Fungal Genomics

at Utrecht University

General Properties

Protein IDHirsu2|406
Gene name
LocationContig_108:23460..24981
Strand-
Gene length (bp)1521
Transcript length (bp)1521
Coding sequence length (bp)1521
Protein length (aa) 507

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PFAM Domains

PFAM Domain ID Short name Long name E-value Start End
PF13738 Pyr_redox_3 Pyridine nucleotide-disulphide oxidoreductase 1.0E-14 13 227
PF07992 Pyr_redox_2 Pyridine nucleotide-disulphide oxidoreductase 7.9E-09 11 207
PF13450 NAD_binding_8 NAD(P)-binding Rossmann-like domain 5.5E-07 14 80
PF00743 FMO-like Flavin-binding monooxygenase-like 1.8E-06 11 215

Swissprot hits

[Show all]
Swissprot ID Swissprot Description Start End E-value
sp|Q9RKB5|BVMO2_STRCO Baeyer-Villiger monooxygenase OS=Streptomyces coelicolor (strain ATCC BAA-471 / A3(2) / M145) GN=SCO3172 PE=1 SV=1 7 503 5.0E-75
sp|Q9I3H5|BVMO_PSEAE Baeyer-Villiger monooxygenase OS=Pseudomonas aeruginosa (strain ATCC 15692 / PAO1 / 1C / PRS 101 / LMG 12228) GN=PA1538 PE=1 SV=1 11 453 3.0E-71
sp|P9WNG1|Y892_MYCTU Uncharacterized monooxygenase Rv0892 OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=Rv0892 PE=1 SV=1 12 485 2.0E-67
sp|P9WNG0|Y892_MYCTO Uncharacterized monooxygenase MT0916 OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=MT0916 PE=3 SV=1 12 485 2.0E-67
sp|P64746|Y916_MYCBO Uncharacterized monooxygenase Mb0916 OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=Mb0916 PE=3 SV=1 12 485 2.0E-67
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Swissprot ID Swissprot Description Start End E-value
sp|Q9RKB5|BVMO2_STRCO Baeyer-Villiger monooxygenase OS=Streptomyces coelicolor (strain ATCC BAA-471 / A3(2) / M145) GN=SCO3172 PE=1 SV=1 7 503 5.0E-75
sp|Q9I3H5|BVMO_PSEAE Baeyer-Villiger monooxygenase OS=Pseudomonas aeruginosa (strain ATCC 15692 / PAO1 / 1C / PRS 101 / LMG 12228) GN=PA1538 PE=1 SV=1 11 453 3.0E-71
sp|P9WNG1|Y892_MYCTU Uncharacterized monooxygenase Rv0892 OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=Rv0892 PE=1 SV=1 12 485 2.0E-67
sp|P9WNG0|Y892_MYCTO Uncharacterized monooxygenase MT0916 OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=MT0916 PE=3 SV=1 12 485 2.0E-67
sp|P64746|Y916_MYCBO Uncharacterized monooxygenase Mb0916 OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=Mb0916 PE=3 SV=1 12 485 2.0E-67
sp|Q93TJ5|HAPMO_PSEFL 4-hydroxyacetophenone monooxygenase OS=Pseudomonas fluorescens GN=hapE PE=1 SV=1 6 503 6.0E-62
sp|P55487|Y4ID_RHISN Uncharacterized monooxygenase y4iD OS=Rhizobium sp. (strain NGR234) GN=NGR_a03290 PE=3 SV=1 12 503 1.0E-51
sp|E3VWK3|PENE_STREX Pentalenolactone D synthase OS=Streptomyces exfoliatus GN=penE PE=1 SV=1 11 469 1.0E-48
