Fungal Genomics

at Utrecht University

General Properties

Protein IDOphun1|2799
Gene name
LocationContig_25:19105..21097
Strand+
Gene length (bp)1992
Transcript length (bp)1737
Coding sequence length (bp)1737
Protein length (aa) 579

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 7.4E-12 43 266
PF00743 FMO-like Flavin-binding monooxygenase-like 2.4E-10 45 230
PF13450 NAD_binding_8 NAD(P)-binding Rossmann-like domain 9.8E-08 45 90

Swissprot hits

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Swissprot ID Swissprot Description Start End E-value
sp|A7HU16|BVMO_PARL1 Baeyer-Villiger monooxygenase OS=Parvibaculum lavamentivorans (strain DS-1 / DSM 13023 / NCIMB 13966) GN=Plav_1781 PE=1 SV=1 41 570 1.0E-161
sp|Q8GAW0|CPMO_COMS9 Cyclopentanone 1,2-monooxygenase OS=Comamonas sp. (strain NCIMB 9872) GN=cpnB PE=1 SV=3 35 571 4.0E-139
sp|A3U3H1|BVMO_OCEBH Baeyer-Villiger monooxygenase OS=Oceanicola batsensis (strain ATCC BAA-863 / DSM 15984 / HTCC2597) GN=OB2597_18631 PE=1 SV=1 37 574 3.0E-104
sp|Q47PU3|PAMO_THEFY Phenylacetone monooxygenase OS=Thermobifida fusca (strain YX) GN=pamO PE=1 SV=1 38 570 1.0E-101
sp|P12015|CHMO_ACISP Cyclohexanone 1,2-monooxygenase OS=Acinetobacter sp. PE=1 SV=2 39 576 5.0E-98
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Swissprot ID Swissprot Description Start End E-value
sp|A7HU16|BVMO_PARL1 Baeyer-Villiger monooxygenase OS=Parvibaculum lavamentivorans (strain DS-1 / DSM 13023 / NCIMB 13966) GN=Plav_1781 PE=1 SV=1 41 570 1.0E-161
sp|Q8GAW0|CPMO_COMS9 Cyclopentanone 1,2-monooxygenase OS=Comamonas sp. (strain NCIMB 9872) GN=cpnB PE=1 SV=3 35 571 4.0E-139
sp|A3U3H1|BVMO_OCEBH Baeyer-Villiger monooxygenase OS=Oceanicola batsensis (strain ATCC BAA-863 / DSM 15984 / HTCC2597) GN=OB2597_18631 PE=1 SV=1 37 574 3.0E-104
sp|Q47PU3|PAMO_THEFY Phenylacetone monooxygenase OS=Thermobifida fusca (strain YX) GN=pamO PE=1 SV=1 38 570 1.0E-101
sp|P12015|CHMO_ACISP Cyclohexanone 1,2-monooxygenase OS=Acinetobacter sp. PE=1 SV=2 39 576 5.0E-98
sp|H3JQW0|OTEMO_PSEPU 2-oxo-Delta(3)-4,5,5-trimethylcyclopentenylacetyl-CoA monooxygenase OS=Pseudomonas putida GN=otemo PE=1 SV=1 41 525 1.0E-89
sp|P64746|Y916_MYCBO Uncharacterized monooxygenase Mb0916 OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=Mb0916 PE=3 SV=1 45 553 3.0E-48
sp|P9WNG1|Y892_MYCTU Uncharacterized monooxygenase Rv0892 OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=Rv0892 PE=1 SV=1 45 553 3.0E-48
sp|P9WNG0|Y892_MYCTO Uncharacterized monooxygenase MT0916 OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=MT0916 PE=3 SV=1 45 553 3.0E-48
sp|Q9RKB5|BVMO2_STRCO Baeyer-Villiger monooxygenase OS=Streptomyces coelicolor (strain ATCC BAA-471 / A3(2) / M145) GN=SCO3172 PE=1 SV=1 45 527 7.0E-43
sp|E3VWI7|PNTE_STRAE Pentalenolactone D synthase OS=Streptomyces arenae GN=pntE PE=1 SV=1 40 570 4.0E-42
sp|E3VWK3|PENE_STREX Pentalenolactone D synthase OS=Streptomyces exfoliatus GN=penE PE=1 SV=1 40 570 4.0E-42
