Fungal Genomics

at Utrecht University

General Properties

Protein IDOphun1|6630
Gene name
LocationContig_74:17089..20765
Strand+
Gene length (bp)3676
Transcript length (bp)2643
Coding sequence length (bp)2643
Protein length (aa) 881

Overview

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PFAM Domains

PFAM Domain ID Short name Long name E-value Start End
PF07859 Abhydrolase_3 alpha/beta hydrolase fold 6.5E-41 171 391
PF00891 Methyltransf_2 O-methyltransferase domain 6.8E-22 652 853
PF20434 BD-FAE BD-FAE 1.1E-17 155 255

Swissprot hits

[Show all]
Swissprot ID Swissprot Description Start End E-value
sp|P55790|OMTA_ASPFL Sterigmatocystin 8-O-methyltransferase OS=Aspergillus flavus GN=omtA PE=3 SV=1 550 863 4.0E-22
sp|A1DA61|FTMD_NEOFI 6-hydroxytryprostatin B O-methyltransferase OS=Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / FGSC A1164 / NRRL 181) GN=ftmMT PE=3 SV=1 490 814 9.0E-22
sp|Q12120|OMTA_ASPPA Sterigmatocystin 8-O-methyltransferase OS=Aspergillus parasiticus GN=omtA PE=1 SV=1 550 863 2.0E-21
sp|Q9P900|OMTB_ASPFL Demethylsterigmatocystin 6-O-methyltransferase OS=Aspergillus flavus GN=omtB PE=3 SV=1 535 857 3.0E-20
sp|B9WZX2|FTMD_ASPFM 6-hydroxytryprostatin B O-methyltransferase OS=Neosartorya fumigata GN=ftmMT PE=1 SV=1 527 814 7.0E-20
[Show all]
[Show less]
Swissprot ID Swissprot Description Start End E-value
sp|P55790|OMTA_ASPFL Sterigmatocystin 8-O-methyltransferase OS=Aspergillus flavus GN=omtA PE=3 SV=1 550 863 4.0E-22
sp|A1DA61|FTMD_NEOFI 6-hydroxytryprostatin B O-methyltransferase OS=Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / FGSC A1164 / NRRL 181) GN=ftmMT PE=3 SV=1 490 814 9.0E-22
sp|Q12120|OMTA_ASPPA Sterigmatocystin 8-O-methyltransferase OS=Aspergillus parasiticus GN=omtA PE=1 SV=1 550 863 2.0E-21
sp|Q9P900|OMTB_ASPFL Demethylsterigmatocystin 6-O-methyltransferase OS=Aspergillus flavus GN=omtB PE=3 SV=1 535 857 3.0E-20
sp|B9WZX2|FTMD_ASPFM 6-hydroxytryprostatin B O-methyltransferase OS=Neosartorya fumigata GN=ftmMT PE=1 SV=1 527 814 7.0E-20
sp|Q9UQY0|OMTB_ASPPA Demethylsterigmatocystin 6-O-methyltransferase OS=Aspergillus parasiticus GN=omtB PE=1 SV=2 535 857 9.0E-20
sp|Q4WAW6|FTMD_ASPFU 6-hydroxytryprostatin B O-methyltransferase OS=Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) GN=ftmMT PE=1 SV=1 527 814 7.0E-19
sp|Q0P5B7|AAAD_BOVIN Arylacetamide deacetylase OS=Bos taurus GN=AADAC PE=2 SV=1 133 390 2.0E-17
sp|P42712|DMPM_STRAD O-demethylpuromycin-O-methyltransferase OS=Streptomyces alboniger GN=dmpM PE=3 SV=1 567 863 3.0E-17
sp|Q5UQ83|YR526_MIMIV Putative alpha/beta hydrolase R526 OS=Acanthamoeba polyphaga mimivirus GN=MIMI_R526 PE=1 SV=1 168 372 4.0E-16
