© 2023 - Robin Ohm - Utrecht University - The Netherlands
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| Protein ID | OphauB2|78 |
| Gene name | |
| Location | Contig_1:193099..195084 |
| Strand | + |
| Gene length (bp) | 1985 |
| Transcript length (bp) | 1692 |
| Coding sequence length (bp) | 1692 |
| Protein length (aa) | 564 |
| PFAM Domain ID | Short name | Long name | E-value | Start | End |
|---|---|---|---|---|---|
| PF00743 | FMO-like | Flavin-binding monooxygenase-like | 2.5E-13 | 38 | 227 |
| PF07992 | Pyr_redox_2 | Pyridine nucleotide-disulphide oxidoreductase | 3.5E-13 | 35 | 241 |
| PF13738 | Pyr_redox_3 | Pyridine nucleotide-disulphide oxidoreductase | 1.2E-08 | 37 | 235 |
| PF13450 | NAD_binding_8 | NAD(P)-binding Rossmann-like domain | 2.3E-06 | 38 | 83 |
| PF13434 | Lys_Orn_oxgnase | L-lysine 6-monooxygenase/L-ornithine 5-monooxygenase | 2.9E-06 | 104 | 232 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|A7HU16|BVMO_PARL1 | Baeyer-Villiger monooxygenase OS=Parvibaculum lavamentivorans (strain DS-1 / DSM 13023 / NCIMB 13966) GN=Plav_1781 PE=1 SV=1 | 35 | 558 | 7.0E-163 |
| sp|Q8GAW0|CPMO_COMS9 | Cyclopentanone 1,2-monooxygenase OS=Comamonas sp. (strain NCIMB 9872) GN=cpnB PE=1 SV=3 | 34 | 544 | 2.0E-142 |
| sp|Q47PU3|PAMO_THEFY | Phenylacetone monooxygenase OS=Thermobifida fusca (strain YX) GN=pamO PE=1 SV=1 | 33 | 560 | 2.0E-103 |
| sp|A3U3H1|BVMO_OCEBH | Baeyer-Villiger monooxygenase OS=Oceanicola batsensis (strain ATCC BAA-863 / DSM 15984 / HTCC2597) GN=OB2597_18631 PE=1 SV=1 | 33 | 548 | 2.0E-99 |
| sp|P12015|CHMO_ACISP | Cyclohexanone 1,2-monooxygenase OS=Acinetobacter sp. PE=1 SV=2 | 29 | 544 | 2.0E-98 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|A7HU16|BVMO_PARL1 | Baeyer-Villiger monooxygenase OS=Parvibaculum lavamentivorans (strain DS-1 / DSM 13023 / NCIMB 13966) GN=Plav_1781 PE=1 SV=1 | 35 | 558 | 7.0E-163 |
| sp|Q8GAW0|CPMO_COMS9 | Cyclopentanone 1,2-monooxygenase OS=Comamonas sp. (strain NCIMB 9872) GN=cpnB PE=1 SV=3 | 34 | 544 | 2.0E-142 |
| sp|Q47PU3|PAMO_THEFY | Phenylacetone monooxygenase OS=Thermobifida fusca (strain YX) GN=pamO PE=1 SV=1 | 33 | 560 | 2.0E-103 |
| sp|A3U3H1|BVMO_OCEBH | Baeyer-Villiger monooxygenase OS=Oceanicola batsensis (strain ATCC BAA-863 / DSM 15984 / HTCC2597) GN=OB2597_18631 PE=1 SV=1 | 33 | 548 | 2.0E-99 |
| sp|P12015|CHMO_ACISP | Cyclohexanone 1,2-monooxygenase OS=Acinetobacter sp. PE=1 SV=2 | 29 | 544 | 2.0E-98 |
| sp|H3JQW0|OTEMO_PSEPU | 2-oxo-Delta(3)-4,5,5-trimethylcyclopentenylacetyl-CoA monooxygenase OS=Pseudomonas putida GN=otemo PE=1 SV=1 | 34 | 560 | 4.0E-93 |
