ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
KDLFIFCD_00001 | 6e-29 | rimI | 2.3.1.128 | K | Ribosomal-protein-alanine acetyltransferase | |
KDLFIFCD_00002 | 2.4e-133 | yeaZ | 2.3.1.234 | O | Universal bacterial protein YeaZ | |
KDLFIFCD_00003 | 2.2e-85 | S | ECF transporter, substrate-specific component | |||
KDLFIFCD_00004 | 1.4e-130 | fat | 3.1.2.21 | I | Acyl-ACP thioesterase | |
KDLFIFCD_00005 | 5.1e-156 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
KDLFIFCD_00006 | 1.8e-59 | yabA | L | Involved in initiation control of chromosome replication | ||
KDLFIFCD_00007 | 1.5e-155 | holB | 2.7.7.7 | L | DNA polymerase III | |
KDLFIFCD_00008 | 2e-52 | yaaQ | S | Cyclic-di-AMP receptor | ||
KDLFIFCD_00009 | 1.6e-114 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
KDLFIFCD_00010 | 1.1e-34 | S | Protein of unknown function (DUF2508) | |||
KDLFIFCD_00011 | 1.6e-108 | 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 | ||
KDLFIFCD_00012 | 8.2e-41 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
KDLFIFCD_00013 | 1.2e-35 | M | lipopolysaccharide 3-alpha-galactosyltransferase activity | |||
KDLFIFCD_00014 | 5.7e-106 | 2.4.1.58 | GT8 | M | family 8 | |
KDLFIFCD_00015 | 0.0 | dnaX | 2.7.7.7 | L | DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
KDLFIFCD_00016 | 2.2e-90 | tadA | 3.5.4.33 | F | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
KDLFIFCD_00017 | 9e-26 | |||||
KDLFIFCD_00018 | 1.3e-116 | rsmC | 2.1.1.172 | J | Methyltransferase | |
KDLFIFCD_00019 | 8.7e-140 | potC | 2.1.1.172, 2.1.1.80, 3.1.1.61 | J | Ion channel | |
KDLFIFCD_00020 | 1.8e-54 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
KDLFIFCD_00021 | 7e-84 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
KDLFIFCD_00022 | 1.5e-11 | GT2,GT4 | M | family 8 | ||
KDLFIFCD_00023 | 7.8e-140 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
KDLFIFCD_00024 | 3.6e-111 | G | Phosphoglycerate mutase family | |||
KDLFIFCD_00025 | 0.0 | ppsA | 2.7.9.2 | H | Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate | |
KDLFIFCD_00026 | 4.2e-150 | rluA | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
KDLFIFCD_00027 | 0.0 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
KDLFIFCD_00028 | 7.2e-56 | yheA | S | Belongs to the UPF0342 family | ||
KDLFIFCD_00029 | 1e-226 | yhaO | L | Ser Thr phosphatase family protein | ||
KDLFIFCD_00030 | 0.0 | L | AAA domain | |||
KDLFIFCD_00031 | 1.9e-186 | cbf | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
KDLFIFCD_00032 | 2.9e-23 | |||||
KDLFIFCD_00033 | 2.4e-51 | S | Domain of unknown function DUF1829 | |||
KDLFIFCD_00034 | 1.1e-265 | |||||
KDLFIFCD_00035 | 1.9e-72 | eda | 4.1.2.14, 4.1.3.42 | G | KDPG and KHG aldolase | |
KDLFIFCD_00036 | 4.3e-153 | prsA | 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
KDLFIFCD_00037 | 3.9e-25 | |||||
KDLFIFCD_00038 | 8.3e-78 | hit | FG | Scavenger mRNA decapping enzyme C-term binding | ||
KDLFIFCD_00039 | 5.7e-135 | ecsA | V | ABC transporter, ATP-binding protein | ||
KDLFIFCD_00040 | 6.5e-221 | ecsB | U | ABC transporter | ||
KDLFIFCD_00041 | 3.3e-126 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
KDLFIFCD_00043 | 2.8e-54 | ytpP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
KDLFIFCD_00044 | 1.4e-122 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
KDLFIFCD_00045 | 9.7e-247 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
KDLFIFCD_00046 | 6.9e-218 | mepA | V | MATE efflux family protein | ||
KDLFIFCD_00047 | 1.8e-176 | S | SLAP domain | |||
KDLFIFCD_00048 | 4.4e-283 | M | Peptidase family M1 domain | |||
KDLFIFCD_00049 | 4.5e-188 | S | Bacteriocin helveticin-J | |||
KDLFIFCD_00050 | 8e-51 | L | RelB antitoxin | |||
KDLFIFCD_00051 | 7.4e-105 | qmcA | O | prohibitin homologues | ||
KDLFIFCD_00052 | 3.5e-25 | qmcA | O | prohibitin homologues | ||
KDLFIFCD_00053 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
KDLFIFCD_00054 | 4.2e-155 | 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 | |
KDLFIFCD_00055 | 1.3e-105 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
KDLFIFCD_00056 | 3.5e-82 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
KDLFIFCD_00057 | 5.1e-251 | dnaB | L | Replication initiation and membrane attachment | ||
KDLFIFCD_00058 | 2.1e-168 | dnaI | L | Primosomal protein DnaI | ||
KDLFIFCD_00059 | 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) | |
KDLFIFCD_00060 | 1.2e-74 | |||||
KDLFIFCD_00061 | 3e-37 | |||||
KDLFIFCD_00062 | 2.4e-110 | K | WHG domain | |||
KDLFIFCD_00063 | 6.4e-96 | nqr | 1.5.1.36 | S | NADPH-dependent FMN reductase | |
KDLFIFCD_00064 | 2e-97 | azr | 1.5.1.36 | S | NADPH-dependent FMN reductase | |
KDLFIFCD_00065 | 6e-151 | 3.1.3.48 | T | Tyrosine phosphatase family | ||
KDLFIFCD_00066 | 2.5e-180 | apbE | 2.7.1.180 | H | Flavin transferase that catalyzes the transfer of the FMN moiety of FAD and its covalent binding to the hydroxyl group of a threonine residue in a target flavoprotein | |
KDLFIFCD_00068 | 3e-53 | cvpA | S | Colicin V production protein | ||
KDLFIFCD_00069 | 5.5e-148 | S | cog cog1373 | |||
KDLFIFCD_00070 | 0.0 | 4.2.1.53 | S | Myosin-crossreactive antigen | ||
KDLFIFCD_00071 | 2e-91 | yxdD | K | Bacterial regulatory proteins, tetR family | ||
KDLFIFCD_00072 | 1.9e-259 | emrY | EGP | Major facilitator Superfamily | ||
KDLFIFCD_00077 | 1.1e-94 | MA20_25245 | K | Acetyltransferase (GNAT) domain | ||
KDLFIFCD_00078 | 4.9e-254 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
KDLFIFCD_00079 | 6.3e-201 | pbpX | V | Beta-lactamase | ||
KDLFIFCD_00080 | 2.8e-244 | nhaC | C | Na H antiporter NhaC | ||
KDLFIFCD_00081 | 3.2e-135 | I | transferase activity, transferring acyl groups other than amino-acyl groups | |||
KDLFIFCD_00082 | 2.6e-57 | |||||
KDLFIFCD_00083 | 4.3e-108 | ybhL | S | Belongs to the BI1 family | ||
KDLFIFCD_00084 | 2.7e-171 | yegS | 2.7.1.107 | G | Lipid kinase | |
KDLFIFCD_00085 | 2.7e-274 | gatB | 6.1.1.12, 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | |
KDLFIFCD_00086 | 2.9e-268 | 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) | |
KDLFIFCD_00087 | 1.5e-49 | 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) | |
KDLFIFCD_00088 | 5.8e-203 | camS | S | sex pheromone | ||
KDLFIFCD_00089 | 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 | |
KDLFIFCD_00090 | 0.0 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
KDLFIFCD_00091 | 5.2e-84 | acmC | 3.2.1.17, 3.2.1.96 | NU | mannosyl-glycoprotein | |
KDLFIFCD_00093 | 4.1e-83 | ydcK | S | Belongs to the SprT family | ||
KDLFIFCD_00094 | 7.7e-134 | M | Glycosyltransferase sugar-binding region containing DXD motif | |||
KDLFIFCD_00095 | 6e-258 | epsU | S | Polysaccharide biosynthesis protein | ||
KDLFIFCD_00096 | 7e-225 | M | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | |||
KDLFIFCD_00097 | 0.0 | pacL | 3.6.3.8 | P | P-type ATPase | |
KDLFIFCD_00098 | 1.4e-204 | tnpB | L | Putative transposase DNA-binding domain | ||
KDLFIFCD_00099 | 3.3e-152 | nadE | 6.3.1.5 | F | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
KDLFIFCD_00100 | 2.4e-286 | pncB | 6.3.4.21 | F | Catalyzes the synthesis of beta-nicotinate D- ribonucleotide from nicotinate and 5-phospho-D-ribose 1-phosphate at the expense of ATP | |
KDLFIFCD_00101 | 1.7e-204 | csaB | M | Glycosyl transferases group 1 | ||
KDLFIFCD_00102 | 2.1e-134 | tagA | 2.4.1.187 | GT26 | F | Catalyzes the conversion of GlcNAc-PP-undecaprenol into ManNAc-GlcNAc-PP-undecaprenol, the first committed lipid intermediate in the de novo synthesis of teichoic acid |
KDLFIFCD_00103 | 5.1e-71 | tagD | 2.7.7.15, 2.7.7.39 | IM | Glycerol-3-phosphate cytidylyltransferase | |
KDLFIFCD_00104 | 1.3e-125 | gntR1 | K | UTRA | ||
KDLFIFCD_00105 | 3.3e-179 | |||||
KDLFIFCD_00106 | 3.4e-45 | oppA2 | E | ABC transporter, substratebinding protein | ||
KDLFIFCD_00107 | 4.4e-239 | oppA2 | E | ABC transporter, substratebinding protein | ||
KDLFIFCD_00110 | 3.2e-240 | npr | 1.11.1.1 | C | NADH oxidase | |
KDLFIFCD_00111 | 6.6e-11 | |||||
KDLFIFCD_00112 | 1.3e-22 | 3.6.4.12 | S | transposase or invertase | ||
KDLFIFCD_00113 | 6.7e-228 | slpX | S | SLAP domain | ||
KDLFIFCD_00114 | 4.4e-144 | K | SIS domain | |||
KDLFIFCD_00115 | 8.1e-120 | rpiA | 5.3.1.6 | G | Ribose 5-phosphate isomerase A (phosphoriboisomerase A) | |
KDLFIFCD_00116 | 2.7e-185 | XK27_10475 | S | Oxidoreductase family, NAD-binding Rossmann fold | ||
KDLFIFCD_00117 | 6.5e-210 | patA | 2.6.1.1, 2.6.1.57 | E | Aminotransferase | |
KDLFIFCD_00119 | 0.0 | mgtA | 3.6.3.2 | P | COG0474 Cation transport ATPase | |
KDLFIFCD_00121 | 1.2e-115 | glpQ1 | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
KDLFIFCD_00122 | 6.6e-119 | VY92_08690 | 5.3.1.32 | G | Antibiotic biosynthesis monooxygenase | |
KDLFIFCD_00123 | 2.6e-89 | G | Histidine phosphatase superfamily (branch 1) | |||
KDLFIFCD_00124 | 1.2e-105 | G | Phosphoglycerate mutase family | |||
KDLFIFCD_00125 | 3.1e-158 | D | nuclear chromosome segregation | |||
