© 2023 - Robin Ohm - Utrecht University - The Netherlands
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| Protein ID | OphauB2|2591 |
| Gene name | |
| Location | Contig_182:35098..37060 |
| Strand | - |
| Gene length (bp) | 1962 |
| Transcript length (bp) | 1740 |
| Coding sequence length (bp) | 1740 |
| Protein length (aa) | 580 |
| PFAM Domain ID | Short name | Long name | E-value | Start | End |
|---|---|---|---|---|---|
| PF00743 | FMO-like | Flavin-binding monooxygenase-like | 8.8E-39 | 11 | 348 |
| PF07992 | Pyr_redox_2 | Pyridine nucleotide-disulphide oxidoreductase | 1.9E-14 | 12 | 235 |
| PF13738 | Pyr_redox_3 | Pyridine nucleotide-disulphide oxidoreductase | 1.0E-11 | 15 | 218 |
| PF13450 | NAD_binding_8 | NAD(P)-binding Rossmann-like domain | 6.9E-06 | 15 | 68 |
| PF13434 | Lys_Orn_oxgnase | L-lysine 6-monooxygenase/L-ornithine 5-monooxygenase | 9.1E-05 | 106 | 211 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|Q04799|FMO5_RABIT | Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Oryctolagus cuniculus GN=FMO5 PE=1 SV=2 | 10 | 547 | 2.0E-30 |
| sp|Q6IRI9|FMO2_RAT | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Rattus norvegicus GN=Fmo2 PE=2 SV=3 | 11 | 458 | 6.0E-30 |
| sp|P36367|FMO4_RABIT | Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Oryctolagus cuniculus GN=FMO4 PE=2 SV=2 | 10 | 539 | 2.0E-29 |
| sp|P97872|FMO5_MOUSE | Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Mus musculus GN=Fmo5 PE=1 SV=4 | 11 | 547 | 2.0E-29 |
| sp|Q8K4C0|FMO5_RAT | Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Rattus norvegicus GN=Fmo5 PE=1 SV=3 | 11 | 547 | 2.0E-29 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|Q04799|FMO5_RABIT | Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Oryctolagus cuniculus GN=FMO5 PE=1 SV=2 | 10 | 547 | 2.0E-30 |
| sp|Q6IRI9|FMO2_RAT | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Rattus norvegicus GN=Fmo2 PE=2 SV=3 | 11 | 458 | 6.0E-30 |
| sp|P36367|FMO4_RABIT | Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Oryctolagus cuniculus GN=FMO4 PE=2 SV=2 | 10 | 539 | 2.0E-29 |
| sp|P97872|FMO5_MOUSE | Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Mus musculus GN=Fmo5 PE=1 SV=4 | 11 | 547 | 2.0E-29 |
| sp|Q8K4C0|FMO5_RAT | Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Rattus norvegicus GN=Fmo5 PE=1 SV=3 | 11 | 547 | 2.0E-29 |
