Fungal Genomics

at Utrecht University

General Properties

Protein IDOphio5|5212
Gene name
Locationscaffold_42:48536..49952
Strand-
Gene length (bp)1416
Transcript length (bp)1416
Coding sequence length (bp)1413
Protein length (aa) 471

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 1.4E-14 100 263
PF00743 FMO-like Flavin-binding monooxygenase-like 3.3E-11 289 393
PF07992 Pyr_redox_2 Pyridine nucleotide-disulphide oxidoreductase 1.1E-12 12 266
PF13454 NAD_binding_9 FAD-NAD(P)-binding 8.3E-05 15 54
PF13434 Lys_Orn_oxgnase L-lysine 6-monooxygenase/L-ornithine 5-monooxygenase 1.0E-06 144 258
PF13450 NAD_binding_8 NAD(P)-binding Rossmann-like domain 4.9E-07 16 50

Swissprot hits

[Show all]
Swissprot ID Swissprot Description Start End E-value
sp|Q9HFE4|FMO1_SCHPO Thiol-specific monooxygenase OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=fmo1 PE=1 SV=1 11 451 1.0E-72
sp|Q9FF12|GSXL9_ARATH Flavin-containing monooxygenase FMO GS-OX-like 9 OS=Arabidopsis thaliana GN=At5g07800 PE=2 SV=1 7 387 2.0E-41
sp|Q9SXE1|GSOX3_ARATH Flavin-containing monooxygenase FMO GS-OX3 OS=Arabidopsis thaliana GN=FMOGS-OX3 PE=2 SV=1 12 424 1.0E-39
sp|Q9SXD5|GSXL3_ARATH Flavin-containing monooxygenase FMO GS-OX-like 3 OS=Arabidopsis thaliana GN=At1g62620 PE=2 SV=2 3 427 3.0E-39
sp|Q9FWW9|GSXL2_ARATH Flavin-containing monooxygenase FMO GS-OX-like 2 OS=Arabidopsis thaliana GN=At1g12200 PE=2 SV=1 39 418 2.0E-38
[Show all]
[Show less]
Swissprot ID Swissprot Description Start End E-value
sp|Q9HFE4|FMO1_SCHPO Thiol-specific monooxygenase OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=fmo1 PE=1 SV=1 11 451 1.0E-72
sp|Q9FF12|GSXL9_ARATH Flavin-containing monooxygenase FMO GS-OX-like 9 OS=Arabidopsis thaliana GN=At5g07800 PE=2 SV=1 7 387 2.0E-41
sp|Q9SXE1|GSOX3_ARATH Flavin-containing monooxygenase FMO GS-OX3 OS=Arabidopsis thaliana GN=FMOGS-OX3 PE=2 SV=1 12 424 1.0E-39
sp|Q9SXD5|GSXL3_ARATH Flavin-containing monooxygenase FMO GS-OX-like 3 OS=Arabidopsis thaliana GN=At1g62620 PE=2 SV=2 3 427 3.0E-39
sp|Q9FWW9|GSXL2_ARATH Flavin-containing monooxygenase FMO GS-OX-like 2 OS=Arabidopsis thaliana GN=At1g12200 PE=2 SV=1 39 418 2.0E-38
sp|Q9C8U0|GSXL5_ARATH Flavin-containing monooxygenase FMO GS-OX-like 5 OS=Arabidopsis thaliana GN=At1g63370 PE=2 SV=2 3 387 2.0E-38
sp|Q9FLK4|GSXL8_ARATH Flavin-containing monooxygenase FMO GS-OX-like 8 OS=Arabidopsis thaliana GN=At5g61290 PE=2 SV=1 6 387 4.0E-37
sp|P38866|FMO1_YEAST Thiol-specific monooxygenase OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FMO1 PE=1 SV=2 39 435 2.0E-36
sp|Q9SS04|GSOX1_ARATH Flavin-containing monooxygenase FMO GS-OX1 OS=Arabidopsis thaliana GN=FMOGS-OX1 PE=2 SV=1 12 452 3.0E-36
