Fungal Genomics

at Utrecht University

General Properties

Protein IDOphauG2|2786
Gene name
LocationContig_206:2905..4874
Strand-
Gene length (bp)1969
Transcript length (bp)1797
Coding sequence length (bp)1797
Protein length (aa) 599

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PFAM Domains

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 hits

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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
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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
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GO

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

[Help with interpreting these statistics]
SignalP signal predicted Location
(based on Ymax)		 D score
(significance: > 0.45)
No 1 - 11 0.45

Transmembrane Domains

Domain # Start End Length
1 552 574 22

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 >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

© 2022 - Robin Ohm - Utrecht University - The Netherlands

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