Fungal Genomics

at Utrecht University

General Properties

Protein IDOphio5|7924
Gene name
Locationscaffold_82:23197..25015
Strand+
Gene length (bp)1818
Transcript length (bp)1761
Coding sequence length (bp)1758
Protein length (aa) 586

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PFAM Domains

PFAM Domain ID Short name Long name E-value Start End
PF01794 Ferric_reduct Ferric reductase like transmembrane component 3.6E-23 150 269
PF08030 NAD_binding_6 Ferric reductase NAD binding domain 2.8E-11 437 516
PF08022 FAD_binding_8 FAD-binding domain 3.0E-06 315 428

Swissprot hits

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Swissprot ID Swissprot Description Start End E-value
sp|P36033|FRE2_YEAST Ferric/cupric reductase transmembrane component 2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FRE2 PE=1 SV=1 87 586 4.0E-41
sp|Q08905|FRE3_YEAST Ferric reductase transmembrane component 3 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FRE3 PE=1 SV=1 87 586 2.0E-40
sp|P53746|FRE4_YEAST Ferric reductase transmembrane component 4 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FRE4 PE=2 SV=1 87 586 1.0E-32
sp|Q08908|FRE5_YEAST Ferric reductase transmembrane component 5 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FRE5 PE=2 SV=1 79 586 1.0E-30
sp|Q5A446|FRE1_CANAL Ferric/cupric reductase transmembrane component 1 OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=CFL1 PE=2 SV=1 79 568 5.0E-30
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Swissprot ID Swissprot Description Start End E-value
sp|P36033|FRE2_YEAST Ferric/cupric reductase transmembrane component 2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FRE2 PE=1 SV=1 87 586 4.0E-41
sp|Q08905|FRE3_YEAST Ferric reductase transmembrane component 3 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FRE3 PE=1 SV=1 87 586 2.0E-40
sp|P53746|FRE4_YEAST Ferric reductase transmembrane component 4 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FRE4 PE=2 SV=1 87 586 1.0E-32
sp|Q08908|FRE5_YEAST Ferric reductase transmembrane component 5 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FRE5 PE=2 SV=1 79 586 1.0E-30
sp|Q5A446|FRE1_CANAL Ferric/cupric reductase transmembrane component 1 OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=CFL1 PE=2 SV=1 79 568 5.0E-30
sp|P78588|FREL_CANAX Probable ferric reductase transmembrane component OS=Candida albicans GN=CFL1 PE=3 SV=1 79 568 6.0E-30
sp|P32791|FRE1_YEAST Ferric/cupric reductase transmembrane component 1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FRE1 PE=1 SV=1 147 586 3.0E-26
sp|Q12473|FRE6_YEAST Ferric reductase transmembrane component 6 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FRE6 PE=1 SV=1 79 586 1.0E-25
sp|Q12333|FRE7_YEAST Ferric/cupric reductase transmembrane component 7 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FRE7 PE=1 SV=2 148 530 5.0E-14
sp|A6ZN61|FRE7_YEAS7 Ferric/cupric reductase transmembrane component 7 OS=Saccharomyces cerevisiae (strain YJM789) GN=FRE7 PE=3 SV=1 148 530 8.0E-14
sp|Q04800|FRP1_SCHPO Ferric reductase transmembrane component 1 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=frp1 PE=1 SV=1 132 582 2.0E-13
sp|O94727|FRP2_SCHPO Ferric/cupric reductase transmembrane component 2 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=frp2 PE=3 SV=1 30 568 4.0E-12
sp|Q9ES45|DUOX2_RAT Dual oxidase 2 OS=Rattus norvegicus GN=Duox2 PE=2 SV=1 150 580 2.0E-11
sp|Q8HZK2|DUOX2_PIG Dual oxidase 2 OS=Sus scrofa GN=DUOX2 PE=1 SV=2 150 580 6.0E-10
sp|C8Z891|AIM14_YEAS8 Probable metalloreductase AIM14 OS=Saccharomyces cerevisiae (strain Lalvin EC1118 / Prise de mousse) GN=AIM14 PE=3 SV=1 184 511 3.0E-09
sp|A6ZU25|AIM14_YEAS7 Probable metalloreductase AIM14 OS=Saccharomyces cerevisiae (strain YJM789) GN=AIM14 PE=3 SV=1 184 511 6.0E-09
sp|B3LHL3|AIM14_YEAS1 Probable metalloreductase AIM14 OS=Saccharomyces cerevisiae (strain RM11-1a) GN=AIM14 PE=3 SV=1 184 511 6.0E-09
sp|P53109|AIM14_YEAST Probable metalloreductase AIM14 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=AIM14 PE=1 SV=1 184 511 1.0E-08
sp|C7GPP6|AIM14_YEAS2 Probable metalloreductase AIM14 OS=Saccharomyces cerevisiae (strain JAY291) GN=AIM14 PE=3 SV=1 184 511 1.0E-08
sp|P92949|FRO2_ARATH Ferric reduction oxidase 2 OS=Arabidopsis thaliana GN=FRO2 PE=1 SV=2 148 522 1.0E-06
sp|A7TQE6|AIM14_VANPO Probable metalloreductase AIM14 OS=Vanderwaltozyma polyspora (strain ATCC 22028 / DSM 70294) GN=AIM14 PE=3 SV=1 137 512 1.0E-06
sp|F4I4K7|FRO3_ARATH Ferric reduction oxidase 3, mitochondrial OS=Arabidopsis thaliana GN=FRO3 PE=2 SV=1 165 514 4.0E-06
sp|Q8HZK3|DUOX1_PIG Dual oxidase 1 OS=Sus scrofa GN=DUOX1 PE=2 SV=1 150 579 4.0E-06
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GO