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 67 559 3.0E-38
sp|U5S003|BVMO4_DIESD Baeyer-Villiger monooxygenase 4 OS=Dietzia sp. (strain D5) PE=1 SV=1 70 539 4.0E-38
sp|Q9RL17|BVMO1_STRCO Baeyer-Villiger monooxygenase OS=Streptomyces coelicolor (strain ATCC BAA-471 / A3(2) / M145) GN=SCO0300 PE=1 SV=1 59 559 4.0E-37
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 12 498 1.0E-36
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 45 518 2.0E-36
sp|Q93TJ5|HAPMO_PSEFL 4-hydroxyacetophenone monooxygenase OS=Pseudomonas fluorescens GN=hapE PE=1 SV=1 40 466 6.0E-36
sp|P55487|Y4ID_RHISN Uncharacterized monooxygenase y4iD OS=Rhizobium sp. (strain NGR234) GN=NGR_a03290 PE=3 SV=1 26 466 8.0E-36
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 41 576 1.0E-32
sp|P9WNF9|ETHA_MYCTU FAD-containing monooxygenase EthA OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ethA PE=1 SV=1 40 466 2.0E-23
sp|P9WNF8|ETHA_MYCTO FAD-containing monooxygenase EthA OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=ethA PE=3 SV=1 40 466 2.0E-23
sp|Q7TVI2|ETHA_MYCBO FAD-containing monooxygenase EthA OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=ethA PE=1 SV=1 40 466 2.0E-23
sp|A0R665|ETHA_MYCS2 FAD-containing monooxygenase EthA OS=Mycobacterium smegmatis (strain ATCC 700084 / mc(2)155) GN=ethA PE=3 SV=1 40 466 5.0E-23
sp|P9WNF7|MYMA_MYCTU Putative FAD-containing monooxygenase MymA OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=mymA PE=1 SV=1 40 466 1.0E-21
sp|P9WNF6|MYMA_MYCTO Putative FAD-containing monooxygenase MymA OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=mymA PE=3 SV=1 40 466 1.0E-21
sp|Q88J44|BVMO_PSEPK Baeyer-Villiger monooxygenase OS=Pseudomonas putida (strain KT2440) GN=PP_2805 PE=1 SV=1 36 249 9.0E-21
sp|Q9LFM5|YUC4_ARATH Probable indole-3-pyruvate monooxygenase YUCCA4 OS=Arabidopsis thaliana GN=YUC4 PE=1 SV=1 44 227 1.0E-11
sp|O64489|YUC9_ARATH Probable indole-3-pyruvate monooxygenase YUCCA9 OS=Arabidopsis thaliana GN=YUC9 PE=2 SV=1 44 250 3.0E-11
sp|Q9SZY8|YUC1_ARATH Probable indole-3-pyruvate monooxygenase YUCCA1 OS=Arabidopsis thaliana GN=YUC1 PE=1 SV=1 44 227 1.0E-10
sp|Q9SVU0|YUC8_ARATH Probable indole-3-pyruvate monooxygenase YUCCA8 OS=Arabidopsis thaliana GN=YUC8 PE=2 SV=1 44 250 5.0E-10
sp|Q9SVQ1|YUC2_ARATH Indole-3-pyruvate monooxygenase YUCCA2 OS=Arabidopsis thaliana GN=YUC2 PE=1 SV=1 44 249 5.0E-10
sp|P16549|FMO1_PIG Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Sus scrofa GN=FMO1 PE=1 SV=3 45 239 5.0E-10
sp|Q01740|FMO1_HUMAN Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Homo sapiens GN=FMO1 PE=2 SV=3 45 239 5.0E-10
sp|Q9LKC0|YUC5_ARATH Probable indole-3-pyruvate monooxygenase YUCCA5 OS=Arabidopsis thaliana GN=YUC5 PE=2 SV=1 44 250 4.0E-09
sp|P97872|FMO5_MOUSE Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Mus musculus GN=Fmo5 PE=1 SV=4 45 224 4.0E-09
sp|P49109|FMO5_CAVPO Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Cavia porcellus GN=FMO5 PE=2 SV=2 45 224 7.0E-09
