Protein ID | OphauB2|3062 |
Gene name | |
Location | Contig_20:26339..28207 |
Strand | + |
Gene length (bp) | 1868 |
Transcript length (bp) | 1620 |
Coding sequence length (bp) | 1620 |
Protein length (aa) | 540 |
PFAM Domain ID | Short name | Long name | E-value | Start | End |
---|---|---|---|---|---|
PF00891 | Methyltransf_2 | O-methyltransferase domain | 8.4E-25 | 295 | 505 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|A1DA61|FTMD_NEOFI | 6-hydroxytryprostatin B O-methyltransferase OS=Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / FGSC A1164 / NRRL 181) GN=ftmMT PE=3 SV=1 | 157 | 530 | 6.0E-30 |
sp|Q4WAW6|FTMD_ASPFU | 6-hydroxytryprostatin B O-methyltransferase OS=Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) GN=ftmMT PE=1 SV=1 | 185 | 530 | 7.0E-28 |
sp|B9WZX2|FTMD_ASPFM | 6-hydroxytryprostatin B O-methyltransferase OS=Neosartorya fumigata GN=ftmMT PE=1 SV=1 | 185 | 530 | 5.0E-27 |
sp|Q12120|OMTA_ASPPA | Sterigmatocystin 8-O-methyltransferase OS=Aspergillus parasiticus GN=omtA PE=1 SV=1 | 150 | 509 | 9.0E-27 |
sp|P55790|OMTA_ASPFL | Sterigmatocystin 8-O-methyltransferase OS=Aspergillus flavus GN=omtA PE=3 SV=1 | 159 | 509 | 8.0E-26 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|A1DA61|FTMD_NEOFI | 6-hydroxytryprostatin B O-methyltransferase OS=Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / FGSC A1164 / NRRL 181) GN=ftmMT PE=3 SV=1 | 157 | 530 | 6.0E-30 |
sp|Q4WAW6|FTMD_ASPFU | 6-hydroxytryprostatin B O-methyltransferase OS=Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) GN=ftmMT PE=1 SV=1 | 185 | 530 | 7.0E-28 |
sp|B9WZX2|FTMD_ASPFM | 6-hydroxytryprostatin B O-methyltransferase OS=Neosartorya fumigata GN=ftmMT PE=1 SV=1 | 185 | 530 | 5.0E-27 |
sp|Q12120|OMTA_ASPPA | Sterigmatocystin 8-O-methyltransferase OS=Aspergillus parasiticus GN=omtA PE=1 SV=1 | 150 | 509 | 9.0E-27 |
sp|P55790|OMTA_ASPFL | Sterigmatocystin 8-O-methyltransferase OS=Aspergillus flavus GN=omtA PE=3 SV=1 | 159 | 509 | 8.0E-26 |
sp|Q9P900|OMTB_ASPFL | Demethylsterigmatocystin 6-O-methyltransferase OS=Aspergillus flavus GN=omtB PE=3 SV=1 | 137 | 505 | 8.0E-20 |
sp|Q9UQY0|OMTB_ASPPA | Demethylsterigmatocystin 6-O-methyltransferase OS=Aspergillus parasiticus GN=omtB PE=1 SV=2 | 137 | 505 | 6.0E-19 |
