Protein ID | OphauG2|2786 |
Gene name | |
Location | Contig_206:2905..4874 |
Strand | - |
Gene length (bp) | 1969 |
Transcript length (bp) | 1797 |
Coding sequence length (bp) | 1797 |
Protein length (aa) | 599 |
PFAM Domain ID | Short name | Long name | E-value | Start | End |
---|---|---|---|---|---|
PF00743 | FMO-like | Flavin-binding monooxygenase-like | 6.0E-18 | 3 | 213 |
PF00743 | FMO-like | Flavin-binding monooxygenase-like | 1.3E-05 | 369 | 537 |
PF13738 | Pyr_redox_3 | Pyridine nucleotide-disulphide oxidoreductase | 2.5E-11 | 6 | 210 |
PF07992 | Pyr_redox_2 | Pyridine nucleotide-disulphide oxidoreductase | 2.9E-11 | 3 | 214 |
PF13434 | Lys_Orn_oxgnase | L-lysine 6-monooxygenase/L-ornithine 5-monooxygenase | 2.6E-06 | 84 | 211 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|Q8HZ69|FMO2_GORGO | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Gorilla gorilla gorilla GN=FMO2 PE=3 SV=3 | 3 | 562 | 3.0E-27 |
sp|Q5REK0|FMO2_PONAB | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Pongo abelii GN=FMO2 PE=2 SV=3 | 3 | 562 | 2.0E-26 |
sp|Q8HZ70|FMO2_PANTR | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Pan troglodytes GN=FMO2 PE=3 SV=3 | 3 | 562 | 2.0E-25 |
sp|Q28505|FMO2_MACMU | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Macaca mulatta GN=FMO2 PE=2 SV=2 | 3 | 550 | 6.0E-25 |
sp|Q99518|FMO2_HUMAN | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Homo sapiens GN=FMO2 PE=1 SV=4 | 3 | 502 | 1.0E-22 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|Q8HZ69|FMO2_GORGO | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Gorilla gorilla gorilla GN=FMO2 PE=3 SV=3 | 3 | 562 | 3.0E-27 |
sp|Q5REK0|FMO2_PONAB | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Pongo abelii GN=FMO2 PE=2 SV=3 | 3 | 562 | 2.0E-26 |
sp|Q8HZ70|FMO2_PANTR | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Pan troglodytes GN=FMO2 PE=3 SV=3 | 3 | 562 | 2.0E-25 |
sp|Q28505|FMO2_MACMU | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Macaca mulatta GN=FMO2 PE=2 SV=2 | 3 | 550 | 6.0E-25 |
sp|Q99518|FMO2_HUMAN | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Homo sapiens GN=FMO2 PE=1 SV=4 | 3 | 502 | 1.0E-22 |
sp|P17635|FMO2_RABIT | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Oryctolagus cuniculus GN=FMO2 PE=1 SV=3 | 3 | 550 | 2.0E-22 |
sp|P36366|FMO2_CAVPO | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Cavia porcellus GN=FMO2 PE=2 SV=2 | 3 | 536 | 2.0E-21 |
sp|Q8K2I3|FMO2_MOUSE | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Mus musculus GN=Fmo2 PE=1 SV=3 | 3 | 536 | 6.0E-21 |
