© 2022 - Robin Ohm - Utrecht University - The Netherlands
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| Protein ID | AgabiH97|022100 |
| Gene name | |
| Location | scaffold_11:158985..160660 |
| Strand | - |
| Gene length (bp) | 1675 |
| Transcript length (bp) | 1104 |
| Coding sequence length (bp) | 1104 |
| Protein length (aa) | 368 |
| PFAM Domain ID | Short name | Long name | E-value | Start | End |
|---|---|---|---|---|---|
| PF01370 | Epimerase | NAD dependent epimerase/dehydratase family | 3.0E-15 | 10 | 276 |
| PF01073 | 3Beta_HSD | 3-beta hydroxysteroid dehydrogenase/isomerase family | 9.9E-11 | 11 | 279 |
| PF13460 | NAD_binding_10 | NAD(P)H-binding | 2.1E-07 | 14 | 136 |
| PF07993 | NAD_binding_4 | Male sterility protein | 3.0E-06 | 67 | 221 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|Q12068|GRE2_YEAST | NADPH-dependent methylglyoxal reductase GRE2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=GRE2 PE=1 SV=1 | 10 | 336 | 3.0E-50 |
| sp|Q9UT59|YKJ7_SCHPO | Putative uncharacterized oxidoreductase C513.07 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC513.07 PE=3 SV=1 | 10 | 279 | 3.0E-45 |
| sp|Q03049|YD541_YEAST | Putative uncharacterized oxidoreductase YDR541C OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=YDR541C PE=3 SV=2 | 10 | 336 | 4.0E-44 |
| sp|P83775|GRP2_CANAL | Putative NADPH-dependent methylglyoxal reductase GRP2 OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=GRP2 PE=1 SV=2 | 10 | 329 | 3.0E-42 |
| sp|P53111|ARI1_YEAST | NADPH-dependent aldehyde reductase ARI1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=ARI1 PE=1 SV=1 | 10 | 329 | 3.0E-41 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|Q12068|GRE2_YEAST | NADPH-dependent methylglyoxal reductase GRE2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=GRE2 PE=1 SV=1 | 10 | 336 | 3.0E-50 |
| sp|Q9UT59|YKJ7_SCHPO | Putative uncharacterized oxidoreductase C513.07 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC513.07 PE=3 SV=1 | 10 | 279 | 3.0E-45 |
| sp|Q03049|YD541_YEAST | Putative uncharacterized oxidoreductase YDR541C OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=YDR541C PE=3 SV=2 | 10 | 336 | 4.0E-44 |
| sp|P83775|GRP2_CANAL | Putative NADPH-dependent methylglyoxal reductase GRP2 OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=GRP2 PE=1 SV=2 | 10 | 329 | 3.0E-42 |
