ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
KKNCFHKG_00002 | 2e-266 | dapE | 3.5.1.16, 3.5.1.18 | E | Peptidase dimerisation domain | |
KKNCFHKG_00003 | 1.9e-178 | yjlA | EG | Putative multidrug resistance efflux transporter | ||
KKNCFHKG_00004 | 8.2e-190 | acoA | C | COG1071 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, alpha subunit | ||
KKNCFHKG_00005 | 1.6e-188 | acoB | C | COG0022 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, beta subunit | ||
KKNCFHKG_00006 | 3.4e-214 | acoC | 2.3.1.12, 2.3.1.61 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
KKNCFHKG_00007 | 1.7e-257 | acoL | 1.8.1.4 | C | COG1249 Pyruvate 2-oxoglutarate dehydrogenase complex, dihydrolipoamide dehydrogenase (E3) component, and related enzymes | |
KKNCFHKG_00008 | 0.0 | acoR | KQ | COG3284 Transcriptional activator of acetoin glycerol metabolism | ||
KKNCFHKG_00009 | 9.7e-181 | kefA | M | Mechanosensitive ion channel | ||
KKNCFHKG_00010 | 1.9e-191 | S | COG0491 Zn-dependent hydrolases, including glyoxylases | |||
KKNCFHKG_00011 | 2.9e-09 | I | SCP-2 sterol transfer family | |||
KKNCFHKG_00012 | 5.7e-103 | S | Appr-1'-p processing enzyme | |||
KKNCFHKG_00013 | 7.5e-25 | sspH | S | small acid-soluble spore protein | ||
KKNCFHKG_00014 | 1.7e-131 | IQ | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
KKNCFHKG_00015 | 6.1e-185 | 6.2.1.3 | IQ | COG0318 Acyl-CoA synthetases (AMP-forming) AMP-acid ligases II | ||
KKNCFHKG_00016 | 1.9e-62 | rtp | K | Plays a role in DNA replication and termination (fork arrest mechanism). Two dimers of rtp bind to the two inverted repeat regions (IRI and IRII) present in the termination site. The binding of each dimer is centered on an 8 bp direct repeat | ||
KKNCFHKG_00017 | 3.3e-141 | S | Sucrose-6F-phosphate phosphohydrolase | |||
KKNCFHKG_00018 | 2.5e-104 | yozB | S | membrane | ||
KKNCFHKG_00019 | 9e-60 | |||||
KKNCFHKG_00020 | 1.9e-75 | mltG | S | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
KKNCFHKG_00021 | 8.5e-179 | ldh1 | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
KKNCFHKG_00022 | 3.2e-24 | kch | P | Ion channel | ||
KKNCFHKG_00023 | 1.1e-59 | arsR | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
KKNCFHKG_00024 | 1.1e-179 | arsB | 1.20.4.1 | P | Sodium Bile acid symporter family | |
KKNCFHKG_00025 | 1.1e-74 | arsC | 1.20.4.1 | T | Catalyzes the reduction of arsenate As(V) to arsenite As(III) | |
KKNCFHKG_00026 | 1e-75 | K | helix_turn_helix multiple antibiotic resistance protein | |||
KKNCFHKG_00027 | 1.9e-142 | S | Predicted permease | |||
KKNCFHKG_00029 | 6e-52 | ywnH | 2.3.1.183 | M | Acetyltransferase (GNAT) domain | |
KKNCFHKG_00030 | 1e-131 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
KKNCFHKG_00031 | 3.4e-214 | fsr | P | COG0477 Permeases of the major facilitator superfamily | ||
KKNCFHKG_00032 | 7.2e-74 | sleB | 3.5.1.28 | M | Cell wall | |
KKNCFHKG_00033 | 3e-147 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
KKNCFHKG_00034 | 1.6e-26 | 1.1.1.31, 1.1.1.60 | I | COG2084 3-hydroxyisobutyrate dehydrogenase and related beta-hydroxyacid dehydrogenases | ||
KKNCFHKG_00035 | 1.7e-281 | glgA | 2.4.1.21 | GT5 | G | Synthesizes alpha-1,4-glucan chains using ADP-glucose |
KKNCFHKG_00036 | 1.7e-183 | glgD | 2.4.1.21, 2.7.7.27 | GT5 | G | Glucose-1-phosphate adenylyltransferase, GlgD subunit |
KKNCFHKG_00037 | 1.3e-207 | glgC | 2.7.7.27 | G | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
KKNCFHKG_00038 | 0.0 | glgB | 2.4.1.18, 3.2.1.141, 3.2.1.20 | CBM48,GH13,GH31 | G | Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position |
KKNCFHKG_00039 | 6.1e-193 | G | Glycosyl hydrolases family 15 | |||
KKNCFHKG_00040 | 7.3e-21 | S | YpzG-like protein | |||
KKNCFHKG_00041 | 5e-82 | Q | protein disulfide oxidoreductase activity | |||
KKNCFHKG_00042 | 3.2e-89 | ywnH | 2.3.1.183 | M | COG1247 Sortase and related acyltransferases | |
KKNCFHKG_00043 | 3.7e-119 | nudL | L | COG0494 NTP pyrophosphohydrolases including oxidative damage repair enzymes | ||
KKNCFHKG_00044 | 3.9e-224 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
KKNCFHKG_00045 | 2.1e-76 | dps | P | Ferritin-like domain | ||
KKNCFHKG_00046 | 1.7e-81 | V | VanZ like family | |||
KKNCFHKG_00047 | 2.5e-167 | yhcI | S | ABC-2 family transporter protein | ||
KKNCFHKG_00048 | 1.5e-169 | ydbJ | V | ABC transporter, ATP-binding protein | ||
KKNCFHKG_00049 | 6.3e-57 | |||||
KKNCFHKG_00050 | 1.2e-166 | murB | 1.3.1.98 | M | cell wall formation | |
KKNCFHKG_00051 | 4e-79 | S | Protein of unknown function (DUF1189) | |||
KKNCFHKG_00052 | 6.9e-37 | S | Protein of unknown function (DUF1450) | |||
KKNCFHKG_00053 | 5.7e-269 | gnd | 1.1.1.343, 1.1.1.44 | G | Catalyzes the oxidative decarboxylation of 6- phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NADP to NADPH | |
KKNCFHKG_00054 | 1e-55 | I | MaoC like domain | |||
KKNCFHKG_00056 | 1.7e-198 | selU | S | tRNA 2-selenouridine synthase | ||
KKNCFHKG_00057 | 1.1e-192 | selD | 2.7.9.3 | E | Synthesizes selenophosphate from selenide and ATP | |
KKNCFHKG_00058 | 3.9e-133 | T | Calcineurin-like phosphoesterase superfamily domain | |||
KKNCFHKG_00060 | 3.1e-187 | yraQ | S | Predicted permease | ||
KKNCFHKG_00061 | 2.4e-226 | proA | 1.2.1.41, 1.2.1.81 | 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 | |
KKNCFHKG_00062 | 1.4e-195 | proB | 2.7.2.11 | E | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
KKNCFHKG_00063 | 6.4e-73 | yjlC | S | Protein of unknown function (DUF1641) | ||
KKNCFHKG_00064 | 7.4e-222 | yjlD | 1.6.99.3 | C | NADH dehydrogenase | |
KKNCFHKG_00065 | 3.7e-229 | nrnB | S | phosphohydrolase (DHH superfamily) | ||
KKNCFHKG_00066 | 4.5e-126 | rpiA | 2.7.1.12, 2.7.1.15, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
KKNCFHKG_00067 | 9.7e-129 | yvpB | NU | protein conserved in bacteria | ||
KKNCFHKG_00068 | 9.2e-50 | tnrA | K | transcriptional | ||
KKNCFHKG_00069 | 4.2e-109 | def | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions | |
KKNCFHKG_00070 | 1.9e-23 | S | Virus attachment protein p12 family | |||
KKNCFHKG_00071 | 0.0 | feoB | P | transporter of a GTP-driven Fe(2 ) uptake system | ||
KKNCFHKG_00072 | 4.9e-37 | feoA | P | COG1918 Fe2 transport system protein A | ||
KKNCFHKG_00073 | 2e-219 | dapL | 2.6.1.83 | E | Aminotransferase | |
KKNCFHKG_00074 | 1.2e-263 | argH | 4.3.2.1 | E | argininosuccinate lyase | |
KKNCFHKG_00075 | 6.2e-232 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
KKNCFHKG_00076 | 3.1e-178 | 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 | |
KKNCFHKG_00077 | 0.0 | carB | 6.3.5.5 | EF | Carbamoyl-phosphate synthetase ammonia chain | |
KKNCFHKG_00078 | 1.5e-205 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
KKNCFHKG_00079 | 4e-223 | argD | 2.6.1.11, 2.6.1.17 | E | acetylornithine aminotransferase | |
KKNCFHKG_00080 | 1.1e-139 | argB | 2.7.2.8 | E | Belongs to the acetylglutamate kinase family. ArgB subfamily | |
KKNCFHKG_00081 | 4.4e-233 | 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 | |
KKNCFHKG_00082 | 4.6e-199 | 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 | |
KKNCFHKG_00084 | 5.5e-80 | |||||
KKNCFHKG_00085 | 1.1e-36 | P | catalase activity | |||
KKNCFHKG_00086 | 1.6e-79 | |||||
KKNCFHKG_00087 | 2.3e-30 | cspD | K | Cold shock | ||
KKNCFHKG_00089 | 2.3e-170 | 3.4.17.13 | V | proteins, homologs of microcin C7 resistance protein MccF | ||
KKNCFHKG_00090 | 3.9e-276 | dacC | 3.4.16.4 | M | D-alanyl-D-alanine carboxypeptidase | |
KKNCFHKG_00091 | 1.7e-105 | plsC | 2.3.1.51 | I | Belongs to the 1-acyl-sn-glycerol-3-phosphate acyltransferase family | |
KKNCFHKG_00092 | 1.3e-76 | yneK | S | Protein of unknown function (DUF2621) | ||
KKNCFHKG_00093 | 3e-76 | yneJ | O | COG4846 Membrane protein involved in cytochrome C biogenesis | ||
KKNCFHKG_00094 | 1.6e-58 | cheB | 3.1.1.61, 3.5.1.44 | T | cheY-homologous receiver domain | |
KKNCFHKG_00095 | 1.9e-127 | ccdA | O | cytochrome c biogenesis protein | ||
KKNCFHKG_00096 | 6.8e-28 | yneF | S | UPF0154 protein | ||
KKNCFHKG_00097 | 3.1e-72 | yneE | S | Sporulation inhibitor of replication protein sirA | ||
KKNCFHKG_00098 | 0.0 | tkt | 2.2.1.1 | G | Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate | |
KKNCFHKG_00099 | 3.4e-33 | ynzC | S | UPF0291 protein | ||
KKNCFHKG_00100 | 5.2e-116 | yneB | L | resolvase | ||
KKNCFHKG_00101 | 6.1e-52 | yneA | D | Inhibits cell division during the SOS response. Affects a later stage of the cell division protein assembly, after the assembly of the Z ring, by probably suppressing recruitment of FtsL and or DivIC to the division machinery | ||
KKNCFHKG_00102 | 1.2e-109 | 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 | |
KKNCFHKG_00103 | 1.9e-261 | glnA | 6.3.1.2 | E | glutamine synthetase | |
KKNCFHKG_00104 | 5.2e-63 | glnR | K | transcriptional | ||
KKNCFHKG_00105 | 0.0 | S | Dynamin family | |||
KKNCFHKG_00106 | 5.5e-32 | |||||
KKNCFHKG_00107 | 3.2e-142 | f42a | O | prohibitin homologues | ||
KKNCFHKG_00108 | 2.6e-231 | pbuX | F | xanthine | ||
KKNCFHKG_00109 | 1.6e-100 | 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 | |
KKNCFHKG_00110 | 1.4e-297 | ypwA | 3.4.17.19 | E | Broad specificity carboxypetidase that releases amino acids sequentially from the C-terminus, including neutral, aromatic, polar and basic residues | |
KKNCFHKG_00111 | 6.5e-223 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
KKNCFHKG_00112 | 3.4e-46 | gpsB | D | Divisome component that associates with the complex late in its assembly, after the Z-ring is formed, and is dependent on DivIC and PBP2B for its recruitment to the divisome. Together with EzrA, is a key component of the system that regulates PBP1 localization during cell cycle progression. Its main role could be the removal of PBP1 from the cell pole after pole maturation is completed. Also contributes to the recruitment of PBP1 to the division complex. Not essential for septum formation | ||
KKNCFHKG_00113 | 1.2e-97 | ypsA | S | Belongs to the UPF0398 family | ||
KKNCFHKG_00114 | 4.1e-45 | cotD | S | Inner spore coat protein D | ||
KKNCFHKG_00115 | 8.4e-251 | yprB | L | RNase_H superfamily | ||
KKNCFHKG_00116 | 0.0 | yprA | L | COG1205 Distinct helicase family with a unique C-terminal domain including a metal-binding cysteine cluster | ||
KKNCFHKG_00117 | 1e-75 | hspX | O | Belongs to the small heat shock protein (HSP20) family | ||
KKNCFHKG_00119 | 4.1e-65 | yppG | S | YppG-like protein | ||
KKNCFHKG_00120 | 3.6e-58 | yppE | S | Bacterial domain of unknown function (DUF1798) | ||
KKNCFHKG_00123 | 1.1e-112 | recU | L | Endonuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves mobile four-strand junctions by introducing symmetrical nicks in paired strands. Promotes annealing of linear ssDNA with homologous dsDNA. Required for DNA repair, homologous recombination and chromosome segregation | ||
KKNCFHKG_00124 | 0.0 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
KKNCFHKG_00125 | 5.4e-121 | 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 | |
KKNCFHKG_00126 | 2.8e-128 | dnaD | L | DNA replication protein DnaD | ||
KKNCFHKG_00127 | 3.4e-252 | asnS | 6.1.1.22 | J | asparaginyl-tRNA | |
KKNCFHKG_00128 | 9.5e-217 | aspB | 2.6.1.1, 2.6.1.14 | E | Aminotransferase | |
KKNCFHKG_00129 | 3.3e-77 | ypmB | S | protein conserved in bacteria | ||
KKNCFHKG_00130 | 0.0 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
KKNCFHKG_00131 | 1.8e-63 | panD | 4.1.1.11 | H | Catalyzes the pyruvoyl-dependent decarboxylation of aspartate to produce beta-alanine | |
KKNCFHKG_00132 | 2.3e-159 | panC | 2.7.4.25, 6.3.2.1 | H | Catalyzes the condensation of pantoate with beta-alanine in an ATP-dependent reaction via a pantoyl-adenylate intermediate | |
KKNCFHKG_00133 | 7.1e-150 | panB | 2.1.2.11 | H | Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is transferred onto alpha-ketoisovalerate to form ketopantoate | |
KKNCFHKG_00134 | 3e-176 | birA | 6.3.4.15 | K | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
KKNCFHKG_00135 | 3.6e-224 | cca | 2.7.7.19, 2.7.7.72 | J | Catalyzes the addition and repair of the essential 3'- terminal CCA sequence in tRNAs without using a nucleic acid template. Adds these three nucleotides in the order of C, C, and A to the tRNA nucleotide-73, using CTP and ATP as substrates and producing inorganic pyrophosphate | |
KKNCFHKG_00136 | 2e-214 | bshA | GT4 | M | N-acetyl-alpha-D-glucosaminyl L-malate synthase | |
KKNCFHKG_00137 | 6.2e-131 | bshB1 | S | proteins, LmbE homologs | ||
KKNCFHKG_00138 | 7.4e-149 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
KKNCFHKG_00139 | 1.7e-57 | ypjD | 2.5.1.19 | S | Nucleotide pyrophosphohydrolase | |
KKNCFHKG_00140 | 2.4e-161 | ypjC | S | Uncharacterized protein conserved in bacteria (DUF2179) | ||
KKNCFHKG_00141 | 6.8e-81 | queT | S | QueT transporter | ||
KKNCFHKG_00142 | 3.4e-102 | yugP | S | Zn-dependent protease | ||
KKNCFHKG_00143 | 6e-143 | ypjB | S | sporulation protein | ||
KKNCFHKG_00144 | 2.5e-109 | ypjA | S | membrane | ||
KKNCFHKG_00145 | 1.1e-146 | qcrC | C | Menaquinol-cytochrome c reductase cytochrome b c subunit | ||
KKNCFHKG_00146 | 1.2e-126 | petB | C | COG1290 Cytochrome b subunit of the bc complex | ||
KKNCFHKG_00147 | 1.9e-97 | qcrA | C | Menaquinol-cytochrome c reductase | ||
KKNCFHKG_00148 | 1.9e-80 | ypiF | S | Protein of unknown function (DUF2487) | ||
KKNCFHKG_00149 | 5.9e-97 | ypiB | S | Belongs to the UPF0302 family | ||
KKNCFHKG_00150 | 1.2e-238 | S | COG0457 FOG TPR repeat | |||
KKNCFHKG_00151 | 2.5e-231 | aroA | 1.3.1.12, 1.3.1.43, 2.5.1.19 | E | Catalyzes the transfer of the enolpyruvyl moiety of phosphoenolpyruvate (PEP) to the 5-hydroxyl of shikimate-3- phosphate (S3P) to produce enolpyruvyl shikimate-3-phosphate and inorganic phosphate | |
KKNCFHKG_00152 | 1.2e-202 | tyrA | 1.3.1.12, 1.3.1.43 | E | prephenate dehydrogenase | |
KKNCFHKG_00153 | 7.9e-210 | hisC | 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
KKNCFHKG_00154 | 3.8e-60 | aroH | 2.7.4.25, 5.4.99.5 | E | Catalyzes the Claisen rearrangement of chorismate to prephenate. Probably involved in the aromatic amino acid biosynthesis | |
KKNCFHKG_00155 | 4.4e-205 | aroB | 2.7.1.71, 4.2.3.4 | E | Catalyzes the conversion of 3-deoxy-D-arabino- heptulosonate 7-phosphate (DAHP) to dehydroquinate (DHQ) | |
KKNCFHKG_00156 | 1.1e-220 | 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 | |
KKNCFHKG_00157 | 2.4e-144 | cheR | 2.1.1.80 | NT | COG1352 Methylase of chemotaxis methyl-accepting proteins | |
KKNCFHKG_00158 | 7.2e-77 | ndk | 2.7.4.6 | F | Major role in the synthesis of nucleoside triphosphates other than ATP. The ATP gamma phosphate is transferred to the NDP beta phosphate via a ping-pong mechanism, using a phosphorylated active-site intermediate | |
KKNCFHKG_00159 | 4.1e-170 | hepT | 2.5.1.30, 2.5.1.83, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
KKNCFHKG_00160 | 6.4e-128 | menG | 2.1.1.163, 2.1.1.201 | H | Methyltransferase required for the conversion of demethylmenaquinol (DMKH2) to menaquinol (MKH2) | |
KKNCFHKG_00161 | 3.3e-144 | hepS | 2.5.1.30 | H | Heptaprenyl diphosphate synthase (HEPPP synthase) subunit 1 | |
KKNCFHKG_00162 | 1.9e-33 | mtrB | K | Required for transcription attenuation control in the Trp operon. This trans-acting factor seems to recognize a 10 bases nucleotide sequence in the Trp leader transcript causing transcription termination. Binds the leader RNA only in presence of L-tryptophan | ||
KKNCFHKG_00163 | 3.9e-41 | hup | L | Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions | ||
KKNCFHKG_00164 | 8.3e-279 | spoIVA | S | ATPase. Has a role at an early stage in the morphogenesis of the spore coat | ||
KKNCFHKG_00165 | 1.7e-136 | yphF | ||||
KKNCFHKG_00166 | 3.2e-08 | yphE | S | Protein of unknown function (DUF2768) | ||
KKNCFHKG_00167 | 4.6e-191 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
KKNCFHKG_00168 | 5.5e-250 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
KKNCFHKG_00169 | 2.4e-19 | yphA | ||||
KKNCFHKG_00170 | 7.3e-14 | S | YpzI-like protein | |||
KKNCFHKG_00171 | 9.4e-206 | rpsA | 1.17.7.4 | J | Ribosomal protein S1 | |
KKNCFHKG_00172 | 1.1e-119 | cmk | 1.17.7.4, 2.5.1.19, 2.7.1.26, 2.7.4.25, 2.7.7.2, 6.3.2.1 | F | Belongs to the cytidylate kinase family. Type 1 subfamily | |
KKNCFHKG_00173 | 2.3e-116 | ypfA | M | Flagellar protein YcgR | ||
KKNCFHKG_00174 | 2.9e-254 | hemX | 2.1.1.107, 4.2.1.75 | H | sporulation protein | |
KKNCFHKG_00175 | 2.6e-146 | sleB | 3.5.1.28 | M | Spore cortex-lytic enzyme | |
KKNCFHKG_00176 | 7e-124 | prsW | S | Involved in the degradation of specific anti-sigma factors | ||
KKNCFHKG_00177 | 5.1e-184 | ypdA | 1.18.1.2, 1.19.1.1, 1.8.1.9 | O | COG0492 Thioredoxin reductase | |
KKNCFHKG_00178 | 4.4e-244 | gudB | 1.4.1.2, 1.4.1.3 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
KKNCFHKG_00179 | 3.8e-96 | mecB | NOT | Negative regulator of genetic competence (MecA) | ||
KKNCFHKG_00180 | 1.8e-144 | ypbG | S | Calcineurin-like phosphoesterase superfamily domain | ||
KKNCFHKG_00181 | 2.6e-30 | cotJA | S | Spore coat associated protein JA (CotJA) | ||
KKNCFHKG_00182 | 1.2e-44 | cotJB | S | CotJB protein | ||
KKNCFHKG_00183 | 1.5e-103 | cotJC | P | Spore Coat | ||
KKNCFHKG_00184 | 1.2e-79 | ypbF | S | Protein of unknown function (DUF2663) | ||
KKNCFHKG_00186 | 1.2e-100 | ypbD | S | metal-dependent membrane protease | ||
KKNCFHKG_00187 | 5.4e-278 | recQ | 3.6.4.12 | L | DNA helicase | |
KKNCFHKG_00188 | 1.1e-203 | ypbB | 5.1.3.1 | S | protein conserved in bacteria | |
KKNCFHKG_00189 | 7.8e-41 | fer | C | Ferredoxin | ||
KKNCFHKG_00190 | 2.4e-96 | fmnP | 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 | ||
KKNCFHKG_00191 | 3.2e-127 | M | COG0739 Membrane proteins related to metalloendopeptidases | |||
KKNCFHKG_00192 | 0.0 | resE | 2.7.13.3 | T | Histidine kinase | |
KKNCFHKG_00193 | 3.3e-132 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
KKNCFHKG_00194 | 2.2e-229 | ccsA | O | 'COG0755 ABC-type transport system involved in cytochrome c biogenesis, permease component' | ||
KKNCFHKG_00195 | 0.0 | ccs1 | O | COG1333 ResB protein required for cytochrome c biosynthesis | ||
KKNCFHKG_00196 | 2.8e-99 | resA | CO | Thiol-disulfide oxidoreductase which is required in disulfide reduction during c-type cytochrome synthesis. May accept reducing equivalents from CcdA, leading to breakage of disulfide bonds in apocytochrome c | ||
KKNCFHKG_00197 | 1.1e-130 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
KKNCFHKG_00198 | 1.4e-87 | spmB | S | Spore maturation protein | ||
KKNCFHKG_00199 | 5.2e-96 | spmA | S | Spore maturation protein | ||
KKNCFHKG_00200 | 3.6e-202 | dacB | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
KKNCFHKG_00201 | 1.2e-106 | 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 | ||
KKNCFHKG_00202 | 1.7e-131 | 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 | ||
KKNCFHKG_00204 | 2.2e-60 | ribT | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
KKNCFHKG_00205 | 1.6e-250 | lysA | 4.1.1.19, 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
KKNCFHKG_00206 | 5e-268 | spoVAF | EG | Stage V sporulation protein AF | ||
KKNCFHKG_00207 | 8e-105 | spoVAEA | S | Stage V sporulation protein AE | ||
KKNCFHKG_00208 | 4.6e-65 | spoVAB | S | Stage V sporulation protein AB | ||
KKNCFHKG_00209 | 6.5e-108 | spoVAA | S | Stage V sporulation protein AA | ||
KKNCFHKG_00210 | 1.4e-133 | sigF | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
KKNCFHKG_00211 | 8.8e-75 | spoIIAB | 2.7.11.1 | F | Binds to sigma F and blocks its ability to form an RNA polymerase holoenzyme (E-sigma F). Phosphorylates SpoIIAA on a serine residue. This phosphorylation may enable SpoIIAA to act as an anti-anti-sigma factor that counteracts SpoIIAB and thus releases sigma F from inhibition | |
KKNCFHKG_00212 | 2.5e-56 | spoIIAA | T | Belongs to the anti-sigma-factor antagonist family | ||
KKNCFHKG_00213 | 7.6e-211 | dacF | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
KKNCFHKG_00215 | 3.6e-168 | xerD | L | recombinase XerD | ||
KKNCFHKG_00216 | 3.7e-34 | S | Protein of unknown function (DUF4227) | |||
KKNCFHKG_00217 | 3.5e-85 | fur | P | Belongs to the Fur family | ||
KKNCFHKG_00218 | 1.5e-104 | spoIIM | S | Required for complete septum migration and engulfment of the forespore compartment during sporulation. Required for stabilizing and recruiting of SpoIIP to the septal membrane | ||
KKNCFHKG_00219 | 1.1e-228 | yqxK | 3.6.4.12 | L | DNA helicase | |
KKNCFHKG_00220 | 1.6e-97 | nudF | 3.6.1.13 | L | Belongs to the Nudix hydrolase family | |
KKNCFHKG_00222 | 1.4e-167 | yqkF | C | oxidoreductases (related to aryl-alcohol dehydrogenases) | ||
KKNCFHKG_00223 | 1e-08 | S | Protein of unknown function (DUF3886) | |||
KKNCFHKG_00224 | 5.6e-110 | xpaC | S | 5-bromo-4-chloroindolyl phosphate hydrolysis protein | ||
KKNCFHKG_00225 | 1.3e-213 | yaaN | P | Belongs to the TelA family | ||
KKNCFHKG_00226 | 8.2e-176 | yqkD | S | COG1073 Hydrolases of the alpha beta superfamily | ||
KKNCFHKG_00227 | 2.4e-235 | yaaH_2 | M | Glycoside Hydrolase Family | ||
KKNCFHKG_00228 | 6.6e-54 | S | YolD-like protein | |||
KKNCFHKG_00229 | 1.3e-240 | polYB | 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 | |
KKNCFHKG_00230 | 1.1e-144 | yqjQ | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | ||
KKNCFHKG_00231 | 2.6e-144 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
KKNCFHKG_00232 | 5.9e-174 | rnz | 3.1.26.11 | S | Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA | |
KKNCFHKG_00233 | 6.4e-295 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
KKNCFHKG_00234 | 8.7e-226 | 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 | |
KKNCFHKG_00235 | 2.9e-76 | cheW | NT | COG0835 Chemotaxis signal transduction protein | ||
KKNCFHKG_00236 | 2.1e-202 | yqjE | 3.4.11.4 | E | COG2195 Di- and tripeptidases | |
KKNCFHKG_00237 | 3.6e-93 | yqjB | S | protein conserved in bacteria | ||
KKNCFHKG_00238 | 2.1e-76 | yqiW | S | Belongs to the UPF0403 family | ||
KKNCFHKG_00239 | 3.4e-166 | fruK | 2.7.1.11, 2.7.1.56 | G | Belongs to the carbohydrate kinase PfkB family | |
KKNCFHKG_00240 | 3e-216 | bfmBB | 2.3.1.168, 2.3.1.61 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
KKNCFHKG_00241 | 3.9e-184 | bfmBAB | 1.2.4.1, 1.2.4.4 | C | COG0022 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, beta subunit | |
KKNCFHKG_00242 | 5e-187 | bfmBAA | 1.2.4.4 | C | COG1071 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, alpha subunit | |
KKNCFHKG_00243 | 4.4e-261 | lpdA | 1.8.1.4 | C | COG1249 Pyruvate 2-oxoglutarate dehydrogenase complex, dihydrolipoamide dehydrogenase (E3) component, and related enzymes | |
KKNCFHKG_00244 | 1.5e-208 | ldh | 1.4.1.9 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
KKNCFHKG_00245 | 4.4e-18 | T | transcription factor binding | |||
KKNCFHKG_00246 | 9.2e-66 | bkdR | 2.7.13.3 | KT | Transcriptional regulator | |
KKNCFHKG_00247 | 9.8e-36 | yqzF | S | Protein of unknown function (DUF2627) | ||
KKNCFHKG_00248 | 1e-131 | yqiK | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
KKNCFHKG_00249 | 4.4e-138 | KT | May play the central regulatory role in sporulation. It may be an element of the effector pathway responsible for the activation of sporulation genes in response to nutritional stress. Spo0A may act in concert with spo0H (a sigma factor) to control the expression of some genes that are critical to the sporulation process | |||
KKNCFHKG_00250 | 3.5e-233 | rseP | 3.4.21.116 | M | Stage IV sporulation protein B | |
KKNCFHKG_00251 | 9.5e-295 | recN | L | May be involved in recombinational repair of damaged DNA | ||
KKNCFHKG_00252 | 5.4e-80 | argR | K | Regulates arginine biosynthesis genes | ||
KKNCFHKG_00253 | 8.5e-148 | rrmJ | 2.1.1.226, 2.1.1.227 | J | rRNA methylase | |
KKNCFHKG_00254 | 0.0 | dxs | 2.2.1.7 | H | Catalyzes the acyloin condensation reaction between C atoms 2 and 3 of pyruvate and glyceraldehyde 3-phosphate to yield 1-deoxy-D-xylulose-5-phosphate (DXP) | |
KKNCFHKG_00255 | 7.5e-155 | ispA | 2.5.1.1, 2.5.1.10, 2.5.1.29, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
KKNCFHKG_00256 | 3.1e-31 | 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 | |
KKNCFHKG_00257 | 3.5e-228 | 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 | |
KKNCFHKG_00258 | 1.6e-157 | 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 | |
KKNCFHKG_00259 | 1.6e-64 | 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 | ||
KKNCFHKG_00260 | 1.1e-68 | yqhY | S | protein conserved in bacteria | ||
KKNCFHKG_00261 | 6.2e-257 | accC | 6.3.4.14, 6.4.1.2 | I | An AccC homodimer forms the biotin carboxylase subunit of the acetyl CoA carboxylase, an enzyme that catalyzes the formation of malonyl-CoA, which in turn controls the rate of fatty acid metabolism | |
KKNCFHKG_00262 | 6.8e-81 | accB | 2.3.1.12, 4.1.1.3 | I | first, biotin carboxylase catalyzes the carboxylation of the carrier protein and then the transcarboxylase transfers the carboxyl group to form malonyl-CoA | |
KKNCFHKG_00263 | 5.5e-79 | spoIIIAH | S | SpoIIIAH-like protein | ||
KKNCFHKG_00264 | 6.6e-111 | spoIIIAG | S | stage III sporulation protein AG | ||
KKNCFHKG_00265 | 1.8e-105 | spoIIIAF | S | Stage III sporulation protein AF (Spore_III_AF) | ||
KKNCFHKG_00266 | 1.2e-174 | spoIIIAE | S | stage III sporulation protein AE | ||
KKNCFHKG_00267 | 2.3e-58 | spoIIIAD | S | Stage III sporulation protein AD | ||
KKNCFHKG_00268 | 1.4e-27 | spoIIIAC | S | stage III sporulation protein AC | ||
KKNCFHKG_00269 | 3.7e-85 | spoIIIAB | S | Stage III sporulation protein | ||
KKNCFHKG_00270 | 2.1e-171 | spoIIIAA | S | stage III sporulation protein AA | ||
KKNCFHKG_00271 | 6.4e-99 | efp | J | Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase | ||
KKNCFHKG_00272 | 9.2e-155 | yqhT | 3.4.11.9, 3.4.13.9 | E | COG0006 Xaa-Pro aminopeptidase | |
KKNCFHKG_00273 | 2.5e-77 | aroQ | 4.2.1.10 | E | Catalyzes a trans-dehydration via an enolate intermediate | |
KKNCFHKG_00274 | 8.7e-90 | yqhR | S | Conserved membrane protein YqhR | ||
KKNCFHKG_00275 | 8e-163 | yqhQ | S | Protein of unknown function (DUF1385) | ||
KKNCFHKG_00276 | 4.3e-11 | yqhP | ||||
KKNCFHKG_00277 | 4.1e-164 | yqhO | S | esterase of the alpha-beta hydrolase superfamily | ||
KKNCFHKG_00278 | 2.3e-71 | bktB | 2.3.1.9 | I | Belongs to the thiolase family | |
KKNCFHKG_00279 | 0.0 | nrdA | 1.17.4.1 | F | Catalyzes the reduction of ribonucleotides to deoxyribonucleotides. May function to provide a pool of deoxyribonucleotide precursors for DNA repair during oxygen limitation and or for immediate growth after restoration of oxygen | |
KKNCFHKG_00280 | 6.8e-161 | lipM | 6.3.1.20 | H | Catalyzes the transfer of endogenously produced octanoic acid from octanoyl-acyl-carrier-protein onto the lipoyl domain of GcvH, an intermediate carrier during protein lipoylation | |
KKNCFHKG_00281 | 2.2e-66 | yqhL | P | COG0607 Rhodanese-related sulfurtransferase | ||
KKNCFHKG_00282 | 1.8e-286 | gcvPB | 1.4.4.2 | E | The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor | |
KKNCFHKG_00283 | 5.3e-256 | gcvPA | 1.4.4.2 | E | The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor | |
KKNCFHKG_00284 | 1.2e-213 | gcvT | 1.4.4.2, 2.1.2.10 | E | The glycine cleavage system catalyzes the degradation of glycine | |
KKNCFHKG_00285 | 0.0 | yqhH | L | COG0553 Superfamily II DNA RNA helicases, SNF2 family | ||
KKNCFHKG_00286 | 1.6e-151 | yqhG | S | Bacterial protein YqhG of unknown function | ||
KKNCFHKG_00287 | 1.1e-09 | yqzE | S | YqzE-like protein | ||
KKNCFHKG_00288 | 5.4e-98 | aroK | 2.7.1.71, 4.2.3.4 | F | Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate | |
KKNCFHKG_00289 | 4e-57 | S | ComG operon protein 7 | |||
KKNCFHKG_00290 | 4.9e-79 | comGF | U | COG4940 Competence protein ComGF | ||
KKNCFHKG_00292 | 9.7e-74 | gspH | NU | COG2165 Type II secretory pathway, pseudopilin PulG | ||
KKNCFHKG_00293 | 9.9e-49 | comGC | U | Required for transformation and DNA binding | ||
KKNCFHKG_00294 | 8.3e-171 | comGB | NU | COG1459 Type II secretory pathway, component PulF | ||
KKNCFHKG_00295 | 1.1e-203 | comGA | NU | COG2804 Type II secretory pathway, ATPase PulE Tfp pilus assembly pathway, ATPase PilB | ||
KKNCFHKG_00296 | 1e-128 | K | Helix-turn-helix domain | |||
KKNCFHKG_00297 | 5.7e-36 | yqgY | S | Protein of unknown function (DUF2626) | ||
KKNCFHKG_00298 | 5e-124 | ycbL | 3.1.2.6 | S | COG0491 Zn-dependent hydrolases, including glyoxylases | |
KKNCFHKG_00299 | 2.9e-21 | yqgW | S | Protein of unknown function (DUF2759) | ||
KKNCFHKG_00300 | 1.6e-169 | glcK | 2.7.1.2 | G | Glucokinase | |
KKNCFHKG_00301 | 2.8e-29 | yqgQ | S | protein conserved in bacteria | ||
KKNCFHKG_00302 | 5.4e-201 | gluP | 3.4.21.105 | O | membrane protein (homolog of Drosophila rhomboid) | |
KKNCFHKG_00304 | 1.6e-20 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
KKNCFHKG_00305 | 9.8e-56 | yqzD | ||||
KKNCFHKG_00306 | 0.0 | mrdA | 3.4.16.4 | M | penicillin-binding protein | |
KKNCFHKG_00307 | 1.2e-219 | yqgE | EGP | Major facilitator superfamily | ||
KKNCFHKG_00308 | 3.7e-116 | sodA | 1.15.1.1 | P | radicals which are normally produced within the cells and which are toxic to biological systems | |
KKNCFHKG_00309 | 3.4e-55 | fimV | NU | Tfp pilus assembly protein FimV | ||
KKNCFHKG_00310 | 6.8e-201 | 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 | |
KKNCFHKG_00311 | 4.4e-114 | yqfW | S | Belongs to the 5'(3')-deoxyribonucleotidase family | ||
KKNCFHKG_00312 | 2.2e-75 | zur | P | Belongs to the Fur family | ||
KKNCFHKG_00313 | 4e-140 | znuB | P | COG1108 ABC-type Mn2 Zn2 transport systems, permease components | ||
KKNCFHKG_00314 | 3.2e-141 | zurA | P | 'COG1121 ABC-type Mn Zn transport systems, ATPase component' | ||
KKNCFHKG_00315 | 1e-19 | yqfT | S | Protein of unknown function (DUF2624) | ||
KKNCFHKG_00316 | 3.4e-125 | cwlO | CBM50 | M | protein conserved in bacteria | |
KKNCFHKG_00317 | 1.1e-169 | nfo | 3.1.21.2 | L | Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin | |
KKNCFHKG_00318 | 7.2e-242 | cshB | 3.6.4.13 | JKL | DEAD-box RNA helicase. May work in conjunction with the cold shock proteins to ensure proper initiation of transcription at low and optimal temperatures | |
KKNCFHKG_00320 | 1.5e-133 | modA | P | Molybdenum ABC transporter | ||
KKNCFHKG_00321 | 1e-120 | P | COG4149 ABC-type molybdate transport system, permease component | |||
KKNCFHKG_00322 | 1.5e-129 | modC | 3.6.3.29 | P | ATPases associated with a variety of cellular activities | |
KKNCFHKG_00323 | 7.8e-188 | moaA | 4.1.99.22, 4.6.1.17 | H | Catalyzes the cyclization of GTP to (8S)-3',8-cyclo-7,8- dihydroguanosine 5'-triphosphate | |
KKNCFHKG_00324 | 1.4e-84 | moaB | 2.7.7.75 | H | May be involved in the biosynthesis of molybdopterin | |
KKNCFHKG_00325 | 7.8e-123 | mobA | 2.7.7.77 | H | Transfers a GMP moiety from GTP to Mo-molybdopterin (Mo- MPT) cofactor (Moco or molybdenum cofactor) to form Mo- molybdopterin guanine dinucleotide (Mo-MGD) cofactor | |
KKNCFHKG_00326 | 3.7e-235 | moeA | 2.10.1.1 | H | molybdopterin | |
KKNCFHKG_00327 | 1.9e-86 | mobB | 2.10.1.1, 2.7.7.77 | H | molybdopterin-guanine dinucleotide biosynthesis protein | |
KKNCFHKG_00328 | 1.2e-79 | moaE | 2.8.1.12 | H | COG0314 Molybdopterin converting factor, large subunit | |
KKNCFHKG_00329 | 1.1e-33 | moaD | 2.8.1.12 | H | Involved in sulfur transfer in the conversion of molybdopterin precursor Z to molybdopterin | |
KKNCFHKG_00330 | 2.7e-85 | moaC | 4.6.1.17 | H | Catalyzes the conversion of (8S)-3',8-cyclo-7,8- dihydroguanosine 5'-triphosphate to cyclic pyranopterin monophosphate (cPMP) | |
KKNCFHKG_00331 | 4e-192 | moeB | 2.7.7.80 | H | COG0476 Dinucleotide-utilizing enzymes involved in molybdopterin and thiamine biosynthesis family 2 | |
KKNCFHKG_00332 | 5.7e-89 | yrhD | S | Protein of unknown function (DUF1641) | ||
KKNCFHKG_00333 | 0.0 | yjgC | 1.17.1.10, 1.17.1.9 | C | formate dehydrogenase, alpha subunit | |
KKNCFHKG_00334 | 3.3e-152 | fdhD | C | Required for formate dehydrogenase (FDH) activity. Acts as a sulfur carrier protein that transfers sulfur from IscS to the molybdenum cofactor prior to its insertion into FDH | ||
KKNCFHKG_00335 | 3.2e-239 | tyrS | 6.1.1.1 | J | Catalyzes the attachment of tyrosine to tRNA(Tyr) in a two-step reaction tyrosine is first activated by ATP to form Tyr- AMP and then transferred to the acceptor end of tRNA(Tyr) | |
KKNCFHKG_00336 | 1.7e-254 | prdR | KT | Transcriptional regulator | ||
KKNCFHKG_00337 | 3.7e-298 | rocA | 1.2.1.88, 1.5.5.2 | C | Belongs to the aldehyde dehydrogenase family. RocA subfamily | |
KKNCFHKG_00338 | 4e-184 | putA | E | Proline dehydrogenase | ||
KKNCFHKG_00339 | 2e-126 | |||||
KKNCFHKG_00340 | 1.3e-145 | |||||
KKNCFHKG_00341 | 1.9e-109 | 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 | ||
KKNCFHKG_00342 | 0.0 | ytrP | 2.7.7.65 | T | COG2199 FOG GGDEF domain | |
KKNCFHKG_00343 | 5.4e-86 | ytsP | 1.8.4.14 | T | GAF domain-containing protein | |
KKNCFHKG_00344 | 4.6e-117 | yttP | K | Transcriptional regulator | ||
KKNCFHKG_00345 | 3.4e-308 | ezrA | D | modulates the frequency and position of FtsZ ring formation. Inhibits FtsZ ring formation at polar sites. Interacts either with FtsZ or with one of its binding partners to promote depolymerization | ||
