Fungal Genomics

at Utrecht University

General Properties

Protein IDOphio5|3096
Gene name
Locationscaffold_246:22994..25502
Strand+
Gene length (bp)2508
Transcript length (bp)2319
Coding sequence length (bp)2316
Protein length (aa) 772

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PFAM Domains

PFAM Domain ID Short name Long name E-value Start End
PF00443 UCH Ubiquitin carboxyl-terminal hydrolase 3.0E-37 303 769
PF17807 zf-UBP_var Variant UBP zinc finger 4.6E-22 16 79
PF02148 zf-UBP Zn-finger in ubiquitin-hydrolases and other protein 5.9E-20 176 248
PF00627 UBA UBA/TS-N domain 2.2E-11 584 621
PF00627 UBA UBA/TS-N domain 1.9E-05 643 678
PF13423 UCH_1 Ubiquitin carboxyl-terminal hydrolase 7.5E-14 431 751

Swissprot hits

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Swissprot ID Swissprot Description Start End E-value
sp|Q11119|UBP14_SCHPO Ubiquitin carboxyl-terminal hydrolase 14 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ubp14 PE=1 SV=2 1 772 0.0E+00
sp|Q8L6Y1|UBP14_ARATH Ubiquitin carboxyl-terminal hydrolase 14 OS=Arabidopsis thaliana GN=UBP14 PE=1 SV=1 16 772 8.0E-139
sp|P56399|UBP5_MOUSE Ubiquitin carboxyl-terminal hydrolase 5 OS=Mus musculus GN=Usp5 PE=1 SV=1 16 772 6.0E-137
sp|P45974|UBP5_HUMAN Ubiquitin carboxyl-terminal hydrolase 5 OS=Homo sapiens GN=USP5 PE=1 SV=2 16 772 1.0E-135
sp|Q5R407|UBP5_PONAB Ubiquitin carboxyl-terminal hydrolase 5 OS=Pongo abelii GN=UBP5 PE=2 SV=1 16 772 6.0E-134
[Show all]
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Swissprot ID Swissprot Description Start End E-value
sp|Q11119|UBP14_SCHPO Ubiquitin carboxyl-terminal hydrolase 14 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ubp14 PE=1 SV=2 1 772 0.0E+00
sp|Q8L6Y1|UBP14_ARATH Ubiquitin carboxyl-terminal hydrolase 14 OS=Arabidopsis thaliana GN=UBP14 PE=1 SV=1 16 772 8.0E-139
sp|P56399|UBP5_MOUSE Ubiquitin carboxyl-terminal hydrolase 5 OS=Mus musculus GN=Usp5 PE=1 SV=1 16 772 6.0E-137
sp|P45974|UBP5_HUMAN Ubiquitin carboxyl-terminal hydrolase 5 OS=Homo sapiens GN=USP5 PE=1 SV=2 16 772 1.0E-135
sp|Q5R407|UBP5_PONAB Ubiquitin carboxyl-terminal hydrolase 5 OS=Pongo abelii GN=UBP5 PE=2 SV=1 16 772 6.0E-134
sp|P38237|UBP14_YEAST Ubiquitin carboxyl-terminal hydrolase 14 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=UBP14 PE=1 SV=2 22 771 1.0E-125
sp|E1BMF7|UBP13_BOVIN Ubiquitin carboxyl-terminal hydrolase 13 OS=Bos taurus GN=USP13 PE=3 SV=2 1 772 1.0E-116
