© 2022 - Robin Ohm - Utrecht University - The Netherlands
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| Protein ID | Ophio5|5773 |
| Gene name | |
| Location | scaffold_483:1365..3429 |
| Strand | + |
| Gene length (bp) | 2064 |
| Transcript length (bp) | 1812 |
| Coding sequence length (bp) | 1809 |
| Protein length (aa) | 603 |
| PFAM Domain ID | Short name | Long name | E-value | Start | End |
|---|---|---|---|---|---|
| PF00743 | FMO-like | Flavin-binding monooxygenase-like | 4.2E-20 | 2 | 211 |
| PF00743 | FMO-like | Flavin-binding monooxygenase-like | 7.2E-09 | 368 | 541 |
| PF13738 | Pyr_redox_3 | Pyridine nucleotide-disulphide oxidoreductase | 1.0E-09 | 5 | 209 |
| PF07992 | Pyr_redox_2 | Pyridine nucleotide-disulphide oxidoreductase | 1.7E-09 | 1 | 213 |
| PF13434 | Lys_Orn_oxgnase | L-lysine 6-monooxygenase/L-ornithine 5-monooxygenase | 1.6E-05 | 95 | 210 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|P17635|FMO2_RABIT | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Oryctolagus cuniculus GN=FMO2 PE=1 SV=3 | 2 | 541 | 1.0E-29 |
| sp|Q8K2I3|FMO2_MOUSE | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Mus musculus GN=Fmo2 PE=1 SV=3 | 2 | 541 | 2.0E-29 |
| sp|Q28505|FMO2_MACMU | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Macaca mulatta GN=FMO2 PE=2 SV=2 | 2 | 541 | 3.0E-29 |
| sp|P49109|FMO5_CAVPO | Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Cavia porcellus GN=FMO5 PE=2 SV=2 | 2 | 541 | 8.0E-20 |
| sp|P36366|FMO2_CAVPO | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Cavia porcellus GN=FMO2 PE=2 SV=2 | 2 | 217 | 9.0E-20 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|P17635|FMO2_RABIT | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Oryctolagus cuniculus GN=FMO2 PE=1 SV=3 | 2 | 541 | 1.0E-29 |
| sp|Q8K2I3|FMO2_MOUSE | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Mus musculus GN=Fmo2 PE=1 SV=3 | 2 | 541 | 2.0E-29 |
| sp|Q28505|FMO2_MACMU | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Macaca mulatta GN=FMO2 PE=2 SV=2 | 2 | 541 | 3.0E-29 |
| sp|P49109|FMO5_CAVPO | Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Cavia porcellus GN=FMO5 PE=2 SV=2 | 2 | 541 | 8.0E-20 |
| sp|P36366|FMO2_CAVPO | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Cavia porcellus GN=FMO2 PE=2 SV=2 | 2 | 217 | 9.0E-20 |