sp|Q8K4C0|FMO5_RAT Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Rattus norvegicus GN=Fmo5 PE=1 SV=3 45 224 1.0E-08
sp|Q8K2I3|FMO2_MOUSE Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Mus musculus GN=Fmo2 PE=1 SV=3 43 243 1.0E-08
sp|Q04799|FMO5_RABIT Dimethylaniline monooxygenase [N-oxide-forming] 5 OS=Oryctolagus cuniculus GN=FMO5 PE=1 SV=2 45 224 1.0E-08
sp|Q99518|FMO2_HUMAN Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Homo sapiens GN=FMO2 PE=1 SV=4 45 243 3.0E-08
sp|Q8MP06|SNO1_TYRJA Senecionine N-oxygenase OS=Tyria jacobaeae GN=sno1 PE=1 SV=1 45 228 6.0E-08
sp|Q95LA2|FMO1_CANLF Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Canis lupus familiaris GN=FMO1 PE=2 SV=3 45 227 7.0E-08
sp|O23024|YUC3_ARATH Probable indole-3-pyruvate monooxygenase YUCCA3 OS=Arabidopsis thaliana GN=YUC3 PE=2 SV=1 44 227 8.0E-08
sp|P36365|FMO1_RAT Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Rattus norvegicus GN=Fmo1 PE=1 SV=2 45 239 1.0E-07
sp|P17636|FMO1_RABIT Dimethylaniline monooxygenase [N-oxide-forming] 1 OS=Oryctolagus cuniculus GN=FMO1 PE=1 SV=3 45 239 2.0E-07
sp|P36366|FMO2_CAVPO Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Cavia porcellus GN=FMO2 PE=2 SV=2 45 244 2.0E-07
sp|Q28505|FMO2_MACMU Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Macaca mulatta GN=FMO2 PE=2 SV=2 45 243 2.0E-07
sp|Q8HZ70|FMO2_PANTR Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Pan troglodytes GN=FMO2 PE=3 SV=3 45 243 2.0E-07
sp|Q5REK0|FMO2_PONAB Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Pongo abelii GN=FMO2 PE=2 SV=3 45 243 2.0E-07
sp|Q8HZ69|FMO2_GORGO Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Gorilla gorilla gorilla GN=FMO2 PE=3 SV=3 45 243 2.0E-07
sp|Q6IRI9|FMO2_RAT Dimethylaniline monooxygenase [N-oxide-forming] 2 OS=Rattus norvegicus GN=Fmo2 PE=2 SV=3 45 243 6.0E-07
sp|O49312|YUC7_ARATH Probable indole-3-pyruvate monooxygenase YUCCA7 OS=Arabidopsis thaliana GN=YUC7 PE=2 SV=1 44 227 1.0E-06
sp|Q8K4B7|FMO4_RAT Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Rattus norvegicus GN=Fmo4 PE=2 SV=3 45 244 1.0E-06
sp|P31512|FMO4_HUMAN Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Homo sapiens GN=FMO4 PE=1 SV=3 45 244 2.0E-06
sp|Q8VZ59|YUC6_ARATH Indole-3-pyruvate monooxygenase YUCCA6 OS=Arabidopsis thaliana GN=YUC6 PE=1 SV=1 26 249 2.0E-06
sp|P64766|Y968_MYCBO Uncharacterized protein Mb0968c OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=Mb0968c PE=4 SV=1 392 505 3.0E-06
sp|P9WKN7|Y943_MYCTU Uncharacterized protein Rv0943c OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=Rv0943c PE=4 SV=1 392 505 3.0E-06
sp|P9WKN6|Y943_MYCTO Uncharacterized protein MT0969 OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=MT0969 PE=4 SV=1 392 505 3.0E-06
sp|Q8VHG0|FMO4_MOUSE Dimethylaniline monooxygenase [N-oxide-forming] 4 OS=Mus musculus GN=Fmo4 PE=1 SV=3 45 244 3.0E-06
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GO