KKNCFHKG_00346 | 2.8e-213 | iscS2 | 2.8.1.7 | E | Cysteine desulfurase | |
KKNCFHKG_00347 | 1.9e-225 | thiI | 2.8.1.4 | H | Catalyzes the ATP-dependent transfer of a sulfur to tRNA to produce 4-thiouridine in position 8 of tRNAs, which functions as a near-UV photosensor. Also catalyzes the transfer of sulfur to the sulfur carrier protein ThiS, forming ThiS-thiocarboxylate. This is a step in the synthesis of thiazole, in the thiamine biosynthesis pathway. The sulfur is donated as persulfide by IscS | |
KKNCFHKG_00348 | 1.4e-27 | sspB | S | spore protein | ||
KKNCFHKG_00349 | 2.2e-311 | acsA | 6.2.1.1, 6.2.1.2 | I | COG0365 Acyl-coenzyme A synthetases AMP-(fatty) acid ligases | |
KKNCFHKG_00350 | 6.7e-179 | sppA | OU | signal peptide peptidase SppA | ||
KKNCFHKG_00351 | 4.2e-84 | yteJ | S | RDD family | ||
KKNCFHKG_00352 | 2e-118 | ytfI | S | Protein of unknown function (DUF2953) | ||
KKNCFHKG_00353 | 2e-66 | ytfJ | S | Sporulation protein YtfJ | ||
KKNCFHKG_00354 | 2.2e-90 | tpx | 1.11.1.15 | O | Thiol-specific peroxidase that catalyzes the reduction of hydrogen peroxide and organic hydroperoxides to water and alcohols, respectively. Plays a role in cell protection against oxidative stress by detoxifying peroxides | |
KKNCFHKG_00355 | 2.4e-176 | ytxK | 2.1.1.72 | L | DNA methylase | |
KKNCFHKG_00356 | 3e-218 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
KKNCFHKG_00357 | 2.7e-149 | S | EcsC protein family | |||
KKNCFHKG_00358 | 3.1e-78 | uspA | T | Belongs to the universal stress protein A family | ||
KKNCFHKG_00359 | 1.3e-196 | ald | 1.4.1.1 | E | Belongs to the AlaDH PNT family | |
KKNCFHKG_00360 | 1.6e-178 | pepQ | 3.4.13.9 | E | COG0006 Xaa-Pro aminopeptidase | |
KKNCFHKG_00361 | 1.1e-129 | ytkL | S | Belongs to the UPF0173 family | ||
KKNCFHKG_00362 | 2.3e-240 | ytoI | K | transcriptional regulator containing CBS domains | ||
KKNCFHKG_00363 | 2.7e-38 | ytpI | S | YtpI-like protein | ||
KKNCFHKG_00364 | 3.5e-175 | nrnA | 3.1.13.3, 3.1.3.7 | S | COG0618 Exopolyphosphatase-related proteins | |
KKNCFHKG_00365 | 6.7e-87 | ytrI | ||||
KKNCFHKG_00366 | 1.6e-41 | ytrH | S | Sporulation protein YtrH | ||
KKNCFHKG_00367 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase | |
KKNCFHKG_00368 | 6.8e-226 | ytsJ | 1.1.1.38 | C | Malate dehydrogenase | |
KKNCFHKG_00369 | 2.4e-164 | accD | 2.1.3.15, 6.4.1.2 | I | Component of the acetyl coenzyme A carboxylase (ACC) complex. Biotin carboxylase (BC) catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the transcarboxylase to acetyl-CoA to form malonyl- CoA | |
KKNCFHKG_00370 | 1e-176 | accA | 2.1.3.15, 6.4.1.2 | I | Component of the acetyl coenzyme A carboxylase (ACC) complex. First, biotin carboxylase catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the carboxyltransferase to acetyl-CoA to form malonyl-CoA | |
KKNCFHKG_00371 | 2.7e-177 | pfkA | 2.7.1.11 | F | Catalyzes the phosphorylation of D-fructose 6-phosphate to fructose 1,6-bisphosphate by ATP, the first committing step of glycolysis | |
KKNCFHKG_00372 | 0.0 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
KKNCFHKG_00373 | 1e-156 | ytvI | S | sporulation integral membrane protein YtvI | ||
KKNCFHKG_00374 | 1e-73 | yeaL | S | Membrane | ||
KKNCFHKG_00375 | 4.1e-206 | citZ | 2.3.3.1 | C | Belongs to the citrate synthase family | |
KKNCFHKG_00376 | 4e-245 | icd | 1.1.1.42 | C | isocitrate | |
KKNCFHKG_00377 | 2.9e-168 | mdh | 1.1.1.37 | C | Catalyzes the reversible oxidation of malate to oxaloacetate | |
KKNCFHKG_00378 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
KKNCFHKG_00379 | 8.5e-156 | fpg | 3.2.2.23, 4.2.99.18 | L | Involved in base excision repair of DNA damaged by oxidation or by mutagenic agents. Acts as DNA glycosylase that recognizes and removes damaged bases. Has a preference for oxidized purines, such as 7,8-dihydro-8-oxoguanine (8-oxoG). Has AP (apurinic apyrimidinic) lyase activity and introduces nicks in the DNA strand. Cleaves the DNA backbone by beta-delta elimination to generate a single-strand break at the site of the removed base with both 3'- and 5'-phosphates | |
KKNCFHKG_00380 | 1.3e-106 | ytaF | P | Probably functions as a manganese efflux pump | ||
KKNCFHKG_00381 | 1e-102 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
KKNCFHKG_00382 | 3.5e-191 | gapB | 1.2.1.12, 1.2.1.59 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
KKNCFHKG_00383 | 3.2e-86 | 2.3.1.178 | J | Benzoate transporter | ||
KKNCFHKG_00384 | 2.1e-79 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
KKNCFHKG_00385 | 2.1e-260 | dnaB | L | Membrane attachment protein | ||
KKNCFHKG_00386 | 8.4e-176 | dnaI | L | Primosomal protein DnaI | ||
KKNCFHKG_00387 | 2.4e-150 | ytxC | S | YtxC-like family | ||
KKNCFHKG_00388 | 0.0 | thrS | 6.1.1.3 | J | Catalyzes the attachment of threonine to tRNA(Thr) in a two-step reaction L-threonine is first activated by ATP to form Thr-AMP and then transferred to the acceptor end of tRNA(Thr) | |
KKNCFHKG_00389 | 7.1e-71 | G | Transmembrane secretion effector | |||
KKNCFHKG_00390 | 5.1e-108 | 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 | ||
KKNCFHKG_00391 | 3.4e-26 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
KKNCFHKG_00392 | 3.3e-56 | rplT | J | Binds directly to 23S ribosomal RNA and is necessary for the in vitro assembly process of the 50S ribosomal subunit. It is not involved in the protein synthesizing functions of that subunit | ||
KKNCFHKG_00394 | 3.3e-80 | 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 | |
KKNCFHKG_00395 | 1.2e-96 | ypdE | 4.4.1.5 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |
KKNCFHKG_00396 | 2.3e-101 | yieF | S | NAD(P)H-dependent FMN reductase | ||
KKNCFHKG_00397 | 2.2e-176 | panE | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
KKNCFHKG_00398 | 1.1e-126 | queC | 6.3.4.20 | F | Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) | |
KKNCFHKG_00399 | 4e-11 | S | NADPH-dependent FMN reductase | |||
KKNCFHKG_00400 | 1.8e-56 | K | Transcriptional regulator | |||
KKNCFHKG_00401 | 6.3e-120 | M1-1017 | S | Protein of unknown function (DUF1129) | ||
KKNCFHKG_00402 | 1.2e-29 | sidE | D | nuclear chromosome segregation | ||
KKNCFHKG_00403 | 8.9e-136 | |||||
KKNCFHKG_00404 | 8.3e-31 | sspI | S | Belongs to the SspI family | ||
KKNCFHKG_00405 | 1.5e-135 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
KKNCFHKG_00406 | 9.6e-181 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
KKNCFHKG_00407 | 0.0 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
KKNCFHKG_00408 | 1.4e-86 | V | Mate efflux family protein | |||
KKNCFHKG_00409 | 5.5e-45 | KT | Transcriptional | |||
KKNCFHKG_00410 | 2.2e-168 | rnhC | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
KKNCFHKG_00411 | 1.6e-42 | zapA | D | Activator of cell division through the inhibition of FtsZ GTPase activity, therefore promoting FtsZ assembly into bundles of protofilaments necessary for the formation of the division Z ring. It is recruited early at mid-cell but it is not essential for cell division | ||
KKNCFHKG_00412 | 1.4e-87 | cvpA | S | membrane protein, required for colicin V production | ||
KKNCFHKG_00413 | 0.0 | polX | L | COG1796 DNA polymerase IV (family X) | ||
KKNCFHKG_00414 | 0.0 | mutS2 | L | Endonuclease that is involved in the suppression of homologous recombination and may therefore have a key role in the control of bacterial genetic diversity | ||
KKNCFHKG_00415 | 0.0 | lcfA | 6.2.1.3 | IQ | COG0318 Acyl-CoA synthetases (AMP-forming) AMP-acid ligases II | |
KKNCFHKG_00416 | 6.6e-102 | fadR | K | Transcriptional regulator | ||
KKNCFHKG_00417 | 4.4e-138 | fadB | 4.2.1.17 | I | Belongs to the enoyl-CoA hydratase isomerase family | |
KKNCFHKG_00418 | 4.8e-129 | etfB | C | Electron transfer flavoprotein | ||
KKNCFHKG_00419 | 6.9e-173 | etfA | C | Electron transfer flavoprotein | ||
KKNCFHKG_00420 | 5.1e-53 | trxA | O | Belongs to the thioredoxin family | ||
KKNCFHKG_00421 | 0.0 | uvrC | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrC both incises the 5' and 3' sides of the lesion. The N-terminal half is responsible for the 3' incision and the C-terminal half is responsible for the 5' incision | ||
KKNCFHKG_00422 | 2e-222 | lysC | 1.1.1.3, 2.7.2.4 | E | Belongs to the aspartokinase family | |
KKNCFHKG_00423 | 7.9e-79 | yslB | S | Protein of unknown function (DUF2507) | ||
KKNCFHKG_00424 | 2.5e-104 | sdhC | C | succinate dehydrogenase | ||
KKNCFHKG_00425 | 0.0 | sdhA | 1.3.5.1, 1.3.5.4 | C | succinate dehydrogenase | |
KKNCFHKG_00426 | 6.5e-150 | sdhB | 1.3.5.1, 1.3.5.4 | C | succinate dehydrogenase | |
KKNCFHKG_00427 | 6.7e-89 | ysmA | S | thioesterase | ||
KKNCFHKG_00428 | 2.3e-31 | gerE | K | Transcriptional regulator | ||
KKNCFHKG_00430 | 3.2e-187 | S | Predicted membrane protein (DUF2157) | |||
KKNCFHKG_00431 | 2.9e-85 | S | GDYXXLXY protein | |||
KKNCFHKG_00432 | 3.9e-78 | ysmB | 2.4.2.28 | K | transcriptional | |
KKNCFHKG_00433 | 6.2e-151 | murI | 3.6.1.66, 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
KKNCFHKG_00435 | 1.5e-189 | gerM | S | COG5401 Spore germination protein | ||
KKNCFHKG_00436 | 6.6e-105 | rdgB | 3.6.1.66 | 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 | |
KKNCFHKG_00437 | 7e-92 | ysnB | S | Phosphoesterase | ||
KKNCFHKG_00439 | 1.5e-46 | |||||
KKNCFHKG_00440 | 5.9e-71 | S | Protein of unknown function (DUF2512) | |||
KKNCFHKG_00441 | 6.8e-184 | trxA2 | O | COG0457 FOG TPR repeat | ||
KKNCFHKG_00442 | 1.2e-209 | 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 | ||
KKNCFHKG_00443 | 1.8e-234 | 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 | ||
KKNCFHKG_00444 | 5.9e-310 | lonB | 2.7.7.7, 3.4.21.53 | LO | Belongs to the peptidase S16 family | |
KKNCFHKG_00445 | 0.0 | lon | 3.4.21.53 | O | ATP-dependent serine protease that mediates the selective degradation of mutant and abnormal proteins as well as certain short-lived regulatory proteins. Required for cellular homeostasis and for survival from DNA damage and developmental changes induced by stress. Degrades polypeptides processively to yield small peptide fragments that are 5 to 10 amino acids long. Binds to DNA in a double-stranded, site-specific manner | |
KKNCFHKG_00446 | 1.3e-105 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
KKNCFHKG_00447 | 2.2e-87 | ysxD | ||||
KKNCFHKG_00448 | 2.1e-241 | hemA | 1.2.1.70 | H | Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA) | |
KKNCFHKG_00449 | 1.7e-148 | hemX | O | cytochrome C | ||
KKNCFHKG_00450 | 4.6e-166 | hemC | 2.1.1.107, 2.5.1.61, 4.2.1.75 | H | Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps | |
KKNCFHKG_00451 | 1.9e-144 | hemD | 2.1.1.107, 4.2.1.75 | H | Uroporphyrinogen-III synthase | |
KKNCFHKG_00452 | 7.1e-186 | hemB | 4.2.1.24 | H | Belongs to the ALAD family | |
KKNCFHKG_00453 | 3.5e-249 | hemL | 5.4.3.8 | H | Glutamate-1-semialdehyde aminotransferase | |
KKNCFHKG_00454 | 7.4e-192 | spoVID | M | stage VI sporulation protein D | ||
KKNCFHKG_00455 | 7.6e-191 | ysxE | S | A protein kinase that phosphorylates Ser and Thr residues. Probably acts to suppress the effects of stress linked to accumulation of reactive oxygen species. Probably involved in the extracytoplasmic stress response | ||
KKNCFHKG_00456 | 3.3e-26 | |||||
KKNCFHKG_00457 | 0.0 | valS | 6.1.1.9 | J | amino acids such as threonine, to avoid such errors, it has a posttransfer editing activity that hydrolyzes mischarged Thr-tRNA(Val) in a tRNA-dependent manner | |
KKNCFHKG_00458 | 3.6e-249 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
KKNCFHKG_00460 | 6.7e-87 | |||||
KKNCFHKG_00461 | 1.1e-223 | NU | Pilus assembly protein PilX | |||
KKNCFHKG_00462 | 3.7e-188 | |||||
KKNCFHKG_00463 | 3.9e-128 | S | PRC-barrel domain | |||
KKNCFHKG_00464 | 2.3e-217 | V | G5 | |||
KKNCFHKG_00465 | 1.2e-294 | pilB | NU | COG2804 Type II secretory pathway, ATPase PulE Tfp pilus assembly pathway, ATPase PilB | ||
KKNCFHKG_00466 | 2.6e-194 | pilT | NU | twitching motility protein | ||
KKNCFHKG_00467 | 2.3e-202 | pilC | NU | type II secretion system | ||
KKNCFHKG_00468 | 4.6e-52 | NU | cell adhesion | |||
KKNCFHKG_00469 | 5.6e-186 | NU | COG4972 Tfp pilus assembly protein, ATPase PilM | |||
KKNCFHKG_00470 | 7.3e-86 | pilN | NU | PFAM Fimbrial assembly family protein | ||
KKNCFHKG_00471 | 4.2e-103 | |||||
KKNCFHKG_00472 | 4.2e-133 | comC | 3.4.23.43 | NOU | COG1989 Type II secretory pathway, prepilin signal peptidase PulO and related peptidases | |
KKNCFHKG_00473 | 1.7e-171 | spoIIB | ||||
KKNCFHKG_00474 | 1.1e-121 | radC | E | Belongs to the UPF0758 family | ||
KKNCFHKG_00475 | 6.9e-184 | mreB | D | Rod shape-determining protein MreB | ||
KKNCFHKG_00476 | 4.4e-139 | mreC | M | Involved in formation and maintenance of cell shape | ||
KKNCFHKG_00477 | 2.4e-87 | mreD | M | shape-determining protein | ||
KKNCFHKG_00478 | 8.8e-122 | minC | D | Cell division inhibitor that blocks the formation of polar Z ring septums. Rapidly oscillates between the poles of the cell to destabilize FtsZ filaments that have formed before they mature into polar Z rings. Prevents FtsZ polymerization | ||
KKNCFHKG_00479 | 1e-145 | minD | D | Belongs to the ParA family | ||
KKNCFHKG_00480 | 1.5e-135 | spoIVFA | M | COG0739 Membrane proteins related to metalloendopeptidases | ||
KKNCFHKG_00481 | 9.8e-163 | spoIVFB | S | Stage IV sporulation protein | ||
KKNCFHKG_00482 | 2.9e-279 | rng | J | ribonuclease, Rne Rng family | ||
KKNCFHKG_00483 | 1.7e-48 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
KKNCFHKG_00484 | 1.6e-52 | ysxB | J | ribosomal protein | ||
KKNCFHKG_00485 | 1.1e-46 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
KKNCFHKG_00486 | 3e-98 | spo0B | T | Sporulation initiation phospho-transferase B, C-terminal | ||
KKNCFHKG_00487 | 9.9e-244 | 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 | ||
KKNCFHKG_00488 | 1.2e-74 | pheB | 5.4.99.5 | S | Belongs to the UPF0735 family | |
KKNCFHKG_00489 | 1.1e-158 | pheA | 4.2.1.51 | E | Prephenate dehydratase | |
KKNCFHKG_00490 | 1.1e-95 | niaR | S | small molecule binding protein (contains 3H domain) | ||
KKNCFHKG_00491 | 4.3e-143 | safA | M | spore coat assembly protein SafA | ||
KKNCFHKG_00492 | 3.1e-189 | 1.1.1.34, 2.7.1.89 | M | choline kinase involved in LPS biosynthesis | ||
KKNCFHKG_00493 | 1.7e-128 | yebC | K | transcriptional regulatory protein | ||
KKNCFHKG_00494 | 1.7e-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 | |
KKNCFHKG_00495 | 2e-183 | 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 | |
KKNCFHKG_00496 | 5.4e-27 | yrzS | S | Protein of unknown function (DUF2905) | ||
KKNCFHKG_00497 | 1.1e-192 | queA | 2.4.99.17 | J | Transfers and isomerizes the ribose moiety from AdoMet to the 7-aminomethyl group of 7-deazaguanine (preQ1-tRNA) to give epoxyqueuosine (oQ-tRNA) | |
KKNCFHKG_00498 | 6.9e-225 | 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) | |
KKNCFHKG_00499 | 1.2e-44 | yajC | U | Preprotein translocase subunit YajC | ||
KKNCFHKG_00500 | 4.9e-61 | yrzE | S | Protein of unknown function (DUF3792) | ||
KKNCFHKG_00501 | 6e-104 | yrbG | S | membrane | ||
KKNCFHKG_00502 | 1.9e-270 | spoVB | S | COG2244 Membrane protein involved in the export of O-antigen and teichoic acid | ||
KKNCFHKG_00503 | 3.6e-60 | yrzD | S | Post-transcriptional regulator | ||
KKNCFHKG_00504 | 0.0 | secF | U | Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. SecDF uses the proton motive force (PMF) to complete protein translocation after the ATP-dependent function of SecA | ||
KKNCFHKG_00505 | 6e-174 | spoVK | O | stage V sporulation protein K | ||
KKNCFHKG_00506 | 3.7e-227 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
KKNCFHKG_00507 | 6.1e-246 | ynbB | 4.4.1.1 | P | COG4100 Cystathionine beta-lyase family protein involved in aluminum resistance | |
KKNCFHKG_00508 | 4.6e-171 | polA | 2.7.7.7 | L | 5'3' exonuclease | |
KKNCFHKG_00509 | 3.6e-27 | ypeQ | S | Zinc-finger | ||
KKNCFHKG_00511 | 1.2e-31 | cspD | K | Cold-shock protein | ||
KKNCFHKG_00512 | 3e-72 | mntR | K | Involved in manganese homeostasis. Might activate the transcription of the mntABCD operon | ||
KKNCFHKG_00513 | 0.0 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
KKNCFHKG_00514 | 7.3e-86 | |||||
KKNCFHKG_00515 | 0.0 | yfmR | S | COG0488 ATPase components of ABC transporters with duplicated ATPase domains | ||
KKNCFHKG_00516 | 7e-153 | ypgR | C | COG0694 Thioredoxin-like proteins and domains | ||
KKNCFHKG_00517 | 2.3e-75 | yphP | S | Belongs to the UPF0403 family | ||
KKNCFHKG_00518 | 8.7e-107 | ypjP | S | YpjP-like protein | ||
KKNCFHKG_00519 | 4.3e-157 | 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 | |
KKNCFHKG_00520 | 1.2e-93 | folA | 1.1.1.262, 1.5.1.3 | H | Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis | |
KKNCFHKG_00521 | 2.9e-111 | hlyIII | S | protein, Hemolysin III | ||
KKNCFHKG_00522 | 3.4e-146 | ypmR | E | COG2755 Lysophospholipase L1 and related esterases | ||
KKNCFHKG_00523 | 9.3e-98 | ypmS | S | protein conserved in bacteria | ||
KKNCFHKG_00524 | 2.3e-275 | rsmF | 2.1.1.176, 2.1.1.178 | J | RNA-binding PUA-like domain of methyltransferase RsmF | |
KKNCFHKG_00525 | 4.3e-100 | msrA | 1.8.4.11, 1.8.4.12 | O | Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine | |
KKNCFHKG_00526 | 7.3e-79 | msrB | 1.8.4.11, 1.8.4.12 | O | peptide methionine sulfoxide reductase | |
KKNCFHKG_00527 | 1.2e-09 | S | Protein of unknown function (Tiny_TM_bacill) | |||
KKNCFHKG_00528 | 8.5e-193 | NT | CHASE3 domain | |||
KKNCFHKG_00529 | 5.7e-35 | yozE | S | Belongs to the UPF0346 family | ||
KKNCFHKG_00530 | 2.1e-114 | yodN | ||||
KKNCFHKG_00531 | 7.5e-25 | yozD | S | YozD-like protein | ||
KKNCFHKG_00532 | 2e-143 | vanY | 3.4.17.14 | M | D-alanyl-D-alanine carboxypeptidase | |
KKNCFHKG_00533 | 3.7e-271 | ctpA | 3.4.21.102 | M | Belongs to the peptidase S41A family | |
KKNCFHKG_00534 | 6.1e-65 | ypoP | K | transcriptional | ||
KKNCFHKG_00536 | 2.9e-99 | ykwD | J | protein with SCP PR1 domains | ||
KKNCFHKG_00537 | 3.5e-239 | norM | V | Multidrug efflux pump | ||
KKNCFHKG_00539 | 3.3e-186 | dapF | 5.1.1.7 | E | Catalyzes the stereoinversion of LL-2,6- diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso- DAP), a precursor of L-lysine and an essential component of the bacterial peptidoglycan | |
KKNCFHKG_00540 | 8.9e-72 | ligD | 6.5.1.1 | L | ATP-dependent DNA ligase | |
KKNCFHKG_00541 | 1.3e-132 | ku | L | With LigD forms a non-homologous end joining (NHEJ) DNA repair enzyme, which repairs dsDNA breaks with reduced fidelity. Binds linear dsDNA with 5'- and 3'- overhangs but not closed circular dsDNA nor ssDNA. Recruits and stimulates the ligase activity of LigD | ||
KKNCFHKG_00542 | 2.2e-111 | 3.6.1.27 | I | COG0671 Membrane-associated phospholipid phosphatase | ||
KKNCFHKG_00543 | 0.0 | ltaS | 2.7.8.20 | M | Belongs to the LTA synthase family | |
KKNCFHKG_00544 | 0.0 | yyaL | O | COG1331 Highly conserved protein containing a thioredoxin domain | ||
KKNCFHKG_00545 | 3.6e-222 | ymfD | EGP | Major facilitator Superfamily | ||
KKNCFHKG_00546 | 3e-122 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
KKNCFHKG_00547 | 2.4e-251 | arlS | 2.7.13.3 | T | Histidine kinase | |
KKNCFHKG_00548 | 7.5e-74 | yozR | S | COG0071 Molecular chaperone (small heat shock protein) | ||
KKNCFHKG_00549 | 0.0 | sucA | 1.2.4.2, 4.1.1.71 | C | The 2-oxoglutarate dehydrogenase complex catalyzes the overall conversion of 2-oxoglutarate to succinyl-CoA and CO(2). It contains multiple copies of three enzymatic components 2- oxoglutarate dehydrogenase (E1), dihydrolipoamide succinyltransferase (E2) and lipoamide dehydrogenase (E3) | |
KKNCFHKG_00550 | 4.4e-204 | sucB | 2.3.1.61 | C | The 2-oxoglutarate dehydrogenase complex catalyzes the overall conversion of 2-oxoglutarate to succinyl-CoA and CO(2) | |
KKNCFHKG_00551 | 5.4e-228 | dhaS | 1.2.1.3, 1.2.1.39 | C | Belongs to the aldehyde dehydrogenase family | |
KKNCFHKG_00552 | 1.8e-80 | rok | S | Repressor of ComK | ||
KKNCFHKG_00553 | 5.2e-115 | yidC | U | Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins | ||
KKNCFHKG_00555 | 7.2e-161 | yqfU | S | Uncharacterized protein conserved in bacteria (DUF2179) | ||
KKNCFHKG_00556 | 0.0 | topB | 5.99.1.2 | L | Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone | |
KKNCFHKG_00557 | 7.8e-193 | yceA | S | Belongs to the UPF0176 family | ||
KKNCFHKG_00558 | 1.1e-129 | yoqW | S | Belongs to the SOS response-associated peptidase family | ||
KKNCFHKG_00559 | 1.1e-104 | thiT | S | Proton-coupled thiamine transporter YuaJ | ||
KKNCFHKG_00560 | 7.6e-168 | yflN | S | COG0491 Zn-dependent hydrolases, including glyoxylases | ||
KKNCFHKG_00561 | 2.1e-79 | S | Domain in cystathionine beta-synthase and other proteins. | |||
KKNCFHKG_00562 | 4.3e-116 | yhfW | CE | COG0665 Glycine D-amino acid oxidases (deaminating) | ||
KKNCFHKG_00563 | 9.1e-107 | yocH | CBM50 | M | COG1388 FOG LysM repeat | |
KKNCFHKG_00564 | 0.0 | topB2 | 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 | |
KKNCFHKG_00565 | 4e-243 | ycgH | E | COG1113 Gamma-aminobutyrate permease and related permeases | ||
KKNCFHKG_00566 | 3.8e-148 | corA | P | Mg2 transporter protein | ||
KKNCFHKG_00567 | 7.1e-64 | S | CHY zinc finger | |||
KKNCFHKG_00568 | 6.2e-218 | hisZ | 2.4.2.17, 6.1.1.21 | E | Required for the first step of histidine biosynthesis. May allow the feedback regulation of ATP phosphoribosyltransferase activity by histidine | |
KKNCFHKG_00569 | 1.8e-110 | hisG | 2.4.2.17 | E | Catalyzes the condensation of ATP and 5-phosphoribose 1- diphosphate to form N'-(5'-phosphoribosyl)-ATP (PR-ATP). Has a crucial role in the pathway because the rate of histidine biosynthesis seems to be controlled primarily by regulation of HisG enzymatic activity | |
KKNCFHKG_00570 | 5.1e-232 | 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 | |
KKNCFHKG_00571 | 2.9e-105 | hisB | 1.1.1.23, 2.6.1.9, 3.1.3.15, 4.2.1.19 | E | imidazoleglycerol-phosphate dehydratase | |
KKNCFHKG_00572 | 6.1e-111 | hisH | E | IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisH subunit provides the glutamine amidotransferase activity that produces the ammonia necessary to HisF for the synthesis of IGP and AICAR | ||
KKNCFHKG_00573 | 1.4e-127 | hisA | 5.3.1.16 | E | 1-(5-phosphoribosyl)-5- 5-phosphoribosylamino)methylideneamino imidazole-4-carboxamide isomerase | |
KKNCFHKG_00574 | 1.3e-134 | hisF | 3.5.4.19, 3.6.1.31 | E | IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisF subunit catalyzes the cyclization activity that produces IGP and AICAR from PRFAR using the ammonia provided by the HisH subunit | |
KKNCFHKG_00575 | 3.1e-116 | hisE | 3.5.4.19, 3.5.4.25, 3.6.1.31, 5.3.1.16 | E | belongs to the PRA-CH family | |
KKNCFHKG_00576 | 1.1e-39 | yedF | O | Belongs to the sulfur carrier protein TusA family | ||
KKNCFHKG_00577 | 1.8e-239 | yedE | S | Sulphur transport | ||
KKNCFHKG_00578 | 6.1e-161 | rarD | S | -transporter | ||
KKNCFHKG_00579 | 6.5e-219 | ktrB | P | COG0168 Trk-type K transport systems, membrane components | ||
KKNCFHKG_00580 | 1.9e-121 | P | COG0569 K transport systems, NAD-binding component | |||
KKNCFHKG_00581 | 8.3e-134 | ykrK | S | Domain of unknown function (DUF1836) | ||
KKNCFHKG_00582 | 4.6e-15 | |||||
KKNCFHKG_00583 | 1.1e-44 | yxcD | S | Protein of unknown function (DUF2653) | ||
KKNCFHKG_00584 | 5.2e-215 | yeaN | P | COG2807 Cyanate permease | ||
KKNCFHKG_00585 | 2.1e-310 | ubiB | S | ABC1 family | ||
KKNCFHKG_00586 | 4.7e-24 | S | ATP synthase, subunit b | |||
KKNCFHKG_00587 | 7.7e-102 | 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 | |
KKNCFHKG_00589 | 2.7e-31 | cspB | K | Cold shock | ||
KKNCFHKG_00590 | 3.2e-118 | folE | 3.5.4.16 | H | GTP cyclohydrolase | |
KKNCFHKG_00591 | 1e-173 | trxB_2 | 1.8.1.9 | C | FAD dependent oxidoreductase | |
KKNCFHKG_00592 | 2.8e-45 | S | Protein of unknown function (DUF1292) | |||
KKNCFHKG_00593 | 5.2e-47 | yxiS | ||||
KKNCFHKG_00594 | 0.0 | bceB | V | ABC transporter (permease) | ||
KKNCFHKG_00595 | 1.2e-135 | bceA | V | ABC transporter, ATP-binding protein | ||
KKNCFHKG_00596 | 2e-183 | bceS | 2.7.13.3 | T | Signal transduction histidine kinase | |
KKNCFHKG_00597 | 1.6e-128 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
KKNCFHKG_00598 | 6.7e-230 | yifK | E | COG1113 Gamma-aminobutyrate permease and related permeases | ||
KKNCFHKG_00599 | 3.2e-190 | yetN | S | Protein of unknown function (DUF3900) | ||
KKNCFHKG_00600 | 3.1e-232 | ywoD | EGP | Major facilitator superfamily | ||
KKNCFHKG_00601 | 5.9e-49 | iscA | S | Heme biosynthesis protein HemY | ||
KKNCFHKG_00602 | 0.0 | yheI | V | COG1132 ABC-type multidrug transport system, ATPase and permease components | ||
KKNCFHKG_00603 | 0.0 | yheH | V | COG1132 ABC-type multidrug transport system, ATPase and permease components | ||
KKNCFHKG_00604 | 9.4e-43 | S | Small, acid-soluble spore proteins, alpha/beta type | |||
KKNCFHKG_00605 | 6.4e-61 | S | Increases the activity of extracellular murein hydrolases possibly by mediating their export via hole formation. Inhibited by the antiholin-like proteins LrgAB. In an unstressed cell, the LrgAB products probably inhibit the function of the CidA protein. When a cell is stressed by the addition of antibiotics or by other factors in the environment, CidA possibly oligomerizes within the bacterial cell membrane, creating lesions that disrupt the proton motive force, which in turn results in loss of cell viability. These lesions are also hypothesized to regulate the subsequent cell lysis by either allowing the murein hydrolases access to the cell wall substrate and or regulating their activity by a | |||
KKNCFHKG_00606 | 2e-110 | M | effector of murein hydrolase | |||
KKNCFHKG_00607 | 0.0 | alkK | IQ | COG0318 Acyl-CoA synthetases (AMP-forming) AMP-acid ligases II | ||
KKNCFHKG_00608 | 4.4e-109 | M | lytic transglycosylase activity | |||
KKNCFHKG_00609 | 1.1e-08 | S | membrane | |||
KKNCFHKG_00610 | 8.6e-19 | sspP | S | Belongs to the SspP family | ||
KKNCFHKG_00611 | 4.5e-39 | |||||
KKNCFHKG_00612 | 7.1e-239 | pepS | E | COG2309 Leucyl aminopeptidase (aminopeptidase T) | ||
KKNCFHKG_00613 | 4.4e-18 | sspO | S | Belongs to the SspO family | ||
KKNCFHKG_00614 | 0.0 | acnA | 4.2.1.3 | C | Catalyzes the isomerization of citrate to isocitrate via cis-aconitate | |
KKNCFHKG_00616 | 4.1e-31 | tlp | S | Belongs to the Tlp family | ||
KKNCFHKG_00617 | 2.2e-75 | yneP | S | thioesterase | ||
KKNCFHKG_00618 | 5.5e-52 | yneQ | ||||
KKNCFHKG_00619 | 5.3e-52 | yneR | S | Belongs to the HesB IscA family | ||
KKNCFHKG_00620 | 5e-97 | plsY | 2.3.1.15, 3.5.1.104 | I | Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP | |
KKNCFHKG_00621 | 7.2e-71 | yccU | S | CoA-binding protein | ||
KKNCFHKG_00622 | 0.0 | parE | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
KKNCFHKG_00623 | 0.0 | parC | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
KKNCFHKG_00624 | 6.3e-145 | |||||
KKNCFHKG_00625 | 7.1e-215 | yjjL | G | Major facilitator superfamily | ||
KKNCFHKG_00626 | 7.6e-149 | yqfL | 2.7.11.33, 2.7.4.28 | S | Bifunctional serine threonine kinase and phosphorylase involved in the regulation of the pyruvate, phosphate dikinase (PPDK) by catalyzing its phosphorylation dephosphorylation | |
KKNCFHKG_00627 | 0.0 | ppdK | 2.7.3.13, 2.7.9.1 | G | Belongs to the PEP-utilizing enzyme family | |
KKNCFHKG_00630 | 3.1e-198 | yrpB | 1.13.12.16 | S | COG2070 Dioxygenases related to 2-nitropropane dioxygenase | |
KKNCFHKG_00633 | 3.6e-102 | 5.1.3.34 | S | oxidoreductase activity | ||
KKNCFHKG_00634 | 9.1e-95 | sipT | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
KKNCFHKG_00636 | 2.6e-197 | leuB1 | 1.1.1.85 | CE | Isocitrate/isopropylmalate dehydrogenase | |
KKNCFHKG_00637 | 2.7e-162 | 2.1.1.144, 2.1.1.197 | S | Methyltransferase domain | ||
KKNCFHKG_00638 | 2.1e-08 | |||||
KKNCFHKG_00641 | 1e-136 | spoIISA | S | Toxin SpoIISA, type II toxin-antitoxin system | ||
KKNCFHKG_00642 | 9.1e-81 | yvbK | 3.1.3.25 | K | acetyltransferase | |
KKNCFHKG_00643 | 2.5e-74 | MA20_02285 | 2.3.1.57 | K | Acetyltransferase (GNAT) family | |
KKNCFHKG_00644 | 1.2e-132 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
KKNCFHKG_00645 | 3e-121 | thiM | 2.7.1.50 | H | Catalyzes the phosphorylation of the hydroxyl group of 4-methyl-5-beta-hydroxyethylthiazole (THZ) | |
KKNCFHKG_00646 | 2.3e-145 | thiD | 2.5.1.3, 2.7.1.35, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
KKNCFHKG_00647 | 2.6e-112 | thiE | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Condenses 4-methyl-5-(beta-hydroxyethyl)thiazole monophosphate (THZ-P) and 2-methyl-4-amino-5-hydroxymethyl pyrimidine pyrophosphate (HMP-PP) to form thiamine monophosphate (TMP) | |
KKNCFHKG_00648 | 3.3e-08 | ykyB | S | YkyB-like protein | ||
KKNCFHKG_00649 | 5.2e-124 | yflK | S | protein conserved in bacteria | ||
KKNCFHKG_00650 | 9.9e-10 | hsdS | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | |
KKNCFHKG_00651 | 4.9e-246 | rocR | KT | COG3829 Transcriptional regulator containing PAS, AAA-type ATPase, and DNA-binding domains | ||
KKNCFHKG_00652 | 4.8e-232 | rocD | 2.6.1.11, 2.6.1.13, 2.6.1.17 | E | Catalyzes the interconversion of ornithine to glutamate semialdehyde | |
KKNCFHKG_00653 | 1.8e-80 | K | Acetyltransferase (GNAT) domain | |||
KKNCFHKG_00654 | 4.7e-97 | O | HI0933-like protein | |||
KKNCFHKG_00655 | 8.9e-29 | rpsN | J | Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site | ||
KKNCFHKG_00656 | 0.0 | yjcD | 3.6.4.12 | L | DNA helicase | |
KKNCFHKG_00657 | 1.6e-225 | ywdJ | F | Xanthine uracil | ||
KKNCFHKG_00658 | 3.1e-165 | ytnM | S | membrane transporter protein | ||
KKNCFHKG_00659 | 1.6e-236 | E | COG1113 Gamma-aminobutyrate permease and related permeases | |||
KKNCFHKG_00660 | 3.6e-137 | nfrA | 1.5.1.38, 1.5.1.39 | C | Oxidoreductase | |
KKNCFHKG_00661 | 0.0 | KQ | COG3284 Transcriptional activator of acetoin glycerol metabolism | |||
KKNCFHKG_00662 | 6.3e-190 | amiE | 3.5.1.4 | S | Carbon-nitrogen hydrolase | |
KKNCFHKG_00663 | 6.9e-309 | F | COG1457 Purine-cytosine permease and related proteins | |||
KKNCFHKG_00664 | 1.8e-200 | amiF | 3.5.1.49 | S | Is an aliphatic amidase with a restricted substrate specificity, as it only hydrolyzes formamide | |
KKNCFHKG_00665 | 3.7e-48 | ureA | 3.5.1.5 | E | Belongs to the urease gamma subunit family | |
KKNCFHKG_00666 | 6.7e-56 | ureB | 3.5.1.5 | E | Belongs to the urease beta subunit family | |
KKNCFHKG_00667 | 0.0 | ureC | 3.5.1.5 | E | Belongs to the metallo-dependent hydrolases superfamily. Urease alpha subunit family | |
KKNCFHKG_00668 | 6e-79 | ureE | O | Involved in urease metallocenter assembly. Binds nickel. Probably functions as a nickel donor during metallocenter assembly | ||
KKNCFHKG_00669 | 1.6e-104 | ureF | O | Required for maturation of urease via the functional incorporation of the urease nickel metallocenter | ||
KKNCFHKG_00670 | 7.3e-112 | ureG | KO | Facilitates the functional incorporation of the urease nickel metallocenter. This process requires GTP hydrolysis, probably effectuated by UreG | ||
KKNCFHKG_00671 | 2e-157 | ureD | O | Required for maturation of urease via the functional incorporation of the urease nickel metallocenter | ||
KKNCFHKG_00672 | 6.1e-112 | ureH | S | PFAM Nickel cobalt transporter, high-affinity | ||
KKNCFHKG_00673 | 1.8e-171 | pfoS | S | Phosphotransferase system, EIIC | ||
KKNCFHKG_00674 | 2.3e-184 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dihydroxyacetone kinase DhaK, subunit | |
KKNCFHKG_00675 | 3.6e-100 | dhaL | 2.7.1.121 | S | Dak2 | |
KKNCFHKG_00676 | 2.6e-59 | dhaM | 2.7.1.121 | S | PTS system fructose IIA component | |
KKNCFHKG_00677 | 3.5e-247 | gabT | 2.6.1.19, 2.6.1.22 | E | Belongs to the class-III pyridoxal-phosphate-dependent aminotransferase family | |
KKNCFHKG_00678 | 1.6e-123 | ywaC | 2.7.6.5 | S | protein conserved in bacteria | |
KKNCFHKG_00679 | 1.3e-70 | ywnF | S | Family of unknown function (DUF5392) | ||
KKNCFHKG_00681 | 2.2e-204 | rlmN | 2.1.1.192 | J | Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs | |
KKNCFHKG_00682 | 4.7e-253 | iolT | EGP | Major facilitator Superfamily | ||
KKNCFHKG_00683 | 7.8e-85 | G | phosphoenolpyruvate-dependent sugar phosphotransferase system | |||
KKNCFHKG_00684 | 3.5e-57 | ygbA | S | Nitrous oxide-stimulated promoter | ||
KKNCFHKG_00685 | 2.5e-152 | yidA | S | hydrolases of the HAD superfamily | ||
KKNCFHKG_00686 | 8.2e-32 | |||||
KKNCFHKG_00687 | 1.1e-22 | D | Hemerythrin HHE cation binding | |||
KKNCFHKG_00688 | 1.8e-47 | D | Hemerythrin HHE cation binding | |||
KKNCFHKG_00689 | 3.2e-203 | gldA | 1.1.1.6 | C | COG0371 Glycerol dehydrogenase and related enzymes | |
KKNCFHKG_00690 | 1.3e-131 | fruR | K | Transcriptional regulator | ||
KKNCFHKG_00691 | 0.0 | fruA | 2.7.1.202 | GT | COG1762 Phosphotransferase system mannitol fructose-specific IIA domain (Ntr-type) | |
KKNCFHKG_00692 | 0.0 | yjcE | P | COG0025 NhaP-type Na H and K H antiporters | ||
KKNCFHKG_00693 | 6e-35 | yoeD | G | Helix-turn-helix domain | ||
KKNCFHKG_00694 | 5.7e-118 | nanE | 5.1.3.9 | G | Converts N-acetylmannosamine-6-phosphate (ManNAc-6-P) to N-acetylglucosamine-6-phosphate (GlcNAc-6-P) | |