| sp|Q95LA1|FMO3_CANLF | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Canis lupus familiaris GN=FMO3 PE=2 SV=3 | 10 | 539 | 5.0E-29 |
| sp|Q8K2I3|FMO2_MOUSE | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Mus musculus GN=Fmo2 PE=1 SV=3 | 10 | 347 | 7.0E-29 |
| sp|Q8SPQ7|FMO3_MACMU | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Macaca mulatta GN=FMO3 PE=2 SV=3 | 10 | 539 | 4.0E-28 |
| sp|P36366|FMO2_CAVPO | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Cavia porcellus GN=FMO2 PE=2 SV=2 | 10 | 543 | 5.0E-28 |
| sp|Q8VHG0|FMO4_MOUSE | Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Mus musculus GN=Fmo4 PE=1 SV=3 | 10 | 348 | 5.0E-27 |
| sp|P49109|FMO5_CAVPO | Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Cavia porcellus GN=FMO5 PE=2 SV=2 | 11 | 547 | 1.0E-26 |
| sp|P31512|FMO4_HUMAN | Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Homo sapiens GN=FMO4 PE=1 SV=3 | 10 | 539 | 5.0E-26 |
| sp|Q8K4B7|FMO4_RAT | Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Rattus norvegicus GN=Fmo4 PE=2 SV=3 | 10 | 539 | 6.0E-26 |
| sp|Q99518|FMO2_HUMAN | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Homo sapiens GN=FMO2 PE=1 SV=4 | 10 | 347 | 8.0E-26 |
| sp|P97501|FMO3_MOUSE | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Mus musculus GN=Fmo3 PE=1 SV=1 | 11 | 566 | 8.0E-26 |
| sp|Q8HZ70|FMO2_PANTR | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Pan troglodytes GN=FMO2 PE=3 SV=3 | 10 | 347 | 1.0E-25 |
| sp|Q5REK0|FMO2_PONAB | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Pongo abelii GN=FMO2 PE=2 SV=3 | 10 | 449 | 1.0E-25 |
| sp|Q28505|FMO2_MACMU | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Macaca mulatta GN=FMO2 PE=2 SV=2 | 10 | 347 | 2.0E-25 |
| sp|Q8HZ69|FMO2_GORGO | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Gorilla gorilla gorilla GN=FMO2 PE=3 SV=3 | 10 | 347 | 2.0E-25 |
| sp|Q95LA2|FMO1_CANLF | Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Canis lupus familiaris GN=FMO1 PE=2 SV=3 | 10 | 560 | 7.0E-25 |
| sp|P17635|FMO2_RABIT | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Oryctolagus cuniculus GN=FMO2 PE=1 SV=3 | 10 | 347 | 1.0E-24 |
| sp|O60774|FMO6_HUMAN | Putative dimethylaniline monooxygenase [N-oxide-forming] 6 OS=Homo sapiens GN=FMO6P PE=5 SV=1 | 10 | 539 | 1.0E-24 |
