase III alpha subunit | |
GCKIAGNM_02193 | 3.1e-68 | yneG | S | Domain of unknown function (DUF4186) | ||
GCKIAGNM_02194 | 7.4e-156 | dkgA | 1.1.1.346 | C | Aldo/keto reductase family | |
GCKIAGNM_02195 | 1.9e-28 | 4.2.1.53 | S | MCRA family | ||
GCKIAGNM_02196 | 0.0 | 4.2.1.53 | S | MCRA family | ||
GCKIAGNM_02197 | 2.3e-20 | nagE | 2.7.1.193, 2.7.1.199 | G | phosphotransferase system, EIIB | |
GCKIAGNM_02198 | 7.5e-86 | 2.7.1.208 | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | ||
GCKIAGNM_02199 | 1.5e-18 | pacL2 | 3.6.3.8 | P | Cation transporter/ATPase, N-terminus | |
GCKIAGNM_02200 | 4.3e-78 | pacL2 | 3.6.3.8 | P | Cation transporter/ATPase, N-terminus | |
GCKIAGNM_02201 | 0.0 | pacL2 | 3.6.3.8 | P | Cation transporter/ATPase, N-terminus | |
GCKIAGNM_02202 | 6.2e-33 | |||||
GCKIAGNM_02203 | 9e-112 | dcd | 3.5.4.13 | F | Belongs to the dCTP deaminase family | |
GCKIAGNM_02204 | 4e-73 | |||||
GCKIAGNM_02205 | 1.2e-64 | |||||
GCKIAGNM_02206 | 1.6e-43 | ypfH | S | Phospholipase/Carboxylesterase | ||
GCKIAGNM_02207 | 3e-56 | ypfH | S | Phospholipase/Carboxylesterase | ||
GCKIAGNM_02208 | 4.5e-99 | S | membrane transporter protein | |||
GCKIAGNM_02209 | 2e-22 | yjcE | P | Sodium/hydrogen exchanger family | ||
GCKIAGNM_02210 | 1.8e-54 | yjcE | P | Sodium/hydrogen exchanger family | ||
GCKIAGNM_02211 | 4.3e-196 | yjcE | P | Sodium/hydrogen exchanger family | ||
GCKIAGNM_02212 | 1.3e-49 | yjcE | P | Sodium/hydrogen exchanger family | ||
GCKIAGNM_02213 | 2.6e-79 | tadA | 3.5.4.1, 3.5.4.33, 3.8.1.5, 6.3.4.19 | FJ | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
GCKIAGNM_02214 | 1.7e-133 | 3.2.1.22 | G | Glycosyl hydrolase family 36 N-terminal domain | ||
GCKIAGNM_02215 | 4.3e-230 | 3.2.1.22 | G | Glycosyl hydrolase family 36 N-terminal domain | ||
GCKIAGNM_02216 | 5e-47 | 3.2.1.22 | G | Glycosyl hydrolase family 36 N-terminal domain | ||
GCKIAGNM_02217 | 2.2e-45 | nagC | GK | ROK family | ||
GCKIAGNM_02218 | 2e-147 | nagC | GK | ROK family | ||
GCKIAGNM_02219 | 3.8e-11 | msmE7 | G | Bacterial extracellular solute-binding protein | ||
GCKIAGNM_02220 | 8e-134 | msmE7 | G | Bacterial extracellular solute-binding protein | ||
GCKIAGNM_02221 | 3e-110 | malC | G | Binding-protein-dependent transport system inner membrane component | ||
GCKIAGNM_02222 | 1.3e-17 | G | Binding-protein-dependent transport system inner membrane component | |||
GCKIAGNM_02223 | 2.9e-137 | G | Binding-protein-dependent transport system inner membrane component | |||
GCKIAGNM_02224 | 9.6e-126 | 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) | |
GCKIAGNM_02225 | 1e-31 | 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) | |
GCKIAGNM_02226 | 1.4e-59 | degP | O | Domain present in PSD-95, Dlg, and ZO-1/2. | ||
GCKIAGNM_02227 | 1.2e-171 | degP | O | Domain present in PSD-95, Dlg, and ZO-1/2. | ||
GCKIAGNM_02229 | 8e-24 | cadA | P | E1-E2 ATPase | ||
GCKIAGNM_02230 | 1.4e-140 | cadA | P | E1-E2 ATPase | ||
GCKIAGNM_02231 | 4.6e-42 | cadA | P | E1-E2 ATPase | ||
GCKIAGNM_02232 | 3.7e-38 | cadA | P | E1-E2 ATPase | ||
GCKIAGNM_02233 | 1.3e-46 | cadA | P | E1-E2 ATPase | ||
GCKIAGNM_02234 | 3.6e-50 | fprA | 1.18.1.2, 1.19.1.1 | C | Pyridine nucleotide-disulphide oxidoreductase | |
GCKIAGNM_02235 | 1.2e-125 | fprA | 1.18.1.2, 1.19.1.1 | C | Pyridine nucleotide-disulphide oxidoreductase | |
GCKIAGNM_02236 | 3.4e-52 | fprA | 1.18.1.2, 1.19.1.1 | C | Pyridine nucleotide-disulphide oxidoreductase | |
GCKIAGNM_02237 | 9.6e-44 | htpX | O | Belongs to the peptidase M48B family | ||
GCKIAGNM_02238 | 6.2e-117 | htpX | O | Belongs to the peptidase M48B family | ||
GCKIAGNM_02240 | 7.8e-103 | yicL | EG | EamA-like transporter family | ||
GCKIAGNM_02241 | 1.1e-90 | fbaA | 4.1.2.13 | G | Fructose-bisphosphate aldolase class-II | |
GCKIAGNM_02242 | 1.2e-79 | fbaA | 4.1.2.13 | G | Fructose-bisphosphate aldolase class-II | |
GCKIAGNM_02243 | 2.2e-137 | 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 | |
GCKIAGNM_02244 | 9.1e-95 | 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 | |
GCKIAGNM_02245 | 1.1e-125 | clcA | P | Voltage gated chloride channel | ||
GCKIAGNM_02246 | 3.2e-133 | clcA | P | Voltage gated chloride channel | ||
GCKIAGNM_02247 | 7.9e-23 | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | |||
GCKIAGNM_02248 | 9.3e-25 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
GCKIAGNM_02249 | 1.1e-23 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
GCKIAGNM_02251 | 1e-201 | K | helix_turn _helix lactose operon repressor | |||
GCKIAGNM_02253 | 6.4e-170 | gtfA | 2.4.1.329, 2.4.1.7 | GH13 | G | Domain of unknown function (DUF1964) |
GCKIAGNM_02254 | 5.7e-80 | gtfA | 2.4.1.329, 2.4.1.7 | GH13 | G | Domain of unknown function (DUF1964) |
GCKIAGNM_02255 | 5e-133 | yihS | 5.1.3.11 | G | N-acylglucosamine 2-epimerase (GlcNAc 2-epimerase) | |
GCKIAGNM_02256 | 4.1e-35 | yihS | 5.1.3.11 | G | N-acylglucosamine 2-epimerase (GlcNAc 2-epimerase) | |
GCKIAGNM_02257 | 7.8e-111 | S | Metal-independent alpha-mannosidase (GH125) | |||
GCKIAGNM_02258 | 1.3e-123 | S | Metal-independent alpha-mannosidase (GH125) | |||
GCKIAGNM_02260 | 4.5e-16 | |||||
GCKIAGNM_02261 | 1.4e-114 | C | Putative TM nitroreductase | |||
GCKIAGNM_02262 | 2.5e-144 | EG | EamA-like transporter family | |||
GCKIAGNM_02263 | 2e-70 | pdxH | S | Pfam:Pyridox_oxidase | ||
GCKIAGNM_02264 | 2.7e-233 | L | ribosomal rna small subunit methyltransferase | |||
GCKIAGNM_02265 | 3.7e-71 | 3.1.3.85, 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | ||
GCKIAGNM_02266 | 9.9e-37 | 3.1.3.85, 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | ||
GCKIAGNM_02267 | 6.4e-147 | corA | P | CorA-like Mg2+ transporter protein | ||
GCKIAGNM_02268 | 6.2e-85 | ET | Bacterial periplasmic substrate-binding proteins | |||
GCKIAGNM_02269 | 2.6e-52 | ET | Bacterial periplasmic substrate-binding proteins | |||
GCKIAGNM_02270 | 6.7e-290 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
GCKIAGNM_02271 | 9.2e-130 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
GCKIAGNM_02272 | 2.4e-90 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
GCKIAGNM_02273 | 2.1e-30 | comEA | 2.4.1.21 | GT5 | L | Helix-hairpin-helix motif |
GCKIAGNM_02274 | 6.2e-74 | comE | S | Competence protein | ||
GCKIAGNM_02275 | 6.1e-163 | comE | S | Competence protein | ||
GCKIAGNM_02276 | 5.5e-105 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
GCKIAGNM_02277 | 2.7e-58 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
GCKIAGNM_02278 | 5.9e-44 | ydiB | 2.7.1.221, 5.1.1.1 | S | Threonylcarbamoyl adenosine biosynthesis protein TsaE | |
GCKIAGNM_02279 | 1.2e-227 | 3.1.1.31 | G | Lactonase, 7-bladed beta-propeller | ||
GCKIAGNM_02280 | 4.5e-59 | |||||
GCKIAGNM_02281 | 5.4e-13 | |||||
GCKIAGNM_02282 | 5.3e-89 | 3.1.3.3, 3.1.3.73 | G | Phosphoglycerate mutase family | ||
GCKIAGNM_02283 | 1.1e-235 | EGP | Major facilitator Superfamily | |||
GCKIAGNM_02284 | 3.3e-55 | S | GtrA-like protein | |||
GCKIAGNM_02285 | 9.7e-34 | S | GtrA-like protein | |||
GCKIAGNM_02286 | 3.3e-61 | S | Macrophage migration inhibitory factor (MIF) | |||
GCKIAGNM_02287 | 4e-50 | fhs | 1.5.1.5, 3.5.4.9, 6.3.4.3 | F | Formate-tetrahydrofolate ligase | |
GCKIAGNM_02288 | 2.1e-185 | fhs | 1.5.1.5, 3.5.4.9, 6.3.4.3 | F | Formate-tetrahydrofolate ligase | |
GCKIAGNM_02289 | 6.9e-21 | fhs | 1.5.1.5, 3.5.4.9, 6.3.4.3 | F | Formate-tetrahydrofolate ligase | |
GCKIAGNM_02290 | 5.9e-63 | pepD | E | Peptidase family C69 | ||
GCKIAGNM_02291 | 3.9e-182 | pepD | E | Peptidase family C69 | ||
GCKIAGNM_02292 | 2.3e-62 | S | Phosphatidylethanolamine-binding protein | |||
GCKIAGNM_02293 | 1.3e-08 | S | Phosphatidylethanolamine-binding protein | |||
GCKIAGNM_02294 | 7.1e-21 | D | nuclear chromosome segregation | |||
GCKIAGNM_02295 | 4.2e-30 | 3.4.17.14 | M | domain, Protein | ||
GCKIAGNM_02296 | 2.1e-117 | 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) | |
GCKIAGNM_02297 | 1.5e-42 | 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) | |
GCKIAGNM_02298 | 4.6e-25 | 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) | |
GCKIAGNM_02299 | 1.4e-20 | 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) | |
