Protein ID | Ophio5|3405 |
Gene name | |
Location | scaffold_27:47124..48246 |
Strand | - |
Gene length (bp) | 1122 |
Transcript length (bp) | 1062 |
Coding sequence length (bp) | 1059 |
Protein length (aa) | 353 |
PFAM Domain ID | Short name | Long name | E-value | Start | End |
---|---|---|---|---|---|
PF01370 | Epimerase | NAD dependent epimerase/dehydratase family | 1.1E-15 | 10 | 193 |
PF16363 | GDP_Man_Dehyd | GDP-mannose 4,6 dehydratase | 1.4E-11 | 11 | 131 |
PF01073 | 3Beta_HSD | 3-beta hydroxysteroid dehydrogenase/isomerase family | 9.9E-10 | 11 | 158 |
PF07993 | NAD_binding_4 | Male sterility protein | 2.1E-07 | 12 | 195 |
PF13460 | NAD_binding_10 | NAD(P)H-binding | 7.7E-09 | 14 | 135 |
PF05368 | NmrA | NmrA-like family | 4.4E-06 | 10 | 130 |
PF02719 | Polysacc_synt_2 | Polysaccharide biosynthesis protein | 2.0E-05 | 10 | 135 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|Q9UUN9|ALD2_SPOSA | Aldehyde reductase 2 OS=Sporidiobolus salmonicolor PE=1 SV=3 | 4 | 341 | 4.0E-79 |
sp|Q9UT59|YKJ7_SCHPO | Putative uncharacterized oxidoreductase C513.07 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC513.07 PE=3 SV=1 | 6 | 285 | 3.0E-33 |
sp|P83775|GRP2_CANAL | Putative NADPH-dependent methylglyoxal reductase GRP2 OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=GRP2 PE=1 SV=2 | 4 | 285 | 1.0E-27 |
sp|Q9XES5|DFRA_MALDO | Bifunctional dihydroflavonol 4-reductase/flavanone 4-reductase OS=Malus domestica GN=DFR PE=1 SV=1 | 10 | 216 | 7.0E-25 |
sp|Q84KP0|DFRA_PYRCO | Bifunctional dihydroflavonol 4-reductase/flavanone 4-reductase OS=Pyrus communis GN=DFR PE=1 SV=1 | 10 | 216 | 9.0E-25 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|Q9UUN9|ALD2_SPOSA | Aldehyde reductase 2 OS=Sporidiobolus salmonicolor PE=1 SV=3 | 4 | 341 | 4.0E-79 |
sp|Q9UT59|YKJ7_SCHPO | Putative uncharacterized oxidoreductase C513.07 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC513.07 PE=3 SV=1 | 6 | 285 | 3.0E-33 |
sp|P83775|GRP2_CANAL | Putative NADPH-dependent methylglyoxal reductase GRP2 OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=GRP2 PE=1 SV=2 | 4 | 285 | 1.0E-27 |
sp|Q9XES5|DFRA_MALDO | Bifunctional dihydroflavonol 4-reductase/flavanone 4-reductase OS=Malus domestica GN=DFR PE=1 SV=1 | 10 | 216 | 7.0E-25 |
sp|Q84KP0|DFRA_PYRCO | Bifunctional dihydroflavonol 4-reductase/flavanone 4-reductase OS=Pyrus communis GN=DFR PE=1 SV=1 | 10 | 216 | 9.0E-25 |
sp|P51102|DFRA_ARATH | Dihydroflavonol-4-reductase OS=Arabidopsis thaliana GN=DFRA PE=1 SV=2 | 10 | 216 | 2.0E-24 |
sp|P51110|DFRA_VITVI | Dihydroflavonol-4-reductase OS=Vitis vinifera GN=DFR PE=1 SV=1 | 10 | 216 | 2.0E-23 |
sp|O94563|YGD4_SCHPO | Putative uncharacterized oxidoreductase C1773.04 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPBC1773.04 PE=1 SV=1 | 9 | 282 | 3.0E-23 |