| sp|Q04799|FMO5_RABIT | Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Oryctolagus cuniculus GN=FMO5 PE=1 SV=2 | 2 | 544 | 2.0E-19 |
| sp|Q8HZ69|FMO2_GORGO | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Gorilla gorilla gorilla GN=FMO2 PE=3 SV=3 | 2 | 217 | 3.0E-19 |
| sp|Q8HZ70|FMO2_PANTR | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Pan troglodytes GN=FMO2 PE=3 SV=3 | 2 | 217 | 4.0E-19 |
| sp|Q6IRI9|FMO2_RAT | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Rattus norvegicus GN=Fmo2 PE=2 SV=3 | 2 | 217 | 5.0E-19 |
| sp|Q99518|FMO2_HUMAN | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Homo sapiens GN=FMO2 PE=1 SV=4 | 2 | 217 | 8.0E-19 |
| sp|P31512|FMO4_HUMAN | Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Homo sapiens GN=FMO4 PE=1 SV=3 | 2 | 210 | 1.0E-18 |
| sp|Q5REK0|FMO2_PONAB | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Pongo abelii GN=FMO2 PE=2 SV=3 | 2 | 217 | 2.0E-18 |
| sp|P49326|FMO5_HUMAN | Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Homo sapiens GN=FMO5 PE=1 SV=2 | 2 | 560 | 4.0E-18 |
| sp|P36367|FMO4_RABIT | Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Oryctolagus cuniculus GN=FMO4 PE=2 SV=2 | 2 | 210 | 2.0E-16 |
| sp|Q8VHG0|FMO4_MOUSE | Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Mus musculus GN=Fmo4 PE=1 SV=3 | 2 | 210 | 1.0E-15 |
| sp|P16549|FMO1_PIG | Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Sus scrofa GN=FMO1 PE=1 SV=3 | 2 | 195 | 2.0E-15 |
| sp|P36365|FMO1_RAT | Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Rattus norvegicus GN=Fmo1 PE=1 SV=2 | 2 | 195 | 2.0E-15 |
| sp|Q8K4B7|FMO4_RAT | Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Rattus norvegicus GN=Fmo4 PE=2 SV=3 | 2 | 210 | 2.0E-15 |
| sp|P17636|FMO1_RABIT | Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Oryctolagus cuniculus GN=FMO1 PE=1 SV=3 | 2 | 192 | 3.0E-15 |
| sp|Q01740|FMO1_HUMAN | Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Homo sapiens GN=FMO1 PE=2 SV=3 | 2 | 195 | 8.0E-15 |
| sp|Q8SPQ7|FMO3_MACMU | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Macaca mulatta GN=FMO3 PE=2 SV=3 | 2 | 210 | 1.0E-14 |
| sp|P50285|FMO1_MOUSE | Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Mus musculus GN=Fmo1 PE=1 SV=1 | 2 | 195 | 2.0E-14 |