GCKIAGNM_02301 | 5.6e-23 | ptsH | G | PTS HPr component phosphorylation site | ||
GCKIAGNM_02302 | 1.2e-08 | K | helix_turn _helix lactose operon repressor | |||
GCKIAGNM_02303 | 3.7e-82 | K | helix_turn _helix lactose operon repressor | |||
GCKIAGNM_02304 | 1.2e-158 | holB | 2.7.7.7 | L | DNA polymerase III | |
GCKIAGNM_02305 | 7.3e-29 | holB | 2.7.7.7 | L | DNA polymerase III | |
GCKIAGNM_02306 | 1.6e-115 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
GCKIAGNM_02307 | 1.1e-152 | S | Domain of unknown function (DUF4143) | |||
GCKIAGNM_02308 | 2.5e-42 | XAC3035 | O | Glutaredoxin | ||
GCKIAGNM_02309 | 2.2e-114 | metC | 2.5.1.48, 4.4.1.8 | E | Cys/Met metabolism PLP-dependent enzyme | |
GCKIAGNM_02310 | 2.8e-68 | metC | 2.5.1.48, 4.4.1.8 | E | Cys/Met metabolism PLP-dependent enzyme | |
GCKIAGNM_02311 | 3.4e-59 | ypfH | S | Phospholipase/Carboxylesterase | ||
GCKIAGNM_02312 | 8.7e-92 | tetP | J | Elongation factor G, domain IV | ||
GCKIAGNM_02313 | 4.8e-17 | tetP | J | Elongation factor G, domain IV | ||
GCKIAGNM_02314 | 3.7e-282 | tetP | J | Elongation factor G, domain IV | ||
GCKIAGNM_02316 | 2.3e-59 | dnaQ | 2.7.7.7 | L | Exonuclease, DNA polymerase III, epsilon subunit family | |
GCKIAGNM_02317 | 1.4e-104 | gmk | 2.7.4.8, 4.1.1.23 | F | Essential for recycling GMP and indirectly, cGMP | |
GCKIAGNM_02318 | 2.5e-19 | pyrF | 2.4.2.10, 4.1.1.23 | F | Essential for recycling GMP and indirectly, cGMP | |
GCKIAGNM_02319 | 1.8e-133 | pyrF | 2.4.2.10, 4.1.1.23 | F | Essential for recycling GMP and indirectly, cGMP | |
GCKIAGNM_02320 | 7.8e-39 | carB | 6.3.5.5 | EF | Carbamoyl-phosphate synthetase large chain, oligomerisation domain | |
GCKIAGNM_02321 | 0.0 | carB | 6.3.5.5 | EF | Carbamoyl-phosphate synthetase large chain, oligomerisation domain | |
GCKIAGNM_02322 | 5.5e-14 | carB | 6.3.5.5 | EF | Carbamoyl-phosphate synthetase large chain, oligomerisation domain | |
GCKIAGNM_02323 | 3.7e-187 | carA | 6.3.5.5 | F | Belongs to the CarA family | |
GCKIAGNM_02324 | 1.4e-39 | carA | 6.3.5.5 | F | Belongs to the CarA family | |
GCKIAGNM_02325 | 2e-90 | 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 | ||
GCKIAGNM_02326 | 2.7e-62 | 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 | ||
GCKIAGNM_02327 | 1.1e-12 | ybbL | V | ATPases associated with a variety of cellular activities | ||
GCKIAGNM_02328 | 7.9e-106 | glpR | K | DeoR C terminal sensor domain | ||
GCKIAGNM_02329 | 1.9e-44 | pyrD | 1.3.1.14, 1.3.5.2, 1.3.98.1 | F | Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor | |
GCKIAGNM_02330 | 2.1e-63 | pyrD | 1.3.1.14, 1.3.5.2, 1.3.98.1 | F | Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor | |
GCKIAGNM_02331 | 4.8e-75 | pyrD | 1.3.1.14, 1.3.5.2, 1.3.98.1 | F | Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor | |
GCKIAGNM_02332 | 5.5e-29 | namA | 1.6.99.1 | C | NADH:flavin oxidoreductase / NADH oxidase family | |
GCKIAGNM_02333 | 1.6e-55 | namA | 1.6.99.1 | C | NADH:flavin oxidoreductase / NADH oxidase family | |
GCKIAGNM_02334 | 4.3e-109 | namA | 1.6.99.1 | C | NADH:flavin oxidoreductase / NADH oxidase family | |
GCKIAGNM_02335 | 2.3e-126 | pon1 | 2.4.1.129, 3.4.16.4 | GT51 | M | Transglycosylase |
GCKIAGNM_02336 | 3.5e-169 | pon1 | 2.4.1.129, 3.4.16.4 | GT51 | M | Transglycosylase |
GCKIAGNM_02337 | 5.9e-89 | pon1 | 2.4.1.129, 3.4.16.4 | GT51 | M | Transglycosylase |
GCKIAGNM_02338 | 1.4e-50 | glxR | K | helix_turn_helix, cAMP Regulatory protein | ||
GCKIAGNM_02339 | 1.1e-55 | glxR | K | helix_turn_helix, cAMP Regulatory protein | ||
GCKIAGNM_02340 | 4.8e-215 | lplA | 6.3.1.20 | H | Biotin/lipoate A/B protein ligase family | |
GCKIAGNM_02341 | 2.1e-29 | leuB | 1.1.1.85 | CE | Catalyzes the oxidation of 3-carboxy-2-hydroxy-4- methylpentanoate (3-isopropylmalate) to 3-carboxy-4-methyl-2- oxopentanoate. The product decarboxylates to 4-methyl-2 oxopentanoate | |
GCKIAGNM_02342 | 3.7e-90 | ptrB | 3.4.21.83 | E | Peptidase, S9A B C family, catalytic domain protein | |
GCKIAGNM_02343 | 1.3e-163 | ptrB | 3.4.21.83 | E | Peptidase, S9A B C family, catalytic domain protein | |
GCKIAGNM_02344 | 1.4e-64 | ptrB | 3.4.21.83 | E | Peptidase, S9A B C family, catalytic domain protein | |
GCKIAGNM_02345 | 4.1e-159 | ptrB | 3.4.21.83 | E | Peptidase, S9A B C family, catalytic domain protein | |
GCKIAGNM_02346 | 3.3e-103 | S | Uncharacterized conserved protein (DUF2183) | |||
GCKIAGNM_02347 | 8.8e-87 | S | Uncharacterized conserved protein (DUF2183) | |||
GCKIAGNM_02348 | 3e-30 | gcvH | E | The glycine cleavage system catalyzes the degradation of glycine. The H protein shuttles the methylamine group of glycine from the P protein to the T protein | ||
GCKIAGNM_02349 | 1.3e-24 | gcvH | E | The glycine cleavage system catalyzes the degradation of glycine. The H protein shuttles the methylamine group of glycine from the P protein to the T protein | ||
GCKIAGNM_02350 | 2.8e-90 | nudC | 1.3.7.1, 3.6.1.22 | L | NADH pyrophosphatase zinc ribbon domain | |
GCKIAGNM_02351 | 1.7e-96 | nudC | 1.3.7.1, 3.6.1.22 | L | NADH pyrophosphatase zinc ribbon domain | |
GCKIAGNM_02352 | 3.3e-150 | mhpC | I | Alpha/beta hydrolase family | ||
GCKIAGNM_02353 | 5.1e-50 | K | helix_turn_helix, arabinose operon control protein | |||
GCKIAGNM_02355 | 2.6e-154 | araN | G | Bacterial extracellular solute-binding protein | ||
GCKIAGNM_02356 | 9.5e-121 | lacF | P | Binding-protein-dependent transport system inner membrane component | ||
GCKIAGNM_02357 | 1.3e-114 | araQ | U | Binding-protein-dependent transport system inner membrane component | ||
GCKIAGNM_02358 | 2e-13 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
GCKIAGNM_02359 | 2.6e-97 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
GCKIAGNM_02360 | 6.8e-63 | tyrA | 5.4.99.5 | E | Chorismate mutase type II | |
GCKIAGNM_02361 | 2.4e-107 | S | domain protein | |||
GCKIAGNM_02362 | 7e-49 | S | domain protein | |||
GCKIAGNM_02363 | 1.8e-119 | S | domain protein | |||
GCKIAGNM_02364 | 9.5e-236 | 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 | |
GCKIAGNM_02365 | 2.8e-40 | 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 | |
GCKIAGNM_02366 | 2.7e-111 | 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 | |
GCKIAGNM_02367 | 7.1e-79 | 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 | |
GCKIAGNM_02368 | 5.7e-138 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | |||
GCKIAGNM_02369 | 1.2e-112 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | |||
GCKIAGNM_02370 | 1.3e-127 | 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 | |
GCKIAGNM_02371 | 1.5e-128 | KT | Transcriptional regulatory protein, C terminal | |||
GCKIAGNM_02372 | 3.4e-68 | |||||
GCKIAGNM_02373 | 5e-125 | pyrE | 2.4.2.10 | F | Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) | |
GCKIAGNM_02374 | 3.4e-28 | |||||
GCKIAGNM_02375 | 7.3e-219 | MA20_36090 | S | Psort location Cytoplasmic, score 8.87 | ||
GCKIAGNM_02376 | 5.1e-133 | cpsY | K | Bacterial regulatory helix-turn-helix protein, lysR family | ||
GCKIAGNM_02377 | 9e-24 | cpsY | K | Bacterial regulatory helix-turn-helix protein, lysR family | ||
GCKIAGNM_02378 | 9.4e-123 | 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | ||
GCKIAGNM_02379 | 1.4e-87 | 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 | |
GCKIAGNM_02380 | 6.4e-165 | 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 | |
GCKIAGNM_02381 | 9.3e-21 | 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 | |
GCKIAGNM_02382 | 1e-232 | ybiT | S | ABC transporter | ||
GCKIAGNM_02383 | 9.4e-43 | ybiT | S | ABC transporter | ||
GCKIAGNM_02384 | 3.3e-91 | S | Enoyl-(Acyl carrier protein) reductase | |||
GCKIAGNM_02385 | 5.2e-56 | P | ABC transporter | |||
GCKIAGNM_02386 | 8.3e-24 | P | ABC transporter | |||
GCKIAGNM_02387 | 1.4e-26 | P | ABC transporter | |||
GCKIAGNM_02388 | 2.2e-22 | XK27_08585 | S | Hypothetical bacterial integral membrane protein (Trep_Strep) | ||
GCKIAGNM_02389 | 9.4e-28 | XK27_08585 | S | Hypothetical bacterial integral membrane protein (Trep_Strep) | ||
GCKIAGNM_02390 | 2.6e-202 | yhdR | 2.6.1.1 | E | Psort location Cytoplasmic, score 8.87 | |