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

Deeploc

Deeploc data not available for this genome

SignalP

(None)

Transmembrane Domains

(None)

Transcription Factor Class

(None)

CAZymes

(None)

Secondary Metabolism

Gene cluster ID Type of secondary metabolism gene
Cluster 14 Decorating

Expression data

No expression data available for this genome

Orthologs

Orthofinder run ID4
Orthogroup418
Change Orthofinder run
Species Protein ID
Ophiocordyceps australis 1348a (Ghana) OphauG2|1203
Ophiocordyceps australis 1348a (Ghana) OphauG2|5874
Ophiocordyceps australis map64 (Brazil) OphauB2|78
Ophiocordyceps camponoti-floridani Ophcf2|00015
Ophiocordyceps camponoti-rufipedis Ophun1|2799 (this protein)
Ophiocordyceps kimflemingae Ophio5|1784
Ophiocordyceps kimflemingae Ophio5|4092
Ophiocordyceps subramaniannii Hirsu2|3631
Ophiocordyceps subramaniannii Hirsu2|7961

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 >Ophun1|2799
MGDASSFFGFRTELTDPRSGTDSGLHSGSTPPALDGVPVELDALIIGAGFAGVFMLKTLRDRGYRVLVYEAGHDL
GGTWRWNGYPGAGVDSEVPLYEFSWPEVWRDWTWTTNYPEYGEIRAYFDHVDAVVGIKKDVRFGAVVVGAKFDTE
AGLWSVETADGRTTRTKYLILGTGFAAKRYVPDWPGMADFKGTIHHSSFWPSDKPDQVPIEGKRCGIIGTGASGV
QMVQAWAPKAGHLSVFQRTPNLAVPMRRRPLTAKAQQQAKAHYPELFRYRERTFSGFCYDWHERKPDEDTAEERR
DLLERCWELGGFRTWLCSYIEVMSDETLNRELYELWLRKTRPRIQDERKRDLLAPLEMPHFFAIKRPCLEQTYFE
EFNRPTVDIVDVKADPIERFTETGVMLKSGEHHELDVIAIATGFDVSTGAMTQLGLTSIQGRSLQDFWAKGAETY
LGITVPGFPNMFHLYGTHAPTLLCNGPSCIEVQGRWIADMMDKAERRGIKYIDARPEAARAWKDELLRFYGTTLF
PTTRSTYMGGNVPGKPFEPVTYGSGLAKYASTIRAVVGKMEGFELVYRDSNKV*
Coding >Ophun1|2799
ATGGGCGATGCATCCTCTTTTTTCGGCTTCCGCACCGAGTTGACCGACCCCCGCTCCGGCACCGACTCCGGTCTC
CACTCCGGCTCCACTCCGCCGGCCCTCGACGGCGTTCCGGTCGAGCTAGACGCGCTCATCATCGGCGCCGGCTTT
GCCGGCGTCTTCATGCTCAAGACGCTCCGTGATCGCGGATACCGCGTGCTCGTCTACGAGGCCGGCCACGACCTC