sp|Q92995|UBP13_HUMAN Ubiquitin carboxyl-terminal hydrolase 13 OS=Homo sapiens GN=USP13 PE=1 SV=2 1 772 1.0E-115
sp|P54201|UBPA_DICDI Ubiquitin carboxyl-terminal hydrolase A OS=Dictyostelium discoideum GN=ubpA PE=2 SV=2 16 771 2.0E-115
sp|E1BY77|UBP13_CHICK Ubiquitin carboxyl-terminal hydrolase 13 OS=Gallus gallus GN=USP13 PE=3 SV=1 16 772 2.0E-114
sp|Q5BKP2|UBP13_MOUSE Ubiquitin carboxyl-terminal hydrolase 13 OS=Mus musculus GN=Usp13 PE=1 SV=1 1 772 3.0E-113
sp|F1QFS9|UBP13_DANRE Ubiquitin carboxyl-terminal hydrolase 13 OS=Danio rerio GN=usp13 PE=2 SV=1 16 772 6.0E-112
sp|F6V6I0|UBP13_XENTR Ubiquitin carboxyl-terminal hydrolase 13 OS=Xenopus tropicalis GN=usp13 PE=3 SV=2 16 571 6.0E-76
sp|Q8R5K2|UBP33_MOUSE Ubiquitin carboxyl-terminal hydrolase 33 OS=Mus musculus GN=Usp33 PE=1 SV=2 154 420 7.0E-14
sp|Q8TEY7|UBP33_HUMAN Ubiquitin carboxyl-terminal hydrolase 33 OS=Homo sapiens GN=USP33 PE=1 SV=2 154 352 5.0E-13
sp|Q5REG5|UBP33_PONAB Ubiquitin carboxyl-terminal hydrolase 33 OS=Pongo abelii GN=USP33 PE=2 SV=1 154 352 1.0E-12
sp|A6QNM7|UBP33_BOVIN Ubiquitin carboxyl-terminal hydrolase 33 OS=Bos taurus GN=USP33 PE=2 SV=1 154 352 4.0E-12
sp|F6V6I0|UBP13_XENTR Ubiquitin carboxyl-terminal hydrolase 13 OS=Xenopus tropicalis GN=usp13 PE=3 SV=2 652 772 8.0E-12
sp|A5PMR2|UBP33_DANRE Ubiquitin carboxyl-terminal hydrolase 33 OS=Danio rerio GN=usp33 PE=2 SV=1 154 331 6.0E-10
sp|Q9Y6I4|UBP3_HUMAN Ubiquitin carboxyl-terminal hydrolase 3 OS=Homo sapiens GN=USP3 PE=1 SV=2 176 550 2.0E-09
sp|Q91W36|UBP3_MOUSE Ubiquitin carboxyl-terminal hydrolase 3 OS=Mus musculus GN=Usp3 PE=2 SV=1 176 550 7.0E-09
sp|Q09738|UBP8_SCHPO Probable ubiquitin carboxyl-terminal hydrolase 8 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ubp8 PE=3 SV=1 176 550 1.0E-08
sp|D2HBJ8|UBP44_AILME Ubiquitin carboxyl-terminal hydrolase 44 OS=Ailuropoda melanoleuca GN=USP44 PE=3 SV=1 154 248 1.0E-08
sp|Q8C6M1|UBP20_MOUSE Ubiquitin carboxyl-terminal hydrolase 20 OS=Mus musculus GN=Usp20 PE=1 SV=1 154 331 1.0E-08
sp|A0JM59|UBP20_XENTR Ubiquitin carboxyl-terminal hydrolase 20 OS=Xenopus tropicalis GN=usp20 PE=2 SV=1 154 325 2.0E-08
sp|Q9H0E7|UBP44_HUMAN Ubiquitin carboxyl-terminal hydrolase 44 OS=Homo sapiens GN=USP44 PE=1 SV=2 154 248 2.0E-08
sp|Q70EK9|UBP51_HUMAN Ubiquitin carboxyl-terminal hydrolase 51 OS=Homo sapiens GN=USP51 PE=2 SV=1 176 601 5.0E-08
