Fungal Genomics

at Utrecht University

General Properties

Protein IDOphauG2|1432
Gene name
LocationContig_143:5735..6946
Strand-
Gene length (bp)1211
Transcript length (bp)1083
Coding sequence length (bp)1083
Protein length (aa) 361

Overview

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PFAM Domains

PFAM Domain ID Short name Long name E-value Start End
PF19445 eIF3h_C C-terminal region of eIF3h 1.8E-17 146 207
PF19445 eIF3h_C C-terminal region of eIF3h 4.8E-23 238 352
PF01398 JAB JAB1/Mov34/MPN/PAD-1 ubiquitin protease 4.4E-07 10 133

Swissprot hits

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Swissprot ID Swissprot Description Start End E-value
sp|A7E7B3|EIF3H_SCLS1 Eukaryotic translation initiation factor 3 subunit H OS=Sclerotinia sclerotiorum (strain ATCC 18683 / 1980 / Ss-1) GN=SS1G_01190 PE=3 SV=1 6 360 0.0E+00
sp|A6RQZ9|EIF3H_BOTFB Eukaryotic translation initiation factor 3 subunit H OS=Botryotinia fuckeliana (strain B05.10) GN=BC1G_03240 PE=3 SV=1 4 360 3.0E-180
sp|Q7S9Y9|EIF3H_NEUCR Eukaryotic translation initiation factor 3 subunit H OS=Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) GN=eif3h PE=3 SV=1 1 360 6.0E-180
sp|Q2GZK0|EIF3H_CHAGB Eukaryotic translation initiation factor 3 subunit H OS=Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) GN=CHGG_05046 PE=3 SV=1 26 360 5.0E-178
sp|A4QT78|EIF3H_MAGO7 Eukaryotic translation initiation factor 3 subunit H OS=Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) GN=MGG_05156 PE=3 SV=1 1 360 5.0E-171
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Swissprot ID Swissprot Description Start End E-value
sp|A7E7B3|EIF3H_SCLS1 Eukaryotic translation initiation factor 3 subunit H OS=Sclerotinia sclerotiorum (strain ATCC 18683 / 1980 / Ss-1) GN=SS1G_01190 PE=3 SV=1 6 360 0.0E+00
sp|A6RQZ9|EIF3H_BOTFB Eukaryotic translation initiation factor 3 subunit H OS=Botryotinia fuckeliana (strain B05.10) GN=BC1G_03240 PE=3 SV=1 4 360 3.0E-180
sp|Q7S9Y9|EIF3H_NEUCR Eukaryotic translation initiation factor 3 subunit H OS=Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) GN=eif3h PE=3 SV=1 1 360 6.0E-180
sp|Q2GZK0|EIF3H_CHAGB Eukaryotic translation initiation factor 3 subunit H OS=Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) GN=CHGG_05046 PE=3 SV=1 26 360 5.0E-178
sp|A4QT78|EIF3H_MAGO7 Eukaryotic translation initiation factor 3 subunit H OS=Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) GN=MGG_05156 PE=3 SV=1 1 360 5.0E-171
sp|Q0UMR2|EIF3H_PHANO Eukaryotic translation initiation factor 3 subunit H OS=Phaeosphaeria nodorum (strain SN15 / ATCC MYA-4574 / FGSC 10173) GN=SNOG_06952 PE=3 SV=3 1 359 7.0E-170
sp|Q1DHB6|EIF3H_COCIM Eukaryotic translation initiation factor 3 subunit H OS=Coccidioides immitis (strain RS) GN=CIMG_10297 PE=3 SV=2 4 359 2.0E-161
sp|A1CQB4|EIF3H_ASPCL Eukaryotic translation initiation factor 3 subunit H OS=Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1) GN=ACLA_025520 PE=3 SV=1 4 359 6.0E-160
sp|Q2U2J1|EIF3H_ASPOR Eukaryotic translation initiation factor 3 subunit H OS=Aspergillus oryzae (strain ATCC 42149 / RIB 40) GN=AO090038000435 PE=3 SV=1 4 359 1.0E-158
sp|Q4WTA6|EIF3H_ASPFU Eukaryotic translation initiation factor 3 subunit H OS=Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) GN=AFUA_1G09970 PE=3 SV=1 4 359 9.0E-158
sp|B0XQB9|EIF3H_ASPFC Eukaryotic translation initiation factor 3 subunit H OS=Neosartorya fumigata (strain CEA10 / CBS 144.89 / FGSC A1163) GN=AFUB_009410 PE=3 SV=1 4 359 9.0E-158
sp|Q0D1J4|EIF3H_ASPTN Eukaryotic translation initiation factor 3 subunit H OS=Aspergillus terreus (strain NIH 2624 / FGSC A1156) GN=ATEG_00190 PE=3 SV=1 4 359 9.0E-157
sp|A2QQA2|EIF3H_ASPNC Eukaryotic translation initiation factor 3 subunit H OS=Aspergillus niger (strain CBS 513.88 / FGSC A1513) GN=An08g01790 PE=3 SV=1 4 359 3.0E-155
sp|Q5BDW0|EIF3H_EMENI Eukaryotic translation initiation factor 3 subunit H OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=AN1270 PE=3 SV=2 9 359 4.0E-155
sp|A1D379|EIF3H_NEOFI Eukaryotic translation initiation factor 3 subunit H OS=Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / FGSC A1164 / NRRL 181) GN=NFIA_015650 PE=3 SV=1 21 359 2.0E-150
sp|Q6C1I3|EIF3H_YARLI Eukaryotic translation initiation factor 3 subunit H OS=Yarrowia lipolytica (strain CLIB 122 / E 150) GN=YALI0F16005g PE=3 SV=1 13 358 5.0E-83
sp|Q9UT48|EIF3H_SCHPO Eukaryotic translation initiation factor 3 subunit H OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=eif3h PE=1 SV=1 5 354 5.0E-74
