© 2022 - Robin Ohm - Utrecht University - The Netherlands
Built with Python Django and Wagtail
| Protein ID | OphauG2|1484 |
| Gene name | |
| Location | Contig_145:1511..3615 |
| Strand | + |
| Gene length (bp) | 2104 |
| Transcript length (bp) | 1947 |
| Coding sequence length (bp) | 1947 |
| Protein length (aa) | 649 |
| PFAM Domain ID | Short name | Long name | E-value | Start | End |
|---|---|---|---|---|---|
| PF00132 | Hexapep | Bacterial transferase hexapeptide (six repeats) | 1.1E-07 | 592 | 627 |
| PF00172 | Zn_clus | Fungal Zn(2)-Cys(6) binuclear cluster domain | 1.0E-09 | 212 | 247 |
| PF14602 | Hexapep_2 | Hexapeptide repeat of succinyl-transferase | 9.5E-08 | 593 | 627 |
| PF12464 | Mac | Maltose acetyltransferase | 1.6E-06 | 445 | 495 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|P08632|NODL_RHILV | Nodulation protein L OS=Rhizobium leguminosarum bv. viciae GN=nodL PE=3 SV=1 | 439 | 645 | 2.0E-37 |
| sp|P37515|MAA_BACSU | Probable maltose O-acetyltransferase OS=Bacillus subtilis (strain 168) GN=maa PE=3 SV=1 | 439 | 644 | 3.0E-37 |
| sp|P28266|NODL_RHIME | Nodulation protein L OS=Rhizobium meliloti (strain 1021) GN=nodL PE=3 SV=1 | 439 | 642 | 2.0E-35 |
| sp|Q4L967|ATRF2_STAHJ | Putative acetyltransferase SH0499 OS=Staphylococcus haemolyticus (strain JCSC1435) GN=SH0499 PE=3 SV=1 | 440 | 646 | 2.0E-34 |
| sp|Q6GDP3|ATRF2_STAAR | Putative acetyltransferase SAR2635 OS=Staphylococcus aureus (strain MRSA252) GN=SAR2635 PE=3 SV=1 | 440 | 646 | 8.0E-33 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|P08632|NODL_RHILV | Nodulation protein L OS=Rhizobium leguminosarum bv. viciae GN=nodL PE=3 SV=1 | 439 | 645 | 2.0E-37 |
| sp|P37515|MAA_BACSU | Probable maltose O-acetyltransferase OS=Bacillus subtilis (strain 168) GN=maa PE=3 SV=1 | 439 | 644 | 3.0E-37 |
| sp|P28266|NODL_RHIME | Nodulation protein L OS=Rhizobium meliloti (strain 1021) GN=nodL PE=3 SV=1 | 439 | 642 | 2.0E-35 |
| sp|Q4L967|ATRF2_STAHJ | Putative acetyltransferase SH0499 OS=Staphylococcus haemolyticus (strain JCSC1435) GN=SH0499 PE=3 SV=1 | 440 | 646 | 2.0E-34 |
| sp|Q6GDP3|ATRF2_STAAR | Putative acetyltransferase SAR2635 OS=Staphylococcus aureus (strain MRSA252) GN=SAR2635 PE=3 SV=1 | 440 | 646 | 8.0E-33 |
| sp|P77791|MAA_ECOLI | Maltose O-acetyltransferase OS=Escherichia coli (strain K12) GN=maa PE=1 SV=3 | 440 | 644 | 1.0E-32 |
| sp|Q7A3E8|ATRF2_STAAN | Putative acetyltransferase SA2342 OS=Staphylococcus aureus (strain N315) GN=SA2342 PE=1 SV=1 | 440 | 646 | 5.0E-32 |
| sp|Q7A2K9|ATRF2_STAAM | Putative acetyltransferase SAV2555 OS=Staphylococcus aureus (strain Mu50 / ATCC 700699) GN=SAV2555 PE=3 SV=1 | 440 | 646 | 5.0E-32 |
| sp|Q9KWJ8|ATRF2_STAA1 | Putative acetyltransferase OS=Staphylococcus aureus (strain Mu3 / ATCC 700698) GN=SAHV_2539 PE=3 SV=1 | 440 | 646 | 5.0E-32 |
| sp|Q8NUR1|ATRF2_STAAW | Putative acetyltransferase MW2476 OS=Staphylococcus aureus (strain MW2) GN=MW2476 PE=3 SV=1 | 440 | 646 | 6.0E-32 |
| sp|Q6G6B9|ATRF2_STAAS | Putative acetyltransferase SAS2441 OS=Staphylococcus aureus (strain MSSA476) GN=SAS2441 PE=3 SV=1 | 440 | 646 | 6.0E-32 |
| sp|Q5HCZ5|ATRF2_STAAC | Putative acetyltransferase SACOL2570 OS=Staphylococcus aureus (strain COL) GN=SACOL2570 PE=1 SV=1 | 440 | 646 | 6.0E-32 |
| sp|P40892|YJV8_YEAST | Putative acetyltransferase YJL218W OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=YJL218W PE=1 SV=1 | 514 | 646 | 2.0E-31 |
| sp|Q09707|YA39_SCHPO | Putative acetyltransferase C18B11.09c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC18B11.09c PE=3 SV=2 | 523 | 646 | 5.0E-28 |
| sp|Q552S7|Y5913_DICDI | Putative acetyltransferase DDB_G0275913 OS=Dictyostelium discoideum GN=DDB_G0275913 PE=3 SV=1 | 438 | 648 | 1.0E-27 |
| sp|Q86A05|Y5507_DICDI | Putative acetyltransferase DDB_G0275507 OS=Dictyostelium discoideum GN=DDB_G0275507 PE=3 SV=1 | 515 | 644 | 2.0E-27 |
| sp|P52984|THGA_LACLA | Galactoside O-acetyltransferase OS=Lactococcus lactis subsp. lactis (strain IL1403) GN=lacA PE=3 SV=1 | 438 | 646 | 4.0E-26 |
| sp|P07464|THGA_ECOLI | Galactoside O-acetyltransferase OS=Escherichia coli (strain K12) GN=lacA PE=1 SV=1 | 500 | 646 | 5.0E-23 |
| sp|Q54UU2|Y0825_DICDI | Putative acetyltransferase DDB_G0280825 OS=Dictyostelium discoideum GN=DDB_G0280825 PE=3 SV=1 | 440 | 648 | 2.0E-21 |
| sp|B9K867|DAPH_THENN | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Thermotoga neapolitana (strain ATCC 49049 / DSM 4359 / NS-E) GN=dapH PE=3 SV=1 | 537 | 644 | 3.0E-15 |
| sp|B7GIC1|DAPH_ANOFW | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Anoxybacillus flavithermus (strain DSM 21510 / WK1) GN=dapH PE=3 SV=1 | 516 | 644 | 2.0E-14 |
