Fungal Genomics

at Utrecht University

General Properties

Protein IDOphio5|2386
Gene name
Locationscaffold_20:13464..15171
Strand-
Gene length (bp)1707
Transcript length (bp)1272
Coding sequence length (bp)1272
Protein length (aa) 424

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PFAM Domains

PFAM Domain ID Short name Long name E-value Start End
PF00891 Methyltransf_2 O-methyltransferase domain 6.8E-22 245 394

Swissprot hits

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Swissprot ID Swissprot Description Start End E-value
sp|Q12120|OMTA_ASPPA Sterigmatocystin 8-O-methyltransferase OS=Aspergillus parasiticus GN=omtA PE=1 SV=1 89 418 2.0E-27
sp|P55790|OMTA_ASPFL Sterigmatocystin 8-O-methyltransferase OS=Aspergillus flavus GN=omtA PE=3 SV=1 89 418 1.0E-26
sp|B9WZX2|FTMD_ASPFM 6-hydroxytryprostatin B O-methyltransferase OS=Neosartorya fumigata GN=ftmMT PE=1 SV=1 64 356 2.0E-23
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 64 356 2.0E-22
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 30 356 2.0E-22
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Swissprot ID Swissprot Description Start End E-value
sp|Q12120|OMTA_ASPPA Sterigmatocystin 8-O-methyltransferase OS=Aspergillus parasiticus GN=omtA PE=1 SV=1 89 418 2.0E-27
sp|P55790|OMTA_ASPFL Sterigmatocystin 8-O-methyltransferase OS=Aspergillus flavus GN=omtA PE=3 SV=1 89 418 1.0E-26
sp|B9WZX2|FTMD_ASPFM 6-hydroxytryprostatin B O-methyltransferase OS=Neosartorya fumigata GN=ftmMT PE=1 SV=1 64 356 2.0E-23
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 64 356 2.0E-22
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 30 356 2.0E-22
sp|Q9P900|OMTB_ASPFL Demethylsterigmatocystin 6-O-methyltransferase OS=Aspergillus flavus GN=omtB PE=3 SV=1 71 398 6.0E-22
sp|Q9UQY0|OMTB_ASPPA Demethylsterigmatocystin 6-O-methyltransferase OS=Aspergillus parasiticus GN=omtB PE=1 SV=2 74 398 3.0E-21
sp|P42712|DMPM_STRAD O-demethylpuromycin-O-methyltransferase OS=Streptomyces alboniger GN=dmpM PE=3 SV=1 195 404 2.0E-15
sp|Q7XB10|4OMT2_PAPSO 3'-hydroxy-N-methyl-(S)-coclaurine 4'-O-methyltransferase 2 OS=Papaver somniferum GN=4'OMT2 PE=1 SV=1 70 394 2.0E-15
sp|Q6WUC1|6OMT_PAPSO (RS)-norcoclaurine 6-O-methyltransferase OS=Papaver somniferum GN=6OMT PE=1 SV=1 195 402 7.0E-15
sp|P59049|OMT1_CHRAE Quercetin 3-O-methyltransferase 1 OS=Chrysosplenium americanum GN=OMT1 PE=1 SV=1 244 400 2.0E-14
sp|Q42653|OMT2_CHRAE Quercetin 3-O-methyltransferase 2 OS=Chrysosplenium americanum GN=OMT2 PE=1 SV=1 244 400 2.0E-14
sp|Q43046|COMT1_POPKI Caffeic acid 3-O-methyltransferase 1 OS=Populus kitakamiensis GN=HOMT1 PE=3 SV=1 244 406 5.0E-14
sp|O22309|7OMT9_MEDSA Isoflavone-7-O-methyltransferase 9 OS=Medicago sativa PE=2 SV=1 195 404 1.0E-13
sp|O22308|7OMT6_MEDSA Isoflavone-7-O-methyltransferase 6 OS=Medicago sativa PE=2 SV=1 195 404 1.0E-13
sp|Q8GU25|COMT1_ROSCH Caffeic acid 3-O-methyltransferase OS=Rosa chinensis GN=COMT1 PE=2 SV=1 244 399 2.0E-13
