ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
KFEKAFMK_00001 | 7.2e-51 | natB | E | Receptor family ligand binding region | ||
KFEKAFMK_00002 | 9.2e-147 | K | helix_turn _helix lactose operon repressor | |||
KFEKAFMK_00003 | 9.7e-299 | gtfA | 2.4.1.329, 2.4.1.7 | GH13 | G | Domain of unknown function (DUF1964) |
KFEKAFMK_00004 | 1.3e-277 | scrT | G | Transporter major facilitator family protein | ||
KFEKAFMK_00005 | 2.8e-180 | K | helix_turn _helix lactose operon repressor | |||
KFEKAFMK_00006 | 1.8e-251 | yhjE | EGP | Sugar (and other) transporter | ||
KFEKAFMK_00007 | 9e-203 | ilvC | 1.1.1.86 | H | Involved in the biosynthesis of branched-chain amino acids (BCAA). Catalyzes an alkyl-migration followed by a ketol- acid reduction of (S)-2-acetolactate (S2AL) to yield (R)-2,3- dihydroxy-isovalerate. In the isomerase reaction, S2AL is rearranged via a Mg-dependent methyl migration to produce 3- hydroxy-3-methyl-2-ketobutyrate (HMKB). In the reductase reaction, this 2-ketoacid undergoes a metal-dependent reduction by NADPH to yield (R)-2,3-dihydroxy-isovalerate | |
KFEKAFMK_00008 | 3.7e-204 | ilvC | 1.1.1.86 | H | Involved in the biosynthesis of branched-chain amino acids (BCAA). Catalyzes an alkyl-migration followed by a ketol- acid reduction of (S)-2-acetolactate (S2AL) to yield (R)-2,3- dihydroxy-isovalerate. In the isomerase reaction, S2AL is rearranged via a Mg-dependent methyl migration to produce 3- hydroxy-3-methyl-2-ketobutyrate (HMKB). In the reductase reaction, this 2-ketoacid undergoes a metal-dependent reduction by NADPH to yield (R)-2,3-dihydroxy-isovalerate | |
KFEKAFMK_00009 | 1.7e-145 | S | Psort location Cytoplasmic, score | |||
KFEKAFMK_00010 | 2.7e-191 | K | Transcriptional regulator | |||
KFEKAFMK_00011 | 0.0 | 3.2.1.10, 3.2.1.20, 3.2.1.93 | GH13,GH31 | G | Alpha-amylase domain | |
KFEKAFMK_00012 | 5.2e-187 | K | Psort location Cytoplasmic, score | |||
KFEKAFMK_00014 | 0.0 | M | cell wall anchor domain protein | |||
KFEKAFMK_00015 | 0.0 | M | domain protein | |||
KFEKAFMK_00016 | 1.8e-173 | 3.4.22.70 | M | Sortase family | ||
KFEKAFMK_00017 | 0.0 | malQ | 2.4.1.18, 2.4.1.25, 3.2.1.196, 5.4.99.15 | CBM48,GH13,GH77 | G | 4-alpha-glucanotransferase |
KFEKAFMK_00018 | 0.0 | malL | 3.2.1.1, 5.4.99.16 | GH13 | G | Alpha-amylase domain |
KFEKAFMK_00019 | 8.3e-232 | malE | G | Bacterial extracellular solute-binding protein | ||
KFEKAFMK_00020 | 1.7e-252 | malF | G | Binding-protein-dependent transport system inner membrane component | ||
KFEKAFMK_00021 | 4e-162 | malG | G | Binding-protein-dependent transport system inner membrane component | ||
KFEKAFMK_00022 | 0.0 | pulA | 3.2.1.41 | CBM48,GH13 | G | Belongs to the glycosyl hydrolase 13 family |
KFEKAFMK_00023 | 2e-172 | S | HAD-hyrolase-like | |||
KFEKAFMK_00024 | 3.2e-144 | traX | S | TraX protein | ||
KFEKAFMK_00025 | 2.6e-194 | K | Psort location Cytoplasmic, score | |||
KFEKAFMK_00026 | 0.0 | pulA | 3.2.1.1, 3.2.1.41 | CBM48,GH13 | M | Aamy_C |
KFEKAFMK_00027 | 0.0 | dnaK | O | Heat shock 70 kDa protein | ||
KFEKAFMK_00028 | 1.5e-57 | grpE | O | Participates actively in the response to hyperosmotic and heat shock by preventing the aggregation of stress-denatured proteins, in association with DnaK and GrpE. It is the nucleotide exchange factor for DnaK and may function as a thermosensor. Unfolded proteins bind initially to DnaJ | ||
KFEKAFMK_00029 | 9.4e-157 | dnaJ1 | O | DnaJ molecular chaperone homology domain | ||
KFEKAFMK_00030 | 2.7e-103 | hspR | K | transcriptional regulator, MerR family | ||
KFEKAFMK_00031 | 1.2e-16 | F | Psort location CytoplasmicMembrane, score 10.00 | |||
KFEKAFMK_00032 | 6.2e-113 | luxC | 1.2.1.50 | C | Acyl-CoA reductase (LuxC) | |
KFEKAFMK_00033 | 1.2e-140 | IQ | Oxidoreductase, short chain dehydrogenase reductase family protein | |||
KFEKAFMK_00034 | 5.7e-126 | S | HAD hydrolase, family IA, variant 3 | |||
KFEKAFMK_00035 | 2.1e-134 | dedA | S | SNARE associated Golgi protein | ||
KFEKAFMK_00036 | 2.9e-124 | cpaE | D | bacterial-type flagellum organization | ||
KFEKAFMK_00037 | 2.9e-190 | cpaF | U | Type II IV secretion system protein | ||
KFEKAFMK_00038 | 1.2e-74 | U | Type ii secretion system | |||
KFEKAFMK_00039 | 5.8e-115 | gspF | NU | Type II secretion system (T2SS), protein F | ||
KFEKAFMK_00040 | 1.1e-41 | S | Protein of unknown function (DUF4244) | |||
KFEKAFMK_00041 | 7.6e-59 | U | TadE-like protein | |||
KFEKAFMK_00042 | 1.9e-53 | S | TIGRFAM helicase secretion neighborhood TadE-like protein | |||
KFEKAFMK_00043 | 1.6e-213 | dagK | 2.7.1.107 | I | Diacylglycerol kinase catalytic domain protein | |
KFEKAFMK_00044 | 3.2e-96 | K | Bacterial regulatory proteins, tetR family | |||
KFEKAFMK_00045 | 0.0 | dnaX | 2.7.7.7 | L | DNA polymerase III subunit gamma tau | |
KFEKAFMK_00046 | 8.7e-110 | recR | L | May play a role in DNA repair. It seems to be involved in an RecBC-independent recombinational process of DNA repair. It may act with RecF and RecO | ||
KFEKAFMK_00047 | 3e-31 | S | ATPase domain predominantly from Archaea | |||
KFEKAFMK_00048 | 2e-198 | 3.4.22.70 | M | Sortase family | ||
KFEKAFMK_00049 | 9.5e-65 | V | Abi-like protein | |||
KFEKAFMK_00050 | 9.4e-106 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
KFEKAFMK_00051 | 6e-65 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
KFEKAFMK_00052 | 1.3e-134 | ask | 1.1.1.3, 2.7.2.4 | E | Amino acid kinase family | |
KFEKAFMK_00053 | 1.8e-96 | askB | 1.1.1.3, 2.7.2.4 | E | ACT domain | |
KFEKAFMK_00054 | 1.6e-210 | asd | 1.2.1.11, 1.2.1.12 | E | Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate | |
KFEKAFMK_00055 | 9.6e-112 | |||||
KFEKAFMK_00056 | 6.9e-175 | L | Domain of unknown function (DUF4862) | |||
KFEKAFMK_00057 | 3.7e-169 | 2.7.1.2 | GK | ROK family | ||
KFEKAFMK_00058 | 8.2e-125 | nanE | 5.1.3.9 | G | Converts N-acetylmannosamine-6-phosphate (ManNAc-6-P) to N-acetylglucosamine-6-phosphate (GlcNAc-6-P) | |
KFEKAFMK_00059 | 2.2e-159 | 3.5.1.106 | I | carboxylic ester hydrolase activity | ||
KFEKAFMK_00060 | 1.6e-301 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | |||
KFEKAFMK_00061 | 4.6e-153 | oppB6 | EP | Binding-protein-dependent transport system inner membrane component | ||
KFEKAFMK_00062 | 0.0 | oppD | EP | Oligopeptide/dipeptide transporter, C-terminal region | ||
KFEKAFMK_00063 | 1.6e-146 | oppF | E | ATPases associated with a variety of cellular activities | ||
KFEKAFMK_00064 | 3.7e-179 | nanL | 4.1.2.28, 4.3.3.7 | EM | Dihydrodipicolinate synthetase family | |
KFEKAFMK_00065 | 3.5e-146 | nagB | 3.1.1.31, 3.5.99.6 | G | Catalyzes the reversible isomerization-deamination of glucosamine 6-phosphate (GlcN6P) to form fructose 6-phosphate (Fru6P) and ammonium ion | |
KFEKAFMK_00067 | 0.0 | nanI | 3.2.1.18 | GH33 | G | BNR repeat-like domain |
KFEKAFMK_00068 | 4.4e-244 | P | Domain of unknown function (DUF4143) | |||
KFEKAFMK_00069 | 1e-151 | K | FCD | |||
KFEKAFMK_00070 | 1.7e-271 | S | Calcineurin-like phosphoesterase | |||
KFEKAFMK_00071 | 0.0 | leuA | 2.3.3.13 | E | Catalyzes the condensation of the acetyl group of acetyl-CoA with 3-methyl-2-oxobutanoate (2-oxoisovalerate) to form 3-carboxy-3-hydroxy-4-methylpentanoate (2-isopropylmalate) | |
KFEKAFMK_00072 | 0.0 | mrcB | 2.4.1.129, 3.4.16.4 | GT51 | M | Transglycosylase |
KFEKAFMK_00073 | 2.3e-164 | 3.6.1.27 | I | PAP2 superfamily | ||
KFEKAFMK_00074 | 0.0 | topA | 5.99.1.2 | L | Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone | |
KFEKAFMK_00075 | 1.6e-115 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
KFEKAFMK_00076 | 1e-207 | holB | 2.7.7.7 | L | DNA polymerase III | |
KFEKAFMK_00077 | 1.5e-104 | K | helix_turn _helix lactose operon repressor | |||
KFEKAFMK_00078 | 3.3e-37 | ptsH | G | PTS HPr component phosphorylation site | ||
KFEKAFMK_00080 | 6e-294 | 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) | |
KFEKAFMK_00081 | 2.5e-106 | S | Phosphatidylethanolamine-binding protein | |||
KFEKAFMK_00082 | 2.7e-310 | pepD | E | Peptidase family C69 | ||
KFEKAFMK_00083 | 1.1e-286 | fhs | 1.5.1.5, 3.5.4.9, 6.3.4.3 | F | Formate-tetrahydrofolate ligase | |
KFEKAFMK_00084 | 6.7e-62 | S | Macrophage migration inhibitory factor (MIF) | |||
KFEKAFMK_00085 | 4.1e-95 | S | GtrA-like protein | |||
KFEKAFMK_00086 | 9.7e-248 | EGP | Major facilitator Superfamily | |||
KFEKAFMK_00087 | 9.9e-123 | 3.1.3.3, 3.1.3.73 | G | Phosphoglycerate mutase family | ||
KFEKAFMK_00088 | 2.8e-118 | |||||
KFEKAFMK_00089 | 1.9e-50 | 3.1.1.31 | G | Lactonase, 7-bladed beta-propeller | ||
KFEKAFMK_00090 | 1.1e-135 | S | Protein of unknown function (DUF805) | |||
KFEKAFMK_00092 | 1.2e-293 | gltX | 6.1.1.17 | J | Catalyzes the attachment of glutamate to tRNA(Glu) in a two-step reaction glutamate is first activated by ATP to form Glu-AMP and then transferred to the acceptor end of tRNA(Glu) | |
KFEKAFMK_00096 | 0.0 | efeU_1 | P | Iron permease FTR1 family | ||
KFEKAFMK_00097 | 1.6e-99 | tpd | P | Fe2+ transport protein | ||
KFEKAFMK_00098 | 1.6e-230 | S | Predicted membrane protein (DUF2318) | |||
KFEKAFMK_00099 | 2.5e-226 | macB_2 | V | ABC transporter permease | ||
KFEKAFMK_00100 | 1.6e-199 | Z012_06715 | V | FtsX-like permease family | ||
KFEKAFMK_00101 | 4.5e-146 | macB | V | ABC transporter, ATP-binding protein | ||
KFEKAFMK_00102 | 1.7e-67 | S | FMN_bind | |||
KFEKAFMK_00103 | 6e-100 | K | Psort location Cytoplasmic, score 8.87 | |||
KFEKAFMK_00104 | 2.3e-306 | pip | S | YhgE Pip domain protein | ||
KFEKAFMK_00105 | 0.0 | pip | S | YhgE Pip domain protein | ||
KFEKAFMK_00106 | 8.1e-180 | S | Putative ABC-transporter type IV | |||
KFEKAFMK_00107 | 4.6e-51 | S | Putative ABC-transporter type IV | |||
KFEKAFMK_00108 | 5.7e-272 | 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 | |
KFEKAFMK_00109 | 3.6e-138 | pgl | 3.1.1.31, 3.5.99.6 | G | Glucosamine-6-phosphate isomerases/6-phosphogluconolactonase | |
KFEKAFMK_00110 | 8.2e-193 | opcA | G | Glucose-6-phosphate dehydrogenase subunit | ||
KFEKAFMK_00111 | 1e-303 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
KFEKAFMK_00112 | 4.7e-275 | 3.5.2.6 | V | Beta-lactamase enzyme family | ||
KFEKAFMK_00114 | 7.4e-299 | pepD | E | Peptidase family C69 | ||
KFEKAFMK_00115 | 2.8e-196 | XK27_01805 | M | Glycosyltransferase like family 2 | ||
KFEKAFMK_00116 | 1.4e-150 | icaR | K | Bacterial regulatory proteins, tetR family | ||
KFEKAFMK_00117 | 2.9e-171 | ftsY | U | Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Acts as a receptor for the complex formed by the signal recognition particle (SRP) and the ribosome-nascent chain (RNC) | ||
