Fungal Genomics

at Utrecht University

General Properties

Protein IDOphauB2|3062
Gene name
LocationContig_20:26339..28207
Strand+
Gene length (bp)1868
Transcript length (bp)1620
Coding sequence length (bp)1620
Protein length (aa) 540

Overview

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PFAM Domains

PFAM Domain ID Short name Long name E-value Start End
PF00891 Methyltransf_2 O-methyltransferase domain 8.4E-25 295 505

Swissprot hits

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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
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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
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GO

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

Deeploc

Deeploc data not available for this genome

SignalP

(None)

Transmembrane Domains

(None)

Transcription Factor Class

(None)

CAZymes

(None)

Secondary Metabolism

Gene cluster ID Type of secondary metabolism gene
Cluster 16 Decorating

Expression data

No expression data available for this genome

Orthologs

Orthofinder run ID4
Orthogroup781
Change Orthofinder run
Species Protein ID
Ophiocordyceps australis 1348a (Ghana) OphauG2|501
Ophiocordyceps australis map64 (Brazil) OphauB2|3062 (this protein)
Ophiocordyceps camponoti-floridani Ophcf2|00878
Ophiocordyceps camponoti-rufipedis Ophun1|5296
Ophiocordyceps kimflemingae Ophio5|1570
Ophiocordyceps subramaniannii Hirsu2|2972

Sequences

Type of sequenceSequence
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

© 2023 - Robin Ohm - Utrecht University - The Netherlands

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