ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
KKGFHILH_00001 | 1.2e-210 | S | Bacterial protein of unknown function (DUF871) | |||
KKGFHILH_00003 | 2.3e-43 | ybhL | S | Belongs to the BI1 family | ||
KKGFHILH_00004 | 1.2e-225 | lacE | 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 | ||
KKGFHILH_00005 | 1.5e-31 | lacE | 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 | ||
KKGFHILH_00006 | 3.9e-46 | pbg6 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
KKGFHILH_00007 | 1.5e-203 | pbg6 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
KKGFHILH_00010 | 1.7e-195 | ampC | V | Beta-lactamase | ||
KKGFHILH_00011 | 4.9e-217 | EGP | Major facilitator Superfamily | |||
KKGFHILH_00012 | 3.2e-253 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
KKGFHILH_00013 | 1.1e-104 | vanZ | V | VanZ like family | ||
KKGFHILH_00014 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
KKGFHILH_00015 | 7.2e-267 | yclK | 2.7.13.3, 4.6.1.1 | T | Histidine kinase | |
KKGFHILH_00016 | 4.4e-129 | K | Transcriptional regulatory protein, C terminal | |||
KKGFHILH_00017 | 7.7e-67 | S | SdpI/YhfL protein family | |||
KKGFHILH_00018 | 7.2e-191 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
KKGFHILH_00019 | 9.9e-227 | patB | 4.4.1.8 | E | Aminotransferase, class I | |
KKGFHILH_00020 | 2.5e-89 | M | Protein of unknown function (DUF3737) | |||
KKGFHILH_00022 | 1e-15 | S | Domain of Unknown Function with PDB structure (DUF3850) | |||
KKGFHILH_00023 | 1.2e-299 | I | Protein of unknown function (DUF2974) | |||
KKGFHILH_00024 | 2.1e-194 | pbpX1 | V | Beta-lactamase | ||
KKGFHILH_00025 | 2.6e-197 | asd | 1.2.1.11 | E | Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate | |
KKGFHILH_00026 | 2.7e-216 | aspC | 2.6.1.1 | E | Aminotransferase | |
KKGFHILH_00027 | 7e-144 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
KKGFHILH_00028 | 9.8e-177 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
KKGFHILH_00029 | 2e-219 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
KKGFHILH_00030 | 2.8e-75 | dapD | 2.3.1.117, 2.3.1.89 | E | Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate | |
KKGFHILH_00031 | 1.3e-246 | lysA | 4.1.1.19, 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
KKGFHILH_00032 | 1.3e-259 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
KKGFHILH_00033 | 2.3e-192 | 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 | |
KKGFHILH_00034 | 3.4e-175 | yjeM | E | Amino Acid | ||
KKGFHILH_00035 | 7.8e-39 | yjeM | E | Amino Acid | ||
KKGFHILH_00036 | 0.0 | uvrA3 | L | excinuclease ABC, A subunit | ||
KKGFHILH_00037 | 1.1e-189 | mmuM | 1.5.1.20, 2.1.1.10 | H | homocysteine S-methyltransferase | |
KKGFHILH_00038 | 2.1e-114 | 3.6.1.27 | I | Acid phosphatase homologues | ||
KKGFHILH_00039 | 7.4e-205 | L | COG2826 Transposase and inactivated derivatives, IS30 family | |||
KKGFHILH_00040 | 1.9e-80 | yvbK | 3.1.3.25 | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | |
KKGFHILH_00041 | 1.4e-115 | lacA | 2.3.1.79 | S | Transferase hexapeptide repeat | |
KKGFHILH_00042 | 9.3e-204 | pbpX1 | V | Beta-lactamase | ||
KKGFHILH_00043 | 2.8e-98 | pdxK | 2.7.1.35 | H | Phosphomethylpyrimidine kinase | |
KKGFHILH_00044 | 7.5e-95 | S | ECF-type riboflavin transporter, S component | |||
KKGFHILH_00045 | 1.3e-229 | S | Putative peptidoglycan binding domain | |||
KKGFHILH_00046 | 9e-83 | K | Acetyltransferase (GNAT) domain | |||
KKGFHILH_00047 | 1.7e-251 | pepT2 | 3.4.11.14, 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
KKGFHILH_00048 | 2e-216 | mnaA | 5.1.3.14 | G | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
KKGFHILH_00050 | 4.7e-249 | celB | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
KKGFHILH_00051 | 2.8e-211 | yfmL | 3.6.4.13 | L | DEAD DEAH box helicase | |
KKGFHILH_00052 | 1.3e-61 | M | Glycosyl hydrolases family 25 | |||
KKGFHILH_00053 | 2.6e-61 | M | Glycosyl hydrolases family 25 | |||
KKGFHILH_00054 | 0.0 | L | PLD-like domain | |||
KKGFHILH_00055 | 4.8e-42 | S | SnoaL-like domain | |||
KKGFHILH_00056 | 5.4e-53 | hipB | K | sequence-specific DNA binding | ||
KKGFHILH_00057 | 8e-22 | rpiB | 5.3.1.6 | G | Ribose/Galactose Isomerase | |
KKGFHILH_00058 | 3.4e-27 | |||||
KKGFHILH_00059 | 1.3e-133 | hxlA | 6.2.1.3 | H | Aldolase/RraA | |
KKGFHILH_00060 | 5.7e-272 | P | Sodium:sulfate symporter transmembrane region | |||
KKGFHILH_00061 | 1.7e-153 | ydjP | I | Alpha/beta hydrolase family | ||
KKGFHILH_00062 | 6.9e-195 | citC | 6.2.1.22 | H | Acetylation of prosthetic group (2-(5''-phosphoribosyl)- 3'-dephosphocoenzyme-A) of the gamma subunit of citrate lyase | |
KKGFHILH_00063 | 1.2e-43 | citD | C | Covalent carrier of the coenzyme of citrate lyase | ||
KKGFHILH_00064 | 2.4e-167 | citE | 4.1.3.25, 4.1.3.34 | G | Belongs to the HpcH HpaI aldolase family | |
KKGFHILH_00065 | 2.1e-288 | citF | 2.8.3.10 | H | Citrate (pro-3S)-lyase alpha chain | |
KKGFHILH_00066 | 9.3e-72 | yeaL | S | Protein of unknown function (DUF441) | ||
KKGFHILH_00067 | 3.5e-21 | |||||
KKGFHILH_00068 | 3.6e-146 | cbiQ | P | cobalt transport | ||
KKGFHILH_00069 | 0.0 | ykoD | P | ABC transporter, ATP-binding protein | ||
KKGFHILH_00070 | 1.5e-95 | S | UPF0397 protein | |||
KKGFHILH_00071 | 2.9e-66 | S | Domain of unknown function DUF1828 | |||
KKGFHILH_00072 | 5.5e-09 | |||||
KKGFHILH_00073 | 1.5e-50 | |||||
KKGFHILH_00074 | 2.6e-177 | citR | K | Putative sugar-binding domain | ||
KKGFHILH_00075 | 6.5e-249 | yjjP | S | Putative threonine/serine exporter | ||
KKGFHILH_00077 | 5.9e-37 | M | domain protein | |||
KKGFHILH_00078 | 8.2e-85 | ybaK | S | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
KKGFHILH_00079 | 6.5e-176 | prmA | J | Ribosomal protein L11 methyltransferase | ||
KKGFHILH_00080 | 8.5e-60 | |||||
KKGFHILH_00081 | 0.0 | relA | 2.7.6.5 | KT | In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance | |
KKGFHILH_00082 | 6e-76 | 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 | ||
KKGFHILH_00083 | 5.8e-244 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
KKGFHILH_00084 | 0.0 | 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) | |
KKGFHILH_00085 | 1.2e-222 | patA | 2.6.1.1 | E | Aminotransferase | |
KKGFHILH_00086 | 9.4e-46 | |||||
KKGFHILH_00087 | 1.8e-38 | D | Alpha beta | |||
KKGFHILH_00088 | 3.7e-122 | D | Alpha beta | |||
KKGFHILH_00089 | 3e-262 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
KKGFHILH_00090 | 1.5e-144 | recX | 2.4.1.337 | GT4 | S | Regulatory protein RecX |
KKGFHILH_00091 | 1.6e-85 | |||||
KKGFHILH_00092 | 2.7e-74 | |||||
KKGFHILH_00093 | 1.4e-140 | hlyX | S | Transporter associated domain | ||
KKGFHILH_00094 | 9.4e-305 | prfC | J | Increases the formation of ribosomal termination complexes and stimulates activities of RF-1 and RF-2. It binds guanine nucleotides and has strong preference for UGA stop codons. It may interact directly with the ribosome. The stimulation of RF- 1 and RF-2 is significantly reduced by GTP and GDP, but not by GMP | ||
KKGFHILH_00095 | 2.3e-44 | XK27_09445 | S | Domain of unknown function (DUF1827) | ||
KKGFHILH_00096 | 0.0 | clpE | O | Belongs to the ClpA ClpB family | ||
KKGFHILH_00098 | 5.2e-104 | |||||
KKGFHILH_00099 | 1.3e-159 | degV | S | EDD domain protein, DegV family | ||
KKGFHILH_00100 | 1.1e-66 | |||||
KKGFHILH_00101 | 0.0 | FbpA | K | Fibronectin-binding protein | ||
KKGFHILH_00102 | 2.9e-86 | V | N-6 DNA Methylase | |||
KKGFHILH_00103 | 3.1e-150 | xerD | L | Phage integrase, N-terminal SAM-like domain | ||
KKGFHILH_00104 | 3e-66 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
KKGFHILH_00105 | 1e-63 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
KKGFHILH_00106 | 5e-13 | mmuM | 1.5.1.20, 2.1.1.10 | H | homocysteine S-methyltransferase | |
KKGFHILH_00107 | 1.4e-115 | mmuP | E | amino acid | ||
KKGFHILH_00108 | 1.4e-272 | pepV | 3.5.1.18 | E | dipeptidase PepV | |
KKGFHILH_00109 | 6.3e-93 | XK26_02160 | C | Pyridoxamine 5'-phosphate oxidase | ||
KKGFHILH_00110 | 1.7e-284 | E | Amino acid permease | |||
KKGFHILH_00111 | 0.0 | yaaO | 4.1.1.17, 4.1.1.19 | E | Orn/Lys/Arg decarboxylase, C-terminal domain | |
KKGFHILH_00112 | 2.3e-245 | ynbB | 4.4.1.1 | P | aluminum resistance | |
KKGFHILH_00113 | 2e-234 | mepA | V | MATE efflux family protein | ||
KKGFHILH_00114 | 3.5e-71 | yjaB | 2.3.1.181 | K | Acetyltransferase (GNAT) domain | |
KKGFHILH_00115 | 1.8e-58 | S | Putative adhesin | |||
KKGFHILH_00116 | 5.6e-101 | yihX | 3.1.3.10, 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | |
KKGFHILH_00117 | 3.8e-20 | 1.3.5.4 | C | FAD dependent oxidoreductase | ||
KKGFHILH_00118 | 1.1e-83 | dps | P | Belongs to the Dps family | ||
KKGFHILH_00119 | 2e-178 | MA20_14895 | S | Conserved hypothetical protein 698 | ||
KKGFHILH_00121 | 5.6e-191 | cbh | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
KKGFHILH_00122 | 3e-119 | VY92_08690 | 5.3.1.32 | G | Antibiotic biosynthesis monooxygenase | |
KKGFHILH_00123 | 9e-98 | |||||
KKGFHILH_00124 | 4.9e-108 | K | LysR substrate binding domain | |||
KKGFHILH_00125 | 1e-20 | |||||
KKGFHILH_00126 | 2.3e-215 | S | Sterol carrier protein domain | |||
KKGFHILH_00127 | 9.2e-95 | citX | 2.4.2.52, 2.7.7.61 | HI | Apo-citrate lyase phosphoribosyl-dephospho-CoA transferase | |
KKGFHILH_00128 | 2e-105 | argF | 2.1.3.3, 2.7.2.2 | E | Belongs to the carbamate kinase family | |
KKGFHILH_00129 | 4.3e-66 | argF | 2.1.3.3, 2.7.2.2 | E | Reversibly catalyzes the transfer of the carbamoyl group from carbamoyl phosphate (CP) to the N(epsilon) atom of ornithine (ORN) to produce L-citrulline | |
KKGFHILH_00130 | 5.7e-233 | arcA | 3.5.3.6 | E | Arginine | |
KKGFHILH_00131 | 9e-137 | lysR5 | K | LysR substrate binding domain | ||
KKGFHILH_00132 | 0.0 | mgtA | 3.6.3.2, 3.6.3.6 | P | Cation transporter/ATPase, N-terminus | |
KKGFHILH_00133 | 1e-48 | S | Metal binding domain of Ada | |||
KKGFHILH_00134 | 1.9e-47 | yhjH | 3.1.4.52 | T | Putative diguanylate phosphodiesterase | |
KKGFHILH_00135 | 1e-149 | D | Alpha beta | |||
KKGFHILH_00136 | 1e-297 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family | |
