| ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
|---|---|---|---|---|---|---|
| AAONGNKJ_00001 | 1.7e-75 | pepT | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
| AAONGNKJ_00002 | 5.1e-71 | alkD | L | DNA alkylation repair enzyme | ||
| AAONGNKJ_00003 | 6.4e-136 | EG | EamA-like transporter family | |||
| AAONGNKJ_00004 | 1.1e-149 | S | Tetratricopeptide repeat protein | |||
| AAONGNKJ_00005 | 5.3e-205 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
| AAONGNKJ_00006 | 2.5e-298 | 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) | |
| AAONGNKJ_00007 | 2.7e-126 | corA | P | CorA-like Mg2+ transporter protein | ||
| AAONGNKJ_00008 | 7.2e-160 | nhaC | C | Na H antiporter NhaC | ||
| AAONGNKJ_00009 | 7.2e-130 | dapF | 5.1.1.7 | E | Catalyzes the stereoinversion of LL-2,6- diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso- DAP), a precursor of L-lysine and an essential component of the bacterial peptidoglycan | |
| AAONGNKJ_00010 | 2.6e-81 | nudF | 3.6.1.13 | L | ADP-ribose pyrophosphatase | |
| AAONGNKJ_00012 | 3.2e-92 | 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 | |
| AAONGNKJ_00013 | 2.6e-155 | iscS | 2.8.1.7 | E | Aminotransferase class V | |
| AAONGNKJ_00014 | 3.7e-41 | XK27_04120 | S | Putative amino acid metabolism | ||
| AAONGNKJ_00015 | 4.3e-203 | 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 | |
| AAONGNKJ_00016 | 0.0 | clpB | O | Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE | ||
| AAONGNKJ_00017 | 4.3e-15 | S | Protein of unknown function (DUF2929) | |||
| AAONGNKJ_00018 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase | |
| AAONGNKJ_00019 | 1.5e-167 | pfkA | 2.7.1.11 | F | Catalyzes the phosphorylation of D-fructose 6-phosphate to fructose 1,6-bisphosphate by ATP, the first committing step of glycolysis | |
| AAONGNKJ_00020 | 6.3e-310 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
| AAONGNKJ_00022 | 1e-39 | ypaA | S | Protein of unknown function (DUF1304) | ||
| AAONGNKJ_00023 | 4.2e-83 | 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 | |
| AAONGNKJ_00024 | 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 | |
| AAONGNKJ_00025 | 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 | |
| AAONGNKJ_00026 | 2.9e-203 | FbpA | K | Fibronectin-binding protein | ||
| AAONGNKJ_00027 | 3e-37 | K | Transcriptional regulator | |||
| AAONGNKJ_00028 | 1.8e-116 | degV | S | EDD domain protein, DegV family | ||
| AAONGNKJ_00029 | 3e-70 | lepB | 3.4.21.89 | U | Signal peptidase, peptidase S26 | |
| AAONGNKJ_00030 | 1.2e-39 | 6.3.3.2 | S | ASCH | ||
| AAONGNKJ_00031 | 5.7e-188 | glyA | 2.1.2.1 | E | Catalyzes the reversible interconversion of serine and glycine with tetrahydrofolate (THF) serving as the one-carbon carrier. This reaction serves as the major source of one-carbon groups required for the biosynthesis of purines, thymidylate, methionine, and other important biomolecules. Also exhibits THF- independent aldolase activity toward beta-hydroxyamino acids, producing glycine and aldehydes, via a retro-aldol mechanism | |
| AAONGNKJ_00032 | 5.9e-80 | yjjH | S | Calcineurin-like phosphoesterase | ||
| AAONGNKJ_00033 | 1.4e-95 | EG | EamA-like transporter family | |||
| AAONGNKJ_00034 | 2.1e-83 | natB | CP | ABC-type Na efflux pump, permease component | ||
| AAONGNKJ_00035 | 2.4e-111 | natA | S | Domain of unknown function (DUF4162) | ||
| AAONGNKJ_00036 | 6.6e-92 | L | Transposase, IS605 OrfB family | |||
| AAONGNKJ_00037 | 1.4e-40 | tlpA2 | L | Transposase IS200 like | ||
| AAONGNKJ_00038 | 3.1e-22 | K | Acetyltransferase (GNAT) domain | |||
| AAONGNKJ_00040 | 8.5e-36 | hup | L | Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions | ||
| AAONGNKJ_00041 | 7.7e-228 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
| AAONGNKJ_00042 | 4.6e-171 | rpsA | 1.17.7.4 | J | Ribosomal protein S1 | |
| AAONGNKJ_00043 | 2e-57 | arsC | 1.20.4.1 | T | Low molecular weight phosphatase family | |
| AAONGNKJ_00044 | 5.7e-151 | dltD | M | Protein involved in D-alanine esterification of lipoteichoic acid and wall teichoic acid (D-alanine transfer protein) | ||
| AAONGNKJ_00045 | 4.9e-29 | dltC | 6.1.1.13 | J | Carrier protein involved in the D-alanylation of lipoteichoic acid (LTA). The loading of thioester-linked D-alanine onto DltC is catalyzed by D-alanine--D-alanyl carrier protein ligase DltA. The DltC-carried D-alanyl group is further transferred to cell membrane phosphatidylglycerol (PG) by forming an ester bond, probably catalyzed by DltD. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
| AAONGNKJ_00046 | 3.1e-175 | dltB | M | MBOAT, membrane-bound O-acyltransferase family | ||
| AAONGNKJ_00047 | 9e-220 | dltA | 6.1.1.13 | H | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
