Fungal Genomics

at Utrecht University

General Properties

Protein IDOphio5|1984
Gene name
Locationscaffold_179:19681..21973
Strand+
Gene length (bp)2292
Transcript length (bp)1896
Coding sequence length (bp)1893
Protein length (aa) 631

Overview

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PFAM Domains

PFAM Domain ID Short name Long name E-value Start End
PF00743 FMO-like Flavin-binding monooxygenase-like 1.9E-48 5 380
PF13738 Pyr_redox_3 Pyridine nucleotide-disulphide oxidoreductase 2.7E-14 99 232
PF07992 Pyr_redox_2 Pyridine nucleotide-disulphide oxidoreductase 3.0E-13 5 241
PF13434 Lys_Orn_oxgnase L-lysine 6-monooxygenase/L-ornithine 5-monooxygenase 8.0E-08 106 223
PF13450 NAD_binding_8 NAD(P)-binding Rossmann-like domain 4.1E-05 8 48

Swissprot hits

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Swissprot ID Swissprot Description Start End E-value
sp|Q8K4C0|FMO5_RAT Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Rattus norvegicus GN=Fmo5 PE=1 SV=3 1 589 2.0E-50
sp|Q04799|FMO5_RABIT Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Oryctolagus cuniculus GN=FMO5 PE=1 SV=2 1 589 3.0E-50
sp|P49109|FMO5_CAVPO Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Cavia porcellus GN=FMO5 PE=2 SV=2 1 589 8.0E-50
sp|Q8K2I3|FMO2_MOUSE Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Mus musculus GN=Fmo2 PE=1 SV=3 5 618 1.0E-49
sp|P97872|FMO5_MOUSE Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Mus musculus GN=Fmo5 PE=1 SV=4 1 589 6.0E-49
[Show all]
[Show less]
Swissprot ID Swissprot Description Start End E-value
sp|Q8K4C0|FMO5_RAT Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Rattus norvegicus GN=Fmo5 PE=1 SV=3 1 589 2.0E-50
sp|Q04799|FMO5_RABIT Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Oryctolagus cuniculus GN=FMO5 PE=1 SV=2 1 589 3.0E-50
sp|P49109|FMO5_CAVPO Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Cavia porcellus GN=FMO5 PE=2 SV=2 1 589 8.0E-50
sp|Q8K2I3|FMO2_MOUSE Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Mus musculus GN=Fmo2 PE=1 SV=3 5 618 1.0E-49
sp|P97872|FMO5_MOUSE Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Mus musculus GN=Fmo5 PE=1 SV=4 1 589 6.0E-49
sp|Q8HZ70|FMO2_PANTR Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Pan troglodytes GN=FMO2 PE=3 SV=3 5 584 3.0E-48
sp|P17635|FMO2_RABIT Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Oryctolagus cuniculus GN=FMO2 PE=1 SV=3 5 584 6.0E-48
sp|Q8HZ69|FMO2_GORGO Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Gorilla gorilla gorilla GN=FMO2 PE=3 SV=3 5 584 7.0E-48
sp|Q5REK0|FMO2_PONAB Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Pongo abelii GN=FMO2 PE=2 SV=3 5 584 8.0E-48
sp|P36366|FMO2_CAVPO Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Cavia porcellus GN=FMO2 PE=2 SV=2 5 584 2.0E-47
sp|Q28505|FMO2_MACMU Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Macaca mulatta GN=FMO2 PE=2 SV=2 5 584 4.0E-47
sp|Q6IRI9|FMO2_RAT Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Rattus norvegicus GN=Fmo2 PE=2 SV=3 5 584 8.0E-46
sp|Q99518|FMO2_HUMAN Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Homo sapiens GN=FMO2 PE=1 SV=4 5 557 1.0E-45
sp|Q8K4B7|FMO4_RAT Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Rattus norvegicus GN=Fmo4 PE=2 SV=3 5 589 5.0E-45
sp|P49326|FMO5_HUMAN Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Homo sapiens GN=FMO5 PE=1 SV=2 1 613 1.0E-44
sp|Q8VHG0|FMO4_MOUSE Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Mus musculus GN=Fmo4 PE=1 SV=3 5 589 4.0E-42
sp|Q01740|FMO1_HUMAN Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Homo sapiens GN=FMO1 PE=2 SV=3 5 601 7.0E-42
sp|P36367|FMO4_RABIT Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Oryctolagus cuniculus GN=FMO4 PE=2 SV=2 5 589 2.0E-40