| sp|P53111|ARI1_YEAST | NADPH-dependent aldehyde reductase ARI1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=ARI1 PE=1 SV=1 | 10 | 329 | 3.0E-41 |
| sp|P53183|YGD9_YEAST | Putative uncharacterized oxidoreductase YGL039W OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=YGL039W PE=1 SV=1 | 10 | 336 | 9.0E-40 |
| sp|Q500U8|TKPR1_ARATH | Tetraketide alpha-pyrone reductase 1 OS=Arabidopsis thaliana GN=TKPR1 PE=1 SV=1 | 8 | 273 | 2.0E-32 |
| sp|Q9CA28|TKPR2_ARATH | Tetraketide alpha-pyrone reductase 2 OS=Arabidopsis thaliana GN=TKPR2 PE=1 SV=1 | 8 | 312 | 9.0E-32 |
| sp|P51102|DFRA_ARATH | Dihydroflavonol-4-reductase OS=Arabidopsis thaliana GN=DFRA PE=1 SV=2 | 3 | 300 | 1.0E-31 |
| sp|Q9S9N9|CCR1_ARATH | Cinnamoyl-CoA reductase 1 OS=Arabidopsis thaliana GN=CCR1 PE=1 SV=1 | 5 | 297 | 7.0E-30 |
| sp|Q9UUN9|ALD2_SPOSA | Aldehyde reductase 2 OS=Sporidiobolus salmonicolor PE=1 SV=3 | 3 | 211 | 1.0E-28 |
| sp|Q9SAH9|CCR2_ARATH | Cinnamoyl-CoA reductase 2 OS=Arabidopsis thaliana GN=CCR2 PE=1 SV=1 | 10 | 330 | 6.0E-28 |
| sp|P51104|DFRA_DIACA | Dihydroflavonol-4-reductase OS=Dianthus caryophyllus GN=A PE=2 SV=1 | 10 | 300 | 7.0E-26 |
| sp|P51105|DFRA_GERHY | Dihydroflavonol-4-reductase OS=Gerbera hybrida GN=DFR PE=2 SV=1 | 7 | 282 | 9.0E-26 |
| sp|P14721|DFRA_ANTMA | Dihydroflavonol-4-reductase OS=Antirrhinum majus GN=DFRA PE=2 SV=1 | 5 | 282 | 4.0E-25 |
| sp|P14720|DFRA_PETHY | Dihydroflavonol-4-reductase OS=Petunia hybrida GN=DFRA PE=2 SV=2 | 5 | 281 | 8.0E-25 |
| sp|Q84KP0|DFRA_PYRCO | Bifunctional dihydroflavonol 4-reductase/flavanone 4-reductase OS=Pyrus communis GN=DFR PE=1 SV=1 | 10 | 273 | 8.0E-25 |
| sp|Q9XES5|DFRA_MALDO | Bifunctional dihydroflavonol 4-reductase/flavanone 4-reductase OS=Malus domestica GN=DFR PE=1 SV=1 | 10 | 273 | 8.0E-25 |
| sp|O22133|BEN1_ARATH | Protein BRI1-5 ENHANCED 1 OS=Arabidopsis thaliana GN=BEN1 PE=2 SV=1 | 10 | 330 | 1.0E-24 |
| sp|P51107|DFRA_SOLLC | Dihydroflavonol-4-reductase OS=Solanum lycopersicum PE=2 SV=1 | 5 | 281 | 5.0E-24 |
| sp|P51110|DFRA_VITVI | Dihydroflavonol-4-reductase OS=Vitis vinifera GN=DFR PE=1 SV=1 | 10 | 273 | 3.0E-23 |
| sp|O94563|YGD4_SCHPO | Putative uncharacterized oxidoreductase C1773.04 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPBC1773.04 PE=1 SV=1 | 10 | 343 | 7.0E-23 |