| sp|Q9RKB5|BVMO2_STRCO | Baeyer-Villiger monooxygenase OS=Streptomyces coelicolor (strain ATCC BAA-471 / A3(2) / M145) GN=SCO3172 PE=1 SV=1 | 34 | 517 | 1.0E-44 |
| sp|Q93TJ5|HAPMO_PSEFL | 4-hydroxyacetophenone monooxygenase OS=Pseudomonas fluorescens GN=hapE PE=1 SV=1 | 29 | 533 | 2.0E-42 |
| 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 | 38 | 495 | 4.0E-37 |
| 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 | 21 | 454 | 2.0E-34 |
| sp|E3VWK3|PENE_STREX | Pentalenolactone D synthase OS=Streptomyces exfoliatus GN=penE PE=1 SV=1 | 33 | 528 | 4.0E-33 |
| 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 | 37 | 507 | 9.0E-33 |
| sp|E3VWI7|PNTE_STRAE | Pentalenolactone D synthase OS=Streptomyces arenae GN=pntE PE=1 SV=1 | 33 | 528 | 9.0E-33 |
| sp|U5S003|BVMO4_DIESD | Baeyer-Villiger monooxygenase 4 OS=Dietzia sp. (strain D5) PE=1 SV=1 | 61 | 548 | 3.0E-32 |
| sp|P55487|Y4ID_RHISN | Uncharacterized monooxygenase y4iD OS=Rhizobium sp. (strain NGR234) GN=NGR_a03290 PE=3 SV=1 | 20 | 531 | 3.0E-32 |
| sp|Q9RL17|BVMO1_STRCO | Baeyer-Villiger monooxygenase OS=Streptomyces coelicolor (strain ATCC BAA-471 / A3(2) / M145) GN=SCO0300 PE=1 SV=1 | 52 | 549 | 8.0E-32 |
| sp|P9WNG1|Y892_MYCTU | Uncharacterized monooxygenase Rv0892 OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=Rv0892 PE=1 SV=1 | 38 | 240 | 1.0E-31 |
| sp|P9WNG0|Y892_MYCTO | Uncharacterized monooxygenase MT0916 OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=MT0916 PE=3 SV=1 | 38 | 240 | 1.0E-31 |
| sp|P64746|Y916_MYCBO | Uncharacterized monooxygenase Mb0916 OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=Mb0916 PE=3 SV=1 | 38 | 240 | 1.0E-31 |
| sp|Q82IY8|PTLE_STRAW | Neopentalenolactone D synthase OS=Streptomyces avermitilis (strain ATCC 31267 / DSM 46492 / JCM 5070 / NBRC 14893 / NCIMB 12804 / NRRL 8165 / MA-4680) GN=ptlE PE=1 SV=1 | 67 | 514 | 6.0E-29 |
| sp|P9WNF9|ETHA_MYCTU | FAD-containing monooxygenase EthA OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ethA PE=1 SV=1 | 34 | 456 | 1.0E-25 |
| sp|P9WNF8|ETHA_MYCTO | FAD-containing monooxygenase EthA OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=ethA PE=3 SV=1 | 34 | 456 | 1.0E-25 |
| sp|Q7TVI2|ETHA_MYCBO | FAD-containing monooxygenase EthA OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=ethA PE=1 SV=1 | 34 | 456 | 1.0E-25 |
| sp|A0R665|ETHA_MYCS2 | FAD-containing monooxygenase EthA OS=Mycobacterium smegmatis (strain ATCC 700084 / mc(2)155) GN=ethA PE=3 SV=1 | 35 | 456 | 2.0E-25 |