sp|Q8SPQ7|FMO3_MACMU Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Macaca mulatta GN=FMO3 PE=2 SV=3 5 589 5.0E-40
sp|Q9EQ76|FMO3_RAT Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Rattus norvegicus GN=Fmo3 PE=1 SV=1 5 589 1.0E-39
sp|P31512|FMO4_HUMAN Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Homo sapiens GN=FMO4 PE=1 SV=3 5 589 2.0E-39
sp|Q95LA2|FMO1_CANLF Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Canis lupus familiaris GN=FMO1 PE=2 SV=3 5 589 2.0E-39
sp|P97501|FMO3_MOUSE Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Mus musculus GN=Fmo3 PE=1 SV=1 5 601 9.0E-38
sp|P16549|FMO1_PIG Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Sus scrofa GN=FMO1 PE=1 SV=3 5 589 5.0E-37
sp|O60774|FMO6_HUMAN Putative dimethylaniline monooxygenase [N-oxide-forming] 6 OS=Homo sapiens GN=FMO6P PE=5 SV=1 3 584 2.0E-36
sp|Q95LA1|FMO3_CANLF Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Canis lupus familiaris GN=FMO3 PE=2 SV=3 5 589 2.0E-36
sp|P50285|FMO1_MOUSE Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Mus musculus GN=Fmo1 PE=1 SV=1 5 589 2.0E-36
sp|P36365|FMO1_RAT Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Rattus norvegicus GN=Fmo1 PE=1 SV=2 5 589 2.0E-36
sp|P31513|FMO3_HUMAN Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Homo sapiens GN=FMO3 PE=1 SV=5 5 589 3.0E-35
sp|Q7YS44|FMO3_PANTR Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Pan troglodytes GN=FMO3 PE=3 SV=3 5 589 5.0E-35
sp|P17636|FMO1_RABIT Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Oryctolagus cuniculus GN=FMO1 PE=1 SV=3 5 589 6.0E-34
sp|P32417|FMO3_RABIT Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Oryctolagus cuniculus GN=FMO3 PE=1 SV=3 5 589 5.0E-33
sp|Q8HYJ9|FMO3_BOVIN Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Bos taurus GN=FMO3 PE=2 SV=1 5 589 4.0E-30
sp|Q8VZ59|YUC6_ARATH Indole-3-pyruvate monooxygenase YUCCA6 OS=Arabidopsis thaliana GN=YUC6 PE=1 SV=1 7 374 2.0E-25
sp|O64489|YUC9_ARATH Probable indole-3-pyruvate monooxygenase YUCCA9 OS=Arabidopsis thaliana GN=YUC9 PE=2 SV=1 7 372 3.0E-25
sp|Q9LKC0|YUC5_ARATH Probable indole-3-pyruvate monooxygenase YUCCA5 OS=Arabidopsis thaliana GN=YUC5 PE=2 SV=1 7 372 4.0E-25
sp|Q9SVU0|YUC8_ARATH Probable indole-3-pyruvate monooxygenase YUCCA8 OS=Arabidopsis thaliana GN=YUC8 PE=2 SV=1 7 372 1.0E-24
sp|O23024|YUC3_ARATH Probable indole-3-pyruvate monooxygenase YUCCA3 OS=Arabidopsis thaliana GN=YUC3 PE=2 SV=1 7 372 2.0E-23
sp|O49312|YUC7_ARATH Probable indole-3-pyruvate monooxygenase YUCCA7 OS=Arabidopsis thaliana GN=YUC7 PE=2 SV=1 7 372 3.0E-23
sp|Q9SZY8|YUC1_ARATH Probable indole-3-pyruvate monooxygenase YUCCA1 OS=Arabidopsis thaliana GN=YUC1 PE=1 SV=1 7 374 7.0E-23
sp|Q9FWW6|GSXL1_ARATH Flavin-containing monooxygenase FMO GS-OX-like 1 OS=Arabidopsis thaliana GN=At1g12160 PE=2 SV=1 6 227 1.0E-21
sp|Q9LFM5|YUC4_ARATH Probable indole-3-pyruvate monooxygenase YUCCA4 OS=Arabidopsis thaliana GN=YUC4 PE=1 SV=1 7 374 2.0E-21
sp|Q9SVQ1|YUC2_ARATH Indole-3-pyruvate monooxygenase YUCCA2 OS=Arabidopsis thaliana GN=YUC2 PE=1 SV=1 7 374 2.0E-20
sp|Q9SXE1|GSOX3_ARATH Flavin-containing monooxygenase FMO GS-OX3 OS=Arabidopsis thaliana GN=FMOGS-OX3 PE=2 SV=1 1 229 4.0E-20
sp|Q9FF12|GSXL9_ARATH Flavin-containing monooxygenase FMO GS-OX-like 9 OS=Arabidopsis thaliana GN=At5g07800 PE=2 SV=1 3 229 4.0E-19
sp|Q9SS04|GSOX1_ARATH Flavin-containing monooxygenase FMO GS-OX1 OS=Arabidopsis thaliana GN=FMOGS-OX1 PE=2 SV=1 3 229 5.0E-19
sp|A8MRX0|GSOX5_ARATH Flavin-containing monooxygenase FMO GS-OX5 OS=Arabidopsis thaliana GN=FMOGS-OX5 PE=2 SV=2 1 229 2.0E-18
sp|Q93Y23|GSOX4_ARATH Flavin-containing monooxygenase FMO GS-OX4 OS=Arabidopsis thaliana GN=FMOGS-OX4 PE=2 SV=1 1 232 3.0E-18
