Fungal Genomics

at Utrecht University

General Properties

Protein IDOphio5|4928
Gene name
Locationscaffold_398:2640..4212
Strand+
Gene length (bp)1572
Transcript length (bp)1572
Coding sequence length (bp)1569
Protein length (aa) 523

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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 1.1E-18 94 211
PF08030 NAD_binding_6 Ferric reductase NAD binding domain 2.4E-11 372 503
PF08022 FAD_binding_8 FAD-binding domain 3.4E-05 254 358

Swissprot hits

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Swissprot ID Swissprot Description Start End E-value
sp|O94727|FRP2_SCHPO Ferric/cupric reductase transmembrane component 2 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=frp2 PE=3 SV=1 93 520 8.0E-32
sp|A3LN69|AIM14_PICST Probable metalloreductase AIM14 OS=Scheffersomyces stipitis (strain ATCC 58785 / CBS 6054 / NBRC 10063 / NRRL Y-11545) GN=AIM14 PE=3 SV=2 65 519 2.0E-23
sp|Q04800|FRP1_SCHPO Ferric reductase transmembrane component 1 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=frp1 PE=1 SV=1 93 520 2.0E-22
sp|A5DE11|AIM14_PICGU Probable metalloreductase AIM14 OS=Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) GN=AIM14 PE=3 SV=2 92 505 3.0E-19
sp|P32791|FRE1_YEAST Ferric/cupric reductase transmembrane component 1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FRE1 PE=1 SV=1 91 523 4.0E-16
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Swissprot ID Swissprot Description Start End E-value
sp|O94727|FRP2_SCHPO Ferric/cupric reductase transmembrane component 2 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=frp2 PE=3 SV=1 93 520 8.0E-32
sp|A3LN69|AIM14_PICST Probable metalloreductase AIM14 OS=Scheffersomyces stipitis (strain ATCC 58785 / CBS 6054 / NBRC 10063 / NRRL Y-11545) GN=AIM14 PE=3 SV=2 65 519 2.0E-23
sp|Q04800|FRP1_SCHPO Ferric reductase transmembrane component 1 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=frp1 PE=1 SV=1 93 520 2.0E-22
sp|A5DE11|AIM14_PICGU Probable metalloreductase AIM14 OS=Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) GN=AIM14 PE=3 SV=2 92 505 3.0E-19
sp|P32791|FRE1_YEAST Ferric/cupric reductase transmembrane component 1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FRE1 PE=1 SV=1 91 523 4.0E-16
sp|C5M5S1|AIM14_CANTT Probable metalloreductase AIM14 OS=Candida tropicalis (strain ATCC MYA-3404 / T1) GN=AIM14 PE=3 SV=1 65 438 3.0E-15
sp|Q5A446|FRE1_CANAL Ferric/cupric reductase transmembrane component 1 OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=CFL1 PE=2 SV=1 130 523 8.0E-13
sp|Q08905|FRE3_YEAST Ferric reductase transmembrane component 3 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FRE3 PE=1 SV=1 93 509 2.0E-12
sp|P78588|FREL_CANAX Probable ferric reductase transmembrane component OS=Candida albicans GN=CFL1 PE=3 SV=1 130 523 3.0E-12
