Fungal Genomics

at Utrecht University

General Properties

Protein IDOphio5|7338
Gene name
Locationscaffold_70:7120..9340
Strand-
Gene length (bp)2220
Transcript length (bp)1959
Coding sequence length (bp)1956
Protein length (aa) 652

Overview

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PFAM Domains

PFAM Domain ID Short name Long name E-value Start End
PF00394 Cu-oxidase Multicopper oxidase 1.8E-29 161 318
PF07732 Cu-oxidase_3 Multicopper oxidase 2.2E-28 36 151
PF07731 Cu-oxidase_2 Multicopper oxidase 5.1E-22 428 566

Swissprot hits

[Show all]
Swissprot ID Swissprot Description Start End E-value
sp|P14133|ASO_CUCSA L-ascorbate oxidase OS=Cucumis sativus PE=1 SV=1 43 565 7.0E-68
sp|P37064|ASO_CUCPM L-ascorbate oxidase OS=Cucurbita pepo var. melopepo PE=1 SV=1 43 585 6.0E-65
sp|P24792|ASO_CUCMA L-ascorbate oxidase OS=Cucurbita maxima GN=AAO PE=1 SV=2 43 585 1.0E-64
sp|Q40588|ASO_TOBAC L-ascorbate oxidase OS=Nicotiana tabacum GN=AAO PE=2 SV=1 43 585 1.0E-58
sp|Q84J37|LAC15_ARATH Laccase-15 OS=Arabidopsis thaliana GN=TT10 PE=1 SV=1 44 566 2.0E-42
[Show all]
[Show less]
Swissprot ID Swissprot Description Start End E-value
sp|P14133|ASO_CUCSA L-ascorbate oxidase OS=Cucumis sativus PE=1 SV=1 43 565 7.0E-68
sp|P37064|ASO_CUCPM L-ascorbate oxidase OS=Cucurbita pepo var. melopepo PE=1 SV=1 43 585 6.0E-65
sp|P24792|ASO_CUCMA L-ascorbate oxidase OS=Cucurbita maxima GN=AAO PE=1 SV=2 43 585 1.0E-64
sp|Q40588|ASO_TOBAC L-ascorbate oxidase OS=Nicotiana tabacum GN=AAO PE=2 SV=1 43 585 1.0E-58
sp|Q84J37|LAC15_ARATH Laccase-15 OS=Arabidopsis thaliana GN=TT10 PE=1 SV=1 44 566 2.0E-42
sp|Q2R0L2|LAC19_ORYSJ Laccase-19 OS=Oryza sativa subsp. japonica GN=LAC19 PE=2 SV=1 44 569 7.0E-37
sp|Q0DHL5|LAC11_ORYSJ Putative laccase-11 OS=Oryza sativa subsp. japonica GN=LAC11 PE=5 SV=2 44 581 1.0E-36
sp|A2XCN6|LAC18_ORYSI Putative laccase-18 OS=Oryza sativa subsp. indica GN=LAC18 PE=3 SV=1 44 569 2.0E-36
sp|Q9LMS3|LAC1_ARATH Laccase-1 OS=Arabidopsis thaliana GN=LAC1 PE=2 SV=1 44 571 2.0E-36
sp|Q0IP28|LAC25_ORYSJ Laccase-25 OS=Oryza sativa subsp. japonica GN=LAC25 PE=3 SV=1 6 581 2.0E-36
sp|Q9ZPY2|LAC6_ARATH Laccase-6 OS=Arabidopsis thaliana GN=LAC6 PE=2 SV=1 5 581 3.0E-36
sp|Q0DHL2|LAC12_ORYSJ Laccase-12/13 OS=Oryza sativa subsp. japonica GN=LAC12 PE=2 SV=1 1 569 3.0E-36
sp|A2Y9C5|LAC19_ORYSI Putative laccase-19 OS=Oryza sativa subsp. indica GN=LAC19 PE=3 SV=1 44 569 5.0E-36
sp|Q1PDH6|LAC16_ARATH Laccase-16 OS=Arabidopsis thaliana GN=LAC16 PE=2 SV=2 31 566 8.0E-36
sp|O81081|LAC2_ARATH Laccase-2 OS=Arabidopsis thaliana GN=LAC2 PE=2 SV=1 44 571 1.0E-35
sp|Q53LU4|LAC18_ORYSJ Laccase-18 OS=Oryza sativa subsp. japonica GN=LAC18 PE=2 SV=1 44 569 2.0E-35
sp|Q99056|LAC5_TRAVI Laccase-5 OS=Trametes villosa GN=LCC5 PE=3 SV=2 29 565 2.0E-35
sp|Q10ND7|LAC10_ORYSJ Laccase-10 OS=Oryza sativa subsp. japonica GN=LAC10 PE=2 SV=1 44 571 3.0E-35