KDLFIFCD_00126 | 5.8e-78 | M | LysM domain protein | |||
KDLFIFCD_00127 | 2.8e-86 | celB | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
KDLFIFCD_00128 | 4.1e-78 | celB | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
KDLFIFCD_00129 | 1.5e-16 | celB | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
KDLFIFCD_00130 | 6.2e-12 | |||||
KDLFIFCD_00131 | 2.3e-172 | pphA | 3.1.3.16 | T | Calcineurin-like phosphoesterase | |
KDLFIFCD_00132 | 2.3e-30 | |||||
KDLFIFCD_00134 | 2.9e-69 | S | Iron-sulphur cluster biosynthesis | |||
KDLFIFCD_00135 | 6.5e-113 | yncA | 2.3.1.79 | S | Maltose acetyltransferase | |
KDLFIFCD_00136 | 6.2e-59 | psiE | S | Phosphate-starvation-inducible E | ||
KDLFIFCD_00138 | 4.4e-135 | nfrA | 1.5.1.38, 1.5.1.39 | C | nitroreductase | |
KDLFIFCD_00139 | 4.3e-228 | amtB | P | ammonium transporter | ||
KDLFIFCD_00140 | 1.4e-60 | |||||
KDLFIFCD_00141 | 0.0 | lhr | L | DEAD DEAH box helicase | ||
KDLFIFCD_00142 | 1.4e-245 | P | P-loop Domain of unknown function (DUF2791) | |||
KDLFIFCD_00143 | 2.6e-138 | S | TerB-C domain | |||
KDLFIFCD_00144 | 2.6e-61 | M | Glycosyl hydrolases family 25 | |||
KDLFIFCD_00145 | 1.3e-61 | M | Glycosyl hydrolases family 25 | |||
KDLFIFCD_00146 | 2.8e-211 | yfmL | 3.6.4.13 | L | DEAD DEAH box helicase | |
KDLFIFCD_00147 | 4.7e-249 | celB | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
KDLFIFCD_00149 | 2e-216 | mnaA | 5.1.3.14 | G | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
KDLFIFCD_00150 | 2.2e-200 | L | Transposase DDE domain | |||
KDLFIFCD_00151 | 7e-87 | gtcA | S | Teichoic acid glycosylation protein | ||
KDLFIFCD_00152 | 4.1e-80 | fld | C | Flavodoxin | ||
KDLFIFCD_00153 | 1.4e-163 | map | 3.4.11.18 | E | Methionine Aminopeptidase | |
KDLFIFCD_00154 | 3.6e-163 | yihY | S | Belongs to the UPF0761 family | ||
KDLFIFCD_00155 | 2.1e-168 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
KDLFIFCD_00156 | 2.5e-214 | atoB | 1.1.1.88, 2.3.1.9 | I | Belongs to the thiolase family | |
KDLFIFCD_00157 | 3.6e-215 | mvaS | 2.3.3.10 | I | Hydroxymethylglutaryl-CoA synthase | |
KDLFIFCD_00158 | 7e-43 | yfdE | 2.8.3.16, 2.8.3.19 | C | Involved in the catabolism of oxalate and in the adapatation to low pH via the induction of the oxalate-dependent acid tolerance response (ATR). Catalyzes the transfer of the CoA moiety from formyl-CoA to oxalate | |
KDLFIFCD_00159 | 6.6e-182 | frc | 2.8.3.16, 2.8.3.19 | C | Involved in the catabolism of oxalate and in the adapatation to low pH via the induction of the oxalate-dependent acid tolerance response (ATR). Catalyzes the transfer of the CoA moiety from formyl-CoA to oxalate | |
KDLFIFCD_00160 | 3.4e-284 | oxc | 4.1.1.8 | EH | Belongs to the TPP enzyme family | |
KDLFIFCD_00161 | 0.0 | uup | S | ABC transporter, ATP-binding protein | ||
KDLFIFCD_00162 | 5.8e-112 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
KDLFIFCD_00163 | 3.2e-10 | S | Domain of unknown function DUF87 | |||
KDLFIFCD_00164 | 9.5e-64 | S | SIR2-like domain | |||
KDLFIFCD_00165 | 5.7e-99 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | ||
KDLFIFCD_00166 | 1.9e-259 | hsdM | 2.1.1.72 | V | type I restriction-modification system | |
KDLFIFCD_00167 | 3.4e-42 | S | RloB-like protein | |||
KDLFIFCD_00168 | 1.2e-164 | S | AAA domain, putative AbiEii toxin, Type IV TA system | |||
KDLFIFCD_00169 | 0.0 | hsdR | 3.1.21.3 | L | DEAD/DEAH box helicase | |
KDLFIFCD_00170 | 0.0 | S | SLAP domain | |||
KDLFIFCD_00172 | 1.1e-236 | XK27_01810 | S | Calcineurin-like phosphoesterase | ||
KDLFIFCD_00173 | 1e-60 | pdxH | S | Pyridoxamine 5'-phosphate oxidase | ||
KDLFIFCD_00174 | 1.9e-37 | G | Bacterial extracellular solute-binding protein | |||
KDLFIFCD_00175 | 7.1e-19 | |||||
KDLFIFCD_00177 | 1e-180 | M | Glycosyl hydrolases family 25 | |||
KDLFIFCD_00178 | 7.7e-30 | |||||
KDLFIFCD_00179 | 2e-17 | |||||
KDLFIFCD_00181 | 8.1e-08 | |||||
KDLFIFCD_00182 | 1.1e-18 | S | Phage uncharacterised protein (Phage_XkdX) | |||
KDLFIFCD_00183 | 2e-23 | |||||
KDLFIFCD_00189 | 2.2e-34 | |||||
KDLFIFCD_00190 | 1.4e-09 | |||||
KDLFIFCD_00191 | 3.9e-114 | Z012_12235 | S | Baseplate J-like protein | ||
KDLFIFCD_00192 | 6.4e-31 | |||||
KDLFIFCD_00193 | 1.2e-37 | |||||
KDLFIFCD_00194 | 9.6e-102 | |||||
KDLFIFCD_00195 | 2.3e-45 | |||||
KDLFIFCD_00196 | 1.3e-59 | M | LysM domain | |||
KDLFIFCD_00197 | 2.5e-227 | 3.4.14.13 | M | Phage tail tape measure protein TP901 | ||
KDLFIFCD_00199 | 2.9e-09 | |||||
KDLFIFCD_00200 | 4.2e-29 | |||||
KDLFIFCD_00201 | 9.2e-104 | Z012_02110 | S | Protein of unknown function (DUF3383) | ||
KDLFIFCD_00202 | 2.5e-31 | |||||
KDLFIFCD_00203 | 3.9e-24 | |||||
KDLFIFCD_00204 | 6.5e-29 | |||||
KDLFIFCD_00205 | 9.2e-20 | S | Protein of unknown function (DUF4054) | |||
KDLFIFCD_00206 | 3.7e-94 | Z012_11565 | S | Uncharacterized protein conserved in bacteria (DUF2184) | ||
KDLFIFCD_00207 | 1.8e-34 | |||||
KDLFIFCD_00208 | 1.6e-57 | S | Uncharacterized protein conserved in bacteria (DUF2213) | |||
KDLFIFCD_00209 | 6.5e-12 | S | Lysin motif | |||
KDLFIFCD_00210 | 1.3e-47 | S | Phage Mu protein F like protein | |||
KDLFIFCD_00211 | 1.4e-134 | S | Protein of unknown function (DUF1073) | |||
KDLFIFCD_00212 | 4.1e-201 | S | Terminase-like family | |||
KDLFIFCD_00213 | 4e-19 | ps333 | L | Terminase small subunit | ||
KDLFIFCD_00216 | 3.3e-09 | arpU | S | Phage transcriptional regulator, ArpU family | ||
KDLFIFCD_00219 | 3.2e-218 | XK27_11280 | S | Psort location CytoplasmicMembrane, score | ||
KDLFIFCD_00221 | 5.5e-49 | S | VRR_NUC | |||
KDLFIFCD_00233 | 5.8e-20 | L | Psort location Cytoplasmic, score | |||
KDLFIFCD_00234 | 2.1e-42 | S | Protein of unknown function (DUF1071) | |||
KDLFIFCD_00236 | 7.7e-48 | |||||
KDLFIFCD_00239 | 6.8e-08 | |||||
KDLFIFCD_00241 | 3.1e-88 | S | AntA/AntB antirepressor | |||
KDLFIFCD_00243 | 3.7e-13 | |||||
KDLFIFCD_00244 | 3.1e-12 | |||||
KDLFIFCD_00245 | 3.7e-18 | ps115 | K | sequence-specific DNA binding | ||
KDLFIFCD_00246 | 3e-14 | S | Pfam:Peptidase_M78 | |||
KDLFIFCD_00247 | 1.2e-54 | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
KDLFIFCD_00248 | 4.8e-12 | |||||
KDLFIFCD_00252 | 6.3e-176 | sip | L | Belongs to the 'phage' integrase family | ||
KDLFIFCD_00253 | 2e-183 | G | Bacterial extracellular solute-binding protein | |||
KDLFIFCD_00254 | 6.3e-17 | |||||
KDLFIFCD_00255 | 2.5e-287 | treC | 3.2.1.93 | GH13 | G | Alpha amylase, catalytic domain protein |
KDLFIFCD_00256 | 8.9e-101 | treR | K | UTRA | ||
KDLFIFCD_00257 | 1.5e-283 | treB | G | phosphotransferase system | ||
KDLFIFCD_00258 | 8.2e-64 | spxA_2 | 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 | |
KDLFIFCD_00259 | 1.9e-191 | yrvN | L | AAA C-terminal domain | ||
KDLFIFCD_00260 | 2.2e-251 | pepT2 | 3.4.11.14, 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
KDLFIFCD_00261 | 9e-83 | K | Acetyltransferase (GNAT) domain | |||
KDLFIFCD_00262 | 1.3e-229 | S | Putative peptidoglycan binding domain | |||
KDLFIFCD_00263 | 7.5e-95 | S | ECF-type riboflavin transporter, S component | |||
KDLFIFCD_00264 | 2.8e-98 | pdxK | 2.7.1.35 | H | Phosphomethylpyrimidine kinase | |
KDLFIFCD_00265 | 9.3e-204 | pbpX1 | V | Beta-lactamase | ||
KDLFIFCD_00266 | 1.4e-115 | lacA | 2.3.1.79 | S | Transferase hexapeptide repeat | |
KDLFIFCD_00267 | 1.9e-80 | yvbK | 3.1.3.25 | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | |
KDLFIFCD_00268 | 7.4e-205 | L | COG2826 Transposase and inactivated derivatives, IS30 family | |||
KDLFIFCD_00269 | 2.1e-114 | 3.6.1.27 | I | Acid phosphatase homologues | ||
KDLFIFCD_00270 | 1.1e-189 | mmuM | 1.5.1.20, 2.1.1.10 | H | homocysteine S-methyltransferase | |
KDLFIFCD_00271 | 0.0 | uvrA3 | L | excinuclease ABC, A subunit | ||
KDLFIFCD_00272 | 9.9e-82 | C | Flavodoxin | |||
KDLFIFCD_00273 | 3.4e-129 | S | (CBS) domain | |||
KDLFIFCD_00274 | 1.5e-183 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
KDLFIFCD_00275 | 5.1e-104 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
KDLFIFCD_00276 | 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 | ||
KDLFIFCD_00277 | 7.4e-40 | yabO | J | S4 domain protein | ||
KDLFIFCD_00278 | 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) | |
KDLFIFCD_00279 | 8.4e-287 | gntK | 2.7.1.12, 2.7.1.17 | G | Belongs to the FGGY kinase family | |
KDLFIFCD_00280 | 1.7e-34 | |||||
KDLFIFCD_00281 | 1.2e-94 | sigH | K | Belongs to the sigma-70 factor family | ||
KDLFIFCD_00282 | 1.7e-139 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
KDLFIFCD_00283 | 5.1e-75 | 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) | ||
KDLFIFCD_00284 | 7.5e-277 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
KDLFIFCD_00285 | 1.6e-290 | 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) | |
KDLFIFCD_00286 | 2.3e-254 | radA | O | DNA-dependent ATPase involved in processing of recombination intermediates, plays a role in repairing DNA breaks. Stimulates the branch migration of RecA-mediated strand transfer reactions, allowing the 3' invading strand to extend heteroduplex DNA faster. Binds ssDNA in the presence of ADP but not other nucleotides, has ATPase activity that is stimulated by ssDNA and various branched DNA structures, but inhibited by SSB. Does not have RecA's homology-searching function | ||