GO Term Description Terminal node
GO:0016491 oxidoreductase activity Yes
GO:0003824 catalytic activity No
GO:0003674 molecular_function No

SignalP

[Help with interpreting these statistics]
SignalP signal predicted Location
(based on Ymax)		 D score
(significance: > 0.45)
No 1 - 58 0.5

Transmembrane Domains

Domain # Start End Length
1 27 49 22
2 112 134 22
3 149 171 22
4 191 213 22
5 223 245 22
6 250 272 22

Transcription Factor Class

(None)

Expression data

Analysis 1: Expression analysis during behavioral modification. Published in De Bekker et al., 2017.

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Sequences

Type of sequenceSequence
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 >Ophio5|7924
MDPSPSLQIRQADGTEDKPLNMIFKDVIWWTLGIVALTVLVVRILEILWAKLRQVSAMSQPRDKQAYWKVSQWNW
MPPLKKHLIYAPLLHKRHNREFRLSTAFNVGTLPSRLHTLLLLLYVGSNIAYLIALNWSVENKFAICAELRGRSG
TLAVVNMIPLIILAGRNNPLIPLLKVSFDTYNLLHRWMGRIVVAEVVVHTIAWAVPAVASSGWSAALAKTYKSIF
IGSGFWAAVAMMLLLLLAVSPFRHAFYETFLNLHIILAMASLIGTWIHCASGDLPALPWVVAVVGLWMADRLARL
SRLLFANWSSRGFTDALVEALPGEVSRVTLYLPRYVSIQPGTHAYLRFWGVRPWESHPFSVAWVEYDAANSLPTS
EKEPLTAVDRKTASTSVSFIIGAQTGMTRMLYNQASKSSSGIRARAAMEGPYAGHHNLDSYGHVVLFAGSTGITH
QISHVRHLLEGYNEGMVATRRLTLVWIIRTYETLEWVRPYMDMILRIPNRKDVLRIQVFVTRPQNPRDIVSASST
VKMFPGRPNIPLLLVKEVQDQIGAMSVSVCGPGGLADDVRGAVRAVQGDSVIDFIEESFTW
Coding >Ophio5|7924
ATGGATCCCTCACCTTCCCTGCAAATACGGCAGGCCGACGGCACTGAGGATAAGCCGTTGAATATGATATTCAAA
GACGTCATCTGGTGGACTCTGGGCATCGTCGCCCTGACTGTGCTCGTCGTCCGGATCCTGGAGATCCTGTGGGCG
AAGCTGCGTCAGGTGTCGGCCATGTCCCAACCACGGGACAAGCAGGCTTACTGGAAGGTGTCGCAATGGAACTGG
ATGCCGCCGCTGAAGAAGCATCTGATATACGCACCCCTTCTTCACAAGCGCCACAATCGAGAGTTCCGCCTCTCG
ACGGCCTTCAATGTCGGCACCCTGCCGTCACGGTTGCACACGCTGCTGCTGCTCCTCTACGTCGGCAGCAACATC
