Fungal Genomics

at Utrecht University

General Properties

Protein IDOphio5|1837
Gene name
Locationscaffold_17:63070..64515
Strand-
Gene length (bp)1445
Transcript length (bp)1332
Coding sequence length (bp)1329
Protein length (aa) 443

Overview

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PFAM Domains

PFAM Domain ID Short name Long name E-value Start End
PF02535 Zip ZIP Zinc transporter 1.8E-55 50 439

Swissprot hits

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Swissprot ID Swissprot Description Start End E-value
sp|Q12436|ZRT2_YEAST Zinc-regulated transporter 2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=ZRT2 PE=1 SV=1 52 443 3.0E-49
sp|Q8W246|ZIP7_ARATH Zinc transporter 7 OS=Arabidopsis thaliana GN=ZIP7 PE=2 SV=1 58 443 1.0E-37
sp|P32804|ZRT1_YEAST Zinc-regulated transporter 1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=ZRT1 PE=1 SV=1 50 443 3.0E-37
sp|Q6L8G0|ZIP5_ORYSJ Zinc transporter 5 OS=Oryza sativa subsp. japonica GN=ZIP5 PE=2 SV=1 52 443 4.0E-30
sp|O94639|ZRT1_SCHPO Zinc-regulated transporter 1 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=zrt1 PE=1 SV=1 282 443 1.0E-25
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Swissprot ID Swissprot Description Start End E-value
sp|Q12436|ZRT2_YEAST Zinc-regulated transporter 2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=ZRT2 PE=1 SV=1 52 443 3.0E-49
sp|Q8W246|ZIP7_ARATH Zinc transporter 7 OS=Arabidopsis thaliana GN=ZIP7 PE=2 SV=1 58 443 1.0E-37
sp|P32804|ZRT1_YEAST Zinc-regulated transporter 1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=ZRT1 PE=1 SV=1 50 443 3.0E-37
sp|Q6L8G0|ZIP5_ORYSJ Zinc transporter 5 OS=Oryza sativa subsp. japonica GN=ZIP5 PE=2 SV=1 52 443 4.0E-30
sp|O94639|ZRT1_SCHPO Zinc-regulated transporter 1 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=zrt1 PE=1 SV=1 282 443 1.0E-25
sp|A3BI11|ZIP8_ORYSJ Zinc transporter 8 OS=Oryza sativa subsp. japonica GN=ZIP8 PE=2 SV=1 279 443 1.0E-23
sp|O23039|ZIP5_ARATH Zinc transporter 5 OS=Arabidopsis thaliana GN=ZIP5 PE=2 SV=1 275 443 8.0E-23
sp|Q75HB1|IRT1_ORYSJ Fe(2+) transport protein 1 OS=Oryza sativa subsp. japonica GN=IRT1 PE=2 SV=1 277 443 1.0E-22
sp|Q6L8F9|ZIP6_ORYSJ Zinc transporter 6 OS=Oryza sativa subsp. japonica GN=ZIP6 PE=2 SV=1 54 443 2.0E-22
sp|Q8W245|ZIP10_ARATH Probable zinc transporter 10 OS=Arabidopsis thaliana GN=ZIP10 PE=1 SV=2 280 443 6.0E-22
sp|Q9SLG3|ZIP3_ARATH Zinc transporter 3 OS=Arabidopsis thaliana GN=ZIP3 PE=2 SV=1 280 443 2.0E-20
sp|Q38856|IRT1_ARATH Fe(2+) transport protein 1 OS=Arabidopsis thaliana GN=IRT1 PE=1 SV=2 280 437 3.0E-20
sp|O81850|IRT2_ARATH Fe(2+) transport protein 2 OS=Arabidopsis thaliana GN=IRT2 PE=1 SV=1 280 443 5.0E-20
sp|Q6L8G1|IRT2_ORYSJ Fe(2+) transport protein 2 OS=Oryza sativa subsp. japonica GN=IRT2 PE=2 SV=1 277 443 8.0E-20