| sp|Q8K4C0|FMO5_RAT | Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Rattus norvegicus GN=Fmo5 PE=1 SV=3 | 2 | 210 | 3.0E-14 |
| sp|Q8MP06|SNO1_TYRJA | Senecionine N-oxygenase OS=Tyria jacobaeae GN=sno1 PE=1 SV=1 | 2 | 192 | 3.0E-14 |
| sp|Q95LA2|FMO1_CANLF | Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Canis lupus familiaris GN=FMO1 PE=2 SV=3 | 2 | 192 | 3.0E-14 |
| sp|P97501|FMO3_MOUSE | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Mus musculus GN=Fmo3 PE=1 SV=1 | 2 | 210 | 9.0E-14 |
| sp|O60774|FMO6_HUMAN | Putative dimethylaniline monooxygenase [N-oxide-forming] 6 OS=Homo sapiens GN=FMO6P PE=5 SV=1 | 2 | 192 | 9.0E-14 |
| sp|Q95LA1|FMO3_CANLF | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Canis lupus familiaris GN=FMO3 PE=2 SV=3 | 2 | 192 | 1.0E-13 |
| sp|Q9EQ76|FMO3_RAT | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Rattus norvegicus GN=Fmo3 PE=1 SV=1 | 2 | 192 | 1.0E-12 |
| sp|P97872|FMO5_MOUSE | Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Mus musculus GN=Fmo5 PE=1 SV=4 | 2 | 210 | 2.0E-11 |
| sp|Q8HZ69|FMO2_GORGO | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Gorilla gorilla gorilla GN=FMO2 PE=3 SV=3 | 374 | 541 | 6.0E-11 |
| sp|Q8HZ70|FMO2_PANTR | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Pan troglodytes GN=FMO2 PE=3 SV=3 | 374 | 541 | 1.0E-10 |
| sp|Q5REK0|FMO2_PONAB | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Pongo abelii GN=FMO2 PE=2 SV=3 | 374 | 541 | 5.0E-10 |
| sp|Q9SZY8|YUC1_ARATH | Probable indole-3-pyruvate monooxygenase YUCCA1 OS=Arabidopsis thaliana GN=YUC1 PE=1 SV=1 | 5 | 218 | 5.0E-10 |
| sp|Q9LKC0|YUC5_ARATH | Probable indole-3-pyruvate monooxygenase YUCCA5 OS=Arabidopsis thaliana GN=YUC5 PE=2 SV=1 | 5 | 218 | 8.0E-10 |
| sp|Q8HYJ9|FMO3_BOVIN | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Bos taurus GN=FMO3 PE=2 SV=1 | 2 | 192 | 1.0E-09 |
| sp|O64489|YUC9_ARATH | Probable indole-3-pyruvate monooxygenase YUCCA9 OS=Arabidopsis thaliana GN=YUC9 PE=2 SV=1 | 5 | 198 | 1.0E-09 |
| sp|O49312|YUC7_ARATH | Probable indole-3-pyruvate monooxygenase YUCCA7 OS=Arabidopsis thaliana GN=YUC7 PE=2 SV=1 | 5 | 209 | 1.0E-09 |
| sp|Q9SVU0|YUC8_ARATH | Probable indole-3-pyruvate monooxygenase YUCCA8 OS=Arabidopsis thaliana GN=YUC8 PE=2 SV=1 | 4 | 192 | 2.0E-09 |