KKGFHILH_00137 | 0.0 | bglP | 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
KKGFHILH_00138 | 8.3e-143 | licT | K | CAT RNA binding domain | ||
KKGFHILH_00139 | 3.8e-207 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
KKGFHILH_00140 | 7.4e-85 | ptpA | 3.1.3.48 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
KKGFHILH_00141 | 1.6e-118 | |||||
KKGFHILH_00142 | 1.8e-75 | K | Penicillinase repressor | |||
KKGFHILH_00143 | 1.4e-147 | S | hydrolase | |||
KKGFHILH_00144 | 1.5e-255 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
KKGFHILH_00145 | 2e-172 | ybbR | S | YbbR-like protein | ||
KKGFHILH_00146 | 6.4e-151 | dacA | 2.7.7.85 | S | Catalyzes the condensation of 2 ATP molecules into cyclic di-AMP (c-di-AMP), a second messenger used to regulate differing processes in different bacteria | |
KKGFHILH_00147 | 7.3e-208 | potD | P | ABC transporter | ||
KKGFHILH_00148 | 4.8e-127 | potC | P | ABC transporter permease | ||
KKGFHILH_00149 | 1.3e-129 | potB | P | ABC transporter permease | ||
KKGFHILH_00150 | 1.8e-206 | potA | 3.6.3.30, 3.6.3.31 | P | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | |
KKGFHILH_00151 | 2e-163 | murB | 1.3.1.98 | M | Cell wall formation | |
KKGFHILH_00152 | 4e-98 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
KKGFHILH_00153 | 7e-86 | ydiB | 2.7.1.221, 5.1.1.1 | O | Hydrolase, P-loop family | |
KKGFHILH_00154 | 4.1e-181 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
KKGFHILH_00155 | 9.7e-137 | ung | 3.2.2.27 | L | Excises uracil residues from the DNA which can arise as a result of misincorporation of dUMP residues by DNA polymerase or due to deamination of cytosine | |
KKGFHILH_00156 | 3.4e-155 | ycsE | S | Sucrose-6F-phosphate phosphohydrolase | ||
KKGFHILH_00157 | 1.2e-94 | |||||
KKGFHILH_00158 | 1.4e-94 | |||||
KKGFHILH_00159 | 3.5e-252 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
KKGFHILH_00160 | 3.1e-170 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
KKGFHILH_00161 | 1.9e-261 | frdC | 1.3.5.4 | C | FAD binding domain | |
KKGFHILH_00162 | 9e-267 | fumC | 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
KKGFHILH_00163 | 3.4e-73 | metI | P | ABC transporter permease | ||
KKGFHILH_00164 | 2.6e-189 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
KKGFHILH_00165 | 5.9e-160 | metQ2 | P | Belongs to the nlpA lipoprotein family | ||
KKGFHILH_00166 | 2.4e-175 | F | DNA/RNA non-specific endonuclease | |||
KKGFHILH_00167 | 0.0 | aha1 | P | E1-E2 ATPase | ||
KKGFHILH_00168 | 1.5e-91 | folA | 1.5.1.3 | H | Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis | |
KKGFHILH_00169 | 1.3e-179 | 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 | |
KKGFHILH_00170 | 1.2e-250 | yifK | E | Amino acid permease | ||
KKGFHILH_00171 | 3.7e-263 | V | ABC-type multidrug transport system, ATPase and permease components | |||
KKGFHILH_00172 | 3.9e-128 | S | CAAX protease self-immunity | |||
KKGFHILH_00173 | 8e-224 | S | SLAP domain | |||
KKGFHILH_00174 | 1.2e-54 | S | Abi-like protein | |||
KKGFHILH_00175 | 1.5e-72 | S | Aminoacyl-tRNA editing domain | |||
KKGFHILH_00176 | 2.2e-163 | 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 | ||
KKGFHILH_00177 | 2.9e-44 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
KKGFHILH_00178 | 5e-134 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
KKGFHILH_00179 | 8.8e-62 | yodB | K | Transcriptional regulator, HxlR family | ||
KKGFHILH_00181 | 9.6e-110 | papP | P | ABC transporter, permease protein | ||
KKGFHILH_00182 | 2e-110 | P | ABC transporter permease | |||
KKGFHILH_00183 | 1.8e-133 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
KKGFHILH_00184 | 3e-53 | cjaA | ET | ABC transporter substrate-binding protein | ||
KKGFHILH_00185 | 8.1e-91 | cjaA | ET | ABC transporter substrate-binding protein | ||
KKGFHILH_00186 | 2.9e-277 | V | ABC transporter transmembrane region | |||
KKGFHILH_00187 | 3.9e-178 | pip | 3.4.11.5 | E | Releases the N-terminal proline from various substrates | |
KKGFHILH_00188 | 3.1e-130 | T | Transcriptional regulatory protein, C terminal | |||
KKGFHILH_00189 | 5.2e-187 | T | GHKL domain | |||
KKGFHILH_00190 | 3.4e-76 | S | Peptidase propeptide and YPEB domain | |||
KKGFHILH_00191 | 2.5e-72 | S | Peptidase propeptide and YPEB domain | |||
KKGFHILH_00192 | 4.7e-83 | paiA | 2.3.1.57 | K | Acetyltransferase (GNAT) domain | |
KKGFHILH_00193 | 3.8e-65 | yybA | 2.3.1.57 | K | Transcriptional regulator | |
KKGFHILH_00194 | 7e-68 | V | ABC transporter transmembrane region | |||
KKGFHILH_00195 | 9e-161 | V | ABC transporter transmembrane region | |||
KKGFHILH_00196 | 2.8e-309 | cpdB | 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
KKGFHILH_00197 | 2.3e-23 | S | Protein of unknown function (DUF2929) | |||
KKGFHILH_00198 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase | |
KKGFHILH_00199 | 3.3e-183 | pfkA | 2.7.1.11 | F | Catalyzes the phosphorylation of D-fructose 6-phosphate to fructose 1,6-bisphosphate by ATP, the first committing step of glycolysis | |
KKGFHILH_00200 | 0.0 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
KKGFHILH_00201 | 1e-167 | cvfB | S | S1 domain | ||
KKGFHILH_00202 | 2.9e-165 | xerD | D | recombinase XerD | ||
KKGFHILH_00203 | 2.6e-61 | ribT | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
KKGFHILH_00204 | 7.6e-132 | scpA | D | Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpB that pull DNA away from mid-cell into both cell halves | ||
KKGFHILH_00205 | 4.1e-104 | scpB | D | Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpA that pull DNA away from mid-cell into both cell halves | ||
KKGFHILH_00206 | 3.1e-130 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
KKGFHILH_00207 | 2.2e-112 | U | Mediates riboflavin uptake, may also transport FMN and roseoflavin. Probably a riboflavin-binding protein that interacts with the energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates. The substrates themselves are bound by transmembrane, not extracytoplasmic soluble proteins | |||
KKGFHILH_00208 | 2.7e-18 | M | Lysin motif | |||
KKGFHILH_00209 | 2.2e-114 | cmk | 1.17.7.4, 2.5.1.19, 2.7.1.26, 2.7.4.25, 2.7.7.2, 6.3.2.1 | F | Belongs to the cytidylate kinase family. Type 1 subfamily | |
KKGFHILH_00210 | 1.4e-24 | rpsA | 1.17.7.4 | J | Ribosomal protein S1 | |
KKGFHILH_00211 | 4.3e-247 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
KKGFHILH_00212 | 2.3e-41 | hup | L | Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions | ||
KKGFHILH_00213 | 3.9e-229 | S | Tetratricopeptide repeat protein | |||
KKGFHILH_00214 | 1.3e-237 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
KKGFHILH_00215 | 2e-75 | S | cog cog0433 | |||
KKGFHILH_00216 | 1.9e-110 | F | DNA/RNA non-specific endonuclease | |||
KKGFHILH_00217 | 2.7e-34 | S | YSIRK type signal peptide | |||
KKGFHILH_00219 | 5.5e-53 | |||||
KKGFHILH_00220 | 1.8e-285 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
KKGFHILH_00221 | 8e-79 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
KKGFHILH_00222 | 9.6e-169 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
KKGFHILH_00223 | 1e-198 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
KKGFHILH_00224 | 0.0 | carB1 | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
KKGFHILH_00225 | 5.3e-26 | |||||
KKGFHILH_00226 | 8.5e-41 | ptsH | G | phosphocarrier protein HPR | ||
KKGFHILH_00227 | 0.0 | ptsI | 2.7.3.9 | G | General (non sugar-specific) component of the phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS). This major carbohydrate active-transport system catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. Enzyme I transfers the phosphoryl group from phosphoenolpyruvate (PEP) to the phosphoryl carrier protein (HPr) | |
KKGFHILH_00228 | 3.9e-66 | spxA | 1.20.4.1 | K | Interferes with activator-stimulated transcription by interaction with the RNA polymerase alpha-CTD. May function to globally reduce transcription of genes involved in growth- and development-promoting processes and to increase transcription of genes involved in thiol homeostasis, during periods of extreme stress | |
KKGFHILH_00229 | 8.5e-139 | mecA | NOT | Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis | ||
KKGFHILH_00230 | 1.4e-158 | coiA | 3.6.4.12 | S | Competence protein | |
KKGFHILH_00231 | 4.6e-114 | yjbH | Q | Thioredoxin | ||
KKGFHILH_00232 | 6.8e-110 | yjbK | S | CYTH | ||
KKGFHILH_00233 | 1.2e-114 | yjbM | 2.7.6.5 | S | RelA SpoT domain protein | |
KKGFHILH_00234 | 3.8e-153 | nadK | 2.7.1.23 | F | Involved in the regulation of the intracellular balance of NAD and NADP, and is a key enzyme in the biosynthesis of NADP. Catalyzes specifically the phosphorylation on 2'-hydroxyl of the adenosine moiety of NAD to yield NADP | |
KKGFHILH_00235 | 6.4e-173 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
KKGFHILH_00236 | 0.0 | mycA | 4.2.1.53 | S | Myosin-crossreactive antigen | |
KKGFHILH_00237 | 4.2e-92 | S | SNARE associated Golgi protein | |||
KKGFHILH_00238 | 1.8e-200 | pgl | 3.1.1.31 | G | Lactonase, 7-bladed beta-propeller | |
KKGFHILH_00239 | 2.2e-66 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
KKGFHILH_00240 | 2.6e-214 | yubA | S | AI-2E family transporter | ||
KKGFHILH_00241 | 4.2e-106 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
KKGFHILH_00242 | 1.7e-69 | WQ51_03320 | S | Protein of unknown function (DUF1149) | ||
KKGFHILH_00243 | 0.0 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
KKGFHILH_00244 | 9e-223 | 2.7.1.26, 2.7.7.2 | S | Peptidase M16 inactive domain protein | ||
KKGFHILH_00245 | 1.9e-236 | S | Peptidase M16 | |||
KKGFHILH_00246 | 2.3e-133 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
KKGFHILH_00247 | 5.2e-97 | ymfM | S | Helix-turn-helix domain | ||
KKGFHILH_00248 | 1.1e-95 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
KKGFHILH_00249 | 4.2e-195 | recA | L | Can catalyze the hydrolysis of ATP in the presence of single-stranded DNA, the ATP-dependent uptake of single-stranded DNA by duplex DNA, and the ATP-dependent hybridization of homologous single-stranded DNAs. It interacts with LexA causing its activation and leading to its autocatalytic cleavage | ||