KKNCFHKG_00695 | 1.7e-207 | fni | 5.3.3.2 | C | Involved in the biosynthesis of isoprenoids. Catalyzes the 1,3-allylic rearrangement of the homoallylic substrate isopentenyl (IPP) to its allylic isomer, dimethylallyl diphosphate (DMAPP) | |
KKNCFHKG_00697 | 2e-88 | 1.8.5.2 | S | DoxX | ||
KKNCFHKG_00698 | 8e-108 | C | Nitroreductase family | |||
KKNCFHKG_00699 | 0.0 | snf | 2.7.11.1 | L | COG0553 Superfamily II DNA RNA helicases, SNF2 family | |
KKNCFHKG_00700 | 1.6e-126 | cas6 | L | CRISPR (clustered regularly interspaced short palindromic repeat) is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA) | ||
KKNCFHKG_00701 | 0.0 | csh | ||||
KKNCFHKG_00702 | 1.2e-177 | L | CRISPR-associated protein Cas7 | |||
KKNCFHKG_00703 | 3e-144 | cas5h | S | CRISPR-associated protein Cas5 | ||
KKNCFHKG_00704 | 0.0 | cas3 | L | CRISPR-associated helicase, Cas3 | ||
KKNCFHKG_00705 | 1.1e-70 | cas4 | 3.1.12.1 | L | Domain of unknown function DUF83 | |
KKNCFHKG_00706 | 7e-189 | cas1 | L | CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Acts as a dsDNA endonuclease. Involved in the integration of spacer DNA into the CRISPR cassette | ||
KKNCFHKG_00707 | 1.1e-28 | cas2 | L | CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Functions as a ssRNA-specific endoribonuclease. Involved in the integration of spacer DNA into the CRISPR cassette | ||
KKNCFHKG_00708 | 5.1e-219 | L | Transposase DDE domain group 1 | |||
KKNCFHKG_00709 | 2.3e-72 | K | sequence-specific DNA binding | |||
KKNCFHKG_00710 | 2e-117 | cobC | 3.1.3.3, 3.1.3.73, 5.4.2.12 | G | Histidine phosphatase superfamily (branch 1) | |
KKNCFHKG_00711 | 2.1e-225 | gltP | C | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
KKNCFHKG_00712 | 9.4e-222 | cpdB | 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
KKNCFHKG_00713 | 1.4e-150 | K | RpiR family transcriptional regulator | |||
KKNCFHKG_00714 | 7.4e-161 | ypuA | S | Secreted protein | ||
KKNCFHKG_00715 | 9.7e-113 | |||||
KKNCFHKG_00716 | 3.1e-69 | S | response to pH | |||
KKNCFHKG_00717 | 3.8e-105 | che | ||||
KKNCFHKG_00718 | 2.8e-293 | K | helix_turn_helix, Lux Regulon | |||
KKNCFHKG_00721 | 2e-89 | 3.5.1.28 | M | n-acetylmuramoyl-L-alanine amidase | ||
KKNCFHKG_00722 | 1.1e-21 | 3.5.1.28 | M | n-acetylmuramoyl-L-alanine amidase | ||
KKNCFHKG_00723 | 2.8e-102 | 4.2.1.1 | P | Reversible hydration of carbon dioxide | ||
KKNCFHKG_00724 | 1.8e-116 | yrrT | 4.4.1.21 | Q | Could be a S-adenosyl-L-methionine-dependent methyltransferase | |
KKNCFHKG_00725 | 6.2e-87 | luxS | 4.4.1.21 | T | 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) | |
KKNCFHKG_00726 | 9.7e-169 | mccA | 2.5.1.134, 2.5.1.47 | E | Cysteine synthase | |
KKNCFHKG_00727 | 1.3e-210 | mccB | 2.5.1.48, 4.4.1.1, 4.4.1.2, 4.4.1.8 | E | cystathionine | |
KKNCFHKG_00728 | 6.7e-88 | yuaF | OU | Membrane protein implicated in regulation of membrane protease activity | ||
KKNCFHKG_00729 | 5.5e-169 | yuaG | S | protein conserved in bacteria | ||
KKNCFHKG_00730 | 1.7e-182 | mreB | D | Rod-share determining protein MreBH | ||
KKNCFHKG_00731 | 1.3e-85 | ykhA | 3.1.2.20 | I | Acyl-CoA hydrolase | |
KKNCFHKG_00732 | 2.5e-146 | dksA | T | COG1734 DnaK suppressor protein | ||
KKNCFHKG_00733 | 8.2e-227 | EGP | Major facilitator Superfamily | |||
KKNCFHKG_00734 | 3.7e-60 | yeaO | S | Protein of unknown function, DUF488 | ||
KKNCFHKG_00736 | 1.3e-57 | yhdN | S | Domain of unknown function (DUF1992) | ||
KKNCFHKG_00737 | 6.6e-137 | motA | N | flagellar motor | ||
KKNCFHKG_00738 | 1.9e-139 | motB | N | Flagellar motor protein | ||
KKNCFHKG_00739 | 3.5e-91 | yfkM | 3.5.1.124 | S | protease | |
KKNCFHKG_00740 | 3.4e-143 | map | 3.4.11.18 | E | Methionine aminopeptidase | |
KKNCFHKG_00741 | 7.3e-33 | yfkK | S | Belongs to the UPF0435 family | ||
KKNCFHKG_00742 | 1.1e-147 | yihY | S | Belongs to the UPF0761 family | ||
KKNCFHKG_00743 | 1e-218 | yfkF | EGP | Major facilitator Superfamily | ||
KKNCFHKG_00744 | 2.9e-172 | cax | P | COG0387 Ca2 H antiporter | ||
KKNCFHKG_00745 | 9e-147 | yfkD | S | YfkD-like protein | ||
KKNCFHKG_00746 | 1.5e-26 | yfjT | ||||
KKNCFHKG_00747 | 1.3e-148 | pdaA | G | deacetylase | ||
KKNCFHKG_00748 | 8.5e-167 | yfjP | 3.2.2.21 | L | COG0122 3-methyladenine DNA glycosylase 8-oxoguanine DNA glycosylase | |
KKNCFHKG_00749 | 1.1e-251 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
KKNCFHKG_00750 | 2.8e-100 | K | DNA-binding transcription factor activity | |||
KKNCFHKG_00751 | 5.6e-298 | lmrA | 3.6.3.44 | V | ABC transporter | |
KKNCFHKG_00753 | 4.5e-120 | L | Transposase IS4 family protein | |||
KKNCFHKG_00754 | 1.1e-291 | mqo | 1.1.5.4 | S | malate quinone oxidoreductase | |
KKNCFHKG_00755 | 3.4e-115 | papP | E | amino acid ABC transporter | ||
KKNCFHKG_00756 | 1.4e-103 | E | amino acid ABC transporter | |||
KKNCFHKG_00757 | 1.6e-129 | glnQ | 3.6.3.21 | E | ATPases associated with a variety of cellular activities | |
KKNCFHKG_00758 | 6.2e-138 | cjaA | ET | Belongs to the bacterial solute-binding protein 3 family | ||
KKNCFHKG_00759 | 8.7e-215 | 5.1.1.12 | E | Alanine racemase, N-terminal domain | ||
KKNCFHKG_00760 | 8.1e-207 | S | Domain of unknown function (DUF1611_N) Rossmann-like domain | |||
KKNCFHKG_00761 | 4.9e-223 | nspC | 4.1.1.96 | E | Pyridoxal-dependent decarboxylase, C-terminal sheet domain | |
KKNCFHKG_00762 | 8.9e-239 | LYS1 | 1.5.1.7 | E | Saccharopine dehydrogenase | |
KKNCFHKG_00763 | 8.6e-145 | T | COG1366 Anti-anti-sigma regulatory factor (antagonist of anti-sigma factor) | |||
KKNCFHKG_00764 | 2.5e-15 | S | Ribbon-helix-helix protein, copG family | |||
KKNCFHKG_00765 | 1.9e-59 | asp | S | protein conserved in bacteria | ||
KKNCFHKG_00766 | 6.7e-301 | yloV | S | kinase related to dihydroxyacetone kinase | ||
KKNCFHKG_00767 | 1.3e-119 | sdaAB | 4.3.1.17 | E | L-serine dehydratase | |
KKNCFHKG_00768 | 3.5e-155 | sdaAA | 4.3.1.17 | E | L-serine dehydratase | |
KKNCFHKG_00769 | 0.0 | recG | 3.6.4.12 | L | Critical role in recombination and DNA repair. Helps process Holliday junction intermediates to mature products by catalyzing branch migration. Has a DNA unwinding activity characteristic of a DNA helicase with a 3'- to 5'- polarity. Unwinds branched duplex DNA (Y-DNA) | |
KKNCFHKG_00770 | 8.8e-99 | fapR | 5.3.1.23 | Q | Transcriptional factor involved in regulation of membrane lipid biosynthesis by repressing genes involved in fatty acid and phospholipid metabolism | |
KKNCFHKG_00771 | 2.5e-178 | plsX | 2.3.1.15 | I | Catalyzes the reversible formation of acyl-phosphate (acyl-PO(4)) from acyl- acyl-carrier-protein (acyl-ACP). This enzyme utilizes acyl-ACP as fatty acyl donor, but not acyl-CoA | |
KKNCFHKG_00772 | 4.2e-159 | fabD | 2.3.1.39 | I | malonyl CoA-acyl carrier protein transacylase | |
KKNCFHKG_00773 | 2.1e-129 | IQ | reductase | |||
KKNCFHKG_00774 | 3.7e-32 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
KKNCFHKG_00775 | 1.5e-132 | 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 | |
KKNCFHKG_00776 | 0.0 | smc | D | Required for chromosome condensation and partitioning | ||
KKNCFHKG_00777 | 1.3e-179 | ftsY | U | Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Acts as a receptor for the complex formed by the signal recognition particle (SRP) and the ribosome-nascent chain (RNC) | ||
KKNCFHKG_00778 | 2.9e-51 | ylxM | S | Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY ffh. May be a regulatory protein | ||
KKNCFHKG_00779 | 8.7e-243 | 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 | |
KKNCFHKG_00780 | 1.7e-44 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
KKNCFHKG_00781 | 5.5e-36 | ylqC | S | Belongs to the UPF0109 family | ||
KKNCFHKG_00782 | 7.1e-60 | ylqD | S | YlqD protein | ||
KKNCFHKG_00783 | 4.4e-94 | 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 | ||
KKNCFHKG_00784 | 2e-140 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
KKNCFHKG_00785 | 2.4e-56 | rplS | J | This protein is located at the 30S-50S ribosomal subunit interface and may play a role in the structure and function of the aminoacyl-tRNA binding site | ||
KKNCFHKG_00786 | 1.2e-102 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
KKNCFHKG_00787 | 4.7e-154 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
KKNCFHKG_00788 | 1.7e-129 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
KKNCFHKG_00789 | 2.8e-227 | CP_1081 | D | nuclear chromosome segregation | ||
KKNCFHKG_00790 | 3.1e-44 | ylqH | S | homolog of the cytoplasmic domain of flagellar protein FhlB | ||
KKNCFHKG_00791 | 1.6e-213 | sucC | 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 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 | |
KKNCFHKG_00792 | 1.7e-165 | 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 | |
KKNCFHKG_00793 | 4.6e-160 | dprA | LU | Rossmann fold nucleotide-binding protein involved in DNA uptake | ||
KKNCFHKG_00794 | 0.0 | topA | 5.99.1.2 | L | Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone | |
KKNCFHKG_00795 | 4.3e-169 | xerC | L | tyrosine recombinase XerC | ||
KKNCFHKG_00796 | 7.4e-92 | hslV | 3.4.25.2 | O | Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery | |
KKNCFHKG_00797 | 2.1e-226 | hslU | O | this subunit has chaperone activity. The binding of ATP and its subsequent hydrolysis by HslU are essential for unfolding of protein substrates subsequently hydrolyzed by HslV. HslU recognizes the N-terminal part of its protein substrates and unfolds these before they are guided to HslV for hydrolysis | ||
KKNCFHKG_00798 | 7.3e-133 | codY | K | DNA-binding protein that represses the expression of many genes that are induced as cells make the transition from rapid exponential growth to stationary phase. It is a GTP-binding protein that senses the intracellular GTP concentration as an indicator of nutritional limitations. At low GTP concentration it no longer binds GTP and stop to act as a transcriptional repressor | ||
KKNCFHKG_00799 | 7e-60 | flgB | N | Structural component of flagellum, the bacterial motility apparatus. Part of the rod structure of flagellar basal body | ||
KKNCFHKG_00800 | 4e-75 | flgC | N | Belongs to the flagella basal body rod proteins family | ||
KKNCFHKG_00801 | 6.4e-40 | fliE | N | Flagellar hook-basal body complex protein FliE | ||
KKNCFHKG_00802 | 1.3e-242 | fliF | N | The M ring may be actively involved in energy transduction | ||
KKNCFHKG_00803 | 2e-162 | fliG | N | One of the proteins that forms a switch complex that is proposed to be located at the base of the basal body. This complex interacts with chemotaxis proteins (such as CheY) in addition to contacting components of the motor that determine the direction of flagellar rotation | ||
KKNCFHKG_00804 | 2.1e-124 | fliH | NU | COG1317 Flagellar biosynthesis type III secretory pathway protein | ||
KKNCFHKG_00805 | 1.2e-241 | fliI | 3.6.3.14 | NU | COG1157 Flagellar biosynthesis type III secretory pathway ATPase | |
KKNCFHKG_00806 | 3.5e-68 | fliJ | N | Flagellar biosynthesis chaperone | ||
KKNCFHKG_00807 | 5.4e-38 | ylxF | S | MgtE intracellular N domain | ||
KKNCFHKG_00808 | 1.3e-293 | fliK | N | Flagellar hook-length control | ||
KKNCFHKG_00809 | 2.3e-108 | flgD | N | Flagellar basal body rod modification protein | ||
KKNCFHKG_00810 | 3.2e-72 | flg | N | Putative flagellar | ||
KKNCFHKG_00811 | 3.1e-115 | flgG | N | Flagellar basal body rod | ||
KKNCFHKG_00812 | 1.3e-64 | fliL | N | Controls the rotational direction of flagella during chemotaxis | ||
KKNCFHKG_00813 | 4.9e-182 | fliM | N | One of the proteins that forms a switch complex that is proposed to be located at the base of the basal body. This complex interacts with chemotaxis proteins (such as CheY) in addition to contacting components of the motor that determine the direction of flagellar rotation | ||
KKNCFHKG_00814 | 1.2e-173 | fliN | N | FliN is one of three proteins (FliG, FliN, FliM) that form the rotor-mounted switch complex (C ring), located at the base of the basal body. This complex interacts with the CheY and CheZ chemotaxis proteins, in addition to contacting components of the motor that determine the direction of flagellar rotation | ||
KKNCFHKG_00815 | 2.1e-58 | cheB | 3.1.1.61, 3.5.1.44 | T | response regulator | |
KKNCFHKG_00816 | 3.2e-116 | fliZ | N | Flagellar biosynthesis protein, FliO | ||
KKNCFHKG_00817 | 2.6e-107 | fliP | N | Plays a role in the flagellum-specific transport system | ||
KKNCFHKG_00818 | 1.5e-37 | fliQ | N | Role in flagellar biosynthesis | ||
KKNCFHKG_00819 | 8.6e-134 | fliR | N | Flagellar biosynthetic protein FliR | ||
KKNCFHKG_00820 | 3.5e-186 | flhB | N | Required for formation of the rod structure in the basal body of the flagellar apparatus. Together with FliI and FliH, may constitute the export apparatus of flagellin | ||
KKNCFHKG_00821 | 0.0 | flhA | N | Required for formation of the rod structure of the flagellar apparatus. Together with FliI and FliH, may constitute the export apparatus of flagellin | ||
KKNCFHKG_00822 | 2.1e-197 | flhF | N | Flagellar biosynthesis regulator FlhF | ||
KKNCFHKG_00823 | 1.2e-144 | flhG | D | Belongs to the ParA family | ||
KKNCFHKG_00824 | 1.4e-113 | cheB | 3.1.1.61, 3.5.1.44 | NT | catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR | |
KKNCFHKG_00825 | 0.0 | cheA | 2.7.13.3 | NT | COG0643 Chemotaxis protein histidine kinase and related kinases | |
KKNCFHKG_00826 | 8.2e-70 | cheW | NT | COG0835 Chemotaxis signal transduction protein | ||
KKNCFHKG_00827 | 1.2e-112 | cheC | NT | COG1776 Chemotaxis protein CheC, inhibitor of MCP methylation | ||
KKNCFHKG_00828 | 8.9e-84 | cheD | 3.5.1.44 | NT | Deamidates glutamine residues to glutamate on methyl- accepting chemotaxis receptors (MCPs). CheD-mediated MCP deamidation is required for productive communication of the conformational signals of the chemoreceptors to the CheA kinase | |
KKNCFHKG_00829 | 1.1e-136 | sigD | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
KKNCFHKG_00830 | 1.4e-69 | ylxL | ||||
KKNCFHKG_00831 | 1.5e-135 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
KKNCFHKG_00832 | 1.8e-156 | 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 | ||
KKNCFHKG_00833 | 1.1e-127 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
KKNCFHKG_00834 | 6.9e-93 | frr | J | Responsible for the release of ribosomes from messenger RNA at the termination of protein biosynthesis. May increase the efficiency of translation by recycling ribosomes from one round of translation to another | ||
KKNCFHKG_00835 | 1.1e-147 | uppS | 2.5.1.31 | I | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
KKNCFHKG_00836 | 3.2e-144 | cdsA | 2.7.7.41 | S | Belongs to the CDS family | |
KKNCFHKG_00837 | 1.7e-194 | 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) | |
KKNCFHKG_00838 | 3.3e-236 | rasP | M | zinc metalloprotease | ||
KKNCFHKG_00839 | 0.0 | proS | 6.1.1.15 | J | Catalyzes the attachment of proline to tRNA(Pro) in a two-step reaction proline is first activated by ATP to form Pro- AMP and then transferred to the acceptor end of tRNA(Pro). As ProRS can inadvertently accommodate and process non-cognate amino acids such as alanine and cysteine, to avoid such errors it has two additional distinct editing activities against alanine. One activity is designated as 'pretransfer' editing and involves the tRNA(Pro)-independent hydrolysis of activated Ala-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Ala-tRNA(Pro). The misacylated Cys- tRNA(Pro) is not edited by ProRS | |
KKNCFHKG_00840 | 0.0 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
KKNCFHKG_00841 | 7.1e-83 | rimP | S | Required for maturation of 30S ribosomal subunits | ||
KKNCFHKG_00842 | 8.1e-224 | nusA | K | Participates in both transcription termination and antitermination | ||
KKNCFHKG_00843 | 8.2e-45 | ylxR | K | nucleic-acid-binding protein implicated in transcription termination | ||
KKNCFHKG_00844 | 2.9e-48 | ylxQ | J | ribosomal protein | ||
KKNCFHKG_00845 | 0.0 | infB | J | One of the essential components for the initiation of protein synthesis. Protects formylmethionyl-tRNA from spontaneous hydrolysis and promotes its binding to the 30S ribosomal subunits. Also involved in the hydrolysis of GTP during the formation of the 70S ribosomal complex | ||
KKNCFHKG_00846 | 8.6e-44 | ylxP | S | protein conserved in bacteria | ||
KKNCFHKG_00847 | 3.2e-56 | 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 | ||
KKNCFHKG_00848 | 2.4e-172 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
KKNCFHKG_00849 | 3.6e-182 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
KKNCFHKG_00850 | 1e-41 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
KKNCFHKG_00851 | 0.0 | pnp | 2.7.7.8 | J | Involved in mRNA degradation. Catalyzes the phosphorolysis of single-stranded polyribonucleotides processively in the 3'- to 5'-direction | |
KKNCFHKG_00852 | 1.2e-208 | ylxY | 3.5.1.104 | G | Sporulation protein, polysaccharide deacetylase | |
KKNCFHKG_00853 | 2.4e-231 | pepR | S | Belongs to the peptidase M16 family | ||
KKNCFHKG_00854 | 1.4e-37 | ymxH | S | YlmC YmxH family | ||
KKNCFHKG_00855 | 2.5e-186 | dpaA | 1.1.1.29, 1.1.1.399, 1.1.1.95 | CH | Dipicolinate synthase subunit A | |
KKNCFHKG_00856 | 2.6e-109 | spoVFB | H | Together with DpaA, catalyzes the conversion of dihydrodipicolinate to dipicolinate (DPA) | ||
KKNCFHKG_00857 | 9.9e-194 | asd | 1.2.1.11 | E | Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate | |
KKNCFHKG_00858 | 1.1e-228 | dapG | 1.1.1.3, 2.7.2.4 | E | Belongs to the aspartokinase family | |
KKNCFHKG_00859 | 3.9e-159 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
KKNCFHKG_00860 | 0.0 | rnjB | S | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
KKNCFHKG_00861 | 2.2e-131 | tepA | 3.4.21.92 | OU | COG0740 Protease subunit of ATP-dependent Clp proteases | |
KKNCFHKG_00862 | 4.3e-35 | S | YlzJ-like protein | |||
KKNCFHKG_00863 | 0.0 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
KKNCFHKG_00864 | 9.1e-195 | tcsA | S | ABC-type transport system, periplasmic component surface lipoprotein | ||
KKNCFHKG_00865 | 8e-285 | xylG | 3.6.3.17 | S | ABC transporter, ATP-binding protein | |
KKNCFHKG_00866 | 5.8e-186 | yufP | S | Belongs to the binding-protein-dependent transport system permease family | ||
KKNCFHKG_00867 | 1.8e-170 | yufQ | S | Belongs to the binding-protein-dependent transport system permease family | ||
KKNCFHKG_00868 | 2.1e-238 | ymfF | S | Peptidase M16 | ||
KKNCFHKG_00869 | 2e-244 | ymfH | S | zinc protease | ||
KKNCFHKG_00870 | 5e-128 | 1.1.1.100 | S | Catalyzes the first of the two reduction steps in the elongation cycle of fatty acid synthesis | ||
KKNCFHKG_00871 | 6.4e-41 | ymfJ | S | Protein of unknown function (DUF3243) | ||
KKNCFHKG_00872 | 1e-142 | ymfK | S | Protein of unknown function (DUF3388) | ||
KKNCFHKG_00873 | 9.9e-137 | ymfM | S | protein conserved in bacteria | ||
KKNCFHKG_00874 | 1.3e-99 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
KKNCFHKG_00875 | 2.4e-223 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
KKNCFHKG_00876 | 4.9e-188 | 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 | ||
KKNCFHKG_00878 | 2.3e-147 | yvaK | 3.1.1.1 | S | BAAT / Acyl-CoA thioester hydrolase C terminal | |
KKNCFHKG_00880 | 7.2e-138 | I | alpha/beta hydrolase fold | |||
KKNCFHKG_00881 | 2.6e-95 | 1.5.1.38 | S | FMN reductase | ||
KKNCFHKG_00882 | 2.5e-27 | K | sequence-specific DNA binding | |||
KKNCFHKG_00883 | 2.2e-240 | yhaO | L | Calcineurin-like phosphoesterase superfamily domain | ||
KKNCFHKG_00884 | 0.0 | L | AAA domain | |||
KKNCFHKG_00885 | 8.5e-57 | mmgB | 1.1.1.157 | I | Dehydrogenase | |
KKNCFHKG_00886 | 4.8e-53 | mmgB | 1.1.1.157 | I | Dehydrogenase | |
KKNCFHKG_00887 | 5.7e-245 | yeeO | V | Mate efflux family protein | ||
KKNCFHKG_00889 | 5.7e-112 | yhbD | K | Protein of unknown function (DUF4004) | ||
KKNCFHKG_00890 | 1.4e-225 | yhdR | 2.6.1.1 | E | Aminotransferase | |
KKNCFHKG_00891 | 1.5e-109 | proA_2 | H | Methyltransferase | ||
KKNCFHKG_00892 | 0.0 | rafA | 3.2.1.22 | G | Alpha-galactosidase | |
KKNCFHKG_00893 | 1.1e-50 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
KKNCFHKG_00894 | 4.7e-268 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
KKNCFHKG_00895 | 1.7e-16 | G | Peptidase_C39 like family | |||
KKNCFHKG_00896 | 2.7e-81 | thiW | S | Thiamine-precursor transporter protein (ThiW) | ||
KKNCFHKG_00897 | 4.1e-26 | yjhE | S | Phage tail protein | ||
KKNCFHKG_00898 | 1.5e-146 | hel | M | 5'-nucleotidase, lipoprotein e(P4) | ||
KKNCFHKG_00901 | 1.8e-209 | ydbM | 1.3.8.1 | I | acyl-CoA dehydrogenase | |
KKNCFHKG_00902 | 2.5e-35 | K | ArsR family transcriptional regulator | |||
KKNCFHKG_00903 | 2.5e-225 | galK | 2.7.1.6 | G | Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) | |
KKNCFHKG_00904 | 3.6e-193 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
KKNCFHKG_00905 | 8.3e-279 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
KKNCFHKG_00906 | 4.1e-200 | galM | 2.7.1.6, 5.1.3.3 | G | Converts alpha-aldose to the beta-anomer | |
KKNCFHKG_00907 | 1.1e-181 | K | Transcriptional regulator | |||
KKNCFHKG_00909 | 1.5e-31 | S | Cold-inducible protein YdjO | |||
KKNCFHKG_00910 | 5.7e-14 | |||||
KKNCFHKG_00912 | 1.2e-165 | cvfB | S | protein conserved in bacteria | ||
KKNCFHKG_00913 | 4.4e-70 | yaeR | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | ||
KKNCFHKG_00914 | 5.1e-189 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
KKNCFHKG_00915 | 6.2e-176 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to L- homoserine, forming acetyl-L-homoserine | |
KKNCFHKG_00916 | 6.2e-274 | yusP | P | Major facilitator superfamily | ||
KKNCFHKG_00917 | 1.8e-212 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
KKNCFHKG_00918 | 8.3e-131 | 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 | |
KKNCFHKG_00919 | 2.8e-123 | gntR1 | K | transcriptional | ||
KKNCFHKG_00920 | 4.1e-170 | sle1 | 3.5.1.28 | CBM50 | M | COG1388 FOG LysM repeat |
KKNCFHKG_00921 | 5.9e-240 | NT | Methyl-accepting chemotaxis-like domains (chemotaxis sensory transducer). | |||
KKNCFHKG_00922 | 0.0 | pbpC | 3.4.16.4 | M | Penicillin-binding Protein | |
KKNCFHKG_00923 | 3.5e-167 | tagO | 2.7.8.33, 2.7.8.35 | M | COG0472 UDP-N-acetylmuramyl pentapeptide phosphotransferase UDP-N-acetylglucosamine-1-phosphate transferase | |
KKNCFHKG_00924 | 4e-113 | yvyE | 3.4.13.9 | S | Domain of unknown function (DUF1949) | |
KKNCFHKG_00925 | 5.1e-207 | degS | 2.7.13.3 | T | Member of the two-component regulatory system DegS DegU, which plays an important role in the transition growth phase | |
KKNCFHKG_00926 | 1.4e-124 | degU | KT | COG2197 Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
KKNCFHKG_00927 | 6.4e-260 | yfnA | E | amino acid | ||
KKNCFHKG_00928 | 1.4e-153 | degV | S | protein conserved in bacteria | ||
KKNCFHKG_00929 | 1.9e-253 | comFA | L | COG4098 Superfamily II DNA RNA helicase required for DNA uptake (late competence protein) | ||
KKNCFHKG_00930 | 1.5e-132 | comFC | S | Phosphoribosyl transferase domain | ||
KKNCFHKG_00931 | 4.2e-68 | yvyF | S | flagellar protein | ||
KKNCFHKG_00932 | 8.8e-38 | flgM | KNU | Negative regulator of flagellin synthesis | ||
KKNCFHKG_00933 | 6.5e-68 | flgN | NOU | FlgN protein | ||
KKNCFHKG_00934 | 1.5e-286 | flgK | N | flagellar hook-associated protein | ||
KKNCFHKG_00935 | 4.3e-153 | flgL | N | Belongs to the bacterial flagellin family | ||
KKNCFHKG_00936 | 9.5e-77 | fliW | S | Binds to the C-terminal region of flagellin, which is implicated in polymerization, and participates in the assembly of the flagellum | ||
KKNCFHKG_00937 | 1.8e-34 | csrA | T | Could accelerate the degradation of some genes transcripts potentially through selective RNA binding | ||
KKNCFHKG_00938 | 5e-129 | fliC | N | Flagellin is the subunit protein which polymerizes to form the filaments of bacterial flagella | ||
KKNCFHKG_00939 | 3.8e-07 | fliC | N | Bacterial flagellin C-terminal helical region | ||
KKNCFHKG_00940 | 3e-96 | K | Glycerol-3-phosphate responsive antiterminator | |||
KKNCFHKG_00941 | 1.5e-113 | sapB | S | MgtC SapB transporter | ||
KKNCFHKG_00942 | 2.2e-151 | araL | 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
KKNCFHKG_00943 | 6.3e-145 | G | myo-inosose-2 dehydratase activity | |||
KKNCFHKG_00944 | 5.5e-245 | EGP | Sugar (and other) transporter | |||
KKNCFHKG_00946 | 3.5e-178 | E | COG1113 Gamma-aminobutyrate permease and related permeases | |||
KKNCFHKG_00947 | 0.0 | ycbZ | 3.4.21.53 | O | AAA domain | |
KKNCFHKG_00949 | 3e-110 | mpg | 3.2.2.21 | L | Belongs to the DNA glycosylase MPG family | |
KKNCFHKG_00950 | 7.8e-61 | flaG | N | flagellar protein FlaG | ||
KKNCFHKG_00951 | 2.3e-234 | fliD | N | morphogenesis and for the elongation of the flagellar filament by facilitating polymerization of the flagellin monomers at the tip of growing filament. Forms a capping structure, which prevents flagellin subunits (transported through the central channel of the flagellum) from leaking out without polymerization at the distal end | ||
KKNCFHKG_00952 | 1.6e-67 | fliS | N | flagellar protein FliS | ||
KKNCFHKG_00953 | 5.7e-53 | fliT | S | bacterial-type flagellum organization | ||
KKNCFHKG_00954 | 1.3e-96 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
KKNCFHKG_00955 | 2.6e-306 | ggtA | 2.3.2.2, 3.4.19.13 | E | gamma-glutamyltransferase | |
KKNCFHKG_00956 | 0.0 | secA | U | Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. Has a central role in coupling the hydrolysis of ATP to the transfer of proteins into and across the cell membrane, serving as an ATP-driven molecular motor driving the stepwise translocation of polypeptide chains across the membrane | ||
KKNCFHKG_00957 | 1.8e-168 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
KKNCFHKG_00958 | 2.6e-155 | yvjA | S | Uncharacterized protein conserved in bacteria (DUF2179) | ||
KKNCFHKG_00959 | 5.5e-50 | cccB | C | COG2010 Cytochrome c, mono- and diheme variants | ||
KKNCFHKG_00960 | 7.1e-124 | ftsE | D | cell division ATP-binding protein FtsE | ||
KKNCFHKG_00961 | 4.5e-155 | ftsX | D | Part of the ABC transporter FtsEX involved in asymmetric cellular division facilitating the initiation of sporulation | ||
KKNCFHKG_00962 | 2.2e-89 | D | peptidase | |||
KKNCFHKG_00963 | 6.2e-271 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
KKNCFHKG_00964 | 4.3e-247 | metY | 2.5.1.49 | E | O-acetylhomoserine | |
KKNCFHKG_00965 | 3.3e-183 | 1.1.1.3 | E | homoserine dehydrogenase | ||
KKNCFHKG_00966 | 9.2e-267 | ctpB | 3.4.21.102 | M | Belongs to the peptidase S41A family | |
KKNCFHKG_00967 | 1.8e-199 | minJ | O | COG0265 Trypsin-like serine proteases, typically periplasmic, contain C-terminal PDZ domain | ||
KKNCFHKG_00968 | 2.6e-164 | yclN | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
KKNCFHKG_00969 | 7.4e-164 | fatC | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
KKNCFHKG_00970 | 6.2e-137 | yclP | 3.6.3.34 | P | ABC transporter, ATP-binding protein | |
KKNCFHKG_00971 | 5.9e-169 | yclQ | P | COG4607 ABC-type enterochelin transport system, periplasmic component | ||
KKNCFHKG_00972 | 1.6e-82 | |||||
KKNCFHKG_00973 | 3.6e-20 | |||||
KKNCFHKG_00974 | 8.4e-32 | S | Family of unknown function (DUF5316) | |||
KKNCFHKG_00975 | 0.0 | phoR | 2.7.13.3 | T | Signal transduction histidine kinase | |
KKNCFHKG_00976 | 1.6e-123 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
KKNCFHKG_00977 | 4.1e-28 | S | Family of unknown function (DUF5316) | |||
KKNCFHKG_00978 | 0.0 | essC | D | COG1674 DNA segregation ATPase FtsK SpoIIIE and related proteins | ||
KKNCFHKG_00979 | 4.4e-218 | essB | S | WXG100 protein secretion system (Wss), protein YukC | ||
KKNCFHKG_00980 | 1.8e-38 | yukD | S | WXG100 protein secretion system (Wss), protein YukD | ||
KKNCFHKG_00981 | 3.3e-234 | esaA | S | domain protein | ||
KKNCFHKG_00982 | 2.5e-211 | yxjG | 2.1.1.14 | E | Methionine synthase | |
KKNCFHKG_00983 | 7e-223 | ackA | 2.7.2.1, 2.7.2.15 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
KKNCFHKG_00984 | 1.4e-148 | pocR | K | Sensory domain found in PocR | ||
KKNCFHKG_00986 | 1.4e-37 | L | Belongs to the 'phage' integrase family | |||
KKNCFHKG_00987 | 3.6e-82 | ywrC | K | Transcriptional regulator | ||
KKNCFHKG_00988 | 6.3e-100 | chrA | P | COG2059 Chromate transport protein ChrA | ||
KKNCFHKG_00989 | 1.3e-91 | ywrA | P | COG2059 Chromate transport protein ChrA | ||
KKNCFHKG_00990 | 0.0 | 6.2.1.1, 6.2.1.16 | I | AMP-dependent synthetase | ||
KKNCFHKG_00991 | 7e-34 | ykuS | S | Belongs to the UPF0180 family | ||
KKNCFHKG_00992 | 0.0 | pepF2 | E | COG1164 Oligoendopeptidase F | ||
KKNCFHKG_00993 | 7.3e-258 | pepC | 3.4.22.40 | E | Papain family cysteine protease | |
KKNCFHKG_00994 | 1e-213 | yhaP | CP | COG1668 ABC-type Na efflux pump, permease component | ||
KKNCFHKG_00995 | 3.6e-168 | yhaQ | S | ABC transporter, ATP-binding protein | ||
KKNCFHKG_00996 | 4.8e-79 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
KKNCFHKG_00997 | 1.7e-167 | gmuE | 2.7.1.2, 2.7.1.4 | GK | COG1940 Transcriptional regulator sugar kinase | |
KKNCFHKG_01003 | 8.1e-134 | yjcH | P | COG2382 Enterochelin esterase and related enzymes | ||
KKNCFHKG_01004 | 4.8e-93 | yjcG | J | Belongs to the 2H phosphoesterase superfamily. YjcG family | ||
KKNCFHKG_01005 | 7.9e-73 | yjcF | S | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
KKNCFHKG_01007 | 4.5e-39 | spoVIF | S | Stage VI sporulation protein F | ||
KKNCFHKG_01009 | 3.3e-56 | spoVAE | S | stage V sporulation protein | ||
KKNCFHKG_01010 | 1.8e-187 | spoVAD | I | Stage V sporulation protein AD | ||
KKNCFHKG_01011 | 3.6e-82 | spoVAC | S | stage V sporulation protein AC | ||
KKNCFHKG_01012 | 3.6e-79 | S | Sporulation lipoprotein YhcN/YlaJ (Spore_YhcN_YlaJ) | |||
KKNCFHKG_01014 | 8.4e-60 | S | Protein of unknown function (DUF1360) | |||
KKNCFHKG_01015 | 9.6e-82 | cotY | S | Spore coat protein | ||
KKNCFHKG_01018 | 7.3e-141 | fabI | 1.3.1.10, 1.3.1.9 | I | Enoyl- acyl-carrier-protein reductase NADH | |
KKNCFHKG_01019 | 4.5e-137 | prpE | 3.6.1.41 | T | Asymmetrically hydrolyzes Ap4p to yield AMP and ATP | |
KKNCFHKG_01020 | 1.5e-163 | yjbO | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
KKNCFHKG_01021 | 4.9e-153 | nadK | 2.7.1.23 | G | 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 | |
KKNCFHKG_01022 | 1.2e-120 | yjbM | 2.7.6.5 | S | GTP pyrophosphokinase | |
KKNCFHKG_01023 | 4.9e-66 | yjbL | S | Belongs to the UPF0738 family | ||
KKNCFHKG_01024 | 5.5e-101 | yjbK | S | protein conserved in bacteria | ||
KKNCFHKG_01025 | 2.6e-98 | yjbJ | M | COG0741 Soluble lytic murein transglycosylase and related regulatory proteins (some contain LysM invasin domains) | ||
KKNCFHKG_01026 | 1.5e-73 | yjbI | S | COG2346 Truncated hemoglobins | ||
KKNCFHKG_01027 | 5e-159 | yjbH | Q | dithiol-disulfide isomerase involved in polyketide biosynthesis | ||
KKNCFHKG_01029 | 0.0 | pepF | E | oligoendopeptidase F | ||
KKNCFHKG_01030 | 5.1e-226 | yjbF | S | Competence protein | ||
KKNCFHKG_01031 | 1.7e-119 | mecA | NOT | Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis. Acts negatively in the development of competence by binding ComK and recruiting it to the ClpCP protease. When overexpressed, inhibits sporulation. Also involved in Spx degradation by ClpC | ||
KKNCFHKG_01032 | 1.6e-67 | spxA | 1.20.4.1 | K | Interferes with activator-stimulated transcription by interaction with the RNA polymerase alpha-CTD. May function to globally reduce transcription of genes involved in growth- and development-promoting processes and to increase transcription of genes involved in thiol homeostasis, during periods of extreme stress | |
KKNCFHKG_01033 | 1.1e-172 | oppF | E | Belongs to the ABC transporter superfamily | ||
KKNCFHKG_01034 | 1.1e-195 | oppD | P | Belongs to the ABC transporter superfamily | ||
KKNCFHKG_01035 | 6.1e-180 | oppC | EP | COG1173 ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
KKNCFHKG_01036 | 6.4e-152 | oppB | P | COG0601 ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
KKNCFHKG_01037 | 1.3e-299 | dppE_1 | E | ABC transporter substrate-binding protein | ||
KKNCFHKG_01038 | 3.1e-48 | S | Domain of unknown function (DUF3899) | |||
KKNCFHKG_01039 | 1.7e-182 | trpS | 6.1.1.2 | J | Tryptophanyl-tRNA synthetase | |
KKNCFHKG_01040 | 5e-147 | yjbA | S | Belongs to the UPF0736 family | ||
KKNCFHKG_01041 | 0.0 | oppA1 | E | COG0747 ABC-type dipeptide transport system, periplasmic component | ||
KKNCFHKG_01042 | 4.5e-134 | oppC | EP | binding-protein-dependent transport systems inner membrane component | ||
KKNCFHKG_01043 | 1.1e-167 | oppB | P | COG0601 ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
KKNCFHKG_01044 | 1.3e-176 | oppF | P | Belongs to the ABC transporter superfamily | ||
KKNCFHKG_01045 | 1.2e-191 | oppD | P | Belongs to the ABC transporter superfamily | ||
KKNCFHKG_01046 | 2.8e-148 | yjaZ | O | Zn-dependent protease | ||
KKNCFHKG_01047 | 1.8e-234 | fabF | 2.3.1.179 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP | |
KKNCFHKG_01048 | 3.3e-172 | fabH | 2.3.1.180 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids | |
KKNCFHKG_01050 | 5.1e-147 | 5.1.3.2 | GM | ADP-glyceromanno-heptose 6-epimerase activity | ||
