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.

Expression values

Label Description Expression (RPKM) Confidence interval (low) Confidence interval (high)
SC16a Pure fungal culture 68.01 36.99 99.03
CcL In ants, during behavior modification 276.74 120.87 432.61
CcD In ants, recently dead 131.90 68.26 195.55

Differential expression

Label1 Label2 Q-value Significant difference
SC16a CcL 0.000286 yes
SC16a CcD 0.003389 yes
CcL CcD 0.003199 yes

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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