sp|Q6IRI9|FMO2_RAT | Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Rattus norvegicus GN=Fmo2 PE=2 SV=3 | 3 | 536 | 5.0E-19 |
sp|P31512|FMO4_HUMAN | Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Homo sapiens GN=FMO4 PE=1 SV=3 | 3 | 211 | 1.0E-15 |
sp|Q9SVU0|YUC8_ARATH | Probable indole-3-pyruvate monooxygenase YUCCA8 OS=Arabidopsis thaliana GN=YUC8 PE=2 SV=1 | 6 | 217 | 6.0E-15 |
sp|P49109|FMO5_CAVPO | Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Cavia porcellus GN=FMO5 PE=2 SV=2 | 3 | 527 | 3.0E-14 |
sp|Q9LKC0|YUC5_ARATH | Probable indole-3-pyruvate monooxygenase YUCCA5 OS=Arabidopsis thaliana GN=YUC5 PE=2 SV=1 | 6 | 219 | 8.0E-14 |
sp|Q04799|FMO5_RABIT | Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Oryctolagus cuniculus GN=FMO5 PE=1 SV=2 | 3 | 443 | 1.0E-13 |
sp|O64489|YUC9_ARATH | Probable indole-3-pyruvate monooxygenase YUCCA9 OS=Arabidopsis thaliana GN=YUC9 PE=2 SV=1 | 6 | 219 | 3.0E-13 |
sp|O23024|YUC3_ARATH | Probable indole-3-pyruvate monooxygenase YUCCA3 OS=Arabidopsis thaliana GN=YUC3 PE=2 SV=1 | 6 | 219 | 4.0E-13 |
sp|O60774|FMO6_HUMAN | Putative dimethylaniline monooxygenase [N-oxide-forming] 6 OS=Homo sapiens GN=FMO6P PE=5 SV=1 | 3 | 193 | 5.0E-13 |
sp|P36367|FMO4_RABIT | Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Oryctolagus cuniculus GN=FMO4 PE=2 SV=2 | 3 | 211 | 5.0E-13 |
sp|Q95LA2|FMO1_CANLF | Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Canis lupus familiaris GN=FMO1 PE=2 SV=3 | 3 | 193 | 5.0E-13 |
sp|Q9SVQ1|YUC2_ARATH | Indole-3-pyruvate monooxygenase YUCCA2 OS=Arabidopsis thaliana GN=YUC2 PE=1 SV=1 | 6 | 193 | 8.0E-13 |
sp|P16549|FMO1_PIG | Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Sus scrofa GN=FMO1 PE=1 SV=3 | 3 | 196 | 9.0E-13 |
sp|O49312|YUC7_ARATH | Probable indole-3-pyruvate monooxygenase YUCCA7 OS=Arabidopsis thaliana GN=YUC7 PE=2 SV=1 | 6 | 217 | 2.0E-12 |
sp|P50285|FMO1_MOUSE | Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Mus musculus GN=Fmo1 PE=1 SV=1 | 3 | 196 | 4.0E-12 |
sp|Q01740|FMO1_HUMAN | Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Homo sapiens GN=FMO1 PE=2 SV=3 | 3 | 196 | 4.0E-12 |
sp|Q9EQ76|FMO3_RAT | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Rattus norvegicus GN=Fmo3 PE=1 SV=1 | 3 | 193 | 4.0E-12 |
sp|Q9FVQ0|YUC10_ARATH | Probable indole-3-pyruvate monooxygenase YUCCA10 OS=Arabidopsis thaliana GN=YUC10 PE=2 SV=1 | 4 | 193 | 4.0E-12 |