sp|Q54GZ0|OMT9_DICDI | O-methyltransferase 9 OS=Dictyostelium discoideum GN=omt9 PE=3 SV=1 | 220 | 508 | 1.0E-14 |
sp|Q54S95|OMT7_DICDI | O-methyltransferase 7 OS=Dictyostelium discoideum GN=omt7 PE=3 SV=1 | 184 | 508 | 1.0E-13 |
sp|Q54B59|OMT12_DICDI | O-methyltransferase 12 OS=Dictyostelium discoideum GN=omt12 PE=1 SV=1 | 221 | 505 | 6.0E-13 |
sp|P16559|TCMN_STRGA | Multifunctional cyclase-dehydratase-3-O-methyl transferase TcmN OS=Streptomyces glaucescens GN=tcmN PE=1 SV=2 | 191 | 506 | 9.0E-12 |
sp|Q38J50|FOMT2_WHEAT | Tricetin 3',4',5'-O-trimethyltransferase OS=Triticum aestivum GN=OMT2 PE=1 SV=1 | 297 | 505 | 6.0E-11 |
sp|Q8GU25|COMT1_ROSCH | Caffeic acid 3-O-methyltransferase OS=Rosa chinensis GN=COMT1 PE=2 SV=1 | 297 | 501 | 1.0E-10 |
sp|Q43046|COMT1_POPKI | Caffeic acid 3-O-methyltransferase 1 OS=Populus kitakamiensis GN=HOMT1 PE=3 SV=1 | 297 | 501 | 1.0E-10 |
sp|Q8GSN1|MOMT_CATRO | Myricetin O-methyltransferase OS=Catharanthus roseus PE=1 SV=1 | 209 | 505 | 1.0E-10 |
sp|Q43609|COMT1_PRUDU | Caffeic acid 3-O-methyltransferase OS=Prunus dulcis GN=COMT1 PE=2 SV=1 | 297 | 505 | 3.0E-10 |
sp|Q00763|COMT1_POPTM | Caffeic acid 3-O-methyltransferase 1 OS=Populus tremuloides GN=OMT1 PE=1 SV=1 | 297 | 505 | 7.0E-10 |
sp|B0EXJ8|HTOMT_CATRO | Tabersonine 16-O-methyltransferase OS=Catharanthus roseus GN=16OMT PE=1 SV=1 | 355 | 505 | 8.0E-10 |
sp|Q41086|COMT2_POPTM | Caffeic acid 3-O-methyltransferase 2 OS=Populus tremuloides GN=OMT2 PE=3 SV=1 | 185 | 513 | 1.0E-09 |
sp|Q43047|COMT3_POPKI | Caffeic acid 3-O-methyltransferase 3 OS=Populus kitakamiensis GN=HOMT3 PE=3 SV=1 | 297 | 513 | 1.0E-09 |
sp|Q43239|COMT1_ZINVI | Caffeic acid 3-O-methyltransferase OS=Zinnia violacea PE=2 SV=1 | 297 | 516 | 1.0E-09 |
sp|Q9LEL6|6OMT_COPJA | (RS)-norcoclaurine 6-O-methyltransferase OS=Coptis japonica PE=1 SV=1 | 166 | 527 | 1.0E-09 |
sp|Q8T638|DMTA_DICDI | Des-methyl DIF-1 methyltransferase A OS=Dictyostelium discoideum GN=dmtA PE=1 SV=1 | 182 | 505 | 2.0E-09 |
sp|Q9FK25|OMT1_ARATH | Flavone 3'-O-methyltransferase 1 OS=Arabidopsis thaliana GN=OMT1 PE=1 SV=1 | 185 | 514 | 2.0E-09 |
sp|Q9FQY8|COMT1_CAPAN | Caffeic acid 3-O-methyltransferase OS=Capsicum annuum GN=COMT PE=2 SV=2 | 297 | 516 | 3.0E-09 |
sp|Q9XGW0|COMT1_OCIBA | Caffeic acid 3-O-methyltransferase 1 OS=Ocimum basilicum GN=COMT1 PE=2 SV=1 | 297 | 505 | 4.0E-09 |