| sp|A7GS09|DAPH_BACCN | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Bacillus cytotoxicus (strain DSM 22905 / CIP 110041 / 391-98 / NVH 391-98) GN=dapH PE=3 SV=1 | 516 | 646 | 2.0E-14 |
| sp|Q58464|Y1064_METJA | Uncharacterized acetyltransferase MJ1064 OS=Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) GN=MJ1064 PE=3 SV=1 | 534 | 644 | 3.0E-13 |
| sp|Q6T1W7|FDTC_ANETH | dTDP-3-amino-3,6-dideoxy-alpha-D-galactopyranose 3-N-acetyltransferase OS=Aneurinibacillus thermoaerophilus GN=fdtC PE=1 SV=1 | 529 | 642 | 4.0E-13 |
| sp|Q8ERA4|DAPH_OCEIH | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Oceanobacillus iheyensis (strain DSM 14371 / JCM 11309 / KCTC 3954 / HTE831) GN=dapH PE=3 SV=1 | 536 | 644 | 2.0E-12 |
| sp|Q5FKR1|DAPH_LACAC | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Lactobacillus acidophilus (strain ATCC 700396 / NCK56 / N2 / NCFM) GN=dapH PE=3 SV=1 | 517 | 646 | 4.0E-12 |
| sp|A1ADJ6|NEUO_ECOK1 | Polysialic acid O-acetyltransferase OS=Escherichia coli O1:K1 / APEC GN=neuO PE=1 SV=1 | 512 | 644 | 6.0E-12 |
| sp|Q8RBI7|DAPH_CALS4 | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Caldanaerobacter subterraneus subsp. tengcongensis (strain DSM 15242 / JCM 11007 / NBRC 100824 / MB4) GN=dapH PE=3 SV=1 | 516 | 646 | 1.0E-11 |
| sp|Q39218|SAT3_ARATH | Serine acetyltransferase 3, mitochondrial OS=Arabidopsis thaliana GN=SAT3 PE=1 SV=3 | 527 | 645 | 4.0E-11 |
| sp|B0K4I5|DAPH_THEPX | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Thermoanaerobacter sp. (strain X514) GN=dapH PE=3 SV=1 | 516 | 646 | 4.0E-11 |
| sp|P0ACD3|WCAF_SHIFL | Putative colanic acid biosynthesis acetyltransferase WcaF OS=Shigella flexneri GN=wcaF PE=3 SV=1 | 515 | 644 | 5.0E-11 |
| sp|P0ACD2|WCAF_ECOLI | Putative colanic acid biosynthesis acetyltransferase WcaF OS=Escherichia coli (strain K12) GN=wcaF PE=3 SV=1 | 515 | 644 | 5.0E-11 |
| sp|B0KAL9|DAPH_THEP3 | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Thermoanaerobacter pseudethanolicus (strain ATCC 33223 / 39E) GN=dapH PE=3 SV=1 | 537 | 646 | 5.0E-11 |
| sp|P23364|CAT4_AGRFC | Chloramphenicol acetyltransferase OS=Agrobacterium fabrum (strain C58 / ATCC 33970) GN=cat PE=3 SV=1 | 574 | 644 | 5.0E-11 |
| sp|Q06750|CYSE_BACSU | Serine acetyltransferase OS=Bacillus subtilis (strain 168) GN=cysE PE=1 SV=1 | 543 | 643 | 8.0E-11 |
| sp|A9BHR6|DAPH_PETMO | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Petrotoga mobilis (strain DSM 10674 / SJ95) GN=dapH PE=3 SV=1 | 542 | 646 | 8.0E-11 |
| sp|P50868|CAT4_ENTAE | Chloramphenicol acetyltransferase OS=Enterobacter aerogenes GN=catB4 PE=3 SV=1 | 550 | 644 | 9.0E-11 |
| sp|Q2YXZ7|DAPH_STAAB | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Staphylococcus aureus (strain bovine RF122 / ET3-1) GN=dapH PE=3 SV=1 | 537 | 644 | 1.0E-10 |
| sp|P26838|CAT4_ECOLX | Chloramphenicol acetyltransferase OS=Escherichia coli GN=catB2 PE=3 SV=2 | 550 | 644 | 1.0E-10 |
| sp|Q03CW1|DAPH_LACC3 | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Lactobacillus casei (strain ATCC 334) GN=dapH PE=3 SV=1 | 535 | 646 | 2.0E-10 |
| sp|A8F961|CYSE_BACP2 | Serine acetyltransferase OS=Bacillus pumilus (strain SAFR-032) GN=cysE PE=3 SV=1 | 543 | 643 | 3.0E-10 |
| sp|B1IMX1|DAPH_CLOBK | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Clostridium botulinum (strain Okra / Type B1) GN=dapH PE=3 SV=1 | 535 | 648 | 3.0E-10 |
| sp|Q8W0E4|SAT1_ORYSJ | Probable serine acetyltransferase 1 OS=Oryza sativa subsp. japonica GN=SAT1 PE=2 SV=1 | 543 | 645 | 3.0E-10 |
| sp|A6LP60|DAPH_THEM4 | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Thermosipho melanesiensis (strain DSM 12029 / CIP 104789 / BI429) GN=dapH PE=3 SV=1 | 536 | 646 | 3.0E-10 |
| sp|A7GI22|DAPH_CLOBL | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Clostridium botulinum (strain Langeland / NCTC 10281 / Type F) GN=dapH PE=3 SV=1 | 535 | 648 | 3.0E-10 |
| sp|C3KTL7|DAPH_CLOB6 | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Clostridium botulinum (strain 657 / Type Ba4) GN=dapH PE=3 SV=1 | 535 | 648 | 3.0E-10 |
| sp|C5CHX7|DAPH_KOSOT | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Kosmotoga olearia (strain TBF 19.5.1) GN=dapH PE=3 SV=1 | 536 | 644 | 4.0E-10 |
| sp|P50869|CAT4_MORMO | Chloramphenicol acetyltransferase OS=Morganella morganii GN=cat PE=3 SV=1 | 550 | 644 | 5.0E-10 |
| sp|Q7A0X6|DAPH_STAAW | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Staphylococcus aureus (strain MW2) GN=dapH PE=3 SV=1 | 537 | 644 | 5.0E-10 |
| sp|Q9EZ10|DAPH_STAAU | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Staphylococcus aureus GN=dapH PE=3 SV=1 | 537 | 644 | 5.0E-10 |