sp|Q6WUC1|6OMT_PAPSO (RS)-norcoclaurine 6-O-methyltransferase OS=Papaver somniferum GN=6OMT PE=1 SV=1 647 853 3.0E-14
sp|P22760|AAAD_HUMAN Arylacetamide deacetylase OS=Homo sapiens GN=AADAC PE=1 SV=5 151 378 5.0E-14
sp|Q84KK5|D7OMT_GLYEC Isoflavone 7-O-methyltransferase OS=Glycyrrhiza echinata GN=D7OMT PE=1 SV=1 565 853 2.0E-13
sp|Q9US38|YFZ3_SCHPO AB hydrolase superfamily protein C1039.03 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC1039.03 PE=3 SV=1 149 389 4.0E-13
sp|P9WK87|NLHH_MYCTU Carboxylesterase NlhH OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=nlhH PE=1 SV=1 112 372 4.0E-13
sp|P9WK86|NLHH_MYCTO Carboxylesterase NlhH OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=nlhH PE=3 SV=1 112 372 4.0E-13
sp|Q8GU25|COMT1_ROSCH Caffeic acid 3-O-methyltransferase OS=Rosa chinensis GN=COMT1 PE=2 SV=1 703 858 7.0E-13
sp|Q43046|COMT1_POPKI Caffeic acid 3-O-methyltransferase 1 OS=Populus kitakamiensis GN=HOMT1 PE=3 SV=1 703 864 7.0E-13
sp|A8J6X1|BMT_GLELI Bergaptol O-methyltransferase OS=Glehnia littoralis GN=BMT PE=1 SV=1 647 857 9.0E-13
sp|Q99PG0|AAAD_MOUSE Arylacetamide deacetylase OS=Mus musculus GN=Aadac PE=1 SV=3 152 373 9.0E-13
sp|P59049|OMT1_CHRAE Quercetin 3-O-methyltransferase 1 OS=Chrysosplenium americanum GN=OMT1 PE=1 SV=1 697 859 1.0E-12
sp|Q42653|OMT2_CHRAE Quercetin 3-O-methyltransferase 2 OS=Chrysosplenium americanum GN=OMT2 PE=1 SV=1 703 859 2.0E-12
sp|Q9QZH8|AAAD_RAT Arylacetamide deacetylase OS=Rattus norvegicus GN=Aadac PE=2 SV=3 152 390 2.0E-12
sp|C6TAY1|SOMT2_SOYBN Flavonoid 4'-O-methyltransferase OS=Glycine max PE=1 SV=1 565 858 3.0E-12
sp|O24529|7OMT8_MEDSA Isoflavone-7-O-methyltransferase 8 OS=Medicago sativa PE=1 SV=1 653 858 4.0E-12
sp|O22309|7OMT9_MEDSA Isoflavone-7-O-methyltransferase 9 OS=Medicago sativa PE=2 SV=1 653 858 5.0E-12
sp|O22308|7OMT6_MEDSA Isoflavone-7-O-methyltransferase 6 OS=Medicago sativa PE=2 SV=1 653 858 5.0E-12
sp|Q00763|COMT1_POPTM Caffeic acid 3-O-methyltransferase 1 OS=Populus tremuloides GN=OMT1 PE=1 SV=1 703 864 7.0E-12
sp|Q6P093|ADCL2_HUMAN Arylacetamide deacetylase-like 2 OS=Homo sapiens GN=AADACL2 PE=2 SV=3 152 378 7.0E-12
sp|Q43609|COMT1_PRUDU Caffeic acid 3-O-methyltransferase OS=Prunus dulcis GN=COMT1 PE=2 SV=1 703 858 9.0E-12
sp|Q9XGV9|COMT2_OCIBA Caffeic acid 3-O-methyltransferase 2 OS=Ocimum basilicum GN=COMT2 PE=2 SV=1 564 854 1.0E-11
sp|Q9FK25|OMT1_ARATH Flavone 3'-O-methyltransferase 1 OS=Arabidopsis thaliana GN=OMT1 PE=1 SV=1 703 858 1.0E-11
sp|A2A7Z8|ADCL3_MOUSE Arylacetamide deacetylase-like 3 OS=Mus musculus GN=Aadacl3 PE=3 SV=1 152 373 1.0E-11
sp|B6VJS4|ROMT_VITVI Trans-resveratrol di-O-methyltransferase OS=Vitis vinifera GN=ROMT PE=1 SV=2 567 858 2.0E-11
