Fungal Genomics

at Utrecht University

General Properties

Protein IDHirsu2|6531
Gene name
LocationContig_338:3709..5467
Strand-
Gene length (bp)1758
Transcript length (bp)1542
Coding sequence length (bp)1542
Protein length (aa) 514

Overview

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PFAM Domains

PFAM Domain ID Short name Long name E-value Start End
PF07992 Pyr_redox_2 Pyridine nucleotide-disulphide oxidoreductase 2.4E-08 45 238
PF13738 Pyr_redox_3 Pyridine nucleotide-disulphide oxidoreductase 6.7E-09 48 239
PF13434 Lys_Orn_oxgnase L-lysine 6-monooxygenase/L-ornithine 5-monooxygenase 1.8E-06 126 238
PF00743 FMO-like Flavin-binding monooxygenase-like 1.3E-05 162 385
PF13450 NAD_binding_8 NAD(P)-binding Rossmann-like domain 1.8E-06 48 92

Swissprot hits

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Swissprot ID Swissprot Description Start End E-value
sp|P9WNG1|Y892_MYCTU Uncharacterized monooxygenase Rv0892 OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=Rv0892 PE=1 SV=1 42 242 6.0E-18
sp|P64746|Y916_MYCBO Uncharacterized monooxygenase Mb0916 OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=Mb0916 PE=3 SV=1 42 242 6.0E-18
sp|P9WNG0|Y892_MYCTO Uncharacterized monooxygenase MT0916 OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=MT0916 PE=3 SV=1 42 242 6.0E-18
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 27 243 7.0E-18
sp|Q93TJ5|HAPMO_PSEFL 4-hydroxyacetophenone monooxygenase OS=Pseudomonas fluorescens GN=hapE PE=1 SV=1 18 313 1.0E-16
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Swissprot ID Swissprot Description Start End E-value
sp|P9WNG1|Y892_MYCTU Uncharacterized monooxygenase Rv0892 OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=Rv0892 PE=1 SV=1 42 242 6.0E-18
sp|P64746|Y916_MYCBO Uncharacterized monooxygenase Mb0916 OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=Mb0916 PE=3 SV=1 42 242 6.0E-18
sp|P9WNG0|Y892_MYCTO Uncharacterized monooxygenase MT0916 OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=MT0916 PE=3 SV=1 42 242 6.0E-18
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 27 243 7.0E-18
sp|Q93TJ5|HAPMO_PSEFL 4-hydroxyacetophenone monooxygenase OS=Pseudomonas fluorescens GN=hapE PE=1 SV=1 18 313 1.0E-16
sp|Q9RKB5|BVMO2_STRCO Baeyer-Villiger monooxygenase OS=Streptomyces coelicolor (strain ATCC BAA-471 / A3(2) / M145) GN=SCO3172 PE=1 SV=1 45 243 1.0E-15
sp|P49109|FMO5_CAVPO Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Cavia porcellus GN=FMO5 PE=2 SV=2 41 439 3.0E-15