sp|Q94BV5|GSXL4_ARATH Flavin-containing monooxygenase FMO GS-OX-like 4 OS=Arabidopsis thaliana GN=At1g62600 PE=2 SV=1 3 394 8.0E-33
sp|A8MRX0|GSOX5_ARATH Flavin-containing monooxygenase FMO GS-OX5 OS=Arabidopsis thaliana GN=FMOGS-OX5 PE=2 SV=2 39 387 1.0E-31
sp|Q9FWW6|GSXL1_ARATH Flavin-containing monooxygenase FMO GS-OX-like 1 OS=Arabidopsis thaliana GN=At1g12160 PE=2 SV=1 1 397 1.0E-31
sp|Q94K43|GSOX2_ARATH Flavin-containing monooxygenase FMO GS-OX2 OS=Arabidopsis thaliana GN=FMOGS-OX2 PE=2 SV=1 39 393 2.0E-30
sp|Q93Y23|GSOX4_ARATH Flavin-containing monooxygenase FMO GS-OX4 OS=Arabidopsis thaliana GN=FMOGS-OX4 PE=2 SV=1 5 463 2.0E-30
sp|Q9SXD9|GSXL7_ARATH Flavin-containing monooxygenase FMO GS-OX-like 7 OS=Arabidopsis thaliana GN=At1g62580 PE=3 SV=2 39 386 6.0E-30
sp|Q9FWW3|GSXL6_ARATH Flavin-containing monooxygenase FMO GS-OX-like 6 OS=Arabidopsis thaliana GN=At1g12130 PE=2 SV=1 39 387 4.0E-28
sp|Q9C8T8|GSXLX_ARATH Putative flavin-containing monooxygenase FMO GS-OX-like 10 OS=Arabidopsis thaliana GN=At1g63340 PE=5 SV=3 39 378 5.0E-27
sp|Q8MP06|SNO1_TYRJA Senecionine N-oxygenase OS=Tyria jacobaeae GN=sno1 PE=1 SV=1 13 387 7.0E-27
sp|P36367|FMO4_RABIT Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Oryctolagus cuniculus GN=FMO4 PE=2 SV=2 12 388 1.0E-13
sp|P97501|FMO3_MOUSE Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Mus musculus GN=Fmo3 PE=1 SV=1 12 261 2.0E-13
sp|Q04799|FMO5_RABIT Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Oryctolagus cuniculus GN=FMO5 PE=1 SV=2 12 255 3.0E-13
sp|Q9EQ76|FMO3_RAT Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Rattus norvegicus GN=Fmo3 PE=1 SV=1 12 255 4.0E-13
sp|Q8HZ69|FMO2_GORGO Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Gorilla gorilla gorilla GN=FMO2 PE=3 SV=3 12 251 2.0E-12
sp|Q8K4B7|FMO4_RAT Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Rattus norvegicus GN=Fmo4 PE=2 SV=3 12 275 2.0E-12
sp|Q99518|FMO2_HUMAN Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Homo sapiens GN=FMO2 PE=1 SV=4 12 251 2.0E-12
sp|P49109|FMO5_CAVPO Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Cavia porcellus GN=FMO5 PE=2 SV=2 12 266 3.0E-12
sp|Q8HZ70|FMO2_PANTR Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Pan troglodytes GN=FMO2 PE=3 SV=3 12 251 3.0E-12
sp|Q28505|FMO2_MACMU Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Macaca mulatta GN=FMO2 PE=2 SV=2 12 266 3.0E-12
sp|Q8K4C0|FMO5_RAT Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Rattus norvegicus GN=Fmo5 PE=1 SV=3 12 255 4.0E-12
sp|Q8VHG0|FMO4_MOUSE Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Mus musculus GN=Fmo4 PE=1 SV=3 12 266 4.0E-12
sp|P16549|FMO1_PIG Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Sus scrofa GN=FMO1 PE=1 SV=3 12 265 5.0E-12
