© 2022 - Robin Ohm - Utrecht University - The Netherlands
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| Protein ID | OphauB2|295 |
| Gene name | |
| Location | Contig_101:6142..8413 |
| Strand | + |
| Gene length (bp) | 2271 |
| Transcript length (bp) | 1974 |
| Coding sequence length (bp) | 1974 |
| Protein length (aa) | 658 |
| PFAM Domain ID | Short name | Long name | E-value | Start | End |
|---|---|---|---|---|---|
| PF00447 | HSF_DNA-bind | HSF-type DNA-binding | 5.4E-28 | 156 | 257 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|Q02953|HSF_SCHPO | Heat shock factor protein OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=hsf1 PE=1 SV=2 | 149 | 372 | 2.0E-31 |
| sp|Q03933|HSF2_HUMAN | Heat shock factor protein 2 OS=Homo sapiens GN=HSF2 PE=1 SV=1 | 153 | 373 | 3.0E-26 |
| sp|P38533|HSF2_MOUSE | Heat shock factor protein 2 OS=Mus musculus GN=Hsf2 PE=2 SV=2 | 153 | 373 | 6.0E-26 |
| sp|P38531|HSF3_CHICK | Heat shock factor protein 3 OS=Gallus gallus GN=HSF3 PE=2 SV=1 | 153 | 373 | 2.0E-25 |
| sp|P41154|HSF_XENLA | Heat shock factor protein OS=Xenopus laevis GN=hsf1 PE=2 SV=1 | 153 | 373 | 4.0E-24 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|Q02953|HSF_SCHPO | Heat shock factor protein OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=hsf1 PE=1 SV=2 | 149 | 372 | 2.0E-31 |
| sp|Q03933|HSF2_HUMAN | Heat shock factor protein 2 OS=Homo sapiens GN=HSF2 PE=1 SV=1 | 153 | 373 | 3.0E-26 |
| sp|P38533|HSF2_MOUSE | Heat shock factor protein 2 OS=Mus musculus GN=Hsf2 PE=2 SV=2 | 153 | 373 | 6.0E-26 |
| sp|P38531|HSF3_CHICK | Heat shock factor protein 3 OS=Gallus gallus GN=HSF3 PE=2 SV=1 | 153 | 373 | 2.0E-25 |
| sp|P41154|HSF_XENLA | Heat shock factor protein OS=Xenopus laevis GN=hsf1 PE=2 SV=1 | 153 | 373 | 4.0E-24 |
| sp|Q5AQ33|HSF_CANAL | Heat shock transcription factor OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=CTA8 PE=1 SV=1 | 139 | 372 | 4.0E-23 |
| sp|P22121|HSF_KLULA | Heat shock factor protein OS=Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) GN=HSF PE=1 SV=1 | 142 | 372 | 8.0E-23 |
| sp|P38530|HSF2_CHICK | Heat shock factor protein 2 OS=Gallus gallus GN=HSF2 PE=2 SV=1 | 153 | 373 | 9.0E-23 |
| sp|P38532|HSF1_MOUSE | Heat shock factor protein 1 OS=Mus musculus GN=Hsf1 PE=1 SV=2 | 153 | 406 | 8.0E-22 |
| sp|P10961|HSF_YEAST | Heat shock factor protein OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=HSF1 PE=1 SV=1 | 140 | 371 | 9.0E-22 |
| sp|Q08DJ8|HSF1_BOVIN | Heat shock factor protein 1 OS=Bos taurus GN=HSF1 PE=2 SV=1 | 153 | 455 | 2.0E-21 |
