Protein ID | Ophio5|17 |
Gene name | |
Location | scaffold_1:36282..38834 |
Strand | + |
Gene length (bp) | 2552 |
Transcript length (bp) | 2259 |
Coding sequence length (bp) | 2256 |
Protein length (aa) | 752 |
PFAM Domain ID | Short name | Long name | E-value | Start | End |
---|---|---|---|---|---|
PF19834 | DUF6314 | Family of unknown function (DUF6314) | 5.6E-31 | 571 | 746 |
PF00743 | FMO-like | Flavin-binding monooxygenase-like | 4.4E-14 | 10 | 216 |
PF13454 | NAD_binding_9 | FAD-NAD(P)-binding | 2.6E-08 | 14 | 158 |
PF07992 | Pyr_redox_2 | Pyridine nucleotide-disulphide oxidoreductase | 6.3E-10 | 10 | 218 |
PF13450 | NAD_binding_8 | NAD(P)-binding Rossmann-like domain | 4.8E-07 | 14 | 59 |
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 | 7 | 508 | 5.0E-18 |
sp|P97501|FMO3_MOUSE | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Mus musculus GN=Fmo3 PE=1 SV=1 | 10 | 508 | 1.0E-16 |
sp|Q9EQ76|FMO3_RAT | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Rattus norvegicus GN=Fmo3 PE=1 SV=1 | 10 | 508 | 5.0E-16 |
sp|P49109|FMO5_CAVPO | Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Cavia porcellus GN=FMO5 PE=2 SV=2 | 7 | 551 | 1.0E-14 |
sp|Q8SPQ7|FMO3_MACMU | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Macaca mulatta GN=FMO3 PE=2 SV=3 | 10 | 431 | 1.0E-14 |
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 | 7 | 508 | 5.0E-18 |
sp|P97501|FMO3_MOUSE | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Mus musculus GN=Fmo3 PE=1 SV=1 | 10 | 508 | 1.0E-16 |
sp|Q9EQ76|FMO3_RAT | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Rattus norvegicus GN=Fmo3 PE=1 SV=1 | 10 | 508 | 5.0E-16 |
sp|P49109|FMO5_CAVPO | Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Cavia porcellus GN=FMO5 PE=2 SV=2 | 7 | 551 | 1.0E-14 |
sp|Q8SPQ7|FMO3_MACMU | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Macaca mulatta GN=FMO3 PE=2 SV=3 | 10 | 431 | 1.0E-14 |
sp|Q95LA1|FMO3_CANLF | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Canis lupus familiaris GN=FMO3 PE=2 SV=3 | 10 | 504 | 3.0E-14 |
sp|P97872|FMO5_MOUSE | Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Mus musculus GN=Fmo5 PE=1 SV=4 | 7 | 559 | 4.0E-14 |
sp|Q6IRI9|FMO2_RAT | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Rattus norvegicus GN=Fmo2 PE=2 SV=3 | 9 | 508 | 5.0E-14 |
sp|Q99518|FMO2_HUMAN | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Homo sapiens GN=FMO2 PE=1 SV=4 | 10 | 508 | 6.0E-14 |
