Protein ID | Ophun1|1908 |
Gene name | |
Location | Contig_186:20350..22762 |
Strand | + |
Gene length (bp) | 2412 |
Transcript length (bp) | 2412 |
Coding sequence length (bp) | 2412 |
Protein length (aa) | 804 |
PFAM Domain ID | Short name | Long name | E-value | Start | End |
---|---|---|---|---|---|
PF01794 | Ferric_reduct | Ferric reductase like transmembrane component | 2.3E-17 | 224 | 347 |
PF08030 | NAD_binding_6 | Ferric reductase NAD binding domain | 6.1E-14 | 504 | 778 |
PF08022 | FAD_binding_8 | FAD-binding domain | 1.8E-11 | 397 | 495 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|Q12333|FRE7_YEAST | Ferric/cupric reductase transmembrane component 7 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FRE7 PE=1 SV=2 | 138 | 559 | 6.0E-48 |
sp|A6ZN61|FRE7_YEAS7 | Ferric/cupric reductase transmembrane component 7 OS=Saccharomyces cerevisiae (strain YJM789) GN=FRE7 PE=3 SV=1 | 138 | 565 | 1.0E-46 |
sp|P53746|FRE4_YEAST | Ferric reductase transmembrane component 4 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FRE4 PE=2 SV=1 | 220 | 551 | 3.0E-21 |
sp|Q08905|FRE3_YEAST | Ferric reductase transmembrane component 3 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FRE3 PE=1 SV=1 | 220 | 564 | 1.0E-20 |
sp|P78588|FREL_CANAX | Probable ferric reductase transmembrane component OS=Candida albicans GN=CFL1 PE=3 SV=1 | 220 | 571 | 2.0E-20 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|Q12333|FRE7_YEAST | Ferric/cupric reductase transmembrane component 7 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FRE7 PE=1 SV=2 | 138 | 559 | 6.0E-48 |
sp|A6ZN61|FRE7_YEAS7 | Ferric/cupric reductase transmembrane component 7 OS=Saccharomyces cerevisiae (strain YJM789) GN=FRE7 PE=3 SV=1 | 138 | 565 | 1.0E-46 |
sp|P53746|FRE4_YEAST | Ferric reductase transmembrane component 4 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FRE4 PE=2 SV=1 | 220 | 551 | 3.0E-21 |
sp|Q08905|FRE3_YEAST | Ferric reductase transmembrane component 3 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FRE3 PE=1 SV=1 | 220 | 564 | 1.0E-20 |