GCKIAGNM_02391 | 1.4e-22 | yhdR | 2.6.1.1 | E | Psort location Cytoplasmic, score 8.87 | |
GCKIAGNM_02392 | 1.5e-13 | 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 | ||
GCKIAGNM_02393 | 8.2e-204 | 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 | ||
GCKIAGNM_02394 | 3.6e-164 | 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 | ||
GCKIAGNM_02395 | 9.4e-106 | 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 | ||
GCKIAGNM_02396 | 5.5e-37 | 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 | ||
GCKIAGNM_02397 | 7.8e-177 | 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 | ||
GCKIAGNM_02398 | 1.7e-125 | trxB2 | 1.8.1.9 | C | Thioredoxin domain | |
GCKIAGNM_02399 | 4e-91 | 5.1.3.2 | GM | ADP-glyceromanno-heptose 6-epimerase activity | ||
GCKIAGNM_02400 | 1.6e-214 | 5.1.3.2 | GM | ADP-glyceromanno-heptose 6-epimerase activity | ||
GCKIAGNM_02401 | 8.5e-165 | |||||
GCKIAGNM_02402 | 2.1e-95 | S | Uncharacterised protein conserved in bacteria (DUF2194) | |||
GCKIAGNM_02403 | 7.1e-195 | S | Uncharacterised protein conserved in bacteria (DUF2194) | |||
GCKIAGNM_02404 | 7e-134 | pelF | GT4 | M | Domain of unknown function (DUF3492) | |
GCKIAGNM_02405 | 8e-48 | pelF | GT4 | M | Domain of unknown function (DUF3492) | |
GCKIAGNM_02406 | 8.9e-26 | pelF | GT4 | M | Domain of unknown function (DUF3492) | |
GCKIAGNM_02407 | 7.6e-40 | pelG | S | Putative exopolysaccharide Exporter (EPS-E) | ||
GCKIAGNM_02408 | 6.9e-117 | pelG | S | Putative exopolysaccharide Exporter (EPS-E) | ||
GCKIAGNM_02409 | 1.2e-71 | pelG | S | Putative exopolysaccharide Exporter (EPS-E) | ||
GCKIAGNM_02410 | 0.0 | cotH | M | CotH kinase protein | ||
GCKIAGNM_02411 | 4.1e-158 | P | VTC domain | |||
GCKIAGNM_02412 | 4.2e-110 | S | Domain of unknown function (DUF4956) | |||
GCKIAGNM_02413 | 3.5e-52 | yliE | T | Putative diguanylate phosphodiesterase | ||
GCKIAGNM_02414 | 0.0 | yliE | T | Putative diguanylate phosphodiesterase | ||
GCKIAGNM_02415 | 3.5e-74 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
GCKIAGNM_02416 | 2.5e-17 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
GCKIAGNM_02417 | 8.5e-11 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
GCKIAGNM_02418 | 4.9e-146 | ywiC | S | YwiC-like protein | ||
GCKIAGNM_02419 | 6.8e-129 | budA | 4.1.1.5 | H | Alpha-acetolactate decarboxylase | |
GCKIAGNM_02420 | 8e-51 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
GCKIAGNM_02421 | 1e-46 | 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 | ||
GCKIAGNM_02422 | 4e-27 | 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 | ||
GCKIAGNM_02423 | 8.2e-33 | rplD | J | Forms part of the polypeptide exit tunnel | ||
GCKIAGNM_02424 | 1.9e-11 | rplD | J | Forms part of the polypeptide exit tunnel | ||
GCKIAGNM_02425 | 3.2e-40 | rplD | J | Forms part of the polypeptide exit tunnel | ||
GCKIAGNM_02426 | 7.5e-46 | 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 | ||
GCKIAGNM_02427 | 1.8e-153 | rplB | J | One of the primary rRNA binding proteins. Required for association of the 30S and 50S subunits to form the 70S ribosome, for tRNA binding and peptide bond formation. It has been suggested to have peptidyltransferase activity | ||
GCKIAGNM_02428 | 3.7e-47 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
GCKIAGNM_02429 | 2.8e-57 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
GCKIAGNM_02430 | 2.6e-36 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
GCKIAGNM_02431 | 2.2e-75 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
GCKIAGNM_02432 | 1.4e-19 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
GCKIAGNM_02433 | 1.9e-23 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
GCKIAGNM_02434 | 6.6e-60 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
GCKIAGNM_02435 | 1.3e-51 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
GCKIAGNM_02436 | 4.4e-103 | 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 | ||
GCKIAGNM_02437 | 9.2e-18 | 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 | ||
GCKIAGNM_02438 | 5.5e-68 | 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 | ||
GCKIAGNM_02439 | 9.1e-82 | 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 | ||
GCKIAGNM_02440 | 7.1e-61 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
GCKIAGNM_02441 | 7.4e-26 | rpmD | J | Ribosomal protein L30p/L7e | ||
GCKIAGNM_02442 | 8.1e-76 | rplO | J | binds to the 23S rRNA | ||
GCKIAGNM_02443 | 2e-222 | 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 | ||
GCKIAGNM_02444 | 6.7e-14 | 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 | ||
GCKIAGNM_02445 | 2.7e-70 | 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 | |
GCKIAGNM_02446 | 1e-134 | tam | 2.1.1.144, 2.1.1.197 | S | Methyltransferase domain | |
GCKIAGNM_02447 | 2.7e-45 | hbd2 | 1.1.1.157 | I | 3-hydroxyacyl-CoA dehydrogenase, C-terminal domain | |
GCKIAGNM_02448 | 1.2e-96 | hbd2 | 1.1.1.157 | I | 3-hydroxyacyl-CoA dehydrogenase, C-terminal domain | |
GCKIAGNM_02449 | 1.2e-31 | 4.1.1.44 | S | Cupin domain | ||
GCKIAGNM_02450 | 5.8e-39 | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | ||
GCKIAGNM_02451 | 2.7e-77 | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | ||
GCKIAGNM_02452 | 8.7e-32 | S | Membrane transport protein | |||
GCKIAGNM_02453 | 2.6e-141 | S | Membrane transport protein | |||
GCKIAGNM_02454 | 1.3e-41 | lacA | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
GCKIAGNM_02455 | 9.7e-110 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
GCKIAGNM_02457 | 9.2e-124 | magIII | L | endonuclease III | ||
GCKIAGNM_02458 | 1.1e-95 | vbsD | V | MatE | ||
GCKIAGNM_02459 | 1.2e-107 | vbsD | V | MatE | ||
GCKIAGNM_02460 | 2.1e-238 | uvrA3 | 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 | ||
GCKIAGNM_02461 | 2e-220 | uvrA3 | 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 | ||
GCKIAGNM_02462 | 1.9e-52 | K | LysR substrate binding domain | |||
GCKIAGNM_02463 | 1.3e-38 | K | LysR substrate binding domain | |||
GCKIAGNM_02464 | 1.5e-144 | K | LysR substrate binding domain | |||
GCKIAGNM_02465 | 1.5e-175 | K | helix_turn _helix lactose operon repressor | |||
GCKIAGNM_02466 | 1.9e-119 | P | Phosphate transporter family | |||
GCKIAGNM_02467 | 2.2e-108 | guaB | 1.1.1.205 | F | Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate- limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth | |
GCKIAGNM_02468 | 3e-54 | tagO | 2.7.8.33, 2.7.8.35 | M | Glycosyl transferase family 4 | |
GCKIAGNM_02469 | 2.5e-109 | tagO | 2.7.8.33, 2.7.8.35 | M | Glycosyl transferase family 4 | |
GCKIAGNM_02470 | 3.9e-84 | ywlC | 2.7.7.87 | J | Belongs to the SUA5 family | |
GCKIAGNM_02471 | 5e-38 | livF | E | ATPases associated with a variety of cellular activities | ||
GCKIAGNM_02472 | 2e-32 | livF | E | ATPases associated with a variety of cellular activities | ||
GCKIAGNM_02473 | 1.6e-34 | livF | E | ATPases associated with a variety of cellular activities | ||
GCKIAGNM_02474 | 1.6e-79 | E | Branched-chain amino acid ATP-binding cassette transporter | |||
GCKIAGNM_02475 | 5.7e-27 | E | Branched-chain amino acid ATP-binding cassette transporter | |||
GCKIAGNM_02476 | 1.5e-24 | livM | U | Belongs to the binding-protein-dependent transport system permease family | ||
GCKIAGNM_02477 | 7.9e-121 | livM | U | Belongs to the binding-protein-dependent transport system permease family | ||
GCKIAGNM_02478 | 7.8e-63 | U | Belongs to the binding-protein-dependent transport system permease family | |||
GCKIAGNM_02479 | 1.3e-45 | U | Belongs to the binding-protein-dependent transport system permease family | |||
GCKIAGNM_02480 | 2.2e-99 | livK | E | Receptor family ligand binding region | ||
GCKIAGNM_02481 | 3.3e-36 | livK | E | Receptor family ligand binding region | ||
GCKIAGNM_02482 | 8.2e-165 | prmC | 2.1.1.297 | J | Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif | |
GCKIAGNM_02483 | 3.7e-191 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
GCKIAGNM_02484 | 1.3e-36 | rpmE | J | Binds the 23S rRNA | ||
GCKIAGNM_02486 | 4.4e-101 | yebQ | EGP | Major facilitator Superfamily | ||
GCKIAGNM_02487 | 7.1e-152 | |||||