sp|Q28CN3|UBP33_XENTR Ubiquitin carboxyl-terminal hydrolase 33 OS=Xenopus tropicalis GN=usp33 PE=2 SV=2 154 325 6.0E-08
sp|Q5R5Z6|UBP20_PONAB Ubiquitin carboxyl-terminal hydrolase 20 OS=Pongo abelii GN=USP20 PE=2 SV=1 154 331 9.0E-08
sp|P38748|ETP1_YEAST RING finger protein ETP1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=ETP1 PE=1 SV=1 154 225 1.0E-07
sp|Q7ZUM8|UBP44_DANRE Ubiquitin carboxyl-terminal hydrolase 44 OS=Danio rerio GN=usp44 PE=2 SV=1 154 248 1.0E-07
sp|E7F6T8|UBP37_DANRE Ubiquitin carboxyl-terminal hydrolase 37 OS=Danio rerio GN=usp37 PE=2 SV=1 300 556 2.0E-07
sp|Q922Y1|UBXN1_MOUSE UBX domain-containing protein 1 OS=Mus musculus GN=Ubxn1 PE=1 SV=1 588 654 2.0E-07
sp|Q0V9G5|UBP44_XENTR Ubiquitin carboxyl-terminal hydrolase 44 OS=Xenopus tropicalis GN=usp44 PE=2 SV=1 154 248 2.0E-07
sp|Q6NTR6|UP44A_XENLA Ubiquitin carboxyl-terminal hydrolase 44-A OS=Xenopus laevis GN=usp44-a PE=2 SV=1 154 248 3.0E-07
sp|Q5XGZ2|UP44B_XENLA Ubiquitin carboxyl-terminal hydrolase 44-B OS=Xenopus laevis GN=usp44-b PE=2 SV=1 154 248 3.0E-07
sp|Q499N6|UBXN1_RAT UBX domain-containing protein 1 OS=Rattus norvegicus GN=Ubxn1 PE=3 SV=2 588 654 3.0E-07
sp|Q8C2S0|UBP44_MOUSE Ubiquitin carboxyl-terminal hydrolase 44 OS=Mus musculus GN=Usp44 PE=2 SV=3 154 248 4.0E-07
sp|Q04323|UBXN1_HUMAN UBX domain-containing protein 1 OS=Homo sapiens GN=UBXN1 PE=1 SV=2 588 635 1.0E-06
sp|Q8C0R0|UBP37_MOUSE Ubiquitin carboxyl-terminal hydrolase 37 OS=Mus musculus GN=Usp37 PE=1 SV=1 302 550 1.0E-06
sp|A7Z056|UBP20_BOVIN Ubiquitin carboxyl-terminal hydrolase 20 OS=Bos taurus GN=USP20 PE=2 SV=1 154 331 2.0E-06
sp|F1SRY5|UBP37_PIG Ubiquitin carboxyl-terminal hydrolase 37 OS=Sus scrofa GN=USP37 PE=3 SV=1 302 550 3.0E-06
sp|Q9LEW0|UBP22_ARATH Ubiquitin carboxyl-terminal hydrolase 22 OS=Arabidopsis thaliana GN=UBP22 PE=2 SV=1 168 562 3.0E-06
sp|Q9Y2K6|UBP20_HUMAN Ubiquitin carboxyl-terminal hydrolase 20 OS=Homo sapiens GN=USP20 PE=1 SV=2 154 331 3.0E-06
sp|Q4R6X7|UBP16_MACFA Ubiquitin carboxyl-terminal hydrolase 16 OS=Macaca fascicularis GN=USP16 PE=2 SV=2 185 329 4.0E-06
sp|Q32KW2|UBXN1_BOVIN UBX domain-containing protein 1 OS=Bos taurus GN=UBXN1 PE=2 SV=1 588 634 5.0E-06
sp|Q86T82|UBP37_HUMAN Ubiquitin carboxyl-terminal hydrolase 37 OS=Homo sapiens GN=USP37 PE=1 SV=2 304 550 6.0E-06
sp|E2RK09|UBP37_CANLF Ubiquitin carboxyl-terminal hydrolase 37 OS=Canis lupus familiaris GN=USP37 PE=3 SV=1 304 550 8.0E-06
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GO

