| ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
|---|---|---|---|---|---|---|
| BBIHAHMK_00001 | 9.6e-38 | V | ATPases associated with a variety of cellular activities | |||
| BBIHAHMK_00003 | 2e-94 | 2.3.1.128, 5.2.1.8 | J | Acetyltransferase (GNAT) domain | ||
| BBIHAHMK_00004 | 1.8e-175 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
| BBIHAHMK_00005 | 0.0 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
| BBIHAHMK_00006 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
| BBIHAHMK_00007 | 1.3e-195 | 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 | ||
| BBIHAHMK_00008 | 1.7e-128 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
| BBIHAHMK_00009 | 1.8e-147 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
| BBIHAHMK_00010 | 2.8e-310 | V | ABC transporter transmembrane region | |||
| BBIHAHMK_00011 | 1e-271 | V | (ABC) transporter | |||
| BBIHAHMK_00012 | 7.3e-26 | dmpI | 5.3.2.6 | G | Belongs to the 4-oxalocrotonate tautomerase family | |
| BBIHAHMK_00013 | 2.8e-60 | yitW | S | Iron-sulfur cluster assembly protein | ||
| BBIHAHMK_00014 | 2e-140 | |||||
| BBIHAHMK_00015 | 4.7e-174 | |||||
| BBIHAHMK_00016 | 1.3e-262 | rsmF | 2.1.1.176, 2.1.1.178 | J | NOL1 NOP2 sun family protein | |
| BBIHAHMK_00017 | 3.6e-196 | 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) | |
| BBIHAHMK_00018 | 2.1e-177 | mvaD | 4.1.1.33 | I | diphosphomevalonate decarboxylase | |
| BBIHAHMK_00019 | 4.6e-166 | mvk | 1.1.1.88, 2.3.3.10, 2.7.1.36 | I | mevalonate kinase | |
| BBIHAHMK_00020 | 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 | |
| BBIHAHMK_00021 | 0.0 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
| BBIHAHMK_00022 | 0.0 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
| BBIHAHMK_00023 | 2.1e-85 | ypmB | S | Protein conserved in bacteria | ||
| BBIHAHMK_00024 | 2.4e-220 | aspB | 2.6.1.1, 2.6.1.14 | E | Aminotransferase | |
| BBIHAHMK_00025 | 1.2e-257 | asnS | 6.1.1.22 | J | Asparaginyl-tRNA synthetase | |
| BBIHAHMK_00026 | 2.4e-110 | dnaD | L | DnaD domain protein | ||
| BBIHAHMK_00027 | 2.4e-113 | 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 | |
| BBIHAHMK_00028 | 1.2e-85 | comEB | 3.5.4.12 | F | ComE operon protein 2 | |
| BBIHAHMK_00029 | 0.0 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
| BBIHAHMK_00030 | 1.5e-120 | 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 | ||
| BBIHAHMK_00031 | 1.9e-106 | ypsA | S | Belongs to the UPF0398 family | ||
| BBIHAHMK_00032 | 1.8e-66 | 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 | ||
| BBIHAHMK_00034 | 3.7e-218 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
| BBIHAHMK_00035 | 7.8e-174 | pdxB | 1.1.1.399, 1.1.1.95 | EH | D-isomer specific 2-hydroxyacid dehydrogenase, NAD binding domain | |
| BBIHAHMK_00036 | 1.9e-33 | |||||
| BBIHAHMK_00037 | 1.6e-193 | lplA | 6.3.1.20 | H | Lipoate-protein ligase | |
| BBIHAHMK_00038 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
| BBIHAHMK_00039 | 4.1e-164 | K | Transcriptional regulator | |||
| BBIHAHMK_00041 | 1.2e-188 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
| BBIHAHMK_00042 | 0.0 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
| BBIHAHMK_00043 | 4.5e-38 | nrdH | O | Glutaredoxin | ||
| BBIHAHMK_00044 | 1.6e-271 | K | Mga helix-turn-helix domain | |||
| BBIHAHMK_00046 | 9.7e-55 | |||||
| BBIHAHMK_00047 | 1.8e-281 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
| BBIHAHMK_00048 | 1.5e-109 | XK27_02070 | S | Nitroreductase family | ||
| BBIHAHMK_00049 | 1.1e-68 | rnhA | 3.1.26.4 | L | Ribonuclease HI | |
| BBIHAHMK_00050 | 2.4e-63 | S | Family of unknown function (DUF5322) | |||
| BBIHAHMK_00051 | 0.0 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
| BBIHAHMK_00052 | 9.2e-82 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
| BBIHAHMK_00053 | 5e-173 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
| BBIHAHMK_00054 | 1.7e-96 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
| BBIHAHMK_00055 | 2.6e-236 | pyrP | F | Permease | ||
| BBIHAHMK_00056 | 2.8e-179 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
| BBIHAHMK_00057 | 2.5e-239 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
| BBIHAHMK_00058 | 1e-209 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
| BBIHAHMK_00059 | 0.0 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
| BBIHAHMK_00060 | 2.1e-152 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
| BBIHAHMK_00061 | 8e-126 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
| BBIHAHMK_00062 | 2.9e-111 | 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) | |