sp|P78588|FREL_CANAX | Probable ferric reductase transmembrane component OS=Candida albicans GN=CFL1 PE=3 SV=1 | 220 | 571 | 2.0E-20 |
sp|Q5A446|FRE1_CANAL | Ferric/cupric reductase transmembrane component 1 OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=CFL1 PE=2 SV=1 | 220 | 571 | 2.0E-20 |
sp|P36033|FRE2_YEAST | Ferric/cupric reductase transmembrane component 2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FRE2 PE=1 SV=1 | 220 | 565 | 6.0E-20 |
sp|Q08908|FRE5_YEAST | Ferric reductase transmembrane component 5 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FRE5 PE=2 SV=1 | 135 | 646 | 1.0E-16 |
sp|O94727|FRP2_SCHPO | Ferric/cupric reductase transmembrane component 2 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=frp2 PE=3 SV=1 | 220 | 537 | 7.0E-15 |
sp|P32791|FRE1_YEAST | Ferric/cupric reductase transmembrane component 1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FRE1 PE=1 SV=1 | 220 | 572 | 4.0E-13 |
sp|Q8HZK2|DUOX2_PIG | Dual oxidase 2 OS=Sus scrofa GN=DUOX2 PE=1 SV=2 | 187 | 613 | 6.0E-13 |
sp|Q9FLW2|FRO5_ARATH | Ferric reduction oxidase 5 OS=Arabidopsis thaliana GN=FRO5 PE=2 SV=1 | 241 | 588 | 6.0E-11 |
sp|Q3KTM0|FRO7_ARATH | Ferric reduction oxidase 7, chloroplastic OS=Arabidopsis thaliana GN=FRO7 PE=2 SV=1 | 221 | 576 | 1.0E-10 |
sp|Q8VY13|FRO8_ARATH | Ferric reduction oxidase 8, mitochondrial OS=Arabidopsis thaliana GN=FRO8 PE=2 SV=1 | 220 | 553 | 3.0E-10 |
sp|Q9FIJ0|RBOHD_ARATH | Respiratory burst oxidase homolog protein D OS=Arabidopsis thaliana GN=RBOHD PE=1 SV=1 | 302 | 556 | 3.0E-10 |
sp|Q924V1|NOX4_RAT | NADPH oxidase 4 OS=Rattus norvegicus GN=Nox4 PE=1 SV=2 | 411 | 561 | 5.0E-10 |
sp|Q8RWS6|FRO6_ARATH | Ferric reduction oxidase 6 OS=Arabidopsis thaliana GN=FRO6 PE=2 SV=1 | 221 | 576 | 6.0E-10 |
sp|O81210|RBOHC_ARATH | Respiratory burst oxidase homolog protein C OS=Arabidopsis thaliana GN=RBOHC PE=2 SV=2 | 307 | 579 | 7.0E-10 |
sp|Q86GL4|NOXB_DICDI | Superoxide-generating NADPH oxidase heavy chain subunit B OS=Dictyostelium discoideum GN=noxB PE=2 SV=1 | 319 | 596 | 8.0E-10 |
sp|Q8W110|FRO4_ARATH | Ferric reduction oxidase 4 OS=Arabidopsis thaliana GN=FRO4 PE=2 SV=1 | 241 | 570 | 8.0E-10 |