sp|Q9C5Z2|EIF3H_ARATH Eukaryotic translation initiation factor 3 subunit H OS=Arabidopsis thaliana GN=TIF3H1 PE=1 SV=2 2 354 5.0E-65
sp|Q4PI64|EIF3H_USTMA Eukaryotic translation initiation factor 3 subunit H OS=Ustilago maydis (strain 521 / FGSC 9021) GN=UMAG_00199 PE=3 SV=1 10 339 4.0E-63
sp|Q9GV27|EIF3H_BOMMO Eukaryotic translation initiation factor 3 subunit H OS=Bombyx mori PE=2 SV=1 7 351 5.0E-58
sp|B5RI54|EIF3H_SALSA Eukaryotic translation initiation factor 3 subunit H OS=Salmo salar GN=eif3h PE=2 SV=1 4 351 3.0E-57
sp|A7SA47|EIF3H_NEMVE Eukaryotic translation initiation factor 3 subunit H OS=Nematostella vectensis GN=v1g168210 PE=3 SV=1 13 351 1.0E-56
sp|B0WDA9|EIF3H_CULQU Eukaryotic translation initiation factor 3 subunit H OS=Culex quinquefasciatus GN=CPIJ005299 PE=3 SV=1 7 351 1.0E-55
sp|Q5PPY6|EIF3H_XENLA Eukaryotic translation initiation factor 3 subunit H OS=Xenopus laevis GN=eif3h PE=2 SV=1 5 351 1.0E-55
sp|Q170C2|EIF3H_AEDAE Eukaryotic translation initiation factor 3 subunit H OS=Aedes aegypti GN=AAEL007945 PE=2 SV=1 7 351 8.0E-55
sp|Q6AXJ2|EI3HA_DANRE Eukaryotic translation initiation factor 3 subunit H-A OS=Danio rerio GN=eif3ha PE=2 SV=1 7 351 6.0E-54
sp|Q5PR67|EI3HB_DANRE Eukaryotic translation initiation factor 3 subunit H-B OS=Danio rerio GN=eif3hb PE=2 SV=2 2 351 5.0E-53
sp|O15372|EIF3H_HUMAN Eukaryotic translation initiation factor 3 subunit H OS=Homo sapiens GN=EIF3H PE=1 SV=1 7 351 5.0E-53
sp|Q6P381|EIF3H_XENTR Eukaryotic translation initiation factor 3 subunit H OS=Xenopus tropicalis GN=eif3h PE=2 SV=1 4 351 8.0E-53
sp|Q56JZ5|EIF3H_BOVIN Eukaryotic translation initiation factor 3 subunit H OS=Bos taurus GN=EIF3H PE=2 SV=1 7 351 1.0E-52
sp|Q91WK2|EIF3H_MOUSE Eukaryotic translation initiation factor 3 subunit H OS=Mus musculus GN=Eif3h PE=1 SV=1 7 351 3.0E-52
sp|Q6P9U8|EIF3H_RAT Eukaryotic translation initiation factor 3 subunit H OS=Rattus norvegicus GN=Eif3h PE=1 SV=1 7 351 7.0E-52
sp|Q54UD0|EIF3H_DICDI Eukaryotic translation initiation factor 3 subunit H OS=Dictyostelium discoideum GN=eif3H PE=3 SV=1 7 355 1.0E-51
sp|B5FY35|EIF3H_TAEGU Eukaryotic translation initiation factor 3 subunit H OS=Taeniopygia guttata GN=EIF3H PE=2 SV=1 7 351 3.0E-51
sp|Q7PVR3|EIF3H_ANOGA Eukaryotic translation initiation factor 3 subunit H OS=Anopheles gambiae GN=AGAP009204 PE=3 SV=3 7 351 3.0E-51
sp|Q5ZLE6|EIF3H_CHICK Eukaryotic translation initiation factor 3 subunit H OS=Gallus gallus GN=EIF3H PE=2 SV=1 7 351 3.0E-50
sp|B4I1C2|EIF3H_DROSE Eukaryotic translation initiation factor 3 subunit H OS=Drosophila sechellia GN=eIF-3p40 PE=3 SV=1 7 351 1.0E-48
sp|Q9U9Q4|EIF3H_DROME Eukaryotic translation initiation factor 3 subunit H OS=Drosophila melanogaster GN=eIF-3p40 PE=2 SV=2 7 351 5.0E-48
sp|B3N4F1|EIF3H_DROER Eukaryotic translation initiation factor 3 subunit H OS=Drosophila erecta GN=eIF-3p40 PE=3 SV=1 7 351 4.0E-47
sp|B3MP94|EIF3H_DROAN Eukaryotic translation initiation factor 3 subunit H OS=Drosophila ananassae GN=eIF-3p40 PE=3 SV=1 7 351 7.0E-47
sp|B4LTW0|EIF3H_DROVI Eukaryotic translation initiation factor 3 subunit H OS=Drosophila virilis GN=eIF-3p40 PE=3 SV=1 7 351 7.0E-47
sp|B4KGS4|EIF3H_DROMO Eukaryotic translation initiation factor 3 subunit H OS=Drosophila mojavensis GN=eIF-3p40 PE=3 SV=1 13 351 2.0E-46
sp|B4JAS7|EIF3H_DROGR Eukaryotic translation initiation factor 3 subunit H OS=Drosophila grimshawi GN=eIF-3p40 PE=3 SV=1 13 351 5.0E-46
sp|B5DJJ2|EIF3H_DROPS Eukaryotic translation initiation factor 3 subunit H OS=Drosophila pseudoobscura pseudoobscura GN=eIF-3p40 PE=3 SV=1 7 351 6.0E-46
sp|B4P3T9|EIF3H_DROYA Eukaryotic translation initiation factor 3 subunit H OS=Drosophila yakuba GN=eIF-3p40 PE=3 SV=1 7 351 7.0E-46
sp|B4N116|EIF3H_DROWI Eukaryotic translation initiation factor 3 subunit H OS=Drosophila willistoni GN=eIF-3p40 PE=3 SV=1 13 351 3.0E-45
sp|A9V3P1|EIF3H_MONBE Eukaryotic translation initiation factor 3 subunit H OS=Monosiga brevicollis GN=9558 PE=3 SV=1 13 354 3.0E-38
sp|A8QCY3|EIF3H_BRUMA Eukaryotic translation initiation factor 3 subunit H OS=Brugia malayi GN=Bm1_50170 PE=3 SV=1 11 329 4.0E-26
sp|O01974|EIF3H_CAEEL Eukaryotic translation initiation factor 3 subunit H OS=Caenorhabditis elegans GN=eif-3.H PE=3 SV=2 13 328 9.0E-24
sp|A8WVY9|EIF3H_CAEBR Eukaryotic translation initiation factor 3 subunit H OS=Caenorhabditis briggsae GN=eif-3.H PE=3 SV=3 13 328 1.0E-22
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GO