sp|O23760|COMT1_CLABR | Caffeic acid 3-O-methyltransferase OS=Clarkia breweri GN=COMT PE=1 SV=1 | 297 | 501 | 5.0E-09 |
sp|O81646|COMT1_CAPCH | Caffeic acid 3-O-methyltransferase OS=Capsicum chinense GN=COMT PE=2 SV=1 | 297 | 501 | 6.0E-09 |
sp|A8J6X1|BMT_GLELI | Bergaptol O-methyltransferase OS=Glehnia littoralis GN=BMT PE=1 SV=1 | 294 | 515 | 6.0E-09 |
sp|P28002|COMT1_MEDSA | Caffeic acid 3-O-methyltransferase OS=Medicago sativa PE=1 SV=1 | 185 | 505 | 7.0E-09 |
sp|Q6T1F5|COMT1_AMMMJ | Caffeic acid 3-O-methyltransferase OS=Ammi majus GN=COMT PE=1 SV=1 | 297 | 505 | 8.0E-09 |
sp|O82054|COMT1_SACOF | Caffeic acid 3-O-methyltransferase OS=Saccharum officinarum GN=COMT PE=2 SV=1 | 297 | 505 | 1.0E-08 |
sp|P46484|COMT1_EUCGU | Caffeic acid 3-O-methyltransferase OS=Eucalyptus gunnii GN=OMT PE=2 SV=1 | 297 | 505 | 2.0E-08 |
sp|Q8W013|COMT1_CATRO | Caffeic acid 3-O-methyltransferase OS=Catharanthus roseus GN=COMT1 PE=2 SV=1 | 297 | 512 | 2.0E-08 |
sp|B0CN39|SFMM3_STRLA | O-methyltransferase SfmM3 OS=Streptomyces lavendulae GN=sfmM3 PE=3 SV=1 | 190 | 510 | 3.0E-08 |
sp|Q54B60|OMT11_DICDI | Probable inactive O-methyltransferase 11 OS=Dictyostelium discoideum GN=omt11 PE=3 SV=1 | 332 | 505 | 4.0E-08 |
sp|Q9XGV9|COMT2_OCIBA | Caffeic acid 3-O-methyltransferase 2 OS=Ocimum basilicum GN=COMT2 PE=2 SV=1 | 297 | 501 | 4.0E-08 |
sp|Q8H9A8|COOMT_COPJA | Columbamine O-methyltransferase OS=Coptis japonica PE=1 SV=1 | 347 | 506 | 5.0E-08 |
sp|Q8LL87|COMT1_COFCA | Caffeic acid 3-O-methyltransferase OS=Coffea canephora PE=2 SV=1 | 297 | 505 | 5.0E-08 |
sp|Q06509|COMT1_MAIZE | Caffeic acid 3-O-methyltransferase OS=Zea mays PE=3 SV=1 | 297 | 505 | 7.0E-08 |
sp|O04385|IEMT_CLABR | (Iso)eugenol O-methyltransferase OS=Clarkia breweri GN=IEMT1 PE=1 SV=2 | 347 | 501 | 1.0E-07 |
sp|Q6WUC1|6OMT_PAPSO | (RS)-norcoclaurine 6-O-methyltransferase OS=Papaver somniferum GN=6OMT PE=1 SV=1 | 356 | 527 | 1.0E-07 |
sp|Q54527|RDMB_STREF | Aclacinomycin 10-hydroxylase RdmB OS=Streptomyces purpurascens GN=rdmB PE=1 SV=1 | 357 | 497 | 2.0E-07 |
sp|Q42653|OMT2_CHRAE | Quercetin 3-O-methyltransferase 2 OS=Chrysosplenium americanum GN=OMT2 PE=1 SV=1 | 297 | 505 | 4.0E-07 |
sp|C7SDN9|N7OMT_PAPSO | Norreticuline-7-O-methyltransferase OS=Papaver somniferum PE=1 SV=1 | 171 | 510 | 2.0E-06 |
