Fungal Genomics

at Utrecht University

General Properties

Protein IDOphio5|7128
Gene name
Locationscaffold_667:3986..6448
Strand+
Gene length (bp)2462
Transcript length (bp)2349
Coding sequence length (bp)2346
Protein length (aa) 782

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PFAM Domains

PFAM Domain ID Short name Long name E-value Start End
PF16209 PhoLip_ATPase_N Phospholipid-translocating ATPase N-terminal 1.7E-14 128 179
PF00122 E1-E2_ATPase E1-E2 ATPase 5.7E-10 228 432
PF13246 Cation_ATPase Cation transport ATPase (P-type) 2.1E-09 582 662

Swissprot hits

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Swissprot ID Swissprot Description Start End E-value
sp|Q9UT43|YFRD_SCHPO Putative phospholipid-transporting ATPase C821.13c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC821.13c PE=1 SV=2 230 782 4.0E-117
sp|P39524|ATC3_YEAST Probable phospholipid-transporting ATPase DRS2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DRS2 PE=1 SV=2 124 663 2.0E-92
sp|Q9XIE6|ALA3_ARATH Phospholipid-transporting ATPase 3 OS=Arabidopsis thaliana GN=ALA3 PE=1 SV=2 132 677 3.0E-87
sp|Q9LK90|ALA8_ARATH Probable phospholipid-transporting ATPase 8 OS=Arabidopsis thaliana GN=ALA8 PE=3 SV=1 123 682 2.0E-86
sp|C7EXK4|AT8A2_BOVIN Phospholipid-transporting ATPase IB OS=Bos taurus GN=ATP8A2 PE=1 SV=4 129 664 4.0E-84
[Show all]
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Swissprot ID Swissprot Description Start End E-value
sp|Q9UT43|YFRD_SCHPO Putative phospholipid-transporting ATPase C821.13c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC821.13c PE=1 SV=2 230 782 4.0E-117
sp|P39524|ATC3_YEAST Probable phospholipid-transporting ATPase DRS2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DRS2 PE=1 SV=2 124 663 2.0E-92
sp|Q9XIE6|ALA3_ARATH Phospholipid-transporting ATPase 3 OS=Arabidopsis thaliana GN=ALA3 PE=1 SV=2 132 677 3.0E-87
sp|Q9LK90|ALA8_ARATH Probable phospholipid-transporting ATPase 8 OS=Arabidopsis thaliana GN=ALA8 PE=3 SV=1 123 682 2.0E-86
sp|C7EXK4|AT8A2_BOVIN Phospholipid-transporting ATPase IB OS=Bos taurus GN=ATP8A2 PE=1 SV=4 129 664 4.0E-84
sp|Q9NTI2|AT8A2_HUMAN Phospholipid-transporting ATPase IB OS=Homo sapiens GN=ATP8A2 PE=1 SV=2 131 664 3.0E-83
sp|Q29449|AT8A1_BOVIN Probable phospholipid-transporting ATPase IA OS=Bos taurus GN=ATP8A1 PE=1 SV=2 129 664 4.0E-83
sp|Q148W0|AT8B1_MOUSE Phospholipid-transporting ATPase IC OS=Mus musculus GN=Atp8b1 PE=1 SV=2 129 663 5.0E-83
sp|P70704|AT8A1_MOUSE Phospholipid-transporting ATPase IA OS=Mus musculus GN=Atp8a1 PE=1 SV=2 129 664 9.0E-83
sp|O94296|YOOC_SCHPO Probable phospholipid-transporting ATPase C887.12 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPBC887.12 PE=3 SV=1 80 664 1.0E-82