sp|Q9FWW9|GSXL2_ARATH Flavin-containing monooxygenase FMO GS-OX-like 2 OS=Arabidopsis thaliana GN=At1g12200 PE=2 SV=1 2 229 5.0E-18
sp|Q9SXD5|GSXL3_ARATH Flavin-containing monooxygenase FMO GS-OX-like 3 OS=Arabidopsis thaliana GN=At1g62620 PE=2 SV=2 3 229 1.0E-17
sp|Q9C8U0|GSXL5_ARATH Flavin-containing monooxygenase FMO GS-OX-like 5 OS=Arabidopsis thaliana GN=At1g63370 PE=2 SV=2 3 229 2.0E-17
sp|Q94K43|GSOX2_ARATH Flavin-containing monooxygenase FMO GS-OX2 OS=Arabidopsis thaliana GN=FMOGS-OX2 PE=2 SV=1 1 229 3.0E-17
sp|Q9RKB5|BVMO2_STRCO Baeyer-Villiger monooxygenase OS=Streptomyces coelicolor (strain ATCC BAA-471 / A3(2) / M145) GN=SCO3172 PE=1 SV=1 4 372 4.0E-17
sp|Q8MP06|SNO1_TYRJA Senecionine N-oxygenase OS=Tyria jacobaeae GN=sno1 PE=1 SV=1 5 229 4.0E-17
sp|Q9FLK4|GSXL8_ARATH Flavin-containing monooxygenase FMO GS-OX-like 8 OS=Arabidopsis thaliana GN=At5g61290 PE=2 SV=1 2 229 5.0E-17
sp|Q9FWW3|GSXL6_ARATH Flavin-containing monooxygenase FMO GS-OX-like 6 OS=Arabidopsis thaliana GN=At1g12130 PE=2 SV=1 1 225 2.0E-16
sp|Q9HFE4|FMO1_SCHPO Thiol-specific monooxygenase OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=fmo1 PE=1 SV=1 5 231 2.0E-15
sp|Q93TJ5|HAPMO_PSEFL 4-hydroxyacetophenone monooxygenase OS=Pseudomonas fluorescens GN=hapE PE=1 SV=1 4 224 1.0E-14
sp|Q9FVQ0|YUC10_ARATH Probable indole-3-pyruvate monooxygenase YUCCA10 OS=Arabidopsis thaliana GN=YUC10 PE=2 SV=1 6 372 4.0E-14
sp|Q9LMA1|FMO1_ARATH Probable flavin-containing monooxygenase 1 OS=Arabidopsis thaliana GN=FMO1 PE=2 SV=1 1 372 7.0E-14
sp|Q9LPL3|YUC11_ARATH Probable indole-3-pyruvate monooxygenase YUCCA11 OS=Arabidopsis thaliana GN=YUC11 PE=2 SV=1 4 372 1.0E-13
sp|Q94BV5|GSXL4_ARATH Flavin-containing monooxygenase FMO GS-OX-like 4 OS=Arabidopsis thaliana GN=At1g62600 PE=2 SV=1 1 229 3.0E-13
sp|Q9C8T8|GSXLX_ARATH Putative flavin-containing monooxygenase FMO GS-OX-like 10 OS=Arabidopsis thaliana GN=At1g63340 PE=5 SV=3 3 232 2.0E-12
sp|P64746|Y916_MYCBO Uncharacterized monooxygenase Mb0916 OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=Mb0916 PE=3 SV=1 6 420 4.0E-12
sp|P9WNG1|Y892_MYCTU Uncharacterized monooxygenase Rv0892 OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=Rv0892 PE=1 SV=1 6 420 4.0E-12
sp|P9WNG0|Y892_MYCTO Uncharacterized monooxygenase MT0916 OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=MT0916 PE=3 SV=1 6 420 4.0E-12
sp|Q9SXD9|GSXL7_ARATH Flavin-containing monooxygenase FMO GS-OX-like 7 OS=Arabidopsis thaliana GN=At1g62580 PE=3 SV=2 3 232 5.0E-12
sp|A0R665|ETHA_MYCS2 FAD-containing monooxygenase EthA OS=Mycobacterium smegmatis (strain ATCC 700084 / mc(2)155) GN=ethA PE=3 SV=1 6 403 9.0E-11
sp|P55487|Y4ID_RHISN Uncharacterized monooxygenase y4iD OS=Rhizobium sp. (strain NGR234) GN=NGR_a03290 PE=3 SV=1 4 380 2.0E-10
sp|A3U3H1|BVMO_OCEBH Baeyer-Villiger monooxygenase OS=Oceanicola batsensis (strain ATCC BAA-863 / DSM 15984 / HTCC2597) GN=OB2597_18631 PE=1 SV=1 7 235 3.0E-10
sp|P9WNF9|ETHA_MYCTU FAD-containing monooxygenase EthA OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ethA PE=1 SV=1 4 373 1.0E-08
sp|P9WNF8|ETHA_MYCTO FAD-containing monooxygenase EthA OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=ethA PE=3 SV=1 4 373 1.0E-08
sp|Q7TVI2|ETHA_MYCBO FAD-containing monooxygenase EthA OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=ethA PE=1 SV=1 4 373 1.0E-08
sp|P38866|FMO1_YEAST Thiol-specific monooxygenase OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FMO1 PE=1 SV=2 26 247 2.0E-06
sp|Q9SH25|GSXLY_ARATH Putative flavin-containing monooxygenase FMO GS-OX-like 11 OS=Arabidopsis thaliana GN=At1g63390 PE=5 SV=1 1 144 3.0E-06
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GO