sp|A8QW52|OMT1_SORBI | Eugenol O-methyltransferase OS=Sorghum bicolor GN=EOMT PE=1 SV=1 | 289 | 505 | 2.0E-06 |
sp|D3KU66|ASMT_MOUSE | Acetylserotonin O-methyltransferase OS=Mus musculus GN=Asmt PE=2 SV=1 | 356 | 505 | 3.0E-06 |
sp|Q55216|DNRK_STRS5 | Carminomycin 4-O-methyltransferase DauK OS=Streptomyces sp. (strain C5) GN=dauK PE=1 SV=1 | 205 | 505 | 3.0E-06 |
sp|D3KU67|ASMT_MUSMM | Acetylserotonin O-methyltransferase OS=Mus musculus molossinus GN=Asmt PE=2 SV=1 | 356 | 505 | 3.0E-06 |
GO Term | Description | Terminal node |
---|---|---|
GO:0008171 | O-methyltransferase activity | Yes |
GO:0003824 | catalytic activity | No |
GO:0003674 | molecular_function | No |
GO:0008168 | methyltransferase activity | No |
GO:0016740 | transferase activity | No |
GO:0016741 | transferase activity, transferring one-carbon groups | No |
Gene cluster ID | Type of secondary metabolism gene |
---|---|
Cluster 16 | Decorating |
Orthofinder run ID | 4 |
Orthogroup | 781 |
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|3062 MSTPLLTGARAGRRSLSQYPRLGHTALAMAKFKMPSWLHSTTSMGDAKKHPRRSFAGFSPTKAKHEAMATQHTAM SKHSDMTVVKSNVSSAQSQLSPPPPPPPPSAVSPMRLLAIKIGLDADVLDEYISSNNLPEPGLDAKAPDEFPRLS AQMQTRRQELILAVRELLALLRGPRESIRLGAWGALDVAALQVINNYGIAQLVPLDSAIALTELQAKSDMNPVTL TRVLRFVMTNNIFHEPSPGFIAHTAASRVLAQDAALRDWVGFNTEEVFPASAHVLDALKRDARATSLTATGFNVA FGTVGSETIFETLGKDPQRARRMVGTMSSMTGSQGYETHYLVDNVDLSKENELEGTLVDIGGSHGLVCVELAQRW DKMKFVVQDLDKTVQSTPQPICDDPAVAQRIQMQVHDFFQEQPVKNADVYLFRWIIHNYSTPYAVKLLRNLIPAL KPGARIIINEHCIRTAGAETPWDERLMRSMDMVMMVLLNAEEREENEFRALFEQADARFTFKGVTRTEGCRMSIV EAVWEPEKMQATKT* |
Coding | >OphauB2|3062 ATGTCGACGCCTCTGCTAACGGGTGCGCGCGCAGGTCGACGTAGCTTATCGCAGTATCCGCGCCTCGGCCACACA GCACTGGCCATGGCCAAGTTCAAGATGCCTTCATGGCTGCACTCGACAACAAGCATGGGCGATGCCAAGAAGCAT CCTCGCCGCTCCTTTGCTGGCTTTTCTCCGACCAAGGCCAAGCACGAGGCCATGGCCACCCAGCACACCGCCATG TCAAAGCACAGCGACATGACGGTTGTCAAGAGCAACGTGTCGTCGGCGCAGAGCCAGCTGTCGCCCCCGCCCCCG CCCCCGCCCCCGAGCGCGGTCTCTCCCATGCGCCTTCTGGCAATCAAGATCGGCCTCGACGCAGACGTGTTGGAT GAGTACATTAGCAGCAACAATCTGCCAGAGCCAGGACTAGACGCCAAGGCCCCCGACGAGTTTCCTCGTCTGTCT GCCCAGATGCAGACGAGGAGACAGGAGCTTATTCTAGCCGTCAGAGAGCTCCTTGCTCTGTTGCGGGGCCCGCGC GAGAGCATAAGACTTGGAGCTTGGGGTGCTCTCGACGTGGCCGCCCTGCAAGTCATCAACAACTATGGCATAGCA CAACTCGTTCCCTTGGATTCTGCCATTGCATTGACAGAGCTTCAGGCCAAGTCTGATATGAACCCAGTAACGCTG