| sp|Q9EQ76|FMO3_RAT | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Rattus norvegicus GN=Fmo3 PE=1 SV=1 | 12 | 556 | 2.0E-24 |
| sp|Q01740|FMO1_HUMAN | Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Homo sapiens GN=FMO1 PE=2 SV=3 | 10 | 347 | 5.0E-24 |
| sp|Q8HYJ9|FMO3_BOVIN | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Bos taurus GN=FMO3 PE=2 SV=1 | 11 | 539 | 1.0E-23 |
| sp|P49326|FMO5_HUMAN | Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Homo sapiens GN=FMO5 PE=1 SV=2 | 11 | 547 | 2.0E-23 |
| sp|P16549|FMO1_PIG | Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Sus scrofa GN=FMO1 PE=1 SV=3 | 10 | 560 | 3.0E-22 |
| sp|P36365|FMO1_RAT | Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Rattus norvegicus GN=Fmo1 PE=1 SV=2 | 12 | 539 | 1.0E-20 |
| sp|P17636|FMO1_RABIT | Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Oryctolagus cuniculus GN=FMO1 PE=1 SV=3 | 10 | 246 | 2.0E-20 |
| sp|Q7YS44|FMO3_PANTR | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Pan troglodytes GN=FMO3 PE=3 SV=3 | 10 | 539 | 4.0E-20 |
| sp|P50285|FMO1_MOUSE | Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Mus musculus GN=Fmo1 PE=1 SV=1 | 11 | 347 | 4.0E-20 |
| sp|P32417|FMO3_RABIT | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Oryctolagus cuniculus GN=FMO3 PE=1 SV=3 | 10 | 539 | 6.0E-20 |
| sp|P31513|FMO3_HUMAN | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Homo sapiens GN=FMO3 PE=1 SV=5 | 10 | 539 | 6.0E-20 |
| sp|O64489|YUC9_ARATH | Probable indole-3-pyruvate monooxygenase YUCCA9 OS=Arabidopsis thaliana GN=YUC9 PE=2 SV=1 | 11 | 391 | 1.0E-19 |
| sp|Q9SVU0|YUC8_ARATH | Probable indole-3-pyruvate monooxygenase YUCCA8 OS=Arabidopsis thaliana GN=YUC8 PE=2 SV=1 | 11 | 348 | 1.0E-18 |
| sp|Q9LKC0|YUC5_ARATH | Probable indole-3-pyruvate monooxygenase YUCCA5 OS=Arabidopsis thaliana GN=YUC5 PE=2 SV=1 | 11 | 391 | 3.0E-18 |
| sp|Q8MP06|SNO1_TYRJA | Senecionine N-oxygenase OS=Tyria jacobaeae GN=sno1 PE=1 SV=1 | 2 | 218 | 3.0E-16 |
| sp|O23024|YUC3_ARATH | Probable indole-3-pyruvate monooxygenase YUCCA3 OS=Arabidopsis thaliana GN=YUC3 PE=2 SV=1 | 11 | 391 | 4.0E-16 |
| sp|O49312|YUC7_ARATH | Probable indole-3-pyruvate monooxygenase YUCCA7 OS=Arabidopsis thaliana GN=YUC7 PE=2 SV=1 | 11 | 347 | 2.0E-14 |
| sp|Q9SXD5|GSXL3_ARATH | Flavin-containing monooxygenase FMO GS-OX-like 3 OS=Arabidopsis thaliana GN=At1g62620 PE=2 SV=2 | 1 | 208 | 7.0E-14 |