sp|Q95LA2|FMO1_CANLF Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Canis lupus familiaris GN=FMO1 PE=2 SV=3 12 265 9.0E-12
sp|Q8SPQ7|FMO3_MACMU Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Macaca mulatta GN=FMO3 PE=2 SV=3 12 251 1.0E-11
sp|Q5REK0|FMO2_PONAB Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Pongo abelii GN=FMO2 PE=2 SV=3 12 251 1.0E-11
sp|P97872|FMO5_MOUSE Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Mus musculus GN=Fmo5 PE=1 SV=4 12 255 2.0E-11
sp|P36366|FMO2_CAVPO Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Cavia porcellus GN=FMO2 PE=2 SV=2 12 251 2.0E-11
sp|P31512|FMO4_HUMAN Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Homo sapiens GN=FMO4 PE=1 SV=3 12 266 2.0E-11
sp|O60774|FMO6_HUMAN Putative dimethylaniline monooxygenase [N-oxide-forming] 6 OS=Homo sapiens GN=FMO6P PE=5 SV=1 12 266 5.0E-11
sp|P17636|FMO1_RABIT Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Oryctolagus cuniculus GN=FMO1 PE=1 SV=3 12 265 6.0E-11
sp|Q95LA1|FMO3_CANLF Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Canis lupus familiaris GN=FMO3 PE=2 SV=3 12 251 1.0E-10
sp|P32417|FMO3_RABIT Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Oryctolagus cuniculus GN=FMO3 PE=1 SV=3 268 418 1.0E-09
sp|Q6IRI9|FMO2_RAT Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Rattus norvegicus GN=Fmo2 PE=2 SV=3 11 251 1.0E-09
sp|Q9SVQ1|YUC2_ARATH Indole-3-pyruvate monooxygenase YUCCA2 OS=Arabidopsis thaliana GN=YUC2 PE=1 SV=1 101 260 2.0E-09
sp|Q8K2I3|FMO2_MOUSE Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Mus musculus GN=Fmo2 PE=1 SV=3 12 254 2.0E-09
sp|Q04799|FMO5_RABIT Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Oryctolagus cuniculus GN=FMO5 PE=1 SV=2 294 399 3.0E-09
sp|Q5REK0|FMO2_PONAB Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Pongo abelii GN=FMO2 PE=2 SV=3 268 387 7.0E-09
sp|P32417|FMO3_RABIT Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Oryctolagus cuniculus GN=FMO3 PE=1 SV=3 12 251 9.0E-09
sp|Q99518|FMO2_HUMAN Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Homo sapiens GN=FMO2 PE=1 SV=4 268 387 1.0E-08
sp|Q8HZ70|FMO2_PANTR Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Pan troglodytes GN=FMO2 PE=3 SV=3 268 387 1.0E-08
sp|Q8HZ69|FMO2_GORGO Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Gorilla gorilla gorilla GN=FMO2 PE=3 SV=3 268 387 1.0E-08
sp|Q28505|FMO2_MACMU Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Macaca mulatta GN=FMO2 PE=2 SV=2 268 387 2.0E-08
sp|Q7YS44|FMO3_PANTR Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Pan troglodytes GN=FMO3 PE=3 SV=3 12 266 3.0E-08
sp|P36366|FMO2_CAVPO Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Cavia porcellus GN=FMO2 PE=2 SV=2 294 416 3.0E-08