KFEKAFMK_00118 | 1.3e-227 | amt | U | Ammonium Transporter Family | ||
KFEKAFMK_00119 | 1e-54 | glnB | K | Nitrogen regulatory protein P-II | ||
KFEKAFMK_00120 | 0.0 | 2.7.7.19, 2.7.7.59 | O | Nucleotidyltransferase domain | ||
KFEKAFMK_00121 | 3e-238 | dinF | V | MatE | ||
KFEKAFMK_00122 | 1.6e-256 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
KFEKAFMK_00123 | 2e-261 | murD | 3.4.21.10, 6.3.2.13, 6.3.2.9 | M | Domain of unknown function (DUF1727) | |
KFEKAFMK_00124 | 1.6e-140 | cobQ | S | CobB/CobQ-like glutamine amidotransferase domain | ||
KFEKAFMK_00125 | 5.5e-38 | S | granule-associated protein | |||
KFEKAFMK_00126 | 0.0 | ubiB | S | ABC1 family | ||
KFEKAFMK_00127 | 1e-70 | K | Periplasmic binding protein domain | |||
KFEKAFMK_00128 | 5e-189 | 3.2.1.185 | GH127 | S | Beta-L-arabinofuranosidase, GH127 | |
KFEKAFMK_00129 | 2.6e-48 | 3.2.1.185 | GH127 | S | Beta-L-arabinofuranosidase, GH127 | |
KFEKAFMK_00130 | 1.9e-153 | yggS | S | Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis | ||
KFEKAFMK_00131 | 1.3e-187 | prs | 2.7.6.1 | F | Involved in the biosynthesis of the central metabolite phospho-alpha-D-ribosyl-1-pyrophosphate (PRPP) via the transfer of pyrophosphoryl group from ATP to 1-hydroxyl of ribose-5-phosphate (Rib-5-P) | |
KFEKAFMK_00132 | 4.6e-48 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
KFEKAFMK_00133 | 4e-76 | ssb1 | L | Single-stranded DNA-binding protein | ||
KFEKAFMK_00134 | 2e-36 | rpsR | J | Binds as a heterodimer with protein S6 to the central domain of the 16S rRNA, where it helps stabilize the platform of the 30S subunit | ||
KFEKAFMK_00135 | 2.7e-71 | rplI | J | Binds to the 23S rRNA | ||
KFEKAFMK_00137 | 6.9e-117 | gla | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
KFEKAFMK_00138 | 0.0 | pacS | 1.9.3.1, 3.6.3.54 | P | E1-E2 ATPase | |
KFEKAFMK_00139 | 3.3e-43 | csoR | S | Metal-sensitive transcriptional repressor | ||
KFEKAFMK_00140 | 6.1e-210 | rmuC | S | RmuC family | ||
KFEKAFMK_00141 | 2e-109 | pyrE | 2.4.2.10 | F | Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) | |
KFEKAFMK_00142 | 2.4e-159 | spoU | 2.1.1.185 | J | RNA methyltransferase TrmH family | |
KFEKAFMK_00143 | 6.4e-168 | V | ABC transporter | |||
KFEKAFMK_00144 | 1.1e-179 | |||||
KFEKAFMK_00145 | 8.7e-161 | K | Psort location Cytoplasmic, score | |||
KFEKAFMK_00146 | 2.4e-47 | 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) | |
KFEKAFMK_00147 | 1.6e-285 | gatA | 6.3.5.6, 6.3.5.7 | F | Allows the formation of correctly charged Gln-tRNA(Gln) through the transamidation of misacylated Glu-tRNA(Gln) in organisms which lack glutaminyl-tRNA synthetase. The reaction takes place in the presence of glutamine and ATP through an activated gamma-phospho-Glu-tRNA(Gln) | |
KFEKAFMK_00148 | 6e-285 | gatB | 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | |
KFEKAFMK_00149 | 4e-195 | 2.3.1.57 | J | Acetyltransferase (GNAT) domain | ||
KFEKAFMK_00150 | 3.3e-52 | S | Protein of unknown function (DUF2469) | |||
KFEKAFMK_00151 | 0.0 | 5.4.99.9 | H | Flavin containing amine oxidoreductase | ||
KFEKAFMK_00152 | 1.7e-279 | rho | K | Facilitates transcription termination by a mechanism that involves Rho binding to the nascent RNA, activation of Rho's RNA-dependent ATPase activity, and release of the mRNA from the DNA template | ||
KFEKAFMK_00153 | 1.1e-45 | pabC | 2.6.1.42, 4.1.3.38 | EH | Amino-transferase class IV | |
KFEKAFMK_00154 | 1.6e-127 | L | Transposase | |||
KFEKAFMK_00155 | 1.5e-49 | K | helix_turn_helix, arabinose operon control protein | |||
KFEKAFMK_00156 | 4.4e-154 | araN | G | Bacterial extracellular solute-binding protein | ||
KFEKAFMK_00157 | 2.5e-121 | lacF | P | Binding-protein-dependent transport system inner membrane component | ||
KFEKAFMK_00158 | 1e-114 | araQ | U | Binding-protein-dependent transport system inner membrane component | ||
KFEKAFMK_00159 | 1.2e-130 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
KFEKAFMK_00160 | 1.1e-28 | L | Helix-turn-helix domain | |||
KFEKAFMK_00161 | 3.8e-51 | pabC | 2.6.1.42, 4.1.3.38 | EH | Amino-transferase class IV | |
KFEKAFMK_00162 | 5.2e-63 | tyrA | 5.4.99.5 | E | Chorismate mutase type II | |
KFEKAFMK_00163 | 0.0 | S | domain protein | |||
KFEKAFMK_00164 | 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 | |
KFEKAFMK_00165 | 1.6e-280 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | |||
KFEKAFMK_00166 | 1.9e-126 | nth | 4.2.99.18 | L | DNA repair enzyme that has both DNA N-glycosylase activity and AP-lyase activity. The DNA N-glycosylase activity releases various damaged pyrimidines from DNA by cleaving the N- glycosidic bond, leaving an AP (apurinic apyrimidinic) site. The AP-lyase activity cleaves the phosphodiester bond 3' to the AP site by a beta-elimination, leaving a 3'-terminal unsaturated sugar and a product with a terminal 5'-phosphate | |
KFEKAFMK_00167 | 1.1e-136 | KT | Transcriptional regulatory protein, C terminal | |||
KFEKAFMK_00168 | 1.1e-116 | |||||
KFEKAFMK_00169 | 2.6e-87 | mntP | P | Probably functions as a manganese efflux pump | ||
KFEKAFMK_00170 | 8.8e-92 | ppa | 3.6.1.1 | C | Catalyzes the hydrolysis of inorganic pyrophosphate (PPi) forming two phosphate ions | |
KFEKAFMK_00171 | 0.0 | glgE | 2.4.99.16 | GH13 | G | Maltosyltransferase that uses maltose 1-phosphate (M1P) as the sugar donor to elongate linear or branched alpha-(1- 4)- glucans. Is involved in a branched alpha-glucan biosynthetic pathway from trehalose, together with TreS, Mak and GlgB |
KFEKAFMK_00172 | 0.0 | K | RNA polymerase II activating transcription factor binding | |||
KFEKAFMK_00174 | 1.6e-207 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to L- homoserine, forming acetyl-L-homoserine | |
KFEKAFMK_00175 | 2.4e-147 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
KFEKAFMK_00176 | 4.4e-30 | 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 | ||
KFEKAFMK_00177 | 1.4e-63 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
KFEKAFMK_00178 | 2.2e-151 | 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 | ||
KFEKAFMK_00179 | 1.3e-309 | 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 | |
KFEKAFMK_00180 | 5.5e-164 | atpG | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The gamma chain is believed to be important in regulating ATPase activity and the flow of protons through the CF(0) complex | ||
KFEKAFMK_00181 | 2.1e-282 | atpD | 3.6.3.14 | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The catalytic sites are hosted primarily by the beta subunits | |
KFEKAFMK_00182 | 9.4e-49 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
KFEKAFMK_00183 | 1.4e-130 | nucS | L | Cleaves both 3' and 5' ssDNA extremities of branched DNA structures | ||
KFEKAFMK_00184 | 9.4e-159 | fkbB | 5.2.1.8 | M | FKBP-type peptidyl-prolyl cis-trans isomerase | |
KFEKAFMK_00185 | 5.4e-183 | |||||
KFEKAFMK_00186 | 1.9e-178 | |||||
KFEKAFMK_00187 | 1.7e-171 | trxA2 | O | Tetratricopeptide repeat | ||
KFEKAFMK_00188 | 2.9e-116 | cyaA | 4.6.1.1 | S | CYTH | |
KFEKAFMK_00191 | 3.6e-64 | psp1 | 3.5.99.10 | J | Endoribonuclease L-PSP | |
KFEKAFMK_00192 | 8.8e-189 | plsC2 | 2.3.1.51 | I | Phosphate acyltransferases | |
KFEKAFMK_00193 | 1.5e-178 | gpsA | 1.1.1.94 | I | NAD-dependent glycerol-3-phosphate dehydrogenase C-terminus | |
KFEKAFMK_00194 | 4.1e-228 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
KFEKAFMK_00195 | 3.8e-218 | P | Bacterial extracellular solute-binding protein | |||
KFEKAFMK_00196 | 9.9e-161 | U | Binding-protein-dependent transport system inner membrane component | |||
KFEKAFMK_00197 | 1.4e-151 | U | Binding-protein-dependent transport system inner membrane component | |||
KFEKAFMK_00198 | 8.2e-238 | 3.6.3.30 | E | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | ||
KFEKAFMK_00199 | 9.9e-186 | S | CAAX protease self-immunity | |||
KFEKAFMK_00200 | 2.5e-136 | M | Mechanosensitive ion channel | |||
KFEKAFMK_00201 | 8.6e-273 | aspA | 4.3.1.1 | E | Fumarase C C-terminus | |
KFEKAFMK_00202 | 5e-11 | L | Transposase DDE domain | |||
KFEKAFMK_00203 | 6.1e-235 | S | AAA domain | |||
KFEKAFMK_00204 | 1.7e-202 | EGP | Major Facilitator Superfamily | |||
KFEKAFMK_00205 | 6.1e-54 | L | Transposase DDE domain | |||
KFEKAFMK_00206 | 1.3e-106 | K | Bacterial regulatory proteins, tetR family | |||
KFEKAFMK_00207 | 1.1e-253 | MA20_36090 | S | Psort location Cytoplasmic, score 8.87 | ||
KFEKAFMK_00208 | 1.8e-89 | ogt | 2.1.1.63, 3.2.2.20 | L | Involved in the cellular defense against the biological effects of O6-methylguanine (O6-MeG) and O4-methylthymine (O4-MeT) in DNA. Repairs the methylated nucleobase in DNA by stoichiometrically transferring the methyl group to a cysteine residue in the enzyme. This is a suicide reaction the enzyme is irreversibly inactivated | |
KFEKAFMK_00209 | 2.5e-81 | acpS | 2.7.8.7, 3.2.1.52 | I | Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein | |
KFEKAFMK_00210 | 1.2e-75 | ams | 2.4.1.4, 3.2.1.1, 5.4.99.16 | GH13 | G | Alpha amylase, catalytic domain |
KFEKAFMK_00211 | 1.2e-113 | P | Sodium/hydrogen exchanger family | |||
KFEKAFMK_00213 | 4.8e-07 | |||||
KFEKAFMK_00214 | 1.8e-80 | |||||
KFEKAFMK_00215 | 0.0 | 1.3.98.1, 3.2.1.21 | GH3 | M | Conserved repeat domain | |
KFEKAFMK_00216 | 2.2e-274 | M | LPXTG cell wall anchor motif | |||
KFEKAFMK_00218 | 6.4e-51 | |||||
KFEKAFMK_00219 | 7.6e-110 | |||||
KFEKAFMK_00220 | 1e-41 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
KFEKAFMK_00221 | 0.0 | pnp | 2.7.7.8 | J | Involved in mRNA degradation. Catalyzes the phosphorolysis of single-stranded polyribonucleotides processively in the 3'- to 5'-direction | |
KFEKAFMK_00222 | 1.3e-89 | lemA | S | LemA family | ||
KFEKAFMK_00223 | 0.0 | S | Predicted membrane protein (DUF2207) | |||
KFEKAFMK_00225 | 1.7e-26 | S | Predicted membrane protein (DUF2207) | |||
KFEKAFMK_00226 | 7.7e-143 | S | Predicted membrane protein (DUF2207) | |||
KFEKAFMK_00227 | 1.1e-20 | |||||
KFEKAFMK_00228 | 3.8e-167 | 1.1.1.65 | C | Oxidoreductase, aldo keto reductase family protein | ||
KFEKAFMK_00229 | 2.9e-201 | iunH1 | 3.2.2.1 | F | Inosine-uridine preferring nucleoside hydrolase | |
KFEKAFMK_00230 | 6.4e-108 | rimM | J | An accessory protein needed during the final step in the assembly of 30S ribosomal subunit, possibly for assembly of the head region. Probably interacts with S19. Essential for efficient processing of 16S rRNA. May be needed both before and after RbfA during the maturation of 16S rRNA. It has affinity for free ribosomal 30S subunits but not for 70S ribosomes | ||