GCCTACTTGATTGCCCTCAACTGGAGCGTCGAAAACAAGTTCGCCATCTGCGCCGAGCTGCGCGGCCGCTCCGGC
ACGCTCGCCGTCGTCAACATGATCCCGCTCATCATACTGGCCGGCCGCAACAATCCCTTGATCCCGCTACTCAAG
GTCAGCTTCGACACTTACAACCTGTTGCATCGGTGGATGGGCCGCATCGTCGTGGCCGAGGTCGTCGTTCACACC
ATCGCCTGGGCTGTACCCGCCGTGGCCAGCTCGGGCTGGTCGGCCGCCCTCGCCAAGACGTACAAAAGCATCTTC
ATCGGGTCCGGCTTCTGGGCCGCCGTCGCCATGATGTTGCTACTGCTGCTCGCCGTCTCGCCCTTCCGTCACGCC
TTTTACGAGACGTTTCTCAACCTGCACATCATACTCGCCATGGCCTCGCTCATAGGCACTTGGATACACTGTGCC
TCCGGTGACCTCCCGGCTCTGCCATGGGTCGTCGCTGTTGTCGGGCTATGGATGGCCGACCGCCTCGCGCGGCTG
TCCCGCCTGTTGTTCGCTAACTGGTCCAGTCGTGGCTTCACCGACGCGCTCGTCGAGGCCCTGCCTGGCGAAGTC
AGTCGCGTCACGCTCTATCTCCCGCGCTACGTCAGCATCCAACCCGGTACGCACGCCTATCTGCGCTTTTGGGGC
GTCCGGCCGTGGGAGAGCCATCCGTTTTCGGTCGCTTGGGTGGAATACGACGCGGCCAACTCGCTCCCGACGTCG
GAAAAGGAGCCCCTCACGGCCGTGGACCGCAAGACGGCGTCGACGTCGGTTTCGTTCATCATCGGCGCCCAGACG
GGCATGACGCGCATGCTCTACAACCAGGCCAGCAAGTCGTCGTCGGGTATCCGAGCCCGGGCCGCCATGGAAGGG
CCTTATGCCGGGCACCATAACCTCGACTCGTACGGCCACGTCGTCTTGTTCGCCGGGTCGACGGGCATCACGCAT
CAGATCTCGCACGTGCGGCACTTGCTGGAGGGCTACAACGAAGGCATGGTGGCGACGCGGAGGTTGACACTGGTC
TGGATCATCCGGACGTACGAGACGCTCGAGTGGGTGCGTCCCTACATGGACATGATCCTGCGGATACCGAATCGC
AAGGACGTGCTCCGGATCCAGGTGTTTGTGACACGACCTCAAAACCCGCGCGACATTGTCAGCGCCAGCTCGACG
GTCAAGATGTTTCCTGGTCGGCCCAACATCCCGCTGCTCCTGGTCAAGGAAGTGCAGGACCAGATCGGGGCCATG
TCAGTGAGCGTTTGCGGGCCTGGCGGTCTGGCCGATGACGTACGGGGCGCCGTTCGGGCGGTGCAAGGCGATAGC
GTCATTGACTTTATCGAGGAGAGTTTTACGTGG
Transcript >Ophio5|7924
ATGGATCCCTCACCTTCCCTGCAAATACGGCAGGCCGACGGCACTGAGGATAAGCCGTTGAATATGATATTCAAA
GACGTCATCTGGTGGACTCTGGGCATCGTCGCCCTGACTGTGCTCGTCGTCCGGATCCTGGAGATCCTGTGGGCG
AAGCTGCGTCAGGTGTCGGCCATGTCCCAACCACGGGACAAGCAGGCTTACTGGAAGGTGTCGCAATGGAACTGG
ATGCCGCCGCTGAAGAAGCATCTGATATACGCACCCCTTCTTCACAAGCGCCACAATCGAGAGTTCCGCCTCTCG