| sp|A8Z3X5|DAPH_STAAT | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Staphylococcus aureus (strain USA300 / TCH1516) GN=dapH PE=3 SV=1 | 537 | 644 | 5.0E-10 |
| sp|Q6G9G4|DAPH_STAAS | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Staphylococcus aureus (strain MSSA476) GN=dapH PE=3 SV=1 | 537 | 644 | 5.0E-10 |
| sp|Q7A5P7|DAPH_STAAN | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Staphylococcus aureus (strain N315) GN=dapH PE=3 SV=1 | 537 | 644 | 5.0E-10 |
| sp|Q7A2S0|DAPH_STAAM | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Staphylococcus aureus (strain Mu50 / ATCC 700699) GN=dapH PE=1 SV=1 | 537 | 644 | 5.0E-10 |
| sp|Q5HG23|DAPH_STAAC | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Staphylococcus aureus (strain COL) GN=dapH PE=3 SV=1 | 537 | 644 | 5.0E-10 |
| sp|A5ISS9|DAPH_STAA9 | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Staphylococcus aureus (strain JH9) GN=dapH PE=3 SV=1 | 537 | 644 | 5.0E-10 |
| sp|Q2FYN7|DAPH_STAA8 | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Staphylococcus aureus (strain NCTC 8325) GN=dapH PE=3 SV=1 | 537 | 644 | 5.0E-10 |
| sp|Q2FH41|DAPH_STAA3 | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Staphylococcus aureus (strain USA300) GN=dapH PE=3 SV=1 | 537 | 644 | 5.0E-10 |
| sp|A6U1L8|DAPH_STAA2 | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Staphylococcus aureus (strain JH1) GN=dapH PE=3 SV=1 | 537 | 644 | 5.0E-10 |
| sp|A7X274|DAPH_STAA1 | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Staphylococcus aureus (strain Mu3 / ATCC 700698) GN=dapH PE=3 SV=1 | 537 | 644 | 5.0E-10 |
| sp|A5I6N5|DAPH_CLOBH | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Clostridium botulinum (strain Hall / ATCC 3502 / NCTC 13319 / Type A) GN=dapH PE=3 SV=1 | 535 | 648 | 5.0E-10 |
| sp|A7FYA5|DAPH_CLOB1 | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Clostridium botulinum (strain ATCC 19397 / Type A) GN=dapH PE=3 SV=1 | 535 | 648 | 5.0E-10 |
| sp|C1FL32|DAPH_CLOBJ | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Clostridium botulinum (strain Kyoto / Type A2) GN=dapH PE=3 SV=1 | 535 | 648 | 6.0E-10 |
| sp|Q6GH11|DAPH_STAAR | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Staphylococcus aureus (strain MRSA252) GN=dapH PE=3 SV=1 | 537 | 644 | 6.0E-10 |
| sp|B1L0V4|DAPH_CLOBM | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Clostridium botulinum (strain Loch Maree / Type A3) GN=dapH PE=3 SV=1 | 535 | 648 | 6.0E-10 |
| sp|O74308|YOG2_SCHPO | Uncharacterized transcriptional regulatory protein C15D4.02 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPBC15D4.02 PE=3 SV=3 | 203 | 285 | 7.0E-10 |
| sp|B3W7E7|DAPH_LACCB | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Lactobacillus casei (strain BL23) GN=dapH PE=3 SV=1 | 535 | 646 | 7.0E-10 |
| sp|Q88V23|DAPH_LACPL | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Lactobacillus plantarum (strain ATCC BAA-793 / NCIMB 8826 / WCFS1) GN=dapH PE=3 SV=1 | 535 | 646 | 7.0E-10 |
| sp|C4L2D4|DAPH_EXISA | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Exiguobacterium sp. (strain ATCC BAA-1283 / AT1b) GN=dapH PE=3 SV=1 | 537 | 644 | 8.0E-10 |
| sp|Q65PC9|CYSE_BACLD | Serine acetyltransferase OS=Bacillus licheniformis (strain ATCC 14580 / DSM 13 / JCM 2505 / NBRC 12200 / NCIMB 9375 / NRRL NRS-1264 / Gibson 46) GN=cysE PE=3 SV=1 | 543 | 643 | 1.0E-09 |
| sp|Q42588|SAT1_ARATH | Serine acetyltransferase 1, chloroplastic OS=Arabidopsis thaliana GN=SAT1 PE=1 SV=2 | 543 | 645 | 1.0E-09 |
| sp|Q6LAN4|DAPH_LISIV | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Listeria ivanovii GN=dapH PE=3 SV=1 | 517 | 644 | 2.0E-09 |
| sp|B7IF15|DAPH_THEAB | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Thermosipho africanus (strain TCF52B) GN=dapH PE=3 SV=1 | 537 | 646 | 2.0E-09 |
| sp|A6QGU8|DAPH_STAAE | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Staphylococcus aureus (strain Newman) GN=dapH PE=3 SV=1 | 537 | 644 | 3.0E-09 |
| sp|Q7A1G0|ATRF1_STAAW | Putative acetyltransferase MW0724 OS=Staphylococcus aureus (strain MW2) GN=MW0724 PE=3 SV=1 | 534 | 639 | 4.0E-09 |
| sp|Q6GB68|ATRF1_STAAS | Putative acetyltransferase SAS0727 OS=Staphylococcus aureus (strain MSSA476) GN=SAS0727 PE=3 SV=1 | 534 | 639 | 4.0E-09 |
| sp|Q6GIM9|ATRF1_STAAR | Putative acetyltransferase SAR0816 OS=Staphylococcus aureus (strain MRSA252) GN=SAR0816 PE=3 SV=1 | 534 | 639 | 4.0E-09 |
| sp|Q7A6Q9|ATRF1_STAAN | Putative acetyltransferase SA0717 OS=Staphylococcus aureus (strain N315) GN=SA0717 PE=3 SV=1 | 534 | 639 | 4.0E-09 |
| sp|Q99VL4|ATRF1_STAAM | Putative acetyltransferase SAV0762 OS=Staphylococcus aureus (strain Mu50 / ATCC 700699) GN=SAV0762 PE=3 SV=1 | 534 | 639 | 4.0E-09 |