KDLFIFCD_00287 | 1.8e-101 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | dUTP diphosphatase | |
KDLFIFCD_00288 | 4.1e-52 | |||||
KDLFIFCD_00289 | 1e-267 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
KDLFIFCD_00290 | 7.3e-44 | |||||
KDLFIFCD_00291 | 2.4e-183 | S | AAA domain | |||
KDLFIFCD_00292 | 3.4e-126 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
KDLFIFCD_00293 | 1.4e-23 | |||||
KDLFIFCD_00294 | 7.3e-161 | czcD | P | cation diffusion facilitator family transporter | ||
KDLFIFCD_00295 | 3.7e-125 | gpmB | G | Belongs to the phosphoglycerate mutase family | ||
KDLFIFCD_00296 | 6e-132 | S | membrane transporter protein | |||
KDLFIFCD_00297 | 1.9e-118 | 3.1.3.18, 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | ||
KDLFIFCD_00298 | 6.3e-105 | thiJ | 2.7.11.1, 3.5.1.124 | S | DJ-1/PfpI family | |
KDLFIFCD_00299 | 1.2e-49 | S | Protein of unknown function (DUF3021) | |||
KDLFIFCD_00300 | 2.8e-65 | K | LytTr DNA-binding domain | |||
KDLFIFCD_00301 | 9.1e-54 | papP | P | ABC transporter, permease protein | ||
KDLFIFCD_00302 | 5.3e-116 | P | ABC transporter permease | |||
KDLFIFCD_00303 | 1.5e-127 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
KDLFIFCD_00304 | 6.8e-156 | cjaA | ET | ABC transporter substrate-binding protein | ||
KDLFIFCD_00305 | 7.1e-200 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
KDLFIFCD_00306 | 0.0 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
KDLFIFCD_00307 | 2e-61 | 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 | ||
KDLFIFCD_00308 | 4.3e-169 | ldh | 1.1.1.27 | C | lactate/malate dehydrogenase, alpha/beta C-terminal domain | |
KDLFIFCD_00309 | 7.1e-158 | metQ1 | P | Belongs to the nlpA lipoprotein family | ||
KDLFIFCD_00310 | 1.9e-25 | |||||
KDLFIFCD_00311 | 0.0 | mco | Q | Multicopper oxidase | ||
KDLFIFCD_00312 | 1.2e-151 | S | Sucrose-6F-phosphate phosphohydrolase | |||
KDLFIFCD_00313 | 0.0 | oppA | E | ABC transporter | ||
KDLFIFCD_00314 | 3.2e-228 | Q | Imidazolonepropionase and related amidohydrolases | |||
KDLFIFCD_00315 | 2.7e-246 | 3.5.1.47 | S | Peptidase dimerisation domain | ||
KDLFIFCD_00316 | 1e-137 | S | Protein of unknown function (DUF3100) | |||
KDLFIFCD_00317 | 9.7e-83 | S | An automated process has identified a potential problem with this gene model | |||
KDLFIFCD_00318 | 1.1e-183 | scrR | K | helix_turn _helix lactose operon repressor | ||
KDLFIFCD_00319 | 3.7e-295 | scrB | 3.2.1.26 | GH32 | G | invertase |
KDLFIFCD_00320 | 0.0 | scrA | 2.7.1.208, 2.7.1.211, 5.3.1.1 | G | phosphotransferase system | |
KDLFIFCD_00321 | 2.3e-181 | M | CHAP domain | |||
KDLFIFCD_00322 | 3.5e-75 | |||||
KDLFIFCD_00323 | 1.4e-41 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
KDLFIFCD_00324 | 5.9e-294 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
KDLFIFCD_00325 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
KDLFIFCD_00326 | 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 | ||
KDLFIFCD_00327 | 1.7e-102 | 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 | |
KDLFIFCD_00328 | 1.5e-186 | 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 | |
KDLFIFCD_00329 | 9.6e-41 | yajC | U | Preprotein translocase | ||
KDLFIFCD_00330 | 9.6e-288 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
KDLFIFCD_00331 | 6.2e-210 | 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 | |
KDLFIFCD_00332 | 1.4e-181 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
KDLFIFCD_00333 | 5.2e-227 | 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 | |
KDLFIFCD_00334 | 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 | |
KDLFIFCD_00335 | 2e-42 | yrzL | S | Belongs to the UPF0297 family | ||
KDLFIFCD_00336 | 6.1e-73 | yqgF | J | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
KDLFIFCD_00337 | 1.1e-50 | yrzB | S | Belongs to the UPF0473 family | ||
KDLFIFCD_00338 | 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 | ||
KDLFIFCD_00339 | 3.5e-54 | trxA | O | Belongs to the thioredoxin family | ||
KDLFIFCD_00367 | 7.9e-224 | mgs | 2.4.1.337 | GT4 | M | Glycosyl transferase 4-like domain |
KDLFIFCD_00368 | 7.6e-202 | cpoA | GT4 | M | Glycosyltransferase, group 1 family protein | |
KDLFIFCD_00369 | 1.4e-176 | mprF | S | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms | ||
KDLFIFCD_00370 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
KDLFIFCD_00371 | 1.7e-29 | secG | U | Preprotein translocase | ||
KDLFIFCD_00372 | 0.0 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
KDLFIFCD_00373 | 5.1e-78 | smpB | J | the 2 termini fold to resemble tRNA(Ala) and it encodes a tag peptide , a short internal open reading frame. During trans-translation Ala- aminoacylated tmRNA acts like a tRNA, entering the A-site of stalled ribosomes, displacing the stalled mRNA. The ribosome then switches to translate the ORF on the tmRNA | ||
KDLFIFCD_00374 | 8.3e-210 | guaB | 1.1.1.205 | F | Catalyzes the irreversible NADPH-dependent deamination of GMP to IMP. It functions in the conversion of nucleobase, nucleoside and nucleotide derivatives of G to A nucleotides, and in maintaining the intracellular balance of A and G nucleotides | |
KDLFIFCD_00375 | 1.1e-146 | oppB | P | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
KDLFIFCD_00376 | 8.9e-187 | oppC | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
KDLFIFCD_00377 | 2.7e-199 | oppD | P | Belongs to the ABC transporter superfamily | ||
KDLFIFCD_00378 | 1.9e-175 | oppF | P | Belongs to the ABC transporter superfamily | ||
KDLFIFCD_00379 | 1.4e-256 | pepC | 3.4.22.40 | E | aminopeptidase | |
KDLFIFCD_00380 | 3.9e-72 | hsp | O | Belongs to the small heat shock protein (HSP20) family | ||
KDLFIFCD_00381 | 1.3e-28 | 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 | ||
KDLFIFCD_00382 | 2.9e-109 | nanE | 5.1.3.9 | G | Converts N-acetylmannosamine-6-phosphate (ManNAc-6-P) to N-acetylglucosamine-6-phosphate (GlcNAc-6-P) | |
KDLFIFCD_00383 | 1.7e-36 | axe1 | 3.1.1.41 | Q | Acetyl xylan esterase (AXE1) | |
KDLFIFCD_00384 | 1.1e-59 | axe1 | 3.1.1.41 | Q | Acetyl xylan esterase (AXE1) | |
KDLFIFCD_00385 | 1e-220 | nanT | E | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
KDLFIFCD_00386 | 1.9e-121 | napA | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
KDLFIFCD_00387 | 2.3e-56 | G | Xylose isomerase domain protein TIM barrel | |||
KDLFIFCD_00388 | 8.4e-90 | nanK | GK | ROK family | ||
KDLFIFCD_00389 | 2.9e-122 | nanA | 4.1.3.3, 4.3.3.7 | EM | Neu5Ac) to form pyruvate and N-acetylmannosamine (ManNAc) via a Schiff base intermediate | |
KDLFIFCD_00390 | 3.7e-66 | K | Helix-turn-helix domain, rpiR family | |||
KDLFIFCD_00391 | 7.1e-263 | E | ABC transporter, substratebinding protein | |||
KDLFIFCD_00392 | 9.1e-10 | K | peptidyl-tyrosine sulfation | |||
KDLFIFCD_00394 | 1.2e-128 | S | interspecies interaction between organisms | |||
KDLFIFCD_00395 | 2.7e-34 | |||||
KDLFIFCD_00398 | 1.9e-21 | |||||
KDLFIFCD_00399 | 6e-148 | |||||
KDLFIFCD_00400 | 1.5e-169 | |||||
KDLFIFCD_00401 | 2e-263 | glnA | 6.3.1.2 | E | glutamine synthetase | |
KDLFIFCD_00402 | 7.6e-225 | ynbB | 4.4.1.1 | P | aluminum resistance | |
KDLFIFCD_00403 | 1.5e-167 | miaA | 2.5.1.75 | F | Catalyzes the transfer of a dimethylallyl group onto the adenine at position 37 in tRNAs that read codons beginning with uridine, leading to the formation of N6-(dimethylallyl)adenosine (i(6)A) | |
KDLFIFCD_00404 | 1.5e-65 | yqhL | P | Rhodanese-like protein | ||
KDLFIFCD_00405 | 9.7e-36 | yqgQ | S | Bacterial protein of unknown function (DUF910) | ||
KDLFIFCD_00406 | 4e-119 | gluP | 3.4.21.105 | S | Rhomboid family | |
KDLFIFCD_00407 | 2.7e-97 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
KDLFIFCD_00408 | 1.2e-20 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
KDLFIFCD_00409 | 0.0 | pbp2b | 3.4.16.4 | M | Penicillin-binding Protein | |
KDLFIFCD_00410 | 0.0 | S | membrane | |||
KDLFIFCD_00411 | 5.2e-170 | 2.7.1.59 | G | BadF/BadG/BcrA/BcrD ATPase family | ||
KDLFIFCD_00412 | 1.3e-38 | S | RelB antitoxin | |||
KDLFIFCD_00413 | 3.4e-51 | S | Bacterial toxin of type II toxin-antitoxin system, YafQ | |||
KDLFIFCD_00414 | 6.7e-44 | 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 | ||
KDLFIFCD_00415 | 6.7e-139 | fhuC | 3.6.3.34 | HP | abc transporter atp-binding protein | |
KDLFIFCD_00416 | 9.5e-148 | isdF | U | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
KDLFIFCD_00417 | 8.7e-159 | isdE | P | Periplasmic binding protein | ||
KDLFIFCD_00418 | 6.3e-123 | M | Iron Transport-associated domain | |||
KDLFIFCD_00419 | 3e-09 | isdH | M | Iron Transport-associated domain | ||
KDLFIFCD_00420 | 8.4e-89 | |||||
KDLFIFCD_00421 | 6.4e-113 | S | SLAP domain | |||
KDLFIFCD_00422 | 1.2e-51 | L | PFAM RNA-directed DNA polymerase (Reverse transcriptase) | |||