GO Term Description Terminal node
GO:0016491 oxidoreductase activity Yes
GO:0050660 flavin adenine dinucleotide binding Yes
GO:0050661 NADP binding Yes
GO:0004499 N,N-dimethylaniline monooxygenase activity Yes
GO:0004497 monooxygenase activity No
GO:0016705 oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen No
GO:0097159 organic cyclic compound binding No
GO:1901265 nucleoside phosphate binding No
GO:0005488 binding No
GO:0016709 oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen No
GO:0000166 nucleotide binding No
GO:0003824 catalytic activity No
GO:0003674 molecular_function No
GO:0043167 ion binding No
GO:0043168 anion binding No
GO:1901363 heterocyclic compound binding No
GO:0036094 small molecule 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
Cytoplasm 0.5867 0.3115 0.0743 0.1142 0.4826 0.1531 0.3404 0.2892 0.2409 0.0793

SignalP

(None)

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
Orthogroup410
Change Orthofinder run
Species Protein ID
Ophiocordyceps australis 1348a (Ghana) OphauG2|6712
Ophiocordyceps australis map64 (Brazil) OphauB2|6202
Ophiocordyceps camponoti-floridani Ophcf2|03398
Ophiocordyceps camponoti-rufipedis Ophun1|1265
Ophiocordyceps kimflemingae Ophio5|1984 (this protein)
Ophiocordyceps kimflemingae Ophio5|1985
Ophiocordyceps subramaniannii Hirsu2|2331