KKGFHILH_00250 | 7.4e-220 | rny | S | Endoribonuclease that initiates mRNA decay | ||
KKGFHILH_00251 | 1.3e-210 | tagO | 2.7.8.33, 2.7.8.35 | M | transferase | |
KKGFHILH_00252 | 5.1e-119 | yvyE | 3.4.13.9 | S | YigZ family | |
KKGFHILH_00253 | 4.7e-246 | comFA | L | Helicase C-terminal domain protein | ||
KKGFHILH_00254 | 9.4e-132 | comFC | S | Competence protein | ||
KKGFHILH_00255 | 1.6e-94 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
KKGFHILH_00256 | 0.0 | secA | U | Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. Has a central role in coupling the hydrolysis of ATP to the transfer of proteins into and across the cell membrane, serving as an ATP-driven molecular motor driving the stepwise translocation of polypeptide chains across the membrane | ||
KKGFHILH_00257 | 4.6e-188 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
KKGFHILH_00258 | 5.1e-17 | |||||
KKGFHILH_00259 | 5.8e-180 | hprK | F | Catalyzes the ATP- as well as the pyrophosphate- dependent phosphorylation of a specific serine residue in HPr, a phosphocarrier protein of the phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS). HprK P also catalyzes the pyrophosphate-producing, inorganic phosphate-dependent dephosphorylation (phosphorolysis) of seryl-phosphorylated HPr (P- Ser-HPr). The two antagonistic activities of HprK P are regulated by several intracellular metabolites, which change their concentration in response to the absence or presence of rapidly metabolisable carbon sources (glucose, fructose, etc.) in the growth medium. Therefore, by controlling the phosphorylation state of HPr, HPrK P is a sensor enzyme that plays a major role in the regulation of carbon metabolism and sugar transport it mediates carbon catabolite repression (CCR), and regulates PTS-catalyzed carbohydrate uptake and inducer exclusion | ||
KKGFHILH_00260 | 9.2e-158 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
KKGFHILH_00261 | 1.1e-186 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
KKGFHILH_00262 | 1.5e-180 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
KKGFHILH_00263 | 0.0 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase phosphomannomutase, alpha beta alpha domain | |
KKGFHILH_00264 | 0.0 | uvrB | L | damaged site, the DNA wraps around one UvrB monomer. DNA wrap is dependent on ATP binding by UvrB and probably causes local melting of the DNA helix, facilitating insertion of UvrB beta-hairpin between the DNA strands. Then UvrB probes one DNA strand for the presence of a lesion. If a lesion is found the UvrA subunits dissociate and the UvrB-DNA preincision complex is formed. This complex is subsequently bound by UvrC and the second UvrB is released. If no lesion is found, the DNA wraps around the other UvrB subunit that will check the other stand for damage | ||
KKGFHILH_00265 | 0.0 | uvrA | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrA is an ATPase and a DNA-binding protein. A damage recognition complex composed of 2 UvrA and 2 UvrB subunits scans DNA for abnormalities. When the presence of a lesion has been verified by UvrB, the UvrA molecules dissociate | ||
KKGFHILH_00266 | 4.1e-90 | S | Short repeat of unknown function (DUF308) | |||
KKGFHILH_00267 | 6.2e-165 | rapZ | S | Displays ATPase and GTPase activities | ||
KKGFHILH_00268 | 4e-195 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
KKGFHILH_00269 | 2.1e-171 | whiA | K | May be required for sporulation | ||
KKGFHILH_00270 | 2.3e-99 | clpP | 3.4.21.92 | O | Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins | |
KKGFHILH_00271 | 0.0 | S | SH3-like domain | |||
KKGFHILH_00272 | 3.9e-51 | V | ABC-type multidrug transport system, ATPase and permease components | |||
KKGFHILH_00273 | 2.6e-275 | V | ABC-type multidrug transport system, ATPase and permease components | |||
KKGFHILH_00274 | 8.4e-56 | S | Domain of unknown function (DUF4767) | |||
KKGFHILH_00275 | 5.8e-244 | eno | 4.2.1.11 | G | Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis | |
KKGFHILH_00276 | 2.5e-147 | yitS | S | Uncharacterised protein, DegV family COG1307 | ||
KKGFHILH_00277 | 3.2e-101 | 3.6.1.27 | I | Acid phosphatase homologues | ||
KKGFHILH_00278 | 2.8e-216 | coaBC | 4.1.1.36, 6.3.2.5 | H | Catalyzes two steps in the biosynthesis of coenzyme A. In the first step cysteine is conjugated to 4'-phosphopantothenate to form 4-phosphopantothenoylcysteine, in the latter compound is decarboxylated to form 4'-phosphopantotheine | |
KKGFHILH_00279 | 4.8e-34 | S | reductase | |||
KKGFHILH_00280 | 4.4e-39 | S | reductase | |||
KKGFHILH_00281 | 2.7e-32 | S | reductase | |||
KKGFHILH_00282 | 1.3e-148 | yxeH | S | hydrolase | ||
KKGFHILH_00283 | 6.8e-181 | gyaR | 1.1.1.26, 2.7.1.165 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
KKGFHILH_00284 | 1.1e-243 | yfnA | E | Amino Acid | ||
KKGFHILH_00285 | 6.8e-110 | dedA | 3.1.3.1 | S | SNARE associated Golgi protein | |
KKGFHILH_00286 | 0.0 | uvrC | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrC both incises the 5' and 3' sides of the lesion. The N-terminal half is responsible for the 3' incision and the C-terminal half is responsible for the 5' incision | ||
KKGFHILH_00287 | 1.7e-243 | obg | S | An essential GTPase which binds GTP, GDP and possibly (p)ppGpp with moderate affinity, with high nucleotide exchange rates and a fairly low GTP hydrolysis rate. Plays a role in control of the cell cycle, stress response, ribosome biogenesis and in those bacteria that undergo differentiation, in morphogenesis control | ||
KKGFHILH_00288 | 2.2e-292 | I | Acyltransferase | |||
KKGFHILH_00289 | 5.4e-175 | rnz | 3.1.26.11 | J | Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA | |
KKGFHILH_00290 | 5.1e-142 | XK27_05435 | 1.1.1.100 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
KKGFHILH_00291 | 1.5e-34 | yrvD | S | Lipopolysaccharide assembly protein A domain | ||
KKGFHILH_00292 | 1.3e-27 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
KKGFHILH_00293 | 1.6e-15 | L | hmm pf00665 | |||
KKGFHILH_00294 | 2.9e-15 | M | LysM domain protein | |||
KKGFHILH_00295 | 3.8e-48 | M | LysM domain protein | |||
KKGFHILH_00296 | 1.4e-86 | C | Aldo keto reductase | |||
KKGFHILH_00297 | 4.8e-181 | lacX | 5.1.3.3 | G | Aldose 1-epimerase | |
KKGFHILH_00298 | 8.2e-236 | 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 | ||
KKGFHILH_00299 | 1.9e-89 | hslV | 3.4.25.2 | O | Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery | |
KKGFHILH_00300 | 5e-141 | xerC | D | Phage integrase, N-terminal SAM-like domain | ||
KKGFHILH_00301 | 1.4e-248 | trmFO | 2.1.1.74 | J | Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs | |
KKGFHILH_00302 | 0.0 | topA | 5.99.1.2 | L | Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone | |
KKGFHILH_00303 | 5.8e-152 | dprA | LU | DNA protecting protein DprA | ||
KKGFHILH_00304 | 4.6e-132 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
KKGFHILH_00305 | 2.8e-154 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
KKGFHILH_00306 | 1.9e-94 | yjcE | P | Sodium proton antiporter | ||
KKGFHILH_00307 | 1.5e-40 | yjcE | P | Sodium proton antiporter | ||
KKGFHILH_00308 | 1.1e-66 | yjcE | P | NhaP-type Na H and K H | ||
KKGFHILH_00309 | 7.1e-36 | yozE | S | Belongs to the UPF0346 family | ||
KKGFHILH_00310 | 2e-144 | DegV | S | Uncharacterised protein, DegV family COG1307 | ||
KKGFHILH_00311 | 1.2e-107 | hlyIII | S | protein, hemolysin III | ||
KKGFHILH_00312 | 3.3e-225 | cca | 2.7.7.19, 2.7.7.72 | J | Catalyzes the addition and repair of the essential 3'- terminal CCA sequence in tRNAs without using a nucleic acid template. Adds these three nucleotides in the order of C, C, and A to the tRNA nucleotide-73, using CTP and ATP as substrates and producing inorganic pyrophosphate | |
KKGFHILH_00313 | 8.8e-159 | ypjC | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
KKGFHILH_00314 | 4.3e-86 | 3.4.21.96 | S | SLAP domain | ||
KKGFHILH_00315 | 8.4e-128 | yagE | E | Amino acid permease | ||
KKGFHILH_00316 | 9.7e-65 | yagE | E | amino acid | ||
KKGFHILH_00317 | 2.2e-113 | S | SLAP domain | |||
KKGFHILH_00318 | 2.9e-53 | L | PFAM RNA-directed DNA polymerase (Reverse transcriptase) | |||
KKGFHILH_00319 | 5.7e-46 | S | An automated process has identified a potential problem with this gene model | |||
KKGFHILH_00320 | 3e-137 | S | Protein of unknown function (DUF3100) | |||
KKGFHILH_00321 | 4e-245 | 3.5.1.47 | S | Peptidase dimerisation domain | ||
KKGFHILH_00322 | 5.8e-230 | Q | Imidazolonepropionase and related amidohydrolases | |||
KKGFHILH_00323 | 0.0 | oppA | E | ABC transporter | ||
KKGFHILH_00324 | 1.2e-151 | S | Sucrose-6F-phosphate phosphohydrolase | |||
KKGFHILH_00325 | 0.0 | mco | Q | Multicopper oxidase | ||
KKGFHILH_00326 | 1.9e-25 | |||||
KKGFHILH_00327 | 1.9e-158 | metQ1 | P | Belongs to the nlpA lipoprotein family | ||
KKGFHILH_00328 | 4.3e-169 | ldh | 1.1.1.27 | C | lactate/malate dehydrogenase, alpha/beta C-terminal domain | |
KKGFHILH_00329 | 2.4e-62 | 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 | ||
KKGFHILH_00330 | 0.0 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
KKGFHILH_00331 | 7.1e-200 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
KKGFHILH_00333 | 3.2e-139 | ribD | 1.1.1.193, 3.5.4.26 | H | Converts 2,5-diamino-6-(ribosylamino)-4(3h)-pyrimidinone 5'-phosphate into 5-amino-6-(ribosylamino)-2,4(1h,3h)- pyrimidinedione 5'-phosphate | |
KKGFHILH_00334 | 8.7e-86 | ribE | 2.5.1.9, 3.5.4.25, 4.1.99.12 | H | Riboflavin synthase | |
KKGFHILH_00335 | 1.5e-197 | ribBA | 3.5.4.25, 4.1.99.12 | H | Catalyzes the conversion of GTP to 2,5-diamino-6- ribosylamino-4(3H)-pyrimidinone 5'-phosphate (DARP), formate and pyrophosphate | |
KKGFHILH_00336 | 5.1e-78 | smpB | J | the 2 termini fold to resemble tRNA(Ala) and it encodes a tag peptide , a short internal open reading frame. During trans-translation Ala- aminoacylated tmRNA acts like a tRNA, entering the A-site of stalled ribosomes, displacing the stalled mRNA. The ribosome then switches to translate the ORF on the tmRNA | ||