sp|E3VWI7|PNTE_STRAE Pentalenolactone D synthase OS=Streptomyces arenae GN=pntE PE=1 SV=1 11 469 1.0E-44
sp|Q82IY8|PTLE_STRAW Neopentalenolactone D synthase OS=Streptomyces avermitilis (strain ATCC 31267 / DSM 46492 / JCM 5070 / NBRC 14893 / NCIMB 12804 / NRRL 8165 / MA-4680) GN=ptlE PE=1 SV=1 38 479 1.0E-40
sp|P12015|CHMO_ACISP Cyclohexanone 1,2-monooxygenase OS=Acinetobacter sp. PE=1 SV=2 5 403 2.0E-40
sp|Q47PU3|PAMO_THEFY Phenylacetone monooxygenase OS=Thermobifida fusca (strain YX) GN=pamO PE=1 SV=1 11 438 3.0E-40
sp|Q00730|STCW_EMENI Putative sterigmatocystin biosynthesis monooxygenase stcW OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=stcW PE=3 SV=2 12 503 4.0E-40
sp|A3U3H1|BVMO_OCEBH Baeyer-Villiger monooxygenase OS=Oceanicola batsensis (strain ATCC BAA-863 / DSM 15984 / HTCC2597) GN=OB2597_18631 PE=1 SV=1 5 461 2.0E-39
sp|U5S003|BVMO4_DIESD Baeyer-Villiger monooxygenase 4 OS=Dietzia sp. (strain D5) PE=1 SV=1 28 480 1.0E-38
sp|A1CLY7|CCSB_ASPCL Ketocytochalasin monooxygenase OS=Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1) GN=ccsB PE=1 SV=1 7 410 7.0E-38
sp|H3JQW0|OTEMO_PSEPU 2-oxo-Delta(3)-4,5,5-trimethylcyclopentenylacetyl-CoA monooxygenase OS=Pseudomonas putida GN=otemo PE=1 SV=1 11 405 1.0E-37
sp|A7HU16|BVMO_PARL1 Baeyer-Villiger monooxygenase OS=Parvibaculum lavamentivorans (strain DS-1 / DSM 13023 / NCIMB 13966) GN=Plav_1781 PE=1 SV=1 2 461 2.0E-37
sp|Q8GAW0|CPMO_COMS9 Cyclopentanone 1,2-monooxygenase OS=Comamonas sp. (strain NCIMB 9872) GN=cpnB PE=1 SV=3 11 409 5.0E-34
sp|Q9RL17|BVMO1_STRCO Baeyer-Villiger monooxygenase OS=Streptomyces coelicolor (strain ATCC BAA-471 / A3(2) / M145) GN=SCO0300 PE=1 SV=1 27 479 2.0E-32
sp|P9WNF9|ETHA_MYCTU FAD-containing monooxygenase EthA OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ethA PE=1 SV=1 5 502 5.0E-28
sp|P9WNF8|ETHA_MYCTO FAD-containing monooxygenase EthA OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=ethA PE=3 SV=1 5 502 5.0E-28
sp|Q7TVI2|ETHA_MYCBO FAD-containing monooxygenase EthA OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=ethA PE=1 SV=1 5 502 5.0E-28
sp|A0R665|ETHA_MYCS2 FAD-containing monooxygenase EthA OS=Mycobacterium smegmatis (strain ATCC 700084 / mc(2)155) GN=ethA PE=3 SV=1 8 438 6.0E-27
sp|Q88J44|BVMO_PSEPK Baeyer-Villiger monooxygenase OS=Pseudomonas putida (strain KT2440) GN=PP_2805 PE=1 SV=1 11 426 7.0E-25
sp|Q9SVU0|YUC8_ARATH Probable indole-3-pyruvate monooxygenase YUCCA8 OS=Arabidopsis thaliana GN=YUC8 PE=2 SV=1 13 353 6.0E-20
sp|Q9SZY8|YUC1_ARATH Probable indole-3-pyruvate monooxygenase YUCCA1 OS=Arabidopsis thaliana GN=YUC1 PE=1 SV=1 10 352 3.0E-19
sp|P9WNF7|MYMA_MYCTU Putative FAD-containing monooxygenase MymA OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=mymA PE=1 SV=1 11 426 8.0E-18