GO Term Description Terminal node
GO:0008270 zinc ion binding Yes
GO:0004843 cysteine-type deubiquitinase activity Yes
GO:0016579 protein deubiquitination Yes
GO:0071704 organic substance metabolic process No
GO:0043170 macromolecule metabolic process No
GO:0008150 biological_process No
GO:1901564 organonitrogen compound metabolic process No
GO:0044238 primary metabolic process No
GO:0006508 proteolysis No
GO:0046872 metal ion binding No
GO:0101005 deubiquitinase activity No
GO:0043412 macromolecule modification No
GO:0043167 ion binding No
GO:0043169 cation binding No
GO:0008152 metabolic process No
GO:0003674 molecular_function No
GO:0008233 peptidase activity No
GO:0070646 protein modification by small protein removal No
GO:0140096 catalytic activity, acting on a protein No
GO:0005488 binding No
GO:0016787 hydrolase activity No
GO:0070647 protein modification by small protein conjugation or removal No
GO:0019538 protein metabolic process No
GO:0036211 protein modification process No
GO:0046914 transition metal ion binding No
GO:0006807 nitrogen compound metabolic process No
GO:0019783 ubiquitin-like protein peptidase activity No
GO:0003824 catalytic activity No
GO:0008234 cysteine-type peptidase activity No