sp|P36365|FMO1_RAT | Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Rattus norvegicus GN=Fmo1 PE=1 SV=2 | 3 | 196 | 6.0E-12 |
sp|P97501|FMO3_MOUSE | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Mus musculus GN=Fmo3 PE=1 SV=1 | 3 | 211 | 7.0E-12 |
sp|Q8VZ59|YUC6_ARATH | Indole-3-pyruvate monooxygenase YUCCA6 OS=Arabidopsis thaliana GN=YUC6 PE=1 SV=1 | 6 | 193 | 8.0E-12 |
sp|Q8K4B7|FMO4_RAT | Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Rattus norvegicus GN=Fmo4 PE=2 SV=3 | 3 | 211 | 9.0E-12 |
sp|P17636|FMO1_RABIT | Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Oryctolagus cuniculus GN=FMO1 PE=1 SV=3 | 3 | 193 | 3.0E-11 |
sp|Q8MP06|SNO1_TYRJA | Senecionine N-oxygenase OS=Tyria jacobaeae GN=sno1 PE=1 SV=1 | 3 | 192 | 5.0E-11 |
sp|Q8SPQ7|FMO3_MACMU | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Macaca mulatta GN=FMO3 PE=2 SV=3 | 3 | 211 | 6.0E-11 |
sp|Q8K4C0|FMO5_RAT | Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Rattus norvegicus GN=Fmo5 PE=1 SV=3 | 3 | 211 | 1.0E-10 |
sp|Q9LFM5|YUC4_ARATH | Probable indole-3-pyruvate monooxygenase YUCCA4 OS=Arabidopsis thaliana GN=YUC4 PE=1 SV=1 | 6 | 193 | 1.0E-09 |
sp|Q9LPL3|YUC11_ARATH | Probable indole-3-pyruvate monooxygenase YUCCA11 OS=Arabidopsis thaliana GN=YUC11 PE=2 SV=1 | 4 | 210 | 2.0E-09 |
sp|P97872|FMO5_MOUSE | Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Mus musculus GN=Fmo5 PE=1 SV=4 | 3 | 211 | 2.0E-08 |
sp|Q95LA1|FMO3_CANLF | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Canis lupus familiaris GN=FMO3 PE=2 SV=3 | 3 | 211 | 3.0E-08 |
sp|Q9FKE7|FMO2_ARATH | Putative flavin-containing monooxygenase 2 OS=Arabidopsis thaliana GN=FMO2 PE=3 SV=2 | 3 | 193 | 3.0E-08 |
sp|P49326|FMO5_HUMAN | Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Homo sapiens GN=FMO5 PE=1 SV=2 | 3 | 211 | 6.0E-08 |
sp|Q5L2G3|CZCO_GEOKA | Uncharacterized oxidoreductase CzcO-like OS=Geobacillus kaustophilus (strain HTA426) GN=GK0582 PE=4 SV=1 | 1 | 213 | 9.0E-08 |
sp|Q9SXD5|GSXL3_ARATH | Flavin-containing monooxygenase FMO GS-OX-like 3 OS=Arabidopsis thaliana GN=At1g62620 PE=2 SV=2 | 4 | 193 | 3.0E-07 |
sp|Q9C8U0|GSXL5_ARATH | Flavin-containing monooxygenase FMO GS-OX-like 5 OS=Arabidopsis thaliana GN=At1g63370 PE=2 SV=2 | 4 | 196 | 3.0E-07 |
sp|Q9SXE1|GSOX3_ARATH | Flavin-containing monooxygenase FMO GS-OX3 OS=Arabidopsis thaliana GN=FMOGS-OX3 PE=2 SV=1 | 4 | 193 | 5.0E-07 |
sp|Q9LMA1|FMO1_ARATH | Probable flavin-containing monooxygenase 1 OS=Arabidopsis thaliana GN=FMO1 PE=2 SV=1 | 3 | 193 | 1.0E-06 |