sp|Q500U8|TKPR1_ARATH | Tetraketide alpha-pyrone reductase 1 OS=Arabidopsis thaliana GN=TKPR1 PE=1 SV=1 | 10 | 341 | 4.0E-22 |
sp|Q12068|GRE2_YEAST | NADPH-dependent methylglyoxal reductase GRE2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=GRE2 PE=1 SV=1 | 10 | 283 | 4.0E-21 |
sp|P51106|DFRA_HORVU | Dihydroflavonol-4-reductase OS=Hordeum vulgare GN=ANT18 PE=3 SV=1 | 6 | 216 | 2.0E-20 |
sp|Q9CA28|TKPR2_ARATH | Tetraketide alpha-pyrone reductase 2 OS=Arabidopsis thaliana GN=TKPR2 PE=1 SV=1 | 11 | 351 | 5.0E-20 |
sp|P51105|DFRA_GERHY | Dihydroflavonol-4-reductase OS=Gerbera hybrida GN=DFR PE=2 SV=1 | 10 | 216 | 7.0E-20 |
sp|P51109|DFRA_MEDSA | Dihydroflavonol-4-reductase (Fragment) OS=Medicago sativa GN=DFR1 PE=2 SV=1 | 20 | 216 | 9.0E-20 |
sp|P53183|YGD9_YEAST | Putative uncharacterized oxidoreductase YGL039W OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=YGL039W PE=1 SV=1 | 8 | 320 | 1.0E-19 |
sp|P53111|ARI1_YEAST | NADPH-dependent aldehyde reductase ARI1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=ARI1 PE=1 SV=1 | 8 | 283 | 6.0E-19 |
sp|P51107|DFRA_SOLLC | Dihydroflavonol-4-reductase OS=Solanum lycopersicum PE=2 SV=1 | 5 | 216 | 3.0E-18 |
sp|P14720|DFRA_PETHY | Dihydroflavonol-4-reductase OS=Petunia hybrida GN=DFRA PE=2 SV=2 | 3 | 216 | 5.0E-18 |
sp|P51104|DFRA_DIACA | Dihydroflavonol-4-reductase OS=Dianthus caryophyllus GN=A PE=2 SV=1 | 4 | 216 | 7.0E-18 |
sp|Q03049|YD541_YEAST | Putative uncharacterized oxidoreductase YDR541C OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=YDR541C PE=3 SV=2 | 10 | 285 | 3.0E-17 |
sp|P14721|DFRA_ANTMA | Dihydroflavonol-4-reductase OS=Antirrhinum majus GN=DFRA PE=2 SV=1 | 3 | 216 | 3.0E-17 |
sp|P51108|DFRA_MAIZE | Dihydroflavonol-4-reductase OS=Zea mays GN=A1 PE=3 SV=1 | 10 | 151 | 8.0E-17 |
sp|Q9SEV0|BAN_ARATH | Anthocyanidin reductase OS=Arabidopsis thaliana GN=BAN PE=1 SV=2 | 12 | 201 | 1.0E-15 |
sp|Q40316|VESTR_MEDSA | Vestitone reductase OS=Medicago sativa PE=1 SV=1 | 10 | 266 | 1.0E-14 |
sp|Q9SAH9|CCR2_ARATH | Cinnamoyl-CoA reductase 2 OS=Arabidopsis thaliana GN=CCR2 PE=1 SV=1 | 6 | 184 | 2.0E-14 |
sp|Q9S9N9|CCR1_ARATH | Cinnamoyl-CoA reductase 1 OS=Arabidopsis thaliana GN=CCR1 PE=1 SV=1 | 3 | 151 | 8.0E-14 |
sp|P51103|DFRA_CALCH | Dihydroflavonol-4-reductase OS=Callistephus chinensis GN=F PE=2 SV=1 | 10 | 216 | 9.0E-14 |
sp|O22133|BEN1_ARATH | Protein BRI1-5 ENHANCED 1 OS=Arabidopsis thaliana GN=BEN1 PE=2 SV=1 | 9 | 216 | 5.0E-09 |
sp|P73212|DFRA_SYNY3 | Putative dihydroflavonol-4-reductase OS=Synechocystis sp. (strain PCC 6803 / Kazusa) GN=dfrA PE=3 SV=1 | 11 | 201 | 3.0E-08 |
GO Term | Description | Terminal node |
---|---|---|