ACTCGCGTCTTGCGCTTTGTAATGACCAATAATATCTTCCACGAGCCTTCACCTGGCTTCATTGCGCATACGGCT GCCTCGCGAGTTCTCGCTCAAGACGCTGCCTTGCGCGACTGGGTTGGCTTCAACACGGAAGAAGTGTTTCCCGCC TCGGCCCATGTCCTTGACGCCCTCAAGAGAGACGCCCGAGCCACGTCGCTGACGGCAACCGGCTTCAATGTTGCT TTTGGTACTGTTGGCAGCGAGACAATTTTTGAGACTCTGGGCAAAGACCCGCAGCGAGCAAGGCGCATGGTGGGA ACAATGTCGAGCATGACGGGCTCCCAAGGTTACGAGACACACTACCTGGTCGATAATGTTGATTTATCCAAGGAG AATGAGCTCGAGGGAACACTGGTTGACATTGGAGGCAGCCATGGCCTAGTCTGTGTCGAGCTGGCCCAGAGGTGG GACAAGATGAAATTTGTCGTTCAGGATCTCGACAAGACAGTGCAAAGCACGCCACAGCCAATCTGTGACGACCCA GCCGTGGCTCAAAGGATACAAATGCAGGTGCACGACTTCTTCCAAGAGCAGCCCGTCAAGAATGCCGATGTCTAC CTTTTCCGCTGGATCATCCACAATTACTCGACGCCGTACGCCGTCAAGCTGCTCCGAAACCTGATACCGGCGCTC AAGCCTGGAGCGCGAATCATCATCAACGAACACTGTATTCGCACGGCAGGTGCCGAGACGCCGTGGGACGAAAGA TTGATGCGAAGCATGGACATGGTCATGATGGTGCTGCTCAATGCTGAGGAGCGCGAGGAGAATGAGTTTCGGGCT CTCTTTGAACAGGCTGACGCACGCTTCACTTTCAAGGGCGTCACACGGACCGAGGGCTGCCGAATGAGCATCGTG GAAGCCGTCTGGGAACCAGAAAAGATGCAAGCAACCAAGACTTGA |
Transcript | >OphauB2|3062 ATGTCGACGCCTCTGCTAACGGGTGCGCGCGCAGGTCGACGTAGCTTATCGCAGTATCCGCGCCTCGGCCACACA GCACTGGCCATGGCCAAGTTCAAGATGCCTTCATGGCTGCACTCGACAACAAGCATGGGCGATGCCAAGAAGCAT CCTCGCCGCTCCTTTGCTGGCTTTTCTCCGACCAAGGCCAAGCACGAGGCCATGGCCACCCAGCACACCGCCATG TCAAAGCACAGCGACATGACGGTTGTCAAGAGCAACGTGTCGTCGGCGCAGAGCCAGCTGTCGCCCCCGCCCCCG CCCCCGCCCCCGAGCGCGGTCTCTCCCATGCGCCTTCTGGCAATCAAGATCGGCCTCGACGCAGACGTGTTGGAT GAGTACATTAGCAGCAACAATCTGCCAGAGCCAGGACTAGACGCCAAGGCCCCCGACGAGTTTCCTCGTCTGTCT GCCCAGATGCAGACGAGGAGACAGGAGCTTATTCTAGCCGTCAGAGAGCTCCTTGCTCTGTTGCGGGGCCCGCGC GAGAGCATAAGACTTGGAGCTTGGGGTGCTCTCGACGTGGCCGCCCTGCAAGTCATCAACAACTATGGCATAGCA CAACTCGTTCCCTTGGATTCTGCCATTGCATTGACAGAGCTTCAGGCCAAGTCTGATATGAACCCAGTAACGCTG ACTCGCGTCTTGCGCTTTGTAATGACCAATAATATCTTCCACGAGCCTTCACCTGGCTTCATTGCGCATACGGCT GCCTCGCGAGTTCTCGCTCAAGACGCTGCCTTGCGCGACTGGGTTGGCTTCAACACGGAAGAAGTGTTTCCCGCC TCGGCCCATGTCCTTGACGCCCTCAAGAGAGACGCCCGAGCCACGTCGCTGACGGCAACCGGCTTCAATGTTGCT TTTGGTACTGTTGGCAGCGAGACAATTTTTGAGACTCTGGGCAAAGACCCGCAGCGAGCAAGGCGCATGGTGGGA ACAATGTCGAGCATGACGGGCTCCCAAGGTTACGAGACACACTACCTGGTCGATAATGTTGATTTATCCAAGGAG AATGAGCTCGAGGGAACACTGGTTGACATTGGAGGCAGCCATGGCCTAGTCTGTGTCGAGCTGGCCCAGAGGTGG GACAAGATGAAATTTGTCGTTCAGGATCTCGACAAGACAGTGCAAAGCACGCCACAGCCAATCTGTGACGACCCA GCCGTGGCTCAAAGGATACAAATGCAGGTGCACGACTTCTTCCAAGAGCAGCCCGTCAAGAATGCCGATGTCTAC