| sp|P9WNF7|MYMA_MYCTU | Putative FAD-containing monooxygenase MymA OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=mymA PE=1 SV=1 | 35 | 500 | 3.0E-21 |
| sp|P9WNF6|MYMA_MYCTO | Putative FAD-containing monooxygenase MymA OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=mymA PE=3 SV=1 | 35 | 500 | 3.0E-21 |
| sp|Q88J44|BVMO_PSEPK | Baeyer-Villiger monooxygenase OS=Pseudomonas putida (strain KT2440) GN=PP_2805 PE=1 SV=1 | 34 | 236 | 2.0E-19 |
| sp|Q9LFM5|YUC4_ARATH | Probable indole-3-pyruvate monooxygenase YUCCA4 OS=Arabidopsis thaliana GN=YUC4 PE=1 SV=1 | 37 | 218 | 5.0E-16 |
| sp|Q9SZY8|YUC1_ARATH | Probable indole-3-pyruvate monooxygenase YUCCA1 OS=Arabidopsis thaliana GN=YUC1 PE=1 SV=1 | 7 | 218 | 2.0E-14 |
| sp|Q8K4C0|FMO5_RAT | Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Rattus norvegicus GN=Fmo5 PE=1 SV=3 | 38 | 214 | 1.0E-12 |
| sp|Q04799|FMO5_RABIT | Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Oryctolagus cuniculus GN=FMO5 PE=1 SV=2 | 38 | 410 | 1.0E-12 |
| sp|Q8VZ59|YUC6_ARATH | Indole-3-pyruvate monooxygenase YUCCA6 OS=Arabidopsis thaliana GN=YUC6 PE=1 SV=1 | 37 | 218 | 3.0E-12 |
| sp|P49109|FMO5_CAVPO | Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Cavia porcellus GN=FMO5 PE=2 SV=2 | 38 | 289 | 7.0E-12 |
| sp|P97872|FMO5_MOUSE | Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Mus musculus GN=Fmo5 PE=1 SV=4 | 38 | 214 | 7.0E-12 |
| sp|P9WNG1|Y892_MYCTU | Uncharacterized monooxygenase Rv0892 OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=Rv0892 PE=1 SV=1 | 354 | 506 | 7.0E-12 |
| sp|P64746|Y916_MYCBO | Uncharacterized monooxygenase Mb0916 OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=Mb0916 PE=3 SV=1 | 354 | 506 | 7.0E-12 |
| sp|P9WNG0|Y892_MYCTO | Uncharacterized monooxygenase MT0916 OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=MT0916 PE=3 SV=1 | 354 | 506 | 7.0E-12 |
| sp|Q9LKC0|YUC5_ARATH | Probable indole-3-pyruvate monooxygenase YUCCA5 OS=Arabidopsis thaliana GN=YUC5 PE=2 SV=1 | 37 | 409 | 1.0E-11 |
| sp|Q9SVQ1|YUC2_ARATH | Indole-3-pyruvate monooxygenase YUCCA2 OS=Arabidopsis thaliana GN=YUC2 PE=1 SV=1 | 37 | 218 | 2.0E-11 |
| sp|P16549|FMO1_PIG | Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Sus scrofa GN=FMO1 PE=1 SV=3 | 38 | 217 | 3.0E-11 |
| sp|Q9SVU0|YUC8_ARATH | Probable indole-3-pyruvate monooxygenase YUCCA8 OS=Arabidopsis thaliana GN=YUC8 PE=2 SV=1 | 37 | 218 | 3.0E-11 |
| sp|Q99518|FMO2_HUMAN | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Homo sapiens GN=FMO2 PE=1 SV=4 | 38 | 233 | 4.0E-11 |
| sp|O64489|YUC9_ARATH | Probable indole-3-pyruvate monooxygenase YUCCA9 OS=Arabidopsis thaliana GN=YUC9 PE=2 SV=1 | 37 | 218 | 5.0E-11 |