KFEKAFMK_00231 | 1e-34 | CP_0960 | S | Belongs to the UPF0109 family | ||
KFEKAFMK_00232 | 7e-62 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
KFEKAFMK_00233 | 1.3e-203 | S | Endonuclease/Exonuclease/phosphatase family | |||
KFEKAFMK_00234 | 5.5e-263 | ffh | 3.6.5.4 | U | Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Binds to the hydrophobic signal sequence of the ribosome-nascent chain (RNC) as it emerges from the ribosomes. The SRP-RNC complex is then targeted to the cytoplasmic membrane where it interacts with the SRP receptor FtsY | |
KFEKAFMK_00235 | 1.8e-159 | P | Cation efflux family | |||
KFEKAFMK_00236 | 0.0 | cysS | 6.1.1.16 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
KFEKAFMK_00237 | 1.6e-136 | guaA1 | 6.3.5.2 | F | Peptidase C26 | |
KFEKAFMK_00238 | 0.0 | yjjK | S | ABC transporter | ||
KFEKAFMK_00239 | 3.9e-72 | vapC | S | Toxic component of a toxin-antitoxin (TA) module. An RNase | ||
KFEKAFMK_00240 | 8.6e-44 | stbC | S | Plasmid stability protein | ||
KFEKAFMK_00241 | 9e-93 | ilvN | 2.2.1.6 | E | ACT domain | |
KFEKAFMK_00242 | 0.0 | ilvB | 2.2.1.6 | H | Thiamine pyrophosphate enzyme, central domain | |
KFEKAFMK_00243 | 9.7e-135 | rnc | 3.1.26.3 | J | Digests double-stranded RNA. Involved in the processing of primary rRNA transcript to yield the immediate precursors to the large and small rRNAs (23S and 16S). Processes some mRNAs, and tRNAs when they are encoded in the rRNA operon. Processes pre- crRNA and tracrRNA of type II CRISPR loci if present in the organism | |
KFEKAFMK_00244 | 9.3e-21 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
KFEKAFMK_00245 | 7.6e-117 | yceD | S | Uncharacterized ACR, COG1399 | ||
KFEKAFMK_00246 | 3.3e-64 | |||||
KFEKAFMK_00247 | 6e-88 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
KFEKAFMK_00248 | 5.8e-48 | S | Protein of unknown function (DUF3039) | |||
KFEKAFMK_00249 | 1.9e-197 | yghZ | C | Aldo/keto reductase family | ||
KFEKAFMK_00250 | 1.4e-77 | soxR | K | MerR, DNA binding | ||
KFEKAFMK_00251 | 4.5e-117 | |||||
KFEKAFMK_00252 | 4e-248 | 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 | |
KFEKAFMK_00253 | 7e-144 | rph | 2.7.7.56, 3.6.1.66 | J | Phosphorolytic exoribonuclease that removes nucleotide residues following the -CCA terminus of tRNA and adds nucleotides to the ends of RNA molecules by using nucleoside diphosphates as substrates | |
KFEKAFMK_00254 | 1.8e-128 | rdgB | 3.6.1.66, 5.1.1.3 | F | Pyrophosphatase that catalyzes the hydrolysis of nucleoside triphosphates to their monophosphate derivatives, with a high preference for the non-canonical purine nucleotides XTP (xanthosine triphosphate), dITP (deoxyinosine triphosphate) and ITP. Seems to function as a house-cleaning enzyme that removes non-canonical purine nucleotides from the nucleotide pool, thus preventing their incorporation into DNA RNA and avoiding chromosomal lesions | |
KFEKAFMK_00255 | 2.4e-176 | S | Auxin Efflux Carrier | |||
KFEKAFMK_00258 | 1.1e-207 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
KFEKAFMK_00259 | 1.4e-158 | S | Fic/DOC family | |||
KFEKAFMK_00260 | 1.8e-16 | S | Psort location Cytoplasmic, score 8.87 | |||
KFEKAFMK_00261 | 1.5e-175 | V | Abi-like protein | |||
KFEKAFMK_00262 | 7.9e-102 | ppiA | 5.2.1.8 | G | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
KFEKAFMK_00263 | 0.0 | relA | 2.7.6.5, 3.1.7.2 | KT | In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance | |
KFEKAFMK_00264 | 6.5e-84 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | This enzyme is involved in nucleotide metabolism it produces dUMP, the immediate precursor of thymidine nucleotides and it decreases the intracellular concentration of dUTP so that uracil cannot be incorporated into DNA | |
KFEKAFMK_00265 | 1.4e-47 | S | Domain of unknown function (DUF4193) | |||
KFEKAFMK_00266 | 1.4e-142 | S | Protein of unknown function (DUF3071) | |||
KFEKAFMK_00267 | 1.5e-233 | S | Type I phosphodiesterase / nucleotide pyrophosphatase | |||
KFEKAFMK_00268 | 0.0 | gyrA | 5.99.1.3 | L | DNA topoisomerase (ATP-hydrolyzing) | |
KFEKAFMK_00269 | 1.9e-09 | E | GDSL-like Lipase/Acylhydrolase | |||
KFEKAFMK_00270 | 3e-110 | G | Bacterial extracellular solute-binding protein | |||
KFEKAFMK_00271 | 7e-44 | K | AraC-like ligand binding domain | |||
KFEKAFMK_00272 | 5.2e-43 | K | Psort location Cytoplasmic, score | |||
KFEKAFMK_00273 | 1.2e-48 | K | Psort location Cytoplasmic, score | |||
KFEKAFMK_00274 | 0.0 | lhr | L | DEAD DEAH box helicase | ||
KFEKAFMK_00275 | 9.8e-172 | rbsK | 2.7.1.15 | H | Catalyzes the phosphorylation of ribose at O-5 in a reaction requiring ATP and magnesium. The resulting D-ribose-5- phosphate can then be used either for sythesis of nucleotides, histidine, and tryptophan, or as a component of the pentose phosphate pathway | |
KFEKAFMK_00276 | 4.5e-222 | G | Major Facilitator Superfamily | |||
KFEKAFMK_00277 | 0.0 | gyrB2 | 5.99.1.3 | L | DNA topoisomerase (ATP-hydrolyzing) | |
KFEKAFMK_00278 | 8.2e-191 | sigA | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released. This sigma factor is the primary sigma factor during exponential growth | ||
KFEKAFMK_00279 | 1.8e-113 | |||||
KFEKAFMK_00280 | 3.2e-195 | crtE | 2.5.1.1, 2.5.1.10, 2.5.1.29 | H | Belongs to the FPP GGPP synthase family | |
KFEKAFMK_00281 | 0.0 | pknL | 2.7.11.1 | KLT | PASTA | |
KFEKAFMK_00282 | 6.2e-131 | plsC2 | 2.3.1.51 | I | Phosphate acyltransferases | |
KFEKAFMK_00283 | 5.3e-119 | |||||
KFEKAFMK_00284 | 2.5e-189 | trpD | 2.4.2.18, 4.1.3.27 | F | Catalyzes the transfer of the phosphoribosyl group of 5- phosphorylribose-1-pyrophosphate (PRPP) to anthranilate to yield N-(5'-phosphoribosyl)-anthranilate (PRA) | |
KFEKAFMK_00285 | 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 | ||
KFEKAFMK_00286 | 2.4e-113 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
KFEKAFMK_00287 | 1.8e-102 | recX | S | Modulates RecA activity | ||
KFEKAFMK_00288 | 3.5e-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 | ||
KFEKAFMK_00289 | 7e-39 | S | Protein of unknown function (DUF3046) | |||
KFEKAFMK_00290 | 1.1e-76 | K | Helix-turn-helix XRE-family like proteins | |||
KFEKAFMK_00291 | 2.2e-91 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
KFEKAFMK_00292 | 4.6e-117 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
KFEKAFMK_00293 | 0.0 | ftsK | D | FtsK SpoIIIE family protein | ||
KFEKAFMK_00294 | 4.8e-151 | fic | D | Fic/DOC family | ||
KFEKAFMK_00295 | 1.2e-177 | 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) | |
KFEKAFMK_00296 | 1.3e-276 | miaB | 2.8.4.3 | H | Catalyzes the methylthiolation of N6- (dimethylallyl)adenosine (i(6)A), leading to the formation of 2- methylthio-N6-(dimethylallyl)adenosine (ms(2)i(6)A) at position 37 in tRNAs that read codons beginning with uridine | |
KFEKAFMK_00297 | 8.8e-150 | relA2 | 2.7.6.5 | S | Region found in RelA / SpoT proteins | |
KFEKAFMK_00298 | 1.1e-164 | ydeD | EG | EamA-like transporter family | ||
KFEKAFMK_00299 | 9.7e-136 | ybhL | S | Belongs to the BI1 family | ||
KFEKAFMK_00300 | 1.1e-81 | K | helix_turn_helix, Lux Regulon | |||
KFEKAFMK_00301 | 8.4e-119 | E | Psort location Cytoplasmic, score 8.87 | |||
KFEKAFMK_00302 | 0.0 | acnA | 4.2.1.3 | C | Catalyzes the isomerization of citrate to isocitrate via cis-aconitate | |
KFEKAFMK_00303 | 0.0 | ctpE | P | E1-E2 ATPase | ||
KFEKAFMK_00304 | 1.1e-93 | |||||
KFEKAFMK_00305 | 1.5e-241 | trmA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
KFEKAFMK_00306 | 3.8e-134 | S | Protein of unknown function (DUF3159) | |||
KFEKAFMK_00307 | 2.8e-154 | S | Protein of unknown function (DUF3710) | |||
KFEKAFMK_00308 | 4.8e-170 | exoA | 3.1.11.2 | L | Endonuclease/Exonuclease/phosphatase family | |
KFEKAFMK_00309 | 0.0 | dppD | EP | Oligopeptide/dipeptide transporter, C-terminal region | ||
KFEKAFMK_00310 | 1e-171 | dppC | EP | N-terminal TM domain of oligopeptide transport permease C | ||
KFEKAFMK_00311 | 2e-153 | dppB | EP | Binding-protein-dependent transport system inner membrane component | ||
KFEKAFMK_00312 | 1e-309 | E | ABC transporter, substrate-binding protein, family 5 | |||
KFEKAFMK_00313 | 6.1e-188 | xerC | D | Belongs to the 'phage' integrase family. XerC subfamily | ||
KFEKAFMK_00314 | 4.1e-147 | V | ABC transporter, ATP-binding protein | |||
KFEKAFMK_00315 | 0.0 | MV | MacB-like periplasmic core domain | |||
KFEKAFMK_00316 | 4.5e-42 | |||||
KFEKAFMK_00317 | 5.5e-189 | tyrA | 1.3.1.12, 1.3.1.43 | E | Prephenate dehydrogenase | |
KFEKAFMK_00318 | 1.5e-188 | pheA | 1.3.1.12, 4.2.1.51, 5.4.99.5 | E | Prephenate dehydratase | |
KFEKAFMK_00319 | 1.2e-77 | |||||
KFEKAFMK_00320 | 0.0 | typA | T | Elongation factor G C-terminus | ||
KFEKAFMK_00321 | 7e-107 | K | Virulence activator alpha C-term | |||
KFEKAFMK_00322 | 4.8e-137 | V | ATPases associated with a variety of cellular activities | |||
KFEKAFMK_00323 | 0.0 | V | FtsX-like permease family | |||
KFEKAFMK_00324 | 6.7e-243 | naiP | U | Sugar (and other) transporter | ||
KFEKAFMK_00325 | 6.9e-237 | iscS1 | 2.8.1.7 | E | Aminotransferase class-V | |
KFEKAFMK_00326 | 8.6e-162 | nadC | 1.4.3.16, 2.4.2.19 | H | Quinolinate phosphoribosyl transferase, N-terminal domain | |
KFEKAFMK_00327 | 4.4e-302 | nadB | 1.3.5.4, 1.4.3.16, 2.4.2.19 | H | Catalyzes the oxidation of L-aspartate to iminoaspartate | |
KFEKAFMK_00328 | 4.1e-250 | nadA | 2.5.1.72 | H | Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate | |
KFEKAFMK_00329 | 3.4e-160 | nrtR | 3.6.1.55 | F | NUDIX hydrolase | |
KFEKAFMK_00330 | 2.9e-114 | 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 | ||
KFEKAFMK_00331 | 1.9e-150 | 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 | ||
KFEKAFMK_00332 | 3.8e-152 | soj | D | CobQ CobB MinD ParA nucleotide binding domain protein | ||
KFEKAFMK_00333 | 4e-154 | xerD | D | recombinase XerD | ||
KFEKAFMK_00334 | 5.4e-193 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
KFEKAFMK_00335 | 1.3e-61 | rplT | J | Binds directly to 23S ribosomal RNA and is necessary for the in vitro assembly process of the 50S ribosomal subunit. It is not involved in the protein synthesizing functions of that subunit | ||
KFEKAFMK_00336 | 6.2e-25 | rpmI | J | Ribosomal protein L35 | ||
KFEKAFMK_00337 | 1.5e-112 | 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 | ||
KFEKAFMK_00338 | 2.3e-32 | S | Spermine/spermidine synthase domain | |||
KFEKAFMK_00339 | 1.5e-21 | S | Spermine/spermidine synthase domain | |||
KFEKAFMK_00340 | 4.2e-135 | 2.7.6.2 | H | Thiamin pyrophosphokinase, vitamin B1 binding domain | ||
KFEKAFMK_00341 | 1.3e-196 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