sp|Q8K4C0|FMO5_RAT Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Rattus norvegicus GN=Fmo5 PE=1 SV=3 41 392 2.0E-14
sp|P97872|FMO5_MOUSE Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Mus musculus GN=Fmo5 PE=1 SV=4 41 392 6.0E-14
sp|H3JQW0|OTEMO_PSEPU 2-oxo-Delta(3)-4,5,5-trimethylcyclopentenylacetyl-CoA monooxygenase OS=Pseudomonas putida GN=otemo PE=1 SV=1 48 242 1.0E-13
sp|Q04799|FMO5_RABIT Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Oryctolagus cuniculus GN=FMO5 PE=1 SV=2 45 392 1.0E-13
sp|Q9FVQ0|YUC10_ARATH Probable indole-3-pyruvate monooxygenase YUCCA10 OS=Arabidopsis thaliana GN=YUC10 PE=2 SV=1 46 365 2.0E-13
sp|P9WNF9|ETHA_MYCTU FAD-containing monooxygenase EthA OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ethA PE=1 SV=1 46 356 3.0E-13
sp|Q7TVI2|ETHA_MYCBO FAD-containing monooxygenase EthA OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=ethA PE=1 SV=1 46 356 3.0E-13
sp|P9WNF8|ETHA_MYCTO FAD-containing monooxygenase EthA OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=ethA PE=3 SV=1 46 356 3.0E-13
sp|A7HU16|BVMO_PARL1 Baeyer-Villiger monooxygenase OS=Parvibaculum lavamentivorans (strain DS-1 / DSM 13023 / NCIMB 13966) GN=Plav_1781 PE=1 SV=1 48 242 8.0E-12
sp|Q9LFM5|YUC4_ARATH Probable indole-3-pyruvate monooxygenase YUCCA4 OS=Arabidopsis thaliana GN=YUC4 PE=1 SV=1 44 368 1.0E-11
sp|Q9SXE1|GSOX3_ARATH Flavin-containing monooxygenase FMO GS-OX3 OS=Arabidopsis thaliana GN=FMOGS-OX3 PE=2 SV=1 37 246 2.0E-11
sp|P9WNF7|MYMA_MYCTU Putative FAD-containing monooxygenase MymA OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=mymA PE=1 SV=1 46 356 1.0E-10
sp|P9WNF6|MYMA_MYCTO Putative FAD-containing monooxygenase MymA OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=mymA PE=3 SV=1 46 356 1.0E-10
sp|P55487|Y4ID_RHISN Uncharacterized monooxygenase y4iD OS=Rhizobium sp. (strain NGR234) GN=NGR_a03290 PE=3 SV=1 45 242 4.0E-10
sp|A0R665|ETHA_MYCS2 FAD-containing monooxygenase EthA OS=Mycobacterium smegmatis (strain ATCC 700084 / mc(2)155) GN=ethA PE=3 SV=1 46 240 6.0E-10
sp|Q95LA2|FMO1_CANLF Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Canis lupus familiaris GN=FMO1 PE=2 SV=3 45 403 1.0E-09
sp|Q9SS04|GSOX1_ARATH Flavin-containing monooxygenase FMO GS-OX1 OS=Arabidopsis thaliana GN=FMOGS-OX1 PE=2 SV=1 45 239 1.0E-09
sp|U5S003|BVMO4_DIESD Baeyer-Villiger monooxygenase 4 OS=Dietzia sp. (strain D5) PE=1 SV=1 110 244 2.0E-09
sp|Q9C8U0|GSXL5_ARATH Flavin-containing monooxygenase FMO GS-OX-like 5 OS=Arabidopsis thaliana GN=At1g63370 PE=2 SV=2 40 237 2.0E-09
