Protein ID | Ophio5|5212 |
Gene name | |
Location | scaffold_42:48536..49952 |
Strand | - |
Gene length (bp) | 1416 |
Transcript length (bp) | 1416 |
Coding sequence length (bp) | 1413 |
Protein length (aa) | 471 |
PFAM Domain ID | Short name | Long name | E-value | Start | End |
---|---|---|---|---|---|
PF00743 | FMO-like | Flavin-binding monooxygenase-like | 1.4E-14 | 100 | 263 |
PF00743 | FMO-like | Flavin-binding monooxygenase-like | 3.3E-11 | 289 | 393 |
PF07992 | Pyr_redox_2 | Pyridine nucleotide-disulphide oxidoreductase | 1.1E-12 | 12 | 266 |
PF13454 | NAD_binding_9 | FAD-NAD(P)-binding | 8.3E-05 | 15 | 54 |
PF13434 | Lys_Orn_oxgnase | L-lysine 6-monooxygenase/L-ornithine 5-monooxygenase | 1.0E-06 | 144 | 258 |
PF13450 | NAD_binding_8 | NAD(P)-binding Rossmann-like domain | 4.9E-07 | 16 | 50 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|Q9HFE4|FMO1_SCHPO | Thiol-specific monooxygenase OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=fmo1 PE=1 SV=1 | 11 | 451 | 1.0E-72 |
sp|Q9FF12|GSXL9_ARATH | Flavin-containing monooxygenase FMO GS-OX-like 9 OS=Arabidopsis thaliana GN=At5g07800 PE=2 SV=1 | 7 | 387 | 2.0E-41 |
sp|Q9SXE1|GSOX3_ARATH | Flavin-containing monooxygenase FMO GS-OX3 OS=Arabidopsis thaliana GN=FMOGS-OX3 PE=2 SV=1 | 12 | 424 | 1.0E-39 |
sp|Q9SXD5|GSXL3_ARATH | Flavin-containing monooxygenase FMO GS-OX-like 3 OS=Arabidopsis thaliana GN=At1g62620 PE=2 SV=2 | 3 | 427 | 3.0E-39 |
sp|Q9FWW9|GSXL2_ARATH | Flavin-containing monooxygenase FMO GS-OX-like 2 OS=Arabidopsis thaliana GN=At1g12200 PE=2 SV=1 | 39 | 418 | 2.0E-38 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|Q9HFE4|FMO1_SCHPO | Thiol-specific monooxygenase OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=fmo1 PE=1 SV=1 | 11 | 451 | 1.0E-72 |
sp|Q9FF12|GSXL9_ARATH | Flavin-containing monooxygenase FMO GS-OX-like 9 OS=Arabidopsis thaliana GN=At5g07800 PE=2 SV=1 | 7 | 387 | 2.0E-41 |
sp|Q9SXE1|GSOX3_ARATH | Flavin-containing monooxygenase FMO GS-OX3 OS=Arabidopsis thaliana GN=FMOGS-OX3 PE=2 SV=1 | 12 | 424 | 1.0E-39 |
sp|Q9SXD5|GSXL3_ARATH | Flavin-containing monooxygenase FMO GS-OX-like 3 OS=Arabidopsis thaliana GN=At1g62620 PE=2 SV=2 | 3 | 427 | 3.0E-39 |
sp|Q9FWW9|GSXL2_ARATH | Flavin-containing monooxygenase FMO GS-OX-like 2 OS=Arabidopsis thaliana GN=At1g12200 PE=2 SV=1 | 39 | 418 | 2.0E-38 |
sp|Q9C8U0|GSXL5_ARATH | Flavin-containing monooxygenase FMO GS-OX-like 5 OS=Arabidopsis thaliana GN=At1g63370 PE=2 SV=2 | 3 | 387 | 2.0E-38 |