KDLFIFCD_00423 | 9.2e-262 | emrY | EGP | Major facilitator Superfamily | ||
KDLFIFCD_00424 | 8.8e-90 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
KDLFIFCD_00425 | 7.6e-239 | pyrP | F | Permease | ||
KDLFIFCD_00426 | 1.9e-22 | K | Putative DNA-binding domain | |||
KDLFIFCD_00427 | 2.3e-93 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
KDLFIFCD_00428 | 5.7e-103 | 3.2.2.20 | K | acetyltransferase | ||
KDLFIFCD_00430 | 4.3e-226 | 2.7.1.207 | 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 | ||
KDLFIFCD_00431 | 4.9e-82 | rarA | L | MgsA AAA+ ATPase C terminal | ||
KDLFIFCD_00432 | 4.1e-21 | K | Helix-turn-helix domain, rpiR family | |||
KDLFIFCD_00433 | 1.3e-71 | K | Helix-turn-helix domain, rpiR family | |||
KDLFIFCD_00434 | 9.7e-136 | dapE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
KDLFIFCD_00435 | 5.4e-242 | lctO | C | L-lactate dehydrogenase (FMN-dependent) and related alpha-hydroxy acid dehydrogenases | ||
KDLFIFCD_00436 | 1.7e-221 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
KDLFIFCD_00437 | 3.2e-278 | yjeM | E | Amino Acid | ||
KDLFIFCD_00438 | 4.5e-49 | S | Fic/DOC family | |||
KDLFIFCD_00439 | 2.8e-08 | S | Fic/DOC family | |||
KDLFIFCD_00440 | 3.1e-278 | |||||
KDLFIFCD_00441 | 3.2e-77 | |||||
KDLFIFCD_00442 | 2.3e-87 | S | Protein of unknown function (DUF805) | |||
KDLFIFCD_00443 | 5.6e-68 | O | OsmC-like protein | |||
KDLFIFCD_00444 | 6.7e-207 | EGP | Major facilitator Superfamily | |||
KDLFIFCD_00445 | 2.6e-141 | sptS | 2.7.13.3 | T | Histidine kinase | |
KDLFIFCD_00446 | 5.9e-57 | sptS | 2.7.13.3 | T | Histidine kinase | |
KDLFIFCD_00447 | 1.3e-65 | K | response regulator | |||
KDLFIFCD_00448 | 6e-27 | K | response regulator | |||
KDLFIFCD_00449 | 7.5e-109 | 2.7.6.5 | T | Region found in RelA / SpoT proteins | ||
KDLFIFCD_00450 | 6.2e-271 | gtfA | 2.4.1.7 | GH13 | G | Sucrose glucosyltransferase |
KDLFIFCD_00451 | 0.0 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
KDLFIFCD_00452 | 2.8e-210 | msmX | P | Belongs to the ABC transporter superfamily | ||
KDLFIFCD_00453 | 2e-152 | msmG | P | Binding-protein-dependent transport system inner membrane component | ||
KDLFIFCD_00454 | 4.8e-157 | msmF | P | Binding-protein-dependent transport system inner membrane component | ||
KDLFIFCD_00455 | 3.2e-172 | msmE | G | Bacterial extracellular solute-binding protein | ||
KDLFIFCD_00456 | 4.9e-35 | msmE | G | Bacterial extracellular solute-binding protein | ||
KDLFIFCD_00457 | 1.6e-158 | scrR | K | Periplasmic binding protein domain | ||
KDLFIFCD_00458 | 5.5e-36 | |||||
KDLFIFCD_00459 | 8.3e-198 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
KDLFIFCD_00460 | 1.8e-200 | pgl | 3.1.1.31 | G | Lactonase, 7-bladed beta-propeller | |
KDLFIFCD_00461 | 2.2e-66 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
KDLFIFCD_00462 | 2.6e-214 | yubA | S | AI-2E family transporter | ||
KDLFIFCD_00463 | 4.2e-106 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
KDLFIFCD_00464 | 1.7e-69 | WQ51_03320 | S | Protein of unknown function (DUF1149) | ||
KDLFIFCD_00465 | 0.0 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
KDLFIFCD_00466 | 9e-223 | 2.7.1.26, 2.7.7.2 | S | Peptidase M16 inactive domain protein | ||
KDLFIFCD_00467 | 1.9e-236 | S | Peptidase M16 | |||
KDLFIFCD_00468 | 2.3e-133 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
KDLFIFCD_00469 | 5.2e-97 | ymfM | S | Helix-turn-helix domain | ||
KDLFIFCD_00470 | 1.1e-95 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
KDLFIFCD_00471 | 4.2e-195 | 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 | ||
KDLFIFCD_00472 | 7.4e-220 | rny | S | Endoribonuclease that initiates mRNA decay | ||
KDLFIFCD_00473 | 1.3e-210 | tagO | 2.7.8.33, 2.7.8.35 | M | transferase | |
KDLFIFCD_00474 | 5.1e-119 | yvyE | 3.4.13.9 | S | YigZ family | |
KDLFIFCD_00475 | 4.7e-246 | comFA | L | Helicase C-terminal domain protein | ||
KDLFIFCD_00476 | 9.4e-132 | comFC | S | Competence protein | ||
KDLFIFCD_00477 | 1.6e-94 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
KDLFIFCD_00478 | 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 | ||
KDLFIFCD_00479 | 4.6e-188 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
KDLFIFCD_00480 | 5.1e-17 | |||||
KDLFIFCD_00481 | 5.8e-180 | hprK | F | Catalyzes the ATP- as well as the pyrophosphate- dependent phosphorylation of a specific serine residue in HPr, a phosphocarrier protein of the phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS). HprK P also catalyzes the pyrophosphate-producing, inorganic phosphate-dependent dephosphorylation (phosphorolysis) of seryl-phosphorylated HPr (P- Ser-HPr). The two antagonistic activities of HprK P are regulated by several intracellular metabolites, which change their concentration in response to the absence or presence of rapidly metabolisable carbon sources (glucose, fructose, etc.) in the growth medium. Therefore, by controlling the phosphorylation state of HPr, HPrK P is a sensor enzyme that plays a major role in the regulation of carbon metabolism and sugar transport it mediates carbon catabolite repression (CCR), and regulates PTS-catalyzed carbohydrate uptake and inducer exclusion | ||
KDLFIFCD_00482 | 9.2e-158 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
KDLFIFCD_00483 | 1.1e-186 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
KDLFIFCD_00484 | 3.9e-181 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
KDLFIFCD_00485 | 0.0 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase phosphomannomutase, alpha beta alpha domain | |
KDLFIFCD_00486 | 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 | ||
KDLFIFCD_00487 | 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 | ||
KDLFIFCD_00488 | 9.1e-90 | S | Short repeat of unknown function (DUF308) | |||
KDLFIFCD_00489 | 6.2e-165 | rapZ | S | Displays ATPase and GTPase activities | ||
KDLFIFCD_00490 | 4e-195 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
KDLFIFCD_00491 | 2.1e-171 | whiA | K | May be required for sporulation | ||
KDLFIFCD_00492 | 2.3e-99 | clpP | 3.4.21.92 | O | Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins | |
KDLFIFCD_00493 | 0.0 | S | SH3-like domain | |||
KDLFIFCD_00494 | 4.9e-111 | ybbL | S | ABC transporter, ATP-binding protein | ||
KDLFIFCD_00495 | 2.5e-130 | ybbM | S | Uncharacterised protein family (UPF0014) | ||
KDLFIFCD_00496 | 1.2e-94 | |||||
KDLFIFCD_00497 | 3.4e-155 | ycsE | S | Sucrose-6F-phosphate phosphohydrolase | ||
KDLFIFCD_00498 | 9.7e-137 | 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 | |
KDLFIFCD_00499 | 4.1e-181 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
KDLFIFCD_00500 | 7e-86 | ydiB | 2.7.1.221, 5.1.1.1 | O | Hydrolase, P-loop family | |
KDLFIFCD_00501 | 4e-98 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
KDLFIFCD_00502 | 2e-163 | murB | 1.3.1.98 | M | Cell wall formation | |
KDLFIFCD_00503 | 1.8e-206 | 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 | |
KDLFIFCD_00504 | 1.3e-129 | potB | P | ABC transporter permease | ||
KDLFIFCD_00505 | 4.8e-127 | potC | P | ABC transporter permease | ||
KDLFIFCD_00506 | 7.3e-208 | potD | P | ABC transporter | ||
KDLFIFCD_00507 | 6.4e-151 | 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 | |
KDLFIFCD_00508 | 2e-172 | ybbR | S | YbbR-like protein | ||
KDLFIFCD_00509 | 4.5e-255 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
KDLFIFCD_00510 | 1.4e-147 | S | hydrolase | |||
KDLFIFCD_00511 | 1.8e-75 | K | Penicillinase repressor | |||
KDLFIFCD_00512 | 1.6e-118 | |||||
KDLFIFCD_00513 | 7.4e-85 | ptpA | 3.1.3.48 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
KDLFIFCD_00514 | 3.8e-207 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
KDLFIFCD_00515 | 8.3e-143 | licT | K | CAT RNA binding domain | ||
KDLFIFCD_00516 | 0.0 | bglP | 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
KDLFIFCD_00517 | 1e-297 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family | |
KDLFIFCD_00518 | 1e-149 | D | Alpha beta | |||
KDLFIFCD_00519 | 1.2e-92 | yhjH | 3.1.4.52 | T | Putative diguanylate phosphodiesterase | |
KDLFIFCD_00520 | 3.7e-26 | queD | 4.1.2.50, 4.2.3.12 | H | 6-pyruvoyl tetrahydropterin synthase | |
KDLFIFCD_00521 | 5.2e-112 | ica2 | GT2 | M | Glycosyl transferase family group 2 | |
KDLFIFCD_00522 | 8.2e-36 | |||||
KDLFIFCD_00523 | 2.2e-90 | 2.7.7.65 | T | GGDEF domain | ||
KDLFIFCD_00524 | 8.8e-82 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
KDLFIFCD_00526 | 2e-310 | E | Amino acid permease | |||
KDLFIFCD_00527 | 5.8e-100 | L | Helix-turn-helix domain | |||
KDLFIFCD_00528 | 1.3e-160 | L | hmm pf00665 | |||
KDLFIFCD_00530 | 3.7e-27 | 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 | ||
KDLFIFCD_00531 | 3.5e-101 | ylbE | GM | NAD(P)H-binding | ||
KDLFIFCD_00532 | 7.6e-94 | S | VanZ like family | |||
KDLFIFCD_00533 | 8.9e-133 | yebC | K | Transcriptional regulatory protein | ||