sp|Q9XGW0|COMT1_OCIBA Caffeic acid 3-O-methyltransferase 1 OS=Ocimum basilicum GN=COMT1 PE=2 SV=1 564 854 2.0E-11
sp|O23760|COMT1_CLABR Caffeic acid 3-O-methyltransferase OS=Clarkia breweri GN=COMT PE=1 SV=1 707 858 3.0E-11
sp|Q6T1F5|COMT1_AMMMJ Caffeic acid 3-O-methyltransferase OS=Ammi majus GN=COMT PE=1 SV=1 699 854 3.0E-11
sp|Q43239|COMT1_ZINVI Caffeic acid 3-O-methyltransferase OS=Zinnia violacea PE=2 SV=1 702 854 3.0E-11
sp|Q9FQY8|COMT1_CAPAN Caffeic acid 3-O-methyltransferase OS=Capsicum annuum GN=COMT PE=2 SV=2 703 857 4.0E-11
sp|O04385|IEMT_CLABR (Iso)eugenol O-methyltransferase OS=Clarkia breweri GN=IEMT1 PE=1 SV=2 703 864 4.0E-11
sp|P16559|TCMN_STRGA Multifunctional cyclase-dehydratase-3-O-methyl transferase TcmN OS=Streptomyces glaucescens GN=tcmN PE=1 SV=2 531 856 4.0E-11
sp|Q9LEL5|4OMT_COPJA 3'-hydroxy-N-methyl-(S)-coclaurine 4'-O-methyltransferase OS=Coptis japonica PE=1 SV=1 626 858 8.0E-11
sp|Q9LEL6|6OMT_COPJA (RS)-norcoclaurine 6-O-methyltransferase OS=Coptis japonica PE=1 SV=1 644 852 1.0E-10
sp|Q7M370|AAAD_RABIT Arylacetamide deacetylase OS=Oryctolagus cuniculus GN=AADAC PE=1 SV=1 151 309 1.0E-10
sp|Q54GZ0|OMT9_DICDI O-methyltransferase 9 OS=Dictyostelium discoideum GN=omt9 PE=3 SV=1 526 858 1.0E-10
sp|Q6WUC2|7OMT_PAPSO (R,S)-reticuline 7-O-methyltransferase OS=Papaver somniferum GN=7OMT PE=1 SV=1 707 866 2.0E-10
sp|Q6T1F6|BMT_AMMMJ Bergaptol O-methyltransferase OS=Ammi majus GN=BMT PE=1 SV=1 662 854 2.0E-10
sp|P93324|CHOMT_MEDSA Isoliquiritigenin 2'-O-methyltransferase OS=Medicago sativa PE=1 SV=1 565 858 2.0E-10
sp|B0CN39|SFMM3_STRLA O-methyltransferase SfmM3 OS=Streptomyces lavendulae GN=sfmM3 PE=3 SV=1 707 862 4.0E-10
sp|P28002|COMT1_MEDSA Caffeic acid 3-O-methyltransferase OS=Medicago sativa PE=1 SV=1 703 858 4.0E-10
sp|Q8LL87|COMT1_COFCA Caffeic acid 3-O-methyltransferase OS=Coffea canephora PE=2 SV=1 703 857 6.0E-10
sp|B0EXJ8|HTOMT_CATRO Tabersonine 16-O-methyltransferase OS=Catharanthus roseus GN=16OMT PE=1 SV=1 626 859 7.0E-10
sp|O81646|COMT1_CAPCH Caffeic acid 3-O-methyltransferase OS=Capsicum chinense GN=COMT PE=2 SV=1 703 849 8.0E-10
sp|P24484|LIP2_MORS1 Lipase 2 OS=Moraxella sp. (strain TA144) GN=lip2 PE=1 SV=1 169 391 9.0E-10
sp|Q43047|COMT3_POPKI Caffeic acid 3-O-methyltransferase 3 OS=Populus kitakamiensis GN=HOMT3 PE=3 SV=1 703 864 1.0E-09
sp|Q9HDX3|YKN2_SCHPO AB hydrolase superfamily protein B1A11.02 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAPB1A11.02 PE=3 SV=1 156 389 2.0E-09
sp|Q8W013|COMT1_CATRO Caffeic acid 3-O-methyltransferase OS=Catharanthus roseus GN=COMT1 PE=2 SV=1 703 853 2.0E-09
sp|Q41086|COMT2_POPTM Caffeic acid 3-O-methyltransferase 2 OS=Populus tremuloides GN=OMT2 PE=3 SV=1 648 864 4.0E-09