sp|P36366|FMO2_CAVPO | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Cavia porcellus GN=FMO2 PE=2 SV=2 | 10 | 218 | 6.0E-14 |
sp|Q8K2I3|FMO2_MOUSE | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Mus musculus GN=Fmo2 PE=1 SV=3 | 10 | 508 | 1.0E-13 |
sp|Q8HZ70|FMO2_PANTR | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Pan troglodytes GN=FMO2 PE=3 SV=3 | 10 | 508 | 1.0E-13 |
sp|P31512|FMO4_HUMAN | Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Homo sapiens GN=FMO4 PE=1 SV=3 | 10 | 503 | 2.0E-13 |
sp|P17635|FMO2_RABIT | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Oryctolagus cuniculus GN=FMO2 PE=1 SV=3 | 10 | 223 | 2.0E-13 |
sp|Q8HZ69|FMO2_GORGO | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Gorilla gorilla gorilla GN=FMO2 PE=3 SV=3 | 10 | 218 | 3.0E-13 |
sp|Q8K4C0|FMO5_RAT | Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Rattus norvegicus GN=Fmo5 PE=1 SV=3 | 7 | 508 | 4.0E-13 |
sp|Q28505|FMO2_MACMU | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Macaca mulatta GN=FMO2 PE=2 SV=2 | 10 | 212 | 6.0E-13 |
sp|Q5REK0|FMO2_PONAB | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Pongo abelii GN=FMO2 PE=2 SV=3 | 10 | 218 | 1.0E-12 |
sp|Q9SXE1|GSOX3_ARATH | Flavin-containing monooxygenase FMO GS-OX3 OS=Arabidopsis thaliana GN=FMOGS-OX3 PE=2 SV=1 | 7 | 226 | 2.0E-12 |
sp|Q8K4B7|FMO4_RAT | Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Rattus norvegicus GN=Fmo4 PE=2 SV=3 | 10 | 383 | 4.0E-12 |
sp|P36367|FMO4_RABIT | Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Oryctolagus cuniculus GN=FMO4 PE=2 SV=2 | 10 | 223 | 5.0E-12 |
sp|Q8HYJ9|FMO3_BOVIN | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Bos taurus GN=FMO3 PE=2 SV=1 | 9 | 504 | 6.0E-12 |
sp|Q95LA2|FMO1_CANLF | Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Canis lupus familiaris GN=FMO1 PE=2 SV=3 | 10 | 212 | 1.0E-11 |
sp|O60774|FMO6_HUMAN | Putative dimethylaniline monooxygenase [N-oxide-forming] 6 OS=Homo sapiens GN=FMO6P PE=5 SV=1 | 9 | 212 | 1.0E-11 |
sp|Q9LMA1|FMO1_ARATH | Probable flavin-containing monooxygenase 1 OS=Arabidopsis thaliana GN=FMO1 PE=2 SV=1 | 7 | 431 | 3.0E-11 |
sp|Q8VHG0|FMO4_MOUSE | Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Mus musculus GN=Fmo4 PE=1 SV=3 | 10 | 223 | 6.0E-11 |
sp|P50285|FMO1_MOUSE | Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Mus musculus GN=Fmo1 PE=1 SV=1 | 9 | 220 | 6.0E-11 |
