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

Overview

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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

[Show all]
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
[Show all]
[Show less]
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

Deeploc

Deeploc data not available for this genome

SignalP

(None)

Transmembrane Domains

Domain # Start End Length
1 552 574 22

Transcription Factor Class

(None)

CAZymes

(None)

Secondary Metabolism

(None)

Expression data

No expression data available for this genome

Orthologs

Orthofinder run ID4
Orthogroup950
Change Orthofinder run
Species Protein ID
Ophiocordyceps australis 1348a (Ghana) OphauG2|2786 (this protein)
Ophiocordyceps australis map64 (Brazil) OphauB2|2822
Ophiocordyceps camponoti-floridani Ophcf2|03701
Ophiocordyceps camponoti-rufipedis Ophun1|6259
Ophiocordyceps kimflemingae Ophio5|5773
Ophiocordyceps subramaniannii Hirsu2|705
Ophiocordyceps subramaniannii Hirsu2|9428

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 >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

© 2023 - Robin Ohm - Utrecht University - The Netherlands

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