| sp|Q8K2I3|FMO2_MOUSE | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Mus musculus GN=Fmo2 PE=1 SV=3 | 36 | 233 | 5.0E-11 |
| sp|Q01740|FMO1_HUMAN | Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Homo sapiens GN=FMO1 PE=2 SV=3 | 38 | 217 | 7.0E-11 |
| sp|P36366|FMO2_CAVPO | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Cavia porcellus GN=FMO2 PE=2 SV=2 | 38 | 233 | 1.0E-10 |
| sp|P17635|FMO2_RABIT | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Oryctolagus cuniculus GN=FMO2 PE=1 SV=3 | 38 | 233 | 2.0E-10 |
| sp|Q8HZ70|FMO2_PANTR | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Pan troglodytes GN=FMO2 PE=3 SV=3 | 38 | 233 | 2.0E-10 |
| sp|Q5REK0|FMO2_PONAB | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Pongo abelii GN=FMO2 PE=2 SV=3 | 38 | 233 | 3.0E-10 |
| sp|Q28505|FMO2_MACMU | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Macaca mulatta GN=FMO2 PE=2 SV=2 | 38 | 233 | 3.0E-10 |
| sp|Q8HZ69|FMO2_GORGO | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Gorilla gorilla gorilla GN=FMO2 PE=3 SV=3 | 38 | 233 | 3.0E-10 |
| sp|Q6IRI9|FMO2_RAT | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Rattus norvegicus GN=Fmo2 PE=2 SV=3 | 38 | 233 | 7.0E-10 |
| sp|Q95LA2|FMO1_CANLF | Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Canis lupus familiaris GN=FMO1 PE=2 SV=3 | 38 | 217 | 1.0E-09 |
| sp|P97501|FMO3_MOUSE | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Mus musculus GN=Fmo3 PE=1 SV=1 | 38 | 234 | 2.0E-09 |
| sp|P17636|FMO1_RABIT | Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Oryctolagus cuniculus GN=FMO1 PE=1 SV=3 | 38 | 217 | 2.0E-09 |
| sp|Q8MP06|SNO1_TYRJA | Senecionine N-oxygenase OS=Tyria jacobaeae GN=sno1 PE=1 SV=1 | 38 | 218 | 2.0E-09 |
| sp|Q9EQ76|FMO3_RAT | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Rattus norvegicus GN=Fmo3 PE=1 SV=1 | 38 | 234 | 4.0E-09 |
| sp|O60774|FMO6_HUMAN | Putative dimethylaniline monooxygenase [N-oxide-forming] 6 OS=Homo sapiens GN=FMO6P PE=5 SV=1 | 38 | 410 | 4.0E-09 |
| sp|Q8HYJ9|FMO3_BOVIN | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Bos taurus GN=FMO3 PE=2 SV=1 | 38 | 234 | 5.0E-09 |
| sp|Q95LA1|FMO3_CANLF | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Canis lupus familiaris GN=FMO3 PE=2 SV=3 | 38 | 234 | 7.0E-09 |
| sp|Q8SPQ7|FMO3_MACMU | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Macaca mulatta GN=FMO3 PE=2 SV=3 | 38 | 234 | 2.0E-08 |
| sp|P31512|FMO4_HUMAN | Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Homo sapiens GN=FMO4 PE=1 SV=3 | 38 | 234 | 2.0E-08 |