sp|Q9SS04|GSOX1_ARATH | Flavin-containing monooxygenase FMO GS-OX1 OS=Arabidopsis thaliana GN=FMOGS-OX1 PE=2 SV=1 | 7 | 223 | 3.0E-10 |
sp|P38866|FMO1_YEAST | Thiol-specific monooxygenase OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FMO1 PE=1 SV=2 | 37 | 227 | 7.0E-10 |
sp|P49326|FMO5_HUMAN | Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Homo sapiens GN=FMO5 PE=1 SV=2 | 7 | 157 | 2.0E-09 |
sp|Q7YS44|FMO3_PANTR | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Pan troglodytes GN=FMO3 PE=3 SV=3 | 10 | 447 | 3.0E-09 |
sp|O64489|YUC9_ARATH | Probable indole-3-pyruvate monooxygenase YUCCA9 OS=Arabidopsis thaliana GN=YUC9 PE=2 SV=1 | 14 | 249 | 4.0E-09 |
sp|P32417|FMO3_RABIT | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Oryctolagus cuniculus GN=FMO3 PE=1 SV=3 | 10 | 502 | 8.0E-09 |
sp|P31513|FMO3_HUMAN | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Homo sapiens GN=FMO3 PE=1 SV=5 | 10 | 447 | 2.0E-08 |
sp|Q9SVU0|YUC8_ARATH | Probable indole-3-pyruvate monooxygenase YUCCA8 OS=Arabidopsis thaliana GN=YUC8 PE=2 SV=1 | 14 | 221 | 4.0E-08 |
sp|Q9FWW6|GSXL1_ARATH | Flavin-containing monooxygenase FMO GS-OX-like 1 OS=Arabidopsis thaliana GN=At1g12160 PE=2 SV=1 | 10 | 221 | 2.0E-07 |
sp|Q9FWW3|GSXL6_ARATH | Flavin-containing monooxygenase FMO GS-OX-like 6 OS=Arabidopsis thaliana GN=At1g12130 PE=2 SV=1 | 7 | 216 | 2.0E-06 |
sp|Q94K43|GSOX2_ARATH | Flavin-containing monooxygenase FMO GS-OX2 OS=Arabidopsis thaliana GN=FMOGS-OX2 PE=2 SV=1 | 5 | 223 | 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 | Nuclear localization signal | 0.6815 | 0.6154 | 0.0763 | 0.057 | 0.3322 | 0.0415 | 0.0526 | 0.095 | 0.1081 | 0.1191 |
Orthofinder run ID | 4 |
Orthogroup | 1643 |
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|17 MAQGKPMTTKSVCVVGAGPSGLVAAKTLLHNAPKEAFRVTVLDRQGAIGGLWPSSVADRRRQIDPLMLANQSRHT MHFSDLAWDVDAPPVPRAFELGKYLHRYLDRYLTPHPAFELRLQTQLVRAKPSPGGAWELLLEAGGRDETAVFDY LLVASGHFGKPMPLPDSLALPQAVPVIHSCQYRDLKSLLGSRPPAHGKVLVVGGQMSGVEIAGTIAAHLSSAAHS PGETLIPGIDGYSVHHIVQRPSWVFPIFTTPEPEAAAPHFLPLDFSRFNSNNRPLPLANTQGHIGREAAQAVHAH LHGSLGGDQSVFSPLLRVDDEARTEPPYLVVSDWYCDFVRSGLITLSKGKLESLQASTAIVSPDGAEVHNVAAVV LANGFDPSPSLNFLPEDILRKLHHSSRHPSQPLALSFHGTHHPEVPGLGFVGFYRSPYWGVMQMQARFLTQLWSE PSAHPKALQRKLAIDDSVGHTLALRDDARVSQFPMGDYPWLMQEFAEALSIEPQTVSLERLPLLPHNGLPLDMLT PSRYVSPTDDGPARDEAAKSILNTVDATATSLTSPKFVARAVFRSLLGSWKLDRSLISRLPSHPSGHFSGTAKFL LREATADGMRCVGEASTDDEVVSGGPAMEYLYVEEGEFKTDTGLAFRATRRYVWRYDERRDVLSAWFAKTDDPSR ADYLFHEMEFQPRQGGSDDGWKATAGHLCIDDYYDVRYNFAFKAVNLGGWNIEYTVKGPKKDYSIRGTYSRLADG RR |
