ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
LKEPKNME_00001 | 1e-29 | E | IrrE N-terminal-like domain | |||
LKEPKNME_00006 | 2.3e-60 | NU | StbA protein | |||
LKEPKNME_00008 | 2e-18 | yefM | 2.3.1.15 | D | Antitoxin component of a toxin-antitoxin (TA) module | |
LKEPKNME_00014 | 2.3e-14 | |||||
LKEPKNME_00016 | 2.1e-89 | L | Lactococcus lactis RepB C-terminus | |||
LKEPKNME_00017 | 8.6e-08 | pi112 | 3.6.4.12 | L | PDDEXK-like domain of unknown function (DUF3799) | |
LKEPKNME_00019 | 8.7e-214 | ltrA_1 | 2.7.7.49 | L | PFAM RNA-directed DNA polymerase (Reverse transcriptase) | |
LKEPKNME_00030 | 1.5e-28 | yedF | O | Belongs to the sulfur carrier protein TusA family | ||
LKEPKNME_00031 | 3.2e-148 | yedE | S | Sulphur transport | ||
LKEPKNME_00032 | 3.7e-97 | tnp2 | L | Transposase | ||
LKEPKNME_00033 | 3.2e-56 | ydiB | 2.7.1.221, 5.1.1.1 | O | Hydrolase, P-loop family | |
LKEPKNME_00034 | 1.9e-73 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
LKEPKNME_00035 | 1.6e-54 | L | Helix-turn-helix domain | |||
LKEPKNME_00037 | 3.7e-23 | K | Acetyltransferase (GNAT) domain | |||
LKEPKNME_00038 | 6.2e-112 | natA | S | Domain of unknown function (DUF4162) | ||
LKEPKNME_00039 | 2.2e-56 | L | Helix-turn-helix domain | |||
LKEPKNME_00041 | 8.6e-08 | pi112 | 3.6.4.12 | L | PDDEXK-like domain of unknown function (DUF3799) | |
LKEPKNME_00042 | 2.1e-89 | L | Lactococcus lactis RepB C-terminus | |||
LKEPKNME_00044 | 2.3e-14 | |||||
LKEPKNME_00050 | 2e-18 | yefM | 2.3.1.15 | D | Antitoxin component of a toxin-antitoxin (TA) module | |
LKEPKNME_00052 | 2.3e-60 | NU | StbA protein | |||
LKEPKNME_00057 | 1e-29 | E | IrrE N-terminal-like domain | |||
LKEPKNME_00058 | 0.0 | asnB | 6.3.5.4 | E | Asparagine synthase | |
LKEPKNME_00059 | 5.7e-64 | D | peptidase | |||
LKEPKNME_00060 | 2.8e-116 | S | Glycosyl transferase family 2 | |||
LKEPKNME_00061 | 7.3e-110 | glxR | 1.1.1.31, 1.1.1.60 | I | Dehydrogenase | |
LKEPKNME_00062 | 6.2e-35 | rpsR | J | Binds as a heterodimer with protein S6 to the central domain of the 16S rRNA, where it helps stabilize the platform of the 30S subunit | ||
LKEPKNME_00063 | 2.5e-63 | ssb | L | Plays an important role in DNA replication, recombination and repair. Binds to ssDNA and to an array of partner proteins to recruit them to their sites of action during DNA metabolism | ||
LKEPKNME_00064 | 4.8e-45 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
LKEPKNME_00065 | 0.0 | gyrA | 5.99.1.3 | L | A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner | |
LKEPKNME_00066 | 0.0 | gyrB | 5.99.1.3 | L | A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner | |
LKEPKNME_00067 | 2.9e-154 | recF | L | it is required for DNA replication and normal SOS inducibility. RecF binds preferentially to single-stranded, linear DNA. It also seems to bind ATP | ||
LKEPKNME_00068 | 9e-20 | yaaA | S | S4 domain protein YaaA | ||
LKEPKNME_00069 | 1.4e-15 | dnaN | 2.7.7.7 | L | Confers DNA tethering and processivity to DNA polymerases and other proteins. Acts as a clamp, forming a ring around DNA (a reaction catalyzed by the clamp-loading complex) which diffuses in an ATP-independent manner freely and bidirectionally along dsDNA. Initially characterized for its ability to contact the catalytic subunit of DNA polymerase III (Pol III), a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria | |
LKEPKNME_00076 | 3.3e-41 | O | Belongs to the ClpA ClpB family | |||
LKEPKNME_00082 | 5e-91 | cps1D | M | Domain of unknown function (DUF4422) | ||
LKEPKNME_00083 | 9e-114 | K | response regulator | |||
LKEPKNME_00084 | 7.3e-272 | vicK | 2.7.13.3 | T | Histidine kinase | |
LKEPKNME_00085 | 6e-103 | yycH | S | YycH protein | ||
LKEPKNME_00086 | 4.3e-80 | yycI | S | YycH protein | ||
LKEPKNME_00087 | 8e-31 | yyaQ | S | YjbR | ||
LKEPKNME_00088 | 1.3e-116 | vicX | 3.1.26.11 | S | domain protein | |
LKEPKNME_00089 | 6.2e-145 | htrA | 3.4.21.107 | O | serine protease | |
LKEPKNME_00090 | 4.4e-72 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
LKEPKNME_00091 | 1.4e-44 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
LKEPKNME_00093 | 1.2e-207 | G | glycerol-3-phosphate transporter | |||
LKEPKNME_00094 | 9.2e-137 | S | interspecies interaction between organisms | |||
LKEPKNME_00095 | 5.8e-12 | sbcD | L | SbcCD cleaves DNA hairpin structures. These structures can inhibit DNA replication and are intermediates in certain DNA recombination reactions. The complex acts as a 3'- 5' double strand exonuclease that can open hairpins. It also has a 5' single-strand endonuclease activity | ||
LKEPKNME_00096 | 2.8e-103 | sbcC | L | Putative exonuclease SbcCD, C subunit | ||
LKEPKNME_00097 | 2.9e-57 | S | LexA-binding, inner membrane-associated putative hydrolase | |||
LKEPKNME_00098 | 7.2e-53 | perR | P | Belongs to the Fur family | ||
LKEPKNME_00099 | 7.1e-71 | mltD | CBM50 | M | NlpC P60 family protein | |
LKEPKNME_00100 | 1.1e-129 | serC | 2.6.1.52 | E | Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine | |
LKEPKNME_00101 | 4.9e-165 | serA | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
LKEPKNME_00102 | 3.1e-75 | ung2 | 3.2.2.27 | L | Uracil-DNA glycosylase | |
LKEPKNME_00103 | 1e-47 | traP | 1.14.99.57, 6.2.1.3 | S | enzyme involved in biosynthesis of extracellular polysaccharides | |
LKEPKNME_00104 | 1.6e-43 | M | Prophage endopeptidase tail | |||
LKEPKNME_00105 | 5.1e-10 | |||||
LKEPKNME_00109 | 1.3e-16 | 3.4.21.88 | K | Peptidase S24-like | ||
LKEPKNME_00112 | 9.1e-15 | sdrF | M | domain protein | ||
LKEPKNME_00115 | 5.4e-19 | S | Replication initiator protein A (RepA) N-terminus | |||
LKEPKNME_00116 | 4.3e-70 | pdxK | 2.7.1.35 | H | Phosphomethylpyrimidine kinase | |
LKEPKNME_00117 | 3.9e-47 | hmpT | S | ECF-type riboflavin transporter, S component | ||
LKEPKNME_00118 | 4.4e-41 | wecD | K | Acetyltransferase GNAT Family | ||
LKEPKNME_00120 | 2.3e-252 | XK27_06780 | V | ABC transporter permease | ||
LKEPKNME_00121 | 5.8e-177 | L | Probable transposase | |||
LKEPKNME_00122 | 0.0 | pacL | 3.6.3.8 | P | P-type ATPase | |
LKEPKNME_00123 | 3.4e-111 | 3.1.4.46 | C | phosphodiesterase | ||
LKEPKNME_00124 | 1.2e-126 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
LKEPKNME_00125 | 1.2e-20 | sdrF | M | domain protein | ||
LKEPKNME_00126 | 1.1e-108 | L | Belongs to the 'phage' integrase family | |||
LKEPKNME_00128 | 2.6e-26 | D | nuclear chromosome segregation | |||
LKEPKNME_00129 | 1.3e-78 | sspC | 2.7.7.7 | DM | Glucan-binding protein C | |
LKEPKNME_00130 | 8.4e-104 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
LKEPKNME_00131 | 1.4e-49 | dhaM | 2.7.1.121 | S | PTS system fructose IIA component | |
LKEPKNME_00132 | 2.8e-68 | dhaL | 2.7.1.121 | S | Dak2 | |
LKEPKNME_00133 | 2e-151 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dak1 domain | |
LKEPKNME_00134 | 1.6e-113 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dak1 domain | |
LKEPKNME_00135 | 1.7e-61 | K | Bacterial regulatory proteins, tetR family | |||
LKEPKNME_00136 | 8.5e-209 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
LKEPKNME_00138 | 1.7e-111 | endA | F | DNA RNA non-specific endonuclease | ||
LKEPKNME_00139 | 4.1e-75 | XK27_02070 | S | Nitroreductase family | ||
LKEPKNME_00140 | 1.1e-193 | cadA | 3.6.3.3, 3.6.3.5 | P | P-type ATPase | |
LKEPKNME_00141 | 2e-83 | pgmB | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | S | beta-phosphoglucomutase |
LKEPKNME_00142 | 0.0 | mapA | 2.4.1.8 | GH65 | G | hydrolase, family 65, central catalytic |
LKEPKNME_00143 | 3.8e-78 | galM | 5.1.3.3 | G | Aldose 1-epimerase | |
LKEPKNME_00144 | 1.8e-208 | malT | G | Transporter, major facilitator family protein | ||
LKEPKNME_00145 | 2.1e-100 | malR | K | Transcriptional regulator, LacI family | ||
LKEPKNME_00146 | 2.1e-73 | kup | P | Transport of potassium into the cell | ||
LKEPKNME_00147 | 1.5e-186 | kup | P | Transport of potassium into the cell | ||
LKEPKNME_00149 | 5.2e-21 | S | Domain of unknown function (DUF3284) | |||
LKEPKNME_00150 | 3.9e-160 | yfmL | L | DEAD DEAH box helicase | ||
LKEPKNME_00151 | 7e-128 | mocA | S | Oxidoreductase | ||
LKEPKNME_00152 | 5.2e-25 | S | Domain of unknown function (DUF4828) | |||
LKEPKNME_00153 | 9.7e-74 | xpt | 2.4.2.22, 2.4.2.7 | F | Converts the preformed base xanthine, a product of nucleic acid breakdown, to xanthosine 5'-monophosphate (XMP), so it can be reused for RNA or DNA synthesis | |
LKEPKNME_00154 | 6.3e-61 | acmC | 3.2.1.96 | NU | mannosyl-glycoprotein | |
LKEPKNME_00155 | 3.2e-64 | S | ECF transporter, substrate-specific component | |||
LKEPKNME_00156 | 3.3e-127 | mleP | S | Sodium Bile acid symporter family | ||
LKEPKNME_00157 | 1.7e-248 | sfcA | 1.1.1.38, 4.1.1.101 | C | Malic enzyme | |
LKEPKNME_00158 | 4.3e-73 | mleR | K | LysR family | ||
LKEPKNME_00159 | 8.1e-57 | K | transcriptional | |||
LKEPKNME_00160 | 2.6e-41 | K | Bacterial regulatory proteins, tetR family | |||
LKEPKNME_00161 | 1.8e-59 | T | Belongs to the universal stress protein A family | |||
LKEPKNME_00162 | 5.6e-45 | K | Copper transport repressor CopY TcrY | |||
LKEPKNME_00164 | 5.6e-136 | fhaB | M | Rib/alpha-like repeat | ||
LKEPKNME_00165 | 7.8e-46 | S | Short repeat of unknown function (DUF308) | |||
LKEPKNME_00166 | 1.2e-29 | tetR | K | Transcriptional regulator C-terminal region | ||
LKEPKNME_00167 | 1.3e-150 | yfeX | P | Peroxidase | ||
LKEPKNME_00168 | 1.1e-16 | S | Protein of unknown function (DUF3021) | |||
LKEPKNME_00169 | 2.4e-40 | K | LytTr DNA-binding domain | |||
LKEPKNME_00170 | 3.6e-115 | mmuM | 1.5.1.20, 2.1.1.10 | H | homocysteine S-methyltransferase | |
LKEPKNME_00171 | 3.8e-209 | mmuP | E | amino acid | ||
LKEPKNME_00172 | 2.7e-15 | psiE | S | Phosphate-starvation-inducible E | ||
LKEPKNME_00173 | 3.7e-155 | oppF | P | Belongs to the ABC transporter superfamily | ||
LKEPKNME_00174 | 7.4e-181 | oppD | P | Belongs to the ABC transporter superfamily | ||
LKEPKNME_00175 | 2.2e-169 | oppC | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
LKEPKNME_00176 | 7.9e-142 | oppB | P | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
LKEPKNME_00177 | 2.6e-142 | oppA | E | ABC transporter, substratebinding protein | ||
LKEPKNME_00178 | 0.0 | rpoB | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
LKEPKNME_00179 | 0.0 | rpoC | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
LKEPKNME_00180 | 7.4e-23 | pilD | 3.4.23.43 | NOU | aspartic-type endopeptidase activity | |
LKEPKNME_00181 | 6.1e-70 | rpsL | J | Interacts with and stabilizes bases of the 16S rRNA that are involved in tRNA selection in the A site and with the mRNA backbone. Located at the interface of the 30S and 50S subunits, it traverses the body of the 30S subunit contacting proteins on the other side and probably holding the rRNA structure together. The combined cluster of proteins S8, S12 and S17 appears to hold together the shoulder and platform of the 30S subunit | ||
LKEPKNME_00182 | 1.3e-81 | rpsG | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the head domain of the 30S subunit. Is located at the subunit interface close to the decoding center, probably blocks exit of the E-site tRNA | ||
LKEPKNME_00183 | 0.0 | fusA | J | Catalyzes the GTP-dependent ribosomal translocation step during translation elongation. During this step, the ribosome changes from the pre-translocational (PRE) to the post- translocational (POST) state as the newly formed A-site-bound peptidyl-tRNA and P-site-bound deacylated tRNA move to the P and E sites, respectively. Catalyzes the coordinated movement of the two tRNA molecules, the mRNA and conformational changes in the ribosome | ||
LKEPKNME_00184 | 1.3e-91 | cobB | K | NAD-dependent protein deacetylase which modulates the activities of several enzymes which are inactive in their acetylated form | ||
LKEPKNME_00185 | 1.4e-98 | baeS | T | Histidine kinase | ||
LKEPKNME_00186 | 3.9e-79 | baeR | K | Bacterial regulatory proteins, luxR family | ||
LKEPKNME_00187 | 2.4e-120 | G | Bacterial extracellular solute-binding protein | |||
LKEPKNME_00188 | 2.4e-71 | S | Protein of unknown function (DUF554) | |||
LKEPKNME_00189 | 4.7e-71 | S | RRXRR protein | |||
LKEPKNME_00190 | 1.8e-37 | yaeR | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | ||
LKEPKNME_00191 | 7.1e-32 | merR | K | MerR HTH family regulatory protein | ||
LKEPKNME_00192 | 3.6e-197 | lmrB | EGP | Major facilitator Superfamily | ||
LKEPKNME_00193 | 1.2e-33 | S | Domain of unknown function (DUF4811) | |||
LKEPKNME_00194 | 1.7e-60 | yceE | S | haloacid dehalogenase-like hydrolase | ||
LKEPKNME_00195 | 7.6e-74 | glcR | K | DeoR C terminal sensor domain | ||
LKEPKNME_00196 | 8.4e-61 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
LKEPKNME_00199 | 1.5e-57 | repB | L | Initiator Replication protein | ||
LKEPKNME_00201 | 3e-40 | ysdA | CP | ABC-type Na efflux pump, permease component | ||
LKEPKNME_00202 | 1.7e-72 | natA | S | Domain of unknown function (DUF4162) | ||
LKEPKNME_00204 | 3.4e-57 | S | MobA/MobL family | |||
LKEPKNME_00205 | 1.1e-85 | efp | J | Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase | ||
LKEPKNME_00206 | 1.5e-56 | ybjI | 3.1.3.102, 3.1.3.104, 3.1.3.23 | S | Sucrose-6F-phosphate phosphohydrolase | |
LKEPKNME_00207 | 1.7e-66 | pgm3 | G | phosphoglycerate mutase family | ||
LKEPKNME_00208 | 4.8e-145 | C | Aldo/keto reductase family | |||
LKEPKNME_00209 | 5.5e-251 | ctpA | 3.6.3.54 | P | P-type ATPase | |
LKEPKNME_00210 | 3.3e-21 | silP | 1.9.3.1, 3.6.3.54 | S | Cupredoxin-like domain | |
LKEPKNME_00211 | 1.5e-43 | silP | 1.9.3.1, 3.6.3.54 | S | Cupredoxin-like domain | |
LKEPKNME_00212 | 6.7e-151 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
LKEPKNME_00213 | 4.8e-182 | EG | GntP family permease | |||
LKEPKNME_00214 | 3.6e-56 | pepL | 3.4.11.5 | E | Releases the N-terminal proline from various substrates | |
LKEPKNME_00215 | 1.7e-200 | oppA2 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | ||
LKEPKNME_00216 | 8.6e-141 | cysK | 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
LKEPKNME_00217 | 3.3e-80 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to | |
LKEPKNME_00218 | 2e-64 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | ||
LKEPKNME_00219 | 5.4e-107 | G | PTS system sorbose-specific iic component | |||
LKEPKNME_00220 | 5.4e-123 | G | PTS system mannose/fructose/sorbose family IID component | |||
LKEPKNME_00221 | 2e-39 | 2.7.1.191 | G | PTS system fructose IIA component | ||
LKEPKNME_00222 | 4e-229 | malL | 3.2.1.10 | GH13 | G | Psort location Cytoplasmic, score |
LKEPKNME_00223 | 1.8e-112 | lacI3 | K | helix_turn _helix lactose operon repressor | ||
LKEPKNME_00225 | 2.4e-57 | glpQ | 3.1.4.46 | C | phosphodiesterase | |
LKEPKNME_00226 | 2.1e-82 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
LKEPKNME_00227 | 9.1e-92 | rfbP | M | Bacterial sugar transferase | ||
LKEPKNME_00228 | 3.9e-143 | rfbA | 2.7.7.24 | H | Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis | |
LKEPKNME_00229 | 3.6e-100 | rfbC | 5.1.3.13 | M | Catalyzes the epimerization of the C3' and C5'positions of dTDP-6-deoxy-D-xylo-4-hexulose, forming dTDP-6-deoxy-L-lyxo-4- hexulose | |
LKEPKNME_00230 | 1.6e-164 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
LKEPKNME_00231 | 9.8e-128 | rfbD | 1.1.1.133, 5.1.3.13 | M | Catalyzes the reduction of dTDP-6-deoxy-L-lyxo-4- hexulose to yield dTDP-L-rhamnose | |
LKEPKNME_00232 | 9e-65 | S | Psort location Cytoplasmic, score 8.96 | |||
LKEPKNME_00233 | 3.8e-14 | |||||
LKEPKNME_00235 | 1.5e-64 | rny | D | Peptidase family M23 | ||
LKEPKNME_00236 | 2.4e-74 | rluA | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
LKEPKNME_00237 | 9.6e-132 | bacI | V | MacB-like periplasmic core domain | ||
LKEPKNME_00238 | 4.3e-97 | V | ABC transporter | |||
LKEPKNME_00239 | 1.5e-64 | bacG | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | ||
LKEPKNME_00240 | 1.4e-156 | gmuE | 2.7.1.2, 2.7.1.4 | GK | ROK family | |
LKEPKNME_00241 | 1.4e-139 | V | MatE | |||
LKEPKNME_00242 | 1.2e-43 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |||
LKEPKNME_00243 | 2.3e-87 | S | Alpha beta hydrolase | |||
LKEPKNME_00244 | 2.3e-94 | 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 | |
LKEPKNME_00245 | 1.6e-173 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
LKEPKNME_00246 | 3.4e-10 | S | Mor transcription activator family | |||
LKEPKNME_00248 | 6.2e-09 | S | zinc-ribbon domain | |||
LKEPKNME_00252 | 1.6e-116 | V | domain protein | |||
LKEPKNME_00253 | 1.3e-119 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
LKEPKNME_00254 | 2e-17 | |||||
LKEPKNME_00255 | 1.3e-102 | azlC | E | AzlC protein | ||
LKEPKNME_00256 | 1.3e-38 | azlD | S | branched-chain amino acid | ||
LKEPKNME_00257 | 5.6e-67 | I | alpha/beta hydrolase fold | |||
LKEPKNME_00258 | 9.1e-21 | S | dextransucrase activity | |||
LKEPKNME_00259 | 1.5e-139 | gldA | 1.1.1.6 | C | Iron-containing alcohol dehydrogenase | |
LKEPKNME_00260 | 3.1e-28 | 2.7.1.194, 2.7.1.200 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
LKEPKNME_00261 | 7.6e-37 | 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
LKEPKNME_00262 | 7.6e-71 | K | DeoR C terminal sensor domain | |||
LKEPKNME_00263 | 2.6e-170 | gatC | G | PTS system sugar-specific permease component | ||
LKEPKNME_00264 | 4.8e-119 | IQ | KR domain | |||
LKEPKNME_00265 | 2.9e-115 | yihT | 4.1.2.40, 4.1.2.57 | G | Belongs to the aldolase LacD family | |
LKEPKNME_00266 | 7.5e-92 | lacC | 2.7.1.11, 2.7.1.144, 2.7.1.56 | H | pfkB family carbohydrate kinase | |
LKEPKNME_00267 | 3.8e-62 | msrB | 1.8.4.11, 1.8.4.12 | O | peptide methionine sulfoxide reductase | |
LKEPKNME_00268 | 2.8e-24 | relB | L | RelB antitoxin | ||
LKEPKNME_00276 | 1.5e-159 | L | transposase, IS605 OrfB family | |||
LKEPKNME_00277 | 9.5e-58 | tlpA2 | L | Transposase IS200 like | ||
LKEPKNME_00278 | 8.9e-14 | M | domain protein | |||
LKEPKNME_00280 | 3.2e-67 | yxkH | G | Polysaccharide deacetylase | ||
LKEPKNME_00281 | 2.1e-08 | |||||
LKEPKNME_00282 | 1.7e-53 | K | LysR substrate binding domain | |||
LKEPKNME_00283 | 1.5e-122 | MA20_14895 | S | Conserved hypothetical protein 698 | ||
LKEPKNME_00284 | 1.1e-199 | nupG | F | Nucleoside | ||
LKEPKNME_00285 | 4.1e-105 | yidC | U | Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins | ||
LKEPKNME_00286 | 2.2e-49 | rnpA | 3.1.26.5 | J | RNaseP catalyzes the removal of the 5'-leader sequence from pre-tRNA to produce the mature 5'-terminus. It can also cleave other RNA substrates such as 4.5S RNA. The protein component plays an auxiliary but essential role in vivo by binding to the 5'-leader sequence and broadening the substrate specificity of the ribozyme | |