| sp|Q00613|HSF1_HUMAN | Heat shock factor protein 1 OS=Homo sapiens GN=HSF1 PE=1 SV=1 | 153 | 406 | 2.0E-21 |
| sp|P22335|HSF24_SOLPE | Heat shock factor protein HSF24 OS=Solanum peruvianum GN=HSF24 PE=2 SV=1 | 155 | 366 | 2.0E-21 |
| sp|P38529|HSF1_CHICK | Heat shock factor protein 1 OS=Gallus gallus GN=HSF1 PE=2 SV=1 | 153 | 406 | 6.0E-21 |
| sp|Q1HGE8|HSF4_CANLF | Heat shock factor protein 4 OS=Canis lupus familiaris GN=HSF4 PE=2 SV=1 | 153 | 381 | 7.0E-20 |
| sp|P22813|HSF_DROME | Heat shock factor protein OS=Drosophila melanogaster GN=Hsf PE=1 SV=1 | 135 | 373 | 2.0E-19 |
| sp|Q9R0L1|HSF4_MOUSE | Heat shock factor protein 4 OS=Mus musculus GN=Hsf4 PE=1 SV=2 | 153 | 368 | 2.0E-19 |
| sp|Q9ULV5|HSF4_HUMAN | Heat shock factor protein 4 OS=Homo sapiens GN=HSF4 PE=1 SV=2 | 153 | 397 | 4.0E-19 |
| sp|Q5A4X5|SKN7_CANAL | Transcription factor SKN7 OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=SKN7 PE=3 SV=1 | 156 | 369 | 5.0E-19 |
| sp|Q96320|HSFB1_ARATH | Heat stress transcription factor B-1 OS=Arabidopsis thaliana GN=HSFB1 PE=2 SV=2 | 148 | 253 | 1.0E-17 |
| sp|Q9LQM7|HFA1D_ARATH | Heat stress transcription factor A-1d OS=Arabidopsis thaliana GN=HSFA1D PE=1 SV=2 | 154 | 369 | 5.0E-17 |
| sp|Q9SCW4|HFB2A_ARATH | Heat stress transcription factor B-2a OS=Arabidopsis thaliana GN=HSFB2A PE=2 SV=1 | 145 | 260 | 6.0E-17 |
| sp|O14283|PRR1_SCHPO | Transcription factor prr1 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=prr1 PE=1 SV=2 | 156 | 218 | 7.0E-17 |
| sp|D0VYS2|HSF3_MOUSE | Heat shock factor protein 3 OS=Mus musculus GN=Hsf3 PE=2 SV=1 | 147 | 372 | 2.0E-16 |
| sp|O22230|HSFB3_ARATH | Heat stress transcription factor B-3 OS=Arabidopsis thaliana GN=HSFB3 PE=2 SV=1 | 154 | 337 | 7.0E-16 |
| sp|Q40152|HSF8_SOLLC | Heat shock factor protein HSF8 OS=Solanum lycopersicum GN=HSF8 PE=3 SV=1 | 156 | 374 | 8.0E-16 |
| sp|Q652B0|HFB2C_ORYSJ | Heat stress transcription factor B-2c OS=Oryza sativa subsp. japonica GN=HSFB2C PE=2 SV=1 | 148 | 260 | 1.0E-15 |
| sp|Q9FK72|HFA4C_ARATH | Heat stress transcription factor A-4c OS=Arabidopsis thaliana GN=HSFA4C PE=2 SV=1 | 153 | 336 | 2.0E-15 |
| sp|Q6Z9C8|HFB2B_ORYSJ | Heat stress transcription factor B-2b OS=Oryza sativa subsp. japonica GN=HSFB2B PE=2 SV=1 | 146 | 260 | 3.0E-15 |
| sp|Q7XRX3|HFB2A_ORYSJ | Heat stress transcription factor B-2a OS=Oryza sativa subsp. japonica GN=HSFB2A PE=2 SV=2 | 154 | 260 | 4.0E-15 |