SignalP

[Help with interpreting these statistics]
SignalP signal predicted Location
(based on Ymax)
D score
(significance: > 0.45)
No 1 - 20 0.45

Transmembrane Domains

(None)

Transcription Factor Class

(None)

Expression data

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

Expression values

Label Description Expression (RPKM) Confidence interval (low) Confidence interval (high)
SC16a Pure fungal culture 44.51 24.11 64.91
CcL In ants, during behavior modification 48.07 26.05 70.10
CcD In ants, recently dead 55.85 30.18 81.53

Differential expression

Label1 Label2 Q-value Significant difference
SC16a CcL 0.778607 no
SC16a CcD 0.355418 no
CcL CcD 0.558622 no

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|3096
MTCPHLDALGAELSPPSASQSVYREDCTQCFDSIDEPSGLDVCLQCFNGACAGARLHNGLHASLWKHPLALNIRR
TRKPMVRDEPPTKMSKLAIVAESDEDRYDTALSAKCLDCDASLDMTDARLAPIVDGILKANTFARKEEVKAWEQE
LTGCEHILMLQQHESRNIQQGDLGHCSACDLRENLWLCLECGNLGCGRKQMGGVDGNSHALAHATESAHGVAVKL
GSITPEGTADVYCYKCDDERLDDQLGPHLAHWGIMLADRRKTEMSLTEMQIEQNLKWDFSMTTDDGKLLKPLYGP
GLTGLKNLGNSCYLASVAQCLFDLPSFRERYYRPTDSPPQVQEPAADLETQLRKLADGLLSGRYAKPDDDDAGPE
PDVVHQQKGLAPAMLKHLIGRGHTEFSTMRQQDAFELFQHLVKLITRWPHGPGLDDPTRPFRFLLEQRLQCMGCG
KVRYSEQEQDSIFINVPLEKLPRAEGDTGDQYKPVTLKQCLDTLTGAEKVELACSACRSTKGFTKQSLFKTFPDV
LAVNANKMSVVNWVPVKVDVPVLVPDEPFLLDDYMSKGLQASEEPLPDEPEAPAPAFVPDAAALGQLEAMGFPRN
RCEKALHATGNSDANAAMEWLFARMEDADIDAPLDLDASPVADPAKIETLGAMGFDAPLAGKALKETGGDVQRAI
EWLFNHPDETGLVEEEVAPAAAREPAGSRSLPASFQLRSIVCHKGTSIHAGHYVAFIRKQLAGQGAQWVLFNDEK
VVEAHDFEEMRKFAYVYFFERV
Coding >Ophio5|3096
ATGACGTGCCCACACCTCGACGCGCTCGGCGCAGAGCTCTCCCCGCCCAGCGCCAGCCAGTCGGTCTATCGCGAA
GACTGTACTCAGTGCTTCGATTCCATCGACGAGCCCAGCGGCCTCGATGTCTGTCTCCAGTGCTTCAACGGCGCC
TGCGCGGGTGCCAGGCTGCACAACGGCCTCCACGCCAGTCTCTGGAAGCATCCTTTAGCGCTCAACATCCGCCGC
ACGCGTAAGCCCATGGTCCGAGATGAGCCCCCTACCAAAATGTCCAAGCTGGCCATCGTGGCCGAGTCGGACGAG
GATCGATACGACACGGCCCTCTCTGCAAAATGCCTTGATTGCGATGCCTCGCTCGATATGACCGACGCCCGCCTC
GCTCCCATCGTCGACGGCATCCTCAAGGCCAACACGTTCGCGCGGAAAGAGGAGGTCAAGGCCTGGGAGCAGGAG
TTGACGGGCTGCGAGCACATCCTCATGCTGCAGCAGCACGAGTCGCGCAATATCCAACAGGGTGACCTCGGCCAC
TGCTCTGCCTGCGACCTGCGCGAGAACCTGTGGCTCTGCCTCGAATGCGGAAACTTGGGCTGTGGCCGCAAACAG
ATGGGGGGCGTCGACGGCAACTCGCACGCCCTCGCACACGCGACCGAGTCGGCACACGGCGTCGCCGTCAAGCTC