sp|Q9FLK4|GSXL8_ARATH | Flavin-containing monooxygenase FMO GS-OX-like 8 OS=Arabidopsis thaliana GN=At5g61290 PE=2 SV=1 | 6 | 387 | 4.0E-37 |
sp|P38866|FMO1_YEAST | Thiol-specific monooxygenase OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FMO1 PE=1 SV=2 | 39 | 435 | 2.0E-36 |
sp|Q9SS04|GSOX1_ARATH | Flavin-containing monooxygenase FMO GS-OX1 OS=Arabidopsis thaliana GN=FMOGS-OX1 PE=2 SV=1 | 12 | 452 | 3.0E-36 |
sp|Q94BV5|GSXL4_ARATH | Flavin-containing monooxygenase FMO GS-OX-like 4 OS=Arabidopsis thaliana GN=At1g62600 PE=2 SV=1 | 3 | 394 | 8.0E-33 |
sp|A8MRX0|GSOX5_ARATH | Flavin-containing monooxygenase FMO GS-OX5 OS=Arabidopsis thaliana GN=FMOGS-OX5 PE=2 SV=2 | 39 | 387 | 1.0E-31 |
sp|Q9FWW6|GSXL1_ARATH | Flavin-containing monooxygenase FMO GS-OX-like 1 OS=Arabidopsis thaliana GN=At1g12160 PE=2 SV=1 | 1 | 397 | 1.0E-31 |
sp|Q94K43|GSOX2_ARATH | Flavin-containing monooxygenase FMO GS-OX2 OS=Arabidopsis thaliana GN=FMOGS-OX2 PE=2 SV=1 | 39 | 393 | 2.0E-30 |
sp|Q93Y23|GSOX4_ARATH | Flavin-containing monooxygenase FMO GS-OX4 OS=Arabidopsis thaliana GN=FMOGS-OX4 PE=2 SV=1 | 5 | 463 | 2.0E-30 |
sp|Q9SXD9|GSXL7_ARATH | Flavin-containing monooxygenase FMO GS-OX-like 7 OS=Arabidopsis thaliana GN=At1g62580 PE=3 SV=2 | 39 | 386 | 6.0E-30 |
sp|Q9FWW3|GSXL6_ARATH | Flavin-containing monooxygenase FMO GS-OX-like 6 OS=Arabidopsis thaliana GN=At1g12130 PE=2 SV=1 | 39 | 387 | 4.0E-28 |
sp|Q9C8T8|GSXLX_ARATH | Putative flavin-containing monooxygenase FMO GS-OX-like 10 OS=Arabidopsis thaliana GN=At1g63340 PE=5 SV=3 | 39 | 378 | 5.0E-27 |
sp|Q8MP06|SNO1_TYRJA | Senecionine N-oxygenase OS=Tyria jacobaeae GN=sno1 PE=1 SV=1 | 13 | 387 | 7.0E-27 |
sp|P36367|FMO4_RABIT | Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Oryctolagus cuniculus GN=FMO4 PE=2 SV=2 | 12 | 388 | 1.0E-13 |
sp|P97501|FMO3_MOUSE | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Mus musculus GN=Fmo3 PE=1 SV=1 | 12 | 261 | 2.0E-13 |
sp|Q04799|FMO5_RABIT | Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Oryctolagus cuniculus GN=FMO5 PE=1 SV=2 | 12 | 255 | 3.0E-13 |
sp|Q9EQ76|FMO3_RAT | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Rattus norvegicus GN=Fmo3 PE=1 SV=1 | 12 | 255 | 4.0E-13 |
sp|Q8HZ69|FMO2_GORGO | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Gorilla gorilla gorilla GN=FMO2 PE=3 SV=3 | 12 | 251 | 2.0E-12 |