sp|Q9JHI8|NOX4_MOUSE | NADPH oxidase 4 OS=Mus musculus GN=Nox4 PE=1 SV=1 | 411 | 561 | 9.0E-10 |
sp|Q9XYS3|NOXA_DICDI | Superoxide-generating NADPH oxidase heavy chain subunit A OS=Dictyostelium discoideum GN=noxA PE=2 SV=1 | 306 | 555 | 1.0E-09 |
sp|Q5ZAJ0|RBOHB_ORYSJ | Respiratory burst oxidase homolog protein B OS=Oryza sativa subsp. japonica GN=RBOHB PE=1 SV=1 | 302 | 606 | 1.0E-09 |
sp|Q6J2K5|RBOHB_ORYSI | Respiratory burst oxidase homolog protein B OS=Oryza sativa subsp. indica GN=RBOHB PE=2 SV=1 | 302 | 606 | 1.0E-09 |
sp|Q9SBI0|RBOHB_ARATH | Respiratory burst oxidase homolog protein B OS=Arabidopsis thaliana GN=RBOHB PE=2 SV=1 | 306 | 606 | 2.0E-09 |
sp|Q04800|FRP1_SCHPO | Ferric reductase transmembrane component 1 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=frp1 PE=1 SV=1 | 220 | 606 | 2.0E-09 |
sp|Q9NPH5|NOX4_HUMAN | NADPH oxidase 4 OS=Homo sapiens GN=NOX4 PE=1 SV=2 | 411 | 567 | 2.0E-09 |
sp|Q5R5C5|NOX4_PONAB | NADPH oxidase 4 OS=Pongo abelii GN=NOX4 PE=2 SV=2 | 411 | 567 | 2.0E-09 |
sp|O61213|DUOX1_CAEEL | Dual oxidase 1 OS=Caenorhabditis elegans GN=bli-3 PE=1 SV=2 | 306 | 578 | 3.0E-09 |
sp|Q9SW17|RBOHG_ARATH | Putative respiratory burst oxidase homolog protein G OS=Arabidopsis thaliana GN=RBOHG PE=2 SV=2 | 306 | 557 | 3.0E-09 |
sp|Q948T9|RBOHB_SOLTU | Respiratory burst oxidase homolog protein B OS=Solanum tuberosum GN=RBOHB PE=1 SV=1 | 306 | 556 | 3.0E-09 |
sp|O81209|RBOHA_ARATH | Respiratory burst oxidase homolog protein A OS=Arabidopsis thaliana GN=RBOHA PE=2 SV=2 | 299 | 600 | 3.0E-09 |
sp|O48538|RBOHF_ARATH | Respiratory burst oxidase homolog protein F OS=Arabidopsis thaliana GN=RBOHF PE=1 SV=1 | 323 | 532 | 6.0E-09 |
sp|Q8CIZ9|NOX1_MOUSE | NADPH oxidase 1 OS=Mus musculus GN=Nox1 PE=1 SV=2 | 410 | 565 | 1.0E-08 |
sp|Q9ES45|DUOX2_RAT | Dual oxidase 2 OS=Rattus norvegicus GN=Duox2 PE=2 SV=1 | 306 | 613 | 2.0E-08 |
sp|Q9VQH2|DUOX_DROME | Dual oxidase OS=Drosophila melanogaster GN=Duox PE=1 SV=2 | 306 | 578 | 2.0E-08 |
sp|Q948U0|RBOHA_SOLTU | Respiratory burst oxidase homolog protein A OS=Solanum tuberosum GN=RBOHA PE=1 SV=1 | 406 | 530 | 4.0E-08 |