KFEKAFMK_00342 | 4.2e-89 | ybaK | J | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
KFEKAFMK_00343 | 7.5e-183 | ispH | 1.17.7.4, 2.7.4.25 | IM | Catalyzes the conversion of 1-hydroxy-2-methyl-2-(E)- butenyl 4-diphosphate (HMBPP) into a mixture of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP). Acts in the terminal step of the DOXP MEP pathway for isoprenoid precursor biosynthesis | |
KFEKAFMK_00344 | 2.1e-190 | galM | 5.1.3.3 | G | Aldose 1-epimerase | |
KFEKAFMK_00345 | 5.8e-185 | galM | 5.1.3.3 | G | Aldose 1-epimerase | |
KFEKAFMK_00346 | 9.5e-52 | |||||
KFEKAFMK_00347 | 1.8e-136 | sigH | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
KFEKAFMK_00348 | 9e-284 | murE | 6.3.2.13, 6.3.2.7 | M | Catalyzes the addition of an amino acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
KFEKAFMK_00349 | 6.9e-192 | V | Acetyltransferase (GNAT) domain | |||
KFEKAFMK_00350 | 3.3e-47 | V | Acetyltransferase (GNAT) domain | |||
KFEKAFMK_00351 | 0.0 | smc | D | Required for chromosome condensation and partitioning | ||
KFEKAFMK_00352 | 1.3e-298 | folC | 6.3.2.12, 6.3.2.17 | H | Mur ligase middle domain | |
KFEKAFMK_00353 | 3.3e-310 | pepP | 3.4.11.9 | E | Aminopeptidase P, N-terminal domain | |
KFEKAFMK_00354 | 3.1e-95 | 3.6.1.55 | F | NUDIX domain | ||
KFEKAFMK_00355 | 3.2e-247 | nagA | 3.5.1.25 | G | Amidohydrolase family | |
KFEKAFMK_00356 | 2.1e-151 | nagB | 3.1.1.31, 3.5.99.6 | G | Catalyzes the reversible isomerization-deamination of glucosamine 6-phosphate (GlcN6P) to form fructose 6-phosphate (Fru6P) and ammonium ion | |
KFEKAFMK_00357 | 9.9e-208 | GK | ROK family | |||
KFEKAFMK_00358 | 3.2e-164 | 2.7.1.2 | GK | ROK family | ||
KFEKAFMK_00359 | 1e-221 | GK | ROK family | |||
KFEKAFMK_00360 | 8.9e-167 | 2.7.1.4 | G | pfkB family carbohydrate kinase | ||
KFEKAFMK_00361 | 8.6e-86 | G | Major Facilitator Superfamily | |||
KFEKAFMK_00362 | 1.1e-44 | G | Major Facilitator Superfamily | |||
KFEKAFMK_00363 | 2.2e-87 | dtd | J | rejects L-amino acids rather than detecting D-amino acids in the active site. By recycling D-aminoacyl-tRNA to D-amino acids and free tRNA molecules, this enzyme counteracts the toxicity associated with the formation of D-aminoacyl-tRNA entities in vivo and helps enforce protein L-homochirality | ||
KFEKAFMK_00364 | 7e-15 | |||||
KFEKAFMK_00365 | 6.2e-172 | ftsQ | 6.3.2.4 | D | Cell division protein FtsQ | |
KFEKAFMK_00366 | 4.9e-282 | murC | 6.3.2.8 | M | Belongs to the MurCDEF family | |
KFEKAFMK_00367 | 6.5e-218 | 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) |
KFEKAFMK_00368 | 5.7e-225 | ftsW | 2.4.1.227 | GT28 | D | Belongs to the SEDS family |
KFEKAFMK_00369 | 1.5e-272 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
KFEKAFMK_00370 | 8.6e-204 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
KFEKAFMK_00371 | 3e-241 | murF | 6.3.2.10 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
KFEKAFMK_00372 | 2.9e-154 | yqeC | 6.3.2.10, 6.3.2.13 | M | Catalyzes the addition of meso-diaminopimelic acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
KFEKAFMK_00373 | 0.0 | ftsI | 3.4.16.4 | M | Penicillin-binding protein, transpeptidase domain protein | |
KFEKAFMK_00374 | 1.4e-67 | ftsL | D | Essential cell division protein. May link together the upstream cell division proteins, which are predominantly cytoplasmic, with the downstream cell division proteins, which are predominantly periplasmic | ||
KFEKAFMK_00375 | 6.7e-190 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
KFEKAFMK_00376 | 1.3e-93 | mraZ | K | Belongs to the MraZ family | ||
KFEKAFMK_00377 | 0.0 | L | DNA helicase | |||
KFEKAFMK_00378 | 2.6e-230 | serA | 1.1.1.399, 1.1.1.95 | EH | D-isomer specific 2-hydroxyacid dehydrogenase, catalytic domain | |
KFEKAFMK_00379 | 8.4e-78 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
KFEKAFMK_00380 | 4.3e-46 | M | Lysin motif | |||
KFEKAFMK_00381 | 8.4e-128 | lexA | 3.4.21.88 | K | Represses a number of genes involved in the response to DNA damage (SOS response), including recA and lexA. In the presence of single-stranded DNA, RecA interacts with LexA causing an autocatalytic cleavage which disrupts the DNA-binding part of LexA, leading to derepression of the SOS regulon and eventually DNA repair | |
KFEKAFMK_00382 | 1.4e-162 | czcD | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
KFEKAFMK_00383 | 1.7e-176 | ldh | 1.1.1.27, 1.1.1.37 | C | Belongs to the LDH MDH superfamily. LDH family | |
KFEKAFMK_00384 | 3.5e-272 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
KFEKAFMK_00385 | 7.5e-123 | rsmC | 2.1.1.172 | J | Ribosomal protein L11 methyltransferase (PrmA) | |
KFEKAFMK_00386 | 0.0 | hrpA | 3.6.4.13 | L | Helicase associated domain (HA2) Add an annotation | |
KFEKAFMK_00387 | 1.5e-217 | EGP | Major facilitator Superfamily | |||
KFEKAFMK_00388 | 4.7e-265 | glnA2 | 6.3.1.2 | E | glutamine synthetase | |
KFEKAFMK_00389 | 2.3e-278 | S | Uncharacterized protein conserved in bacteria (DUF2252) | |||
KFEKAFMK_00390 | 4.1e-130 | hisA | 5.3.1.16, 5.3.1.24 | E | Histidine biosynthesis protein | |
KFEKAFMK_00391 | 9.1e-121 | hisH | E | IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisH subunit provides the glutamine amidotransferase activity that produces the ammonia necessary to HisF for the synthesis of IGP and AICAR | ||
KFEKAFMK_00392 | 1.4e-96 | |||||
KFEKAFMK_00393 | 3.5e-111 | hisB | 1.1.1.23, 2.6.1.9, 3.1.3.15, 4.2.1.19 | E | Imidazoleglycerol-phosphate dehydratase | |
KFEKAFMK_00394 | 6.8e-220 | hisC | 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
KFEKAFMK_00395 | 1.2e-252 | hisD | 1.1.1.23, 1.1.1.308 | E | Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine | |
KFEKAFMK_00396 | 3.1e-53 | acyP | 3.6.1.7 | C | Acylphosphatase | |
KFEKAFMK_00397 | 1.9e-155 | yvgN | 1.1.1.346 | S | Aldo/keto reductase family | |
KFEKAFMK_00398 | 0.0 | 2.4.1.230, 3.2.1.51 | GH65,GH95 | G | Glycosyl hydrolase family 65, N-terminal domain | |
KFEKAFMK_00399 | 6.3e-165 | dapA | 4.1.2.28, 4.3.3.7 | EM | Dihydrodipicolinate synthetase family | |
KFEKAFMK_00400 | 1e-133 | S | Amidohydrolase | |||
KFEKAFMK_00401 | 1.1e-49 | 4.2.1.68 | M | Enolase C-terminal domain-like | ||
KFEKAFMK_00404 | 1.5e-46 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
KFEKAFMK_00405 | 5e-133 | |||||
KFEKAFMK_00406 | 5.7e-85 | rimJ | 2.3.1.128 | J | Acetyltransferase (GNAT) domain | |
KFEKAFMK_00407 | 7.3e-56 | fthC | 6.3.3.2 | H | 5-formyltetrahydrofolate cyclo-ligase family | |
KFEKAFMK_00408 | 4.3e-31 | fmdB | S | Putative regulatory protein | ||
KFEKAFMK_00409 | 5.9e-92 | flgA | NO | SAF | ||
KFEKAFMK_00410 | 6.6e-19 | L | Superfamily I DNA and RNA helicases and helicase subunits | |||
KFEKAFMK_00411 | 0.0 | L | Superfamily I DNA and RNA helicases and helicase subunits | |||
KFEKAFMK_00412 | 6.3e-191 | T | Forkhead associated domain | |||
KFEKAFMK_00413 | 9.3e-49 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
KFEKAFMK_00414 | 2.4e-87 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
KFEKAFMK_00415 | 2.5e-144 | 3.2.1.8 | S | alpha beta | ||
KFEKAFMK_00416 | 1.1e-251 | pbuO | S | Permease family | ||
KFEKAFMK_00417 | 2.1e-148 | pstB | 3.6.3.27 | P | Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system | |
KFEKAFMK_00418 | 1.3e-171 | pstA | P | Phosphate transport system permease | ||
KFEKAFMK_00419 | 1.2e-156 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
KFEKAFMK_00420 | 1.3e-202 | pstS | P | Part of the ABC transporter complex PstSACB involved in phosphate import | ||
KFEKAFMK_00421 | 3.8e-142 | KT | Transcriptional regulatory protein, C terminal | |||
KFEKAFMK_00422 | 3.9e-208 | senX3 | 2.7.13.3 | T | His Kinase A (phosphoacceptor) domain | |
KFEKAFMK_00423 | 1.1e-240 | EGP | Sugar (and other) transporter | |||
KFEKAFMK_00424 | 6.3e-123 | mtnN | 3.2.2.9 | E | Catalyzes the irreversible cleavage of the glycosidic bond in both 5'-methylthioadenosine (MTA) and S- adenosylhomocysteine (SAH AdoHcy) to adenine and the corresponding thioribose, 5'-methylthioribose and S-ribosylhomocysteine, respectively | |
KFEKAFMK_00425 | 1.9e-236 | aroG | 2.5.1.54 | E | Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) | |
KFEKAFMK_00426 | 2e-216 | aroG | 2.5.1.54 | E | Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) | |
KFEKAFMK_00427 | 4.1e-86 | ebgC | G | YhcH YjgK YiaL family protein | ||
KFEKAFMK_00428 | 0.0 | ebgA | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
KFEKAFMK_00429 | 5.6e-115 | pgmB | 5.4.2.6 | S | phosphonoacetaldehyde hydrolase activity | |
KFEKAFMK_00430 | 9.4e-156 | EG | EamA-like transporter family | |||
KFEKAFMK_00431 | 0.0 | kojP | 2.4.1.230 | GH65 | G | Glycosyl hydrolase family 65 central catalytic domain |
KFEKAFMK_00432 | 1.9e-152 | P | Binding-protein-dependent transport system inner membrane component | |||
KFEKAFMK_00433 | 5.3e-170 | malC | U | Binding-protein-dependent transport system inner membrane component | ||
KFEKAFMK_00434 | 1.5e-236 | G | Bacterial extracellular solute-binding protein | |||
KFEKAFMK_00435 | 4.6e-188 | K | Periplasmic binding protein domain | |||
KFEKAFMK_00436 | 2e-98 | U | MarC family integral membrane protein | |||
KFEKAFMK_00437 | 1.8e-264 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
KFEKAFMK_00438 | 1e-267 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
KFEKAFMK_00439 | 2.4e-44 | D | nuclear chromosome segregation | |||
KFEKAFMK_00440 | 2.6e-126 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
KFEKAFMK_00441 | 4.2e-150 | ispD | 1.1.1.405, 2.7.7.40, 2.7.7.60, 4.6.1.12 | I | Catalyzes the formation of 4-diphosphocytidyl-2-C- methyl-D-erythritol from CTP and 2-C-methyl-D-erythritol 4- phosphate (MEP) | |
KFEKAFMK_00442 | 1.3e-196 | yfiH | Q | Multi-copper polyphenol oxidoreductase laccase | ||
KFEKAFMK_00443 | 8.1e-301 | yegQ | O | Peptidase family U32 C-terminal domain | ||
KFEKAFMK_00444 | 6.3e-179 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
KFEKAFMK_00445 | 2.2e-102 | rsmD | 2.1.1.171 | L | Conserved hypothetical protein 95 | |
KFEKAFMK_00446 | 0.0 | recG | 3.6.4.12 | L | helicase superfamily c-terminal domain | |
KFEKAFMK_00447 | 2.5e-29 | rpmB | J | Ribosomal L28 family | ||
KFEKAFMK_00448 | 1.9e-194 | yegV | G | pfkB family carbohydrate kinase | ||
KFEKAFMK_00449 | 5.5e-234 | yxiO | S | Vacuole effluxer Atg22 like | ||
KFEKAFMK_00450 | 1.5e-181 | K | Helix-turn-helix XRE-family like proteins | |||
KFEKAFMK_00451 | 8.3e-62 | S | Alpha/beta hydrolase family | |||
KFEKAFMK_00455 | 4e-44 | XK27_04590 | S | NADPH-dependent FMN reductase | ||