sp|P31513|FMO3_HUMAN Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Homo sapiens GN=FMO3 PE=1 SV=5 12 266 4.0E-08
sp|Q6IRI9|FMO2_RAT Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Rattus norvegicus GN=Fmo2 PE=2 SV=3 287 388 6.0E-08
sp|O60774|FMO6_HUMAN Putative dimethylaniline monooxygenase [N-oxide-forming] 6 OS=Homo sapiens GN=FMO6P PE=5 SV=1 268 404 6.0E-08
sp|P49109|FMO5_CAVPO Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Cavia porcellus GN=FMO5 PE=2 SV=2 294 399 6.0E-08
sp|Q8K4C0|FMO5_RAT Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Rattus norvegicus GN=Fmo5 PE=1 SV=3 294 399 7.0E-08
sp|P49326|FMO5_HUMAN Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Homo sapiens GN=FMO5 PE=1 SV=2 294 420 8.0E-08
sp|P97872|FMO5_MOUSE Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Mus musculus GN=Fmo5 PE=1 SV=4 294 399 1.0E-07
sp|P17635|FMO2_RABIT Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Oryctolagus cuniculus GN=FMO2 PE=1 SV=3 294 430 1.0E-07
sp|P31512|FMO4_HUMAN Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Homo sapiens GN=FMO4 PE=1 SV=3 268 430 2.0E-07
sp|Q9FVQ0|YUC10_ARATH Probable indole-3-pyruvate monooxygenase YUCCA10 OS=Arabidopsis thaliana GN=YUC10 PE=2 SV=1 162 260 2.0E-07
sp|Q9EQ76|FMO3_RAT Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Rattus norvegicus GN=Fmo3 PE=1 SV=1 268 430 2.0E-07
sp|P49326|FMO5_HUMAN Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Homo sapiens GN=FMO5 PE=1 SV=2 12 265 3.0E-07
sp|Q8HYJ9|FMO3_BOVIN Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Bos taurus GN=FMO3 PE=2 SV=1 272 430 3.0E-07
sp|P97501|FMO3_MOUSE Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Mus musculus GN=Fmo3 PE=1 SV=1 268 430 3.0E-07
sp|Q9LFM5|YUC4_ARATH Probable indole-3-pyruvate monooxygenase YUCCA4 OS=Arabidopsis thaliana GN=YUC4 PE=1 SV=1 100 250 5.0E-07
sp|Q9SZY8|YUC1_ARATH Probable indole-3-pyruvate monooxygenase YUCCA1 OS=Arabidopsis thaliana GN=YUC1 PE=1 SV=1 93 250 6.0E-07
sp|Q8K2I3|FMO2_MOUSE Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Mus musculus GN=Fmo2 PE=1 SV=3 287 388 8.0E-07
sp|Q8VZ59|YUC6_ARATH Indole-3-pyruvate monooxygenase YUCCA6 OS=Arabidopsis thaliana GN=YUC6 PE=1 SV=1 2 250 1.0E-06
sp|O64489|YUC9_ARATH Probable indole-3-pyruvate monooxygenase YUCCA9 OS=Arabidopsis thaliana GN=YUC9 PE=2 SV=1 100 262 3.0E-06
sp|Q8HYJ9|FMO3_BOVIN Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Bos taurus GN=FMO3 PE=2 SV=1 178 266 5.0E-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|Nucleus Peroxisomal targeting signal 0.8228 0.5412 0.0519 0.053 0.4673 0.034 0.0409 0.198 0.1271 0.7163

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