sp|Q5BL50|AT8B1_XENTR Phospholipid-transporting ATPase IC OS=Xenopus tropicalis GN=atp8b1 PE=2 SV=1 129 663 1.0E-82
sp|P98200|AT8A2_MOUSE Phospholipid-transporting ATPase IB OS=Mus musculus GN=Atp8a2 PE=1 SV=1 129 664 2.0E-82
sp|Q9Y2Q0|AT8A1_HUMAN Phospholipid-transporting ATPase IA OS=Homo sapiens GN=ATP8A1 PE=1 SV=1 129 664 3.0E-82
sp|O43520|AT8B1_HUMAN Phospholipid-transporting ATPase IC OS=Homo sapiens GN=ATP8B1 PE=1 SV=3 129 663 7.0E-82
sp|Q9SGG3|ALA5_ARATH Probable phospholipid-transporting ATPase 5 OS=Arabidopsis thaliana GN=ALA5 PE=3 SV=1 121 664 3.0E-81
sp|P57792|ALA12_ARATH Probable phospholipid-transporting ATPase 12 OS=Arabidopsis thaliana GN=ALA12 PE=2 SV=1 129 664 2.0E-80
sp|Q9LNQ4|ALA4_ARATH Probable phospholipid-transporting ATPase 4 OS=Arabidopsis thaliana GN=ALA4 PE=3 SV=2 121 664 3.0E-80
sp|Q9SX33|ALA9_ARATH Putative phospholipid-transporting ATPase 9 OS=Arabidopsis thaliana GN=ALA9 PE=3 SV=1 129 685 5.0E-79
sp|A3FIN4|AT8B5_MOUSE Phospholipid-transporting ATPase FetA OS=Mus musculus GN=Atp8b5 PE=2 SV=1 127 663 2.0E-77
sp|Q9LI83|ALA10_ARATH Phospholipid-transporting ATPase 10 OS=Arabidopsis thaliana GN=ALA10 PE=3 SV=1 129 664 2.0E-77
sp|Q6UQ17|AT8B3_MOUSE Phospholipid-transporting ATPase IK OS=Mus musculus GN=Atp8b3 PE=1 SV=1 129 676 7.0E-77
sp|Q8TF62|AT8B4_HUMAN Probable phospholipid-transporting ATPase IM OS=Homo sapiens GN=ATP8B4 PE=1 SV=3 127 663 1.0E-75
sp|Q9SAF5|ALA11_ARATH Probable phospholipid-transporting ATPase 11 OS=Arabidopsis thaliana GN=ALA11 PE=2 SV=1 129 664 3.0E-75
sp|O60423|AT8B3_HUMAN Phospholipid-transporting ATPase IK OS=Homo sapiens GN=ATP8B3 PE=2 SV=4 129 670 2.0E-73
sp|Q9U280|TAT1_CAEEL Phospholipid-transporting ATPase tat-1 OS=Caenorhabditis elegans GN=tat-1 PE=3 SV=3 129 663 9.0E-73
sp|P98198|AT8B2_HUMAN Phospholipid-transporting ATPase ID OS=Homo sapiens GN=ATP8B2 PE=1 SV=2 98 663 4.0E-71
sp|P98199|AT8B2_MOUSE Phospholipid-transporting ATPase ID OS=Mus musculus GN=Atp8b2 PE=2 SV=2 98 663 1.0E-70
sp|P98204|ALA1_ARATH Phospholipid-transporting ATPase 1 OS=Arabidopsis thaliana GN=ALA1 PE=2 SV=1 119 657 2.0E-69
sp|P98205|ALA2_ARATH Phospholipid-transporting ATPase 2 OS=Arabidopsis thaliana GN=ALA2 PE=1 SV=1 122 660 4.0E-67
sp|Q9QZW0|AT11C_MOUSE Phospholipid-transporting ATPase 11C OS=Mus musculus GN=Atp11c PE=1 SV=2 113 706 1.0E-64
sp|Q8NB49|AT11C_HUMAN Phospholipid-transporting ATPase IG OS=Homo sapiens GN=ATP11C PE=1 SV=3 101 687 1.0E-64
sp|Q12674|ATC8_YEAST Probable phospholipid-transporting ATPase DNF3 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF3 PE=1 SV=1 234 531 2.0E-64