sp|B9WB34|AIM14_CANDC Probable metalloreductase AIM14 OS=Candida dubliniensis (strain CD36 / ATCC MYA-646 / CBS 7987 / NCPF 3949 / NRRL Y-17841) GN=AIM14 PE=3 SV=1 65 502 5.0E-12
sp|C4Y9R6|AIM14_CLAL4 Probable metalloreductase AIM14 OS=Clavispora lusitaniae (strain ATCC 42720) GN=AIM14 PE=3 SV=1 80 501 4.0E-11
sp|C7GPP6|AIM14_YEAS2 Probable metalloreductase AIM14 OS=Saccharomyces cerevisiae (strain JAY291) GN=AIM14 PE=3 SV=1 67 458 5.0E-11
sp|C5E4F2|AIM14_ZYGRC Probable metalloreductase AIM14 OS=Zygosaccharomyces rouxii (strain ATCC 2623 / CBS 732 / NBRC 1130 / NCYC 568 / NRRL Y-229) GN=AIM14 PE=3 SV=1 131 502 6.0E-11
sp|B3LHL3|AIM14_YEAS1 Probable metalloreductase AIM14 OS=Saccharomyces cerevisiae (strain RM11-1a) GN=AIM14 PE=3 SV=1 67 458 2.0E-10
sp|A6ZU25|AIM14_YEAS7 Probable metalloreductase AIM14 OS=Saccharomyces cerevisiae (strain YJM789) GN=AIM14 PE=3 SV=1 67 458 2.0E-10
sp|C8Z891|AIM14_YEAS8 Probable metalloreductase AIM14 OS=Saccharomyces cerevisiae (strain Lalvin EC1118 / Prise de mousse) GN=AIM14 PE=3 SV=1 67 458 3.0E-10
sp|P53109|AIM14_YEAST Probable metalloreductase AIM14 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=AIM14 PE=1 SV=1 67 458 4.0E-10
sp|Q75CQ8|FRE8_ASHGO Probable ferric reductase transmembrane component OS=Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) GN=FRE8 PE=3 SV=1 91 412 6.0E-10
sp|P36033|FRE2_YEAST Ferric/cupric reductase transmembrane component 2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FRE2 PE=1 SV=1 93 509 1.0E-09
sp|Q6C188|AIM14_YARLI Probable metalloreductase AIM14 OS=Yarrowia lipolytica (strain CLIB 122 / E 150) GN=AIM14 PE=3 SV=1 65 470 5.0E-09
sp|P92949|FRO2_ARATH Ferric reduction oxidase 2 OS=Arabidopsis thaliana GN=FRO2 PE=1 SV=2 93 455 1.0E-08
sp|Q12209|FRE8_YEAST Probable ferric reductase transmembrane component 8 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FRE8 PE=1 SV=1 86 442 2.0E-08
sp|C5E398|AIM14_LACTC Probable metalloreductase AIM14 OS=Lachancea thermotolerans (strain ATCC 56472 / CBS 6340 / NRRL Y-8284) GN=AIM14 PE=3 SV=1 169 481 8.0E-07
sp|F4I4K7|FRO3_ARATH Ferric reduction oxidase 3, mitochondrial OS=Arabidopsis thaliana GN=FRO3 PE=2 SV=1 119 459 9.0E-07
sp|Q8VY13|FRO8_ARATH Ferric reduction oxidase 8, mitochondrial OS=Arabidopsis thaliana GN=FRO8 PE=2 SV=1 93 412 1.0E-06
sp|P53746|FRE4_YEAST Ferric reductase transmembrane component 4 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FRE4 PE=2 SV=1 89 509 2.0E-06
sp|Q9LMM2|FRO1_ARATH Probable ferric reduction oxidase 1 OS=Arabidopsis thaliana GN=FRO1 PE=2 SV=1 93 390 3.0E-06
sp|Q12473|FRE6_YEAST Ferric reductase transmembrane component 6 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FRE6 PE=1 SV=1 93 504 9.0E-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)
Yes 1 - 20 0.45