| sp|Q9C8U0|GSXL5_ARATH | Flavin-containing monooxygenase FMO GS-OX-like 5 OS=Arabidopsis thaliana GN=At1g63370 PE=2 SV=2 | 1 | 208 | 2.0E-13 |
| sp|Q9FVQ0|YUC10_ARATH | Probable indole-3-pyruvate monooxygenase YUCCA10 OS=Arabidopsis thaliana GN=YUC10 PE=2 SV=1 | 13 | 405 | 3.0E-13 |
| sp|Q9HFE4|FMO1_SCHPO | Thiol-specific monooxygenase OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=fmo1 PE=1 SV=1 | 8 | 230 | 7.0E-13 |
| sp|Q9SVQ1|YUC2_ARATH | Indole-3-pyruvate monooxygenase YUCCA2 OS=Arabidopsis thaliana GN=YUC2 PE=1 SV=1 | 15 | 356 | 1.0E-12 |
| sp|Q9FWW6|GSXL1_ARATH | Flavin-containing monooxygenase FMO GS-OX-like 1 OS=Arabidopsis thaliana GN=At1g12160 PE=2 SV=1 | 13 | 201 | 3.0E-12 |
| sp|Q9SS04|GSOX1_ARATH | Flavin-containing monooxygenase FMO GS-OX1 OS=Arabidopsis thaliana GN=FMOGS-OX1 PE=2 SV=1 | 8 | 201 | 7.0E-12 |
| sp|Q9FF12|GSXL9_ARATH | Flavin-containing monooxygenase FMO GS-OX-like 9 OS=Arabidopsis thaliana GN=At5g07800 PE=2 SV=1 | 10 | 201 | 8.0E-12 |
| sp|Q8VZ59|YUC6_ARATH | Indole-3-pyruvate monooxygenase YUCCA6 OS=Arabidopsis thaliana GN=YUC6 PE=1 SV=1 | 15 | 347 | 3.0E-11 |
| sp|P55487|Y4ID_RHISN | Uncharacterized monooxygenase y4iD OS=Rhizobium sp. (strain NGR234) GN=NGR_a03290 PE=3 SV=1 | 8 | 215 | 3.0E-11 |
| sp|Q9FWW3|GSXL6_ARATH | Flavin-containing monooxygenase FMO GS-OX-like 6 OS=Arabidopsis thaliana GN=At1g12130 PE=2 SV=1 | 7 | 201 | 1.0E-10 |
| sp|Q9SXE1|GSOX3_ARATH | Flavin-containing monooxygenase FMO GS-OX3 OS=Arabidopsis thaliana GN=FMOGS-OX3 PE=2 SV=1 | 13 | 201 | 2.0E-10 |
| sp|Q9LMA1|FMO1_ARATH | Probable flavin-containing monooxygenase 1 OS=Arabidopsis thaliana GN=FMO1 PE=2 SV=1 | 1 | 201 | 3.0E-10 |
| sp|Q00730|STCW_EMENI | Putative sterigmatocystin biosynthesis monooxygenase stcW OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=stcW PE=3 SV=2 | 12 | 225 | 1.0E-09 |
| sp|Q47PU3|PAMO_THEFY | Phenylacetone monooxygenase OS=Thermobifida fusca (strain YX) GN=pamO PE=1 SV=1 | 7 | 211 | 2.0E-09 |
| sp|Q9SZY8|YUC1_ARATH | Probable indole-3-pyruvate monooxygenase YUCCA1 OS=Arabidopsis thaliana GN=YUC1 PE=1 SV=1 | 15 | 391 | 3.0E-09 |
| sp|Q9FLK4|GSXL8_ARATH | Flavin-containing monooxygenase FMO GS-OX-like 8 OS=Arabidopsis thaliana GN=At5g61290 PE=2 SV=1 | 13 | 204 | 6.0E-09 |
| sp|Q9FWW9|GSXL2_ARATH | Flavin-containing monooxygenase FMO GS-OX-like 2 OS=Arabidopsis thaliana GN=At1g12200 PE=2 SV=1 | 1 | 234 | 1.0E-08 |
