| ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
|---|---|---|---|---|---|---|
| PEFLCPBG_00001 | 9.8e-73 | S | SnoaL-like polyketide cyclase | |||
| PEFLCPBG_00004 | 0.0 | uvrA3 | 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 | ||
| PEFLCPBG_00005 | 1.1e-166 | ybaJ | Q | ubiE/COQ5 methyltransferase family | ||
| PEFLCPBG_00006 | 1.1e-125 | |||||
| PEFLCPBG_00007 | 5.8e-106 | XK27_04590 | S | NADPH-dependent FMN reductase | ||
| PEFLCPBG_00008 | 7.4e-101 | |||||
| PEFLCPBG_00009 | 5.6e-20 | |||||
| PEFLCPBG_00010 | 7.5e-58 | K | Acetyltransferase (GNAT) domain | |||
| PEFLCPBG_00011 | 2.8e-25 | |||||
| PEFLCPBG_00012 | 8.3e-59 | S | T5orf172 | |||
| PEFLCPBG_00013 | 0.0 | L | Restriction endonuclease | |||
| PEFLCPBG_00014 | 5.6e-26 | exoX | 2.7.7.7, 3.6.4.12 | L | EXOIII | |
| PEFLCPBG_00015 | 0.0 | 3.6.4.12 | L | Protein conserved in bacteria | ||
| PEFLCPBG_00018 | 4.5e-94 | paiA | 2.3.1.57 | K | Acetyltransferase (GNAT) domain | |
| PEFLCPBG_00019 | 1.4e-23 | |||||
| PEFLCPBG_00025 | 2.3e-158 | S | PAC2 family | |||
| PEFLCPBG_00026 | 2.6e-150 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
| PEFLCPBG_00027 | 4.2e-160 | G | Fructosamine kinase | |||
| PEFLCPBG_00028 | 2.8e-218 | 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 | ||
| PEFLCPBG_00029 | 6.8e-201 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
| PEFLCPBG_00030 | 0.0 | tkt | 2.2.1.1 | H | Belongs to the transketolase family | |
| PEFLCPBG_00031 | 1.4e-201 | tal | 2.2.1.2 | H | Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway | |
| PEFLCPBG_00032 | 1.5e-62 | S | PFAM Pentapeptide repeats (8 copies) | |||
| PEFLCPBG_00033 | 5.8e-230 | yugH | 2.6.1.1 | E | Aminotransferase class I and II | |
| PEFLCPBG_00034 | 1e-90 | alaR | K | helix_turn_helix ASNC type | ||
| PEFLCPBG_00035 | 4.1e-306 | alaA | 2.6.1.2, 2.6.1.66 | E | Aminotransferase, class I II | |
| PEFLCPBG_00036 | 1.1e-160 | S | Sucrose-6F-phosphate phosphohydrolase | |||
| PEFLCPBG_00037 | 4.7e-25 | secG | U | Preprotein translocase SecG subunit | ||
| PEFLCPBG_00038 | 9.5e-152 | tpiA | 2.7.2.3, 5.3.1.1 | G | Involved in the gluconeogenesis. Catalyzes stereospecifically the conversion of dihydroxyacetone phosphate (DHAP) to D-glyceraldehyde-3-phosphate (G3P) | |
| PEFLCPBG_00039 | 3.1e-223 | pgk | 2.7.2.3, 5.3.1.1 | F | Phosphoglycerate kinase | |
| PEFLCPBG_00040 | 1.2e-174 | whiA | K | May be required for sporulation | ||
| PEFLCPBG_00041 | 3e-173 | rapZ | S | Displays ATPase and GTPase activities | ||
| PEFLCPBG_00042 | 9.8e-177 | aroE | 1.1.1.25 | E | Shikimate dehydrogenase substrate binding domain | |
| PEFLCPBG_00043 | 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 | ||
| PEFLCPBG_00044 | 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 | ||
| PEFLCPBG_00045 | 7e-32 | 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 | ||
| PEFLCPBG_00046 | 2.9e-179 | wcoO | ||||
| PEFLCPBG_00047 | 2.1e-99 | mug | 3.2.2.28 | L | Uracil DNA glycosylase superfamily | |
| PEFLCPBG_00048 | 6.1e-122 | S | Phospholipase/Carboxylesterase | |||
| PEFLCPBG_00049 | 4.1e-300 | ybiT | S | ABC transporter | ||
| PEFLCPBG_00050 | 1.9e-195 | cat | P | Cation efflux family | ||
| PEFLCPBG_00051 | 6.3e-145 | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | ||