LKEPKNME_00287 | 3.4e-14 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
LKEPKNME_00289 | 1.1e-203 | dnaA | L | it binds specifically double-stranded DNA at a 9 bp consensus (dnaA box) 5'-TTATC CA A CA A-3'. DnaA binds to ATP and to acidic phospholipids | ||
LKEPKNME_00290 | 3.6e-33 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
LKEPKNME_00291 | 1.5e-55 | S | ECF transporter, substrate-specific component | |||
LKEPKNME_00292 | 1.6e-95 | znuB | U | ABC 3 transport family | ||
LKEPKNME_00293 | 3.8e-98 | fhuC | P | ABC transporter | ||
LKEPKNME_00294 | 2.7e-104 | psaA | P | Belongs to the bacterial solute-binding protein 9 family | ||
LKEPKNME_00295 | 1.2e-125 | |||||
LKEPKNME_00296 | 1.8e-64 | L | Transposase IS200 like | |||
LKEPKNME_00297 | 1.9e-206 | cshA | 3.6.4.13 | F | DEAD-box RNA helicase possibly involved in RNA degradation. Unwinds dsRNA in both 5'- and 3'-directions, has RNA- dependent ATPase activity | |
LKEPKNME_00298 | 5.3e-179 | 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 | |
LKEPKNME_00300 | 3.2e-42 | G | Transmembrane secretion effector | |||
LKEPKNME_00301 | 7.5e-179 | metC | 4.4.1.1, 4.4.1.2, 4.4.1.8 | E | cystathionine | |
LKEPKNME_00302 | 2.3e-109 | mccA | 2.5.1.134, 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
LKEPKNME_00303 | 2.7e-223 | pepF | E | Oligopeptidase F | ||
LKEPKNME_00304 | 2.9e-96 | yicL | EG | EamA-like transporter family | ||
LKEPKNME_00306 | 5.9e-42 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
LKEPKNME_00318 | 2.5e-12 | |||||
LKEPKNME_00322 | 1.4e-161 | tkt | 2.2.1.1 | H | Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate | |
LKEPKNME_00323 | 1.5e-91 | tal | 2.2.1.2 | F | Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway | |
LKEPKNME_00324 | 3e-190 | ulaA | 2.7.1.194 | S | PTS system sugar-specific permease component | |
LKEPKNME_00325 | 2.6e-38 | ulaB | 2.7.1.194 | G | Phosphotransferase system galactitol-specific IIB component | |
LKEPKNME_00326 | 2.6e-34 | 2.7.1.194, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
LKEPKNME_00327 | 2.2e-91 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
LKEPKNME_00328 | 3.1e-69 | 2.3.1.178 | J | Acetyltransferase (GNAT) domain | ||
LKEPKNME_00329 | 8.1e-164 | yjjP | S | Putative threonine/serine exporter | ||
LKEPKNME_00330 | 3.1e-64 | C | FMN binding | |||
LKEPKNME_00331 | 7.4e-231 | purA | 6.3.4.4 | F | Plays an important role in the de novo pathway of purine nucleotide biosynthesis. Catalyzes the first committed step in the biosynthesis of AMP from IMP | |
LKEPKNME_00333 | 3.3e-156 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
LKEPKNME_00334 | 2.8e-59 | ykhA | 3.1.2.20 | I | Thioesterase superfamily | |
LKEPKNME_00335 | 5.1e-11 | S | CAAX protease self-immunity | |||
LKEPKNME_00336 | 2.5e-82 | S | Belongs to the UPF0246 family | |||
LKEPKNME_00337 | 3.5e-100 | nfrA | 1.5.1.38, 1.5.1.39 | C | nitroreductase | |
LKEPKNME_00338 | 7.6e-87 | rnmV | 3.1.26.8 | J | Required for correct processing of both the 5' and 3' ends of 5S rRNA precursor. Cleaves both sides of a double-stranded region yielding mature 5S rRNA in one step | |
LKEPKNME_00339 | 4.1e-104 | tatD | L | hydrolase, TatD family | ||
LKEPKNME_00340 | 1.1e-158 | metG | 6.1.1.10, 6.1.1.20 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
LKEPKNME_00341 | 1.3e-165 | metG | 6.1.1.10, 6.1.1.20 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
LKEPKNME_00342 | 1.1e-127 | |||||
LKEPKNME_00343 | 6.7e-152 | mvaA | 1.1.1.34, 1.1.1.88, 2.3.1.9 | C | Belongs to the HMG-CoA reductase family | |
LKEPKNME_00344 | 3.6e-42 | VPA1512 | ET | Bacterial extracellular solute-binding proteins, family 3 | ||
LKEPKNME_00348 | 2.2e-56 | L | Helix-turn-helix domain | |||
LKEPKNME_00349 | 3.4e-114 | kdgK | 2.7.1.45 | G | pfkB family carbohydrate kinase | |
LKEPKNME_00350 | 5.1e-63 | eda | 4.1.2.14, 4.1.3.42 | G | KDPG and KHG aldolase | |
LKEPKNME_00351 | 5.6e-110 | glcU | U | sugar transport | ||
LKEPKNME_00352 | 2.6e-15 | yobS | K | transcriptional regulator | ||
LKEPKNME_00353 | 1.7e-152 | mdtG | EGP | Major facilitator Superfamily | ||
LKEPKNME_00354 | 6.5e-104 | racD | 5.1.1.13 | M | Belongs to the aspartate glutamate racemases family | |
LKEPKNME_00355 | 4.5e-225 | yxbA | 6.3.1.12 | S | ATP-grasp enzyme | |
LKEPKNME_00356 | 5.5e-97 | 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 | |
LKEPKNME_00357 | 2.3e-112 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
LKEPKNME_00358 | 5.6e-190 | glnPH2 | P | ABC transporter permease | ||
LKEPKNME_00359 | 9.4e-214 | yjeM | E | Amino Acid | ||
LKEPKNME_00360 | 1.8e-32 | yvdC | S | MazG nucleotide pyrophosphohydrolase domain | ||
LKEPKNME_00361 | 2.1e-136 | tetA | EGP | Major facilitator Superfamily | ||
LKEPKNME_00362 | 6.1e-63 | S | Glycosyltransferase like family 2 | |||
LKEPKNME_00363 | 3.1e-68 | cps1D | M | Domain of unknown function (DUF4422) | ||
LKEPKNME_00364 | 2.8e-98 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
LKEPKNME_00365 | 8.2e-34 | S | CAAX protease self-immunity | |||
LKEPKNME_00366 | 2.4e-33 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
LKEPKNME_00367 | 1.3e-272 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
LKEPKNME_00368 | 1e-264 | aha1 | P | TIGRFAM ATPase, P-type (transporting), HAD superfamily, subfamily IC | ||
LKEPKNME_00369 | 1.9e-49 | kdgR | K | FCD domain | ||
LKEPKNME_00370 | 3.8e-208 | mtlD | 1.1.1.17, 1.1.1.57 | G | Mannitol dehydrogenase C-terminal domain | |
LKEPKNME_00371 | 2.6e-173 | uxuA | 4.2.1.8 | G | Catalyzes the dehydration of D-mannonate | |
LKEPKNME_00372 | 8.7e-193 | uxaC | 5.3.1.12 | G | glucuronate isomerase | |
LKEPKNME_00373 | 1.4e-225 | uxuT | G | MFS/sugar transport protein | ||
LKEPKNME_00374 | 8.4e-24 | S | PFAM Archaeal ATPase | |||
LKEPKNME_00375 | 1e-88 | asp1 | S | Accessory Sec system protein Asp1 | ||
LKEPKNME_00376 | 3.5e-65 | secY2 | U | SecY translocase | ||
LKEPKNME_00377 | 3.5e-14 | |||||
LKEPKNME_00378 | 1.7e-95 | RB5993 | 3.1.1.3 | I | Pfam Lipase (class 3) | |
LKEPKNME_00379 | 1.4e-13 | |||||
LKEPKNME_00380 | 1.4e-83 | ppiB | 5.2.1.8 | G | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
LKEPKNME_00381 | 1e-109 | puuD | S | peptidase C26 | ||
LKEPKNME_00382 | 1.1e-200 | gshF | 6.3.2.2 | H | Belongs to the glutamate--cysteine ligase type 1 family | |
LKEPKNME_00383 | 1.1e-25 | |||||
LKEPKNME_00384 | 0.0 | clpL | O | C-terminal, D2-small domain, of ClpB protein | ||
LKEPKNME_00385 | 6.6e-60 | uspA | T | Universal stress protein family | ||
LKEPKNME_00386 | 3.8e-43 | marR | K | Transcriptional regulator, MarR family | ||
LKEPKNME_00387 | 4.9e-102 | fabH | 2.3.1.180 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids | |
LKEPKNME_00388 | 2.2e-27 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
LKEPKNME_00389 | 1.9e-103 | fabD | 2.3.1.39 | I | Malonyl CoA-acyl carrier protein transacylase | |
LKEPKNME_00390 | 8.4e-99 | IQ | reductase | |||
LKEPKNME_00391 | 3.7e-195 | fabF | 2.3.1.179 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP | |
LKEPKNME_00392 | 2.9e-49 | fabZ | 3.5.1.108, 4.2.1.59 | I | Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs | |
LKEPKNME_00393 | 7.1e-216 | accC | 6.3.4.14, 6.4.1.2 | I | Acetyl-CoA carboxylase biotin carboxylase subunit | |
LKEPKNME_00394 | 9e-152 | manL | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
LKEPKNME_00395 | 6.4e-116 | manY | G | PTS system sorbose-specific iic component | ||
LKEPKNME_00396 | 1.6e-147 | manN | G | system, mannose fructose sorbose family IID component | ||
LKEPKNME_00397 | 3.2e-52 | manO | S | Domain of unknown function (DUF956) | ||
LKEPKNME_00398 | 6.8e-77 | XK27_02480 | EGP | Major Facilitator Superfamily | ||
LKEPKNME_00399 | 3.5e-24 | K | Helix-turn-helix XRE-family like proteins | |||
LKEPKNME_00400 | 1.2e-60 | ubiG | 2.1.1.265 | H | Methyltransferase domain | |
LKEPKNME_00401 | 6.7e-84 | adc | 4.1.1.4 | Q | Acetoacetate decarboxylase (ADC) | |
LKEPKNME_00402 | 2.9e-106 | fadB4 | 1.1.1.157 | I | 3-hydroxyacyl-CoA dehydrogenase | |
LKEPKNME_00403 | 9e-171 | npr | 1.11.1.1 | S | Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain | |
LKEPKNME_00404 | 4.3e-265 | yaaO | 4.1.1.17, 4.1.1.19 | E | Orn/Lys/Arg decarboxylase, C-terminal domain | |
LKEPKNME_00406 | 1.7e-72 | alr | 5.1.1.1 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
LKEPKNME_00407 | 1.4e-13 | |||||
LKEPKNME_00408 | 3.4e-48 | ndoA | L | Toxic component of a toxin-antitoxin (TA) module | ||
LKEPKNME_00409 | 5.1e-92 | yunF | F | Protein of unknown function DUF72 | ||
LKEPKNME_00410 | 1.1e-155 | nrnB | S | DHHA1 domain | ||
LKEPKNME_00411 | 3.7e-43 | def | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins | |
LKEPKNME_00412 | 9.9e-60 | |||||
LKEPKNME_00413 | 1.1e-09 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic domain | |
LKEPKNME_00415 | 5.9e-22 | S | Cytochrome B5 | |||
LKEPKNME_00416 | 8.1e-20 | sigH | K | DNA-templated transcription, initiation | ||
LKEPKNME_00418 | 2.5e-140 | yabM | S | Polysaccharide biosynthesis protein | ||
LKEPKNME_00419 | 3.6e-31 | yabO | J | S4 domain protein | ||
LKEPKNME_00420 | 2.2e-21 | divIC | D | Septum formation initiator | ||
LKEPKNME_00421 | 1.1e-40 | yabR | J | RNA binding | ||
LKEPKNME_00422 | 5.6e-96 | 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 | |
LKEPKNME_00423 | 1.5e-76 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
LKEPKNME_00424 | 2.1e-56 | 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 | ||
LKEPKNME_00425 | 1.4e-75 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
LKEPKNME_00426 | 1.4e-89 | prmB | 2.1.1.297, 2.1.1.298 | J | Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif | |
LKEPKNME_00427 | 1e-134 | ywlC | 2.7.7.87, 3.1.3.48 | J | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine | |
LKEPKNME_00428 | 5e-100 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
LKEPKNME_00429 | 2.6e-97 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
LKEPKNME_00430 | 1.8e-15 | 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 | ||
LKEPKNME_00431 | 2.4e-39 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
LKEPKNME_00432 | 4.1e-58 | 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 | ||
LKEPKNME_00434 | 1.7e-23 | yktA | S | Belongs to the UPF0223 family | ||
LKEPKNME_00435 | 9.7e-77 | suhB | 3.1.3.25 | G | Belongs to the inositol monophosphatase superfamily | |
LKEPKNME_00436 | 0.0 | typA | T | GTP-binding protein TypA | ||
LKEPKNME_00437 | 1.6e-148 | manL | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
LKEPKNME_00438 | 1.9e-115 | manY | G | PTS system | ||
LKEPKNME_00439 | 8.6e-141 | manN | G | system, mannose fructose sorbose family IID component | ||
LKEPKNME_00440 | 2.2e-191 | tnpB | L | Putative transposase DNA-binding domain | ||
LKEPKNME_00441 | 1.3e-155 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
LKEPKNME_00442 | 4.8e-53 | rplQ | J | Ribosomal protein L17 | ||
LKEPKNME_00443 | 1.8e-100 | ecfA1 | P | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
LKEPKNME_00444 | 6.7e-111 | ecfA2 | 3.6.3.55 | P | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | |
LKEPKNME_00445 | 2.8e-108 | ecfT | U | Transmembrane (T) component of an energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
LKEPKNME_00446 | 1.9e-125 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
LKEPKNME_00447 | 5.5e-77 | rplM | J | This protein is one of the early assembly proteins of the 50S ribosomal subunit, although it is not seen to bind rRNA by itself. It is important during the early stages of 50S assembly | ||
LKEPKNME_00448 | 1.1e-60 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
LKEPKNME_00458 | 7.6e-64 | Z012_12235 | S | Baseplate J-like protein | ||
LKEPKNME_00459 | 4.5e-47 | |||||
LKEPKNME_00461 | 4.7e-18 | S | Bacteriophage holin family | |||
LKEPKNME_00462 | 3.7e-115 | M | Glycosyl hydrolases family 25 | |||
LKEPKNME_00463 | 7.3e-120 | gatD | 1.1.1.14 | E | Alcohol dehydrogenase GroES-like domain | |
LKEPKNME_00464 | 1.4e-181 | gatC | G | PTS system sugar-specific permease component | ||
LKEPKNME_00465 | 9.2e-36 | 2.7.1.194, 2.7.1.200 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
LKEPKNME_00466 | 2.7e-39 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
LKEPKNME_00467 | 2.9e-60 | K | DeoR C terminal sensor domain | |||
LKEPKNME_00468 | 1.4e-23 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
LKEPKNME_00469 | 4.3e-57 | racA | K | Domain of unknown function (DUF1836) | ||
LKEPKNME_00470 | 4.7e-116 | queH | 1.17.99.6, 3.1.26.4 | C | Catalyzes the conversion of epoxyqueuosine (oQ) to queuosine (Q), which is a hypermodified base found in the wobble positions of tRNA(Asp), tRNA(Asn), tRNA(His) and tRNA(Tyr) | |
LKEPKNME_00471 | 4.3e-147 | ald | 1.4.1.1 | C | Belongs to the AlaDH PNT family | |
LKEPKNME_00472 | 5.6e-168 | potE2 | E | amino acid | ||
LKEPKNME_00473 | 1.2e-29 | |||||
LKEPKNME_00474 | 1.5e-44 | O | ATPase family associated with various cellular activities (AAA) | |||
LKEPKNME_00475 | 5e-34 | S | Protein of unknown function (DUF3644) | |||
LKEPKNME_00476 | 1.8e-103 | trsE | S | COG0433 Predicted ATPase | ||
LKEPKNME_00478 | 2.6e-60 | M | Peptidase family M23 | |||
LKEPKNME_00481 | 4e-118 | S | Uncharacterised protein family (UPF0236) | |||
LKEPKNME_00482 | 1.1e-233 | gatA | 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Gln-tRNA(Gln) through the transamidation of misacylated Glu-tRNA(Gln) in organisms which lack glutaminyl-tRNA synthetase. The reaction takes place in the presence of glutamine and ATP through an activated gamma-phospho-Glu-tRNA(Gln) | |
LKEPKNME_00483 | 1.9e-256 | gatB | 6.1.1.12, 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | |
LKEPKNME_00484 | 3.4e-146 | yegS | 2.7.1.107 | G | Lipid kinase | |
LKEPKNME_00485 | 4.8e-212 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
LKEPKNME_00486 | 1.9e-67 | XK27_09620 | S | NADPH-dependent FMN reductase | ||
LKEPKNME_00487 | 2e-156 | XK27_09615 | S | reductase | ||
LKEPKNME_00488 | 3.4e-39 | 2.7.7.65 | T | phosphorelay sensor kinase activity | ||
LKEPKNME_00489 | 5.5e-146 | iunH | 3.2.2.1 | F | Inosine-uridine preferring nucleoside hydrolase | |
LKEPKNME_00490 | 3.6e-14 | |||||
LKEPKNME_00491 | 2.2e-32 | M | Dolichyl-phosphate-mannose-protein mannosyltransferase | |||
LKEPKNME_00492 | 8.6e-39 | S | Acyltransferase family | |||
LKEPKNME_00493 | 4.5e-43 | S | Peptidase_C39 like family | |||
LKEPKNME_00494 | 2.5e-63 | M | Glycosyltransferase like family 2 | |||
LKEPKNME_00495 | 6.2e-74 | M | LicD family | |||
LKEPKNME_00496 | 5.3e-20 | cps3F | ||||
LKEPKNME_00497 | 7.5e-72 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |||
LKEPKNME_00498 | 2.3e-120 | ytbE | S | reductase | ||
LKEPKNME_00499 | 4.2e-43 | ytcD | K | HxlR-like helix-turn-helix | ||
LKEPKNME_00500 | 1.5e-101 | ybbM | S | Uncharacterised protein family (UPF0014) | ||
LKEPKNME_00501 | 2.2e-66 | ybbL | S | ABC transporter | ||
LKEPKNME_00502 | 3.7e-163 | oxlT | P | Major Facilitator Superfamily | ||
LKEPKNME_00503 | 4.1e-151 | pfkB | 2.7.1.11, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
LKEPKNME_00504 | 2.2e-86 | fruR | K | DeoR C terminal sensor domain | ||
LKEPKNME_00505 | 2.1e-220 | XK27_08635 | S | UPF0210 protein | ||
LKEPKNME_00506 | 4.1e-27 | gcvR | T | Belongs to the UPF0237 family | ||
LKEPKNME_00507 | 1e-38 | |||||
LKEPKNME_00508 | 2.8e-52 | E | GDSL-like Lipase/Acylhydrolase family | |||
LKEPKNME_00509 | 1.6e-88 | yvyE | 3.4.13.9 | S | YigZ family | |
LKEPKNME_00510 | 1.7e-58 | S | Haloacid dehalogenase-like hydrolase | |||
LKEPKNME_00511 | 5.8e-154 | EGP | Major facilitator Superfamily | |||
LKEPKNME_00513 | 1.8e-68 | ypgQ | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
LKEPKNME_00514 | 7e-28 | adhR | K | Transcriptional regulator | ||
LKEPKNME_00515 | 3.5e-90 | S | NADPH-dependent FMN reductase | |||
LKEPKNME_00516 | 6.7e-19 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
LKEPKNME_00518 | 7.2e-56 | nss | M | transferase activity, transferring glycosyl groups | ||
LKEPKNME_00519 | 4.3e-109 | gtf2 | M | A stabilizing protein that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon. Stabilizes the glycosylation activity of Gtf1 | ||
LKEPKNME_00520 | 5.5e-39 | cpsJ | S | Glycosyltransferase like family 2 | ||
LKEPKNME_00521 | 2.6e-38 | cpsJ | S | Glycosyltransferase like family 2 | ||
LKEPKNME_00523 | 1.1e-50 | nudG | 3.6.1.55, 3.6.1.65 | L | NUDIX domain | |
LKEPKNME_00524 | 5.1e-38 | yhjH | 3.1.4.52 | T | Putative diguanylate phosphodiesterase | |
LKEPKNME_00525 | 2.7e-112 | 2.7.7.65 | T | diguanylate cyclase activity | ||
LKEPKNME_00526 | 0.0 | ydaN | S | Bacterial cellulose synthase subunit | ||
LKEPKNME_00527 | 3e-111 | ydaM | M | Glycosyl transferase family group 2 | ||
LKEPKNME_00528 | 8.9e-61 | EG | EamA-like transporter family | |||
LKEPKNME_00529 | 5.3e-118 | K | AI-2E family transporter | |||
LKEPKNME_00530 | 8.4e-173 | malY | 4.4.1.8 | E | Aminotransferase, class I | |
LKEPKNME_00531 | 6e-123 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
LKEPKNME_00532 | 1.7e-59 | yfjR | K | WYL domain | ||
LKEPKNME_00533 | 3.3e-243 | 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 | |
LKEPKNME_00534 | 3.6e-130 | nadE | 6.3.1.5 | F | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
LKEPKNME_00535 | 1.6e-249 | yhgF | K | Tex-like protein N-terminal domain protein | ||
LKEPKNME_00536 | 5.2e-53 | S | HicB_like antitoxin of bacterial toxin-antitoxin system | |||
LKEPKNME_00537 | 6.4e-19 | N | HicA toxin of bacterial toxin-antitoxin, | |||
LKEPKNME_00538 | 1.2e-31 | arpU | S | Phage transcriptional regulator, ArpU family | ||
LKEPKNME_00546 | 4.5e-33 | rusA | L | Endodeoxyribonuclease RusA | ||
LKEPKNME_00549 | 6.3e-20 | dnaC | 3.4.21.53 | L | DNA replication protein | |
LKEPKNME_00550 | 1.5e-188 | iolF | EGP | Major facilitator Superfamily | ||
LKEPKNME_00551 | 2.8e-76 | rhaR | K | helix_turn_helix, arabinose operon control protein | ||
LKEPKNME_00552 | 4.9e-50 | S | Membrane | |||
LKEPKNME_00553 | 6.7e-180 | adhC | 1.1.1.90 | C | Zn-dependent alcohol dehydrogenases, class III | |
LKEPKNME_00554 | 1.1e-14 | S | COG NOG19168 non supervised orthologous group | |||
LKEPKNME_00556 | 2.3e-168 | 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) | |
LKEPKNME_00557 | 1.5e-20 | rimL | 1.1.1.25 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | |
LKEPKNME_00559 | 1.2e-112 | dkg | S | reductase | ||