Transmembrane Domains

Domain # Start End Length
1 65 84 19
2 94 116 22
3 137 159 22
4 163 185 22
5 197 219 22

Transcription Factor Class

(None)

Expression data

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

Click here for more information

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|4928
MLAGLIRLLSWLLVRDSSSYVAVPTSPVAKARRRLDGRRLRYENVVSRIAWWLDDRLGFGRRDEWLIGFVWFFWL
LALCLHHTGTDFLHFTKRLGAVAVSQLPVLYLLSLKGLNPFALAFGSSHERLNRFHGVLGRLVGLLLVLHAACYN
YFFVVAGIWPRRLLDWIVVCGVVAALGLAALGATAMASVRRASYRVFFVTHVLVALMLPLLIFFHAPSVRIYLIE
ALLALLFDLGVRKLRSVHSPSTLVLRPDANLVAVEAPVPPHMLRAVSASAGSHVYLSIPPGSGRSASGPRALDLF
DFLYNPFTVAAVDHQRASITLVARVRHGPMTRTLARLASSTPAARKVSLTIDGPYGSMARQLRHLVAWSPTRVLV
IAGGVGATFSLPIYRFLREQLPSARIRLIWSVRGLADAAWASDAGLLPEDDRDVQLFISGGASAPYDTADTDSAV
EMRSLRQASSPRHRLGRPDLETIVDDVFRQGLEEPVAVLVCGPAEMAAEVRRRVRPWVMLGRDVWWHSESFGW
Coding >Ophio5|4928
ATGTTGGCGGGACTGATACGGCTCTTGAGCTGGCTACTCGTCCGCGACTCGTCCTCGTACGTCGCTGTGCCGACG
TCTCCGGTAGCCAAGGCACGACGACGCTTGGATGGGCGACGATTACGATACGAGAATGTCGTGTCCAGGATAGCT
TGGTGGCTTGATGACCGTCTTGGCTTCGGTCGTCGTGACGAATGGCTTATTGGCTTCGTCTGGTTCTTTTGGCTA
CTTGCTCTTTGCCTTCATCATACGGGCACCGATTTCTTGCACTTTACCAAGCGTCTAGGCGCCGTCGCTGTCTCT
CAGCTTCCGGTGCTGTATCTGCTTTCCCTCAAGGGCTTGAATCCCTTTGCGCTGGCGTTTGGCTCGTCGCATGAG
CGACTCAATCGCTTTCATGGCGTGCTGGGTCGCCTCGTTGGTCTCTTGCTCGTGCTTCACGCTGCTTGCTACAAT
TACTTCTTCGTCGTCGCCGGTATCTGGCCCAGGAGACTGTTGGACTGGATCGTCGTCTGTGGCGTCGTTGCCGCT
CTTGGGCTCGCTGCTCTCGGTGCCACGGCCATGGCGTCGGTTCGACGCGCCTCGTATCGCGTCTTCTTCGTCACT
CACGTCCTCGTCGCCTTGATGCTTCCGCTACTCATCTTCTTTCATGCTCCTTCGGTTCGCATCTATCTGATCGAG
GCCCTACTGGCGCTACTGTTCGACCTCGGCGTCCGCAAGCTGCGTTCCGTCCATTCTCCCTCGACGCTCGTCCTC
CGCCCCGATGCTAATCTCGTCGCTGTTGAGGCTCCTGTGCCGCCTCACATGTTGCGCGCCGTGTCCGCCTCGGCC
GGCTCTCATGTCTATCTCAGCATTCCGCCCGGCAGCGGCCGCTCTGCCTCTGGGCCGCGCGCCTTGGATTTGTTC
GACTTCCTCTACAACCCCTTTACCGTCGCCGCTGTCGACCACCAGCGCGCCTCCATCACCCTCGTCGCGCGTGTA
CGCCATGGGCCTATGACTCGAACGCTGGCTCGTCTGGCCTCTTCTACGCCCGCCGCCCGAAAGGTGTCTCTCACC