KKGFHILH_00337 | 0.0 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
KKGFHILH_00338 | 1.7e-29 | secG | U | Preprotein translocase | ||
KKGFHILH_00339 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
KKGFHILH_00340 | 1.4e-176 | mprF | S | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms | ||
KKGFHILH_00341 | 7.6e-202 | cpoA | GT4 | M | Glycosyltransferase, group 1 family protein | |
KKGFHILH_00342 | 7.9e-224 | mgs | 2.4.1.337 | GT4 | M | Glycosyl transferase 4-like domain |
KKGFHILH_00349 | 0.0 | V | FtsX-like permease family | |||
KKGFHILH_00350 | 4.1e-133 | cysA | V | ABC transporter, ATP-binding protein | ||
KKGFHILH_00351 | 3.4e-23 | |||||
KKGFHILH_00352 | 2.5e-288 | pipD | E | Dipeptidase | ||
KKGFHILH_00353 | 3.6e-161 | 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) | ||
KKGFHILH_00354 | 0.0 | smc | D | Required for chromosome condensation and partitioning | ||
KKGFHILH_00355 | 1.9e-124 | 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 | |
KKGFHILH_00356 | 2.1e-308 | oppA | E | ABC transporter substrate-binding protein | ||
KKGFHILH_00357 | 3.1e-240 | oppA | E | ABC transporter substrate-binding protein | ||
KKGFHILH_00358 | 0.0 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
KKGFHILH_00359 | 3.3e-61 | 3.6.1.55 | F | NUDIX domain | ||
KKGFHILH_00360 | 1e-79 | S | AAA domain | |||
KKGFHILH_00361 | 2.9e-117 | fbiB | 6.3.2.12, 6.3.2.17, 6.3.2.31, 6.3.2.34 | S | F420-0:Gamma-glutamyl ligase | |
KKGFHILH_00362 | 1.3e-277 | arlS | 2.7.13.3 | T | Histidine kinase | |
KKGFHILH_00363 | 1.2e-126 | K | response regulator | |||
KKGFHILH_00364 | 4.7e-97 | yceD | S | Uncharacterized ACR, COG1399 | ||
KKGFHILH_00365 | 1.7e-215 | ylbM | S | Belongs to the UPF0348 family | ||
KKGFHILH_00366 | 5.3e-59 | rsfS | J | Functions as a ribosomal silencing factor. Interacts with ribosomal protein L14 (rplN), blocking formation of intersubunit bridge B8. Prevents association of the 30S and 50S ribosomal subunits and the formation of functional ribosomes, thus repressing translation | ||
KKGFHILH_00367 | 4.3e-109 | nadD | 2.7.6.3, 2.7.7.18 | H | Hydrolase, HD family | |
KKGFHILH_00368 | 4.4e-123 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
KKGFHILH_00369 | 4.4e-200 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
KKGFHILH_00370 | 4.2e-84 | yqeG | S | HAD phosphatase, family IIIA | ||
KKGFHILH_00371 | 9.2e-201 | tnpB | L | Putative transposase DNA-binding domain | ||
KKGFHILH_00372 | 6.9e-152 | add | 3.5.4.4 | F | Catalyzes the hydrolytic deamination of adenine to hypoxanthine. Plays an important role in the purine salvage pathway and in nitrogen catabolism | |
KKGFHILH_00373 | 3e-57 | rplT | J | Binds directly to 23S ribosomal RNA and is necessary for the in vitro assembly process of the 50S ribosomal subunit. It is not involved in the protein synthesizing functions of that subunit | ||
KKGFHILH_00374 | 8.1e-28 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
KKGFHILH_00375 | 3.2e-72 | infC | J | IF-3 binds to the 30S ribosomal subunit and shifts the equilibrum between 70S ribosomes and their 50S and 30S subunits in favor of the free subunits, thus enhancing the availability of 30S subunits on which protein synthesis initiation begins | ||
KKGFHILH_00376 | 4e-98 | rihB | 3.2.2.1 | F | Nucleoside | |
KKGFHILH_00377 | 2.7e-258 | yfnA | E | amino acid | ||
KKGFHILH_00378 | 6e-55 | 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 | ||
KKGFHILH_00379 | 4.9e-228 | 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 | |
KKGFHILH_00380 | 7.6e-45 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
KKGFHILH_00381 | 3.4e-94 | rimM | J | An accessory protein needed during the final step in the assembly of 30S ribosomal subunit, possibly for assembly of the head region. Probably interacts with S19. Essential for efficient processing of 16S rRNA. May be needed both before and after RbfA during the maturation of 16S rRNA. It has affinity for free ribosomal 30S subunits but not for 70S ribosomes | ||
KKGFHILH_00382 | 3.2e-135 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
KKGFHILH_00383 | 1.1e-56 | rplS | J | This protein is located at the 30S-50S ribosomal subunit interface and may play a role in the structure and function of the aminoacyl-tRNA binding site | ||
KKGFHILH_00384 | 4.6e-213 | S | SLAP domain | |||
KKGFHILH_00385 | 5.4e-121 | ung2 | 3.2.2.27 | L | Uracil-DNA glycosylase | |
KKGFHILH_00386 | 9.8e-146 | E | GDSL-like Lipase/Acylhydrolase family | |||
KKGFHILH_00387 | 2e-112 | 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 | |
KKGFHILH_00388 | 3e-38 | ynzC | S | UPF0291 protein | ||
KKGFHILH_00389 | 5.5e-30 | yneF | S | Uncharacterised protein family (UPF0154) | ||
KKGFHILH_00390 | 0.0 | mdlA | V | ABC transporter | ||
KKGFHILH_00391 | 0.0 | mdlB | V | ABC transporter | ||
KKGFHILH_00392 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
KKGFHILH_00393 | 3.9e-223 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
KKGFHILH_00394 | 2.9e-116 | plsC | 2.3.1.51 | I | Acyltransferase | |
KKGFHILH_00395 | 3e-195 | yabB | 2.1.1.223 | L | Methyltransferase small domain | |
KKGFHILH_00396 | 3.7e-137 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
KKGFHILH_00397 | 3.1e-184 | 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 | ||
KKGFHILH_00398 | 1.4e-130 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
KKGFHILH_00399 | 5.3e-93 | frr | J | Responsible for the release of ribosomes from messenger RNA at the termination of protein biosynthesis. May increase the efficiency of translation by recycling ribosomes from one round of translation to another | ||
KKGFHILH_00400 | 5.4e-138 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
KKGFHILH_00401 | 8.4e-140 | cdsA | 2.7.7.41 | I | Belongs to the CDS family | |
KKGFHILH_00402 | 5.7e-196 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
KKGFHILH_00403 | 0.0 | proS | 6.1.1.15 | J | Catalyzes the attachment of proline to tRNA(Pro) in a two-step reaction proline is first activated by ATP to form Pro- AMP and then transferred to the acceptor end of tRNA(Pro). As ProRS can inadvertently accommodate and process non-cognate amino acids such as alanine and cysteine, to avoid such errors it has two additional distinct editing activities against alanine. One activity is designated as 'pretransfer' editing and involves the tRNA(Pro)-independent hydrolysis of activated Ala-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Ala-tRNA(Pro). The misacylated Cys- tRNA(Pro) is not edited by ProRS | |
KKGFHILH_00404 | 0.0 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
KKGFHILH_00405 | 2.5e-83 | rimP | J | Required for maturation of 30S ribosomal subunits | ||
KKGFHILH_00406 | 1.4e-196 | nusA | K | Participates in both transcription termination and antitermination | ||
KKGFHILH_00407 | 1.5e-43 | ylxR | K | Protein of unknown function (DUF448) | ||
KKGFHILH_00408 | 3.2e-47 | rplGA | J | ribosomal protein | ||
KKGFHILH_00409 | 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 | ||
KKGFHILH_00410 | 1.1e-59 | 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 | ||
KKGFHILH_00411 | 1.6e-155 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
KKGFHILH_00412 | 3.2e-175 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
KKGFHILH_00413 | 4.9e-193 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
KKGFHILH_00414 | 8e-68 | 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 | ||
KKGFHILH_00415 | 0.0 | dnaK | O | Heat shock 70 kDa protein | ||
KKGFHILH_00416 | 2.2e-202 | 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 | ||
KKGFHILH_00417 | 0.0 | lepA | M | Required for accurate and efficient protein synthesis under certain stress conditions. May act as a fidelity factor of the translation reaction, by catalyzing a one-codon backward translocation of tRNAs on improperly translocated ribosomes. Back- translocation proceeds from a post-translocation (POST) complex to a pre-translocation (PRE) complex, thus giving elongation factor G a second chance to translocate the tRNAs correctly. Binds to ribosomes in a GTP-dependent manner | ||
KKGFHILH_00418 | 1.5e-102 | srtA | 3.4.22.70 | M | sortase family | |
KKGFHILH_00419 | 4.7e-26 | K | FCD | |||
KKGFHILH_00420 | 1.6e-60 | clcA | P | chloride | ||
KKGFHILH_00421 | 8.8e-41 | clcA | P | chloride | ||
KKGFHILH_00422 | 8.7e-60 | chbA | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose Cellobiose specific IIA subunit | |
KKGFHILH_00423 | 1e-54 | celA1 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
KKGFHILH_00424 | 6.4e-128 | K | UTRA domain | |||
KKGFHILH_00425 | 9.9e-293 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
KKGFHILH_00426 | 2e-85 | alkD | L | DNA alkylation repair enzyme | ||
KKGFHILH_00427 | 1.3e-176 | iunH | 3.2.2.1 | F | inosine-uridine preferring nucleoside hydrolase | |
KKGFHILH_00428 | 1.2e-80 | |||||
KKGFHILH_00429 | 3.6e-39 | C | FMN_bind | |||
KKGFHILH_00430 | 1.2e-188 | K | Periplasmic binding protein-like domain | |||
KKGFHILH_00431 | 2e-106 | K | Transcriptional regulator, AbiEi antitoxin | |||
KKGFHILH_00432 | 7.6e-163 | S | Nucleotidyl transferase AbiEii toxin, Type IV TA system | |||
KKGFHILH_00433 | 5.3e-189 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
KKGFHILH_00434 | 3.5e-145 | lacM | 3.2.1.23, 3.2.1.35, 3.2.1.51, 3.2.1.97 | GH101,GH29 | G | beta-galactosidase |
KKGFHILH_00435 | 0.0 | lacL | 3.2.1.23 | G | Belongs to the glycosyl hydrolase 2 family | |
KKGFHILH_00436 | 3.2e-165 | lacR | K | Transcriptional regulator | ||
KKGFHILH_00437 | 0.0 | lacS | G | Transporter | ||
KKGFHILH_00438 | 0.0 | lacZ | 3.2.1.23 | G | -beta-galactosidase | |
KKGFHILH_00439 | 1.1e-220 | 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) | |
KKGFHILH_00440 | 1.1e-288 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
KKGFHILH_00441 | 2e-196 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
KKGFHILH_00442 | 5.5e-36 | |||||
KKGFHILH_00443 | 6.4e-71 | scrR | K | Periplasmic binding protein domain | ||
KKGFHILH_00444 | 2.7e-94 | mreD | ||||
KKGFHILH_00445 | 2e-147 | mreC | M | Involved in formation and maintenance of cell shape | ||