sp|Q9LVK9|ALA7_ARATH Probable phospholipid-transporting ATPase 7 OS=Arabidopsis thaliana GN=ALA7 PE=3 SV=3 127 514 3.0E-63
sp|Q9SLK6|ALA6_ARATH Phospholipid-transporting ATPase 6 OS=Arabidopsis thaliana GN=ALA6 PE=1 SV=2 129 514 9.0E-62
sp|O36028|ATCZ_SCHPO Putative phospholipid-transporting ATPase C4F10.16c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC4F10.16c PE=3 SV=1 240 682 1.0E-61
sp|Q09891|ATCX_SCHPO Putative phospholipid-transporting ATPase C24B11.12c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC24B11.12c PE=3 SV=1 235 670 6.0E-61
sp|Q9Y2G3|AT11B_HUMAN Probable phospholipid-transporting ATPase IF OS=Homo sapiens GN=ATP11B PE=1 SV=2 129 672 1.0E-60
sp|P98197|AT11A_MOUSE Probable phospholipid-transporting ATPase IH OS=Mus musculus GN=Atp11a PE=1 SV=1 103 687 1.0E-60
sp|O60312|AT10A_HUMAN Probable phospholipid-transporting ATPase VA OS=Homo sapiens GN=ATP10A PE=2 SV=2 102 524 1.0E-60
sp|P98196|AT11A_HUMAN Probable phospholipid-transporting ATPase IH OS=Homo sapiens GN=ATP11A PE=1 SV=3 103 687 9.0E-60
sp|Q12675|ATC4_YEAST Phospholipid-transporting ATPase DNF2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF2 PE=1 SV=1 235 663 1.0E-59
sp|P32660|ATC5_YEAST Phospholipid-transporting ATPase DNF1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF1 PE=1 SV=2 235 673 3.0E-59
sp|Q8K2X1|AT10D_MOUSE Probable phospholipid-transporting ATPase VD OS=Mus musculus GN=Atp10d PE=2 SV=2 104 526 5.0E-59
sp|O54827|AT10A_MOUSE Probable phospholipid-transporting ATPase VA OS=Mus musculus GN=Atp10a PE=1 SV=4 131 524 9.0E-59
sp|Q9N0Z4|AT11B_RABIT Probable phospholipid-transporting ATPase IF (Fragment) OS=Oryctolagus cuniculus GN=ATP11B PE=1 SV=2 129 672 1.0E-58
sp|Q9P241|AT10D_HUMAN Probable phospholipid-transporting ATPase VD OS=Homo sapiens GN=ATP10D PE=2 SV=3 104 526 8.0E-57
sp|O94823|AT10B_HUMAN Probable phospholipid-transporting ATPase VB OS=Homo sapiens GN=ATP10B PE=2 SV=2 129 556 2.0E-53
sp|O75110|ATP9A_HUMAN Probable phospholipid-transporting ATPase IIA OS=Homo sapiens GN=ATP9A PE=1 SV=3 106 759 8.0E-47
sp|Q10309|YD56_SCHPO Putative phospholipid-transporting ATPase C6C3.06c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC6C3.06c PE=3 SV=1 129 659 1.0E-46
sp|O70228|ATP9A_MOUSE Probable phospholipid-transporting ATPase IIA OS=Mus musculus GN=Atp9a PE=1 SV=3 129 759 2.0E-46
sp|P40527|ATC7_YEAST Probable phospholipid-transporting ATPase NEO1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=NEO1 PE=1 SV=1 129 679 7.0E-43
sp|A1A4J6|ATP9B_BOVIN Probable phospholipid-transporting ATPase IIB OS=Bos taurus GN=ATP9B PE=2 SV=1 132 759 1.0E-40