sp|O23024|YUC3_ARATH Probable indole-3-pyruvate monooxygenase YUCCA3 OS=Arabidopsis thaliana GN=YUC3 PE=2 SV=1 48 368 5.0E-09
sp|Q8VZ59|YUC6_ARATH Indole-3-pyruvate monooxygenase YUCCA6 OS=Arabidopsis thaliana GN=YUC6 PE=1 SV=1 48 383 5.0E-09
sp|Q9SXD5|GSXL3_ARATH Flavin-containing monooxygenase FMO GS-OX-like 3 OS=Arabidopsis thaliana GN=At1g62620 PE=2 SV=2 40 237 8.0E-09
sp|O64489|YUC9_ARATH Probable indole-3-pyruvate monooxygenase YUCCA9 OS=Arabidopsis thaliana GN=YUC9 PE=2 SV=1 48 256 1.0E-08
sp|Q9SZY8|YUC1_ARATH Probable indole-3-pyruvate monooxygenase YUCCA1 OS=Arabidopsis thaliana GN=YUC1 PE=1 SV=1 48 307 2.0E-08
sp|P17635|FMO2_RABIT Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Oryctolagus cuniculus GN=FMO2 PE=1 SV=3 45 403 3.0E-08
sp|Q9SVU0|YUC8_ARATH Probable indole-3-pyruvate monooxygenase YUCCA8 OS=Arabidopsis thaliana GN=YUC8 PE=2 SV=1 47 368 6.0E-08
sp|E3VWK3|PENE_STREX Pentalenolactone D synthase OS=Streptomyces exfoliatus GN=penE PE=1 SV=1 35 217 9.0E-08
sp|Q8MP06|SNO1_TYRJA Senecionine N-oxygenase OS=Tyria jacobaeae GN=sno1 PE=1 SV=1 45 219 2.0E-07
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 35 244 4.0E-07
sp|Q9SVQ1|YUC2_ARATH Indole-3-pyruvate monooxygenase YUCCA2 OS=Arabidopsis thaliana GN=YUC2 PE=1 SV=1 19 307 6.0E-07
sp|Q9LKC0|YUC5_ARATH Probable indole-3-pyruvate monooxygenase YUCCA5 OS=Arabidopsis thaliana GN=YUC5 PE=2 SV=1 48 366 1.0E-06
sp|Q9FF12|GSXL9_ARATH Flavin-containing monooxygenase FMO GS-OX-like 9 OS=Arabidopsis thaliana GN=At5g07800 PE=2 SV=1 42 231 1.0E-06
sp|Q9FWW9|GSXL2_ARATH Flavin-containing monooxygenase FMO GS-OX-like 2 OS=Arabidopsis thaliana GN=At1g12200 PE=2 SV=1 40 236 3.0E-06
sp|E3VWI7|PNTE_STRAE Pentalenolactone D synthase OS=Streptomyces arenae GN=pntE PE=1 SV=1 35 217 3.0E-06
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 42 239 4.0E-06
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=1 104 244 5.0E-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:0003674 molecular_function No
GO:0036094 small molecule binding No
GO:0043167 ion binding No
GO:1901363 heterocyclic compound binding No
GO:0005488 binding No
GO:0097159 organic cyclic compound binding No
GO:0003824 catalytic activity 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:0000166 nucleotide binding No
GO:1901265 nucleoside phosphate binding No
GO:0016705 oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen No
GO:0004497 monooxygenase activity No
GO:0043168 anion binding No