KKNCFHKG_01051 | 0.0 | clpB | O | Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE | ||
KKNCFHKG_01052 | 6.2e-27 | yjzC | S | YjzC-like protein | ||
KKNCFHKG_01053 | 9.5e-52 | yitW | S | metal-sulfur cluster biosynthetic enzyme | ||
KKNCFHKG_01054 | 2.7e-154 | yitU | 3.1.3.104 | S | hydrolases of the HAD superfamily | |
KKNCFHKG_01055 | 6.3e-25 | S | Protein of unknown function (DUF3813) | |||
KKNCFHKG_01056 | 3.6e-157 | yitS | S | protein conserved in bacteria | ||
KKNCFHKG_01057 | 1.5e-103 | yisN | S | Protein of unknown function (DUF2777) | ||
KKNCFHKG_01058 | 3.3e-59 | yisL | S | UPF0344 protein | ||
KKNCFHKG_01059 | 1.3e-162 | yisK | Q | COG0179 2-keto-4-pentenoate hydratase 2-oxohepta-3-ene-1,7-dioic acid hydratase (catechol pathway) | ||
KKNCFHKG_01060 | 1.9e-222 | P | Protein of unknown function (DUF418) | |||
KKNCFHKG_01061 | 1.6e-32 | gerPA | S | Spore germination protein | ||
KKNCFHKG_01062 | 1.4e-97 | gerPC | S | Spore germination protein | ||
KKNCFHKG_01063 | 2e-25 | gerPD | S | Spore germination protein | ||
KKNCFHKG_01064 | 2.9e-70 | gerPE | S | Spore germination protein GerPE | ||
KKNCFHKG_01065 | 4.7e-29 | gerPF | S | Spore germination protein gerPA/gerPF | ||
KKNCFHKG_01066 | 0.0 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
KKNCFHKG_01067 | 0.0 | addB | 3.1.21.3, 3.6.4.12 | L | ATP-dependent helicase deoxyribonuclease subunit B | |
KKNCFHKG_01069 | 1.8e-142 | S | Mitochondrial biogenesis AIM24 | |||
KKNCFHKG_01070 | 8.2e-96 | comK | K | Competence transcription factor | ||
KKNCFHKG_01071 | 3.7e-08 | S | IDEAL | |||
KKNCFHKG_01072 | 8.4e-208 | yhfN | 3.4.24.84 | O | Peptidase M48 | |
KKNCFHKG_01073 | 5.7e-41 | azlD | S | branched-chain amino acid | ||
KKNCFHKG_01074 | 7.9e-118 | azlC | E | AzlC protein | ||
KKNCFHKG_01075 | 1.1e-294 | fadD | 6.2.1.3 | IQ | Activates fatty acids by binding to coenzyme A | |
KKNCFHKG_01076 | 8.5e-187 | lplJ | 6.3.1.20 | H | Lipoate-protein ligase | |
KKNCFHKG_01077 | 3.1e-64 | ytkA | S | YtkA-like | ||
KKNCFHKG_01078 | 9.7e-103 | ypmQ | S | protein SCO1 SenC PrrC, involved in biogenesis of respiratory and photosynthetic systems | ||
KKNCFHKG_01079 | 1.5e-17 | aldA | 1.2.1.21, 1.2.1.22 | C | Catalyzes the oxidation of malonate semialdehyde (MSA) and methylmalonate semialdehyde (MMSA) into acetyl-CoA and propanoyl-CoA, respectively | |
KKNCFHKG_01080 | 4.1e-162 | EG | EamA-like transporter family | |||
KKNCFHKG_01081 | 2.9e-58 | EGP | Major facilitator Superfamily | |||
KKNCFHKG_01082 | 2.3e-146 | yhgE | S | YhgE Pip N-terminal domain protein | ||
KKNCFHKG_01083 | 2.4e-101 | yhgD | K | Transcriptional regulator | ||
KKNCFHKG_01084 | 6.8e-104 | 2.7.1.202 | K | transcriptional regulator, MtlR | ||
KKNCFHKG_01085 | 1.7e-35 | 2.7.1.202 | K | transcriptional regulator, MtlR | ||
KKNCFHKG_01086 | 1.5e-31 | 2.7.1.196, 2.7.1.205 | G | phosphotransferase system | ||
KKNCFHKG_01087 | 3.5e-161 | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | |||
KKNCFHKG_01088 | 1.2e-64 | S | Protein of unknown function (DUF2512) | |||
KKNCFHKG_01089 | 2.5e-18 | L | PFAM Transposase, IS116 IS110 IS902 | |||
KKNCFHKG_01090 | 2.5e-155 | kdsA | 2.5.1.55 | M | Belongs to the KdsA family | |
KKNCFHKG_01091 | 1.1e-175 | kdsD | 5.3.1.13 | M | Belongs to the SIS family. GutQ KpsF subfamily | |
KKNCFHKG_01092 | 2.9e-219 | metB | 2.5.1.48, 4.4.1.1, 4.4.1.2, 4.4.1.8 | E | cystathionine | |
KKNCFHKG_01093 | 3.9e-215 | metC | 2.5.1.48, 4.4.1.1, 4.4.1.2, 4.4.1.8 | E | cystathionine | |
KKNCFHKG_01094 | 0.0 | treP | 2.4.1.64 | GH65 | G | Glycoside hydrolase, family 65 |
KKNCFHKG_01095 | 3.2e-147 | G | Binding-protein-dependent transport system inner membrane component | |||
KKNCFHKG_01096 | 2e-217 | sugA | G | Binding-protein-dependent transport system inner membrane component | ||
KKNCFHKG_01097 | 1.7e-224 | G | Bacterial extracellular solute-binding protein | |||
KKNCFHKG_01098 | 9.4e-130 | K | helix_turn_helix, arabinose operon control protein | |||
KKNCFHKG_01099 | 1.6e-137 | gumM | 2.4.1.187, 2.4.1.252 | GT26,GT4 | M | Catalyzes the conversion of GlcNAc-PP-undecaprenol into ManNAc-GlcNAc-PP-undecaprenol, the first committed lipid intermediate in the de novo synthesis of teichoic acid |
KKNCFHKG_01100 | 1.5e-52 | S | Iron-sulphur cluster biosynthesis | |||
KKNCFHKG_01101 | 1.1e-175 | yhfP | 1.1.1.1 | C | Quinone oxidoreductase | |
KKNCFHKG_01102 | 1.3e-159 | yeaB | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
KKNCFHKG_01103 | 0.0 | pmmB | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase | |
KKNCFHKG_01104 | 1.9e-72 | 3.4.21.121 | O | Belongs to the peptidase S8 family | ||
KKNCFHKG_01105 | 2e-83 | |||||
KKNCFHKG_01106 | 6e-146 | tagH | 3.6.3.38, 3.6.3.40 | GM | Part of the ABC transporter complex TagGH involved in teichoic acids export. Responsible for energy coupling to the transport system | |
KKNCFHKG_01107 | 9.5e-29 | IQ | Short-chain dehydrogenase reductase sdr | |||
KKNCFHKG_01108 | 2.3e-28 | qoxD | 1.10.3.12, 1.9.3.1 | C | quinol oxidase, subunit | |
KKNCFHKG_01109 | 5.2e-110 | cyoC | 1.10.3.12, 1.9.3.1 | C | quinol oxidase, subunit | |
KKNCFHKG_01110 | 0.0 | qoxB | 1.10.3.12, 1.9.3.1 | C | Cytochrome c oxidase is the component of the respiratory chain that catalyzes the reduction of oxygen to water. Subunits 1- 3 form the functional core of the enzyme complex. CO I is the catalytic subunit of the enzyme. Electrons originating in cytochrome c are transferred via the copper A center of subunit 2 and heme A of subunit 1 to the bimetallic center formed by heme A3 and copper B | |
KKNCFHKG_01111 | 6.6e-157 | cyoA | 1.10.3.10, 1.10.3.12 | C | Catalyzes quinol oxidation with the concomitant reduction of oxygen to water. Subunit II transfers the electrons from a quinol to the binuclear center of the catalytic subunit I | |
KKNCFHKG_01112 | 1.2e-123 | yhcW | 5.4.2.6 | S | hydrolase | |
KKNCFHKG_01113 | 2.5e-164 | lytR_1 | K | May catalyze the final step in cell wall teichoic acid biosynthesis, the transfer of the anionic cell wall polymers (APs) from their lipid-linked precursor to the cell wall peptidoglycan (PG) | ||
KKNCFHKG_01114 | 1.3e-125 | pgmB | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | S | Haloacid dehalogenase-like hydrolase |
KKNCFHKG_01115 | 0.0 | mapA | 2.4.1.8 | GH65 | G | Glycoside hydrolase, family 65 |
KKNCFHKG_01116 | 6.3e-260 | G | Major facilitator Superfamily | |||
KKNCFHKG_01117 | 3.2e-186 | malR | K | Transcriptional regulator | ||
KKNCFHKG_01118 | 9.7e-21 | T | PhoQ Sensor | |||
KKNCFHKG_01119 | 2.2e-19 | |||||
KKNCFHKG_01120 | 0.0 | ppc | 4.1.1.31 | C | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
KKNCFHKG_01122 | 9.9e-177 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
KKNCFHKG_01123 | 9.1e-74 | yabE | S | 3D domain | ||
KKNCFHKG_01124 | 2e-32 | relA_2 | 2.7.6.5, 3.1.7.2 | KT | HD domain | |
KKNCFHKG_01125 | 0.0 | pip | S | YhgE Pip N-terminal domain protein | ||
KKNCFHKG_01126 | 2.9e-48 | yqgV | S | Thiamine-binding protein | ||
KKNCFHKG_01127 | 4.2e-200 | pgl | 3.1.1.31 | G | 6-phosphogluconolactonase | |
KKNCFHKG_01128 | 0.0 | S | ATPase. Has a role at an early stage in the morphogenesis of the spore coat | |||
KKNCFHKG_01129 | 0.0 | levR | K | PTS system fructose IIA component | ||
KKNCFHKG_01130 | 4e-84 | manX | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
KKNCFHKG_01131 | 1.6e-177 | manL | 2.7.1.191 | G | PTS system mannose fructose sorbose family | |
KKNCFHKG_01132 | 1.2e-117 | manY | G | COG3715 Phosphotransferase system, mannose fructose N-acetylgalactosamine-specific component IIC | ||
KKNCFHKG_01133 | 9e-167 | manN | G | COG3716 Phosphotransferase system, mannose fructose N-acetylgalactosamine-specific component IID | ||
KKNCFHKG_01135 | 1.6e-64 | manO | S | Domain of unknown function (DUF956) | ||
KKNCFHKG_01136 | 5.6e-211 | prpC | 2.3.3.1, 2.3.3.5 | C | Belongs to the citrate synthase family | |
KKNCFHKG_01137 | 6.9e-278 | prpD | 4.2.1.79 | S | 2-methylcitrate dehydratase | |
KKNCFHKG_01138 | 1.9e-164 | prpB | 4.1.3.30 | G | Catalyzes the thermodynamically favored C-C bond cleavage of (2R,3S)-2-methylisocitrate to yield pyruvate and succinate | |
KKNCFHKG_01139 | 2.7e-85 | S | Heat induced stress protein YflT | |||
KKNCFHKG_01140 | 1.5e-253 | nylA | 3.5.1.4 | J | Belongs to the amidase family | |
KKNCFHKG_01141 | 1.4e-50 | M1-594 | S | Thiamine-binding protein | ||
KKNCFHKG_01142 | 8.4e-137 | ssuC_1 | P | binding-protein-dependent transport systems inner membrane component | ||
KKNCFHKG_01143 | 2.9e-182 | M1-596 | P | COG0715 ABC-type nitrate sulfonate bicarbonate transport systems, periplasmic components | ||
KKNCFHKG_01144 | 6.3e-134 | P | ABC transporter, ATP-binding protein | |||
KKNCFHKG_01145 | 3.1e-159 | thrB | 2.7.1.39 | E | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
KKNCFHKG_01146 | 5.2e-190 | thrC | 4.2.3.1 | E | Catalyzes the gamma-elimination of phosphate from L- phosphohomoserine and the beta-addition of water to produce L- threonine | |
KKNCFHKG_01147 | 4.6e-241 | hom | 1.1.1.3 | E | homoserine dehydrogenase | |
KKNCFHKG_01148 | 1.6e-148 | 3.5.3.1, 3.5.3.11 | E | Belongs to the arginase family | ||
KKNCFHKG_01149 | 8.6e-16 | S | Protein of unknown function (DUF4064) | |||
KKNCFHKG_01150 | 5e-284 | nnrD | 4.2.1.136, 5.1.99.6 | G | Bifunctional enzyme that catalyzes the epimerization of the S- and R-forms of NAD(P)HX and the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. This allows the repair of both epimers of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration | |
KKNCFHKG_01151 | 9.1e-164 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
KKNCFHKG_01152 | 9.6e-48 | yhdT | S | Sodium pantothenate symporter | ||
KKNCFHKG_01153 | 8.8e-233 | panF | H | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
KKNCFHKG_01156 | 4.5e-169 | corA | P | Mg2 transporter protein CorA family protein | ||
KKNCFHKG_01157 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
KKNCFHKG_01158 | 8.5e-199 | yfmL | 3.6.4.13 | L | COG0513 Superfamily II DNA and RNA helicases | |
KKNCFHKG_01159 | 3.2e-76 | |||||
KKNCFHKG_01160 | 3.6e-76 | lytE | CBM50 | M | COG0791 Cell wall-associated hydrolases (invasion-associated proteins) | |
KKNCFHKG_01161 | 1.1e-138 | map | 3.4.11.18 | E | Methionine aminopeptidase | |
KKNCFHKG_01162 | 7.9e-100 | bioY | S | Biotin biosynthesis protein | ||
KKNCFHKG_01163 | 1.7e-187 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
KKNCFHKG_01164 | 8.5e-148 | aacC | 2.3.1.81 | V | aminoglycoside | |
KKNCFHKG_01165 | 8.1e-217 | ykvU | S | COG2244 Membrane protein involved in the export of O-antigen and teichoic acid | ||
KKNCFHKG_01166 | 2.8e-70 | yxiE | T | Belongs to the universal stress protein A family | ||
KKNCFHKG_01167 | 2.4e-27 | |||||
KKNCFHKG_01168 | 1.1e-73 | |||||
KKNCFHKG_01169 | 6.3e-226 | yfkA | S | YfkB-like domain | ||
KKNCFHKG_01170 | 6.2e-68 | gutA | G | MFS/sugar transport protein | ||
KKNCFHKG_01171 | 8.8e-136 | IQ | Short-chain dehydrogenase reductase sdr | |||
KKNCFHKG_01172 | 2.3e-72 | cymR | K | Transcriptional regulator | ||
KKNCFHKG_01173 | 2.6e-208 | iscS | 2.8.1.7 | E | Cysteine desulfurase | |
KKNCFHKG_01174 | 9.8e-224 | mnmA | 2.8.1.13 | J | Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 | |
KKNCFHKG_01175 | 1.3e-125 | S | COG0457 FOG TPR repeat | |||
KKNCFHKG_01176 | 0.0 | recD2 | 3.1.11.5 | L | DNA-dependent ATPase and ATP-dependent 5'-3' DNA helicase. Has no activity on blunt DNA or DNA with 3'-overhangs, requires at least 10 bases of 5'-ssDNA for helicase activity | |
KKNCFHKG_01177 | 2.8e-73 | yndM | S | Protein of unknown function (DUF2512) | ||
KKNCFHKG_01178 | 4e-29 | yrzR | ||||
KKNCFHKG_01180 | 4.2e-171 | yrrI | S | AI-2E family transporter | ||
KKNCFHKG_01181 | 0.0 | alaS | 6.1.1.7 | J | Catalyzes the attachment of alanine to tRNA(Ala) in a two-step reaction alanine is first activated by ATP to form Ala- AMP and then transferred to the acceptor end of tRNA(Ala). Also edits incorrectly charged Ser-tRNA(Ala) and Gly-tRNA(Ala) via its editing domain | |
KKNCFHKG_01182 | 1.1e-43 | yrzL | S | Belongs to the UPF0297 family | ||
KKNCFHKG_01183 | 6.8e-69 | yqgF | L | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
KKNCFHKG_01184 | 1.5e-41 | yrzB | S | Belongs to the UPF0473 family | ||
KKNCFHKG_01185 | 8e-202 | mltG | S | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
KKNCFHKG_01186 | 3.7e-114 | yrrM | 2.1.1.104 | S | O-methyltransferase | |
KKNCFHKG_01187 | 1.7e-111 | udk | 2.7.1.48 | F | Cytidine monophosphokinase | |
KKNCFHKG_01188 | 1.2e-77 | 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 | ||
KKNCFHKG_01189 | 7.9e-58 | yrrS | S | Protein of unknown function (DUF1510) | ||
KKNCFHKG_01190 | 6.4e-28 | yrzA | S | Protein of unknown function (DUF2536) | ||
KKNCFHKG_01191 | 4.6e-123 | 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 | |
KKNCFHKG_01192 | 2.9e-10 | S | YrhC-like protein | |||
KKNCFHKG_01194 | 3.8e-107 | ahpC | 1.11.1.15 | O | Alkyl hydroperoxide reductase | |
KKNCFHKG_01195 | 6.2e-293 | ahpF | O | Alkyl hydroperoxide reductase | ||
KKNCFHKG_01196 | 1.8e-125 | sigK | K | sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
KKNCFHKG_01197 | 6.7e-93 | pssA | 2.7.8.8 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
KKNCFHKG_01198 | 7.2e-15 | sda | S | Sporulation inhibitor A | ||
KKNCFHKG_01199 | 1.7e-149 | czcD | P | COG1230 Co Zn Cd efflux system component | ||
KKNCFHKG_01200 | 9.1e-119 | S | VIT family | |||
KKNCFHKG_01201 | 3.3e-60 | crcB | D | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
KKNCFHKG_01202 | 1.2e-58 | crcB | D | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
KKNCFHKG_01203 | 6.5e-78 | lemA | S | LemA family | ||
KKNCFHKG_01204 | 1.3e-116 | S | TPM domain | |||
KKNCFHKG_01205 | 1.2e-98 | CO | alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen | |||
KKNCFHKG_01206 | 2.7e-22 | S | Short C-terminal domain | |||
KKNCFHKG_01207 | 3.9e-75 | hsp18 | O | Belongs to the small heat shock protein (HSP20) family | ||
KKNCFHKG_01208 | 5.1e-225 | mco | 1.16.3.3 | Q | multicopper oxidases | |
KKNCFHKG_01209 | 1.6e-205 | ysfB | KT | regulator | ||
KKNCFHKG_01210 | 7.7e-258 | glcD | 1.1.3.15 | C | Glycolate oxidase subunit | |
KKNCFHKG_01211 | 8.1e-257 | glcF | C | Glycolate oxidase | ||
KKNCFHKG_01212 | 3.8e-93 | yqeG | S | hydrolase of the HAD superfamily | ||
KKNCFHKG_01213 | 9.1e-214 | yqeH | S | In Bacillus subtilis this enzyme appears to be involved in 30S ribosomal RNA subunit biogenesis | ||
KKNCFHKG_01214 | 8.1e-162 | aroE | 1.1.1.25 | E | Involved in the biosynthesis of the chorismate, which leads to the biosynthesis of aromatic amino acids. Catalyzes the reversible NADPH linked reduction of 3-dehydroshikimate (DHSA) to yield shikimate (SA) | |
KKNCFHKG_01215 | 2.4e-44 | yhbY | J | RNA-binding protein containing KH domain, possibly ribosomal protein | ||
KKNCFHKG_01216 | 5e-107 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
KKNCFHKG_01217 | 3.4e-103 | nadD | 2.7.6.3, 2.7.7.18 | H | HD superfamily hydrolase involved in NAD metabolism | |
KKNCFHKG_01218 | 1.4e-59 | rsfS | J | Functions as a ribosomal silencing factor. Interacts with ribosomal protein L14 (rplN), blocking formation of intersubunit bridge B8. Prevents association of the 30S and 50S ribosomal subunits and the formation of functional ribosomes, thus repressing translation | ||
KKNCFHKG_01219 | 2.5e-146 | cmoA | S | Methyltransferase domain | ||
KKNCFHKG_01220 | 1.1e-147 | comER | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | ||
KKNCFHKG_01221 | 8.8e-93 | comEA | L | COG1555 DNA uptake protein and related DNA-binding proteins | ||
KKNCFHKG_01222 | 2.1e-111 | comEB | 3.5.4.12 | F | COG2131 Deoxycytidylate deaminase | |
KKNCFHKG_01223 | 0.0 | comEC | S | Competence protein ComEC | ||
KKNCFHKG_01225 | 1e-187 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
KKNCFHKG_01226 | 3.7e-33 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
KKNCFHKG_01227 | 4.7e-202 | gpr | 3.4.24.78 | C | Initiates the rapid degradation of small, acid-soluble proteins during spore germination | |
KKNCFHKG_01228 | 3.8e-221 | spoIIP | M | stage II sporulation protein P | ||
KKNCFHKG_01229 | 0.0 | lepA | M | Required for accurate and efficient protein synthesis under certain stress conditions. May act as a fidelity factor of the translation reaction, by catalyzing a one-codon backward translocation of tRNAs on improperly translocated ribosomes. Back- translocation proceeds from a post-translocation (POST) complex to a pre-translocation (PRE) complex, thus giving elongation factor G a second chance to translocate the tRNAs correctly. Binds to ribosomes in a GTP-dependent manner | ||
KKNCFHKG_01230 | 9.7e-219 | hemN | H | Involved in the biosynthesis of porphyrin-containing compound | ||
KKNCFHKG_01231 | 6.3e-185 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
KKNCFHKG_01232 | 2.1e-88 | 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 | ||
KKNCFHKG_01233 | 1.4e-307 | dnaK | O | Heat shock 70 kDa protein | ||
KKNCFHKG_01234 | 4.2e-206 | 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 | ||
KKNCFHKG_01235 | 1.5e-172 | prmA | J | Methylates ribosomal protein L11 | ||
KKNCFHKG_01236 | 7.8e-140 | 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 | |
KKNCFHKG_01237 | 4.2e-261 | yqeV | 2.8.4.5 | J | ribosomal protein S12 methylthiotransferase | |
KKNCFHKG_01238 | 1.6e-155 | yqeW | P | COG1283 Na phosphate symporter | ||
KKNCFHKG_01239 | 2.6e-48 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
KKNCFHKG_01240 | 1.2e-19 | rpsU | J | Belongs to the bacterial ribosomal protein bS21 family | ||
KKNCFHKG_01241 | 6.6e-70 | yqeY | S | Yqey-like protein | ||
KKNCFHKG_01242 | 3.2e-46 | yqfC | S | sporulation protein YqfC | ||
KKNCFHKG_01243 | 1.2e-224 | yqfD | 3.1.3.102, 3.1.3.104 | S | Stage IV sporulation | |
KKNCFHKG_01244 | 6.1e-174 | phoH | T | Phosphate starvation-inducible protein PhoH | ||
KKNCFHKG_01245 | 5.4e-55 | yqfF | S | membrane-associated HD superfamily hydrolase | ||
KKNCFHKG_01246 | 2.9e-162 | yqfF | S | membrane-associated HD superfamily hydrolase | ||
KKNCFHKG_01247 | 4.2e-83 | 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 | |
KKNCFHKG_01248 | 7.9e-67 | dgkA | 2.7.1.107, 2.7.1.66 | M | Diacylglycerol kinase | |
KKNCFHKG_01249 | 5.6e-169 | era | S | An essential GTPase that binds both GDP and GTP, with rapid nucleotide exchange. Plays a role in 16S rRNA processing and 30S ribosomal subunit biogenesis and possibly also in cell cycle regulation and energy metabolism | ||
KKNCFHKG_01250 | 3e-08 | S | YqzL-like protein | |||
KKNCFHKG_01251 | 1.6e-145 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
KKNCFHKG_01252 | 2.2e-111 | ccpN | K | CBS domain | ||
KKNCFHKG_01253 | 5.5e-144 | yqfL | 2.7.11.33, 2.7.4.28 | S | Bifunctional serine threonine kinase and phosphorylase involved in the regulation of the pyruvate, phosphate dikinase (PPDK) by catalyzing its phosphorylation dephosphorylation | |
KKNCFHKG_01254 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
KKNCFHKG_01255 | 2.8e-202 | 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 | ||
KKNCFHKG_01256 | 5.8e-89 | |||||
KKNCFHKG_01257 | 1.5e-64 | cccA | C | Cytochrome C oxidase, cbb3-type, subunit III | ||
KKNCFHKG_01258 | 6.6e-119 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
KKNCFHKG_01259 | 8.4e-207 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
KKNCFHKG_01260 | 9.8e-180 | 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 | |
KKNCFHKG_01261 | 2.2e-63 | erpA | S | Belongs to the HesB IscA family | ||
KKNCFHKG_01262 | 1.1e-59 | yuzD | S | protein conserved in bacteria | ||
KKNCFHKG_01263 | 8.6e-37 | nifU | O | COG0694 Thioredoxin-like proteins and domains | ||
KKNCFHKG_01264 | 3.1e-200 | yutH | S | Spore coat protein | ||
KKNCFHKG_01265 | 1.1e-84 | pgpA | 3.1.3.27 | I | COG1267 Phosphatidylglycerophosphatase A and related proteins | |
KKNCFHKG_01266 | 7.4e-138 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
KKNCFHKG_01267 | 4.3e-74 | yutE | S | Protein of unknown function DUF86 | ||
KKNCFHKG_01268 | 2.6e-48 | yutD | S | protein conserved in bacteria | ||
KKNCFHKG_01269 | 1e-173 | lipA | 2.8.1.8 | H | Catalyzes the radical-mediated insertion of two sulfur atoms into the C-6 and C-8 positions of the octanoyl moiety bound to the lipoyl domains of lipoate-dependent enzymes, thereby converting the octanoylated domains into lipoylated derivatives | |
KKNCFHKG_01270 | 6.7e-200 | lytH | M | Peptidase, M23 | ||
KKNCFHKG_01271 | 1e-125 | yunB | S | Sporulation protein YunB (Spo_YunB) | ||
KKNCFHKG_01272 | 5.3e-47 | yunC | S | Domain of unknown function (DUF1805) | ||
KKNCFHKG_01273 | 3.4e-277 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
KKNCFHKG_01274 | 2.2e-273 | sufB | O | FeS cluster assembly | ||
KKNCFHKG_01275 | 1.4e-75 | nifU | C | COG0822 NifU homolog involved in Fe-S cluster formation | ||
KKNCFHKG_01276 | 1.3e-237 | 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 | |
KKNCFHKG_01277 | 2.3e-240 | sufD | O | assembly protein SufD | ||
KKNCFHKG_01278 | 1.3e-142 | sufC | O | COG0396 ABC-type transport system involved in Fe-S cluster assembly, ATPase component | ||
KKNCFHKG_01280 | 1.5e-49 | traF | CO | Thioredoxin | ||
KKNCFHKG_01281 | 5.1e-63 | gcvH | E | Is also involved in protein lipoylation via its role as an octanoyl lipoyl carrier protein intermediate | ||
KKNCFHKG_01282 | 3.1e-62 | arsC | 1.20.4.1 | P | Belongs to the ArsC family | |
KKNCFHKG_01283 | 0.0 | fadE | 1.3.8.1 | I | acyl-CoA dehydrogenase | |
KKNCFHKG_01284 | 1.5e-214 | fadA | 2.3.1.16 | I | Belongs to the thiolase family | |
KKNCFHKG_01285 | 0.0 | fadB | 1.1.1.35, 4.2.1.17, 5.1.2.3 | I | 3-hydroxyacyl-CoA dehydrogenase | |
KKNCFHKG_01286 | 2.6e-14 | S | YuzL-like protein | |||
KKNCFHKG_01287 | 2.4e-40 | |||||
KKNCFHKG_01288 | 7.1e-56 | yusN | M | Coat F domain | ||
KKNCFHKG_01289 | 1.3e-213 | rodA | D | Belongs to the SEDS family | ||
KKNCFHKG_01290 | 5.7e-70 | ydbP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
KKNCFHKG_01291 | 4.3e-280 | cls2 | I | PLD-like domain | ||
KKNCFHKG_01293 | 0.0 | swrC | V | Belongs to the resistance-nodulation-cell division (RND) (TC 2.A.6) family | ||
KKNCFHKG_01294 | 5.6e-189 | M1-600 | T | Putative diguanylate phosphodiesterase | ||
KKNCFHKG_01295 | 1.1e-297 | katA | 1.11.1.6 | P | serves to protect cells from the toxic effects of hydrogen peroxide | |
KKNCFHKG_01296 | 3.5e-100 | bcrC | 3.6.1.27 | I | COG0671 Membrane-associated phospholipid phosphatase | |
KKNCFHKG_01297 | 2.9e-139 | pgdA | 3.5.1.104, 3.5.1.41 | G | Polysaccharide deacetylase | |
KKNCFHKG_01298 | 4.5e-241 | ugtP | 2.4.1.315 | GT28 | M | Monogalactosyldiacylglycerol (MGDG) synthase |
KKNCFHKG_01299 | 1.7e-122 | |||||
KKNCFHKG_01300 | 3.4e-83 | S | Putative zinc-finger | |||
KKNCFHKG_01301 | 3.7e-88 | K | Belongs to the sigma-70 factor family. ECF subfamily | |||
KKNCFHKG_01302 | 6.9e-220 | ykoN | 2.4.1.315 | GT28 | M | COG0707 UDP-N-acetylglucosamine LPS N-acetylglucosamine transferase |
KKNCFHKG_01303 | 0.0 | M | Dolichyl-phosphate-mannose-protein mannosyltransferase | |||
KKNCFHKG_01304 | 2.7e-235 | NU | cell adhesion | |||
KKNCFHKG_01306 | 3.3e-21 | eda | 4.1.2.14, 4.1.3.42 | G | 2-dehydro-3-deoxy-phosphogluconate aldolase | |
KKNCFHKG_01307 | 1.9e-75 | K | helix_turn_helix isocitrate lyase regulation | |||
KKNCFHKG_01308 | 1.7e-19 | L | Winged helix-turn helix | |||
KKNCFHKG_01309 | 2.9e-36 | uraH | 3.5.2.17 | S | Belongs to the transthyretin family. 5-hydroxyisourate hydrolase subfamily | |
KKNCFHKG_01310 | 2.1e-210 | P | Monooxygenase | |||
KKNCFHKG_01311 | 2.2e-42 | uraD | 1.7.3.3, 3.5.1.41, 4.1.1.97 | S | OHCU decarboxylase | |
KKNCFHKG_01312 | 3e-155 | pbuX | F | Permease family | ||
KKNCFHKG_01313 | 6e-166 | pucR | QT | COG2508 Regulator of polyketide synthase expression | ||
KKNCFHKG_01314 | 1e-144 | pucF | 3.5.1.6, 3.5.1.87, 3.5.3.9 | E | COG0624 Acetylornithine deacetylase Succinyl-diaminopimelate desuccinylase and related deacylases | |
KKNCFHKG_01315 | 7.7e-201 | pucG | 2.6.1.112, 2.6.1.44, 2.6.1.45, 2.6.1.51 | E | COG0075 Serine-pyruvate aminotransferase archaeal aspartate aminotransferase | |
KKNCFHKG_01316 | 5.2e-182 | allB | 3.5.2.5 | F | Catalyzes the conversion of allantoin (5- ureidohydantoin) to allantoic acid by hydrolytic cleavage of the five-member hydantoin ring | |
KKNCFHKG_01317 | 2.9e-19 | G | M42 glutamyl aminopeptidase | |||
KKNCFHKG_01318 | 1.6e-280 | yfmM | S | COG0488 ATPase components of ABC transporters with duplicated ATPase domains | ||
KKNCFHKG_01320 | 2.8e-18 | |||||
KKNCFHKG_01321 | 5.7e-10 | S | transposase or invertase | |||
KKNCFHKG_01322 | 5e-81 | smpB | O | Required for rescue of stalled ribosomes mediated by trans-translation. Binds to transfer-messenger RNA (tmRNA), required for stable association of tmRNA with ribosomes. tmRNA and SmpB together mimic tRNA shape, replacing the anticodon stem-loop with SmpB. tmRNA is encoded by the ssrA gene | ||
KKNCFHKG_01323 | 0.0 | rnr | K | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
KKNCFHKG_01324 | 3.4e-143 | est | 3.1.1.1 | S | Carboxylesterase | |
KKNCFHKG_01325 | 2.5e-28 | secG | U | Preprotein translocase subunit SecG | ||
KKNCFHKG_01326 | 1.3e-240 | 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 | |
KKNCFHKG_01328 | 2.3e-300 | gpmI | 5.4.2.12 | G | Catalyzes the interconversion of 2-phosphoglycerate and | |
KKNCFHKG_01329 | 2.5e-122 | 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) | |
KKNCFHKG_01330 | 2.9e-218 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
KKNCFHKG_01331 | 7.6e-183 | gapA | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
KKNCFHKG_01332 | 1.4e-184 | cggR | K | COG2390 Transcriptional regulator, contains sigma factor-related N-terminal domain | ||
KKNCFHKG_01333 | 2.3e-39 | XAC3035 | O | Has a glutathione-disulfide oxidoreductase activity in the presence of NADPH and glutathione reductase. Reduces low molecular weight disulfides and proteins | ||
KKNCFHKG_01334 | 1.6e-244 | rpoN | K | COG1508 DNA-directed RNA polymerase specialized sigma subunit, sigma54 homolog | ||
KKNCFHKG_01336 | 1.3e-07 | S | Heavy-metal-associated domain | |||
KKNCFHKG_01337 | 1.7e-82 | S | Protein of unknown function (DUF1641) | |||
KKNCFHKG_01339 | 0.0 | yjgC | 1.17.1.10, 1.17.1.9 | C | formate dehydrogenase, alpha subunit | |
KKNCFHKG_01340 | 1.7e-31 | |||||
KKNCFHKG_01341 | 0.0 | acsA | 6.2.1.1 | I | COG0365 Acyl-coenzyme A synthetases AMP-(fatty) acid ligases | |
KKNCFHKG_01342 | 2.5e-123 | acuA | K | Part of the acuABC operon, which is possibly involved in the breakdown of acetoin and butanediol. Acts as an acetyltransferase inactivating acetyl-CoA synthetase AcsA via acetylation at a Lys residue | ||
KKNCFHKG_01343 | 3.8e-119 | acuB | S | Acetoin utilization protein AcuB | ||
KKNCFHKG_01344 | 1.6e-232 | acuC | BQ | histone deacetylase | ||
KKNCFHKG_01345 | 2.2e-182 | ccpA | K | catabolite control protein A | ||
KKNCFHKG_01346 | 1.4e-190 | aroF | 2.5.1.54, 5.4.99.5 | E | Catalyzes the formation of 3-deoxy-D-aribino-hept-2-ulosonate 7-phosphate from phosphoenolpyruvate and D-erythrose 4-phosphate and the formation of prephenate from chorismate | |
KKNCFHKG_01347 | 1.7e-34 | XK27_07760 | S | COG4980 Gas vesicle protein | ||
KKNCFHKG_01348 | 2.5e-44 | ytxG | S | protein containing a divergent version of the methyl-accepting chemotaxis-like domain | ||
KKNCFHKG_01349 | 2.2e-254 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
KKNCFHKG_01350 | 0.0 | sftA | D | Belongs to the FtsK SpoIIIE SftA family | ||
KKNCFHKG_01351 | 1.2e-66 | yhcN | S | Sporulation lipoprotein YhcN/YlaJ (Spore_YhcN_YlaJ) | ||
KKNCFHKG_01352 | 1.1e-109 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
KKNCFHKG_01353 | 4.8e-148 | ytpQ | S | Belongs to the UPF0354 family | ||
KKNCFHKG_01354 | 1.9e-55 | ytpP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
KKNCFHKG_01355 | 8.8e-196 | rsbU | 3.1.3.3 | T | response regulator | |
KKNCFHKG_01356 | 8.9e-153 | cheR | 2.1.1.80 | NT | chemotaxis | |
KKNCFHKG_01357 | 0.0 | T | PhoQ Sensor | |||
KKNCFHKG_01358 | 6.6e-53 | ytzB | S | small secreted protein | ||
KKNCFHKG_01359 | 1.5e-171 | ytnP | S | COG0491 Zn-dependent hydrolases, including glyoxylases | ||
KKNCFHKG_01361 | 5.1e-130 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
KKNCFHKG_01362 | 2.7e-55 | ytzH | S | YtzH-like protein | ||
KKNCFHKG_01363 | 4.8e-156 | ytmP | 2.7.1.89 | M | Phosphotransferase | |
KKNCFHKG_01365 | 5.4e-146 | ytlQ | ||||
KKNCFHKG_01366 | 7.7e-108 | ligT | 3.1.4.58, 3.5.1.42 | J | Hydrolyzes RNA 2',3'-cyclic phosphodiester to an RNA 2'- phosphomonoester | |
KKNCFHKG_01368 | 1.2e-160 | dat | 2.6.1.21 | E | Acts on the D-isomers of alanine, leucine, aspartate, glutamate, aminobutyrate, norvaline and asparagine. The enzyme transfers an amino group from a substrate D-amino acid to the pyridoxal phosphate cofactor to form pyridoxamine and an alpha- keto acid in the first half-reaction | |
KKNCFHKG_01369 | 1e-273 | pepV | 3.5.1.18 | E | Dipeptidase | |
KKNCFHKG_01370 | 1.2e-32 | ytzE | K | COG1349 Transcriptional regulators of sugar metabolism | ||
KKNCFHKG_01371 | 2.6e-286 | ytgP | S | COG2244 Membrane protein involved in the export of O-antigen and teichoic acid | ||
KKNCFHKG_01372 | 6.4e-27 | yteV | S | Sporulation protein Cse60 | ||
KKNCFHKG_01374 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
KKNCFHKG_01375 | 1.6e-187 | yttB | EGP | Major facilitator Superfamily | ||
KKNCFHKG_01376 | 9.4e-43 | ytzC | S | Protein of unknown function (DUF2524) | ||
KKNCFHKG_01377 | 8.3e-102 | ytqB | J | Putative rRNA methylase | ||
KKNCFHKG_01378 | 1.7e-207 | ytpB | 4.2.3.130 | S | Tetraprenyl-beta-curcumene synthase | |
KKNCFHKG_01379 | 1.7e-153 | ytpA | 3.1.1.5 | I | Alpha beta hydrolase | |
KKNCFHKG_01380 | 5.6e-73 | ytoA | S | COG0663 Carbonic anhydrases acetyltransferases, isoleucine patch superfamily | ||
KKNCFHKG_01381 | 0.0 | asnB | 6.3.5.4 | E | Asparagine synthase | |
KKNCFHKG_01382 | 9.3e-220 | metK | 2.5.1.6 | H | Catalyzes the formation of S-adenosylmethionine (AdoMet) from methionine and ATP. The overall synthetic reaction is composed of two sequential steps, AdoMet formation and the subsequent tripolyphosphate hydrolysis which occurs prior to release of AdoMet from the enzyme | |
KKNCFHKG_01383 | 1.7e-309 | pckA | 4.1.1.49 | C | Involved in the gluconeogenesis. Catalyzes the conversion of oxaloacetate (OAA) to phosphoenolpyruvate (PEP) through direct phosphoryl transfer between the nucleoside triphosphate and OAA | |
KKNCFHKG_01384 | 2.8e-55 | 3.6.1.55 | F | GDP-mannose mannosyl hydrolase activity | ||
KKNCFHKG_01385 | 1.9e-208 | ytmA | E | COG1506 Dipeptidyl aminopeptidases acylaminoacyl-peptidases | ||
KKNCFHKG_01386 | 1.9e-100 | ywqN | S | NAD(P)H-dependent | ||
KKNCFHKG_01387 | 3.1e-56 | gntK | 2.7.1.12, 2.7.1.17 | G | FGGY family of carbohydrate kinases, N-terminal domain | |
KKNCFHKG_01388 | 1.9e-186 | ytlA | P | COG0715 ABC-type nitrate sulfonate bicarbonate transport systems, periplasmic components | ||
KKNCFHKG_01389 | 3e-139 | ytlC | P | ABC transporter | ||
KKNCFHKG_01390 | 1.6e-127 | ytlD | P | COG0600 ABC-type nitrate sulfonate bicarbonate transport system, permease component | ||
KKNCFHKG_01391 | 9.8e-85 | ytkD | 3.6.1.55 | L | COG0494 NTP pyrophosphohydrolases including oxidative damage repair enzymes | |
KKNCFHKG_01392 | 7.4e-39 | |||||
KKNCFHKG_01393 | 2.8e-76 | dps | P | Belongs to the Dps family | ||
KKNCFHKG_01394 | 6.4e-40 | yidD | S | Could be involved in insertion of integral membrane proteins into the membrane | ||
KKNCFHKG_01396 | 1.2e-158 | adcA | P | Belongs to the bacterial solute-binding protein 9 family | ||
KKNCFHKG_01397 | 7.5e-208 | menC | 4.2.1.113 | H | Converts 2-succinyl-6-hydroxy-2,4-cyclohexadiene-1- carboxylate (SHCHC) to 2-succinylbenzoate (OSB) | |
KKNCFHKG_01398 | 4e-278 | menE | 6.2.1.26 | H | Belongs to the ATP-dependent AMP-binding enzyme family. MenE subfamily | |
KKNCFHKG_01399 | 1.9e-155 | menB | 4.1.3.36 | H | Converts o-succinylbenzoyl-CoA (OSB-CoA) to 1,4- dihydroxy-2-naphthoyl-CoA (DHNA-CoA) | |
KKNCFHKG_01400 | 1.5e-152 | menH | 4.2.99.20 | S | Catalyzes a proton abstraction reaction that results in 2,5-elimination of pyruvate from 2-succinyl-5-enolpyruvyl-6- hydroxy-3-cyclohexene-1-carboxylate (SEPHCHC) and the formation of 2-succinyl-6-hydroxy-2,4-cyclohexadiene-1-carboxylate (SHCHC) | |
KKNCFHKG_01401 | 0.0 | menD | 2.2.1.9 | H | Catalyzes the thiamine diphosphate-dependent decarboxylation of 2-oxoglutarate and the subsequent addition of the resulting succinic semialdehyde-thiamine pyrophosphate anion to isochorismate to yield 2-succinyl-5-enolpyruvyl-6-hydroxy-3- cyclohexene-1-carboxylate (SEPHCHC) | |
KKNCFHKG_01402 | 3.9e-251 | menF | 5.4.4.2 | HQ | Isochorismate synthase | |
KKNCFHKG_01403 | 9.4e-164 | menA | 2.5.1.74 | H | Belongs to the MenA family. Type 1 subfamily | |
KKNCFHKG_01413 | 3e-09 | |||||
KKNCFHKG_01419 | 5.1e-08 | |||||
KKNCFHKG_01420 | 1.6e-08 | |||||
KKNCFHKG_01424 | 1.6e-42 | |||||
KKNCFHKG_01427 | 4.3e-42 | S | COG NOG14552 non supervised orthologous group | |||