ACGGCCTTCAATGTCGGCACCCTGCCGTCACGGTTGCACACGCTGCTGCTGCTCCTCTACGTCGGCAGCAACATC
GCCTACTTGATTGCCCTCAACTGGAGCGTCGAAAACAAGTTCGCCATCTGCGCCGAGCTGCGCGGCCGCTCCGGC
ACGCTCGCCGTCGTCAACATGATCCCGCTCATCATACTGGCCGGCCGCAACAATCCCTTGATCCCGCTACTCAAG
GTCAGCTTCGACACTTACAACCTGTTGCATCGGTGGATGGGCCGCATCGTCGTGGCCGAGGTCGTCGTTCACACC
ATCGCCTGGGCTGTACCCGCCGTGGCCAGCTCGGGCTGGTCGGCCGCCCTCGCCAAGACGTACAAAAGCATCTTC
ATCGGGTCCGGCTTCTGGGCCGCCGTCGCCATGATGTTGCTACTGCTGCTCGCCGTCTCGCCCTTCCGTCACGCC
TTTTACGAGACGTTTCTCAACCTGCACATCATACTCGCCATGGCCTCGCTCATAGGCACTTGGATACACTGTGCC
TCCGGTGACCTCCCGGCTCTGCCATGGGTCGTCGCTGTTGTCGGGCTATGGATGGCCGACCGCCTCGCGCGGCTG
TCCCGCCTGTTGTTCGCTAACTGGTCCAGTCGTGGCTTCACCGACGCGCTCGTCGAGGCCCTGCCTGGCGAAGTC
AGTCGCGTCACGCTCTATCTCCCGCGCTACGTCAGCATCCAACCCGGTACGCACGCCTATCTGCGCTTTTGGGGC
GTCCGGCCGTGGGAGAGCCATCCGTTTTCGGTCGCTTGGGTGGAATACGACGCGGCCAACTCGCTCCCGACGTCG
GAAAAGGAGCCCCTCACGGCCGTGGACCGCAAGACGGCGTCGACGTCGGTTTCGTTCATCATCGGCGCCCAGACG
GGCATGACGCGCATGCTCTACAACCAGGCCAGCAAGTCGTCGTCGGGTATCCGAGCCCGGGCCGCCATGGAAGGG
CCTTATGCCGGGCACCATAACCTCGACTCGTACGGCCACGTCGTCTTGTTCGCCGGGTCGACGGGCATCACGCAT
CAGATCTCGCACGTGCGGCACTTGCTGGAGGGCTACAACGAAGGCATGGTGGCGACGCGGAGGTTGACACTGGTC
TGGATCATCCGGACGTACGAGACGCTCGAGTGGGTGCGTCCCTACATGGACATGATCCTGCGGATACCGAATCGC
AAGGACGTGCTCCGGATCCAGGTGTTTGTGACACGACCTCAAAACCCGCGCGACATTGTCAGCGCCAGCTCGACG
GTCAAGATGTTTCCTGGTCGGCCCAACATCCCGCTGCTCCTGGTCAAGGAAGTGCAGGACCAGATCGGGGCCATG
TCAGTGAGCGTTTGCGGGCCTGGCGGTCTGGCCGATGACGTACGGGGCGCCGTTCGGGCGGTGCAAGGCGATAGC
GTCATTGACTTTATCGAGGAGAGTTTTACGTGGTGA
Gene >Ophio5|7924
ATGGATCCCTCACCTTCCCTGCAAATACGGCAGGCCGACGGCACTGAGGATAAGGTACAGCCTAGCTCGACGATT
GCCCCGTTTGCCACGGCGCTAAATGGAGTAAATCAGCCGTTGAATATGATATTCAAAGACGTCATCTGGTGGACT
CTGGGCATCGTCGCCCTGACTGTGCTCGTCGTCCGGATCCTGGAGATCCTGTGGGCGAAGCTGCGTCAGGTGTCG