sp|Q12473|FRE6_YEAST | Ferric reductase transmembrane component 6 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FRE6 PE=1 SV=1 | 220 | 565 | 5.0E-08 |
sp|Q9HBY0|NOX3_HUMAN | NADPH oxidase 3 OS=Homo sapiens GN=NOX3 PE=1 SV=1 | 419 | 559 | 6.0E-08 |
sp|Q9NRD8|DUOX2_HUMAN | Dual oxidase 2 OS=Homo sapiens GN=DUOX2 PE=1 SV=2 | 187 | 613 | 7.0E-08 |
sp|Q9WV87|NOX1_RAT | NADPH oxidase 1 OS=Rattus norvegicus GN=Nox1 PE=2 SV=1 | 358 | 578 | 9.0E-08 |
sp|Q8CIY2|DUOX1_RAT | Dual oxidase 1 OS=Rattus norvegicus GN=Duox1 PE=1 SV=1 | 259 | 613 | 1.0E-07 |
sp|Q96PH1|NOX5_HUMAN | NADPH oxidase 5 OS=Homo sapiens GN=NOX5 PE=1 SV=1 | 211 | 581 | 1.0E-07 |
sp|O81211|RBOHE_ARATH | Respiratory burst oxidase homolog protein E OS=Arabidopsis thaliana GN=RBOHE PE=2 SV=2 | 323 | 532 | 1.0E-07 |
sp|Q2HXK9|RBOHD_SOLTU | Respiratory burst oxidase homolog protein D OS=Solanum tuberosum GN=RBOHD PE=1 SV=2 | 323 | 556 | 2.0E-07 |
sp|Q9MZF4|DUOX1_CANLF | Dual oxidase 1 OS=Canis lupus familiaris GN=DUOX1 PE=1 SV=1 | 412 | 613 | 3.0E-07 |
sp|Q9Y5S8|NOX1_HUMAN | NADPH oxidase 1 OS=Homo sapiens GN=NOX1 PE=1 SV=2 | 420 | 559 | 4.0E-07 |
sp|Q672K1|NOX3_RAT | NADPH oxidase 3 OS=Rattus norvegicus GN=Nox3 PE=2 SV=1 | 419 | 559 | 4.0E-07 |
sp|Q2HXL0|RBOHC_SOLTU | Respiratory burst oxidase homolog protein C OS=Solanum tuberosum GN=RBOHC PE=1 SV=2 | 306 | 531 | 9.0E-07 |
sp|Q672J9|NOX3_MOUSE | NADPH oxidase 3 OS=Mus musculus GN=Nox3 PE=1 SV=2 | 419 | 559 | 1.0E-06 |
sp|Q9NRD9|DUOX1_HUMAN | Dual oxidase 1 OS=Homo sapiens GN=DUOX1 PE=1 SV=1 | 407 | 613 | 2.0E-06 |
sp|P92949|FRO2_ARATH | Ferric reduction oxidase 2 OS=Arabidopsis thaliana GN=FRO2 PE=1 SV=2 | 221 | 548 | 3.0E-06 |
sp|Q8HZK3|DUOX1_PIG | Dual oxidase 1 OS=Sus scrofa GN=DUOX1 PE=2 SV=1 | 179 | 613 | 4.0E-06 |
sp|Q9SUT8|RBOHI_ARATH | Probable respiratory burst oxidase homolog protein I OS=Arabidopsis thaliana GN=RBOHI PE=3 SV=2 | 406 | 606 | 7.0E-06 |
GO Term | Description | Terminal node |
---|---|---|
GO:0016491 | oxidoreductase activity | Yes |
GO:0003674 | molecular_function | No |
GO:0003824 | catalytic activity | No |
SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
---|---|---|
No | 1 - 24 | 0.5 |