KDLFIFCD_00534 | 1.7e-179 | comGA | NU | Type II IV secretion system protein | ||
KDLFIFCD_00535 | 1.7e-171 | comGB | NU | type II secretion system | ||
KDLFIFCD_00536 | 3.1e-43 | comGC | U | competence protein ComGC | ||
KDLFIFCD_00537 | 1.8e-69 | |||||
KDLFIFCD_00538 | 2.3e-41 | |||||
KDLFIFCD_00539 | 3.8e-77 | comGF | U | Putative Competence protein ComGF | ||
KDLFIFCD_00540 | 4.7e-172 | V | ABC-type multidrug transport system, ATPase and permease components | |||
KDLFIFCD_00541 | 1.5e-64 | arsC | 1.20.4.1 | P | Belongs to the ArsC family | |
KDLFIFCD_00542 | 1.5e-177 | I | Carboxylesterase family | |||
KDLFIFCD_00544 | 1.7e-205 | M | Glycosyl hydrolases family 25 | |||
KDLFIFCD_00545 | 1.3e-157 | cinI | S | Serine hydrolase (FSH1) | ||
KDLFIFCD_00546 | 2.7e-300 | S | Predicted membrane protein (DUF2207) | |||
KDLFIFCD_00547 | 1.6e-27 | dmpI | 5.3.2.6 | G | Belongs to the 4-oxalocrotonate tautomerase family | |
KDLFIFCD_00549 | 7.8e-255 | S | Uncharacterized protein conserved in bacteria (DUF2325) | |||
KDLFIFCD_00550 | 3.7e-151 | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | |||
KDLFIFCD_00551 | 5.8e-49 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
KDLFIFCD_00552 | 1.3e-47 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
KDLFIFCD_00553 | 1e-196 | pepP | 3.4.11.9, 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
KDLFIFCD_00554 | 4.9e-102 | 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 | ||
KDLFIFCD_00555 | 3.4e-71 | yqhY | S | Asp23 family, cell envelope-related function | ||
KDLFIFCD_00556 | 1.1e-63 | 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 | ||
KDLFIFCD_00557 | 6.7e-156 | 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 | |
KDLFIFCD_00558 | 2.9e-193 | 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 | |
KDLFIFCD_00559 | 3.7e-35 | 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 | |
KDLFIFCD_00560 | 3.9e-159 | 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 | |
KDLFIFCD_00561 | 2.3e-153 | rrmJ | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
KDLFIFCD_00562 | 2.6e-300 | recN | L | May be involved in recombinational repair of damaged DNA | ||
KDLFIFCD_00563 | 1.1e-77 | 6.3.3.2 | S | ASCH | ||
KDLFIFCD_00564 | 2.1e-111 | gmk | 2.7.4.8, 4.1.1.23 | F | Essential for recycling GMP and indirectly, cGMP | |
KDLFIFCD_00565 | 1.1e-33 | 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 | |
KDLFIFCD_00566 | 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 | ||
KDLFIFCD_00567 | 5.7e-172 | 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 | |
KDLFIFCD_00568 | 1.6e-244 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
KDLFIFCD_00569 | 1.1e-138 | stp | 3.1.3.16 | T | phosphatase | |
KDLFIFCD_00570 | 0.0 | prkC | 2.7.11.1 | KLT | serine threonine protein kinase | |
KDLFIFCD_00571 | 4.5e-163 | 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 | |
KDLFIFCD_00572 | 2.9e-119 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
KDLFIFCD_00573 | 4.1e-124 | thiN | 2.7.6.2 | H | thiamine pyrophosphokinase | |
KDLFIFCD_00574 | 1.4e-30 | |||||
KDLFIFCD_00575 | 9.9e-118 | L | Belongs to the 'phage' integrase family | |||
KDLFIFCD_00577 | 2.2e-15 | E | Pfam:DUF955 | |||
KDLFIFCD_00579 | 4.7e-18 | K | Helix-turn-helix XRE-family like proteins | |||
KDLFIFCD_00580 | 4.4e-79 | S | Phage antirepressor protein KilAC domain | |||
KDLFIFCD_00581 | 3.5e-46 | |||||
KDLFIFCD_00587 | 1.1e-36 | S | AAA domain | |||
KDLFIFCD_00590 | 4.4e-17 | CO | COG0526, thiol-disulfide isomerase and thioredoxins | |||
KDLFIFCD_00593 | 1.2e-32 | M | Peptidase family M23 | |||
KDLFIFCD_00594 | 1.8e-159 | trsE | S | COG0433 Predicted ATPase | ||
KDLFIFCD_00595 | 4.9e-15 | |||||
KDLFIFCD_00597 | 1e-32 | I | mechanosensitive ion channel activity | |||
KDLFIFCD_00598 | 1.2e-140 | U | TraM recognition site of TraD and TraG | |||
KDLFIFCD_00602 | 6.6e-38 | M | domain protein | |||
KDLFIFCD_00603 | 1.6e-42 | M | domain protein | |||
KDLFIFCD_00605 | 1.4e-24 | srtA | 3.4.22.70 | M | sortase family | |
KDLFIFCD_00606 | 1.8e-21 | S | SLAP domain | |||
KDLFIFCD_00611 | 2.6e-11 | ssb | L | Single-strand binding protein family | ||
KDLFIFCD_00619 | 3.2e-24 | S | Domain of unknown function (DUF771) | |||
KDLFIFCD_00620 | 8.9e-32 | K | Helix-turn-helix domain | |||
KDLFIFCD_00621 | 1.2e-21 | XK27_07105 | K | Helix-turn-helix XRE-family like proteins | ||
KDLFIFCD_00622 | 1.2e-23 | K | Helix-turn-helix domain | |||
KDLFIFCD_00623 | 5e-08 | S | Pfam:DUF955 | |||
KDLFIFCD_00624 | 1.4e-153 | L | Belongs to the 'phage' integrase family | |||
KDLFIFCD_00626 | 1.8e-220 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
KDLFIFCD_00627 | 1.9e-186 | ytxK | 2.1.1.72 | L | N-6 DNA Methylase | |
KDLFIFCD_00628 | 6e-85 | hipB | K | Helix-turn-helix | ||
KDLFIFCD_00629 | 1.4e-15 | S | cog cog1373 | |||
KDLFIFCD_00630 | 1e-30 | S | cog cog1373 | |||
KDLFIFCD_00631 | 7.6e-91 | F | Nucleoside 2-deoxyribosyltransferase | |||
KDLFIFCD_00632 | 3.3e-261 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Belongs to the aldehyde dehydrogenase family | |
KDLFIFCD_00633 | 1.1e-141 | yfeO | P | Voltage gated chloride channel | ||
KDLFIFCD_00634 | 1.4e-184 | 5.3.3.2 | C | FMN-dependent dehydrogenase | ||
KDLFIFCD_00635 | 1.4e-51 | |||||
KDLFIFCD_00636 | 2.1e-42 | |||||
KDLFIFCD_00637 | 6.4e-232 | 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 | |
KDLFIFCD_00638 | 1.1e-295 | ybeC | E | amino acid | ||
KDLFIFCD_00639 | 2.6e-157 | S | Sucrose-6F-phosphate phosphohydrolase | |||
KDLFIFCD_00640 | 0.0 | dexB | 3.2.1.10, 3.2.1.70 | GH13 | G | Alpha amylase, catalytic domain protein |
KDLFIFCD_00641 | 2.5e-39 | rpmE2 | J | Ribosomal protein L31 | ||
KDLFIFCD_00642 | 8e-260 | murF | 6.3.2.10, 6.3.2.13 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
KDLFIFCD_00643 | 4e-249 | cshA | 3.6.4.13 | F | DEAD-box RNA helicase possibly involved in RNA degradation. Unwinds dsRNA in both 5'- and 3'-directions, has RNA- dependent ATPase activity | |
KDLFIFCD_00644 | 1.7e-60 | acpS | 2.7.6.3, 2.7.8.7, 5.1.1.1 | I | Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein | |
KDLFIFCD_00645 | 1e-215 | alr | 5.1.1.1 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
KDLFIFCD_00646 | 9.7e-46 | oppA | E | ABC transporter substrate-binding protein | ||
KDLFIFCD_00647 | 5.6e-132 | oppC | P | Binding-protein-dependent transport system inner membrane component | ||
KDLFIFCD_00648 | 2.6e-172 | oppB | P | ABC transporter permease | ||
KDLFIFCD_00649 | 1.5e-170 | oppF | P | Belongs to the ABC transporter superfamily | ||
KDLFIFCD_00650 | 1.1e-192 | oppD | P | Belongs to the ABC transporter superfamily | ||
KDLFIFCD_00651 | 4.9e-35 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
KDLFIFCD_00652 | 3.7e-182 | 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 | |
KDLFIFCD_00653 | 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) | |
KDLFIFCD_00654 | 7.6e-305 | yloV | S | DAK2 domain fusion protein YloV | ||
KDLFIFCD_00655 | 4e-57 | asp | S | Asp23 family, cell envelope-related function | ||
KDLFIFCD_00656 | 1.4e-26 | rpmB | J | Belongs to the bacterial ribosomal protein bL28 family | ||
KDLFIFCD_00658 | 4e-87 | M | hydrolase, family 25 | |||
KDLFIFCD_00659 | 7.6e-39 | S | Bacteriophage holin of superfamily 6 (Holin_LLH) | |||
KDLFIFCD_00668 | 6e-136 | S | Phage minor structural protein | |||
KDLFIFCD_00669 | 4.5e-34 | S | phage tail | |||
KDLFIFCD_00670 | 8.1e-129 | M | Phage tail tape measure protein TP901 | |||
KDLFIFCD_00673 | 3.1e-13 | S | Pfam:Phage_TTP_1 | |||
KDLFIFCD_00675 | 8.6e-14 | S | Bacteriophage HK97-gp10, putative tail-component | |||
KDLFIFCD_00677 | 5.2e-17 | S | Phage gp6-like head-tail connector protein | |||
KDLFIFCD_00678 | 2e-55 | S | Phage capsid family | |||
KDLFIFCD_00679 | 5.5e-87 | clpP | 3.4.21.92 | OU | Belongs to the peptidase S14 family | |
KDLFIFCD_00680 | 9.1e-135 | S | Phage portal protein | |||
KDLFIFCD_00682 | 2.8e-210 | S | Phage Terminase | |||
KDLFIFCD_00683 | 9e-47 | S | HicB_like antitoxin of bacterial toxin-antitoxin system | |||
KDLFIFCD_00684 | 3.4e-18 | N | HicA toxin of bacterial toxin-antitoxin, | |||
KDLFIFCD_00685 | 1.6e-55 | L | Phage terminase, small subunit | |||
KDLFIFCD_00686 | 2.1e-49 | S | HNH endonuclease | |||
KDLFIFCD_00688 | 1.2e-13 | arpU | S | Phage transcriptional regulator, ArpU family | ||
KDLFIFCD_00689 | 2.7e-268 | aglB | 3.2.1.122, 3.2.1.86 | GH4,GT4 | G | Family 4 glycosyl hydrolase C-terminal domain |
KDLFIFCD_00690 | 5.3e-136 | glvR | K | Helix-turn-helix domain, rpiR family | ||
KDLFIFCD_00691 | 9.4e-186 | ansA | 3.5.1.1 | EJ | L-asparaginase, type I | |
KDLFIFCD_00692 | 5.9e-09 | |||||
KDLFIFCD_00693 | 4.4e-43 | |||||
KDLFIFCD_00694 | 8.7e-66 | 2.7.1.191 | G | PTS system fructose IIA component | ||
KDLFIFCD_00695 | 0.0 | 3.6.3.8 | P | P-type ATPase | ||
KDLFIFCD_00696 | 4.9e-125 | |||||
KDLFIFCD_00697 | 1.2e-241 | S | response to antibiotic | |||