GCKIAGNM_02488 | 3.5e-70 | def2 | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins | |
GCKIAGNM_02489 | 5.1e-120 | dkgB | S | Oxidoreductase, aldo keto reductase family protein | ||
GCKIAGNM_02490 | 1.5e-18 | lmrB | U | Major Facilitator Superfamily | ||
GCKIAGNM_02491 | 4.8e-88 | K | Winged helix DNA-binding domain | |||
GCKIAGNM_02492 | 1e-51 | S | Appr-1'-p processing enzyme | |||
GCKIAGNM_02493 | 6e-74 | S | von Willebrand factor (vWF) type A domain | |||
GCKIAGNM_02494 | 6e-85 | 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 | ||
GCKIAGNM_02495 | 0.0 | 3.2.1.24 | GH38 | G | Alpha mannosidase, middle domain | |
GCKIAGNM_02496 | 1.6e-215 | 3.2.1.24 | GH38 | G | Alpha mannosidase, middle domain | |
GCKIAGNM_02497 | 7.4e-284 | 3.2.1.24 | GH38 | G | Alpha mannosidase, middle domain | |
GCKIAGNM_02498 | 8.5e-12 | 3.2.1.24 | GH38 | G | Alpha mannosidase, middle domain | |
GCKIAGNM_02499 | 3.8e-179 | srrA1 | G | Bacterial extracellular solute-binding protein | ||
GCKIAGNM_02500 | 6.2e-08 | G | Binding-protein-dependent transport system inner membrane component | |||
GCKIAGNM_02501 | 1.1e-69 | G | Binding-protein-dependent transport system inner membrane component | |||
GCKIAGNM_02502 | 9.4e-13 | G | Binding-protein-dependent transport system inner membrane component | |||
GCKIAGNM_02503 | 5.9e-125 | lacG | G | Binding-protein-dependent transport system inner membrane component | ||
GCKIAGNM_02504 | 1.8e-221 | G | Belongs to the glycosyl hydrolase 5 (cellulase A) family | |||
GCKIAGNM_02505 | 4.2e-139 | K | helix_turn _helix lactose operon repressor | |||
GCKIAGNM_02506 | 2.7e-08 | 2.5.1.49 | E | Cys/Met metabolism PLP-dependent enzyme | ||
GCKIAGNM_02507 | 7e-114 | XK27_08050 | O | prohibitin homologues | ||
GCKIAGNM_02508 | 1.4e-25 | S | Domain of unknown function (DUF4143) | |||
GCKIAGNM_02509 | 1.1e-10 | S | Domain of unknown function (DUF4143) | |||
GCKIAGNM_02510 | 1.2e-115 | S | Patatin-like phospholipase | |||
GCKIAGNM_02511 | 9.7e-17 | S | Patatin-like phospholipase | |||
GCKIAGNM_02512 | 5.7e-149 | murI | 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
GCKIAGNM_02513 | 2.7e-171 | 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 | |
GCKIAGNM_02514 | 5.4e-107 | S | Vitamin K epoxide reductase | |||
GCKIAGNM_02515 | 2.9e-102 | PPA1328 | 3.1.3.97 | S | DNA polymerase alpha chain like domain | |
GCKIAGNM_02516 | 2.9e-47 | PPA1328 | 3.1.3.97 | S | DNA polymerase alpha chain like domain | |
GCKIAGNM_02517 | 2.1e-64 | mphA | S | Aminoglycoside phosphotransferase | ||
GCKIAGNM_02518 | 2.5e-158 | mphA | S | Aminoglycoside phosphotransferase | ||
GCKIAGNM_02519 | 7.8e-89 | uvrD2 | 3.6.4.12 | L | DNA helicase | |
GCKIAGNM_02520 | 9.4e-86 | uvrD2 | 3.6.4.12 | L | DNA helicase | |
GCKIAGNM_02521 | 2.1e-11 | uvrD2 | 3.6.4.12 | L | DNA helicase | |
GCKIAGNM_02522 | 2.3e-144 | S | Zincin-like metallopeptidase | |||
GCKIAGNM_02523 | 9.5e-32 | S | Zincin-like metallopeptidase | |||
GCKIAGNM_02524 | 4.6e-88 | S | Zincin-like metallopeptidase | |||
GCKIAGNM_02525 | 1.5e-175 | lon | T | Belongs to the peptidase S16 family | ||
GCKIAGNM_02526 | 1.6e-73 | S | Protein of unknown function (DUF3052) | |||
GCKIAGNM_02528 | 8.6e-37 | 2.7.11.1 | NU | Tfp pilus assembly protein FimV | ||
GCKIAGNM_02529 | 3e-114 | der | 1.1.1.399, 1.1.1.95, 2.7.4.25 | F | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
GCKIAGNM_02530 | 1.8e-94 | der | 1.1.1.399, 1.1.1.95, 2.7.4.25 | F | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
GCKIAGNM_02531 | 1.9e-141 | rluB | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
GCKIAGNM_02532 | 2.9e-120 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
GCKIAGNM_02533 | 1.3e-32 | |||||
GCKIAGNM_02534 | 5.9e-163 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
GCKIAGNM_02535 | 5.3e-118 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
GCKIAGNM_02536 | 3.4e-53 | |||||
GCKIAGNM_02537 | 1.8e-134 | |||||
GCKIAGNM_02538 | 1.2e-155 | sucD | 6.2.1.5 | C | Succinyl-CoA synthetase functions in the citric acid cycle (TCA), coupling the hydrolysis of succinyl-CoA to the synthesis of either ATP or GTP and thus represents the only step of substrate-level phosphorylation in the TCA. The alpha subunit of the enzyme binds the substrates coenzyme A and phosphate, while succinate binding and nucleotide specificity is provided by the beta subunit | |
GCKIAGNM_02539 | 6e-177 | sucC | 6.2.1.5 | F | Succinyl-CoA synthetase functions in the citric acid cycle (TCA), coupling the hydrolysis of succinyl-CoA to the synthesis of either ATP or GTP and thus represents the only step of substrate-level phosphorylation in the TCA. The beta subunit provides nucleotide specificity of the enzyme and binds the substrate succinate, while the binding sites for coenzyme A and phosphate are found in the alpha subunit | |
GCKIAGNM_02540 | 9.3e-50 | 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 | |
GCKIAGNM_02541 | 9.8e-21 | 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 | |
GCKIAGNM_02542 | 3.6e-52 | yajC | U | Preprotein translocase subunit | ||
GCKIAGNM_02543 | 2.9e-28 | 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 | |
GCKIAGNM_02544 | 1.4e-150 | 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 | |
GCKIAGNM_02545 | 3e-105 | ruvA | 3.6.4.12 | L | The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing. RuvA stimulates, in the presence of DNA, the weak ATPase activity of RuvB | |
GCKIAGNM_02546 | 1.7e-89 | ruvC | 3.1.22.4 | L | Nuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves the cruciform structure in supercoiled DNA by nicking to strands with the same polarity at sites symmetrically opposed at the junction in the homologous arms and leaves a 5'-terminal phosphate and a 3'-terminal hydroxyl group | |
GCKIAGNM_02547 | 9.6e-13 | yebC | K | transcriptional regulatory protein | ||
GCKIAGNM_02548 | 6.9e-65 | yebC | K | transcriptional regulatory protein | ||
GCKIAGNM_02549 | 6.6e-29 | hit | 2.7.7.53 | FG | HIT domain | |
GCKIAGNM_02550 | 2.6e-73 | hit | 2.7.7.53 | FG | HIT domain | |
GCKIAGNM_02551 | 2.4e-65 | 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) | |
GCKIAGNM_02552 | 1.7e-36 | EGP | Major facilitator Superfamily | |||
GCKIAGNM_02553 | 1.6e-140 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
GCKIAGNM_02554 | 5.9e-168 | yeaD | 4.2.1.9, 5.1.3.15 | G | Aldose 1-epimerase | |
GCKIAGNM_02555 | 4.2e-302 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
GCKIAGNM_02556 | 1.7e-122 | KLT | Domain of unknown function (DUF4032) | |||
GCKIAGNM_02557 | 2.7e-127 | KLT | Domain of unknown function (DUF4032) | |||
GCKIAGNM_02558 | 8.9e-108 | |||||
GCKIAGNM_02559 | 1.4e-17 | tnp7109-21 | L | Integrase core domain | ||
GCKIAGNM_02560 | 2.2e-53 | K | helix_turn _helix lactose operon repressor | |||
GCKIAGNM_02561 | 1.5e-69 | K | helix_turn _helix lactose operon repressor | |||
GCKIAGNM_02562 | 9.5e-116 | G | Periplasmic binding protein domain | |||
GCKIAGNM_02563 | 7.7e-171 | 3.6.3.17 | G | ATPases associated with a variety of cellular activities | ||
GCKIAGNM_02564 | 5e-142 | U | Branched-chain amino acid transport system / permease component | |||
GCKIAGNM_02565 | 5.2e-157 | |||||
GCKIAGNM_02566 | 3.8e-188 | 3.2.1.10, 3.2.1.20, 3.2.1.93 | GH13,GH31 | G | Alpha-amylase domain | |
GCKIAGNM_02567 | 1e-23 | 3.2.1.10, 3.2.1.20, 3.2.1.93 | GH13,GH31 | G | Alpha-amylase domain | |
GCKIAGNM_02568 | 2e-132 | K | Psort location Cytoplasmic, score | |||
GCKIAGNM_02569 | 4.9e-18 | K | Psort location Cytoplasmic, score | |||
GCKIAGNM_02570 | 2.5e-282 | M | cell wall anchor domain protein | |||
GCKIAGNM_02571 | 0.0 | M | cell wall anchor domain protein | |||
GCKIAGNM_02572 | 1.6e-180 | M | domain protein | |||
GCKIAGNM_02573 | 1.9e-43 | M | domain protein | |||
GCKIAGNM_02574 | 2.2e-25 | M | domain protein | |||
GCKIAGNM_02575 | 3.6e-174 | 3.4.22.70 | M | Sortase family | ||
GCKIAGNM_02576 | 1.3e-262 | malQ | 2.4.1.18, 2.4.1.25, 3.2.1.196, 5.4.99.15 | CBM48,GH13,GH77 | G | 4-alpha-glucanotransferase |
GCKIAGNM_02577 | 1.3e-115 | malQ | 2.4.1.18, 2.4.1.25, 3.2.1.196, 5.4.99.15 | CBM48,GH13,GH77 | G | 4-alpha-glucanotransferase |