GO Term Description Terminal node
GO:0005515 protein binding Yes
GO:0070122 obsolete isopeptidase activity Yes
GO:0140492 metal-dependent deubiquitinase activity Yes
GO:0019783 ubiquitin-like protein peptidase activity No
GO:0003674 molecular_function No
GO:0008237 metallopeptidase activity No
GO:0016787 hydrolase activity No
GO:0003824 catalytic activity No
GO:0005488 binding No
GO:0101005 deubiquitinase activity No
GO:0008233 peptidase activity No
GO:0140096 catalytic activity, acting on a protein No

Deeploc

Deeploc data not available for this genome

SignalP

(None)

Transmembrane Domains

(None)

Transcription Factor Class

(None)

CAZymes

(None)

Secondary Metabolism

(None)

Expression data

No expression data available for this genome

Orthologs

Orthofinder run ID4
Orthogroup2884
Change Orthofinder run
Species Protein ID
Ophiocordyceps australis 1348a (Ghana) OphauG2|1432 (this protein)
Ophiocordyceps australis map64 (Brazil) OphauB2|6042
Ophiocordyceps camponoti-floridani Ophcf2|06400
Ophiocordyceps camponoti-rufipedis Ophun1|3482
Ophiocordyceps kimflemingae Ophio5|6401
Ophiocordyceps subramaniannii Hirsu2|479