GO:0016616 | oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor | Yes |
GO:0006694 | steroid biosynthetic process | Yes |
GO:0003854 | 3-beta-hydroxy-delta5-steroid dehydrogenase activity | Yes |
GO:1901360 | organic cyclic compound metabolic process | No |
GO:0009058 | biosynthetic process | No |
GO:0008150 | biological_process | No |
GO:0016614 | oxidoreductase activity, acting on CH-OH group of donors | No |
GO:0044238 | primary metabolic process | No |
GO:0016491 | oxidoreductase activity | No |
GO:0016229 | steroid dehydrogenase activity | No |
GO:1901576 | organic substance biosynthetic process | No |
GO:0008152 | metabolic process | No |
GO:0003674 | molecular_function | No |
GO:0033764 | steroid dehydrogenase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor | No |
GO:0008202 | steroid metabolic process | No |
GO:0071704 | organic substance metabolic process | No |
GO:0006629 | lipid metabolic process | No |
GO:0008610 | lipid biosynthetic process | No |
GO:1901362 | organic cyclic compound biosynthetic process | No |
GO:0003824 | catalytic activity | No |
Localizations | Signals | Cytoplasm | Nucleus | Extracellular | Cell membrane | Mitochondrion | Plastid | Endoplasmic reticulum | Lysosome vacuole | Golgi apparatus | Peroxisome |
---|---|---|---|---|---|---|---|---|---|---|---|
Cytoplasm | Peroxisomal targeting signal | 0.5551 | 0.2411 | 0.3822 | 0.1219 | 0.1909 | 0.0158 | 0.308 | 0.203 | 0.196 | 0.2755 |
Orthofinder run ID | 4 |
Orthogroup | 969 |
Change Orthofinder run |
Type of sequence | Sequence |
---|---|
Locus | Download genbank file of locus
Download genbank file of locus (reverse complement)
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 | >Ophio5|3405 MPAIPNGSLILVTGVNGYIGSHVAEQLLEHGFRVRGTVRDAYKAEYMRAIFDEKYGKDAFEVRTVEDMATSGAFD DVMKGCTGVMHVASDLTLNPDPHKVIPMVVSGVQNVLAAAAREPSVKRFVFTSSSAAATPPISNKRFHVDAETWN DEEIEVAWAPPPYNDDRKLAVYAASKTLAEKECWRFMQEEKPSFVLNTVLPNCNIGRILSEDQPASTGGWYKKLW EGDEEILDLLWNFPPQHFVNTTDTALLHLAALREEDVVGERLLAFAGPFNFNDTVDVLEKIQADGFGDGSKRFTK ISSTAKDLKIVDTKRSQELLRRYNRPGFASLEESLKEVVESCRVFAQKRSLQG |
Coding | >Ophio5|3405 ATGCCGGCCATCCCGAATGGATCCCTCATCCTTGTTACAGGCGTAAATGGATACATCGGCAGTCATGTCGCCGAA CAACTCCTCGAGCATGGCTTTCGCGTTCGTGGCACCGTCCGTGATGCCTACAAGGCCGAGTACATGCGTGCAATT TTCGATGAGAAGTACGGCAAAGATGCTTTTGAAGTTCGCACAGTCGAGGATATGGCCACAAGCGGCGCCTTTGAC GATGTTATGAAGGGCTGTACAGGCGTCATGCACGTTGCTTCTGATCTTACGCTCAATCCGGATCCTCACAAAGTC ATACCTATGGTGGTTTCTGGTGTTCAAAACGTACTCGCAGCAGCGGCACGGGAACCAAGCGTGAAACGCTTCGTC TTCACTTCATCGAGCGCCGCGGCAACACCACCTATTTCAAACAAGAGGTTTCACGTCGATGCGGAAACGTGGAAC GACGAAGAAATCGAAGTAGCGTGGGCGCCCCCGCCCTATAACGACGACAGGAAGCTGGCTGTGTATGCAGCGAGC AAGACGCTAGCAGAGAAGGAGTGTTGGCGCTTTATGCAGGAAGAGAAGCCGTCATTCGTTCTCAACACCGTTTTG