GCKIAGNM_02578 | 7.8e-79 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
GCKIAGNM_02579 | 1.3e-76 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
GCKIAGNM_02580 | 8.1e-131 | K | Bacterial regulatory proteins, tetR family | |||
GCKIAGNM_02581 | 8e-222 | G | Transmembrane secretion effector | |||
GCKIAGNM_02582 | 4.7e-193 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
GCKIAGNM_02583 | 8.7e-38 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
GCKIAGNM_02584 | 5.2e-113 | nox | 1.6.3.4 | C | Pyridine nucleotide-disulphide oxidoreductase | |
GCKIAGNM_02585 | 9.9e-11 | ET | Bacterial periplasmic substrate-binding proteins | |||
GCKIAGNM_02586 | 1.6e-70 | ET | Bacterial periplasmic substrate-binding proteins | |||
GCKIAGNM_02587 | 6.6e-47 | ET | Bacterial periplasmic substrate-binding proteins | |||
GCKIAGNM_02588 | 3.7e-120 | ytmL | P | Binding-protein-dependent transport system inner membrane component | ||
GCKIAGNM_02589 | 1.2e-138 | P | Binding-protein-dependent transport system inner membrane component | |||
GCKIAGNM_02590 | 3.5e-105 | S | L-2-amino-thiazoline-4-carboxylic acid hydrolase | |||
GCKIAGNM_02591 | 1.3e-131 | yxeO | 3.6.3.21 | E | ATPases associated with a variety of cellular activities | |
GCKIAGNM_02592 | 1.9e-186 | pyrD | 1.3.1.14, 1.3.98.1 | F | Dihydroorotate dehydrogenase | |
GCKIAGNM_02593 | 2.2e-84 | S | Fic/DOC family | |||
GCKIAGNM_02594 | 1.3e-251 | S | HipA-like C-terminal domain | |||
GCKIAGNM_02596 | 2.3e-74 | |||||
GCKIAGNM_02598 | 1.6e-97 | L | Phage integrase family | |||
GCKIAGNM_02599 | 3.9e-48 | L | Phage integrase family | |||
GCKIAGNM_02600 | 3.7e-141 | fic | D | Fic/DOC family | ||
GCKIAGNM_02601 | 9.5e-26 | |||||
GCKIAGNM_02602 | 6.9e-13 | |||||
GCKIAGNM_02603 | 1.9e-26 | |||||
GCKIAGNM_02604 | 2.6e-64 | |||||
GCKIAGNM_02607 | 8.4e-155 | topB | 5.99.1.2 | L | DNA topoisomerase | |
GCKIAGNM_02608 | 3.9e-123 | topB | 5.99.1.2 | L | DNA topoisomerase | |
GCKIAGNM_02609 | 2.7e-68 | |||||
GCKIAGNM_02610 | 5.3e-31 | |||||
GCKIAGNM_02612 | 1.6e-32 | infA | J | One of the essential components for the initiation of protein synthesis. Stabilizes the binding of IF-2 and IF-3 on the 30S subunit to which N-formylmethionyl-tRNA(fMet) subsequently binds. Helps modulate mRNA selection, yielding the 30S pre- initiation complex (PIC). Upon addition of the 50S ribosomal subunit IF-1, IF-2 and IF-3 are released leaving the mature 70S translation initation complex | ||
GCKIAGNM_02613 | 8.4e-14 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
GCKIAGNM_02614 | 9.5e-62 | 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 | ||
GCKIAGNM_02615 | 7.8e-42 | 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 | ||
GCKIAGNM_02616 | 9.5e-24 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
GCKIAGNM_02617 | 6.3e-61 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
GCKIAGNM_02618 | 9.3e-46 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
GCKIAGNM_02619 | 5.2e-60 | rplQ | J | Ribosomal protein L17 | ||
GCKIAGNM_02620 | 8.7e-170 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
GCKIAGNM_02621 | 3.6e-177 | gcs2 | S | A circularly permuted ATPgrasp | ||
GCKIAGNM_02622 | 6e-121 | gcs2 | S | A circularly permuted ATPgrasp | ||
GCKIAGNM_02623 | 1.6e-94 | gcs2 | S | A circularly permuted ATPgrasp | ||
GCKIAGNM_02624 | 3.3e-146 | E | Transglutaminase/protease-like homologues | |||
GCKIAGNM_02626 | 2.9e-100 | K | helix_turn _helix lactose operon repressor | |||
GCKIAGNM_02627 | 2.7e-84 | |||||
GCKIAGNM_02628 | 5.8e-116 | nusA | K | Participates in both transcription termination and antitermination | ||
GCKIAGNM_02629 | 3.5e-23 | 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 | ||
GCKIAGNM_02630 | 1.4e-104 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
GCKIAGNM_02631 | 4.9e-112 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
GCKIAGNM_02632 | 3.1e-91 | yjjP | S | Threonine/Serine exporter, ThrE | ||
GCKIAGNM_02633 | 2.4e-43 | yjjP | S | Threonine/Serine exporter, ThrE | ||
GCKIAGNM_02634 | 1.9e-112 | yjjP | S | Threonine/Serine exporter, ThrE | ||
GCKIAGNM_02635 | 1.8e-298 | putP | E | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
GCKIAGNM_02636 | 1.5e-18 | gmk | 1.1.1.23, 2.7.4.8 | S | Protein conserved in bacteria | |
GCKIAGNM_02637 | 2.2e-115 | gmk | 1.1.1.23, 2.7.4.8 | S | Protein conserved in bacteria | |
GCKIAGNM_02638 | 2.3e-76 | S | Amidohydrolase family | |||
GCKIAGNM_02639 | 2.4e-50 | S | Amidohydrolase family | |||
GCKIAGNM_02640 | 1.3e-103 | S | Amidohydrolase family | |||
GCKIAGNM_02641 | 5.5e-203 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
GCKIAGNM_02642 | 1.9e-20 | F | Domain of unknown function (DUF4916) | |||
GCKIAGNM_02643 | 1.9e-59 | trxA | 1.8.1.8, 1.8.1.9 | O | Belongs to the thioredoxin family | |
GCKIAGNM_02644 | 1.6e-37 | S | G5 | |||
GCKIAGNM_02645 | 1.1e-121 | S | G5 | |||
GCKIAGNM_02646 | 5.5e-27 | |||||
GCKIAGNM_02647 | 1.3e-110 | |||||
GCKIAGNM_02648 | 8.8e-88 | wcoI | DM | Psort location CytoplasmicMembrane, score | ||
GCKIAGNM_02649 | 1.4e-92 | wcoI | DM | Psort location CytoplasmicMembrane, score | ||
GCKIAGNM_02650 | 3.2e-46 | |||||
GCKIAGNM_02651 | 1.4e-251 | S | Psort location CytoplasmicMembrane, score 9.99 | |||
GCKIAGNM_02652 | 3e-08 | L | transposase and inactivated derivatives, IS30 family | |||
GCKIAGNM_02653 | 1.4e-10 | K | Transposase IS116 IS110 IS902 | |||
GCKIAGNM_02654 | 1.5e-177 | I | alpha/beta hydrolase fold | |||
GCKIAGNM_02655 | 5e-90 | S | Appr-1'-p processing enzyme | |||
GCKIAGNM_02656 | 1.1e-39 | S | phosphoesterase or phosphohydrolase | |||
GCKIAGNM_02657 | 1.8e-90 | S | phosphoesterase or phosphohydrolase | |||
GCKIAGNM_02658 | 2e-140 | tenA | 3.5.99.2 | K | Catalyzes an amino-pyrimidine hydrolysis reaction at the C5' of the pyrimidine moiety of thiamine compounds, a reaction that is part of a thiamine salvage pathway | |
GCKIAGNM_02660 | 1.3e-133 | S | Phospholipase/Carboxylesterase | |||
GCKIAGNM_02661 | 1.3e-183 | trmI | 2.1.1.219, 2.1.1.220 | J | Catalyzes the S-adenosyl-L-methionine-dependent formation of N(1)-methyladenine at position 58 (m1A58) in tRNA | |
GCKIAGNM_02662 | 4.5e-35 | sixA | 3.6.1.55 | T | Phosphoglycerate mutase family | |
GCKIAGNM_02664 | 1.1e-190 | metE | 2.1.1.14 | E | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | |
GCKIAGNM_02665 | 2.4e-54 | 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 | |
GCKIAGNM_02666 | 9e-130 | 3.6.1.27 | I | PAP2 superfamily | ||
GCKIAGNM_02667 | 1.4e-55 | mrcB | 2.4.1.129, 3.4.16.4 | GT51 | M | Transglycosylase |
GCKIAGNM_02668 | 4.6e-282 | mrcB | 2.4.1.129, 3.4.16.4 | GT51 | M | Transglycosylase |
GCKIAGNM_02669 | 0.0 | leuA | 2.3.3.13 | E | Catalyzes the condensation of the acetyl group of acetyl-CoA with 3-methyl-2-oxobutanoate (2-oxoisovalerate) to form 3-carboxy-3-hydroxy-4-methylpentanoate (2-isopropylmalate) | |
GCKIAGNM_02670 | 3.6e-67 | glnE | 2.7.7.42, 2.7.7.89 | H | Involved in the regulation of glutamine synthetase GlnA, a key enzyme in the process to assimilate ammonia. When cellular nitrogen levels are high, the C-terminal adenylyl transferase (AT) inactivates GlnA by covalent transfer of an adenylyl group from ATP to specific tyrosine residue of GlnA, thus reducing its activity. Conversely, when nitrogen levels are low, the N-terminal adenylyl removase (AR) activates GlnA by removing the adenylyl group by phosphorolysis, increasing its activity. The regulatory region of GlnE binds the signal transduction protein PII (GlnB) which indicates the nitrogen status of the cell | |
GCKIAGNM_02671 | 5e-137 | glnE | 2.7.7.42, 2.7.7.89 | H | Involved in the regulation of glutamine synthetase GlnA, a key enzyme in the process to assimilate ammonia. When cellular nitrogen levels are high, the C-terminal adenylyl transferase (AT) inactivates GlnA by covalent transfer of an adenylyl group from ATP to specific tyrosine residue of GlnA, thus reducing its activity. Conversely, when nitrogen levels are low, the N-terminal adenylyl removase (AR) activates GlnA by removing the adenylyl group by phosphorolysis, increasing its activity. The regulatory region of GlnE binds the signal transduction protein PII (GlnB) which indicates the nitrogen status of the cell | |