sp|P9WNF6|MYMA_MYCTO Putative FAD-containing monooxygenase MymA OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=mymA PE=3 SV=1 11 426 8.0E-18
sp|O64489|YUC9_ARATH Probable indole-3-pyruvate monooxygenase YUCCA9 OS=Arabidopsis thaliana GN=YUC9 PE=2 SV=1 13 380 2.0E-17
sp|Q8VZ59|YUC6_ARATH Indole-3-pyruvate monooxygenase YUCCA6 OS=Arabidopsis thaliana GN=YUC6 PE=1 SV=1 13 377 4.0E-16
sp|Q9LKC0|YUC5_ARATH Probable indole-3-pyruvate monooxygenase YUCCA5 OS=Arabidopsis thaliana GN=YUC5 PE=2 SV=1 13 380 5.0E-16
sp|O23024|YUC3_ARATH Probable indole-3-pyruvate monooxygenase YUCCA3 OS=Arabidopsis thaliana GN=YUC3 PE=2 SV=1 13 352 4.0E-15
sp|Q9FVQ0|YUC10_ARATH Probable indole-3-pyruvate monooxygenase YUCCA10 OS=Arabidopsis thaliana GN=YUC10 PE=2 SV=1 12 352 2.0E-14
sp|O49312|YUC7_ARATH Probable indole-3-pyruvate monooxygenase YUCCA7 OS=Arabidopsis thaliana GN=YUC7 PE=2 SV=1 13 377 7.0E-14
sp|Q9LPL3|YUC11_ARATH Probable indole-3-pyruvate monooxygenase YUCCA11 OS=Arabidopsis thaliana GN=YUC11 PE=2 SV=1 12 353 1.0E-13
sp|Q9LFM5|YUC4_ARATH Probable indole-3-pyruvate monooxygenase YUCCA4 OS=Arabidopsis thaliana GN=YUC4 PE=1 SV=1 13 352 1.0E-12
sp|Q8MP06|SNO1_TYRJA Senecionine N-oxygenase OS=Tyria jacobaeae GN=sno1 PE=1 SV=1 12 202 1.0E-11
sp|Q04799|FMO5_RABIT Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Oryctolagus cuniculus GN=FMO5 PE=1 SV=2 12 240 6.0E-10
sp|P49109|FMO5_CAVPO Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Cavia porcellus GN=FMO5 PE=2 SV=2 8 239 9.0E-09
sp|P97872|FMO5_MOUSE Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Mus musculus GN=Fmo5 PE=1 SV=4 12 213 6.0E-08
sp|Q8K2I3|FMO2_MOUSE Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Mus musculus GN=Fmo2 PE=1 SV=3 11 215 6.0E-08
sp|P17635|FMO2_RABIT Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Oryctolagus cuniculus GN=FMO2 PE=1 SV=3 11 215 1.0E-07
sp|P36366|FMO2_CAVPO Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Cavia porcellus GN=FMO2 PE=2 SV=2 11 215 1.0E-07
sp|O07085|CZCO_BACSU Uncharacterized oxidoreductase CzcO OS=Bacillus subtilis (strain 168) GN=czcO PE=1 SV=1 10 198 2.0E-07
sp|Q28505|FMO2_MACMU Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Macaca mulatta GN=FMO2 PE=2 SV=2 11 215 5.0E-07
sp|Q8HZ70|FMO2_PANTR Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Pan troglodytes GN=FMO2 PE=3 SV=3 11 215 7.0E-07
sp|Q8HZ69|FMO2_GORGO Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Gorilla gorilla gorilla GN=FMO2 PE=3 SV=3 11 215 8.0E-07
sp|Q6IRI9|FMO2_RAT Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Rattus norvegicus GN=Fmo2 PE=2 SV=3 11 215 3.0E-06
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GO