GGCTCCATCACTCCCGAGGGCACCGCCGACGTCTACTGCTACAAGTGCGACGACGAGCGCCTCGACGACCAGCTC
GGCCCCCATCTCGCCCACTGGGGCATCATGCTGGCTGACCGCCGCAAGACGGAGATGAGCCTGACGGAGATGCAG
ATCGAGCAGAATCTCAAGTGGGACTTTAGCATGACTACCGACGACGGCAAGCTTCTGAAGCCCCTCTACGGCCCG
GGCCTTACCGGCCTCAAGAACCTGGGCAACAGCTGCTACCTGGCCAGCGTCGCGCAGTGCCTCTTCGACCTGCCG
TCCTTCCGAGAGCGCTACTACAGACCTACCGATTCCCCGCCTCAAGTCCAGGAGCCGGCGGCCGATCTGGAGACG
CAGCTGCGCAAGCTTGCCGATGGCCTCTTGTCGGGGCGCTATGCCAAGCCGGACGACGACGACGCGGGCCCGGAA
CCAGACGTCGTCCACCAACAAAAGGGCCTGGCGCCGGCCATGCTGAAGCATCTCATCGGCAGAGGTCACACCGAG
TTCTCCACTATGCGGCAGCAGGACGCCTTCGAGCTGTTCCAGCACCTCGTCAAGCTCATCACGCGATGGCCGCAC
GGCCCCGGCCTCGACGACCCGACCAGGCCCTTCCGCTTTCTCCTAGAGCAGAGGCTGCAGTGTATGGGCTGCGGC
AAGGTGCGGTACAGCGAGCAAGAGCAGGACAGCATCTTCATCAACGTGCCGCTCGAGAAGCTGCCCCGGGCCGAG
GGCGATACGGGCGACCAGTACAAGCCCGTCACCCTGAAGCAGTGCCTCGACACCTTGACGGGGGCGGAAAAGGTG
GAACTGGCCTGCTCGGCCTGCCGGAGCACCAAGGGCTTCACCAAGCAGTCGCTTTTCAAGACGTTTCCCGACGTG
CTCGCGGTCAACGCCAACAAAATGTCCGTCGTCAACTGGGTGCCCGTCAAGGTCGACGTCCCCGTCCTCGTCCCG
GACGAGCCCTTTCTACTGGACGACTACATGTCCAAGGGCTTGCAGGCGTCGGAGGAGCCTCTGCCGGACGAGCCC
GAGGCGCCGGCGCCGGCCTTTGTACCCGATGCCGCCGCCCTCGGCCAGCTGGAGGCCATGGGATTCCCGCGCAAC
CGCTGCGAGAAGGCGCTGCACGCCACCGGAAACTCGGACGCCAACGCCGCCATGGAGTGGCTCTTTGCGCGCATG
GAGGATGCCGACATCGACGCGCCTCTCGATCTGGACGCCAGCCCCGTCGCCGATCCGGCCAAGATTGAGACGCTG
GGCGCCATGGGCTTCGACGCGCCTCTTGCCGGAAAGGCCCTCAAGGAGACGGGCGGCGACGTGCAGCGCGCCATC
GAATGGCTCTTTAACCATCCGGATGAAACGGGCTTGGTCGAGGAAGAGGTGGCCCCCGCAGCTGCTAGGGAGCCC
GCCGGCAGTCGGTCGCTCCCCGCCAGCTTCCAGCTGCGGTCCATTGTCTGCCACAAGGGGACCAGTATCCATGCG
GGGCACTACGTGGCCTTTATCCGGAAGCAGCTCGCAGGGCAGGGCGCCCAGTGGGTGCTGTTCAACGACGAAAAG
GTTGTCGAGGCGCACGATTTCGAAGAGATGCGGAAATTTGCCTACGTGTATTTTTTCGAGCGCGTA
Transcript >Ophio5|3096
ATGACGTGCCCACACCTCGACGCGCTCGGCGCAGAGCTCTCCCCGCCCAGCGCCAGCCAGTCGGTCTATCGCGAA
GACTGTACTCAGTGCTTCGATTCCATCGACGAGCCCAGCGGCCTCGATGTCTGTCTCCAGTGCTTCAACGGCGCC
TGCGCGGGTGCCAGGCTGCACAACGGCCTCCACGCCAGTCTCTGGAAGCATCCTTTAGCGCTCAACATCCGCCGC
ACGCGTAAGCCCATGGTCCGAGATGAGCCCCCTACCAAAATGTCCAAGCTGGCCATCGTGGCCGAGTCGGACGAG
GATCGATACGACACGGCCCTCTCTGCAAAATGCCTTGATTGCGATGCCTCGCTCGATATGACCGACGCCCGCCTC
GCTCCCATCGTCGACGGCATCCTCAAGGCCAACACGTTCGCGCGGAAAGAGGAGGTCAAGGCCTGGGAGCAGGAG
TTGACGGGCTGCGAGCACATCCTCATGCTGCAGCAGCACGAGTCGCGCAATATCCAACAGGGTGACCTCGGCCAC