sp|P56193|LAC1_THACU Laccase-1 OS=Thanatephorus cucumeris GN=LCC1 PE=1 SV=1 1 580 3.0E-35
sp|Q9FY79|LAC14_ARATH Laccase-14 OS=Arabidopsis thaliana GN=LAC14 PE=2 SV=1 6 581 4.0E-35
sp|Q9LFD1|LAC9_ARATH Laccase-9 OS=Arabidopsis thaliana GN=LAC9 PE=2 SV=1 44 581 1.0E-34
sp|Q02079|LAC3_THACU Laccase-3 OS=Thanatephorus cucumeris GN=LCC3 PE=2 SV=1 1 596 2.0E-34
sp|Q5N7A3|LAC6_ORYSJ Laccase-6 OS=Oryza sativa subsp. japonica GN=LAC6 PE=2 SV=1 2 565 2.0E-34
sp|Q02075|LAC2_THACU Laccase-2 OS=Thanatephorus cucumeris GN=LCC2 PE=2 SV=1 30 282 4.0E-34
sp|Q5ZCW1|LAC1_ORYSJ Putative laccase-1 OS=Oryza sativa subsp. japonica GN=LAC1 PE=3 SV=1 44 581 6.0E-34
sp|Q12717|LAC5_TRAVE Laccase-5 OS=Trametes versicolor GN=LCC5 PE=2 SV=1 29 565 1.0E-33
sp|Q2QZ80|LAC21_ORYSJ Laccase-21 OS=Oryza sativa subsp. japonica GN=LAC21 PE=2 SV=1 6 581 1.0E-33
sp|A2Y9C2|LAC20_ORYSI Laccase-20 OS=Oryza sativa subsp. indica GN=LAC20 PE=3 SV=1 44 569 2.0E-33
sp|Q2R0L0|LAC20_ORYSJ Laccase-20 OS=Oryza sativa subsp. japonica GN=LAC20 PE=2 SV=1 44 569 4.0E-33
sp|Q0IQU1|LAC22_ORYSJ Laccase-22 OS=Oryza sativa subsp. japonica GN=LAC22 PE=2 SV=2 10 566 8.0E-33
sp|O80434|LAC4_ARATH Laccase-4 OS=Arabidopsis thaliana GN=IRX12 PE=2 SV=2 11 566 2.0E-32
sp|Q02081|LAC4_THACU Laccase-4 OS=Thanatephorus cucumeris GN=LCC4 PE=1 SV=1 7 553 2.0E-32
sp|Q9SR40|LAC7_ARATH Laccase-7 OS=Arabidopsis thaliana GN=LAC7 PE=2 SV=1 44 566 2.0E-32
sp|Q9FLB5|LAC12_ARATH Laccase-12 OS=Arabidopsis thaliana GN=LAC12 PE=2 SV=1 44 566 5.0E-32
sp|Q99055|LAC4_TRAVI Laccase-4 OS=Trametes villosa GN=LCC4 PE=3 SV=1 29 565 9.0E-32
sp|Q8RYM9|LAC2_ORYSJ Laccase-2 OS=Oryza sativa subsp. japonica GN=LAC2 PE=2 SV=1 31 569 1.0E-31
sp|Q12719|LAC4_TRAVE Laccase-4 OS=Trametes versicolor GN=LCC4 PE=3 SV=1 29 565 2.0E-31
sp|Q99049|LAC3_TRAVI Laccase-3 OS=Trametes villosa GN=LCC3 PE=3 SV=1 7 377 2.0E-31
sp|Q8VZA1|LAC11_ARATH Laccase-11 OS=Arabidopsis thaliana GN=LAC11 PE=2 SV=1 31 573 3.0E-31
sp|Q5N7B4|LAC7_ORYSJ Laccase-7 OS=Oryza sativa subsp. japonica GN=LAC7 PE=2 SV=1 44 571 3.0E-31
sp|Q99046|LAC2_TRAVI Laccase-2 OS=Trametes villosa GN=LCC2 PE=3 SV=1 5 565 4.0E-31
sp|Q69L99|LAC14_ORYSJ Laccase-14 OS=Oryza sativa subsp. japonica GN=LAC14 PE=3 SV=1 45 571 5.0E-31
sp|P78591|FET3_CANAX Iron transport multicopper oxidase FET3 OS=Candida albicans GN=FET3 PE=3 SV=1 47 566 7.0E-31
sp|Q12718|LAC2_TRAVE Laccase-2 OS=Trametes versicolor GN=LCC2 PE=1 SV=1 5 565 1.0E-30
sp|Q9SIY8|LAC5_ARATH Laccase-5 OS=Arabidopsis thaliana GN=LAC5 PE=2 SV=1 1 566 2.0E-30
sp|D0VWU3|LAC1_TRAMX Laccase OS=Trametes maxima PE=1 SV=1 43 317 3.0E-30
sp|Q5N9X2|LAC4_ORYSJ Laccase-4 OS=Oryza sativa subsp. japonica GN=LAC4 PE=2 SV=1 44 569 3.0E-30
sp|Q9LYQ2|LAC13_ARATH Laccase-13 OS=Arabidopsis thaliana GN=LAC13 PE=2 SV=1 2 566 4.0E-30
sp|Q6CII3|FET3_KLULA Iron transport multicopper oxidase FET3 OS=Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) GN=FET3 PE=3 SV=1 38 566 5.0E-30