Deeploc

[Help with interpreting the results of Deeploc 2.0]
Localizations Signals Cytoplasm Nucleus Extracellular Cell membrane Mitochondrion Plastid Endoplasmic reticulum Lysosome vacuole Golgi apparatus Peroxisome
Endoplasmic reticulum Signal peptide|Peroxisomal targeting signal 0.3235 0.2594 0.1651 0.1191 0.3316 0.0973 0.8435 0.2586 0.5406 0.3322

SignalP

(None)

Transmembrane Domains

Domain # Start End Length
1 7 26 19

Transcription Factor Class

(None)

CAZymes

(None)

Secondary Metabolism

(None)

Expression data

No expression data available for this genome

Orthologs

Orthofinder run ID4
Orthogroup3435
Change Orthofinder run
Species Protein ID
Ophiocordyceps australis 1348a (Ghana) OphauG2|6557
Ophiocordyceps australis map64 (Brazil) OphauB2|218
Ophiocordyceps camponoti-floridani Ophcf2|04959
Ophiocordyceps camponoti-rufipedis Ophun1|5590
Ophiocordyceps kimflemingae Ophio5|6109
Ophiocordyceps subramaniannii Hirsu2|6531 (this protein)

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 >Hirsu2|6531
MTSKSQVANPLLSPLLFLFQLIQWVLDKALSPSAPRADRPLRRPRIAVVGAGITGVTAASHICGHGFDVVIFEAG
PEEQLGGIWSRVNDTSGLQLHSLMYRFHPSVKWEQGYPDRDQILGQVRQLWRRYGLQDKTRFNFRVDRVYQDERG
RWIVNSPAHGRFDGLIAAVGTCGEAKMPHIPDMDKFGGSIFHSSELTGKDAKGKKVAIIGGGASAIEALEFADAA
QAAHVSVLSRSDKWIIPRDILVDALLSLNVLGQETSLSVVPEFLLRKLFYRDLEHLAPPASKGLFTDTPMVNSAL
MGKLRDGRADWVRCDIDGFTASGVVVNRRARGVPKGGPGHREVVEADMVVMATGFKRPSLAFLPDDCFREPYQSP
NWYLQTFPPQHPSVSAINCTYVSGIGSVGNWHIGIYTRLLLMFVLDPLTRPSPFWMHRWIDMTRLLKRNSPVAAF
DFFTYLELLWWFAFCVSINPFRWKWALFVLTGLGLSWPQAFVSREEKILNGDGYRFRDQGSSF*
Coding >Hirsu2|6531
ATGACGTCCAAGTCGCAGGTGGCCAACCCGCTGCTGAGCCCGCTGCTCTTCCTCTTCCAGCTGATCCAATGGGTG
CTGGACAAGGCGCTGTCGCCGAGCGCGCCGCGGGCGGACCGGCCGCTGCGGCGGCCGCGCATCGCCGTCGTCGGC
GCCGGCATCACGGGCGTCACGGCGGCGTCGCACATCTGCGGGCACGGCTTCGACGTCGTCATCTTCGAGGCCGGG
CCGGAGGAGCAGCTGGGCGGCATCTGGAGTAGGGTCAACGACACTTCGGGCCTGCAGCTGCACAGCCTCATGTAC
CGCTTCCACCCGTCCGTCAAGTGGGAGCAGGGCTACCCGGACCGCGACCAGATCCTCGGCCAGGTGCGGCAGCTG
TGGCGGCGGTACGGCCTGCAGGACAAGACGCGCTTCAACTTCCGCGTCGACCGGGTCTACCAGGACGAGCGCGGC
CGGTGGATCGTCAACAGCCCGGCGCATGGCCGCTTCGACGGCCTGATCGCCGCCGTGGGCACCTGCGGCGAGGCC
AAGATGCCGCACATCCCGGACATGGACAAGTTTGGCGGCTCCATCTTCCACTCGAGCGAGCTGACGGGCAAGGAC