KKGFHILH_00446 | 2.4e-176 | mreB | D | cell shape determining protein MreB | ||
KKGFHILH_00447 | 2.3e-108 | radC | L | DNA repair protein | ||
KKGFHILH_00448 | 5.7e-126 | S | Haloacid dehalogenase-like hydrolase | |||
KKGFHILH_00449 | 1.5e-239 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
KKGFHILH_00450 | 0.0 | valS | 6.1.1.9 | J | amino acids such as threonine, to avoid such errors, it has a posttransfer editing activity that hydrolyzes mischarged Thr-tRNA(Val) in a tRNA-dependent manner | |
KKGFHILH_00451 | 2.5e-52 | |||||
KKGFHILH_00452 | 1.1e-132 | S | AAA domain, putative AbiEii toxin, Type IV TA system | |||
KKGFHILH_00453 | 0.0 | 3.6.3.8 | P | P-type ATPase | ||
KKGFHILH_00455 | 6.5e-44 | |||||
KKGFHILH_00456 | 1.5e-94 | S | Protein of unknown function (DUF3990) | |||
KKGFHILH_00457 | 5.2e-170 | yfdH | 2.4.2.53 | GT2 | M | Glycosyltransferase, group 2 family protein |
KKGFHILH_00458 | 2.1e-65 | 2.4.1.83 | GT2 | S | GtrA-like protein | |
KKGFHILH_00459 | 5.5e-44 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
KKGFHILH_00460 | 3.2e-119 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
KKGFHILH_00461 | 1.7e-184 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
KKGFHILH_00462 | 2e-225 | thiI | 2.8.1.4 | H | Catalyzes the ATP-dependent transfer of a sulfur to tRNA to produce 4-thiouridine in position 8 of tRNAs, which functions as a near-UV photosensor. Also catalyzes the transfer of sulfur to the sulfur carrier protein ThiS, forming ThiS-thiocarboxylate. This is a step in the synthesis of thiazole, in the thiamine biosynthesis pathway. The sulfur is donated as persulfide by IscS | |
KKGFHILH_00463 | 4.8e-213 | iscS2 | 2.8.1.7 | E | Aminotransferase class V | |
KKGFHILH_00464 | 2.1e-294 | ezrA | D | modulates the frequency and position of FtsZ ring formation. Inhibits FtsZ ring formation at polar sites. Interacts either with FtsZ or with one of its binding partners to promote depolymerization | ||
KKGFHILH_00465 | 1.4e-110 | rpsD | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the body of the 30S subunit | ||
KKGFHILH_00466 | 1.3e-84 | yueI | S | Protein of unknown function (DUF1694) | ||
KKGFHILH_00467 | 6.3e-238 | rarA | L | recombination factor protein RarA | ||
KKGFHILH_00468 | 8.4e-39 | |||||
KKGFHILH_00469 | 1.8e-78 | usp6 | T | universal stress protein | ||
KKGFHILH_00470 | 4.7e-216 | rodA | D | Belongs to the SEDS family | ||
KKGFHILH_00471 | 3.3e-33 | S | Protein of unknown function (DUF2969) | |||
KKGFHILH_00472 | 1e-50 | yidD | S | Could be involved in insertion of integral membrane proteins into the membrane | ||
KKGFHILH_00473 | 1.2e-177 | mbl | D | Cell shape determining protein MreB Mrl | ||
KKGFHILH_00474 | 2e-30 | ywzB | S | Protein of unknown function (DUF1146) | ||
KKGFHILH_00475 | 9e-72 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
KKGFHILH_00476 | 3.3e-240 | atpD | 3.6.3.14 | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The catalytic sites are hosted primarily by the beta subunits | |
KKGFHILH_00477 | 8.9e-173 | 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 | ||
KKGFHILH_00478 | 2.5e-283 | 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 | |
KKGFHILH_00479 | 1.3e-91 | atpH | C | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
KKGFHILH_00480 | 4.4e-46 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
KKGFHILH_00481 | 3.5e-27 | atpE | C | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
KKGFHILH_00482 | 1e-128 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
KKGFHILH_00483 | 6.8e-113 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
KKGFHILH_00484 | 1.9e-189 | 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 | |
KKGFHILH_00485 | 7.3e-155 | prmB | 2.1.1.297, 2.1.1.298 | J | Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif | |
KKGFHILH_00486 | 3.1e-182 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
KKGFHILH_00487 | 1.7e-113 | tdk | 2.7.1.21 | F | thymidine kinase | |
KKGFHILH_00488 | 8.4e-262 | murF | 6.3.2.10, 6.3.2.13 | M | Domain of unknown function (DUF1727) | |
KKGFHILH_00490 | 5e-29 | |||||
KKGFHILH_00491 | 5.7e-171 | M | Glycosyl hydrolases family 25 | |||
KKGFHILH_00494 | 1.3e-122 | S | haloacid dehalogenase-like hydrolase | |||
KKGFHILH_00495 | 4.5e-291 | V | ABC-type multidrug transport system, ATPase and permease components | |||
KKGFHILH_00496 | 2.9e-277 | V | ABC-type multidrug transport system, ATPase and permease components | |||
KKGFHILH_00497 | 1.5e-64 | arsC | 1.20.4.1 | P | Belongs to the ArsC family | |
KKGFHILH_00498 | 8.5e-178 | I | Carboxylesterase family | |||
KKGFHILH_00500 | 1e-205 | M | Glycosyl hydrolases family 25 | |||
KKGFHILH_00501 | 1.2e-155 | cinI | S | Serine hydrolase (FSH1) | ||
KKGFHILH_00502 | 4.3e-298 | S | Predicted membrane protein (DUF2207) | |||
KKGFHILH_00503 | 1.6e-27 | dmpI | 5.3.2.6 | G | Belongs to the 4-oxalocrotonate tautomerase family | |
KKGFHILH_00505 | 7.8e-255 | S | Uncharacterized protein conserved in bacteria (DUF2325) | |||
KKGFHILH_00506 | 3.7e-151 | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | |||
KKGFHILH_00507 | 5.8e-49 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
KKGFHILH_00508 | 1.3e-47 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
KKGFHILH_00509 | 1e-196 | pepP | 3.4.11.9, 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
KKGFHILH_00510 | 4.9e-102 | efp | J | Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase | ||
KKGFHILH_00511 | 3.4e-71 | yqhY | S | Asp23 family, cell envelope-related function | ||
KKGFHILH_00512 | 1.1e-63 | nusB | K | Involved in transcription antitermination. Required for transcription of ribosomal RNA (rRNA) genes. Binds specifically to the boxA antiterminator sequence of the ribosomal RNA (rrn) operons | ||
KKGFHILH_00513 | 6.7e-156 | folD | 1.5.1.5, 3.5.4.9 | F | Catalyzes the oxidation of 5,10- methylenetetrahydrofolate to 5,10-methenyltetrahydrofolate and then the hydrolysis of 5,10-methenyltetrahydrofolate to 10- formyltetrahydrofolate | |
KKGFHILH_00514 | 2.9e-193 | xseA | 3.1.11.6 | L | Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides | |
KKGFHILH_00515 | 3.7e-35 | xseB | 3.1.11.6 | L | Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides | |
KKGFHILH_00516 | 1e-159 | ispA | 2.5.1.1, 2.5.1.10, 2.5.1.29, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
KKGFHILH_00517 | 2.3e-153 | rrmJ | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
KKGFHILH_00518 | 2.6e-300 | recN | L | May be involved in recombinational repair of damaged DNA | ||
KKGFHILH_00519 | 1.1e-77 | 6.3.3.2 | S | ASCH | ||
KKGFHILH_00520 | 2.1e-111 | gmk | 2.7.4.8, 4.1.1.23 | F | Essential for recycling GMP and indirectly, cGMP | |
KKGFHILH_00521 | 1.1e-33 | rpoZ | 2.7.7.6 | K | Promotes RNA polymerase assembly. Latches the N- and C- terminal regions of the beta' subunit thereby facilitating its interaction with the beta and alpha subunits | |
KKGFHILH_00522 | 0.0 | priA | L | Involved in the restart of stalled replication forks. Recognizes and binds the arrested nascent DNA chain at stalled replication forks. It can open the DNA duplex, via its helicase activity, and promote assembly of the primosome and loading of the major replicative helicase DnaB onto DNA | ||
KKGFHILH_00523 | 5.7e-172 | fmt | 2.1.2.9 | J | Attaches a formyl group to the free amino group of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by promoting its recognition by IF2 and preventing the misappropriation of this tRNA by the elongation apparatus | |
KKGFHILH_00524 | 1.6e-244 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
KKGFHILH_00525 | 1.1e-138 | stp | 3.1.3.16 | T | phosphatase | |
KKGFHILH_00526 | 0.0 | prkC | 2.7.11.1 | KLT | serine threonine protein kinase | |
KKGFHILH_00527 | 4.5e-163 | rsgA | 3.1.3.100 | S | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Helps release RbfA from mature subunits. May play a role in the assembly of ribosomal proteins into the subunit. Circularly permuted GTPase that catalyzes slow GTP hydrolysis, GTPase activity is stimulated by the 30S ribosomal subunit | |
KKGFHILH_00528 | 2.9e-119 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
KKGFHILH_00529 | 4.1e-124 | thiN | 2.7.6.2 | H | thiamine pyrophosphokinase | |
KKGFHILH_00530 | 1.4e-30 | |||||
KKGFHILH_00531 | 9.9e-118 | L | Belongs to the 'phage' integrase family | |||
KKGFHILH_00533 | 2.2e-15 | E | Pfam:DUF955 | |||
KKGFHILH_00535 | 4.7e-18 | K | Helix-turn-helix XRE-family like proteins | |||
KKGFHILH_00536 | 4.4e-79 | S | Phage antirepressor protein KilAC domain | |||
KKGFHILH_00537 | 3.5e-46 | |||||
KKGFHILH_00543 | 1.6e-70 | S | AAA domain | |||
KKGFHILH_00545 | 4.7e-148 | res | L | Helicase C-terminal domain protein | ||
KKGFHILH_00546 | 1.7e-30 | S | Protein of unknown function (DUF669) | |||
KKGFHILH_00547 | 2.7e-268 | S | Phage plasmid primase, P4 | |||
KKGFHILH_00558 | 3.3e-37 | S | VRR_NUC | |||
KKGFHILH_00560 | 9.8e-12 | |||||
KKGFHILH_00561 | 3.1e-14 | arpU | S | Phage transcriptional regulator, ArpU family | ||
KKGFHILH_00563 | 3.5e-49 | L | HNH nucleases | |||
KKGFHILH_00564 | 1.6e-55 | L | Phage terminase, small subunit | |||
KKGFHILH_00565 | 3.4e-18 | N | HicA toxin of bacterial toxin-antitoxin, | |||
KKGFHILH_00566 | 9e-47 | S | HicB_like antitoxin of bacterial toxin-antitoxin system | |||
KKGFHILH_00567 | 2.8e-210 | S | Phage Terminase | |||
KKGFHILH_00568 | 3.6e-140 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
KKGFHILH_00569 | 4.3e-52 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
KKGFHILH_00570 | 4.1e-156 | crtI | 1.3.99.23, 5.2.1.13 | Q | HI0933-like protein | |
KKGFHILH_00571 | 2.6e-65 | C | 2Fe-2S iron-sulfur cluster binding domain | |||
KKGFHILH_00572 | 1.9e-22 | K | Putative DNA-binding domain | |||
KKGFHILH_00573 | 7.6e-239 | pyrP | F | Permease | ||
KKGFHILH_00574 | 8.8e-90 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
KKGFHILH_00575 | 9.2e-262 | emrY | EGP | Major facilitator Superfamily | ||
KKGFHILH_00576 | 1.9e-138 | 2.4.2.3 | F | Phosphorylase superfamily | ||