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|1984
MNSIRIVVIGLGPAGLTALKCLRDEGFDVVALERRSEVGGLWSYNPDGSYTSVIRGTVSNISKFVSGFSDFPIPK
GKASPLSCPVLFSTPLTVDIEYPPYLSGAQMAEYMQSYARHFNLEPHMRFNTSVQKVKRDTTRNAWRVELVGPAG
EEVAFFDKVVFGTGSERLPIWPSMPGRDEFRGIVIHGQSYRSPEQFAGKRVMVVGIGNTACDVALNLTGHASHVY
QSYRRGRILVSRYLDSGLPVDSTMAWPTLRLKYLLDDKMSWLSRPLVDRFMRRKMTTDAARQEPTGDGSRKSRRR
RRARERLNDWRLMTGPSMAHTHPAVQEDFIAALYAGLVLPVTGFRRFVGAEGVVVDDGSVVEVDAVVFCTGYSNG
FGIMPELEMDGAGDVPLKTAQEVESDETACSSAPHIPRLYQMIFPPRYASSVAFLSWMAPQESVWTVCELASTAI
SQIWAAETGRQLDLVPPDSRPSLLPCRARMEESVDEYHEWWRKQWKREPSMRDGLVRSHDFYRFLHRMAGTAMYD
NLDHLFSGVGWKLWWRDRDLYRCLASGPMNSYAWRLFDTNPDRIPGCGRAAWAGARQAVQEAYDTYGGYKAAVLS
KKLVRGPASSSTLKPIDSDTYHKTDSGDTWS
Coding >Ophio5|1984
ATGAATAGCATCAGAATCGTCGTCATCGGTCTCGGCCCCGCCGGCCTGACGGCCCTGAAATGTCTTCGAGACGAG
GGCTTCGATGTCGTGGCCCTGGAGAGGCGCAGCGAGGTTGGCGGCCTCTGGTCGTACAACCCGGATGGCAGCTAT
ACGTCCGTCATTCGTGGCACCGTCTCCAATATTAGCAAGTTTGTCTCCGGCTTTAGCGACTTTCCAATCCCCAAA
GGCAAAGCCTCGCCCCTGTCCTGTCCTGTCCTATTTTCGACTCCTCTGACGGTGGATATAGAATATCCGCCCTAC
CTCTCCGGTGCTCAGATGGCGGAATACATGCAATCGTACGCCCGCCATTTCAACCTCGAGCCTCACATGCGCTTC
AACACATCAGTTCAAAAAGTCAAGCGCGACACGACACGAAACGCATGGAGAGTTGAGCTGGTGGGCCCGGCGGGC
GAAGAGGTAGCCTTCTTCGACAAGGTAGTCTTCGGCACCGGCTCCGAAAGACTCCCTATTTGGCCGTCGATGCCC
GGCCGTGACGAGTTCCGCGGCATCGTCATACACGGACAGAGCTACCGGAGTCCGGAGCAGTTCGCCGGCAAACGC
GTCATGGTGGTAGGCATCGGCAACACAGCCTGCGACGTGGCCCTCAACCTGACCGGCCACGCCTCGCACGTATAT
CAATCCTACCGCCGGGGCCGAATACTGGTATCCCGCTACCTCGACAGCGGACTACCAGTCGACAGCACCATGGCC
TGGCCGACACTGCGTCTCAAATACCTACTGGACGATAAGATGTCGTGGCTCTCCCGGCCGCTCGTCGACCGCTTC
ATGCGGCGCAAGATGACGACGGACGCGGCGCGCCAAGAGCCCACCGGTGACGGGTCGCGAAAGAGTCGGCGCAGA
CGAAGGGCTCGCGAGAGGTTAAACGACTGGCGACTGATGACGGGACCGAGTATGGCGCATACGCATCCGGCTGTA
CAGGAGGACTTTATCGCCGCTCTCTACGCCGGTCTCGTCTTACCCGTCACTGGCTTTCGACGGTTTGTTGGCGCA
