| ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
|---|---|---|---|---|---|---|
| OEJBJGDD_00001 | 3.7e-41 | 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 | |
| OEJBJGDD_00002 | 4.9e-78 | 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 | |
| OEJBJGDD_00003 | 9.7e-109 | 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 | |
| OEJBJGDD_00004 | 6.6e-125 | 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 | ||
| OEJBJGDD_00005 | 9.2e-62 | 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 | |
| OEJBJGDD_00006 | 1.3e-64 | 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 | |
| OEJBJGDD_00007 | 1.4e-63 | 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 | |
| OEJBJGDD_00008 | 1.9e-38 | 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 | ||
| OEJBJGDD_00009 | 6.1e-09 | 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 | ||
| OEJBJGDD_00010 | 4.1e-20 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
| OEJBJGDD_00011 | 1.3e-11 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
| OEJBJGDD_00012 | 1.6e-26 | 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 | ||
| OEJBJGDD_00013 | 3.8e-65 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
| OEJBJGDD_00014 | 4.2e-26 | atpI | S | ATP synthase | ||
| OEJBJGDD_00015 | 2e-13 | atpI | S | ATP synthase | ||
| OEJBJGDD_00016 | 7.5e-70 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
| OEJBJGDD_00017 | 4.1e-24 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
| OEJBJGDD_00018 | 3.9e-162 | 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 | |
| OEJBJGDD_00019 | 3.9e-22 | 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 | |
| OEJBJGDD_00020 | 1e-96 | ywlG | S | Belongs to the UPF0340 family | ||
| OEJBJGDD_00021 | 6.3e-09 | rpiB | 5.3.1.6 | G | Ribose 5-phosphate isomerase | |
| OEJBJGDD_00022 | 1.3e-76 | ywlE | 3.1.3.48, 3.9.1.2, 5.3.1.6 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
| OEJBJGDD_00023 | 2e-38 | mntP | P | Probably functions as a manganese efflux pump | ||
| OEJBJGDD_00024 | 1.5e-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 | |
| OEJBJGDD_00025 | 1.1e-74 | ywlB | 1.20.4.1, 2.3.1.1 | E | Belongs to the acetyltransferase family. ArgA subfamily | |
| OEJBJGDD_00026 | 8.9e-119 | spoIIR | S | stage II sporulation protein R | ||
| OEJBJGDD_00027 | 1.4e-60 | ywlA | S | Uncharacterised protein family (UPF0715) | ||
| OEJBJGDD_00029 | 4.8e-154 | prmC | 2.1.1.297 | J | Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif | |
| OEJBJGDD_00030 | 1.9e-192 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
| OEJBJGDD_00031 | 2e-67 | yaeR | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | ||
| OEJBJGDD_00032 | 2.2e-94 | racA | K | Required for the formation of axial filaments and for anchoring the origin regions at the cell poles in sporulating cells, thus ensuring proper chromosome segregation in the prespore. Binds in a dispersed manner throughout the chromosome but preferentially to sites clustered in the origin portion of the chromosome, causing condensation of the chromosome and its remodeling into an elongated, anchored structure | ||
| OEJBJGDD_00033 | 6.8e-157 | ywkB | S | Membrane transport protein | ||
| OEJBJGDD_00034 | 0.0 | sfcA | 1.1.1.38 | C | malic enzyme | |
| OEJBJGDD_00035 | 2.5e-101 | tdk | 2.7.1.21 | F | thymidine kinase | |
| OEJBJGDD_00036 | 1.1e-32 | rpmE | J | Binds the 23S rRNA | ||
| OEJBJGDD_00037 | 4.3e-239 | rho | K | Facilitates transcription termination by a mechanism that involves Rho binding to the nascent RNA, activation of Rho's RNA-dependent ATPase activity, and release of the mRNA from the DNA template | ||