| sp|A8MRX0|GSOX5_ARATH | Flavin-containing monooxygenase FMO GS-OX5 OS=Arabidopsis thaliana GN=FMOGS-OX5 PE=2 SV=2 | 12 | 201 | 3.0E-08 |
| sp|Q93TJ5|HAPMO_PSEFL | 4-hydroxyacetophenone monooxygenase OS=Pseudomonas fluorescens GN=hapE PE=1 SV=1 | 12 | 211 | 5.0E-08 |
| sp|Q9C8T8|GSXLX_ARATH | Putative flavin-containing monooxygenase FMO GS-OX-like 10 OS=Arabidopsis thaliana GN=At1g63340 PE=5 SV=3 | 1 | 243 | 1.0E-07 |
| sp|Q9SXD9|GSXL7_ARATH | Flavin-containing monooxygenase FMO GS-OX-like 7 OS=Arabidopsis thaliana GN=At1g62580 PE=3 SV=2 | 1 | 188 | 3.0E-07 |
| sp|Q94BV5|GSXL4_ARATH | Flavin-containing monooxygenase FMO GS-OX-like 4 OS=Arabidopsis thaliana GN=At1g62600 PE=2 SV=1 | 1 | 220 | 7.0E-07 |
| sp|Q93Y23|GSOX4_ARATH | Flavin-containing monooxygenase FMO GS-OX4 OS=Arabidopsis thaliana GN=FMOGS-OX4 PE=2 SV=1 | 1 | 201 | 7.0E-07 |
| sp|Q8ENX4|FENR2_OCEIH | Ferredoxin--NADP reductase 2 OS=Oceanobacillus iheyensis (strain DSM 14371 / JCM 11309 / KCTC 3954 / HTE831) GN=OB2351 PE=3 SV=1 | 13 | 223 | 7.0E-07 |
| sp|Q9I3H5|BVMO_PSEAE | Baeyer-Villiger monooxygenase OS=Pseudomonas aeruginosa (strain ATCC 15692 / PAO1 / 1C / PRS 101 / LMG 12228) GN=PA1538 PE=1 SV=1 | 3 | 207 | 1.0E-06 |
| sp|A1CLY7|CCSB_ASPCL | Ketocytochalasin monooxygenase OS=Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1) GN=ccsB PE=1 SV=1 | 3 | 230 | 2.0E-06 |
| sp|Q94K43|GSOX2_ARATH | Flavin-containing monooxygenase FMO GS-OX2 OS=Arabidopsis thaliana GN=FMOGS-OX2 PE=2 SV=1 | 1 | 222 | 6.0E-06 |
| sp|P64746|Y916_MYCBO | Uncharacterized monooxygenase Mb0916 OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=Mb0916 PE=3 SV=1 | 13 | 356 | 6.0E-06 |
| sp|P9WNG1|Y892_MYCTU | Uncharacterized monooxygenase Rv0892 OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=Rv0892 PE=1 SV=1 | 13 | 356 | 6.0E-06 |
| sp|P9WNG0|Y892_MYCTO | Uncharacterized monooxygenase MT0916 OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=MT0916 PE=3 SV=1 | 13 | 356 | 6.0E-06 |
| GO Term | Description | Terminal node |
|---|---|---|
| GO:0050661 | NADP binding | Yes |
| GO:0016491 | oxidoreductase activity | Yes |
| GO:0050660 | flavin adenine dinucleotide binding | Yes |
| GO:0004499 | N,N-dimethylaniline monooxygenase activity | Yes |
| GO:1901265 | nucleoside phosphate binding | No |