| PEFLCPBG_00052 | 1.4e-183 | cbh | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
| PEFLCPBG_00053 | 0.0 | nnrD | 4.2.1.136, 5.1.99.6 | H | Catalyzes the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. Together with NAD(P)HX epimerase, which catalyzes the epimerization of the S- and R-forms, the enzyme allows the repair of both epimers of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration | |
| PEFLCPBG_00054 | 2e-108 | ahpC | 1.11.1.15 | O | C-terminal domain of 1-Cys peroxiredoxin | |
| PEFLCPBG_00055 | 0.0 | trxB1 | 1.8.1.9 | C | Thioredoxin domain | |
| PEFLCPBG_00056 | 5e-173 | cpsY | K | Bacterial regulatory helix-turn-helix protein, lysR family | ||
| PEFLCPBG_00057 | 1.1e-123 | 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | ||
| PEFLCPBG_00058 | 1.2e-188 | gmk | 1.1.1.23, 2.7.4.8 | S | Protein conserved in bacteria | |
| PEFLCPBG_00059 | 1.2e-182 | draG | O | ADP-ribosylglycohydrolase | ||
| PEFLCPBG_00060 | 2.6e-58 | ytfH | K | HxlR-like helix-turn-helix | ||
| PEFLCPBG_00061 | 2.8e-51 | 3.6.1.55 | L | NUDIX domain | ||
| PEFLCPBG_00062 | 8.9e-80 | 2.3.1.1 | K | Psort location Cytoplasmic, score 8.87 | ||
| PEFLCPBG_00063 | 3.6e-123 | pyrE | 2.4.2.10 | F | Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) | |
| PEFLCPBG_00064 | 7.7e-188 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
| PEFLCPBG_00065 | 3.5e-157 | pyrK | 1.18.1.2, 1.19.1.1, 1.4.1.13, 1.4.1.14 | C | Iron-sulfur cluster binding domain of dihydroorotate dehydrogenase B | |
| PEFLCPBG_00066 | 4.5e-177 | pyrF | 2.4.2.10, 4.1.1.23 | F | Belongs to the OMP decarboxylase family. Type 2 subfamily | |
| PEFLCPBG_00067 | 3.8e-281 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
| PEFLCPBG_00068 | 2e-73 | pyrI | 2.1.3.2 | F | Aspartate carbamoyltransferase regulatory chain, allosteric domain protein | |
| PEFLCPBG_00069 | 1.6e-177 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
| PEFLCPBG_00070 | 2e-88 | yneG | S | Domain of unknown function (DUF4186) | ||
| PEFLCPBG_00071 | 0.0 | glnE | 2.7.7.42, 2.7.7.89 | H | Involved in the regulation of glutamine synthetase GlnA, a key enzyme in the process to assimilate ammonia. When cellular nitrogen levels are high, the C-terminal adenylyl transferase (AT) inactivates GlnA by covalent transfer of an adenylyl group from ATP to specific tyrosine residue of GlnA, thus reducing its activity. Conversely, when nitrogen levels are low, the N-terminal adenylyl removase (AR) activates GlnA by removing the adenylyl group by phosphorolysis, increasing its activity. The regulatory region of GlnE binds the signal transduction protein PII (GlnB) which indicates the nitrogen status of the cell | |
| PEFLCPBG_00072 | 1.5e-160 | metF | 1.5.1.20 | E | Methylenetetrahydrofolate reductase | |
| PEFLCPBG_00073 | 0.0 | metE | 2.1.1.14 | E | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | |
| PEFLCPBG_00074 | 1.7e-99 | sixA | 3.6.1.55 | T | Phosphoglycerate mutase family | |
| PEFLCPBG_00075 | 8.8e-198 | trmI | 2.1.1.219, 2.1.1.220 | J | Catalyzes the S-adenosyl-L-methionine-dependent formation of N(1)-methyladenine at position 58 (m1A58) in tRNA | |
| PEFLCPBG_00076 | 3.4e-160 | modF | 3.6.3.21, 3.6.3.34 | P | ATPases associated with a variety of cellular activities | |