KFEKAFMK_00456 | 0.0 | fas | 2.3.1.179 | I | Beta-ketoacyl synthase, C-terminal domain | |
KFEKAFMK_00457 | 1.8e-279 | pccB | I | Carboxyl transferase domain | ||
KFEKAFMK_00458 | 0.0 | accA | 6.3.4.14, 6.4.1.2, 6.4.1.3 | I | Carbamoyl-phosphate synthase L chain, ATP binding domain protein | |
KFEKAFMK_00459 | 9e-91 | bioY | S | BioY family | ||
KFEKAFMK_00460 | 5.5e-161 | birA | 2.7.1.33, 6.3.4.15 | H | Biotin/lipoate A/B protein ligase family | |
KFEKAFMK_00461 | 0.0 | |||||
KFEKAFMK_00462 | 1e-162 | QT | PucR C-terminal helix-turn-helix domain | |||
KFEKAFMK_00463 | 1.4e-122 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
KFEKAFMK_00464 | 1e-72 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
KFEKAFMK_00465 | 7e-110 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
KFEKAFMK_00466 | 4.7e-32 | secE | U | Essential subunit of the Sec protein translocation channel SecYEG. Clamps together the 2 halves of SecY. May contact the channel plug during translocation | ||
KFEKAFMK_00468 | 3.8e-229 | aspC | E | DegT/DnrJ/EryC1/StrS aminotransferase family | ||
KFEKAFMK_00469 | 4e-221 | G | polysaccharide deacetylase | |||
KFEKAFMK_00470 | 8.3e-199 | proB | 2.7.2.11 | E | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
KFEKAFMK_00471 | 2.3e-311 | 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 | ||
KFEKAFMK_00472 | 5.8e-39 | rpmA | J | Ribosomal L27 protein | ||
KFEKAFMK_00473 | 1.4e-47 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
KFEKAFMK_00474 | 0.0 | rne | 3.1.26.12 | J | Ribonuclease E/G family | |
KFEKAFMK_00475 | 4e-231 | dapE | 3.5.1.18 | E | Peptidase dimerisation domain | |
KFEKAFMK_00476 | 1.9e-167 | mdcF | S | Transporter, auxin efflux carrier (AEC) family protein | ||
KFEKAFMK_00477 | 5.7e-166 | dapA | 4.1.2.28, 4.3.3.7 | EM | Dihydrodipicolinate synthetase family | |
KFEKAFMK_00478 | 3.2e-149 | S | Amidohydrolase | |||
KFEKAFMK_00479 | 2e-201 | fucP | G | Major Facilitator Superfamily | ||
KFEKAFMK_00480 | 2.8e-148 | IQ | KR domain | |||
KFEKAFMK_00481 | 1.1e-250 | 4.2.1.68 | M | Enolase C-terminal domain-like | ||
KFEKAFMK_00482 | 1.2e-191 | K | Bacterial regulatory proteins, lacI family | |||
KFEKAFMK_00483 | 2.7e-218 | V | Efflux ABC transporter, permease protein | |||
KFEKAFMK_00484 | 6.1e-130 | V | ATPases associated with a variety of cellular activities | |||
KFEKAFMK_00485 | 1.6e-28 | S | Protein of unknown function (DUF1778) | |||
KFEKAFMK_00486 | 2.7e-88 | K | Acetyltransferase (GNAT) family | |||
KFEKAFMK_00487 | 1.8e-278 | maf | 1.1.1.25, 2.1.1.190, 3.6.1.55, 3.6.1.67 | DF | Maf-like protein | |
KFEKAFMK_00488 | 1.7e-207 | thrB | 2.7.1.39 | E | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
KFEKAFMK_00489 | 2.8e-238 | hom | 1.1.1.3 | E | Homoserine dehydrogenase | |
KFEKAFMK_00490 | 1.1e-54 | nagE | 2.7.1.193, 2.7.1.199 | G | phosphotransferase system, EIIB | |
KFEKAFMK_00491 | 2.1e-56 | 2.7.1.208 | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | ||
KFEKAFMK_00492 | 1.1e-303 | lysA | 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
KFEKAFMK_00493 | 0.0 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
KFEKAFMK_00494 | 1.3e-128 | K | Bacterial regulatory proteins, tetR family | |||
KFEKAFMK_00495 | 1.1e-218 | G | Transmembrane secretion effector | |||
KFEKAFMK_00496 | 6.8e-256 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
KFEKAFMK_00497 | 4.9e-254 | nox | 1.6.3.4 | C | Pyridine nucleotide-disulphide oxidoreductase | |
KFEKAFMK_00498 | 3.8e-218 | pyrD | 1.3.1.14, 1.3.98.1 | F | Dihydroorotate dehydrogenase | |
KFEKAFMK_00499 | 1.2e-34 | 2.7.13.3 | T | Histidine kinase | ||
KFEKAFMK_00500 | 6e-14 | S | Bacterial PH domain | |||
KFEKAFMK_00501 | 3.2e-132 | leuD | 4.2.1.33, 4.2.1.35 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
KFEKAFMK_00502 | 4.9e-273 | leuC | 4.2.1.33, 4.2.1.35 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
KFEKAFMK_00503 | 2.2e-140 | ltbR | K | Transcriptional regulator, IclR family, C-terminal domain protein | ||
KFEKAFMK_00504 | 5.6e-258 | S | Calcineurin-like phosphoesterase | |||
KFEKAFMK_00505 | 0.0 | ppk | 2.7.4.1 | P | Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) | |
KFEKAFMK_00506 | 4.6e-234 | mutT | 3.6.1.13, 3.6.1.55 | LT | Phosphoglycerate mutase family | |
KFEKAFMK_00507 | 1.2e-130 | |||||
KFEKAFMK_00509 | 0.0 | G | N-terminal domain of (some) glycogen debranching enzymes | |||
KFEKAFMK_00510 | 9.1e-140 | P | Binding-protein-dependent transport system inner membrane component | |||
KFEKAFMK_00511 | 4.4e-209 | U | Binding-protein-dependent transport system inner membrane component | |||
KFEKAFMK_00512 | 1.9e-207 | G | Bacterial extracellular solute-binding protein | |||
KFEKAFMK_00513 | 1.1e-128 | K | helix_turn _helix lactose operon repressor | |||
KFEKAFMK_00514 | 3.9e-116 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
KFEKAFMK_00515 | 1e-81 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
KFEKAFMK_00516 | 4.9e-215 | ugpQ | 3.1.4.46 | C | Glycerophosphoryl diester phosphodiesterase family | |
KFEKAFMK_00517 | 1e-217 | gluQ | 6.1.1.17 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
KFEKAFMK_00519 | 0.0 | clpB | O | Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE | ||
KFEKAFMK_00520 | 1.4e-162 | S | Auxin Efflux Carrier | |||
KFEKAFMK_00521 | 2e-157 | fahA | Q | Fumarylacetoacetate (FAA) hydrolase family | ||
KFEKAFMK_00522 | 3.4e-92 | S | Domain of unknown function (DUF4190) | |||
KFEKAFMK_00523 | 7.9e-57 | |||||
KFEKAFMK_00524 | 5.5e-89 | |||||
KFEKAFMK_00525 | 8.6e-234 | glf | 5.4.99.9 | M | UDP-galactopyranose mutase | |
KFEKAFMK_00526 | 4.8e-64 | K | Helix-turn-helix domain | |||
KFEKAFMK_00527 | 3.7e-07 | S | PIN domain | |||
KFEKAFMK_00528 | 1e-46 | 5.3.1.27 | G | sugar phosphate isomerase involved in capsule formation | ||
KFEKAFMK_00529 | 8.3e-58 | G | Branched-chain amino acid transport system / permease component | |||
KFEKAFMK_00530 | 1.9e-72 | P | branched-chain amino acid ABC transporter, permease protein | |||
KFEKAFMK_00531 | 6.3e-120 | G | ATPases associated with a variety of cellular activities | |||
KFEKAFMK_00532 | 2.1e-79 | G | ABC-type sugar transport system periplasmic component | |||
KFEKAFMK_00533 | 8.6e-167 | xylB | 1.1.1.57, 2.7.1.17 | G | Belongs to the FGGY kinase family | |
KFEKAFMK_00534 | 4.7e-76 | xylR | GK | ROK family | ||
KFEKAFMK_00535 | 9.1e-74 | |||||
KFEKAFMK_00536 | 6.4e-111 | K | helix_turn_helix, mercury resistance | |||
KFEKAFMK_00537 | 6.7e-75 | garA | T | Inner membrane component of T3SS, cytoplasmic domain | ||
KFEKAFMK_00538 | 1.1e-139 | S | Bacterial protein of unknown function (DUF881) | |||
KFEKAFMK_00539 | 3.9e-35 | sbp | S | Protein of unknown function (DUF1290) | ||
KFEKAFMK_00540 | 1.5e-167 | S | Bacterial protein of unknown function (DUF881) | |||
KFEKAFMK_00541 | 8.7e-105 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
KFEKAFMK_00542 | 8.7e-156 | hisG | 2.4.2.17 | F | ATP phosphoribosyltransferase | |
KFEKAFMK_00543 | 9.9e-42 | hisE | 3.5.4.19, 3.6.1.31, 5.3.1.16 | E | Phosphoribosyl-ATP pyrophosphohydrolase | |
KFEKAFMK_00544 | 9.4e-113 | rpe | 5.1.3.1 | G | Ribulose-phosphate 3-epimerase | |
KFEKAFMK_00545 | 7e-186 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
KFEKAFMK_00546 | 9.2e-161 | trpA | 4.2.1.20 | E | The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate | |
KFEKAFMK_00547 | 0.0 | trpB | 4.1.1.48, 4.2.1.20 | E | The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine | |
KFEKAFMK_00548 | 6.5e-133 | S | SOS response associated peptidase (SRAP) | |||
KFEKAFMK_00549 | 9.4e-158 | nfo | 3.1.21.2 | L | Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin | |
KFEKAFMK_00550 | 7.6e-258 | mmuP | E | amino acid | ||
KFEKAFMK_00551 | 1.2e-188 | V | VanZ like family | |||
KFEKAFMK_00552 | 4.8e-14 | cefD | 5.1.1.17 | E | Aminotransferase, class V | |
KFEKAFMK_00553 | 4.2e-46 | cefD | 5.1.1.17 | E | Aminotransferase class-V | |
KFEKAFMK_00554 | 3.3e-100 | S | Acetyltransferase (GNAT) domain | |||
KFEKAFMK_00555 | 6.5e-46 | V | MacB-like periplasmic core domain | |||
KFEKAFMK_00556 | 4.6e-39 | relB | L | RelB antitoxin | ||
KFEKAFMK_00557 | 9.4e-49 | S | Bacterial toxin of type II toxin-antitoxin system, YafQ | |||
KFEKAFMK_00558 | 3.5e-26 | G | Transporter major facilitator family protein | |||
KFEKAFMK_00559 | 1.4e-292 | mmuP | E | amino acid | ||
KFEKAFMK_00561 | 2.5e-64 | yeaO | K | Protein of unknown function, DUF488 | ||
KFEKAFMK_00562 | 5.5e-74 | |||||
KFEKAFMK_00563 | 2.1e-172 | 3.6.4.12 | ||||
KFEKAFMK_00564 | 6.4e-92 | yijF | S | Domain of unknown function (DUF1287) | ||
KFEKAFMK_00565 | 3.2e-297 | trpE | 4.1.3.27 | E | Part of a heterotetrameric complex that catalyzes the two-step biosynthesis of anthranilate, an intermediate in the biosynthesis of L-tryptophan. In the first step, the glutamine- binding beta subunit (TrpG) of anthranilate synthase (AS) provides the glutamine amidotransferase activity which generates ammonia as a substrate that, along with chorismate, is used in the second step, catalyzed by the large alpha subunit of AS (TrpE) to produce anthranilate. In the absence of TrpG, TrpE can synthesize anthranilate directly from chorismate and high concentrations of ammonia | |
KFEKAFMK_00566 | 5.3e-71 | hisI | 3.5.4.19, 3.6.1.31 | E | Catalyzes the hydrolysis of the adenine ring of phosphoribosyl-AMP | |
KFEKAFMK_00567 | 6.1e-140 | hisF | 4.1.3.27 | E | IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisF subunit catalyzes the cyclization activity that produces IGP and AICAR from PRFAR using the ammonia provided by the HisH subunit | |
KFEKAFMK_00568 | 7.2e-77 | 3.5.1.124 | S | DJ-1/PfpI family | ||
KFEKAFMK_00569 | 1.8e-223 | rlmN | 2.1.1.192 | J | Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs | |
KFEKAFMK_00570 | 1.1e-173 | cdsA | 2.7.7.41, 2.7.7.67 | I | Cytidylyltransferase family | |
KFEKAFMK_00571 | 7.5e-92 | frr | J | Responsible for the release of ribosomes from messenger RNA at the termination of protein biosynthesis. May increase the efficiency of translation by recycling ribosomes from one round of translation to another | ||
KFEKAFMK_00572 | 2.8e-134 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
KFEKAFMK_00573 | 1.4e-145 | tsf | J | Associates with the EF-Tu.GDP complex and induces the exchange of GDP to GTP. It remains bound to the aminoacyl-tRNA.EF- Tu.GTP complex up to the GTP hydrolysis stage on the ribosome | ||
KFEKAFMK_00574 | 5.8e-144 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