sp|O24529|7OMT8_MEDSA Isoflavone-7-O-methyltransferase 8 OS=Medicago sativa PE=1 SV=1 195 404 2.0E-13
sp|C6TAY1|SOMT2_SOYBN Flavonoid 4'-O-methyltransferase OS=Glycine max PE=1 SV=1 195 399 4.0E-13
sp|Q00763|COMT1_POPTM Caffeic acid 3-O-methyltransferase 1 OS=Populus tremuloides GN=OMT1 PE=1 SV=1 244 406 5.0E-13
sp|Q43609|COMT1_PRUDU Caffeic acid 3-O-methyltransferase OS=Prunus dulcis GN=COMT1 PE=2 SV=1 244 399 1.0E-12
sp|Q9FK25|OMT1_ARATH Flavone 3'-O-methyltransferase 1 OS=Arabidopsis thaliana GN=OMT1 PE=1 SV=1 244 399 1.0E-12
sp|Q6T1F5|COMT1_AMMMJ Caffeic acid 3-O-methyltransferase OS=Ammi majus GN=COMT PE=1 SV=1 204 395 2.0E-12
sp|O24305|M3OM1_PEA (+)-6a-hydroxymaackiain 3-O-methyltransferase 1 OS=Pisum sativum GN=HMM1 PE=1 SV=1 58 404 3.0E-12
sp|Q9LEL6|6OMT_COPJA (RS)-norcoclaurine 6-O-methyltransferase OS=Coptis japonica PE=1 SV=1 195 402 3.0E-12
sp|O81646|COMT1_CAPCH Caffeic acid 3-O-methyltransferase OS=Capsicum chinense GN=COMT PE=2 SV=1 244 390 5.0E-12
sp|Q9XGV9|COMT2_OCIBA Caffeic acid 3-O-methyltransferase 2 OS=Ocimum basilicum GN=COMT2 PE=2 SV=1 70 395 6.0E-12
sp|Q54S95|OMT7_DICDI O-methyltransferase 7 OS=Dictyostelium discoideum GN=omt7 PE=3 SV=1 155 396 6.0E-12
sp|Q43239|COMT1_ZINVI Caffeic acid 3-O-methyltransferase OS=Zinnia violacea PE=2 SV=1 243 395 6.0E-12
sp|Q6WUC2|7OMT_PAPSO (R,S)-reticuline 7-O-methyltransferase OS=Papaver somniferum GN=7OMT PE=1 SV=1 247 404 7.0E-12
sp|B0CN39|SFMM3_STRLA O-methyltransferase SfmM3 OS=Streptomyces lavendulae GN=sfmM3 PE=3 SV=1 185 403 1.0E-11
sp|Q9XGW0|COMT1_OCIBA Caffeic acid 3-O-methyltransferase 1 OS=Ocimum basilicum GN=COMT1 PE=2 SV=1 205 395 1.0E-11
sp|Q8W013|COMT1_CATRO Caffeic acid 3-O-methyltransferase OS=Catharanthus roseus GN=COMT1 PE=2 SV=1 70 394 2.0E-11
sp|O23760|COMT1_CLABR Caffeic acid 3-O-methyltransferase OS=Clarkia breweri GN=COMT PE=1 SV=1 247 399 2.0E-11
sp|P28002|COMT1_MEDSA Caffeic acid 3-O-methyltransferase OS=Medicago sativa PE=1 SV=1 244 399 2.0E-11
sp|Q54GZ0|OMT9_DICDI O-methyltransferase 9 OS=Dictyostelium discoideum GN=omt9 PE=3 SV=1 74 399 2.0E-11
sp|Q9FQY8|COMT1_CAPAN Caffeic acid 3-O-methyltransferase OS=Capsicum annuum GN=COMT PE=2 SV=2 244 398 4.0E-11
sp|C7SDN9|N7OMT_PAPSO Norreticuline-7-O-methyltransferase OS=Papaver somniferum PE=1 SV=1 248 413 5.0E-11
sp|Q7XB11|4OMT1_PAPSO 3'-hydroxy-N-methyl-(S)-coclaurine 4'-O-methyltransferase 1 OS=Papaver somniferum GN=4'OMT1 PE=2 SV=1 199 394 2.0E-10
sp|Q41086|COMT2_POPTM Caffeic acid 3-O-methyltransferase 2 OS=Populus tremuloides GN=OMT2 PE=3 SV=1 244 406 2.0E-10
sp|Q8LL87|COMT1_COFCA Caffeic acid 3-O-methyltransferase OS=Coffea canephora PE=2 SV=1 244 398 2.0E-10
sp|A8J6X1|BMT_GLELI Bergaptol O-methyltransferase OS=Glehnia littoralis GN=BMT PE=1 SV=1 244 398 2.0E-10
sp|Q43047|COMT3_POPKI Caffeic acid 3-O-methyltransferase 3 OS=Populus kitakamiensis GN=HOMT3 PE=3 SV=1 244 406 2.0E-10