KDLFIFCD_00698 | 6.2e-276 | gnd | 1.1.1.343, 1.1.1.44 | H | Catalyzes the oxidative decarboxylation of 6- phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NADP to NADPH | |
KDLFIFCD_00699 | 0.0 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
KDLFIFCD_00700 | 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 | ||
KDLFIFCD_00701 | 2.1e-252 | 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 | ||
KDLFIFCD_00702 | 8.4e-146 | 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 | ||
KDLFIFCD_00703 | 3.5e-61 | 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 | |
KDLFIFCD_00704 | 1.1e-15 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
KDLFIFCD_00705 | 6.8e-60 | divIC | D | Septum formation initiator | ||
KDLFIFCD_00706 | 1.8e-62 | yabR | J | S1 RNA binding domain | ||
KDLFIFCD_00707 | 2.6e-241 | tilS | 2.4.2.8, 6.3.4.19 | J | Ligates lysine onto the cytidine present at position 34 of the AUA codon-specific tRNA(Ile) that contains the anticodon CAU, in an ATP-dependent manner. Cytidine is converted to lysidine, thus changing the amino acid specificity of the tRNA from methionine to isoleucine | |
KDLFIFCD_00708 | 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 | ||
KDLFIFCD_00709 | 9.7e-166 | 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 | ||
KDLFIFCD_00710 | 2e-194 | dus | J | Catalyzes the synthesis of 5,6-dihydrouridine (D), a modified base found in the D-loop of most tRNAs, via the reduction of the C5-C6 double bond in target uridines | ||
KDLFIFCD_00711 | 1.1e-297 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
KDLFIFCD_00712 | 1.4e-83 | K | FR47-like protein | |||
KDLFIFCD_00713 | 7.1e-237 | L | transposase, IS605 OrfB family | |||
KDLFIFCD_00714 | 2.1e-28 | S | Peptidase propeptide and YPEB domain | |||
KDLFIFCD_00715 | 2.4e-60 | ypaA | S | Protein of unknown function (DUF1304) | ||
KDLFIFCD_00716 | 2.3e-309 | oppA3 | E | ABC transporter, substratebinding protein | ||
KDLFIFCD_00717 | 9e-161 | V | ABC transporter transmembrane region | |||
KDLFIFCD_00718 | 7e-68 | V | ABC transporter transmembrane region | |||
KDLFIFCD_00719 | 3.8e-65 | yybA | 2.3.1.57 | K | Transcriptional regulator | |
KDLFIFCD_00720 | 4.7e-83 | paiA | 2.3.1.57 | K | Acetyltransferase (GNAT) domain | |
KDLFIFCD_00721 | 2.5e-72 | S | Peptidase propeptide and YPEB domain | |||
KDLFIFCD_00722 | 3.4e-76 | S | Peptidase propeptide and YPEB domain | |||
KDLFIFCD_00723 | 5.2e-187 | T | GHKL domain | |||
KDLFIFCD_00724 | 3.1e-130 | T | Transcriptional regulatory protein, C terminal | |||
KDLFIFCD_00725 | 2.1e-179 | pip | 3.4.11.5 | E | Releases the N-terminal proline from various substrates | |
KDLFIFCD_00726 | 2.9e-277 | V | ABC transporter transmembrane region | |||
KDLFIFCD_00727 | 0.0 | clpE | O | Belongs to the ClpA ClpB family | ||
KDLFIFCD_00728 | 2.3e-44 | XK27_09445 | S | Domain of unknown function (DUF1827) | ||
KDLFIFCD_00729 | 9.4e-305 | 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 | ||
KDLFIFCD_00730 | 1.4e-140 | hlyX | S | Transporter associated domain | ||
KDLFIFCD_00731 | 2.7e-74 | |||||
KDLFIFCD_00732 | 1.6e-85 | |||||
KDLFIFCD_00733 | 1.5e-144 | recX | 2.4.1.337 | GT4 | S | Regulatory protein RecX |
KDLFIFCD_00734 | 4.6e-263 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
KDLFIFCD_00735 | 1.4e-118 | D | Alpha beta | |||
KDLFIFCD_00736 | 1.8e-38 | D | Alpha beta | |||
KDLFIFCD_00737 | 9.4e-46 | |||||
KDLFIFCD_00738 | 1.1e-282 | phoR | 2.7.13.3 | T | Histidine kinase | |
KDLFIFCD_00739 | 9.5e-121 | T | Transcriptional regulatory protein, C terminal | |||
KDLFIFCD_00740 | 4e-105 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
KDLFIFCD_00741 | 1.3e-139 | pstB | 3.6.3.27 | P | Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system | |
KDLFIFCD_00742 | 1.2e-152 | pstA | P | Phosphate transport system permease protein PstA | ||
KDLFIFCD_00743 | 1.1e-159 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
KDLFIFCD_00744 | 4.2e-145 | pstS | P | Phosphate | ||
KDLFIFCD_00745 | 1.3e-30 | |||||
KDLFIFCD_00746 | 1.4e-191 | oppA | E | ABC transporter, substratebinding protein | ||
KDLFIFCD_00747 | 4.7e-275 | ytgP | S | Polysaccharide biosynthesis protein | ||
KDLFIFCD_00748 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
KDLFIFCD_00749 | 1.1e-121 | 3.6.1.27 | I | Acid phosphatase homologues | ||
KDLFIFCD_00750 | 2.8e-168 | K | LysR substrate binding domain | |||
KDLFIFCD_00751 | 2.3e-84 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
KDLFIFCD_00752 | 6.2e-43 | 1.3.5.4 | C | FAD binding domain | ||
KDLFIFCD_00753 | 2.4e-231 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
KDLFIFCD_00754 | 1.1e-161 | menA | 2.5.1.74 | H | 1,4-dihydroxy-2-naphthoate | |
KDLFIFCD_00755 | 6.1e-177 | hepT | 2.5.1.30, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
KDLFIFCD_00756 | 2.2e-128 | menG | 2.1.1.163, 2.1.1.201 | H | Methyltransferase required for the conversion of demethylmenaquinol (DMKH2) to menaquinol (MKH2) | |
KDLFIFCD_00757 | 4.1e-269 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydC | ||
KDLFIFCD_00758 | 0.0 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydD | ||
KDLFIFCD_00759 | 8.2e-177 | cydB | 1.10.3.14 | C | Cytochrome d ubiquinol oxidase subunit II | |
KDLFIFCD_00760 | 1.5e-272 | cydA | 1.10.3.14 | C | ubiquinol oxidase | |
KDLFIFCD_00761 | 3.7e-130 | ybbH_2 | K | rpiR family | ||
KDLFIFCD_00762 | 2.6e-126 | S | Bacterial protein of unknown function (DUF871) | |||
KDLFIFCD_00763 | 2.2e-54 | oppA | E | ABC transporter substrate-binding protein | ||
KDLFIFCD_00764 | 1.3e-149 | oppA | E | ABC transporter substrate-binding protein | ||
KDLFIFCD_00765 | 1.7e-142 | 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) | |
KDLFIFCD_00766 | 1e-226 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
KDLFIFCD_00767 | 6.5e-190 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
KDLFIFCD_00768 | 3.3e-189 | cggR | K | Putative sugar-binding domain | ||
KDLFIFCD_00770 | 2.8e-290 | |||||
KDLFIFCD_00771 | 4.6e-274 | ycaM | E | amino acid | ||
KDLFIFCD_00772 | 3.1e-139 | S | Cysteine-rich secretory protein family | |||
KDLFIFCD_00773 | 4.2e-77 | K | MerR HTH family regulatory protein | |||
KDLFIFCD_00774 | 1.4e-262 | lmrB | EGP | Major facilitator Superfamily | ||
KDLFIFCD_00775 | 3.1e-48 | S | Domain of unknown function (DUF4811) | |||
KDLFIFCD_00776 | 4e-08 | |||||
KDLFIFCD_00777 | 6.6e-56 | |||||
KDLFIFCD_00778 | 2.7e-57 | |||||
KDLFIFCD_00779 | 1.6e-11 | |||||
KDLFIFCD_00780 | 8.1e-126 | S | PAS domain | |||
KDLFIFCD_00781 | 2.8e-216 | coaBC | 4.1.1.36, 6.3.2.5 | H | Catalyzes two steps in the biosynthesis of coenzyme A. In the first step cysteine is conjugated to 4'-phosphopantothenate to form 4-phosphopantothenoylcysteine, in the latter compound is decarboxylated to form 4'-phosphopantotheine | |
KDLFIFCD_00782 | 4.8e-34 | S | reductase | |||
KDLFIFCD_00783 | 4.4e-39 | S | reductase | |||
KDLFIFCD_00784 | 2.7e-32 | S | reductase | |||
KDLFIFCD_00785 | 1.3e-148 | yxeH | S | hydrolase | ||
KDLFIFCD_00786 | 6.8e-181 | gyaR | 1.1.1.26, 2.7.1.165 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
KDLFIFCD_00787 | 1.1e-243 | yfnA | E | Amino Acid | ||
KDLFIFCD_00788 | 6.8e-110 | dedA | 3.1.3.1 | S | SNARE associated Golgi protein | |
KDLFIFCD_00789 | 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 | ||
KDLFIFCD_00790 | 8.5e-243 | 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 | ||
KDLFIFCD_00791 | 2.2e-292 | I | Acyltransferase | |||
KDLFIFCD_00792 | 5.4e-175 | rnz | 3.1.26.11 | J | Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA | |
KDLFIFCD_00793 | 5.1e-142 | XK27_05435 | 1.1.1.100 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
KDLFIFCD_00794 | 1.5e-34 | yrvD | S | Lipopolysaccharide assembly protein A domain | ||
KDLFIFCD_00795 | 1.3e-27 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
KDLFIFCD_00796 | 2.6e-310 | cpdB | 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
KDLFIFCD_00797 | 2.3e-23 | S | Protein of unknown function (DUF2929) | |||
KDLFIFCD_00798 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase | |
KDLFIFCD_00799 | 3.3e-183 | 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 | |
KDLFIFCD_00800 | 0.0 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
KDLFIFCD_00801 | 1e-167 | cvfB | S | S1 domain | ||
KDLFIFCD_00802 | 2.9e-165 | xerD | D | recombinase XerD | ||
KDLFIFCD_00803 | 6.2e-54 | ribT | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
KDLFIFCD_00804 | 7.6e-132 | 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 | ||
KDLFIFCD_00805 | 4.1e-104 | 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 | ||
KDLFIFCD_00806 | 3.1e-130 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
KDLFIFCD_00807 | 5.7e-113 | 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 | |||
KDLFIFCD_00808 | 2.7e-18 | M | Lysin motif | |||
KDLFIFCD_00809 | 5e-114 | 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 | |
KDLFIFCD_00810 | 5.5e-212 | rpsA | 1.17.7.4 | J | Ribosomal protein S1 | |