sp|Q5Z653|ZIP10_ORYSJ Zinc transporter 10 OS=Oryza sativa subsp. japonica GN=ZIP10 PE=3 SV=2 283 412 2.0E-19
sp|O04089|ZIP4_ARATH Zinc transporter 4, chloroplastic OS=Arabidopsis thaliana GN=ZIP4 PE=2 SV=1 279 443 3.0E-19
sp|Q8LE59|IRT3_ARATH Fe(2+) transport protein 3, chloroplastic OS=Arabidopsis thaliana GN=IRT3 PE=2 SV=3 283 443 3.0E-19
sp|Q7XLD4|ZIP3_ORYSJ Zinc transporter 3 OS=Oryza sativa subsp. japonica GN=ZIP3 PE=1 SV=2 248 443 7.0E-19
sp|Q8S3W4|ZIP8_ARATH Probable zinc transporter 8 OS=Arabidopsis thaliana GN=ZIP8 PE=2 SV=1 279 409 7.0E-19
sp|Q6L8F7|ZIP7_ORYSJ Zinc transporter 7 OS=Oryza sativa subsp. japonica GN=ZIP7 PE=2 SV=1 275 443 4.0E-18
sp|O82643|ZIP9_ARATH Zinc transporter 9 OS=Arabidopsis thaliana GN=ZIP9 PE=2 SV=1 283 412 2.0E-17
sp|O64738|ZIP6_ARATH Zinc transporter 6, chloroplastic OS=Arabidopsis thaliana GN=ZIP6 PE=3 SV=1 281 443 5.0E-16
sp|Q9FIS2|ZIP12_ARATH Probable zinc transporter 12 OS=Arabidopsis thaliana GN=ZIP12 PE=3 SV=1 283 443 7.0E-16
sp|O81123|ZIP1_ARATH Zinc transporter 1 OS=Arabidopsis thaliana GN=ZIP1 PE=2 SV=1 275 443 1.0E-15
sp|Q6ZJ91|ZIP4_ORYSJ Zinc transporter 4 OS=Oryza sativa subsp. japonica GN=ZIP4 PE=2 SV=1 264 443 3.0E-15
sp|Q0DHE3|ZIP9_ORYSJ Zinc transporter 9 OS=Oryza sativa subsp. japonica GN=ZIP9 PE=3 SV=3 317 443 1.0E-12
sp|A3BI11|ZIP8_ORYSJ Zinc transporter 8 OS=Oryza sativa subsp. japonica GN=ZIP8 PE=2 SV=1 51 148 2.0E-11
sp|Q0DHE3|ZIP9_ORYSJ Zinc transporter 9 OS=Oryza sativa subsp. japonica GN=ZIP9 PE=3 SV=3 52 148 5.0E-11
sp|O81123|ZIP1_ARATH Zinc transporter 1 OS=Arabidopsis thaliana GN=ZIP1 PE=2 SV=1 57 171 3.0E-10
sp|Q9FIS2|ZIP12_ARATH Probable zinc transporter 12 OS=Arabidopsis thaliana GN=ZIP12 PE=3 SV=1 34 209 4.0E-10
sp|Q8W245|ZIP10_ARATH Probable zinc transporter 10 OS=Arabidopsis thaliana GN=ZIP10 PE=1 SV=2 54 169 8.0E-09
sp|Q9SLG3|ZIP3_ARATH Zinc transporter 3 OS=Arabidopsis thaliana GN=ZIP3 PE=2 SV=1 68 213 3.0E-08
sp|O23039|ZIP5_ARATH Zinc transporter 5 OS=Arabidopsis thaliana GN=ZIP5 PE=2 SV=1 31 170 3.0E-08
sp|Q7XLD4|ZIP3_ORYSJ Zinc transporter 3 OS=Oryza sativa subsp. japonica GN=ZIP3 PE=1 SV=2 55 156 4.0E-08
sp|O94639|ZRT1_SCHPO Zinc-regulated transporter 1 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=zrt1 PE=1 SV=1 26 131 8.0E-08
sp|Q75HB1|IRT1_ORYSJ Fe(2+) transport protein 1 OS=Oryza sativa subsp. japonica GN=IRT1 PE=2 SV=1 58 147 1.0E-07
sp|Q6L8G1|IRT2_ORYSJ Fe(2+) transport protein 2 OS=Oryza sativa subsp. japonica GN=IRT2 PE=2 SV=1 36 176 2.0E-07
sp|O04089|ZIP4_ARATH Zinc transporter 4, chloroplastic OS=Arabidopsis thaliana GN=ZIP4 PE=2 SV=1 68 144 1.0E-06
sp|Q8LE59|IRT3_ARATH Fe(2+) transport protein 3, chloroplastic OS=Arabidopsis thaliana GN=IRT3 PE=2 SV=3 68 168 2.0E-06
sp|Q6L8F7|ZIP7_ORYSJ Zinc transporter 7 OS=Oryza sativa subsp. japonica GN=ZIP7 PE=2 SV=1 54 150 8.0E-06
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GO