sp|O04385|IEMT_CLABR (Iso)eugenol O-methyltransferase OS=Clarkia breweri GN=IEMT1 PE=1 SV=2 244 406 8.0E-10
sp|B0EXJ8|HTOMT_CATRO Tabersonine 16-O-methyltransferase OS=Catharanthus roseus GN=16OMT PE=1 SV=1 244 400 1.0E-09
sp|P46484|COMT1_EUCGU Caffeic acid 3-O-methyltransferase OS=Eucalyptus gunnii GN=OMT PE=2 SV=1 244 399 2.0E-09
sp|Q6T1F6|BMT_AMMMJ Bergaptol O-methyltransferase OS=Ammi majus GN=BMT PE=1 SV=1 244 395 3.0E-09
sp|Q06509|COMT1_MAIZE Caffeic acid 3-O-methyltransferase OS=Zea mays PE=3 SV=1 210 408 5.0E-09
sp|Q54B59|OMT12_DICDI O-methyltransferase 12 OS=Dictyostelium discoideum GN=omt12 PE=1 SV=1 248 399 6.0E-09
sp|Q86I40|OMT4_DICDI O-methyltransferase 4 OS=Dictyostelium discoideum GN=omt4 PE=3 SV=1 195 399 7.0E-09
sp|O82054|COMT1_SACOF Caffeic acid 3-O-methyltransferase OS=Saccharum officinarum GN=COMT PE=2 SV=1 205 408 9.0E-09
sp|P93324|CHOMT_MEDSA Isoliquiritigenin 2'-O-methyltransferase OS=Medicago sativa PE=1 SV=1 244 399 1.0E-08
sp|P45986|IMT1_MESCR Inositol 4-methyltransferase OS=Mesembryanthemum crystallinum GN=IMT1 PE=1 SV=1 248 399 1.0E-08
sp|Q39522|SMT_COPJA (S)-scoulerine 9-O-methyltransferase OS=Coptis japonica GN=SMT PE=1 SV=1 247 402 1.0E-08
sp|Q8GSN1|MOMT_CATRO Myricetin O-methyltransferase OS=Catharanthus roseus PE=1 SV=1 244 400 2.0E-08
sp|A8QW52|OMT1_SORBI Eugenol O-methyltransferase OS=Sorghum bicolor GN=EOMT PE=1 SV=1 248 394 2.0E-08
sp|Q38J50|FOMT2_WHEAT Tricetin 3',4',5'-O-trimethyltransferase OS=Triticum aestivum GN=OMT2 PE=1 SV=1 205 408 2.0E-08
sp|Q8T638|DMTA_DICDI Des-methyl DIF-1 methyltransferase A OS=Dictyostelium discoideum GN=dmtA PE=1 SV=1 82 418 4.0E-08
sp|P16559|TCMN_STRGA Multifunctional cyclase-dehydratase-3-O-methyl transferase TcmN OS=Streptomyces glaucescens GN=tcmN PE=1 SV=2 247 397 4.0E-08
sp|Q84KK4|I4OMT_LOTJA Isoflavone 4'-O-methyltransferase OS=Lotus japonicus GN=HI4'OMT PE=1 SV=1 58 404 5.0E-08
sp|B6VJS4|ROMT_VITVI Trans-resveratrol di-O-methyltransferase OS=Vitis vinifera GN=ROMT PE=1 SV=2 58 404 7.0E-08
sp|Q9SWC2|COMT1_EUCGL Caffeic acid 3-O-methyltransferase (Fragment) OS=Eucalyptus globulus GN=COMT1 PE=3 SV=1 244 381 8.0E-08
sp|D3KU67|ASMT_MUSMM Acetylserotonin O-methyltransferase OS=Mus musculus molossinus GN=Asmt PE=2 SV=1 248 395 2.0E-07
sp|D3KU66|ASMT_MOUSE Acetylserotonin O-methyltransferase OS=Mus musculus GN=Asmt PE=2 SV=1 248 395 2.0E-07
sp|A9X7L0|ANMT_RUTGR Anthranilate N-methyltransferase OS=Ruta graveolens PE=1 SV=1 247 395 3.0E-07
sp|P0DH60|M3OM2_PEA (+)-6a-hydroxymaackiain 3-O-methyltransferase 2 OS=Pisum sativum GN=HMM2 PE=1 SV=1 58 404 1.0E-06
sp|Q92056|ASMT_CHICK Acetylserotonin O-methyltransferase OS=Gallus gallus GN=ASMT PE=2 SV=1 274 399 1.0E-06
sp|Q8HZJ0|ASMT_MACMU Acetylserotonin O-methyltransferase OS=Macaca mulatta GN=ASMT PE=2 SV=1 248 394 1.0E-06
sp|P10950|ASMT_BOVIN Acetylserotonin O-methyltransferase OS=Bos taurus GN=ASMT PE=1 SV=2 248 408 2.0E-06
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GO