sp|D4ABB8|ATP9B_RAT Probable phospholipid-transporting ATPase IIB OS=Rattus norvegicus GN=Atp9b PE=3 SV=1 132 759 2.0E-40
sp|O43861|ATP9B_HUMAN Probable phospholipid-transporting ATPase IIB OS=Homo sapiens GN=ATP9B PE=2 SV=4 132 678 2.0E-39
sp|P98195|ATP9B_MOUSE Probable phospholipid-transporting ATPase IIB OS=Mus musculus GN=Atp9b PE=1 SV=4 132 759 2.0E-39
sp|F1Q4S1|ATP9B_DANRE Probable phospholipid-transporting ATPase IIB OS=Danio rerio GN=atp9b PE=3 SV=1 123 759 6.0E-38
sp|Q12674|ATC8_YEAST Probable phospholipid-transporting ATPase DNF3 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF3 PE=1 SV=1 540 697 9.0E-35
sp|Q12674|ATC8_YEAST Probable phospholipid-transporting ATPase DNF3 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF3 PE=1 SV=1 108 228 3.0E-22
sp|Q9UT43|YFRD_SCHPO Putative phospholipid-transporting ATPase C821.13c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC821.13c PE=1 SV=2 121 218 8.0E-16
sp|Q9LVK9|ALA7_ARATH Probable phospholipid-transporting ATPase 7 OS=Arabidopsis thaliana GN=ALA7 PE=3 SV=3 559 664 2.0E-15
sp|Q9SLK6|ALA6_ARATH Phospholipid-transporting ATPase 6 OS=Arabidopsis thaliana GN=ALA6 PE=1 SV=2 563 664 5.0E-14
sp|O94823|AT10B_HUMAN Probable phospholipid-transporting ATPase VB OS=Homo sapiens GN=ATP10B PE=2 SV=2 579 663 1.0E-09
sp|Q12675|ATC4_YEAST Phospholipid-transporting ATPase DNF2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF2 PE=1 SV=1 118 236 6.0E-09
sp|Q9GKS6|AT10D_MACFA Probable phospholipid-transporting ATPase VD (Fragment) OS=Macaca fascicularis GN=ATP10D PE=2 SV=1 578 696 1.0E-08
sp|Q9P241|AT10D_HUMAN Probable phospholipid-transporting ATPase VD OS=Homo sapiens GN=ATP10D PE=2 SV=3 570 687 2.0E-08
sp|O54827|AT10A_MOUSE Probable phospholipid-transporting ATPase VA OS=Mus musculus GN=Atp10a PE=1 SV=4 575 663 5.0E-08
sp|Q8K2X1|AT10D_MOUSE Probable phospholipid-transporting ATPase VD OS=Mus musculus GN=Atp10d PE=2 SV=2 579 665 5.0E-08
sp|O60312|AT10A_HUMAN Probable phospholipid-transporting ATPase VA OS=Homo sapiens GN=ATP10A PE=2 SV=2 572 663 2.0E-07
sp|P32660|ATC5_YEAST Phospholipid-transporting ATPase DNF1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF1 PE=1 SV=2 118 236 3.0E-07
sp|O36028|ATCZ_SCHPO Putative phospholipid-transporting ATPase C4F10.16c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC4F10.16c PE=3 SV=1 122 259 7.0E-07
sp|O34431|ATCL_BACSU Calcium-transporting ATPase OS=Bacillus subtilis (strain 168) GN=yloB PE=1 SV=1 480 662 3.0E-06
sp|Q09891|ATCX_SCHPO Putative phospholipid-transporting ATPase C24B11.12c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC24B11.12c PE=3 SV=1 132 253 5.0E-06
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GO