| sp|Q5HHQ6|ATRF1_STAAC | Putative acetyltransferase SACOL0827 OS=Staphylococcus aureus (strain COL) GN=SACOL0827 PE=3 SV=1 | 534 | 639 | 4.0E-09 |
| sp|Q03YE4|DAPH_LEUMM | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Leuconostoc mesenteroides subsp. mesenteroides (strain ATCC 8293 / NCDO 523) GN=dapH PE=3 SV=1 | 537 | 644 | 4.0E-09 |
| sp|P32003|CYSE_BUCAP | Serine acetyltransferase OS=Buchnera aphidicola subsp. Schizaphis graminum (strain Sg) GN=cysE PE=3 SV=1 | 547 | 646 | 4.0E-09 |
| sp|B9DP25|DAPH_STACT | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Staphylococcus carnosus (strain TM300) GN=dapH PE=3 SV=1 | 537 | 644 | 6.0E-09 |
| sp|A4ILT5|DAPH_GEOTN | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Geobacillus thermodenitrificans (strain NG80-2) GN=dapH PE=3 SV=1 | 516 | 644 | 6.0E-09 |
| sp|B2G6M7|DAPH_LACRJ | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Lactobacillus reuteri (strain JCM 1112) GN=dapH PE=3 SV=1 | 535 | 646 | 6.0E-09 |
| sp|A5VJ56|DAPH_LACRD | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Lactobacillus reuteri (strain DSM 20016) GN=dapH PE=3 SV=1 | 535 | 646 | 6.0E-09 |
| sp|B1YJ41|DAPH_EXIS2 | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Exiguobacterium sibiricum (strain DSM 17290 / JCM 13490 / 255-15) GN=dapH PE=3 SV=1 | 535 | 644 | 7.0E-09 |
| sp|A3CQT5|DAPH_STRSV | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Streptococcus sanguinis (strain SK36) GN=dapH PE=3 SV=1 | 537 | 644 | 7.0E-09 |
| sp|A8YUT1|DAPH_LACH4 | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Lactobacillus helveticus (strain DPC 4571) GN=dapH PE=3 SV=1 | 517 | 646 | 8.0E-09 |
| sp|Q42538|SAT5_ARATH | Serine acetyltransferase 5 OS=Arabidopsis thaliana GN=SAT5 PE=1 SV=1 | 543 | 645 | 8.0E-09 |
| sp|P50870|VATD_ENTFC | Streptogramin A acetyltransferase OS=Enterococcus faecium GN=vatD PE=1 SV=1 | 549 | 644 | 9.0E-09 |
| sp|P26841|CAT4_PSEAE | Chloramphenicol acetyltransferase OS=Pseudomonas aeruginosa (strain ATCC 15692 / PAO1 / 1C / PRS 101 / LMG 12228) GN=cat PE=1 SV=3 | 586 | 644 | 1.0E-08 |
| sp|C1CH25|DAPH_STRZJ | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Streptococcus pneumoniae (strain JJA) GN=dapH PE=3 SV=1 | 537 | 644 | 1.0E-08 |
| sp|Q8DN54|DAPH_STRR6 | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Streptococcus pneumoniae (strain ATCC BAA-255 / R6) GN=dapH PE=3 SV=1 | 537 | 644 | 1.0E-08 |
| sp|B8ZPL9|DAPH_STRPJ | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Streptococcus pneumoniae (strain ATCC 700669 / Spain 23F-1) GN=dapH PE=3 SV=1 | 537 | 644 | 1.0E-08 |
| sp|B1I9G3|DAPH_STRPI | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Streptococcus pneumoniae (strain Hungary19A-6) GN=dapH PE=3 SV=1 | 537 | 644 | 1.0E-08 |
| sp|C1CAS4|DAPH_STRP7 | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Streptococcus pneumoniae (strain 70585) GN=dapH PE=3 SV=1 | 537 | 644 | 1.0E-08 |
| sp|B5E3A4|DAPH_STRP4 | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Streptococcus pneumoniae serotype 19F (strain G54) GN=dapH PE=3 SV=1 | 537 | 644 | 1.0E-08 |
| sp|Q04I77|DAPH_STRP2 | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Streptococcus pneumoniae serotype 2 (strain D39 / NCTC 7466) GN=dapH PE=3 SV=1 | 537 | 644 | 1.0E-08 |
| sp|B2IN15|DAPH_STRPS | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Streptococcus pneumoniae (strain CGSP14) GN=dapH PE=3 SV=1 | 537 | 644 | 1.0E-08 |
| sp|P39856|CAPG_STAAU | Protein CapG OS=Staphylococcus aureus GN=capG PE=3 SV=1 | 593 | 646 | 1.0E-08 |
| sp|Q9UT46|MOC3_SCHPO | Transcriptional regulatory protein moc3 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=moc3 PE=1 SV=4 | 199 | 245 | 1.0E-08 |
| sp|A8AUL9|DAPH_STRGC | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Streptococcus gordonii (strain Challis / ATCC 35105 / CH1 / DL1 / V288) GN=dapH PE=3 SV=1 | 537 | 644 | 1.0E-08 |
| sp|C1CN43|DAPH_STRZP | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Streptococcus pneumoniae (strain P1031) GN=dapH PE=3 SV=1 | 537 | 644 | 2.0E-08 |
| sp|Q97NE6|DAPH_STRPN | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Streptococcus pneumoniae serotype 4 (strain ATCC BAA-334 / TIGR4) GN=dapH PE=3 SV=1 | 537 | 644 | 2.0E-08 |
| sp|C1CU00|DAPH_STRZT | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Streptococcus pneumoniae (strain Taiwan19F-14) GN=dapH PE=3 SV=1 | 537 | 644 | 2.0E-08 |
| sp|Q4L6A2|DAPH_STAHJ | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Staphylococcus haemolyticus (strain JCSC1435) GN=dapH PE=3 SV=1 | 537 | 644 | 2.0E-08 |
| sp|P37750|WBBJ_ECOLI | Putative lipopolysaccharide biosynthesis O-acetyl transferase WbbJ OS=Escherichia coli (strain K12) GN=wbbJ PE=3 SV=2 | 535 | 644 | 2.0E-08 |