sp|Q01679|LAC1_PHLRA Laccase OS=Phlebia radiata GN=LAC PE=1 SV=2 6 565 2.0E-29
sp|O59896|LAC1_PYCCI Laccase OS=Pycnoporus cinnabarinus GN=LCC3-1 PE=1 SV=1 5 571 2.0E-29
sp|Q09920|FIO1_SCHPO Iron transport multicopper oxidase fio1 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=fio1 PE=3 SV=1 45 566 1.0E-28
sp|Q96WT3|FET3_CANGA Iron transport multicopper oxidase FET3 OS=Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) GN=FET3 PE=3 SV=1 38 566 2.0E-28
sp|Q99044|LAC1_TRAVI Laccase-1 OS=Trametes villosa GN=LCC1 PE=3 SV=1 10 325 2.0E-28
sp|Q12542|LAC2_AGABI Laccase-2 OS=Agaricus bisporus GN=lcc2 PE=1 SV=1 8 565 6.0E-28
sp|Q339K6|LAC15_ORYSJ Laccase-15 OS=Oryza sativa subsp. japonica GN=LAC15 PE=2 SV=1 44 274 6.0E-27
sp|Q0JHP8|LAC8_ORYSJ Laccase-8 OS=Oryza sativa subsp. japonica GN=LAC8 PE=3 SV=2 44 565 4.0E-26
sp|Q02497|LAC1_TRAHI Laccase OS=Trametes hirsuta PE=1 SV=1 29 317 1.0E-25
sp|P38993|FET3_YEAST Iron transport multicopper oxidase FET3 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FET3 PE=1 SV=2 1 556 4.0E-25
sp|P78722|LAC2_PODAS Laccase-2 OS=Podospora anserina GN=LAC2 PE=2 SV=1 46 566 1.0E-24
sp|Q2QUN2|LAC24_ORYSJ Laccase-24 OS=Oryza sativa subsp. japonica GN=LAC24 PE=2 SV=1 32 274 5.0E-24
sp|Q9FJD5|LAC17_ARATH Laccase-17 OS=Arabidopsis thaliana GN=LAC17 PE=2 SV=1 10 285 7.0E-24
sp|Q12739|LAC2_PLEOS Laccase-2 OS=Pleurotus ostreatus GN=POX2 PE=1 SV=1 57 317 3.0E-23
sp|Q12729|LAC1_PLEOS Laccase-1 OS=Pleurotus ostreatus GN=POX1 PE=2 SV=1 71 317 5.0E-23
sp|Q70KY3|LAC1_MELAO Laccase-1 OS=Melanocarpus albomyces GN=LAC1 PE=1 SV=1 46 563 6.0E-23
sp|Q12541|LAC1_AGABI Laccase-1 OS=Agaricus bisporus GN=lcc1 PE=1 SV=1 8 299 8.0E-23
sp|P06811|LAC1_NEUCR Laccase OS=Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) GN=lacc PE=1 SV=3 50 561 2.0E-22
sp|P43561|FET5_YEAST Iron transport multicopper oxidase FET5 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FET5 PE=1 SV=1 45 574 5.0E-22
sp|Q6Z8L2|LAC9_ORYSJ Putative laccase-9 OS=Oryza sativa subsp. japonica GN=LAC9 PE=3 SV=1 44 283 8.0E-22
sp|P17489|LAC1_EMENI Laccase-1 OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=yA PE=2 SV=3 47 561 1.0E-21
sp|Q6ID18|LAC10_ARATH Laccase-10 OS=Arabidopsis thaliana GN=LAC10 PE=2 SV=1 1 282 8.0E-21
sp|Q5N9W4|LAC5_ORYSJ Putative laccase-5 OS=Oryza sativa subsp. japonica GN=LAC5 PE=3 SV=1 44 280 2.0E-20
sp|Q9LFD2|LAC8_ARATH Laccase-8 OS=Arabidopsis thaliana GN=LAC8 PE=2 SV=1 44 285 2.0E-20
sp|Q96WM9|LAC2_BOTFU Laccase-2 OS=Botryotinia fuckeliana GN=lcc2 PE=2 SV=1 30 325 1.0E-19
sp|Q941X2|LAC3_ORYSJ Laccase-3 OS=Oryza sativa subsp. japonica GN=LAC3 PE=2 SV=1 44 274 2.0E-19
sp|Q00624|ASOL_BRANA L-ascorbate oxidase homolog OS=Brassica napus GN=Bp10 PE=2 SV=1 50 560 2.0E-19
sp|Q56YT0|LAC3_ARATH Laccase-3 OS=Arabidopsis thaliana GN=LAC3 PE=2 SV=2 6 283 2.0E-19
sp|Q8VXX5|SKS1_ARATH Monocopper oxidase-like protein SKS1 OS=Arabidopsis thaliana GN=SKS1 PE=1 SV=1 5 551 8.0E-19