GGCGGCACCTGGCGCTGGAACGGTTATCCCGGCGCCGGGGTCGACAGCGAAGTGCCACTTTACGAGTTCTCGTGG
CCCGAGGTTTGGCGGGACTGGACCTGGACGACCAACTATCCCGAGTACGGCGAGATCCGGGCTTATTTCGACCAC
GTCGATGCTGTGGTGGGCATCAAGAAGGACGTCCGCTTCGGGGCCGTCGTCGTGGGAGCCAAGTTTGATACCGAG
GCCGGCCTCTGGAGCGTTGAGACGGCGGACGGACGGACGACGCGGACCAAGTATCTGATTCTGGGGACGGGGTTT
GCTGCGAAACGCTATGTCCCCGACTGGCCCGGTATGGCCGACTTCAAGGGTACCATTCACCACTCCTCCTTCTGG
CCTTCCGACAAGCCAGACCAAGTCCCCATCGAGGGCAAACGCTGCGGCATCATCGGCACCGGCGCCTCGGGCGTC
CAGATGGTTCAGGCCTGGGCCCCCAAAGCCGGCCACCTCTCCGTCTTCCAGCGGACGCCCAACCTGGCCGTCCCC
ATGCGTCGCCGCCCCCTGACAGCCAAAGCCCAACAGCAGGCAAAGGCCCATTACCCGGAGCTGTTCCGCTACCGT
GAGCGCACCTTTTCCGGCTTCTGCTACGACTGGCATGAGAGGAAGCCCGACGAGGACACGGCTGAGGAGCGGAGG
GACCTGCTGGAGCGCTGCTGGGAACTCGGCGGGTTCCGCACCTGGCTGTGCTCGTATATCGAGGTGATGAGCGAC
GAGACGCTCAACCGCGAGCTTTACGAGTTGTGGCTGCGCAAGACGAGGCCAAGGATCCAGGACGAGCGGAAGCGG
GATCTGTTGGCTCCGCTCGAGATGCCGCATTTCTTCGCCATCAAGAGGCCGTGTCTGGAACAGACCTACTTTGAG
GAATTTAACCGGCCGACTGTGGATATCGTCGACGTCAAGGCTGATCCGATCGAGCGATTCACCGAGACGGGTGTG
ATGCTGAAGAGCGGCGAGCATCACGAGCTGGATGTCATTGCCATCGCCACGGGCTTTGACGTCTCTACAGGAGCC
ATGACCCAACTTGGCCTCACAAGCATCCAGGGCCGCTCCCTCCAAGATTTCTGGGCCAAAGGGGCAGAAACCTAC
CTCGGCATCACCGTCCCCGGCTTCCCCAACATGTTCCACCTATACGGCACGCACGCTCCGACACTCCTCTGCAAT
GGCCCGTCGTGTATCGAGGTCCAGGGCCGGTGGATAGCCGACATGATGGACAAGGCGGAGCGGCGCGGCATCAAG
TACATCGATGCCCGGCCCGAGGCGGCGCGGGCCTGGAAGGACGAGCTGCTGCGCTTTTACGGGACGACGCTCTTC
CCGACGACCCGCTCGACTTACATGGGGGGCAACGTTCCGGGGAAGCCGTTTGAGCCGGTGACGTACGGGTCCGGG
CTGGCCAAGTATGCGAGCACCATTCGGGCTGTGGTCGGGAAGATGGAAGGCTTCGAGCTGGTGTATAGAGACTCG
AACAAGGTGTAG
Transcript >Ophun1|2799
ATGGGCGATGCATCCTCTTTTTTCGGCTTCCGCACCGAGTTGACCGACCCCCGCTCCGGCACCGACTCCGGTCTC
CACTCCGGCTCCACTCCGCCGGCCCTCGACGGCGTTCCGGTCGAGCTAGACGCGCTCATCATCGGCGCCGGCTTT
GCCGGCGTCTTCATGCTCAAGACGCTCCGTGATCGCGGATACCGCGTGCTCGTCTACGAGGCCGGCCACGACCTC
GGCGGCACCTGGCGCTGGAACGGTTATCCCGGCGCCGGGGTCGACAGCGAAGTGCCACTTTACGAGTTCTCGTGG