GCKIAGNM_02672 | 1.4e-26 | glnE | 2.7.7.42, 2.7.7.89 | H | Involved in the regulation of glutamine synthetase GlnA, a key enzyme in the process to assimilate ammonia. When cellular nitrogen levels are high, the C-terminal adenylyl transferase (AT) inactivates GlnA by covalent transfer of an adenylyl group from ATP to specific tyrosine residue of GlnA, thus reducing its activity. Conversely, when nitrogen levels are low, the N-terminal adenylyl removase (AR) activates GlnA by removing the adenylyl group by phosphorolysis, increasing its activity. The regulatory region of GlnE binds the signal transduction protein PII (GlnB) which indicates the nitrogen status of the cell | |
GCKIAGNM_02673 | 2.3e-67 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
GCKIAGNM_02674 | 3.2e-65 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
GCKIAGNM_02675 | 1.9e-08 | pyrI | 2.1.3.2 | F | Aspartate carbamoyltransferase regulatory chain, allosteric domain protein | |
GCKIAGNM_02676 | 7.1e-52 | pyrI | 2.1.3.2 | F | Aspartate carbamoyltransferase regulatory chain, allosteric domain protein | |
GCKIAGNM_02677 | 5.4e-278 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
GCKIAGNM_02678 | 4.2e-161 | pyrF | 2.4.2.10, 4.1.1.23 | F | Belongs to the OMP decarboxylase family. Type 2 subfamily | |
GCKIAGNM_02679 | 4.9e-159 | pyrK | 1.18.1.2, 1.19.1.1, 1.4.1.13, 1.4.1.14 | C | Iron-sulfur cluster binding domain of dihydroorotate dehydrogenase B | |
GCKIAGNM_02680 | 2.2e-76 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
GCKIAGNM_02681 | 1.5e-11 | 2.7.13.3 | T | Histidine kinase | ||
GCKIAGNM_02682 | 5.1e-26 | 2.7.13.3 | T | Histidine kinase | ||
GCKIAGNM_02683 | 3.2e-49 | S | Bacterial toxin of type II toxin-antitoxin system, YafQ | |||
GCKIAGNM_02684 | 3.2e-78 | V | MacB-like periplasmic core domain | |||
GCKIAGNM_02685 | 5.1e-45 | V | MacB-like periplasmic core domain | |||
GCKIAGNM_02686 | 6.5e-27 | lolD | Q | ATPases associated with a variety of cellular activities | ||
GCKIAGNM_02687 | 3.9e-71 | lolD | Q | ATPases associated with a variety of cellular activities | ||
GCKIAGNM_02688 | 1.1e-33 | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | |||
GCKIAGNM_02689 | 1.2e-46 | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | |||
GCKIAGNM_02690 | 3e-95 | |||||
GCKIAGNM_02691 | 1.6e-52 | K | helix_turn_helix, Lux Regulon | |||
GCKIAGNM_02692 | 3e-38 | K | helix_turn_helix, Lux Regulon | |||
GCKIAGNM_02693 | 9.1e-41 | 2.7.13.3 | T | Histidine kinase | ||
GCKIAGNM_02694 | 1.6e-82 | 2.7.13.3 | T | Histidine kinase | ||
GCKIAGNM_02695 | 9.9e-59 | 2.7.13.3 | T | Histidine kinase | ||
GCKIAGNM_02696 | 4.5e-20 | 2.7.13.3 | T | Histidine kinase | ||
GCKIAGNM_02697 | 4e-09 | K | helix_turn_helix, Lux Regulon | |||
GCKIAGNM_02698 | 6.4e-43 | ilvC | 1.1.1.86 | H | Involved in the biosynthesis of branched-chain amino acids (BCAA). Catalyzes an alkyl-migration followed by a ketol- acid reduction of (S)-2-acetolactate (S2AL) to yield (R)-2,3- dihydroxy-isovalerate. In the isomerase reaction, S2AL is rearranged via a Mg-dependent methyl migration to produce 3- hydroxy-3-methyl-2-ketobutyrate (HMKB). In the reductase reaction, this 2-ketoacid undergoes a metal-dependent reduction by NADPH to yield (R)-2,3-dihydroxy-isovalerate | |
GCKIAGNM_02699 | 2e-82 | ilvC | 1.1.1.86 | H | Involved in the biosynthesis of branched-chain amino acids (BCAA). Catalyzes an alkyl-migration followed by a ketol- acid reduction of (S)-2-acetolactate (S2AL) to yield (R)-2,3- dihydroxy-isovalerate. In the isomerase reaction, S2AL is rearranged via a Mg-dependent methyl migration to produce 3- hydroxy-3-methyl-2-ketobutyrate (HMKB). In the reductase reaction, this 2-ketoacid undergoes a metal-dependent reduction by NADPH to yield (R)-2,3-dihydroxy-isovalerate | |
GCKIAGNM_02700 | 3.6e-69 | ilvC | 1.1.1.86 | H | Involved in the biosynthesis of branched-chain amino acids (BCAA). Catalyzes an alkyl-migration followed by a ketol- acid reduction of (S)-2-acetolactate (S2AL) to yield (R)-2,3- dihydroxy-isovalerate. In the isomerase reaction, S2AL is rearranged via a Mg-dependent methyl migration to produce 3- hydroxy-3-methyl-2-ketobutyrate (HMKB). In the reductase reaction, this 2-ketoacid undergoes a metal-dependent reduction by NADPH to yield (R)-2,3-dihydroxy-isovalerate | |
GCKIAGNM_02701 | 2.1e-41 | yhjE | EGP | Sugar (and other) transporter | ||
GCKIAGNM_02702 | 1.1e-87 | yhjE | EGP | Sugar (and other) transporter | ||
GCKIAGNM_02703 | 5.2e-68 | yhjE | EGP | Sugar (and other) transporter | ||
GCKIAGNM_02705 | 2.1e-163 | K | helix_turn _helix lactose operon repressor | |||
GCKIAGNM_02706 | 1.7e-39 | scrT | G | Transporter major facilitator family protein | ||
GCKIAGNM_02707 | 3.8e-175 | scrT | G | Transporter major facilitator family protein | ||
GCKIAGNM_02708 | 3.7e-21 | 2.7.13.3 | T | Histidine kinase | ||
GCKIAGNM_02709 | 6.1e-22 | S | Bacterial PH domain | |||
GCKIAGNM_02710 | 1.1e-118 | leuD | 4.2.1.33, 4.2.1.35 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
GCKIAGNM_02711 | 2.5e-74 | leuC | 4.2.1.33, 4.2.1.35 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
GCKIAGNM_02712 | 6.7e-51 | leuC | 4.2.1.33, 4.2.1.35 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
GCKIAGNM_02713 | 6.6e-33 | leuC | 4.2.1.33, 4.2.1.35 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
GCKIAGNM_02714 | 3e-56 | leuC | 4.2.1.33, 4.2.1.35 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
GCKIAGNM_02715 | 4.1e-139 | ltbR | K | Transcriptional regulator, IclR family, C-terminal domain protein | ||
GCKIAGNM_02716 | 3e-153 | S | Calcineurin-like phosphoesterase | |||
GCKIAGNM_02717 | 4.4e-37 | S | Calcineurin-like phosphoesterase | |||
GCKIAGNM_02718 | 1.6e-76 | |||||
GCKIAGNM_02720 | 5.2e-100 | K | DNA binding | |||
GCKIAGNM_02721 | 4.8e-102 | dam2 | 2.1.1.72 | L | D12 class N6 adenine-specific DNA methyltransferase | |
GCKIAGNM_02723 | 2.3e-57 | U | Type IV secretory system Conjugative DNA transfer | |||
GCKIAGNM_02724 | 1.8e-249 | U | Type IV secretory system Conjugative DNA transfer | |||
GCKIAGNM_02725 | 4.4e-44 | |||||
GCKIAGNM_02726 | 6.1e-51 | |||||
GCKIAGNM_02728 | 1.8e-68 | 2.7.7.49 | L | Transposase, Mutator family | ||
GCKIAGNM_02729 | 1.5e-55 | L | Transposase, Mutator family | |||
GCKIAGNM_02730 | 6.8e-67 | |||||
GCKIAGNM_02731 | 3.3e-75 | |||||
GCKIAGNM_02732 | 2.8e-15 | L | PFAM Integrase catalytic | |||
GCKIAGNM_02733 | 1.4e-10 | L | HTH-like domain | |||
GCKIAGNM_02735 | 3.9e-07 | |||||
GCKIAGNM_02736 | 3e-60 | L | Transposase, Mutator family | |||
GCKIAGNM_02737 | 1e-48 | |||||
GCKIAGNM_02738 | 5.4e-162 | yfiL | V | ATPases associated with a variety of cellular activities | ||
GCKIAGNM_02739 | 2e-70 | |||||
GCKIAGNM_02740 | 2.4e-23 | |||||
GCKIAGNM_02741 | 3.4e-24 | |||||
GCKIAGNM_02742 | 4.5e-147 | S | EamA-like transporter family | |||
GCKIAGNM_02743 | 1.4e-99 | |||||
GCKIAGNM_02744 | 7.7e-103 | |||||
GCKIAGNM_02745 | 4.1e-121 | V | ATPases associated with a variety of cellular activities | |||
GCKIAGNM_02746 | 2.2e-48 | P | Domain of unknown function (DUF4976) | |||
GCKIAGNM_02747 | 1.2e-102 | P | Domain of unknown function (DUF4976) | |||
GCKIAGNM_02748 | 4.7e-141 | gtr | U | Sugar (and other) transporter | ||
GCKIAGNM_02749 | 4.4e-50 | gtr | U | Sugar (and other) transporter | ||
GCKIAGNM_02750 | 3.5e-140 | yeaD | 4.2.1.9, 5.1.3.15 | G | Aldose 1-epimerase | |
GCKIAGNM_02751 | 2.2e-11 | yeaD | 4.2.1.9, 5.1.3.15 | G | Aldose 1-epimerase | |
GCKIAGNM_02752 | 3.1e-220 | GK | ROK family | |||
GCKIAGNM_02753 | 3.4e-152 | K | FCD | |||
GCKIAGNM_02754 | 2.2e-251 | P | Domain of unknown function (DUF4143) | |||
GCKIAGNM_02755 | 1.5e-54 | nanI | 3.2.1.18 | GH33 | G | BNR repeat-like domain |
GCKIAGNM_02756 | 1.4e-53 | nanI | 3.2.1.18 | GH33 | G | BNR repeat-like domain |
GCKIAGNM_02757 | 1.9e-181 | nanI | 3.2.1.18 | GH33 | G | BNR repeat-like domain |
GCKIAGNM_02758 | 4.1e-08 | |||||