| sp|P49326|FMO5_HUMAN | Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Homo sapiens GN=FMO5 PE=1 SV=2 | 38 | 190 | 3.0E-08 |
| sp|Q7YS44|FMO3_PANTR | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Pan troglodytes GN=FMO3 PE=3 SV=3 | 38 | 234 | 9.0E-08 |
| sp|P31513|FMO3_HUMAN | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Homo sapiens GN=FMO3 PE=1 SV=5 | 38 | 234 | 9.0E-08 |
| sp|P50285|FMO1_MOUSE | Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Mus musculus GN=Fmo1 PE=1 SV=1 | 38 | 217 | 2.0E-07 |
| sp|P36365|FMO1_RAT | Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Rattus norvegicus GN=Fmo1 PE=1 SV=2 | 38 | 217 | 2.0E-07 |
| sp|Q9LMA1|FMO1_ARATH | Probable flavin-containing monooxygenase 1 OS=Arabidopsis thaliana GN=FMO1 PE=2 SV=1 | 38 | 240 | 2.0E-07 |
| sp|P32417|FMO3_RABIT | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Oryctolagus cuniculus GN=FMO3 PE=1 SV=3 | 38 | 234 | 2.0E-07 |
| sp|Q9FLK4|GSXL8_ARATH | Flavin-containing monooxygenase FMO GS-OX-like 8 OS=Arabidopsis thaliana GN=At5g61290 PE=2 SV=1 | 38 | 240 | 7.0E-07 |
| sp|Q8K4B7|FMO4_RAT | Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Rattus norvegicus GN=Fmo4 PE=2 SV=3 | 38 | 214 | 1.0E-06 |
| sp|Q8VHG0|FMO4_MOUSE | Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Mus musculus GN=Fmo4 PE=1 SV=3 | 38 | 234 | 2.0E-06 |
| sp|O49312|YUC7_ARATH | Probable indole-3-pyruvate monooxygenase YUCCA7 OS=Arabidopsis thaliana GN=YUC7 PE=2 SV=1 | 37 | 218 | 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 |
| Orthofinder run ID | 4 |
| Orthogroup | 418 |
| Change Orthofinder run |
| 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|78 MGDQSSLENFKINLTDYSAPVRTPDGPYASDLDVDALIIGAGFGGVFMLKTLRDRGYKTVIYEAGDDIGGTWRWN CYPGAAVDSEVPEYEFSWPEVWKTWNWTTNYPGYKELRAYFDHVDKAVGIKKDCAFNTVVVGADFDTNQGKWNVR TKDGRTATTKFLILATGMASKRYVPSWPGMDKFKGTIHHSSFWPDYEVDVSSKKCAVIGTGASGVQITQAWGPKA QELKVLQRTPNLALPVRRRDLTVEEQEAGKKWYPHLFEYRERTFGGFIFDWLEKNTSDDTIEEQKATYEKAWETG GFRLWIGMYKDVLLDGAANKPIYDFWASKTRQRIQDARKRDILAPLEMPHYFGTKRPCLEFDYYEQFNRPSVDVV DLKNNPIKEFTETGITLEDGTHHEFDVVAVATGFDVVTGGMTQLGLESITGEKLDDEWKTGATTYLGLTVSGYPN MFHMYGTHAPTLLANGPSLVEIQGRWIVDCMDKMKHSNIKYIDAKPESAQAWKKLIVDVNNATLFPTTRSTYMGG NVQGKVQEPMCYANGVNKYAKEVRLALDSMEGFEMVQN* |