CCCGAGGTTTGGCGGGACTGGACCTGGACGACCAACTATCCCGAGTACGGCGAGATCCGGGCTTATTTCGACCAC
GTCGATGCTGTGGTGGGCATCAAGAAGGACGTCCGCTTCGGGGCCGTCGTCGTGGGAGCCAAGTTTGATACCGAG
GCCGGCCTCTGGAGCGTTGAGACGGCGGACGGACGGACGACGCGGACCAAGTATCTGATTCTGGGGACGGGGTTT
GCTGCGAAACGCTATGTCCCCGACTGGCCCGGTATGGCCGACTTCAAGGGTACCATTCACCACTCCTCCTTCTGG
CCTTCCGACAAGCCAGACCAAGTCCCCATCGAGGGCAAACGCTGCGGCATCATCGGCACCGGCGCCTCGGGCGTC
CAGATGGTTCAGGCCTGGGCCCCCAAAGCCGGCCACCTCTCCGTCTTCCAGCGGACGCCCAACCTGGCCGTCCCC
ATGCGTCGCCGCCCCCTGACAGCCAAAGCCCAACAGCAGGCAAAGGCCCATTACCCGGAGCTGTTCCGCTACCGT
GAGCGCACCTTTTCCGGCTTCTGCTACGACTGGCATGAGAGGAAGCCCGACGAGGACACGGCTGAGGAGCGGAGG
GACCTGCTGGAGCGCTGCTGGGAACTCGGCGGGTTCCGCACCTGGCTGTGCTCGTATATCGAGGTGATGAGCGAC
GAGACGCTCAACCGCGAGCTTTACGAGTTGTGGCTGCGCAAGACGAGGCCAAGGATCCAGGACGAGCGGAAGCGG
GATCTGTTGGCTCCGCTCGAGATGCCGCATTTCTTCGCCATCAAGAGGCCGTGTCTGGAACAGACCTACTTTGAG
GAATTTAACCGGCCGACTGTGGATATCGTCGACGTCAAGGCTGATCCGATCGAGCGATTCACCGAGACGGGTGTG
ATGCTGAAGAGCGGCGAGCATCACGAGCTGGATGTCATTGCCATCGCCACGGGCTTTGACGTCTCTACAGGAGCC
ATGACCCAACTTGGCCTCACAAGCATCCAGGGCCGCTCCCTCCAAGATTTCTGGGCCAAAGGGGCAGAAACCTAC
CTCGGCATCACCGTCCCCGGCTTCCCCAACATGTTCCACCTATACGGCACGCACGCTCCGACACTCCTCTGCAAT
GGCCCGTCGTGTATCGAGGTCCAGGGCCGGTGGATAGCCGACATGATGGACAAGGCGGAGCGGCGCGGCATCAAG
TACATCGATGCCCGGCCCGAGGCGGCGCGGGCCTGGAAGGACGAGCTGCTGCGCTTTTACGGGACGACGCTCTTC
CCGACGACCCGCTCGACTTACATGGGGGGCAACGTTCCGGGGAAGCCGTTTGAGCCGGTGACGTACGGGTCCGGG
CTGGCCAAGTATGCGAGCACCATTCGGGCTGTGGTCGGGAAGATGGAAGGCTTCGAGCTGGTGTATAGAGACTCG
AACAAGGTGTAG
Gene >Ophun1|2799
ATGGGCGATGCATCCTCTTTTTTCGGCTTCCGCACCGAGTTGACCGACCCCCGCTCCGGCACCGACTCCGGTCTC
CACTCCGGCTCCACTCCGCCGGCCCTCGACGGCGTTCCGGTCGAGCTAGACGCGCTCATCATCGGCGCCGGCTTT
GGTCCGTCCTCTTCTCCTGCGTCAGATTCTCTTGAGCTTACCTTGTGGCAATAGCCGGCGTCTTCATGCTCAAGA
CGCTCCGTGATCGCGGATACCGCGTGCTCGTCTACGAGGCCGGCCACGACCTCGGCGGCACCTGGCGCTGGAACG