| GO:0036094 | small molecule binding | No |
| GO:0043168 | anion binding | No |
| GO:0004497 | monooxygenase activity | No |
| GO:0005488 | binding | No |
| GO:0003674 | molecular_function | No |
| GO:1901363 | heterocyclic compound binding | No |
| GO:0003824 | catalytic 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:0043167 | ion 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 |
| Gene cluster ID | Type of secondary metabolism gene |
|---|---|
| Cluster 15 | Decorating |
| Orthofinder run ID | 4 |
| Orthogroup | 7811 |
| Change Orthofinder run |
| Species | Protein ID |
|---|---|
| Ophiocordyceps australis 1348a (Ghana) | OphauG2|1530 |
| Ophiocordyceps australis map64 (Brazil) | OphauB2|2591 (this protein) |
| Type of sequence | Sequence |
|---|---|
| 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 | >OphauB2|2591 MASVHPPPPGNKVCVVGAGPIGLVTIKNLTEQGLAVTAFERDGGFGGTWLQSEVVDKPMALPTTVFMNGKNGTSY TDFPMGDDYPAQLSARHLVKYFGEYASHFELQQYIVLHTAVIDVRRDEKDTTWLVQTRHMQTGEETRHAFDRVVI ACGNFGRKRMRYMEAAHVFAGTVLHSCDVRDTVQYKGKNVLVVGGGPTAVDYVESLHRNGAATIYISHGGKFRFL PESFRGYLWDDVYTLRTEMIISALAHMSQIIMFWIFDRIALLMCRLMFPALSFWPSFFDNIPNRQRQPHVFVFFN DYFLSIVEQGQVEIKAAFGKFTGPRSVVLADGEQLDDVDAVIVCSGYHEVPMPLSGPGIPTDPALSPERSERLIK SPYYDPKSPFPRLYHGLLSETWPESLACVGRLSVPRSTMVIYDVATMALASVWSGKHPLPEQAEMKRVIDARHDF VISVLEKGPIIYTGITLDMSETYWWWNEAAGTGINERLGSWGLQGWKFWLTEPILYEMIMDGAFCPAVYRLFETG KGRRAWPGARQTIVRVQQDARRSNRAWKQKVKREGIKKSRSWGEALFSLSHWRG* |
| Coding | >OphauB2|2591 ATGGCCTCTGTGCATCCTCCACCGCCCGGCAACAAGGTCTGCGTCGTCGGGGCGGGACCGATAGGCCTTGTAACC ATCAAGAACCTGACGGAGCAGGGCCTTGCTGTGACGGCGTTTGAACGAGATGGAGGCTTTGGCGGCACTTGGCTG CAGTCCGAGGTGGTGGACAAGCCCATGGCTCTTCCCACCACTGTCTTTATGAATGGGAAAAACGGGACCTCATAC ACTGATTTCCCCATGGGAGATGACTATCCCGCGCAGCTTTCGGCGAGACATCTCGTAAAGTACTTTGGCGAATAC GCAAGCCATTTCGAGCTTCAACAGTACATAGTTTTACACACGGCCGTCATTGACGTCCGCCGTGACGAAAAGGAC ACGACTTGGCTGGTGCAGACGCGCCACATGCAGACTGGCGAGGAAACACGGCATGCTTTTGATAGAGTCGTGATT GCTTGTGGCAACTTTGGCCGCAAGCGCATGCGCTACATGGAGGCGGCCCATGTCTTTGCCGGCACAGTCTTGCAC TCTTGCGATGTTCGTGACACGGTGCAGTACAAGGGCAAGAATGTCCTGGTTGTCGGCGGAGGCCCAACAGCCGTT GACTATGTCGAGTCGCTTCACCGCAACGGCGCTGCCACCATTTACATTAGCCACGGCGGCAAATTTCGCTTTCTA CCTGAATCTTTTCGTGGCTATCTTTGGGATGACGTCTATACCCTTCGCACCGAAATGATTATTAGCGCCCTAGCT CACATGAGTCAAATCATCATGTTTTGGATATTTGACAGGATTGCCCTGCTAATGTGTAGACTAATGTTTCCCGCT CTATCCTTTTGGCCCTCCTTTTTCGACAATATCCCCAACAGGCAGCGACAGCCACACGTCTTTGTTTTTTTCAAT