Domain # | Start | End | Length |
---|---|---|---|
1 | 36 | 58 | 22 |
2 | 185 | 207 | 22 |
3 | 227 | 249 | 22 |
4 | 262 | 284 | 22 |
5 | 299 | 321 | 22 |
6 | 328 | 350 | 22 |
7 | 360 | 379 | 19 |
8 | 501 | 523 | 22 |
Type of sequence | Sequence |
---|---|
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 | >Ophun1|1908 MAGLARRINIPLTPTSPPGLVQADAVDPWSRAGRYGLGWTYLALAVVGVVVVVRIWHLWQDKIRQAIYKEAVEEH YRGQGEQQRHHQDQQHHQQQHQVHQEQHHQQQHRQDHQHQPDHQHHHQHQHQHQHNNHFSLFPTTPSFRPRAHFS SVTCVNDTLALFRWVFYRPIPDLVWRKHRFTSSSLAVLACAVLAVIVVTLYCFLQQPLYWQSIRFGSPPVAIRAG MMAVAMTPWIVATSMKANLLTLIVGIGPDRLNVIHRWLGYLCLLLVLVHMVPFYVQPVWRDGGMSVFDQLFPDGS GFVYGTGIACFVPLVWLCVGSLPWLRRAAFEAFALLHAPAGAVYVGLLFWHTKNYLLSWSYLYATIAIWAVCYLA RFVFKLNWSRPGRLSFLVGDEAAITLLADNAIKLTIPTQMRWRPGQYIYLRMPAVSLMGNHPFTIASLCSDDFPS DYGDSYRDCVLVFKPYHGFTHRLLQTAIANGPLHTYRAFLDGPYGGMRRELAAFDTCILIAGGSGITSLMSQLLN LVKRMRDGKAITRKVMVVWALKRFEAMDWFREELRICQESAPPESVVCKFFLTSAVRHRPLDDGPTMTMAQDQQH NPRALNHMLHDKLDGFVAGIASKRNSALIVAEAQGDVERERELRAEDEDRITALPQQCYLQPHQPEPLPVRAPEL AHLRQPGDLDKRRPVSTFGPPAGFDFGFPTTPTEFQKSLMRFAFPIPHQMDGGWTIEYGRPQLGHMLRQWATGGS DGRGILGRRTAVFVCGPPSMREGVANTVARLQAAIWGDDELEELFLHTENFAL* |
Coding | >Ophun1|1908 ATGGCCGGCCTCGCGCGACGCATCAACATCCCGCTGACGCCGACCAGCCCTCCGGGGCTGGTGCAGGCCGATGCC GTCGATCCGTGGTCCCGGGCCGGACGGTACGGCTTGGGCTGGACGTACCTGGCGCTGGCCGTCGTGGGCGTCGTG GTGGTTGTGCGCATCTGGCACCTGTGGCAGGACAAGATACGGCAGGCCATATATAAGGAGGCGGTGGAGGAGCAT TACCGAGGGCAGGGGGAGCAGCAGCGGCATCATCAAGACCAGCAGCATCATCAACAGCAGCATCAAGTCCATCAA GAGCAGCATCATCAGCAGCAGCATCGTCAAGATCATCAACACCAGCCTGACCATCAACACCATCACCAACACCAA CACCAACACCAGCACAACAACCACTTCTCCCTCTTCCCTACTACCCCCAGCTTCCGTCCCCGCGCCCACTTCTCC TCCGTCACCTGCGTCAACGATACCCTCGCCCTCTTCCGATGGGTCTTCTACCGCCCCATCCCGGACCTCGTCTGG CGCAAGCACCGCTTCACCTCGTCTTCCCTGGCAGTACTGGCCTGCGCCGTCCTGGCCGTCATCGTGGTGACGCTC TACTGCTTCCTCCAACAGCCGCTCTACTGGCAGAGCATCCGCTTCGGGTCGCCGCCCGTCGCCATCCGGGCCGGC ATGATGGCCGTCGCCATGACGCCGTGGATCGTGGCCACCAGCATGAAGGCCAACCTGCTGACGCTTATAGTCGGC ATCGGCCCGGACCGCCTCAACGTCATCCACCGCTGGCTGGGATACTTGTGTCTGCTGCTGGTGCTGGTCCATATG GTGCCCTTTTACGTCCAGCCTGTATGGCGAGACGGCGGCATGTCCGTCTTCGACCAGCTGTTCCCGGACGGCAGC GGCTTCGTCTACGGCACGGGCATCGCCTGCTTCGTGCCGCTGGTCTGGCTGTGTGTCGGCTCGCTTCCTTGGCTT