| sp|Q338B0|HFA2C_ORYSJ | Heat stress transcription factor A-2c OS=Oryza sativa subsp. japonica GN=HSFA2C PE=1 SV=2 | 154 | 260 | 8.0E-15 |
| sp|Q9SCW5|HFA1E_ARATH | Heat stress transcription factor A-1e OS=Arabidopsis thaliana GN=HSFA1E PE=2 SV=2 | 144 | 218 | 2.0E-14 |
| sp|Q6H6Q7|HSFA3_ORYSJ | Heat stress transcription factor A-3 OS=Oryza sativa subsp. japonica GN=HSFA3 PE=2 SV=1 | 145 | 386 | 2.0E-14 |
| sp|P41151|HFA1A_ARATH | Heat stress transcription factor A-1a OS=Arabidopsis thaliana GN=HSFA1A PE=1 SV=2 | 154 | 369 | 3.0E-14 |
| sp|Q9T0D3|HFB2B_ARATH | Heat stress transcription factor B-2b OS=Arabidopsis thaliana GN=HSFB2B PE=2 SV=1 | 150 | 260 | 3.0E-14 |
| sp|Q9LUH8|HFA6B_ARATH | Heat stress transcription factor A-6b OS=Arabidopsis thaliana GN=HSFA6b PE=2 SV=1 | 154 | 265 | 4.0E-14 |
| sp|P38889|SKN7_YEAST | Transcription factor SKN7 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=SKN7 PE=1 SV=1 | 156 | 218 | 4.0E-14 |
| sp|Q84T61|HSFA1_ORYSJ | Heat stress transcription factor A-1 OS=Oryza sativa subsp. japonica GN=HSFA1 PE=2 SV=1 | 154 | 369 | 4.0E-14 |
| sp|Q94J16|HFA4B_ORYSJ | Heat stress transcription factor A-4b OS=Oryza sativa subsp. japonica GN=HSFA4B PE=2 SV=1 | 153 | 358 | 6.0E-14 |
| sp|P41153|HSF8_SOLPE | Heat shock factor protein HSF8 OS=Solanum peruvianum GN=HSF8 PE=2 SV=1 | 156 | 369 | 6.0E-14 |
| sp|P41152|HSF30_SOLPE | Heat shock factor protein HSF30 OS=Solanum peruvianum GN=HSF30 PE=2 SV=1 | 154 | 218 | 7.0E-14 |
| sp|O81821|HFA1B_ARATH | Heat stress transcription factor A-1b OS=Arabidopsis thaliana GN=HSFA1B PE=2 SV=2 | 153 | 260 | 8.0E-14 |
| sp|Q8GYY1|HSFA3_ARATH | Heat stress transcription factor A-3 OS=Arabidopsis thaliana GN=HSFA3 PE=2 SV=2 | 153 | 373 | 9.0E-14 |
| sp|Q942D6|HFC1B_ORYSJ | Heat stress transcription factor C-1b OS=Oryza sativa subsp. japonica GN=HSFC1B PE=2 SV=1 | 153 | 291 | 2.0E-13 |
| sp|Q6VBA4|HFC1A_ORYSJ | Heat stress transcription factor C-1a OS=Oryza sativa subsp. japonica GN=HSFC1A PE=2 SV=2 | 150 | 218 | 4.0E-13 |
| sp|Q7XHZ0|HFB4B_ORYSJ | Heat stress transcription factor B-4b OS=Oryza sativa subsp. japonica GN=HSFB4B PE=1 SV=1 | 151 | 260 | 6.0E-13 |
| sp|Q84MN7|HFA2A_ORYSJ | Heat stress transcription factor A-2a OS=Oryza sativa subsp. japonica GN=HSFA2A PE=2 SV=1 | 154 | 218 | 7.0E-13 |
| sp|Q67TP9|HSFB1_ORYSJ | Heat stress transcription factor B-1 OS=Oryza sativa subsp. japonica GN=HSFB1 PE=2 SV=1 | 155 | 260 | 7.0E-13 |
| sp|Q9C635|HSFB4_ARATH | Heat stress transcription factor B-4 OS=Arabidopsis thaliana GN=HSFB4 PE=2 SV=1 | 140 | 262 | 8.0E-13 |