GACTACTTCCTCTCCATTGTCGAGCAAGGCCAGGTGGAGATCAAGGCAGCCTTTGGAAAATTCACCGGCCCTCGC TCTGTCGTGTTGGCTGATGGAGAGCAGCTCGACGACGTGGATGCCGTTATTGTCTGTAGCGGCTACCACGAGGTC CCCATGCCCCTGTCGGGCCCAGGCATCCCAACGGACCCGGCACTGTCACCGGAGCGAAGCGAAAGGCTAATCAAG TCACCCTACTACGACCCCAAGAGCCCCTTTCCTCGCCTCTATCACGGCCTCTTGTCCGAAACCTGGCCCGAGTCA CTGGCTTGCGTGGGGCGCTTATCGGTACCCAGATCGACCATGGTGATATACGACGTTGCCACAATGGCACTGGCC AGCGTCTGGTCTGGCAAGCACCCACTTCCTGAGCAAGCAGAGATGAAGCGAGTCATTGATGCGCGTCATGATTTC GTGATAAGCGTCTTGGAAAAGGGCCCCATTATCTACACGGGCATCACATTGGACATGTCGGAGACGTATTGGTGG TGGAATGAGGCAGCAGGTACGGGCATCAATGAAAGGCTGGGCAGCTGGGGCCTCCAAGGATGGAAGTTTTGGTTG ACGGAGCCCATTTTGTACGAGATGATTATGGATGGCGCCTTTTGCCCCGCTGTCTACCGGCTGTTTGAGACGGGC AAAGGGCGAAGAGCCTGGCCTGGTGCGCGGCAGACGATTGTCAGGGTGCAACAAGATGCAAGAAGATCTAATCGG GCCTGGAAGCAAAAGGTTAAGAGGGAAGGCATCAAAAAGTCGAGGTCATGGGGGGAAGCATTGTTCTCCTTGAGT CACTGGAGGGGTTGA |
| Transcript | >OphauB2|2591 ATGGCCTCTGTGCATCCTCCACCGCCCGGCAACAAGGTCTGCGTCGTCGGGGCGGGACCGATAGGCCTTGTAACC ATCAAGAACCTGACGGAGCAGGGCCTTGCTGTGACGGCGTTTGAACGAGATGGAGGCTTTGGCGGCACTTGGCTG CAGTCCGAGGTGGTGGACAAGCCCATGGCTCTTCCCACCACTGTCTTTATGAATGGGAAAAACGGGACCTCATAC ACTGATTTCCCCATGGGAGATGACTATCCCGCGCAGCTTTCGGCGAGACATCTCGTAAAGTACTTTGGCGAATAC GCAAGCCATTTCGAGCTTCAACAGTACATAGTTTTACACACGGCCGTCATTGACGTCCGCCGTGACGAAAAGGAC ACGACTTGGCTGGTGCAGACGCGCCACATGCAGACTGGCGAGGAAACACGGCATGCTTTTGATAGAGTCGTGATT GCTTGTGGCAACTTTGGCCGCAAGCGCATGCGCTACATGGAGGCGGCCCATGTCTTTGCCGGCACAGTCTTGCAC TCTTGCGATGTTCGTGACACGGTGCAGTACAAGGGCAAGAATGTCCTGGTTGTCGGCGGAGGCCCAACAGCCGTT GACTATGTCGAGTCGCTTCACCGCAACGGCGCTGCCACCATTTACATTAGCCACGGCGGCAAATTTCGCTTTCTA CCTGAATCTTTTCGTGGCTATCTTTGGGATGACGTCTATACCCTTCGCACCGAAATGATTATTAGCGCCCTAGCT CACATGAGTCAAATCATCATGTTTTGGATATTTGACAGGATTGCCCTGCTAATGTGTAGACTAATGTTTCCCGCT CTATCCTTTTGGCCCTCCTTTTTCGACAATATCCCCAACAGGCAGCGACAGCCACACGTCTTTGTTTTTTTCAAT GACTACTTCCTCTCCATTGTCGAGCAAGGCCAGGTGGAGATCAAGGCAGCCTTTGGAAAATTCACCGGCCCTCGC TCTGTCGTGTTGGCTGATGGAGAGCAGCTCGACGACGTGGATGCCGTTATTGTCTGTAGCGGCTACCACGAGGTC CCCATGCCCCTGTCGGGCCCAGGCATCCCAACGGACCCGGCACTGTCACCGGAGCGAAGCGAAAGGCTAATCAAG TCACCCTACTACGACCCCAAGAGCCCCTTTCCTCGCCTCTATCACGGCCTCTTGTCCGAAACCTGGCCCGAGTCA CTGGCTTGCGTGGGGCGCTTATCGGTACCCAGATCGACCATGGTGATATACGACGTTGCCACAATGGCACTGGCC AGCGTCTGGTCTGGCAAGCACCCACTTCCTGAGCAAGCAGAGATGAAGCGAGTCATTGATGCGCGTCATGATTTC GTGATAAGCGTCTTGGAAAAGGGCCCCATTATCTACACGGGCATCACATTGGACATGTCGGAGACGTATTGGTGG TGGAATGAGGCAGCAGGTACGGGCATCAATGAAAGGCTGGGCAGCTGGGGCCTCCAAGGATGGAAGTTTTGGTTG ACGGAGCCCATTTTGTACGAGATGATTATGGATGGCGCCTTTTGCCCCGCTGTCTACCGGCTGTTTGAGACGGGC AAAGGGCGAAGAGCCTGGCCTGGTGCGCGGCAGACGATTGTCAGGGTGCAACAAGATGCAAGAAGATCTAATCGG GCCTGGAAGCAAAAGGTTAAGAGGGAAGGCATCAAAAAGTCGAGGTCATGGGGGGAAGCATTGTTCTCCTTGAGT CACTGGAGGGGTTGA |