KKNCFHKG_01428 | 0.0 | cydD | V | ATP-binding protein | ||
KKNCFHKG_01429 | 0.0 | cydD | V | ATP-binding | ||
KKNCFHKG_01430 | 2.2e-182 | cydB | 1.10.3.14 | C | Cytochrome d ubiquinol oxidase, subunit II | |
KKNCFHKG_01431 | 4.3e-261 | cydA | 1.10.3.14 | C | oxidase, subunit | |
KKNCFHKG_01432 | 2.6e-30 | |||||
KKNCFHKG_01433 | 5.5e-138 | pdaB | 3.5.1.104 | G | xylanase chitin deacetylase | |
KKNCFHKG_01434 | 4.9e-76 | |||||
KKNCFHKG_01435 | 1.2e-58 | yrkC | G | Cupin domain | ||
KKNCFHKG_01436 | 1.3e-173 | K | Transcriptional regulator | |||
KKNCFHKG_01437 | 1.4e-211 | S | Acyl-coenzyme A:6-aminopenicillanic acid acyl-transferase | |||
KKNCFHKG_01438 | 1.6e-101 | kbaA | 2.7.8.43 | S | Involved in the activation of the KinB signaling pathway of sporulation | |
KKNCFHKG_01439 | 1.4e-61 | gerD | S | Spore gernimation protein | ||
KKNCFHKG_01440 | 1.9e-197 | mrp | D | Binds and transfers iron-sulfur (Fe-S) clusters to target apoproteins. Can hydrolyze ATP | ||
KKNCFHKG_01441 | 2.4e-130 | cwlD | 3.5.1.28 | M | n-acetylmuramoyl-L-alanine amidase | |
KKNCFHKG_01442 | 2.8e-81 | ybaK | S | Protein of unknown function (DUF2521) | ||
KKNCFHKG_01443 | 1.1e-273 | lysP | E | amino acid | ||
KKNCFHKG_01444 | 2.8e-111 | cysC | 2.7.1.25, 2.7.7.4 | P | Catalyzes the synthesis of activated sulfate | |
KKNCFHKG_01445 | 3.7e-226 | sat | 2.7.7.4 | P | Belongs to the sulfate adenylyltransferase family | |
KKNCFHKG_01447 | 6.7e-10 | S | Protein conserved in bacteria | |||
KKNCFHKG_01448 | 1.6e-64 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
KKNCFHKG_01449 | 6.4e-78 | rplM | J | This protein is one of the early assembly proteins of the 50S ribosomal subunit, although it is not seen to bind rRNA by itself. It is important during the early stages of 50S assembly | ||
KKNCFHKG_01450 | 1.4e-138 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
KKNCFHKG_01451 | 4.6e-138 | ecfT | P | Transmembrane (T) component of an energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
KKNCFHKG_01452 | 2.2e-162 | ecfA2 | 3.6.3.55 | P | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | |
KKNCFHKG_01453 | 2.4e-156 | cbiO | P | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
KKNCFHKG_01454 | 5.8e-65 | rplQ | J | Ribosomal protein L17 | ||
KKNCFHKG_01455 | 5.8e-169 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
KKNCFHKG_01456 | 2e-62 | rpsK | J | Located on the platform of the 30S subunit, it bridges several disparate RNA helices of the 16S rRNA. Forms part of the Shine-Dalgarno cleft in the 70S ribosome | ||
KKNCFHKG_01457 | 1.8e-57 | 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 | ||
KKNCFHKG_01458 | 2.4e-33 | infA | J | One of the essential components for the initiation of protein synthesis. Stabilizes the binding of IF-2 and IF-3 on the 30S subunit to which N-formylmethionyl-tRNA(fMet) subsequently binds. Helps modulate mRNA selection, yielding the 30S pre- initiation complex (PIC). Upon addition of the 50S ribosomal subunit IF-1, IF-2 and IF-3 are released leaving the mature 70S translation initation complex | ||
KKNCFHKG_01459 | 9.7e-123 | 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 | |
KKNCFHKG_01460 | 6.9e-229 | secY | U | The central subunit of the protein translocation channel SecYEG. Consists of two halves formed by TMs 1-5 and 6-10. These two domains form a lateral gate at the front which open onto the bilayer between TMs 2 and 7, and are clamped together by SecE at the back. The channel is closed by both a pore ring composed of hydrophobic SecY resides and a short helix (helix 2A) on the extracellular side of the membrane which forms a plug. The plug probably moves laterally to allow the channel to open. The ring and the pore may move independently | ||
KKNCFHKG_01461 | 4.5e-71 | rplO | J | binds to the 23S rRNA | ||
KKNCFHKG_01462 | 4.1e-23 | rpmD | J | Ribosomal protein L30 | ||
KKNCFHKG_01463 | 6.2e-85 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
KKNCFHKG_01464 | 8.8e-57 | rplR | J | This is one of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance | ||
KKNCFHKG_01465 | 1e-93 | rplF | J | This protein binds to the 23S rRNA, and is important in its secondary structure. It is located near the subunit interface in the base of the L7 L12 stalk, and near the tRNA binding site of the peptidyltransferase center | ||
KKNCFHKG_01466 | 1e-66 | rpsH | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA central domain where it helps coordinate assembly of the platform of the 30S subunit | ||
KKNCFHKG_01467 | 5.8e-28 | 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 | ||
KKNCFHKG_01468 | 1.6e-94 | 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 | ||
KKNCFHKG_01469 | 9.6e-52 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
KKNCFHKG_01470 | 1.5e-59 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
KKNCFHKG_01471 | 6e-39 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
KKNCFHKG_01472 | 2.7e-26 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
KKNCFHKG_01473 | 9.2e-77 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
KKNCFHKG_01474 | 1.4e-116 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
KKNCFHKG_01475 | 6.6e-54 | rplV | J | The globular domain of the protein is located near the polypeptide exit tunnel on the outside of the subunit, while an extended beta-hairpin is found that lines the wall of the exit tunnel in the center of the 70S ribosome | ||
KKNCFHKG_01476 | 2.2e-47 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
KKNCFHKG_01477 | 1.5e-155 | 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 | ||
KKNCFHKG_01478 | 6.3e-42 | 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 | ||
KKNCFHKG_01479 | 1.1e-107 | rplD | J | Forms part of the polypeptide exit tunnel | ||
KKNCFHKG_01480 | 2.6e-112 | rplC | J | One of the primary rRNA binding proteins, it binds directly near the 3'-end of the 23S rRNA, where it nucleates assembly of the 50S subunit | ||
KKNCFHKG_01481 | 3.4e-49 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
KKNCFHKG_01482 | 1.4e-223 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
KKNCFHKG_01483 | 0.0 | fusA | J | Catalyzes the GTP-dependent ribosomal translocation step during translation elongation. During this step, the ribosome changes from the pre-translocational (PRE) to the post- translocational (POST) state as the newly formed A-site-bound peptidyl-tRNA and P-site-bound deacylated tRNA move to the P and E sites, respectively. Catalyzes the coordinated movement of the two tRNA molecules, the mRNA and conformational changes in the ribosome | ||
KKNCFHKG_01484 | 9.3e-83 | rpsG | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the head domain of the 30S subunit. Is located at the subunit interface close to the decoding center, probably blocks exit of the E-site tRNA | ||
KKNCFHKG_01485 | 8.6e-72 | 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 | ||
KKNCFHKG_01486 | 1.3e-35 | rplGB | J | Belongs to the eukaryotic ribosomal protein eL8 family | ||
KKNCFHKG_01487 | 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 | |
KKNCFHKG_01488 | 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 | |
KKNCFHKG_01489 | 2.5e-112 | rsmC | 2.1.1.172 | J | Methyltransferase | |
KKNCFHKG_01490 | 3e-52 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
KKNCFHKG_01491 | 5.4e-81 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
KKNCFHKG_01492 | 1e-08 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
KKNCFHKG_01493 | 4.3e-124 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
KKNCFHKG_01494 | 1.4e-69 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
KKNCFHKG_01495 | 9.2e-95 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
KKNCFHKG_01496 | 8.6e-24 | 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 | ||
KKNCFHKG_01497 | 7.2e-110 | sigH | K | Belongs to the sigma-70 factor family | ||
KKNCFHKG_01498 | 9.6e-89 | yacP | S | RNA-binding protein containing a PIN domain | ||
KKNCFHKG_01499 | 1.3e-134 | trmH | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
KKNCFHKG_01500 | 3e-69 | mrnC | J | Involved in correct processing of both the 5' and 3' ends of 23S rRNA precursor. Processes 30S rRNA precursor transcript even in absence of ribonuclease 3 (Rnc) | ||
KKNCFHKG_01501 | 2.9e-273 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
KKNCFHKG_01502 | 1.4e-113 | cysE | 2.3.1.30 | E | Serine acetyltransferase | |
KKNCFHKG_01503 | 1.9e-283 | gltX | 6.1.1.17, 6.1.1.24 | J | Catalyzes the attachment of glutamate to tRNA(Glu) in a two-step reaction glutamate is first activated by ATP to form Glu-AMP and then transferred to the acceptor end of tRNA(Glu) | |
KKNCFHKG_01504 | 2.1e-82 | ispF | 2.1.1.228, 2.7.7.60, 4.6.1.12 | I | Involved in the biosynthesis of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP), two major building blocks of isoprenoid compounds. Catalyzes the conversion of 4- diphosphocytidyl-2-C-methyl-D-erythritol 2-phosphate (CDP-ME2P) to 2-C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-CPP) with a corresponding release of cytidine 5-monophosphate (CMP) | |
KKNCFHKG_01505 | 7.5e-118 | ispD | 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) | |
KKNCFHKG_01506 | 6.9e-198 | yacL | S | COG4956 Integral membrane protein (PIN domain superfamily) | ||
KKNCFHKG_01507 | 1.1e-253 | radA | O | DNA-dependent ATPase involved in processing of recombination intermediates, plays a role in repairing DNA breaks. Stimulates the branch migration of RecA-mediated strand transfer reactions, allowing the 3' invading strand to extend heteroduplex DNA faster. Binds ssDNA in the presence of ADP but not other nucleotides, has ATPase activity that is stimulated by ssDNA and various branched DNA structures, but inhibited by SSB. Does not have RecA's homology-searching function | ||
KKNCFHKG_01508 | 0.0 | clpC | O | Belongs to the ClpA ClpB family | ||
KKNCFHKG_01509 | 2.8e-191 | mcsB | 2.7.14.1, 2.7.3.2, 2.7.3.3 | E | Catalyzes the specific phosphorylation of arginine residues in a large number of proteins. Is part of the bacterial stress response system. Protein arginine phosphorylation has a physiologically important role and is involved in the regulation of many critical cellular processes, such as protein homeostasis, motility, competence, and stringent and stress responses, by regulating gene expression and protein activity | |
KKNCFHKG_01510 | 8.2e-99 | mcsA | 2.7.14.1 | S | protein with conserved CXXC pairs | |
KKNCFHKG_01511 | 5.4e-75 | ctsR | K | Belongs to the CtsR family | ||
KKNCFHKG_01512 | 1.9e-90 | 4.1.1.44 | S | Antioxidant protein with alkyl hydroperoxidase activity. Required for the reduction of the AhpC active site cysteine residues and for the regeneration of the AhpC enzyme activity | ||
KKNCFHKG_01513 | 2.3e-38 | gcvR | T | Belongs to the UPF0237 family | ||
KKNCFHKG_01514 | 1.4e-248 | XK27_08635 | S | UPF0210 protein | ||
KKNCFHKG_01517 | 2.4e-36 | ptxS | K | transcriptional | ||
KKNCFHKG_01518 | 2.9e-91 | hxlB | 4.1.2.14, 4.1.2.43, 4.1.3.42, 5.3.1.27 | M | SIS domain | |
KKNCFHKG_01519 | 4e-84 | cotF | M | Spore coat protein | ||
KKNCFHKG_01520 | 1.1e-175 | iolS | C | Aldo keto reductase | ||
KKNCFHKG_01521 | 1.2e-97 | ydjA | C | Nitroreductase family | ||
KKNCFHKG_01522 | 2.6e-250 | E | COG1113 Gamma-aminobutyrate permease and related permeases | |||
KKNCFHKG_01523 | 2.4e-273 | dtpT | E | amino acid peptide transporter | ||
KKNCFHKG_01524 | 1e-276 | lysP | E | amino acid | ||
KKNCFHKG_01526 | 4.3e-98 | puuR | K | Cupin domain | ||
KKNCFHKG_01527 | 2.3e-209 | potA | 3.6.3.30, 3.6.3.31 | P | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | |
KKNCFHKG_01528 | 9e-139 | potB | E | COG1176 ABC-type spermidine putrescine transport system, permease component I | ||
KKNCFHKG_01529 | 5.4e-139 | potC | E | COG1177 ABC-type spermidine putrescine transport system, permease component II | ||
KKNCFHKG_01530 | 9.8e-205 | potD | E | COG0687 Spermidine putrescine-binding periplasmic protein | ||
KKNCFHKG_01531 | 1.4e-248 | H | HemY protein | |||
KKNCFHKG_01532 | 3.7e-252 | E | amino acid | |||
KKNCFHKG_01533 | 2.7e-134 | lutC | S | Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source | ||
KKNCFHKG_01534 | 2.5e-272 | lutB | C | Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source. Has probably a role as an electron transporter during oxidation of L-lactate | ||
KKNCFHKG_01535 | 5e-136 | lutA | C | Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source | ||
KKNCFHKG_01536 | 6.9e-251 | E | Amino acid permease | |||
KKNCFHKG_01537 | 3.9e-223 | yugJ | C | oxidoreductases, Fe-dependent alcohol dehydrogenase family | ||
KKNCFHKG_01538 | 1.2e-233 | amt | P | Ammonium transporter | ||
KKNCFHKG_01539 | 1.1e-15 | S | Ribbon-helix-helix protein, copG family | |||
KKNCFHKG_01540 | 4.9e-79 | citH | C | Citrate transporter | ||
KKNCFHKG_01541 | 4.2e-181 | ykoT | GT2 | M | COG0463 Glycosyltransferases involved in cell wall biogenesis | |
KKNCFHKG_01542 | 0.0 | helD | 3.6.4.12 | L | DNA helicase | |
KKNCFHKG_01546 | 5.5e-128 | L | Archaeal putative transposase ISC1217 | |||
KKNCFHKG_01547 | 2.2e-19 | |||||
KKNCFHKG_01550 | 2.5e-98 | glpP | K | Regulates expression of the glpD operon. In the presence of glycerol 3-phosphate (G3P) causes antitermination of transcription of glpD at the inverted repeat of the leader region to enhance its transcription. Binds and stabilizes glpD leader mRNA | ||
KKNCFHKG_01551 | 3.6e-151 | glpF | G | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
KKNCFHKG_01552 | 1.1e-289 | glpK | 2.7.1.30 | C | Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate | |
KKNCFHKG_01553 | 0.0 | glpD | 1.1.5.3 | C | Belongs to the FAD-dependent glycerol-3-phosphate dehydrogenase family | |
KKNCFHKG_01554 | 8.3e-211 | dctA | U | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
KKNCFHKG_01555 | 2.5e-15 | S | Ribbon-helix-helix protein, copG family | |||
KKNCFHKG_01556 | 1.6e-120 | K | COG0664 cAMP-binding proteins - catabolite gene activator and regulatory subunit of cAMP-dependent protein kinases | |||
KKNCFHKG_01557 | 5.2e-122 | ric | D | Di-iron-containing protein involved in the repair of iron-sulfur clusters | ||
KKNCFHKG_01558 | 4e-90 | S | Belongs to the UPF0312 family | |||
KKNCFHKG_01559 | 2.2e-215 | yqiG | C | COG1902 NADH flavin oxidoreductases, Old Yellow Enzyme family | ||
KKNCFHKG_01561 | 2.5e-189 | T | HD domain | |||
KKNCFHKG_01562 | 2.3e-278 | glyQS | 6.1.1.14 | J | Catalyzes the attachment of glycine to tRNA(Gly) | |
KKNCFHKG_01563 | 0.0 | ydaO | E | amino acid | ||
KKNCFHKG_01564 | 1.4e-145 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
KKNCFHKG_01565 | 3e-24 | tatA | U | Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. TatA could form the protein-conducting channel of the Tat system | ||
KKNCFHKG_01566 | 1.1e-173 | ydbI | S | AI-2E family transporter | ||
KKNCFHKG_01567 | 1.9e-130 | glnQ | 3.6.3.21 | E | COG1126 ABC-type polar amino acid transport system, ATPase component | |
KKNCFHKG_01568 | 4.7e-135 | glnH | ET | Belongs to the bacterial solute-binding protein 3 family | ||
KKNCFHKG_01569 | 6.1e-109 | gluC | P | ABC transporter | ||
KKNCFHKG_01570 | 2.1e-115 | glnP | P | ABC transporter | ||
KKNCFHKG_01571 | 1.3e-218 | ggt | 2.3.2.2, 3.4.19.13 | E | gamma-glutamyltransferase | |
KKNCFHKG_01572 | 5.2e-165 | EGP | MFS_1 like family | |||
KKNCFHKG_01573 | 3.8e-55 | ywrC | K | Transcriptional regulator | ||
KKNCFHKG_01574 | 8.4e-230 | S | PFAM Uncharacterised protein family UPF0236 | |||
KKNCFHKG_01575 | 3.4e-13 | S | PFAM Uncharacterised protein family UPF0236 | |||
KKNCFHKG_01577 | 2.7e-253 | ybhI | P | Sodium:sulfate symporter transmembrane region | ||
KKNCFHKG_01578 | 2e-89 | endA | 3.1.21.1 | L | Endonuclease I | |
KKNCFHKG_01579 | 0.0 | XK27_11280 | S | Psort location CytoplasmicMembrane, score | ||
KKNCFHKG_01581 | 4e-129 | |||||
KKNCFHKG_01582 | 9.2e-127 | yhcG | V | ABC transporter, ATP-binding protein | ||
KKNCFHKG_01583 | 1.6e-58 | yhcF | K | Transcriptional regulator | ||
KKNCFHKG_01584 | 4.3e-95 | padR | K | transcriptional | ||
KKNCFHKG_01585 | 5.6e-94 | padC | Q | Phenolic acid decarboxylase | ||
KKNCFHKG_01586 | 6.9e-113 | ywnB | S | NAD(P)H-binding | ||
KKNCFHKG_01587 | 4.4e-86 | folT | 2.7.13.3 | T | ECF transporter, substrate-specific component | |
KKNCFHKG_01588 | 1.5e-35 | yeeD | O | Belongs to the sulfur carrier protein TusA family | ||
KKNCFHKG_01589 | 9.4e-192 | yeeE | S | Sulphur transport | ||
KKNCFHKG_01590 | 1.8e-220 | yihS | 5.1.3.11, 5.3.1.9 | G | N-acylglucosamine 2-epimerase (GlcNAc 2-epimerase) | |
KKNCFHKG_01591 | 2.5e-169 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
KKNCFHKG_01592 | 1.3e-94 | pucA | 1.17.1.4 | O | COG1975 Xanthine and CO dehydrogenases maturation factor, XdhC CoxF family | |
KKNCFHKG_01593 | 8.3e-42 | pucB | 1.1.1.328, 1.17.1.4, 2.7.7.76 | S | MobA-like NTP transferase domain | |
KKNCFHKG_01594 | 1.7e-61 | ygfM | 1.17.1.4, 1.2.5.3 | C | COG1319 Aerobic-type carbon monoxide dehydrogenase, middle subunit CoxM CutM homologs | |
KKNCFHKG_01595 | 5.6e-274 | xdhA | 1.17.1.4 | C | COG1529 Aerobic-type carbon monoxide dehydrogenase, large subunit CoxL CutL homologs | |
KKNCFHKG_01596 | 9.1e-55 | 1.17.1.4, 1.2.5.3, 1.3.99.16 | C | COG2080 Aerobic-type carbon monoxide dehydrogenase, small subunit CoxS CutS homologs | ||
KKNCFHKG_01598 | 2.5e-155 | E | Amino acid permease | |||
KKNCFHKG_01600 | 1.3e-279 | tynA | 1.4.3.21 | Q | amine oxidase | |
KKNCFHKG_01601 | 4.6e-40 | K | helix_turn_helix, arabinose operon control protein | |||
KKNCFHKG_01602 | 2.8e-152 | yeaN | P | COG2807 Cyanate permease | ||
KKNCFHKG_01603 | 5.8e-187 | ubiB | S | ABC1 family | ||
KKNCFHKG_01604 | 1.9e-62 | ubiB | S | ABC1 family | ||
KKNCFHKG_01605 | 4e-15 | S | ATP synthase, subunit b | |||
KKNCFHKG_01606 | 1.1e-16 | gmuE | 2.7.1.2, 2.7.1.4 | GK | COG1940 Transcriptional regulator sugar kinase | |
KKNCFHKG_01607 | 5.8e-280 | scrA | 2.7.1.211, 5.3.1.1 | G | pts system | |
KKNCFHKG_01608 | 4.8e-202 | scrB | 3.2.1.26 | GH32 | G | invertase |
KKNCFHKG_01609 | 1.4e-136 | scrR | K | helix_turn _helix lactose operon repressor | ||
KKNCFHKG_01610 | 3.1e-93 | |||||
KKNCFHKG_01612 | 1.4e-27 | K | Helix-turn-helix domain | |||
KKNCFHKG_01613 | 6.1e-31 | |||||
KKNCFHKG_01614 | 2.7e-31 | S | Domain of unknown function (DUF4177) | |||
KKNCFHKG_01615 | 1.2e-299 | guaA | 2.3.1.128, 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
KKNCFHKG_01616 | 5.2e-153 | nadE | 6.3.1.5 | H | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
KKNCFHKG_01617 | 9.4e-283 | pncB | 6.3.4.21 | H | Catalyzes the synthesis of beta-nicotinate D- ribonucleotide from nicotinate and 5-phospho-D-ribose 1-phosphate at the expense of ATP | |
KKNCFHKG_01618 | 2.4e-106 | pncA | Q | COG1335 Amidases related to nicotinamidase | ||
KKNCFHKG_01619 | 1.8e-198 | ykfB | 5.1.1.20 | M | Belongs to the mandelate racemase muconate lactonizing enzyme family | |
KKNCFHKG_01620 | 0.0 | ykoS | ||||
KKNCFHKG_01621 | 1.5e-186 | ykoT | GT2 | M | COG0463 Glycosyltransferases involved in cell wall biogenesis | |
KKNCFHKG_01622 | 4.1e-68 | yngA | S | GtrA-like protein | ||
KKNCFHKG_01623 | 3.2e-284 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
KKNCFHKG_01624 | 5.7e-43 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
KKNCFHKG_01625 | 1.9e-122 | ydiL | S | CAAX protease self-immunity | ||
KKNCFHKG_01626 | 4.7e-28 | S | Domain of unknown function (DUF4305) | |||
KKNCFHKG_01627 | 5.1e-131 | tatC | U | Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes | ||
KKNCFHKG_01628 | 7.8e-123 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
KKNCFHKG_01629 | 1.1e-09 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
KKNCFHKG_01630 | 0.0 | ydiF | S | ABC transporter | ||
KKNCFHKG_01631 | 2.3e-184 | 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 | |
KKNCFHKG_01632 | 2.2e-81 | rimI | 2.3.1.128 | K | This enzyme acetylates the N-terminal alanine of ribosomal protein S18 | |
KKNCFHKG_01633 | 1.4e-127 | yeaZ | 2.3.1.234 | O | COG1214 Inactive homolog of metal-dependent proteases | |
KKNCFHKG_01634 | 5.3e-83 | ydiB | 2.7.1.221, 5.1.1.1 | S | ATPase or kinase | |
KKNCFHKG_01636 | 1.1e-64 | argO | S | Lysine exporter protein LysE YggA | ||
KKNCFHKG_01637 | 1.3e-190 | yfjN | 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 | ||
KKNCFHKG_01638 | 6.2e-31 | yhcC | S | nucleic-acid-binding protein containing a Zn-ribbon domain | ||
KKNCFHKG_01639 | 9.9e-83 | S | AAA domain | |||
KKNCFHKG_01640 | 2.1e-85 | S | Bacterial PH domain | |||
KKNCFHKG_01641 | 1.4e-273 | ydbT | S | Bacterial PH domain | ||
KKNCFHKG_01642 | 8.6e-76 | yqgC | S | protein conserved in bacteria | ||
KKNCFHKG_01643 | 9.6e-237 | ydjN | U | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
KKNCFHKG_01644 | 4.2e-43 | |||||
KKNCFHKG_01645 | 1.6e-69 | yoaS | S | Protein of unknown function (DUF2975) | ||
KKNCFHKG_01646 | 5.1e-28 | yozG | K | Transcriptional regulator | ||
KKNCFHKG_01647 | 1.6e-13 | yoaT | S | Protein of unknown function (DUF817) | ||
KKNCFHKG_01648 | 3e-260 | S | Protein of unknown function (DUF2397) | |||
KKNCFHKG_01650 | 8.9e-228 | S | Protein of unknown function (DUF2398) | |||
KKNCFHKG_01651 | 0.0 | D | Putative exonuclease SbcCD, C subunit | |||
KKNCFHKG_01652 | 5.1e-248 | S | Protein of unknown function N-terminus (DUF3323) | |||
KKNCFHKG_01653 | 2.7e-55 | yhgE | S | YhgE Pip N-terminal domain protein | ||
KKNCFHKG_01654 | 3.1e-20 | yhgD | K | Transcriptional regulator | ||
KKNCFHKG_01655 | 0.0 | cotA | 1.10.3.4, 1.16.3.3 | Q | multicopper oxidases | |
KKNCFHKG_01656 | 7.2e-194 | ansA | 3.5.1.1 | EJ | L-asparaginase | |
KKNCFHKG_01657 | 2.2e-307 | ypdA | 2.7.13.3 | T | Signal transduction histidine kinase | |
KKNCFHKG_01658 | 2.1e-137 | ypdB | KT | LytTr DNA-binding domain | ||
KKNCFHKG_01659 | 5.8e-92 | yhjX | P | Major facilitator superfamily | ||
KKNCFHKG_01660 | 1.6e-115 | yhjX | P | Major facilitator superfamily | ||
KKNCFHKG_01661 | 1.7e-215 | yxjG | 2.1.1.14 | E | Methionine synthase | |
KKNCFHKG_01662 | 2.6e-104 | yetJ | S | Belongs to the BI1 family | ||
KKNCFHKG_01663 | 1.1e-38 | cypC | 1.11.2.4, 1.14.14.1 | Q | Cytochrome P450 | |
KKNCFHKG_01664 | 1e-245 | |||||
KKNCFHKG_01665 | 3.8e-151 | T | STAS domain | |||
KKNCFHKG_01666 | 3.5e-244 | braB | E | Component of the transport system for branched-chain amino acids | ||
KKNCFHKG_01667 | 0.0 | ilvD | 4.2.1.9 | E | Belongs to the IlvD Edd family | |
KKNCFHKG_01668 | 0.0 | ilvB | 2.2.1.6 | E | Acetolactate synthase | |
KKNCFHKG_01669 | 1.1e-84 | ilvN | 2.2.1.6 | E | Acetolactate synthase | |
KKNCFHKG_01670 | 1.8e-195 | ilvC | 1.1.1.86 | EH | Involved in the biosynthesis of branched-chain amino acids (BCAA). Catalyzes an alkyl-migration followed by a ketol- acid reduction of (S)-2-acetolactate (S2AL) to yield (R)-2,3- dihydroxy-isovalerate. In the isomerase reaction, S2AL is rearranged via a Mg-dependent methyl migration to produce 3- hydroxy-3-methyl-2-ketobutyrate (HMKB). In the reductase reaction, this 2-ketoacid undergoes a metal-dependent reduction by NADPH to yield (R)-2,3-dihydroxy-isovalerate | |
KKNCFHKG_01671 | 5.8e-283 | leuA | 2.3.3.13 | E | Catalyzes the condensation of the acetyl group of acetyl-CoA with 3-methyl-2-oxobutanoate (2-oxoisovalerate) to form 3-carboxy-3-hydroxy-4-methylpentanoate (2-isopropylmalate) | |
KKNCFHKG_01672 | 1.7e-199 | 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 | |
KKNCFHKG_01673 | 2.6e-269 | 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 | |
KKNCFHKG_01674 | 7.8e-111 | leuD | 4.2.1.33, 4.2.1.35, 4.2.1.36 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
KKNCFHKG_01675 | 7.4e-189 | ilvA | 4.3.1.19 | E | Catalyzes the anaerobic formation of alpha-ketobutyrate and ammonia from threonine in a two-step reaction. The first step involved a dehydration of threonine and a production of enamine intermediates (aminocrotonate), which tautomerizes to its imine form (iminobutyrate). Both intermediates are unstable and short- lived. The second step is the nonenzymatic hydrolysis of the enamine imine intermediates to form 2-ketobutyrate and free ammonia. In the low water environment of the cell, the second step is accelerated by RidA | |
KKNCFHKG_01676 | 3.3e-219 | 2.6.1.9 | S | HAD-hyrolase-like | ||
KKNCFHKG_01677 | 1.5e-178 | S | Phosphotransferase system, EIIC | |||
KKNCFHKG_01678 | 1.7e-301 | serA | 1.1.1.399, 1.1.1.95 | E | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
KKNCFHKG_01679 | 1.5e-219 | dhsS | 1.12.1.2 | E | COG0075 Serine-pyruvate aminotransferase archaeal aspartate aminotransferase | |
KKNCFHKG_01680 | 4.3e-183 | serA1 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | ||
KKNCFHKG_01681 | 3e-239 | mcpA | NT | chemotaxis protein | ||
KKNCFHKG_01684 | 0.0 | glgP | 2.4.1.1 | GT35 | G | Phosphorylase is an important allosteric enzyme in carbohydrate metabolism. Enzymes from different sources differ in their regulatory mechanisms and in their natural substrates. However, all known phosphorylases share catalytic and structural properties |
KKNCFHKG_01685 | 1.3e-48 | bacI | V | COG0577 ABC-type antimicrobial peptide transport system, permease component | ||
KKNCFHKG_01686 | 1.3e-41 | |||||
KKNCFHKG_01688 | 0.0 | nrdA | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
KKNCFHKG_01689 | 5.6e-88 | fld | C | Flavodoxin | ||
KKNCFHKG_01690 | 2.2e-193 | nrdB | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
KKNCFHKG_01691 | 3.6e-103 | plsY | 2.3.1.15 | I | Belongs to the PlsY family | |
KKNCFHKG_01692 | 3.3e-208 | crtQ | M | Glycosyl transferase family 21 | ||
KKNCFHKG_01693 | 7.6e-23 | S | transposase or invertase | |||
KKNCFHKG_01694 | 1e-92 | Q | Thioesterase superfamily | |||
KKNCFHKG_01695 | 2.2e-48 | sugE | P | Multidrug resistance protein | ||
KKNCFHKG_01696 | 4.9e-49 | ykkC | P | Multidrug resistance protein | ||
KKNCFHKG_01697 | 1e-134 | yfcA | S | membrane transporter protein | ||
KKNCFHKG_01698 | 9.1e-176 | fhuG | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
KKNCFHKG_01699 | 2.4e-179 | fhuB | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
KKNCFHKG_01700 | 1.6e-169 | fhuD | P | Periplasmic binding protein | ||
KKNCFHKG_01701 | 1.6e-151 | fhuC | 3.6.3.34 | HP | ABC transporter | |
KKNCFHKG_01702 | 7.2e-197 | ycgT | 1.18.1.2, 1.19.1.1 | C | Ferredoxin--NADP reductase | |
KKNCFHKG_01703 | 7e-93 | |||||
KKNCFHKG_01704 | 1.2e-97 | |||||
KKNCFHKG_01705 | 3.2e-127 | yeeN | K | transcriptional regulatory protein | ||
KKNCFHKG_01706 | 1.5e-186 | T | Anti-anti-sigma regulatory factor (Antagonist of anti-sigma factor) | |||
KKNCFHKG_01707 | 5.4e-251 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Catalyzes the oxidation of malonate semialdehyde (MSA) and methylmalonate semialdehyde (MMSA) into acetyl-CoA and propanoyl-CoA, respectively | |
KKNCFHKG_01708 | 8.4e-100 | glnH | ET | COG0834 ABC-type amino acid transport signal transduction systems, periplasmic component domain | ||
KKNCFHKG_01709 | 9.9e-83 | yecS_2 | E | COG0765 ABC-type amino acid transport system, permease component | ||
KKNCFHKG_01710 | 9.5e-111 | artM_2 | 3.6.3.21 | E | ABC transporter | |
KKNCFHKG_01711 | 4.7e-239 | yobO | M | Pectate lyase superfamily protein | ||
KKNCFHKG_01712 | 2.3e-141 | cysH | 1.8.4.10, 1.8.4.8, 2.7.1.25 | EH | Belongs to the PAPS reductase family. CysH subfamily | |
KKNCFHKG_01713 | 3.7e-142 | hemD | 2.1.1.107, 4.2.1.75 | H | Belongs to the precorrin methyltransferase family | |
KKNCFHKG_01714 | 6.3e-126 | cbiX | 4.99.1.3, 4.99.1.4, 5.4.99.60, 5.4.99.61 | S | Sirohydrochlorin ferrochelatase | |
KKNCFHKG_01715 | 3.8e-100 | cysG | 1.3.1.76, 4.99.1.4 | H | Siroheme synthase | |
KKNCFHKG_01716 | 5.4e-95 | ywhH | S | Aminoacyl-tRNA editing domain | ||
KKNCFHKG_01717 | 1.1e-203 | gldA | 1.1.1.6 | C | COG0371 Glycerol dehydrogenase and related enzymes | |
KKNCFHKG_01718 | 3.7e-309 | IQ | COG0318 Acyl-CoA synthetases (AMP-forming) AMP-acid ligases II | |||
KKNCFHKG_01719 | 8.7e-182 | 2.7.7.65 | T | Diguanylate cyclase, GGDEF domain | ||
KKNCFHKG_01721 | 7.8e-166 | EG | COG0697 Permeases of the drug metabolite transporter (DMT) superfamily | |||
KKNCFHKG_01722 | 6.6e-178 | S | Nuclease-related domain | |||
KKNCFHKG_01723 | 1.1e-18 | |||||
KKNCFHKG_01724 | 2.2e-50 | |||||
KKNCFHKG_01725 | 2.6e-169 | czcD | P | COG1230 Co Zn Cd efflux system component | ||
KKNCFHKG_01726 | 9e-209 | T | Osmosensitive K+ channel His kinase sensor domain | |||
KKNCFHKG_01727 | 1.3e-99 | kdpC | 3.6.3.12 | P | Part of the high-affinity ATP-driven potassium transport (or Kdp) system, which catalyzes the hydrolysis of ATP coupled with the electrogenic transport of potassium into the cytoplasm. This subunit acts as a catalytic chaperone that increases the ATP- binding affinity of the ATP-hydrolyzing subunit KdpB by the formation of a transient KdpB KdpC ATP ternary complex | |
KKNCFHKG_01728 | 0.0 | kdpB | 3.6.3.12 | P | of the high-affinity ATP-driven potassium transport (or KDP) system, which catalyzes the hydrolysis of ATP coupled with the | |
KKNCFHKG_01729 | 1.9e-303 | kdpA | 3.6.3.12 | P | Part of the high-affinity ATP-driven potassium transport (or Kdp) system, which catalyzes the hydrolysis of ATP coupled with the electrogenic transport of potassium into the cytoplasm. This subunit binds and transports the potassium across the cytoplasmic membrane | |
KKNCFHKG_01730 | 2.3e-83 | L | PFAM transposase IS4 family protein | |||
KKNCFHKG_01731 | 2.5e-19 | L | PFAM transposase IS4 family protein | |||
KKNCFHKG_01732 | 8.5e-14 | ma_1747 | S | ABC transporter | ||
KKNCFHKG_01733 | 0.0 | glmS | 2.6.1.16 | M | Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source | |
KKNCFHKG_01734 | 1e-292 | M | Glycosyltransferase like family 2 | |||
KKNCFHKG_01735 | 1.1e-170 | mvk | 1.1.1.88, 2.3.3.10, 2.7.1.36 | I | GHMP kinases C terminal | |
KKNCFHKG_01736 | 6.9e-181 | mvaD | 4.1.1.33 | I | GHMP kinases N terminal domain | |
KKNCFHKG_01737 | 1.4e-201 | mvaK2 | 2.7.1.36, 2.7.1.43, 2.7.4.2 | I | GHMP kinases C terminal | |
KKNCFHKG_01738 | 9.7e-115 | yhfK | GM | NmrA-like family | ||
KKNCFHKG_01739 | 2.2e-31 | csfB | S | Inhibitor of sigma-G Gin | ||
KKNCFHKG_01740 | 3.6e-282 | adiA | 4.1.1.17, 4.1.1.18, 4.1.1.19 | E | Orn Lys Arg decarboxylase | |
KKNCFHKG_01741 | 2.3e-119 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
KKNCFHKG_01742 | 9.8e-55 | yaaQ | S | protein conserved in bacteria | ||
KKNCFHKG_01743 | 1.5e-71 | yaaR | S | protein conserved in bacteria | ||
KKNCFHKG_01744 | 8.9e-184 | holB | 2.7.7.7 | L | DNA polymerase III | |
KKNCFHKG_01745 | 1.7e-148 | yaaT | S | stage 0 sporulation protein | ||
KKNCFHKG_01746 | 3.3e-61 | yabA | L | Involved in initiation control of chromosome replication | ||
KKNCFHKG_01747 | 1.6e-137 | yabB | 2.1.1.223 | S | Conserved hypothetical protein 95 | |
KKNCFHKG_01748 | 1.2e-48 | yazA | L | endonuclease containing a URI domain | ||
KKNCFHKG_01749 | 2.6e-163 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
KKNCFHKG_01750 | 4.7e-48 | abrB | K | COG2002 Regulators of stationary sporulation gene expression | ||
KKNCFHKG_01751 | 0.0 | metG | 6.1.1.10 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
KKNCFHKG_01752 | 8e-148 | tatD | L | hydrolase, TatD | ||
KKNCFHKG_01753 | 1.1e-104 | rnmV | 3.1.26.8 | J | Required for correct processing of both the 5' and 3' ends of 5S rRNA precursor. Cleaves both sides of a double-stranded region yielding mature 5S rRNA in one step | |
KKNCFHKG_01754 | 2.7e-160 | ksgA | 2.1.1.182 | J | Specifically dimethylates two adjacent adenosines (A1518 and A1519) in the loop of a conserved hairpin near the 3'-end of 16S rRNA in the 30S particle. May play a critical role in biogenesis of 30S subunits | |
KKNCFHKG_01755 | 1.4e-161 | yabG | S | peptidase | ||
KKNCFHKG_01756 | 2.4e-37 | veg | S | protein conserved in bacteria | ||
KKNCFHKG_01757 | 1.9e-26 | sspF | S | DNA topological change | ||
KKNCFHKG_01758 | 7.3e-158 | ispE | 2.1.1.182, 2.7.1.148 | I | Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol | |
KKNCFHKG_01759 | 1.3e-152 | purR | 2.4.2.22, 2.4.2.7 | F | pur operon repressor | |
KKNCFHKG_01760 | 1.2e-61 | yabJ | 3.5.99.10 | J | translation initiation inhibitor, yjgF family | |
KKNCFHKG_01761 | 1.4e-47 | spoVG | D | Essential for sporulation. Interferes with or is a negative regulator of the pathway leading to asymmetric septation | ||
KKNCFHKG_01763 | 2.5e-15 | S | Ribbon-helix-helix protein, copG family | |||
KKNCFHKG_01764 | 3.1e-19 | L | Transposase, IS605 OrfB family | |||
KKNCFHKG_01765 | 1.6e-239 | 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 | |
KKNCFHKG_01766 | 1.2e-174 | 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) | |
KKNCFHKG_01767 | 1.7e-108 | 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 | ||
KKNCFHKG_01768 | 2.7e-105 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
KKNCFHKG_01769 | 5.7e-38 | yabK | S | Peptide ABC transporter permease | ||
KKNCFHKG_01770 | 0.0 | mfd | L | Couples transcription and DNA repair by recognizing RNA polymerase (RNAP) stalled at DNA lesions. Mediates ATP-dependent release of RNAP and its truncated transcript from the DNA, and recruitment of nucleotide excision repair machinery to the damaged site | ||