| sp|P51109|DFRA_MEDSA | Dihydroflavonol-4-reductase (Fragment) OS=Medicago sativa GN=DFR1 PE=2 SV=1 | 22 | 227 | 2.0E-22 |
| sp|Q40316|VESTR_MEDSA | Vestitone reductase OS=Medicago sativa PE=1 SV=1 | 8 | 269 | 2.0E-21 |
| sp|P51103|DFRA_CALCH | Dihydroflavonol-4-reductase OS=Callistephus chinensis GN=F PE=2 SV=1 | 7 | 282 | 4.0E-21 |
| sp|P51106|DFRA_HORVU | Dihydroflavonol-4-reductase OS=Hordeum vulgare GN=ANT18 PE=3 SV=1 | 10 | 224 | 8.0E-21 |
| sp|Q9SEV0|BAN_ARATH | Anthocyanidin reductase OS=Arabidopsis thaliana GN=BAN PE=1 SV=2 | 9 | 298 | 1.0E-20 |
| sp|P51108|DFRA_MAIZE | Dihydroflavonol-4-reductase OS=Zea mays GN=A1 PE=3 SV=1 | 10 | 331 | 3.0E-19 |
| sp|P73212|DFRA_SYNY3 | Putative dihydroflavonol-4-reductase OS=Synechocystis sp. (strain PCC 6803 / Kazusa) GN=dfrA PE=3 SV=1 | 11 | 274 | 4.0E-09 |
| sp|P27365|3BHS1_MACMU | 3 beta-hydroxysteroid dehydrogenase/Delta 5-->4-isomerase type 1 OS=Macaca mulatta GN=HSD3B1 PE=2 SV=2 | 10 | 263 | 3.0E-06 |
| sp|O46516|3BHS_HORSE | 3 beta-hydroxysteroid dehydrogenase/Delta 5-->4-isomerase OS=Equus caballus GN=HSD3B PE=2 SV=3 | 10 | 263 | 5.0E-06 |
| sp|P14060|3BHS1_HUMAN | 3 beta-hydroxysteroid dehydrogenase/Delta 5-->4-isomerase type 1 OS=Homo sapiens GN=HSD3B1 PE=1 SV=2 | 10 | 263 | 9.0E-06 |
| GO Term | Description | Terminal node |
|---|---|---|
| GO:0016616 | oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor | Yes |
| GO:0003854 | 3-beta-hydroxy-delta5-steroid dehydrogenase activity | Yes |
| GO:0006694 | steroid biosynthetic process | Yes |
| GO:1901576 | organic substance biosynthetic process | No |
| GO:0033764 | steroid dehydrogenase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor | No |
| GO:0009058 | biosynthetic process | No |
| GO:1901360 | organic cyclic compound metabolic process | No |
| GO:0071704 | organic substance metabolic process | No |
| GO:0008150 | biological_process | No |
| GO:0016229 | steroid dehydrogenase activity | No |
| GO:0008202 | steroid metabolic process | No |
| GO:0016614 | oxidoreductase activity, acting on CH-OH group of donors | No |
| GO:0008152 | metabolic process | No |
| GO:0003674 | molecular_function | No |
| GO:1901362 | organic cyclic compound biosynthetic process | No |
| GO:0044238 | primary metabolic process | No |
| GO:0008610 | lipid biosynthetic process | No |
| GO:0003824 | catalytic activity | No |