CGGAGAGCGGCCTTTGAGGCCTTTGCCCTGTTACACGCTCCAGCGGGAGCCGTCTACGTCGGGCTGCTGTTCTGG CACACCAAGAACTACCTGCTGTCGTGGTCGTATCTGTACGCCACCATCGCCATCTGGGCCGTCTGTTACCTCGCT CGCTTCGTCTTCAAGCTCAACTGGAGTCGGCCTGGGCGGTTGTCGTTCCTGGTGGGCGACGAGGCTGCCATCACG CTGCTGGCAGACAACGCCATCAAGCTGACCATCCCGACACAGATGCGCTGGCGACCGGGCCAATACATCTATCTA CGTATGCCGGCTGTCTCGTTGATGGGGAACCATCCGTTTACCATTGCGTCTCTGTGCAGCGACGACTTTCCCTCC GACTACGGCGATAGCTACCGCGACTGTGTCCTCGTCTTCAAGCCCTATCATGGCTTCACTCACCGCCTACTCCAG ACGGCCATCGCCAACGGGCCGCTTCACACCTATCGCGCCTTTCTCGACGGACCATATGGTGGCATGAGGCGAGAG CTGGCTGCCTTTGATACGTGCATCCTCATCGCCGGCGGCAGCGGCATCACCTCTCTCATGTCACAGCTGCTCAAC CTGGTCAAGCGCATGCGCGATGGCAAGGCAATAACCCGCAAGGTCATGGTCGTCTGGGCGCTGAAGCGGTTCGAG GCCATGGACTGGTTCCGCGAGGAGCTGCGCATCTGTCAGGAGTCTGCTCCCCCGGAGAGCGTCGTCTGCAAGTTC TTCCTGACGTCTGCTGTGCGCCATCGCCCGCTCGATGACGGACCGACCATGACCATGGCCCAGGATCAACAGCAT AATCCGAGGGCGCTCAACCACATGCTGCACGATAAGCTCGACGGCTTCGTCGCCGGCATCGCTTCCAAGCGCAAC TCGGCCTTGATCGTGGCCGAGGCTCAGGGCGACGTCGAGCGAGAGCGCGAACTCCGGGCCGAGGACGAGGATCGT ATCACGGCGCTGCCGCAGCAGTGTTACCTGCAGCCTCACCAGCCGGAGCCGCTCCCGGTGCGGGCTCCGGAGCTG GCCCACCTTCGGCAACCCGGCGATCTCGACAAGCGACGGCCCGTCTCCACTTTCGGTCCGCCCGCCGGCTTCGAC TTTGGCTTCCCCACGACGCCGACCGAGTTTCAGAAGAGCCTGATGCGGTTCGCCTTTCCGATTCCGCACCAGATG GACGGCGGTTGGACCATCGAATACGGCCGTCCGCAGCTGGGACACATGCTCCGTCAGTGGGCCACGGGGGGGTCC GACGGCCGGGGGATCCTGGGCCGGAGGACGGCCGTCTTTGTGTGCGGGCCGCCGTCGATGCGCGAGGGCGTCGCC AATACGGTGGCCAGGTTGCAGGCTGCCATCTGGGGGGACGACGAGCTGGAGGAGCTGTTTCTGCATACCGAGAAC TTTGCCCTGTGA |
Transcript | >Ophun1|1908 ATGGCCGGCCTCGCGCGACGCATCAACATCCCGCTGACGCCGACCAGCCCTCCGGGGCTGGTGCAGGCCGATGCC GTCGATCCGTGGTCCCGGGCCGGACGGTACGGCTTGGGCTGGACGTACCTGGCGCTGGCCGTCGTGGGCGTCGTG GTGGTTGTGCGCATCTGGCACCTGTGGCAGGACAAGATACGGCAGGCCATATATAAGGAGGCGGTGGAGGAGCAT TACCGAGGGCAGGGGGAGCAGCAGCGGCATCATCAAGACCAGCAGCATCATCAACAGCAGCATCAAGTCCATCAA GAGCAGCATCATCAGCAGCAGCATCGTCAAGATCATCAACACCAGCCTGACCATCAACACCATCACCAACACCAA CACCAACACCAGCACAACAACCACTTCTCCCTCTTCCCTACTACCCCCAGCTTCCGTCCCCGCGCCCACTTCTCC TCCGTCACCTGCGTCAACGATACCCTCGCCCTCTTCCGATGGGTCTTCTACCGCCCCATCCCGGACCTCGTCTGG CGCAAGCACCGCTTCACCTCGTCTTCCCTGGCAGTACTGGCCTGCGCCGTCCTGGCCGTCATCGTGGTGACGCTC