sp|Q8T638|DMTA_DICDI Des-methyl DIF-1 methyltransferase A OS=Dictyostelium discoideum GN=dmtA PE=1 SV=1 535 862 4.0E-09
sp|A8QW53|OMT3_SORBI 5-pentadecatrienyl resorcinol O-methyltransferase OS=Sorghum bicolor GN=OMT3 PE=1 SV=1 632 858 5.0E-09
sp|B5EXN3|AES_SALA4 Acetyl esterase OS=Salmonella agona (strain SL483) GN=aes PE=3 SV=1 158 391 5.0E-09
sp|B4TMG8|AES_SALSV Acetyl esterase OS=Salmonella schwarzengrund (strain CVM19633) GN=aes PE=3 SV=1 158 391 5.0E-09
sp|A9MW81|AES_SALPB Acetyl esterase OS=Salmonella paratyphi B (strain ATCC BAA-1250 / SPB7) GN=aes PE=3 SV=1 158 391 5.0E-09
sp|Q8GSN1|MOMT_CATRO Myricetin O-methyltransferase OS=Catharanthus roseus PE=1 SV=1 703 859 6.0E-09
sp|Q39522|SMT_COPJA (S)-scoulerine 9-O-methyltransferase OS=Coptis japonica GN=SMT PE=1 SV=1 706 853 6.0E-09
sp|P46484|COMT1_EUCGU Caffeic acid 3-O-methyltransferase OS=Eucalyptus gunnii GN=OMT PE=2 SV=1 703 858 6.0E-09
sp|Q9LFR7|CXE17_ARATH Probable carboxylesterase 17 OS=Arabidopsis thaliana GN=CXE17 PE=2 SV=1 156 391 7.0E-09
sp|C7SDN9|N7OMT_PAPSO Norreticuline-7-O-methyltransferase OS=Papaver somniferum PE=1 SV=1 653 853 8.0E-09
sp|Q0T7A9|AES_SHIF8 Acetyl esterase OS=Shigella flexneri serotype 5b (strain 8401) GN=aes PE=3 SV=1 158 391 1.0E-08
sp|P0DH60|M3OM2_PEA (+)-6a-hydroxymaackiain 3-O-methyltransferase 2 OS=Pisum sativum GN=HMM2 PE=1 SV=1 654 858 2.0E-08
sp|Q5VUY0|ADCL3_HUMAN Arylacetamide deacetylase-like 3 OS=Homo sapiens GN=AADACL3 PE=2 SV=4 167 309 2.0E-08
sp|Q5PFJ2|AES_SALPA Acetyl esterase OS=Salmonella paratyphi A (strain ATCC 9150 / SARB42) GN=aes PE=3 SV=1 158 391 2.0E-08
sp|B4SWY4|AES_SALNS Acetyl esterase OS=Salmonella newport (strain SL254) GN=aes PE=3 SV=1 158 391 2.0E-08
sp|Q83M39|AES_SHIFL Acetyl esterase OS=Shigella flexneri GN=aes PE=3 SV=2 158 391 2.0E-08
sp|B5BD42|AES_SALPK Acetyl esterase OS=Salmonella paratyphi A (strain AKU_12601) GN=aes PE=3 SV=1 158 391 2.0E-08
sp|Q8ZRA1|AES_SALTY Acetyl esterase OS=Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) GN=aes PE=1 SV=1 158 391 2.0E-08
sp|Q0TKG5|AES_ECOL5 Acetyl esterase OS=Escherichia coli O6:K15:H31 (strain 536 / UPEC) GN=aes PE=3 SV=1 167 391 2.0E-08
sp|Q8Z8T1|AES_SALTI Acetyl esterase OS=Salmonella typhi GN=aes PE=3 SV=1 158 391 2.0E-08
sp|Q86I40|OMT4_DICDI O-methyltransferase 4 OS=Dictyostelium discoideum GN=omt4 PE=3 SV=1 654 858 2.0E-08
sp|O82054|COMT1_SACOF Caffeic acid 3-O-methyltransferase OS=Saccharum officinarum GN=COMT PE=2 SV=1 703 853 2.0E-08
sp|Q8FK82|AES_ECOL6 Acetyl esterase OS=Escherichia coli O6:H1 (strain CFT073 / ATCC 700928 / UPEC) GN=aes PE=3 SV=1 167 391 3.0E-08
sp|Q7XB11|4OMT1_PAPSO 3'-hydroxy-N-methyl-(S)-coclaurine 4'-O-methyltransferase 1 OS=Papaver somniferum GN=4'OMT1 PE=2 SV=1 546 853 3.0E-08