KKNCFHKG_01771 | 4.7e-91 | spoVT | K | stage V sporulation protein | ||
KKNCFHKG_01772 | 2.3e-274 | yabM | S | COG2244 Membrane protein involved in the export of O-antigen and teichoic acid | ||
KKNCFHKG_01773 | 1.4e-190 | mazG | 3.6.1.66, 3.6.1.9 | S | COG3956 Protein containing tetrapyrrole methyltransferase domain and MazG-like | |
KKNCFHKG_01774 | 3.1e-41 | yabO | J | COG1188 Ribosome-associated heat shock protein implicated in the recycling of the 50S subunit (S4 paralog) | ||
KKNCFHKG_01775 | 3e-50 | yabP | S | Sporulation protein YabP | ||
KKNCFHKG_01776 | 8e-106 | yabQ | S | spore cortex biosynthesis protein | ||
KKNCFHKG_01777 | 1.9e-60 | divIC | D | Septum formation initiator | ||
KKNCFHKG_01778 | 3.7e-54 | yabR | J | RNA binding protein (contains ribosomal protein S1 domain) | ||
KKNCFHKG_01780 | 0.0 | spoIIE | 3.1.3.16, 3.1.3.3 | KT | stage II sporulation protein E | |
KKNCFHKG_01782 | 8.7e-120 | yabS | S | protein containing a von Willebrand factor type A (vWA) domain | ||
KKNCFHKG_01783 | 2.8e-166 | KLT | serine threonine protein kinase | |||
KKNCFHKG_01784 | 8.9e-278 | tilS | 2.4.2.8, 6.3.4.19 | D | Ligates lysine onto the cytidine present at position 34 of the AUA codon-specific tRNA(Ile) that contains the anticodon CAU, in an ATP-dependent manner. Cytidine is converted to lysidine, thus changing the amino acid specificity of the tRNA from methionine to isoleucine | |
KKNCFHKG_01785 | 2.9e-96 | hpt | 2.4.2.8, 6.3.4.19 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
KKNCFHKG_01786 | 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 | ||
KKNCFHKG_01787 | 1.7e-159 | coaX | 2.7.1.33 | F | Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis | |
KKNCFHKG_01788 | 8.4e-162 | hslO | O | Redox regulated molecular chaperone. Protects both thermally unfolding and oxidatively damaged proteins from irreversible aggregation. Plays an important role in the bacterial defense system toward oxidative stress | ||
KKNCFHKG_01789 | 8.9e-170 | cysK | 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
KKNCFHKG_01790 | 1.7e-156 | folP | 2.5.1.15, 2.7.6.3 | 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 | |
KKNCFHKG_01791 | 3.2e-62 | folB | 1.13.11.81, 2.5.1.15, 2.7.6.3, 4.1.2.25, 5.1.99.8 | H | Catalyzes the conversion of 7,8-dihydroneopterin to 6- hydroxymethyl-7,8-dihydropterin | |
KKNCFHKG_01792 | 1.1e-97 | folK | 1.13.11.81, 2.5.1.15, 2.7.6.3, 3.5.4.16, 4.1.2.25, 5.1.99.8 | H | 2-amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase | |
KKNCFHKG_01794 | 2.7e-285 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
KKNCFHKG_01795 | 4.5e-43 | xfp | 4.1.2.22, 4.1.2.9 | G | D-xylulose 5-phosphate/D-fructose 6-phosphate phosphoketolase | |
KKNCFHKG_01796 | 1e-289 | amy | 3.2.1.1 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
KKNCFHKG_01797 | 6.4e-98 | queF | 1.7.1.13 | S | Catalyzes the NADPH-dependent reduction of 7-cyano-7- deazaguanine (preQ0) to 7-aminomethyl-7-deazaguanine (preQ1) | |
KKNCFHKG_01798 | 2.3e-111 | yhhQ_2 | S | Involved in the import of queuosine (Q) precursors, required for Q precursor salvage | ||
KKNCFHKG_01799 | 7.4e-43 | atsK | 1.14.11.17 | Q | Taurine catabolism dioxygenase TauD, TfdA family | |
KKNCFHKG_01801 | 6.5e-107 | mmuM | 1.5.1.20, 2.1.1.10 | H | Homocysteine | |
KKNCFHKG_01802 | 9.3e-203 | mmuP | E | Permease | ||
KKNCFHKG_01803 | 8.9e-160 | L | Transposase IS4 family protein | |||
KKNCFHKG_01804 | 1.8e-50 | L | Transposase IS4 family protein | |||
KKNCFHKG_01805 | 1.3e-117 | deoC | 4.1.2.4 | F | Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate | |
KKNCFHKG_01806 | 0.0 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
KKNCFHKG_01807 | 7.8e-225 | uraA | F | Xanthine uracil | ||
KKNCFHKG_01808 | 1.2e-14 | S | Leucine-rich repeat (LRR) protein | |||
KKNCFHKG_01809 | 5e-50 | S | Leucine-rich repeat (LRR) protein | |||
KKNCFHKG_01810 | 1e-271 | EGP | Major facilitator Superfamily | |||
KKNCFHKG_01813 | 4.9e-232 | pepT | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
KKNCFHKG_01814 | 4.9e-153 | M | Glycosyl transferase family 8 | |||
KKNCFHKG_01815 | 3.1e-240 | yisQ | V | Mate efflux family protein | ||
KKNCFHKG_01816 | 1.8e-220 | pilM | NU | Pilus assembly protein | ||
KKNCFHKG_01817 | 8.9e-96 | |||||
KKNCFHKG_01818 | 4.7e-140 | modF | 3.6.3.21, 3.6.3.34 | P | COG1119 ABC-type molybdenum transport system, ATPase component photorepair protein PhrA | |
KKNCFHKG_01819 | 3.3e-189 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
KKNCFHKG_01820 | 2.9e-98 | metI | P | COG2011 ABC-type metal ion transport system, permease component | ||
KKNCFHKG_01821 | 2.1e-154 | metQ | M | Belongs to the nlpA lipoprotein family | ||
KKNCFHKG_01822 | 0.0 | cstA | T | Carbon starvation protein | ||
KKNCFHKG_01823 | 1.6e-207 | ilvE | 2.6.1.42 | E | Branched-chain amino acid aminotransferase | |
KKNCFHKG_01824 | 3e-128 | thrE | S | Putative threonine/serine exporter | ||
KKNCFHKG_01825 | 1e-70 | S | Threonine/Serine exporter, ThrE | |||
KKNCFHKG_01826 | 3.5e-127 | S | Protein of unknown function (DUF1646) | |||
KKNCFHKG_01827 | 0.0 | asnO | 6.3.5.4 | E | Asparagine synthase | |
KKNCFHKG_01828 | 2.9e-176 | ywbI | K | Transcriptional regulator | ||
KKNCFHKG_01829 | 2.3e-55 | ywbH | S | LrgA family | ||
KKNCFHKG_01830 | 3.8e-117 | ywbG | M | effector of murein hydrolase | ||
KKNCFHKG_01832 | 7.3e-115 | ybaK | S | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
KKNCFHKG_01833 | 1.4e-77 | |||||
KKNCFHKG_01834 | 4.4e-126 | T | Two component transcriptional regulator, winged helix family | |||
KKNCFHKG_01835 | 4.2e-231 | T | His Kinase A (phosphoacceptor) domain | |||
KKNCFHKG_01836 | 7.7e-14 | |||||
KKNCFHKG_01837 | 3.2e-161 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
KKNCFHKG_01838 | 3.4e-152 | ybbH_2 | K | Transcriptional regulator | ||
KKNCFHKG_01839 | 2.1e-230 | phoA | 3.1.3.1 | P | Belongs to the alkaline phosphatase family | |
KKNCFHKG_01840 | 0.0 | recQ | 3.6.4.12 | L | DNA helicase | |
KKNCFHKG_01841 | 9.8e-163 | ycsE | S | hydrolases of the HAD superfamily | ||
KKNCFHKG_01842 | 6.2e-128 | bshB2 | S | deacetylase | ||
KKNCFHKG_01843 | 5.7e-61 | yojF | S | Protein of unknown function (DUF1806) | ||
KKNCFHKG_01844 | 2.4e-150 | thiD | 2.5.1.3, 2.7.1.35, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
KKNCFHKG_01845 | 3e-165 | 2.1.1.72 | V | site-specific DNA-methyltransferase (adenine-specific) activity | ||
KKNCFHKG_01846 | 2.8e-111 | 2.1.1.72 | L | Belongs to the N(4) N(6)-methyltransferase family | ||
KKNCFHKG_01847 | 7e-78 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
KKNCFHKG_01848 | 2e-225 | htrA | 3.4.21.107 | O | COG0265 Trypsin-like serine proteases, typically periplasmic, contain C-terminal PDZ domain | |
KKNCFHKG_01849 | 9e-147 | vicX | 3.1.26.11 | S | COG1235 Metal-dependent hydrolases of the beta-lactamase superfamily I | |
KKNCFHKG_01850 | 4.3e-141 | yycI | S | protein conserved in bacteria | ||
KKNCFHKG_01851 | 8.3e-243 | yycH | S | protein conserved in bacteria | ||
KKNCFHKG_01852 | 0.0 | vicK | 2.7.13.3 | T | Histidine kinase | |
KKNCFHKG_01853 | 1.7e-133 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
KKNCFHKG_01857 | 1.9e-247 | purA | 6.3.4.4 | F | Plays an important role in the de novo pathway of purine nucleotide biosynthesis. Catalyzes the first committed step in the biosynthesis of AMP from IMP | |
KKNCFHKG_01858 | 1.4e-248 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
KKNCFHKG_01859 | 1.2e-71 | rplI | J | binds to the 23S rRNA | ||
KKNCFHKG_01860 | 0.0 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
KKNCFHKG_01861 | 4.6e-158 | yybS | S | membrane | ||
KKNCFHKG_01862 | 3e-37 | 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 | ||
KKNCFHKG_01863 | 2.2e-82 | ssb | L | Plays an important role in DNA replication, recombination and repair. Binds to ssDNA and to an array of partner proteins to recruit them to their sites of action during DNA metabolism | ||
KKNCFHKG_01864 | 5e-47 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
KKNCFHKG_01865 | 2.5e-80 | ribH | 2.5.1.78 | H | Catalyzes the formation of 6,7-dimethyl-8- ribityllumazine by condensation of 5-amino-6-(D- ribitylamino)uracil with 3,4-dihydroxy-2-butanone 4-phosphate. This is the penultimate step in the biosynthesis of riboflavin | |
KKNCFHKG_01866 | 8.9e-223 | ribBA | 3.5.4.25, 4.1.99.12 | H | Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate | |
KKNCFHKG_01867 | 2.3e-116 | ribE | 2.5.1.9 | H | Riboflavin synthase | |
KKNCFHKG_01868 | 8.9e-209 | ribD | 1.1.1.193, 3.5.4.26 | H | Converts 2,5-diamino-6-(ribosylamino)-4(3h)-pyrimidinone 5'-phosphate into 5-amino-6-(ribosylamino)-2,4(1h,3h)- pyrimidinedione 5'-phosphate | |
KKNCFHKG_01869 | 1.1e-203 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
KKNCFHKG_01870 | 1.1e-32 | yyzM | S | protein conserved in bacteria | ||
KKNCFHKG_01871 | 1.5e-136 | ykuT | M | Mechanosensitive ion channel | ||
KKNCFHKG_01872 | 1.5e-112 | yyaC | S | Sporulation protein YyaC | ||
KKNCFHKG_01873 | 2.3e-117 | ydfK | S | Protein of unknown function (DUF554) | ||
KKNCFHKG_01874 | 1.5e-150 | spo0J | K | Belongs to the ParB family | ||
KKNCFHKG_01875 | 6.9e-136 | soj | D | COG1192 ATPases involved in chromosome partitioning | ||
KKNCFHKG_01876 | 3.5e-152 | noc | D | Effects nucleoid occlusion by binding relatively nonspecifically to DNA and preventing the assembly of the division machinery in the vicinity of the nucleoid, especially under conditions that disturb the cell cycle. It helps to coordinate cell division and chromosome segregation by preventing the formation of the Z ring through the nucleoid, which would cause chromosome breakage | ||
KKNCFHKG_01877 | 2.5e-132 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of guanine in position 535 of 16S rRNA | |
KKNCFHKG_01878 | 0.0 | gidA | D | NAD-binding protein involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA-cmnm(5)s(2)U34 | ||
KKNCFHKG_01879 | 3.4e-251 | mnmE | S | Exhibits a very high intrinsic GTPase hydrolysis rate. Involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA- cmnm(5)s(2)U34 | ||
KKNCFHKG_01880 | 5.9e-109 | jag | S | single-stranded nucleic acid binding R3H | ||
KKNCFHKG_01881 | 3.2e-128 | yidC | U | Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins | ||
KKNCFHKG_01882 | 4.2e-56 | rnpA | 3.1.26.5 | J | RNaseP catalyzes the removal of the 5'-leader sequence from pre-tRNA to produce the mature 5'-terminus. It can also cleave other RNA substrates such as 4.5S RNA. The protein component plays an auxiliary but essential role in vivo by binding to the 5'-leader sequence and broadening the substrate specificity of the ribozyme | |
KKNCFHKG_01883 | 9e-256 | dnaA | L | it binds specifically double-stranded DNA at a 9 bp consensus (dnaA box) 5'-TTATC CA A CA A-3'. DnaA binds to ATP and to acidic phospholipids | ||
KKNCFHKG_01884 | 3.8e-207 | dnaN | 2.7.7.7 | L | Confers DNA tethering and processivity to DNA polymerases and other proteins. Acts as a clamp, forming a ring around DNA (a reaction catalyzed by the clamp-loading complex) which diffuses in an ATP-independent manner freely and bidirectionally along dsDNA. Initially characterized for its ability to contact the catalytic subunit of DNA polymerase III (Pol III), a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria | |
KKNCFHKG_01885 | 4.5e-32 | yaaA | S | S4 domain | ||
KKNCFHKG_01886 | 7.8e-205 | 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 | ||
KKNCFHKG_01887 | 6.2e-10 | yaaB | S | Domain of unknown function (DUF370) | ||
KKNCFHKG_01888 | 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 | |
KKNCFHKG_01889 | 0.0 | gyrA | 5.99.1.3 | L | A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner | |
KKNCFHKG_01890 | 2.2e-196 | M1-161 | T | HD domain | ||
KKNCFHKG_01891 | 9.1e-89 | ylaL | S | Part of the MsrPQ system that repairs oxidized periplasmic proteins containing methionine sulfoxide residues (Met-O), using respiratory chain electrons. Thus protects these proteins from oxidative-stress damage caused by reactive species of oxygen and chlorine generated by the host defense mechanisms. MsrPQ is essential for the maintenance of envelope integrity under bleach stress, rescuing a wide series of structurally unrelated periplasmic proteins from methionine oxidation. The catalytic subunit MsrP is non-stereospecific, being able to reduce both (R-) and (S-) diastereoisomers of methionine sulfoxide | ||
KKNCFHKG_01892 | 2e-247 | phoH | T | ATPase related to phosphate starvation-inducible protein PhoH | ||
KKNCFHKG_01893 | 3e-51 | ylaH | S | YlaH-like protein | ||
KKNCFHKG_01894 | 0.0 | typA | T | GTP-binding protein TypA | ||
KKNCFHKG_01895 | 6e-25 | S | Family of unknown function (DUF5325) | |||
KKNCFHKG_01896 | 1.3e-145 | suhB | 3.1.3.25 | G | Inositol monophosphatase | |
KKNCFHKG_01897 | 1.4e-24 | |||||
KKNCFHKG_01898 | 2.9e-116 | yktB | S | Belongs to the UPF0637 family | ||
KKNCFHKG_01899 | 6.1e-45 | yktA | S | Belongs to the UPF0223 family | ||
KKNCFHKG_01901 | 6.1e-274 | speA | 4.1.1.19 | E | Arginine | |
KKNCFHKG_01903 | 1.6e-33 | |||||
KKNCFHKG_01904 | 6.3e-260 | lpdA | 1.8.1.4 | C | COG1249 Pyruvate 2-oxoglutarate dehydrogenase complex, dihydrolipoamide dehydrogenase (E3) component, and related enzymes | |
KKNCFHKG_01905 | 1e-224 | pdhC | 2.3.1.12 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
KKNCFHKG_01906 | 4.5e-180 | pdhB | 1.2.4.1, 1.2.4.4 | C | COG0022 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, beta subunit | |
KKNCFHKG_01907 | 1.2e-202 | pdhA | 1.2.4.1, 1.2.4.4 | C | COG1071 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, alpha subunit | |
KKNCFHKG_01909 | 1.2e-29 | ykzG | S | Belongs to the UPF0356 family | ||
KKNCFHKG_01910 | 0.0 | rnjA | S | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
KKNCFHKG_01911 | 1.8e-18 | S | YhfH-like protein | |||
KKNCFHKG_01912 | 3.6e-218 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
KKNCFHKG_01913 | 1.2e-70 | dapD | 2.3.1.117, 2.3.1.89 | E | Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate | |
KKNCFHKG_01914 | 2.3e-156 | ccpC | K | Transcriptional regulator | ||
KKNCFHKG_01915 | 6.5e-78 | ykuL | S | CBS domain | ||
KKNCFHKG_01916 | 5.8e-39 | ykuJ | S | protein conserved in bacteria | ||
KKNCFHKG_01917 | 4.3e-161 | 3.5.1.4 | C | Acetamidase | ||
KKNCFHKG_01918 | 2.1e-140 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
KKNCFHKG_01919 | 1e-31 | |||||
KKNCFHKG_01920 | 1e-32 | T | Diguanylate cyclase | |||
KKNCFHKG_01921 | 3e-16 | T | Diguanylate cyclase | |||
KKNCFHKG_01922 | 0.0 | ydgH | S | drug exporters of the RND superfamily | ||
KKNCFHKG_01923 | 2.6e-85 | ykyB | S | YkyB-like protein | ||
KKNCFHKG_01924 | 6.4e-165 | cheV | 2.7.13.3 | T | Chemotaxis protein CheV | |
KKNCFHKG_01925 | 4.4e-219 | patA | 2.6.1.1 | E | Aminotransferase | |
KKNCFHKG_01926 | 5e-159 | glxR | 1.1.1.31, 1.1.1.60 | I | COG2084 3-hydroxyisobutyrate dehydrogenase and related beta-hydroxyacid dehydrogenases | |
KKNCFHKG_01927 | 6.2e-140 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
KKNCFHKG_01928 | 0.0 | ptsI | 2.7.3.9 | G | General (non sugar-specific) component of the phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS). This major carbohydrate active-transport system catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. Enzyme I transfers the phosphoryl group from phosphoenolpyruvate (PEP) to the phosphoryl carrier protein (HPr) | |
KKNCFHKG_01929 | 3.2e-40 | ptsH | G | phosphocarrier protein HPr | ||
KKNCFHKG_01930 | 5e-26 | |||||
KKNCFHKG_01931 | 4.2e-26 | ykvS | S | protein conserved in bacteria | ||
KKNCFHKG_01932 | 7.3e-104 | S | Abortive infection protein | |||
KKNCFHKG_01933 | 1.1e-179 | ykvI | S | membrane | ||
KKNCFHKG_01934 | 0.0 | clpE | O | Belongs to the ClpA ClpB family | ||
KKNCFHKG_01936 | 4.3e-71 | XK27_09985 | S | Protein of unknown function (DUF1232) | ||
KKNCFHKG_01937 | 4e-78 | ogt | 2.1.1.63 | L | Involved in the cellular defense against the biological effects of O6-methylguanine (O6-MeG) and O4-methylthymine (O4-MeT) in DNA. Repairs the methylated nucleobase in DNA by stoichiometrically transferring the methyl group to a cysteine residue in the enzyme. This is a suicide reaction the enzyme is irreversibly inactivated | |
KKNCFHKG_01938 | 5.1e-284 | kinE | 2.7.13.3 | T | Histidine kinase | |
KKNCFHKG_01940 | 4.3e-19 | S | Stage 0 Sporulation Regulatory protein | |||
KKNCFHKG_01941 | 2.8e-28 | sspD | S | small acid-soluble spore protein | ||
KKNCFHKG_01942 | 8.6e-129 | ykoY | P | COG0861 Membrane protein TerC, possibly involved in tellurium resistance | ||
KKNCFHKG_01943 | 3.1e-78 | |||||
KKNCFHKG_01944 | 1.5e-43 | ylaN | S | Belongs to the UPF0358 family | ||
KKNCFHKG_01945 | 8.8e-218 | ftsW | D | Belongs to the SEDS family | ||
KKNCFHKG_01946 | 3.6e-174 | ctaA | 2.5.1.141 | O | Catalyzes the oxidation of the C8 methyl side group on heme O porphyrin ring into a formyl group | |
KKNCFHKG_01947 | 1.6e-163 | ctaB | 2.5.1.141 | O | Converts heme B (protoheme IX) to heme O by substitution of the vinyl group on carbon 2 of heme B porphyrin ring with a hydroxyethyl farnesyl side group | |
KKNCFHKG_01948 | 4.9e-196 | ctaC | 1.9.3.1 | C | Subunits I and II form the functional core of the enzyme complex. Electrons originating in cytochrome c are transferred via heme a and Cu(A) to the binuclear center formed by heme a3 and Cu(B) | |
KKNCFHKG_01949 | 0.0 | ctaD | 1.10.3.12, 1.9.3.1 | C | Cytochrome c oxidase is the component of the respiratory chain that catalyzes the reduction of oxygen to water. Subunits 1- 3 form the functional core of the enzyme complex. CO I is the catalytic subunit of the enzyme. Electrons originating in cytochrome c are transferred via the copper A center of subunit 2 and heme A of subunit 1 to the bimetallic center formed by heme A3 and copper B | |
KKNCFHKG_01950 | 2.1e-114 | cyoC | 1.10.3.12, 1.9.3.1 | C | COG1845 Heme copper-type cytochrome quinol oxidase, subunit 3 | |
KKNCFHKG_01951 | 1.4e-53 | ctaF | 1.10.3.12, 1.9.3.1 | C | COG3125 Heme copper-type cytochrome quinol oxidase, subunit 4 | |
KKNCFHKG_01952 | 1.7e-168 | ctaG | S | cytochrome c oxidase | ||
KKNCFHKG_01953 | 9.6e-64 | ylbA | S | YugN-like family | ||
KKNCFHKG_01954 | 2.3e-167 | ylbC | S | protein with SCP PR1 domains | ||
KKNCFHKG_01955 | 1.7e-84 | yiiD | Q | protein, possibly involved in aromatic compounds catabolism | ||
KKNCFHKG_01956 | 2e-70 | ylbD | S | Putative coat protein | ||
KKNCFHKG_01957 | 7.9e-38 | ylbE | S | YlbE-like protein | ||
KKNCFHKG_01958 | 3.3e-62 | |||||
KKNCFHKG_01959 | 2.8e-73 | ylbF | S | Belongs to the UPF0342 family | ||
KKNCFHKG_01960 | 4.1e-45 | ylbG | S | UPF0298 protein | ||
KKNCFHKG_01961 | 7.7e-67 | S | Methylthioribose kinase | |||
KKNCFHKG_01962 | 2.3e-105 | rsmD | 2.1.1.171 | L | Methyltransferase | |
KKNCFHKG_01963 | 6.6e-84 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
KKNCFHKG_01964 | 5.5e-220 | ylbJ | S | Sporulation integral membrane protein YlbJ | ||
KKNCFHKG_01965 | 7.6e-138 | ylbK | S | esterase of the alpha-beta hydrolase superfamily | ||
KKNCFHKG_01966 | 6.5e-193 | ylbL | T | Belongs to the peptidase S16 family | ||
KKNCFHKG_01967 | 8.2e-224 | ylbM | S | Belongs to the UPF0348 family | ||
KKNCFHKG_01968 | 1.2e-93 | yceD | S | metal-binding, possibly nucleic acid-binding protein | ||
KKNCFHKG_01969 | 1.1e-25 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
KKNCFHKG_01970 | 1.6e-80 | rsfA | S | SANT SWI3, ADA2, N-CoR and TFIIIB'' DNA-binding domains | ||
KKNCFHKG_01971 | 2.3e-92 | ylbP | K | n-acetyltransferase | ||
KKNCFHKG_01972 | 1.1e-158 | panE | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
KKNCFHKG_01973 | 0.0 | bshC | S | Involved in bacillithiol (BSH) biosynthesis. May catalyze the last step of the pathway, the addition of cysteine to glucosamine malate (GlcN-Mal) to generate BSH | ||
KKNCFHKG_01974 | 1.4e-77 | mraZ | K | Belongs to the MraZ family | ||
KKNCFHKG_01975 | 3.3e-172 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
KKNCFHKG_01976 | 1.7e-39 | ftsL | D | Essential cell division protein | ||
KKNCFHKG_01977 | 0.0 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
KKNCFHKG_01978 | 0.0 | ftsI | 3.4.16.4 | M | stage V sporulation protein D | |
KKNCFHKG_01979 | 4.8e-279 | murE | 6.3.2.10, 6.3.2.13 | M | Catalyzes the addition of meso-diaminopimelic acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
KKNCFHKG_01980 | 1.7e-78 | murF | 6.3.2.10 | M | UDP-N-acetylmuramoyl-tripeptide-D-alanyl-D-alanine ligase activity | |
KKNCFHKG_01981 | 2.5e-170 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
KKNCFHKG_01982 | 1.3e-257 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
KKNCFHKG_01983 | 7.7e-189 | spoVE | D | Belongs to the SEDS family | ||
KKNCFHKG_01984 | 7.7e-205 | 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) |
KKNCFHKG_01985 | 1.1e-117 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
KKNCFHKG_01987 | 6.4e-219 | ftsA | D | Cell division protein that is involved in the assembly of the Z ring. May serve as a membrane anchor for the Z ring | ||
KKNCFHKG_01988 | 3.6e-189 | 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 | ||
KKNCFHKG_01989 | 7.3e-164 | spoIIGA | M | aspartic protease that is responsible for the proteolytic cleavage of the RNA polymerase sigma E factor (SigE spoIIGB) to yield the active peptide in the mother cell during sporulation. Responds to a signal from the forespore that is triggered by the extracellular signal protein SpoIIR | ||
KKNCFHKG_01990 | 3.5e-113 | sigE | K | sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
KKNCFHKG_01991 | 3.7e-137 | sigG | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
KKNCFHKG_01992 | 2.4e-99 | cwlS | 3.5.1.28 | CBM50 | M | COG1388 FOG LysM repeat |
KKNCFHKG_01994 | 1.6e-101 | P | Integral membrane protein TerC family | |||
KKNCFHKG_01995 | 7.8e-304 | yhcX | K | Nitrilase cyanide hydratase and apolipoprotein N-acyltransferase | ||
KKNCFHKG_01996 | 7e-23 | S | Uncharacterized small protein (DUF2292) | |||
KKNCFHKG_01997 | 3.3e-08 | ssuE | 1.5.1.38 | S | FMN reductase | |
KKNCFHKG_01998 | 4.2e-77 | ssuD | 1.14.14.5 | C | Catalyzes the desulfonation of aliphatic sulfonates | |
KKNCFHKG_01999 | 8.5e-187 | guaC | 1.1.1.205, 1.7.1.7 | F | Catalyzes the irreversible NADPH-dependent deamination of GMP to IMP. It functions in the conversion of nucleobase, nucleoside and nucleotide derivatives of G to A nucleotides, and in maintaining the intracellular balance of A and G nucleotides | |
KKNCFHKG_02000 | 0.0 | metE | 2.1.1.14 | E | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | |
KKNCFHKG_02001 | 4e-71 | cdd | 2.4.2.2, 3.5.4.5 | F | This enzyme scavenges exogenous and endogenous cytidine and 2'-deoxycytidine for UMP synthesis | |
KKNCFHKG_02002 | 1.4e-110 | deoC | 4.1.2.4, 5.4.2.8 | F | Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate | |
KKNCFHKG_02003 | 1.4e-234 | pdp | 2.4.2.2, 2.4.2.4 | F | phosphorylase | |
KKNCFHKG_02004 | 1.1e-233 | deoB | 5.4.2.7 | G | Phosphotransfer between the C1 and C5 carbon atoms of pentose | |
KKNCFHKG_02005 | 5.7e-172 | deoR | K | COG2390 Transcriptional regulator, contains sigma factor-related N-terminal domain | ||
KKNCFHKG_02006 | 4.9e-128 | deoD | 2.4.2.1, 2.4.2.28 | F | Purine nucleoside phosphorylase | |
KKNCFHKG_02007 | 1.1e-207 | nupG | F | Belongs to the concentrative nucleoside transporter (CNT) (TC 2.A.41) family | ||
KKNCFHKG_02008 | 1.4e-224 | pbuO_1 | S | permease | ||
KKNCFHKG_02009 | 3e-116 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
KKNCFHKG_02010 | 1.5e-164 | S | Protein of unknown function (DUF979) | |||
KKNCFHKG_02011 | 6.5e-117 | S | Protein of unknown function (DUF969) | |||
KKNCFHKG_02012 | 2.2e-137 | ycsF | S | Belongs to the UPF0271 (lamB) family | ||
KKNCFHKG_02013 | 1.6e-185 | kipA | 6.3.4.6 | E | Allophanate hydrolase subunit 2 | |
KKNCFHKG_02014 | 1.2e-131 | kipI | 3.5.1.54, 6.3.4.6 | E | Allophanate hydrolase subunit 1 | |
KKNCFHKG_02015 | 1.7e-213 | EGP | Major facilitator Superfamily | |||
KKNCFHKG_02016 | 3.9e-78 | ymaD | O | redox protein, regulator of disulfide bond formation | ||
KKNCFHKG_02017 | 5e-128 | artM | 3.6.3.21 | E | COG1126 ABC-type polar amino acid transport system, ATPase component | |
KKNCFHKG_02018 | 5.8e-115 | artQ | E | COG0765 ABC-type amino acid transport system, permease component | ||
KKNCFHKG_02019 | 6.7e-131 | artP | ET | COG0834 ABC-type amino acid transport signal transduction systems, periplasmic component domain | ||
KKNCFHKG_02020 | 5e-210 | hipO3 | 3.5.1.47 | S | amidohydrolase | |
KKNCFHKG_02021 | 0.0 | htpG | O | Molecular chaperone. Has ATPase activity | ||
KKNCFHKG_02022 | 8.2e-183 | M | FFAT motif binding | |||
KKNCFHKG_02023 | 9.1e-56 | I | Domain of unknown function (DUF4430) | |||
KKNCFHKG_02024 | 4.2e-90 | S | Psort location CytoplasmicMembrane, score | |||
KKNCFHKG_02025 | 1.8e-115 | crtF | 2.1.1.210, 2.1.1.281, 2.1.1.79 | M | Methyltransferase | |
KKNCFHKG_02026 | 4.3e-211 | yurR | 1.4.5.1 | E | COG0665 Glycine D-amino acid oxidases (deaminating) | |
KKNCFHKG_02027 | 1.6e-29 | S | Nucleotidyltransferase domain | |||
KKNCFHKG_02028 | 3.8e-190 | adhP | 1.1.1.1 | C | alcohol dehydrogenase | |
KKNCFHKG_02030 | 1.1e-149 | S | LXG domain of WXG superfamily | |||
KKNCFHKG_02031 | 4.4e-41 | S | LXG domain of WXG superfamily | |||
KKNCFHKG_02034 | 3.8e-140 | S | Protein of unknown function | |||
KKNCFHKG_02035 | 1.1e-189 | aglB | 3.2.1.122, 3.2.1.86 | GH4,GT4 | G | Family 4 glycosyl hydrolase C-terminal domain |
KKNCFHKG_02036 | 1.7e-197 | glvC | 2.7.1.199, 2.7.1.208 | G | pts system | |
KKNCFHKG_02037 | 3.8e-33 | glvR | K | Helix-turn-helix domain, rpiR family | ||
KKNCFHKG_02039 | 1.8e-41 | nagE | 2.7.1.193, 2.7.1.208 | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | |
KKNCFHKG_02040 | 1.1e-118 | frnE | Q | dithiol-disulfide isomerase involved in polyketide biosynthesis | ||
KKNCFHKG_02041 | 2.4e-90 | yebE | S | UPF0316 protein | ||
KKNCFHKG_02042 | 2.9e-31 | yebG | S | NETI protein | ||
KKNCFHKG_02043 | 1.3e-82 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
KKNCFHKG_02044 | 4.6e-216 | purK | 6.3.4.18 | F | Catalyzes the ATP-dependent conversion of 5- aminoimidazole ribonucleotide (AIR) and HCO(3)(-) to N5- carboxyaminoimidazole ribonucleotide (N5-CAIR) | |
KKNCFHKG_02045 | 4.3e-247 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
KKNCFHKG_02046 | 2.5e-124 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
KKNCFHKG_02047 | 7.1e-37 | purS | 6.3.2.6, 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
KKNCFHKG_02048 | 3.8e-125 | purQ | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
KKNCFHKG_02049 | 0.0 | purL | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
KKNCFHKG_02050 | 4.2e-272 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
KKNCFHKG_02051 | 2.1e-191 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
KKNCFHKG_02052 | 4.1e-104 | purN | 2.1.2.2 | F | Catalyzes the transfer of a formyl group from 10- formyltetrahydrofolate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR) and tetrahydrofolate | |
KKNCFHKG_02053 | 2e-288 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
KKNCFHKG_02054 | 1.6e-230 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
KKNCFHKG_02055 | 3.2e-36 | S | Protein of unknown function (DUF2892) | |||
KKNCFHKG_02056 | 0.0 | yerA | 3.5.4.2 | F | adenine deaminase | |
KKNCFHKG_02057 | 4.2e-189 | yerB | S | Protein of unknown function (DUF3048) C-terminal domain | ||
KKNCFHKG_02058 | 2.2e-54 | yerC | S | protein conserved in bacteria | ||
KKNCFHKG_02059 | 4.8e-128 | pcrB | I | 35 carbon atoms) to the C3 hydroxyl of sn-glycerol-1-phosphate (G1P), producing heptaprenylglyceryl phosphate (HepGP). This reaction is an ether-bond-formation step in the biosynthesis of archaea-type G1P-based membrane lipids found in Bacillales | ||
KKNCFHKG_02060 | 0.0 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
KKNCFHKG_02061 | 0.0 | ligA | 6.5.1.2 | L | DNA ligase that catalyzes the formation of phosphodiester linkages between 5'-phosphoryl and 3'-hydroxyl groups in double-stranded DNA using NAD as a coenzyme and as the energy source for the reaction. It is essential for DNA replication and repair of damaged DNA | |
KKNCFHKG_02062 | 1.3e-215 | camS | S | COG4851 Protein involved in sex pheromone biosynthesis | ||
KKNCFHKG_02063 | 0.0 | aceB | 2.3.3.9 | C | Belongs to the malate synthase family | |
KKNCFHKG_02064 | 1.5e-244 | aceA | 4.1.3.1 | C | Isocitrate lyase | |
KKNCFHKG_02066 | 7.3e-46 | 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) | |
KKNCFHKG_02067 | 4.6e-274 | gatA | 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Gln-tRNA(Gln) through the transamidation of misacylated Glu-tRNA(Gln) in organisms which lack glutaminyl-tRNA synthetase. The reaction takes place in the presence of glutamine and ATP through an activated gamma-phospho-Glu-tRNA(Gln) | |
KKNCFHKG_02068 | 3.3e-272 | gatB | 6.1.1.12, 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | |
KKNCFHKG_02071 | 5.2e-150 | Q | N-acetyltransferase | |||
KKNCFHKG_02072 | 3.5e-171 | yegS | 2.7.1.107 | I | COG1597 Sphingosine kinase and enzymes related to eukaryotic diacylglycerol kinase | |
KKNCFHKG_02073 | 9.5e-267 | putP | E | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
KKNCFHKG_02074 | 4.4e-242 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
KKNCFHKG_02075 | 1.8e-81 | |||||
KKNCFHKG_02076 | 6.3e-132 | ypmR1 | E | G-D-S-L family | ||
KKNCFHKG_02077 | 5.6e-169 | bcrA | V | ABC transporter, ATP-binding protein | ||
KKNCFHKG_02078 | 5.7e-175 | bcrB | S | ABC transporter (permease) | ||
KKNCFHKG_02079 | 6.4e-88 | |||||
KKNCFHKG_02080 | 7.4e-95 | 1.5.1.38 | S | FMN reductase | ||
KKNCFHKG_02081 | 2.1e-145 | pflA | 1.97.1.4 | C | Activation of pyruvate formate-lyase under anaerobic conditions by generation of an organic free radical, using S- adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine | |
KKNCFHKG_02082 | 0.0 | pflB | 2.3.1.54 | C | formate acetyltransferase | |
KKNCFHKG_02085 | 3.5e-149 | focA | P | Formate/nitrite transporter | ||
KKNCFHKG_02086 | 1.8e-22 | tcyC | 3.6.3.21 | E | COG1126 ABC-type polar amino acid transport system, ATPase component | |
KKNCFHKG_02087 | 6.2e-66 | tcyC | 3.6.3.21 | E | COG1126 ABC-type polar amino acid transport system, ATPase component | |
KKNCFHKG_02088 | 4.2e-116 | tcyB | P | COG0765 ABC-type amino acid transport system, permease component | ||
KKNCFHKG_02089 | 5e-145 | tcyA | ET | Belongs to the bacterial solute-binding protein 3 family | ||
KKNCFHKG_02090 | 2.4e-83 | S | Rubrerythrin | |||
KKNCFHKG_02091 | 4.6e-166 | ppaC | 3.6.1.1 | C | Inorganic pyrophosphatase | |
KKNCFHKG_02092 | 8.2e-103 | yvbG | U | UPF0056 membrane protein | ||
KKNCFHKG_02093 | 6e-221 | queG | 1.17.99.6 | C | Catalyzes the conversion of epoxyqueuosine (oQ) to queuosine (Q), which is a hypermodified base found in the wobble positions of tRNA(Asp), tRNA(Asn), tRNA(His) and tRNA(Tyr) | |
KKNCFHKG_02094 | 1.1e-161 | yhbB | S | Putative amidase domain | ||
KKNCFHKG_02095 | 2e-88 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
KKNCFHKG_02096 | 0.0 | prkA | T | Ser protein kinase | ||
KKNCFHKG_02097 | 8.1e-221 | yhbH | S | Belongs to the UPF0229 family | ||
KKNCFHKG_02099 | 1.9e-98 | 2.3.1.128 | J | Acetyltransferase (GNAT) domain | ||
KKNCFHKG_02100 | 3.4e-175 | pit | P | phosphate transporter | ||
KKNCFHKG_02101 | 5.6e-112 | ykaA | P | COG1392 Phosphate transport regulator (distant homolog of PhoU) | ||
KKNCFHKG_02102 | 1.2e-10 | yhcU | S | Family of unknown function (DUF5365) | ||
KKNCFHKG_02103 | 3.9e-66 | yhcU | S | Family of unknown function (DUF5365) | ||
KKNCFHKG_02104 | 5.8e-88 | bdbA | CO | Thioredoxin | ||
KKNCFHKG_02105 | 2.1e-73 | bdbC | O | Required for disulfide bond formation in some proteins | ||
KKNCFHKG_02106 | 1.6e-134 | 3.2.1.18 | GH33 | E | GDSL-like Lipase/Acylhydrolase | |
KKNCFHKG_02107 | 4.1e-181 | ykrP | G | COG3594 Fucose 4-O-acetylase and related acetyltransferases | ||
KKNCFHKG_02108 | 6.9e-275 | ycgB | S | Stage V sporulation protein R | ||
KKNCFHKG_02110 | 1.8e-46 | yhdB | S | YhdB-like protein | ||
KKNCFHKG_02111 | 2.5e-183 | corA | P | Mediates influx of magnesium ions | ||
KKNCFHKG_02112 | 6e-126 | S | Peptidase C26 | |||
KKNCFHKG_02113 | 4.1e-159 | dppB | P | COG0601 ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
KKNCFHKG_02114 | 6.5e-168 | dppC | EP | COG1173 ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
KKNCFHKG_02115 | 4.6e-188 | dppD | P | Belongs to the ABC transporter superfamily | ||
KKNCFHKG_02116 | 0.0 | dppE | E | ABC transporter substrate-binding protein | ||
KKNCFHKG_02117 | 1.5e-177 | ykfC | 3.4.14.13 | M | COG0791 Cell wall-associated hydrolases (invasion-associated proteins) | |
KKNCFHKG_02118 | 6.9e-192 | ykfD | E | Belongs to the ABC transporter superfamily | ||
KKNCFHKG_02120 | 9.6e-86 | uspF | T | Universal stress protein | ||
KKNCFHKG_02121 | 0.0 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