| sp|Q1PDN3|HFA6A_ARATH | Heat stress transcription factor A-6a OS=Arabidopsis thaliana GN=HSFA6A PE=2 SV=1 | 151 | 275 | 1.0E-12 |
| sp|O80982|HSFA2_ARATH | Heat stress transcription factor A-2 OS=Arabidopsis thaliana GN=HSFA2 PE=1 SV=1 | 154 | 218 | 1.0E-12 |
| sp|Q6VBB2|HFA2B_ORYSJ | Heat stress transcription factor A-2b OS=Oryza sativa subsp. japonica GN=HSFA2B PE=2 SV=1 | 154 | 260 | 1.0E-12 |
| sp|Q6F388|HFA2E_ORYSJ | Heat stress transcription factor A-2e OS=Oryza sativa subsp. japonica GN=HSFA2E PE=2 SV=1 | 154 | 260 | 3.0E-12 |
| sp|Q6EUG4|HFC2A_ORYSJ | Heat stress transcription factor C-2a OS=Oryza sativa subsp. japonica GN=HSFC2A PE=2 SV=1 | 153 | 342 | 3.0E-12 |
| sp|Q8H7Y6|HFA2D_ORYSJ | Heat stress transcription factor A-2d OS=Oryza sativa subsp. japonica GN=HSFA2D PE=2 SV=2 | 154 | 260 | 4.0E-12 |
| sp|Q10KX8|HFB4D_ORYSJ | Heat stress transcription factor B-4d OS=Oryza sativa subsp. japonica GN=HSFB4D PE=3 SV=1 | 156 | 260 | 5.0E-12 |
| sp|Q9S7U5|HSFA8_ARATH | Heat stress transcription factor A-8 OS=Arabidopsis thaliana GN=HSFA8 PE=2 SV=1 | 153 | 339 | 8.0E-12 |
| sp|Q9LVW2|HSFA9_ARATH | Heat stress transcription factor A-9 OS=Arabidopsis thaliana GN=HSFA9 PE=2 SV=1 | 153 | 218 | 2.0E-11 |
| sp|Q67U94|HFB4C_ORYSJ | Heat stress transcription factor B-4c OS=Oryza sativa subsp. japonica GN=HSFB4C PE=3 SV=1 | 155 | 260 | 2.0E-11 |
| sp|Q94BZ5|HSFA5_ARATH | Heat stress transcription factor A-5 OS=Arabidopsis thaliana GN=HSFA5 PE=2 SV=1 | 156 | 218 | 2.0E-11 |
| sp|Q9LV52|HSFC1_ARATH | Heat stress transcription factor C-1 OS=Arabidopsis thaliana GN=HSFC1 PE=2 SV=1 | 153 | 315 | 2.0E-11 |
| sp|Q0DBL6|HFC2B_ORYSJ | Heat stress transcription factor C-2b OS=Oryza sativa subsp. japonica GN=HSFC2B PE=3 SV=1 | 155 | 218 | 2.0E-11 |
| sp|Q5A287|SFL1_CANAL | Transcription factor SFL1 OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=SFL1 PE=1 SV=1 | 156 | 218 | 3.0E-11 |
| sp|Q9SV12|HFA7A_ARATH | Heat stress transcription factor A-7a OS=Arabidopsis thaliana GN=HSFA7A PE=2 SV=1 | 154 | 218 | 3.0E-11 |
| sp|Q6K6S5|HSFA5_ORYSJ | Heat stress transcription factor A-5 OS=Oryza sativa subsp. japonica GN=HSFA5 PE=2 SV=1 | 155 | 260 | 6.0E-11 |
| sp|P20134|SFL1_YEAST | Flocculation suppression protein OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=SFL1 PE=1 SV=3 | 156 | 218 | 8.0E-11 |
| sp|Q93VB5|HFA4D_ORYSJ | Heat stress transcription factor A-4d OS=Oryza sativa subsp. japonica GN=HSFA4D PE=1 SV=1 | 156 | 260 | 9.0E-11 |