GO Term Description Terminal node
GO:0016020 membrane Yes
GO:0046873 metal ion transmembrane transporter activity Yes
GO:0030001 metal ion transport Yes
GO:0055085 transmembrane transport Yes
GO:0015075 ion transmembrane transporter activity No
GO:0008150 biological_process No
GO:0051234 establishment of localization No
GO:0006810 transport No
GO:0051179 localization No
GO:0003674 molecular_function No
GO:0005215 transporter activity No
GO:0022890 inorganic cation transmembrane transporter activity No
GO:0022857 transmembrane transporter activity No
GO:0110165 cellular anatomical entity No
GO:0009987 cellular process No
GO:0005575 cellular_component No
GO:0008324 cation transmembrane transporter activity No
GO:0006811 ion transport No
GO:0006812 cation transport No
GO:0015318 inorganic molecular entity transmembrane transporter activity No

Deeploc

[Help with interpreting the results of Deeploc 2.0]
Localizations Signals Cytoplasm Nucleus Extracellular Cell membrane Mitochondrion Plastid Endoplasmic reticulum Lysosome vacuole Golgi apparatus Peroxisome
Cell membrane Signal peptide|Transmembrane domain 0.09 0.0716 0.0684 0.556 0.0524 0.0182 0.4631 0.5159 0.4644 0.01

SignalP

(None)

Transmembrane Domains

Domain # Start End Length
1 50 72 22
2 85 107 22
3 127 149 22
4 289 311 22
5 316 338 22
6 345 367 22
7 382 404 22
8 425 442 17

Transcription Factor Class

(None)

CAZymes

(None)

Secondary Metabolism

(None)

Expression data

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

Click here for more information

Orthologs

Orthofinder run ID4
Orthogroup53
Change Orthofinder run
Species Protein ID
Ophiocordyceps australis 1348a (Ghana) OphauG2|4441
Ophiocordyceps australis 1348a (Ghana) OphauG2|3674
Ophiocordyceps australis 1348a (Ghana) OphauG2|3874
Ophiocordyceps australis map64 (Brazil) OphauB2|30
Ophiocordyceps australis map64 (Brazil) OphauB2|371
Ophiocordyceps australis map64 (Brazil) OphauB2|7557
Ophiocordyceps camponoti-floridani Ophcf2|06924
Ophiocordyceps camponoti-floridani Ophcf2|02705
Ophiocordyceps camponoti-floridani Ophcf2|01026
Ophiocordyceps camponoti-rufipedis Ophun1|1933
Ophiocordyceps camponoti-rufipedis Ophun1|6647
Ophiocordyceps camponoti-rufipedis Ophun1|2734
Ophiocordyceps kimflemingae Ophio5|1837 (this protein)
Ophiocordyceps kimflemingae Ophio5|2651
Ophiocordyceps kimflemingae Ophio5|5120
Ophiocordyceps subramaniannii Hirsu2|8868
Ophiocordyceps subramaniannii Hirsu2|5985
Ophiocordyceps subramaniannii Hirsu2|5953
Ophiocordyceps subramaniannii Hirsu2|10402