sp|P32417|FMO3_RABIT | Dimethylaniline monooxygenase [N-oxide-forming] 3 OS=Oryctolagus cuniculus GN=FMO3 PE=1 SV=3 | 3 | 218 | 3.0E-06 |
GO Term | Description | Terminal node |
---|---|---|
GO:0016491 | oxidoreductase activity | Yes |
GO:0004499 | N,N-dimethylaniline monooxygenase activity | Yes |
GO:0050661 | NADP binding | Yes |
GO:0050660 | flavin adenine dinucleotide binding | Yes |
GO:1901265 | nucleoside phosphate binding | No |
GO:0003674 | molecular_function | 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:0097159 | organic cyclic compound binding | No |
GO:0043167 | ion binding | No |
GO:0004497 | monooxygenase activity | No |
GO:0005488 | binding | No |
GO:0043168 | anion binding | No |
GO:0036094 | small molecule binding | No |
GO:0003824 | catalytic activity | No |
GO:0016705 | oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen | No |
GO:1901363 | heterocyclic compound binding | No |
GO:0000166 | nucleotide binding | No |
SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
---|---|---|
No | 1 - 11 | 0.45 |
Domain # | Start | End | Length |
---|---|---|---|
1 | 552 | 574 | 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 | >OphauG2|2786 MLKVAVIGGGPAGLATLKFLATAHRFFPIPRIEARLFEAEDQIGGTFVHRIYEDAELVSSKYLTAFSDFRLPLDA PDFVTPQVYVQYLVDYVARFELEPMIECQAKVTRVRRGEGGLGHVVQVSKPMGQGFDYVCDAVAICSGINVNPMM PKIKGIDRVATVLHSSKLKSRQQFGQGTHVVVCGAGETGMDIAHLAVTSPTASVTLCHRAGFFCAPKIIPTPVHR SQKAGARPNKPVDASVASLFDTAYAHPILQRSQLLWTAYDQWVKKMHLVVSGTEEGPDQWVGHMSRERKHLDSIF LCKSDKALPYISEGHRSQSLWNRVRSWLLNVPIKKTFGRRIQVRQWPTKIDKQGWMHFGHGDATRVRPDVIVFAT GYKSQFDFLDADYPLLSQADVHGIYKTNHVSVGYMGFVRPSIGAIPPLAELQAQLWVLRLLQASFPSQVPQTPGP DAVEPYQLDYALHARQGYDLFANKRGVDHESYAYQLALDMGSAPTICHVASKGWRVLFTWAMGSNFNPKFRLVGP WRDEACAEHIMRGELYRVVKRSGGFVYLVTYSIIPMLVFGVLSMVLYALTGIKEAVVSSCKAQRLFKAAKTRC* |
Coding | >OphauG2|2786 ATGCTCAAGGTTGCCGTTATTGGTGGCGGCCCGGCTGGGCTGGCAACGCTCAAGTTTCTGGCCACTGCCCACCGC TTTTTCCCTATTCCTCGCATTGAGGCTCGTCTGTTTGAGGCTGAGGACCAAATTGGCGGGACATTTGTCCACCGC ATCTATGAAGACGCCGAGCTCGTCTCGTCCAAGTACCTCACAGCGTTTTCCGACTTTCGTCTCCCGCTCGACGCG CCCGACTTTGTCACGCCACAGGTATACGTGCAGTATCTGGTGGACTATGTTGCCCGGTTCGAGCTCGAGCCCATG ATTGAGTGCCAGGCCAAGGTGACGCGGGTGCGGCGCGGCGAGGGAGGCCTGGGCCATGTTGTGCAAGTCAGCAAG CCAATGGGCCAGGGCTTTGACTATGTCTGCGACGCGGTAGCCATCTGCTCGGGCATCAACGTCAATCCCATGATG CCCAAGATCAAGGGCATCGACAGGGTGGCCACGGTGCTTCACTCGTCCAAGCTCAAGAGCCGGCAGCAGTTTGGC CAAGGCACTCATGTTGTTGTCTGCGGCGCGGGCGAGACTGGCATGGACATTGCCCATCTGGCTGTGACGTCGCCC ACTGCCTCGGTCACGCTGTGCCATCGAGCCGGCTTCTTCTGTGCCCCCAAGATCATCCCCACGCCGGTGCATCGG