GCCAAGGGCAAAAAGGTGGCCATCATCGGCGGCGGCGCCAGCGCCATCGAGGCCCTCGAGTTCGCCGACGCGGCC
CAGGCGGCGCACGTCTCGGTGCTCTCCCGGTCCGACAAATGGATCATCCCGCGCGACATCCTGGTGGACGCGCTG
CTGAGCCTCAACGTGCTGGGCCAGGAGACGAGCCTGTCGGTCGTGCCCGAGTTCCTGCTGCGCAAGCTCTTCTAC
CGCGACCTCGAGCACCTGGCGCCGCCGGCCAGCAAGGGCCTCTTCACCGACACGCCCATGGTCAACTCGGCCCTG
ATGGGCAAGCTGCGCGACGGCCGGGCCGACTGGGTCCGCTGCGACATCGACGGCTTCACGGCCTCGGGCGTCGTC
GTCAACCGCCGCGCCCGCGGCGTGCCCAAGGGCGGGCCGGGTCACCGCGAGGTCGTCGAGGCCGACATGGTCGTC
ATGGCCACCGGCTTCAAGCGGCCGTCGCTGGCCTTCCTGCCCGACGACTGCTTCCGCGAGCCGTACCAGAGCCCC
AACTGGTACCTGCAGACCTTCCCGCCCCAGCACCCGTCCGTCTCGGCCATCAACTGCACCTACGTCTCCGGCATC
GGCAGCGTCGGCAACTGGCACATCGGCATCTACACCCGCCTGCTGCTCATGTTCGTCCTCGACCCGCTGACCCGG
CCCAGCCCGTTCTGGATGCACCGCTGGATCGACATGACGCGTCTGCTCAAGCGCAACAGCCCGGTCGCCGCCTTC
GACTTCTTCACCTACCTCGAGCTGCTCTGGTGGTTCGCCTTCTGCGTCTCCATCAACCCCTTCCGCTGGAAATGG
GCCCTGTTCGTCCTCACCGGCCTCGGCCTCTCCTGGCCCCAGGCCTTTGTGAGTCGTGAGGAGAAGATCCTCAAC
GGCGACGGCTACCGCTTCCGGGACCAGGGCTCCAGCTTCTAG
Transcript >Hirsu2|6531
ATGACGTCCAAGTCGCAGGTGGCCAACCCGCTGCTGAGCCCGCTGCTCTTCCTCTTCCAGCTGATCCAATGGGTG
CTGGACAAGGCGCTGTCGCCGAGCGCGCCGCGGGCGGACCGGCCGCTGCGGCGGCCGCGCATCGCCGTCGTCGGC
GCCGGCATCACGGGCGTCACGGCGGCGTCGCACATCTGCGGGCACGGCTTCGACGTCGTCATCTTCGAGGCCGGG
CCGGAGGAGCAGCTGGGCGGCATCTGGAGTAGGGTCAACGACACTTCGGGCCTGCAGCTGCACAGCCTCATGTAC
CGCTTCCACCCGTCCGTCAAGTGGGAGCAGGGCTACCCGGACCGCGACCAGATCCTCGGCCAGGTGCGGCAGCTG
TGGCGGCGGTACGGCCTGCAGGACAAGACGCGCTTCAACTTCCGCGTCGACCGGGTCTACCAGGACGAGCGCGGC
CGGTGGATCGTCAACAGCCCGGCGCATGGCCGCTTCGACGGCCTGATCGCCGCCGTGGGCACCTGCGGCGAGGCC
AAGATGCCGCACATCCCGGACATGGACAAGTTTGGCGGCTCCATCTTCCACTCGAGCGAGCTGACGGGCAAGGAC
GCCAAGGGCAAAAAGGTGGCCATCATCGGCGGCGGCGCCAGCGCCATCGAGGCCCTCGAGTTCGCCGACGCGGCC
CAGGCGGCGCACGTCTCGGTGCTCTCCCGGTCCGACAAATGGATCATCCCGCGCGACATCCTGGTGGACGCGCTG
CTGAGCCTCAACGTGCTGGGCCAGGAGACGAGCCTGTCGGTCGTGCCCGAGTTCCTGCTGCGCAAGCTCTTCTAC
CGCGACCTCGAGCACCTGGCGCCGCCGGCCAGCAAGGGCCTCTTCACCGACACGCCCATGGTCAACTCGGCCCTG
ATGGGCAAGCTGCGCGACGGCCGGGCCGACTGGGTCCGCTGCGACATCGACGGCTTCACGGCCTCGGGCGTCGTC
GTCAACCGCCGCGCCCGCGGCGTGCCCAAGGGCGGGCCGGGTCACCGCGAGGTCGTCGAGGCCGACATGGTCGTC
ATGGCCACCGGCTTCAAGCGGCCGTCGCTGGCCTTCCTGCCCGACGACTGCTTCCGCGAGCCGTACCAGAGCCCC
AACTGGTACCTGCAGACCTTCCCGCCCCAGCACCCGTCCGTCTCGGCCATCAACTGCACCTACGTCTCCGGCATC
GGCAGCGTCGGCAACTGGCACATCGGCATCTACACCCGCCTGCTGCTCATGTTCGTCCTCGACCCGCTGACCCGG