| GO:0016491 | oxidoreductase activity | No |
| GO:0006629 | lipid metabolic process | No |
| SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
|---|---|---|
| No | 1 - 34 | 0.5 |
| 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 | >AgabiH97|022100 MTIVPPPAKVLVTGANGYIAIWVVRLLLEQGYSVRGTVRSAGKGKYLSEYFGKLGFGDKLEIVVVEDITKEGAFD QAVQGVDAIEHTASPFITSLVNLSDFVDPAVRGTVGVLQSAIKHAPNVKRIVITSSCGAVMAPPPQPTIFSETDW NTSSQVDIDKNGVNADPLSKYRVSKTLAEKAAWEFYEKHKGSIGWELVVINPPFVFGPPIQEITGGPESLNTSLK PFYDALVGDGPKTEKLLSTSNSWVDVRDTALSHILAIQKEAAAGERIIVCGGAYLWQEWFDAANTIQPYPLPNHP PAKGMPGITAPYVIQYNAAKADKLLGIRYKTKAETIPRIEDSLKLYVLKLYTLLKRLLWTKIYVFLT* |
| Coding | >AgabiH97|022100 ATGACTATTGTTCCTCCGCCTGCTAAAGTCTTAGTCACCGGTGCAAATGGCTATATCGCCATTTGGGTCGTTCGG CTACTGCTTGAACAAGGTTATTCAGTCAGAGGAACGGTCCGGTCCGCGGGGAAAGGGAAGTACTTGTCCGAATAC TTCGGCAAGCTAGGTTTTGGCGATAAGCTTGAAATAGTGGTAGTCGAGGATATCACAAAGGAAGGCGCATTCGAT CAAGCTGTGCAAGGCGTTGATGCTATTGAACACACGGCCTCTCCGTTTATAACCAGCCTTGTTAATCTATCTGAT TTCGTCGATCCCGCCGTCCGAGGAACAGTTGGTGTCCTTCAGAGCGCAATCAAGCATGCTCCAAACGTGAAGCGT ATCGTGATCACCTCTTCATGTGGTGCTGTTATGGCTCCTCCACCTCAGCCGACGATATTCTCGGAAACAGATTGG AATACCAGTTCCCAAGTGGACATTGACAAGAATGGCGTCAACGCTGACCCTCTATCCAAGTATCGCGTATCCAAG ACTCTTGCAGAAAAGGCCGCATGGGAGTTTTACGAAAAGCATAAAGGCAGTATTGGATGGGAACTAGTGGTTATC AACCCTCCATTTGTATTTGGACCTCCAATTCAAGAAATAACCGGCGGACCGGAAAGCCTTAATACATCTCTCAAA CCTTTCTATGACGCTCTCGTAGGCGATGGGCCGAAAACGGAAAAACTCTTGTCTACGTCTAATTCGTGGGTAGAC GTCCGAGATACTGCATTAAGCCATATACTGGCTATTCAAAAAGAAGCTGCTGCCGGTGAGAGGATTATCGTATGT GGTGGGGCGTATCTTTGGCAAGAATGGTTCGACGCTGCGAATACGATCCAACCGTACCCACTCCCGAATCATCCT CCCGCGAAAGGCATGCCAGGAATTACAGCACCCTATGTTATTCAATACAACGCGGCGAAAGCGGATAAACTTTTA GGAATCAGATACAAGACGAAGGCAGAGACTATCCCAAGAATTGAGGATTCATTAAAGTTATATGTGTTAAAACTG TATACCTTATTGAAAAGACTGCTGTGGACGAAAATCTATGTTTTTTTGACCTGA |
| Transcript | >AgabiH97|022100 ATGACTATTGTTCCTCCGCCTGCTAAAGTCTTAGTCACCGGTGCAAATGGCTATATCGCCATTTGGGTCGTTCGG CTACTGCTTGAACAAGGTTATTCAGTCAGAGGAACGGTCCGGTCCGCGGGGAAAGGGAAGTACTTGTCCGAATAC TTCGGCAAGCTAGGTTTTGGCGATAAGCTTGAAATAGTGGTAGTCGAGGATATCACAAAGGAAGGCGCATTCGAT CAAGCTGTGCAAGGCGTTGATGCTATTGAACACACGGCCTCTCCGTTTATAACCAGCCTTGTTAATCTATCTGAT TTCGTCGATCCCGCCGTCCGAGGAACAGTTGGTGTCCTTCAGAGCGCAATCAAGCATGCTCCAAACGTGAAGCGT ATCGTGATCACCTCTTCATGTGGTGCTGTTATGGCTCCTCCACCTCAGCCGACGATATTCTCGGAAACAGATTGG AATACCAGTTCCCAAGTGGACATTGACAAGAATGGCGTCAACGCTGACCCTCTATCCAAGTATCGCGTATCCAAG