| sp|A6LUD2|DAPH_CLOB8 | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Clostridium beijerinckii (strain ATCC 51743 / NCIMB 8052) GN=dapH PE=3 SV=1 | 517 | 646 | 3.0E-08 |
| sp|B9DVY7|DAPH_STRU0 | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Streptococcus uberis (strain ATCC BAA-854 / 0140J) GN=dapH PE=3 SV=1 | 535 | 644 | 3.0E-08 |
| sp|Q0DGG8|SAT5_ORYSJ | Probable serine acetyltransferase 5 OS=Oryza sativa subsp. japonica GN=SAT5 PE=2 SV=2 | 533 | 643 | 4.0E-08 |
| sp|Q03IN0|DAPH_STRTD | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Streptococcus thermophilus (strain ATCC BAA-491 / LMD-9) GN=dapH PE=3 SV=1 | 536 | 644 | 5.0E-08 |
| sp|Q5M2I4|DAPH_STRT2 | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Streptococcus thermophilus (strain ATCC BAA-250 / LMG 18311) GN=dapH PE=3 SV=1 | 536 | 644 | 5.0E-08 |
| sp|Q5LXY2|DAPH_STRT1 | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Streptococcus thermophilus (strain CNRZ 1066) GN=dapH PE=3 SV=1 | 536 | 644 | 5.0E-08 |
| sp|C5D826|DAPH_GEOSW | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Geobacillus sp. (strain WCH70) GN=dapH PE=3 SV=1 | 516 | 644 | 5.0E-08 |
| sp|Q8S895|SAT2_ARATH | Serine acetyltransferase 2 OS=Arabidopsis thaliana GN=SAT2 PE=1 SV=2 | 515 | 644 | 5.0E-08 |
| sp|A4VY24|DAPH_STRSY | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Streptococcus suis (strain 05ZYH33) GN=dapH PE=3 SV=2 | 535 | 644 | 5.0E-08 |
| sp|A4W4B5|DAPH_STRS2 | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Streptococcus suis (strain 98HAH33) GN=dapH PE=3 SV=1 | 535 | 644 | 5.0E-08 |
| sp|P0A9D7|CYSE_SHIFL | Serine acetyltransferase OS=Shigella flexneri GN=cysE PE=3 SV=1 | 535 | 643 | 6.0E-08 |
| sp|P0A9D4|CYSE_ECOLI | Serine acetyltransferase OS=Escherichia coli (strain K12) GN=cysE PE=1 SV=1 | 535 | 643 | 6.0E-08 |
| sp|P0A9D5|CYSE_ECOL6 | Serine acetyltransferase OS=Escherichia coli O6:H1 (strain CFT073 / ATCC 700928 / UPEC) GN=cysE PE=3 SV=1 | 535 | 643 | 6.0E-08 |
| sp|P0A9D6|CYSE_ECO57 | Serine acetyltransferase OS=Escherichia coli O157:H7 GN=cysE PE=3 SV=1 | 535 | 643 | 6.0E-08 |
| sp|Q032G9|DAPH_LACLS | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Lactococcus lactis subsp. cremoris (strain SK11) GN=dapH PE=3 SV=1 | 535 | 644 | 6.0E-08 |
| sp|Q8DVY7|DAPH_STRMU | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Streptococcus mutans serotype c (strain ATCC 700610 / UA159) GN=dapH PE=3 SV=1 | 521 | 644 | 6.0E-08 |
| sp|P29847|CYSE_SALTY | Serine acetyltransferase OS=Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) GN=cysE PE=1 SV=1 | 535 | 643 | 6.0E-08 |
| sp|A2RI05|DAPH_LACLM | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Lactococcus lactis subsp. cremoris (strain MG1363) GN=dapH PE=3 SV=1 | 535 | 644 | 6.0E-08 |
| sp|Q9CIS5|DAPH_LACLA | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Lactococcus lactis subsp. lactis (strain IL1403) GN=dapH PE=3 SV=1 | 535 | 644 | 7.0E-08 |
| sp|P26839|VATA_STAAU | Virginiamycin A acetyltransferase OS=Staphylococcus aureus GN=vat PE=1 SV=2 | 593 | 644 | 8.0E-08 |
| sp|Q9X1K7|DAPH_THEMA | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Thermotoga maritima (strain ATCC 43589 / MSB8 / DSM 3109 / JCM 10099) GN=dapH PE=3 SV=1 | 537 | 644 | 1.0E-07 |
| sp|A6TT15|DAPH_ALKMQ | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Alkaliphilus metalliredigens (strain QYMF) GN=dapH PE=3 SV=1 | 516 | 644 | 1.0E-07 |
| sp|B1LBQ9|DAPH_THESQ | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Thermotoga sp. (strain RQ2) GN=dapH PE=3 SV=1 | 537 | 644 | 1.0E-07 |
| sp|A5IM64|DAPH_THEP1 | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Thermotoga petrophila (strain RKU-1 / ATCC BAA-488 / DSM 13995) GN=dapH PE=3 SV=1 | 537 | 644 | 2.0E-07 |
| sp|B2V5B7|DAPH_CLOBA | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Clostridium botulinum (strain Alaska E43 / Type E3) GN=dapH PE=3 SV=1 | 517 | 646 | 2.0E-07 |
| sp|P26840|MATA_LYSSH | Probable macrolide acetyltransferase (Fragment) OS=Lysinibacillus sphaericus PE=3 SV=1 | 536 | 644 | 2.0E-07 |
| sp|B1MZN0|DAPH_LEUCK | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Leuconostoc citreum (strain KM20) GN=dapH PE=3 SV=1 | 535 | 644 | 3.0E-07 |
| sp|G3XD01|WBPD_PSEAE | UDP-2-acetamido-3-amino-2,3-dideoxy-D-glucuronate N-acetyltransferase OS=Pseudomonas aeruginosa (strain ATCC 15692 / PAO1 / 1C / PRS 101 / LMG 12228) GN=wbpD PE=1 SV=1 | 515 | 641 | 3.0E-07 |
| sp|B2TS78|DAPH_CLOBB | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Clostridium botulinum (strain Eklund 17B / Type B) GN=dapH PE=3 SV=1 | 517 | 646 | 3.0E-07 |