sp|Q57S73|AES_SALCH Acetyl esterase OS=Salmonella choleraesuis (strain SC-B67) GN=aes PE=3 SV=1 158 391 5.0E-08
sp|Q1RF59|AES_ECOUT Acetyl esterase OS=Escherichia coli (strain UTI89 / UPEC) GN=aes PE=3 SV=1 173 391 6.0E-08
sp|A1A8E2|AES_ECOK1 Acetyl esterase OS=Escherichia coli O1:K1 / APEC GN=aes PE=3 SV=1 173 391 6.0E-08
sp|B7MDZ8|AES_ECO45 Acetyl esterase OS=Escherichia coli O45:K1 (strain S88 / ExPEC) GN=aes PE=3 SV=1 173 391 6.0E-08
sp|B1IZB8|AES_ECOLC Acetyl esterase OS=Escherichia coli (strain ATCC 8739 / DSM 1576 / Crooks) GN=aes PE=3 SV=1 158 391 6.0E-08
sp|B5QU79|AES_SALEP Acetyl esterase OS=Salmonella enteritidis PT4 (strain P125109) GN=aes PE=3 SV=1 158 391 6.0E-08
sp|B5FLK0|AES_SALDC Acetyl esterase OS=Salmonella dublin (strain CT_02021853) GN=aes PE=3 SV=1 158 391 6.0E-08
sp|P10950|ASMT_BOVIN Acetylserotonin O-methyltransferase OS=Bos taurus GN=ASMT PE=1 SV=2 707 867 7.0E-08
sp|B1LJN4|AES_ECOSM Acetyl esterase OS=Escherichia coli (strain SMS-3-5 / SECEC) GN=aes PE=3 SV=1 158 391 7.0E-08
sp|P23872|AES_ECOLI Acetyl esterase OS=Escherichia coli (strain K12) GN=aes PE=1 SV=3 158 391 7.0E-08
sp|B1XFR3|AES_ECODH Acetyl esterase OS=Escherichia coli (strain K12 / DH10B) GN=aes PE=3 SV=1 158 391 7.0E-08
sp|C4ZUT0|AES_ECOBW Acetyl esterase OS=Escherichia coli (strain K12 / MC4100 / BW2952) GN=aes PE=3 SV=1 158 391 7.0E-08
sp|B7NIF4|AES_ECO7I Acetyl esterase OS=Escherichia coli O7:K1 (strain IAI39 / ExPEC) GN=aes PE=3 SV=1 158 391 7.0E-08
sp|B7N929|AES_ECOLU Acetyl esterase OS=Escherichia coli O17:K52:H18 (strain UMN026 / ExPEC) GN=aes PE=3 SV=1 158 391 7.0E-08
sp|Q3Z4S3|AES_SHISS Acetyl esterase OS=Shigella sonnei (strain Ss046) GN=aes PE=3 SV=1 158 391 8.0E-08
sp|B7M3W8|AES_ECO8A Acetyl esterase OS=Escherichia coli O8 (strain IAI1) GN=aes PE=3 SV=1 158 391 8.0E-08
sp|B7MQJ1|AES_ECO81 Acetyl esterase OS=Escherichia coli O81 (strain ED1a) GN=aes PE=3 SV=1 173 391 8.0E-08
sp|A7ZXD4|AES_ECOHS Acetyl esterase OS=Escherichia coli O9:H4 (strain HS) GN=aes PE=3 SV=1 158 391 9.0E-08
sp|B5Z3Y7|AES_ECO5E Acetyl esterase OS=Escherichia coli O157:H7 (strain EC4115 / EHEC) GN=aes PE=3 SV=1 158 391 1.0E-07
sp|Q8XD38|AES_ECO57 Acetyl esterase OS=Escherichia coli O157:H7 GN=aes PE=3 SV=1 158 391 1.0E-07
sp|B7UKF6|AES_ECO27 Acetyl esterase OS=Escherichia coli O127:H6 (strain E2348/69 / EPEC) GN=aes PE=3 SV=1 173 391 1.0E-07
sp|A8QW52|OMT1_SORBI Eugenol O-methyltransferase OS=Sorghum bicolor GN=EOMT PE=1 SV=1 707 853 1.0E-07
sp|Q54S95|OMT7_DICDI O-methyltransferase 7 OS=Dictyostelium discoideum GN=omt7 PE=3 SV=1 653 816 1.0E-07
sp|D3KU67|ASMT_MUSMM Acetylserotonin O-methyltransferase OS=Mus musculus molossinus GN=Asmt PE=2 SV=1 643 853 1.0E-07