sp|Q9SU40|SKU5_ARATH Monocopper oxidase-like protein SKU5 OS=Arabidopsis thaliana GN=SKU5 PE=1 SV=1 11 333 1.0E-18
sp|D4APX3|LAC1_ARTBC Laccase ARB_05828 OS=Arthroderma benhamiae (strain ATCC MYA-4681 / CBS 112371) GN=ARB_05828 PE=1 SV=1 31 299 1.0E-18
sp|P12374|COPA_PSEUB Copper resistance protein A OS=Pseudomonas syringae pv. tomato GN=copA PE=1 SV=1 32 286 1.0E-17
sp|Q9FHN6|SKS2_ARATH Monocopper oxidase-like protein SKS2 OS=Arabidopsis thaliana GN=SKS2 PE=1 SV=1 20 321 2.0E-17
sp|Q96UM2|LAC3_BOTFU Laccase-3 (Fragment) OS=Botryotinia fuckeliana GN=lcc3 PE=3 SV=1 57 561 6.0E-17
sp|Q2RBK2|LAC17_ORYSJ Putative laccase-17 OS=Oryza sativa subsp. japonica GN=LAC17 PE=3 SV=1 44 274 1.0E-16
sp|Q2QYS3|LAC23_ORYSJ Laccase-23 OS=Oryza sativa subsp. japonica GN=LAC23 PE=3 SV=1 44 274 2.0E-16
sp|Q339K6|LAC15_ORYSJ Laccase-15 OS=Oryza sativa subsp. japonica GN=LAC15 PE=2 SV=1 436 581 5.0E-16
sp|Q12570|LAC1_BOTFU Laccase-1 OS=Botryotinia fuckeliana GN=lcc1 PE=2 SV=3 28 299 2.0E-15
sp|P29162|ASOL_TOBAC L-ascorbate oxidase homolog OS=Nicotiana tabacum PE=2 SV=1 31 560 1.0E-14
sp|P59571|COPA_PSESM Copper resistance protein A homolog OS=Pseudomonas syringae pv. tomato (strain DC3000) GN=copA PE=3 SV=1 30 286 4.0E-14
sp|Q03966|LAC1_CRYPA Laccase OS=Cryphonectria parasitica GN=LAC-1 PE=3 SV=1 50 294 4.0E-13
sp|I6WZK7|MMCO_MYCTU Multicopper oxidase MmcO OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=mmcO PE=1 SV=1 48 282 3.0E-12
sp|Q47452|PCOA_ECOLX Copper resistance protein A OS=Escherichia coli GN=pcoA PE=3 SV=1 31 334 9.0E-12
sp|Q941X2|LAC3_ORYSJ Laccase-3 OS=Oryza sativa subsp. japonica GN=LAC3 PE=2 SV=1 448 569 2.0E-11
sp|Q56YT0|LAC3_ARATH Laccase-3 OS=Arabidopsis thaliana GN=LAC3 PE=2 SV=2 448 566 7.0E-11
sp|Q7XE50|LAC16_ORYSJ Putative laccase-16 OS=Oryza sativa subsp. japonica GN=LAC16 PE=5 SV=1 448 581 4.0E-10
sp|Q6Z8L2|LAC9_ORYSJ Putative laccase-9 OS=Oryza sativa subsp. japonica GN=LAC9 PE=3 SV=1 448 581 6.0E-10
sp|Q6ID18|LAC10_ARATH Laccase-10 OS=Arabidopsis thaliana GN=LAC10 PE=2 SV=1 448 566 3.0E-09
sp|Q9LFD2|LAC8_ARATH Laccase-8 OS=Arabidopsis thaliana GN=LAC8 PE=2 SV=1 445 581 5.0E-09
sp|Q9FJD5|LAC17_ARATH Laccase-17 OS=Arabidopsis thaliana GN=LAC17 PE=2 SV=1 476 571 6.0E-09
sp|Q5N9W4|LAC5_ORYSJ Putative laccase-5 OS=Oryza sativa subsp. japonica GN=LAC5 PE=3 SV=1 476 571 6.0E-09
sp|Q2RBK2|LAC17_ORYSJ Putative laccase-17 OS=Oryza sativa subsp. japonica GN=LAC17 PE=3 SV=1 448 569 1.0E-08
sp|Q2QYS3|LAC23_ORYSJ Laccase-23 OS=Oryza sativa subsp. japonica GN=LAC23 PE=3 SV=1 448 569 1.0E-08
sp|Q2QUN2|LAC24_ORYSJ Laccase-24 OS=Oryza sativa subsp. japonica GN=LAC24 PE=2 SV=1 416 565 2.0E-08
sp|Q12570|LAC1_BOTFU Laccase-1 OS=Botryotinia fuckeliana GN=lcc1 PE=2 SV=3 476 561 1.0E-06
sp|Q96WM9|LAC2_BOTFU Laccase-2 OS=Botryotinia fuckeliana GN=lcc2 PE=2 SV=1 476 584 3.0E-06
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GO