sp|Q8K4B7|FMO4_RAT | Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Rattus norvegicus GN=Fmo4 PE=2 SV=3 | 12 | 275 | 2.0E-12 |
sp|Q99518|FMO2_HUMAN | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Homo sapiens GN=FMO2 PE=1 SV=4 | 12 | 251 | 2.0E-12 |
sp|P49109|FMO5_CAVPO | Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Cavia porcellus GN=FMO5 PE=2 SV=2 | 12 | 266 | 3.0E-12 |
sp|Q8HZ70|FMO2_PANTR | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Pan troglodytes GN=FMO2 PE=3 SV=3 | 12 | 251 | 3.0E-12 |
sp|Q28505|FMO2_MACMU | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Macaca mulatta GN=FMO2 PE=2 SV=2 | 12 | 266 | 3.0E-12 |
sp|Q8K4C0|FMO5_RAT | Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Rattus norvegicus GN=Fmo5 PE=1 SV=3 | 12 | 255 | 4.0E-12 |
sp|Q8VHG0|FMO4_MOUSE | Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Mus musculus GN=Fmo4 PE=1 SV=3 | 12 | 266 | 4.0E-12 |
sp|P16549|FMO1_PIG | Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Sus scrofa GN=FMO1 PE=1 SV=3 | 12 | 265 | 5.0E-12 |
sp|Q95LA2|FMO1_CANLF | Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Canis lupus familiaris GN=FMO1 PE=2 SV=3 | 12 | 265 | 9.0E-12 |
sp|Q8SPQ7|FMO3_MACMU | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Macaca mulatta GN=FMO3 PE=2 SV=3 | 12 | 251 | 1.0E-11 |
sp|Q5REK0|FMO2_PONAB | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Pongo abelii GN=FMO2 PE=2 SV=3 | 12 | 251 | 1.0E-11 |
sp|P97872|FMO5_MOUSE | Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Mus musculus GN=Fmo5 PE=1 SV=4 | 12 | 255 | 2.0E-11 |
sp|P36366|FMO2_CAVPO | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Cavia porcellus GN=FMO2 PE=2 SV=2 | 12 | 251 | 2.0E-11 |
sp|P31512|FMO4_HUMAN | Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Homo sapiens GN=FMO4 PE=1 SV=3 | 12 | 266 | 2.0E-11 |
sp|O60774|FMO6_HUMAN | Putative dimethylaniline monooxygenase [N-oxide-forming] 6 OS=Homo sapiens GN=FMO6P PE=5 SV=1 | 12 | 266 | 5.0E-11 |
sp|P17636|FMO1_RABIT | Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Oryctolagus cuniculus GN=FMO1 PE=1 SV=3 | 12 | 265 | 6.0E-11 |
sp|Q95LA1|FMO3_CANLF | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Canis lupus familiaris GN=FMO3 PE=2 SV=3 | 12 | 251 | 1.0E-10 |
sp|P32417|FMO3_RABIT | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Oryctolagus cuniculus GN=FMO3 PE=1 SV=3 | 268 | 418 | 1.0E-09 |