| sp|Q97GI6|DAPH_CLOAB | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Clostridium acetobutylicum (strain ATCC 824 / DSM 792 / JCM 1419 / LMG 5710 / VKM B-1787) GN=dapH PE=3 SV=1 | 517 | 646 | 3.0E-07 |
| sp|A9VUE3|DAPH_BACWK | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Bacillus weihenstephanensis (strain KBAB4) GN=dapH PE=3 SV=1 | 516 | 646 | 4.0E-07 |
| sp|Q9XCW3|VIOB_ECOLX | dTDP-4-amino-4,6-dideoxy-D-glucose acyltransferase OS=Escherichia coli GN=vioB PE=1 SV=1 | 517 | 641 | 4.0E-07 |
| sp|Q6HEI4|DAPH_BACHK | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Bacillus thuringiensis subsp. konkukian (strain 97-27) GN=dapH PE=3 SV=1 | 516 | 646 | 6.0E-07 |
| sp|Q635U7|DAPH_BACCZ | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Bacillus cereus (strain ZK / E33L) GN=dapH PE=3 SV=1 | 516 | 646 | 6.0E-07 |
| sp|B9IW61|DAPH_BACCQ | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Bacillus cereus (strain Q1) GN=dapH PE=3 SV=1 | 516 | 646 | 6.0E-07 |
| sp|C1EPZ5|DAPH_BACC3 | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Bacillus cereus (strain 03BB102) GN=dapH PE=3 SV=1 | 516 | 646 | 6.0E-07 |
| sp|Q731Y5|DAPH_BACC1 | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Bacillus cereus (strain ATCC 10987 / NRS 248) GN=dapH PE=3 SV=1 | 516 | 646 | 6.0E-07 |
| sp|B7JKV5|DAPH_BACC0 | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Bacillus cereus (strain AH820) GN=dapH PE=3 SV=1 | 516 | 646 | 6.0E-07 |
| sp|Q81MQ2|DAPH_BACAN | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Bacillus anthracis GN=dapH PE=1 SV=1 | 516 | 646 | 6.0E-07 |
| sp|C3LI47|DAPH_BACAC | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Bacillus anthracis (strain CDC 684 / NRRL 3495) GN=dapH PE=3 SV=1 | 516 | 646 | 6.0E-07 |
| sp|C3P6Y8|DAPH_BACAA | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Bacillus anthracis (strain A0248) GN=dapH PE=3 SV=1 | 516 | 646 | 6.0E-07 |
| sp|Q819J5|DAPH_BACCR | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Bacillus cereus (strain ATCC 14579 / DSM 31 / JCM 2152 / NBRC 15305 / NCIMB 9373 / NRRL B-3711) GN=dapH PE=3 SV=1 | 516 | 646 | 6.0E-07 |
| sp|B7H6W8|DAPH_BACC4 | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Bacillus cereus (strain B4264) GN=dapH PE=3 SV=1 | 516 | 646 | 6.0E-07 |
| sp|B7IVL8|DAPH_BACC2 | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Bacillus cereus (strain G9842) GN=dapH PE=3 SV=1 | 516 | 646 | 6.0E-07 |
| sp|B7HMV2|DAPH_BACC7 | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Bacillus cereus (strain AH187) GN=dapH PE=3 SV=1 | 516 | 646 | 7.0E-07 |
| sp|Q10S58|SAT2_ORYSJ | Probable serine acetyltransferase 2 OS=Oryza sativa subsp. japonica GN=SAT2 PE=2 SV=1 | 502 | 643 | 8.0E-07 |
| sp|A0RHZ3|DAPH_BACAH | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Bacillus thuringiensis (strain Al Hakam) GN=dapH PE=3 SV=1 | 516 | 644 | 8.0E-07 |
| sp|O34993|YVOF_BACSU | Putative acetyltransferase YvoF OS=Bacillus subtilis (strain 168) GN=yvoF PE=3 SV=1 | 554 | 643 | 1.0E-06 |
| sp|Q8TY70|DAPH_METKA | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Methanopyrus kandleri (strain AV19 / DSM 6324 / JCM 9639 / NBRC 100938) GN=dapH PE=3 SV=1 | 516 | 646 | 2.0E-06 |
| sp|Q5ANB1|WOR2_CANAL | White-opaque regulator 1 OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=WOR2 PE=1 SV=1 | 213 | 244 | 2.0E-06 |
| sp|Q65K85|DAPH_BACLD | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Bacillus licheniformis (strain ATCC 14580 / DSM 13 / JCM 2505 / NBRC 12200 / NCIMB 9375 / NRRL NRS-1264 / Gibson 46) GN=dapH PE=3 SV=1 | 516 | 646 | 3.0E-06 |
| sp|A7Z432|DAPH_BACMF | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Bacillus methylotrophicus (strain DSM 23117 / BGSC 10A6 / FZB42) GN=dapH PE=3 SV=1 | 516 | 646 | 3.0E-06 |
| sp|A8FCN1|DAPH_BACP2 | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Bacillus pumilus (strain SAFR-032) GN=dapH PE=3 SV=1 | 516 | 646 | 3.0E-06 |
| sp|O34981|DAPH_BACSU | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Bacillus subtilis (strain 168) GN=dapH PE=1 SV=2 | 516 | 646 | 3.0E-06 |
| sp|Q5L146|DAPH_GEOKA | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Geobacillus kaustophilus (strain HTA426) GN=dapH PE=3 SV=1 | 516 | 644 | 4.0E-06 |
| sp|A7HJ58|DAPH_FERNB | 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-acetyltransferase OS=Fervidobacterium nodosum (strain ATCC 35602 / DSM 5306 / Rt17-B1) GN=dapH PE=3 SV=1 | 517 | 646 | 5.0E-06 |
| sp|O53281|Y3034_MYCTU | Putative acetyltransferase Rv3034c OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=Rv3034c PE=1 SV=1 | 537 | 644 | 5.0E-06 |