| sp|Q9M1V5|HFA7B_ARATH | Heat stress transcription factor A-7b OS=Arabidopsis thaliana GN=HSFA7B PE=2 SV=1 | 155 | 218 | 1.0E-10 |
| sp|Q6Z9R8|HFB4A_ORYSJ | Putative heat stress transcription factor B-4a OS=Oryza sativa subsp. japonica GN=HSFB4A PE=3 SV=1 | 156 | 265 | 3.0E-10 |
| sp|O49403|HFA4A_ARATH | Heat stress transcription factor A-4a OS=Arabidopsis thaliana GN=HSFA4A PE=2 SV=1 | 153 | 260 | 2.0E-09 |
| sp|Q10PR4|HSFA9_ORYSJ | Heat stress transcription factor A-9 OS=Oryza sativa subsp. japonica GN=HSFA9 PE=2 SV=1 | 149 | 218 | 2.0E-09 |
| sp|Q657C0|HFA6B_ORYSJ | Heat stress transcription factor A-6a OS=Oryza sativa subsp. japonica GN=HSFA6B PE=2 SV=1 | 155 | 218 | 9.0E-09 |
| sp|Q5Z6A4|HFA6A_ORYSJ | Putative heat stress transcription factor A-6a OS=Oryza sativa subsp. japonica GN=HSFA6A PE=3 SV=1 | 155 | 218 | 9.0E-08 |
| sp|Q96LI6|HSFY1_HUMAN | Heat shock transcription factor, Y-linked OS=Homo sapiens GN=HSFY1 PE=1 SV=1 | 156 | 261 | 1.0E-06 |
| sp|B7XIV9|HSF_ENTBH | Probable heat shock factor protein homolog OS=Enterocytozoon bieneusi (strain H348) GN=HSF PE=3 SV=1 | 148 | 261 | 2.0E-06 |
| sp|P47175|HMS2_YEAST | Probable transcription factor HMS2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=HMS2 PE=1 SV=1 | 145 | 218 | 8.0E-06 |
| GO Term | Description | Terminal node |
|---|---|---|
| GO:0043565 | sequence-specific DNA binding | Yes |
| GO:0003700 | DNA-binding transcription factor activity | Yes |
| GO:0006355 | regulation of transcription, DNA-templated | Yes |
| GO:0065007 | biological regulation | No |
| GO:0010468 | regulation of gene expression | No |
| GO:0140110 | transcription regulator activity | No |
| GO:0008150 | biological_process | No |
| GO:0005488 | binding | No |
| GO:0003674 | molecular_function | No |
| GO:0009889 | regulation of biosynthetic process | No |
| GO:0010556 | regulation of macromolecule biosynthetic process | No |
| GO:0060255 | regulation of macromolecule metabolic process | No |
| GO:0050789 | regulation of biological process | No |
| GO:0031323 | regulation of cellular metabolic process | No |
| GO:0003677 | DNA binding | No |
| GO:0051171 | regulation of nitrogen compound metabolic process | No |
| GO:0097159 | organic cyclic compound binding | No |
| GO:2001141 | regulation of RNA biosynthetic process | No |
| GO:1901363 | heterocyclic compound binding | No |
| GO:0050794 | regulation of cellular process | No |
| GO:0051252 | regulation of RNA metabolic process | No |
| GO:0031326 | regulation of cellular biosynthetic process | No |