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 >OphauG2|1432
MNEAVKDAPFQAVQVEALVAMKIAKHCSLTFPTTATGAVVGMDQKGLLEVTNSFPFPSAEGAVVDNHPNDPSAIA
AAAPRQKSNAAYQVDMIRNLKEVNVDANSVGWYTSATMGNFVNMSFIENQFFYQKDNERTIALVYDTSKSSQGSL
TLRAFRLTTTFMNAYKEGKFTTESLQKSKLSFRDIIAELPIVIHNSHLLTSFLHQMPAPPLQDEIEQPESLADLK
RSAIRPPLYPSIENLDLSIDPFLEKTCDLLLESIESHYTDLNNFQFYQRQLGREQAKINQWQAKRKAENAQRAVA
KQPLLPEDEWQRLFKLPQEPSRLEGMLNAKQVEQYGKQVDGFTANISAKMFAVREDLLPQ*
Coding >OphauG2|1432
ATGAACGAAGCTGTCAAAGATGCGCCCTTCCAGGCGGTCCAGGTTGAGGCGCTGGTTGCAATGAAAATTGCAAAA
CATTGCTCCCTGACTTTTCCGACGACAGCCACGGGCGCTGTGGTCGGAATGGACCAAAAGGGCCTTTTGGAAGTC
ACCAATTCCTTTCCATTTCCCTCGGCCGAAGGTGCCGTTGTCGACAACCATCCAAACGATCCCTCGGCGATTGCA
GCAGCCGCTCCCCGGCAAAAATCCAATGCAGCGTACCAGGTGGACATGATTCGAAATCTCAAAGAGGTCAATGTG
GACGCCAACAGCGTCGGCTGGTACACCAGTGCCACCATGGGGAACTTTGTCAACATGAGCTTCATCGAGAACCAA
TTCTTCTACCAGAAAGACAATGAGCGCACCATTGCTCTCGTTTACGACACGAGCAAGAGCTCTCAGGGAAGCCTG
ACCCTCAGGGCGTTTCGCCTGACGACAACCTTTATGAACGCCTACAAGGAGGGCAAGTTTACCACGGAGAGCCTT
CAAAAGTCCAAGCTCTCTTTCCGCGACATAATCGCCGAGCTACCCATTGTGATACACAACTCGCATCTTCTCACC
TCGTTCCTCCACCAAATGCCTGCTCCTCCATTGCAGGACGAAATTGAGCAACCCGAGTCACTAGCCGACCTAAAG
CGCAGCGCCATCAGGCCCCCACTGTACCCCTCCATCGAGAACCTCGATCTATCTATCGATCCTTTTCTTGAAAAG
ACGTGCGATCTTTTACTTGAAAGCATCGAGTCGCATTACACAGACCTCAACAACTTTCAGTTTTACCAAAGGCAG
CTCGGGCGTGAGCAGGCCAAGATTAATCAGTGGCAAGCCAAGCGCAAGGCCGAAAACGCGCAGCGTGCTGTGGCC
AAGCAACCGCTGCTCCCCGAAGACGAGTGGCAGCGACTCTTCAAGCTACCGCAAGAACCCAGTCGCCTCGAGGGA
ATGCTCAATGCCAAGCAGGTGGAGCAGTATGGCAAGCAGGTTGATGGCTTCACCGCAAATATTAGTGCCAAGATG
TTTGCCGTAAGAGAAGATTTATTGCCTCAGTAG
Transcript >OphauG2|1432
ATGAACGAAGCTGTCAAAGATGCGCCCTTCCAGGCGGTCCAGGTTGAGGCGCTGGTTGCAATGAAAATTGCAAAA
CATTGCTCCCTGACTTTTCCGACGACAGCCACGGGCGCTGTGGTCGGAATGGACCAAAAGGGCCTTTTGGAAGTC
ACCAATTCCTTTCCATTTCCCTCGGCCGAAGGTGCCGTTGTCGACAACCATCCAAACGATCCCTCGGCGATTGCA
GCAGCCGCTCCCCGGCAAAAATCCAATGCAGCGTACCAGGTGGACATGATTCGAAATCTCAAAGAGGTCAATGTG
GACGCCAACAGCGTCGGCTGGTACACCAGTGCCACCATGGGGAACTTTGTCAACATGAGCTTCATCGAGAACCAA
TTCTTCTACCAGAAAGACAATGAGCGCACCATTGCTCTCGTTTACGACACGAGCAAGAGCTCTCAGGGAAGCCTG