| OEJBJGDD_00038 | 5.6e-175 | glpX | 3.1.3.11, 3.1.3.37 | G | fructose-1,6-bisphosphatase | |
| OEJBJGDD_00039 | 2e-39 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
| OEJBJGDD_00040 | 1.5e-189 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
| OEJBJGDD_00041 | 1.9e-110 | tal | 2.2.1.2 | G | Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway | |
| OEJBJGDD_00042 | 5.5e-158 | fbaA | 4.1.2.13, 4.1.2.29 | G | Aldolase | |
| OEJBJGDD_00043 | 8.5e-63 | spo0F | T | COG0784 FOG CheY-like receiver | ||
| OEJBJGDD_00044 | 4.2e-92 | ywjG | S | Domain of unknown function (DUF2529) | ||
| OEJBJGDD_00045 | 0.0 | pyrG | 6.3.4.2 | F | Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen. Regulates intracellular CTP levels through interactions with the four ribonucleotide triphosphates | |
| OEJBJGDD_00046 | 2.4e-47 | rpoE | K | Participates in both the initiation and recycling phases of transcription. In the presence of the delta subunit, RNAP displays an increased specificity of transcription, a decreased affinity for nucleic acids, and an increased efficiency of RNA synthesis because of enhanced recycling | ||
| OEJBJGDD_00047 | 0.0 | fadF | C | COG0247 Fe-S oxidoreductase | ||
| OEJBJGDD_00048 | 2.3e-218 | clsB | I | Belongs to the phospholipase D family. Cardiolipin synthase subfamily | ||
| OEJBJGDD_00049 | 2.2e-179 | uvsE | L | Component in a DNA repair pathway. Removal of UV-light damaged nucleotides. Recognizes pyrimidine dimers and cleave a phosphodiester bond immediately 5' to the lesion | ||
| OEJBJGDD_00050 | 4.2e-43 | ywjC | ||||
| OEJBJGDD_00051 | 1.6e-288 | ywjA | V | ABC transporter | ||
| OEJBJGDD_00052 | 7.7e-18 | ywjA | V | ABC transporter | ||
| OEJBJGDD_00053 | 1.6e-296 | ywiE | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
| OEJBJGDD_00054 | 3.4e-104 | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | |||
| OEJBJGDD_00055 | 2.1e-120 | narI | 1.7.5.1 | C | nitrate reductase, gamma | |
| OEJBJGDD_00056 | 1.7e-91 | narJ | 1.7.5.1 | C | nitrate reductase | |
| OEJBJGDD_00057 | 3.7e-295 | narH | 1.7.5.1 | C | Nitrate reductase, beta | |
| OEJBJGDD_00058 | 0.0 | narG | 1.7.5.1 | C | Belongs to the prokaryotic molybdopterin-containing oxidoreductase family | |
| OEJBJGDD_00059 | 1.7e-84 | arfM | T | cyclic nucleotide binding | ||
| OEJBJGDD_00060 | 2.8e-139 | ywiC | S | YwiC-like protein | ||
| OEJBJGDD_00061 | 8.5e-128 | fnr | K | helix_turn_helix, cAMP Regulatory protein | ||
| OEJBJGDD_00062 | 5.4e-212 | narK | P | COG2223 Nitrate nitrite transporter | ||
| OEJBJGDD_00063 | 0.0 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
| OEJBJGDD_00064 | 2.9e-43 | ywiB | S | protein conserved in bacteria | ||
| OEJBJGDD_00065 | 4.7e-72 | S | aspartate phosphatase | |||
| OEJBJGDD_00067 | 9.7e-29 | ydcG | K | sequence-specific DNA binding | ||
| OEJBJGDD_00068 | 1.6e-31 | |||||
| OEJBJGDD_00070 | 1.3e-74 | CP | Membrane | |||
| OEJBJGDD_00073 | 7.8e-168 | speB | 3.5.3.11 | E | Belongs to the arginase family | |
| OEJBJGDD_00074 | 4.1e-158 | speE | 2.5.1.16 | E | Catalyzes the irreversible transfer of a propylamine group from the amino donor S-adenosylmethioninamine (decarboxy- AdoMet) to putrescine (1,4-diaminobutane) to yield spermidine | |
| OEJBJGDD_00075 | 0.0 | pbpG | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
| OEJBJGDD_00076 | 1.8e-80 | |||||
| OEJBJGDD_00077 | 1.9e-92 | ywhD | S | YwhD family | ||
| OEJBJGDD_00078 | 1.2e-117 | ywhC | S | Peptidase family M50 | ||
| OEJBJGDD_00079 | 1.3e-24 | dmpI | 5.3.2.6 | G | 4-oxalocrotonate tautomerase | |
| OEJBJGDD_00080 | 4.9e-67 | ywhA | K | Transcriptional regulator | ||
| OEJBJGDD_00081 | 5.8e-75 | yhdG_1 | E | C-terminus of AA_permease | ||