CCCAGCCCGTTCTGGATGCACCGCTGGATCGACATGACGCGTCTGCTCAAGCGCAACAGCCCGGTCGCCGCCTTC
GACTTCTTCACCTACCTCGAGCTGCTCTGGTGGTTCGCCTTCTGCGTCTCCATCAACCCCTTCCGCTGGAAATGG
GCCCTGTTCGTCCTCACCGGCCTCGGCCTCTCCTGGCCCCAGGCCTTTGTGAGTCGTGAGGAGAAGATCCTCAAC
GGCGACGGCTACCGCTTCCGGGACCAGGGCTCCAGCTTCTAG
Gene >Hirsu2|6531
ATGACGTCCAAGTCGCAGGTGGCCAACCCGCTGCTGAGCCCGCTGCTCTTCCTCTTCCAGCTGATCCAATGGGTG
CTGGACAAGGCGCTGTCGCCGAGCGCGCCGCGGGCGGACCGGCCGCTGCGGCGGCCGCGCATCGCCGTCGTCGGC
GCCGGCATCACGGGCGTCACGGCGGCGTCGCACATCTGCGGGCACGGCTTCGACGTCGTCATCTTCGAGGCCGGG
CCGGAGGAGCAGCTGGGCGGCATCTGGAGTGTAGGTCTTGTCCTCTTCTCTGTTGCAGCGCTCAGCGGTCGGACG
GAGGCGGCCGAGAGAATCAAAGAGAGAGCTGACCGGGACCGTTGATACCTGCAGAGGGTCAACGACACTTCGGGC
CTGCAGCTGCACAGCCTCATGTACCGCTTCCACCCGTCCGTCAAGTGGGAGCAGGGCTACCCGGACCGCGACCAG
ATCCTCGGCCAGGTGCGGCAGCTGTGGCGGCGGTACGGCCTGCAGGACAAGACGCGCTTCAACTTCCGCGTCGAC
CGGGTCTACCAGGACGAGCGCGGCCGGTGGATCGTCAACAGCCCGGCGCATGGCCGCTTCGACGGCCTGATCGCC
GCCGTGGGCACCTGCGGCGAGGCCAAGATGCCGCACATCCCGGACATGGACAAGTTTGGCGGCTCCATCTTCCAC
TCGAGCGAGCTGACGGGGTGAGTGAAAGTTGTTGTGCCCAAGTCCATGTCCAGTCGTCATCGTCATCCTTTGTTC
TATACACCCACCTTCTTCTCCCTCCTCCCCTCCTCTTTTGTTCTGACAAGCGACCGCAGCAAGGACGCCAAGGGC
AAAAAGGTGGCCATCATCGGCGGCGGCGCCAGCGCCATCGAGGCCCTCGAGTTCGCCGACGCGGCCCAGGCGGCG
CACGTCTCGGTGCTCTCCCGGTCCGACAAATGGATCATCCCGCGCGACATCCTGGTGGACGCGCTGCTGAGCCTC
AACGTGCTGGGCCAGGAGACGAGCCTGTCGGTCGTGCCCGAGTTCCTGCTGCGCAAGCTCTTCTACCGCGACCTC
GAGCACCTGGCGCCGCCGGCCAGCAAGGGCCTCTTCACCGACACGCCCATGGTCAACTCGGCCCTGATGGGCAAG
CTGCGCGACGGCCGGGCCGACTGGGTCCGCTGCGACATCGACGGCTTCACGGCCTCGGGCGTCGTCGTCAACCGC
CGCGCCCGCGGCGTGCCCAAGGGCGGGCCGGGTCACCGCGAGGTCGTCGAGGCCGACATGGTCGTCATGGCCACC
GGCTTCAAGCGGCCGTCGCTGGCCTTCCTGCCCGACGACTGCTTCCGCGAGCCGTACCAGAGCCCCAACTGGTAC
CTGCAGACCTTCCCGCCCCAGCACCCGTCCGTCTCGGCCATCAACTGCACCTACGTCTCCGGCATCGGCAGCGTC
GGCAACTGGCACATCGGCATCTACACCCGCCTGCTGCTCATGTTCGTCCTCGACCCGCTGACCCGGCCCAGCCCG
TTCTGGATGCACCGCTGGATCGACATGACGCGTCTGCTCAAGCGCAACAGCCCGGTCGCCGCCTTCGACTTCTTC
ACCTACCTCGAGCTGCTCTGGTGGTTCGCCTTCTGCGTCTCCATCAACCCCTTCCGCTGGAAATGGGCCCTGTTC
GTCCTCACCGGCCTCGGCCTCTCCTGGCCCCAGGCCTTTGTGAGTCGTGAGGAGAAGATCCTCAACGGCGACGGC
TACCGCTTCCGGGACCAGGGCTCCAGCTTCTAG

© 2023 - Robin Ohm - Utrecht University - The Netherlands

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