GCKIAGNM_02760 | 1.1e-27 | oppD | EP | Oligopeptide/dipeptide transporter, C-terminal region | ||
GCKIAGNM_02761 | 6.5e-73 | oppD | EP | Oligopeptide/dipeptide transporter, C-terminal region | ||
GCKIAGNM_02762 | 4.6e-153 | oppB6 | EP | Binding-protein-dependent transport system inner membrane component | ||
GCKIAGNM_02763 | 1.6e-145 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | |||
GCKIAGNM_02764 | 6.1e-132 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | |||
GCKIAGNM_02765 | 9.8e-160 | 3.5.1.106 | I | carboxylic ester hydrolase activity | ||
GCKIAGNM_02766 | 7.7e-51 | nanE | 5.1.3.9 | G | Converts N-acetylmannosamine-6-phosphate (ManNAc-6-P) to N-acetylglucosamine-6-phosphate (GlcNAc-6-P) | |
GCKIAGNM_02767 | 4.1e-56 | deaD | 3.6.4.13 | JKL | helicase superfamily c-terminal domain | |
GCKIAGNM_02768 | 1.1e-08 | L | helicase activity | |||
GCKIAGNM_02769 | 2.2e-259 | nplT | G | Alpha amylase, catalytic domain | ||
GCKIAGNM_02770 | 3.1e-187 | pit | P | Phosphate transporter family | ||
GCKIAGNM_02771 | 1e-113 | MA20_27875 | P | Protein of unknown function DUF47 | ||
GCKIAGNM_02772 | 3.4e-84 | K | helix_turn_helix, Lux Regulon | |||
GCKIAGNM_02773 | 2.6e-24 | T | Histidine kinase | |||
GCKIAGNM_02774 | 1.3e-108 | EGP | Major facilitator Superfamily | |||
GCKIAGNM_02775 | 7.9e-108 | 3.1.3.27 | E | haloacid dehalogenase-like hydrolase | ||
GCKIAGNM_02776 | 2e-74 | 3.1.3.73 | G | Phosphoglycerate mutase family | ||
GCKIAGNM_02777 | 1.3e-69 | 3.1.3.73 | G | Phosphoglycerate mutase family | ||
GCKIAGNM_02778 | 5.3e-86 | rutG | F | Permease family | ||
GCKIAGNM_02779 | 1.8e-63 | rutG | F | Permease family | ||
GCKIAGNM_02780 | 1.1e-181 | deaD | 3.6.4.13 | JKL | helicase superfamily c-terminal domain | |
GCKIAGNM_02781 | 1.1e-53 | sprF | 4.6.1.1 | M | Cell surface antigen C-terminus | |
GCKIAGNM_02782 | 2.5e-66 | sprF | 4.6.1.1 | M | Cell surface antigen C-terminus | |
GCKIAGNM_02783 | 4.9e-286 | XK27_00515 | D | Cell surface antigen C-terminus | ||
GCKIAGNM_02784 | 8.3e-44 | XK27_00515 | D | Cell surface antigen C-terminus | ||
GCKIAGNM_02785 | 6.9e-41 | |||||
GCKIAGNM_02786 | 2.3e-89 | G | Transmembrane secretion effector | |||
GCKIAGNM_02787 | 6.4e-60 | K | Bacterial regulatory proteins, tetR family | |||
GCKIAGNM_02788 | 2.7e-16 | K | Bacterial regulatory proteins, tetR family | |||
GCKIAGNM_02789 | 2.2e-11 | |||||
GCKIAGNM_02790 | 9.8e-151 | cysB | 4.2.1.22 | EGP | Major facilitator Superfamily | |
GCKIAGNM_02791 | 1.8e-103 | cysB | 4.2.1.22 | EGP | Major facilitator Superfamily | |
GCKIAGNM_02792 | 4.7e-67 | cysB | 4.2.1.22 | EGP | Major facilitator Superfamily | |
GCKIAGNM_02793 | 1.2e-13 | EGP | Transmembrane secretion effector | |||
GCKIAGNM_02794 | 7e-50 | V | ABC transporter | |||
GCKIAGNM_02795 | 3.1e-37 | V | Efflux ABC transporter, permease protein | |||
GCKIAGNM_02796 | 1.1e-190 | V | Efflux ABC transporter, permease protein | |||
GCKIAGNM_02797 | 1.4e-88 | T | Histidine kinase | |||
GCKIAGNM_02798 | 3.5e-126 | T | Histidine kinase | |||
GCKIAGNM_02799 | 2.5e-93 | K | Bacterial regulatory proteins, luxR family | |||
GCKIAGNM_02800 | 4e-24 | L | Transposase and inactivated derivatives IS30 family | |||
GCKIAGNM_02801 | 2.8e-120 | tsaD | 2.3.1.234 | O | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaE and TsaB. TsaD likely plays a direct catalytic role in this reaction | |
GCKIAGNM_02803 | 6.2e-22 | K | helix_turn_helix, Lux Regulon | |||
GCKIAGNM_02804 | 1.8e-48 | K | helix_turn_helix, Lux Regulon | |||
GCKIAGNM_02805 | 7.9e-20 | K | helix_turn_helix, Lux Regulon | |||
GCKIAGNM_02806 | 3.3e-239 | T | Histidine kinase | |||
GCKIAGNM_02808 | 6.7e-60 | |||||
GCKIAGNM_02809 | 7.2e-24 | 3.2.1.10 | GH13 | G | Alpha amylase, catalytic domain protein | |
GCKIAGNM_02810 | 1e-73 | 3.2.1.10 | GH13 | G | Alpha amylase, catalytic domain protein | |
GCKIAGNM_02811 | 5.7e-73 | 3.2.1.10 | GH13 | G | Alpha amylase, catalytic domain protein | |
GCKIAGNM_02812 | 8.2e-16 | tdcB | 4.3.1.19 | E | Pyridoxal-phosphate dependent enzyme | |
GCKIAGNM_02813 | 7.5e-22 | tdcB | 4.3.1.19 | E | Pyridoxal-phosphate dependent enzyme | |
GCKIAGNM_02814 | 4.8e-51 | tdcB | 4.3.1.19 | E | Pyridoxal-phosphate dependent enzyme | |
GCKIAGNM_02815 | 1.6e-56 | tdcB | 4.3.1.19 | E | Pyridoxal-phosphate dependent enzyme | |
GCKIAGNM_02816 | 2.6e-12 | cobB2 | K | Sir2 family | ||
GCKIAGNM_02817 | 7.2e-118 | cobB2 | K | Sir2 family | ||
GCKIAGNM_02818 | 5.3e-126 | glnE | 2.7.7.42, 2.7.7.89 | H | Involved in the regulation of glutamine synthetase GlnA, a key enzyme in the process to assimilate ammonia. When cellular nitrogen levels are high, the C-terminal adenylyl transferase (AT) inactivates GlnA by covalent transfer of an adenylyl group from ATP to specific tyrosine residue of GlnA, thus reducing its activity. Conversely, when nitrogen levels are low, the N-terminal adenylyl removase (AR) activates GlnA by removing the adenylyl group by phosphorolysis, increasing its activity. The regulatory region of GlnE binds the signal transduction protein PII (GlnB) which indicates the nitrogen status of the cell | |
GCKIAGNM_02819 | 1.7e-187 | cbh | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
GCKIAGNM_02820 | 2.8e-162 | metF | 1.5.1.20 | E | Methylenetetrahydrofolate reductase | |
GCKIAGNM_02821 | 8.7e-148 | metE | 2.1.1.14 | E | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | |
GCKIAGNM_02822 | 3.1e-195 | trsE | U | type IV secretory pathway VirB4 | ||
GCKIAGNM_02823 | 2.6e-136 | trsE | U | type IV secretory pathway VirB4 | ||
GCKIAGNM_02824 | 8.8e-62 | S | PrgI family protein | |||
GCKIAGNM_02825 | 5.3e-145 | |||||
GCKIAGNM_02826 | 8.9e-26 | |||||
GCKIAGNM_02827 | 1.3e-159 | ksgA | 2.1.1.182 | J | Methyltransferase domain | |
GCKIAGNM_02828 | 9.1e-60 | yccF | S | Inner membrane component domain | ||
GCKIAGNM_02829 | 3.1e-234 | XK27_00240 | K | Fic/DOC family | ||
GCKIAGNM_02830 | 3.6e-112 | K | COG2197 Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | |||
GCKIAGNM_02831 | 1e-82 | 2.7.13.3 | T | Histidine kinase | ||
GCKIAGNM_02832 | 3.6e-82 | 2.7.13.3 | T | Histidine kinase | ||
GCKIAGNM_02833 | 3.3e-162 | EGP | Major Facilitator Superfamily | |||
GCKIAGNM_02834 | 1.3e-91 | G | Transmembrane secretion effector | |||
GCKIAGNM_02835 | 1.1e-32 | K | addiction module antidote protein HigA | |||
GCKIAGNM_02836 | 3.3e-244 | S | HipA-like C-terminal domain | |||
GCKIAGNM_02837 | 1.1e-37 | L | RelB antitoxin | |||
GCKIAGNM_02838 | 3.8e-38 | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
GCKIAGNM_02839 | 5.2e-47 | S | Cupin 2, conserved barrel domain protein | |||
GCKIAGNM_02840 | 1.8e-105 | V | ATPases associated with a variety of cellular activities | |||
GCKIAGNM_02841 | 1.6e-28 | S | Protein of unknown function (DUF1778) | |||
GCKIAGNM_02842 | 1.5e-56 | K | Acetyltransferase (GNAT) family | |||
GCKIAGNM_02843 | 5.7e-241 | maf | 1.1.1.25, 2.1.1.190, 3.6.1.55, 3.6.1.67 | DF | Maf-like protein | |
GCKIAGNM_02844 | 1.9e-24 | maf | 1.1.1.25, 2.1.1.190, 3.6.1.55, 3.6.1.67 | DF | Maf-like protein | |
GCKIAGNM_02845 | 1.3e-31 | thrB | 2.7.1.39 | E | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
GCKIAGNM_02846 | 6.7e-233 | mutT | 3.6.1.13, 3.6.1.55 | LT | Phosphoglycerate mutase family | |
GCKIAGNM_02847 | 5.6e-150 | ppk | 2.7.4.1 | P | Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) | |
GCKIAGNM_02848 | 6.8e-153 | ppk | 2.7.4.1 | P | Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) | |
GCKIAGNM_02849 | 3.1e-29 | |||||
GCKIAGNM_02850 | 5e-52 | |||||
GCKIAGNM_02851 | 1.2e-13 | |||||
GCKIAGNM_02852 | 3.3e-30 | |||||
GCKIAGNM_02853 | 5.4e-97 | |||||
GCKIAGNM_02854 | 2.8e-17 | 3.4.22.70 | S | Sortase family | ||
GCKIAGNM_02855 | 8.2e-37 | L | PFAM Integrase catalytic | |||
GCKIAGNM_02856 | 6.4e-107 | S | Bacterial protein of unknown function (DUF881) | |||
GCKIAGNM_02857 | 4.3e-55 | crgA | D | Involved in cell division | ||
GCKIAGNM_02858 | 3.9e-120 | gluP | 3.4.21.105 | S | Rhomboid family | |
GCKIAGNM_02859 | 2.6e-35 | |||||
GCKIAGNM_02860 | 3.3e-91 | |||||
GCKIAGNM_02861 | 8.6e-70 | |||||
GCKIAGNM_02862 | 7.9e-108 | S | Protein of unknown function (DUF3801) | |||