(None)

SignalP

[Help with interpreting these statistics]
SignalP signal predicted Location
(based on Ymax)
D score
(significance: > 0.45)
No 1 - 11 0.45

Transmembrane Domains

Domain # Start End Length
1 385 407 22
2 427 449 22

Transcription Factor Class

(None)

Expression data

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

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Sequences

Type of sequenceSequence
Locus Download genbank file of locus
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|7128
MPLSRGQFCVVDASSLESGSLSRGGGQRARLVPYGSSHHLFTDTEPEWLVSTAAAMKLPDRDTVVPVPNSGEPTY
VTNLSLTTRLRLRANLLARDLGWNFALPPPGKGRRIPLLAGEEDLLDERTGLPYIDNFVRSTRHTIGSFFPQQLY
FQFSRLNNCYFLFLVSLNFMPGSKPTDKWHLLGPLLLYVGLSMAKEALGDYRRHRLDKRENESVTFVLARAANDE
ETEDWIAIKWRYVRVGDVVRLRRDDAVPADMLVLCAKGPNGVAYIDTMALDGETNLKIKHPPEPLAKRCTTVADI
RAAAALITSEDPNPDLYNYDGMLTVDGKTLPLTQNNVVYRGSTLRNTNEAIGLVFNSGEECKIRVSAHLDVRAKK
PALHAVVDGVIIIQLFVVYVLAIILITSHMAWRRGVEANLWYLAHASMPMHLICIGHLTMSATLIPLSLYISMEL
LKVMQLYMMHDVEMYDPVSNTPMVSNTIDALADLGQVTHVFSDKTGTMTENVMRFRKMTVGGVACLHDMNEPKVE
DKADDGGLEMKTEALLTYIRRHPDTAFSRKARHLLLCIALCHTCLPERMDDGRIAFLAASPDELALVEAARDLGL
LLIDRSAQAMTLRMGDDSVETYQVLDVIEFSSGRKRMSVVVLMPDGKIEVVCKGADTVIMERLALREVAERKAKQ
MGQRNSERKTMELERERRKTLELTPSPDWSRRATLEPSRERRRTFELGRMSSRDDRRRRPTTVDETLASDEEAVL
GRCLHHVDDFSAEGLRTLVYASRVMGQERYEA
Coding >Ophio5|7128
ATGCCTCTTTCTCGGGGCCAGTTTTGTGTCGTGGATGCCTCTTCTCTGGAGAGCGGCAGCCTGTCTCGGGGAGGG
GGGCAGCGAGCCCGTCTCGTTCCATATGGCTCATCTCATCACTTGTTCACGGACACGGAGCCTGAATGGCTCGTC
TCTACTGCCGCGGCCATGAAGCTCCCTGACCGCGACACCGTCGTGCCGGTTCCAAACAGCGGCGAGCCGACGTAC
GTGACAAACCTCTCCCTGACGACGCGTTTACGCCTCCGGGCCAATCTCTTGGCCCGCGACCTCGGCTGGAATTTT
GCGCTGCCGCCGCCAGGAAAAGGGCGGCGCATCCCGTTACTGGCCGGCGAAGAGGATCTGCTGGATGAGAGAACT
GGTCTGCCCTACATCGACAACTTTGTTCGCTCCACTCGGCACACCATCGGCTCCTTCTTCCCCCAGCAGTTATAC
TTTCAATTCAGCCGGCTGAACAACTGTTACTTTCTTTTCCTGGTATCGTTGAATTTCATGCCGGGCTCGAAACCG
ACTGATAAGTGGCATCTTCTGGGGCCTCTGCTTCTTTATGTAGGCCTTAGTATGGCCAAAGAAGCGCTTGGTGAT
TACCGTCGGCATCGGCTCGACAAGCGAGAGAACGAAAGTGTCACCTTCGTGCTGGCCCGGGCAGCCAACGACGAG
GAGACAGAAGACTGGATCGCCATCAAATGGAGGTACGTCCGCGTCGGCGACGTGGTCCGACTGCGGCGCGACGAT
GCCGTTCCAGCAGACATGCTCGTCCTGTGCGCCAAGGGCCCCAACGGCGTCGCTTACATCGACACCATGGCCCTC