TGCTCTGCCTGCGACCTGCGCGAGAACCTGTGGCTCTGCCTCGAATGCGGAAACTTGGGCTGTGGCCGCAAACAG
ATGGGGGGCGTCGACGGCAACTCGCACGCCCTCGCACACGCGACCGAGTCGGCACACGGCGTCGCCGTCAAGCTC
GGCTCCATCACTCCCGAGGGCACCGCCGACGTCTACTGCTACAAGTGCGACGACGAGCGCCTCGACGACCAGCTC
GGCCCCCATCTCGCCCACTGGGGCATCATGCTGGCTGACCGCCGCAAGACGGAGATGAGCCTGACGGAGATGCAG
ATCGAGCAGAATCTCAAGTGGGACTTTAGCATGACTACCGACGACGGCAAGCTTCTGAAGCCCCTCTACGGCCCG
GGCCTTACCGGCCTCAAGAACCTGGGCAACAGCTGCTACCTGGCCAGCGTCGCGCAGTGCCTCTTCGACCTGCCG
TCCTTCCGAGAGCGCTACTACAGACCTACCGATTCCCCGCCTCAAGTCCAGGAGCCGGCGGCCGATCTGGAGACG
CAGCTGCGCAAGCTTGCCGATGGCCTCTTGTCGGGGCGCTATGCCAAGCCGGACGACGACGACGCGGGCCCGGAA
CCAGACGTCGTCCACCAACAAAAGGGCCTGGCGCCGGCCATGCTGAAGCATCTCATCGGCAGAGGTCACACCGAG
TTCTCCACTATGCGGCAGCAGGACGCCTTCGAGCTGTTCCAGCACCTCGTCAAGCTCATCACGCGATGGCCGCAC
GGCCCCGGCCTCGACGACCCGACCAGGCCCTTCCGCTTTCTCCTAGAGCAGAGGCTGCAGTGTATGGGCTGCGGC
AAGGTGCGGTACAGCGAGCAAGAGCAGGACAGCATCTTCATCAACGTGCCGCTCGAGAAGCTGCCCCGGGCCGAG
GGCGATACGGGCGACCAGTACAAGCCCGTCACCCTGAAGCAGTGCCTCGACACCTTGACGGGGGCGGAAAAGGTG
GAACTGGCCTGCTCGGCCTGCCGGAGCACCAAGGGCTTCACCAAGCAGTCGCTTTTCAAGACGTTTCCCGACGTG
CTCGCGGTCAACGCCAACAAAATGTCCGTCGTCAACTGGGTGCCCGTCAAGGTCGACGTCCCCGTCCTCGTCCCG
GACGAGCCCTTTCTACTGGACGACTACATGTCCAAGGGCTTGCAGGCGTCGGAGGAGCCTCTGCCGGACGAGCCC
GAGGCGCCGGCGCCGGCCTTTGTACCCGATGCCGCCGCCCTCGGCCAGCTGGAGGCCATGGGATTCCCGCGCAAC
CGCTGCGAGAAGGCGCTGCACGCCACCGGAAACTCGGACGCCAACGCCGCCATGGAGTGGCTCTTTGCGCGCATG
GAGGATGCCGACATCGACGCGCCTCTCGATCTGGACGCCAGCCCCGTCGCCGATCCGGCCAAGATTGAGACGCTG
GGCGCCATGGGCTTCGACGCGCCTCTTGCCGGAAAGGCCCTCAAGGAGACGGGCGGCGACGTGCAGCGCGCCATC
GAATGGCTCTTTAACCATCCGGATGAAACGGGCTTGGTCGAGGAAGAGGTGGCCCCCGCAGCTGCTAGGGAGCCC
GCCGGCAGTCGGTCGCTCCCCGCCAGCTTCCAGCTGCGGTCCATTGTCTGCCACAAGGGGACCAGTATCCATGCG
GGGCACTACGTGGCCTTTATCCGGAAGCAGCTCGCAGGGCAGGGCGCCCAGTGGGTGCTGTTCAACGACGAAAAG
GTTGTCGAGGCGCACGATTTCGAAGAGATGCGGAAATTTGCCTACGTGTATTTTTTCGAGCGCGTATGA
Gene >Ophio5|3096
ATGACGTGCCCACACCTCGACGCGCTCGGCGCAGGTACGTCCTGCTGATCCTACTCGGCTCCCGCTGGTCACGTC
CGAGGCTCACGCAGCGTCCAGAGCTCTCCCCGCCCAGCGCCAGCCAGTCGGTCTATCGCGAAGACTGTACTCAGT
GCTTCGATTCCATCGTGCGTCGGCCGCTGACGCTACCCTCTCTCGCCTTGAAAGTGGCTGACATGCCCCCTGCCT
CAGGACGAGCCCAGCGGCCTCGATGTCTGTCTCCAGTGCTTCAACGGCGCCTGCGCGGGTGCCAGGCTGCACAAC
GGCCTCCACGCCAGTCTCTGGAAGCATCCTTTAGCGCTCAACATCCGCCGCACGCGTAAGCCCATGGTCCGAGAT
GAGCCCCCTACCAAAATGTCCAAGCTGGCCATCGTGGCCGAGTCGGACGAGGATCGATACGACACGGCCCTCTCT