GO Term Description Terminal node
GO:0004499 N,N-dimethylaniline monooxygenase activity Yes
GO:0050660 flavin adenine dinucleotide binding Yes
GO:0055114 oxidation-reduction process Yes
GO:0016491 oxidoreductase activity Yes
GO:0050661 NADP binding Yes
GO:0003674 molecular_function No
GO:0036094 small molecule binding No
GO:0008150 biological_process No
GO:0008152 metabolic process No
GO:1901265 nucleoside phosphate binding No
GO:0005488 binding No
GO:0097159 organic cyclic compound binding No
GO:0048037 cofactor binding No
GO:0050662 coenzyme binding No
GO:0016705 oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen No
GO:0003824 catalytic activity No
GO:0043168 anion binding No
GO:0004497 monooxygenase activity No
GO:0043167 ion binding No
GO:0000166 nucleotide 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:1901363 heterocyclic compound binding No

SignalP

[Help with interpreting these statistics]
SignalP signal predicted Location
(based on Ymax)
D score
(significance: > 0.45)
No 1 - 25 0.45

Transmembrane Domains

(None)

Transcription Factor Class

(None)

Expression data

No expression data available for this genome

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 >Hirsu2|406
MAASTSHTDHEVVVIGAGPGGICAGVRLKEANVQDFVILERDAEIGGSWRDNRYPDIGVDIPCCLYQYSFARNPN
WSRLFPKGAEVLAYHKDVVRKYALEPHMRYHSHVIGQAWDETAGHWELTMATGQVMTAKFVISAVGAFLVAKEDP
GIEGWLEFKGKVLRPTDWDYGYSLAGKRVAIIGTGASSVQITPVLAKQASHLDVYQRTPVWCLPKPDVILGPKTQ
RMLAFPLVQTLINGLSLIIVDVVLRIVIYSPLFLFIRLARAFDAISKYAYRRYLRAVVKEARDRAALLPDYGLLG
KRPTISGQFLQTFNRSNVSLITAPIWRITPAGVRTANGEHRQYDALVLATGYHLFSDPESYATGAIVGRDGFDLG
TFYNSKGLQAYESVSVPGLPNRWTVIGPYSWTGISWHTMVEISTRHIVNVLLEARCRGAKSVEVSEAAHRAYHDK
IRRLATNMTFYFTYINKGLRTYYLNSQGQVPFIRPTTLLSALRSSRQVKFDDYVFT*
Coding >Hirsu2|406
ATGGCAGCATCGACATCGCACACTGACCATGAAGTCGTCGTCATCGGAGCCGGGCCCGGCGGCATCTGCGCAGGC
GTGCGGCTGAAAGAGGCCAACGTTCAGGACTTCGTCATCCTCGAGCGAGACGCGGAAATTGGGGGCAGCTGGCGA
GATAACCGCTATCCAGATATAGGTGTAGACATCCCATGTTGTCTGTACCAGTATAGCTTCGCGCGCAACCCGAAT
TGGTCGCGCCTCTTCCCCAAGGGCGCCGAGGTGCTGGCCTACCACAAGGACGTGGTCCGCAAGTATGCCCTAGAG
CCGCACATGCGCTACCATTCGCACGTCATCGGCCAGGCCTGGGACGAAACGGCAGGCCATTGGGAGCTCACCATG
GCGACAGGGCAAGTCATGACAGCCAAGTTCGTCATATCCGCGGTTGGGGCCTTCCTGGTCGCAAAGGAGGACCCG