GACGGCGAGACAAACCTCAAGATCAAGCATCCTCCTGAGCCGCTCGCTAAACGCTGCACCACCGTGGCCGACATC
CGCGCCGCCGCCGCGCTCATCACTTCGGAGGACCCCAATCCGGATCTGTACAACTATGACGGCATGCTGACGGTC
GACGGGAAGACGCTGCCGCTTACACAGAACAACGTTGTCTATCGCGGCTCGACGTTGCGCAATACCAACGAGGCC
ATCGGACTCGTCTTCAACTCGGGCGAGGAGTGCAAGATTCGCGTCAGCGCCCATCTCGACGTTCGCGCCAAGAAG
CCGGCCTTGCACGCCGTCGTCGACGGGGTGATTATCATTCAGCTTTTCGTTGTCTACGTGCTGGCGATCATTCTG
ATAACCTCCCACATGGCGTGGCGGCGAGGGGTTGAGGCGAATTTGTGGTATTTGGCTCACGCAAGCATGCCGATG
CACCTCATCTGTATTGGACACTTGACCATGTCCGCGACGCTGATTCCGCTGTCTCTTTACATTTCCATGGAGCTT
TTAAAGGTCATGCAGCTGTATATGATGCATGACGTCGAGATGTATGACCCGGTTTCCAACACGCCCATGGTCTCC
AACACCATCGATGCCCTGGCCGACTTGGGGCAGGTGACGCATGTCTTTTCCGACAAGACGGGGACCATGACGGAG
AACGTGATGCGCTTTCGCAAGATGACGGTTGGTGGTGTCGCCTGTCTACACGACATGAACGAACCCAAGGTCGAG
GACAAGGCTGACGACGGGGGCCTCGAGATGAAGACGGAGGCCCTCCTCACCTATATTCGCCGCCATCCCGACACG
GCTTTTTCCCGGAAGGCGAGACACTTGCTGCTGTGCATTGCCCTGTGCCACACCTGTCTCCCCGAAAGGATGGAC
GACGGACGCATCGCGTTCCTGGCGGCGTCGCCAGACGAGCTGGCCCTGGTAGAAGCGGCGCGTGACTTGGGACTG
CTGTTGATCGACCGGTCGGCGCAGGCGATGACACTGCGGATGGGCGATGACAGTGTCGAGACGTACCAAGTGCTG
GACGTGATTGAGTTTAGCAGCGGGCGCAAGAGGATGTCTGTCGTGGTGCTGATGCCGGACGGGAAGATCGAAGTC
GTATGCAAGGGCGCGGACACGGTCATTATGGAGAGGCTGGCTCTACGGGAGGTGGCGGAGAGGAAGGCGAAGCAG
ATGGGCCAGCGGAACAGCGAGCGCAAGACGATGGAGCTGGAGCGGGAGAGGAGGAAGACGCTGGAGCTGACGCCG
AGCCCGGACTGGTCGAGGCGGGCGACGCTGGAGCCGAGTCGGGAGAGGCGCAGGACCTTTGAGCTGGGCCGGATG
AGCAGCAGGGACGACAGGCGACGACGGCCAACGACGGTCGACGAGACGCTGGCGAGCGACGAAGAGGCGGTCCTG
GGCCGTTGCCTGCATCACGTCGACGACTTTTCAGCCGAGGGCCTGCGGACGCTCGTCTACGCCTCTCGAGTTATG
GGCCAAGAGAGATATGAAGCC
Transcript >Ophio5|7128
ATGCCTCTTTCTCGGGGCCAGTTTTGTGTCGTGGATGCCTCTTCTCTGGAGAGCGGCAGCCTGTCTCGGGGAGGG
GGGCAGCGAGCCCGTCTCGTTCCATATGGCTCATCTCATCACTTGTTCACGGACACGGAGCCTGAATGGCTCGTC
TCTACTGCCGCGGCCATGAAGCTCCCTGACCGCGACACCGTCGTGCCGGTTCCAAACAGCGGCGAGCCGACGTAC
GTGACAAACCTCTCCCTGACGACGCGTTTACGCCTCCGGGCCAATCTCTTGGCCCGCGACCTCGGCTGGAATTTT
GCGCTGCCGCCGCCAGGAAAAGGGCGGCGCATCCCGTTACTGGCCGGCGAAGAGGATCTGCTGGATGAGAGAACT
GGTCTGCCCTACATCGACAACTTTGTTCGCTCCACTCGGCACACCATCGGCTCCTTCTTCCCCCAGCAGTTATAC
TTTCAATTCAGCCGGCTGAACAACTGTTACTTTCTTTTCCTGGTATCGTTGAATTTCATGCCGGGCTCGAAACCG
ACTGATAAGTGGCATCTTCTGGGGCCTCTGCTTCTTTATGTAGGCCTTAGTATGGCCAAAGAAGCGCTTGGTGAT