ATCGACGGCCCCTACGGCTCCATGGCCCGCCAGCTGCGTCACCTCGTCGCCTGGTCCCCCACTCGCGTTCTCGTC
ATCGCCGGCGGCGTCGGCGCAACCTTCTCGTTACCCATCTACCGCTTCCTGCGCGAGCAGCTACCTTCCGCCCGC
ATCCGCCTCATCTGGTCCGTCCGCGGCCTCGCCGACGCCGCATGGGCCTCCGACGCCGGCCTTCTTCCCGAAGAC
GACCGAGACGTCCAGCTCTTCATATCGGGTGGCGCCTCCGCTCCCTACGACACCGCCGACACCGACTCGGCTGTC
GAGATGCGATCCCTCCGCCAGGCTTCCTCGCCTCGCCACCGCCTCGGCCGACCCGACCTCGAGACCATCGTCGAC
GATGTCTTCCGCCAAGGCCTGGAGGAACCCGTCGCTGTTCTCGTCTGCGGACCGGCCGAGATGGCGGCCGAAGTG
AGGCGACGCGTGCGCCCGTGGGTTATGCTGGGGAGAGACGTGTGGTGGCACAGTGAGAGCTTTGGCTGG
Transcript >Ophio5|4928
ATGTTGGCGGGACTGATACGGCTCTTGAGCTGGCTACTCGTCCGCGACTCGTCCTCGTACGTCGCTGTGCCGACG
TCTCCGGTAGCCAAGGCACGACGACGCTTGGATGGGCGACGATTACGATACGAGAATGTCGTGTCCAGGATAGCT
TGGTGGCTTGATGACCGTCTTGGCTTCGGTCGTCGTGACGAATGGCTTATTGGCTTCGTCTGGTTCTTTTGGCTA
CTTGCTCTTTGCCTTCATCATACGGGCACCGATTTCTTGCACTTTACCAAGCGTCTAGGCGCCGTCGCTGTCTCT
CAGCTTCCGGTGCTGTATCTGCTTTCCCTCAAGGGCTTGAATCCCTTTGCGCTGGCGTTTGGCTCGTCGCATGAG
CGACTCAATCGCTTTCATGGCGTGCTGGGTCGCCTCGTTGGTCTCTTGCTCGTGCTTCACGCTGCTTGCTACAAT
TACTTCTTCGTCGTCGCCGGTATCTGGCCCAGGAGACTGTTGGACTGGATCGTCGTCTGTGGCGTCGTTGCCGCT
CTTGGGCTCGCTGCTCTCGGTGCCACGGCCATGGCGTCGGTTCGACGCGCCTCGTATCGCGTCTTCTTCGTCACT
CACGTCCTCGTCGCCTTGATGCTTCCGCTACTCATCTTCTTTCATGCTCCTTCGGTTCGCATCTATCTGATCGAG
GCCCTACTGGCGCTACTGTTCGACCTCGGCGTCCGCAAGCTGCGTTCCGTCCATTCTCCCTCGACGCTCGTCCTC
CGCCCCGATGCTAATCTCGTCGCTGTTGAGGCTCCTGTGCCGCCTCACATGTTGCGCGCCGTGTCCGCCTCGGCC
GGCTCTCATGTCTATCTCAGCATTCCGCCCGGCAGCGGCCGCTCTGCCTCTGGGCCGCGCGCCTTGGATTTGTTC
GACTTCCTCTACAACCCCTTTACCGTCGCCGCTGTCGACCACCAGCGCGCCTCCATCACCCTCGTCGCGCGTGTA
CGCCATGGGCCTATGACTCGAACGCTGGCTCGTCTGGCCTCTTCTACGCCCGCCGCCCGAAAGGTGTCTCTCACC
ATCGACGGCCCCTACGGCTCCATGGCCCGCCAGCTGCGTCACCTCGTCGCCTGGTCCCCCACTCGCGTTCTCGTC
ATCGCCGGCGGCGTCGGCGCAACCTTCTCGTTACCCATCTACCGCTTCCTGCGCGAGCAGCTACCTTCCGCCCGC
ATCCGCCTCATCTGGTCCGTCCGCGGCCTCGCCGACGCCGCATGGGCCTCCGACGCCGGCCTTCTTCCCGAAGAC
GACCGAGACGTCCAGCTCTTCATATCGGGTGGCGCCTCCGCTCCCTACGACACCGCCGACACCGACTCGGCTGTC