| GO:0019222 | regulation of metabolic process | No |
| GO:0003676 | nucleic acid binding | No |
| GO:0080090 | regulation of primary metabolic process | No |
| GO:0019219 | regulation of nucleobase-containing compound metabolic process | No |
| GO:1903506 | regulation of nucleic acid-templated transcription | No |
| SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
|---|---|---|
| No | 1 - 13 | 0.45 |
| 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 | >OphauB2|295 MSGQNPRKRPAPGASPIAPYTQSLPSPYGVETALSDPVAKWNIGPSDTLGHIDANSYAVNNQLGSVSDSQQYIQP APMPSNSLTRRSMNQALIATNPRSNLESAIEPWSGFGDENTLLQTNDGEGAMEQENIEVLEERSQKAKREAQAKR KQIPPFVQKLRSFLEDRKNEDFIRWSEKGDSFIVIDEDEFAKTLIPELFKHNNYASFVRQLNMYGFHKRVGLSDN SMRASERKNKSPSEYFNPYFRRGHPNLMWLITKAKGGSKSKKGGRSAEGEAESEEDNVPEDATTQAANSASTSLP AAESQALPKKEMTMIRDELNKIREQQKMILGAINQLQRNNNELYSQALRFQNQHDRHQNSINAILNFLANVFRKT LEDGSSQNVGDIISSIMSNQANPPSHQQGSIFDLGDLVQNATEPEQTKPSRAPSAASTPYHPIGHMSPEMGHVTE LVDGSEATPNLRQELEKNPQERMMKIINDHNATNTSNLALPDAAEIVAKAPQTLNLAQGSHPSAPPMGMIPQSPV ENSINSNQIDLDQLHRLQNDQDAKIQEIGEMLGPLSPSGQIPGLGDGHGHLFDPPNVDLDQYFDSNAFLHDASFT GDGNDFNFSLDTGDSLGTANGADAKSVISPRDTDNYQDNDPAGATNADADCKRRRII* |
| Coding | >OphauB2|295 ATGTCAGGTCAAAATCCAAGAAAGCGCCCTGCGCCGGGCGCATCGCCTATTGCCCCCTACACTCAGTCATTACCC TCGCCCTACGGTGTGGAAACTGCATTGTCGGACCCTGTTGCGAAATGGAATATTGGACCAAGCGACACCTTGGGT CATATAGACGCGAATAGCTATGCTGTCAACAACCAGCTGGGCTCAGTCTCTGACTCGCAGCAATACATACAGCCC GCCCCGATGCCTTCCAACTCGCTCACTCGACGATCTATGAACCAGGCGCTGATAGCAACCAATCCGCGTTCCAAT CTCGAATCGGCAATTGAACCCTGGTCCGGCTTCGGCGACGAGAATACCTTATTGCAAACAAATGATGGCGAAGGA GCTATGGAGCAGGAGAATATCGAGGTTCTTGAAGAGAGATCTCAAAAAGCCAAGCGTGAGGCCCAAGCGAAAAGA AAACAGATACCCCCCTTCGTACAGAAGCTCAGAAGCTTTCTTGAAGATCGCAAAAACGAAGATTTTATTCGGTGG TCAGAAAAGGGCGATTCCTTCATTGTTATAGACGAGGACGAATTTGCAAAGACCCTGATACCCGAACTTTTCAAG CATAACAACTACGCATCATTTGTCCGCCAGCTCAACATGTACGGCTTTCACAAACGCGTTGGTCTGTCCGACAAT AGCATGCGTGCAAGTGAACGCAAGAACAAGAGCCCTAGCGAATATTTTAATCCCTACTTTCGTCGCGGTCATCCG AATTTGATGTGGCTTATTACCAAAGCCAAAGGGGGAAGCAAATCTAAAAAAGGGGGCAGAAGCGCCGAAGGCGAG GCCGAAAGTGAGGAGGACAATGTACCGGAAGACGCGACGACTCAAGCAGCCAACAGCGCCAGTACTTCGCTGCCA GCTGCCGAGTCCCAAGCATTACCAAAAAAGGAAATGACCATGATAAGAGACGAGCTGAACAAGATTCGCGAACAA CAGAAGATGATTCTGGGTGCCATCAATCAGTTGCAGCGCAACAATAACGAACTGTATAGCCAAGCCCTCAGGTTT CAGAACCAGCACGACCGCCACCAAAACTCGATCAACGCCATACTCAACTTCCTGGCTAATGTCTTCAGGAAGACT CTAGAGGATGGCAGCAGTCAGAATGTTGGCGATATCATCTCGAGCATCATGTCAAACCAAGCCAACCCGCCGTCT CATCAGCAAGGTAGTATCTTTGACCTGGGAGACCTGGTTCAAAATGCGACGGAACCTGAGCAGACGAAACCGAGC AGAGCTCCGTCAGCGGCTAGCACACCATACCATCCAATTGGTCACATGTCGCCCGAAATGGGGCACGTCACCGAA