Coding | >Ophio5|17 ATGGCACAAGGAAAGCCAATGACAACAAAATCCGTCTGCGTCGTCGGCGCCGGCCCCTCTGGTCTCGTGGCCGCC AAGACGCTCCTCCACAATGCGCCCAAGGAAGCTTTTCGTGTCACCGTTCTGGACCGGCAGGGCGCCATTGGAGGC TTGTGGCCTTCGTCGGTCGCCGACCGTCGACGTCAGATCGACCCCCTGATGCTCGCCAACCAGAGCCGGCACACG ATGCACTTTAGCGACCTGGCCTGGGATGTCGACGCACCGCCGGTCCCTCGCGCCTTCGAGCTTGGCAAATATCTG CATCGCTATCTTGACCGCTACTTGACGCCACATCCGGCTTTTGAACTGCGGCTGCAGACGCAACTGGTACGCGCC AAGCCGAGCCCTGGTGGTGCCTGGGAATTGCTCCTCGAAGCCGGCGGCAGAGACGAGACGGCCGTCTTTGACTAT CTCTTGGTCGCTTCAGGGCACTTCGGGAAGCCCATGCCGCTGCCAGATTCTCTGGCGCTGCCGCAGGCTGTTCCC GTCATCCACAGCTGCCAATATCGCGATCTGAAGAGCTTGCTGGGCAGCCGCCCGCCCGCACACGGCAAAGTGCTT GTTGTCGGAGGACAGATGTCTGGCGTCGAGATCGCCGGCACCATCGCAGCTCACCTGTCCTCGGCTGCTCACTCG CCCGGCGAGACTCTGATTCCCGGCATCGACGGATACTCGGTTCACCACATCGTTCAACGGCCGTCATGGGTCTTT CCCATCTTCACCACCCCCGAGCCCGAGGCCGCGGCACCGCACTTTTTACCCCTGGACTTTTCACGCTTCAACTCC AACAATCGGCCCCTGCCGCTGGCCAACACACAGGGCCACATTGGGCGAGAAGCCGCCCAGGCTGTTCACGCTCAT TTGCATGGCAGCCTGGGCGGCGATCAGTCCGTCTTCTCCCCGCTCTTGCGCGTCGACGACGAGGCTAGGACGGAA CCACCGTATCTGGTTGTCAGCGACTGGTATTGCGACTTTGTGCGATCCGGGCTCATCACCCTTTCTAAAGGCAAA CTCGAGTCGCTGCAGGCATCCACGGCCATCGTCTCTCCAGACGGTGCAGAGGTGCACAATGTCGCCGCCGTCGTG CTTGCCAACGGCTTCGATCCGTCACCTAGCCTGAACTTCCTCCCGGAAGACATACTTCGCAAGCTGCACCACTCA TCTCGCCATCCAAGCCAGCCACTGGCCCTGTCCTTCCACGGGACGCATCACCCGGAAGTCCCCGGGCTGGGATTC GTCGGCTTCTATCGCTCACCTTACTGGGGTGTCATGCAGATGCAGGCGAGATTCCTTACTCAGCTCTGGTCAGAG CCGAGCGCGCATCCCAAGGCGTTACAGCGCAAGCTCGCAATCGACGACTCCGTCGGACACACGCTGGCCCTGCGG GATGACGCCCGTGTTTCGCAGTTCCCCATGGGCGACTATCCCTGGCTCATGCAAGAGTTTGCCGAGGCGCTCTCC ATCGAGCCCCAGACTGTCTCGCTCGAGAGACTACCGCTCTTACCTCACAATGGCCTGCCCCTGGATATGCTGACG CCCTCTCGATATGTCTCGCCTACGGATGATGGCCCGGCCAGAGACGAGGCTGCGAAATCAATCCTGAACACGGTT GACGCCACAGCCACCAGCCTTACATCGCCCAAATTTGTCGCTCGCGCTGTCTTCCGCAGCCTGCTAGGTAGCTGG AAGCTGGACCGTAGTCTTATCAGCAGGCTGCCATCACATCCTAGCGGACACTTCAGCGGCACCGCTAAATTCCTA CTGCGTGAAGCGACGGCCGACGGCATGCGCTGTGTGGGCGAAGCTTCGACGGACGACGAGGTTGTTTCGGGTGGA CCGGCTATGGAGTATCTTTACGTCGAAGAAGGCGAATTCAAGACGGATACAGGACTTGCATTCCGAGCAACAAGG CGATACGTCTGGCGCTACGATGAGCGGAGAGATGTGCTGAGCGCCTGGTTCGCCAAGACAGACGATCCCAGTCGA GCCGACTACCTCTTCCACGAGATGGAGTTCCAGCCGCGCCAGGGAGGCAGCGACGACGGCTGGAAGGCCACCGCG GGCCATCTCTGCATCGACGACTACTATGATGTCCGCTACAATTTTGCCTTTAAAGCCGTGAATCTCGGTGGGTGG AATATAGAGTACACGGTCAAGGGGCCGAAGAAGGACTATTCAATCCGCGGGACGTACAGCCGGTTGGCCGATGGA CGAAGG |