Sequences

Type of sequenceSequence
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|1837
MGGENDAAAQDAAWSSLSTELLLHELRRREEQGERPQCGGRRMGWYDTSAHVCALFLILTLSTLACGLPLISRRA
AAGKLQKTIIFYCQHVGTGVLLATAFVHLLPTAFESLTDPCLPHFFSQGYKPLPGLVAMVAAVSVVGVESYLTAR
RAGHSHSHAHDYFGESDSEDHLDNEARRPSRRRSTGRRPPEISLHDVEATEGLVAGVSPLPEATPTSVGSPRTPD
SSAHDEDSDLDLDANDLNTVGNRADHFSSIKPSGRDAPAPAIQEVPQCLGPTPEQQRRQLLQCLLLEAGILFHSV
FIGMAVSVATGPAFMVFLVAICFHQSFEGLALGSRIAAIQFSRNSLRPWLMVLAYGVTTPLGQAIGMAVHKMYDP
ASMGGLLVVGFMNAVSAGLLLYAGLVQLLAEDFLTEKSYKVLKGKKRLRAYLAVVGGAVLMALVGAFA
Coding >Ophio5|1837
ATGGGCGGCGAAAATGATGCGGCGGCGCAAGACGCCGCCTGGTCGTCCCTCTCTACCGAATTGCTGCTCCACGAA
CTCCGGCGCCGGGAGGAGCAGGGCGAAAGGCCTCAGTGCGGAGGACGGCGGATGGGATGGTACGACACATCGGCG
CACGTGTGTGCGCTGTTCCTGATACTGACGCTGAGCACGCTTGCTTGTGGACTTCCCTTGATCTCGCGACGCGCA
GCGGCTGGTAAGCTGCAAAAAACCATCATCTTCTACTGCCAGCATGTCGGCACCGGCGTCCTCCTGGCCACGGCC
TTCGTCCACCTCCTACCGACGGCTTTCGAGTCCCTTACGGACCCCTGCCTTCCCCATTTCTTCAGCCAAGGCTAC
AAACCTCTTCCAGGTCTCGTGGCCATGGTGGCCGCCGTTTCCGTCGTCGGCGTCGAATCGTATTTGACGGCCCGT
AGAGCCGGTCACTCCCATTCGCACGCACACGACTACTTCGGCGAGTCCGACAGCGAAGACCACCTTGACAACGAA
GCGCGCCGTCCTTCGAGGCGCAGGTCCACCGGCCGACGGCCGCCGGAAATCTCGCTGCACGATGTCGAGGCCACA
GAGGGTCTCGTCGCCGGTGTCTCACCCTTACCCGAGGCGACGCCCACTAGCGTCGGCTCGCCAAGAACTCCTGAT
TCTTCGGCTCACGATGAGGACTCAGACCTGGACCTAGACGCCAACGACCTCAACACCGTCGGTAATCGAGCCGAC
CATTTCTCCTCCATCAAGCCCAGCGGCCGAGACGCGCCCGCCCCGGCAATCCAGGAGGTGCCGCAGTGCCTTGGG
CCGACGCCGGAGCAGCAGAGGCGACAGCTGCTGCAATGCCTGCTGCTCGAGGCCGGCATCCTCTTCCACAGCGTC
TTCATCGGCATGGCCGTGTCCGTGGCCACGGGGCCGGCCTTTATGGTCTTCCTCGTCGCCATCTGCTTCCACCAG
TCGTTCGAGGGCCTGGCGCTCGGCAGCCGGATCGCGGCCATTCAGTTCTCGCGGAACTCGCTGCGGCCCTGGCTG
ATGGTGCTCGCGTACGGAGTGACGACGCCGCTGGGGCAGGCCATCGGCATGGCCGTGCACAAAATGTACGACCCG
GCTTCGATGGGCGGCCTGCTGGTCGTGGGCTTCATGAACGCCGTCTCGGCCGGCCTGCTGCTCTACGCCGGGCTC
GTCCAGCTACTGGCCGAGGACTTTTTGACGGAGAAGAGCTACAAGGTGCTCAAGGGGAAGAAGAGGCTCCGTGCC
TATCTTGCCGTCGTCGGCGGAGCGGTCCTCATGGCCTTGGTGGGGGCTTTTGCC
Transcript >Ophio5|1837
ATGGGCGGCGAAAATGATGCGGCGGCGCAAGACGCCGCCTGGTCGTCCCTCTCTACCGAATTGCTGCTCCACGAA
CTCCGGCGCCGGGAGGAGCAGGGCGAAAGGCCTCAGTGCGGAGGACGGCGGATGGGATGGTACGACACATCGGCG
CACGTGTGTGCGCTGTTCCTGATACTGACGCTGAGCACGCTTGCTTGTGGACTTCCCTTGATCTCGCGACGCGCA
GCGGCTGGTAAGCTGCAAAAAACCATCATCTTCTACTGCCAGCATGTCGGCACCGGCGTCCTCCTGGCCACGGCC
TTCGTCCACCTCCTACCGACGGCTTTCGAGTCCCTTACGGACCCCTGCCTTCCCCATTTCTTCAGCCAAGGCTAC
AAACCTCTTCCAGGTCTCGTGGCCATGGTGGCCGCCGTTTCCGTCGTCGGCGTCGAATCGTATTTGACGGCCCGT
AGAGCCGGTCACTCCCATTCGCACGCACACGACTACTTCGGCGAGTCCGACAGCGAAGACCACCTTGACAACGAA