GO Term Description Terminal node
GO:0005507 copper ion binding Yes
GO:0016491 oxidoreductase activity Yes
GO:0046914 transition metal ion binding No
GO:0046872 metal ion binding No
GO:0005488 binding No
GO:0003824 catalytic activity No
GO:0003674 molecular_function No
GO:0043169 cation binding No
GO:0043167 ion binding 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
Extracellular Signal peptide 0.1385 0.0842 0.792 0.2075 0.0754 0.0222 0.3036 0.2662 0.1394 0.0023

SignalP

SignalP signal predicted Location Score
Yes 1 - 18 0.999719

Transmembrane Domains

(None)

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
Orthogroup273
Change Orthofinder run
Species Protein ID
Ophiocordyceps australis 1348a (Ghana) OphauG2|88
Ophiocordyceps australis map64 (Brazil) OphauB2|4831
Ophiocordyceps camponoti-floridani Ophcf2|02493
Ophiocordyceps camponoti-floridani Ophcf2|02994
Ophiocordyceps camponoti-rufipedis Ophun1|4061
Ophiocordyceps camponoti-rufipedis Ophun1|5337
Ophiocordyceps kimflemingae Ophio5|7338 (this protein)
Ophiocordyceps kimflemingae Ophio5|8186
Ophiocordyceps kimflemingae Ophio5|8234
Ophiocordyceps subramaniannii Hirsu2|2347
Ophiocordyceps subramaniannii Hirsu2|8700