KKGFHILH_00577 | 9e-144 | 2.4.2.3 | F | Phosphorylase superfamily | ||
KKGFHILH_00578 | 3.6e-151 | aacC | 2.3.1.81 | V | Aminoglycoside 3-N-acetyltransferase | |
KKGFHILH_00579 | 8.1e-126 | S | PAS domain | |||
KKGFHILH_00580 | 1.6e-11 | |||||
KKGFHILH_00581 | 2.7e-57 | |||||
KKGFHILH_00582 | 6.6e-56 | |||||
KKGFHILH_00583 | 4e-08 | |||||
KKGFHILH_00584 | 1.1e-223 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
KKGFHILH_00585 | 3.3e-275 | yjeM | E | Amino Acid | ||
KKGFHILH_00586 | 5.8e-83 | S | Fic/DOC family | |||
KKGFHILH_00587 | 2.7e-285 | |||||
KKGFHILH_00588 | 3.2e-77 | |||||
KKGFHILH_00589 | 2.3e-87 | S | Protein of unknown function (DUF805) | |||
KKGFHILH_00590 | 5.6e-68 | O | OsmC-like protein | |||
KKGFHILH_00591 | 9.4e-209 | EGP | Major facilitator Superfamily | |||
KKGFHILH_00592 | 2.5e-215 | sptS | 2.7.13.3 | T | Histidine kinase | |
KKGFHILH_00593 | 2.2e-85 | S | PFAM Archaeal ATPase | |||
KKGFHILH_00594 | 5.7e-84 | S | PFAM Archaeal ATPase | |||
KKGFHILH_00595 | 7.7e-26 | |||||
KKGFHILH_00596 | 1.1e-71 | 2.5.1.74 | H | UbiA prenyltransferase family | ||
KKGFHILH_00597 | 1.3e-116 | S | Peptidase family M23 | |||
KKGFHILH_00598 | 1.8e-104 | 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 | |
KKGFHILH_00600 | 4.6e-160 | yitT | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
KKGFHILH_00601 | 9.4e-118 | |||||
KKGFHILH_00602 | 2.8e-157 | thrB | 2.7.1.39 | F | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
KKGFHILH_00603 | 6.6e-221 | hom | 1.1.1.3, 2.7.2.4 | E | homoserine dehydrogenase | |
KKGFHILH_00604 | 2.6e-280 | thrC | 4.2.3.1 | E | Threonine synthase | |
KKGFHILH_00605 | 8.8e-259 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
KKGFHILH_00606 | 9.6e-103 | pgm3 | 5.4.2.11 | G | Histidine phosphatase superfamily (branch 1) | |
KKGFHILH_00607 | 5.8e-85 | 2.3.1.128 | K | Acetyltransferase (GNAT) domain | ||
KKGFHILH_00608 | 2e-157 | S | reductase | |||
KKGFHILH_00609 | 9.3e-35 | |||||
KKGFHILH_00611 | 6.4e-54 | S | Protein of unknown function (DUF3397) | |||
KKGFHILH_00612 | 6.3e-78 | mraZ | K | Belongs to the MraZ family | ||
KKGFHILH_00613 | 7.2e-175 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
KKGFHILH_00614 | 1.8e-54 | ftsL | D | Cell division protein FtsL | ||
KKGFHILH_00615 | 0.0 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
KKGFHILH_00616 | 3.3e-175 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
KKGFHILH_00617 | 5e-262 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
KKGFHILH_00618 | 3.7e-207 | murG | 2.4.1.227, 6.3.2.8 | GT28 | M | Cell wall formation. Catalyzes the transfer of a GlcNAc subunit on undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide (lipid intermediate I) to form undecaprenyl-pyrophosphoryl-MurNAc- (pentapeptide)GlcNAc (lipid intermediate II) |
KKGFHILH_00619 | 4.5e-152 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
KKGFHILH_00620 | 6.7e-243 | 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 | ||
KKGFHILH_00621 | 1.7e-206 | ftsZ | D | Essential cell division protein that forms a contractile ring structure (Z ring) at the future cell division site. The regulation of the ring assembly controls the timing and the location of cell division. One of the functions of the FtsZ ring is to recruit other cell division proteins to the septum to produce a new cell wall between the dividing cells. Binds GTP and shows GTPase activity | ||
KKGFHILH_00622 | 7.3e-74 | sepF | D | Cell division protein that is part of the divisome complex and is recruited early to the Z-ring. Probably stimulates Z-ring formation, perhaps through the cross-linking of FtsZ protofilaments. Its function overlaps with FtsA | ||
KKGFHILH_00623 | 1.7e-45 | yggT | S | YGGT family | ||
KKGFHILH_00624 | 5.7e-149 | ylmH | S | S4 domain protein | ||
KKGFHILH_00625 | 2.8e-74 | gpsB | D | DivIVA domain protein | ||
KKGFHILH_00626 | 0.0 | ileS | 6.1.1.5 | J | amino acids such as valine, to avoid such errors it has two additional distinct tRNA(Ile)-dependent editing activities. One activity is designated as 'pretransfer' editing and involves the hydrolysis of activated Val-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Val-tRNA(Ile) | |
KKGFHILH_00627 | 3.6e-31 | cspA | K | 'Cold-shock' DNA-binding domain | ||
KKGFHILH_00628 | 2.8e-102 | nudF | 3.6.1.13 | L | ADP-ribose pyrophosphatase | |
KKGFHILH_00629 | 6.7e-37 | |||||
KKGFHILH_00630 | 1.2e-126 | mtnN | 3.2.2.9 | E | Catalyzes the irreversible cleavage of the glycosidic bond in both 5'-methylthioadenosine (MTA) and S- adenosylhomocysteine (SAH AdoHcy) to adenine and the corresponding thioribose, 5'-methylthioribose and S-ribosylhomocysteine, respectively | |
KKGFHILH_00631 | 3.2e-217 | iscS | 2.8.1.7 | E | Aminotransferase class V | |
KKGFHILH_00632 | 5.4e-56 | XK27_04120 | S | Putative amino acid metabolism | ||
KKGFHILH_00633 | 5.1e-220 | mnmA | 2.8.1.13 | J | Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 | |
KKGFHILH_00634 | 3.9e-127 | pgm6 | 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | |
KKGFHILH_00635 | 2.4e-105 | S | Repeat protein | |||
KKGFHILH_00636 | 0.0 | recD2 | 3.1.11.5 | L | DNA-dependent ATPase and ATP-dependent 5'-3' DNA helicase. Has no activity on blunt DNA or DNA with 3'-overhangs, requires at least 10 bases of 5'-ssDNA for helicase activity | |
KKGFHILH_00637 | 1.6e-294 | L | Nuclease-related domain | |||
KKGFHILH_00638 | 2.3e-164 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic domain | |
KKGFHILH_00639 | 1.4e-26 | rpmB | J | Belongs to the bacterial ribosomal protein bL28 family | ||
KKGFHILH_00640 | 4e-57 | asp | S | Asp23 family, cell envelope-related function | ||
KKGFHILH_00641 | 7.6e-305 | yloV | S | DAK2 domain fusion protein YloV | ||
KKGFHILH_00642 | 0.0 | recG | 3.6.4.12 | L | Critical role in recombination and DNA repair. Helps process Holliday junction intermediates to mature products by catalyzing branch migration. Has a DNA unwinding activity characteristic of a DNA helicase with a 3'- to 5'- polarity. Unwinds branched duplex DNA (Y-DNA) | |
KKGFHILH_00643 | 3.7e-182 | plsX | 2.3.1.15 | I | Catalyzes the reversible formation of acyl-phosphate (acyl-PO(4)) from acyl- acyl-carrier-protein (acyl-ACP). This enzyme utilizes acyl-ACP as fatty acyl donor, but not acyl-CoA | |
KKGFHILH_00644 | 4.9e-35 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
KKGFHILH_00645 | 1.1e-192 | oppD | P | Belongs to the ABC transporter superfamily | ||
KKGFHILH_00646 | 1.5e-170 | oppF | P | Belongs to the ABC transporter superfamily | ||
KKGFHILH_00647 | 2.6e-172 | oppB | P | ABC transporter permease | ||
KKGFHILH_00648 | 5.6e-132 | oppC | P | Binding-protein-dependent transport system inner membrane component | ||
KKGFHILH_00649 | 9.7e-46 | oppA | E | ABC transporter substrate-binding protein | ||
KKGFHILH_00650 | 1.9e-115 | rdgB | 3.6.1.66, 5.1.1.3 | F | Ham1 family | |
KKGFHILH_00651 | 3.4e-79 | |||||
KKGFHILH_00652 | 1e-242 | cpdA | S | Calcineurin-like phosphoesterase | ||
KKGFHILH_00653 | 3.6e-218 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
KKGFHILH_00654 | 1.1e-68 | gpsB | D | Divisome component that associates with the complex late in its assembly, after the Z-ring is formed, and is dependent on DivIC and PBP2B for its recruitment to the divisome. Together with EzrA, is a key component of the system that regulates PBP1 localization during cell cycle progression. Its main role could be the removal of PBP1 from the cell pole after pole maturation is completed. Also contributes to the recruitment of PBP1 to the division complex. Not essential for septum formation | ||
KKGFHILH_00655 | 1e-107 | ypsA | S | Belongs to the UPF0398 family | ||
KKGFHILH_00656 | 4.5e-117 | recU | L | Endonuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves mobile four-strand junctions by introducing symmetrical nicks in paired strands. Promotes annealing of linear ssDNA with homologous dsDNA. Required for DNA repair, homologous recombination and chromosome segregation | ||
KKGFHILH_00657 | 0.0 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
KKGFHILH_00658 | 2.7e-114 | 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 | |
KKGFHILH_00659 | 1.3e-114 | dnaD | L | DnaD domain protein | ||
KKGFHILH_00660 | 5.8e-260 | asnS | 6.1.1.22 | J | Asparaginyl-tRNA synthetase | |
KKGFHILH_00661 | 2.4e-89 | ypmB | S | Protein conserved in bacteria | ||
KKGFHILH_00662 | 3e-22 | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
KKGFHILH_00663 | 9.2e-14 | |||||
KKGFHILH_00664 | 1.6e-121 | M | Glycosyl hydrolases family 25 | |||
KKGFHILH_00665 | 7.4e-128 | citG | 2.4.2.52, 2.7.7.61 | H | 2-(5''-triphosphoribosyl)-3'-dephosphocoenzyme-A synthase | |
KKGFHILH_00666 | 4.5e-192 | I | transferase activity, transferring acyl groups other than amino-acyl groups | |||
KKGFHILH_00667 | 5.6e-179 | S | PFAM Archaeal ATPase | |||
KKGFHILH_00668 | 2.4e-73 | S | cog cog1373 | |||
KKGFHILH_00669 | 2e-169 | celD | 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 | ||
KKGFHILH_00670 | 3.5e-70 | S | Domain of unknown function (DUF3284) | |||
KKGFHILH_00671 | 4.5e-301 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family | |
KKGFHILH_00672 | 5.3e-130 | gmuR | K | UTRA | ||
KKGFHILH_00673 | 7e-214 | pepQ | 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
KKGFHILH_00674 | 3.2e-181 | ccpA | K | catabolite control protein A | ||
KKGFHILH_00675 | 2.3e-267 | ugpQ | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
KKGFHILH_00676 | 4.3e-55 | |||||
KKGFHILH_00677 | 5.8e-274 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
KKGFHILH_00678 | 2.1e-92 | yutD | S | Protein of unknown function (DUF1027) | ||
KKGFHILH_00679 | 3.4e-143 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
KKGFHILH_00680 | 3.7e-100 | S | Protein of unknown function (DUF1461) | |||
KKGFHILH_00681 | 6.8e-116 | dedA | S | SNARE-like domain protein | ||
KKGFHILH_00682 | 7.5e-183 | yumC | 1.18.1.2, 1.19.1.1, 1.8.1.9 | C | Ferredoxin--NADP reductase | |
KKGFHILH_00683 | 1.3e-36 | |||||
KKGFHILH_00684 | 9.5e-10 | WQ51_05790 | S | protein containing a divergent version of the methyl-accepting chemotaxis-like domain | ||