| Coding | >OphauB2|78 ATGGGCGACCAATCTAGCTTGGAAAACTTCAAGATTAACCTGACAGACTATTCTGCGCCTGTCAGAACGCCCGAT GGCCCCTACGCAAGCGATCTTGACGTGGATGCCTTGATTATTGGGGCTGGATTTGGTGGTGTATTTATGCTTAAA ACTTTGCGCGACCGAGGCTATAAGACAGTCATTTATGAAGCGGGTGATGATATTGGGGGAACATGGCGCTGGAAC TGCTATCCAGGTGCCGCCGTCGACTCCGAGGTGCCAGAATATGAATTCTCTTGGCCCGAGGTTTGGAAAACGTGG AACTGGACGACCAATTATCCCGGCTACAAGGAGCTTCGAGCCTACTTTGACCACGTTGACAAGGCGGTGGGTATC AAAAAGGACTGCGCTTTCAATACAGTTGTCGTCGGTGCAGACTTTGATACCAACCAGGGCAAATGGAATGTCCGT ACCAAGGACGGCCGCACTGCCACCACCAAGTTCCTGATTCTGGCAACGGGAATGGCATCAAAGCGCTATGTTCCC AGCTGGCCTGGCATGGACAAATTCAAAGGCACCATCCACCACTCTTCCTTTTGGCCAGACTACGAAGTGGATGTG TCAAGCAAAAAGTGCGCCGTCATTGGCACTGGAGCCTCGGGAGTCCAGATAACCCAGGCGTGGGGCCCCAAAGCC CAAGAGCTCAAGGTCTTGCAGCGCACGCCCAACCTGGCCCTACCCGTGCGTCGACGCGACTTGACAGTCGAAGAG CAAGAGGCGGGCAAAAAGTGGTATCCGCACCTCTTTGAGTACCGCGAGAGGACATTTGGCGGCTTCATCTTTGAC TGGCTCGAGAAGAATACCTCGGACGACACAATAGAGGAGCAGAAAGCAACATATGAAAAGGCGTGGGAAACTGGT GGCTTCCGTCTCTGGATTGGCATGTATAAGGATGTGCTCCTGGACGGGGCGGCAAACAAGCCCATCTACGACTTT TGGGCTTCCAAGACGCGACAACGAATCCAAGACGCTCGCAAGCGGGATATTCTGGCTCCTTTGGAGATGCCTCAT TATTTTGGCACTAAACGTCCGTGTTTGGAATTCGACTATTATGAACAATTCAATCGACCATCTGTCGACGTGGTT GACCTCAAGAACAACCCAATCAAGGAGTTTACCGAAACGGGCATTACCCTTGAAGACGGCACGCACCATGAATTT GATGTTGTTGCCGTTGCGACAGGATTTGACGTTGTGACTGGAGGCATGACACAGTTAGGACTTGAAAGCATCACG GGCGAAAAACTCGATGACGAATGGAAGACGGGGGCTACCACATACCTGGGCCTAACCGTCAGCGGCTACCCCAAC ATGTTCCACATGTATGGCACCCATGCGCCCACGCTTCTCGCCAACGGCCCCTCCCTGGTCGAGATCCAGGGTCGA TGGATCGTCGACTGCATGGATAAGATGAAGCACAGCAATATTAAGTACATCGACGCCAAGCCTGAATCGGCACAG GCCTGGAAGAAGCTCATCGTCGACGTCAATAACGCGACACTCTTCCCCACGACAAGGTCGACCTACATGGGCGGC AACGTTCAGGGCAAGGTTCAAGAGCCAATGTGCTATGCCAATGGCGTCAACAAGTATGCCAAGGAGGTTCGATTG GCACTGGATAGCATGGAAGGATTTGAAATGGTGCAAAACTGA |
| Transcript | >OphauB2|78 ATGGGCGACCAATCTAGCTTGGAAAACTTCAAGATTAACCTGACAGACTATTCTGCGCCTGTCAGAACGCCCGAT GGCCCCTACGCAAGCGATCTTGACGTGGATGCCTTGATTATTGGGGCTGGATTTGGTGGTGTATTTATGCTTAAA ACTTTGCGCGACCGAGGCTATAAGACAGTCATTTATGAAGCGGGTGATGATATTGGGGGAACATGGCGCTGGAAC TGCTATCCAGGTGCCGCCGTCGACTCCGAGGTGCCAGAATATGAATTCTCTTGGCCCGAGGTTTGGAAAACGTGG AACTGGACGACCAATTATCCCGGCTACAAGGAGCTTCGAGCCTACTTTGACCACGTTGACAAGGCGGTGGGTATC AAAAAGGACTGCGCTTTCAATACAGTTGTCGTCGGTGCAGACTTTGATACCAACCAGGGCAAATGGAATGTCCGT ACCAAGGACGGCCGCACTGCCACCACCAAGTTCCTGATTCTGGCAACGGGAATGGCATCAAAGCGCTATGTTCCC AGCTGGCCTGGCATGGACAAATTCAAAGGCACCATCCACCACTCTTCCTTTTGGCCAGACTACGAAGTGGATGTG TCAAGCAAAAAGTGCGCCGTCATTGGCACTGGAGCCTCGGGAGTCCAGATAACCCAGGCGTGGGGCCCCAAAGCC CAAGAGCTCAAGGTCTTGCAGCGCACGCCCAACCTGGCCCTACCCGTGCGTCGACGCGACTTGACAGTCGAAGAG CAAGAGGCGGGCAAAAAGTGGTATCCGCACCTCTTTGAGTACCGCGAGAGGACATTTGGCGGCTTCATCTTTGAC TGGCTCGAGAAGAATACCTCGGACGACACAATAGAGGAGCAGAAAGCAACATATGAAAAGGCGTGGGAAACTGGT GGCTTCCGTCTCTGGATTGGCATGTATAAGGATGTGCTCCTGGACGGGGCGGCAAACAAGCCCATCTACGACTTT TGGGCTTCCAAGACGCGACAACGAATCCAAGACGCTCGCAAGCGGGATATTCTGGCTCCTTTGGAGATGCCTCAT TATTTTGGCACTAAACGTCCGTGTTTGGAATTCGACTATTATGAACAATTCAATCGACCATCTGTCGACGTGGTT