LKEPKNME_00560 | 1.7e-24 | |||||
LKEPKNME_00561 | 4.7e-76 | 2.4.2.3 | F | Phosphorylase superfamily | ||
LKEPKNME_00562 | 4.1e-21 | ebh | 2.1.1.80, 3.1.1.61 | D | interspecies interaction between organisms | |
LKEPKNME_00565 | 1.6e-197 | dtpT | U | amino acid peptide transporter | ||
LKEPKNME_00566 | 5.1e-08 | |||||
LKEPKNME_00572 | 1.4e-218 | pckA | 4.1.1.49 | H | Phosphoenolpyruvate carboxykinase | |
LKEPKNME_00578 | 3.9e-20 | L | Phage regulatory protein | |||
LKEPKNME_00579 | 1.8e-08 | K | Helix-turn-helix XRE-family like proteins | |||
LKEPKNME_00580 | 8.6e-35 | K | Helix-turn-helix XRE-family like proteins | |||
LKEPKNME_00581 | 5.8e-09 | E | IrrE N-terminal-like domain | |||
LKEPKNME_00582 | 2e-39 | K | LytTr DNA-binding domain | |||
LKEPKNME_00587 | 4.1e-70 | xerD | L | Phage integrase, N-terminal SAM-like domain | ||
LKEPKNME_00588 | 7.2e-25 | N | phage tail tape measure protein | |||
LKEPKNME_00589 | 1.7e-54 | rplI | J | Binds to the 23S rRNA | ||
LKEPKNME_00590 | 2.6e-262 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
LKEPKNME_00591 | 4.7e-07 | |||||
LKEPKNME_00592 | 0.0 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
LKEPKNME_00593 | 1.8e-107 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
LKEPKNME_00594 | 3.9e-73 | S | DNA primase | |||
LKEPKNME_00595 | 3.8e-92 | L | Transposase, IS605 OrfB family | |||
LKEPKNME_00596 | 1e-54 | tlpA2 | L | Transposase IS200 like | ||
LKEPKNME_00598 | 3.5e-11 | |||||
LKEPKNME_00599 | 0.0 | lacL | 3.2.1.23 | G | -beta-galactosidase | |
LKEPKNME_00600 | 7e-184 | nplT | 3.2.1.133, 3.2.1.135, 3.2.1.54 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
LKEPKNME_00601 | 1.6e-114 | ntpJ | P | Potassium uptake protein | ||
LKEPKNME_00602 | 2.2e-58 | ktrA | P | TrkA-N domain | ||
LKEPKNME_00603 | 5.7e-54 | XK27_08875 | O | PFAM peptidase M10A and M12B, matrixin and adamalysin | ||
LKEPKNME_00604 | 4.5e-85 | yhcA | V | ABC transporter, ATP-binding protein | ||
LKEPKNME_00605 | 5.8e-35 | K | Bacterial regulatory proteins, tetR family | |||
LKEPKNME_00606 | 4.9e-222 | lmrA | V | ABC transporter, ATP-binding protein | ||
LKEPKNME_00607 | 9.1e-55 | |||||
LKEPKNME_00608 | 1.5e-109 | Z012_02110 | S | Protein of unknown function (DUF3383) | ||
LKEPKNME_00609 | 1.2e-26 | |||||
LKEPKNME_00611 | 9e-48 | Z012_02125 | ||||
LKEPKNME_00612 | 1.3e-25 | |||||
LKEPKNME_00613 | 8.8e-18 | S | LysM domain | |||
LKEPKNME_00614 | 1.9e-18 | |||||
LKEPKNME_00615 | 1.2e-102 | |||||
LKEPKNME_00616 | 2.9e-184 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
LKEPKNME_00617 | 2.3e-63 | srtA | 3.4.22.70 | M | sortase family | |
LKEPKNME_00619 | 5.2e-72 | thiJ | 2.7.11.1, 3.5.1.124 | S | DJ-1/PfpI family | |
LKEPKNME_00620 | 7.9e-62 | yvdD | 3.2.2.10 | S | Possible lysine decarboxylase | |
LKEPKNME_00621 | 4.7e-149 | mtlA | 2.7.1.197 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
LKEPKNME_00622 | 2.8e-65 | mtlF | 2.7.1.197 | G | catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | |
LKEPKNME_00623 | 6.4e-186 | mtlD | 1.1.1.17 | C | mannitol-1-phosphate 5-dehydrogenase activity | |
LKEPKNME_00624 | 1.1e-41 | gntR1 | K | Transcriptional regulator, GntR family | ||
LKEPKNME_00625 | 1.4e-95 | V | ABC transporter, ATP-binding protein | |||
LKEPKNME_00626 | 5.9e-145 | hslU | O | this subunit has chaperone activity. The binding of ATP and its subsequent hydrolysis by HslU are essential for unfolding of protein substrates subsequently hydrolyzed by HslV. HslU recognizes the N-terminal part of its protein substrates and unfolds these before they are guided to HslV for hydrolysis | ||
LKEPKNME_00627 | 4.1e-143 | potA | 3.6.3.30, 3.6.3.31 | P | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | |
LKEPKNME_00628 | 1.5e-120 | potB | P | ABC transporter permease | ||
LKEPKNME_00629 | 4.5e-104 | potC | U | Binding-protein-dependent transport system inner membrane component | ||
LKEPKNME_00630 | 7.8e-19 | nss | M | transferase activity, transferring glycosyl groups | ||
LKEPKNME_00631 | 4e-55 | M | Glycosyltransferase like family 2 | |||
LKEPKNME_00633 | 5.3e-39 | M | family 8 | |||
LKEPKNME_00634 | 9.3e-39 | S | glycosyl transferase family 2 | |||
LKEPKNME_00635 | 5.4e-26 | M | glycosyl transferase family 8 | |||
LKEPKNME_00636 | 2.7e-26 | rplR | J | This is one of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance | ||
LKEPKNME_00637 | 1.3e-82 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
LKEPKNME_00638 | 2.1e-22 | rpmD | J | Ribosomal protein L30 | ||
LKEPKNME_00639 | 1e-67 | rplO | J | Binds to the 23S rRNA | ||
LKEPKNME_00640 | 4.4e-207 | secY | U | The central subunit of the protein translocation channel SecYEG. Consists of two halves formed by TMs 1-5 and 6-10. These two domains form a lateral gate at the front which open onto the bilayer between TMs 2 and 7, and are clamped together by SecE at the back. The channel is closed by both a pore ring composed of hydrophobic SecY resides and a short helix (helix 2A) on the extracellular side of the membrane which forms a plug. The plug probably moves laterally to allow the channel to open. The ring and the pore may move independently | ||
LKEPKNME_00641 | 4.4e-107 | adk | 2.7.4.3 | F | Catalyzes the reversible transfer of the terminal phosphate group between ATP and AMP. Plays an important role in cellular energy homeostasis and in adenine nucleotide metabolism | |
LKEPKNME_00642 | 4.8e-34 | infA | J | One of the essential components for the initiation of protein synthesis. Stabilizes the binding of IF-2 and IF-3 on the 30S subunit to which N-formylmethionyl-tRNA(fMet) subsequently binds. Helps modulate mRNA selection, yielding the 30S pre- initiation complex (PIC). Upon addition of the 50S ribosomal subunit IF-1, IF-2 and IF-3 are released leaving the mature 70S translation initation complex | ||
LKEPKNME_00643 | 2.5e-13 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
LKEPKNME_00644 | 4.4e-56 | rpsM | J | Located at the top of the head of the 30S subunit, it contacts several helices of the 16S rRNA. In the 70S ribosome it contacts the 23S rRNA (bridge B1a) and protein L5 of the 50S subunit (bridge B1b), connecting the 2 subunits | ||
LKEPKNME_00645 | 3.4e-53 | K | Transcriptional regulator C-terminal region | |||
LKEPKNME_00646 | 1e-43 | thiT | S | Thiamine transporter protein (Thia_YuaJ) | ||
LKEPKNME_00647 | 4.8e-287 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
LKEPKNME_00648 | 9.1e-98 | asp2 | 3.4.11.5 | S | Accessory Sec system GspB-transporter | |
LKEPKNME_00649 | 1.2e-30 | asp3 | S | Accessory Sec system protein Asp3 | ||
LKEPKNME_00650 | 3e-246 | secA2 | 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 | ||
LKEPKNME_00651 | 2.3e-79 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
LKEPKNME_00652 | 4.6e-99 | rpiA | 2.7.1.12, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
LKEPKNME_00653 | 5.8e-78 | yvfR | V | ABC transporter | ||
LKEPKNME_00654 | 4.9e-54 | yvfS | V | ABC-2 type transporter | ||
LKEPKNME_00655 | 1.2e-56 | salK | 2.7.13.3 | T | Histidine kinase | |
LKEPKNME_00656 | 8.7e-15 | |||||
LKEPKNME_00657 | 4.4e-81 | sip | L | Belongs to the 'phage' integrase family | ||
LKEPKNME_00658 | 5.8e-123 | 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 | ||
LKEPKNME_00659 | 1.9e-128 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
LKEPKNME_00660 | 1.5e-27 | yazA | L | GIY-YIG catalytic domain protein | ||
LKEPKNME_00662 | 9.5e-18 | ftsK | D | FtsK/SpoIIIE family | ||
LKEPKNME_00664 | 1.2e-22 | drgA | C | nitroreductase | ||
LKEPKNME_00665 | 4.4e-134 | argE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
LKEPKNME_00666 | 2.7e-70 | metI | P | ABC transporter permease | ||
LKEPKNME_00667 | 2.6e-149 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
LKEPKNME_00668 | 7.4e-107 | metQ1 | P | Belongs to the nlpA lipoprotein family | ||
LKEPKNME_00669 | 1e-24 | metK1 | 2.1.1.14 | E | 5-methyltetrahydropteroyltriglutamate--homocysteine methyltransferase | |
LKEPKNME_00670 | 1.3e-40 | |||||
LKEPKNME_00671 | 1.9e-35 | K | GNAT family | |||
LKEPKNME_00672 | 4.5e-210 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Belongs to the aldehyde dehydrogenase family | |
LKEPKNME_00673 | 3.5e-220 | gdhA | 1.4.1.4 | E | Glutamate/Leucine/Phenylalanine/Valine dehydrogenase | |
LKEPKNME_00674 | 1.6e-258 | treB | G | phosphotransferase system | ||
LKEPKNME_00675 | 4.8e-83 | treR | K | UTRA | ||
LKEPKNME_00676 | 9.5e-234 | 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 | |
LKEPKNME_00677 | 2.3e-128 | tpiA | 2.7.2.3, 5.3.1.1 | G | Involved in the gluconeogenesis. Catalyzes stereospecifically the conversion of dihydroxyacetone phosphate (DHAP) to D-glyceraldehyde-3-phosphate (G3P) | |
LKEPKNME_00678 | 1.3e-208 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
LKEPKNME_00679 | 1.7e-108 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
LKEPKNME_00680 | 8.7e-91 | macB2 | V | ABC transporter, ATP-binding protein | ||
LKEPKNME_00681 | 1.5e-71 | T | PhoQ Sensor | |||
LKEPKNME_00682 | 8.4e-61 | K | response regulator | |||
LKEPKNME_00683 | 1.8e-60 | aroD | 1.1.1.25, 4.2.1.10 | E | Involved in the third step of the chorismate pathway, which leads to the biosynthesis of aromatic amino acids. Catalyzes the cis-dehydration of 3-dehydroquinate (DHQ) and introduces the first double bond of the aromatic ring to yield 3- dehydroshikimate | |
LKEPKNME_00684 | 7.7e-179 | galK | 2.7.1.6 | F | Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) | |
LKEPKNME_00685 | 2.3e-163 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
LKEPKNME_00686 | 1.1e-201 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
LKEPKNME_00687 | 6.4e-114 | degV | S | EDD domain protein, DegV family | ||
LKEPKNME_00688 | 1.9e-148 | yfdH | 2.4.2.53 | GT2 | M | Glycosyltransferase, group 2 family protein |
LKEPKNME_00689 | 1.2e-56 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
LKEPKNME_00690 | 2.2e-26 | ydiI | Q | Thioesterase superfamily | ||
LKEPKNME_00691 | 1.5e-144 | menB | 4.1.3.36 | H | Converts o-succinylbenzoyl-CoA (OSB-CoA) to 1,4- dihydroxy-2-naphthoyl-CoA (DHNA-CoA) | |
LKEPKNME_00692 | 1.7e-205 | M | Exporter of polyketide antibiotics | |||
LKEPKNME_00693 | 6e-131 | yjjC | V | ATPases associated with a variety of cellular activities | ||
LKEPKNME_00694 | 1.8e-81 | K | Bacterial regulatory proteins, tetR family | |||
LKEPKNME_00695 | 3e-81 | G | PTS system Galactitol-specific IIC component | |||
LKEPKNME_00696 | 1.9e-101 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
LKEPKNME_00697 | 4.5e-102 | tcyB | E | ABC transporter | ||
LKEPKNME_00698 | 1.5e-33 | M | Glycosyl hydrolases family 25 | |||
LKEPKNME_00699 | 3.6e-188 | nox | S | Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain | ||
LKEPKNME_00700 | 1.4e-14 | |||||
LKEPKNME_00701 | 1.3e-102 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
LKEPKNME_00702 | 1.3e-100 | glnH | ET | ABC transporter | ||
LKEPKNME_00703 | 1.2e-85 | gluC | P | ABC transporter permease | ||
LKEPKNME_00704 | 2.9e-82 | glnP | P | ABC transporter permease | ||
LKEPKNME_00705 | 1.2e-73 | steT | E | amino acid | ||
LKEPKNME_00706 | 3.9e-76 | L | haloacid dehalogenase-like hydrolase | |||
LKEPKNME_00707 | 7.6e-117 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
LKEPKNME_00708 | 1.7e-67 | 1.5.1.38 | S | NADPH-dependent FMN reductase | ||
LKEPKNME_00709 | 8.3e-164 | C | Luciferase-like monooxygenase | |||
LKEPKNME_00710 | 1.4e-40 | K | Transcriptional regulator, HxlR family | |||
LKEPKNME_00711 | 1.1e-99 | glgD | 2.4.1.21, 2.7.7.27 | GT5 | G | Nucleotidyl transferase |
LKEPKNME_00712 | 1e-193 | glgA | 2.4.1.21 | GT5 | F | Synthesizes alpha-1,4-glucan chains using ADP-glucose |
LKEPKNME_00713 | 9.7e-108 | dnaI | L | Primosomal protein DnaI | ||
LKEPKNME_00714 | 3.6e-79 | dnaB | L | replication initiation and membrane attachment | ||
LKEPKNME_00715 | 6.1e-66 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
LKEPKNME_00716 | 2.1e-50 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
LKEPKNME_00717 | 8.3e-63 | fpg | 3.2.2.23, 4.2.99.18 | L | Involved in base excision repair of DNA damaged by oxidation or by mutagenic agents. Acts as DNA glycosylase that recognizes and removes damaged bases. Has a preference for oxidized purines, such as 7,8-dihydro-8-oxoguanine (8-oxoG). Has AP (apurinic apyrimidinic) lyase activity and introduces nicks in the DNA strand. Cleaves the DNA backbone by beta-delta elimination to generate a single-strand break at the site of the removed base with both 3'- and 5'-phosphates | |
LKEPKNME_00718 | 1.2e-87 | glnP | P | ABC transporter | ||
LKEPKNME_00719 | 2.6e-119 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
LKEPKNME_00720 | 1.5e-31 | |||||
LKEPKNME_00721 | 4.1e-112 | ampC | V | Beta-lactamase | ||
LKEPKNME_00722 | 1.6e-110 | cobQ | S | glutamine amidotransferase | ||
LKEPKNME_00723 | 9.2e-60 | murF | 6.3.2.10, 6.3.2.13 | M | Domain of unknown function (DUF1727) | |
LKEPKNME_00724 | 0.0 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
LKEPKNME_00725 | 3.2e-145 | purK2 | 6.3.4.18 | F | Involved in the de novo purine biosynthesis. Catalyzes the transfer of formate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR). Formate is provided by PurU via hydrolysis of 10-formyl-tetrahydrofolate | |
LKEPKNME_00726 | 1.7e-289 | rexB | 3.1.21.3, 3.6.4.12 | L | The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination. This subunit has 5' - 3' nuclease activity | |
LKEPKNME_00727 | 8.4e-12 | sdrF | M | domain protein | ||
LKEPKNME_00730 | 1.4e-44 | 3.4.22.70 | M | Sortase family | ||
LKEPKNME_00731 | 2.8e-89 | M | Gram-positive pilin backbone subunit 2, Cna-B-like domain | |||
LKEPKNME_00732 | 2.7e-79 | ptp2 | 3.1.3.48 | T | Tyrosine phosphatase family | |
LKEPKNME_00733 | 2.1e-180 | yhdP | S | Transporter associated domain | ||
LKEPKNME_00735 | 6.5e-78 | nadK | 2.7.1.23 | F | Involved in the regulation of the intracellular balance of NAD and NADP, and is a key enzyme in the biosynthesis of NADP. Catalyzes specifically the phosphorylation on 2'-hydroxyl of the adenosine moiety of NAD to yield NADP | |
LKEPKNME_00736 | 3.2e-94 | yjbM | 2.7.6.5 | S | RelA SpoT domain protein | |
LKEPKNME_00737 | 6.2e-256 | topB | 5.99.1.2 | L | This gene contains a nucleotide ambiguity which may be the result of a sequencing error | |
LKEPKNME_00738 | 7e-34 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
LKEPKNME_00739 | 3e-85 | coaBC | 4.1.1.36, 6.3.2.5 | H | Catalyzes two steps in the biosynthesis of coenzyme A. In the first step cysteine is conjugated to 4'-phosphopantothenate to form 4-phosphopantothenoylcysteine, in the latter compound is decarboxylated to form 4'-phosphopantotheine | |
LKEPKNME_00740 | 8.3e-289 | 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 | ||
LKEPKNME_00741 | 2.5e-65 | rpsH | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA central domain where it helps coordinate assembly of the platform of the 30S subunit | ||
LKEPKNME_00742 | 4.4e-28 | rpsN | J | Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site | ||
LKEPKNME_00743 | 1.3e-91 | rplE | J | This is 1 of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance. In the 70S ribosome it contacts protein S13 of the 30S subunit (bridge B1b), connecting the 2 subunits | ||
LKEPKNME_00744 | 7e-47 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
LKEPKNME_00745 | 5.1e-60 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
LKEPKNME_00746 | 8e-39 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
LKEPKNME_00747 | 9e-24 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
LKEPKNME_00748 | 6.2e-73 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
LKEPKNME_00749 | 5.2e-116 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
LKEPKNME_00750 | 2.7e-182 | pepS | E | Thermophilic metalloprotease (M29) | ||
LKEPKNME_00751 | 2.1e-168 | mnaA | 5.1.3.14 | G | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
LKEPKNME_00752 | 6.2e-71 | K | Sugar-specific transcriptional regulator TrmB | |||
LKEPKNME_00753 | 4.1e-237 | yloV | S | DAK2 domain fusion protein YloV | ||
LKEPKNME_00754 | 4.5e-53 | asp | S | Asp23 family, cell envelope-related function | ||
LKEPKNME_00755 | 1.4e-26 | rpmB | J | Belongs to the bacterial ribosomal protein bL28 family | ||
LKEPKNME_00756 | 3.8e-58 | thiN | 2.7.6.2 | H | thiamine pyrophosphokinase | |
LKEPKNME_00757 | 8.7e-97 | proB | 2.7.2.11 | F | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
LKEPKNME_00758 | 8.1e-158 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
LKEPKNME_00759 | 4.3e-59 | 1.13.11.2 | S | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | ||
LKEPKNME_00760 | 2.5e-39 | ybjQ | S | Belongs to the UPF0145 family | ||
LKEPKNME_00762 | 3.7e-26 | radC | L | DNA repair protein | ||
LKEPKNME_00767 | 1.3e-225 | cadA | P | P-type ATPase | ||
LKEPKNME_00768 | 1.8e-254 | E | Amino acid permease | |||
LKEPKNME_00769 | 6.6e-89 | D | CobQ CobB MinD ParA nucleotide binding domain protein | |||
LKEPKNME_00771 | 1.4e-35 | |||||
LKEPKNME_00772 | 2e-283 | pepN | 3.4.11.2 | E | aminopeptidase | |
LKEPKNME_00773 | 1.3e-242 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family | |
LKEPKNME_00774 | 9.6e-96 | S | Predicted membrane protein (DUF2207) | |||
LKEPKNME_00775 | 8.3e-90 | sirR | K | Helix-turn-helix diphteria tox regulatory element | ||
LKEPKNME_00776 | 3.1e-27 | cspC | K | Cold shock protein | ||
LKEPKNME_00777 | 4.3e-82 | thrE | S | Putative threonine/serine exporter | ||
LKEPKNME_00778 | 6.3e-49 | S | Threonine/Serine exporter, ThrE | |||
LKEPKNME_00779 | 2.4e-124 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
LKEPKNME_00780 | 2.8e-277 | tkt | 2.2.1.1 | H | Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate | |
LKEPKNME_00781 | 6e-88 | tal | 2.2.1.2 | F | Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway | |
LKEPKNME_00782 | 2.4e-71 | gutB | 1.1.1.1, 1.1.1.14 | E | Dehydrogenase | |
LKEPKNME_00783 | 0.0 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
LKEPKNME_00784 | 5.4e-167 | pbuG | S | permease | ||
LKEPKNME_00785 | 1.2e-80 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
LKEPKNME_00787 | 2.9e-60 | M | ErfK YbiS YcfS YnhG | |||
LKEPKNME_00788 | 2.7e-46 | yqhL | P | Rhodanese-like protein | ||
LKEPKNME_00789 | 9.7e-17 | WQ51_02665 | S | Protein of unknown function (DUF3042) | ||
LKEPKNME_00790 | 1.1e-111 | 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) | |
LKEPKNME_00791 | 8e-206 | ynbB | 4.4.1.1 | P | aluminum resistance | |