KFEKAFMK_00575 | 1.7e-87 | def | 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions | |
KFEKAFMK_00576 | 0.0 | fadD3 | 6.2.1.3 | I | long-chain-fatty acid CoA ligase | |
KFEKAFMK_00577 | 3.3e-91 | |||||
KFEKAFMK_00578 | 1.5e-208 | guaB | 1.1.1.205 | F | IMP dehydrogenase family protein | |
KFEKAFMK_00579 | 2.3e-242 | icd | 1.1.1.42 | C | Belongs to the isocitrate and isopropylmalate dehydrogenases family | |
KFEKAFMK_00580 | 2.3e-256 | G | ABC transporter substrate-binding protein | |||
KFEKAFMK_00581 | 5.2e-36 | M | Peptidase family M23 | |||
KFEKAFMK_00583 | 2.1e-166 | xerH | L | Phage integrase family | ||
KFEKAFMK_00584 | 4.4e-127 | 2.7.11.1 | S | HipA-like C-terminal domain | ||
KFEKAFMK_00588 | 2.4e-57 | ard | S | Antirestriction protein (ArdA) | ||
KFEKAFMK_00590 | 2.5e-86 | M | G5 domain protein | |||
KFEKAFMK_00591 | 7.7e-68 | |||||
KFEKAFMK_00594 | 7.7e-241 | topB | 5.99.1.2 | L | DNA topoisomerase | |
KFEKAFMK_00597 | 2.8e-16 | K | Bacterial mobilisation protein (MobC) | |||
KFEKAFMK_00598 | 2.2e-36 | S | Pfam:CtkA_N | |||
KFEKAFMK_00600 | 7.6e-26 | ecoRIIR | 3.1.21.4 | L | EcoRII C terminal | |
KFEKAFMK_00601 | 4.6e-126 | S | Fic/DOC family | |||
KFEKAFMK_00602 | 4.1e-136 | L | PFAM Relaxase mobilization nuclease family protein | |||
KFEKAFMK_00603 | 4.5e-87 | 2.7.11.1 | S | HipA-like C-terminal domain | ||
KFEKAFMK_00605 | 1.8e-39 | |||||
KFEKAFMK_00606 | 1.2e-49 | S | Domain of unknown function (DUF4913) | |||
KFEKAFMK_00607 | 1e-230 | U | TraM recognition site of TraD and TraG | |||
KFEKAFMK_00608 | 5.6e-22 | |||||
KFEKAFMK_00609 | 2.8e-07 | |||||
KFEKAFMK_00611 | 8.9e-202 | traD | S | COG0433 Predicted ATPase | ||
KFEKAFMK_00612 | 4.4e-187 | |||||
KFEKAFMK_00613 | 1.7e-141 | |||||
KFEKAFMK_00614 | 2.2e-29 | |||||
KFEKAFMK_00615 | 9e-33 | |||||
KFEKAFMK_00616 | 1.8e-08 | |||||
KFEKAFMK_00617 | 8e-21 | |||||
KFEKAFMK_00618 | 0.0 | XK27_00515 | D | Cell surface antigen C-terminus | ||
KFEKAFMK_00619 | 1e-38 | |||||
KFEKAFMK_00621 | 1.4e-30 | parA | D | VirC1 protein | ||
KFEKAFMK_00622 | 5.8e-16 | S | Transcription factor WhiB | |||
KFEKAFMK_00623 | 1.3e-15 | S | Helix-turn-helix domain | |||
KFEKAFMK_00629 | 1.4e-16 | |||||
KFEKAFMK_00631 | 8.1e-196 | tsaD | 2.3.1.234 | O | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaE and TsaB. TsaD likely plays a direct catalytic role in this reaction | |
KFEKAFMK_00632 | 2.1e-103 | rimI | 2.3.1.128, 2.3.1.234 | K | FR47-like protein | |
KFEKAFMK_00633 | 3.9e-159 | yeaZ | 2.3.1.234 | O | Glycoprotease family | |
KFEKAFMK_00634 | 4e-88 | ydiB | 2.7.1.221, 5.1.1.1 | S | Threonylcarbamoyl adenosine biosynthesis protein TsaE | |
KFEKAFMK_00635 | 2.4e-173 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
KFEKAFMK_00636 | 1.5e-308 | comE | S | Competence protein | ||
KFEKAFMK_00637 | 2.3e-77 | comEA | 2.4.1.21 | GT5 | L | Helix-hairpin-helix motif |
KFEKAFMK_00638 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
KFEKAFMK_00639 | 5.5e-161 | ET | Bacterial periplasmic substrate-binding proteins | |||
KFEKAFMK_00640 | 5.3e-170 | corA | P | CorA-like Mg2+ transporter protein | ||
KFEKAFMK_00641 | 2.1e-165 | 3.1.3.85, 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | ||
KFEKAFMK_00642 | 7e-234 | L | ribosomal rna small subunit methyltransferase | |||
KFEKAFMK_00643 | 4.1e-71 | pdxH | S | Pfam:Pyridox_oxidase | ||
KFEKAFMK_00644 | 3.4e-169 | EG | EamA-like transporter family | |||
KFEKAFMK_00645 | 2.1e-131 | C | Putative TM nitroreductase | |||
KFEKAFMK_00646 | 9.5e-31 | |||||
KFEKAFMK_00647 | 1.7e-256 | S | Metal-independent alpha-mannosidase (GH125) | |||
KFEKAFMK_00648 | 4.9e-240 | yihS | 5.1.3.11 | G | N-acylglucosamine 2-epimerase (GlcNAc 2-epimerase) | |
KFEKAFMK_00649 | 7.6e-208 | K | helix_turn _helix lactose operon repressor | |||
KFEKAFMK_00650 | 0.0 | 3.2.1.96 | G | Glycosyl hydrolase family 85 | ||
KFEKAFMK_00651 | 0.0 | 3.2.1.20 | GH31 | G | Belongs to the glycosyl hydrolase 31 family | |
KFEKAFMK_00652 | 7.3e-263 | G | Belongs to the glycosyl hydrolase 5 (cellulase A) family | |||
KFEKAFMK_00653 | 5.2e-156 | lacG | G | Binding-protein-dependent transport system inner membrane component | ||
KFEKAFMK_00654 | 4.3e-172 | malC | G | Binding-protein-dependent transport system inner membrane component | ||
KFEKAFMK_00655 | 3e-245 | srrA1 | G | Bacterial extracellular solute-binding protein | ||
KFEKAFMK_00656 | 0.0 | 3.2.1.24 | GH38 | G | Alpha mannosidase, middle domain | |
KFEKAFMK_00657 | 0.0 | 3.2.1.24 | GH38 | G | Alpha mannosidase, middle domain | |
KFEKAFMK_00658 | 0.0 | 3.2.1.24 | GH38 | G | Alpha mannosidase, middle domain | |
KFEKAFMK_00659 | 7.1e-86 | dtd | J | rejects L-amino acids rather than detecting D-amino acids in the active site. By recycling D-aminoacyl-tRNA to D-amino acids and free tRNA molecules, this enzyme counteracts the toxicity associated with the formation of D-aminoacyl-tRNA entities in vivo and helps enforce protein L-homochirality | ||
KFEKAFMK_00660 | 2.2e-51 | S | Appr-1'-p processing enzyme | |||
KFEKAFMK_00661 | 1.2e-30 | lacS | G | Psort location CytoplasmicMembrane, score 10.00 | ||
KFEKAFMK_00662 | 1.5e-13 | sprF | 4.6.1.1 | M | Cell surface antigen C-terminus | |
KFEKAFMK_00663 | 3.6e-15 | L | Phage integrase family | |||
KFEKAFMK_00665 | 3.8e-160 | trmB | 2.1.1.297, 2.1.1.33, 2.4.99.12, 2.4.99.13, 2.4.99.14, 2.4.99.15 | GT30 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA |
KFEKAFMK_00668 | 1.6e-262 | cma | 2.1.1.79 | M | Mycolic acid cyclopropane synthetase | |
KFEKAFMK_00669 | 5.2e-204 | fucO | 1.1.1.1, 1.1.1.77, 1.1.99.37, 1.2.98.1 | C | Iron-containing alcohol dehydrogenase | |
KFEKAFMK_00670 | 5.2e-178 | 3.4.14.13 | M | Glycosyltransferase like family 2 | ||
KFEKAFMK_00671 | 2.8e-272 | S | AI-2E family transporter | |||
KFEKAFMK_00672 | 4.7e-235 | epsG | M | Glycosyl transferase family 21 | ||
KFEKAFMK_00673 | 1.2e-189 | natA | V | ATPases associated with a variety of cellular activities | ||
KFEKAFMK_00674 | 1.8e-298 | |||||
KFEKAFMK_00675 | 3.7e-250 | dacB | 3.4.16.4 | M | D-Ala-D-Ala carboxypeptidase 3 (S13) family | |
KFEKAFMK_00676 | 2.3e-207 | 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 | |
KFEKAFMK_00677 | 2.7e-97 | hpt | 2.4.2.8, 6.3.4.19 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
KFEKAFMK_00678 | 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 | ||
KFEKAFMK_00679 | 3.6e-117 | folE | 2.7.6.3, 3.5.4.16 | H | GTP cyclohydrolase | |
KFEKAFMK_00680 | 1.1e-156 | folP | 1.13.11.81, 2.5.1.15, 2.7.6.3, 4.1.2.25, 5.1.99.8 | H | Catalyzes the condensation of para-aminobenzoate (pABA) with 6-hydroxymethyl-7,8-dihydropterin diphosphate (DHPt-PP) to form 7,8-dihydropteroate (H2Pte), the immediate precursor of folate derivatives | |
KFEKAFMK_00681 | 4.2e-300 | folK | 1.13.11.81, 2.5.1.15, 2.7.6.3, 3.5.4.16, 3.5.4.39, 4.1.2.25, 5.1.99.8 | H | Catalyzes the conversion of 7,8-dihydroneopterin to 6- hydroxymethyl-7,8-dihydropterin | |
KFEKAFMK_00682 | 2.5e-92 | S | Protein of unknown function (DUF3180) | |||
KFEKAFMK_00683 | 3.3e-169 | tesB | I | Thioesterase-like superfamily | ||
KFEKAFMK_00684 | 0.0 | yjjK | S | ATP-binding cassette protein, ChvD family | ||
KFEKAFMK_00685 | 1.7e-232 | 2.7.11.1 | S | HipA-like C-terminal domain | ||
KFEKAFMK_00686 | 1.4e-38 | K | Helix-turn-helix XRE-family like proteins | |||
KFEKAFMK_00687 | 3.2e-27 | K | transcriptional regulator | |||
KFEKAFMK_00688 | 9.9e-14 | S | Protein of unknown function (DUF1048) | |||
KFEKAFMK_00690 | 7.1e-293 | EGP | Major Facilitator Superfamily | |||
KFEKAFMK_00692 | 7.7e-177 | glkA | 2.7.1.2 | G | ROK family | |
KFEKAFMK_00693 | 3.4e-86 | K | Winged helix DNA-binding domain | |||
KFEKAFMK_00694 | 1.5e-18 | lmrB | U | Major Facilitator Superfamily | ||
KFEKAFMK_00695 | 4.2e-166 | dkgB | S | Oxidoreductase, aldo keto reductase family protein | ||
KFEKAFMK_00696 | 1.8e-69 | def2 | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins | |
KFEKAFMK_00697 | 1.1e-147 | |||||
KFEKAFMK_00698 | 4.2e-75 | EGP | Major facilitator Superfamily | |||
KFEKAFMK_00700 | 1.3e-36 | rpmE | J | Binds the 23S rRNA | ||
KFEKAFMK_00701 | 4.1e-190 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
KFEKAFMK_00702 | 6.5e-154 | prmC | 2.1.1.297 | J | Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif | |
KFEKAFMK_00703 | 2.9e-205 | livK | E | Receptor family ligand binding region | ||
KFEKAFMK_00704 | 5.4e-111 | U | Belongs to the binding-protein-dependent transport system permease family | |||
KFEKAFMK_00705 | 5e-188 | livM | U | Belongs to the binding-protein-dependent transport system permease family | ||
KFEKAFMK_00706 | 1.1e-161 | E | Branched-chain amino acid ATP-binding cassette transporter | |||
KFEKAFMK_00707 | 2.5e-124 | livF | E | ATPases associated with a variety of cellular activities | ||
KFEKAFMK_00708 | 1.5e-118 | ywlC | 2.7.7.87 | J | Belongs to the SUA5 family | |
KFEKAFMK_00709 | 6.7e-213 | tagO | 2.7.8.33, 2.7.8.35 | M | Glycosyl transferase family 4 | |
KFEKAFMK_00710 | 4.8e-293 | guaB | 1.1.1.205 | F | Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate- limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth | |
KFEKAFMK_00711 | 4.8e-122 | orn | L | 3'-to-5' exoribonuclease specific for small oligoribonucleotides | ||
KFEKAFMK_00712 | 2.4e-267 | recD2 | 3.6.4.12 | L | PIF1-like helicase | |
KFEKAFMK_00713 | 2.2e-154 | pflA | 1.97.1.4 | O | Radical SAM superfamily | |
KFEKAFMK_00714 | 0.0 | proS | 6.1.1.15 | J | Catalyzes the attachment of proline to tRNA(Pro) in a two-step reaction proline is first activated by ATP to form Pro- AMP and then transferred to the acceptor end of tRNA(Pro). As ProRS can inadvertently accommodate and process non-cognate amino acids such as alanine and cysteine, to avoid such errors it has two additional distinct editing activities against alanine. One activity is designated as 'pretransfer' editing and involves the tRNA(Pro)-independent hydrolysis of activated Ala-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Ala-tRNA(Pro). The misacylated Cys- tRNA(Pro) is not edited by ProRS | |
KFEKAFMK_00715 | 1e-114 | L | Single-strand binding protein family | |||
KFEKAFMK_00716 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
KFEKAFMK_00717 | 1e-119 | S | Short repeat of unknown function (DUF308) | |||
KFEKAFMK_00718 | 6e-151 | map | 3.4.11.18 | E | Methionine aminopeptidase | |
KFEKAFMK_00719 | 9.2e-250 | gltA | 2.3.3.1 | C | Citrate synthase, C-terminal domain | |
KFEKAFMK_00720 | 3.4e-146 | dapD | 2.3.1.117 | E | Catalyzes the conversion of the cyclic tetrahydrodipicolinate (THDP) into the acyclic N-succinyl-L-2- amino-6-oxopimelate using succinyl-CoA | |