Transcript | >Ophio5|17 ATGGCACAAGGAAAGCCAATGACAACAAAATCCGTCTGCGTCGTCGGCGCCGGCCCCTCTGGTCTCGTGGCCGCC AAGACGCTCCTCCACAATGCGCCCAAGGAAGCTTTTCGTGTCACCGTTCTGGACCGGCAGGGCGCCATTGGAGGC TTGTGGCCTTCGTCGGTCGCCGACCGTCGACGTCAGATCGACCCCCTGATGCTCGCCAACCAGAGCCGGCACACG ATGCACTTTAGCGACCTGGCCTGGGATGTCGACGCACCGCCGGTCCCTCGCGCCTTCGAGCTTGGCAAATATCTG CATCGCTATCTTGACCGCTACTTGACGCCACATCCGGCTTTTGAACTGCGGCTGCAGACGCAACTGGTACGCGCC AAGCCGAGCCCTGGTGGTGCCTGGGAATTGCTCCTCGAAGCCGGCGGCAGAGACGAGACGGCCGTCTTTGACTAT CTCTTGGTCGCTTCAGGGCACTTCGGGAAGCCCATGCCGCTGCCAGATTCTCTGGCGCTGCCGCAGGCTGTTCCC GTCATCCACAGCTGCCAATATCGCGATCTGAAGAGCTTGCTGGGCAGCCGCCCGCCCGCACACGGCAAAGTGCTT GTTGTCGGAGGACAGATGTCTGGCGTCGAGATCGCCGGCACCATCGCAGCTCACCTGTCCTCGGCTGCTCACTCG CCCGGCGAGACTCTGATTCCCGGCATCGACGGATACTCGGTTCACCACATCGTTCAACGGCCGTCATGGGTCTTT CCCATCTTCACCACCCCCGAGCCCGAGGCCGCGGCACCGCACTTTTTACCCCTGGACTTTTCACGCTTCAACTCC AACAATCGGCCCCTGCCGCTGGCCAACACACAGGGCCACATTGGGCGAGAAGCCGCCCAGGCTGTTCACGCTCAT TTGCATGGCAGCCTGGGCGGCGATCAGTCCGTCTTCTCCCCGCTCTTGCGCGTCGACGACGAGGCTAGGACGGAA CCACCGTATCTGGTTGTCAGCGACTGGTATTGCGACTTTGTGCGATCCGGGCTCATCACCCTTTCTAAAGGCAAA CTCGAGTCGCTGCAGGCATCCACGGCCATCGTCTCTCCAGACGGTGCAGAGGTGCACAATGTCGCCGCCGTCGTG CTTGCCAACGGCTTCGATCCGTCACCTAGCCTGAACTTCCTCCCGGAAGACATACTTCGCAAGCTGCACCACTCA TCTCGCCATCCAAGCCAGCCACTGGCCCTGTCCTTCCACGGGACGCATCACCCGGAAGTCCCCGGGCTGGGATTC GTCGGCTTCTATCGCTCACCTTACTGGGGTGTCATGCAGATGCAGGCGAGATTCCTTACTCAGCTCTGGTCAGAG CCGAGCGCGCATCCCAAGGCGTTACAGCGCAAGCTCGCAATCGACGACTCCGTCGGACACACGCTGGCCCTGCGG GATGACGCCCGTGTTTCGCAGTTCCCCATGGGCGACTATCCCTGGCTCATGCAAGAGTTTGCCGAGGCGCTCTCC ATCGAGCCCCAGACTGTCTCGCTCGAGAGACTACCGCTCTTACCTCACAATGGCCTGCCCCTGGATATGCTGACG CCCTCTCGATATGTCTCGCCTACGGATGATGGCCCGGCCAGAGACGAGGCTGCGAAATCAATCCTGAACACGGTT GACGCCACAGCCACCAGCCTTACATCGCCCAAATTTGTCGCTCGCGCTGTCTTCCGCAGCCTGCTAGGTAGCTGG AAGCTGGACCGTAGTCTTATCAGCAGGCTGCCATCACATCCTAGCGGACACTTCAGCGGCACCGCTAAATTCCTA CTGCGTGAAGCGACGGCCGACGGCATGCGCTGTGTGGGCGAAGCTTCGACGGACGACGAGGTTGTTTCGGGTGGA CCGGCTATGGAGTATCTTTACGTCGAAGAAGGCGAATTCAAGACGGATACAGGACTTGCATTCCGAGCAACAAGG CGATACGTCTGGCGCTACGATGAGCGGAGAGATGTGCTGAGCGCCTGGTTCGCCAAGACAGACGATCCCAGTCGA GCCGACTACCTCTTCCACGAGATGGAGTTCCAGCCGCGCCAGGGAGGCAGCGACGACGGCTGGAAGGCCACCGCG GGCCATCTCTGCATCGACGACTACTATGATGTCCGCTACAATTTTGCCTTTAAAGCCGTGAATCTCGGTGGGTGG AATATAGAGTACACGGTCAAGGGGCCGAAGAAGGACTATTCAATCCGCGGGACGTACAGCCGGTTGGCCGATGGA CGAAGGTGA |