KDLFIFCD_00811 | 1.9e-247 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
KDLFIFCD_00812 | 2.3e-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 | ||
KDLFIFCD_00813 | 8.7e-229 | S | Tetratricopeptide repeat protein | |||
KDLFIFCD_00814 | 4e-237 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
KDLFIFCD_00815 | 8.9e-133 | L | Phage integrase family | |||
KDLFIFCD_00816 | 5.1e-66 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
KDLFIFCD_00817 | 5.9e-79 | rplM | J | This protein is one of the early assembly proteins of the 50S ribosomal subunit, although it is not seen to bind rRNA by itself. It is important during the early stages of 50S assembly | ||
KDLFIFCD_00818 | 8.4e-145 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
KDLFIFCD_00819 | 7.2e-136 | ecfT | U | Transmembrane (T) component of an energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
KDLFIFCD_00820 | 3.5e-157 | ecfA | 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 | |
KDLFIFCD_00821 | 1.4e-153 | ecfA1 | P | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
KDLFIFCD_00822 | 1.4e-60 | rplQ | J | Ribosomal protein L17 | ||
KDLFIFCD_00823 | 1.1e-170 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
KDLFIFCD_00824 | 3e-63 | rpsK | J | Located on the platform of the 30S subunit, it bridges several disparate RNA helices of the 16S rRNA. Forms part of the Shine-Dalgarno cleft in the 70S ribosome | ||
KDLFIFCD_00825 | 4.2e-56 | 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 | ||
KDLFIFCD_00826 | 7.8e-15 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
KDLFIFCD_00827 | 8.4e-34 | infA | J | One of the essential components for the initiation of protein synthesis. Stabilizes the binding of IF-2 and IF-3 on the 30S subunit to which N-formylmethionyl-tRNA(fMet) subsequently binds. Helps modulate mRNA selection, yielding the 30S pre- initiation complex (PIC). Upon addition of the 50S ribosomal subunit IF-1, IF-2 and IF-3 are released leaving the mature 70S translation initation complex | ||
KDLFIFCD_00828 | 1e-119 | 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 | |
KDLFIFCD_00829 | 9e-237 | 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 | ||
KDLFIFCD_00830 | 2.6e-71 | rplO | J | Binds to the 23S rRNA | ||
KDLFIFCD_00831 | 2.3e-24 | rpmD | J | Ribosomal protein L30 | ||
KDLFIFCD_00832 | 4.1e-84 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
KDLFIFCD_00833 | 3.6e-55 | 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 | ||
KDLFIFCD_00834 | 3.3e-92 | 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 | ||
KDLFIFCD_00835 | 3.2e-68 | rpsH | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA central domain where it helps coordinate assembly of the platform of the 30S subunit | ||
KDLFIFCD_00836 | 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 | ||
KDLFIFCD_00837 | 5.5e-95 | rplE | J | This is 1 of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance. In the 70S ribosome it contacts protein S13 of the 30S subunit (bridge B1b), connecting the 2 subunits | ||
KDLFIFCD_00838 | 3.4e-33 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
KDLFIFCD_00839 | 1.1e-59 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
KDLFIFCD_00840 | 5e-41 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
KDLFIFCD_00841 | 1.3e-25 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
KDLFIFCD_00842 | 2.1e-76 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
KDLFIFCD_00843 | 2.7e-120 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
KDLFIFCD_00844 | 4e-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 | ||
KDLFIFCD_00845 | 1.1e-46 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
KDLFIFCD_00846 | 3.6e-154 | 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 | ||
KDLFIFCD_00847 | 3.1e-47 | rplW | J | One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome | ||
KDLFIFCD_00848 | 2.1e-106 | rplD | J | Forms part of the polypeptide exit tunnel | ||
KDLFIFCD_00849 | 9e-113 | 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 | ||
KDLFIFCD_00850 | 4.4e-49 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
KDLFIFCD_00851 | 5.9e-45 | |||||
KDLFIFCD_00852 | 3.7e-58 | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
KDLFIFCD_00854 | 2.1e-45 | S | PFAM Archaeal ATPase | |||
KDLFIFCD_00855 | 7.3e-74 | |||||
KDLFIFCD_00856 | 0.0 | kup | P | Transport of potassium into the cell | ||
KDLFIFCD_00857 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
KDLFIFCD_00858 | 1.9e-19 | |||||
KDLFIFCD_00859 | 2.5e-264 | 3.6.3.6 | P | Cation transporter/ATPase, N-terminus | ||
KDLFIFCD_00860 | 4.4e-35 | 3.6.3.2, 3.6.3.6 | P | cation transport ATPase | ||
KDLFIFCD_00861 | 7.8e-10 | 3.6.3.2, 3.6.3.6 | P | cation transport ATPase | ||
KDLFIFCD_00862 | 1.3e-273 | pipD | E | Dipeptidase | ||
KDLFIFCD_00863 | 1.5e-102 | devA | 3.6.3.25 | V | ABC transporter, ATP-binding protein | |
KDLFIFCD_00864 | 3.3e-176 | hrtB | V | ABC transporter permease | ||
KDLFIFCD_00865 | 3.2e-92 | ygfC | K | Bacterial regulatory proteins, tetR family | ||
KDLFIFCD_00866 | 3.5e-111 | G | phosphoglycerate mutase | |||
KDLFIFCD_00867 | 4.1e-141 | aroD | S | Alpha/beta hydrolase family | ||
KDLFIFCD_00868 | 2.2e-142 | S | Belongs to the UPF0246 family | |||
KDLFIFCD_00869 | 3.3e-52 | S | Iron-sulfur cluster assembly protein | |||
KDLFIFCD_00870 | 8.5e-154 | sdaAA | 4.3.1.17 | E | L-serine dehydratase, iron-sulfur-dependent, alpha subunit | |
KDLFIFCD_00871 | 3.4e-123 | sdaAB | 4.3.1.17 | E | Serine dehydratase beta chain | |
KDLFIFCD_00872 | 1.5e-43 | |||||
KDLFIFCD_00873 | 2.7e-285 | lsa | S | ABC transporter | ||
KDLFIFCD_00874 | 1.6e-141 | L | An automated process has identified a potential problem with this gene model | |||
KDLFIFCD_00875 | 7.9e-135 | UW | LPXTG-motif cell wall anchor domain protein | |||
KDLFIFCD_00876 | 1.3e-161 | UW | LPXTG-motif cell wall anchor domain protein | |||
KDLFIFCD_00877 | 3.3e-45 | UW | LPXTG-motif cell wall anchor domain protein | |||
KDLFIFCD_00878 | 9.1e-10 | UW | LPXTG-motif cell wall anchor domain protein | |||
KDLFIFCD_00879 | 1.3e-248 | 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) | |
KDLFIFCD_00880 | 7.5e-100 | J | Acetyltransferase (GNAT) domain | |||
KDLFIFCD_00881 | 1.4e-110 | yjbF | S | SNARE associated Golgi protein | ||
KDLFIFCD_00882 | 2.7e-151 | I | alpha/beta hydrolase fold | |||
KDLFIFCD_00883 | 4.4e-62 | hipB | K | Helix-turn-helix | ||
KDLFIFCD_00884 | 8.3e-24 | papP | P | ABC transporter, permease protein | ||
KDLFIFCD_00886 | 4.5e-58 | yodB | K | Transcriptional regulator, HxlR family | ||
KDLFIFCD_00887 | 2.2e-134 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
KDLFIFCD_00888 | 2.9e-44 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
KDLFIFCD_00889 | 2.4e-162 | yidC | U | Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins | ||
KDLFIFCD_00890 | 5.7e-83 | S | Aminoacyl-tRNA editing domain | |||
KDLFIFCD_00891 | 6.1e-224 | S | SLAP domain | |||
KDLFIFCD_00892 | 1.6e-93 | S | CAAX protease self-immunity | |||
KDLFIFCD_00893 | 1e-12 | |||||
KDLFIFCD_00894 | 1.3e-277 | arlS | 2.7.13.3 | T | Histidine kinase | |
KDLFIFCD_00895 | 1.2e-126 | K | response regulator | |||
KDLFIFCD_00896 | 4.7e-97 | yceD | S | Uncharacterized ACR, COG1399 | ||
KDLFIFCD_00897 | 4.6e-216 | ylbM | S | Belongs to the UPF0348 family | ||
KDLFIFCD_00898 | 5.3e-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 | ||
KDLFIFCD_00899 | 6.6e-110 | nadD | 2.7.6.3, 2.7.7.18 | H | Hydrolase, HD family | |
KDLFIFCD_00900 | 4.4e-123 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
KDLFIFCD_00901 | 4.4e-200 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
KDLFIFCD_00902 | 4.2e-84 | yqeG | S | HAD phosphatase, family IIIA | ||
KDLFIFCD_00903 | 8.6e-199 | tnpB | L | Putative transposase DNA-binding domain | ||
KDLFIFCD_00904 | 3.1e-152 | add | 3.5.4.4 | F | Catalyzes the hydrolytic deamination of adenine to hypoxanthine. Plays an important role in the purine salvage pathway and in nitrogen catabolism | |
KDLFIFCD_00905 | 3e-57 | rplT | J | Binds directly to 23S ribosomal RNA and is necessary for the in vitro assembly process of the 50S ribosomal subunit. It is not involved in the protein synthesizing functions of that subunit | ||
KDLFIFCD_00906 | 8.1e-28 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
KDLFIFCD_00907 | 3.2e-72 | 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 | ||
KDLFIFCD_00908 | 4e-98 | rihB | 3.2.2.1 | F | Nucleoside | |
KDLFIFCD_00909 | 3.8e-103 | potB | E | Binding-protein-dependent transport system inner membrane component | ||
KDLFIFCD_00910 | 1e-15 | S | Domain of Unknown Function with PDB structure (DUF3850) | |||
KDLFIFCD_00912 | 2.5e-89 | M | Protein of unknown function (DUF3737) | |||
KDLFIFCD_00913 | 9.9e-227 | patB | 4.4.1.8 | E | Aminotransferase, class I | |
KDLFIFCD_00914 | 7.2e-191 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
KDLFIFCD_00915 | 7.7e-67 | S | SdpI/YhfL protein family | |||