GO Term Description Terminal node
GO:0008171 O-methyltransferase activity Yes
GO:0008168 methyltransferase activity No
GO:0003824 catalytic activity No
GO:0016740 transferase activity No
GO:0003674 molecular_function No
GO:0016741 transferase activity, transferring one-carbon groups No

SignalP

[Help with interpreting these statistics]
SignalP signal predicted Location
(based on Ymax)
D score
(significance: > 0.45)
No 1 - 39 0.45

Transmembrane Domains

(None)

Transcription Factor Class

(None)

Expression data

Analysis 1: Expression analysis during behavioral modification. Published in De Bekker et al., 2017.

Click here for more information

Sequences

Type of sequenceSequence
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 >Ophio5|2386
MATILSKAQVDEAIQRLLGAAKSYSDTPEPEGHAARVEMLAQVRSLNQSLLTPDMMPFYHGLNMAELVDVRTFMK
LGVLEAIPQRGSISLRRLSHETGVQESLLERMARNLVMSGFLQQTRPDGGEYRHSKFSRAYRIDSSGTGPGHLFL
VLFDYILKPFVDFDDYFAQRGQLQNAREPDDALYSPFSLSRNQGGTCPWTILSQDPEQLRMFQMGMRNLDLAVPA
VGSFDFDCLRNTPEEEAAGRIQLVDVGGGHGVVLGDILDAHPDALRPETCVLQDRPDVIELSKINGALPAEVQRI
HHDFMTEQPVKGAKAYFMRMIIHDWPDAVCVQILAHLAAAMALDSRVLIFDSVLPQRVDEANFFAAVVDHAVMAI
AGKERTEEDFSALLNEAGLELVRVWQVPGNSGAGACIEGRLRRRSERL*
Coding >Ophio5|2386
ATGGCAACGATACTGTCCAAAGCCCAGGTCGACGAGGCCATCCAGAGGCTACTCGGAGCTGCAAAGAGCTACTCG
GATACCCCCGAGCCGGAGGGCCATGCGGCGCGAGTCGAGATGCTCGCGCAGGTGCGGAGCTTGAACCAGTCACTG
CTCACGCCGGACATGATGCCATTCTACCACGGACTCAACATGGCCGAACTTGTCGATGTTCGCACCTTCATGAAG
CTCGGGGTGCTGGAAGCTATCCCCCAACGAGGCTCCATCTCCCTTCGACGGCTGTCTCACGAGACAGGGGTGCAG
GAATCTTTGCTAGAGCGTATGGCACGCAATCTTGTCATGTCCGGCTTCCTCCAACAGACACGACCGGACGGAGGC
GAGTATCGTCACTCCAAGTTCTCTCGCGCCTATCGAATCGACAGCTCGGGCACGGGCCCGGGTCACCTATTCCTA
GTCTTATTTGACTACATTCTGAAGCCTTTCGTCGATTTCGACGACTATTTCGCCCAACGGGGCCAGCTGCAGAAC
GCCCGCGAGCCCGACGACGCCCTCTACAGCCCCTTCAGCCTCTCTCGCAACCAGGGCGGCACGTGCCCTTGGACC
ATCCTGAGCCAGGATCCGGAGCAGCTGCGCATGTTCCAGATGGGCATGCGCAACTTGGACCTCGCCGTCCCTGCC