AGCCAAAAGGCAGGCGCCAGACCCAACAAGCCGGTCGACGCGTCGGTTGCAAGTCTCTTCGACACGGCGTATGCG CACCCCATCCTGCAGCGAAGCCAGCTCCTGTGGACGGCCTACGACCAATGGGTCAAGAAGATGCACCTGGTGGTG TCGGGGACGGAGGAAGGGCCGGACCAGTGGGTCGGGCACATGAGCCGCGAGCGCAAGCATCTCGACTCCATCTTC CTCTGCAAGTCGGACAAGGCGCTGCCCTACATCTCCGAGGGCCATCGTTCGCAGTCGCTGTGGAACCGGGTGCGG TCGTGGCTGCTCAACGTGCCCATCAAGAAGACGTTTGGGCGCCGCATCCAGGTGCGCCAGTGGCCGACCAAGATT GACAAGCAGGGCTGGATGCACTTTGGCCACGGCGACGCGACGCGCGTGCGCCCCGATGTCATTGTCTTTGCCACG GGCTACAAGAGCCAGTTCGACTTTCTCGACGCCGACTACCCGCTGCTGAGCCAGGCCGATGTGCACGGCATCTAC AAGACGAACCATGTGTCGGTCGGCTACATGGGCTTTGTGCGGCCGTCGATTGGGGCCATTCCTCCGCTGGCCGAG CTCCAGGCCCAACTCTGGGTCTTGCGGCTGCTCCAGGCCAGCTTCCCCAGCCAGGTGCCGCAGACGCCAGGGCCC GACGCCGTCGAGCCCTACCAGCTCGACTATGCCCTGCATGCGCGCCAGGGCTACGACTTATTTGCCAACAAGCGC GGCGTGGACCACGAGTCGTATGCCTACCAGCTTGCCCTCGACATGGGATCTGCGCCCACCATCTGCCATGTTGCC AGCAAGGGCTGGAGGGTCTTGTTCACCTGGGCCATGGGCTCCAACTTCAATCCCAAGTTCCGCCTCGTCGGGCCA TGGAGGGACGAGGCCTGCGCCGAGCACATTATGCGTGGCGAGCTGTATCGAGTCGTCAAGCGGTCGGGAGGCTTT GTGTATCTCGTCACCTACTCCATCATCCCAATGCTGGTTTTTGGCGTCTTGAGCATGGTGCTCTACGCCTTGACG GGAATCAAGGAGGCTGTTGTGTCTAGTTGCAAGGCCCAGCGACTTTTCAAAGCCGCCAAGACGCGCTGCTAA |
Transcript | >OphauG2|2786 ATGCTCAAGGTTGCCGTTATTGGTGGCGGCCCGGCTGGGCTGGCAACGCTCAAGTTTCTGGCCACTGCCCACCGC TTTTTCCCTATTCCTCGCATTGAGGCTCGTCTGTTTGAGGCTGAGGACCAAATTGGCGGGACATTTGTCCACCGC ATCTATGAAGACGCCGAGCTCGTCTCGTCCAAGTACCTCACAGCGTTTTCCGACTTTCGTCTCCCGCTCGACGCG CCCGACTTTGTCACGCCACAGGTATACGTGCAGTATCTGGTGGACTATGTTGCCCGGTTCGAGCTCGAGCCCATG ATTGAGTGCCAGGCCAAGGTGACGCGGGTGCGGCGCGGCGAGGGAGGCCTGGGCCATGTTGTGCAAGTCAGCAAG CCAATGGGCCAGGGCTTTGACTATGTCTGCGACGCGGTAGCCATCTGCTCGGGCATCAACGTCAATCCCATGATG CCCAAGATCAAGGGCATCGACAGGGTGGCCACGGTGCTTCACTCGTCCAAGCTCAAGAGCCGGCAGCAGTTTGGC CAAGGCACTCATGTTGTTGTCTGCGGCGCGGGCGAGACTGGCATGGACATTGCCCATCTGGCTGTGACGTCGCCC ACTGCCTCGGTCACGCTGTGCCATCGAGCCGGCTTCTTCTGTGCCCCCAAGATCATCCCCACGCCGGTGCATCGG AGCCAAAAGGCAGGCGCCAGACCCAACAAGCCGGTCGACGCGTCGGTTGCAAGTCTCTTCGACACGGCGTATGCG CACCCCATCCTGCAGCGAAGCCAGCTCCTGTGGACGGCCTACGACCAATGGGTCAAGAAGATGCACCTGGTGGTG TCGGGGACGGAGGAAGGGCCGGACCAGTGGGTCGGGCACATGAGCCGCGAGCGCAAGCATCTCGACTCCATCTTC CTCTGCAAGTCGGACAAGGCGCTGCCCTACATCTCCGAGGGCCATCGTTCGCAGTCGCTGTGGAACCGGGTGCGG TCGTGGCTGCTCAACGTGCCCATCAAGAAGACGTTTGGGCGCCGCATCCAGGTGCGCCAGTGGCCGACCAAGATT GACAAGCAGGGCTGGATGCACTTTGGCCACGGCGACGCGACGCGCGTGCGCCCCGATGTCATTGTCTTTGCCACG GGCTACAAGAGCCAGTTCGACTTTCTCGACGCCGACTACCCGCTGCTGAGCCAGGCCGATGTGCACGGCATCTAC AAGACGAACCATGTGTCGGTCGGCTACATGGGCTTTGTGCGGCCGTCGATTGGGGCCATTCCTCCGCTGGCCGAG CTCCAGGCCCAACTCTGGGTCTTGCGGCTGCTCCAGGCCAGCTTCCCCAGCCAGGTGCCGCAGACGCCAGGGCCC