| AAONGNKJ_00048 | 2.6e-07 | dltX | S | D-Ala-teichoic acid biosynthesis protein | ||
| AAONGNKJ_00049 | 1.5e-90 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
| AAONGNKJ_00050 | 3.5e-155 | 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 | ||
| AAONGNKJ_00051 | 1.1e-29 | dgkA | 2.7.1.107, 2.7.1.66 | M | Diacylglycerol kinase | |
| AAONGNKJ_00052 | 8.6e-60 | 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 | |
| AAONGNKJ_00053 | 4.6e-153 | phoH | T | phosphate starvation-inducible protein PhoH | ||
| AAONGNKJ_00054 | 4.4e-83 | lytH | 3.5.1.28 | M | Ami_3 | |
| AAONGNKJ_00055 | 2.6e-86 | 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 | |
| AAONGNKJ_00056 | 7.7e-12 | M | Lysin motif | |||
| AAONGNKJ_00057 | 6.5e-127 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
| AAONGNKJ_00058 | 9.9e-61 | ypbB | 5.1.3.1 | S | Helix-turn-helix domain | |
| AAONGNKJ_00059 | 6.4e-221 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
| AAONGNKJ_00060 | 1.3e-186 | 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 | ||
| AAONGNKJ_00061 | 1.7e-212 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
| AAONGNKJ_00062 | 7.3e-281 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
| AAONGNKJ_00063 | 3.7e-168 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
| AAONGNKJ_00064 | 2.6e-110 | pepE | 3.4.13.21 | E | Alpha/beta hydrolase of unknown function (DUF915) | |
| AAONGNKJ_00065 | 2e-69 | pts13C | 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 | ||
| AAONGNKJ_00066 | 1.6e-93 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | ||
| AAONGNKJ_00067 | 2.8e-131 | L | Belongs to the 'phage' integrase family | |||
| AAONGNKJ_00068 | 3.7e-64 | hsdS | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | |
| AAONGNKJ_00069 | 1e-210 | hsdM | 2.1.1.72 | V | type I restriction-modification system | |
| AAONGNKJ_00070 | 0.0 | hsdR | 3.1.21.3 | V | Subunit R is required for both nuclease and ATPase activities, but not for modification | |
| AAONGNKJ_00072 | 8.7e-81 | XK27_07525 | 3.6.1.55 | F | Hydrolase, nudix family | |
| AAONGNKJ_00073 | 2.8e-56 | 3.6.1.27 | I | Acid phosphatase homologues | ||
| AAONGNKJ_00074 | 1.8e-68 | maa | 2.3.1.79 | S | Maltose acetyltransferase | |
| AAONGNKJ_00075 | 5.2e-75 | 2.3.1.178 | M | GNAT acetyltransferase | ||
| AAONGNKJ_00077 | 1.1e-197 | ade | 3.5.4.2 | F | Adenine deaminase C-terminal domain | |
| AAONGNKJ_00078 | 7.8e-65 | ypsA | S | Belongs to the UPF0398 family | ||
| AAONGNKJ_00079 | 3.1e-187 | nhaC | C | Na H antiporter NhaC | ||
| AAONGNKJ_00080 | 2.3e-76 | 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 | ||
| AAONGNKJ_00081 | 2.1e-292 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
| AAONGNKJ_00082 | 9.6e-98 | tnp2 | L | Transposase | ||
| AAONGNKJ_00083 | 9.4e-113 | xerD | D | recombinase XerD | ||
| AAONGNKJ_00084 | 9.6e-126 | cvfB | S | S1 domain | ||
| AAONGNKJ_00085 | 5.4e-51 | yeaL | S | Protein of unknown function (DUF441) | ||
| AAONGNKJ_00086 | 3.5e-58 | 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 | |||
| AAONGNKJ_00087 | 3.4e-100 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
| AAONGNKJ_00088 | 1.1e-56 | 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 | ||
| AAONGNKJ_00089 | 1.2e-58 | 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 | ||
| AAONGNKJ_00090 | 4.6e-37 | ribT | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
| AAONGNKJ_00091 | 7.8e-218 | 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 | ||
| AAONGNKJ_00092 | 7e-79 | hslV | 3.4.25.2 | O | Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery | |
| AAONGNKJ_00093 | 6e-123 | xerC | D | Belongs to the 'phage' integrase family. XerC subfamily | ||
| AAONGNKJ_00094 | 1.3e-178 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
| AAONGNKJ_00095 | 5.9e-100 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic domain | |
| AAONGNKJ_00097 | 1.6e-42 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
| AAONGNKJ_00098 | 3.8e-27 | ysxB | J | Cysteine protease Prp | ||
| AAONGNKJ_00099 | 8.3e-48 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
| AAONGNKJ_00102 | 1.2e-71 | S | RRXRR protein | |||
| AAONGNKJ_00105 | 2.2e-08 | S | Protein of unknown function (DUF2922) | |||
| AAONGNKJ_00107 | 7.5e-17 | K | DNA-templated transcription, initiation | |||
| AAONGNKJ_00109 | 7.3e-66 | H | Methyltransferase domain | |||
| AAONGNKJ_00110 | 5.9e-76 | cps2D | 5.1.3.2 | M | RmlD substrate binding domain | |
| AAONGNKJ_00111 | 2.8e-40 | wecD | M | Acetyltransferase (GNAT) family | ||
| AAONGNKJ_00113 | 6.2e-26 | ybl78 | L | Conserved phage C-terminus (Phg_2220_C) |
Showing 1 to 100 of 1,560 entries
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)