ACTCTTGCAGAAAAGGCCGCATGGGAGTTTTACGAAAAGCATAAAGGCAGTATTGGATGGGAACTAGTGGTTATC AACCCTCCATTTGTATTTGGACCTCCAATTCAAGAAATAACCGGCGGACCGGAAAGCCTTAATACATCTCTCAAA CCTTTCTATGACGCTCTCGTAGGCGATGGGCCGAAAACGGAAAAACTCTTGTCTACGTCTAATTCGTGGGTAGAC GTCCGAGATACTGCATTAAGCCATATACTGGCTATTCAAAAAGAAGCTGCTGCCGGTGAGAGGATTATCGTATGT GGTGGGGCGTATCTTTGGCAAGAATGGTTCGACGCTGCGAATACGATCCAACCGTACCCACTCCCGAATCATCCT CCCGCGAAAGGCATGCCAGGAATTACAGCACCCTATGTTATTCAATACAACGCGGCGAAAGCGGATAAACTTTTA GGAATCAGATACAAGACGAAGGCAGAGACTATCCCAAGAATTGAGGATTCATTAAAGTTATATGTGTTAAAACTG TATACCTTATTGAAAAGACTGCTGTGGACGAAAATCTATGTTTTTTTGACCTGA |
| Gene | >AgabiH97|022100 ATGACTATTGTTCCTCCGCCTGCTAAAGTCTTAGTCACCGGTGCAAATGGCTATATCGCCATTTGGGTCGTTCGG CTACTGCTTGAACAAGGTTATTCAGTCAGAGGAACGGTCCGGTCCGCGGGGAAAGGGAAGTACTTGTCCGAATAC TTCGGCAAGCTAGGTTTTGGCGATAAGCTTGAAATAGTGGTAGTCGAGGATATCACAAAGGTGATATATCTTGCC AACGTTATCTCTGTTCAACTCAATTCGTACGGTAACAGGAAGGCGCATTCGATCAAGCTGTGCAAGGCGTTGATG CTATTGAACACACGGCCTCTCCGTTTATAACCAGCCTTGTTAATCTATCTGGTACTTTCCCTATCCCTATCTATC CTATTCTCTATGTTTACAGTCTTGCTTAGATTTCGTCGATCCCGCCGTCCGAGGAACAGTTGGTGTCCTTCAGAG CGCAATCAAGCATGCGTGCGCATCTCCTGGAGCTCTATCTTTGAAGATCATATATGCTGATAACTGCCAATTAGT CCAAACGTGAAGCGTATCGTGATCACCTCTTCATGTGGTGCTGTTATGGCTCCTCCACCTCAGCCGACGATATTC TCGGAAACAGATTGGAATACCAGTTCCCAAGTGGACATTGACAAGAATGGCGTCAACGCTGACCCTCTATCCAAG TATCGCGTATCCAAGACTCTTGCAGAAAAGGGTGCGGCGGTATTCTCAGCCCCAGTCATGAGTTATCTTCTGACA AAATCACAGCCGCATGGGAGTTTTACGAAAAGCATAAAGGCAGTATTGGATGGGAACTAGTGGTTATCAACCCTC CATTTGTACGTTACATTAATCTGTGTCAAGTTTTCTGAACGTGACTCGCTTTCTAGGTATTTGGAGTAAGTTTAC TTGCCAGTATCTTTTAACACCGGATAGGCCTGACGCATACCGTAGCCTCCAATTCAAGAAATAACCGGCGGACCG GAAAGCCTTAATACATCTCTCAAACCTTTCTATGACGCTCTCGTAGGCGATGGGCCGAAAACGGAAAAACTCTTG TCTACGTCTAATTCGTGGGTAGACGTCCGAGATACTGCATTAAGCCATATACTGGCTATTCAAAAAGAAGCTGCT GCCGGTGAGAGGATTATCGTATGTGGTGGTATGTATAGATGATTATGTCAAATTATGATAATCTAACTTATGTCT TATGAATCCCAGGGGCGTATCTTTGGCAAGAATGGTGTATGTCAATTAGCCTCTAGCCCGAAGTATTGATGCGAT TAGAACTGACGTTCTTTTTTTCTTTTTTGGATTTGCTCTACCAGTCGACGCTGCGAATACGATCCAACCGTACCC ACTCCCGAATCATCCTCCCGCGAAAGGCATGCCAGGAATTACAGCACCCTATGTTATTCAATACAACGCGGCGAA AGCGGATAAACTTTTAGGAATCAGATACAAGACGAAGGCAGAGACTATCCGTGATACGTTGGAAATATTCGCTGC GAAAGGATGGTAATGCTAGGTGCAAAGTAGCAAGAATTGAGGTGAGTCGGGACAGTGTTATATACTCAATTTGTG ATTGACGCTCTGGAAGGATTCATTAAAGTTATATGTGTTAAAACTGTATACCTTATTGAAAAGACTGCTGTGGAC GAAAATCTATGTTTTTTTGACCTGA |