GGCATCGAGGGCTGGCTCGAATTCAAGGGAAAGGTGCTGCGGCCTACTGACTGGGACTATGGCTACAGCCTGGCC
GGGAAACGTGTGGCCATCATTGGAACCGGTGCCAGCTCCGTACAGATTACTCCGGTTCTGGCCAAACAGGCGAGC
CACTTGGACGTTTACCAGCGGACTCCGGTCTGGTGTCTGCCCAAGCCAGACGTTATCCTGGGACCCAAGACTCAA
CGCATGCTCGCCTTTCCACTCGTGCAGACTTTGATCAACGGCCTCTCGCTCATCATCGTCGACGTCGTTTTACGC
ATCGTCATCTATTCACCCCTATTCCTCTTTATACGGCTTGCACGGGCTTTCGATGCCATTTCCAAATACGCCTAT
CGCCGCTATCTAAGGGCCGTGGTCAAAGAGGCCCGTGACCGGGCCGCTCTGCTTCCCGACTACGGCCTGCTTGGC
AAGCGGCCGACTATCTCGGGGCAGTTCCTCCAGACCTTCAACCGGTCCAACGTGTCGCTCATCACCGCCCCCATT
TGGCGCATCACGCCCGCCGGAGTGCGAACCGCAAACGGGGAGCATCGCCAGTATGACGCCCTCGTGCTGGCCACC
GGCTACCATCTCTTCTCCGACCCAGAGAGCTACGCCACTGGGGCCATCGTCGGTCGGGACGGCTTCGATCTCGGC
ACCTTTTATAACAGCAAGGGCTTGCAGGCCTACGAGAGCGTGAGCGTTCCCGGCCTGCCCAACCGCTGGACAGTC
ATTGGGCCCTACTCTTGGACAGGCATAAGTTGGCATACCATGGTCGAGATCTCGACCCGCCACATCGTCAACGTC
CTCCTCGAAGCGCGCTGCCGGGGGGCCAAGTCTGTAGAGGTCAGTGAGGCCGCGCACCGTGCCTATCACGACAAG
ATCCGCAGGCTGGCGACCAACATGACGTTCTACTTCACCTACATCAACAAGGGCCTGCGCACCTACTACTTGAAT
TCCCAGGGACAAGTTCCCTTCATACGGCCCACGACGCTGCTGTCCGCTCTGCGAAGCAGCCGCCAAGTCAAGTTC
GACGACTATGTATTCACGTAG
Transcript >Hirsu2|406
ATGGCAGCATCGACATCGCACACTGACCATGAAGTCGTCGTCATCGGAGCCGGGCCCGGCGGCATCTGCGCAGGC
GTGCGGCTGAAAGAGGCCAACGTTCAGGACTTCGTCATCCTCGAGCGAGACGCGGAAATTGGGGGCAGCTGGCGA
GATAACCGCTATCCAGATATAGGTGTAGACATCCCATGTTGTCTGTACCAGTATAGCTTCGCGCGCAACCCGAAT
TGGTCGCGCCTCTTCCCCAAGGGCGCCGAGGTGCTGGCCTACCACAAGGACGTGGTCCGCAAGTATGCCCTAGAG
CCGCACATGCGCTACCATTCGCACGTCATCGGCCAGGCCTGGGACGAAACGGCAGGCCATTGGGAGCTCACCATG
GCGACAGGGCAAGTCATGACAGCCAAGTTCGTCATATCCGCGGTTGGGGCCTTCCTGGTCGCAAAGGAGGACCCG
GGCATCGAGGGCTGGCTCGAATTCAAGGGAAAGGTGCTGCGGCCTACTGACTGGGACTATGGCTACAGCCTGGCC
GGGAAACGTGTGGCCATCATTGGAACCGGTGCCAGCTCCGTACAGATTACTCCGGTTCTGGCCAAACAGGCGAGC
CACTTGGACGTTTACCAGCGGACTCCGGTCTGGTGTCTGCCCAAGCCAGACGTTATCCTGGGACCCAAGACTCAA
CGCATGCTCGCCTTTCCACTCGTGCAGACTTTGATCAACGGCCTCTCGCTCATCATCGTCGACGTCGTTTTACGC
ATCGTCATCTATTCACCCCTATTCCTCTTTATACGGCTTGCACGGGCTTTCGATGCCATTTCCAAATACGCCTAT
CGCCGCTATCTAAGGGCCGTGGTCAAAGAGGCCCGTGACCGGGCCGCTCTGCTTCCCGACTACGGCCTGCTTGGC
AAGCGGCCGACTATCTCGGGGCAGTTCCTCCAGACCTTCAACCGGTCCAACGTGTCGCTCATCACCGCCCCCATT
TGGCGCATCACGCCCGCCGGAGTGCGAACCGCAAACGGGGAGCATCGCCAGTATGACGCCCTCGTGCTGGCCACC