LKEPKNME_00792 | 1.3e-45 | glnR | K | Transcriptional regulator | ||
LKEPKNME_00793 | 3.9e-23 | licT | K | Psort location Cytoplasmic, score 8.87 | ||
LKEPKNME_00794 | 1.3e-28 | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | |||
LKEPKNME_00795 | 2.3e-218 | L | Probable transposase | |||
LKEPKNME_00796 | 5.2e-15 | mreB | D | cell shape determining protein MreB | ||
LKEPKNME_00797 | 2.1e-88 | mreC | M | Involved in formation and maintenance of cell shape | ||
LKEPKNME_00798 | 1.5e-54 | mreD | M | rod shape-determining protein MreD | ||
LKEPKNME_00799 | 1.9e-76 | minC | D | Cell division inhibitor that blocks the formation of polar Z ring septums. Rapidly oscillates between the poles of the cell to destabilize FtsZ filaments that have formed before they mature into polar Z rings. Prevents FtsZ polymerization | ||
LKEPKNME_00800 | 1.8e-126 | minD | D | Belongs to the ParA family | ||
LKEPKNME_00802 | 2.2e-40 | M | family 8 | |||
LKEPKNME_00803 | 2.2e-154 | gtf1 | 2.4.1.52 | GT4 | M | An N-acetylglucosaminyl transferase that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon |
LKEPKNME_00804 | 1.3e-27 | M | Glycosyltransferase like family 2 | |||
LKEPKNME_00805 | 5.3e-189 | 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 | ||
LKEPKNME_00806 | 1e-200 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
LKEPKNME_00808 | 3.2e-231 | S | Virulence-associated protein E | |||
LKEPKNME_00809 | 4.7e-140 | S | Bifunctional DNA primase/polymerase, N-terminal | |||
LKEPKNME_00810 | 3.7e-85 | |||||
LKEPKNME_00811 | 5.6e-117 | L | AAA domain | |||
LKEPKNME_00812 | 5.2e-13 | res | L | Helicase C-terminal domain protein | ||
LKEPKNME_00814 | 1e-285 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
LKEPKNME_00815 | 2e-21 | yheA | S | Belongs to the UPF0342 family | ||
LKEPKNME_00816 | 1.5e-45 | ykuL | S | CBS domain | ||
LKEPKNME_00817 | 3.9e-61 | dapD | 2.3.1.117, 2.3.1.89 | E | Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate | |
LKEPKNME_00818 | 2.4e-177 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
LKEPKNME_00819 | 2.5e-82 | ykuT | M | mechanosensitive ion channel | ||
LKEPKNME_00821 | 7.9e-10 | S | Putative Competence protein ComGF | |||
LKEPKNME_00823 | 9.9e-98 | ytxK | 2.1.1.72 | L | N-6 DNA Methylase | |
LKEPKNME_00824 | 3.2e-184 | cycA | E | Amino acid permease | ||
LKEPKNME_00825 | 1e-48 | V | ABC transporter | |||
LKEPKNME_00826 | 6.8e-89 | S | radical SAM domain protein | |||
LKEPKNME_00829 | 2e-65 | yxaM | EGP | Major Facilitator Superfamily | ||
LKEPKNME_00830 | 1.7e-105 | 2.7.7.73, 2.7.7.80 | H | Involved in molybdopterin and thiamine biosynthesis, family 2 | ||
LKEPKNME_00831 | 3.7e-29 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
LKEPKNME_00832 | 1.7e-108 | S | Acyltransferase family | |||
LKEPKNME_00833 | 7.5e-195 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
LKEPKNME_00834 | 5.1e-103 | 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 | |
LKEPKNME_00835 | 1.4e-36 | nusB | K | Involved in transcription antitermination. Required for transcription of ribosomal RNA (rRNA) genes. Binds specifically to the boxA antiterminator sequence of the ribosomal RNA (rrn) operons | ||
LKEPKNME_00836 | 2.4e-45 | yqhY | S | Asp23 family, cell envelope-related function | ||
LKEPKNME_00837 | 2.1e-94 | efp | J | Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase | ||
LKEPKNME_00838 | 1.8e-29 | dut | S | dUTPase | ||
LKEPKNME_00844 | 9.4e-40 | XK27_10050 | K | Peptidase S24-like | ||
LKEPKNME_00846 | 1.1e-71 | ywlG | S | Belongs to the UPF0340 family | ||
LKEPKNME_00848 | 1e-24 | yjaB_1 | K | Psort location Cytoplasmic, score 8.87 | ||
LKEPKNME_00849 | 1.6e-33 | K | Transcriptional regulator C-terminal region | |||
LKEPKNME_00850 | 2.3e-196 | EGP | Major Facilitator Superfamily | |||
LKEPKNME_00851 | 2.3e-29 | S | Domain of unknown function (DUF4811) | |||
LKEPKNME_00853 | 7.4e-23 | yiiE | S | Protein of unknown function (DUF1211) | ||
LKEPKNME_00854 | 6e-40 | 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 | ||
LKEPKNME_00855 | 2.8e-247 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
LKEPKNME_00857 | 4e-57 | S | CAAX protease self-immunity | |||
LKEPKNME_00858 | 1.9e-99 | K | Psort location Cytoplasmic, score | |||
LKEPKNME_00859 | 6.9e-105 | S | PFAM Archaeal ATPase | |||
LKEPKNME_00860 | 4.1e-109 | ymfF | S | Peptidase M16 inactive domain protein | ||
LKEPKNME_00861 | 1.2e-184 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
LKEPKNME_00863 | 6.4e-90 | nanK | GK | ROK family | ||
LKEPKNME_00864 | 3.9e-127 | nanA | 4.1.3.3, 4.3.3.7 | EM | Neu5Ac) to form pyruvate and N-acetylmannosamine (ManNAc) via a Schiff base intermediate | |
LKEPKNME_00865 | 4.6e-302 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
LKEPKNME_00866 | 2.2e-86 | gla | U | Major intrinsic protein | ||
LKEPKNME_00867 | 1.5e-07 | S | Psort location CytoplasmicMembrane, score | |||
LKEPKNME_00868 | 7.1e-70 | epsB | M | biosynthesis protein | ||
LKEPKNME_00869 | 3.9e-80 | ywqD | 2.7.10.1 | D | Capsular exopolysaccharide family | |
LKEPKNME_00870 | 6e-111 | ywqE | 3.1.3.48 | GM | PHP domain protein | |
LKEPKNME_00871 | 8.6e-211 | lysP | E | amino acid | ||
LKEPKNME_00872 | 2.1e-190 | serS | 6.1.1.11 | J | Catalyzes the attachment of serine to tRNA(Ser). Is also able to aminoacylate tRNA(Sec) with serine, to form the misacylated tRNA L-seryl-tRNA(Sec), which will be further converted into selenocysteinyl-tRNA(Sec) | |
LKEPKNME_00875 | 2.5e-237 | fumC | 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
LKEPKNME_00876 | 5.7e-14 | ybaN | S | Protein of unknown function (DUF454) | ||
LKEPKNME_00877 | 1.7e-143 | merA | 1.16.1.1, 1.8.1.7 | C | Pyridine nucleotide-disulfide oxidoreductase | |
LKEPKNME_00878 | 5.6e-40 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
LKEPKNME_00879 | 1.8e-116 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
LKEPKNME_00880 | 9.2e-266 | rnjB | J | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
LKEPKNME_00881 | 3.6e-42 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
LKEPKNME_00882 | 5e-204 | 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 | |
LKEPKNME_00883 | 7e-40 | ylxM | S | Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY ffh. May be a regulatory protein | ||
LKEPKNME_00884 | 6.2e-150 | 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) | ||
LKEPKNME_00885 | 7.8e-107 | cas1 | L | CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Acts as a dsDNA endonuclease. Involved in the integration of spacer DNA into the CRISPR cassette | ||
LKEPKNME_00886 | 6.5e-37 | cas2 | L | CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Functions as a ssRNA-specific endoribonuclease. Involved in the integration of spacer DNA into the CRISPR cassette | ||
LKEPKNME_00887 | 4.8e-48 | S | CRISPR-associated protein (Cas_Csn2) | |||
LKEPKNME_00888 | 5.8e-153 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
LKEPKNME_00889 | 2.7e-224 | mutL | L | This protein is involved in the repair of mismatches in DNA. It is required for dam-dependent methyl-directed DNA mismatch repair. May act as a molecular matchmaker , a protein that promotes the formation of a stable complex between two or more DNA-binding proteins in an ATP-dependent manner without itself being part of a final effector complex | ||
LKEPKNME_00890 | 2.9e-33 | nfrA | 1.5.1.38, 1.5.1.39 | C | nitroreductase | |
LKEPKNME_00891 | 0.0 | helD | 3.6.4.12 | L | DNA helicase | |
LKEPKNME_00892 | 1e-190 | cycA | E | Amino acid permease | ||
LKEPKNME_00893 | 1.1e-268 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
LKEPKNME_00894 | 0.0 | clpC | O | Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE | ||
LKEPKNME_00895 | 1.6e-55 | ctsR | K | Belongs to the CtsR family | ||
LKEPKNME_00897 | 4.1e-169 | yfnA | E | Amino Acid | ||
LKEPKNME_00898 | 3.2e-53 | zur | P | Belongs to the Fur family | ||
LKEPKNME_00899 | 3.1e-09 | 3.2.1.14 | GH18 | |||
LKEPKNME_00900 | 2e-105 | |||||
LKEPKNME_00901 | 1.2e-31 | K | Transcriptional regulator, MarR family | |||
LKEPKNME_00902 | 8.3e-172 | S | Putative peptidoglycan binding domain | |||
LKEPKNME_00903 | 2.4e-156 | fruA | 2.7.1.202 | GT | Phosphotransferase System | |
LKEPKNME_00904 | 9.1e-50 | cps3F | ||||
LKEPKNME_00905 | 2.7e-83 | S | Membrane | |||
LKEPKNME_00906 | 4.2e-93 | purR | 2.4.2.22, 2.4.2.7 | F | pur operon repressor | |
LKEPKNME_00907 | 5.1e-48 | EGP | Transmembrane secretion effector | |||
LKEPKNME_00908 | 1e-121 | S | overlaps another CDS with the same product name | |||
LKEPKNME_00909 | 5.5e-98 | birA | 6.3.4.15 | H | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
LKEPKNME_00910 | 6.7e-63 | bCE_4747 | S | Beta-lactamase superfamily domain | ||
LKEPKNME_00911 | 1.8e-46 | ybiT | S | ABC transporter, ATP-binding protein | ||
LKEPKNME_00912 | 6.5e-97 | ygaC | J | Belongs to the UPF0374 family | ||
LKEPKNME_00913 | 1.1e-192 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
LKEPKNME_00914 | 1.7e-25 | rhaA | 2.7.1.5, 5.3.1.14 | G | L-rhamnose isomerase (RhaA) | |
LKEPKNME_00915 | 6.9e-110 | rhaD | 4.1.2.17, 4.1.2.19 | H | Catalyzes the reversible cleavage of L-rhamnulose-1- phosphate to dihydroxyacetone phosphate (DHAP) and L-lactaldehyde | |
LKEPKNME_00916 | 2.1e-30 | S | ParE toxin of type II toxin-antitoxin system, parDE | |||
LKEPKNME_00917 | 1.2e-23 | |||||
LKEPKNME_00918 | 2.1e-183 | XK27_11280 | S | Psort location CytoplasmicMembrane, score | ||
LKEPKNME_00919 | 9.1e-43 | yodB | K | Transcriptional regulator, HxlR family | ||
LKEPKNME_00920 | 3e-35 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
LKEPKNME_00921 | 1.9e-121 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
LKEPKNME_00922 | 2.4e-119 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
LKEPKNME_00923 | 1.3e-55 | rbfA | J | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Associates with free 30S ribosomal subunits (but not with 30S subunits that are part of 70S ribosomes or polysomes). Required for efficient processing of 16S rRNA. May interact with the 5'-terminal helix region of 16S rRNA | ||
LKEPKNME_00924 | 0.0 | infB | J | One of the essential components for the initiation of protein synthesis. Protects formylmethionyl-tRNA from spontaneous hydrolysis and promotes its binding to the 30S ribosomal subunits. Also involved in the hydrolysis of GTP during the formation of the 70S ribosomal complex | ||
LKEPKNME_00926 | 6.8e-25 | radC | E | Belongs to the UPF0758 family | ||
LKEPKNME_00927 | 1.4e-46 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
LKEPKNME_00929 | 1.2e-102 | pgm3 | G | phosphoglycerate mutase | ||
LKEPKNME_00930 | 1e-55 | S | CAAX protease self-immunity | |||
LKEPKNME_00931 | 5.7e-48 | C | Flavodoxin | |||
LKEPKNME_00932 | 3.7e-59 | yphH | S | Cupin domain | ||
LKEPKNME_00933 | 3e-45 | yphJ | 4.1.1.44 | S | decarboxylase | |
LKEPKNME_00934 | 7.4e-159 | tyrS | 6.1.1.1 | J | Catalyzes the attachment of tyrosine to tRNA(Tyr) in a two-step reaction tyrosine is first activated by ATP to form Tyr- AMP and then transferred to the acceptor end of tRNA(Tyr) | |
LKEPKNME_00935 | 4e-141 | panE | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
LKEPKNME_00936 | 2.5e-86 | S | (CBS) domain | |||
LKEPKNME_00937 | 1e-138 | EGP | Major facilitator Superfamily | |||
LKEPKNME_00938 | 1.4e-21 | K | helix_turn_helix multiple antibiotic resistance protein | |||
LKEPKNME_00939 | 2.1e-226 | pipD | E | Dipeptidase | ||
LKEPKNME_00940 | 1e-271 | rnjA | J | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
LKEPKNME_00941 | 2.3e-249 | 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 | |
LKEPKNME_00943 | 4.1e-74 | metY | 2.5.1.49 | E | Catalyzes the formation of L-methionine and acetate from O-acetyl-L-homoserine and methanethiol | |
LKEPKNME_00944 | 1.1e-160 | adhB | 1.1.1.1, 1.1.1.14 | E | alcohol dehydrogenase | |
LKEPKNME_00945 | 9.8e-57 | 3.1.3.48 | K | Transcriptional regulator | ||
LKEPKNME_00946 | 2.9e-33 | 1.3.5.4 | C | FMN_bind | ||
LKEPKNME_00947 | 6.5e-197 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
LKEPKNME_00948 | 1.7e-201 | argH | 4.3.2.1 | E | argininosuccinate lyase | |
LKEPKNME_00949 | 2.3e-302 | glmS | 2.6.1.16 | M | Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source | |
LKEPKNME_00950 | 6.8e-90 | mtlR | K | Mga helix-turn-helix domain | ||
LKEPKNME_00951 | 5e-147 | pbuO_1 | S | Permease family | ||
LKEPKNME_00952 | 4.2e-156 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
LKEPKNME_00953 | 4.7e-59 | menA | 2.5.1.74 | H | Belongs to the MenA family. Type 1 subfamily | |
LKEPKNME_00954 | 1.8e-184 | recJ | L | Single-stranded-DNA-specific exonuclease RecJ | ||
LKEPKNME_00955 | 5.8e-101 | XK27_05435 | 1.1.1.100 | S | Enoyl-(Acyl carrier protein) reductase | |
LKEPKNME_00958 | 3.7e-21 | yvaO | K | Helix-turn-helix domain | ||
LKEPKNME_00959 | 2.3e-10 | E | IrrE N-terminal-like domain | |||
LKEPKNME_00962 | 1.1e-21 | |||||
LKEPKNME_00963 | 2.7e-115 | murB | 1.3.1.98 | M | Cell wall formation | |
LKEPKNME_00964 | 2e-70 | S | Protein of unknown function (DUF1361) | |||
LKEPKNME_00965 | 2.9e-127 | dacA | 2.7.7.85 | S | Catalyzes the condensation of 2 ATP molecules into cyclic di-AMP (c-di-AMP), a second messenger used to regulate differing processes in different bacteria | |
LKEPKNME_00966 | 2.2e-192 | |||||
LKEPKNME_00967 | 7.4e-08 | yfiE | K | LysR family | ||
LKEPKNME_00968 | 4.3e-18 | |||||
LKEPKNME_00974 | 3.7e-75 | recT | L | RecT family | ||
LKEPKNME_00975 | 1.2e-88 | pi112 | 3.6.4.12 | L | PDDEXK-like domain of unknown function (DUF3799) | |
LKEPKNME_00977 | 2.4e-224 | dxs | 2.2.1.7 | H | Catalyzes the acyloin condensation reaction between C atoms 2 and 3 of pyruvate and glyceraldehyde 3-phosphate to yield 1-deoxy-D-xylulose-5-phosphate (DXP) | |
LKEPKNME_00978 | 4.2e-29 | |||||
LKEPKNME_00979 | 5.3e-246 | yjbQ | P | TrkA C-terminal domain protein | ||
LKEPKNME_00982 | 9.2e-40 | S | Phage tail assembly chaperone proteins, TAC | |||
LKEPKNME_00983 | 1.2e-103 | pfoS | S | Phosphotransferase system, EIIC | ||
LKEPKNME_00984 | 1.5e-127 | ldhD | 1.1.1.28 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
LKEPKNME_00985 | 7.8e-115 | patA | 2.6.1.1, 2.6.1.57 | E | Aminotransferase | |
LKEPKNME_00987 | 3.5e-63 | bcgIB | 2.1.1.72, 3.1.21.3 | V | type I restriction modification DNA specificity domain | |
LKEPKNME_00988 | 3.7e-99 | 2.1.1.72 | V | N-6 DNA Methylase | ||
LKEPKNME_00989 | 2.9e-247 | gltX | 6.1.1.17, 6.1.1.24 | J | Catalyzes the attachment of glutamate to tRNA(Glu) in a two-step reaction glutamate is first activated by ATP to form Glu-AMP and then transferred to the acceptor end of tRNA(Glu) | |
LKEPKNME_00990 | 5.9e-14 | yacL | S | domain protein | ||
LKEPKNME_00992 | 1.7e-25 | 3.2.1.18 | GH33 | M | Rib/alpha-like repeat | |
LKEPKNME_00994 | 2.5e-76 | hchA | S | intracellular protease amidase | ||
LKEPKNME_00995 | 3.1e-22 | K | transcriptional regulator | |||
LKEPKNME_00996 | 7.5e-40 | KT | Putative sugar diacid recognition | |||
LKEPKNME_00998 | 4.6e-08 | |||||
LKEPKNME_01001 | 5.5e-75 | |||||
LKEPKNME_01007 | 7.6e-177 | 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 | |
LKEPKNME_01008 | 5.5e-54 | ytmP | 2.7.1.89 | M | Choline/ethanolamine kinase | |
LKEPKNME_01009 | 3e-100 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
LKEPKNME_01011 | 4e-45 | ytpP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
LKEPKNME_01012 | 8.1e-77 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
LKEPKNME_01013 | 4.6e-35 | ygfC | K | Bacterial regulatory proteins, tetR family | ||
LKEPKNME_01014 | 1.1e-85 | ddpX | 3.4.13.22 | E | Catalyzes hydrolysis of the D-alanyl-D-alanine dipeptide | |
LKEPKNME_01015 | 9.1e-217 | scrB | 3.2.1.26 | GH32 | G | invertase |
LKEPKNME_01016 | 3.7e-43 | ispA | 2.5.1.1, 2.5.1.10, 2.5.1.29, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
LKEPKNME_01017 | 5.2e-121 | rrmJ | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
LKEPKNME_01018 | 6.6e-49 | argR | K | Regulates arginine biosynthesis genes | ||
LKEPKNME_01019 | 8.2e-33 | M | Glycosyl transferase, family 2 | |||
LKEPKNME_01020 | 4.3e-79 | MA20_43635 | M | Capsular polysaccharide synthesis protein | ||
LKEPKNME_01021 | 7.2e-91 | licD2 | M | LICD family | ||
LKEPKNME_01022 | 2.1e-78 | L | Replication protein | |||
LKEPKNME_01024 | 1.9e-23 | dedA | 3.1.3.1 | S | SNARE associated Golgi protein | |
LKEPKNME_01025 | 1.8e-162 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
LKEPKNME_01026 | 4.1e-18 | yncA | 2.3.1.79 | S | Maltose acetyltransferase | |
LKEPKNME_01027 | 1.3e-84 | yflS | P | Sodium:sulfate symporter transmembrane region | ||
LKEPKNME_01028 | 3.9e-49 | rsfS | J | Functions as a ribosomal silencing factor. Interacts with ribosomal protein L14 (rplN), blocking formation of intersubunit bridge B8. Prevents association of the 30S and 50S ribosomal subunits and the formation of functional ribosomes, thus repressing translation | ||
LKEPKNME_01029 | 1.2e-71 | nadD | 2.7.6.3, 2.7.7.18 | H | Hydrolase, HD family | |
LKEPKNME_01030 | 3.5e-77 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
LKEPKNME_01031 | 6e-30 | yhbY | J | RNA-binding protein | ||
LKEPKNME_01032 | 3.6e-75 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
LKEPKNME_01037 | 3.8e-39 | rplW | J | One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome | ||
LKEPKNME_01038 | 1e-100 | rplD | J | Forms part of the polypeptide exit tunnel | ||
LKEPKNME_01039 | 3.8e-108 | rplC | J | One of the primary rRNA binding proteins, it binds directly near the 3'-end of the 23S rRNA, where it nucleates assembly of the 50S subunit | ||
LKEPKNME_01040 | 2e-49 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
LKEPKNME_01041 | 3.5e-09 | ybhF_2 | V | abc transporter atp-binding protein | ||
LKEPKNME_01042 | 2.1e-47 | ybhF_2 | V | AAA domain, putative AbiEii toxin, Type IV TA system | ||
LKEPKNME_01043 | 4.4e-103 | ppx | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
LKEPKNME_01044 | 4e-61 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
LKEPKNME_01045 | 3.9e-108 | 3.6.3.38, 3.6.3.40 | GM | Part of the ABC transporter complex TagGH involved in teichoic acids export. Responsible for energy coupling to the transport system | ||
LKEPKNME_01046 | 2e-53 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
LKEPKNME_01047 | 1.3e-133 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
LKEPKNME_01048 | 1.1e-43 | E | GDSL-like Lipase/Acylhydrolase | |||
LKEPKNME_01049 | 2.5e-280 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
LKEPKNME_01050 | 7.6e-53 | S | Membrane | |||