KKNCFHKG_02123 | 3.4e-163 | ygxA | S | Nucleotidyltransferase-like | ||
KKNCFHKG_02124 | 2.8e-55 | ygzB | S | UPF0295 protein | ||
KKNCFHKG_02125 | 2.9e-139 | budA | 4.1.1.5 | Q | Alpha-acetolactate decarboxylase | |
KKNCFHKG_02126 | 0.0 | alsS | 2.2.1.6 | EH | Belongs to the TPP enzyme family | |
KKNCFHKG_02127 | 1.5e-163 | alsR | K | Transcriptional regulator | ||
KKNCFHKG_02128 | 5.4e-87 | iprA | K | Transcriptional regulator | ||
KKNCFHKG_02130 | 2.9e-81 | perR | P | Belongs to the Fur family | ||
KKNCFHKG_02131 | 2.3e-101 | yvqK | 1.2.1.88, 1.5.5.2, 2.5.1.17 | S | Adenosyltransferase | |
KKNCFHKG_02132 | 3.4e-65 | P | Ion transport | |||
KKNCFHKG_02133 | 5.6e-247 | gsaB | 5.4.3.8 | H | Glutamate-1-semialdehyde aminotransferase | |
KKNCFHKG_02134 | 1.2e-37 | yqhV | S | Protein of unknown function (DUF2619) | ||
KKNCFHKG_02135 | 3.2e-187 | ygaE | S | Membrane | ||
KKNCFHKG_02136 | 1.2e-147 | K | transcriptional | |||
KKNCFHKG_02137 | 1.6e-250 | sacX | 2.7.1.201, 2.7.1.211 | G | phosphotransferase system | |
KKNCFHKG_02138 | 6.8e-151 | murQ | 4.2.1.126 | G | Specifically catalyzes the cleavage of the D-lactyl ether substituent of MurNAc 6-phosphate, producing GlcNAc 6- phosphate and D-lactate | |
KKNCFHKG_02139 | 2.6e-205 | yleB | 4.2.1.126 | S | Bacterial protein of unknown function (DUF871) | |
KKNCFHKG_02140 | 0.0 | ygaD | V | ABC transporter | ||
KKNCFHKG_02141 | 5.3e-103 | ygaC | J | Belongs to the UPF0374 family | ||
KKNCFHKG_02142 | 1.3e-35 | ygaB | S | YgaB-like protein | ||
KKNCFHKG_02143 | 1.7e-08 | sspE | S | Small, acid-soluble spore protein, gamma-type | ||
KKNCFHKG_02144 | 7.7e-132 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
KKNCFHKG_02145 | 4.9e-165 | gltC | K | Transcriptional regulator | ||
KKNCFHKG_02146 | 0.0 | gltB | 1.4.1.13, 1.4.1.14, 1.4.7.1 | E | glutamate synthase | |
KKNCFHKG_02148 | 1.4e-278 | gltD | 1.4.1.13, 1.4.1.14 | E | COG0493 NADPH-dependent glutamate synthase beta chain and related oxidoreductases | |
KKNCFHKG_02149 | 8.8e-31 | |||||
KKNCFHKG_02150 | 3.1e-198 | mutY | L | A G-specific | ||
KKNCFHKG_02151 | 4.1e-181 | yfhP | S | membrane-bound metal-dependent | ||
KKNCFHKG_02152 | 4.2e-19 | sspK | S | reproduction | ||
KKNCFHKG_02153 | 4.5e-49 | yfhH | S | Protein of unknown function (DUF1811) | ||
KKNCFHKG_02154 | 2.4e-131 | recX | 2.4.1.337 | GT4 | S | Modulates RecA activity |
KKNCFHKG_02156 | 3.8e-24 | yfhD | S | YfhD-like protein | ||
KKNCFHKG_02157 | 6.9e-139 | trpA | 4.2.1.20 | E | The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate | |
KKNCFHKG_02159 | 1.6e-227 | trpB | 4.2.1.20, 5.3.1.24 | E | The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine | |
KKNCFHKG_02160 | 2.8e-247 | trpF | 4.1.1.48, 4.2.1.160, 4.2.1.20, 5.3.1.24 | E | Belongs to the TrpC family | |
KKNCFHKG_02161 | 2.2e-182 | trpD | 2.4.2.18, 4.1.3.27 | E | Catalyzes the transfer of the phosphoribosyl group of 5- phosphorylribose-1-pyrophosphate (PRPP) to anthranilate to yield N-(5'-phosphoribosyl)-anthranilate (PRA) | |
KKNCFHKG_02162 | 1.5e-106 | trpG | 2.4.2.18, 2.6.1.85, 4.1.3.27 | EH | Anthranilate synthase | |
KKNCFHKG_02163 | 4.7e-260 | trpE | 4.1.3.27 | EH | Part of a heterotetrameric complex that catalyzes the two-step biosynthesis of anthranilate, an intermediate in the biosynthesis of L-tryptophan. In the first step, the glutamine- binding beta subunit (TrpG) of anthranilate synthase (AS) provides the glutamine amidotransferase activity which generates ammonia as a substrate that, along with chorismate, is used in the second step, catalyzed by the large alpha subunit of AS (TrpE) to produce anthranilate. In the absence of TrpG, TrpE can synthesize anthranilate directly from chorismate and high concentrations of ammonia | |
KKNCFHKG_02164 | 0.0 | atl | 3.2.1.96, 3.5.1.28 | GH73 | G | Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase |
KKNCFHKG_02166 | 5.5e-29 | yodI | ||||
KKNCFHKG_02167 | 5.9e-120 | yjaZ | O | Zn-dependent protease | ||
KKNCFHKG_02168 | 2.5e-101 | yodH | Q | Methyltransferase | ||
KKNCFHKG_02169 | 8.5e-21 | S | PD-(D/E)XK nuclease family transposase | |||
KKNCFHKG_02170 | 2.1e-111 | S | PD-(D/E)XK nuclease family transposase | |||
KKNCFHKG_02171 | 0.0 | gtfC | 2.4.1.5 | GH13 | M | KxYKxGKxW signal domain protein |
KKNCFHKG_02172 | 1.9e-21 | ygiM | N | Bacterial SH3 domain | ||
KKNCFHKG_02173 | 1.7e-197 | L | High confidence in function and specificity | |||
KKNCFHKG_02174 | 3.5e-68 | G | PTS system fructose IIA component | |||
KKNCFHKG_02175 | 1.3e-143 | G | PTS system mannose/fructose/sorbose family IID component | |||
KKNCFHKG_02176 | 5.9e-138 | agaC | G | PTS system sorbose-specific iic component | ||
KKNCFHKG_02177 | 9.6e-80 | agaB | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
KKNCFHKG_02178 | 1.5e-127 | 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 | |
KKNCFHKG_02179 | 4.6e-129 | K | UTRA | |||
KKNCFHKG_02180 | 3.8e-96 | puuR_2 | K | Cupin domain | ||
KKNCFHKG_02181 | 0.0 | oplaH | 3.5.2.14, 3.5.2.9 | EQ | COG0145 N-methylhydantoinase A acetone carboxylase, beta subunit | |
KKNCFHKG_02182 | 0.0 | 3.5.2.14 | EQ | COG0146 N-methylhydantoinase B acetone carboxylase, alpha subunit | ||
KKNCFHKG_02183 | 3.7e-249 | F | Permease for cytosine/purines, uracil, thiamine, allantoin | |||
KKNCFHKG_02184 | 0.0 | K | PTS system fructose IIA component | |||
KKNCFHKG_02185 | 2.6e-95 | K | PRD domain | |||
KKNCFHKG_02186 | 1.5e-71 | 2.7.1.191 | G | PTS system fructose IIA component | ||
KKNCFHKG_02187 | 2.1e-42 | 2.7.1.191 | G | PTS system mannose fructose sorbose family | ||
KKNCFHKG_02188 | 5.7e-133 | G | PTS system sorbose-specific iic component | |||
KKNCFHKG_02189 | 6.1e-143 | G | PFAM Phosphotransferase system, mannose fructose sorbose family IID component | |||
KKNCFHKG_02190 | 1.2e-169 | M | SIS domain | |||
KKNCFHKG_02191 | 7.6e-12 | M | SIS domain | |||
KKNCFHKG_02192 | 1.3e-170 | 2.7.1.194, 2.7.1.202 | GKT | COG3711 Transcriptional antiterminator | ||
KKNCFHKG_02193 | 1.2e-35 | 2.7.1.197, 2.7.1.200, 2.7.1.202 | G | PTS galactitol transporter subunit IIA | ||
KKNCFHKG_02194 | 4.1e-30 | sgcB | 2.7.1.200 | G | to PTS system galactitol-specific enzyme IIB component | |
KKNCFHKG_02195 | 9.8e-197 | G | PTS system sugar-specific permease component | |||
KKNCFHKG_02197 | 4e-72 | 2.7.1.11, 2.7.1.56 | F | pfkB family carbohydrate kinase | ||
KKNCFHKG_02198 | 7.9e-85 | 4.1.2.17, 4.1.2.19 | G | Class II Aldolase and Adducin N-terminal domain | ||
KKNCFHKG_02199 | 5.7e-284 | K | COG3829 Transcriptional regulator containing PAS, AAA-type ATPase, and DNA-binding domains | |||
KKNCFHKG_02200 | 1.8e-19 | S | transposase or invertase | |||
KKNCFHKG_02202 | 8.3e-105 | clpP | 3.4.21.92 | OU | 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 | |
KKNCFHKG_02203 | 4.3e-40 | crh | G | Phosphocarrier protein Chr | ||
KKNCFHKG_02204 | 5.2e-173 | whiA | K | May be required for sporulation | ||
KKNCFHKG_02205 | 8.5e-179 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
KKNCFHKG_02206 | 3.4e-163 | rapZ | S | Displays ATPase and GTPase activities | ||
KKNCFHKG_02207 | 5.1e-86 | yvcI | 3.6.1.55 | F | Nudix hydrolase | |
KKNCFHKG_02208 | 3.1e-178 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
KKNCFHKG_02209 | 1.3e-250 | S | COG0457 FOG TPR repeat | |||
KKNCFHKG_02210 | 5.2e-71 | yvoF | S | COG0110 Acetyltransferase (isoleucine patch superfamily) | ||
KKNCFHKG_02211 | 1.7e-114 | ppaX | 3.1.3.18, 3.6.1.1 | S | Hydrolyzes pyrophosphate formed during P-Ser-HPr dephosphorylation by HPrK P. Might play a role in controlling the intracellular pyrophosphate pool | |
KKNCFHKG_02212 | 3.5e-154 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
KKNCFHKG_02213 | 1.7e-171 | hprK | F | Catalyzes the ATP- as well as the pyrophosphate- dependent phosphorylation of a specific serine residue in HPr, a phosphocarrier protein of the phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS). HprK P also catalyzes the pyrophosphate-producing, inorganic phosphate-dependent dephosphorylation (phosphorolysis) of seryl-phosphorylated HPr (P- Ser-HPr). The two antagonistic activities of HprK P are regulated by several intracellular metabolites, which change their concentration in response to the absence or presence of rapidly metabolisable carbon sources (glucose, fructose, etc.) in the growth medium. Also phosphorylates dephosphorylates the HPr-like catabolite repression protein crh on a specific serine residue. Therefore, by controlling the phosphorylation state of HPr and crh, HPrK P is a sensor enzyme that plays a major role in the regulation of carbon metabolism and sugar transport it mediates carbon catabolite repression (CCR), and regulates PTS-catalyzed carbohydrate uptake and inducer exclusion | ||
KKNCFHKG_02214 | 3.5e-31 | yvlD | S | Membrane | ||
KKNCFHKG_02215 | 1.7e-170 | yvlB | S | Putative adhesin | ||
KKNCFHKG_02216 | 0.0 | 2.7.8.12 | M | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | ||
KKNCFHKG_02217 | 4.5e-146 | tagG | GM | Transport permease protein | ||
KKNCFHKG_02218 | 2e-230 | tagF | 2.7.8.12 | M | glycosyl glycerophosphate transferases involved in teichoic acid biosynthesis TagF TagB EpsJ RodC | |
KKNCFHKG_02219 | 4.9e-229 | tagB | 2.7.8.14, 2.7.8.44, 2.7.8.47 | M | glycosyl glycerophosphate transferases involved in teichoic acid biosynthesis TagF TagB EpsJ RodC | |
KKNCFHKG_02220 | 2.8e-72 | tagD | 2.7.7.15, 2.7.7.39 | IM | Cytidylyltransferase | |
KKNCFHKG_02221 | 0.0 | uvrA | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrA is an ATPase and a DNA-binding protein. A damage recognition complex composed of 2 UvrA and 2 UvrB subunits scans DNA for abnormalities. When the presence of a lesion has been verified by UvrB, the UvrA molecules dissociate | ||
KKNCFHKG_02222 | 0.0 | uvrB | L | damaged site, the DNA wraps around one UvrB monomer. DNA wrap is dependent on ATP binding by UvrB and probably causes local melting of the DNA helix, facilitating insertion of UvrB beta-hairpin between the DNA strands. Then UvrB probes one DNA strand for the presence of a lesion. If a lesion is found the UvrA subunits dissociate and the UvrB-DNA preincision complex is formed. This complex is subsequently bound by UvrC and the second UvrB is released. If no lesion is found, the DNA wraps around the other UvrB subunit that will check the other stand for damage | ||
KKNCFHKG_02223 | 3.6e-09 | S | Uncharacterized conserved protein (DUF2164) | |||
KKNCFHKG_02224 | 1.2e-33 | csbA | S | protein conserved in bacteria | ||
KKNCFHKG_02225 | 1.6e-117 | yfbR | S | HD containing hydrolase-like enzyme | ||
KKNCFHKG_02226 | 2.1e-49 | S | EamA-like transporter family | |||
KKNCFHKG_02227 | 2.1e-55 | P | EamA-like transporter family | |||
KKNCFHKG_02228 | 0.0 | |||||
KKNCFHKG_02229 | 3.9e-173 | M | Glycosyltransferase like family 2 | |||
KKNCFHKG_02230 | 5.8e-146 | 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 | |
KKNCFHKG_02231 | 1.4e-153 | 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 | |
KKNCFHKG_02232 | 6.9e-156 | pstA | P | Phosphate transport system permease | ||
KKNCFHKG_02233 | 1.6e-158 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
KKNCFHKG_02234 | 1.2e-160 | pstS | P | Phosphate | ||
KKNCFHKG_02235 | 3.3e-261 | hemY2 | 1.3.3.15, 1.3.3.4 | H | Catalyzes the 6-electron oxidation of protoporphyrinogen-IX to form protoporphyrin-IX | |
KKNCFHKG_02236 | 1.4e-40 | fdxA | C | 4Fe-4S binding domain | ||
KKNCFHKG_02237 | 2.5e-15 | S | Ribbon-helix-helix protein, copG family | |||
KKNCFHKG_02238 | 1.5e-269 | hemG | 1.14.19.9, 1.3.3.15, 1.3.3.4 | H | Catalyzes the 6-electron oxidation of protoporphyrinogen-IX to form protoporphyrin-IX | |
KKNCFHKG_02239 | 2.7e-182 | hemH | 4.99.1.1, 4.99.1.9 | H | Catalyzes the ferrous insertion into protoporphyrin IX | |
KKNCFHKG_02240 | 1.1e-197 | hemE | 4.1.1.37 | H | Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III | |
KKNCFHKG_02241 | 7.5e-94 | traP | 1.14.99.57 | S | enzyme involved in biosynthesis of extracellular polysaccharides | |
KKNCFHKG_02243 | 1.8e-238 | yhfA | C | membrane | ||
KKNCFHKG_02244 | 3.7e-229 | yhaA | 3.5.1.47 | E | COG1473 Metal-dependent amidase aminoacylase carboxypeptidase | |
KKNCFHKG_02245 | 7.2e-220 | ecsB | U | ABC transporter | ||
KKNCFHKG_02246 | 1.6e-137 | ecsA | V | transporter (ATP-binding protein) | ||
KKNCFHKG_02247 | 4.1e-74 | hit | FG | COG0537 Diadenosine tetraphosphate (Ap4A) hydrolase and other HIT family hydrolases | ||
KKNCFHKG_02248 | 1.9e-84 | trpP | S | Tryptophan transporter TrpP | ||
KKNCFHKG_02249 | 2.1e-18 | yhaH | S | YtxH-like protein | ||
KKNCFHKG_02250 | 1.2e-103 | hpr | K | Negative regulator of protease production and sporulation | ||
KKNCFHKG_02251 | 1.1e-53 | yhaI | S | Protein of unknown function (DUF1878) | ||
KKNCFHKG_02254 | 3.1e-148 | prsA | 5.2.1.8 | M | plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
KKNCFHKG_02255 | 3e-27 | yhaL | S | Sporulation protein YhaL | ||
KKNCFHKG_02256 | 1.1e-178 | yhaM | L | Shows a 3'-5' exoribonuclease activity | ||
KKNCFHKG_02257 | 0.0 | L | AAA domain | |||
KKNCFHKG_02258 | 2.8e-240 | yhaO | L | DNA repair exonuclease | ||
KKNCFHKG_02259 | 6.9e-153 | ycgQ | S | membrane | ||
KKNCFHKG_02260 | 3.3e-145 | ycgR | S | permeases | ||
KKNCFHKG_02261 | 8.1e-121 | P | Integral membrane protein TerC family | |||
KKNCFHKG_02262 | 4.9e-27 | S | YhzD-like protein | |||
KKNCFHKG_02263 | 2.9e-137 | yhaR | 5.3.3.18 | I | enoyl-CoA hydratase | |
KKNCFHKG_02264 | 3e-159 | yhaX | S | hydrolases of the HAD superfamily | ||
KKNCFHKG_02265 | 6.1e-55 | yheA | S | Belongs to the UPF0342 family | ||
KKNCFHKG_02266 | 9.1e-209 | yheB | S | Belongs to the UPF0754 family | ||
KKNCFHKG_02267 | 1e-259 | gshB | 6.3.2.2, 6.3.2.3 | HJ | YheC/D like ATP-grasp | |
KKNCFHKG_02268 | 9.3e-211 | yheC | HJ | YheC/D like ATP-grasp | ||
KKNCFHKG_02269 | 5.5e-269 | gshB | 6.3.2.2, 6.3.2.3 | HJ | YheC/D like ATP-grasp | |
KKNCFHKG_02270 | 4.1e-228 | HJ | COG0189 Glutathione synthase Ribosomal protein S6 modification enzyme (glutaminyl transferase) | |||
KKNCFHKG_02271 | 6.8e-167 | lrp | QT | PucR C-terminal helix-turn-helix domain | ||
KKNCFHKG_02272 | 5e-204 | msmK | P | Belongs to the ABC transporter superfamily | ||
KKNCFHKG_02273 | 3.4e-29 | sspB | S | spore protein | ||
KKNCFHKG_02274 | 2.7e-263 | fumC | 1.1.1.38, 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
KKNCFHKG_02275 | 1.3e-232 | pgaC | GT2 | M | N-acetylglucosaminyltransferase that catalyzes the polymerization of single monomer units of UDP-N-acetylglucosamine to produce the linear homopolymer poly-beta-1,6-N-acetyl-D- glucosamine (PNAG, also referred to as PIA), a biofilm adhesin polysaccharide. Requires IcaD for full activity | |
KKNCFHKG_02276 | 1.9e-47 | icaD | ||||
KKNCFHKG_02277 | 5.4e-147 | icaB | G | Catalyzes the N-deacetylation of poly-beta-1,6-N-acetyl- D-glucosamine (PNAG, also referred to as PIA), a biofilm adhesin polysaccharide | ||
KKNCFHKG_02278 | 7.3e-173 | icaC | G | transferase activity, transferring acyl groups other than amino-acyl groups | ||
KKNCFHKG_02279 | 6.1e-185 | yumC | 1.18.1.2, 1.19.1.1 | C | reductase | |
KKNCFHKG_02280 | 1.4e-228 | yumB | 1.6.99.3 | C | NADH dehydrogenase | |
KKNCFHKG_02281 | 1.2e-46 | yuiB | S | Putative membrane protein | ||
KKNCFHKG_02282 | 6.4e-108 | yuiC | S | protein conserved in bacteria | ||
KKNCFHKG_02283 | 6.3e-299 | pepA | 3.4.11.1, 3.4.11.5 | E | Presumably involved in the processing and regular turnover of intracellular proteins. Catalyzes the removal of unsubstituted N-terminal amino acids from various peptides | |
KKNCFHKG_02285 | 3.5e-294 | gerKA | EG | Spore germination protein | ||
KKNCFHKG_02286 | 6e-227 | gerKC | S | spore germination | ||
KKNCFHKG_02287 | 1.7e-191 | E | Spore germination protein | |||
KKNCFHKG_02289 | 2.8e-55 | yuzC | ||||
KKNCFHKG_02290 | 9.4e-65 | ydiI | Q | protein, possibly involved in aromatic compounds catabolism | ||
KKNCFHKG_02291 | 8.8e-194 | yuxJ | EGP | Major facilitator Superfamily | ||
KKNCFHKG_02292 | 1.5e-67 | kapB | G | Kinase associated protein B | ||
KKNCFHKG_02293 | 2.7e-111 | ppiB | 5.2.1.8 | O | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
KKNCFHKG_02295 | 6e-238 | S | protein conserved in bacteria | |||
KKNCFHKG_02296 | 9.9e-160 | dkgB | S | Aldo/keto reductase family | ||
KKNCFHKG_02297 | 3.6e-165 | S | reductase | |||
KKNCFHKG_02298 | 8e-196 | namA | C | Catalyzes the reduction of the double bond of an array of alpha,beta-unsaturated aldehydes and ketones. It also reduces the nitro group of nitroester and nitroaromatic compounds. It could have a role in detoxification processes | ||
KKNCFHKG_02299 | 5.9e-29 | K | Helix-turn-helix XRE-family like proteins | |||
KKNCFHKG_02300 | 1.2e-64 | yugI | 5.3.1.9 | J | RNA binding protein (contains ribosomal protein S1 domain) | |
KKNCFHKG_02301 | 4e-86 | K | Bacterial transcription activator, effector binding domain | |||
KKNCFHKG_02302 | 5.1e-34 | yuzA | S | Domain of unknown function (DUF378) | ||
KKNCFHKG_02303 | 1.3e-259 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
KKNCFHKG_02304 | 1.9e-181 | yugO | P | COG1226 Kef-type K transport systems | ||
KKNCFHKG_02307 | 3.7e-168 | 4.3.1.12 | E | ornithine cyclodeaminase | ||
KKNCFHKG_02308 | 5.9e-277 | ycbD | 1.2.1.3 | C | Catalyzes the oxidation of malonate semialdehyde (MSA) and methylmalonate semialdehyde (MMSA) into acetyl-CoA and propanoyl-CoA, respectively | |
KKNCFHKG_02309 | 9.9e-227 | FOXRED | 1.5.3.1 | E | FAD dependent oxidoreductase | |
KKNCFHKG_02310 | 6.1e-221 | solA | 1.5.3.1 | E | FAD dependent oxidoreductase | |
KKNCFHKG_02311 | 9.6e-72 | yuiD | S | protein conserved in bacteria | ||
KKNCFHKG_02312 | 3e-133 | L | PFAM transposase IS4 family protein | |||
KKNCFHKG_02313 | 5.4e-113 | L | PFAM transposase IS4 family protein | |||
KKNCFHKG_02315 | 1.7e-249 | corC1 | S | COG1253 Hemolysins and related proteins containing CBS domains | ||
KKNCFHKG_02316 | 2.7e-74 | cueR | K | transcriptional | ||
KKNCFHKG_02317 | 6.1e-233 | corC1 | S | COG1253 Hemolysins and related proteins containing CBS domains | ||
KKNCFHKG_02318 | 2.1e-148 | |||||
KKNCFHKG_02319 | 5.7e-197 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
KKNCFHKG_02320 | 1.9e-256 | 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 | |
KKNCFHKG_02321 | 0.0 | malL | 3.2.1.10 | GH13 | G | COG0366 Glycosidases |
KKNCFHKG_02322 | 0.0 | yvdK | 2.4.1.8 | GH65 | G | Glycoside hydrolase, family 65 |
KKNCFHKG_02323 | 2.8e-146 | malA | S | Protein of unknown function (DUF1189) | ||
KKNCFHKG_02324 | 6.7e-156 | malD | P | transport | ||
KKNCFHKG_02325 | 3.3e-239 | malC | P | COG1175 ABC-type sugar transport systems, permease components | ||
KKNCFHKG_02326 | 4.4e-236 | mdxE | G | COG2182 Maltose-binding periplasmic proteins domains | ||
KKNCFHKG_02327 | 0.0 | nplT | 3.2.1.133, 3.2.1.135, 3.2.1.54 | GH13 | G | Alpha amylase, N-terminal ig-like domain |
KKNCFHKG_02328 | 0.0 | malL | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | COG0366 Glycosidases |
KKNCFHKG_02329 | 6.1e-174 | yvdE | K | Transcriptional regulator | ||
KKNCFHKG_02330 | 3.3e-121 | otsB2 | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | S | Haloacid dehalogenase-like hydrolase |
KKNCFHKG_02331 | 5.5e-107 | E | Lysine exporter protein LysE YggA | |||
KKNCFHKG_02332 | 9.1e-114 | L | COG2826 Transposase and inactivated derivatives, IS30 family | |||
KKNCFHKG_02333 | 8.4e-254 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
KKNCFHKG_02334 | 6e-171 | gnd | 1.1.1.343, 1.1.1.44 | G | 6-phosphogluconate dehydrogenase | |
KKNCFHKG_02335 | 1.4e-259 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
KKNCFHKG_02336 | 3.7e-50 | hxlR | K | transcriptional | ||
KKNCFHKG_02337 | 6.4e-87 | hxlA | 4.1.2.43 | G | 3-hexulose-6-phosphate synthase | |
KKNCFHKG_02338 | 3.3e-95 | hxlB | 4.1.2.43, 5.3.1.27 | M | sugar phosphate isomerase involved in capsule formation | |
KKNCFHKG_02339 | 7.8e-258 | cshA | 3.6.4.13 | JKL | DEAD-box RNA helicase possibly involved in RNA degradation. Unwinds dsRNA in both 5'- and 3'-directions, has RNA- dependent ATPase activity | |
KKNCFHKG_02340 | 2.1e-192 | S | AI-2E family transporter | |||
KKNCFHKG_02341 | 1.7e-109 | lmrB | EGP | the major facilitator superfamily | ||
KKNCFHKG_02342 | 1.3e-222 | EGP | Major facilitator Superfamily | |||
KKNCFHKG_02343 | 1.3e-102 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
KKNCFHKG_02344 | 1.1e-23 | S | double-stranded DNA endodeoxyribonuclease activity | |||
KKNCFHKG_02346 | 3.8e-75 | mgsA | 2.7.1.24, 4.2.3.3 | G | methylglyoxal synthase | |
KKNCFHKG_02347 | 2.2e-14 | rhaD | 4.1.2.17, 4.1.2.19, 5.1.3.4 | G | Catalyzes the reversible cleavage of L-rhamnulose-1- phosphate to dihydroxyacetone phosphate (DHAP) and L-lactaldehyde | |
KKNCFHKG_02348 | 9.8e-208 | L | Transposase IS4 family protein | |||
KKNCFHKG_02349 | 1.4e-156 | S | Nuclease-related domain | |||
KKNCFHKG_02351 | 3.2e-110 | pyrE | 2.4.2.10, 4.1.1.23 | F | Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) | |
KKNCFHKG_02352 | 1.1e-122 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
KKNCFHKG_02353 | 4e-181 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
KKNCFHKG_02354 | 2.8e-140 | pyrK | C | Responsible for channeling the electrons from the oxidation of dihydroorotate from the FMN redox center in the PyrD type B subunit to the ultimate electron acceptor NAD( ) | ||
KKNCFHKG_02355 | 0.0 | carB | 6.3.5.5 | F | Belongs to the CarB family | |
KKNCFHKG_02356 | 6.5e-212 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
KKNCFHKG_02357 | 1.1e-247 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
KKNCFHKG_02358 | 3.1e-167 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
KKNCFHKG_02359 | 9.7e-92 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
KKNCFHKG_02360 | 7.9e-179 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
KKNCFHKG_02361 | 1.3e-82 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
KKNCFHKG_02363 | 0.0 | ileS | 6.1.1.5 | J | amino acids such as valine, to avoid such errors it has two additional distinct tRNA(Ile)-dependent editing activities. One activity is designated as 'pretransfer' editing and involves the hydrolysis of activated Val-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Val-tRNA(Ile) | |
KKNCFHKG_02364 | 2.5e-65 | divIVA | D | Cell division initiation protein | ||
KKNCFHKG_02365 | 3.7e-145 | ylmH | 5.4.99.23, 5.4.99.24 | S | conserved protein, contains S4-like domain | |
KKNCFHKG_02366 | 1.4e-38 | yggT | S | membrane | ||
KKNCFHKG_02367 | 1.1e-64 | 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 | ||
KKNCFHKG_02368 | 2.3e-122 | ylmE | S | Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis | ||
KKNCFHKG_02369 | 8.2e-159 | yfiH | S | Belongs to the multicopper oxidase YfiH RL5 family | ||
KKNCFHKG_02370 | 2.6e-73 | yocH | CBM50 | M | 3D domain | |
KKNCFHKG_02371 | 1.5e-43 | ylmC | S | sporulation protein | ||
KKNCFHKG_02372 | 9.4e-68 | L | COG2801 Transposase and inactivated derivatives | |||
KKNCFHKG_02373 | 2.8e-34 | S | Protein of unknown function (DUF2971) | |||
KKNCFHKG_02374 | 2.9e-17 | L | Transposase, IS4 family protein | |||
KKNCFHKG_02375 | 5.6e-181 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
KKNCFHKG_02376 | 3.8e-135 | rfbD | 1.1.1.133, 5.1.3.13 | M | Catalyzes the reduction of dTDP-6-deoxy-L-lyxo-4- hexulose to yield dTDP-L-rhamnose | |
KKNCFHKG_02377 | 1.1e-87 | rfbC | 5.1.3.13 | M | Catalyzes the epimerization of the C3' and C5'positions of dTDP-6-deoxy-D-xylo-4-hexulose, forming dTDP-6-deoxy-L-lyxo-4- hexulose | |
KKNCFHKG_02378 | 2.2e-146 | rfbA | 2.7.7.24 | M | Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis | |
KKNCFHKG_02380 | 1.2e-160 | S | polysaccharide biosynthetic process | |||
KKNCFHKG_02381 | 1.3e-38 | L | Transposase, IS4 family protein | |||
KKNCFHKG_02382 | 1.7e-180 | manC | 2.7.7.13, 5.3.1.8 | G | mannose-1-phosphate guanylyltransferase | |
KKNCFHKG_02383 | 8.7e-12 | 3.2.1.15 | M | Right handed beta helix region | ||
KKNCFHKG_02384 | 1e-69 | J | Glycosyl transferase family 2 | |||
KKNCFHKG_02386 | 1.4e-89 | cps4F | 2.4.1.306 | GT4 | M | Glycosyl transferase 4-like |
KKNCFHKG_02387 | 1.2e-23 | M | Glycosyl transferases group 1 | |||
KKNCFHKG_02388 | 3.9e-90 | cpsE | M | COG2148 Sugar transferases involved in lipopolysaccharide synthesis | ||
KKNCFHKG_02389 | 4.7e-152 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
KKNCFHKG_02390 | 1e-139 | ywqE | 3.1.3.48 | GM | COG4464 Capsular polysaccharide biosynthesis protein | |
KKNCFHKG_02391 | 1.3e-110 | ywqD | 2.7.10.1 | D | COG0489 ATPases involved in chromosome partitioning | |
KKNCFHKG_02392 | 1.1e-122 | ywqC | M | biosynthesis protein | ||
KKNCFHKG_02393 | 4.7e-151 | E | lipolytic protein G-D-S-L family | |||
KKNCFHKG_02394 | 8.4e-97 | sigS | 2.7.7.6 | K | Belongs to the sigma-70 factor family. ECF subfamily | |
KKNCFHKG_02395 | 4.3e-88 | K | ComK protein | |||
KKNCFHKG_02397 | 1.2e-09 | csbD | S | Belongs to the UPF0337 (CsbD) family | ||
KKNCFHKG_02398 | 0.0 | metH | 2.1.1.13 | E | Methionine synthase | |
KKNCFHKG_02399 | 0.0 | yitJ | 1.5.1.20, 2.1.1.10, 2.1.1.13 | E | Catalyzes the formation of 5,10-methylenetetrahydrofolate from 5-methyltetrahydrofolate and S-adenosyl-L-homocysteine and methionine from S-adenosyl-L-methionine and L-homocysteine | |
KKNCFHKG_02400 | 1.3e-43 | rpoE | K | Participates in both the initiation and recycling phases of transcription. In the presence of the delta subunit, RNAP displays an increased specificity of transcription, a decreased affinity for nucleic acids, and an increased efficiency of RNA synthesis because of enhanced recycling | ||
KKNCFHKG_02402 | 7.7e-14 | icmF | 5.4.99.13 | EI | Catalyzes the reversible interconversion of isobutyryl- CoA and n-butyryl-CoA, using radical chemistry. Also exhibits GTPase activity, associated with its G-protein domain (MeaI) that functions as a chaperone that assists cofactor delivery and proper holo-enzyme assembly | |
KKNCFHKG_02403 | 2e-92 | icmF | 5.4.99.13 | EI | Catalyzes the reversible interconversion of isobutyryl- CoA and n-butyryl-CoA, using radical chemistry. Also exhibits GTPase activity, associated with its G-protein domain (MeaI) that functions as a chaperone that assists cofactor delivery and proper holo-enzyme assembly | |
KKNCFHKG_02404 | 1.1e-40 | icmF | 5.4.99.13 | EI | Catalyzes the reversible interconversion of isobutyryl- CoA and n-butyryl-CoA, using radical chemistry. Also exhibits GTPase activity, associated with its G-protein domain (MeaI) that functions as a chaperone that assists cofactor delivery and proper holo-enzyme assembly | |
KKNCFHKG_02405 | 1.3e-111 | kstR2_2 | K | Transcriptional regulator | ||
KKNCFHKG_02406 | 3.2e-214 | acdA | 1.3.8.1, 1.3.8.7 | I | acyl-CoA dehydrogenase | |
KKNCFHKG_02407 | 1e-207 | mmgC | I | acyl-CoA dehydrogenase | ||
KKNCFHKG_02408 | 2.9e-218 | mmgA | 2.3.1.9 | I | Catalyzes the synthesis of acetoacetyl coenzyme A from two molecules of acetyl coenzyme A. It can also act as a thiolase, catalyzing the reverse reaction and generating two-carbon units from the four-carbon product of fatty acid oxidation | |
KKNCFHKG_02409 | 0.0 | fadF | C | COG0247 Fe-S oxidoreductase | ||
KKNCFHKG_02410 | 9.3e-212 | cls | I | Belongs to the phospholipase D family. Cardiolipin synthase subfamily | ||
KKNCFHKG_02411 | 0.0 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
KKNCFHKG_02412 | 6.7e-75 | ywiB | S | Domain of unknown function (DUF1934) | ||
KKNCFHKG_02413 | 4.1e-169 | speB | 3.5.3.11 | E | Belongs to the arginase family | |
KKNCFHKG_02414 | 0.0 | pbpG | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
KKNCFHKG_02415 | 1.7e-93 | ywhD | S | YwhD family | ||
KKNCFHKG_02416 | 7.8e-120 | ywhC | S | Peptidase M50 | ||
KKNCFHKG_02417 | 2.7e-25 | dmpI | 5.3.2.6 | G | 4-oxalocrotonate tautomerase | |
KKNCFHKG_02418 | 6e-91 | ywgA | 2.1.1.72, 3.1.21.3 | |||
KKNCFHKG_02419 | 6.1e-257 | ywfO | S | COG1078 HD superfamily phosphohydrolases | ||
KKNCFHKG_02420 | 8.2e-99 | rsfA | S | Transcriptional regulator | ||
KKNCFHKG_02421 | 1.8e-153 | lipL | 2.3.1.200, 2.3.1.204 | H | Catalyzes the amidotransfer (transamidation) of the octanoyl moiety from octanoyl-GcvH to the lipoyl domain of the E2 subunit of lipoate-dependent enzymes | |
KKNCFHKG_02422 | 3.9e-176 | pta | 2.3.1.8, 3.6.3.21 | C | In Salmonella this enzyme is required for ethanolamine catabolism | |
KKNCFHKG_02423 | 9.5e-146 | ywfI | C | May function as heme-dependent peroxidase | ||
KKNCFHKG_02424 | 3.7e-73 | gerQ | S | Essential for the localization of CwlJ in the spore coat and for spore germination triggered by calcium and dipicolinic acid (DPA). Its assembly into the spore coat is dependent on the coat morphogenetic proteins CotE and SpoIVA | ||
KKNCFHKG_02425 | 2.2e-55 | ywdK | S | small membrane protein | ||
KKNCFHKG_02426 | 7.2e-37 | S | Family of unknown function (DUF5327) | |||
KKNCFHKG_02427 | 6.4e-133 | 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 | |
KKNCFHKG_02428 | 1.1e-53 | S | Heat induced stress protein YflT | |||
KKNCFHKG_02429 | 1.9e-31 | |||||
KKNCFHKG_02430 | 1.8e-46 | |||||
KKNCFHKG_02431 | 4.3e-161 | L | PFAM transposase, IS4 family protein | |||
KKNCFHKG_02432 | 3.9e-78 | ywlE | 3.1.3.48, 3.9.1.2, 5.3.1.6 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
KKNCFHKG_02433 | 4.1e-165 | mcpA | NT | Chemotaxis | ||
KKNCFHKG_02434 | 3.1e-80 | rpiB | 5.3.1.6 | G | Ribose 5-phosphate isomerase | |
KKNCFHKG_02435 | 3.7e-94 | ywlG | S | Belongs to the UPF0340 family | ||
KKNCFHKG_02436 | 5.4e-239 | glyA | 2.1.2.1 | E | Catalyzes the reversible interconversion of serine and glycine with tetrahydrofolate (THF) serving as the one-carbon carrier. This reaction serves as the major source of one-carbon groups required for the biosynthesis of purines, thymidylate, methionine, and other important biomolecules. Also exhibits THF- independent aldolase activity toward beta-hydroxyamino acids, producing glycine and aldehydes, via a retro-aldol mechanism | |
KKNCFHKG_02437 | 1e-113 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
KKNCFHKG_02438 | 8e-53 | atpI | S | ATP synthase I chain | ||
KKNCFHKG_02439 | 8.2e-131 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
KKNCFHKG_02440 | 1.3e-26 | 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 | ||
KKNCFHKG_02441 | 1.3e-37 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
KKNCFHKG_02442 | 4.9e-88 | atpH | C | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
KKNCFHKG_02443 | 5.9e-280 | atpA | 3.6.3.14 | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit | |
KKNCFHKG_02444 | 4.7e-149 | 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 | ||
KKNCFHKG_02445 | 4.5e-266 | 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 | |
KKNCFHKG_02446 | 1.8e-53 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
KKNCFHKG_02447 | 6.8e-34 | ywzB | S | membrane | ||
KKNCFHKG_02448 | 3.3e-135 | ywmB | S | TATA-box binding | ||
KKNCFHKG_02449 | 4.8e-238 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
KKNCFHKG_02450 | 3.1e-184 | spoIID | D | Stage II sporulation protein D | ||
KKNCFHKG_02451 | 4.1e-128 | spoIIQ | M | COG0739 Membrane proteins related to metalloendopeptidases | ||
KKNCFHKG_02452 | 6.5e-41 | spoIIID | K | Stage III sporulation protein D | ||
KKNCFHKG_02453 | 1.9e-178 | mbl | D | Rod shape-determining protein | ||
KKNCFHKG_02454 | 1.1e-144 | flhO | N | flagellar basal body | ||
KKNCFHKG_02455 | 1.9e-139 | flhP | N | flagellar basal body | ||
KKNCFHKG_02456 | 8.7e-72 | fabZ | 3.5.1.108, 4.2.1.59 | I | Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs | |
KKNCFHKG_02458 | 3.3e-64 | ssbB | L | Single-stranded DNA-binding protein | ||
KKNCFHKG_02459 | 1.9e-71 | ywpF | S | YwpF-like protein | ||
KKNCFHKG_02460 | 0.0 | cpdB | 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
KKNCFHKG_02461 | 2.1e-207 | ysdC | G | COG1363 Cellulase M and related proteins | ||
KKNCFHKG_02462 | 3.6e-271 | L | RNA-directed DNA polymerase (reverse transcriptase) | |||
KKNCFHKG_02463 | 1.1e-10 | S | double-stranded DNA endodeoxyribonuclease activity | |||
KKNCFHKG_02464 | 4.5e-132 | VVA0018 | T | Histidine kinase | ||
KKNCFHKG_02465 | 4.7e-123 | T | helix_turn_helix, arabinose operon control protein | |||
KKNCFHKG_02466 | 6.3e-07 | E | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | |||
KKNCFHKG_02467 | 3.5e-163 | 3.5.1.4 | C | Acetamidase | ||
KKNCFHKG_02468 | 1.2e-223 | puuP_1 | E | Amino acid permease | ||
KKNCFHKG_02469 | 1.1e-12 | S | Zinc-ribbon containing domain | |||
KKNCFHKG_02470 | 2.4e-298 | yvfH | C | L-lactate permease | ||
KKNCFHKG_02471 | 4.2e-119 | yvfI | K | COG2186 Transcriptional regulators | ||
KKNCFHKG_02472 | 4.4e-230 | lysN | EK | COG1167 Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | ||
KKNCFHKG_02473 | 2.3e-60 | |||||
KKNCFHKG_02475 | 3.3e-175 | lytR_1 | K | May catalyze the final step in cell wall teichoic acid biosynthesis, the transfer of the anionic cell wall polymers (APs) from their lipid-linked precursor to the cell wall peptidoglycan (PG) | ||
KKNCFHKG_02476 | 3.6e-209 | EGP | Major facilitator Superfamily | |||