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|7338
MLCPAFLLSSLLLLGAQAQFQVHGDDFKPDFELEATTGELDIDCQKRLSVLINGQSPGPQLNMTEGKVTWVRVWN
KMSDLNLTMHWHGLSQRAAPFSDGTPLVSQWPIPPGHFFDYEVRPEPGDAGTYFYHSHVGFQLITAHGPLIVQDP
NLEQAEQEYGEDVVMMLADYYAKDDHTIESGLLADPFRWSGEPQAVLVQGHSGKANFGSGNPSCEPYVIDVEPGK
MYRLRMIGATAISVVKLGIEDHSNLTVIEADGSYTEPTEIDHMQLAPGQRFSYRLQAKSAAEIDRMNKTEFWVRY
ESRERPESIQGYALLRYRMDKCEKPPRPKSQLPDKSPIELSTTTNDYLEYQLQPASQQERQKFPRLSEVTRTVTI
QINQMLTSGEYVDGKLQGSLVWVQNGSPWKEDVQAEANQMPYLITVYTANEADNVTMPNYERALENGGFDSETKT
FPARVGEVLDIVWQNNGGITGNFDIHPMHIHGEHAWDLGSGSGTYKAEENEKRFEGFTPARRDTTILYRYTEKDA
PDTTNGWRAWRIRVTEDNVGAWMMHCHIAQHAAMGMNTVWIFGDTPALMSRFPTAPFTEGYLKFGGEAYGSADKS
PVVNHHFGQDEAEEKKAEEEQKTAEEAPPEPPTELDNANEFDVDGEKTKRTQ
Coding >Ophio5|7338
ATGTTGTGTCCGGCTTTTCTGTTGTCGTCCTTGCTGCTGCTCGGGGCGCAGGCTCAGTTCCAGGTTCATGGCGAT
GATTTCAAGCCGGATTTCGAACTCGAGGCCACGACGGGAGAGCTCGATATTGACTGCCAGAAACGCCTTTCCGTC
TTGATCAATGGACAATCGCCGGGGCCGCAGCTAAACATGACTGAGGGTAAAGTCACTTGGGTCCGGGTTTGGAAT
AAGATGAGTGACTTGAACCTGACCATGCACTGGCATGGCCTCTCTCAGAGGGCAGCCCCCTTCTCGGATGGGACC
CCCCTCGTCAGCCAGTGGCCCATCCCGCCTGGGCACTTTTTCGATTACGAGGTCCGGCCGGAGCCGGGTGATGCC
GGCACCTACTTCTACCATTCGCACGTAGGCTTCCAGCTGATTACGGCTCACGGCCCTCTCATCGTCCAAGACCCC
AACCTCGAGCAGGCGGAGCAGGAGTACGGTGAGGATGTAGTAATGATGCTGGCCGACTACTACGCAAAGGACGAC
CACACCATTGAGAGTGGCCTCCTGGCCGATCCCTTCCGCTGGTCAGGCGAGCCGCAGGCCGTACTGGTACAGGGT
CACAGCGGCAAGGCCAACTTTGGCTCCGGGAACCCGTCGTGCGAGCCGTATGTCATCGACGTCGAGCCGGGCAAG
ATGTATCGGTTGCGCATGATCGGCGCCACGGCCATCTCCGTGGTCAAGCTGGGCATCGAGGATCACTCGAACCTC
ACCGTCATCGAGGCCGACGGCAGCTACACGGAGCCAACGGAGATCGACCACATGCAGCTTGCCCCCGGCCAGCGC
TTCAGCTACCGGCTACAGGCCAAGTCGGCCGCCGAGATTGACCGGATGAACAAGACGGAGTTCTGGGTCCGCTAC
GAGAGCCGCGAGCGTCCGGAGAGCATCCAAGGCTATGCCTTGCTGCGCTACCGCATGGACAAGTGCGAGAAGCCC
CCTCGGCCCAAATCTCAGCTGCCGGACAAGTCTCCTATCGAGTTGTCGACGACGACCAACGACTATCTCGAATAT
CAGCTGCAGCCTGCATCGCAGCAGGAGCGTCAGAAGTTCCCTCGTCTGTCTGAGGTGACGCGAACCGTCACCATC
CAGATCAACCAGATGCTCACGAGCGGCGAGTACGTCGACGGCAAGCTCCAGGGCAGCCTGGTTTGGGTGCAAAAC
GGTTCTCCCTGGAAGGAAGACGTTCAGGCAGAGGCCAACCAAATGCCCTACCTAATCACCGTCTATACCGCCAAC
GAGGCCGATAACGTTACCATGCCCAACTACGAGCGCGCCTTGGAGAACGGCGGCTTCGACTCGGAGACCAAGACG
TTCCCGGCCAGAGTAGGCGAGGTGCTGGACATTGTGTGGCAGAACAACGGCGGCATCACAGGAAACTTTGACATC
CATCCGATGCACATCCACGGCGAACACGCGTGGGACCTGGGCTCCGGCTCCGGCACGTACAAGGCCGAAGAGAAC
GAGAAGCGTTTCGAAGGCTTCACGCCCGCCCGGCGAGACACCACCATCCTCTACCGCTACACCGAGAAGGACGCG