LKEPKNME_01051 | 6.7e-98 | spoVK | O | ATPase family associated with various cellular activities (AAA) | ||
LKEPKNME_01052 | 9.7e-231 | V | ABC transporter transmembrane region | |||
LKEPKNME_01053 | 1.6e-106 | yxeH | S | hydrolase | ||
LKEPKNME_01054 | 3.9e-236 | ydaO | E | amino acid | ||
LKEPKNME_01055 | 7.4e-146 | tagO | 2.7.8.33, 2.7.8.35 | M | transferase | |
LKEPKNME_01056 | 2.6e-79 | mgs | 2.4.1.337 | GT4 | M | Glycosyltransferase, group 1 family protein |
LKEPKNME_01057 | 7.2e-119 | cpoA | GT4 | M | Glycosyltransferase, group 1 family protein | |
LKEPKNME_01058 | 4e-131 | mprF | I | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms | ||
LKEPKNME_01059 | 6.2e-112 | natA | S | Domain of unknown function (DUF4162) | ||
LKEPKNME_01060 | 3.7e-23 | K | Acetyltransferase (GNAT) domain | |||
LKEPKNME_01062 | 4.3e-61 | uspA | T | universal stress protein | ||
LKEPKNME_01064 | 7e-28 | yfnA | E | amino acid | ||
LKEPKNME_01067 | 3e-42 | srtB | 3.4.22.70 | S | Sortase family | |
LKEPKNME_01068 | 5.8e-206 | S | Protein conserved in bacteria | |||
LKEPKNME_01069 | 1.5e-24 | |||||
LKEPKNME_01070 | 7.6e-77 | |||||
LKEPKNME_01071 | 5.6e-61 | divIVA | D | DivIVA domain protein | ||
LKEPKNME_01072 | 1e-104 | 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 | ||
LKEPKNME_01073 | 1.6e-199 | oatA | I | Acyltransferase | ||
LKEPKNME_01074 | 1.3e-38 | srlR2 | 2.7.1.202 | GT | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
LKEPKNME_01075 | 4.5e-43 | gutM | K | Glucitol operon activator protein (GutM) | ||
LKEPKNME_01076 | 4.8e-83 | srlA | G | PTS system enzyme II sorbitol-specific factor | ||
LKEPKNME_01077 | 2.1e-135 | srlE | 2.7.1.198 | G | Sorbitol phosphotransferase enzyme II N-terminus | |
LKEPKNME_01078 | 1.7e-58 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | ||
LKEPKNME_01079 | 9.5e-63 | hsdS-1 | 3.1.21.3 | L | Belongs to the 'phage' integrase family | |
LKEPKNME_01080 | 2.9e-24 | L | Addiction module antitoxin, RelB DinJ family | |||
LKEPKNME_01081 | 4.1e-24 | S | Addiction module toxin RelE StbE family | |||
LKEPKNME_01082 | 6.5e-10 | S | D5 N terminal like | |||
LKEPKNME_01084 | 1.2e-10 | |||||
LKEPKNME_01085 | 1.9e-251 | guaB | 1.1.1.205 | F | Catalyzes the irreversible NADPH-dependent deamination of GMP to IMP. It functions in the conversion of nucleobase, nucleoside and nucleotide derivatives of G to A nucleotides, and in maintaining the intracellular balance of A and G nucleotides | |
LKEPKNME_01086 | 8.4e-65 | L | Helicase C-terminal domain protein | |||
LKEPKNME_01087 | 8.7e-133 | hprK | F | Catalyzes the ATP- as well as the pyrophosphate- dependent phosphorylation of a specific serine residue in HPr, a phosphocarrier protein of the phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS). HprK P also catalyzes the pyrophosphate-producing, inorganic phosphate-dependent dephosphorylation (phosphorolysis) of seryl-phosphorylated HPr (P- Ser-HPr). The two antagonistic activities of HprK P are regulated by several intracellular metabolites, which change their concentration in response to the absence or presence of rapidly metabolisable carbon sources (glucose, fructose, etc.) in the growth medium. Therefore, by controlling the phosphorylation state of HPr, HPrK P is a sensor enzyme that plays a major role in the regulation of carbon metabolism and sugar transport it mediates carbon catabolite repression (CCR), and regulates PTS-catalyzed carbohydrate uptake and inducer exclusion | ||
LKEPKNME_01088 | 2.7e-26 | yvlD | S | Mycobacterial 4 TMS phage holin, superfamily IV | ||
LKEPKNME_01089 | 4.1e-08 | KT | PspC domain protein | |||
LKEPKNME_01090 | 4.1e-75 | phoR | 2.7.13.3 | T | Histidine kinase | |
LKEPKNME_01091 | 6.4e-177 | licA | 2.7.1.89 | M | Choline/ethanolamine kinase | |
LKEPKNME_01092 | 5e-38 | thrB | 2.7.1.39 | F | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
LKEPKNME_01093 | 2.7e-66 | rimP | J | Required for maturation of 30S ribosomal subunits | ||
LKEPKNME_01094 | 3.1e-169 | nusA | K | Participates in both transcription termination and antitermination | ||
LKEPKNME_01095 | 1.4e-39 | ylxR | K | Protein of unknown function (DUF448) | ||
LKEPKNME_01096 | 6.8e-26 | ylxQ | J | ribosomal protein | ||
LKEPKNME_01098 | 6.4e-149 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
LKEPKNME_01099 | 7.1e-41 | sbcD | L | SbcCD cleaves DNA hairpin structures. These structures can inhibit DNA replication and are intermediates in certain DNA recombination reactions. The complex acts as a 3'- 5' double strand exonuclease that can open hairpins. It also has a 5' single-strand endonuclease activity | ||
LKEPKNME_01100 | 1.4e-42 | |||||
LKEPKNME_01101 | 4.9e-128 | S | AAA domain, putative AbiEii toxin, Type IV TA system | |||
LKEPKNME_01102 | 3.7e-23 | |||||
LKEPKNME_01103 | 1.5e-14 | |||||
LKEPKNME_01104 | 1.9e-128 | G | Belongs to the glycosyl hydrolase 8 (cellulase D) family | |||
LKEPKNME_01105 | 2e-41 | 2.7.7.65 | T | GGDEF domain | ||
LKEPKNME_01106 | 1.8e-65 | S | Protein of unknown function (DUF806) | |||
LKEPKNME_01107 | 4.3e-65 | S | Bacteriophage HK97-gp10, putative tail-component | |||
LKEPKNME_01108 | 4.6e-58 | S | Phage head-tail joining protein | |||
LKEPKNME_01109 | 4.8e-22 | S | Phage gp6-like head-tail connector protein | |||
LKEPKNME_01110 | 5.4e-192 | S | Phage capsid family | |||
LKEPKNME_01111 | 2.1e-199 | S | Phage Terminase | |||
LKEPKNME_01112 | 4.3e-83 | L | Phage terminase, small subunit | |||
LKEPKNME_01113 | 6.8e-74 | L | HNH nucleases | |||
LKEPKNME_01116 | 1.7e-303 | pyc | 6.4.1.1 | C | Catalyzes a 2-step reaction, involving the ATP-dependent carboxylation of the covalently attached biotin in the first step and the transfer of the carboxyl group to pyruvate in the second | |
LKEPKNME_01117 | 8.1e-18 | ylbG | S | Uncharacterized protein conserved in bacteria (DUF2129) | ||
LKEPKNME_01124 | 1.7e-115 | fabH | 2.3.1.180 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids | |
LKEPKNME_01125 | 5.9e-129 | mleP2 | S | Sodium Bile acid symporter family | ||
LKEPKNME_01126 | 6.2e-114 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
LKEPKNME_01127 | 1.5e-32 | ywjH | S | Protein of unknown function (DUF1634) | ||
LKEPKNME_01128 | 1.7e-119 | yxaA | S | membrane transporter protein | ||
LKEPKNME_01129 | 3.4e-167 | mbl | D | Cell shape determining protein MreB Mrl | ||
LKEPKNME_01130 | 9e-27 | yidD | S | Could be involved in insertion of integral membrane proteins into the membrane | ||
LKEPKNME_01131 | 1.3e-13 | S | Protein of unknown function (DUF2969) | |||
LKEPKNME_01132 | 1.1e-71 | lemA | S | LemA family | ||
LKEPKNME_01133 | 1.3e-114 | htpX | O | Belongs to the peptidase M48B family | ||
LKEPKNME_01135 | 2.8e-87 | helD | 3.6.4.12 | L | DNA helicase | |
LKEPKNME_01139 | 3e-17 | yvaO | K | Helix-turn-helix XRE-family like proteins | ||
LKEPKNME_01140 | 3.2e-15 | S | Pfam:DUF955 | |||
LKEPKNME_01141 | 1.6e-33 | |||||
LKEPKNME_01144 | 4.9e-09 | S | CAAX protease self-immunity | |||
LKEPKNME_01147 | 7e-68 | S | Cell surface protein | |||
LKEPKNME_01148 | 1.4e-117 | yxjG | 2.1.1.14 | E | Cobalamin-independent synthase, Catalytic domain | |
LKEPKNME_01149 | 9.8e-75 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to | |
LKEPKNME_01150 | 1.4e-100 | metY | 2.5.1.49 | E | Catalyzes the formation of L-methionine and acetate from O-acetyl-L-homoserine and methanethiol | |
LKEPKNME_01151 | 4.5e-141 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
LKEPKNME_01152 | 6.5e-79 | K | rpiR family | |||
LKEPKNME_01153 | 3.5e-217 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
LKEPKNME_01154 | 5.2e-93 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
LKEPKNME_01155 | 1.7e-19 | |||||
LKEPKNME_01158 | 2.2e-61 | |||||
LKEPKNME_01159 | 7e-183 | dinG | 3.1.12.1, 3.6.4.12 | KL | DEAD_2 | |
LKEPKNME_01162 | 3.3e-13 | |||||
LKEPKNME_01163 | 1.6e-86 | pepQ | 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
LKEPKNME_01164 | 7.6e-104 | S | Phospholipase/Carboxylesterase | |||
LKEPKNME_01165 | 8.5e-98 | G | PFAM major facilitator superfamily MFS_1 | |||
LKEPKNME_01166 | 2.1e-131 | pdhC | 2.3.1.12 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
LKEPKNME_01167 | 8.8e-230 | lpdA | 1.8.1.4 | C | Dehydrogenase | |
LKEPKNME_01168 | 5.4e-177 | thrC | 4.2.3.1 | E | Threonine synthase | |
LKEPKNME_01169 | 2.3e-49 | XK27_08315 | M | Sulfatase | ||
LKEPKNME_01170 | 5.1e-08 | D | Lytic transglycosylase with a strong preference for naked glycan strands that lack stem peptides | |||
LKEPKNME_01172 | 4.3e-17 | holB | 2.7.7.7 | L | DNA polymerase III | |
LKEPKNME_01173 | 1.4e-40 | yabA | L | Involved in initiation control of chromosome replication | ||
LKEPKNME_01174 | 4.1e-92 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
LKEPKNME_01175 | 2.1e-81 | fat | 3.1.2.21 | I | Acyl-ACP thioesterase | |
LKEPKNME_01176 | 2.6e-50 | lysR5 | K | LysR substrate binding domain | ||
LKEPKNME_01177 | 9.4e-57 | lssY | 3.6.1.27 | I | phosphatidate phosphatase activity | |
LKEPKNME_01178 | 3.2e-14 | 2.3.1.128 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | ||
LKEPKNME_01179 | 1.1e-11 | |||||
LKEPKNME_01182 | 5.1e-115 | glcR | K | DeoR C terminal sensor domain | ||
LKEPKNME_01183 | 4.5e-171 | patA | 2.6.1.1 | E | Aminotransferase | |
LKEPKNME_01184 | 1.5e-42 | K | helix_turn_helix isocitrate lyase regulation | |||
LKEPKNME_01185 | 4e-120 | 1.1.1.28 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | ||
LKEPKNME_01186 | 4.8e-49 | pfoS | S | Phosphotransferase system, EIIC | ||
LKEPKNME_01187 | 2.6e-100 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
LKEPKNME_01188 | 1.3e-57 | 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 | ||
LKEPKNME_01189 | 7.7e-21 | 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 | ||
LKEPKNME_01190 | 1.8e-68 | xerD | L | Phage integrase, N-terminal SAM-like domain | ||
LKEPKNME_01192 | 1.8e-56 | yqeY | S | YqeY-like protein | ||
LKEPKNME_01193 | 4.7e-22 | rpsU | J | Belongs to the bacterial ribosomal protein bS21 family | ||
LKEPKNME_01194 | 1.9e-07 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
LKEPKNME_01195 | 4e-190 | ftsA | D | Cell division protein that is involved in the assembly of the Z ring. May serve as a membrane anchor for the Z ring | ||
LKEPKNME_01196 | 3e-76 | glgP | 2.4.1.1 | GT35 | G | Phosphorylase is an important allosteric enzyme in carbohydrate metabolism. Enzymes from different sources differ in their regulatory mechanisms and in their natural substrates. However, all known phosphorylases share catalytic and structural properties |
LKEPKNME_01197 | 1.5e-16 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
LKEPKNME_01198 | 7.6e-75 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
LKEPKNME_01199 | 1.7e-47 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
LKEPKNME_01200 | 1.4e-54 | |||||
LKEPKNME_01201 | 5.5e-109 | fabI | 1.3.1.10, 1.3.1.9 | I | Enoyl- acyl-carrier-protein reductase NADH | |
LKEPKNME_01202 | 6e-64 | accA | 2.1.3.15, 6.4.1.2 | I | alpha subunit | |
LKEPKNME_01203 | 1.7e-60 | ypbB | 5.1.3.1 | S | Helix-turn-helix domain | |
LKEPKNME_01205 | 1.5e-99 | M | Prophage endopeptidase tail | |||
LKEPKNME_01206 | 8e-70 | S | Uncharacterised protein family (UPF0236) | |||
LKEPKNME_01207 | 1.3e-75 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
LKEPKNME_01208 | 1.9e-168 | ilvE | 2.6.1.42 | E | Branched-chain amino acid aminotransferase | |
LKEPKNME_01209 | 3.5e-132 | ABC-SBP | S | ABC transporter | ||
LKEPKNME_01210 | 8.1e-198 | dnaX | 2.7.7.7 | L | DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
LKEPKNME_01211 | 7e-34 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
LKEPKNME_01213 | 4.7e-294 | lai | 4.2.1.53 | S | Myosin-crossreactive antigen | |
LKEPKNME_01214 | 2.1e-21 | nmtR | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
LKEPKNME_01215 | 2.5e-09 | sftA | D | Belongs to the FtsK SpoIIIE SftA family | ||
LKEPKNME_01217 | 1.1e-150 | rny | S | Endoribonuclease that initiates mRNA decay | ||
LKEPKNME_01218 | 2.9e-16 | M | domain protein | |||
LKEPKNME_01219 | 7.9e-125 | yvgN | C | Aldo keto reductase | ||
LKEPKNME_01223 | 2.8e-36 | repE | K | Primase C terminal 1 (PriCT-1) | ||
LKEPKNME_01224 | 1.8e-17 | S | Bacterial membrane protein YfhO | |||
LKEPKNME_01225 | 2.6e-226 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
LKEPKNME_01226 | 1.1e-60 | ybbR | S | YbbR-like protein | ||
LKEPKNME_01227 | 2.4e-190 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
LKEPKNME_01228 | 1.8e-24 | yyzM | S | Bacterial protein of unknown function (DUF951) | ||
LKEPKNME_01229 | 3e-33 | spo0J | K | Belongs to the ParB family | ||
LKEPKNME_01230 | 1.2e-205 | yeeA | V | Type II restriction enzyme, methylase subunits | ||
LKEPKNME_01231 | 1.7e-57 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
LKEPKNME_01232 | 1.9e-114 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase phosphomannomutase, alpha beta alpha domain | |
LKEPKNME_01233 | 1.3e-147 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase phosphomannomutase, alpha beta alpha domain | |
LKEPKNME_01234 | 8.3e-96 | clcA | P | chloride | ||
LKEPKNME_01235 | 2.8e-19 | secG | U | Preprotein translocase | ||
LKEPKNME_01236 | 6.8e-26 | ykuJ | S | Protein of unknown function (DUF1797) | ||
LKEPKNME_01237 | 1.6e-55 | jag | S | R3H domain protein | ||
LKEPKNME_01238 | 1.6e-120 | sip | L | Belongs to the 'phage' integrase family | ||
LKEPKNME_01239 | 8.8e-90 | KT | Transcriptional regulatory protein, C terminal | |||
LKEPKNME_01240 | 5e-45 | spaC2 | V | Lanthionine synthetase C-like protein | ||
LKEPKNME_01241 | 6.8e-62 | L | Resolvase, N-terminal domain | |||
LKEPKNME_01242 | 2.1e-23 | M1-874 | K | Domain of unknown function (DUF1836) | ||
LKEPKNME_01243 | 2.1e-83 | S | membrane | |||
LKEPKNME_01244 | 1.1e-79 | S | VIT family | |||
LKEPKNME_01245 | 2.4e-24 | fba | 4.1.2.13, 4.1.2.29 | G | Fructose-1,6-bisphosphate aldolase, class II | |
LKEPKNME_01246 | 1.4e-48 | 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 | ||
LKEPKNME_01247 | 5.5e-110 | sufB | O | assembly protein SufB | ||
LKEPKNME_01248 | 1.2e-44 | S | VIT family | |||
LKEPKNME_01249 | 3.4e-33 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
LKEPKNME_01250 | 6.3e-69 | gluP | 3.4.21.105 | S | Peptidase, S54 family | |
LKEPKNME_01251 | 1.5e-25 | yqgQ | S | Bacterial protein of unknown function (DUF910) | ||
LKEPKNME_01252 | 2.2e-145 | KLT | serine threonine protein kinase | |||
LKEPKNME_01253 | 2.3e-168 | hom | 1.1.1.3, 2.7.2.4 | E | homoserine dehydrogenase | |
LKEPKNME_01255 | 4.1e-138 | hprA | 1.1.1.29 | C | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
LKEPKNME_01256 | 4.7e-178 | pdhA | 1.2.4.1, 1.2.4.4 | C | Dehydrogenase E1 component | |
LKEPKNME_01257 | 6e-81 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
LKEPKNME_01258 | 7e-95 | yeaN | P | Major Facilitator Superfamily | ||
LKEPKNME_01261 | 5.1e-282 | V | DNA modification | |||
LKEPKNME_01262 | 1.8e-199 | 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 | ||
LKEPKNME_01263 | 1.1e-83 | luxS | 4.4.1.21 | H | Involved in the synthesis of autoinducer 2 (AI-2) which is secreted by bacteria and is used to communicate both the cell density and the metabolic potential of the environment. The regulation of gene expression in response to changes in cell density is called quorum sensing. Catalyzes the transformation of S-ribosylhomocysteine (RHC) to homocysteine (HC) and 4,5- dihydroxy-2,3-pentadione (DPD) | |
LKEPKNME_01264 | 2.9e-79 | ylbE | GM | NAD dependent epimerase dehydratase family protein | ||
LKEPKNME_01265 | 1.4e-153 | 1.3.5.4 | C | FMN_bind | ||
LKEPKNME_01267 | 1.8e-85 | sip | L | Belongs to the 'phage' integrase family | ||
LKEPKNME_01268 | 1.3e-74 | metQ | M | Belongs to the nlpA lipoprotein family | ||
LKEPKNME_01269 | 5.7e-55 | S | Protein of unknown function (DUF4256) | |||
LKEPKNME_01273 | 1.7e-107 | terC | P | Integral membrane protein TerC family | ||
LKEPKNME_01274 | 3.6e-38 | K | Transcriptional regulator | |||
LKEPKNME_01275 | 1.2e-91 | tcyA | ET | Belongs to the bacterial solute-binding protein 3 family | ||
LKEPKNME_01276 | 5e-67 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
LKEPKNME_01277 | 7.7e-84 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
LKEPKNME_01278 | 2.6e-11 | 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 | ||
LKEPKNME_01279 | 2.1e-20 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
LKEPKNME_01280 | 1.3e-191 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
LKEPKNME_01281 | 4.4e-104 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
LKEPKNME_01282 | 1.8e-82 | pncA | Q | isochorismatase | ||
LKEPKNME_01283 | 1.8e-62 | 3.1.3.73 | G | phosphoglycerate mutase | ||
LKEPKNME_01284 | 9.9e-47 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | ||
LKEPKNME_01285 | 4.6e-47 | hsdR | 3.1.21.3 | V | Subunit R is required for both nuclease and ATPase activities, but not for modification | |
LKEPKNME_01286 | 3.5e-16 | EGP | Major facilitator Superfamily | |||
LKEPKNME_01287 | 4.7e-81 | S | L,D-transpeptidase catalytic domain | |||
LKEPKNME_01288 | 9.4e-109 | menE | 6.2.1.26 | H | Belongs to the ATP-dependent AMP-binding enzyme family. MenE subfamily | |
LKEPKNME_01289 | 7.3e-201 | pflB | 2.3.1.54 | C | Pyruvate formate lyase-like | |
LKEPKNME_01290 | 4.4e-136 | pflA | 1.97.1.4 | C | Activation of pyruvate formate-lyase under anaerobic conditions by generation of an organic free radical, using S- adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine | |
LKEPKNME_01291 | 1.8e-149 | whiA | K | May be required for sporulation | ||
LKEPKNME_01292 | 5.7e-154 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
LKEPKNME_01293 | 7e-79 | hslV | 3.4.25.2 | O | Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery | |
LKEPKNME_01294 | 6e-123 | xerC | D | Belongs to the 'phage' integrase family. XerC subfamily | ||
LKEPKNME_01295 | 1.1e-67 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
LKEPKNME_01296 | 7e-198 | yfnA | E | amino acid | ||
LKEPKNME_01297 | 3.2e-25 | pat | 2.3.1.183 | M | Acetyltransferase GNAT family | |
LKEPKNME_01298 | 6.5e-16 | L | AAA ATPase domain | |||
LKEPKNME_01299 | 2.4e-19 | 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 | ||
LKEPKNME_01300 | 9.9e-94 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | G | Responsible for synthesis of pseudouridine from uracil | |