GAGGGCGTCGTGGTCGACGACGGTTCGGTTGTCGAGGTTGATGCCGTCGTCTTTTGCACCGGTTACTCCAACGGG
TTCGGTATCATGCCTGAGCTGGAGATGGACGGTGCGGGCGACGTGCCCCTGAAGACGGCTCAGGAGGTGGAATCG
GATGAGACGGCCTGCTCGTCGGCACCACACATCCCCCGGCTGTATCAGATGATATTCCCACCACGATACGCCTCC
TCCGTCGCCTTTCTCAGCTGGATGGCGCCGCAAGAGAGCGTGTGGACCGTGTGCGAGCTAGCCTCGACAGCCATC
TCTCAGATCTGGGCGGCCGAAACAGGCCGACAACTCGACCTTGTCCCACCCGACAGTCGACCATCTCTGCTCCCC
TGCCGAGCCAGGATGGAGGAGTCGGTAGACGAATACCACGAATGGTGGCGCAAGCAATGGAAGCGCGAGCCGTCG
ATGCGAGACGGCCTCGTCCGCTCTCACGACTTCTACCGCTTCCTCCACCGCATGGCCGGCACCGCCATGTACGAC
AACCTCGACCATCTCTTTTCCGGCGTCGGTTGGAAACTCTGGTGGCGTGATCGCGACTTGTATCGCTGTCTCGCC
TCCGGGCCCATGAATAGCTACGCCTGGCGCCTCTTCGACACCAACCCGGATCGGATACCGGGCTGTGGACGCGCT
GCTTGGGCTGGTGCGAGACAGGCCGTTCAAGAAGCTTACGACACCTACGGCGGCTACAAGGCCGCTGTTTTGAGC
AAGAAGCTTGTCCGCGGGCCCGCGAGCAGCTCTACATTGAAACCGATCGACTCTGATACGTATCACAAGACGGAC
TCGGGGGATACTTGGTCG
Transcript >Ophio5|1984
ATGAATAGCATCAGAATCGTCGTCATCGGTCTCGGCCCCGCCGGCCTGACGGCCCTGAAATGTCTTCGAGACGAG
GGCTTCGATGTCGTGGCCCTGGAGAGGCGCAGCGAGGTTGGCGGCCTCTGGTCGTACAACCCGGATGGCAGCTAT
ACGTCCGTCATTCGTGGCACCGTCTCCAATATTAGCAAGTTTGTCTCCGGCTTTAGCGACTTTCCAATCCCCAAA
GGCAAAGCCTCGCCCCTGTCCTGTCCTGTCCTATTTTCGACTCCTCTGACGGTGGATATAGAATATCCGCCCTAC
CTCTCCGGTGCTCAGATGGCGGAATACATGCAATCGTACGCCCGCCATTTCAACCTCGAGCCTCACATGCGCTTC
AACACATCAGTTCAAAAAGTCAAGCGCGACACGACACGAAACGCATGGAGAGTTGAGCTGGTGGGCCCGGCGGGC
GAAGAGGTAGCCTTCTTCGACAAGGTAGTCTTCGGCACCGGCTCCGAAAGACTCCCTATTTGGCCGTCGATGCCC
GGCCGTGACGAGTTCCGCGGCATCGTCATACACGGACAGAGCTACCGGAGTCCGGAGCAGTTCGCCGGCAAACGC
GTCATGGTGGTAGGCATCGGCAACACAGCCTGCGACGTGGCCCTCAACCTGACCGGCCACGCCTCGCACGTATAT
CAATCCTACCGCCGGGGCCGAATACTGGTATCCCGCTACCTCGACAGCGGACTACCAGTCGACAGCACCATGGCC
TGGCCGACACTGCGTCTCAAATACCTACTGGACGATAAGATGTCGTGGCTCTCCCGGCCGCTCGTCGACCGCTTC