GCAAAATGCCTTGATTGCGATGCCTCGCTCGATATGACCGACGCCCGCCTCGCTCCCATCGTCGACGGCATCCTC
AAGGCCAACACGTTCGCGCGGAAAGAGGAGGTCAAGGCCTGGGAGCAGGAGTTGACGGGCTGCGAGCACATCCTC
ATGCTGCAGCAGCACGAGTCGCGCAATATCCAACAGGGTGACCTCGGCCACTGCTCTGCCTGCGACCTGCGCGAG
AACCTGTGGCTCTGCCTCGAATGCGGAAACTTGGGCTGTGGCCGCAAACAGATGGGGGGCGTCGACGGCAACTCG
CACGCCCTCGCACACGCGACCGAGTCGGCACACGGCGTCGCCGTCAAGCTCGGCTCCATCACTCCCGAGGGCACC
GCCGACGTCTACTGCTACAAGTGCGACGACGAGCGCCTCGACGACCAGCTCGGCCCCCATCTCGCCCACTGGGGC
ATCATGCTGGCTGACCGCCGCAAGACGGAGATGAGCCTGACGGAGATGCAGATCGAGCAGAATCTCAAGTGGGAC
TTTAGCATGACTACCGACGACGGCAAGCTTCTGAAGCCCCTCTACGGCCCGGGCCTTACCGGCCTCAAGAACCTG
GGCAACAGCTGCTACCTGGCCAGCGTCGCGCAGTGCCTCTTCGACCTGCCGTCCTTCCGAGAGCGCTACTACAGA
CCTACCGATTCCCCGCCTCAAGTCCAGGAGCCGGCGGCCGATCTGGAGACGCAGCTGCGCAAGCTTGCCGATGGC
CTCTTGTCGGGGCGCTATGCCAAGCCGGACGACGACGACGCGGGCCCGGAACCAGACGTCGTCCACCAACAAAAG
GGCCTGGCGCCGGCCATGCTGAAGCATCTCATCGGCAGAGGTCACACCGAGTTCTCCACTATGCGGCAGCAGGAC
GCCTTCGAGCTGTTCCAGCACCTCGTCAAGCTCATCACGCGATGGCCGCACGGCCCCGGCCTCGACGACCCGACC
AGGCCCTTCCGCTTTCTCCTAGAGCAGAGGCTGCAGTGTATGGGCTGCGGCAAGGTGCGGTACAGCGAGCAAGAG
CAGGACAGCATCTTCATCAACGTGCCGCTCGAGAAGCTGCCCCGGGCCGAGGGCGATACGGGCGACCAGTACAAG
CCCGTCACCCTGAAGCAGTGCCTCGACACCTTGACGGGGGCGGAAAAGGTGGAACTGGCCTGCTCGGCCTGCCGG
AGCACCAAGGGCTTCACCAAGCAGTCGCTTTTCAAGACGTTTCCCGACGTGCTCGCGGTCAACGCCAACAAAATG
TCCGTCGTCAACTGGGTGCCCGTCAAGGTCGACGTCCCCGTCCTCGTCCCGGACGAGCCCTTTCTACTGGACGAC
TACATGTCCAAGGGCTTGCAGGCGTCGGAGGAGCCTCTGCCGGACGAGCCCGAGGCGCCGGCGCCGGCCTTTGTA
CCCGATGCCGCCGCCCTCGGCCAGCTGGAGGCCATGGGATTCCCGCGCAACCGCTGCGAGAAGGCGCTGCACGCC
ACCGGAAACTCGGACGCCAACGCCGCCATGGAGTGGCTCTTTGCGCGCATGGAGGATGCCGACATCGACGCGCCT
CTCGATCTGGACGCCAGCCCCGTCGCCGATCCGGCCAAGATTGAGACGCTGGGCGCCATGGGCTTCGACGCGCCT
CTTGCCGGAAAGGCCCTCAAGGAGACGGGCGGCGACGTGCAGCGCGCCATCGAATGGCTCTTTAACCATCCGGAT
GAAACGGGCTTGGTCGAGGAAGAGGTGGCCCCCGCAGCTGCTAGGGAGCCCGCCGGCAGTCGGTCGCTCCCCGCC
AGCTTCCAGCTGCGGTCCATTGTCTGCCACAAGGGGACCAGTATCCATGCGGGGTAGGTCTTCTCGCCGTCCTTG
TGGCGCCAAGCCCCCCTTTCCCCCTTACTGACCCTTTCCAGGCACTACGTGGCCTTTATCCGGAAGCAGCTCGCA
GGGCAGGGCGCCCAGTGGGTGCTGTTCAACGACGAAAAGGTTGTCGAGGCGCACGATTTCGAAGAGATGCGGAAA
TTTGCCTACGTGTATTTTTTCGAGCGCGTATGA

© 2022 - Robin Ohm - Utrecht University - The Netherlands

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