Orthogroup1617
Change Orthofinder run
Species Protein ID
Ophiocordyceps australis 1348a (Ghana) OphauG2|7143
Ophiocordyceps australis map64 (Brazil) OphauB2|3613
Ophiocordyceps camponoti-floridani Ophcf2|05075
Ophiocordyceps camponoti-rufipedis Ophun1|3475
Ophiocordyceps kimflemingae Ophio5|5212 (this protein)
Ophiocordyceps subramaniannii Hirsu2|1276

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|5212
MGSVSPSRFHVKQVAIIGAGPSGLAAAKYLLAQQAFDHIAVFEQQQDIGGVWVPPPAESSPPPPPSTVPQTNPFR
PPETPVPIAEARPHYKPAVYFPSPVYDHLRANIIGPLMQFSDEPFPSSCCVFPSLEDIRASVRRYGREVRHLVRF
GQQVTRLELLQEQGRDRWHLRARDLLSGETADYVFDAVVVASGHYSLPFIPDIKNITDFHRAHPTVVTHSKHYRS
PKSFLDKKVIVVGNGPSGIDIAAQINAVSKVKTLLSVKAATSPETLACIGCDEAPEIVEFLIDQRGVRFKDGSVE
INVDSVVFCTGYLFSYPFLADLQAKLITNGRGVHGLYKHLFTIQHPTLVFLALPMRSVPWPMSECQAAAVATVWS
NQLELPPVEEMLSWSRSLHERVGEALHVMPPGGNCQYINELHDWVMKASHLGKQPPRWSDLSGWQHLHMPEARRR
FQEQGCRATTWTELGFQEALG
Coding >Ophio5|5212
ATGGGGTCCGTATCCCCCAGCCGCTTCCACGTGAAGCAAGTCGCCATCATCGGCGCCGGTCCCTCCGGCCTCGCT
GCAGCCAAGTACCTTCTCGCCCAGCAGGCCTTCGACCACATCGCCGTCTTCGAGCAACAGCAAGATATCGGCGGC
GTCTGGGTTCCTCCTCCCGCCGAATCAAGCCCCCCTCCGCCGCCCAGCACCGTGCCGCAGACGAATCCCTTTCGG
CCTCCCGAAACTCCCGTCCCCATCGCCGAAGCCCGGCCCCACTACAAGCCGGCCGTGTACTTCCCGTCACCCGTC
TACGACCATCTCCGCGCCAACATCATCGGTCCGCTCATGCAGTTCTCCGACGAGCCGTTCCCCTCTTCTTGCTGC
GTCTTTCCGTCGTTGGAGGACATTCGGGCCTCCGTTCGCCGCTACGGCCGGGAGGTCCGTCATCTCGTCCGCTTC
GGCCAGCAGGTCACCAGACTCGAGCTGCTGCAGGAGCAGGGCCGAGACCGATGGCATCTCCGAGCTCGGGATTTG
CTCAGCGGCGAGACGGCTGACTATGTCTTTGATGCTGTCGTCGTCGCTAGCGGACACTATTCTTTACCCTTTATT
CCGGACATCAAAAACATCACCGACTTCCATCGCGCCCACCCTACTGTCGTCACCCATTCGAAGCATTATCGCTCC
CCAAAAAGCTTCCTTGACAAAAAGGTCATTGTCGTAGGCAACGGTCCCTCAGGCATCGACATTGCGGCCCAGATC
AACGCCGTGTCCAAGGTCAAAACTCTCCTCTCTGTCAAAGCCGCCACTTCGCCTGAGACCCTTGCCTGCATCGGT
TGCGATGAGGCTCCAGAGATAGTCGAATTTCTGATCGATCAGCGTGGCGTGCGATTTAAAGATGGAAGCGTCGAG
ATCAACGTCGACTCTGTTGTCTTTTGCACGGGGTACCTCTTCAGCTACCCCTTCCTTGCCGACTTACAGGCCAAG
CTCATCACCAACGGCCGCGGCGTCCACGGCCTTTACAAGCACTTATTTACCATCCAACACCCTACCTTGGTCTTT
CTCGCTCTACCCATGAGATCTGTCCCTTGGCCCATGTCCGAGTGTCAAGCCGCAGCGGTCGCCACAGTTTGGTCC
AATCAGCTCGAGCTGCCTCCGGTGGAGGAGATGCTAAGCTGGAGTAGAAGTTTGCATGAGAGAGTGGGTGAGGCT
CTTCATGTTATGCCACCCGGCGGTAATTGTCAGTACATCAACGAGCTTCATGACTGGGTAATGAAGGCCTCGCAT
CTGGGAAAACAACCTCCGCGATGGAGCGATTTGAGCGGATGGCAACATCTTCACATGCCAGAGGCACGGCGCCGC
TTCCAGGAGCAAGGCTGCCGAGCGACGACTTGGACGGAGCTGGGCTTTCAAGAAGCGCTCGGA
Transcript >Ophio5|5212
ATGGGGTCCGTATCCCCCAGCCGCTTCCACGTGAAGCAAGTCGCCATCATCGGCGCCGGTCCCTCCGGCCTCGCT
GCAGCCAAGTACCTTCTCGCCCAGCAGGCCTTCGACCACATCGCCGTCTTCGAGCAACAGCAAGATATCGGCGGC
GTCTGGGTTCCTCCTCCCGCCGAATCAAGCCCCCCTCCGCCGCCCAGCACCGTGCCGCAGACGAATCCCTTTCGG
CCTCCCGAAACTCCCGTCCCCATCGCCGAAGCCCGGCCCCACTACAAGCCGGCCGTGTACTTCCCGTCACCCGTC