sp|Q8BM81|ADCL4_MOUSE Arylacetamide deacetylase-like 4 OS=Mus musculus GN=Aadacl4 PE=2 SV=2 152 256 1.0E-07
sp|P18773|EST_ACILW Esterase OS=Acinetobacter lwoffii GN=est PE=3 SV=2 170 371 1.0E-07
sp|B6I0B9|AES_ECOSE Acetyl esterase OS=Escherichia coli (strain SE11) GN=aes PE=3 SV=1 158 391 2.0E-07
sp|B7L7A1|AES_ECO55 Acetyl esterase OS=Escherichia coli (strain 55989 / EAEC) GN=aes PE=3 SV=1 158 391 2.0E-07
sp|Q06509|COMT1_MAIZE Caffeic acid 3-O-methyltransferase OS=Zea mays PE=3 SV=1 703 853 2.0E-07
sp|Q84KK4|I4OMT_LOTJA Isoflavone 4'-O-methyltransferase OS=Lotus japonicus GN=HI4'OMT PE=1 SV=1 519 834 2.0E-07
sp|Q8HZJ0|ASMT_MACMU Acetylserotonin O-methyltransferase OS=Macaca mulatta GN=ASMT PE=2 SV=1 668 853 2.0E-07
sp|D3KU66|ASMT_MOUSE Acetylserotonin O-methyltransferase OS=Mus musculus GN=Asmt PE=2 SV=1 643 853 2.0E-07
sp|B2U4S9|AES_SHIB3 Acetyl esterase OS=Shigella boydii serotype 18 (strain CDC 3083-94 / BS512) GN=aes PE=3 SV=1 158 389 2.0E-07
sp|A7ZIN6|AES_ECO24 Acetyl esterase OS=Escherichia coli O139:H28 (strain E24377A / ETEC) GN=aes PE=3 SV=1 158 391 4.0E-07
sp|O95671|ASML_HUMAN N-acetylserotonin O-methyltransferase-like protein OS=Homo sapiens GN=ASMTL PE=1 SV=3 488 863 5.0E-07
sp|Q325C0|AES_SHIBS Acetyl esterase OS=Shigella boydii serotype 4 (strain Sb227) GN=aes PE=3 SV=1 158 391 5.0E-07
sp|Q92056|ASMT_CHICK Acetylserotonin O-methyltransferase OS=Gallus gallus GN=ASMT PE=2 SV=1 549 861 5.0E-07
sp|Q93WU2|EOMT1_OCIBA Eugenol O-methyltransferase OS=Ocimum basilicum GN=EOMT1 PE=1 SV=1 654 863 6.0E-07
sp|Q54527|RDMB_STREF Aclacinomycin 10-hydroxylase RdmB OS=Streptomyces purpurascens GN=rdmB PE=1 SV=1 524 855 6.0E-07
sp|B8RCD3|AIMT1_PIMAN Trans-anol O-methyltransferase 1 OS=Pimpinella anisum GN=AIMT1 PE=1 SV=1 564 853 1.0E-06
sp|Q9SWC2|COMT1_EUCGL Caffeic acid 3-O-methyltransferase (Fragment) OS=Eucalyptus globulus GN=COMT1 PE=3 SV=1 703 840 1.0E-06
sp|Q8VYP9|ICML1_ARATH Probable isoprenylcysteine alpha-carbonyl methylesterase ICMEL1 OS=Arabidopsis thaliana GN=ICMEL1 PE=2 SV=1 153 251 3.0E-06
sp|B4XY98|AZIB2_STREG 3-hydroxy-5-methyl-1-naphthoate 3-O-methyltransferase OS=Streptomyces sahachiroi GN=aziB2 PE=1 SV=1 686 873 3.0E-06
sp|P46597|ASMT_HUMAN Acetylserotonin O-methyltransferase OS=Homo sapiens GN=ASMT PE=1 SV=1 707 853 4.0E-06
sp|Q9LMA7|CXE1_ARATH Probable carboxylesterase 1 OS=Arabidopsis thaliana GN=CXE1 PE=2 SV=1 168 288 5.0E-06
sp|Q05469|LIPS_HUMAN Hormone-sensitive lipase OS=Homo sapiens GN=LIPE PE=1 SV=4 141 259 8.0E-06
sp|Q1PET6|ICML2_ARATH Probable isoprenylcysteine alpha-carbonyl methylesterase ICMEL2 OS=Arabidopsis thaliana GN=ICMEL2 PE=2 SV=1 146 251 8.0E-06
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GO