KDLFIFCD_00916 | 4.4e-129 | K | Transcriptional regulatory protein, C terminal | |||
KDLFIFCD_00917 | 7.2e-267 | yclK | 2.7.13.3, 4.6.1.1 | T | Histidine kinase | |
KDLFIFCD_00918 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
KDLFIFCD_00919 | 3.8e-105 | vanZ | V | VanZ like family | ||
KDLFIFCD_00920 | 3.2e-253 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
KDLFIFCD_00921 | 3.8e-217 | EGP | Major facilitator Superfamily | |||
KDLFIFCD_00922 | 3.9e-195 | ampC | V | Beta-lactamase | ||
KDLFIFCD_00925 | 1.7e-262 | murF | 6.3.2.10, 6.3.2.13 | M | Domain of unknown function (DUF1727) | |
KDLFIFCD_00926 | 1.3e-113 | tdk | 2.7.1.21 | F | thymidine kinase | |
KDLFIFCD_00927 | 3.1e-182 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
KDLFIFCD_00928 | 7.3e-155 | prmB | 2.1.1.297, 2.1.1.298 | J | Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif | |
KDLFIFCD_00929 | 3.7e-190 | 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 | |
KDLFIFCD_00930 | 6.8e-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 | |
KDLFIFCD_00931 | 3.8e-128 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
KDLFIFCD_00932 | 3.5e-27 | atpE | C | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
KDLFIFCD_00933 | 3.4e-46 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
KDLFIFCD_00934 | 2.8e-91 | 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 | ||
KDLFIFCD_00935 | 2.8e-282 | 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 | |
KDLFIFCD_00936 | 2e-172 | 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 | ||
KDLFIFCD_00937 | 3.3e-240 | 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 | |
KDLFIFCD_00938 | 9e-72 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
KDLFIFCD_00939 | 2e-30 | ywzB | S | Protein of unknown function (DUF1146) | ||
KDLFIFCD_00940 | 1.2e-177 | mbl | D | Cell shape determining protein MreB Mrl | ||
KDLFIFCD_00941 | 1e-50 | yidD | S | Could be involved in insertion of integral membrane proteins into the membrane | ||
KDLFIFCD_00942 | 3.3e-33 | S | Protein of unknown function (DUF2969) | |||
KDLFIFCD_00943 | 4.7e-216 | rodA | D | Belongs to the SEDS family | ||
KDLFIFCD_00944 | 1.8e-78 | usp6 | T | universal stress protein | ||
KDLFIFCD_00945 | 8.4e-39 | |||||
KDLFIFCD_00946 | 2.2e-238 | rarA | L | recombination factor protein RarA | ||
KDLFIFCD_00947 | 1.3e-84 | yueI | S | Protein of unknown function (DUF1694) | ||
KDLFIFCD_00948 | 1.4e-110 | 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 | ||
KDLFIFCD_00949 | 2.1e-294 | 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 | ||
KDLFIFCD_00950 | 7.4e-214 | iscS2 | 2.8.1.7 | E | Aminotransferase class V | |
KDLFIFCD_00951 | 2e-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 | |
KDLFIFCD_00952 | 1.7e-184 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
KDLFIFCD_00953 | 3.2e-119 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
KDLFIFCD_00954 | 5.5e-44 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
KDLFIFCD_00955 | 2.1e-65 | 2.4.1.83 | GT2 | S | GtrA-like protein | |
KDLFIFCD_00956 | 5.2e-170 | yfdH | 2.4.2.53 | GT2 | M | Glycosyltransferase, group 2 family protein |
KDLFIFCD_00957 | 1.5e-94 | S | Protein of unknown function (DUF3990) | |||
KDLFIFCD_00958 | 6.5e-44 | |||||
KDLFIFCD_00960 | 0.0 | 3.6.3.8 | P | P-type ATPase | ||
KDLFIFCD_00961 | 1.1e-132 | S | AAA domain, putative AbiEii toxin, Type IV TA system | |||
KDLFIFCD_00962 | 2.5e-52 | |||||
KDLFIFCD_00963 | 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 | |
KDLFIFCD_00964 | 1.5e-239 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
KDLFIFCD_00965 | 5.7e-126 | S | Haloacid dehalogenase-like hydrolase | |||
KDLFIFCD_00966 | 2.3e-108 | radC | L | DNA repair protein | ||
KDLFIFCD_00967 | 2.4e-176 | mreB | D | cell shape determining protein MreB | ||
KDLFIFCD_00968 | 2e-147 | mreC | M | Involved in formation and maintenance of cell shape | ||
KDLFIFCD_00969 | 2.7e-94 | mreD | ||||
KDLFIFCD_00971 | 6.4e-54 | S | Protein of unknown function (DUF3397) | |||
KDLFIFCD_00972 | 6.3e-78 | mraZ | K | Belongs to the MraZ family | ||
KDLFIFCD_00973 | 7.2e-175 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
KDLFIFCD_00974 | 1.8e-54 | ftsL | D | Cell division protein FtsL | ||
KDLFIFCD_00975 | 0.0 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
KDLFIFCD_00976 | 1.5e-175 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
KDLFIFCD_00977 | 5e-262 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
KDLFIFCD_00978 | 3.7e-207 | 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) |
KDLFIFCD_00979 | 4.5e-152 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
KDLFIFCD_00980 | 1.3e-246 | 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 | ||
KDLFIFCD_00981 | 1.7e-206 | 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 | ||
KDLFIFCD_00982 | 7.3e-74 | 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 | ||
KDLFIFCD_00983 | 1.7e-45 | yggT | S | YGGT family | ||
KDLFIFCD_00984 | 5.7e-149 | ylmH | S | S4 domain protein | ||
KDLFIFCD_00985 | 2.8e-74 | gpsB | D | DivIVA domain protein | ||
KDLFIFCD_00986 | 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) | |
KDLFIFCD_00987 | 3.6e-31 | cspA | K | 'Cold-shock' DNA-binding domain | ||
KDLFIFCD_00988 | 2.8e-102 | nudF | 3.6.1.13 | L | ADP-ribose pyrophosphatase | |
KDLFIFCD_00989 | 6.7e-37 | |||||
KDLFIFCD_00990 | 1.2e-126 | 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 | |
KDLFIFCD_00991 | 3.2e-217 | iscS | 2.8.1.7 | E | Aminotransferase class V | |
KDLFIFCD_00992 | 5.4e-56 | XK27_04120 | S | Putative amino acid metabolism | ||
KDLFIFCD_00993 | 1.9e-219 | 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 | |
KDLFIFCD_00994 | 3.9e-127 | pgm6 | 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | |
KDLFIFCD_00995 | 8.3e-106 | S | Repeat protein | |||
KDLFIFCD_00996 | 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 | |
KDLFIFCD_00997 | 1.6e-294 | L | Nuclease-related domain | |||
KDLFIFCD_00998 | 2.3e-164 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic domain | |
KDLFIFCD_00999 | 1.4e-126 | pgm3 | G | Phosphoglycerate mutase family | ||
KDLFIFCD_01000 | 2.7e-124 | XK27_08875 | O | PFAM peptidase M10A and M12B, matrixin and adamalysin | ||
KDLFIFCD_01001 | 0.0 | helD | 3.6.4.12 | L | DNA helicase | |
KDLFIFCD_01002 | 1.5e-107 | glnP | P | ABC transporter permease | ||
KDLFIFCD_01003 | 1e-105 | glnQ | 3.6.3.21 | E | ABC transporter | |
KDLFIFCD_01004 | 1.6e-143 | aatB | ET | ABC transporter substrate-binding protein | ||
KDLFIFCD_01005 | 7.5e-74 | yjcF | S | Acetyltransferase (GNAT) domain | ||
KDLFIFCD_01006 | 7.1e-98 | E | GDSL-like Lipase/Acylhydrolase | |||
KDLFIFCD_01007 | 2.5e-169 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
KDLFIFCD_01008 | 1.3e-102 | 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 | ||
KDLFIFCD_01009 | 8.8e-58 | S | Peptidase propeptide and YPEB domain | |||
KDLFIFCD_01010 | 1e-148 | glcU | U | sugar transport | ||
KDLFIFCD_01011 | 5.1e-44 | |||||
KDLFIFCD_01012 | 6.2e-81 | msrB | 1.8.4.11, 1.8.4.12 | O | peptide methionine sulfoxide reductase | |
KDLFIFCD_01013 | 0.0 | pepX | 3.4.14.11 | E | Removes N-terminal dipeptides sequentially from polypeptides having unsubstituted N-termini provided that the penultimate residue is proline | |
KDLFIFCD_01014 | 1e-23 | S | Alpha beta hydrolase | |||
KDLFIFCD_01015 | 1.3e-65 | S | Alpha beta hydrolase | |||
KDLFIFCD_01016 | 1.9e-37 | |||||
KDLFIFCD_01017 | 2.6e-52 | |||||
KDLFIFCD_01018 | 4e-113 | S | haloacid dehalogenase-like hydrolase | |||
KDLFIFCD_01019 | 2e-291 | V | ABC-type multidrug transport system, ATPase and permease components | |||
KDLFIFCD_01020 | 3.8e-88 | V | ABC-type multidrug transport system, ATPase and permease components | |||
KDLFIFCD_01021 | 5.3e-26 | |||||
KDLFIFCD_01022 | 8.5e-41 | ptsH | G | phosphocarrier protein HPR | ||
KDLFIFCD_01023 | 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) | |
KDLFIFCD_01024 | 3.9e-66 | 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 | |
KDLFIFCD_01025 | 8.5e-139 | mecA | NOT | Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis | ||
KDLFIFCD_01026 | 1.4e-158 | coiA | 3.6.4.12 | S | Competence protein | |
KDLFIFCD_01027 | 4.6e-114 | yjbH | Q | Thioredoxin | ||
KDLFIFCD_01028 | 6.8e-110 | yjbK | S | CYTH | ||
KDLFIFCD_01029 | 1.2e-114 | yjbM | 2.7.6.5 | S | RelA SpoT domain protein | |
KDLFIFCD_01030 | 3.8e-153 | nadK | 2.7.1.23 | F | Involved in the regulation of the intracellular balance of NAD and NADP, and is a key enzyme in the biosynthesis of NADP. Catalyzes specifically the phosphorylation on 2'-hydroxyl of the adenosine moiety of NAD to yield NADP | |
KDLFIFCD_01031 | 7.1e-172 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
KDLFIFCD_01032 | 0.0 | mycA | 4.2.1.53 | S | Myosin-crossreactive antigen | |
KDLFIFCD_01033 | 4.2e-92 | S | SNARE associated Golgi protein |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)