TTGGTCGATGGTTCAGAAGCGACGCCTAATCTACGACAGGAATTAGAGAAGAATCCACAAGAACGTATGATGAAA ATTATCAACGACCACAATGCCACCAACACGTCGAATTTGGCTCTTCCCGATGCCGCCGAGATTGTTGCCAAGGCA CCACAAACTCTGAATTTGGCTCAGGGGTCACATCCATCTGCTCCTCCCATGGGCATGATTCCTCAAAGTCCTGTA GAGAATTCGATCAACTCGAATCAAATTGATCTCGATCAACTCCACCGGCTGCAAAACGATCAAGACGCCAAGATT CAAGAGATCGGTGAGATGCTCGGGCCTCTGAGCCCCTCAGGCCAGATCCCGGGGCTGGGAGATGGTCATGGGCAT CTATTTGATCCACCCAACGTAGATTTGGATCAATACTTTGACAGTAATGCATTTTTGCATGATGCCAGCTTTACC GGGGATGGTAACGACTTTAACTTTAGCCTTGATACCGGCGACTCGCTTGGTACTGCGAATGGGGCCGACGCAAAA TCCGTTATAAGCCCTCGGGACACAGATAATTATCAAGACAATGACCCGGCCGGTGCCACCAATGCGGATGCAGAC TGCAAACGAAGGCGGATCATATAG |
| Transcript | >OphauB2|295 ATGTCAGGTCAAAATCCAAGAAAGCGCCCTGCGCCGGGCGCATCGCCTATTGCCCCCTACACTCAGTCATTACCC TCGCCCTACGGTGTGGAAACTGCATTGTCGGACCCTGTTGCGAAATGGAATATTGGACCAAGCGACACCTTGGGT CATATAGACGCGAATAGCTATGCTGTCAACAACCAGCTGGGCTCAGTCTCTGACTCGCAGCAATACATACAGCCC GCCCCGATGCCTTCCAACTCGCTCACTCGACGATCTATGAACCAGGCGCTGATAGCAACCAATCCGCGTTCCAAT CTCGAATCGGCAATTGAACCCTGGTCCGGCTTCGGCGACGAGAATACCTTATTGCAAACAAATGATGGCGAAGGA GCTATGGAGCAGGAGAATATCGAGGTTCTTGAAGAGAGATCTCAAAAAGCCAAGCGTGAGGCCCAAGCGAAAAGA AAACAGATACCCCCCTTCGTACAGAAGCTCAGAAGCTTTCTTGAAGATCGCAAAAACGAAGATTTTATTCGGTGG TCAGAAAAGGGCGATTCCTTCATTGTTATAGACGAGGACGAATTTGCAAAGACCCTGATACCCGAACTTTTCAAG CATAACAACTACGCATCATTTGTCCGCCAGCTCAACATGTACGGCTTTCACAAACGCGTTGGTCTGTCCGACAAT AGCATGCGTGCAAGTGAACGCAAGAACAAGAGCCCTAGCGAATATTTTAATCCCTACTTTCGTCGCGGTCATCCG AATTTGATGTGGCTTATTACCAAAGCCAAAGGGGGAAGCAAATCTAAAAAAGGGGGCAGAAGCGCCGAAGGCGAG GCCGAAAGTGAGGAGGACAATGTACCGGAAGACGCGACGACTCAAGCAGCCAACAGCGCCAGTACTTCGCTGCCA GCTGCCGAGTCCCAAGCATTACCAAAAAAGGAAATGACCATGATAAGAGACGAGCTGAACAAGATTCGCGAACAA CAGAAGATGATTCTGGGTGCCATCAATCAGTTGCAGCGCAACAATAACGAACTGTATAGCCAAGCCCTCAGGTTT CAGAACCAGCACGACCGCCACCAAAACTCGATCAACGCCATACTCAACTTCCTGGCTAATGTCTTCAGGAAGACT CTAGAGGATGGCAGCAGTCAGAATGTTGGCGATATCATCTCGAGCATCATGTCAAACCAAGCCAACCCGCCGTCT CATCAGCAAGGTAGTATCTTTGACCTGGGAGACCTGGTTCAAAATGCGACGGAACCTGAGCAGACGAAACCGAGC AGAGCTCCGTCAGCGGCTAGCACACCATACCATCCAATTGGTCACATGTCGCCCGAAATGGGGCACGTCACCGAA TTGGTCGATGGTTCAGAAGCGACGCCTAATCTACGACAGGAATTAGAGAAGAATCCACAAGAACGTATGATGAAA ATTATCAACGACCACAATGCCACCAACACGTCGAATTTGGCTCTTCCCGATGCCGCCGAGATTGTTGCCAAGGCA CCACAAACTCTGAATTTGGCTCAGGGGTCACATCCATCTGCTCCTCCCATGGGCATGATTCCTCAAAGTCCTGTA GAGAATTCGATCAACTCGAATCAAATTGATCTCGATCAACTCCACCGGCTGCAAAACGATCAAGACGCCAAGATT CAAGAGATCGGTGAGATGCTCGGGCCTCTGAGCCCCTCAGGCCAGATCCCGGGGCTGGGAGATGGTCATGGGCAT CTATTTGATCCACCCAACGTAGATTTGGATCAATACTTTGACAGTAATGCATTTTTGCATGATGCCAGCTTTACC GGGGATGGTAACGACTTTAACTTTAGCCTTGATACCGGCGACTCGCTTGGTACTGCGAATGGGGCCGACGCAAAA TCCGTTATAAGCCCTCGGGACACAGATAATTATCAAGACAATGACCCGGCCGGTGCCACCAATGCGGATGCAGAC TGCAAACGAAGGCGGATCATATAG |