| Gene | >OphauB2|2591 ATGGCCTCTGTGCATCCTCCACCGCCCGGCAACAAGGTCTGCGTCGTCGGGGCGGGACCGATAGGCCTTGTAACC ATCAAGAACCTGACGGAGCAGGGCCTTGCTGTGACGGCGTTTGAACGAGATGGAGGCTTTGGCGGCACTTGGCTG CAGTCCGAGGTGGTGGACAAGCCCATGGCTCTTCCCACCACTGTCTTTATGAATGGGAAAAACGGGGTGAGTTTT CTTTTTTCTTTTTTTTTTTTAAAAAAATTACAGAAAAAAAAACAATAGCAACAACTTGGTGTCCTGGCGTCATTG ATATTGATAATCCATGCCAGACCTCATACACTGATTTCCCCATGGGAGATGGTAAGCAAAACCACAGCGACGCGC TTGGCACTTGGACTGACTCTAGCCCCTTGTAGACTATCCCGCGCAGCTTTCGGCGAGACATCTCGTAAAGTACTT TGGCGAATACGCAAGCCATTTCGAGCTTCAACAGTACATAGTTTTACACACGGCCGTCATTGACGTCCGCCGTGA CGAAAAGGACACGACTTGGCTGGTGCAGACGCGCCACATGCAGACTGGCGAGGAAACACGGCATGCTTTTGATAG AGTCGTGATTGCTTGTGGCAACTTTGGCCGCAAGCGCATGCGCTACATGGAGGCGGCCCATGTCTTTGCCGGCAC AGTCTTGCACTCTTGCGATGTTCGTGACACGGTGCAGTACAAGGGCAAGAATGTCCTGGTTGTCGGCGGAGGCCC AACAGCCGTTGACTATGTCGAGTCGCTTCACCGCAACGGCGCTGCCACCATTTACATTAGCCACGGCGGCAAATT TCGCTTTGTTGGTCCTCCGTGTCTTTTGCCATGATGGCTTGCTGGCTTGGCTCTTGCTGACCGTGGCAGCTACCT GAATCTTTTCGTGGCTATCTTTGGGATGACGTCTATACCCTTCGCACCGAAATGATTATTAGCGCCCTAGCTCAC ATGAGTCAAATCATCATGTTTTGGATATTTGACAGGATTGCCCTGCTAATGTGTAGACTAATGTTTCCCGCTCTA TCCTTTTGGCCCTCCTTTTTCGACAATATCCCCAACAGGCAGCGACAGCCACACGTCTTTGTTTTTTTCAATGAC TACTTCCTCTCCATTGTCGAGCAAGGCCAGGTGGAGATCAAGGCAGCCTTTGGAAAATTCACCGGCCCTCGCTCT GTCGTGTTGGCTGATGGAGAGCAGCTCGACGACGTGGATGCCGTTATTGTCTGTAGCGGCTACCACGAGGTCCCC ATGCCCCTGTCGGGCCCAGGCATCCCAACGGACCCGGCACTGTCACCGGAGCGAAGCGAAAGGCTAATCAAGTCA CCCTACTACGACCCCAAGAGCCCCTTTCCTCGCCTCTATCACGGCCTCTTGTCCGAAACCTGGCCCGAGTCACTG GCTTGCGTGGGGCGCTTATCGGTACCCAGATCGACCATGGTGATATACGACGTTGCCACAATGGCACTGGCCAGC GTCTGGTCTGGCAAGCACCCACTTCCTGAGCAAGCAGAGATGAAGCGAGTCATTGATGCGCGTCATGATTTCGTG ATAAGCGTCTTGGAAAAGGGCCCCATTATCTACACGGGCATCACATTGGACATGTCGGAGACGTATTGGTGGTGG AATGAGGCAGCAGGTACGGGCATCAATGAAAGGCTGGGCAGCTGGGGCCTCCAAGGATGGAAGTTTTGGTTGACG GAGCCCATTTTGTACGAGATGATTATGGATGGCGCCTTTTGCCCCGCTGTCTACCGGCTGTTTGAGACGGGCAAA GGGCGAAGAGCCTGGCCTGGTGCGCGGCAGACGATTGTCAGGGTGCAACAAGATGCAAGAAGATCTAATCGGGCC TGGAAGCAAAAGGTTAAGAGGGAAGGCATCAAAAAGTCGAGGTCATGGGGGGAAGCATTGTTCTCCTTGAGTCAC TGGAGGGGTTGA |