KKNCFHKG_02478 | 2.2e-16 | S | YvrJ protein family | |||
KKNCFHKG_02479 | 9.8e-11 | S | Protein of unknown function (DUF2922) | |||
KKNCFHKG_02480 | 2.6e-11 | S | Protein of unknown function (DUF1659) | |||
KKNCFHKG_02481 | 0.0 | O | Belongs to the peptidase S8 family | |||
KKNCFHKG_02482 | 7.5e-223 | licH | 3.2.1.86 | GT4 | G | COG1486 Alpha-galactosidases 6-phospho-beta-glucosidases, family 4 of glycosyl hydrolases |
KKNCFHKG_02483 | 1.7e-27 | licA | 2.7.1.196, 2.7.1.205 | G | PTS cellobiose transporter subunit IIA | |
KKNCFHKG_02484 | 3.2e-73 | 2.7.1.199 | G | phosphoenolpyruvate-dependent sugar phosphotransferase system | ||
KKNCFHKG_02485 | 1.5e-146 | yokF | 3.1.31.1 | L | RNA catabolic process | |
KKNCFHKG_02486 | 1.2e-36 | yhjE | S | protein conserved in bacteria | ||
KKNCFHKG_02487 | 1.5e-49 | P | Rhodanese domain protein | |||
KKNCFHKG_02488 | 1.5e-239 | P | Voltage gated chloride channel | |||
KKNCFHKG_02491 | 6e-174 | nodB1 | G | deacetylase | ||
KKNCFHKG_02492 | 4.1e-12 | recN | L | Putative cell-wall binding lipoprotein | ||
KKNCFHKG_02493 | 4.7e-94 | VY92_08700 | S | Enoyl-(Acyl carrier protein) reductase | ||
KKNCFHKG_02494 | 1.4e-90 | ydhK | M | Protein of unknown function (DUF1541) | ||
KKNCFHKG_02495 | 1.5e-126 | KT | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
KKNCFHKG_02496 | 3.8e-249 | T | PhoQ Sensor | |||
KKNCFHKG_02498 | 9.1e-33 | S | Protein of unknown function (DUF2933) | |||
KKNCFHKG_02501 | 9.5e-267 | E | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | |||
KKNCFHKG_02502 | 1.3e-27 | yhjC | S | Protein of unknown function (DUF3311) | ||
KKNCFHKG_02503 | 7.2e-225 | 3.5.1.47 | E | COG1473 Metal-dependent amidase aminoacylase carboxypeptidase | ||
KKNCFHKG_02504 | 9.5e-71 | S | Antioxidant protein with alkyl hydroperoxidase activity. Required for the reduction of the AhpC active site cysteine residues and for the regeneration of the AhpC enzyme activity | |||
KKNCFHKG_02505 | 4.3e-68 | lrpC | K | Transcriptional regulator | ||
KKNCFHKG_02506 | 8.4e-57 | S | protein conserved in bacteria | |||
KKNCFHKG_02507 | 2.4e-30 | P | Copper resistance protein CopZ | |||
KKNCFHKG_02508 | 0.0 | copA | 3.6.3.54 | P | P-type ATPase | |
KKNCFHKG_02509 | 1.7e-58 | EGP | Major facilitator Superfamily | |||
KKNCFHKG_02510 | 1.5e-165 | S | Protein of unknown function (DUF1646) | |||
KKNCFHKG_02511 | 9.3e-116 | sapB | S | MgtC SapB transporter | ||
KKNCFHKG_02512 | 2.9e-149 | EG | COG0697 Permeases of the drug metabolite transporter (DMT) superfamily | |||
KKNCFHKG_02513 | 1e-21 | |||||
KKNCFHKG_02518 | 1.7e-07 | |||||
KKNCFHKG_02520 | 1.7e-07 | |||||
KKNCFHKG_02521 | 1.5e-07 | |||||
KKNCFHKG_02525 | 4.3e-169 | rocF | 3.5.3.1, 3.5.3.11 | E | Belongs to the arginase family | |
KKNCFHKG_02527 | 2.1e-97 | sigW | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
KKNCFHKG_02528 | 1.9e-115 | rsiW | K | Is the anti-sigma factor for SigW. The presence of RsiW leads to the inactivation of SigW, and its proteolytic destruction to sigma-W activation | ||
KKNCFHKG_02529 | 4.7e-146 | dacA | 2.7.7.85 | S | Catalyzes the condensation of 2 ATP molecules into cyclic di-AMP (c-di-AMP), a second messenger used to regulate differing processes in different bacteria | |
KKNCFHKG_02530 | 3.4e-217 | ybbR | S | protein conserved in bacteria | ||
KKNCFHKG_02531 | 5.5e-253 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
KKNCFHKG_02532 | 0.0 | glmS | 2.6.1.16 | M | Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source | |
KKNCFHKG_02533 | 6.4e-70 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
KKNCFHKG_02534 | 3.6e-48 | ykvR | S | Protein of unknown function (DUF3219) | ||
KKNCFHKG_02535 | 2.4e-173 | yceB | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | ||
KKNCFHKG_02537 | 3.1e-237 | mvaA | 1.1.1.34, 1.1.1.88, 2.3.1.9 | I | Hydroxymethylglutaryl-coenzyme A reductase | |
KKNCFHKG_02538 | 9e-220 | mvaS | 2.3.3.10 | I | synthase | |
KKNCFHKG_02539 | 2.6e-211 | atoB | 1.1.1.88, 2.3.1.9 | I | Belongs to the thiolase family | |
KKNCFHKG_02540 | 5e-54 | S | DsrE/DsrF-like family | |||
KKNCFHKG_02541 | 5.6e-74 | |||||
KKNCFHKG_02542 | 5.3e-181 | ghrB | 1.1.1.215, 1.1.1.26, 1.1.1.43, 1.1.1.79, 1.1.1.81 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
KKNCFHKG_02543 | 4.2e-110 | proV | E | COG1125 ABC-type proline glycine betaine transport systems, ATPase components | ||
KKNCFHKG_02544 | 1.5e-151 | L | Transposase domain (DUF772) | |||
KKNCFHKG_02545 | 1.2e-85 | qorB | 1.6.5.2 | GM | NmrA-like family | |
KKNCFHKG_02546 | 1.6e-126 | L | Transposase | |||
KKNCFHKG_02547 | 1.2e-35 | hfq | J | RNA chaperone that binds small regulatory RNA (sRNAs) and mRNAs to facilitate mRNA translational regulation in response to envelope stress, environmental stress and changes in metabolite concentrations. Also binds with high specificity to tRNAs | ||
KKNCFHKG_02548 | 2e-169 | miaA | 2.5.1.75 | J | Catalyzes the transfer of a dimethylallyl group onto the adenine at position 37 in tRNAs that read codons beginning with uridine, leading to the formation of N6-(dimethylallyl)adenosine (i(6)A) | |
KKNCFHKG_02551 | 1e-12 | 2.1.1.80, 3.1.1.61 | S | protein secretion by the type IV secretion system | ||
KKNCFHKG_02552 | 5.5e-40 | yhjA | S | Excalibur calcium-binding domain | ||
KKNCFHKG_02553 | 0.0 | mutL | L | This protein is involved in the repair of mismatches in DNA. It is required for dam-dependent methyl-directed DNA mismatch repair. May act as a molecular matchmaker , a protein that promotes the formation of a stable complex between two or more DNA-binding proteins in an ATP-dependent manner without itself being part of a final effector complex | ||
KKNCFHKG_02554 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
KKNCFHKG_02555 | 6.2e-99 | cotE | S | Outer spore coat protein E (CotE) | ||
KKNCFHKG_02556 | 2.1e-49 | ymcA | 3.6.3.21 | S | Belongs to the UPF0342 family | |
KKNCFHKG_02557 | 5.2e-300 | miaB | 2.8.4.3 | J | Catalyzes the methylthiolation of N6- (dimethylallyl)adenosine (i(6)A), leading to the formation of 2- methylthio-N6-(dimethylallyl)adenosine (ms(2)i(6)A) at position 37 in tRNAs that read codons beginning with uridine | |
KKNCFHKG_02558 | 3.6e-260 | patA | 2.6.1.11, 2.6.1.17, 2.6.1.82 | E | Belongs to the class-III pyridoxal-phosphate-dependent aminotransferase family | |
KKNCFHKG_02559 | 1.5e-288 | gbsA | 1.2.1.8 | C | Belongs to the aldehyde dehydrogenase family | |
KKNCFHKG_02561 | 0.0 | KT | COG3829 Transcriptional regulator containing PAS, AAA-type ATPase, and DNA-binding domains | |||
KKNCFHKG_02562 | 9.4e-245 | E | Amino acid permease | |||
KKNCFHKG_02563 | 2.9e-248 | yegQ | O | COG0826 Collagenase and related proteases | ||
KKNCFHKG_02564 | 1.1e-167 | yegQ | O | Peptidase U32 | ||
KKNCFHKG_02565 | 3.3e-37 | spoVS | S | Stage V sporulation protein S | ||
KKNCFHKG_02566 | 7.2e-152 | ymdB | S | protein conserved in bacteria | ||
KKNCFHKG_02567 | 5.6e-217 | rny | S | Endoribonuclease that initiates mRNA decay | ||
KKNCFHKG_02568 | 1.9e-106 | queE | 1.97.1.4, 4.3.99.3 | H | Catalyzes the complex heterocyclic radical-mediated conversion of 6-carboxy-5,6,7,8-tetrahydropterin (CPH4) to 7- carboxy-7-deazaguanine (CDG), a step common to the biosynthetic pathways of all 7-deazapurine-containing compounds | |
KKNCFHKG_02569 | 9.6e-167 | yocS | S | -transporter | ||
KKNCFHKG_02570 | 0.0 | FbpA | K | RNA-binding protein homologous to eukaryotic snRNP | ||
KKNCFHKG_02571 | 0.0 | yloB | 3.6.3.8 | P | COG0474 Cation transport ATPase | |
KKNCFHKG_02572 | 1.3e-151 | yicC | S | stress-induced protein | ||
KKNCFHKG_02573 | 3.8e-45 | ylzA | S | Belongs to the UPF0296 family | ||
KKNCFHKG_02574 | 3.7e-108 | gmk | 2.7.4.8 | F | Essential for recycling GMP and indirectly, cGMP | |
KKNCFHKG_02575 | 7.6e-29 | 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 | |
KKNCFHKG_02576 | 3.2e-220 | coaBC | 4.1.1.36, 6.3.2.5 | H | Catalyzes two steps in the biosynthesis of coenzyme A. In the first step cysteine is conjugated to 4'-phosphopantothenate to form 4-phosphopantothenoylcysteine, in the latter compound is decarboxylated to form 4'-phosphopantotheine | |
KKNCFHKG_02577 | 0.0 | priA | L | Involved in the restart of stalled replication forks. Recognizes and binds the arrested nascent DNA chain at stalled replication forks. It can open the DNA duplex, via its helicase activity, and promote assembly of the primosome and loading of the major replicative helicase DnaB onto DNA | ||
KKNCFHKG_02578 | 5.1e-84 | def | 2.1.2.9, 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 | |
KKNCFHKG_02579 | 1.7e-179 | fmt | 2.1.2.9 | J | Attaches a formyl group to the free amino group of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by promoting its recognition by IF2 and preventing the misappropriation of this tRNA by the elongation apparatus | |
KKNCFHKG_02580 | 1.7e-254 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
KKNCFHKG_02581 | 1.2e-135 | stp | 3.1.3.16 | T | phosphatase | |
KKNCFHKG_02582 | 0.0 | prkC | 2.7.11.1 | KLT | serine threonine protein kinase | |
KKNCFHKG_02583 | 1.8e-167 | rsgA | 3.1.3.100 | S | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Helps release RbfA from mature subunits. May play a role in the assembly of ribosomal proteins into the subunit. Circularly permuted GTPase that catalyzes slow GTP hydrolysis, GTPase activity is stimulated by the 30S ribosomal subunit | |
KKNCFHKG_02584 | 6.8e-116 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
KKNCFHKG_02585 | 1.5e-123 | thiN | 2.7.6.2 | H | thiamine pyrophosphokinase | |
KKNCFHKG_02586 | 5e-27 | rpmB | J | Belongs to the bacterial ribosomal protein bL28 family | ||
KKNCFHKG_02588 | 9.9e-101 | ycnI | S | Domain of unkown function (DUF1775) | ||
KKNCFHKG_02589 | 4.7e-291 | ycnJ | P | protein, homolog of Cu resistance protein CopC | ||
KKNCFHKG_02590 | 3.5e-26 | |||||
KKNCFHKG_02592 | 4.7e-263 | 2.7.13.3 | T | His Kinase A (phosphoacceptor) domain | ||
KKNCFHKG_02593 | 6.6e-226 | 2.3.1.179 | IQ | Beta-ketoacyl synthase, C-terminal domain | ||
KKNCFHKG_02594 | 4.6e-31 | cspL | K | Cold shock | ||
KKNCFHKG_02595 | 1.9e-178 | ydcZ | S | Putative inner membrane exporter, YdcZ | ||
KKNCFHKG_02596 | 0.0 | nagA | 3.2.1.52 | G | Belongs to the glycosyl hydrolase 3 family | |
KKNCFHKG_02597 | 6.6e-309 | ampC | V | Belongs to the UPF0214 family | ||
KKNCFHKG_02598 | 4.1e-234 | ybbC | 3.2.1.52 | S | protein conserved in bacteria | |
KKNCFHKG_02599 | 0.0 | yfiC | V | COG1132 ABC-type multidrug transport system, ATPase and permease components | ||
KKNCFHKG_02600 | 0.0 | yfiB | V | ABC transporter | ||
KKNCFHKG_02601 | 2.5e-80 | K | helix_turn_helix multiple antibiotic resistance protein | |||
KKNCFHKG_02602 | 5.7e-51 | L | Transposase | |||
KKNCFHKG_02603 | 3.4e-173 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
KKNCFHKG_02604 | 4.9e-193 | bdhA | 1.1.1.303, 1.1.1.4 | E | Dehydrogenase | |
KKNCFHKG_02605 | 2.8e-207 | U | protein localization to endoplasmic reticulum | |||
KKNCFHKG_02606 | 0.0 | nrdD | 1.1.98.6 | F | Ribonucleoside-triphosphate reductase | |
KKNCFHKG_02607 | 9.4e-91 | nrdG | 1.97.1.4 | O | 4Fe-4S single cluster domain | |
KKNCFHKG_02608 | 7.8e-99 | mleR | K | LysR substrate binding domain | ||
KKNCFHKG_02609 | 1.5e-157 | sfcA | 1.1.1.38, 4.1.1.101 | C | Malic enzyme, NAD binding domain | |
KKNCFHKG_02610 | 7.9e-25 | mleP | S | Membrane transport protein | ||
KKNCFHKG_02612 | 7.7e-132 | K | Helix-turn-helix domain, rpiR family | |||
KKNCFHKG_02613 | 1.9e-292 | 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | ||
KKNCFHKG_02614 | 2.7e-260 | 3.2.1.122, 3.2.1.86 | GH4,GT4 | G | COG1486 Alpha-galactosidases 6-phospho-beta-glucosidases, family 4 of glycosyl hydrolases | |
KKNCFHKG_02615 | 4.5e-80 | 2.7.1.199 | G | COG2190 Phosphotransferase system IIA components | ||
KKNCFHKG_02616 | 1.9e-83 | btuE | 1.11.1.9 | O | Belongs to the glutathione peroxidase family | |
KKNCFHKG_02617 | 9.7e-115 | E | LysE type translocator | |||
KKNCFHKG_02618 | 5.7e-26 | |||||
KKNCFHKG_02619 | 1.8e-237 | cshA | L | COG2256 ATPase related to the helicase subunit of the Holliday junction resolvase | ||
KKNCFHKG_02620 | 4.1e-136 | yrvM | H | COG1179 Dinucleotide-utilizing enzymes involved in molybdopterin and thiamine biosynthesis family 1 | ||
KKNCFHKG_02621 | 3.2e-162 | ybaS | 1.1.1.58 | S | Na -dependent transporter | |
KKNCFHKG_02623 | 0.0 | aspS | 6.1.1.12 | J | Aspartyl-tRNA synthetase with relaxed tRNA specificity since it is able to aspartylate not only its cognate tRNA(Asp) but also tRNA(Asn). Reaction proceeds in two steps L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp Asn) | |
KKNCFHKG_02624 | 3e-248 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
KKNCFHKG_02627 | 7.2e-275 | lytH | 3.5.1.28, 6.1.1.12 | M | COG3103 SH3 domain protein | |
KKNCFHKG_02628 | 5.2e-307 | yhcA5 | EGP | Major facilitator Superfamily | ||
KKNCFHKG_02629 | 2.2e-106 | emrA | V | COG1566 Multidrug resistance efflux pump | ||
KKNCFHKG_02630 | 1.3e-67 | K | helix_turn_helix multiple antibiotic resistance protein | |||
KKNCFHKG_02631 | 1.8e-75 | 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 | ||
KKNCFHKG_02632 | 0.0 | relA | 2.7.6.5 | KT | In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance | |
KKNCFHKG_02633 | 5.3e-95 | apt | 2.4.2.22, 2.4.2.7 | F | Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis | |
KKNCFHKG_02634 | 0.0 | recJ | L | Single-stranded-DNA-specific exonuclease RecJ | ||
KKNCFHKG_02635 | 1.1e-175 | phnD | P | Phosphonate ABC transporter | ||
KKNCFHKG_02636 | 6.1e-143 | phnE | 3.6.1.63 | P | ABC transporter | |
KKNCFHKG_02637 | 2.3e-134 | phnE | 3.6.1.63 | P | ABC transporter | |
KKNCFHKG_02638 | 1.2e-135 | phnC | 3.6.3.28 | P | Part of the ABC transporter complex PhnCDE involved in phosphonates import. Responsible for energy coupling to the transport system | |
KKNCFHKG_02639 | 3.8e-195 | S | Metallo-beta-lactamase superfamily | |||
KKNCFHKG_02640 | 9.5e-26 | 6.2.1.3 | IQ | AMP-binding enzyme C-terminal domain | ||
KKNCFHKG_02641 | 6.2e-265 | Otg1 | S | Predicted membrane protein (DUF2339) | ||
KKNCFHKG_02642 | 6.9e-59 | xylS | 3.2.1.20 | GH31 | G | Belongs to the glycosyl hydrolase 31 family |
KKNCFHKG_02643 | 4.3e-163 | salL | 2.5.1.63, 2.5.1.94 | S | S-adenosyl-l-methionine hydroxide adenosyltransferase | |
KKNCFHKG_02644 | 6.8e-93 | S | UPF0397 protein | |||
KKNCFHKG_02645 | 0.0 | ykoD | P | ABC transporter, ATP-binding protein | ||
KKNCFHKG_02646 | 4.3e-150 | cbiQ | P | COG0619 ABC-type cobalt transport system, permease component CbiQ and related transporters | ||
KKNCFHKG_02647 | 1e-142 | focA | P | Formate nitrite | ||
KKNCFHKG_02648 | 1e-88 | S | NYN domain | |||
KKNCFHKG_02649 | 3.4e-76 | L | PFAM Integrase, catalytic core | |||
KKNCFHKG_02650 | 1.6e-86 | mntP | P | Probably functions as a manganese efflux pump | ||
KKNCFHKG_02651 | 1.9e-192 | ywlC | 2.7.7.87, 3.1.3.48 | J | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine | |
KKNCFHKG_02652 | 5.4e-133 | spoIIR | S | Stage II sporulation protein R (spore_II_R) | ||
KKNCFHKG_02653 | 4.1e-161 | 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 | |
KKNCFHKG_02654 | 3e-193 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
KKNCFHKG_02656 | 1.3e-110 | tdk | 2.7.1.21 | F | thymidine kinase | |
KKNCFHKG_02657 | 2.2e-33 | rpmE | J | Ribosomal protein L31 | ||
KKNCFHKG_02658 | 2.7e-230 | 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 | ||
KKNCFHKG_02660 | 2.7e-174 | glpX | 3.1.3.11, 3.1.3.37 | G | fructose-1,6-bisphosphatase | |
KKNCFHKG_02661 | 8.1e-238 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
KKNCFHKG_02662 | 4.4e-115 | tal | 2.2.1.2 | G | Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway | |
KKNCFHKG_02663 | 2.1e-157 | fbaA | 4.1.2.13, 4.1.2.29 | G | Aldolase | |
KKNCFHKG_02664 | 6e-61 | spo0F | T | response regulator | ||
KKNCFHKG_02665 | 2.5e-198 | |||||
KKNCFHKG_02666 | 2.5e-48 | |||||
KKNCFHKG_02667 | 1.8e-102 | ydcA | 3.4.21.105 | S | membrane protein (homolog of Drosophila rhomboid) | |
KKNCFHKG_02668 | 2.1e-55 | acpS | 2.7.6.3, 2.7.8.7, 5.1.1.1 | I | Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein | |
KKNCFHKG_02669 | 1.1e-189 | ydcC | M | COG2834 Outer membrane lipoprotein-sorting protein | ||
KKNCFHKG_02670 | 7.8e-216 | alr | 5.1.1.1, 5.1.1.5 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
KKNCFHKG_02671 | 2e-40 | ndoAI | K | transcriptional regulators containing the CopG Arc MetJ DNA-binding domain and a metal-binding domain | ||
KKNCFHKG_02672 | 6.1e-55 | ndoA | L | Toxic component of a toxin-antitoxin (TA) module | ||
KKNCFHKG_02673 | 2.2e-151 | rsbR | T | Positive regulator of sigma-B | ||
KKNCFHKG_02674 | 8.1e-55 | rsbS | T | antagonist | ||
KKNCFHKG_02675 | 4.5e-70 | rsbT | 2.7.11.1 | T | COG2172 Anti-sigma regulatory factor (Ser Thr protein kinase) | |
KKNCFHKG_02676 | 8.1e-185 | rsbU | 3.1.3.3 | KT | phosphatase | |
KKNCFHKG_02677 | 4e-54 | rsbV | T | Belongs to the anti-sigma-factor antagonist family | ||
KKNCFHKG_02678 | 6.7e-81 | rsbW | 2.7.11.1 | T | Negative regulator of sigma-B activity. Phosphorylates and inactivates its specific antagonist protein, RsbV. Upon phosphorylation of RsbV, RsbW is released and binds to sigma-B, thereby blocking its ability to form an RNA polymerase holoenzyme (E-sigma-B) | |
KKNCFHKG_02679 | 8.6e-134 | sigB | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
KKNCFHKG_02680 | 5.2e-107 | rsbX | 3.1.3.16, 3.1.3.3 | KT | Sigma factor PP2C-like phosphatases | |
KKNCFHKG_02681 | 0.0 | yhgF | K | COG2183 Transcriptional accessory protein | ||
KKNCFHKG_02682 | 3e-92 | ydcK | S | Belongs to the SprT family | ||
KKNCFHKG_02690 | 1.6e-08 | |||||
KKNCFHKG_02695 | 1.5e-155 | galM | 5.1.3.3 | G | Aldose 1-epimerase | |
KKNCFHKG_02697 | 4.1e-51 | |||||
KKNCFHKG_02699 | 9.5e-16 | sqhC | 4.2.1.137, 5.4.99.7 | I | COG1657 Squalene cyclase | |
KKNCFHKG_02700 | 3.3e-161 | fda | 4.1.2.13 | G | Belongs to the class I fructose-bisphosphate aldolase family | |
KKNCFHKG_02701 | 5e-128 | V | COG1131 ABC-type multidrug transport system, ATPase component | |||
KKNCFHKG_02703 | 5e-197 | ybhR | V | COG0842 ABC-type multidrug transport system, permease component | ||
KKNCFHKG_02704 | 3.5e-112 | K | Transcriptional regulator | |||
KKNCFHKG_02705 | 3.7e-271 | lysP | E | amino acid | ||
KKNCFHKG_02706 | 0.0 | hsdR | 3.1.21.3 | L | COG4096 Type I site-specific restriction-modification system, R (restriction) subunit and related helicases | |
KKNCFHKG_02707 | 2.1e-266 | hsdM | 2.1.1.72 | V | Type I restriction-modification system | |
KKNCFHKG_02708 | 4.4e-38 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | ||
KKNCFHKG_02709 | 4.3e-302 | prfC | J | Increases the formation of ribosomal termination complexes and stimulates activities of RF-1 and RF-2. It binds guanine nucleotides and has strong preference for UGA stop codons. It may interact directly with the ribosome. The stimulation of RF- 1 and RF-2 is significantly reduced by GTP and GDP, but not by GMP | ||
KKNCFHKG_02710 | 6.2e-207 | kinC | 2.7.13.3 | T | COG0642 Signal transduction histidine kinase | |
KKNCFHKG_02711 | 1.7e-179 | mocA | S | Oxidoreductase | ||
KKNCFHKG_02712 | 3.4e-74 | dps | P | Ferritin-like domain | ||
KKNCFHKG_02713 | 2.7e-124 | S | membrane transporter protein | |||
KKNCFHKG_02714 | 1.3e-224 | hmp | 1.14.12.17 | C | Is involved in NO detoxification in an aerobic process, termed nitric oxide dioxygenase (NOD) reaction that utilizes O(2) and NAD(P)H to convert NO to nitrate, which protects the bacterium from various noxious nitrogen compounds. Therefore, plays a central role in the inducible response to nitrosative stress | |
KKNCFHKG_02715 | 3.9e-75 | nsrR | K | Transcriptional regulator | ||
KKNCFHKG_02716 | 3.8e-142 | tesE | Q | COG3971 2-keto-4-pentenoate hydratase | ||
KKNCFHKG_02717 | 1.5e-245 | proP | EGP | Transporter | ||
KKNCFHKG_02718 | 1.7e-179 | ldhA | 1.1.1.28 | CH | D-isomer specific 2-hydroxyacid dehydrogenase, NAD binding domain | |
KKNCFHKG_02720 | 4.9e-145 | L | Transposase DDE domain | |||
KKNCFHKG_02721 | 3.6e-205 | nifS | 2.8.1.7 | E | Cysteine desulfurase | |
KKNCFHKG_02722 | 2.8e-304 | nadB | 1.3.5.4, 1.4.3.16 | H | Catalyzes the oxidation of L-aspartate to iminoaspartate | |
KKNCFHKG_02723 | 3.2e-158 | nadC | 1.4.3.16, 2.4.2.19 | H | Belongs to the NadC ModD family | |
KKNCFHKG_02724 | 6.1e-210 | nadA | 2.5.1.72 | H | Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate | |
KKNCFHKG_02725 | 8.7e-201 | gldA | 1.1.1.1, 1.1.1.6 | C | COG0371 Glycerol dehydrogenase and related enzymes | |
KKNCFHKG_02726 | 4.6e-21 | |||||
KKNCFHKG_02727 | 7.6e-148 | S | transposase or invertase | |||
KKNCFHKG_02728 | 2.8e-301 | comM | O | Mg chelatase subunit ChlI | ||
KKNCFHKG_02729 | 1.6e-51 | pnbA | CE10 | I | Belongs to the type-B carboxylesterase lipase family | |
KKNCFHKG_02730 | 5.9e-137 | yflN_1 | S | Metallo-beta-lactamase superfamily | ||
KKNCFHKG_02731 | 3.1e-150 | 3.1.1.5 | E | GDSL-like Lipase/Acylhydrolase | ||
KKNCFHKG_02732 | 4.6e-227 | treC | 3.2.1.93 | GH13 | G | COG0366 Glycosidases |
KKNCFHKG_02733 | 7.4e-132 | treR | K | transcriptional | ||
KKNCFHKG_02734 | 4.2e-65 | EG | COG2610 H gluconate symporter and related permeases | |||
KKNCFHKG_02735 | 3.1e-308 | gntK | 2.7.1.12, 2.7.1.17 | G | Belongs to the FGGY kinase family | |
KKNCFHKG_02736 | 8.5e-125 | gntR | K | transcriptional | ||
KKNCFHKG_02737 | 3.6e-168 | gnd | 1.1.1.343, 1.1.1.44 | G | 6-phosphogluconate dehydrogenase | |
KKNCFHKG_02738 | 5e-81 | fld | C | Flavodoxin | ||
KKNCFHKG_02739 | 6.9e-198 | 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 | ||
KKNCFHKG_02740 | 2.4e-152 | T | PhoQ Sensor | |||
KKNCFHKG_02741 | 2.2e-99 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
KKNCFHKG_02742 | 2.9e-77 | S | COG1277 ABC-type transport system involved in multi-copper enzyme maturation, permease component | |||
KKNCFHKG_02743 | 1.5e-108 | natA | V | COG1131 ABC-type multidrug transport system, ATPase component | ||
KKNCFHKG_02744 | 0.0 | M | Peptidase M30 | |||
KKNCFHKG_02745 | 3.2e-59 | croE | S | Helix-turn-helix | ||
KKNCFHKG_02746 | 3.5e-135 | E | IrrE N-terminal-like domain | |||
KKNCFHKG_02747 | 1.9e-38 | |||||
KKNCFHKG_02748 | 4.2e-245 | yicJ | G | MFS/sugar transport protein | ||
KKNCFHKG_02749 | 1.5e-302 | 2.7.1.12, 2.7.1.17 | G | xylulose kinase | ||
KKNCFHKG_02751 | 5e-223 | adhB | 1.1.1.1, 1.1.1.14, 1.1.1.284 | E | COG1063 Threonine dehydrogenase and related Zn-dependent dehydrogenases | |
KKNCFHKG_02752 | 6.7e-113 | azoR | I | Catalyzes the reductive cleavage of azo bond in aromatic azo compounds to the corresponding amines. Requires NADH, but not NADPH, as an electron donor for its activity | ||
KKNCFHKG_02753 | 2.1e-88 | tadA | 3.5.4.1, 3.5.4.33 | FJ | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
KKNCFHKG_02754 | 2.5e-120 | yaaH | M | Glycoside Hydrolase Family | ||
KKNCFHKG_02755 | 3.8e-37 | yaaH | M | Glycoside Hydrolase Family | ||
KKNCFHKG_02756 | 1.4e-118 | dgk | 2.7.1.113, 2.7.1.74, 2.7.1.76 | F | Deoxyguanosine kinase | |
KKNCFHKG_02757 | 3.3e-126 | dck | 2.7.1.113, 2.7.1.74, 2.7.1.76 | F | Deoxycytidine kinase | |
KKNCFHKG_02758 | 6.5e-09 | |||||
KKNCFHKG_02759 | 3.4e-212 | 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) | |
KKNCFHKG_02760 | 1.3e-102 | 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 | |
KKNCFHKG_02761 | 6.3e-157 | 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 | |
KKNCFHKG_02762 | 1e-240 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
KKNCFHKG_02763 | 1.5e-272 | 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 | |
KKNCFHKG_02764 | 3.6e-179 | yaaC | S | YaaC-like Protein | ||
KKNCFHKG_02765 | 2.8e-26 | S | Protein of unknown function (DUF3006) | |||
KKNCFHKG_02766 | 1.1e-242 | L | Metallo-beta-lactamase superfamily | |||
KKNCFHKG_02767 | 4.2e-65 | S | Protein of unknown function (DUF1648) | |||
KKNCFHKG_02768 | 6.4e-68 | yjbR | S | YjbR | ||
KKNCFHKG_02769 | 4.2e-178 | 1.13.12.16, 1.3.1.9 | S | COG2070 Dioxygenases related to 2-nitropropane dioxygenase | ||
KKNCFHKG_02770 | 2.4e-284 | apc3 | 3.5.2.9 | EQ | Hydantoinase/oxoprolinase | |
KKNCFHKG_02771 | 5e-204 | S | Protein of unknown function (DUF917) | |||
KKNCFHKG_02772 | 1.9e-205 | codB | F | cytosine purines uracil thiamine allantoin | ||
KKNCFHKG_02773 | 8.7e-279 | apc3 | 3.5.2.9 | EQ | Hydantoinase oxoprolinase | |
KKNCFHKG_02774 | 5.8e-200 | S | Protein of unknown function (DUF917) | |||
KKNCFHKG_02775 | 8e-211 | ynfM | EGP | Major facilitator Superfamily | ||
KKNCFHKG_02776 | 0.0 | ywjA | V | ABC transporter | ||
KKNCFHKG_02778 | 4.3e-234 | pbuG | S | permease | ||
KKNCFHKG_02779 | 3.3e-155 | glcT | K | antiterminator | ||
KKNCFHKG_02780 | 0.0 | 2.7.1.201, 2.7.1.211 | G | phosphotransferase system | ||
KKNCFHKG_02781 | 9.3e-223 | gltT | C | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
KKNCFHKG_02783 | 1.5e-11 | ymbI | L | Transposase | ||
KKNCFHKG_02784 | 2.2e-84 | opuCC | M | COG1732 Periplasmic glycine betaine choline-binding (lipo)protein of an ABC-type transport system (osmoprotectant binding protein) | ||
KKNCFHKG_02785 | 5.9e-170 | K | Transcriptional regulator | |||
KKNCFHKG_02786 | 8.7e-210 | EGP | Major facilitator Superfamily | |||
KKNCFHKG_02787 | 4.2e-74 | K | transcriptional | |||
KKNCFHKG_02788 | 1e-193 | ydjE | EGP | Major facilitator superfamily | ||
KKNCFHKG_02789 | 3.1e-74 | G | Glycosyl hydrolases family 39 | |||
KKNCFHKG_02790 | 2.3e-115 | K | helix_turn_helix, arabinose operon control protein | |||
KKNCFHKG_02791 | 6.1e-255 | gph | G | MFS/sugar transport protein | ||
KKNCFHKG_02792 | 1e-17 | K | Acetyltransferase (GNAT) family | |||
KKNCFHKG_02793 | 7.7e-52 | L | IstB-like ATP binding protein | |||
KKNCFHKG_02795 | 2e-22 | EGP | Transmembrane secretion effector | |||
KKNCFHKG_02798 | 3.5e-168 | L | Transposase DDE domain | |||
KKNCFHKG_02799 | 1.1e-62 | cadC | K | transcriptional | ||
KKNCFHKG_02800 | 0.0 | cadA | 3.6.3.3, 3.6.3.5 | P | COG2217 Cation transport ATPase | |
KKNCFHKG_02801 | 5.9e-77 | |||||
KKNCFHKG_02802 | 6.5e-125 | yhcG | V | ABC transporter, ATP-binding protein | ||
KKNCFHKG_02803 | 2e-65 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
KKNCFHKG_02804 | 1.1e-308 | 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 | |
KKNCFHKG_02805 | 2.1e-36 | L | Archaeal putative transposase ISC1217 | |||
KKNCFHKG_02806 | 0.0 | cysJ | 1.8.1.2 | P | Component of the sulfite reductase complex that catalyzes the 6-electron reduction of sulfite to sulfide. This is one of several activities required for the biosynthesis of L- cysteine from sulfate. The flavoprotein component catalyzes the electron flow from NADPH - FAD - FMN to the hemoprotein component | |
KKNCFHKG_02807 | 0.0 | cysI | 1.7.7.1, 1.8.1.2, 1.8.7.1 | P | Component of the sulfite reductase complex that catalyzes the 6-electron reduction of sulfite to sulfide. This is one of several activities required for the biosynthesis of L- cysteine from sulfate | |
KKNCFHKG_02808 | 4.8e-108 | |||||
KKNCFHKG_02809 | 3e-120 | mta | K | transcriptional | ||
KKNCFHKG_02810 | 5.6e-118 | L | Transposase | |||
KKNCFHKG_02811 | 4.1e-96 | L | Bacterial dnaA protein | |||
KKNCFHKG_02813 | 0.0 | 2.1.1.80, 3.1.1.61, 3.4.21.105 | L | DNA recombination | ||
KKNCFHKG_02821 | 1.7e-07 | |||||
KKNCFHKG_02822 | 8.7e-08 | |||||
KKNCFHKG_02826 | 1.6e-08 | |||||
KKNCFHKG_02830 | 2.2e-199 | adhC | 1.1.1.1 | C | Zinc-binding dehydrogenase | |
KKNCFHKG_02831 | 3.8e-190 | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | |||
KKNCFHKG_02833 | 1.9e-71 | L | COG2801 Transposase and inactivated derivatives | |||
KKNCFHKG_02834 | 6.7e-120 | msmE7 | G | Bacterial extracellular solute-binding protein | ||
KKNCFHKG_02835 | 6.2e-122 | msmF3 | U | Binding-protein-dependent transport system inner membrane component | ||
KKNCFHKG_02836 | 2.9e-119 | U | Binding-protein-dependent transport system inner membrane component | |||
KKNCFHKG_02837 | 5.4e-255 | dexB | 3.2.1.10, 3.2.1.70 | GH13 | G | COG0366 Glycosidases |
KKNCFHKG_02838 | 6.6e-306 | ywqB | S | Zinc finger, swim domain protein | ||
KKNCFHKG_02839 | 0.0 | ywqA | L | COG0553 Superfamily II DNA RNA helicases, SNF2 family | ||
KKNCFHKG_02840 | 1.1e-15 | S | Ribbon-helix-helix protein, copG family | |||
KKNCFHKG_02841 | 2.4e-53 | yodB | K | transcriptional | ||
KKNCFHKG_02842 | 6.7e-193 | S | Protein of unknown function (DUF1648) | |||
KKNCFHKG_02843 | 1.5e-68 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
KKNCFHKG_02844 | 7.7e-81 | ywrA | P | COG2059 Chromate transport protein ChrA | ||
KKNCFHKG_02845 | 8.7e-86 | chrA | P | Chromate transporter | ||
KKNCFHKG_02846 | 2.8e-50 | |||||
KKNCFHKG_02848 | 2.8e-174 | K | cell envelope-related transcriptional attenuator | |||
KKNCFHKG_02849 | 2e-305 | dnaX | 2.7.7.7 | L | DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
KKNCFHKG_02850 | 9.2e-34 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
KKNCFHKG_02851 | 1.5e-109 | recR | L | May play a role in DNA repair. It seems to be involved in an RecBC-independent recombinational process of DNA repair. It may act with RecF and RecO | ||
KKNCFHKG_02852 | 3.4e-08 | yaaL | S | Protein of unknown function (DUF2508) | ||
KKNCFHKG_02853 | 4.8e-36 | bofA | S | Sigma-K factor-processing regulatory protein BofA | ||
KKNCFHKG_02854 | 7.3e-151 | msrR | K | COG1316 Transcriptional regulator | ||
KKNCFHKG_02855 | 1.2e-98 | yngC | S | membrane-associated protein | ||
KKNCFHKG_02856 | 1.7e-227 | S | SNARE associated Golgi protein | |||
KKNCFHKG_02857 | 1.4e-35 | 3.2.1.78 | GH26 | O | cellulase activity | |
KKNCFHKG_02858 | 0.0 | ybeC | E | amino acid | ||
KKNCFHKG_02859 | 1e-57 | ulaG | S | L-ascorbate 6-phosphate lactonase | ||
KKNCFHKG_02861 | 3.1e-69 | dgoT | G | COG0477 Permeases of the major facilitator superfamily | ||
KKNCFHKG_02862 | 6.1e-137 | 4.1.99.16, 4.2.3.22, 4.2.3.75 | T | COG0664 cAMP-binding proteins - catabolite gene activator and regulatory subunit of cAMP-dependent protein kinases | ||
KKNCFHKG_02864 | 0.0 | 3.6.3.3, 3.6.3.5 | P | E1-E2 ATPase | ||
KKNCFHKG_02865 | 1.3e-29 | P | Heavy-metal-associated domain | |||
KKNCFHKG_02866 | 1.2e-51 | L | Transposase, IS4 family protein | |||
KKNCFHKG_02867 | 7.9e-295 | S | Immune inhibitor A peptidase M6 | |||
KKNCFHKG_02869 | 1.1e-19 | ydfD | K | COG1167 Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | ||
KKNCFHKG_02870 | 9.9e-125 | mmr | U | Major Facilitator Superfamily | ||
KKNCFHKG_02871 | 1.1e-37 | K | HxlR-like helix-turn-helix | |||
KKNCFHKG_02872 | 1e-151 | yetF1 | S | membrane | ||
KKNCFHKG_02873 | 3.8e-28 | S | Protein of unknown function (DUF1657) | |||
KKNCFHKG_02874 | 7.4e-194 | spoVAD | I | Stage V sporulation protein AD | ||
KKNCFHKG_02875 | 5.1e-25 | S | Protein of unknown function (DUF1657) | |||
KKNCFHKG_02876 | 4.2e-16 | L | Transposase, IS4 family protein | |||
KKNCFHKG_02877 | 3.8e-145 | pdaC | 3.5.1.104 | G | Polysaccharide deacetylase | |
KKNCFHKG_02880 | 5.6e-42 | |||||
KKNCFHKG_02881 | 2.6e-129 | V | ABC transporter | |||
KKNCFHKG_02882 | 2.5e-33 | C | acyl-CoA transferases carnitine dehydratase | |||
KKNCFHKG_02883 | 6.5e-182 | yfmJ | S | N-terminal domain of oxidoreductase | ||
KKNCFHKG_02884 | 2.5e-15 | S | Ribbon-helix-helix protein, copG family | |||
KKNCFHKG_02885 | 1.2e-210 | L | COG4584 Transposase and inactivated derivatives | |||
KKNCFHKG_02886 | 1.9e-111 | L | Bacterial dnaA protein | |||
KKNCFHKG_02887 | 1.5e-230 | patB | 4.4.1.8 | E | COG1168 Bifunctional PLP-dependent enzyme with beta-cystathionase and maltose regulon repressor activities | |
KKNCFHKG_02888 | 2.4e-131 | U | AAA domain | |||
KKNCFHKG_02889 | 3.2e-155 | L | Mu transposase, C-terminal | |||
KKNCFHKG_02890 | 3.4e-214 | EGP | Major facilitator Superfamily | |||
KKNCFHKG_02891 | 5.1e-44 | 2.7.1.202 | K | transcriptional regulator, MtlR | ||
KKNCFHKG_02892 | 1.8e-41 | S | transposase or invertase | |||
KKNCFHKG_02893 | 1.9e-172 | ydhF | S | Oxidoreductase | ||
KKNCFHKG_02895 | 1.7e-69 | L | COG2801 Transposase and inactivated derivatives | |||
KKNCFHKG_02896 | 2.6e-69 | L | COG2801 Transposase and inactivated derivatives | |||
KKNCFHKG_02897 | 3.3e-46 | L | COG2963 Transposase and inactivated derivatives | |||
KKNCFHKG_02900 | 2.2e-75 | 5.4.2.11 | G | Phosphoglycerate mutase family | ||
KKNCFHKG_02901 | 4.3e-18 | L | Helix-turn-helix domain of resolvase | |||
KKNCFHKG_02902 | 2.8e-132 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
KKNCFHKG_02903 | 4.4e-16 | L | Transposase, IS4 family protein | |||
KKNCFHKG_02904 | 8.4e-45 | L | Mu transposase, C-terminal | |||
KKNCFHKG_02905 | 5.3e-71 | L | Transposase, IS4 family protein | |||
KKNCFHKG_02906 | 3.3e-120 | L | Transposase | |||
KKNCFHKG_02907 | 6.3e-73 | L | resolvase | |||
KKNCFHKG_02908 | 8.2e-64 | L | Transposase IS200 like | |||
KKNCFHKG_02909 | 8e-42 | L | Transposase | |||
KKNCFHKG_02910 | 6.9e-64 | L | COG2801 Transposase and inactivated derivatives | |||
KKNCFHKG_02914 | 4e-08 | |||||
KKNCFHKG_02915 | 1.6e-08 | |||||
KKNCFHKG_02916 | 1.6e-37 | |||||
KKNCFHKG_02919 | 1.9e-15 | S | Ribbon-helix-helix protein, copG family |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)