TACCGTCGGCATCGGCTCGACAAGCGAGAGAACGAAAGTGTCACCTTCGTGCTGGCCCGGGCAGCCAACGACGAG
GAGACAGAAGACTGGATCGCCATCAAATGGAGGTACGTCCGCGTCGGCGACGTGGTCCGACTGCGGCGCGACGAT
GCCGTTCCAGCAGACATGCTCGTCCTGTGCGCCAAGGGCCCCAACGGCGTCGCTTACATCGACACCATGGCCCTC
GACGGCGAGACAAACCTCAAGATCAAGCATCCTCCTGAGCCGCTCGCTAAACGCTGCACCACCGTGGCCGACATC
CGCGCCGCCGCCGCGCTCATCACTTCGGAGGACCCCAATCCGGATCTGTACAACTATGACGGCATGCTGACGGTC
GACGGGAAGACGCTGCCGCTTACACAGAACAACGTTGTCTATCGCGGCTCGACGTTGCGCAATACCAACGAGGCC
ATCGGACTCGTCTTCAACTCGGGCGAGGAGTGCAAGATTCGCGTCAGCGCCCATCTCGACGTTCGCGCCAAGAAG
CCGGCCTTGCACGCCGTCGTCGACGGGGTGATTATCATTCAGCTTTTCGTTGTCTACGTGCTGGCGATCATTCTG
ATAACCTCCCACATGGCGTGGCGGCGAGGGGTTGAGGCGAATTTGTGGTATTTGGCTCACGCAAGCATGCCGATG
CACCTCATCTGTATTGGACACTTGACCATGTCCGCGACGCTGATTCCGCTGTCTCTTTACATTTCCATGGAGCTT
TTAAAGGTCATGCAGCTGTATATGATGCATGACGTCGAGATGTATGACCCGGTTTCCAACACGCCCATGGTCTCC
AACACCATCGATGCCCTGGCCGACTTGGGGCAGGTGACGCATGTCTTTTCCGACAAGACGGGGACCATGACGGAG
AACGTGATGCGCTTTCGCAAGATGACGGTTGGTGGTGTCGCCTGTCTACACGACATGAACGAACCCAAGGTCGAG
GACAAGGCTGACGACGGGGGCCTCGAGATGAAGACGGAGGCCCTCCTCACCTATATTCGCCGCCATCCCGACACG
GCTTTTTCCCGGAAGGCGAGACACTTGCTGCTGTGCATTGCCCTGTGCCACACCTGTCTCCCCGAAAGGATGGAC
GACGGACGCATCGCGTTCCTGGCGGCGTCGCCAGACGAGCTGGCCCTGGTAGAAGCGGCGCGTGACTTGGGACTG
CTGTTGATCGACCGGTCGGCGCAGGCGATGACACTGCGGATGGGCGATGACAGTGTCGAGACGTACCAAGTGCTG
GACGTGATTGAGTTTAGCAGCGGGCGCAAGAGGATGTCTGTCGTGGTGCTGATGCCGGACGGGAAGATCGAAGTC
GTATGCAAGGGCGCGGACACGGTCATTATGGAGAGGCTGGCTCTACGGGAGGTGGCGGAGAGGAAGGCGAAGCAG
ATGGGCCAGCGGAACAGCGAGCGCAAGACGATGGAGCTGGAGCGGGAGAGGAGGAAGACGCTGGAGCTGACGCCG
AGCCCGGACTGGTCGAGGCGGGCGACGCTGGAGCCGAGTCGGGAGAGGCGCAGGACCTTTGAGCTGGGCCGGATG
AGCAGCAGGGACGACAGGCGACGACGGCCAACGACGGTCGACGAGACGCTGGCGAGCGACGAAGAGGCGGTCCTG
GGCCGTTGCCTGCATCACGTCGACGACTTTTCAGCCGAGGGCCTGCGGACGCTCGTCTACGCCTCTCGAGTTATG
GGCCAAGAGAGATATGAAGCCTAG
Gene >Ophio5|7128
ATGCCTCTTTCTCGGGGCCAGTTTTGTGTCGTGGATGCCTCTTCTCTGGAGAGCGGCAGCCTGTCTCGGGGAGGG
GGGCAGCGAGCCCGTCTCGTTCCATATGGTCTGTTCTTTTCATCTTTACCTTGCGTATTGCCTCGCCTACTTACG
TACCAACATATCTACTCACTTGTACAAGGCTCATCTCATCACTTGTTCACGGACACGGAGCCTGAATGGCTCGTC
TCTACTGCCGGTGCCAGTAGCAGCCGCCTTGACGGCTTGCTCGACCAGCGGCCATGAAGCTCCCTGACCGCGACA
CCGTCGTGCCGGTTCCAAACAGCGGCGAGCCGACGTACGTGACAAACCTCTCCCTGACGACGCGTTTACGCCTCC
GGGCCAATCTCTTGGCCCGCGACCTCGGCTGGAATTTTGCGCTGCCGCCGCCAGGAAAAGGGCGGCGCATCCCGT