LKEPKNME_01301 | 3.3e-109 | dnaJ | O | ATP binding to DnaK triggers the release of the substrate protein, thus completing the reaction cycle. Several rounds of ATP-dependent interactions between DnaJ, DnaK and GrpE are required for fully efficient folding. Also involved, together with DnaK and GrpE, in the DNA replication of plasmids through activation of initiation proteins | ||
LKEPKNME_01302 | 1.3e-73 | 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 | |
LKEPKNME_01303 | 1.4e-42 | S | Phosphoesterase | |||
LKEPKNME_01305 | 9.7e-37 | ptsH | G | phosphocarrier protein HPR | ||
LKEPKNME_01306 | 1.5e-15 | |||||
LKEPKNME_01307 | 7.2e-181 | cydA | 1.10.3.14 | C | ubiquinol oxidase | |
LKEPKNME_01308 | 1.3e-114 | sip | L | Belongs to the 'phage' integrase family | ||
LKEPKNME_01309 | 1.6e-54 | L | Helix-turn-helix domain | |||
LKEPKNME_01310 | 2.4e-119 | lepA | M | Required for accurate and efficient protein synthesis under certain stress conditions. May act as a fidelity factor of the translation reaction, by catalyzing a one-codon backward translocation of tRNAs on improperly translocated ribosomes. Back- translocation proceeds from a post-translocation (POST) complex to a pre-translocation (PRE) complex, thus giving elongation factor G a second chance to translocate the tRNAs correctly. Binds to ribosomes in a GTP-dependent manner | ||
LKEPKNME_01311 | 1e-196 | alsS | 2.2.1.6 | EH | Belongs to the TPP enzyme family | |
LKEPKNME_01312 | 3.1e-69 | budA | 4.1.1.5 | Q | Alpha-acetolactate decarboxylase | |
LKEPKNME_01313 | 1.8e-22 | 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 | |
LKEPKNME_01314 | 6e-142 | 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 | ||
LKEPKNME_01315 | 8.4e-19 | 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 | |
LKEPKNME_01319 | 1.9e-184 | spaT | V | ATPases associated with a variety of cellular activities | ||
LKEPKNME_01320 | 1.5e-39 | rhaM | 5.1.3.32 | G | Involved in the anomeric conversion of L-rhamnose | |
LKEPKNME_01321 | 1.3e-73 | rhaB | 2.7.1.5, 5.3.1.14 | F | Involved in the catabolism of L-rhamnose (6-deoxy-L- mannose). Catalyzes the transfer of the gamma-phosphate group from ATP to the 1-hydroxyl group of L-rhamnulose to yield L-rhamnulose 1-phosphate | |
LKEPKNME_01323 | 5.8e-188 | rarA | L | recombination factor protein RarA | ||
LKEPKNME_01324 | 4.8e-157 | M | Belongs to the BCCT transporter (TC 2.A.15) family | |||
LKEPKNME_01325 | 1.1e-12 | M | MobA-like NTP transferase domain | |||
LKEPKNME_01326 | 9.8e-95 | ecsA | V | ABC transporter, ATP-binding protein | ||
LKEPKNME_01327 | 5.4e-53 | hit | FG | histidine triad | ||
LKEPKNME_01328 | 8e-136 | mvaS | 2.3.3.10 | I | Hydroxymethylglutaryl-CoA synthase | |
LKEPKNME_01329 | 1.7e-267 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
LKEPKNME_01330 | 4.9e-32 | O | ADP-ribosylglycohydrolase | |||
LKEPKNME_01331 | 2.5e-158 | purK | 6.3.4.18 | F | Catalyzes the ATP-dependent conversion of 5- aminoimidazole ribonucleotide (AIR) and HCO(3)(-) to N5- carboxyaminoimidazole ribonucleotide (N5-CAIR) | |
LKEPKNME_01332 | 4.7e-138 | G | Xylose isomerase-like TIM barrel | |||
LKEPKNME_01334 | 1.3e-87 | endA | F | DNA RNA non-specific endonuclease | ||
LKEPKNME_01335 | 1.3e-189 | mnmE | S | Exhibits a very high intrinsic GTPase hydrolysis rate. Involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA- cmnm(5)s(2)U34 | ||
LKEPKNME_01336 | 9.2e-138 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
LKEPKNME_01337 | 1.7e-10 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
LKEPKNME_01338 | 1.4e-12 | yajC | U | Preprotein translocase | ||
LKEPKNME_01339 | 7.8e-208 | tgt | 2.4.2.29 | F | Catalyzes the base-exchange of a guanine (G) residue with the queuine precursor 7-aminomethyl-7-deazaguanine (PreQ1) at position 34 (anticodon wobble position) in tRNAs with GU(N) anticodons (tRNA-Asp, -Asn, -His and -Tyr). Catalysis occurs through a double-displacement mechanism. The nucleophile active site attacks the C1' of nucleotide 34 to detach the guanine base from the RNA, forming a covalent enzyme-RNA intermediate. The proton acceptor active site deprotonates the incoming PreQ1, allowing a nucleophilic attack on the C1' of the ribose to form the product. After dissociation, two additional enzymatic reactions on the tRNA convert PreQ1 to queuine (Q), resulting in the hypermodified nucleoside queuosine (7-(((4,5-cis-dihydroxy-2- cyclopenten-1-yl)amino)methyl)-7-deazaguanosine) | |
LKEPKNME_01343 | 3.4e-11 | D | Antitoxin component of a toxin-antitoxin (TA) module | |||
LKEPKNME_01344 | 3.5e-22 | S | PIN domain | |||
LKEPKNME_01345 | 2e-43 | XK27_03960 | S | Protein of unknown function (DUF3013) | ||
LKEPKNME_01346 | 8e-21 | iunH2 | 3.2.2.1 | F | nucleoside hydrolase | |
LKEPKNME_01347 | 4.3e-54 | queT | S | QueT transporter | ||
LKEPKNME_01349 | 1.1e-56 | degV | S | Uncharacterised protein, DegV family COG1307 | ||
LKEPKNME_01350 | 5.4e-63 | lacX | 5.1.3.3 | G | Aldose 1-epimerase | |
LKEPKNME_01351 | 2.3e-109 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydD | ||
LKEPKNME_01352 | 2.5e-202 | parE | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
LKEPKNME_01353 | 3.3e-97 | 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) | |
LKEPKNME_01354 | 4.2e-102 | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | |||
LKEPKNME_01355 | 9.3e-59 | 2.4.2.6 | F | Nucleoside 2-deoxyribosyltransferase | ||
LKEPKNME_01356 | 3.4e-50 | K | response regulator | |||
LKEPKNME_01357 | 2.3e-167 | arlS | 2.7.13.3 | T | Histidine kinase | |
LKEPKNME_01358 | 5.1e-260 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
LKEPKNME_01359 | 1.5e-129 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
LKEPKNME_01360 | 2.4e-31 | metI | U | ABC transporter permease | ||
LKEPKNME_01361 | 5e-15 | metQ | M | Belongs to the nlpA lipoprotein family | ||
LKEPKNME_01362 | 1.4e-77 | yhaM | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
LKEPKNME_01363 | 1.2e-112 | prsA | 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
LKEPKNME_01364 | 3.3e-142 | hpk31 | 2.7.13.3 | T | Histidine kinase | |
LKEPKNME_01365 | 7.4e-87 | K | response regulator | |||
LKEPKNME_01366 | 5.4e-70 | napA | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
LKEPKNME_01367 | 9.1e-15 | cvpA | S | Colicin V production protein | ||
LKEPKNME_01368 | 2.9e-100 | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | |||
LKEPKNME_01369 | 8.9e-86 | tdk | 2.7.1.21 | F | thymidine kinase | |
LKEPKNME_01370 | 7.3e-100 | S | Tetratricopeptide repeat protein | |||
LKEPKNME_01371 | 1.2e-32 | ubiX | 2.5.1.129 | H | Flavin prenyltransferase that catalyzes the synthesis of the prenylated FMN cofactor (prenyl-FMN) for 4-hydroxy-3- polyprenylbenzoic acid decarboxylase UbiD. The prenyltransferase is metal-independent and links a dimethylallyl moiety from dimethylallyl monophosphate (DMAP) to the flavin N5 and C6 atoms of FMN | |
LKEPKNME_01372 | 2.8e-32 | |||||
LKEPKNME_01373 | 6.8e-116 | EGP | Major Facilitator Superfamily | |||
LKEPKNME_01374 | 4.9e-24 | |||||
LKEPKNME_01375 | 2.7e-10 | cps3F | ||||
LKEPKNME_01376 | 6.8e-94 | M | transferase activity, transferring glycosyl groups | |||
LKEPKNME_01377 | 4.5e-87 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
LKEPKNME_01378 | 6.1e-07 | XK27_07075 | S | CAAX amino terminal protease family protein | ||
LKEPKNME_01380 | 6e-45 | EGP | Sugar (and other) transporter | |||
LKEPKNME_01381 | 9.3e-79 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
LKEPKNME_01382 | 4.3e-25 | dnaD | L | DnaD domain protein | ||
LKEPKNME_01383 | 3.3e-83 | 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 | |
LKEPKNME_01384 | 2.6e-78 | msrA | 1.8.4.11, 1.8.4.12 | O | Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine | |
LKEPKNME_01385 | 1.4e-167 | recG | 3.6.4.12 | L | Critical role in recombination and DNA repair. Helps process Holliday junction intermediates to mature products by catalyzing branch migration. Has a DNA unwinding activity characteristic of a DNA helicase with a 3'- to 5'- polarity. Unwinds branched duplex DNA (Y-DNA) | |
LKEPKNME_01386 | 2.4e-89 | plsX | 2.3.1.15 | I | Catalyzes the reversible formation of acyl-phosphate (acyl-PO(4)) from acyl- acyl-carrier-protein (acyl-ACP). This enzyme utilizes acyl-ACP as fatty acyl donor, but not acyl-CoA | |
LKEPKNME_01387 | 3.9e-13 | S | Enterocin A Immunity | |||
LKEPKNME_01389 | 1.3e-16 | pspC | KT | PspC domain | ||
LKEPKNME_01391 | 4e-110 | IQ | NAD dependent epimerase/dehydratase family | |||
LKEPKNME_01392 | 1.6e-24 | |||||
LKEPKNME_01393 | 7e-82 | def | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions | |
LKEPKNME_01394 | 2e-202 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
LKEPKNME_01395 | 4.4e-156 | thyA | 2.1.1.45 | F | Catalyzes the reductive methylation of 2'-deoxyuridine- 5'-monophosphate (dUMP) to 2'-deoxythymidine-5'-monophosphate (dTMP) while utilizing 5,10-methylenetetrahydrofolate (mTHF) as the methyl donor and reductant in the reaction, yielding dihydrofolate (DHF) as a by-product. This enzymatic reaction provides an intracellular de novo source of dTMP, an essential precursor for DNA biosynthesis | |
LKEPKNME_01396 | 6.1e-48 | yfmR | S | ABC transporter, ATP-binding protein | ||
LKEPKNME_01397 | 1.7e-89 | xerD | D | recombinase XerD | ||
LKEPKNME_01398 | 8e-117 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
LKEPKNME_01399 | 4.9e-32 | S | CHY zinc finger | |||
LKEPKNME_01400 | 1.6e-39 | K | Transcriptional regulator | |||
LKEPKNME_01401 | 2.1e-52 | qorB | 1.6.5.2 | GM | NmrA-like family | |
LKEPKNME_01402 | 6.4e-23 | napA | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
LKEPKNME_01403 | 9.2e-29 | pepX | 3.4.14.11 | E | Removes N-terminal dipeptides sequentially from polypeptides having unsubstituted N-termini provided that the penultimate residue is proline | |
LKEPKNME_01404 | 1.2e-64 | noc | K | Belongs to the ParB family | ||
LKEPKNME_01405 | 6.5e-118 | soj | D | Sporulation initiation inhibitor | ||
LKEPKNME_01406 | 6.7e-237 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
LKEPKNME_01407 | 1.2e-153 | phoH | T | phosphate starvation-inducible protein PhoH | ||
LKEPKNME_01408 | 3.9e-23 | XK27_09445 | S | Domain of unknown function (DUF1827) | ||
LKEPKNME_01409 | 2.5e-25 | clpE | O | Belongs to the ClpA ClpB family | ||
LKEPKNME_01410 | 3.2e-137 | aroE | 1.1.1.25, 1.1.1.282, 1.3.5.4 | E | Involved in the biosynthesis of the chorismate, which leads to the biosynthesis of aromatic amino acids. Catalyzes the reversible NADPH linked reduction of 3-dehydroshikimate (DHSA) to yield shikimate (SA) | |
LKEPKNME_01411 | 1e-93 | 1.3.5.4 | C | FAD binding domain | ||
LKEPKNME_01412 | 3.5e-215 | sftA | D | Belongs to the FtsK SpoIIIE SftA family | ||
LKEPKNME_01413 | 2.6e-86 | M | Core-2/I-Branching enzyme | |||
LKEPKNME_01414 | 1.5e-119 | yebC | K | Transcriptional regulatory protein | ||
LKEPKNME_01415 | 1.3e-23 | hsdR | 3.1.21.3 | V | Subunit R is required for both nuclease and ATPase activities, but not for modification | |
LKEPKNME_01416 | 1.6e-177 | hsdM | 2.1.1.72 | V | type I restriction-modification system | |
LKEPKNME_01417 | 3.5e-142 | tsaD | 2.3.1.234 | J | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaE and TsaB. TsaD likely plays a direct catalytic role in this reaction | |
LKEPKNME_01418 | 2.3e-66 | uup | S | ABC transporter, ATP-binding protein | ||
LKEPKNME_01419 | 1.3e-30 | dltA | 6.1.1.13 | H | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
LKEPKNME_01420 | 1.4e-175 | dltB | M | MBOAT, membrane-bound O-acyltransferase family | ||
LKEPKNME_01421 | 4.9e-29 | dltC | 6.1.1.13 | J | Carrier protein involved in the D-alanylation of lipoteichoic acid (LTA). The loading of thioester-linked D-alanine onto DltC is catalyzed by D-alanine--D-alanyl carrier protein ligase DltA. The DltC-carried D-alanyl group is further transferred to cell membrane phosphatidylglycerol (PG) by forming an ester bond, probably catalyzed by DltD. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
LKEPKNME_01422 | 1.1e-27 | K | Helix-turn-helix XRE-family like proteins | |||
LKEPKNME_01424 | 1.2e-19 | D | nuclear chromosome segregation | |||
LKEPKNME_01425 | 1.2e-22 | 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 | ||
LKEPKNME_01426 | 3.2e-132 | hslO | O | Redox regulated molecular chaperone. Protects both thermally unfolding and oxidatively damaged proteins from irreversible aggregation. Plays an important role in the bacterial defense system toward oxidative stress | ||
LKEPKNME_01427 | 8e-155 | dapG | 1.1.1.3, 2.7.2.4 | E | Amino acid kinase family | |
LKEPKNME_01428 | 3.4e-08 | S | Protein of unknown function (DUF3397) | |||
LKEPKNME_01430 | 4.7e-53 | gltP | U | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
LKEPKNME_01431 | 4.2e-44 | guaC | 1.1.1.205, 1.7.1.7 | F | Catalyzes the irreversible NADPH-dependent deamination of GMP to IMP. It functions in the conversion of nucleobase, nucleoside and nucleotide derivatives of G to A nucleotides, and in maintaining the intracellular balance of A and G nucleotides | |
LKEPKNME_01432 | 7.8e-71 | lepB | 3.4.21.89 | U | Signal peptidase, peptidase S26 | |
LKEPKNME_01433 | 2.4e-40 | 6.3.3.2 | S | ASCH | ||
LKEPKNME_01434 | 2.2e-42 | glyA | 2.1.2.1 | E | Catalyzes the reversible interconversion of serine and glycine with tetrahydrofolate (THF) serving as the one-carbon carrier. This reaction serves as the major source of one-carbon groups required for the biosynthesis of purines, thymidylate, methionine, and other important biomolecules. Also exhibits THF- independent aldolase activity toward beta-hydroxyamino acids, producing glycine and aldehydes, via a retro-aldol mechanism | |
LKEPKNME_01435 | 1.1e-35 | celB | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
LKEPKNME_01436 | 1.5e-110 | pepE | 3.4.13.21 | E | Alpha/beta hydrolase of unknown function (DUF915) | |
LKEPKNME_01438 | 1.5e-49 | doc | ||||
LKEPKNME_01439 | 2e-34 | arpU | S | Phage transcriptional regulator, ArpU family | ||
LKEPKNME_01440 | 8e-140 | 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 | ||
LKEPKNME_01441 | 2.8e-133 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
LKEPKNME_01442 | 2.5e-43 | isp2 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | ||
LKEPKNME_01443 | 5.6e-69 | radC | L | DNA repair protein | ||
LKEPKNME_01444 | 2.6e-21 | K | Cold shock | |||
LKEPKNME_01445 | 4.8e-132 | pgl | 3.1.1.31 | G | Lactonase, 7-bladed beta-propeller | |
LKEPKNME_01446 | 7.5e-29 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
LKEPKNME_01448 | 1e-52 | pepX | 3.4.14.11 | E | Removes N-terminal dipeptides sequentially from polypeptides having unsubstituted N-termini provided that the penultimate residue is proline | |
LKEPKNME_01449 | 9.3e-43 | pepX | 3.4.14.11 | E | Removes N-terminal dipeptides sequentially from polypeptides having unsubstituted N-termini provided that the penultimate residue is proline | |
LKEPKNME_01450 | 1.2e-142 | mepA | V | MATE efflux family protein | ||
LKEPKNME_01451 | 8.8e-116 | cshB | 3.6.4.13 | JKL | DEAD-box RNA helicase. May work in conjunction with the cold shock proteins to ensure proper initiation of transcription at low and optimal temperatures | |
LKEPKNME_01454 | 4.9e-86 | S | overlaps another CDS with the same product name | |||
LKEPKNME_01455 | 6e-33 | K | helix_turn_helix, mercury resistance | |||
LKEPKNME_01456 | 6.5e-43 | S | Aldo keto reductase | |||
LKEPKNME_01457 | 2.1e-62 | S | Aldo keto reductase | |||
LKEPKNME_01458 | 2e-88 | plsC | 2.3.1.51 | I | Acyltransferase | |
LKEPKNME_01459 | 8.8e-15 | yceD | S | Uncharacterized ACR, COG1399 | ||
LKEPKNME_01461 | 5.9e-27 | yneF | S | UPF0154 protein | ||
LKEPKNME_01462 | 1.6e-92 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
LKEPKNME_01463 | 5.4e-44 | MA20_27270 | S | mazG nucleotide pyrophosphohydrolase | ||
LKEPKNME_01464 | 8.7e-44 | L | Transposase | |||
LKEPKNME_01471 | 8.7e-09 | 2.3.1.19 | K | Cro/C1-type HTH DNA-binding domain | ||
LKEPKNME_01472 | 2.5e-86 | glgB | 2.4.1.18, 3.2.1.141, 3.2.1.20 | CBM48,GH13,GH31 | G | Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position |
LKEPKNME_01473 | 4.9e-105 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
LKEPKNME_01474 | 7.2e-82 | frr | J | Responsible for the release of ribosomes from messenger RNA at the termination of protein biosynthesis. May increase the efficiency of translation by recycling ribosomes from one round of translation to another | ||
LKEPKNME_01475 | 2.4e-12 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
LKEPKNME_01476 | 9.5e-52 | K | LysR substrate binding domain | |||
LKEPKNME_01477 | 1.7e-84 | ubiD | 4.1.1.98 | H | 3-octaprenyl-4-hydroxybenzoate carboxy-lyase | |
LKEPKNME_01478 | 8.2e-66 | 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 | ||
LKEPKNME_01479 | 6.8e-49 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
LKEPKNME_01480 | 5.6e-14 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
LKEPKNME_01481 | 3.2e-148 | yedE | S | Sulphur transport | ||
LKEPKNME_01482 | 1.5e-28 | yedF | O | Belongs to the sulfur carrier protein TusA family | ||
LKEPKNME_01483 | 7.1e-13 | comEA | L | Competence protein ComEA | ||
LKEPKNME_01484 | 2e-69 | comEB | 3.5.4.12 | F | ComE operon protein 2 | |
LKEPKNME_01485 | 1.7e-38 | comEC | S | Competence protein ComEC | ||
LKEPKNME_01486 | 1.5e-39 | glpK | 2.7.1.30 | F | Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate | |
LKEPKNME_01487 | 1.6e-17 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
LKEPKNME_01488 | 4.6e-126 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
LKEPKNME_01489 | 2.7e-173 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
LKEPKNME_01490 | 1.6e-31 | rpsN | J | Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site | ||
LKEPKNME_01492 | 2.8e-111 | yjeM | E | Amino Acid | ||
LKEPKNME_01494 | 3.5e-42 | U | type IV secretory pathway VirB4 | |||
LKEPKNME_01500 | 5.1e-66 | K | Phage regulatory protein | |||
LKEPKNME_01501 | 4e-163 | thiI | 2.8.1.4 | H | Catalyzes the ATP-dependent transfer of a sulfur to tRNA to produce 4-thiouridine in position 8 of tRNAs, which functions as a near-UV photosensor. Also catalyzes the transfer of sulfur to the sulfur carrier protein ThiS, forming ThiS-thiocarboxylate. This is a step in the synthesis of thiazole, in the thiamine biosynthesis pathway. The sulfur is donated as persulfide by IscS | |
LKEPKNME_01502 | 2.6e-40 | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
LKEPKNME_01503 | 8.8e-22 | |||||
LKEPKNME_01504 | 1.9e-07 | |||||
LKEPKNME_01505 | 3.7e-22 | nhaC | C | Na H antiporter NhaC | ||