GAGATGCGATCCCTCCGCCAGGCTTCCTCGCCTCGCCACCGCCTCGGCCGACCCGACCTCGAGACCATCGTCGAC
GATGTCTTCCGCCAAGGCCTGGAGGAACCCGTCGCTGTTCTCGTCTGCGGACCGGCCGAGATGGCGGCCGAAGTG
AGGCGACGCGTGCGCCCGTGGGTTATGCTGGGGAGAGACGTGTGGTGGCACAGTGAGAGCTTTGGCTGGTAA
Gene >Ophio5|4928
ATGTTGGCGGGACTGATACGGCTCTTGAGCTGGCTACTCGTCCGCGACTCGTCCTCGTACGTCGCTGTGCCGACG
TCTCCGGTAGCCAAGGCACGACGACGCTTGGATGGGCGACGATTACGATACGAGAATGTCGTGTCCAGGATAGCT
TGGTGGCTTGATGACCGTCTTGGCTTCGGTCGTCGTGACGAATGGCTTATTGGCTTCGTCTGGTTCTTTTGGCTA
CTTGCTCTTTGCCTTCATCATACGGGCACCGATTTCTTGCACTTTACCAAGCGTCTAGGCGCCGTCGCTGTCTCT
CAGCTTCCGGTGCTGTATCTGCTTTCCCTCAAGGGCTTGAATCCCTTTGCGCTGGCGTTTGGCTCGTCGCATGAG
CGACTCAATCGCTTTCATGGCGTGCTGGGTCGCCTCGTTGGTCTCTTGCTCGTGCTTCACGCTGCTTGCTACAAT
TACTTCTTCGTCGTCGCCGGTATCTGGCCCAGGAGACTGTTGGACTGGATCGTCGTCTGTGGCGTCGTTGCCGCT
CTTGGGCTCGCTGCTCTCGGTGCCACGGCCATGGCGTCGGTTCGACGCGCCTCGTATCGCGTCTTCTTCGTCACT
CACGTCCTCGTCGCCTTGATGCTTCCGCTACTCATCTTCTTTCATGCTCCTTCGGTTCGCATCTATCTGATCGAG
GCCCTACTGGCGCTACTGTTCGACCTCGGCGTCCGCAAGCTGCGTTCCGTCCATTCTCCCTCGACGCTCGTCCTC
CGCCCCGATGCTAATCTCGTCGCTGTTGAGGCTCCTGTGCCGCCTCACATGTTGCGCGCCGTGTCCGCCTCGGCC
GGCTCTCATGTCTATCTCAGCATTCCGCCCGGCAGCGGCCGCTCTGCCTCTGGGCCGCGCGCCTTGGATTTGTTC
GACTTCCTCTACAACCCCTTTACCGTCGCCGCTGTCGACCACCAGCGCGCCTCCATCACCCTCGTCGCGCGTGTA
CGCCATGGGCCTATGACTCGAACGCTGGCTCGTCTGGCCTCTTCTACGCCCGCCGCCCGAAAGGTGTCTCTCACC
ATCGACGGCCCCTACGGCTCCATGGCCCGCCAGCTGCGTCACCTCGTCGCCTGGTCCCCCACTCGCGTTCTCGTC
ATCGCCGGCGGCGTCGGCGCAACCTTCTCGTTACCCATCTACCGCTTCCTGCGCGAGCAGCTACCTTCCGCCCGC
ATCCGCCTCATCTGGTCCGTCCGCGGCCTCGCCGACGCCGCATGGGCCTCCGACGCCGGCCTTCTTCCCGAAGAC
GACCGAGACGTCCAGCTCTTCATATCGGGTGGCGCCTCCGCTCCCTACGACACCGCCGACACCGACTCGGCTGTC
GAGATGCGATCCCTCCGCCAGGCTTCCTCGCCTCGCCACCGCCTCGGCCGACCCGACCTCGAGACCATCGTCGAC
GATGTCTTCCGCCAAGGCCTGGAGGAACCCGTCGCTGTTCTCGTCTGCGGACCGGCCGAGATGGCGGCCGAAGTG
AGGCGACGCGTGCGCCCGTGGGTTATGCTGGGGAGAGACGTGTGGTGGCACAGTGAGAGCTTTGGCTGGTAA

© 2022 - Robin Ohm - Utrecht University - The Netherlands

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