GCKIAGNM_02863 | 2.6e-35 | tnp3512a | L | Transposase | ||
GCKIAGNM_02864 | 8.8e-16 | |||||
GCKIAGNM_02865 | 4.7e-25 | |||||
GCKIAGNM_02866 | 4.5e-81 | M | L,D-transpeptidase catalytic domain | |||
GCKIAGNM_02867 | 1.5e-19 | ybbM | V | Uncharacterised protein family (UPF0014) | ||
GCKIAGNM_02868 | 6e-98 | ybbM | V | Uncharacterised protein family (UPF0014) | ||
GCKIAGNM_02869 | 6.3e-28 | ybbL | V | ATPases associated with a variety of cellular activities | ||
GCKIAGNM_02870 | 1.7e-07 | nagE | 2.7.1.193, 2.7.1.199 | G | phosphotransferase system, EIIB | |
GCKIAGNM_02871 | 1.1e-27 | nagE | 2.7.1.193, 2.7.1.199 | G | phosphotransferase system, EIIB | |
GCKIAGNM_02872 | 1e-111 | hom | 1.1.1.3 | E | Homoserine dehydrogenase | |
GCKIAGNM_02873 | 2.4e-113 | hom | 1.1.1.3 | E | Homoserine dehydrogenase | |
GCKIAGNM_02874 | 3.1e-95 | thrB | 2.7.1.39 | E | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
GCKIAGNM_02875 | 2.1e-44 | S | Domain of unknown function (DUF4160) | |||
GCKIAGNM_02876 | 5.5e-42 | K | Protein of unknown function (DUF2442) | |||
GCKIAGNM_02877 | 1.4e-101 | ltrBE1 | U | Relaxase/Mobilisation nuclease domain | ||
GCKIAGNM_02878 | 2e-39 | ltrBE1 | U | Relaxase/Mobilisation nuclease domain | ||
GCKIAGNM_02879 | 6e-144 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
GCKIAGNM_02880 | 4.6e-20 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
GCKIAGNM_02881 | 3.1e-116 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
GCKIAGNM_02882 | 1.6e-146 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
GCKIAGNM_02883 | 1.7e-148 | oppF | E | ATPases associated with a variety of cellular activities | ||
GCKIAGNM_02884 | 4.6e-23 | nanL | 4.1.2.28, 4.3.3.7 | EM | Dihydrodipicolinate synthetase family | |
GCKIAGNM_02885 | 1.2e-75 | nanL | 4.1.2.28, 4.3.3.7 | EM | Dihydrodipicolinate synthetase family | |
GCKIAGNM_02886 | 4.8e-11 | pacL | 3.6.3.8, 3.6.3.9 | P | Cation transporter/ATPase, N-terminus | |
GCKIAGNM_02887 | 5e-187 | V | ATPases associated with a variety of cellular activities | |||
GCKIAGNM_02888 | 4.1e-22 | V | ABC-2 family transporter protein | |||
GCKIAGNM_02889 | 2.5e-59 | V | ABC-2 family transporter protein | |||
GCKIAGNM_02891 | 6.2e-19 | S | AAA ATPase domain | |||
GCKIAGNM_02892 | 5.6e-10 | S | AAA ATPase domain | |||
GCKIAGNM_02893 | 4.1e-17 | L | PFAM Integrase catalytic | |||
GCKIAGNM_02894 | 2.9e-35 | 2.7.1.208 | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | ||
GCKIAGNM_02895 | 2.1e-227 | lysA | 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
GCKIAGNM_02896 | 5.4e-33 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
GCKIAGNM_02897 | 1e-128 | |||||
GCKIAGNM_02898 | 1.4e-14 | |||||
GCKIAGNM_02899 | 1.4e-14 | |||||
GCKIAGNM_02900 | 4.1e-100 | S | Helix-turn-helix domain | |||
GCKIAGNM_02901 | 1e-61 | galK | 2.7.1.6, 2.7.7.12 | G | Belongs to the GHMP kinase family. GalK subfamily | |
GCKIAGNM_02902 | 4.3e-115 | galK | 2.7.1.6, 2.7.7.12 | G | Belongs to the GHMP kinase family. GalK subfamily | |
GCKIAGNM_02903 | 6.1e-154 | galT | 2.7.7.12 | C | Galactose-1-phosphate uridyl transferase, N-terminal domain | |
GCKIAGNM_02904 | 1e-80 | EGP | Major Facilitator Superfamily | |||
GCKIAGNM_02905 | 1e-60 | EGP | Major Facilitator Superfamily | |||
GCKIAGNM_02906 | 8.4e-42 | EGP | Major Facilitator Superfamily | |||
GCKIAGNM_02907 | 1e-79 | EGP | Major facilitator Superfamily | |||
GCKIAGNM_02908 | 2.2e-07 | EGP | Major facilitator Superfamily | |||
GCKIAGNM_02909 | 1.6e-09 | yccF | S | Inner membrane component domain | ||
GCKIAGNM_02910 | 1.7e-63 | MA20_22310 | 4.4.1.5 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |
GCKIAGNM_02912 | 5.6e-17 | S | Sulfite exporter TauE/SafE | |||
GCKIAGNM_02913 | 3.1e-82 | |||||
GCKIAGNM_02917 | 0.0 | fas | 2.3.1.179 | I | Beta-ketoacyl synthase, C-terminal domain | |
GCKIAGNM_02918 | 7.8e-149 | malC | G | Binding-protein-dependent transport system inner membrane component | ||
GCKIAGNM_02919 | 8.5e-57 | G | ABC transporter permease | |||
GCKIAGNM_02920 | 5.7e-21 | G | ABC transporter permease | |||
GCKIAGNM_02921 | 2.4e-49 | H | Beta-ketoacyl synthase, C-terminal domain | |||
GCKIAGNM_02922 | 1.9e-115 | K | WHG domain | |||
GCKIAGNM_02923 | 1.6e-140 | isp2 | 3.2.1.96 | M | CHAP domain | |
GCKIAGNM_02924 | 1.8e-69 | V | ABC-2 family transporter protein | |||
GCKIAGNM_02925 | 1.6e-36 | V | ABC-2 family transporter protein | |||
GCKIAGNM_02926 | 5.4e-31 | V | ABC-2 family transporter protein | |||
GCKIAGNM_02927 | 3.6e-52 | V | ABC-2 family transporter protein | |||
GCKIAGNM_02928 | 1.5e-186 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
GCKIAGNM_02929 | 1.2e-60 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
GCKIAGNM_02930 | 6.1e-99 | nagA | 3.5.1.25 | G | Amidohydrolase family | |
GCKIAGNM_02932 | 2.9e-164 | aslB | C | Iron-sulfur cluster-binding domain | ||
GCKIAGNM_02933 | 3e-90 | aslB | C | Iron-sulfur cluster-binding domain | ||
GCKIAGNM_02934 | 6e-32 | nagE | 2.7.1.193, 2.7.1.199 | G | phosphotransferase system, EIIB | |
GCKIAGNM_02935 | 8.6e-43 | nagE | 2.7.1.193, 2.7.1.199 | G | phosphotransferase system, EIIB | |
GCKIAGNM_02936 | 3.4e-48 | nagE | 2.7.1.193, 2.7.1.199 | G | phosphotransferase system, EIIB | |
GCKIAGNM_02937 | 1.1e-11 | EGP | Major facilitator Superfamily | |||
GCKIAGNM_02938 | 2.1e-67 | pccB | I | Carboxyl transferase domain | ||
GCKIAGNM_02939 | 5.7e-135 | pccB | I | Carboxyl transferase domain | ||
GCKIAGNM_02940 | 3.8e-105 | rimI | 2.3.1.128, 2.3.1.234 | K | FR47-like protein | |
GCKIAGNM_02941 | 3.7e-74 | yeaZ | 2.3.1.234 | O | Glycoprotease family | |
GCKIAGNM_02942 | 2.3e-26 | 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 |
GCKIAGNM_02943 | 3.7e-52 | 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 |
GCKIAGNM_02944 | 7.7e-69 | L | PFAM Integrase catalytic | |||
GCKIAGNM_02945 | 1.7e-17 | L | PFAM Integrase catalytic | |||
GCKIAGNM_02946 | 4.3e-42 | L | PFAM Integrase catalytic | |||
GCKIAGNM_02947 | 6.7e-47 | 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 |
GCKIAGNM_02948 | 4.3e-73 | fas | 2.3.1.179 | I | Beta-ketoacyl synthase, C-terminal domain | |
GCKIAGNM_02949 | 5.5e-50 | fas | 2.3.1.179 | I | Beta-ketoacyl synthase, C-terminal domain | |
GCKIAGNM_02950 | 6.7e-47 | 3.2.1.10, 3.2.1.20, 3.2.1.93 | GH13,GH31 | G | Alpha-amylase domain | |
GCKIAGNM_02951 | 1.1e-110 | ilvC | 1.1.1.86 | H | Involved in the biosynthesis of branched-chain amino acids (BCAA). Catalyzes an alkyl-migration followed by a ketol- acid reduction of (S)-2-acetolactate (S2AL) to yield (R)-2,3- dihydroxy-isovalerate. In the isomerase reaction, S2AL is rearranged via a Mg-dependent methyl migration to produce 3- hydroxy-3-methyl-2-ketobutyrate (HMKB). In the reductase reaction, this 2-ketoacid undergoes a metal-dependent reduction by NADPH to yield (R)-2,3-dihydroxy-isovalerate | |
GCKIAGNM_02952 | 7.7e-17 | parA | D | AAA domain | ||
GCKIAGNM_02953 | 1.6e-36 | parA | D | AAA domain | ||
GCKIAGNM_02954 | 3e-59 | S | Transcription factor WhiB | |||
GCKIAGNM_02955 | 3.6e-32 | L | Integrase core domain | |||
GCKIAGNM_02956 | 1.2e-08 | L | IstB-like ATP binding protein | |||
GCKIAGNM_02957 | 1.5e-28 | L | IstB-like ATP binding protein | |||
GCKIAGNM_02958 | 2.5e-43 | L | Helix-turn-helix domain | |||
GCKIAGNM_02959 | 2.1e-41 | S | Sulfite exporter TauE/SafE | |||
GCKIAGNM_02961 | 1e-96 | fas | 2.3.1.179 | I | Beta-ketoacyl synthase, C-terminal domain | |
GCKIAGNM_02962 | 5.2e-31 | tnp3503b | 2.7.7.7 | L | Transposase and inactivated derivatives | |
GCKIAGNM_02963 | 9.1e-118 | 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 | |
GCKIAGNM_02964 | 2.6e-52 | L | PFAM Integrase catalytic | |||
GCKIAGNM_02965 | 2e-52 | rpoE4 | K | Sigma-70 region 2 | ||
GCKIAGNM_02966 | 7.8e-31 | 3.2.1.10 | GH13 | G | Alpha amylase, catalytic domain protein | |
GCKIAGNM_02967 | 1.3e-60 | L | IstB-like ATP binding protein | |||
GCKIAGNM_02968 | 5.5e-92 | L | Transposase and inactivated derivatives IS30 family | |||
GCKIAGNM_02969 | 5.5e-27 | |||||
GCKIAGNM_02970 | 1.4e-41 | T | Histidine kinase |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)