| Gene | >OphauB2|295 ATGTCAGGTCAAAATCCAAGAAAGCGCCCTGCGCCGGGCGCATCGCCTATTGCCCCCTACACTCAGTCATTACCC TCGCCCTACGGTGTGGAAACTGCATTGTCGGACCCTGTTGCGAAATGGAATATTGGACCAAGCGACACCTTGGGT CATATAGACGCGAATAGCTATGCTGTCAACAACCAGCTGGGCTCAGTCTCTGACTCGCAGCAATACATACAGCCC GCCCCGATGCCTTCCAACTCGCTCACTCGACGATCTATGAACCAGGCGCTGATAGCAACCAATCCGCGTTCCAAT CTCGAATCGGCAATTGAACCCTGGTCCGGCTTCGGCGACGAGAATACCTTATTGCAAACAAATGATGGCGAAGGA GCTATGGAGCAGGAGAATATCGAGGTTCTTGAAGAGAGATCTCAAAAAGCCAAGCGTGAGGCCCAAGCGAAAAGA AAACAGATACCCCCCTTCGTACAGAAGCTCAGAAGGTAAGCATCATGTAGCAGCAATGTCCATGTCTTCCAGTGC ACTGATGATGTGTGGTTTAGCTTTCTTGAAGATCGCAAAAACGAAGATTTTATTCGGTGGTCAGAAAAGGGCGAT TCCTTCATTGTTATAGACGAGGACGAATTTGCAAAGACCCTGATACCCGAACTTTTCAAGCATAACAACTACGCA TCATTTGTCCGCCAGCTCAACATGTACGGCTTTCACAAACGCGTTGGTCTGTCCGACAATAGCATGCGTGCAAGT GAACGCAAGAACAAGAGCCCTAGCGAATATTTTAATCCCTACTTTCGTCGCGGTCATCCGAATTTGATGTGGCTT ATTACCAAAGCCAAAGGGGGAAGCAAATCTAAAAAAGGGGGCAGAAGCGCCGAAGGCGAGGCCGAAAGTGAGGAG GACAATGTACCGGAAGACGCGACGACTCAAGCAGCCAACAGCGCCAGTACTTCGCTGCCAGCTGCCGAGTCCCAA GCATTACCAAAAAAGGAAATGACCATGATAAGAGACGAGCTGAACAAGATTCGCGAACAACAGAAGATGATTCTG GGTGCCATCAATCAGTTGCAGCGCAACAATAACGAACTGTATAGCCAAGCCCTCAGGTTTCAGAACCAGCACGAC CGCCACCAAAACTCGATCAACGCCATACTCAACTTCCTGGCTAATGTCTTCAGGAAGACTCTAGAGGATGGCAGC AGTCAGAATGTTGGCGATATCATCTCGAGCATCATGTCAAACCAAGCCAACCCGCCGTCTCATCAGCAAGGTAGT ATCTTTGACCTGGGAGACCTGGTTCAAAATGCGACGGAACCGTCAACGCCGCTTGGCGGCACTCATAGGAGAGCT CGTGGCTTGCTTCCACCAATTCCTGACCACAGTGAGCAGACGAAACCGAGCAGAGCTCCGTCAGCGGCTAGCACA CCATACCATCCAATTGGTCACATGTCGCCCGAAATGGGGCACGTCACCGAATTGGTCGATGGTTCAGAAGCGACG CCTAATCTACGACAGGAATTAGAGAAGAATCCACAAGAACGTATGATGAAAATTATCAACGACCACAATGCCACC AACACGTCGAATTTGGCTCTTCCCGATGCCGCCGAGATTGTTGCCAAGGCACCACAAACTCTGAATTTGGCTCAG GGGTCACAGTTGGTCGACTTGATGTCGCATCAAACGCCATCTGGCCTAAATCGGAGGCATATACATGCCTCGACA GGCCAGTCCAGCAGGGAAACACCCCAACAACCGCCTTTTAGTCCATCTGCTCCTCCCATGGGCATGATTCCTCAA AGTCCTGTAGAGAATTCGGTACCTCCGTCTTTATCACCCATCATGCGGTCGCCGGCATTGACACCGCCATCACTG CAACAGATCAACTCGAATCAAATTGATCTCGATCAACTCCACCGGCTGCAAAACGATCAAGACGCCAAGATTCAA GAGATCGGTGAGATGCTCGGGCCTCTGAGCCCCTCAGGCCAGATCCCGGGGCTGGGAGATGGTCATGGGCATCTA TTTGATCCACCCAACGTAGATTTGGATCAATACTTTGACAGTAATGCATTTTTGCATGATGCCAGCTTTACCGGG GATGGTAACGACTTTAACTTTAGCCTTGATACCGGCGACTCGCTTGGTACTGCGAATGGGGCCGACGCAAAATCC GTTATAAGCCCTCGGGACACAGATAATTATCAAGACAATGACCCGGCCGGTGCCACCAATGCGGATGCAGACTGC AAACGAAGGCGGATCATATAG |