CTTTTCCGCTGGATCATCCACAATTACTCGACGCCGTACGCCGTCAAGCTGCTCCGAAACCTGATACCGGCGCTC AAGCCTGGAGCGCGAATCATCATCAACGAACACTGTATTCGCACGGCAGGTGCCGAGACGCCGTGGGACGAAAGA TTGATGCGAAGCATGGACATGGTCATGATGGTGCTGCTCAATGCTGAGGAGCGCGAGGAGAATGAGTTTCGGGCT CTCTTTGAACAGGCTGACGCACGCTTCACTTTCAAGGGCGTCACACGGACCGAGGGCTGCCGAATGAGCATCGTG GAAGCCGTCTGGGAACCAGAAAAGATGCAAGCAACCAAGACTTGA |
Gene | >OphauB2|3062 ATGTCGACGCCTCTGCTAACGGGTGCGCGCGCAGGTCGACGTAGCTTATCGCAGTATCCGCGCCTCGGCCACACA GCACTGGCCATGGCCAAGTTCAAGATGCCTTCATGGCTGCACTCGACAACAAGCATGGGCGATGCCAAGAAGCAT CCTCGCCGCTCCTTTGCTGGCTTTTCTCCGACCAAGGCCAAGCACGAGGCCATGGCCACCCAGCACACCGCCATG TCAAAGCACAGCGACATGACGGTTGTCAAGAGCAACGTGTCGTCGGCGCAGAGCCAGCTGTCGCCCCCGCCCCCG CCCCCGCCCCCGAGCGCGGTCTCTCCCATGCGCCTTCTGGCAATCAAGATCGGCCTCGACGCAGACGTGTTGGAT GAGTACATTAGCAGCAACAATCTGCCAGAGCCAGGACTAGACGCCAAGGCCCCCGACGAGTTTCCTCGTCTGTCT GCCCAGATGCAGACGAGGAGACAGGAGCTTATTCTAGCCGTCAGAGAGCTCCTTGCTCTGTTGCGGGGCCCGCGC GAGAGCATAAGACTTGGAGCTTGGGGTGTAAGGCTTTGCTTTGACGCCTTTTGCTGCTCTTTTGTGGTTGACTCT TCTGCCAGGCTCTCGACGTGGCCGCCCTGCAAGTCATCAACAACTATGGCATAGGTAGCGGCTCTTGTCCCTATG GCTGGCGCCATGTGCTGACCTGGACACTAGCACAACTCGTTCCCTTGGATTCTGCCATTGCATTGACAGAGCTTC AGGCCAAGTCTGATATGAACCCAGTAACGCTGACTCGCGTCTTGCGCTTTGTAATGACCAATAATATCTTCCACG AGCCTTCACCTGGCTTCATTGCGCATACGGCTGCCTCGCGAGTTCTCGCTCAAGACGCTGCCTTGCGCGACTGGG TTGGCTTCAACACGGAAGAAGTGTTTCCCGCCTCGGCCCATGTCCTTGACGCCCTCAAGAGAGACGCCCGAGCCA CGTCGCTGACGGCAACCGGCTTCAATGTTGCTTTTGGTACTGTTGGCAGCGAGACAATTTTTGAGACTCTGGGCA AAGACCCGCAGCGAGCAAGGCGCATGGTGGGAACAATGTCGAGCATGACGGGCTCCCAAGGTTACGAGACACACT ACCTGGTCGATAATGTTGATTTATCCAAGGAGAATGAGCTCGAGGGAACACTGGTTGACATTGGAGGCAGCCATG GCCTAGTCTGTGTCGAGCTGGCCCAGAGGTGGGACAAGATGAAATTTGTCGTTCAGGATCTCGACAAGACAGTGC AAAGCACGCCACAGCCAATCTGTGACGACCCAGCCGTGGCTCAAAGGATACAAATGCAGGTGCACGACTTCTTCC AAGAGCAGCCCGTCAAGAATGCCGATGGTATGGCACCGTCCCCCTTGTCTGTCTCCTGGCACCAAGTCACTGAGC TGACGAGCTTGCCTGGCTCCCAACAGTCTACCTTTTCCGCTGGATCATCCACAATTACTCGACGCCGTACGCCGT CAAGCTGCTCCGAAACCTGATACCGGCGCTCAAGCCTGGAGCGCGAATCATCATCAACGAACACTGTATTCGCAC GGCAGGTGCCGAGACGCCGTGGGACGAAAGATTGATGCGAAGCATGGACATGGTCATGATGGTGCTGCTCAATGC TGAGGAGCGCGAGGAGAATGAGTTTCGGGCTCTCTTTGAACAGGCTGACGCACGCTTCACTTTCAAGGTGACTGG CTGCATGCCTCGTTGTCTTTGGTGTTTTTTTTTTTCTTTTTCGCTGACTTGCAGCCTAGGGCGTCACACGGACCG AGGGCTGCCGAATGAGCATCGTGGAAGCCGTCTGGGAACCAGAAAAGATGCAAGCAACCAAGACTTGA |