CCGGACACGACCAACGGATGGCGAGCGTGGCGAATCCGCGTGACCGAGGATAACGTCGGCGCTTGGATGATGCAC
TGTCACATCGCCCAGCACGCGGCCATGGGCATGAACACGGTCTGGATCTTTGGTGACACGCCGGCCCTCATGAGT
CGCTTCCCGACGGCCCCCTTCACCGAGGGCTATCTGAAATTCGGCGGCGAGGCTTACGGTTCGGCTGACAAAAGC
CCGGTTGTGAACCACCACTTTGGGCAAGACGAGGCAGAAGAGAAGAAGGCTGAAGAGGAGCAAAAGACGGCGGAA
GAAGCGCCTCCTGAGCCGCCGACCGAACTCGACAACGCCAACGAGTTTGATGTCGACGGCGAGAAGACCAAGAGG
ACGCAA
Transcript >Ophio5|7338
ATGTTGTGTCCGGCTTTTCTGTTGTCGTCCTTGCTGCTGCTCGGGGCGCAGGCTCAGTTCCAGGTTCATGGCGAT
GATTTCAAGCCGGATTTCGAACTCGAGGCCACGACGGGAGAGCTCGATATTGACTGCCAGAAACGCCTTTCCGTC
TTGATCAATGGACAATCGCCGGGGCCGCAGCTAAACATGACTGAGGGTAAAGTCACTTGGGTCCGGGTTTGGAAT
AAGATGAGTGACTTGAACCTGACCATGCACTGGCATGGCCTCTCTCAGAGGGCAGCCCCCTTCTCGGATGGGACC
CCCCTCGTCAGCCAGTGGCCCATCCCGCCTGGGCACTTTTTCGATTACGAGGTCCGGCCGGAGCCGGGTGATGCC
GGCACCTACTTCTACCATTCGCACGTAGGCTTCCAGCTGATTACGGCTCACGGCCCTCTCATCGTCCAAGACCCC
AACCTCGAGCAGGCGGAGCAGGAGTACGGTGAGGATGTAGTAATGATGCTGGCCGACTACTACGCAAAGGACGAC
CACACCATTGAGAGTGGCCTCCTGGCCGATCCCTTCCGCTGGTCAGGCGAGCCGCAGGCCGTACTGGTACAGGGT
CACAGCGGCAAGGCCAACTTTGGCTCCGGGAACCCGTCGTGCGAGCCGTATGTCATCGACGTCGAGCCGGGCAAG
ATGTATCGGTTGCGCATGATCGGCGCCACGGCCATCTCCGTGGTCAAGCTGGGCATCGAGGATCACTCGAACCTC
ACCGTCATCGAGGCCGACGGCAGCTACACGGAGCCAACGGAGATCGACCACATGCAGCTTGCCCCCGGCCAGCGC
TTCAGCTACCGGCTACAGGCCAAGTCGGCCGCCGAGATTGACCGGATGAACAAGACGGAGTTCTGGGTCCGCTAC
GAGAGCCGCGAGCGTCCGGAGAGCATCCAAGGCTATGCCTTGCTGCGCTACCGCATGGACAAGTGCGAGAAGCCC
CCTCGGCCCAAATCTCAGCTGCCGGACAAGTCTCCTATCGAGTTGTCGACGACGACCAACGACTATCTCGAATAT
CAGCTGCAGCCTGCATCGCAGCAGGAGCGTCAGAAGTTCCCTCGTCTGTCTGAGGTGACGCGAACCGTCACCATC
CAGATCAACCAGATGCTCACGAGCGGCGAGTACGTCGACGGCAAGCTCCAGGGCAGCCTGGTTTGGGTGCAAAAC
GGTTCTCCCTGGAAGGAAGACGTTCAGGCAGAGGCCAACCAAATGCCCTACCTAATCACCGTCTATACCGCCAAC
GAGGCCGATAACGTTACCATGCCCAACTACGAGCGCGCCTTGGAGAACGGCGGCTTCGACTCGGAGACCAAGACG
TTCCCGGCCAGAGTAGGCGAGGTGCTGGACATTGTGTGGCAGAACAACGGCGGCATCACAGGAAACTTTGACATC
CATCCGATGCACATCCACGGCGAACACGCGTGGGACCTGGGCTCCGGCTCCGGCACGTACAAGGCCGAAGAGAAC
GAGAAGCGTTTCGAAGGCTTCACGCCCGCCCGGCGAGACACCACCATCCTCTACCGCTACACCGAGAAGGACGCG
CCGGACACGACCAACGGATGGCGAGCGTGGCGAATCCGCGTGACCGAGGATAACGTCGGCGCTTGGATGATGCAC
TGTCACATCGCCCAGCACGCGGCCATGGGCATGAACACGGTCTGGATCTTTGGTGACACGCCGGCCCTCATGAGT
CGCTTCCCGACGGCCCCCTTCACCGAGGGCTATCTGAAATTCGGCGGCGAGGCTTACGGTTCGGCTGACAAAAGC
CCGGTTGTGAACCACCACTTTGGGCAAGACGAGGCAGAAGAGAAGAAGGCTGAAGAGGAGCAAAAGACGGCGGAA
GAAGCGCCTCCTGAGCCGCCGACCGAACTCGACAACGCCAACGAGTTTGATGTCGACGGCGAGAAGACCAAGAGG
ACGCAATAA
Gene >Ophio5|7338