ATGCGGCGCAAGATGACGACGGACGCGGCGCGCCAAGAGCCCACCGGTGACGGGTCGCGAAAGAGTCGGCGCAGA
CGAAGGGCTCGCGAGAGGTTAAACGACTGGCGACTGATGACGGGACCGAGTATGGCGCATACGCATCCGGCTGTA
CAGGAGGACTTTATCGCCGCTCTCTACGCCGGTCTCGTCTTACCCGTCACTGGCTTTCGACGGTTTGTTGGCGCA
GAGGGCGTCGTGGTCGACGACGGTTCGGTTGTCGAGGTTGATGCCGTCGTCTTTTGCACCGGTTACTCCAACGGG
TTCGGTATCATGCCTGAGCTGGAGATGGACGGTGCGGGCGACGTGCCCCTGAAGACGGCTCAGGAGGTGGAATCG
GATGAGACGGCCTGCTCGTCGGCACCACACATCCCCCGGCTGTATCAGATGATATTCCCACCACGATACGCCTCC
TCCGTCGCCTTTCTCAGCTGGATGGCGCCGCAAGAGAGCGTGTGGACCGTGTGCGAGCTAGCCTCGACAGCCATC
TCTCAGATCTGGGCGGCCGAAACAGGCCGACAACTCGACCTTGTCCCACCCGACAGTCGACCATCTCTGCTCCCC
TGCCGAGCCAGGATGGAGGAGTCGGTAGACGAATACCACGAATGGTGGCGCAAGCAATGGAAGCGCGAGCCGTCG
ATGCGAGACGGCCTCGTCCGCTCTCACGACTTCTACCGCTTCCTCCACCGCATGGCCGGCACCGCCATGTACGAC
AACCTCGACCATCTCTTTTCCGGCGTCGGTTGGAAACTCTGGTGGCGTGATCGCGACTTGTATCGCTGTCTCGCC
TCCGGGCCCATGAATAGCTACGCCTGGCGCCTCTTCGACACCAACCCGGATCGGATACCGGGCTGTGGACGCGCT
GCTTGGGCTGGTGCGAGACAGGCCGTTCAAGAAGCTTACGACACCTACGGCGGCTACAAGGCCGCTGTTTTGAGC
AAGAAGCTTGTCCGCGGGCCCGCGAGCAGCTCTACATTGAAACCGATCGACTCTGATACGTATCACAAGACGGAC
TCGGGGGATACTTGGTCGTGA
Gene >Ophio5|1984
ATGAATAGCATCAGAATCGTCGTCATCGGTCTCGGTATTCATGCTCCGTTCACTTTGAATAACGCAGTTTTTTCA
TAGACTAACGAGCACTCATCTAGGCCCCGCCGGCCTGACGGCCCTGAAATGTCTTCGAGACGAGGGCTTCGATGT
CGTGGCCCTGGAGAGGCGCAGCGAGGTTGGCGGCCTCTGGTCGTACAACCCGGATGGCAGCTATACGTCCGTCAT
TCGTGGCACCGTCTCCAATATTAGCAAGTTTGTCGTGAGTCGGACACCTACCTCAGCAAAGGACGCAGACGAGAC
GAAAGGAGGGAGACGGGAAAAAAGGGAGAATGACCAACTCTGACATGGAGCAAGCAGTCCGGCTTTAGCGACTTT
CCAATCCCCAAAGGCAAAGCCTCGCCCCTGTCCTGTCCTGTCCTATTTTCGACTCCTCTGACGGTGGATATAGAA
TATCCGCCCTACCTCTCCGGTGCTCAGATGGCGGAATACATGCAATCGTACGCCCGCCATTTCAACCTCGAGCCT
CACATGCGCTTCAACACATCAGTTCAAAAAGTCAAGCGCGACACGACACGAAACGCATGGAGAGTTGAGCTGGTG
GGCCCGGCGGGCGAAGAGGTAGCCTTCTTCGACAAGGTAGTCTTCGGCACCGGCTCCGAAAGACTCCCTATTTGG