| sp|P32417|FMO3_RABIT | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Oryctolagus cuniculus GN=FMO3 PE=1 SV=3 | 2 | 210 | 8.0E-09 |
| sp|Q7YS44|FMO3_PANTR | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Pan troglodytes GN=FMO3 PE=3 SV=3 | 2 | 210 | 1.0E-08 |
| sp|Q6IRI9|FMO2_RAT | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Rattus norvegicus GN=Fmo2 PE=2 SV=3 | 373 | 541 | 2.0E-08 |
| sp|Q9FKE7|FMO2_ARATH | Putative flavin-containing monooxygenase 2 OS=Arabidopsis thaliana GN=FMO2 PE=3 SV=2 | 2 | 192 | 2.0E-08 |
| sp|P31513|FMO3_HUMAN | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Homo sapiens GN=FMO3 PE=1 SV=5 | 2 | 210 | 5.0E-08 |
| sp|Q8VZ59|YUC6_ARATH | Indole-3-pyruvate monooxygenase YUCCA6 OS=Arabidopsis thaliana GN=YUC6 PE=1 SV=1 | 5 | 216 | 1.0E-07 |
| sp|P36366|FMO2_CAVPO | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Cavia porcellus GN=FMO2 PE=2 SV=2 | 374 | 541 | 3.0E-07 |
| sp|Q9SXD5|GSXL3_ARATH | Flavin-containing monooxygenase FMO GS-OX-like 3 OS=Arabidopsis thaliana GN=At1g62620 PE=2 SV=2 | 3 | 192 | 3.0E-07 |
| sp|Q9C8U0|GSXL5_ARATH | Flavin-containing monooxygenase FMO GS-OX-like 5 OS=Arabidopsis thaliana GN=At1g63370 PE=2 SV=2 | 3 | 192 | 9.0E-07 |
| sp|P97501|FMO3_MOUSE | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Mus musculus GN=Fmo3 PE=1 SV=1 | 374 | 541 | 1.0E-06 |
| sp|Q9LFM5|YUC4_ARATH | Probable indole-3-pyruvate monooxygenase YUCCA4 OS=Arabidopsis thaliana GN=YUC4 PE=1 SV=1 | 5 | 192 | 2.0E-06 |
| sp|Q9SVQ1|YUC2_ARATH | Indole-3-pyruvate monooxygenase YUCCA2 OS=Arabidopsis thaliana GN=YUC2 PE=1 SV=1 | 5 | 216 | 2.0E-06 |
| sp|P36365|FMO1_RAT | Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Rattus norvegicus GN=Fmo1 PE=1 SV=2 | 356 | 541 | 2.0E-06 |
| GO Term | Description | Terminal node |
|---|---|---|
| GO:0016491 | oxidoreductase activity | Yes |
| GO:0050660 | flavin adenine dinucleotide binding | Yes |
| GO:0050661 | NADP binding | Yes |
| GO:0004499 | N,N-dimethylaniline monooxygenase activity | Yes |
| GO:0004497 | monooxygenase 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:1901265 | nucleoside phosphate binding | No |
| GO:0005488 | 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 |
| GO:0003824 | catalytic activity | No |
| GO:0003674 | molecular_function | No |