sp|Q6IRI9|FMO2_RAT | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Rattus norvegicus GN=Fmo2 PE=2 SV=3 | 11 | 251 | 1.0E-09 |
sp|Q9SVQ1|YUC2_ARATH | Indole-3-pyruvate monooxygenase YUCCA2 OS=Arabidopsis thaliana GN=YUC2 PE=1 SV=1 | 101 | 260 | 2.0E-09 |
sp|Q8K2I3|FMO2_MOUSE | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Mus musculus GN=Fmo2 PE=1 SV=3 | 12 | 254 | 2.0E-09 |
sp|Q04799|FMO5_RABIT | Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Oryctolagus cuniculus GN=FMO5 PE=1 SV=2 | 294 | 399 | 3.0E-09 |
sp|Q5REK0|FMO2_PONAB | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Pongo abelii GN=FMO2 PE=2 SV=3 | 268 | 387 | 7.0E-09 |
sp|P32417|FMO3_RABIT | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Oryctolagus cuniculus GN=FMO3 PE=1 SV=3 | 12 | 251 | 9.0E-09 |
sp|Q99518|FMO2_HUMAN | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Homo sapiens GN=FMO2 PE=1 SV=4 | 268 | 387 | 1.0E-08 |
sp|Q8HZ70|FMO2_PANTR | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Pan troglodytes GN=FMO2 PE=3 SV=3 | 268 | 387 | 1.0E-08 |
sp|Q8HZ69|FMO2_GORGO | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Gorilla gorilla gorilla GN=FMO2 PE=3 SV=3 | 268 | 387 | 1.0E-08 |
sp|Q28505|FMO2_MACMU | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Macaca mulatta GN=FMO2 PE=2 SV=2 | 268 | 387 | 2.0E-08 |
sp|Q7YS44|FMO3_PANTR | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Pan troglodytes GN=FMO3 PE=3 SV=3 | 12 | 266 | 3.0E-08 |
sp|P36366|FMO2_CAVPO | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Cavia porcellus GN=FMO2 PE=2 SV=2 | 294 | 416 | 3.0E-08 |
sp|P31513|FMO3_HUMAN | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Homo sapiens GN=FMO3 PE=1 SV=5 | 12 | 266 | 4.0E-08 |
sp|Q6IRI9|FMO2_RAT | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Rattus norvegicus GN=Fmo2 PE=2 SV=3 | 287 | 388 | 6.0E-08 |
sp|O60774|FMO6_HUMAN | Putative dimethylaniline monooxygenase [N-oxide-forming] 6 OS=Homo sapiens GN=FMO6P PE=5 SV=1 | 268 | 404 | 6.0E-08 |
sp|P49109|FMO5_CAVPO | Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Cavia porcellus GN=FMO5 PE=2 SV=2 | 294 | 399 | 6.0E-08 |
sp|Q8K4C0|FMO5_RAT | Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Rattus norvegicus GN=Fmo5 PE=1 SV=3 | 294 | 399 | 7.0E-08 |
sp|P49326|FMO5_HUMAN | Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Homo sapiens GN=FMO5 PE=1 SV=2 | 294 | 420 | 8.0E-08 |