GO Term Description Terminal node
GO:0008171 O-methyltransferase activity Yes
GO:0016787 hydrolase activity Yes
GO:0003674 molecular_function No
GO:0008168 methyltransferase activity No
GO:0016740 transferase activity No
GO:0003824 catalytic activity No
GO:0016741 transferase activity, transferring one-carbon groups No

Deeploc

Deeploc data not available for this genome

SignalP

(None)

Transmembrane Domains

(None)

Transcription Factor Class

(None)

CAZymes

(None)

Secondary Metabolism

(None)

Expression data

No expression data available for this genome

Orthologs

Orthofinder run ID4
Orthogroup616
Change Orthofinder run
Species Protein ID
Ophiocordyceps australis 1348a (Ghana) OphauG2|1967
Ophiocordyceps australis map64 (Brazil) OphauB2|7303
Ophiocordyceps camponoti-floridani Ophcf2|04222
Ophiocordyceps camponoti-floridani Ophcf2|04223
Ophiocordyceps camponoti-rufipedis Ophun1|6630 (this protein)
Ophiocordyceps kimflemingae Ophio5|2386
Ophiocordyceps kimflemingae Ophio5|2387
Ophiocordyceps subramaniannii Hirsu2|998

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|6630
MTLIAALDHRGWPSPAAFSGSSPHRAPRLPQRRGDDPSGFHMGESKPTVSSSTSVSVATGIASHVASGVVTPGLS
PLAESPLAESESPPPPEYVNPLEASSRWYLSARASAVRYAASLGFSLSNRSDSTAPSPTRDLWLDSTLSRWSGRR
KIKVDVWVPTRMSAGPRPAVIDLHGGGWILGQGTDDARWAGAVMEALDAVVFSVNYRLAPSYPFPTPIEDCVDAV
LQIANRANELGIDPNNLFLSGFSAGATNALTSWLMIQDPSRWGYDLPSAPPTVAGLILFYPTLDITISRPEKRQM
CARPELTLSPSLTDLIDASYVYPPIPRDQRTDPRLSPGLMSDELLQKLPPLHLCLCEYDMLLAEGFRFAQRLQYH
HKHFSMRVVKGEAHGWDKPPPLVPKESVVIEYGEATRAVAGWLGRDCETDNHSTGSKGHRVMRLLKRPSYLSFRS
RSQTLPSLWTAMTTISSKAEVEEAVQELVEAAKSYSEDAGPAGQAVRAEILAQTRKLTKVLLTPDMMPFYHGLNM
SEIVNIHAFMKLRVLQAIPEQGSISLGKLSQATGVQESLLERMARSLVMSGFLEQTRREGGEYRHSKFSHAYRLD
SMSQGHLFLVLYDFILEPFIHFDGYLQKRDQLQHAREPEDGHNSPYSFSKGQFGTDPWIIMSQDPERVRSFQMSM
AVNKKAVPAVGAFDFDCLRNTAEEAAAGRVQLVDVGGGQGNVLGEIISAHPDALRPETCVLEDRPDVIEISKTNK
ALPEAAQRLAHDFFKEQPVKGAKAYFLRQIIHDYSDAMSVKILSHLAAAMAPDSRVLIFETVLPPQLGEANIPAV
VIDHGVMAIGGKERTEQAFSAILNEAGLELVRVWRAPGNPTAGACVEGKLRGQSV*
Coding >Ophun1|6630
ATGACGCTGATCGCCGCCTTAGACCACCGTGGCTGGCCCTCCCCAGCTGCCTTCTCGGGCTCGTCGCCCCACCGC
GCTCCCCGACTCCCCCAGCGGCGTGGAGACGATCCCTCCGGCTTTCACATGGGCGAATCGAAGCCGACCGTCTCT