GACGCCGTCGAGCCCTACCAGCTCGACTATGCCCTGCATGCGCGCCAGGGCTACGACTTATTTGCCAACAAGCGC GGCGTGGACCACGAGTCGTATGCCTACCAGCTTGCCCTCGACATGGGATCTGCGCCCACCATCTGCCATGTTGCC AGCAAGGGCTGGAGGGTCTTGTTCACCTGGGCCATGGGCTCCAACTTCAATCCCAAGTTCCGCCTCGTCGGGCCA TGGAGGGACGAGGCCTGCGCCGAGCACATTATGCGTGGCGAGCTGTATCGAGTCGTCAAGCGGTCGGGAGGCTTT GTGTATCTCGTCACCTACTCCATCATCCCAATGCTGGTTTTTGGCGTCTTGAGCATGGTGCTCTACGCCTTGACG GGAATCAAGGAGGCTGTTGTGTCTAGTTGCAAGGCCCAGCGACTTTTCAAAGCCGCCAAGACGCGCTGCTAA |
Gene | >OphauG2|2786 ATGCTCAAGGTTGCCGTTATTGGTGGCGGCCCGGCTGGGCTGGCAACGCTCAAGTTTCTGGCCACTGCCCACCGC TTTTTCCCTATTCCTCGCATTGAGGCTCGTCTGTTTGAGGCTGAGGACCAAATTGGCGGGACATTTGTCCACCGC ATCTATGAAGACGCCGAGGCGAGTCTCGTTGCTGTCCTCTGGGCGCGGCTGTCTTGCTCACGCAAAACGCAGCTC GTCTCGTCCAAGTACCTCACAGCGTTTTCCGACTTTCGTCTCCCGCTCGACGCGCCCGACTTTGTCACGCCACAG GTATACGTGCAGTATCTGGTGGACTATGTTGCCCGGTTCGAGCTCGAGCCCATGATTGAGTGCCAGGCCAAGGTG ACGCGGGTGCGGCGCGGCGAGGGAGGCCTGGGCCATGTTGTGCAAGTCAGCAAGCCAATGGGCCAGGGCTTTGAC TATGTCTGCGACGCGGTAGCCATCTGCTCGGGCATCAACGTCAATCCCATGATGCCCAAGATCAAGGGCATCGAC AGGGTGGCCACGGTGCTTCACTCGTCCAAGCTCAAGAGCCGGCAGCAGTTTGGCCAAGGCACTCATGTTGTTGTC TGCGGCGCGGGCGAGACTGGCATGGACATTGCCCATCTGGCTGTGACGTCGCCCACTGCCTCGGTCACGCTGTGC CATCGAGCCGGCTTCTTCTGTGCCCCCAAGGCAAGTGGCCACAGCCATGAAAGGAGAGGCATATCAATCCGAGTG CTCATCATGGCCAATGCTAGATCATCCCCACGCCGGTGCATCGGAGCCAAAAGGCAGGCGCCAGACCCAACAAGC CGGTCGACGCGTCGGTTGCAAGTCTCTTCGACACGGCGTATGCGCACCCCATCCTGCAGCGAAGCCAGCTCCTGT GGACGGCCTACGACCAATGGGTCAAGAAGATGCACCTGGTGGTGTCGGGGACGGAGGAAGGGCCGGACCAGTGGG TCGGGCACATGAGCCGCGAGCGCAAGCATCTCGACTCCATCTTCCTCTGCAAGTCGGACAAGGCGCTGCCCTACA TCTCCGAGGGCCATCGTTCGCAGTCGCTGTGGAACCGGGTGCGGTCGTGGCTGCTCAACGTGCCCATCAAGAAGA CGTTTGGGCGCCGCATCCAGGTGCGCCAGTGGCCGACCAAGATTGACAAGCAGGGCTGGATGCACTTTGGCCACG GCGACGCGACGCGCGTGCGCCCCGATGTCATTGTCTTTGCCACGGGCTACAAGAGCCAGTTCGACTTTCTCGACG CCGACTACCCGCTGCTGAGCCAGGCCGATGTGCACGGCATCTACAAGACGAACCATGTGTCGGTCGGCTACATGG GCTTTGTGCGGCCGTCGATTGGGGCCATTCCTCCGCTGGCCGAGCTCCAGGCCCAACTCTGGGTCTTGCGGCTGC TCCAGGCCAGCTTCCCCAGCCAGGTGCCGCAGACGCCAGGGCCCGACGCCGTCGAGCCCTACCAGCTCGACTATG CCCTGCATGCGCGCCAGGGCTACGACTTATTTGCCAACAAGCGCGGCGTGGACCACGAGTCGTATGCCTACCAGC TTGCCCTCGACATGGGATCTGCGCCCACCATCTGCCATGTTGCCAGCAAGGGCTGGAGGGTCTTGTTCACCTGGG CCATGGGCTCCAACTTCAATCCCAAGTTCCGCCTCGTCGGGCCATGGAGGGACGAGGCCTGCGCCGAGCACATTA TGCGTGGCGAGCTGTATCGAGTCGTCAAGCGGTCGGGAGGCTTTGTGTGTGAGTGCTGGCTTTTTCCCTCTCCCT TTTGCGGCTGACCGACGCCGGAGCAGATCTCGTCACCTACTCCATCATCCCAATGCTGGTTTTTGGCGTCTTGAG CATGGTGCTCTACGCCTTGACGGGAATCAAGGAGGCTGTTGTGTCTAGTTGCAAGGCCCAGCGACTTTTCAAAGC CGCCAAGACGCGCTGCTAA |