GTTATCCCGGCGCCGGGGTCGACAGCGAAGTGCCACTTTACGAGTTCTCGTGGCCCGAGGTTTGGCGGGACTGGA
CCTGGACGACCAACTATCCCGAGTACGGCGAGATCCGGGCTTATTTCGACCACGTCGATGCTGTGGTGGGCATCA
AGAAGGACGTCCGCTTCGGGGCCGTCGTCGTGGGAGCCAAGTTTGATACCGAGGCCGGCCTCTGGAGCGTTGAGA
CGGCGGACGGACGGACGACGCGGACCAAGTATCTGATTCTGGGGACGGGGTTTGTCAGTTTCTCTCTTTCTGGTC
TCCGCCTCTCTCTCATCTCTCTCATCTCCTCTTCTATTCCGCCTGTAAACTGACTTGTCCAGGCTGCGAAACGCT
ATGTCCCCGACTGGCCCGGTATGGCCGACTTCAAGGGTACCATTCACCACTCCTCCTTCTGGCCTTCCGACAAGC
CAGACCAAGTCCCCATCGAGGGCAAACGCTGCGGCATCATCGGCACCGGCGCCTCGGGCGTCCAGATGGTTCAGG
CCTGGGCCCCCAAAGCCGGCCACCTCTCCGTCTTCCAGCGGACGCCCAACCTGGCCGTCCCCATGCGTCGCCGCC
CCCTGACAGCCAAAGCCCAACAGCAGGCAAAGGCCCATTACCCGGAGCTGTTCCGCTACCGTGAGCGCACCTTTT
CCGGCTTCTGCTACGACTGGCATGAGAGGAAGCCCGACGAGGACACGGCTGAGGAGCGGAGGGACCTGCTGGAGC
GCTGCTGGGAACTCGGCGGGTTCCGCACCTGGCTGTGCTCGTATATCGAGGTGATGAGCGACGAGACGCTCAACC
GCGAGCTTTACGAGTTGTGGCTGCGCAAGACGAGGCCAAGGATCCAGGACGAGCGGAAGCGGGATCTGTTGGCTC
CGCTCGAGATGCCGCATTTCTTCGCCATCAAGAGGCCGTGTCTGGAACAGACCTACTTTGAGGAATTTAACCGGC
CGACTGTGGATATCGTCGACGTCAAGGCTGATCCGATCGAGCGATTCACCGAGACGGGTGTGATGCTGAAGAGCG
GCGAGCATCACGAGCTGGATGTCATTGCCATCGCCACGGGCTTTGTGAGTCTAGCACACTTGTAGTAGGACTTCT
CAGACTGACCACGACAACTCGCCTATACAGGACGTCTCTACAGGAGGTATGAAGTCCTCCCCCAAACCCCCTCAC
CCATGACTCCTTCAACTAACAGCCTCAGCCATGACCCAACTTGGCCTCACAAGCATCCAGGGCCGCTCCCTCCAA
GATTTCTGGGCCAAAGGGGCAGAAACCTACCTCGGCATCACCGTCCCCGGCTTCCCCAACATGTTCCACCTATAC
GGCACGCACGCTCCGACACTCCTCTGCAATGGCCCGTCGTGTATCGAGGTCCAGGGCCGGTGGATAGCCGACATG
ATGGACAAGGCGGAGCGGCGCGGCATCAAGTACATCGATGCCCGGCCCGAGGCGGCGCGGGCCTGGAAGGACGAG
CTGCTGCGCTTTTACGGGACGACGCTCTTCCCGACGACCCGCTCGACTTACATGGGGGGCAACGTTCCGGGGAAG
CCGTTTGAGCCGGTGACGTACGGGTCCGGGCTGGCCAAGTATGCGAGCACCATTCGGGCTGTGGTCGGGAAGATG
GAAGGCTTCGAGCTGGTGTATAGAGACTCGAACAAGGTGTAG

© 2023 - Robin Ohm - Utrecht University - The Netherlands

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