| PEFLCPBG_00077 | 3.6e-243 | glgA | 2.4.1.342 | GT4 | G | Starch synthase catalytic domain |
| PEFLCPBG_00078 | 9.9e-88 | bcp | 1.11.1.15 | O | Redoxin | |
| PEFLCPBG_00079 | 6.1e-79 | |||||
| PEFLCPBG_00080 | 1.2e-304 | gltD | 1.4.1.13, 1.4.1.14 | C | Dihydroprymidine dehydrogenase domain II, 4Fe-4S cluster | |
| PEFLCPBG_00081 | 0.0 | gltB | 1.4.1.13, 1.4.1.14, 1.4.7.1 | E | glutamate synthase NADPH large subunit | |
| PEFLCPBG_00082 | 1.8e-261 | hemN | H | Involved in the biosynthesis of porphyrin-containing compound | ||
| PEFLCPBG_00083 | 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 | ||
| PEFLCPBG_00084 | 3.4e-34 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
| PEFLCPBG_00085 | 3e-134 | S | UPF0126 domain | |||
| PEFLCPBG_00086 | 1.5e-227 | ilvE | 2.6.1.42 | E | Amino-transferase class IV | |
| PEFLCPBG_00087 | 7.2e-107 | ctc | J | This is one of the proteins that binds to the 5S RNA in the ribosome where it forms part of the central protuberance | ||
| PEFLCPBG_00088 | 2.6e-183 | S | alpha beta | |||
| PEFLCPBG_00089 | 2.7e-250 | pntB | 1.6.1.2 | C | The transhydrogenation between NADH and NADP is coupled to respiration and ATP hydrolysis and functions as a proton pump across the membrane | |
| PEFLCPBG_00090 | 1.2e-46 | pntA | 1.6.1.2 | C | 4TM region of pyridine nucleotide transhydrogenase, mitoch | |
| PEFLCPBG_00091 | 1.9e-206 | pntAA | 1.6.1.2 | C | NAD(P) transhydrogenase subunit alpha part 1 K00324 | |
| PEFLCPBG_00092 | 0.0 | fadD | 6.2.1.3 | I | AMP-binding enzyme | |
| PEFLCPBG_00093 | 2.9e-182 | 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 | ||
| PEFLCPBG_00094 | 1.6e-247 | corC | S | CBS domain | ||
| PEFLCPBG_00095 | 1.2e-102 | 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 | |
| PEFLCPBG_00096 | 4e-204 | phoH | T | PhoH-like protein | ||
| PEFLCPBG_00097 | 2.5e-58 | hinT | 2.1.1.226, 2.1.1.227 | FG | Scavenger mRNA decapping enzyme C-term binding | |
| PEFLCPBG_00098 | 4.8e-140 | rsmE | 2.1.1.193 | J | Specifically methylates the N3 position of the uracil ring of uridine 1498 (m3U1498) in 16S rRNA. Acts on the fully assembled 30S ribosomal subunit | |
| PEFLCPBG_00100 | 1.7e-159 | spoU | 2.1.1.185 | J | SpoU rRNA Methylase family | |
| PEFLCPBG_00101 | 1.6e-211 | glgC | 2.7.7.27 | H | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
| PEFLCPBG_00102 | 1.2e-89 | yitW | S | Iron-sulfur cluster assembly protein | ||
| PEFLCPBG_00103 | 2.2e-102 | iscU | C | SUF system FeS assembly protein, NifU family | ||
| PEFLCPBG_00104 | 5.4e-234 | sufS | 2.8.1.7, 4.4.1.16 | E | Catalyzes the removal of elemental sulfur and selenium atoms from L-cysteine, L-cystine, L-selenocysteine, and L- selenocystine to produce L-alanine | |
| PEFLCPBG_00105 | 9.5e-141 | sufC | O | FeS assembly ATPase SufC | ||
| PEFLCPBG_00106 | 4.7e-227 | sufD | O | FeS assembly protein SufD | ||
| PEFLCPBG_00107 | 3.1e-289 | sufB | O | FeS assembly protein SufB | ||
| PEFLCPBG_00108 | 0.0 | S | L,D-transpeptidase catalytic domain | |||
| PEFLCPBG_00109 | 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 | |
| PEFLCPBG_00110 | 8.2e-163 | pulA | 3.2.1.41 | CBM48,GH13 | G | Belongs to the glycosyl hydrolase 13 family |
Showing 1 to 100 of 1,540 entries
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)