CCGTCGATGCCCGGCCGTGACGAGTTCCGCGGCATCGTCATACACGGACAGAGCTACCGGAGGTGAGAACAAAAA
CTCGGGAAGAGCGGAGCGATGAAGAGTTTAGTCGAGCTGATATGATAATTCTCTTACCCATGCCCCCCTTAGTCC
GGAGCAGTTCGCCGGCAAACGCGTCATGGTGGTAGGCATCGGCAACACAGCCTGCGACGTGGCCCTCAACCTGAC
CGGCCACGCCTCGCACGTATATCAATCCTACCGCCGGGGCCGAATACTGGTATCCCGCTACCTCGACAGCGGACT
ACCAGTCGACAGCACCATGGCCTGGCCGACACTGCGTCTCAAATACCTACTGGACGATAAGATGTCGTGGCTCTC
CCGGCCGCTCGTCGACCGCTTCATGCGGCGCAAGATGACGACGGACGCGGCGCGCCAAGAGCCCACCGGTGACGG
GTCGCGAAAGAGTCGGCGCAGACGAAGGGCTCGCGAGAGGTTAAACGACTGGCGACTGATGACGGGACCGAGTAT
GGCGCATACGCATCCGGCTGTACAGGAGGACTTTATCGCCGCTCTCTACGCCGGTCTCGTCTTACCCGTCACTGG
CTTTCGACGGTTTGTTGGCGCAGAGGGCGTCGTGGTCGACGACGGTTCGGTTGTCGAGGTTGATGCCGTCGTCTT
TTGCACCGGTTACTCCAACGGGTTCGGTATCATGCCTGAGCTGGAGATGGACGGTGCGGGCGACGTGCCCCTGAA
GACGGCTCAGGAGGTGGAATCGGATGAGACGGCCTGCTCGTCGGCACCACACATCCCCCGGCTGTATCAGATGAT
ATTCCCACCACGATACGCCTCCTCCGTCGCCTTTCTCAGCTGGATGGCGCCGCAAGAGAGCGTGTGGACCGTGTG
CGAGCTAGCCTCGACAGCCATCTCTCAGATCTGGGCGGCCGAAACAGGCCGACAACTCGACCTTGTCCCACCCGA
CAGTCGACCATCTCTGCTCCCCTGCCGAGCCAGGATGGAGGAGTCGGTAGACGAATACCACGAATGGTGGCGCAA
GCAATGGAAGCGCGAGCCGTCGATGCGAGACGGCCTCGTCCGCTCTCACGACTTCTACCGCTTCCTCCACCGCAT
GGCCGGCACCGCCATGTACGACAACCTCGACCATCTCTTTTCCGGCGTCGGTTGGAAACTCTGGTGGCGTGATCG
CGACTTGTATCGCTGTCTCGCCTCCGGGCCCATGAATAGCTACGCCTGGCGCCTCTTCGACACCAACCCGGATCG
GATACCGGGCTGTGGACGCGCTGCTTGGGCTGGTGCGAGACAGGCCGTTCAAGAAGCTGTGAGTTGTCAACCTCC
TTTTCTCTTTCTCTCTCTCTCTCTCTCTCTCTCCCTCTTCCTATCCCTCTCTCTCTTGCTCTCCCCTCTCCCTCT
CTTTAAAGACTTGGGGGCATAGAATCGTTGTTGACTTTACAATCTTGGGCTTTTCAGTACGACACCTACGGCGGC
TACAAGGCCGCTGTTTTGAGCAAGAAGCTTGTCCGCGGGCCCGCGAGCAGCTCTACATTGAAACCGATCGACTCT
GATACGTATCACAAGACGGACTCGGGGGATACTTGGTCGTGA

© 2023 - Robin Ohm - Utrecht University - The Netherlands

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