| sp|Q8W2B8|SAT4_ARATH | Serine acetyltransferase 4 OS=Arabidopsis thaliana GN=SAT4 PE=1 SV=1 | 513 | 643 | 5.0E-06 |
| GO Term | Description | Terminal node |
|---|---|---|
| GO:0006355 | regulation of transcription, DNA-templated | Yes |
| GO:0000981 | DNA-binding transcription factor activity, RNA polymerase II-specific | Yes |
| GO:0016407 | acetyltransferase activity | Yes |
| GO:0008270 | zinc ion binding | Yes |
| GO:0050789 | regulation of biological process | No |
| GO:0008150 | biological_process | No |
| GO:0080090 | regulation of primary metabolic process | No |
| GO:0060255 | regulation of macromolecule metabolic process | No |
| GO:0010468 | regulation of gene expression | No |
| GO:0019219 | regulation of nucleobase-containing compound metabolic process | No |
| GO:0050794 | regulation of cellular process | No |
| GO:0016746 | acyltransferase activity | No |
| GO:0046872 | metal ion binding | No |
| GO:0043167 | ion binding | No |
| GO:0019222 | regulation of metabolic process | No |
| GO:2001141 | regulation of RNA biosynthetic process | No |
| GO:1903506 | regulation of nucleic acid-templated transcription | No |
| GO:0140110 | transcription regulator activity | No |
| GO:0031323 | regulation of cellular metabolic process | No |
| GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | No |
| GO:0009889 | regulation of biosynthetic process | No |
| GO:0065007 | biological regulation | No |
| GO:0005488 | binding | No |
| GO:0046914 | transition metal ion binding | No |
| GO:0016740 | transferase activity | No |
| GO:0003674 | molecular_function | No |
| GO:0051171 | regulation of nitrogen compound metabolic process | No |
| GO:0010556 | regulation of macromolecule biosynthetic process | No |
| GO:0003700 | DNA-binding transcription factor activity | No |
| GO:0043169 | cation binding | No |
| GO:0003824 | catalytic activity | No |
| GO:0051252 | regulation of RNA metabolic process | No |
| GO:0031326 | regulation of cellular biosynthetic process | No |
| SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
|---|---|---|
| No | 1 - 47 | 0.45 |
| Transcription Factor Class (based on PFAM domains) |
|---|
| Fungal Specific TF |
| Type of sequence | Sequence |
|---|---|
| Locus | Download genbank file of locus
The gene with 5 kb flanks (if sufficient flanking sequence is available). For use in cloning design programs. NOTE: features (genes or exons) that are only partially contained within the sequence are completely excluded. |
| Protein | >OphauG2|1484 MSSFTALNGTTPKDKDLAQTADAADKLVNVDDGPRNGAAPRSRKSPILHPNHKESWQERDCASSRPTRGLDMSDC HKRKRSASDDDKREPRYHVQAAPNMSQSTSHRRYNDDFQESKSPSLHRERDDRLAFETQHSSIDSNRGHSEERQA GEARRHTSASQGQSDHSQASPDAEEASVTQYDSSYAAEQRQDSILQHDPKKRKRNFSNRTKTGCLTCRKRKKKCD EQKPECSNCIRGGFVCAGYPPQRGPGWQKPDNKTAAIPLESKDPSYVPPGAYGMPQHGVYAAQPVKREPLPHYRG QALRIDPPQGKSLAVSDDDRHTASTLASASATSPDNKLSAMAYTPNTVFPTPVSANTQPSPPFGEIMAKEYQRMP SLHELSRSRPDVETPHSATSLPHITVLNPTRASSPASHTPTPVSSAQGVAQLALSHTQYPTARRTQKDEMLAGRH FYPLDKELCLERERCMLACWKFNSLTPPPHGVSFEERARLFLDILQPRDPVRLSAAETSTCNKMGRLGRNVALET PFTCDYGYNIFIGNQVLIKRNCTINDAGEVNIGDHCVIGPNVSIFTSSLPVDPKKRQGGLGPQHAKSVSIEQDCW IGGGAIILPGRTIGKGSTVGAGSVVTKDVPPFTVVAGNPARVLRGVGI* |
| Coding | >OphauG2|1484 ATGTCGAGCTTCACAGCCCTCAATGGGACCACGCCCAAGGACAAGGACTTGGCGCAGACAGCCGACGCGGCTGAC AAGTTGGTAAATGTCGATGATGGCCCGCGAAACGGTGCTGCGCCCCGTTCTCGAAAATCGCCCATCCTGCACCCA AACCACAAGGAATCATGGCAGGAGCGGGATTGCGCGTCATCACGTCCAACAAGAGGGCTGGACATGTCTGACTGC CACAAACGGAAACGTTCCGCATCAGACGACGACAAACGTGAGCCGAGATATCATGTGCAAGCTGCCCCAAATATG TCTCAGTCGACTTCACATCGTCGCTACAACGACGACTTTCAAGAGAGCAAATCACCTTCACTGCACCGTGAACGG GACGATAGACTGGCCTTTGAGACGCAACATAGCTCGATTGATTCGAATCGCGGCCACAGTGAGGAGCGTCAAGCT GGAGAGGCCCGGCGGCACACCAGTGCCTCTCAAGGTCAAAGTGACCACAGCCAAGCAAGCCCAGATGCTGAAGAG GCGTCGGTGACTCAGTATGACAGTTCTTATGCGGCGGAGCAGCGCCAGGATTCAATCCTTCAACACGACCCCAAG AAACGCAAGCGCAATTTCAGCAACCGCACCAAGACTGGATGCTTGACTTGTCGCAAACGCAAGAAGAAATGCGAT GAGCAAAAGCCAGAGTGTAGTAACTGTATTCGAGGCGGCTTTGTCTGCGCAGGCTACCCACCACAAAGAGGCCCC GGCTGGCAGAAGCCGGATAACAAAACGGCAGCCATTCCTCTCGAGTCCAAGGACCCTAGTTATGTCCCGCCTGGA GCCTATGGCATGCCACAACATGGCGTTTACGCGGCCCAGCCTGTAAAGCGGGAACCTCTGCCACACTATCGTGGC CAGGCTTTGCGTATCGATCCTCCCCAGGGCAAGTCTTTGGCTGTATCCGACGATGATCGACATACTGCGTCGACT CTGGCAAGTGCATCTGCCACGAGTCCTGACAACAAGCTGTCTGCCATGGCATATACGCCCAACACTGTCTTTCCT ACGCCAGTCAGCGCAAACACGCAGCCATCGCCGCCGTTTGGTGAGATTATGGCCAAGGAATATCAGCGCATGCCT TCGCTCCATGAGCTCAGCCGGAGCAGGCCCGATGTGGAAACTCCTCACTCGGCCACGTCTCTGCCGCACATCACC GTCTTGAACCCAACCCGAGCAAGTAGCCCGGCTTCTCACACCCCCACTCCTGTTTCCAGTGCCCAGGGTGTCGCT CAGCTTGCCCTTTCGCACACGCAGTATCCGACGGCTAGAAGGACACAAAAGGATGAAATGCTTGCTGGACGGCAC TTTTATCCCTTGGATAAGGAGTTGTGTCTGGAACGCGAGCGTTGCATGCTTGCCTGCTGGAAGTTCAACAGCTTA ACTCCGCCTCCCCACGGTGTTTCATTTGAGGAAAGAGCCCGTTTGTTTCTTGACATCTTACAGCCGCGTGATCCC GTGCGTCTTTCGGCGGCTGAGACCTCAACATGTAACAAGATGGGCCGTCTTGGACGCAACGTGGCTCTCGAGACG CCCTTTACCTGCGACTATGGCTACAATATATTTATCGGGAATCAAGTTCTCATTAAGCGCAACTGCACCATTAAT GACGCTGGCGAAGTCAATATTGGTGATCATTGTGTCATTGGCCCCAATGTGAGCATTTTTACCTCGTCTTTGCCA GTGGACCCCAAGAAACGTCAGGGTGGGCTAGGTCCCCAACATGCAAAGAGTGTCAGTATTGAACAAGACTGTTGG ATTGGAGGCGGCGCCATCATTCTGCCCGGCCGCACTATTGGAAAGGGGAGCACTGTTGGCGCCGGGTCTGTGGTG ACAAAGGATGTTCCTCCTTTTACTGTCGTGGCAGGAAATCCCGCCCGCGTTCTTCGCGGCGTCGGTATATGA |