sp|P97872|FMO5_MOUSE | Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Mus musculus GN=Fmo5 PE=1 SV=4 | 294 | 399 | 1.0E-07 |
sp|P17635|FMO2_RABIT | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Oryctolagus cuniculus GN=FMO2 PE=1 SV=3 | 294 | 430 | 1.0E-07 |
sp|P31512|FMO4_HUMAN | Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Homo sapiens GN=FMO4 PE=1 SV=3 | 268 | 430 | 2.0E-07 |
sp|Q9FVQ0|YUC10_ARATH | Probable indole-3-pyruvate monooxygenase YUCCA10 OS=Arabidopsis thaliana GN=YUC10 PE=2 SV=1 | 162 | 260 | 2.0E-07 |
sp|Q9EQ76|FMO3_RAT | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Rattus norvegicus GN=Fmo3 PE=1 SV=1 | 268 | 430 | 2.0E-07 |
sp|P49326|FMO5_HUMAN | Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Homo sapiens GN=FMO5 PE=1 SV=2 | 12 | 265 | 3.0E-07 |
sp|Q8HYJ9|FMO3_BOVIN | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Bos taurus GN=FMO3 PE=2 SV=1 | 272 | 430 | 3.0E-07 |
sp|P97501|FMO3_MOUSE | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Mus musculus GN=Fmo3 PE=1 SV=1 | 268 | 430 | 3.0E-07 |
sp|Q9LFM5|YUC4_ARATH | Probable indole-3-pyruvate monooxygenase YUCCA4 OS=Arabidopsis thaliana GN=YUC4 PE=1 SV=1 | 100 | 250 | 5.0E-07 |
sp|Q9SZY8|YUC1_ARATH | Probable indole-3-pyruvate monooxygenase YUCCA1 OS=Arabidopsis thaliana GN=YUC1 PE=1 SV=1 | 93 | 250 | 6.0E-07 |
sp|Q8K2I3|FMO2_MOUSE | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Mus musculus GN=Fmo2 PE=1 SV=3 | 287 | 388 | 8.0E-07 |
sp|Q8VZ59|YUC6_ARATH | Indole-3-pyruvate monooxygenase YUCCA6 OS=Arabidopsis thaliana GN=YUC6 PE=1 SV=1 | 2 | 250 | 1.0E-06 |
sp|O64489|YUC9_ARATH | Probable indole-3-pyruvate monooxygenase YUCCA9 OS=Arabidopsis thaliana GN=YUC9 PE=2 SV=1 | 100 | 262 | 3.0E-06 |
sp|Q8HYJ9|FMO3_BOVIN | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Bos taurus GN=FMO3 PE=2 SV=1 | 178 | 266 | 5.0E-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 |
Localizations | Signals | Cytoplasm | Nucleus | Extracellular | Cell membrane | Mitochondrion | Plastid | Endoplasmic reticulum | Lysosome vacuole | Golgi apparatus | Peroxisome |
---|---|---|---|---|---|---|---|---|---|---|---|
Cytoplasm|Nucleus | Peroxisomal targeting signal | 0.8228 | 0.5412 | 0.0519 | 0.053 | 0.4673 | 0.034 | 0.0409 | 0.198 | 0.1271 | 0.7163 |
Orthofinder run ID | 4 |
Orthogroup | 1617 |