GGCTACCATCTCTTCTCCGACCCAGAGAGCTACGCCACTGGGGCCATCGTCGGTCGGGACGGCTTCGATCTCGGC
ACCTTTTATAACAGCAAGGGCTTGCAGGCCTACGAGAGCGTGAGCGTTCCCGGCCTGCCCAACCGCTGGACAGTC
ATTGGGCCCTACTCTTGGACAGGCATAAGTTGGCATACCATGGTCGAGATCTCGACCCGCCACATCGTCAACGTC
CTCCTCGAAGCGCGCTGCCGGGGGGCCAAGTCTGTAGAGGTCAGTGAGGCCGCGCACCGTGCCTATCACGACAAG
ATCCGCAGGCTGGCGACCAACATGACGTTCTACTTCACCTACATCAACAAGGGCCTGCGCACCTACTACTTGAAT
TCCCAGGGACAAGTTCCCTTCATACGGCCCACGACGCTGCTGTCCGCTCTGCGAAGCAGCCGCCAAGTCAAGTTC
GACGACTATGTATTCACGTAG
Gene >Hirsu2|406
ATGGCAGCATCGACATCGCACACTGACCATGAAGTCGTCGTCATCGGAGCCGGGCCCGGCGGCATCTGCGCAGGC
GTGCGGCTGAAAGAGGCCAACGTTCAGGACTTCGTCATCCTCGAGCGAGACGCGGAAATTGGGGGCAGCTGGCGA
GATAACCGCTATCCAGATATAGGTGTAGACATCCCATGTTGTCTGTACCAGTATAGCTTCGCGCGCAACCCGAAT
TGGTCGCGCCTCTTCCCCAAGGGCGCCGAGGTGCTGGCCTACCACAAGGACGTGGTCCGCAAGTATGCCCTAGAG
CCGCACATGCGCTACCATTCGCACGTCATCGGCCAGGCCTGGGACGAAACGGCAGGCCATTGGGAGCTCACCATG
GCGACAGGGCAAGTCATGACAGCCAAGTTCGTCATATCCGCGGTTGGGGCCTTCCTGGTCGCAAAGGAGGACCCG
GGCATCGAGGGCTGGCTCGAATTCAAGGGAAAGGTGCTGCGGCCTACTGACTGGGACTATGGCTACAGCCTGGCC
GGGAAACGTGTGGCCATCATTGGAACCGGTGCCAGCTCCGTACAGATTACTCCGGTTCTGGCCAAACAGGCGAGC
CACTTGGACGTTTACCAGCGGACTCCGGTCTGGTGTCTGCCCAAGCCAGACGTTATCCTGGGACCCAAGACTCAA
CGCATGCTCGCCTTTCCACTCGTGCAGACTTTGATCAACGGCCTCTCGCTCATCATCGTCGACGTCGTTTTACGC
ATCGTCATCTATTCACCCCTATTCCTCTTTATACGGCTTGCACGGGCTTTCGATGCCATTTCCAAATACGCCTAT
CGCCGCTATCTAAGGGCCGTGGTCAAAGAGGCCCGTGACCGGGCCGCTCTGCTTCCCGACTACGGCCTGCTTGGC
AAGCGGCCGACTATCTCGGGGCAGTTCCTCCAGACCTTCAACCGGTCCAACGTGTCGCTCATCACCGCCCCCATT
TGGCGCATCACGCCCGCCGGAGTGCGAACCGCAAACGGGGAGCATCGCCAGTATGACGCCCTCGTGCTGGCCACC
GGCTACCATCTCTTCTCCGACCCAGAGAGCTACGCCACTGGGGCCATCGTCGGTCGGGACGGCTTCGATCTCGGC
ACCTTTTATAACAGCAAGGGCTTGCAGGCCTACGAGAGCGTGAGCGTTCCCGGCCTGCCCAACCGCTGGACAGTC
ATTGGGCCCTACTCTTGGACAGGCATAAGTTGGCATACCATGGTCGAGATCTCGACCCGCCACATCGTCAACGTC
CTCCTCGAAGCGCGCTGCCGGGGGGCCAAGTCTGTAGAGGTCAGTGAGGCCGCGCACCGTGCCTATCACGACAAG
ATCCGCAGGCTGGCGACCAACATGACGTTCTACTTCACCTACATCAACAAGGGCCTGCGCACCTACTACTTGAAT
TCCCAGGGACAAGTTCCCTTCATACGGCCCACGACGCTGCTGTCCGCTCTGCGAAGCAGCCGCCAAGTCAAGTTC
GACGACTATGTATTCACGTAG

© 2022 - Robin Ohm - Utrecht University - The Netherlands

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