KFEKAFMK_00721 | 0.0 | snf | 2.7.11.1 | KL | Psort location Cytoplasmic, score 8.87 | |
KFEKAFMK_00722 | 4.5e-100 | XK27_03610 | K | Acetyltransferase (GNAT) domain | ||
KFEKAFMK_00723 | 2.2e-87 | vsr | L | May nick specific sequences that contain T G mispairs resulting from m5C-deamination | ||
KFEKAFMK_00724 | 5.5e-200 | afr_2 | S | Oxidoreductase family, NAD-binding Rossmann fold | ||
KFEKAFMK_00725 | 3.9e-234 | aspB | E | Aminotransferase class-V | ||
KFEKAFMK_00726 | 9.9e-180 | ppx | 3.6.1.11, 3.6.1.40 | FP | Ppx/GppA phosphatase family | |
KFEKAFMK_00727 | 1.6e-200 | S | Endonuclease/Exonuclease/phosphatase family | |||
KFEKAFMK_00729 | 3.7e-78 | F | Nucleoside 2-deoxyribosyltransferase | |||
KFEKAFMK_00730 | 3.2e-65 | mscL | M | Channel that opens in response to stretch forces in the membrane lipid bilayer. May participate in the regulation of osmotic pressure changes within the cell | ||
KFEKAFMK_00731 | 0.0 | fadD | 6.2.1.3 | I | AMP-binding enzyme | |
KFEKAFMK_00732 | 2.4e-90 | ywrO | 1.6.5.2 | S | Flavodoxin-like fold | |
KFEKAFMK_00733 | 3.5e-40 | 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 | |
KFEKAFMK_00734 | 5.3e-256 | 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 | |
KFEKAFMK_00735 | 0.0 | nrdD | 1.1.98.6 | F | Anaerobic ribonucleoside-triphosphate reductase | |
KFEKAFMK_00736 | 6.5e-136 | nrdG | 1.97.1.4 | O | Activation of anaerobic ribonucleoside-triphosphate reductase under anaerobic conditions by generation of an organic free radical, using S-adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine | |
KFEKAFMK_00737 | 0.0 | hgdC | I | CoA enzyme activase uncharacterised domain (DUF2229) | ||
KFEKAFMK_00738 | 4.2e-255 | gshA | 6.3.2.2 | H | Glutamate-cysteine ligase family 2(GCS2) | |
KFEKAFMK_00739 | 2e-140 | K | Bacterial regulatory proteins, tetR family | |||
KFEKAFMK_00740 | 0.0 | bgl2 | 3.2.1.21 | GH3 | G | Fibronectin type III-like domain |
KFEKAFMK_00741 | 3e-37 | S | PIN domain | |||
KFEKAFMK_00742 | 8.3e-23 | K | Antidote-toxin recognition MazE, bacterial antitoxin | |||
KFEKAFMK_00743 | 8.3e-70 | mgtC | S | MgtC family | ||
KFEKAFMK_00744 | 5.8e-20 | yclK | 2.7.13.3 | T | PhoQ Sensor | |
KFEKAFMK_00745 | 3.9e-52 | K | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
KFEKAFMK_00746 | 7.3e-199 | G | Transporter major facilitator family protein | |||
KFEKAFMK_00747 | 4.4e-81 | K | Bacterial regulatory proteins, tetR family | |||
KFEKAFMK_00748 | 8.1e-248 | 2.7.7.7 | S | Protein of unknown function (DUF4038) | ||
KFEKAFMK_00749 | 6.7e-198 | G | Psort location CytoplasmicMembrane, score 10.00 | |||
KFEKAFMK_00750 | 3.3e-46 | S | Nucleotidyltransferase domain | |||
KFEKAFMK_00751 | 1.9e-68 | S | Nucleotidyltransferase substrate binding protein like | |||
KFEKAFMK_00752 | 8.9e-212 | 3.2.1.58 | G | Belongs to the glycosyl hydrolase 5 (cellulase A) family | ||
KFEKAFMK_00753 | 7.6e-43 | shetA | P | Voltage-dependent anion channel | ||
KFEKAFMK_00754 | 6.8e-77 | I | Hydrolase, alpha beta domain protein | |||
KFEKAFMK_00755 | 8e-113 | G | Major Facilitator Superfamily | |||
KFEKAFMK_00756 | 5.8e-32 | K | Bacterial regulatory proteins, tetR family | |||
KFEKAFMK_00757 | 2.5e-85 | K | Bacterial regulatory proteins, tetR family | |||
KFEKAFMK_00758 | 0.0 | bglB | 3.2.1.21 | GH3 | G | Glycosyl hydrolase family 3 N-terminal domain protein |
KFEKAFMK_00759 | 1.9e-87 | K | MarR family | |||
KFEKAFMK_00760 | 0.0 | V | ABC transporter, ATP-binding protein | |||
KFEKAFMK_00761 | 0.0 | V | ABC transporter transmembrane region | |||
KFEKAFMK_00762 | 1.9e-125 | rbsR | K | helix_turn _helix lactose operon repressor | ||
KFEKAFMK_00763 | 2.4e-43 | K | acetyltransferase | |||
KFEKAFMK_00764 | 2.6e-105 | rihB | 3.2.2.1 | F | Inosine-uridine preferring nucleoside hydrolase | |
KFEKAFMK_00765 | 4.7e-162 | dcuD | C | C4-dicarboxylate anaerobic carrier | ||
KFEKAFMK_00766 | 3.9e-152 | rbsK | 2.7.1.15 | H | Catalyzes the phosphorylation of ribose at O-5 in a reaction requiring ATP and magnesium. The resulting D-ribose-5- phosphate can then be used either for sythesis of nucleotides, histidine, and tryptophan, or as a component of the pentose phosphate pathway | |
KFEKAFMK_00767 | 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) | |
KFEKAFMK_00768 | 8.2e-238 | hsdR | 3.1.21.3 | V | Subunit R is required for both nuclease and ATPase activities, but not for modification | |
KFEKAFMK_00770 | 9e-150 | G | Fic/DOC family | |||
KFEKAFMK_00771 | 2.2e-229 | metK | 2.5.1.6 | H | Catalyzes the formation of S-adenosylmethionine (AdoMet) from methionine and ATP. The overall synthetic reaction is composed of two sequential steps, AdoMet formation and the subsequent tripolyphosphate hydrolysis which occurs prior to release of AdoMet from the enzyme | |
KFEKAFMK_00772 | 4.2e-46 | rpoZ | 2.7.7.6 | K | Promotes RNA polymerase assembly. Latches the N- and C- terminal regions of the beta' subunit thereby facilitating its interaction with the beta and alpha subunits | |
KFEKAFMK_00773 | 0.0 | ilvD | 4.2.1.9 | H | Belongs to the IlvD Edd family | |
KFEKAFMK_00774 | 1.3e-185 | fmt | 2.1.1.176, 2.1.2.9 | J | Attaches a formyl group to the free amino group of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by promoting its recognition by IF2 and preventing the misappropriation of this tRNA by the elongation apparatus | |
KFEKAFMK_00775 | 5.6e-132 | 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | ||
KFEKAFMK_00776 | 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 | ||
KFEKAFMK_00777 | 5.5e-119 | serB | 3.1.3.3 | E | haloacid dehalogenase-like hydrolase | |
KFEKAFMK_00778 | 6.5e-125 | apl | 3.1.3.1 | S | SNARE associated Golgi protein | |
KFEKAFMK_00779 | 3.3e-286 | arc | O | AAA ATPase forming ring-shaped complexes | ||
KFEKAFMK_00780 | 6e-134 | 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | ||
KFEKAFMK_00781 | 2.4e-278 | manR | K | PRD domain | ||
KFEKAFMK_00782 | 8.8e-72 | H | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |||
KFEKAFMK_00783 | 2.6e-77 | 2.7.1.194, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
KFEKAFMK_00784 | 2.1e-46 | fruA | 2.7.1.202 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
KFEKAFMK_00785 | 6.9e-161 | G | Phosphotransferase System | |||
KFEKAFMK_00786 | 2.1e-134 | alsE | 5.1.3.1 | G | Ribulose-phosphate 3 epimerase family | |
KFEKAFMK_00787 | 0.0 | dop | 3.5.1.119, 6.3.1.19 | S | Pup-ligase protein | |
KFEKAFMK_00788 | 8.9e-175 | hisN | 3.1.3.25 | G | Inositol monophosphatase family | |
KFEKAFMK_00790 | 8.6e-284 | pafA | 6.3.1.19 | O | Catalyzes the covalent attachment of the prokaryotic ubiquitin-like protein modifier Pup to the proteasomal substrate proteins, thereby targeting them for proteasomal degradation. This tagging system is termed pupylation. The ligation reaction involves the side-chain carboxylate of the C-terminal glutamate of Pup and the side-chain amino group of a substrate lysine | |
KFEKAFMK_00791 | 8.1e-42 | hup | L | Belongs to the bacterial histone-like protein family | ||
KFEKAFMK_00792 | 0.0 | S | Lysylphosphatidylglycerol synthase TM region | |||
KFEKAFMK_00793 | 2e-277 | purB | 4.3.2.2 | F | Adenylosuccinate lyase C-terminal | |
KFEKAFMK_00794 | 1.4e-110 | ykoE | S | ABC-type cobalt transport system, permease component | ||
KFEKAFMK_00795 | 2.9e-253 | S | PGAP1-like protein | |||
KFEKAFMK_00796 | 3.1e-56 | |||||
KFEKAFMK_00797 | 9.3e-152 | S | von Willebrand factor (vWF) type A domain | |||
KFEKAFMK_00798 | 3.3e-189 | S | von Willebrand factor (vWF) type A domain | |||
KFEKAFMK_00799 | 6.1e-86 | |||||
KFEKAFMK_00800 | 3.7e-163 | S | Protein of unknown function DUF58 | |||
KFEKAFMK_00801 | 6.2e-183 | moxR | S | ATPase family associated with various cellular activities (AAA) | ||
KFEKAFMK_00802 | 1.4e-132 | 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 | |
KFEKAFMK_00803 | 9.9e-83 | S | LytR cell envelope-related transcriptional attenuator | |||
KFEKAFMK_00804 | 6.1e-38 | K | 'Cold-shock' DNA-binding domain | |||
KFEKAFMK_00805 | 2.7e-291 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
KFEKAFMK_00806 | 4.2e-33 | S | Proteins of 100 residues with WXG | |||
KFEKAFMK_00807 | 8.7e-100 | |||||
KFEKAFMK_00808 | 4.4e-132 | KT | Response regulator receiver domain protein | |||
KFEKAFMK_00809 | 1.6e-309 | 2.7.13.3 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | ||
KFEKAFMK_00810 | 1.7e-66 | cspB | K | 'Cold-shock' DNA-binding domain | ||
KFEKAFMK_00811 | 4.6e-175 | S | Protein of unknown function (DUF3027) | |||
KFEKAFMK_00812 | 7.4e-178 | uspA | T | Belongs to the universal stress protein A family | ||
KFEKAFMK_00813 | 0.0 | clpC | O | ATPase family associated with various cellular activities (AAA) | ||
KFEKAFMK_00814 | 1.5e-25 | K | helix_turn_helix, arabinose operon control protein | |||
KFEKAFMK_00815 | 3e-132 | xylE | U | Sugar (and other) transporter | ||
KFEKAFMK_00816 | 1.6e-58 | lipA | I | Hydrolase, alpha beta domain protein | ||
KFEKAFMK_00817 | 0.0 | 3.1.3.5 | F | 5'-nucleotidase, C-terminal domain | ||
KFEKAFMK_00818 | 8.2e-223 | 3.1.26.12, 3.2.1.8 | S | Domain of Unknown Function (DUF349) | ||
KFEKAFMK_00819 | 4.5e-261 | hisS | 6.1.1.21 | J | Histidyl-tRNA synthetase | |
KFEKAFMK_00820 | 0.0 | aspS | 6.1.1.12 | J | Aspartyl-tRNA synthetase with relaxed tRNA specificity since it is able to aspartylate not only its cognate tRNA(Asp) but also tRNA(Asn). Reaction proceeds in two steps L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp Asn) | |
KFEKAFMK_00821 | 2e-100 | S | Aminoacyl-tRNA editing domain | |||
KFEKAFMK_00822 | 1.7e-151 | gluA | 3.6.3.21 | E | ATP-binding protein of ABC transporter for glutamate K02028 | |
KFEKAFMK_00823 | 7.7e-146 | gluB | ET | Belongs to the bacterial solute-binding protein 3 family | ||
KFEKAFMK_00824 | 2e-110 | gluC | E | Binding-protein-dependent transport system inner membrane component | ||
KFEKAFMK_00825 | 2.7e-194 | gluD | E | Binding-protein-dependent transport system inner membrane component | ||
KFEKAFMK_00826 | 1.7e-290 | phoN | I | PAP2 superfamily | ||
KFEKAFMK_00827 | 1.3e-111 | argO | S | LysE type translocator | ||
KFEKAFMK_00828 | 1.6e-285 | ydfD | EK | Alanine-glyoxylate amino-transferase | ||
KFEKAFMK_00829 | 1.2e-197 | 2.7.4.1 | S | Polyphosphate kinase 2 (PPK2) | ||
KFEKAFMK_00830 | 0.0 | helY | L | DEAD DEAH box helicase | ||
KFEKAFMK_00831 | 8.9e-251 | rarA | L | Recombination factor protein RarA | ||
KFEKAFMK_00832 | 6.9e-11 | KT | Transcriptional regulatory protein, C terminal | |||