Gene | >Ophio5|17 ATGGCACAAGGGTAAGTCTCCTCATAACTACCTAGCTACCGATCGACAGCCCCCCGCCGCACCCGTGGGGTTTCT CCACCATTGTCATTGGCGATGGCCTCAAATAAGCTCGTGCTCTTGCTCTTTGTCTAACTCTGAGGCAGAAAGCCA ATGACAACAAAATCCGTCTGCGTCGTCGGTGAGTCCATGAGTGTCTTACTTCTGTCTGACCTCGTCATGACGTCT CTCGACCCCTGTGTTCGCTCATCGTCGTCGTTGTGTCCTTTTCCTCAGGCGCCGGCCCCTCTGGTCTCGTGGCCG CCAAGACGCTCCTCCACAATGCGCCCAAGGAAGCTTTTCGTGTCACCGTTCTGGACCGGCAGGGCGCCATTGGAG GCTTGTGGCCTTCGTCGGTCGCCGACCGTCGACGTCAGATCGACCCCCTGATGCTCGCCAACCAGAGCCGGCACA CGATGCACTTTAGCGACCTGGCCTGGGATGTCGACGCACCGCCGGTCCCTCGCGCCTTCGAGCTTGGCAAATATC TGCATCGCTATCTTGACCGCTACTTGACGCCACATCCGGCTTTTGAACTGCGGCTGCAGACGCAACTGGTACGCG CCAAGCCGAGCCCTGGTGGTGCCTGGGAATTGCTCCTCGAAGCCGGCGGCAGAGACGAGACGGCCGTCTTTGACT ATCTCTTGGTCGCTTCAGGGCACTTCGGGAAGCCCATGCCGCTGCCAGATTCTCTGGCGCTGCCGCAGGCTGTTC CCGTCATCCACAGCTGCCAATATCGCGATCTGAAGAGCTTGCTGGGCAGCCGCCCGCCCGCACACGGCAAAGTGC TTGTTGTCGGAGGACAGATGTCTGGCGTCGAGATCGCCGGCACCATCGCAGCTCACCTGTCCTCGGCTGCTCACT CGCCCGGCGAGACTCTGATTCCCGGCATCGACGGATACTCGGTTCACCACATCGTTCAACGGCCGTCATGGGTCT TTCCCATCTTCACCACCCCCGAGGTGATGCATTCCTGTTATTCGCTGCTGGCCACCTAGGTAACGTTCTAGATAC TGACCAAGGAGTAGCCCGAGGCCGCGGCACCGCACTTTTTACCCCTGGACTTTTCACGCTTCAACTCCAACAATC GGCCCCTGCCGCTGGCCAACACACAGGGCCACATTGGGCGAGAAGCCGCCCAGGCTGTTCACGCTCATTTGCATG GCAGCCTGGGCGGCGATCAGTCCGTCTTCTCCCCGCTCTTGCGCGTCGACGACGAGGCTAGGACGGAACCACCGT ATCTGGTTGTCAGCGACTGGTATTGCGACTTTGTGCGATCCGGGCTCATCACCCTTTCTAAAGGCAAACTCGAGT CGCTGCAGGCATCCACGGCCATCGTCTCTCCAGACGGTGCAGAGGTGCACAATGTCGCCGCCGTCGTGCTTGCCA ACGGCTTCGATCCGTCACCTAGCCTGAACTTCCTCCCGGAAGACATACTTCGCAAGCTGCACCACTCATCTCGCC ATCCAAGCCAGCCACTGGCCCTGTCCTTCCACGGGACGCATCACCCGGAAGTCCCCGGGCTGGGATTCGTCGGCT TCTATCGCTCACCTTACTGGGGTGTCATGCAGATGCAGGCGAGATTCCTTACTCAGCTCTGGTCAGAGCCGAGCG CGCATCCCAAGGCGTTACAGCGCAAGCTCGCAATCGACGACTCCGTCGGACACACGCTGGCCCTGCGGGATGACG CCCGTGTTTCGCAGTTCCCCATGGGCGACTATCCCTGGCTCATGCAAGAGTTTGCCGAGGCGCTCTCCATCGAGC CCCAGACTGTCTCGCTCGAGAGACTACCGCTCTTACCTCACAATGGCCTGCCCCTGGATATGCTGACGCCCTCTC GATATGTCTCGCCTACGGATGATGGCCCGGCCAGAGACGAGGCTGCGAAATCAATCCTGAACACGGTTGACGCCA CAGCCACCAGCCTTACATCGCCCAAATTTGTCGCTCGCGCTGTCTTCCGCAGCCTGCTAGGTAGCTGGAAGCTGG ACCGTAGTCTTATCAGCAGGCTGCCATCACATCCTAGCGGACACTTCAGCGGCACCGCTAAATTCCTACTGCGTG AAGCGACGGCCGACGGCATGCGCTGTGTGGGCGAAGCTTCGACGGACGACGAGGTTGTTTCGGGTGGACCGGCTA TGGAGTATCTTTACGTCGAAGAAGGCGAATTCAAGACGGATACAGGACTTGCATTCCGAGCAACAAGGCGATACG TCTGGCGCTACGATGAGCGGAGAGATGTGCTGAGCGCCTGGTTCGCCAAGACAGACGATCCCAGTCGAGCCGACT ACCTCTTCCACGAGATGGAGTTCCAGCCGCGCCAGGGAGGCAGCGACGACGGCTGGAAGGCCACCGCGGGCCATC TCTGCATCGACGACTACTATGATGTCCGCTACAATTTTGCCTTTAAAGCCGTGAATCTCGGTGGGTGGAATATAG AGTACACGGTCAAGGGGCCGAAGAAGGACTATTCAATCCGCGGGACGTACAGCCGGTTGGCCGATGGACGAAGGT GA |