ACCCTCAGGGCGTTTCGCCTGACGACAACCTTTATGAACGCCTACAAGGAGGGCAAGTTTACCACGGAGAGCCTT
CAAAAGTCCAAGCTCTCTTTCCGCGACATAATCGCCGAGCTACCCATTGTGATACACAACTCGCATCTTCTCACC
TCGTTCCTCCACCAAATGCCTGCTCCTCCATTGCAGGACGAAATTGAGCAACCCGAGTCACTAGCCGACCTAAAG
CGCAGCGCCATCAGGCCCCCACTGTACCCCTCCATCGAGAACCTCGATCTATCTATCGATCCTTTTCTTGAAAAG
ACGTGCGATCTTTTACTTGAAAGCATCGAGTCGCATTACACAGACCTCAACAACTTTCAGTTTTACCAAAGGCAG
CTCGGGCGTGAGCAGGCCAAGATTAATCAGTGGCAAGCCAAGCGCAAGGCCGAAAACGCGCAGCGTGCTGTGGCC
AAGCAACCGCTGCTCCCCGAAGACGAGTGGCAGCGACTCTTCAAGCTACCGCAAGAACCCAGTCGCCTCGAGGGA
ATGCTCAATGCCAAGCAGGTGGAGCAGTATGGCAAGCAGGTTGATGGCTTCACCGCAAATATTAGTGCCAAGATG
TTTGCCGTAAGAGAAGATTTATTGCCTCAGTAG
Gene >OphauG2|1432
ATGAACGAAGCTGTCAAAGATGCGCCCTTCCAGGCGGTCCAGGTTGAGGCGCTGGTGAGTCTCCAATCAGCCCCA
CCTTGGCCTTGTGGCCTCATTGCTGCGACTGACAAACAACTGTCGTGGACAGGTTGCAATGAAAATTGCAAAACA
TTGCTCCCTGACTTTTCCGACGACAGCCACGGGCGCTGTGGTCGGAATGGACCAAAAGGGCCTTTTGGAAGTCAC
CAATTCCTTTCCATTTCCCTCGGCCGAAGGTGCCGTTGTCGACAACCATCCAAACGATCCCTCGGCGATTGCAGC
AGCCGCTCCCCGGCAAAAATCCAATGCAGCGTACCAGGTGGACATGATTCGAAATCTCAAAGAGGTCAATGTGGA
CGCCAACAGCGTCGGCTGGTACACCAGTGCCACCATGGGGAACTTTGTCAACATGAGCTTCATCGAGAACCAATT
CTTCTACCAGAAAGACAATGAGCGCACCATTGCTCTCGTTTACGACACGAGCAAGAGCTCTCAGGGAAGCCTGAC
CCTCAGGGCGTTTCGCCTGACGACAACCTTTATGAACGCCTACAAGGAGGGCAAGTTTACCACGGAGAGGTGAGT
TTAGATATAAAACTTGGAACAAAGCAGGCCTGGACTCATACCGTTCCAGCCTTCAAAAGTCCAAGCTCTCTTTCC
GCGACATAATCGCCGAGCTACCCATTGTGATACACAACTCGCATCTTCTCACCTCGTTCCTCCACCAAATGCCTG
CTCCTCCATTGCAGGACGAAATTGAGCAACCCGAGTCACTAGCCGACCTAAAGCGCAGCGCCATCAGGCCCCCAC
TGTACCCCTCCATCGAGAACCTCGATCTATCTATCGATCCTTTTCTTGAAAAGACGTGCGATCTTTTACTTGAAA
GCATCGAGTCGCATTACACAGACCTCAACAACTTTCAGTTTTACCAAAGGCAGCTCGGGCGTGAGCAGGCCAAGA
TTAATCAGTGGCAAGCCAAGCGCAAGGCCGAAAACGCGCAGCGTGCTGTGGCCAAGCAACCGCTGCTCCCCGAAG
ACGAGTGGCAGCGACTCTTCAAGCTACCGCAAGAACCCAGTCGCCTCGAGGGAATGCTCAATGCCAAGCAGGTGG
AGCAGTATGGCAAGCAGGTTGATGGCTTCACCGCAAATATTAGTGCCAAGATGTTTGCCGTAAGAGAAGATTTAT
TGCCTCAGTAG

© 2023 - Robin Ohm - Utrecht University - The Netherlands

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