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 | >Ophio5|5212 MGSVSPSRFHVKQVAIIGAGPSGLAAAKYLLAQQAFDHIAVFEQQQDIGGVWVPPPAESSPPPPPSTVPQTNPFR PPETPVPIAEARPHYKPAVYFPSPVYDHLRANIIGPLMQFSDEPFPSSCCVFPSLEDIRASVRRYGREVRHLVRF GQQVTRLELLQEQGRDRWHLRARDLLSGETADYVFDAVVVASGHYSLPFIPDIKNITDFHRAHPTVVTHSKHYRS PKSFLDKKVIVVGNGPSGIDIAAQINAVSKVKTLLSVKAATSPETLACIGCDEAPEIVEFLIDQRGVRFKDGSVE INVDSVVFCTGYLFSYPFLADLQAKLITNGRGVHGLYKHLFTIQHPTLVFLALPMRSVPWPMSECQAAAVATVWS NQLELPPVEEMLSWSRSLHERVGEALHVMPPGGNCQYINELHDWVMKASHLGKQPPRWSDLSGWQHLHMPEARRR FQEQGCRATTWTELGFQEALG |
Coding | >Ophio5|5212 ATGGGGTCCGTATCCCCCAGCCGCTTCCACGTGAAGCAAGTCGCCATCATCGGCGCCGGTCCCTCCGGCCTCGCT GCAGCCAAGTACCTTCTCGCCCAGCAGGCCTTCGACCACATCGCCGTCTTCGAGCAACAGCAAGATATCGGCGGC GTCTGGGTTCCTCCTCCCGCCGAATCAAGCCCCCCTCCGCCGCCCAGCACCGTGCCGCAGACGAATCCCTTTCGG CCTCCCGAAACTCCCGTCCCCATCGCCGAAGCCCGGCCCCACTACAAGCCGGCCGTGTACTTCCCGTCACCCGTC TACGACCATCTCCGCGCCAACATCATCGGTCCGCTCATGCAGTTCTCCGACGAGCCGTTCCCCTCTTCTTGCTGC GTCTTTCCGTCGTTGGAGGACATTCGGGCCTCCGTTCGCCGCTACGGCCGGGAGGTCCGTCATCTCGTCCGCTTC GGCCAGCAGGTCACCAGACTCGAGCTGCTGCAGGAGCAGGGCCGAGACCGATGGCATCTCCGAGCTCGGGATTTG CTCAGCGGCGAGACGGCTGACTATGTCTTTGATGCTGTCGTCGTCGCTAGCGGACACTATTCTTTACCCTTTATT CCGGACATCAAAAACATCACCGACTTCCATCGCGCCCACCCTACTGTCGTCACCCATTCGAAGCATTATCGCTCC CCAAAAAGCTTCCTTGACAAAAAGGTCATTGTCGTAGGCAACGGTCCCTCAGGCATCGACATTGCGGCCCAGATC AACGCCGTGTCCAAGGTCAAAACTCTCCTCTCTGTCAAAGCCGCCACTTCGCCTGAGACCCTTGCCTGCATCGGT TGCGATGAGGCTCCAGAGATAGTCGAATTTCTGATCGATCAGCGTGGCGTGCGATTTAAAGATGGAAGCGTCGAG ATCAACGTCGACTCTGTTGTCTTTTGCACGGGGTACCTCTTCAGCTACCCCTTCCTTGCCGACTTACAGGCCAAG CTCATCACCAACGGCCGCGGCGTCCACGGCCTTTACAAGCACTTATTTACCATCCAACACCCTACCTTGGTCTTT CTCGCTCTACCCATGAGATCTGTCCCTTGGCCCATGTCCGAGTGTCAAGCCGCAGCGGTCGCCACAGTTTGGTCC AATCAGCTCGAGCTGCCTCCGGTGGAGGAGATGCTAAGCTGGAGTAGAAGTTTGCATGAGAGAGTGGGTGAGGCT CTTCATGTTATGCCACCCGGCGGTAATTGTCAGTACATCAACGAGCTTCATGACTGGGTAATGAAGGCCTCGCAT CTGGGAAAACAACCTCCGCGATGGAGCGATTTGAGCGGATGGCAACATCTTCACATGCCAGAGGCACGGCGCCGC TTCCAGGAGCAAGGCTGCCGAGCGACGACTTGGACGGAGCTGGGCTTTCAAGAAGCGCTCGGA |
Transcript | >Ophio5|5212 ATGGGGTCCGTATCCCCCAGCCGCTTCCACGTGAAGCAAGTCGCCATCATCGGCGCCGGTCCCTCCGGCCTCGCT GCAGCCAAGTACCTTCTCGCCCAGCAGGCCTTCGACCACATCGCCGTCTTCGAGCAACAGCAAGATATCGGCGGC GTCTGGGTTCCTCCTCCCGCCGAATCAAGCCCCCCTCCGCCGCCCAGCACCGTGCCGCAGACGAATCCCTTTCGG CCTCCCGAAACTCCCGTCCCCATCGCCGAAGCCCGGCCCCACTACAAGCCGGCCGTGTACTTCCCGTCACCCGTC TACGACCATCTCCGCGCCAACATCATCGGTCCGCTCATGCAGTTCTCCGACGAGCCGTTCCCCTCTTCTTGCTGC GTCTTTCCGTCGTTGGAGGACATTCGGGCCTCCGTTCGCCGCTACGGCCGGGAGGTCCGTCATCTCGTCCGCTTC