TACGACCATCTCCGCGCCAACATCATCGGTCCGCTCATGCAGTTCTCCGACGAGCCGTTCCCCTCTTCTTGCTGC
GTCTTTCCGTCGTTGGAGGACATTCGGGCCTCCGTTCGCCGCTACGGCCGGGAGGTCCGTCATCTCGTCCGCTTC
GGCCAGCAGGTCACCAGACTCGAGCTGCTGCAGGAGCAGGGCCGAGACCGATGGCATCTCCGAGCTCGGGATTTG
CTCAGCGGCGAGACGGCTGACTATGTCTTTGATGCTGTCGTCGTCGCTAGCGGACACTATTCTTTACCCTTTATT
CCGGACATCAAAAACATCACCGACTTCCATCGCGCCCACCCTACTGTCGTCACCCATTCGAAGCATTATCGCTCC
CCAAAAAGCTTCCTTGACAAAAAGGTCATTGTCGTAGGCAACGGTCCCTCAGGCATCGACATTGCGGCCCAGATC
AACGCCGTGTCCAAGGTCAAAACTCTCCTCTCTGTCAAAGCCGCCACTTCGCCTGAGACCCTTGCCTGCATCGGT
TGCGATGAGGCTCCAGAGATAGTCGAATTTCTGATCGATCAGCGTGGCGTGCGATTTAAAGATGGAAGCGTCGAG
ATCAACGTCGACTCTGTTGTCTTTTGCACGGGGTACCTCTTCAGCTACCCCTTCCTTGCCGACTTACAGGCCAAG
CTCATCACCAACGGCCGCGGCGTCCACGGCCTTTACAAGCACTTATTTACCATCCAACACCCTACCTTGGTCTTT
CTCGCTCTACCCATGAGATCTGTCCCTTGGCCCATGTCCGAGTGTCAAGCCGCAGCGGTCGCCACAGTTTGGTCC
AATCAGCTCGAGCTGCCTCCGGTGGAGGAGATGCTAAGCTGGAGTAGAAGTTTGCATGAGAGAGTGGGTGAGGCT
CTTCATGTTATGCCACCCGGCGGTAATTGTCAGTACATCAACGAGCTTCATGACTGGGTAATGAAGGCCTCGCAT
CTGGGAAAACAACCTCCGCGATGGAGCGATTTGAGCGGATGGCAACATCTTCACATGCCAGAGGCACGGCGCCGC
TTCCAGGAGCAAGGCTGCCGAGCGACGACTTGGACGGAGCTGGGCTTTCAAGAAGCGCTCGGATAA
Gene >Ophio5|5212
ATGGGGTCCGTATCCCCCAGCCGCTTCCACGTGAAGCAAGTCGCCATCATCGGCGCCGGTCCCTCCGGCCTCGCT
GCAGCCAAGTACCTTCTCGCCCAGCAGGCCTTCGACCACATCGCCGTCTTCGAGCAACAGCAAGATATCGGCGGC
GTCTGGGTTCCTCCTCCCGCCGAATCAAGCCCCCCTCCGCCGCCCAGCACCGTGCCGCAGACGAATCCCTTTCGG
CCTCCCGAAACTCCCGTCCCCATCGCCGAAGCCCGGCCCCACTACAAGCCGGCCGTGTACTTCCCGTCACCCGTC
TACGACCATCTCCGCGCCAACATCATCGGTCCGCTCATGCAGTTCTCCGACGAGCCGTTCCCCTCTTCTTGCTGC
GTCTTTCCGTCGTTGGAGGACATTCGGGCCTCCGTTCGCCGCTACGGCCGGGAGGTCCGTCATCTCGTCCGCTTC
GGCCAGCAGGTCACCAGACTCGAGCTGCTGCAGGAGCAGGGCCGAGACCGATGGCATCTCCGAGCTCGGGATTTG
CTCAGCGGCGAGACGGCTGACTATGTCTTTGATGCTGTCGTCGTCGCTAGCGGACACTATTCTTTACCCTTTATT
CCGGACATCAAAAACATCACCGACTTCCATCGCGCCCACCCTACTGTCGTCACCCATTCGAAGCATTATCGCTCC
CCAAAAAGCTTCCTTGACAAAAAGGTCATTGTCGTAGGCAACGGTCCCTCAGGCATCGACATTGCGGCCCAGATC
AACGCCGTGTCCAAGGTCAAAACTCTCCTCTCTGTCAAAGCCGCCACTTCGCCTGAGACCCTTGCCTGCATCGGT
TGCGATGAGGCTCCAGAGATAGTCGAATTTCTGATCGATCAGCGTGGCGTGCGATTTAAAGATGGAAGCGTCGAG
ATCAACGTCGACTCTGTTGTCTTTTGCACGGGGTACCTCTTCAGCTACCCCTTCCTTGCCGACTTACAGGCCAAG
CTCATCACCAACGGCCGCGGCGTCCACGGCCTTTACAAGCACTTATTTACCATCCAACACCCTACCTTGGTCTTT
CTCGCTCTACCCATGAGATCTGTCCCTTGGCCCATGTCCGAGTGTCAAGCCGCAGCGGTCGCCACAGTTTGGTCC
AATCAGCTCGAGCTGCCTCCGGTGGAGGAGATGCTAAGCTGGAGTAGAAGTTTGCATGAGAGAGTGGGTGAGGCT
CTTCATGTTATGCCACCCGGCGGTAATTGTCAGTACATCAACGAGCTTCATGACTGGGTAATGAAGGCCTCGCAT
CTGGGAAAACAACCTCCGCGATGGAGCGATTTGAGCGGATGGCAACATCTTCACATGCCAGAGGCACGGCGCCGC
TTCCAGGAGCAAGGCTGCCGAGCGACGACTTGGACGGAGCTGGGCTTTCAAGAAGCGCTCGGATAA

© 2023 - Robin Ohm - Utrecht University - The Netherlands

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