| GO:0043167 | ion binding | No |
| GO:0043168 | anion binding | No |
| GO:1901363 | heterocyclic compound binding | No |
| GO:0036094 | small molecule binding | No |
| SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
|---|---|---|
| No | 1 - 34 | 0.45 |
| Domain # | Start | End | Length |
|---|---|---|---|
| 1 | 564 | 586 | 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 | >Ophio5|5773 MKVAVVGGGPGGLATLKFLSTAHLFFPIEPIEARLFEAEDRIGGTFVYRVYEDAELVSSKYLTAFSDFRLPADAP DFVTPQAYVAYLGAYVQAFRLAGSIECQARVMSISRRLGGVGHVLTVRKPDGREFRWDCDAVAVCSGLHVHPYVP HIPGIEKVPVVMHSSRLKRREQFGRGTNVVVCGAGETAMDVAHLAVTSPTASVTLCHRDGWFCAPKIIPTPRARR QKGPTRPNKPVDTSVASLFDTAYAHPILQRSRLLWFAYDQWVKKMHLLISGTEEGPDQWQGHISPERKNLDSIFL CKSDRALPYISEGHRSQSWWNRKRSSIINVPLGDTQGRRIDVMKWPSKVDADGFMHVAEDDSSGSGATRRIRADV VVLATGYSTDFGFLDDDYPRPGQADVRGVYKSDDVSLAFIGFVRPAIGAIPPLAELQAQLWVLRLLQARFPTVMP RGPGRDALKTYELDYGLHPRCGYDFFASKGGVDHEAYAYQLALDMGAAPTATYVARKGWRLFFTWAMGSNFNTKF RLVGPWRWEAGAEAVMRGELFAVVRRSGGMLYLMTYTLIPFTIFGTISLALHAWSGVLSLLSAALRVAMRRPRKK RTV |
| Coding | >Ophio5|5773 ATGAAGGTCGCTGTCGTCGGCGGTGGCCCGGGCGGGCTGGCAACGCTCAAGTTTCTATCCACAGCGCACCTCTTC TTTCCCATAGAGCCCATCGAGGCCCGTCTATTTGAAGCAGAAGACCGCATCGGCGGCACCTTTGTCTATCGAGTT TACGAGGACGCCGAGCTCGTGTCGTCCAAGTACCTTACGGCCTTCTCTGACTTCCGGCTGCCGGCAGATGCGCCG GATTTCGTCACGCCCCAGGCCTATGTCGCCTATCTCGGTGCCTATGTCCAGGCCTTTCGTCTAGCCGGCTCTATC GAGTGCCAGGCTCGAGTCATGAGCATCAGTCGGAGGCTAGGAGGCGTCGGACACGTTCTGACCGTCCGCAAGCCC GATGGACGCGAATTTCGCTGGGACTGCGACGCCGTTGCTGTCTGCTCGGGCCTTCATGTCCACCCTTACGTGCCG CATATACCAGGCATCGAAAAAGTGCCGGTGGTGATGCACTCGTCGCGCCTCAAGCGCCGCGAGCAGTTTGGACGC GGCACAAATGTCGTTGTGTGCGGTGCAGGAGAGACGGCCATGGATGTGGCTCATCTGGCCGTCACGTCGCCCACG GCCTCCGTCACCTTGTGTCACCGAGATGGCTGGTTCTGCGCGCCCAAGATTATCCCGACACCGCGCGCTCGCCGG CAAAAGGGTCCAACACGACCTAACAAGCCCGTCGACACATCCGTAGCCAGCCTCTTTGACACGGCCTACGCTCAT CCGATTCTGCAGCGAAGTCGGCTGCTGTGGTTCGCCTATGATCAGTGGGTGAAAAAGATGCACTTGCTCATCTCG GGCACCGAGGAGGGCCCCGATCAGTGGCAGGGTCATATCAGCCCTGAACGAAAGAATCTCGACTCAATCTTTCTC TGCAAGTCGGACCGCGCCTTGCCGTACATCTCCGAGGGCCACCGATCACAGTCGTGGTGGAACCGGAAGCGGTCC AGCATCATCAACGTGCCTCTCGGAGACACTCAGGGCAGACGGATCGACGTCATGAAGTGGCCGAGCAAAGTAGAC GCAGATGGATTCATGCACGTGGCCGAGGACGACTCCAGCGGATCGGGCGCAACGCGGCGCATTCGGGCCGATGTC GTCGTCCTGGCCACGGGCTACTCGACTGACTTTGGCTTCCTCGATGACGACTACCCTCGGCCAGGCCAAGCCGAT