GGCCAGCAGGTCACCAGACTCGAGCTGCTGCAGGAGCAGGGCCGAGACCGATGGCATCTCCGAGCTCGGGATTTG CTCAGCGGCGAGACGGCTGACTATGTCTTTGATGCTGTCGTCGTCGCTAGCGGACACTATTCTTTACCCTTTATT CCGGACATCAAAAACATCACCGACTTCCATCGCGCCCACCCTACTGTCGTCACCCATTCGAAGCATTATCGCTCC CCAAAAAGCTTCCTTGACAAAAAGGTCATTGTCGTAGGCAACGGTCCCTCAGGCATCGACATTGCGGCCCAGATC AACGCCGTGTCCAAGGTCAAAACTCTCCTCTCTGTCAAAGCCGCCACTTCGCCTGAGACCCTTGCCTGCATCGGT TGCGATGAGGCTCCAGAGATAGTCGAATTTCTGATCGATCAGCGTGGCGTGCGATTTAAAGATGGAAGCGTCGAG ATCAACGTCGACTCTGTTGTCTTTTGCACGGGGTACCTCTTCAGCTACCCCTTCCTTGCCGACTTACAGGCCAAG CTCATCACCAACGGCCGCGGCGTCCACGGCCTTTACAAGCACTTATTTACCATCCAACACCCTACCTTGGTCTTT CTCGCTCTACCCATGAGATCTGTCCCTTGGCCCATGTCCGAGTGTCAAGCCGCAGCGGTCGCCACAGTTTGGTCC AATCAGCTCGAGCTGCCTCCGGTGGAGGAGATGCTAAGCTGGAGTAGAAGTTTGCATGAGAGAGTGGGTGAGGCT CTTCATGTTATGCCACCCGGCGGTAATTGTCAGTACATCAACGAGCTTCATGACTGGGTAATGAAGGCCTCGCAT CTGGGAAAACAACCTCCGCGATGGAGCGATTTGAGCGGATGGCAACATCTTCACATGCCAGAGGCACGGCGCCGC TTCCAGGAGCAAGGCTGCCGAGCGACGACTTGGACGGAGCTGGGCTTTCAAGAAGCGCTCGGATAA |
Gene | >Ophio5|5212 ATGGGGTCCGTATCCCCCAGCCGCTTCCACGTGAAGCAAGTCGCCATCATCGGCGCCGGTCCCTCCGGCCTCGCT GCAGCCAAGTACCTTCTCGCCCAGCAGGCCTTCGACCACATCGCCGTCTTCGAGCAACAGCAAGATATCGGCGGC GTCTGGGTTCCTCCTCCCGCCGAATCAAGCCCCCCTCCGCCGCCCAGCACCGTGCCGCAGACGAATCCCTTTCGG CCTCCCGAAACTCCCGTCCCCATCGCCGAAGCCCGGCCCCACTACAAGCCGGCCGTGTACTTCCCGTCACCCGTC TACGACCATCTCCGCGCCAACATCATCGGTCCGCTCATGCAGTTCTCCGACGAGCCGTTCCCCTCTTCTTGCTGC GTCTTTCCGTCGTTGGAGGACATTCGGGCCTCCGTTCGCCGCTACGGCCGGGAGGTCCGTCATCTCGTCCGCTTC GGCCAGCAGGTCACCAGACTCGAGCTGCTGCAGGAGCAGGGCCGAGACCGATGGCATCTCCGAGCTCGGGATTTG CTCAGCGGCGAGACGGCTGACTATGTCTTTGATGCTGTCGTCGTCGCTAGCGGACACTATTCTTTACCCTTTATT CCGGACATCAAAAACATCACCGACTTCCATCGCGCCCACCCTACTGTCGTCACCCATTCGAAGCATTATCGCTCC CCAAAAAGCTTCCTTGACAAAAAGGTCATTGTCGTAGGCAACGGTCCCTCAGGCATCGACATTGCGGCCCAGATC AACGCCGTGTCCAAGGTCAAAACTCTCCTCTCTGTCAAAGCCGCCACTTCGCCTGAGACCCTTGCCTGCATCGGT TGCGATGAGGCTCCAGAGATAGTCGAATTTCTGATCGATCAGCGTGGCGTGCGATTTAAAGATGGAAGCGTCGAG ATCAACGTCGACTCTGTTGTCTTTTGCACGGGGTACCTCTTCAGCTACCCCTTCCTTGCCGACTTACAGGCCAAG CTCATCACCAACGGCCGCGGCGTCCACGGCCTTTACAAGCACTTATTTACCATCCAACACCCTACCTTGGTCTTT CTCGCTCTACCCATGAGATCTGTCCCTTGGCCCATGTCCGAGTGTCAAGCCGCAGCGGTCGCCACAGTTTGGTCC AATCAGCTCGAGCTGCCTCCGGTGGAGGAGATGCTAAGCTGGAGTAGAAGTTTGCATGAGAGAGTGGGTGAGGCT CTTCATGTTATGCCACCCGGCGGTAATTGTCAGTACATCAACGAGCTTCATGACTGGGTAATGAAGGCCTCGCAT CTGGGAAAACAACCTCCGCGATGGAGCGATTTGAGCGGATGGCAACATCTTCACATGCCAGAGGCACGGCGCCGC TTCCAGGAGCAAGGCTGCCGAGCGACGACTTGGACGGAGCTGGGCTTTCAAGAAGCGCTCGGATAA |