LKEPKNME_01506 | 1.1e-130 | dapF | 5.1.1.7 | E | Catalyzes the stereoinversion of LL-2,6- diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso- DAP), a precursor of L-lysine and an essential component of the bacterial peptidoglycan | |
LKEPKNME_01508 | 5e-150 | S | Phage Terminase | |||
LKEPKNME_01509 | 7.8e-48 | S | Domain of unknown function (DUF956) | |||
LKEPKNME_01510 | 6.3e-21 | ogt | 2.1.1.63 | H | 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 | |
LKEPKNME_01513 | 1.3e-69 | |||||
LKEPKNME_01514 | 3.2e-93 | nhaC | C | Na H antiporter NhaC | ||
LKEPKNME_01515 | 2.2e-55 | ade | 3.5.4.2 | F | Adenine deaminase C-terminal domain | |
LKEPKNME_01516 | 5.8e-09 | D | Antitoxin component of a toxin-antitoxin (TA) module | |||
LKEPKNME_01517 | 5.1e-08 | XK27_10540 | S | ParE toxin of type II toxin-antitoxin system, parDE | ||
LKEPKNME_01518 | 4.9e-61 | ybaK | J | Aminoacyl-tRNA editing domain | ||
LKEPKNME_01521 | 1.3e-16 | K | DNA-templated transcription, initiation | |||
LKEPKNME_01522 | 2.8e-12 | mltD | CBM50 | M | Lysin motif | |
LKEPKNME_01523 | 1.3e-151 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
LKEPKNME_01530 | 1.7e-19 | ada | 3.2.2.21 | F | DNA/RNA non-specific endonuclease | |
LKEPKNME_01531 | 1e-136 | ywfO | S | HD domain protein | ||
LKEPKNME_01532 | 4.8e-219 | res | L | Helicase C-terminal domain protein | ||
LKEPKNME_01533 | 4.1e-34 | S | Siphovirus Gp157 | |||
LKEPKNME_01534 | 4.6e-16 | fmt | 2.1.2.9 | J | Attaches a formyl group to the free amino group of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by promoting its recognition by IF2 and preventing the misappropriation of this tRNA by the elongation apparatus | |
LKEPKNME_01535 | 5.2e-141 | XK27_08315 | M | Sulfatase | ||
LKEPKNME_01536 | 6.6e-46 | argR | K | Regulates arginine biosynthesis genes | ||
LKEPKNME_01537 | 4.1e-100 | arcT | 2.6.1.1 | E | Cys/Met metabolism PLP-dependent enzyme | |
LKEPKNME_01538 | 5.9e-48 | L | Uncharacterised protein family (UPF0236) | |||
LKEPKNME_01543 | 1.3e-89 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
LKEPKNME_01548 | 9.5e-94 | 2.7.1.89 | M | Phosphotransferase enzyme family | ||
LKEPKNME_01549 | 4.5e-10 | arsC | 1.20.4.1 | P | ArsC family | |
LKEPKNME_01551 | 6.3e-69 | relA | 2.7.6.5 | KT | In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance | |
LKEPKNME_01552 | 1.1e-53 | dtd | J | rejects L-amino acids rather than detecting D-amino acids in the active site. By recycling D-aminoacyl-tRNA to D-amino acids and free tRNA molecules, this enzyme counteracts the toxicity associated with the formation of D-aminoacyl-tRNA entities in vivo and helps enforce protein L-homochirality | ||
LKEPKNME_01553 | 1e-51 | ps333 | L | Terminase small subunit | ||
LKEPKNME_01555 | 2.5e-183 | pepT | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
LKEPKNME_01556 | 3e-13 | L | Plasmid pRiA4b ORF-3-like protein | |||
LKEPKNME_01557 | 8.7e-214 | ltrA_1 | 2.7.7.49 | L | PFAM RNA-directed DNA polymerase (Reverse transcriptase) | |
LKEPKNME_01558 | 3.1e-144 | 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 | |
LKEPKNME_01559 | 1.1e-107 | lplA | 6.3.1.20 | H | Lipoate-protein ligase | |
LKEPKNME_01560 | 4.7e-45 | hsdR | 3.1.21.3 | L | Subunit R is required for both nuclease and ATPase activities, but not for modification | |
LKEPKNME_01562 | 1e-38 | V | N-6 DNA Methylase | |||
LKEPKNME_01564 | 4e-185 | gidA | D | NAD-binding protein involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA-cmnm(5)s(2)U34 | ||
LKEPKNME_01565 | 1.3e-65 | cas9 | L | CRISPR (clustered regularly interspaced short palindromic repeat) is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). In type II CRISPR systems correct processing of pre-crRNA requires a trans-encoded small RNA (tracrRNA), endogenous ribonuclease 3 (rnc) and this protein. The tracrRNA serves as a guide for ribonuclease 3-aided processing of pre-crRNA. Subsequently Cas9 crRNA tracrRNA endonucleolytically cleaves linear or circular dsDNA target complementary to the spacer | ||
LKEPKNME_01566 | 4.2e-38 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
LKEPKNME_01567 | 1.3e-20 | S | Bacteriophage holin family | |||
LKEPKNME_01570 | 1.9e-53 | yutD | S | Protein of unknown function (DUF1027) | ||
LKEPKNME_01571 | 1.6e-54 | S | Calcineurin-like phosphoesterase | |||
LKEPKNME_01572 | 3.8e-143 | xerS | L | Phage integrase family | ||
LKEPKNME_01573 | 2.1e-90 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
LKEPKNME_01574 | 1.2e-22 | veg | S | Biofilm formation stimulator VEG | ||
LKEPKNME_01575 | 3.7e-142 | rgpAc | GT4 | M | Domain of unknown function (DUF1972) | |
LKEPKNME_01576 | 1.1e-27 | S | Protein of unknown function (DUF3290) | |||
LKEPKNME_01578 | 4.9e-49 | yviA | S | Protein of unknown function (DUF421) | ||
LKEPKNME_01579 | 2.1e-83 | mprF | 2.3.2.3 | S | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms | |
LKEPKNME_01580 | 3.9e-94 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
LKEPKNME_01581 | 3.3e-79 | yjfP | S | COG1073 Hydrolases of the alpha beta superfamily | ||
LKEPKNME_01582 | 1e-36 | S | Protein of unknown function (DUF3644) | |||
LKEPKNME_01583 | 1.9e-25 | K | Transcriptional regulator | |||
LKEPKNME_01584 | 1.8e-143 | ppaC | 3.6.1.1 | C | inorganic pyrophosphatase | |
LKEPKNME_01585 | 2.3e-81 | 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 | |
LKEPKNME_01586 | 4.8e-67 | aspS | 6.1.1.12 | J | Catalyzes the attachment of L-aspartate to tRNA(Asp) in a two-step reaction L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp) | |
LKEPKNME_01587 | 8.5e-132 | dinB | 2.7.7.7 | L | Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII | |
LKEPKNME_01588 | 7.6e-191 | lysA | 4.1.1.19, 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
LKEPKNME_01589 | 5e-46 | S | phosphatase homologous to the C-terminal domain of histone macroH2A1 | |||
LKEPKNME_01590 | 8.3e-98 | pstS | P | Phosphate | ||
LKEPKNME_01592 | 3.1e-34 | |||||
LKEPKNME_01593 | 5.5e-117 | |||||
LKEPKNME_01594 | 5.9e-27 | yqfL | 2.7.11.33, 2.7.4.28 | F | Bifunctional serine threonine kinase and phosphorylase involved in the regulation of the pyruvate, phosphate dikinase (PPDK) by catalyzing its phosphorylation dephosphorylation | |
LKEPKNME_01597 | 6.1e-42 | epsJ1 | M | Glycosyltransferase like family 2 | ||
LKEPKNME_01598 | 1.2e-146 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
LKEPKNME_01600 | 3.6e-113 | NU | StbA protein | |||
LKEPKNME_01601 | 2e-112 | ylbM | S | Belongs to the UPF0348 family | ||
LKEPKNME_01602 | 2.1e-26 | yqeM | Q | Methyltransferase | ||
LKEPKNME_01603 | 2.8e-48 | desR | K | helix_turn_helix, Lux Regulon | ||
LKEPKNME_01604 | 1.6e-71 | ptp3 | 3.1.3.48 | T | Tyrosine phosphatase family | |
LKEPKNME_01605 | 1.4e-15 | zapA | D | Activator of cell division through the inhibition of FtsZ GTPase activity, therefore promoting FtsZ assembly into bundles of protofilaments necessary for the formation of the division Z ring. It is recruited early at mid-cell but it is not essential for cell division | ||
LKEPKNME_01606 | 1.9e-33 | yrzB | S | Belongs to the UPF0473 family | ||
LKEPKNME_01607 | 2.3e-59 | yqgF | J | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
LKEPKNME_01608 | 2.2e-52 | 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 | ||
LKEPKNME_01609 | 1.4e-24 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
LKEPKNME_01610 | 1.3e-79 | 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 | ||
LKEPKNME_01612 | 1.2e-15 | |||||
LKEPKNME_01616 | 3e-87 | S | Haloacid dehalogenase-like hydrolase | |||
LKEPKNME_01618 | 1.9e-167 | pfkA | 2.7.1.11 | F | Catalyzes the phosphorylation of D-fructose 6-phosphate to fructose 1,6-bisphosphate by ATP, the first committing step of glycolysis | |
LKEPKNME_01619 | 3.8e-89 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
LKEPKNME_01620 | 1.2e-70 | L | Belongs to the 'phage' integrase family | |||
LKEPKNME_01621 | 9.3e-174 | hsdM | 2.1.1.72 | V | type I restriction-modification system | |
LKEPKNME_01622 | 8.2e-149 | nanT | E | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
LKEPKNME_01623 | 6.3e-53 | uvrA | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrA is an ATPase and a DNA-binding protein. A damage recognition complex composed of 2 UvrA and 2 UvrB subunits scans DNA for abnormalities. When the presence of a lesion has been verified by UvrB, the UvrA molecules dissociate | ||
LKEPKNME_01624 | 1.5e-75 | sdaAB | 4.3.1.17 | E | Serine dehydratase beta chain | |
LKEPKNME_01625 | 3.8e-189 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
LKEPKNME_01626 | 3.3e-77 | ydcZ | S | Putative inner membrane exporter, YdcZ | ||
LKEPKNME_01627 | 9.5e-39 | S | hydrolase | |||
LKEPKNME_01628 | 2.3e-173 | alaS | 6.1.1.7 | J | Catalyzes the attachment of alanine to tRNA(Ala) in a two-step reaction alanine is first activated by ATP to form Ala- AMP and then transferred to the acceptor end of tRNA(Ala). Also edits incorrectly charged Ser-tRNA(Ala) and Gly-tRNA(Ala) via its editing domain | |
LKEPKNME_01629 | 1.7e-34 | S | Repeat protein | |||
LKEPKNME_01630 | 8.3e-26 | S | Bacterial membrane protein, YfhO | |||
LKEPKNME_01631 | 5.2e-64 | mraZ | K | Belongs to the MraZ family | ||
LKEPKNME_01632 | 4e-170 | scrA | 2.7.1.211, 5.3.1.1 | G | phosphotransferase system | |
LKEPKNME_01633 | 1.1e-73 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
LKEPKNME_01634 | 5.9e-29 | yqkB | S | Belongs to the HesB IscA family | ||
LKEPKNME_01635 | 1.8e-13 | 3.1.11.5 | L | COG0507 ATP-dependent exoDNAse (exonuclease V) alpha subunit - helicase superfamily I member | ||
LKEPKNME_01638 | 2.3e-15 | |||||
LKEPKNME_01640 | 1.2e-74 | purN | 2.1.2.2 | F | Catalyzes the transfer of a formyl group from 10- formyltetrahydrofolate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR) and tetrahydrofolate | |
LKEPKNME_01641 | 4.6e-67 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
LKEPKNME_01645 | 3.6e-38 | yeeB | L | DEAD-like helicases superfamily | ||
LKEPKNME_01646 | 1.1e-33 | lmrB | EGP | Major facilitator Superfamily | ||
LKEPKNME_01647 | 3.7e-45 | lmrB | EGP | Major facilitator Superfamily | ||
LKEPKNME_01648 | 6.6e-08 | S | Uncharacterized protein pXO2-11 | |||
LKEPKNME_01649 | 6.8e-11 | spoVK | O | ATPase family associated with various cellular activities (AAA) | ||
LKEPKNME_01650 | 2e-77 | M | Glycosyltransferase sugar-binding region containing DXD motif | |||
LKEPKNME_01651 | 2.4e-161 | camS | S | sex pheromone | ||
LKEPKNME_01652 | 1.2e-08 | ligA | 6.5.1.2 | L | DNA ligase that catalyzes the formation of phosphodiester linkages between 5'-phosphoryl and 3'-hydroxyl groups in double-stranded DNA using NAD as a coenzyme and as the energy source for the reaction. It is essential for DNA replication and repair of damaged DNA | |
LKEPKNME_01653 | 7.9e-56 | P | Plays a role in the regulation of phosphate uptake | |||
LKEPKNME_01654 | 1.1e-58 | arsC | 1.20.4.1 | T | Low molecular weight phosphatase family | |
LKEPKNME_01655 | 2.8e-106 | comGA | NU | Type II IV secretion system protein | ||
LKEPKNME_01656 | 2.2e-36 | dnaK | O | Heat shock 70 kDa protein | ||
LKEPKNME_01657 | 1.7e-12 | |||||
LKEPKNME_01658 | 1.8e-26 | |||||
LKEPKNME_01660 | 1.4e-65 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
LKEPKNME_01661 | 3.1e-77 | rsmE | 2.1.1.193 | J | Specifically methylates the N3 position of the uracil ring of uridine 1498 (m3U1498) in 16S rRNA. Acts on the fully assembled 30S ribosomal subunit | |
LKEPKNME_01662 | 8.4e-51 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
LKEPKNME_01663 | 1.5e-64 | cdsA | 2.7.7.41 | I | Belongs to the CDS family | |
LKEPKNME_01664 | 7.7e-08 | L | Helix-turn-helix domain | |||
LKEPKNME_01665 | 6e-65 | 2.3.1.178 | M | GNAT acetyltransferase | ||
LKEPKNME_01667 | 3.3e-37 | L | Belongs to the 'phage' integrase family | |||
LKEPKNME_01668 | 5.5e-146 | XK27_10475 | S | Oxidoreductase family, NAD-binding Rossmann fold | ||
LKEPKNME_01669 | 1.3e-44 | S | VRR_NUC | |||
LKEPKNME_01671 | 1.1e-08 | |||||
LKEPKNME_01672 | 4.1e-80 | rbsB | G | sugar-binding domain protein | ||
LKEPKNME_01673 | 2.5e-71 | yqeG | S | HAD phosphatase, family IIIA | ||
LKEPKNME_01674 | 2e-26 | clpE | O | Belongs to the ClpA ClpB family | ||
LKEPKNME_01675 | 1.2e-137 | glnP | P | ABC transporter | ||
LKEPKNME_01677 | 4.7e-09 | M | LysM domain | |||
LKEPKNME_01679 | 5e-157 | ubiD | 4.1.1.98 | H | 3-octaprenyl-4-hydroxybenzoate carboxy-lyase | |
LKEPKNME_01680 | 1.8e-63 | yifK | E | Amino acid permease | ||
LKEPKNME_01681 | 2.5e-129 | 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 | |
LKEPKNME_01682 | 4.5e-135 | cggR | K | Putative sugar-binding domain | ||
LKEPKNME_01683 | 2.8e-21 | |||||
LKEPKNME_01684 | 1.2e-07 | |||||
LKEPKNME_01687 | 6e-23 | GT4 | M | Glycosyltransferase like family 2 | ||
LKEPKNME_01689 | 4.2e-56 | 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 | ||
LKEPKNME_01690 | 2.1e-48 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
LKEPKNME_01694 | 9.1e-178 | asnS | 6.1.1.22 | J | Asparaginyl-tRNA synthetase | |
LKEPKNME_01695 | 2.1e-121 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
LKEPKNME_01696 | 1.8e-38 | yueF | S | AI-2E family transporter | ||
LKEPKNME_01697 | 2e-115 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
LKEPKNME_01700 | 3.5e-82 | mtnU | 3.5.1.3 | S | Carbon-nitrogen hydrolase | |
LKEPKNME_01701 | 1.2e-16 | 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 | |
LKEPKNME_01702 | 2e-25 | 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 | |
LKEPKNME_01703 | 6.3e-36 | |||||
LKEPKNME_01704 | 8.4e-78 | yihY | S | Belongs to the UPF0761 family | ||
LKEPKNME_01706 | 1.4e-24 | XK27_08840 | U | Belongs to the binding-protein-dependent transport system permease family | ||
LKEPKNME_01709 | 4.2e-57 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
LKEPKNME_01710 | 1.4e-19 | 3.4.21.107 | O | Domain present in PSD-95, Dlg, and ZO-1/2. | ||
LKEPKNME_01711 | 6e-86 | K | response regulator | |||
LKEPKNME_01712 | 5.7e-49 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | dUTP diphosphatase | |
LKEPKNME_01713 | 4.3e-15 | S | Protein of unknown function (DUF2929) | |||
LKEPKNME_01714 | 3.9e-101 | 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 | |
LKEPKNME_01715 | 1.7e-29 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
LKEPKNME_01716 | 9.7e-65 | tal | 2.2.1.2 | H | Transaldolase/Fructose-6-phosphate aldolase | |
LKEPKNME_01717 | 3.4e-45 | ylbL | T | Belongs to the peptidase S16 family | ||
LKEPKNME_01718 | 1.2e-09 | lutA | C | Cysteine-rich domain | ||
LKEPKNME_01719 | 1.9e-37 | lutB | C | 4Fe-4S dicluster domain | ||
LKEPKNME_01721 | 2e-63 | ybhR | V | ABC transporter | ||
LKEPKNME_01722 | 1.5e-38 | |||||
LKEPKNME_01723 | 1.9e-73 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
LKEPKNME_01724 | 3.2e-56 | ydiB | 2.7.1.221, 5.1.1.1 | O | Hydrolase, P-loop family | |
LKEPKNME_01725 | 3.2e-19 | XK27_06920 | S | Protein of unknown function (DUF1700) | ||
LKEPKNME_01726 | 2.3e-37 | K | transcriptional regulator PadR family | |||
LKEPKNME_01727 | 5.9e-75 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
LKEPKNME_01728 | 5.2e-23 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
LKEPKNME_01729 | 3e-82 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
LKEPKNME_01730 | 2e-151 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
LKEPKNME_01731 | 4.7e-59 | yjjG | 3.1.3.102, 3.1.3.104, 3.1.3.5, 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | |
LKEPKNME_01732 | 4.3e-69 | 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 | |
LKEPKNME_01733 | 3e-48 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
LKEPKNME_01734 | 2.3e-15 | steT | E | amino acid | ||
LKEPKNME_01735 | 9.1e-97 | pepP | 3.4.11.9, 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
LKEPKNME_01737 | 2.8e-20 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
LKEPKNME_01738 | 2.8e-21 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
LKEPKNME_01739 | 6.5e-17 | trxA | O | Belongs to the thioredoxin family | ||
LKEPKNME_01740 | 1.1e-28 | S | Bacterial membrane protein, YfhO | |||
LKEPKNME_01741 | 4.1e-54 | 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 | ||
LKEPKNME_01742 | 4.3e-28 | rimI | 2.3.1.128 | K | Ribosomal-protein-alanine acetyltransferase | |
LKEPKNME_01743 | 1.4e-30 | yeaZ | 2.3.1.234 | O | Universal bacterial protein YeaZ | |
LKEPKNME_01744 | 9.4e-83 | 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 | |
LKEPKNME_01745 | 2.2e-20 | S | Replication initiator protein A (RepA) N-terminus | |||
LKEPKNME_01746 | 4.6e-22 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family | |
LKEPKNME_01749 | 1.4e-32 | tetR | K | transcriptional regulator | ||
LKEPKNME_01751 | 8.6e-13 | L | hmm pf00665 | |||
LKEPKNME_01752 | 1e-62 | ccpA | K | catabolite control protein A | ||
LKEPKNME_01753 | 9.9e-25 | S | N-acetylmuramoyl-L-alanine amidase activity | |||
LKEPKNME_01754 | 2.9e-08 | cdd | 2.4.2.4, 3.5.4.5 | J | Acetyltransferase (GNAT) domain | |
LKEPKNME_01755 | 3.2e-38 | cdd | 2.4.2.4, 3.5.4.5 | F | Cytidine and deoxycytidylate deaminase zinc-binding region | |
LKEPKNME_01756 | 1.6e-48 | S | Domain of unknown function (DUF4343) | |||
LKEPKNME_01757 | 1.7e-120 | pipD | E | Dipeptidase | ||
LKEPKNME_01758 | 3.8e-102 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
LKEPKNME_01759 | 1.2e-71 | mutS2 | L | Endonuclease that is involved in the suppression of homologous recombination and may therefore have a key role in the control of bacterial genetic diversity | ||
LKEPKNME_01760 | 6.8e-87 | devA | 3.6.3.25 | V | ABC transporter, ATP-binding protein | |
LKEPKNME_01763 | 2e-137 | L | Transposase and inactivated derivatives, IS30 family DNA replication, recombination, and repair | |||
LKEPKNME_01764 | 1.9e-90 | stp | 3.1.3.16 | T | phosphatase | |
LKEPKNME_01765 | 1.8e-10 | S | AAA ATPase domain | |||
LKEPKNME_01766 | 9e-113 | 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 | ||
LKEPKNME_01767 | 1.9e-33 | ecsB | U | ABC transporter | ||
LKEPKNME_01773 | 1.2e-58 | pepV | 3.5.1.18 | E | dipeptidase PepV | |
LKEPKNME_01774 | 2.4e-15 | S | HicB family | |||
LKEPKNME_01776 | 4.2e-56 | ytsP | 1.8.4.14 | T | GAF domain-containing protein | |
LKEPKNME_01777 | 3.2e-32 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
LKEPKNME_01778 | 1.8e-32 | ywiB | S | Domain of unknown function (DUF1934) | ||
LKEPKNME_01781 | 7.6e-120 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
LKEPKNME_01782 | 1.4e-30 | S | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