GCCATGTCCCAACCACGGGACAAGCAGGCTTACTGGAAGGTGTCGCAATGGAACTGGATGCCGCCGCTGAAGAAG
CATCTGATATACGCACCCCTTCTTCACAAGCGCCACAATCGAGAGTTCCGCCTCTCGACGGCCTTCAATGTCGGC
ACCCTGCCGTCACGGTTGCACACGCTGCTGCTGCTCCTCTACGTCGGCAGCAACATCGCCTACTTGATTGCCCTC
AACTGGAGCGTCGAAAACAAGTTCGCCATCTGCGCCGAGCTGCGCGGCCGCTCCGGCACGCTCGCCGTCGTCAAC
ATGATCCCGCTCATCATACTGGCCGGCCGCAACAATCCCTTGATCCCGCTACTCAAGGTCAGCTTCGACACTTAC
AACCTGTTGCATCGGTGGATGGGCCGCATCGTCGTGGCCGAGGTCGTCGTTCACACCATCGCCTGGGCTGTACCC
GCCGTGGCCAGCTCGGGCTGGTCGGCCGCCCTCGCCAAGACGTACAAAAGCATCTTCATCGGGTCCGGCTTCTGG
GCCGCCGTCGCCATGATGTTGCTACTGCTGCTCGCCGTCTCGCCCTTCCGTCACGCCTTTTACGAGACGTTTCTC
AACCTGCACATCATACTCGCCATGGCCTCGCTCATAGGCACTTGGATACACTGTGCCTCCGGTGACCTCCCGGCT
CTGCCATGGGTCGTCGCTGTTGTCGGGCTATGGATGGCCGACCGCCTCGCGCGGCTGTCCCGCCTGTTGTTCGCT
AACTGGTCCAGTCGTGGCTTCACCGACGCGCTCGTCGAGGCCCTGCCTGGCGAAGTCAGTCGCGTCACGCTCTAT
CTCCCGCGCTACGTCAGCATCCAACCCGGTACGCACGCCTATCTGCGCTTTTGGGGCGTCCGGCCGTGGGAGAGC
CATCCGTTTTCGGTCGCTTGGGTGGAATACGACGCGGCCAACTCGCTCCCGACGTCGGAAAAGGAGCCCCTCACG
GCCGTGGACCGCAAGACGGCGTCGACGTCGGTTTCGTTCATCATCGGCGCCCAGACGGGCATGACGCGCATGCTC
TACAACCAGGCCAGCAAGTCGTCGTCGGGTATCCGAGCCCGGGCCGCCATGGAAGGGCCTTATGCCGGGCACCAT
AACCTCGACTCGTACGGCCACGTCGTCTTGTTCGCCGGGTCGACGGGCATCACGCATCAGATCTCGCACGTGCGG
CACTTGCTGGAGGGCTACAACGAAGGCATGGTGGCGACGCGGAGGTTGACACTGGTCTGGATCATCCGGACGTAC
GAGACGCTCGAGTGGGTGCGTCCCTACATGGACATGATCCTGCGGATACCGAATCGCAAGGACGTGCTCCGGATC
CAGGTGTTTGTGACACGACCTCAAAACCCGCGCGACATTGTCAGCGCCAGCTCGACGGTCAAGATGTTTCCTGGT
CGGCCCAACATCCCGCTGCTCCTGGTCAAGGAAGTGCAGGACCAGATCGGGGCCATGTCAGTGAGCGTTTGCGGG
CCTGGCGGTCTGGCCGATGACGTACGGGGCGCCGTTCGGGCGGTGCAAGGCGATAGCGTCATTGACTTTATCGAG
GAGAGTTTTACGTGGTGA

© 2022 - Robin Ohm - Utrecht University - The Netherlands

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