GTCGGCTCCTTCGACTTCGATTGCCTTCGCAACACGCCCGAGGAGGAAGCGGCCGGACGTATCCAGCTTGTCGAC
GTAGGCGGCGGTCATGGCGTTGTCCTCGGCGACATCCTCGACGCTCATCCCGATGCGCTGAGGCCCGAGACCTGC
GTCCTCCAAGATCGGCCGGACGTCATCGAGCTATCCAAGATCAATGGGGCTCTTCCAGCCGAGGTCCAACGTATT
CACCATGACTTTATGACGGAGCAGCCGGTCAAAGGAGCCAAGGCCTACTTCATGCGCATGATCATCCACGACTGG
CCCGATGCCGTGTGCGTTCAGATACTCGCTCATCTGGCTGCCGCCATGGCTCTCGACTCGCGCGTTCTCATCTTC
GATTCCGTGCTTCCACAGCGGGTTGACGAGGCCAATTTCTTCGCAGCAGTCGTTGACCACGCCGTTATGGCCATA
GCCGGTAAGGAACGTACCGAGGAGGACTTCTCCGCGCTCCTCAACGAGGCCGGGCTGGAGCTGGTCAGAGTGTGG
CAAGTTCCGGGTAATTCTGGAGCTGGAGCGTGTATCGAGGGCAGGCTGCGGCGCCGGTCCGAGAGGCTGTAG
Transcript >Ophio5|2386
ATGGCAACGATACTGTCCAAAGCCCAGGTCGACGAGGCCATCCAGAGGCTACTCGGAGCTGCAAAGAGCTACTCG
GATACCCCCGAGCCGGAGGGCCATGCGGCGCGAGTCGAGATGCTCGCGCAGGTGCGGAGCTTGAACCAGTCACTG
CTCACGCCGGACATGATGCCATTCTACCACGGACTCAACATGGCCGAACTTGTCGATGTTCGCACCTTCATGAAG
CTCGGGGTGCTGGAAGCTATCCCCCAACGAGGCTCCATCTCCCTTCGACGGCTGTCTCACGAGACAGGGGTGCAG
GAATCTTTGCTAGAGCGTATGGCACGCAATCTTGTCATGTCCGGCTTCCTCCAACAGACACGACCGGACGGAGGC
GAGTATCGTCACTCCAAGTTCTCTCGCGCCTATCGAATCGACAGCTCGGGCACGGGCCCGGGTCACCTATTCCTA
GTCTTATTTGACTACATTCTGAAGCCTTTCGTCGATTTCGACGACTATTTCGCCCAACGGGGCCAGCTGCAGAAC
GCCCGCGAGCCCGACGACGCCCTCTACAGCCCCTTCAGCCTCTCTCGCAACCAGGGCGGCACGTGCCCTTGGACC
ATCCTGAGCCAGGATCCGGAGCAGCTGCGCATGTTCCAGATGGGCATGCGCAACTTGGACCTCGCCGTCCCTGCC
GTCGGCTCCTTCGACTTCGATTGCCTTCGCAACACGCCCGAGGAGGAAGCGGCCGGACGTATCCAGCTTGTCGAC
GTAGGCGGCGGTCATGGCGTTGTCCTCGGCGACATCCTCGACGCTCATCCCGATGCGCTGAGGCCCGAGACCTGC
GTCCTCCAAGATCGGCCGGACGTCATCGAGCTATCCAAGATCAATGGGGCTCTTCCAGCCGAGGTCCAACGTATT
CACCATGACTTTATGACGGAGCAGCCGGTCAAAGGAGCCAAGGCCTACTTCATGCGCATGATCATCCACGACTGG
CCCGATGCCGTGTGCGTTCAGATACTCGCTCATCTGGCTGCCGCCATGGCTCTCGACTCGCGCGTTCTCATCTTC
GATTCCGTGCTTCCACAGCGGGTTGACGAGGCCAATTTCTTCGCAGCAGTCGTTGACCACGCCGTTATGGCCATA
GCCGGTAAGGAACGTACCGAGGAGGACTTCTCCGCGCTCCTCAACGAGGCCGGGCTGGAGCTGGTCAGAGTGTGG
CAAGTTCCGGGTAATTCTGGAGCTGGAGCGTGTATCGAGGGCAGGCTGCGGCGCCGGTCCGAGAGGCTGTAG