LKEPKNME_01783 | 1.5e-07 | |||||
LKEPKNME_01784 | 1.6e-30 | acpS | 2.7.6.3, 2.7.8.7, 5.1.1.1 | I | Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein | |
LKEPKNME_01785 | 3.1e-74 | EG | EamA-like transporter family | |||
LKEPKNME_01786 | 4.5e-45 | yjcF | K | protein acetylation | ||
LKEPKNME_01788 | 4.9e-17 | mvk | 1.1.1.88, 2.3.3.10, 2.7.1.36 | I | mevalonate kinase | |
LKEPKNME_01789 | 8.5e-22 | ypsA | S | Belongs to the UPF0398 family | ||
LKEPKNME_01790 | 2.6e-18 | pacA | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
LKEPKNME_01792 | 4.5e-53 | K | Helix-turn-helix domain, rpiR family | |||
LKEPKNME_01793 | 1.4e-36 | nanE | 5.1.3.9 | G | Converts N-acetylmannosamine-6-phosphate (ManNAc-6-P) to N-acetylglucosamine-6-phosphate (GlcNAc-6-P) | |
LKEPKNME_01794 | 7.6e-84 | trxB2 | 1.18.1.2, 1.19.1.1 | C | Ferredoxin--NADP reductase | |
LKEPKNME_01795 | 1.1e-46 | ymfM | S | Helix-turn-helix domain | ||
LKEPKNME_01797 | 1e-115 | mtnE | 2.6.1.83 | E | Aminotransferase | |
LKEPKNME_01798 | 3.1e-25 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
LKEPKNME_01799 | 1e-157 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
LKEPKNME_01800 | 7e-86 | L | PFAM transposase IS116 IS110 IS902 | |||
LKEPKNME_01801 | 2.8e-33 | lutB | C | 4Fe-4S dicluster domain | ||
LKEPKNME_01802 | 3.8e-73 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
LKEPKNME_01803 | 9e-49 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
LKEPKNME_01804 | 4e-21 | rsmD | 2.1.1.171 | L | RNA methyltransferase, RsmD family | |
LKEPKNME_01805 | 8.9e-45 | S | Bacterial membrane protein, YfhO | |||
LKEPKNME_01806 | 3.5e-12 | L | PFAM transposase IS200-family protein | |||
LKEPKNME_01807 | 1.2e-111 | ansA | 3.5.1.1 | EJ | Asparaginase | |
LKEPKNME_01808 | 1.5e-46 | 2.7.7.12 | C | Domain of unknown function (DUF4931) | ||
LKEPKNME_01809 | 7.6e-12 | M | Lysin motif | |||
LKEPKNME_01810 | 2.4e-138 | L | Belongs to the 'phage' integrase family | |||
LKEPKNME_01811 | 3.8e-43 | |||||
LKEPKNME_01813 | 3.9e-33 | 2.1.1.72 | V | site-specific DNA-methyltransferase (adenine-specific) activity | ||
LKEPKNME_01814 | 6.2e-49 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
LKEPKNME_01815 | 2e-147 | relA | 2.7.6.5 | KT | In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance | |
LKEPKNME_01816 | 2.1e-19 | nudF | 3.6.1.13 | L | ADP-ribose pyrophosphatase | |
LKEPKNME_01819 | 4.6e-21 | ruvB | 3.6.4.12 | L | four-way junction helicase activity | |
LKEPKNME_01820 | 2.3e-48 | alkD | L | DNA alkylation repair enzyme | ||
LKEPKNME_01821 | 3.1e-45 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
LKEPKNME_01822 | 1.1e-49 | M | transferase activity, transferring glycosyl groups | |||
LKEPKNME_01823 | 3.4e-64 | hly | S | protein, hemolysin III | ||
LKEPKNME_01824 | 1.3e-93 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
LKEPKNME_01825 | 1.6e-93 | ruvB | 3.6.4.12 | L | The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing | |
LKEPKNME_01827 | 1.3e-32 | ypaA | S | Protein of unknown function (DUF1304) | ||
LKEPKNME_01829 | 2e-07 | L | Family membership | |||
LKEPKNME_01830 | 7.1e-110 | frdC | 1.3.5.4 | C | FAD binding domain | |
LKEPKNME_01831 | 8.5e-91 | L | Belongs to the 'phage' integrase family | |||
LKEPKNME_01832 | 1.2e-51 | pyrP | F | Permease | ||
LKEPKNME_01833 | 1.2e-71 | yxeH | S | hydrolase | ||
LKEPKNME_01834 | 4.6e-08 | rsmC | 2.1.1.172 | J | Methyltransferase | |
LKEPKNME_01835 | 3.3e-62 | tadA | 3.5.4.33 | F | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
LKEPKNME_01836 | 1e-83 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
LKEPKNME_01837 | 1.9e-56 | K | LysR substrate binding domain | |||
LKEPKNME_01839 | 2.4e-24 | fabK | 1.3.1.9 | S | Nitronate monooxygenase | |
LKEPKNME_01840 | 3e-32 | azlD | S | Branched-chain amino acid transport protein (AzlD) | ||
LKEPKNME_01841 | 1.5e-28 | ohrR | K | helix_turn_helix multiple antibiotic resistance protein | ||
LKEPKNME_01842 | 1.8e-32 | L | Helix-turn-helix domain | |||
LKEPKNME_01843 | 1.6e-26 | lmrP | E | Major Facilitator Superfamily | ||
LKEPKNME_01844 | 5e-09 | S | SdpI/YhfL protein family | |||
LKEPKNME_01845 | 3.5e-121 | 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 | |
LKEPKNME_01846 | 1.2e-21 | comGB | NU | type II secretion system | ||
LKEPKNME_01847 | 1.8e-26 | comGC | U | competence protein ComGC | ||
LKEPKNME_01848 | 1.6e-61 | XK27_08315 | M | Sulfatase | ||
LKEPKNME_01851 | 8.5e-36 | hup | L | Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions | ||
LKEPKNME_01852 | 1.3e-34 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
LKEPKNME_01853 | 8.1e-91 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydC | ||
LKEPKNME_01854 | 2.5e-26 | pfoS | S | Phosphotransferase system, EIIC | ||
LKEPKNME_01855 | 3.9e-54 | ycsE | S | Sucrose-6F-phosphate phosphohydrolase | ||
LKEPKNME_01856 | 3.2e-28 | mutF | V | AAA domain, putative AbiEii toxin, Type IV TA system | ||
LKEPKNME_01857 | 1.1e-11 | 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 | ||
LKEPKNME_01858 | 8.5e-33 | 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 | ||
LKEPKNME_01863 | 3.3e-52 | ymfH | S | Peptidase M16 | ||
LKEPKNME_01864 | 3e-07 | ruvB | 3.6.4.12 | L | four-way junction helicase activity | |
LKEPKNME_01865 | 8e-31 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic domain | |
LKEPKNME_01866 | 9.8e-66 | fabZ | 3.5.1.108, 4.2.1.59 | I | Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs | |
LKEPKNME_01867 | 2.8e-45 | degV | S | EDD domain protein, DegV family | ||
LKEPKNME_01869 | 9.4e-11 | S | Polysaccharide pyruvyl transferase | |||
LKEPKNME_01870 | 1.5e-49 | trmFO | 2.1.1.74 | J | Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs | |
LKEPKNME_01871 | 7.2e-43 | |||||
LKEPKNME_01872 | 5.1e-54 | fld | C | Flavodoxin | ||
LKEPKNME_01873 | 1.6e-16 | fasB | 2.7.13.3 | T | signal transduction protein with a C-terminal ATPase domain | |
LKEPKNME_01875 | 4.4e-30 | pfoS | S | Phosphotransferase system, EIIC | ||
LKEPKNME_01876 | 7.1e-33 | glpD | 1.1.3.21, 1.1.5.3 | C | C-terminal domain of alpha-glycerophosphate oxidase | |
LKEPKNME_01877 | 2.2e-63 | traI | 5.99.1.2 | L | C-terminal repeat of topoisomerase | |
LKEPKNME_01879 | 6.4e-08 | S | Bacterial membrane protein, YfhO | |||
LKEPKNME_01880 | 2.9e-63 | yitS | S | EDD domain protein, DegV family | ||
LKEPKNME_01882 | 6.2e-117 | prfC | J | Increases the formation of ribosomal termination complexes and stimulates activities of RF-1 and RF-2. It binds guanine nucleotides and has strong preference for UGA stop codons. It may interact directly with the ribosome. The stimulation of RF- 1 and RF-2 is significantly reduced by GTP and GDP, but not by GMP | ||
LKEPKNME_01887 | 1.5e-67 | M | ErfK YbiS YcfS YnhG | |||
LKEPKNME_01888 | 1.4e-57 | sufS | 2.8.1.7, 4.4.1.16 | E | Catalyzes the removal of elemental sulfur and selenium atoms from L-cysteine, L-cystine, L-selenocysteine, and L- selenocystine to produce L-alanine | |
LKEPKNME_01889 | 2.2e-17 | |||||
LKEPKNME_01891 | 9.7e-17 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
LKEPKNME_01892 | 2.5e-11 | ftsL | D | cell division protein FtsL | ||
LKEPKNME_01893 | 4.1e-22 | 2.1.1.72 | L | DNA methylase | ||
LKEPKNME_01894 | 5.3e-11 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
LKEPKNME_01895 | 5.2e-77 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
LKEPKNME_01896 | 4.9e-98 | E | Amino acid permease | |||
LKEPKNME_01897 | 2.9e-65 | trsE | S | COG0433 Predicted ATPase | ||
LKEPKNME_01898 | 5.3e-12 | S | Family of unknown function (DUF5322) | |||
LKEPKNME_01899 | 6.6e-23 | coiA | 3.6.4.12 | S | Competence protein | |
LKEPKNME_01900 | 4.7e-30 | tag | 3.2.2.20 | L | glycosylase | |
LKEPKNME_01901 | 2e-44 | usp6 | T | universal stress protein | ||
LKEPKNME_01902 | 4.2e-51 | mdtG | EGP | Major facilitator Superfamily | ||
LKEPKNME_01903 | 1.1e-65 | iscS | 2.8.1.7 | E | Aminotransferase class V | |
LKEPKNME_01904 | 2.6e-57 | spxA | 1.20.4.1 | K | Interferes with activator-stimulated transcription by interaction with the RNA polymerase alpha-CTD. May function to globally reduce transcription of genes involved in growth- and development-promoting processes and to increase transcription of genes involved in thiol homeostasis, during periods of extreme stress | |
LKEPKNME_01905 | 1.5e-19 | merA | 1.16.1.1, 1.8.1.7 | C | Pyridine nucleotide-disulfide oxidoreductase | |
LKEPKNME_01906 | 6.5e-28 | K | helix_turn_helix, arabinose operon control protein | |||
LKEPKNME_01907 | 1.2e-65 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
LKEPKNME_01908 | 6.6e-62 | cvfB | S | S1 domain | ||
LKEPKNME_01909 | 1.1e-10 | xerD | D | recombinase XerD | ||
LKEPKNME_01911 | 5.6e-13 | S | Thioredoxin | |||
LKEPKNME_01912 | 4.3e-19 | HA62_12640 | S | GCN5-related N-acetyl-transferase | ||
LKEPKNME_01913 | 1.4e-105 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
LKEPKNME_01914 | 1e-35 | 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) |
LKEPKNME_01915 | 6.8e-12 | rplV | J | The globular domain of the protein is located near the polypeptide exit tunnel on the outside of the subunit, while an extended beta-hairpin is found that lines the wall of the exit tunnel in the center of the 70S ribosome | ||
LKEPKNME_01916 | 1e-44 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
LKEPKNME_01917 | 3.5e-21 | rplB | J | rRNA binding | ||
LKEPKNME_01919 | 3.6e-66 | accD | 2.1.3.15, 6.4.1.2 | I | Component of the acetyl coenzyme A carboxylase (ACC) complex. Biotin carboxylase (BC) catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the transcarboxylase to acetyl-CoA to form malonyl- CoA | |
LKEPKNME_01920 | 4.6e-35 | ispE | 2.1.1.182, 2.7.1.148 | F | Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol | |
LKEPKNME_01921 | 6.8e-21 | sufC | O | FeS assembly ATPase SufC | ||
LKEPKNME_01922 | 5e-27 | ysxB | J | Cysteine protease Prp | ||
LKEPKNME_01923 | 5.6e-18 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
LKEPKNME_01924 | 1.4e-34 | V | site-specific DNA-methyltransferase (adenine-specific) activity | |||
LKEPKNME_01925 | 3e-38 | ruvA | 3.6.4.12 | L | The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing. RuvA stimulates, in the presence of DNA, the weak ATPase activity of RuvB | |
LKEPKNME_01927 | 1.6e-16 | sdaAA | 4.3.1.17 | E | L-serine dehydratase, iron-sulfur-dependent, alpha subunit | |
LKEPKNME_01928 | 7.7e-41 | S | Iron-sulfur cluster assembly protein | |||
LKEPKNME_01929 | 2.5e-29 | recD2 | 3.1.11.5 | L | DNA-dependent ATPase and ATP-dependent 5'-3' DNA helicase. Has no activity on blunt DNA or DNA with 3'-overhangs, requires at least 10 bases of 5'-ssDNA for helicase activity | |
LKEPKNME_01931 | 1.9e-65 | plsY | 2.3.1.15, 3.5.1.104 | I | Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP | |
LKEPKNME_01933 | 3.6e-32 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
LKEPKNME_01934 | 2.3e-78 | S | Phage tail tube protein | |||
LKEPKNME_01935 | 4.8e-82 | S | Phage portal protein | |||
LKEPKNME_01936 | 9.9e-83 | clpP | 3.4.21.92 | O | Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins | |
LKEPKNME_01937 | 8.2e-15 | dprA | LU | DNA protecting protein DprA | ||
LKEPKNME_01938 | 1.8e-16 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
LKEPKNME_01939 | 1.1e-12 | nnrD | 4.2.1.136, 5.1.99.6 | H | Catalyzes the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. Together with NAD(P)HX epimerase, which catalyzes the epimerization of the S- and R-forms, the enzyme allows the repair of both epimers of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration | |
LKEPKNME_01944 | 1.3e-14 | K | Transcriptional regulator, LysR family | |||
LKEPKNME_01945 | 3.2e-29 | EGP | Major Facilitator Superfamily | |||
LKEPKNME_01946 | 8.8e-29 | yjjH | S | Calcineurin-like phosphoesterase | ||
LKEPKNME_01947 | 3.1e-40 | K | Transcriptional regulator | |||
LKEPKNME_01948 | 4.7e-17 | ybeY | 2.6.99.2, 3.5.4.5 | S | Single strand-specific metallo-endoribonuclease involved in late-stage 70S ribosome quality control and in maturation of the 3' terminus of the 16S rRNA | |
LKEPKNME_01949 | 1.4e-43 | recQ1 | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
LKEPKNME_01950 | 3.8e-37 | yfjM | S | Protein of unknown function DUF262 | ||
LKEPKNME_01951 | 1.5e-25 | G | Xylose isomerase domain protein TIM barrel | |||
LKEPKNME_01952 | 2.3e-35 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
LKEPKNME_01953 | 7.8e-15 | comFA | L | Helicase C-terminal domain protein | ||
LKEPKNME_01954 | 2.6e-24 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
LKEPKNME_01956 | 3.1e-50 | S | Domain of unknown function (DUF3841) | |||
LKEPKNME_01957 | 2.2e-56 | ftsW | D | Belongs to the SEDS family | ||
LKEPKNME_01958 | 1.3e-27 | aspB | 2.6.1.1, 2.6.1.14 | E | Aminotransferase | |
LKEPKNME_01960 | 2.2e-30 | purS | 6.3.2.6, 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
LKEPKNME_01962 | 3.9e-10 | arbx | M | family 8 | ||
LKEPKNME_01963 | 2.1e-44 | yjaB_1 | K | Acetyltransferase (GNAT) domain | ||
LKEPKNME_01964 | 1.2e-63 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
LKEPKNME_01965 | 1.4e-49 | lacS | G | Transporter | ||
LKEPKNME_01969 | 2.6e-81 | relA | 2.7.6.5 | KT | In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance | |
LKEPKNME_01970 | 2.5e-30 | paiA | 2.3.1.57 | K | Acetyltransferase (GNAT) domain | |
LKEPKNME_01971 | 9.4e-08 | |||||
LKEPKNME_01973 | 2.3e-13 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | ||
LKEPKNME_01975 | 3.5e-35 | FbpA | K | Fibronectin-binding protein | ||
LKEPKNME_01976 | 1.8e-25 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
LKEPKNME_01977 | 1.7e-73 | pyrG | 6.3.4.2 | F | Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen. Regulates intracellular CTP levels through interactions with the four ribonucleotide triphosphates | |
LKEPKNME_01978 | 6.7e-67 | glnA | 6.3.1.2 | E | glutamine synthetase | |
LKEPKNME_01979 | 1.8e-24 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
LKEPKNME_01980 | 8.8e-23 | mvaK2 | 2.7.1.36, 2.7.1.43, 2.7.4.2 | I | GHMP kinases C terminal | |
LKEPKNME_01981 | 6.6e-10 | XK27_04120 | S | Putative amino acid metabolism | ||
LKEPKNME_01983 | 1.8e-15 | 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) | |
LKEPKNME_01984 | 8.5e-25 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
LKEPKNME_01985 | 3.2e-64 | uvrC | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrC both incises the 5' and 3' sides of the lesion. The N-terminal half is responsible for the 3' incision and the C-terminal half is responsible for the 5' incision | ||
LKEPKNME_01986 | 4e-37 | mvk | 1.1.1.88, 2.3.3.10, 2.7.1.36 | I | mevalonate kinase | |
LKEPKNME_01990 | 6.7e-17 | gntR1 | K | UbiC transcription regulator-associated domain protein | ||
LKEPKNME_01991 | 7.7e-22 | yphA | GM | NAD dependent epimerase/dehydratase family | ||
LKEPKNME_01992 | 4.9e-34 | murI | 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
LKEPKNME_01993 | 9e-32 | nplT | 3.2.1.133, 3.2.1.135, 3.2.1.54 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
LKEPKNME_01995 | 2e-40 | L | hmm pf00665 | |||
LKEPKNME_01996 | 3.4e-22 | aspB | 2.6.1.1, 2.6.1.14 | E | Aminotransferase | |
LKEPKNME_01997 | 2.8e-51 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
LKEPKNME_01999 | 2.9e-14 | cro | K | Helix-turn-helix XRE-family like proteins | ||
LKEPKNME_02000 | 7.4e-23 | yitT | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
LKEPKNME_02001 | 5.7e-20 | pstA | P | Phosphate transport system permease protein PstA | ||
LKEPKNME_02003 | 1.8e-58 | yvgN | C | Aldo keto reductase | ||
LKEPKNME_02004 | 2.5e-41 | S | Phage portal protein, SPP1 Gp6-like | |||
LKEPKNME_02005 | 5.3e-09 | S | Single-strand binding protein family | |||
LKEPKNME_02007 | 2.9e-10 | tig | D | Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation. Functions as a peptidyl-prolyl cis-trans isomerase | ||
LKEPKNME_02008 | 2.3e-28 | cbh | 3.5.1.24 | M | Linear amide C-N hydrolases, choloylglycine hydrolase family | |
LKEPKNME_02009 | 9.2e-09 | M | Phage tail tape measure protein TP901 | |||
LKEPKNME_02010 | 7.8e-22 | radA | O | DNA-dependent ATPase involved in processing of recombination intermediates, plays a role in repairing DNA breaks. Stimulates the branch migration of RecA-mediated strand transfer reactions, allowing the 3' invading strand to extend heteroduplex DNA faster. Binds ssDNA in the presence of ADP but not other nucleotides, has ATPase activity that is stimulated by ssDNA and various branched DNA structures, but inhibited by SSB. Does not have RecA's homology-searching function | ||
LKEPKNME_02017 | 2.8e-31 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
LKEPKNME_02019 | 6.9e-26 | maa | 2.3.1.79 | S | Maltose acetyltransferase | |
LKEPKNME_02020 | 1.1e-37 | rodA | D | Belongs to the SEDS family | ||
LKEPKNME_02025 | 1.6e-13 | rssA | S | Phospholipase, patatin family | ||
LKEPKNME_02029 | 2.9e-29 | clpB | O | C-terminal, D2-small domain, of ClpB protein | ||
LKEPKNME_02030 | 2.1e-07 | L | Transposase | |||
LKEPKNME_02034 | 2.3e-23 | yeaL | S | Protein of unknown function (DUF441) | ||
LKEPKNME_02035 | 3.6e-12 | mltG | S | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
LKEPKNME_02036 | 2e-21 | L | Helicase C-terminal domain protein | |||
LKEPKNME_02037 | 1.8e-13 | S | Uncharacterised protein family (UPF0236) | |||
LKEPKNME_02038 | 3e-17 | S | CAAX protease self-immunity | |||
LKEPKNME_02039 | 2e-28 | XK27_06785 | V | ABC transporter, ATP-binding protein | ||
LKEPKNME_02042 | 7.5e-13 | |||||
LKEPKNME_02043 | 5.6e-14 | ade | 3.5.4.2 | F | Adenine deaminase C-terminal domain | |
LKEPKNME_02044 | 7.7e-36 | sufB | O | assembly protein SufB | ||
LKEPKNME_02045 | 4.2e-12 | S | Phage portal protein, SPP1 Gp6-like | |||
LKEPKNME_02046 | 5.6e-12 | ypmS | S | Uncharacterized protein conserved in bacteria (DUF2140) | ||
LKEPKNME_02048 | 7.5e-23 | clpP | 3.4.21.92 | OU | Belongs to the peptidase S14 family | |
LKEPKNME_02051 | 3.3e-08 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
LKEPKNME_02052 | 9.8e-14 | 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 | ||
LKEPKNME_02053 | 7e-25 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
LKEPKNME_02054 | 5.6e-18 | ydhK | M | Protein of unknown function (DUF1541) | ||
LKEPKNME_02055 | 5.8e-22 | hlyX | S | Transporter associated domain | ||
LKEPKNME_02056 | 2.2e-21 | udk | 2.7.1.48 | F | Cytidine monophosphokinase |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)