GCGCGCCGTCCTTCGAGGCGCAGGTCCACCGGCCGACGGCCGCCGGAAATCTCGCTGCACGATGTCGAGGCCACA
GAGGGTCTCGTCGCCGGTGTCTCACCCTTACCCGAGGCGACGCCCACTAGCGTCGGCTCGCCAAGAACTCCTGAT
TCTTCGGCTCACGATGAGGACTCAGACCTGGACCTAGACGCCAACGACCTCAACACCGTCGGTAATCGAGCCGAC
CATTTCTCCTCCATCAAGCCCAGCGGCCGAGACGCGCCCGCCCCGGCAATCCAGGAGGTGCCGCAGTGCCTTGGG
CCGACGCCGGAGCAGCAGAGGCGACAGCTGCTGCAATGCCTGCTGCTCGAGGCCGGCATCCTCTTCCACAGCGTC
TTCATCGGCATGGCCGTGTCCGTGGCCACGGGGCCGGCCTTTATGGTCTTCCTCGTCGCCATCTGCTTCCACCAG
TCGTTCGAGGGCCTGGCGCTCGGCAGCCGGATCGCGGCCATTCAGTTCTCGCGGAACTCGCTGCGGCCCTGGCTG
ATGGTGCTCGCGTACGGAGTGACGACGCCGCTGGGGCAGGCCATCGGCATGGCCGTGCACAAAATGTACGACCCG
GCTTCGATGGGCGGCCTGCTGGTCGTGGGCTTCATGAACGCCGTCTCGGCCGGCCTGCTGCTCTACGCCGGGCTC
GTCCAGCTACTGGCCGAGGACTTTTTGACGGAGAAGAGCTACAAGGTGCTCAAGGGGAAGAAGAGGCTCCGTGCC
TATCTTGCCGTCGTCGGCGGAGCGGTCCTCATGGCCTTGGTGGGGGCTTTTGCCTGA
Gene >Ophio5|1837
ATGGGCGGCGAAAATGATGCGGCGGCGCAAGGTGACTGATGCCGCGCAAATCCCCCCTCCCCGACGACTGATGCT
GACCAGAGAGTCTCGACAAGACGCCGCCTGGTCGTCCCTCTCTACCGAATTGCTGCTCCACGAACTCCGGCGCCG
GGAGGAGCAGGGCGAAAGGCCTCAGTGCGGAGGACGGCGGATGGGATGGTACGACACATCGGCGCACGTGTGTGC
GCTGTTCCTGATACTGACGCTGAGCACGCTTGGTATGTGTTTCTCTTGCGGCGGAGGAAGACGAGTCTGACGGCA
AGACAGCTTGTGGACTTCCCTTGATCTCGCGACGCGCAGCGGCTGGTAAGCTGCAAAAAACCATCATCTTCTACT
GCCAGCATGTCGGCACCGGCGTCCTCCTGGCCACGGCCTTCGTCCACCTCCTACCGACGGCTTTCGAGTCCCTTA
CGGACCCCTGCCTTCCCCATTTCTTCAGCCAAGGCTACAAACCTCTTCCAGGTCTCGTGGCCATGGTGGCCGCCG
TTTCCGTCGTCGGCGTCGAATCGTATTTGACGGCCCGTAGAGCCGGTCACTCCCATTCGCACGCACACGACTACT
TCGGCGAGTCCGACAGCGAAGACCACCTTGACAACGAAGCGCGCCGTCCTTCGAGGCGCAGGTCCACCGGCCGAC
GGCCGCCGGAAATCTCGCTGCACGATGTCGAGGCCACAGAGGGTCTCGTCGCCGGTGTCTCACCCTTACCCGAGG
CGACGCCCACTAGCGTCGGCTCGCCAAGAACTCCTGATTCTTCGGCTCACGATGAGGACTCAGACCTGGACCTAG
ACGCCAACGACCTCAACACCGTCGGTAATCGAGCCGACCATTTCTCCTCCATCAAGCCCAGCGGCCGAGACGCGC
CCGCCCCGGCAATCCAGGAGGTGCCGCAGTGCCTTGGGCCGACGCCGGAGCAGCAGAGGCGACAGCTGCTGCAAT
GCCTGCTGCTCGAGGCCGGCATCCTCTTCCACAGCGTCTTCATCGGCATGGCCGTGTCCGTGGCCACGGGGCCGG
CCTTTATGGTCTTCCTCGTCGCCATCTGCTTCCACCAGTCGTTCGAGGGCCTGGCGCTCGGCAGCCGGATCGCGG
CCATTCAGTTCTCGCGGAACTCGCTGCGGCCCTGGCTGATGGTGCTCGCGTACGGAGTGACGACGCCGCTGGGGC
AGGCCATCGGCATGGCCGTGCACAAAATGTACGACCCGGCTTCGATGGGCGGCCTGCTGGTCGTGGGCTTCATGA
ACGCCGTCTCGGCCGGCCTGCTGCTCTACGCCGGGCTCGTCCAGCTACTGGCCGAGGACTTTTTGACGGAGAAGA
GCTACAAGGTGCTCAAGGGGAAGAAGAGGCTCCGTGCCTATCTTGCCGTCGTCGGCGGAGCGGTCCTCATGGCCT
TGGTGGGGGCTTTTGCCTGA

© 2023 - Robin Ohm - Utrecht University - The Netherlands

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