KFEKAFMK_00833 | 3.3e-35 | KT | Transcriptional regulatory protein, C terminal | |||
KFEKAFMK_00834 | 1.1e-40 | KT | Transcriptional regulatory protein, C terminal | |||
KFEKAFMK_00835 | 1.4e-33 | mtrB | 2.7.13.3 | T | HAMP (Histidine kinases, Adenylyl cyclases, Methyl binding proteins, Phosphatases) domain | |
KFEKAFMK_00836 | 7.3e-251 | EGP | Major facilitator Superfamily | |||
KFEKAFMK_00837 | 1.4e-186 | ghrA | EH | D-isomer specific 2-hydroxyacid dehydrogenase, NAD binding domain | ||
KFEKAFMK_00838 | 1.8e-52 | |||||
KFEKAFMK_00839 | 1.2e-47 | yvlD | S | Mycobacterial 4 TMS phage holin, superfamily IV | ||
KFEKAFMK_00840 | 3.1e-47 | yhbY | J | CRS1_YhbY | ||
KFEKAFMK_00841 | 0.0 | ecfA | GP | ABC transporter, ATP-binding protein | ||
KFEKAFMK_00842 | 3.6e-93 | ribU | U | Mediates riboflavin uptake, may also transport FMN and roseoflavin. Probably a riboflavin-binding protein that interacts with the energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates. The substrates themselves are bound by transmembrane, not extracytoplasmic soluble proteins | ||
KFEKAFMK_00843 | 6e-196 | S | Glycosyltransferase, group 2 family protein | |||
KFEKAFMK_00844 | 7.6e-146 | C | Putative TM nitroreductase | |||
KFEKAFMK_00845 | 3.6e-140 | ppgK | 2.7.1.2, 2.7.1.63 | GK | ROK family | |
KFEKAFMK_00846 | 3e-303 | cscA | 3.2.1.26 | GH32 | G | Belongs to the glycosyl hydrolase 32 family |
KFEKAFMK_00847 | 6.2e-241 | lacY | P | LacY proton/sugar symporter | ||
KFEKAFMK_00848 | 1.8e-195 | K | helix_turn _helix lactose operon repressor | |||
KFEKAFMK_00849 | 2.3e-257 | O | SERine Proteinase INhibitors | |||
KFEKAFMK_00850 | 1.1e-189 | |||||
KFEKAFMK_00851 | 6.1e-123 | K | helix_turn_helix, Lux Regulon | |||
KFEKAFMK_00852 | 8.9e-214 | 2.7.13.3 | T | Histidine kinase | ||
KFEKAFMK_00853 | 7.1e-248 | ydjK | G | Sugar (and other) transporter | ||
KFEKAFMK_00854 | 5.6e-62 | S | Thiamine-binding protein | |||
KFEKAFMK_00855 | 8.7e-145 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
KFEKAFMK_00856 | 5.4e-228 | O | AAA domain (Cdc48 subfamily) | |||
KFEKAFMK_00857 | 0.0 | thiC | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Catalyzes the synthesis of the hydroxymethylpyrimidine phosphate (HMP-P) moiety of thiamine from aminoimidazole ribotide (AIR) in a radical S-adenosyl-L-methionine (SAM)-dependent reaction | |
KFEKAFMK_00858 | 1.1e-167 | thiM | 2.7.1.50 | H | Catalyzes the phosphorylation of the hydroxyl group of 4-methyl-5-beta-hydroxyethylthiazole (THZ) | |
KFEKAFMK_00859 | 4.8e-96 | |||||
KFEKAFMK_00860 | 5.3e-68 | marR5 | K | Winged helix DNA-binding domain | ||
KFEKAFMK_00861 | 9.1e-105 | |||||
KFEKAFMK_00862 | 1.3e-139 | cbiO | V | ATPases associated with a variety of cellular activities | ||
KFEKAFMK_00863 | 2.8e-123 | |||||
KFEKAFMK_00864 | 1.1e-296 | glyQS | 6.1.1.14 | J | Catalyzes the attachment of glycine to tRNA(Gly) | |
KFEKAFMK_00865 | 3.7e-248 | 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 | ||
KFEKAFMK_00866 | 1.2e-211 | 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 | ||
KFEKAFMK_00867 | 6.6e-68 | 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 | ||
KFEKAFMK_00868 | 1.5e-44 | yggT | S | YGGT family | ||
KFEKAFMK_00869 | 5.3e-22 | tccB2 | V | DivIVA protein | ||
KFEKAFMK_00870 | 2.3e-88 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
KFEKAFMK_00871 | 1.7e-176 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
KFEKAFMK_00872 | 3.9e-198 | K | WYL domain | |||
KFEKAFMK_00873 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase III alpha subunit | |
KFEKAFMK_00874 | 1.4e-68 | yneG | S | Domain of unknown function (DUF4186) | ||
KFEKAFMK_00875 | 1.3e-167 | dkgA | 1.1.1.346 | C | Aldo/keto reductase family | |
KFEKAFMK_00876 | 0.0 | 4.2.1.53 | S | MCRA family | ||
KFEKAFMK_00877 | 1.3e-25 | zntR | K | bacterial-type RNA polymerase transcription factor activity, metal ion regulated sequence-specific DNA binding | ||
KFEKAFMK_00878 | 0.0 | glgX | 3.2.1.68 | CBM48,GH13 | G | Belongs to the glycosyl hydrolase 13 family |
KFEKAFMK_00879 | 4e-127 | 3.6.1.13 | L | NUDIX domain | ||
KFEKAFMK_00880 | 2e-177 | yqfO | 3.5.4.16 | L | NIF3 (NGG1p interacting factor 3) | |
KFEKAFMK_00881 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
KFEKAFMK_00882 | 1.2e-122 | pdtaR | T | Response regulator receiver domain protein | ||
KFEKAFMK_00884 | 2.8e-108 | aspA | 3.6.1.13 | L | NUDIX domain | |
KFEKAFMK_00885 | 1.5e-272 | pyk | 2.7.1.40 | G | Pyruvate kinase | |
KFEKAFMK_00886 | 1e-176 | terC | P | Integral membrane protein, TerC family | ||
KFEKAFMK_00887 | 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 | ||
KFEKAFMK_00888 | 2.1e-106 | coaE | 2.7.1.24 | H | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
KFEKAFMK_00889 | 7.1e-254 | rpsA | J | Ribosomal protein S1 | ||
KFEKAFMK_00890 | 5.8e-163 | folD | 1.5.1.5, 3.5.4.9 | F | Catalyzes the oxidation of 5,10- methylenetetrahydrofolate to 5,10-methenyltetrahydrofolate and then the hydrolysis of 5,10-methenyltetrahydrofolate to 10- formyltetrahydrofolate | |
KFEKAFMK_00891 | 1.2e-182 | P | Zinc-uptake complex component A periplasmic | |||
KFEKAFMK_00892 | 8.4e-162 | znuC | P | ATPases associated with a variety of cellular activities | ||
KFEKAFMK_00893 | 7.5e-136 | znuB | U | ABC 3 transport family | ||
KFEKAFMK_00894 | 3.1e-87 | ispF | 2.1.1.228, 2.7.7.60, 4.6.1.12 | H | Involved in the biosynthesis of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP), two major building blocks of isoprenoid compounds. Catalyzes the conversion of 4- diphosphocytidyl-2-C-methyl-D-erythritol 2-phosphate (CDP-ME2P) to 2-C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-CPP) with a corresponding release of cytidine 5-monophosphate (CMP) | |
KFEKAFMK_00895 | 2.1e-100 | carD | K | CarD-like/TRCF domain | ||
KFEKAFMK_00896 | 0.0 | glgB | 2.4.1.18 | CBM48,GH13 | G | Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position |
KFEKAFMK_00897 | 1e-128 | T | Response regulator receiver domain protein | |||
KFEKAFMK_00898 | 4.4e-197 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | |||
KFEKAFMK_00899 | 3.9e-103 | ctsW | S | Phosphoribosyl transferase domain | ||
KFEKAFMK_00900 | 1.8e-147 | cof | 5.2.1.8 | T | Eukaryotic phosphomannomutase | |
KFEKAFMK_00901 | 6.3e-78 | MA20_43655 | 2.7.2.8 | S | Zincin-like metallopeptidase | |
KFEKAFMK_00902 | 2.8e-253 | |||||
KFEKAFMK_00903 | 0.0 | S | Glycosyl transferase, family 2 | |||
KFEKAFMK_00904 | 1.8e-55 | whiB | K | Acts as a transcriptional regulator. Probably redox- responsive. The apo- but not holo-form probably binds DNA | ||
KFEKAFMK_00905 | 3.2e-205 | K | Cell envelope-related transcriptional attenuator domain | |||
KFEKAFMK_00906 | 0.0 | D | FtsK/SpoIIIE family | |||
KFEKAFMK_00907 | 4.9e-47 | whiB | K | Acts as a transcriptional regulator. Probably redox- responsive. The apo- but not holo-form probably binds DNA | ||
KFEKAFMK_00908 | 1.1e-278 | pdtaS | 2.7.13.3 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | |
KFEKAFMK_00909 | 2e-145 | yplQ | S | Haemolysin-III related | ||
KFEKAFMK_00910 | 4.4e-80 | greA | K | Necessary for efficient RNA polymerase transcription elongation past template-encoded arresting sites. The arresting sites in DNA have the property of trapping a certain fraction of elongating RNA polymerases that pass through, resulting in locked ternary complexes. Cleavage of the nascent transcript by cleavage factors such as GreA or GreB allows the resumption of elongation from the new 3'terminus. GreA releases sequences of 2 to 3 nucleotides | ||
KFEKAFMK_00911 | 1.4e-74 | fkbP | 5.2.1.8 | G | Peptidyl-prolyl cis-trans | |
KFEKAFMK_00912 | 1.8e-281 | sdaA | 4.3.1.17 | E | Serine dehydratase alpha chain | |
KFEKAFMK_00913 | 2.7e-92 | |||||
KFEKAFMK_00915 | 1.3e-182 | ppx | 3.6.1.11, 3.6.1.40 | FP | Ppx/GppA phosphatase family | |
KFEKAFMK_00916 | 8.2e-102 | ppx2 | 3.6.1.11, 3.6.1.40 | S | Protein of unknown function (DUF501) | |
KFEKAFMK_00917 | 1.4e-67 | divIC | D | Septum formation initiator | ||
KFEKAFMK_00918 | 2.6e-244 | eno | 4.2.1.11 | G | Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis | |
KFEKAFMK_00919 | 6e-179 | 1.1.1.65 | C | Aldo/keto reductase family | ||
KFEKAFMK_00920 | 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 | ||
KFEKAFMK_00921 | 3.4e-114 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
KFEKAFMK_00922 | 2.5e-90 | 2.3.1.183 | M | Acetyltransferase (GNAT) domain | ||
KFEKAFMK_00923 | 0.0 | S | Uncharacterised protein family (UPF0182) | |||
KFEKAFMK_00924 | 1.4e-17 | ybbD | 3.2.1.52 | G | Glycosyl hydrolase family 3 N-terminal domain protein | |
KFEKAFMK_00925 | 2.2e-91 | ybbD | 3.2.1.52 | G | Glycosyl hydrolase family 3 N-terminal domain protein | |
KFEKAFMK_00926 | 3.2e-138 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
KFEKAFMK_00927 | 1.9e-98 | |||||
KFEKAFMK_00928 | 3.1e-237 | proA | 1.2.1.41 | E | Catalyzes the NADPH-dependent reduction of L-glutamate 5-phosphate into L-glutamate 5-semialdehyde and phosphate. The product spontaneously undergoes cyclization to form 1-pyrroline-5- carboxylate | |
KFEKAFMK_00929 | 4.7e-282 | thrC | 4.2.3.1 | E | Threonine synthase N terminus | |
KFEKAFMK_00930 | 3.1e-196 | S | Protein of unknown function (DUF1648) | |||
KFEKAFMK_00931 | 7.8e-71 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
KFEKAFMK_00932 | 8.8e-25 | pacL2 | 3.6.3.8 | P | ATPase, P-type transporting, HAD superfamily, subfamily IC | |
KFEKAFMK_00933 | 4.8e-107 | |||||
KFEKAFMK_00934 | 9.3e-119 | S | ABC-2 family transporter protein | |||
KFEKAFMK_00935 | 9.4e-172 | V | ATPases associated with a variety of cellular activities | |||
KFEKAFMK_00936 | 1.3e-58 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
KFEKAFMK_00937 | 2.2e-33 | J | Acetyltransferase (GNAT) domain | |||
KFEKAFMK_00938 | 1.5e-11 | J | Acetyltransferase (GNAT) domain | |||
KFEKAFMK_00939 | 2.3e-116 | S | Haloacid dehalogenase-like hydrolase | |||
KFEKAFMK_00940 | 0.0 | recN | L | May be involved in recombinational repair of damaged DNA | ||
KFEKAFMK_00941 | 5.1e-184 | nadK | 2.7.1.23 | H | Involved in the regulation of the intracellular balance of NAD and NADP, and is a key enzyme in the biosynthesis of NADP. Catalyzes specifically the phosphorylation on 2'-hydroxyl of the adenosine moiety of NAD to yield NADP | |
KFEKAFMK_00942 | 1.2e-17 | trkB | P | Cation transport protein | ||
KFEKAFMK_00943 | 8.3e-12 | trkB | P | Cation transport protein | ||
KFEKAFMK_00944 | 8.1e-70 | trkA | P | TrkA-N domain |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)