ATGTTGTGTCCGGCTTTTCTGTTGTCGTCCTTGCTGCTGCTCGGGGCGCAGGCTCAGTTCCAGGTTCATGGCGAT
GATTTCAAGCCGGATTTCGAACTCGAGGCCACGACGGGAGAGCTCGATATTGACTGCCAGAAACGCCTTTCCGTC
TTGATCAATGGACAATCGCCGGGGCCGCAGCTAAACATGACTGAGGGTAAAGTCACTTGGGTCCGGGTTTGGAAT
AAGATGAGTGACTTGAACCTGACCATGGTTTGTTGCCTCTTTTTTTTAAAACACTCACGCATATAATAATTGATA
TCTCTCGTCTGCCCGCGTCTTTCATTCTTCACAATCTATCTTCGGTTACTGCTCTTCTCAGTCCCTTGTTTCTCA
CACTTCCCTATCCTCTTTTCCCAACTTGATCCATGTGACCCGGCTACTGACAGAAATTGCATTGTATAGCACTGG
CATGGCCTCTCTCAGAGGGCAGCCCCCTTCTCGGATGGGACCCCCCTCGTCAGCCAGTGGCCCATCCCGCCTGGG
CACTTTTTCGATTACGAGGTCCGGCCGGAGCCGGGTGATGCCGGCACCTACTTCTACCATTCGCACGTAGGCTTC
CAGCTGATTACGGCTCACGGCCCTCTCATCGTCCAAGACCCCAACCTCGAGCAGGCGGAGCAGGAGTACGGTGAG
GATGTAGTAATGATGCTGGCCGACTACTACGCAAAGGACGACCACACCATTGAGAGTGGCCTCCTGGCCGATCCC
TTCCGCTGGTCAGGCGAGCCGCAGGCCGTACTGGTACAGGGTCACAGCGGCAAGGCCAACTTTGGCTCCGGGAAC
CCGTCGTGCGAGCCGTATGTCATCGACGTCGAGCCGGGCAAGATGTATCGGTTGCGCATGATCGGCGCCACGGCC
ATCTCCGTGGTCAAGCTGGGCATCGAGGATCACTCGAACCTCACCGTCATCGAGGCCGACGGCAGCTACACGGAG
CCAACGGAGATCGACCACATGCAGCTTGCCCCCGGCCAGCGCTTCAGCTACCGGCTACAGGCCAAGTCGGCCGCC
GAGATTGACCGGATGAACAAGACGGAGTTCTGGGTCCGCTACGAGAGCCGCGAGCGTCCGGAGAGCATCCAAGGC
TATGCCTTGCTGCGCTACCGCATGGACAAGTGCGAGAAGCCCCCTCGGCCCAAATCTCAGCTGCCGGACAAGTCT
CCTATCGAGTTGTCGACGACGACCAACGACTATCTCGAATATCAGCTGCAGCCTGCATCGCAGCAGGAGCGTCAG
AAGTTCCCTCGTCTGTCTGAGGTGACGCGAACCGTCACCATCCAGATCAACCAGATGCTCACGAGCGGCGAGTAC
GTCGACGGCAAGCTCCAGGGCAGCCTGGTTTGGGTGTAAGTCTTGACACGCTTTGATGAGCGAGACAAGAAGAAA
AAAAACAAGCTAACCTTGGGGGTTTACAGGCAAAACGGTTCTCCCTGGAAGGAAGACGTTCAGGCAGAGGCCAAC
CAAATGCCCTACCTAATCACCGTCTATACCGCCAACGAGGCCGATAACGTTACCATGCCCAACTACGAGCGCGCC
TTGGAGAACGGCGGCTTCGACTCGGAGACCAAGACGTTCCCGGCCAGAGTAGGCGAGGTGCTGGACATTGTGTGG
CAGAACAACGGCGGCATCACAGGAAACTTTGACATCCATCCGATGCACATCCACGGCGAACACGCGTGGGACCTG
GGCTCCGGCTCCGGCACGTACAAGGCCGAAGAGAACGAGAAGCGTTTCGAAGGCTTCACGCCCGCCCGGCGAGAC
ACCACCATCCTCTACCGCTACACCGAGAAGGACGCGCCGGACACGACCAACGGATGGCGAGCGTGGCGAATCCGC
GTGACCGAGGATAACGTCGGCGCTTGGATGATGCACTGTCACATCGCCCAGCACGCGGCCATGGGCATGAACACG
GTCTGGATCTTTGGTGACACGCCGGCCCTCATGAGTCGCTTCCCGACGGCCCCCTTCACCGAGGGCTATCTGAAA
TTCGGCGGCGAGGCTTACGGTTCGGCTGACAAAAGCCCGGTTGTGAACCACCACTTTGGGCAAGACGAGGCAGAA
GAGAAGAAGGCTGAAGAGGAGCAAAAGACGGCGGAAGAAGCGCCTCCTGAGCCGCCGACCGAACTCGACAACGCC
AACGAGTTTGATGTCGACGGCGAGAAGACCAAGAGGACGCAATAA

© 2023 - Robin Ohm - Utrecht University - The Netherlands

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