| OEJBJGDD_00082 | 1.2e-144 | yhdG_1 | E | C-terminus of AA_permease | ||
| OEJBJGDD_00083 | 4.6e-88 | ywgA | 2.1.1.72, 3.1.21.3 | |||
| OEJBJGDD_00084 | 3e-256 | ywfO | S | COG1078 HD superfamily phosphohydrolases | ||
| OEJBJGDD_00085 | 6.9e-36 | ywzC | S | Belongs to the UPF0741 family | ||
| OEJBJGDD_00086 | 6.6e-110 | rsfA_1 | ||||
| OEJBJGDD_00087 | 9.7e-52 | padR | K | PadR family transcriptional regulator | ||
| OEJBJGDD_00088 | 3.4e-92 | S | membrane | |||
| OEJBJGDD_00089 | 2.1e-163 | V | ABC transporter, ATP-binding protein | |||
| OEJBJGDD_00090 | 7.2e-167 | yhcI | S | ABC transporter (permease) | ||
| OEJBJGDD_00093 | 4.5e-174 | |||||
| OEJBJGDD_00095 | 1.2e-155 | lipL | 2.3.1.200, 2.3.1.204 | H | Catalyzes the amidotransfer (transamidation) of the octanoyl moiety from octanoyl-GcvH to the lipoyl domain of the E2 subunit of lipoate-dependent enzymes | |
| OEJBJGDD_00096 | 1.8e-122 | cysL | K | Transcriptional regulator | ||
| OEJBJGDD_00097 | 6.2e-158 | MA20_14895 | S | Conserved hypothetical protein 698 | ||
| OEJBJGDD_00098 | 5.1e-176 | pta | 2.3.1.19, 2.3.1.8, 3.6.3.21 | C | In Salmonella this enzyme is required for ethanolamine catabolism | |
| OEJBJGDD_00099 | 1.1e-146 | ywfI | C | May function as heme-dependent peroxidase | ||
| OEJBJGDD_00100 | 1.1e-139 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
| OEJBJGDD_00101 | 8.6e-234 | ywfG | 2.6.1.83 | E | Aminotransferase class I and II | |
| OEJBJGDD_00102 | 1e-207 | bacE | EGP | Major facilitator Superfamily | ||
| OEJBJGDD_00103 | 2.4e-267 | purD | 6.3.2.49, 6.3.4.13 | F | Part of the bacABCDEFG operon responsible for the biosynthesis of bacilysin, an irreversible inactivator of the glutaminase domain of glucosamine synthetase. Catalyzes the formation of alpha-dipeptides from various L-amino acids in the presence of ATP. In vivo catalyzes the ligation of L-alanine and L-anticapsin (epoxycyclohexanonyl-Ala) to produce the final bacilysin antibiotic (L-Ala-L-4S-cyclohexenonyl-Ala dipeptide) | |
| OEJBJGDD_00104 | 8.7e-139 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
| OEJBJGDD_00105 | 7.6e-137 | bacB | 5.3.3.19, 5.4.99.5 | S | Part of the bacABCDEF operon responsible for the biosynthesis of the nonribosomally synthesized dipeptide antibiotic bacilysin, composed of L-alanine and L-anticapsin. Bacilysin is an irreversible inactivator of the glutaminase domain of glucosamine synthetase. BacB catalyzes the allylic isomerization of the | |
| OEJBJGDD_00106 | 3.9e-113 | pheA | 1.1.1.3, 1.3.1.12, 4.1.1.100, 4.2.1.51, 5.4.99.5 | E | Part of the bacABCDEF operon responsible for the biosynthesis of the nonribosomally synthesized dipeptide antibiotic bacilysin, composed of L-alanine and L-anticapsin. Bacilysin is an irreversible inactivator of the glutaminase domain of glucosamine synthetase. BacA is an unusual prephenate decarboxylase that avoids the typical aromatization of the cyclohexadienol ring of prephenate. BacA catalyzes the protonation of prephenate (1-carboxy-4-hydroxy-alpha-oxo-2,5-cyclohexadiene-1- propanoic acid) at C6 position, followed by a decarboxylation to produce the endocyclic-delta(4),delta(8)-7R-dihydro- hydroxyphenylpyruvate (en-H2HPP). En-H2HPP is able to undergo a slow nonenzymatic isomerization to produce the exocyclic- delta(3),delta(5)-dihydro-hydroxyphenylpyruvate (ex-H2HPP). BacA isomerizes only the pro-R double bond in prephenate | |
| OEJBJGDD_00107 | 3.5e-222 | ywfA | EGP | Major facilitator Superfamily | ||
| OEJBJGDD_00108 | 2.5e-204 | tcaB | EGP | Major facilitator Superfamily |
Showing 1 to 100 of 3,749 entries
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)