KKGFHILH_00685 | 3.7e-146 | ykuT | M | mechanosensitive ion channel | ||
KKGFHILH_00686 | 6.9e-100 | V | ATPases associated with a variety of cellular activities | |||
KKGFHILH_00687 | 1.7e-139 | |||||
KKGFHILH_00688 | 5.4e-113 | |||||
KKGFHILH_00689 | 4.2e-150 | rluA | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
KKGFHILH_00690 | 0.0 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
KKGFHILH_00691 | 7.2e-56 | yheA | S | Belongs to the UPF0342 family | ||
KKGFHILH_00692 | 1e-226 | yhaO | L | Ser Thr phosphatase family protein | ||
KKGFHILH_00693 | 0.0 | L | AAA domain | |||
KKGFHILH_00694 | 1.9e-186 | cbf | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
KKGFHILH_00695 | 2.9e-23 | |||||
KKGFHILH_00696 | 2.4e-51 | S | Domain of unknown function DUF1829 | |||
KKGFHILH_00697 | 1.1e-265 | |||||
KKGFHILH_00698 | 1.9e-72 | eda | 4.1.2.14, 4.1.3.42 | G | KDPG and KHG aldolase | |
KKGFHILH_00699 | 4.3e-153 | prsA | 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
KKGFHILH_00700 | 3.9e-25 | |||||
KKGFHILH_00701 | 8.3e-78 | hit | FG | Scavenger mRNA decapping enzyme C-term binding | ||
KKGFHILH_00702 | 5.7e-135 | ecsA | V | ABC transporter, ATP-binding protein | ||
KKGFHILH_00703 | 6.5e-221 | ecsB | U | ABC transporter | ||
KKGFHILH_00704 | 3.3e-126 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
KKGFHILH_00706 | 2.8e-54 | ytpP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
KKGFHILH_00707 | 1.4e-122 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
KKGFHILH_00708 | 9.7e-247 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
KKGFHILH_00709 | 6.9e-218 | mepA | V | MATE efflux family protein | ||
KKGFHILH_00710 | 1.8e-176 | S | SLAP domain | |||
KKGFHILH_00711 | 4.4e-283 | M | Peptidase family M1 domain | |||
KKGFHILH_00712 | 4.5e-188 | S | Bacteriocin helveticin-J | |||
KKGFHILH_00713 | 8e-51 | L | RelB antitoxin | |||
KKGFHILH_00714 | 7.4e-105 | qmcA | O | prohibitin homologues | ||
KKGFHILH_00715 | 3.5e-25 | qmcA | O | prohibitin homologues | ||
KKGFHILH_00716 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
KKGFHILH_00717 | 4.2e-155 | fpg | 3.2.2.23, 4.2.99.18 | L | Involved in base excision repair of DNA damaged by oxidation or by mutagenic agents. Acts as DNA glycosylase that recognizes and removes damaged bases. Has a preference for oxidized purines, such as 7,8-dihydro-8-oxoguanine (8-oxoG). Has AP (apurinic apyrimidinic) lyase activity and introduces nicks in the DNA strand. Cleaves the DNA backbone by beta-delta elimination to generate a single-strand break at the site of the removed base with both 3'- and 5'-phosphates | |
KKGFHILH_00718 | 1.3e-105 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
KKGFHILH_00719 | 3.5e-82 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
KKGFHILH_00720 | 5.1e-251 | dnaB | L | Replication initiation and membrane attachment | ||
KKGFHILH_00721 | 1.3e-168 | dnaI | L | Primosomal protein DnaI | ||
KKGFHILH_00722 | 0.0 | thrS | 6.1.1.3 | J | Catalyzes the attachment of threonine to tRNA(Thr) in a two-step reaction L-threonine is first activated by ATP to form Thr-AMP and then transferred to the acceptor end of tRNA(Thr) | |
KKGFHILH_00723 | 4.3e-75 | |||||
KKGFHILH_00724 | 4e-60 | L | Resolvase, N terminal domain | |||
KKGFHILH_00725 | 4.6e-25 | dnaQ | 2.7.7.7 | L | DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. The epsilon subunit contain the editing function and is a proofreading 3'-5' exonuclease | |
KKGFHILH_00726 | 3.2e-103 | L | An automated process has identified a potential problem with this gene model | |||
KKGFHILH_00727 | 7.8e-10 | 3.6.3.2, 3.6.3.6 | P | cation transport ATPase | ||
KKGFHILH_00728 | 4.4e-35 | 3.6.3.2, 3.6.3.6 | P | cation transport ATPase | ||
KKGFHILH_00729 | 3.6e-241 | 3.6.3.6 | P | Cation transporter/ATPase, N-terminus | ||
KKGFHILH_00730 | 1.9e-19 | |||||
KKGFHILH_00731 | 2.2e-142 | S | Belongs to the UPF0246 family | |||
KKGFHILH_00732 | 4.1e-141 | aroD | S | Alpha/beta hydrolase family | ||
KKGFHILH_00733 | 3.5e-111 | G | phosphoglycerate mutase | |||
KKGFHILH_00734 | 3.2e-92 | ygfC | K | Bacterial regulatory proteins, tetR family | ||
KKGFHILH_00735 | 3.3e-176 | hrtB | V | ABC transporter permease | ||
KKGFHILH_00736 | 2e-102 | devA | 3.6.3.25 | V | ABC transporter, ATP-binding protein | |
KKGFHILH_00737 | 1.3e-273 | pipD | E | Dipeptidase | ||
KKGFHILH_00738 | 1.2e-94 | apt | 2.4.2.22, 2.4.2.7 | F | Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis | |
KKGFHILH_00739 | 0.0 | recJ | L | Single-stranded-DNA-specific exonuclease RecJ | ||
KKGFHILH_00740 | 3.1e-107 | ribE | 2.5.1.9, 3.5.4.25, 4.1.99.12 | H | Riboflavin synthase | |
KKGFHILH_00741 | 1.7e-201 | ribD | 1.1.1.193, 3.5.4.26 | H | Converts 2,5-diamino-6-(ribosylamino)-4(3h)-pyrimidinone 5'-phosphate into 5-amino-6-(ribosylamino)-2,4(1h,3h)- pyrimidinedione 5'-phosphate | |
KKGFHILH_00742 | 2.2e-120 | lsa | S | ABC transporter | ||
KKGFHILH_00743 | 6e-46 | L | An automated process has identified a potential problem with this gene model | |||
KKGFHILH_00744 | 2.8e-48 | S | Peptidase propeptide and YPEB domain | |||
KKGFHILH_00745 | 4.1e-33 | adh | 1.1.1.1, 1.1.1.14 | E | alcohol dehydrogenase | |
KKGFHILH_00746 | 1.3e-29 | paiA | 2.3.1.57 | K | Acetyltransferase (GNAT) domain | |
KKGFHILH_00747 | 1.3e-12 | L | TIGRFAM transposase, IS605 OrfB family | |||
KKGFHILH_00748 | 1.2e-11 | S | Transposase C of IS166 homeodomain | |||
KKGFHILH_00749 | 1.4e-59 | XK27_01125 | L | IS66 Orf2 like protein | ||
KKGFHILH_00750 | 4.4e-169 | ppaC | 3.6.1.1 | C | inorganic pyrophosphatase | |
KKGFHILH_00751 | 2.8e-182 | K | Transcriptional regulator | |||
KKGFHILH_00752 | 0.0 | parC | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
KKGFHILH_00753 | 0.0 | parE | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
KKGFHILH_00754 | 3.5e-109 | 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 | |
KKGFHILH_00755 | 0.0 | snf | 2.7.11.1 | KL | domain protein | |
KKGFHILH_00756 | 2e-35 | |||||
KKGFHILH_00758 | 3.8e-104 | pncA | Q | Isochorismatase family | ||
KKGFHILH_00759 | 4.9e-118 | |||||
KKGFHILH_00762 | 3.6e-63 | |||||
KKGFHILH_00763 | 1.4e-34 | |||||
KKGFHILH_00764 | 2.1e-47 | |||||
KKGFHILH_00766 | 5e-07 | K | Helix-turn-helix XRE-family like proteins | |||
KKGFHILH_00767 | 7.2e-10 | |||||
KKGFHILH_00772 | 1.1e-90 | S | AntA/AntB antirepressor | |||
KKGFHILH_00774 | 2e-20 | cro | K | Helix-turn-helix XRE-family like proteins | ||
KKGFHILH_00775 | 2.8e-13 | K | Helix-turn-helix XRE-family like proteins | |||
KKGFHILH_00777 | 3e-59 | |||||
KKGFHILH_00778 | 6e-14 | |||||
KKGFHILH_00782 | 2.5e-13 | |||||
KKGFHILH_00783 | 1.6e-147 | sip | L | Belongs to the 'phage' integrase family | ||
KKGFHILH_00784 | 0.0 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
KKGFHILH_00785 | 0.0 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
KKGFHILH_00786 | 0.0 | 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 | |
KKGFHILH_00787 | 4.8e-136 | mvk | 1.1.1.88, 2.3.3.10, 2.7.1.36 | I | GHMP kinases N terminal domain | |
KKGFHILH_00788 | 1.4e-178 | mvaD | 4.1.1.33 | I | diphosphomevalonate decarboxylase | |
KKGFHILH_00789 | 2.1e-202 | mvaK2 | 2.7.1.36, 2.7.1.43, 2.7.4.2 | I | phosphomevalonate kinase | |
KKGFHILH_00790 | 6.9e-184 | fni | 1.1.1.88, 5.3.3.2 | C | Involved in the biosynthesis of isoprenoids. Catalyzes the 1,3-allylic rearrangement of the homoallylic substrate isopentenyl (IPP) to its allylic isomer, dimethylallyl diphosphate (DMAPP) | |
KKGFHILH_00791 | 1.3e-116 | 3.1.3.102, 3.1.3.104, 3.1.3.23 | G | Sucrose-6F-phosphate phosphohydrolase | ||
KKGFHILH_00792 | 8.3e-265 | rsmF | 2.1.1.176 | J | NOL1 NOP2 sun family protein | |
KKGFHILH_00793 | 9.7e-169 | |||||
KKGFHILH_00794 | 7.5e-143 | |||||
KKGFHILH_00795 | 3.9e-104 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
KKGFHILH_00796 | 1.4e-26 | |||||
KKGFHILH_00797 | 6.7e-145 | |||||
KKGFHILH_00798 | 5.1e-137 | |||||
KKGFHILH_00799 | 4.5e-141 | |||||
KKGFHILH_00800 | 9.6e-124 | skfE | V | ATPases associated with a variety of cellular activities | ||
KKGFHILH_00801 | 1.4e-60 | yvoA_1 | K | Transcriptional regulator, GntR family | ||
KKGFHILH_00802 | 1.7e-240 | pepT | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
KKGFHILH_00803 | 1.4e-152 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
KKGFHILH_00804 | 3.5e-123 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
KKGFHILH_00805 | 4.8e-81 | mutT | 3.6.1.55 | F | NUDIX domain | |
KKGFHILH_00806 | 1.4e-127 | S | Peptidase family M23 | |||
KKGFHILH_00807 | 9.9e-200 | 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 | ||
KKGFHILH_00808 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
KKGFHILH_00809 | 0.0 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
KKGFHILH_00810 | 4.6e-179 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
KKGFHILH_00811 | 4.4e-135 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
KKGFHILH_00812 | 2.1e-168 | era | S | An essential GTPase that binds both GDP and GTP, with rapid nucleotide exchange. Plays a role in 16S rRNA processing and 30S ribosomal subunit biogenesis and possibly also in cell cycle regulation and energy metabolism | ||
KKGFHILH_00813 | 2.2e-93 | 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 | |
KKGFHILH_00814 | 1.1e-175 | phoH | T | phosphate starvation-inducible protein PhoH | ||
KKGFHILH_00815 | 3.5e-71 | yqeY | S | YqeY-like protein | ||
KKGFHILH_00816 | 2e-22 | rpsU | J | Belongs to the bacterial ribosomal protein bS21 family | ||
KKGFHILH_00817 | 1.2e-154 | 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 | |
KKGFHILH_00818 | 1.5e-18 | S | CRISPR-associated protein (Cas_Csn2) | |||
KKGFHILH_00819 | 2.5e-197 | M | Phage tail tape measure protein TP901 | |||
KKGFHILH_00820 | 1.1e-11 | |||||
KKGFHILH_00821 | 1.3e-11 | |||||
KKGFHILH_00822 | 1.7e-133 | Z012_02110 | S | Protein of unknown function (DUF3383) | ||
KKGFHILH_00823 | 1.6e-27 | |||||
KKGFHILH_00824 | 2.7e-10 | |||||
KKGFHILH_00825 | 7.7e-42 | |||||