Gene >Ophio5|2386
ATGGCAACGATACTGTCCAAAGCCCAGGTCGACGAGGCCATCCAGAGGCTACTCGGAGCTGCAAAGAGCTACTCG
GATACCCCCGAGCCGGAGGGCCATGCGGCGCGAGTCGAGATGCTCGCGCAGGTGCGGAGCTTGAACCAGTCACTG
CTCACGCCGGACATGATGCCATTCTACCACGGACTCAACGTTCGTTGTTCCACCCACCTTTTAATTTCTGGCAGT
ACGTCTGCGGTAGGAGACTGAGCTGCGAACGCGGGCATCTGCTGCTTGTAGATGGCCGAACTTGTCGATGTTCGC
ACCTTCATGAAGCTCGGGGTGCTGGAAGCTATCCCCCAACGAGGCTCCATCTCCCTTCGACGGCTGTCTCACGAG
ACAGGGGTGCAGGAATCTTTGCTAGGTGCGACCTTGTTCCTGATCCATCCTCCTCTTGATAGAAAAAAGGCAGAT
GAGTAAGTAACACACGAGTGATGGGACTCGAGACAGAGCGTATGGCACGCAATCTTGGTAGGTTTGTTCTTTCTC
CTTTCTTTCGTGGCCAGACGTTGAATTTCTCGCTGATGGCTTCACCTATCATCTCGCCCCAGTCATGTCCGGCTT
CCTCCAACAGACACGACCGGACGGAGGCGAGTATCGTCACTCCAAGTTCTCTCGCGCCTATCGAATCGACAGCTC
GGGCACGGGCCCGGGTCACCTATTCCTAGTCTTGTAAGCGGAGATCGGAGTCTCACGAGACTAGTCGCTCGTTGC
CATCACTTTGCTCACCCCCTCTCGCTCTCAGATTTGACTACATTCTGAAGCCTTTCGTCGATTTCGACGACTATT
TCGCCCAACGGGGCCAGCTGCAGAACGCCCGCGAGCCCGACGACGCCCTCTACAGCCCCTTCAGCCTCTCTCGCA
ACCAGGGCGGCACGTGCCCTTGGACCATCCTGAGCCAGGATCCGGAGCAGCTGCGCATGTTCCAGATGGGCATGC
GCAACTTGGACCTCGCCGTCCCTGCCGTCGGCTCCTTCGACTTCGATTGCCTTCGCAACACGCCCGAGGAGGAAG
CGGCCGGACGTATCCAGCTTGTCGACGTAGGCGGCGGTCATGGCGTTGTCCTCGGCGACATCCTCGACGCTCATC
CCGATGCGCTGAGGCCCGAGACCTGCGTCCTCCAAGATCGGCCGGACGTCATCGAGCTATCCAAGATCAATGGGG
CTCTTCCAGCCGAGGTCCAACGTATTCACCATGACTTTATGACGGAGCAGCCGGTCAAAGGTGAGCTTTCCGCCT
TCCTCCACTTCTCTCACCTTGGCTCCTCTCCCTCCCGAGCCTAGATGCTTTCTGCTTACCCTTAGACTGACTCGC
CCCATTCCAATGCCGATAGGAGCCAAGGCCTACTTCATGCGCATGATCATCCACGACTGGCCCGATGCCGTGTGC
GTTCAGATACTCGCTCATCTGGCTGCCGCCATGGCTCTCGACTCGCGCGTTCTCATCTTCGATTCCGTGCTTCCA
CAGCGGGTTGACGAGGCCAATTTCTTCGCAGCAGTCGTTGACCACGCCGTTATGGCCATAGCCGGTAAGGAACGT
ACCGAGGAGGACTTCTCCGCGCTCCTCAACGAGGCCGGGCTGGAGCTGGTCAGAGTGTGGCAAGTTCCGGGTAAT
TCTGGAGCTGGAGCGTGTATCGAGGGCAGGCTGCGGCGCCGGTCCGAGAGGCTGTAG

© 2022 - Robin Ohm - Utrecht University - The Netherlands

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