CCTAATTGCAACATTGGTAGAATCCTGTCCGAGGACCAGCCGGCGTCGACGGGCGGTTGGTATAAAAAGCTCTGG GAGGGAGACGAGGAGATCCTCGACCTTTTGTGGAACTTTCCACCTCAACACTTCGTCAACACAACCGACACAGCG CTTTTACACCTCGCAGCTTTACGCGAAGAGGACGTTGTTGGGGAGAGGCTCCTGGCATTTGCGGGCCCGTTCAAC TTTAACGACACGGTGGATGTACTGGAGAAGATCCAGGCCGACGGCTTTGGAGACGGTAGCAAGCGATTCACCAAG ATCTCCAGCACGGCAAAAGACCTGAAGATTGTGGATACGAAGAGATCTCAGGAACTCCTACGGAGATACAACAGG CCGGGATTTGCGAGCTTGGAGGAGTCATTGAAGGAGGTCGTCGAGTCCTGCCGGGTCTTTGCCCAGAAGCGTTCT CTACAGGGC |
Transcript | >Ophio5|3405 ATGCCGGCCATCCCGAATGGATCCCTCATCCTTGTTACAGGCGTAAATGGATACATCGGCAGTCATGTCGCCGAA CAACTCCTCGAGCATGGCTTTCGCGTTCGTGGCACCGTCCGTGATGCCTACAAGGCCGAGTACATGCGTGCAATT TTCGATGAGAAGTACGGCAAAGATGCTTTTGAAGTTCGCACAGTCGAGGATATGGCCACAAGCGGCGCCTTTGAC GATGTTATGAAGGGCTGTACAGGCGTCATGCACGTTGCTTCTGATCTTACGCTCAATCCGGATCCTCACAAAGTC ATACCTATGGTGGTTTCTGGTGTTCAAAACGTACTCGCAGCAGCGGCACGGGAACCAAGCGTGAAACGCTTCGTC TTCACTTCATCGAGCGCCGCGGCAACACCACCTATTTCAAACAAGAGGTTTCACGTCGATGCGGAAACGTGGAAC GACGAAGAAATCGAAGTAGCGTGGGCGCCCCCGCCCTATAACGACGACAGGAAGCTGGCTGTGTATGCAGCGAGC AAGACGCTAGCAGAGAAGGAGTGTTGGCGCTTTATGCAGGAAGAGAAGCCGTCATTCGTTCTCAACACCGTTTTG CCTAATTGCAACATTGGTAGAATCCTGTCCGAGGACCAGCCGGCGTCGACGGGCGGTTGGTATAAAAAGCTCTGG GAGGGAGACGAGGAGATCCTCGACCTTTTGTGGAACTTTCCACCTCAACACTTCGTCAACACAACCGACACAGCG CTTTTACACCTCGCAGCTTTACGCGAAGAGGACGTTGTTGGGGAGAGGCTCCTGGCATTTGCGGGCCCGTTCAAC TTTAACGACACGGTGGATGTACTGGAGAAGATCCAGGCCGACGGCTTTGGAGACGGTAGCAAGCGATTCACCAAG ATCTCCAGCACGGCAAAAGACCTGAAGATTGTGGATACGAAGAGATCTCAGGAACTCCTACGGAGATACAACAGG CCGGGATTTGCGAGCTTGGAGGAGTCATTGAAGGAGGTCGTCGAGTCCTGCCGGGTCTTTGCCCAGAAGCGTTCT CTACAGGGCTGA |
Gene | >Ophio5|3405 ATGCCGGCCATCCCGAATGGATCCCTCATCCTTGTTACAGGCGTAAATGGATACATCGGCAGTCATGTCGCCGAA CAACTCCTCGAGCATGGCTTTCGCGTTCGTGGCACCGTCCGTGATGCCTACAAGGCCGAGTACATGCGTGCAATT TTCGATGAGAAGTACGGCAAAGATGCTTTTGAAGTTCGCACAGTCGAGGATATGGCCACAAGCGGCGCCTTTGAC GATGTTATGAAGGGTGGGATCCCACGCCTCGACACGCAGCCGCAGGAGCCAGATCTAAACTAACACTTTACAGGC TGTACAGGCGTCATGCACGTTGCTTCTGATCTTACGCTCAATCCGGATCCTCACAAAGTCATACCTATGGTGGTT TCTGGTGTTCAAAACGTACTCGCAGCAGCGGCACGGGAACCAAGCGTGAAACGCTTCGTCTTCACTTCATCGAGC GCCGCGGCAACACCACCTATTTCAAACAAGAGGTTTCACGTCGATGCGGAAACGTGGAACGACGAAGAAATCGAA GTAGCGTGGGCGCCCCCGCCCTATAACGACGACAGGAAGCTGGCTGTGTATGCAGCGAGCAAGACGCTAGCAGAG AAGGAGTGTTGGCGCTTTATGCAGGAAGAGAAGCCGTCATTCGTTCTCAACACCGTTTTGCCTAATTGCAACATT GGTAGAATCCTGTCCGAGGACCAGCCGGCGTCGACGGGCGGTTGGTATAAAAAGCTCTGGGAGGGAGACGAGGAG ATCCTCGACCTTTTGTGGAACTTTCCACCTCAACACTTCGTCAACACAACCGACACAGCGCTTTTACACCTCGCA GCTTTACGCGAAGAGGACGTTGTTGGGGAGAGGCTCCTGGCATTTGCGGGCCCGTTCAACTTTAACGACACGGTG GATGTACTGGAGAAGATCCAGGCCGACGGCTTTGGAGACGGTAGCAAGCGATTCACCAAGATCTCCAGCACGGCA AAAGACCTGAAGATTGTGGATACGAAGAGATCTCAGGAACTCCTACGGAGATACAACAGGCCGGGATTTGCGAGC TTGGAGGAGTCATTGAAGGAGGTCGTCGAGTCCTGCCGGGTCTTTGCCCAGAAGCGTTCTCTACAGGGCTGA |