KKGFHILH_00826 | 1.6e-27 | S | Protein of unknown function (DUF4054) | |||
KKGFHILH_00827 | 2.9e-36 | Z012_11565 | S | Uncharacterized protein conserved in bacteria (DUF2184) | ||
KKGFHILH_00828 | 1e-22 | |||||
KKGFHILH_00829 | 1.3e-53 | S | Uncharacterized protein conserved in bacteria (DUF2213) | |||
KKGFHILH_00830 | 4.8e-20 | S | Lysin motif | |||
KKGFHILH_00831 | 1.3e-55 | S | Phage Mu protein F like protein | |||
KKGFHILH_00832 | 3.3e-91 | S | Protein of unknown function (DUF1073) | |||
KKGFHILH_00833 | 9.6e-187 | S | Terminase-like family | |||
KKGFHILH_00836 | 1.1e-20 | S | N-methyltransferase activity | |||
KKGFHILH_00842 | 3.4e-09 | |||||
KKGFHILH_00843 | 5.3e-36 | S | VRR_NUC | |||
KKGFHILH_00845 | 2.2e-67 | S | ORF6C domain | |||
KKGFHILH_00850 | 2.7e-33 | Q | DNA (cytosine-5-)-methyltransferase activity | |||
KKGFHILH_00856 | 1.5e-21 | radC | L | DNA repair protein | ||
KKGFHILH_00857 | 4e-65 | 2.1.1.72 | L | Belongs to the N(4) N(6)-methyltransferase family | ||
KKGFHILH_00858 | 1.6e-31 | 2.1.1.72 | L | Belongs to the N(4) N(6)-methyltransferase family | ||
KKGFHILH_00860 | 2.7e-31 | K | Helix-turn-helix domain | |||
KKGFHILH_00861 | 1.6e-44 | S | ERF superfamily | |||
KKGFHILH_00862 | 2.2e-53 | S | Protein of unknown function (DUF1351) | |||
KKGFHILH_00866 | 3.2e-10 | |||||
KKGFHILH_00869 | 6.6e-11 | K | Helix-turn-helix XRE-family like proteins | |||
KKGFHILH_00870 | 4.8e-17 | S | protein disulfide oxidoreductase activity | |||
KKGFHILH_00873 | 1.4e-95 | sip | L | Belongs to the 'phage' integrase family | ||
KKGFHILH_00874 | 5.1e-12 | S | haloacid dehalogenase-like hydrolase | |||
KKGFHILH_00875 | 7e-50 | |||||
KKGFHILH_00876 | 1.9e-37 | |||||
KKGFHILH_00877 | 1.2e-63 | S | Alpha beta hydrolase | |||
KKGFHILH_00878 | 3.7e-19 | S | Alpha beta hydrolase | |||
KKGFHILH_00879 | 0.0 | pepX | 3.4.14.11 | E | Removes N-terminal dipeptides sequentially from polypeptides having unsubstituted N-termini provided that the penultimate residue is proline | |
KKGFHILH_00880 | 2.8e-81 | msrB | 1.8.4.11, 1.8.4.12 | O | peptide methionine sulfoxide reductase | |
KKGFHILH_00881 | 7.1e-46 | |||||
KKGFHILH_00882 | 3.1e-148 | glcU | U | sugar transport | ||
KKGFHILH_00883 | 3.7e-250 | lctP | C | L-lactate permease | ||
KKGFHILH_00884 | 0.0 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
KKGFHILH_00885 | 6.4e-212 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
KKGFHILH_00886 | 8.8e-245 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
KKGFHILH_00887 | 3.6e-182 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
KKGFHILH_00888 | 7.2e-95 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
KKGFHILH_00889 | 9.1e-167 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
KKGFHILH_00890 | 1.6e-126 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
KKGFHILH_00891 | 1.9e-118 | pyrE | 2.4.2.10, 4.1.1.23 | F | Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) | |
KKGFHILH_00892 | 1.5e-102 | GM | NmrA-like family | |||
KKGFHILH_00893 | 4.2e-63 | lmrB | EGP | Major facilitator Superfamily | ||
KKGFHILH_00894 | 2.9e-122 | rbtT | P | Major Facilitator Superfamily | ||
KKGFHILH_00895 | 2.7e-202 | XK27_00915 | C | Luciferase-like monooxygenase | ||
KKGFHILH_00896 | 2.5e-86 | K | GNAT family | |||
KKGFHILH_00897 | 1.4e-124 | S | Glucose-6-phosphate 1-dehydrogenase (EC 1.1.1.49) | |||
KKGFHILH_00899 | 4.3e-36 | |||||
KKGFHILH_00900 | 6.2e-288 | P | ABC transporter | |||
KKGFHILH_00901 | 2.3e-07 | V | ABC-type multidrug transport system, ATPase and permease components | |||
KKGFHILH_00902 | 3.6e-88 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
KKGFHILH_00903 | 7.7e-10 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
KKGFHILH_00904 | 2.9e-109 | nanE | 5.1.3.9 | G | Converts N-acetylmannosamine-6-phosphate (ManNAc-6-P) to N-acetylglucosamine-6-phosphate (GlcNAc-6-P) | |
KKGFHILH_00905 | 1.7e-36 | axe1 | 3.1.1.41 | Q | Acetyl xylan esterase (AXE1) | |
KKGFHILH_00906 | 1.1e-59 | axe1 | 3.1.1.41 | Q | Acetyl xylan esterase (AXE1) | |
KKGFHILH_00907 | 1e-220 | nanT | E | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
KKGFHILH_00908 | 1.9e-121 | napA | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
KKGFHILH_00909 | 2.3e-56 | G | Xylose isomerase domain protein TIM barrel | |||
KKGFHILH_00910 | 8.4e-90 | nanK | GK | ROK family | ||
KKGFHILH_00911 | 2.9e-122 | nanA | 4.1.3.3, 4.3.3.7 | EM | Neu5Ac) to form pyruvate and N-acetylmannosamine (ManNAc) via a Schiff base intermediate | |
KKGFHILH_00912 | 3.7e-66 | K | Helix-turn-helix domain, rpiR family | |||
KKGFHILH_00913 | 7.1e-263 | E | ABC transporter, substratebinding protein | |||
KKGFHILH_00914 | 9.1e-10 | K | peptidyl-tyrosine sulfation | |||
KKGFHILH_00916 | 4.5e-131 | S | interspecies interaction between organisms | |||
KKGFHILH_00917 | 1.9e-11 | |||||
KKGFHILH_00920 | 1.9e-21 | |||||
KKGFHILH_00921 | 6e-148 | |||||
KKGFHILH_00922 | 6.7e-170 | |||||
KKGFHILH_00923 | 2e-263 | glnA | 6.3.1.2 | E | glutamine synthetase | |
KKGFHILH_00924 | 7.6e-225 | ynbB | 4.4.1.1 | P | aluminum resistance | |
KKGFHILH_00925 | 1.5e-167 | miaA | 2.5.1.75 | F | Catalyzes the transfer of a dimethylallyl group onto the adenine at position 37 in tRNAs that read codons beginning with uridine, leading to the formation of N6-(dimethylallyl)adenosine (i(6)A) | |
KKGFHILH_00926 | 1.5e-65 | yqhL | P | Rhodanese-like protein | ||
KKGFHILH_00927 | 9.7e-36 | yqgQ | S | Bacterial protein of unknown function (DUF910) | ||
KKGFHILH_00928 | 4e-119 | gluP | 3.4.21.105 | S | Rhomboid family | |
KKGFHILH_00929 | 2.7e-97 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
KKGFHILH_00930 | 1.2e-20 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
KKGFHILH_00931 | 0.0 | pbp2b | 3.4.16.4 | M | Penicillin-binding Protein | |
KKGFHILH_00932 | 0.0 | S | membrane | |||
KKGFHILH_00933 | 5.2e-170 | 2.7.1.59 | G | BadF/BadG/BcrA/BcrD ATPase family | ||
KKGFHILH_00934 | 1.3e-38 | S | RelB antitoxin | |||
KKGFHILH_00935 | 3.4e-51 | S | Bacterial toxin of type II toxin-antitoxin system, YafQ | |||
KKGFHILH_00936 | 6.7e-44 | hup | L | Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions | ||
KKGFHILH_00937 | 6.7e-139 | fhuC | 3.6.3.34 | HP | abc transporter atp-binding protein | |
KKGFHILH_00938 | 9.5e-148 | isdF | U | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
KKGFHILH_00939 | 8.7e-159 | isdE | P | Periplasmic binding protein | ||
KKGFHILH_00940 | 6.3e-123 | M | Iron Transport-associated domain | |||
KKGFHILH_00941 | 3e-09 | isdH | M | Iron Transport-associated domain | ||
KKGFHILH_00942 | 2.2e-89 | |||||
KKGFHILH_00943 | 3.7e-243 | lctO | C | L-lactate dehydrogenase (FMN-dependent) and related alpha-hydroxy acid dehydrogenases | ||
KKGFHILH_00944 | 5e-48 | dapE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
KKGFHILH_00945 | 6.9e-116 | dapE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
KKGFHILH_00946 | 9.7e-52 | S | Iron-sulfur cluster assembly protein | |||
KKGFHILH_00947 | 3.8e-154 | sdaAA | 4.3.1.17 | E | L-serine dehydratase, iron-sulfur-dependent, alpha subunit | |
KKGFHILH_00948 | 1.3e-122 | sdaAB | 4.3.1.17 | E | Serine dehydratase beta chain | |
KKGFHILH_00949 | 1.6e-295 | 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 | ||
KKGFHILH_00950 | 5.4e-203 | xerS | L | Belongs to the 'phage' integrase family | ||
KKGFHILH_00951 | 4.1e-67 | |||||
KKGFHILH_00952 | 8e-111 | XK27_00160 | S | Domain of unknown function (DUF5052) | ||
KKGFHILH_00953 | 5.8e-211 | M | Glycosyl hydrolases family 25 | |||
KKGFHILH_00954 | 4.9e-111 | ybbL | S | ABC transporter, ATP-binding protein | ||
KKGFHILH_00955 | 2.5e-130 | ybbM | S | Uncharacterised protein family (UPF0014) | ||
KKGFHILH_00956 | 2.5e-191 | yrvN | L | AAA C-terminal domain | ||
KKGFHILH_00957 | 5.7e-65 | spxA_2 | 1.20.4.1 | K | Interferes with activator-stimulated transcription by interaction with the RNA polymerase alpha-CTD. May function to globally reduce transcription of genes involved in growth- and development-promoting processes and to increase transcription of genes involved in thiol homeostasis, during periods of extreme stress | |
KKGFHILH_00958 | 6.8e-153 | treB | G | phosphotransferase system | ||
KKGFHILH_00959 | 4.5e-111 | treB | G | phosphotransferase system | ||
KKGFHILH_00960 | 1.2e-100 | treR | K | UTRA | ||
KKGFHILH_00961 | 1e-288 | treC | 3.2.1.93 | GH13 | G | Alpha amylase, catalytic domain protein |
KKGFHILH_00962 | 5.7e-18 | |||||
KKGFHILH_00963 | 1.5e-239 | G | Bacterial extracellular solute-binding protein | |||
KKGFHILH_00964 | 1e-60 | pdxH | S | Pyridoxamine 5'-phosphate oxidase | ||
KKGFHILH_00965 | 1.1e-236 | XK27_01810 | S | Calcineurin-like phosphoesterase | ||
KKGFHILH_00967 | 0.0 | S | SLAP domain | |||
KKGFHILH_00968 | 0.0 | hsdR | 3.1.21.3 | L | DEAD/DEAH box helicase | |
KKGFHILH_00969 | 1.2e-164 | S | AAA domain, putative AbiEii toxin, Type IV TA system | |||
KKGFHILH_00970 | 3.4e-42 | S | RloB-like protein | |||
KKGFHILH_00971 | 1.9e-259 | hsdM | 2.1.1.72 | V | type I restriction-modification system | |
KKGFHILH_00972 | 2.3e-51 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | ||
KKGFHILH_00973 | 8.3e-45 | hsdS | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | |
KKGFHILH_00974 | 1.2e-63 | S | SIR2-like domain | |||
KKGFHILH_00975 | 3.2e-10 | S | Domain of unknown function DUF87 | |||
KKGFHILH_00976 | 8.5e-279 | 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 | ||
KKGFHILH_00977 | 1e-30 | S | cog cog1373 | |||
KKGFHILH_00978 | 7.6e-91 | F | Nucleoside 2-deoxyribosyltransferase | |||
KKGFHILH_00979 | 3.3e-261 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Belongs to the aldehyde dehydrogenase family | |
KKGFHILH_00980 | 2.7e-83 | S | Protein of unknown function (DUF1211) | |||
KKGFHILH_00981 | 3.1e-113 | ltrA | S | Bacterial low temperature requirement A protein (LtrA) | ||
KKGFHILH_00982 | 2.8e-119 | 3.6.1.55 | F | NUDIX domain | ||
KKGFHILH_00983 | 3.9e-246 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
KKGFHILH_00984 | 0.0 | L | Plasmid pRiA4b ORF-3-like protein |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)