| Transcript | >OphauG2|1484 ATGTCGAGCTTCACAGCCCTCAATGGGACCACGCCCAAGGACAAGGACTTGGCGCAGACAGCCGACGCGGCTGAC AAGTTGGTAAATGTCGATGATGGCCCGCGAAACGGTGCTGCGCCCCGTTCTCGAAAATCGCCCATCCTGCACCCA AACCACAAGGAATCATGGCAGGAGCGGGATTGCGCGTCATCACGTCCAACAAGAGGGCTGGACATGTCTGACTGC CACAAACGGAAACGTTCCGCATCAGACGACGACAAACGTGAGCCGAGATATCATGTGCAAGCTGCCCCAAATATG TCTCAGTCGACTTCACATCGTCGCTACAACGACGACTTTCAAGAGAGCAAATCACCTTCACTGCACCGTGAACGG GACGATAGACTGGCCTTTGAGACGCAACATAGCTCGATTGATTCGAATCGCGGCCACAGTGAGGAGCGTCAAGCT GGAGAGGCCCGGCGGCACACCAGTGCCTCTCAAGGTCAAAGTGACCACAGCCAAGCAAGCCCAGATGCTGAAGAG GCGTCGGTGACTCAGTATGACAGTTCTTATGCGGCGGAGCAGCGCCAGGATTCAATCCTTCAACACGACCCCAAG AAACGCAAGCGCAATTTCAGCAACCGCACCAAGACTGGATGCTTGACTTGTCGCAAACGCAAGAAGAAATGCGAT GAGCAAAAGCCAGAGTGTAGTAACTGTATTCGAGGCGGCTTTGTCTGCGCAGGCTACCCACCACAAAGAGGCCCC GGCTGGCAGAAGCCGGATAACAAAACGGCAGCCATTCCTCTCGAGTCCAAGGACCCTAGTTATGTCCCGCCTGGA GCCTATGGCATGCCACAACATGGCGTTTACGCGGCCCAGCCTGTAAAGCGGGAACCTCTGCCACACTATCGTGGC CAGGCTTTGCGTATCGATCCTCCCCAGGGCAAGTCTTTGGCTGTATCCGACGATGATCGACATACTGCGTCGACT CTGGCAAGTGCATCTGCCACGAGTCCTGACAACAAGCTGTCTGCCATGGCATATACGCCCAACACTGTCTTTCCT ACGCCAGTCAGCGCAAACACGCAGCCATCGCCGCCGTTTGGTGAGATTATGGCCAAGGAATATCAGCGCATGCCT TCGCTCCATGAGCTCAGCCGGAGCAGGCCCGATGTGGAAACTCCTCACTCGGCCACGTCTCTGCCGCACATCACC GTCTTGAACCCAACCCGAGCAAGTAGCCCGGCTTCTCACACCCCCACTCCTGTTTCCAGTGCCCAGGGTGTCGCT CAGCTTGCCCTTTCGCACACGCAGTATCCGACGGCTAGAAGGACACAAAAGGATGAAATGCTTGCTGGACGGCAC TTTTATCCCTTGGATAAGGAGTTGTGTCTGGAACGCGAGCGTTGCATGCTTGCCTGCTGGAAGTTCAACAGCTTA ACTCCGCCTCCCCACGGTGTTTCATTTGAGGAAAGAGCCCGTTTGTTTCTTGACATCTTACAGCCGCGTGATCCC GTGCGTCTTTCGGCGGCTGAGACCTCAACATGTAACAAGATGGGCCGTCTTGGACGCAACGTGGCTCTCGAGACG CCCTTTACCTGCGACTATGGCTACAATATATTTATCGGGAATCAAGTTCTCATTAAGCGCAACTGCACCATTAAT GACGCTGGCGAAGTCAATATTGGTGATCATTGTGTCATTGGCCCCAATGTGAGCATTTTTACCTCGTCTTTGCCA GTGGACCCCAAGAAACGTCAGGGTGGGCTAGGTCCCCAACATGCAAAGAGTGTCAGTATTGAACAAGACTGTTGG ATTGGAGGCGGCGCCATCATTCTGCCCGGCCGCACTATTGGAAAGGGGAGCACTGTTGGCGCCGGGTCTGTGGTG ACAAAGGATGTTCCTCCTTTTACTGTCGTGGCAGGAAATCCCGCCCGCGTTCTTCGCGGCGTCGGTATATGA |
| Gene | >OphauG2|1484 ATGTCGAGCTTCACAGCCCTCAATGGGACCACGCCCAAGGACAAGGACTTGGCGCAGACAGCCGACGCGGCTGAC AAGTTGGTAAATGTCGATGATGGCCCGCGAAACGGTGCTGCGCCCCGTTCTCGAAAATCGCCCATCCTGCACCCA AACCACAAGGAATCATGGCAGGAGCGGGATTGCGCGTCATCACGTCCAACAAGAGGGCTGGACATGTCTGACTGC CACAAACGGAAACGTTCCGCATCAGACGACGACAAACGTGAGCCGAGATATCATGTGCAAGCTGCCCCAAATATG TCTCAGTCGACTTCACATCGTCGCTACAACGACGACTTTCAAGAGAGCAAATCACCTTCACTGCACCGTGAACGG GACGATAGACTGGCCTTTGAGACGCAACATAGCTCGATTGATTCGAATCGCGGCCACAGTGAGGAGCGTCAAGCT GGAGAGGCCCGGCGGCACACCAGTGCCTCTCAAGGTCAAAGTGACCACAGCCAAGCAAGCCCAGATGCTGAAGAG GCGTCGGTGACTCAGTATGACAGTTCTTATGCGGCGGAGCAGCGCCAGGATTCAATCCTTCAACACGACCCCAAG AAACGCAAGCGCAATTTCAGCAACCGCACCAAGACTGGATGCTTGACTTGTCGCAAACGCAAGAAGAAATGCGAT GAGCAAAAGCCAGAGTGTATGATGGCGCATCTCGTGCATCCATCATTGACACAAGTAGCTCTGAAGCTAATGCTT TGGTCTAGGTAGTAACTGTATTCGAGGCGGCTTTGTCTGCGCAGGCTACCCACCACAAAGAGGCCCCGGCTGGCA GAAGCCGGATAACAAAACGGCAGCCATTCCTCTCGAGTCCAAGGACCCTAGTTATGTCCCGCCTGGAGCCTATGG CATGCCACAACATGGCGTTTACGCGGCCCAGCCTGTAAAGCGGGAACCTCTGCCACACTATCGTGGCCAGGCTTT GCGTATCGATCCTCCCCAGGGCAAGTCTTTGGCTGTATCCGACGATGATCGACATACTGCGTCGACTCTGGCAAG TGCATCTGCCACGAGTCCTGACAACAAGCTGTCTGCCATGGCATATACGCCCAACACTGTCTTTCCTACGCCAGT CAGCGCAAACACGCAGCCATCGCCGCCGTTTGGTGAGATTATGGCCAAGGAATATCAGCGCATGCCTTCGCTCCA TGAGCTCAGCCGGAGCAGGCCCGATGTGGAAACTCCTCACTCGGCCACGTCTCTGCCGCACATCACCGTCTTGAA CCCAACCCGAGCAAGTAGCCCGGCTTCTCACACCCCCACTCCTGTTTCCAGTGCCCAGGGTGTCGCTCAGCTTGC CCTTTCGCACACGCAGTATCCGACGGCTAGAAGGACACAAAAGGATGAAATGCTTGCTGGACGGCACTTTTATCC CTTGGATAAGGAGTTGTGTCTGGAACGCGAGCGTTGCATGCTTGCCTGCTGGAAGTTCAACAGCTTAACTCCGCC TCCCCACGGTGTTTCATTTGAGGAAAGAGCCCGTTTGTTTCTTGACATCTTACAGCCGCGTGATCCCGTGCGTCT TTCGGCGGCTGAGACCTCAACATGTAACAAGATGGGCCGTCTTGGACGCAACGTGGCTCTCGAGACGCCCTTTAC CTGCGACTATGGCTACAATATATTTATCGGGAATCAAGTTCTCATTAAGCGCAACTGCACCATTAATGACGCTGG CGAAGTCAATATTGGTGATCATTGTGTCATTGGCCCCAATGTGAGCATTTTTACCTCGTCTTTGCCAGTGGACCC CAAGAAACGTCAGGGTGGGCTAGGTCCCCAACATGCAAAGAGTGTCAGTATTGAACAAGACTGTTGGATTGGAGG CGGCGCCATCATTCTGCCCGGCCGCACTATTGGAAAGGGGAGCACTGTTGGCGCCGGGTCTGTGGTGACAAAGGT ATGCTTTCTTTCTTTTTCTTTTTTTTTTTTTTTGTTTTTGAATCCATTTGGCAGTTTGCCATTGCGCAGTAGCTG ACCGCCGAGGAAGGATGTTCCTCCTTTTACTGTCGTGGCAGGAAATCCCGCCCGCGTTCTTCGCGGCGTCGGTAT ATGA |