| BBIHAHMK_00063 | 3.2e-193 | pfoS | S | Phosphotransferase system, EIIC | ||
| BBIHAHMK_00064 | 6.2e-51 | S | MazG-like family | |||
| BBIHAHMK_00065 | 0.0 | FbpA | K | Fibronectin-binding protein | ||
| BBIHAHMK_00066 | 8.1e-09 | |||||
| BBIHAHMK_00067 | 3.2e-161 | degV | S | EDD domain protein, DegV family | ||
| BBIHAHMK_00068 | 1.5e-100 | 3.6.1.13 | L | Belongs to the Nudix hydrolase family | ||
| BBIHAHMK_00069 | 2.2e-204 | hisC | 2.6.1.9 | E | Cys/Met metabolism PLP-dependent enzyme | |
| BBIHAHMK_00070 | 9.2e-217 | hisZ | 2.4.2.17, 6.1.1.21 | E | Required for the first step of histidine biosynthesis. May allow the feedback regulation of ATP phosphoribosyltransferase activity by histidine | |
| BBIHAHMK_00071 | 2.7e-109 | hisG | 2.4.2.17 | F | Catalyzes the condensation of ATP and 5-phosphoribose 1- diphosphate to form N'-(5'-phosphoribosyl)-ATP (PR-ATP). Has a crucial role in the pathway because the rate of histidine biosynthesis seems to be controlled primarily by regulation of HisG enzymatic activity | |
| BBIHAHMK_00072 | 3.5e-225 | hisD | 1.1.1.23, 1.1.1.308 | E | Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine | |
| BBIHAHMK_00073 | 2.4e-104 | hisB | 1.1.1.23, 2.6.1.9, 3.1.3.15, 4.2.1.19 | E | imidazoleglycerol-phosphate dehydratase | |
| BBIHAHMK_00074 | 1.5e-112 | hisH | E | IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisH subunit provides the glutamine amidotransferase activity that produces the ammonia necessary to HisF for the synthesis of IGP and AICAR | ||
| BBIHAHMK_00075 | 4.1e-133 | hisA | 5.3.1.16 | E | 1-(5-phosphoribosyl)-5- (5-phosphoribosylamino)methylideneamino imidazole-4-carboxamide isomerase | |
| BBIHAHMK_00076 | 3.2e-133 | hisF | 3.5.4.19, 3.6.1.31 | E | IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisF subunit catalyzes the cyclization activity that produces IGP and AICAR from PRFAR using the ammonia provided by the HisH subunit | |
| BBIHAHMK_00077 | 2.1e-57 | hisI | 3.5.4.19, 3.5.4.25, 3.6.1.31, 5.3.1.16 | E | Catalyzes the hydrolysis of the adenine ring of phosphoribosyl-AMP | |
| BBIHAHMK_00078 | 6e-52 | hisE | 3.5.4.19, 3.6.1.31, 5.3.1.16 | E | phosphoribosyl-ATP diphosphatase activity | |
| BBIHAHMK_00079 | 3.1e-206 | hisC | 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
| BBIHAHMK_00080 | 1.3e-145 | Q | Fumarylacetoacetate (FAA) hydrolase family | |||
| BBIHAHMK_00081 | 2.6e-112 | nfnB | 1.5.1.34 | C | Nitroreductase family | |
| BBIHAHMK_00082 | 5.9e-70 | K | Acetyltransferase (GNAT) domain | |||
| BBIHAHMK_00083 | 7.1e-68 | msi198 | K | Acetyltransferase (GNAT) domain | ||
| BBIHAHMK_00084 | 1.1e-217 | EGP | Transmembrane secretion effector | |||
| BBIHAHMK_00085 | 4.8e-128 | T | Transcriptional regulatory protein, C terminal | |||
| BBIHAHMK_00086 | 5.2e-173 | T | Histidine kinase-like ATPases | |||
| BBIHAHMK_00087 | 3.8e-134 | XK27_05695 | V | ABC transporter, ATP-binding protein | ||
| BBIHAHMK_00088 | 0.0 | ysaB | V | FtsX-like permease family | ||
| BBIHAHMK_00089 | 2.9e-207 | xerS | L | Belongs to the 'phage' integrase family | ||
| BBIHAHMK_00090 | 9.5e-172 | ppaC | 3.6.1.1 | C | inorganic pyrophosphatase | |
| BBIHAHMK_00091 | 1.8e-181 | K | LysR substrate binding domain | |||
| BBIHAHMK_00092 | 4.3e-171 | pflA | 1.97.1.4 | C | Activation of pyruvate formate-lyase under anaerobic conditions by generation of an organic free radical, using S- adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine | |
| BBIHAHMK_00093 | 0.0 | pflB | 2.3.1.54 | C | Pyruvate formate lyase-like | |
| BBIHAHMK_00094 | 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 | |
| BBIHAHMK_00095 | 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 | |
| BBIHAHMK_00096 | 4.5e-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 | |
| BBIHAHMK_00097 | 6.2e-173 | lacX | 5.1.3.3 | G | Aldose 1-epimerase | |
| BBIHAHMK_00098 | 5e-257 | 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 | ||
| BBIHAHMK_00099 | 5.5e-92 | hslV | 3.4.25.2 | O | Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery | |
| BBIHAHMK_00100 | 1.5e-166 | xerC | D | Belongs to the 'phage' integrase family. XerC subfamily | ||
| BBIHAHMK_00101 | 3e-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 | |
| BBIHAHMK_00102 | 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 | |
| BBIHAHMK_00103 | 1.4e-147 | dprA | LU | DNA protecting protein DprA | ||
| BBIHAHMK_00104 | 3.6e-137 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids |
Showing 1 to 100 of 2,588 entries
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)