GTCCGCGGCGTGTACAAGAGCGACGACGTCTCCCTAGCCTTCATCGGTTTCGTACGGCCAGCCATCGGAGCGATC CCGCCGCTGGCCGAGCTGCAGGCTCAACTATGGGTGCTGCGCCTCTTGCAAGCCCGGTTCCCGACTGTGATGCCC CGAGGCCCGGGCCGCGACGCGCTGAAGACGTACGAGCTGGACTATGGGCTTCACCCGCGGTGTGGATACGACTTC TTCGCCTCCAAGGGCGGCGTCGATCACGAAGCTTATGCTTACCAGCTGGCGCTGGACATGGGCGCGGCACCGACG GCAACGTACGTGGCGCGGAAGGGATGGCGCCTGTTCTTCACCTGGGCCATGGGATCCAACTTCAACACCAAATTT CGCCTCGTCGGCCCGTGGCGCTGGGAAGCGGGCGCTGAAGCCGTCATGCGCGGTGAGCTGTTTGCCGTCGTTCGC CGTTCAGGCGGCATGCTGTACTTGATGACTTACACGCTGATTCCGTTTACCATCTTTGGCACCATCAGTCTGGCT CTGCATGCCTGGTCCGGGGTGTTGAGTCTGCTGAGTGCGGCTCTGCGAGTGGCCATGAGACGGCCTCGCAAGAAA CGCACTGTA |
| Transcript | >Ophio5|5773 ATGAAGGTCGCTGTCGTCGGCGGTGGCCCGGGCGGGCTGGCAACGCTCAAGTTTCTATCCACAGCGCACCTCTTC TTTCCCATAGAGCCCATCGAGGCCCGTCTATTTGAAGCAGAAGACCGCATCGGCGGCACCTTTGTCTATCGAGTT TACGAGGACGCCGAGCTCGTGTCGTCCAAGTACCTTACGGCCTTCTCTGACTTCCGGCTGCCGGCAGATGCGCCG GATTTCGTCACGCCCCAGGCCTATGTCGCCTATCTCGGTGCCTATGTCCAGGCCTTTCGTCTAGCCGGCTCTATC GAGTGCCAGGCTCGAGTCATGAGCATCAGTCGGAGGCTAGGAGGCGTCGGACACGTTCTGACCGTCCGCAAGCCC GATGGACGCGAATTTCGCTGGGACTGCGACGCCGTTGCTGTCTGCTCGGGCCTTCATGTCCACCCTTACGTGCCG CATATACCAGGCATCGAAAAAGTGCCGGTGGTGATGCACTCGTCGCGCCTCAAGCGCCGCGAGCAGTTTGGACGC GGCACAAATGTCGTTGTGTGCGGTGCAGGAGAGACGGCCATGGATGTGGCTCATCTGGCCGTCACGTCGCCCACG GCCTCCGTCACCTTGTGTCACCGAGATGGCTGGTTCTGCGCGCCCAAGATTATCCCGACACCGCGCGCTCGCCGG CAAAAGGGTCCAACACGACCTAACAAGCCCGTCGACACATCCGTAGCCAGCCTCTTTGACACGGCCTACGCTCAT CCGATTCTGCAGCGAAGTCGGCTGCTGTGGTTCGCCTATGATCAGTGGGTGAAAAAGATGCACTTGCTCATCTCG GGCACCGAGGAGGGCCCCGATCAGTGGCAGGGTCATATCAGCCCTGAACGAAAGAATCTCGACTCAATCTTTCTC TGCAAGTCGGACCGCGCCTTGCCGTACATCTCCGAGGGCCACCGATCACAGTCGTGGTGGAACCGGAAGCGGTCC AGCATCATCAACGTGCCTCTCGGAGACACTCAGGGCAGACGGATCGACGTCATGAAGTGGCCGAGCAAAGTAGAC GCAGATGGATTCATGCACGTGGCCGAGGACGACTCCAGCGGATCGGGCGCAACGCGGCGCATTCGGGCCGATGTC GTCGTCCTGGCCACGGGCTACTCGACTGACTTTGGCTTCCTCGATGACGACTACCCTCGGCCAGGCCAAGCCGAT GTCCGCGGCGTGTACAAGAGCGACGACGTCTCCCTAGCCTTCATCGGTTTCGTACGGCCAGCCATCGGAGCGATC CCGCCGCTGGCCGAGCTGCAGGCTCAACTATGGGTGCTGCGCCTCTTGCAAGCCCGGTTCCCGACTGTGATGCCC CGAGGCCCGGGCCGCGACGCGCTGAAGACGTACGAGCTGGACTATGGGCTTCACCCGCGGTGTGGATACGACTTC TTCGCCTCCAAGGGCGGCGTCGATCACGAAGCTTATGCTTACCAGCTGGCGCTGGACATGGGCGCGGCACCGACG GCAACGTACGTGGCGCGGAAGGGATGGCGCCTGTTCTTCACCTGGGCCATGGGATCCAACTTCAACACCAAATTT CGCCTCGTCGGCCCGTGGCGCTGGGAAGCGGGCGCTGAAGCCGTCATGCGCGGTGAGCTGTTTGCCGTCGTTCGC CGTTCAGGCGGCATGCTGTACTTGATGACTTACACGCTGATTCCGTTTACCATCTTTGGCACCATCAGTCTGGCT CTGCATGCCTGGTCCGGGGTGTTGAGTCTGCTGAGTGCGGCTCTGCGAGTGGCCATGAGACGGCCTCGCAAGAAA CGCACTGTATAG |