TACTGCTTCCTCCAACAGCCGCTCTACTGGCAGAGCATCCGCTTCGGGTCGCCGCCCGTCGCCATCCGGGCCGGC ATGATGGCCGTCGCCATGACGCCGTGGATCGTGGCCACCAGCATGAAGGCCAACCTGCTGACGCTTATAGTCGGC ATCGGCCCGGACCGCCTCAACGTCATCCACCGCTGGCTGGGATACTTGTGTCTGCTGCTGGTGCTGGTCCATATG GTGCCCTTTTACGTCCAGCCTGTATGGCGAGACGGCGGCATGTCCGTCTTCGACCAGCTGTTCCCGGACGGCAGC GGCTTCGTCTACGGCACGGGCATCGCCTGCTTCGTGCCGCTGGTCTGGCTGTGTGTCGGCTCGCTTCCTTGGCTT CGGAGAGCGGCCTTTGAGGCCTTTGCCCTGTTACACGCTCCAGCGGGAGCCGTCTACGTCGGGCTGCTGTTCTGG CACACCAAGAACTACCTGCTGTCGTGGTCGTATCTGTACGCCACCATCGCCATCTGGGCCGTCTGTTACCTCGCT CGCTTCGTCTTCAAGCTCAACTGGAGTCGGCCTGGGCGGTTGTCGTTCCTGGTGGGCGACGAGGCTGCCATCACG CTGCTGGCAGACAACGCCATCAAGCTGACCATCCCGACACAGATGCGCTGGCGACCGGGCCAATACATCTATCTA CGTATGCCGGCTGTCTCGTTGATGGGGAACCATCCGTTTACCATTGCGTCTCTGTGCAGCGACGACTTTCCCTCC GACTACGGCGATAGCTACCGCGACTGTGTCCTCGTCTTCAAGCCCTATCATGGCTTCACTCACCGCCTACTCCAG ACGGCCATCGCCAACGGGCCGCTTCACACCTATCGCGCCTTTCTCGACGGACCATATGGTGGCATGAGGCGAGAG CTGGCTGCCTTTGATACGTGCATCCTCATCGCCGGCGGCAGCGGCATCACCTCTCTCATGTCACAGCTGCTCAAC CTGGTCAAGCGCATGCGCGATGGCAAGGCAATAACCCGCAAGGTCATGGTCGTCTGGGCGCTGAAGCGGTTCGAG GCCATGGACTGGTTCCGCGAGGAGCTGCGCATCTGTCAGGAGTCTGCTCCCCCGGAGAGCGTCGTCTGCAAGTTC TTCCTGACGTCTGCTGTGCGCCATCGCCCGCTCGATGACGGACCGACCATGACCATGGCCCAGGATCAACAGCAT AATCCGAGGGCGCTCAACCACATGCTGCACGATAAGCTCGACGGCTTCGTCGCCGGCATCGCTTCCAAGCGCAAC TCGGCCTTGATCGTGGCCGAGGCTCAGGGCGACGTCGAGCGAGAGCGCGAACTCCGGGCCGAGGACGAGGATCGT ATCACGGCGCTGCCGCAGCAGTGTTACCTGCAGCCTCACCAGCCGGAGCCGCTCCCGGTGCGGGCTCCGGAGCTG GCCCACCTTCGGCAACCCGGCGATCTCGACAAGCGACGGCCCGTCTCCACTTTCGGTCCGCCCGCCGGCTTCGAC TTTGGCTTCCCCACGACGCCGACCGAGTTTCAGAAGAGCCTGATGCGGTTCGCCTTTCCGATTCCGCACCAGATG GACGGCGGTTGGACCATCGAATACGGCCGTCCGCAGCTGGGACACATGCTCCGTCAGTGGGCCACGGGGGGGTCC GACGGCCGGGGGATCCTGGGCCGGAGGACGGCCGTCTTTGTGTGCGGGCCGCCGTCGATGCGCGAGGGCGTCGCC AATACGGTGGCCAGGTTGCAGGCTGCCATCTGGGGGGACGACGAGCTGGAGGAGCTGTTTCTGCATACCGAGAAC TTTGCCCTGTGA |
Gene | >Ophun1|1908 ATGGCCGGCCTCGCGCGACGCATCAACATCCCGCTGACGCCGACCAGCCCTCCGGGGCTGGTGCAGGCCGATGCC GTCGATCCGTGGTCCCGGGCCGGACGGTACGGCTTGGGCTGGACGTACCTGGCGCTGGCCGTCGTGGGCGTCGTG GTGGTTGTGCGCATCTGGCACCTGTGGCAGGACAAGATACGGCAGGCCATATATAAGGAGGCGGTGGAGGAGCAT TACCGAGGGCAGGGGGAGCAGCAGCGGCATCATCAAGACCAGCAGCATCATCAACAGCAGCATCAAGTCCATCAA