GACCTCAAGAACAACCCAATCAAGGAGTTTACCGAAACGGGCATTACCCTTGAAGACGGCACGCACCATGAATTT GATGTTGTTGCCGTTGCGACAGGATTTGACGTTGTGACTGGAGGCATGACACAGTTAGGACTTGAAAGCATCACG GGCGAAAAACTCGATGACGAATGGAAGACGGGGGCTACCACATACCTGGGCCTAACCGTCAGCGGCTACCCCAAC ATGTTCCACATGTATGGCACCCATGCGCCCACGCTTCTCGCCAACGGCCCCTCCCTGGTCGAGATCCAGGGTCGA TGGATCGTCGACTGCATGGATAAGATGAAGCACAGCAATATTAAGTACATCGACGCCAAGCCTGAATCGGCACAG GCCTGGAAGAAGCTCATCGTCGACGTCAATAACGCGACACTCTTCCCCACGACAAGGTCGACCTACATGGGCGGC AACGTTCAGGGCAAGGTTCAAGAGCCAATGTGCTATGCCAATGGCGTCAACAAGTATGCCAAGGAGGTTCGATTG GCACTGGATAGCATGGAAGGATTTGAAATGGTGCAAAACTGA |
| Gene | >OphauB2|78 ATGGGCGACCAATCTAGCTTGGAAAACTTCAAGATTAACCTGACAGACTATTCTGCGCCTGTCAGAACGCCCGAT GGCCCCTACGCAAGCGATCTTGACGTGGATGCCTTGATTATTGGGGCTGGATTTGGTTGGTGGATTGAACTTGAC ATGTGCATTTTATACGCTGACTGATATGCTATTATAGGTGGTGTATTTATGCTTAAAACTTTGCGCGACCGAGGC TATAAGACAGTCATTTATGAAGCGGGTGATGATATTGGGGGAACATGGCGCTGGAACTGCTATCCAGGTGCCGCC GTCGACTCCGAGGTGCCAGAATATGAATTCTCTTGGCCCGAGGTTTGGAAAACGTGGAACTGGACGACCAATTAT CCCGGCTACAAGGAGCTTCGAGCCTACTTTGACCACGTTGACAAGGCGGTGGGTATCAAAAAGGACTGCGCTTTC AATACAGTTGTCGTCGGTGCAGACTTTGATACCAACCAGGGCAAATGGAATGTCCGTACCAAGGACGGCCGCACT GCCACCACCAAGTTCCTGATTCTGGCAACGGGAATGGTAGGAGCAGCCCAATGGCTAGTGTACTGGGGTCAGTTG CTAAAACAGTTTGTAGGCATCAAAGCGCTATGTTCCCAGCTGGCCTGGCATGGACAAATTCAAAGGCACCATCCA CCACTCTTCCTTTTGGCCAGACTACGAAGTGGATGTGTCAAGCAAAAAGTGCGCCGTCATTGGCACTGGAGCCTC GGGAGTCCAGATAACCCAGGCGTGGGGCCCCAAAGCCCAAGAGCTCAAGGTCTTGCAGCGCACGCCCAACCTGGC CCTACCCGTGCGTCGACGCGACTTGACAGTCGAAGAGCAAGAGGCGGGCAAAAAGTGGTATCCGCACCTCTTTGA GTACCGCGAGAGGACATTTGGCGGCTTCATCTTTGACTGGCTCGAGAAGAATACCTCGGACGACACAATAGAGGA GCAGAAAGCAACATATGAAAAGGCGTGGGAAACTGGTGGCTTCCGTCTCTGGATTGGCATGTATAAGGATGTGCT CCTGGACGGGGCGGCAAACAAGCCCATCTACGACTTTTGGGCTTCCAAGACGCGACAACGAATCCAAGACGCTCG CAAGCGGGATATTCTGGCTCCTTTGGAGATGCCTCATTATTTTGGCACTAAACGTCCGTGTTTGGAATTCGACTA TTATGAACAATTCAATCGACCATCTGTCGACGTGGTTGACCTCAAGAACAACCCAATCAAGGAGTTTACCGAAAC GGGCATTACCCTTGAAGACGGCACGCACCATGAATTTGATGTTGTTGCCGTTGCGACAGGATTTGTAAGTCGCAT CAATGACGAGTATCCCTTGAAATGATGAAGCTTGTCGTACCCCTGAGGGAGCACGAGTCGTTGACAGAAACTGGA AGCTGACTGTTTACGCAGGACGTTGTGACTGGAGGTATGAAGTTGTAGCATGGCATCATGTCATTTTCATCTTGT TGATTATTGATTTACCCCTGCTGACTCGCTTGGCAGGCATGACACAGTTAGGACTTGAAAGCATCACGGGCGAAA AACTCGATGACGAATGGAAGACGGGGGCTACCACATACCTGGGCCTAACCGTCAGCGGCTACCCCAACATGTTCC ACATGTATGGCACCCATGCGCCCACGCTTCTCGCCAACGGCCCCTCCCTGGTCGAGATCCAGGGTCGATGGATCG TCGACTGCATGGATAAGATGAAGCACAGCAATATTAAGTACATCGACGCCAAGCCTGAATCGGCACAGGCCTGGA AGAAGCTCATCGTCGACGTCAATAACGCGACACTCTTCCCCACGACAAGGTCGACCTACATGGGCGGCAACGTTC AGGGCAAGGTTCAAGAGCCAATGTGCTATGCCAATGGCGTCAACAAGTATGCCAAGGAGGTTCGATTGGCACTGG ATAGCATGGAAGGATTTGAAATGGTGCAAAACTGA |