| Gene | >Ophio5|5773 ATGAAGGTCGCTGTCGTCGGCGGTGGCCCGGGCGGGCTGGCAACGCTCAAGTTTCTATCCACAGCGCACCTCTTC TTTCCCATAGAGCCCATCGAGGCCCGTCTATTTGAAGCAGAAGACCGCATCGGCGGCACCTTTGTCTATCGAGTT TACGAGGACGCCGAGGTGCGAGTCTGTTGTCGTCGACCTCTTTGCCGACTGTCTCCCCCTTTTTGGGACCCTGCT GACGTGGAAACGACGCGCAGCTCGTGTCGTCCAAGTACCTTACGGCCTTCTCTGACTTCCGGCTGCCGGCAGATG CGCCGGATTTCGTCACGCCCCAGGCCTATGTCGCCTATCTCGGTGCCTATGTCCAGGCCTTTCGTCTAGCCGGCT CTATCGAGTGCCAGGCTCGAGTCATGAGCATCAGTCGGAGGCTAGGAGGCGTCGGACACGTTCTGACCGTCCGCA AGCCCGATGGACGCGAATTTCGCTGGGACTGCGACGCCGTTGCTGTCTGCTCGGGCCTTCATGTCCACCCTTACG TGCCGCATATACCAGGCATCGAAAAAGTGCCGGTGGTGATGCACTCGTCGCGCCTCAAGCGCCGCGAGCAGTTTG GACGCGGCACAAATGTCGTTGTGTGCGGTGCAGGAGAGACGGCCATGGATGTGGCTCATCTGGCCGTCACGTCGC CCACGGCCTCCGTCACCTTGTGTCACCGAGATGGCTGGTTCTGCGCGCCCAAGGTTGCTCTGGGGCCCTGCGATG GAACGTGAAGCTGTACTGACGTTGTTAACAGATTATCCCGACACCGCGCGCTCGCCGGCAAAAGGGTCCAACACG ACCTAACAAGCCCGTCGACACATCCGTAGCCAGCCTCTTTGACACGGCCTACGCTCATCCGATTCTGCAGCGAAG TCGGCTGCTGTGGTTCGCCTATGATCAGTGGGTGAAAAAGATGCACTTGCTCATCTCGGGCACCGAGGAGGGCCC CGATCAGTGGCAGGGTCATATCAGCCCTGAACGAAAGAATCTCGACTCAAGTGCGTGGCATGTCTCTCGGGAAGA GGAATCATGAACTTATACGGATCATAGTCTTTCTCTGCAAGTCGGACCGCGCCTTGCCGTACATCTCCGAGGGCC ACCGATCACAGTCGTGGTGGAACCGGAAGCGGTCCAGCATCATCAACGTGCCTCTCGGAGACACTCAGGGCAGAC GGATCGACGTCATGAAGTGGCCGAGCAAAGTAGACGCAGATGGATTCATGCACGTGGCCGAGGACGACTCCAGCG GATCGGGCGCAACGCGGCGCATTCGGGCCGATGTCGTCGTCCTGGCCACGGGCTACTCGACTGACTTTGGCTTCC TCGATGACGACTACCCTCGGCCAGGCCAAGCCGATGTCCGCGGCGTGTACAAGAGCGACGACGTCTCCCTAGCCT TCATCGGTTTCGTACGGCCAGCCATCGGAGCGATCCCGCCGCTGGCCGAGCTGCAGGCTCAACTATGGGTGCTGC GCCTCTTGCAAGCCCGGTTCCCGACTGTGATGCCCCGAGGCCCGGGCCGCGACGCGCTGAAGACGTACGAGCTGG ACTATGGGCTTCACCCGCGGTGTGGATACGACTTCTTCGCCTCCAAGGGCGGCGTCGATCACGAAGCTTATGCTT ACCAGCTGGCGCTGGACATGGGCGCGGCACCGACGGCAACGTACGTGGCGCGGAAGGGATGGCGCCTGTTCTTCA CCTGGGCCATGGGATCCAACTTCAACACCAAATTTCGCCTCGTCGGCCCGTGGCGCTGGGAAGCGGGCGCTGAAG CCGTCATGCGCGGTGAGCTGTTTGCCGTCGTTCGCCGTTCAGGCGGCATGCTGTGTAAGTATCGACGAAGTAAGG GGAGGGGAGAGAGAGGCAGAGAGCGTGCGCTGACGGCTGAGGATAGACTTGATGACTTACACGCTGATTCCGTTT ACCATCTTTGGCACCATCAGTCTGGCTCTGCATGCCTGGTCCGGGGTGTTGAGTCTGCTGAGTGCGGCTCTGCGA GTGGCCATGAGACGGCCTCGCAAGAAACGCACTGTATAG |