TACTGGCCGGCGAAGAGGATCTGCTGGATGAGAGAACTGGTCTGCCCTACATCGACAACTTTGTTCGCTCCACTC
GGCACACCATCGGCTCCTTCTTCCCCCAGCAGTTATACTTTCAATTCAGCCGGCTGAACAACTGTTACTTTCTTT
TCCTGGTATCGTTGAATTTCATGCCGGGCTCGAAACCGACTGATAAGTGGCATCTTCTGGGGCCTCTGCTTCTTT
ATGTAGGCCTTAGTATGGCCAAAGAAGCGCTTGGTGATTACCGTCGGCATCGGCTCGACAAGCGAGAGAACGAAA
GTGTCACCTTCGTGCTGGCCCGGGCAGCCAACGACGAGGAGACAGAAGACTGGATCGCCATCAAATGGAGGTACG
TCCGCGTCGGCGACGTGGTCCGACTGCGGCGCGACGATGCCGTTCCAGCAGACATGCTCGTCCTGTGCGCCAAGG
GCCCCAACGGCGTCGCTTACATCGACACCATGGCCCTCGACGGCGAGACAAACCTCAAGATCAAGCATCCTCCTG
AGCCGCTCGCTAAACGCTGCACCACCGTGGCCGACATCCGCGCCGCCGCCGCGCTCATCACTTCGGAGGACCCCA
ATCCGGATCTGTACAACTATGACGGCATGCTGACGGTCGACGGGAAGACGCTGCCGCTTACACAGAACAACGTTG
TCTATCGCGGCTCGACGTTGCGCAATACCAACGAGGCCATCGGACTCGTCTTCAACTCGGGCGAGGAGTGCAAGA
TTCGCGTCAGCGCCCATCTCGACGTTCGCGCCAAGAAGCCGGCCTTGCACGCCGTCGTCGACGGGGTGATTATCA
TTCAGCTTTTCGTTGTCTACGTGCTGGCGATCATTCTGATAACCTCCCACATGGCGTGGCGGCGAGGGGTTGAGG
CGAATTTGTGGTATTTGGCTCACGCAAGCATGCCGATGCACCTCATCTGTATTGGACACTTGACCATGTCCGCGA
CGCTGATTCCGCTGTCTCTTTACATTTCCATGGAGCTTTTAAAGGTCATGCAGCTGTATATGATGCATGACGTCG
AGATGTATGACCCGGTTTCCAACACGCCCATGGTCTCCAACACCATCGATGCCCTGGCCGACTTGGGGCAGGTGA
CGCATGTCTTTTCCGACAAGACGGGGACCATGACGGAGAACGTGATGCGCTTTCGCAAGATGACGGTTGGTGGTG
TCGCCTGTCTACACGACATGAACGAACCCAAGGTCGAGGACAAGGCTGACGACGGGGGCCTCGAGATGAAGACGG
AGGCCCTCCTCACCTATATTCGCCGCCATCCCGACACGGCTTTTTCCCGGAAGGCGAGACACTTGCTGCTGTGCA
TTGCCCTGTGCCACACCTGTCTCCCCGAAAGGATGGACGACGGACGCATCGCGTTCCTGGCGGCGTCGCCAGACG
AGCTGGCCCTGGTAGAAGCGGCGCGTGACTTGGGACTGCTGTTGATCGACCGGTCGGCGCAGGCGATGACACTGC
GGATGGGCGATGACAGTGTCGAGACGTACCAAGTGCTGGACGTGATTGAGTTTAGCAGCGGGCGCAAGAGGATGT
CTGTCGTGGTGCTGATGCCGGACGGGAAGATCGAAGTCGTATGCAAGGGCGCGGACACGGTCATTATGGAGAGGC
TGGCTCTACGGGAGGTGGCGGAGAGGAAGGCGAAGCAGATGGGCCAGCGGAACAGCGAGCGCAAGACGATGGAGC
TGGAGCGGGAGAGGAGGAAGACGCTGGAGCTGACGCCGAGCCCGGACTGGTCGAGGCGGGCGACGCTGGAGCCGA
GTCGGGAGAGGCGCAGGACCTTTGAGCTGGGCCGGATGAGCAGCAGGGACGACAGGCGACGACGGCCAACGACGG
TCGACGAGACGCTGGCGAGCGACGAAGAGGCGGTCCTGGGCCGTTGCCTGCATCACGTCGACGACTTTTCAGCCG
AGGGCCTGCGGACGCTCGTCTACGCCTCTCGAGTTATGGGCCAAGAGAGATATGAAGCCTAG

© 2022 - Robin Ohm - Utrecht University - The Netherlands

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