GAGCAGCATCATCAGCAGCAGCATCGTCAAGATCATCAACACCAGCCTGACCATCAACACCATCACCAACACCAA CACCAACACCAGCACAACAACCACTTCTCCCTCTTCCCTACTACCCCCAGCTTCCGTCCCCGCGCCCACTTCTCC TCCGTCACCTGCGTCAACGATACCCTCGCCCTCTTCCGATGGGTCTTCTACCGCCCCATCCCGGACCTCGTCTGG CGCAAGCACCGCTTCACCTCGTCTTCCCTGGCAGTACTGGCCTGCGCCGTCCTGGCCGTCATCGTGGTGACGCTC TACTGCTTCCTCCAACAGCCGCTCTACTGGCAGAGCATCCGCTTCGGGTCGCCGCCCGTCGCCATCCGGGCCGGC ATGATGGCCGTCGCCATGACGCCGTGGATCGTGGCCACCAGCATGAAGGCCAACCTGCTGACGCTTATAGTCGGC ATCGGCCCGGACCGCCTCAACGTCATCCACCGCTGGCTGGGATACTTGTGTCTGCTGCTGGTGCTGGTCCATATG GTGCCCTTTTACGTCCAGCCTGTATGGCGAGACGGCGGCATGTCCGTCTTCGACCAGCTGTTCCCGGACGGCAGC GGCTTCGTCTACGGCACGGGCATCGCCTGCTTCGTGCCGCTGGTCTGGCTGTGTGTCGGCTCGCTTCCTTGGCTT CGGAGAGCGGCCTTTGAGGCCTTTGCCCTGTTACACGCTCCAGCGGGAGCCGTCTACGTCGGGCTGCTGTTCTGG CACACCAAGAACTACCTGCTGTCGTGGTCGTATCTGTACGCCACCATCGCCATCTGGGCCGTCTGTTACCTCGCT CGCTTCGTCTTCAAGCTCAACTGGAGTCGGCCTGGGCGGTTGTCGTTCCTGGTGGGCGACGAGGCTGCCATCACG CTGCTGGCAGACAACGCCATCAAGCTGACCATCCCGACACAGATGCGCTGGCGACCGGGCCAATACATCTATCTA CGTATGCCGGCTGTCTCGTTGATGGGGAACCATCCGTTTACCATTGCGTCTCTGTGCAGCGACGACTTTCCCTCC GACTACGGCGATAGCTACCGCGACTGTGTCCTCGTCTTCAAGCCCTATCATGGCTTCACTCACCGCCTACTCCAG ACGGCCATCGCCAACGGGCCGCTTCACACCTATCGCGCCTTTCTCGACGGACCATATGGTGGCATGAGGCGAGAG CTGGCTGCCTTTGATACGTGCATCCTCATCGCCGGCGGCAGCGGCATCACCTCTCTCATGTCACAGCTGCTCAAC CTGGTCAAGCGCATGCGCGATGGCAAGGCAATAACCCGCAAGGTCATGGTCGTCTGGGCGCTGAAGCGGTTCGAG GCCATGGACTGGTTCCGCGAGGAGCTGCGCATCTGTCAGGAGTCTGCTCCCCCGGAGAGCGTCGTCTGCAAGTTC TTCCTGACGTCTGCTGTGCGCCATCGCCCGCTCGATGACGGACCGACCATGACCATGGCCCAGGATCAACAGCAT AATCCGAGGGCGCTCAACCACATGCTGCACGATAAGCTCGACGGCTTCGTCGCCGGCATCGCTTCCAAGCGCAAC TCGGCCTTGATCGTGGCCGAGGCTCAGGGCGACGTCGAGCGAGAGCGCGAACTCCGGGCCGAGGACGAGGATCGT ATCACGGCGCTGCCGCAGCAGTGTTACCTGCAGCCTCACCAGCCGGAGCCGCTCCCGGTGCGGGCTCCGGAGCTG GCCCACCTTCGGCAACCCGGCGATCTCGACAAGCGACGGCCCGTCTCCACTTTCGGTCCGCCCGCCGGCTTCGAC TTTGGCTTCCCCACGACGCCGACCGAGTTTCAGAAGAGCCTGATGCGGTTCGCCTTTCCGATTCCGCACCAGATG GACGGCGGTTGGACCATCGAATACGGCCGTCCGCAGCTGGGACACATGCTCCGTCAGTGGGCCACGGGGGGGTCC GACGGCCGGGGGATCCTGGGCCGGAGGACGGCCGTCTTTGTGTGCGGGCCGCCGTCGATGCGCGAGGGCGTCGCC AATACGGTGGCCAGGTTGCAGGCTGCCATCTGGGGGGACGACGAGCTGGAGGAGCTGTTTCTGCATACCGAGAAC TTTGCCCTGTGA |