TCCAGTACCTCGGTAAGCGTGGCAACCGGCATAGCCTCACATGTCGCCTCGGGCGTCGTCACGCCCGGGCTGTCT
CCCTTGGCCGAGTCACCCCTGGCCGAGTCCGAGTCGCCGCCGCCGCCCGAGTACGTGAACCCCCTGGAAGCCAGC
TCGCGATGGTATCTCTCCGCTCGTGCCTCGGCCGTACGCTACGCCGCGAGCCTGGGTTTCAGCCTCTCCAACCGG
TCCGACTCGACGGCTCCATCCCCCACGCGCGATCTTTGGCTCGACTCGACCTTGTCTCGCTGGAGCGGACGTCGG
AAGATCAAGGTTGACGTCTGGGTGCCGACCCGAATGTCGGCCGGGCCTCGCCCCGCCGTCATTGATCTTCACGGC
GGTGGATGGATCCTCGGCCAGGGCACCGACGATGCCCGCTGGGCAGGCGCCGTAATGGAAGCCCTCGATGCCGTC
GTCTTCTCCGTCAACTACCGGCTGGCCCCGAGCTACCCCTTTCCAACTCCCATCGAAGACTGTGTCGATGCCGTG
CTGCAGATTGCCAACCGTGCTAACGAGCTGGGCATCGATCCGAACAACCTCTTCCTCTCGGGTTTCTCAGCCGGC
GCCACCAACGCTCTCACCAGCTGGCTCATGATTCAGGATCCATCACGCTGGGGCTACGACCTGCCTTCTGCGCCC
CCAACCGTCGCCGGCCTTATACTCTTCTATCCTACGCTCGACATCACCATCTCGCGGCCGGAGAAGCGGCAGATG
TGTGCCCGTCCTGAGCTGACGCTGTCTCCCAGCCTAACGGATCTCATCGACGCCTCATATGTCTACCCGCCCATC
CCCCGTGATCAGCGGACCGATCCTCGGCTGTCCCCTGGCCTCATGTCGGATGAGCTTTTGCAGAAGCTGCCTCCG
CTGCATCTCTGCCTCTGCGAGTATGACATGCTCTTGGCCGAGGGCTTCCGATTCGCTCAGCGCCTGCAATACCAT
CATAAGCACTTCTCCATGCGTGTCGTCAAGGGCGAAGCCCACGGTTGGGACAAACCTCCGCCTCTTGTGCCCAAG
GAGAGCGTGGTTATCGAGTACGGCGAGGCGACGCGTGCCGTGGCCGGGTGGTTGGGTCGAGACTGTGAAACGGAC
AATCACAGCACCGGCTCCAAAGGTCATCGGGTTATGCGGCTCCTCAAGCGTCCCAGTTACCTCTCGTTCCGGTCG
AGAAGCCAAACACTGCCTTCACTTTGGACGGCGATGACGACGATATCATCAAAAGCCGAGGTCGAAGAGGCCGTT
CAGGAGCTGGTGGAAGCAGCAAAGAGCTACTCGGAAGATGCTGGACCAGCAGGTCAAGCAGTGAGAGCCGAGATA
CTTGCTCAGACTCGCAAGTTGACCAAGGTTCTCCTGACGCCGGATATGATGCCCTTCTATCACGGACTCAACATG
TCTGAGATTGTCAACATTCACGCCTTTATGAAGCTTCGGGTGCTGCAAGCTATTCCTGAACAGGGATCCATCTCT
CTCGGCAAGCTTTCGCAGGCAACAGGCGTTCAAGAGTCGTTGCTTGAACGCATGGCCCGCAGTCTCGTCATGTCC
GGCTTTCTAGAGCAGACGCGGCGCGAGGGAGGCGAGTACCGGCACTCCAAGTTCTCTCATGCCTATCGTCTAGAC
AGCATGAGTCAAGGCCACCTATTCCTCGTCCTCTACGACTTCATACTAGAACCCTTCATCCACTTCGATGGCTAC
TTACAGAAACGGGACCAGTTGCAGCACGCCCGCGAGCCGGAGGACGGCCACAACAGCCCATACTCCTTCAGCAAA
GGGCAATTCGGGACCGATCCATGGATCATCATGAGTCAAGATCCGGAACGGGTGCGCAGCTTCCAGATGAGCATG
GCAGTTAACAAGAAGGCCGTTCCTGCGGTTGGCGCCTTCGACTTCGACTGCCTTCGCAACACAGCAGAAGAGGCG
GCCGCTGGACGGGTTCAGCTGGTGGACGTGGGAGGCGGTCAAGGCAACGTTCTCGGCGAGATCATCAGCGCCCAT
CCTGACGCGTTGAGGCCTGAGACTTGCGTCCTCGAAGATAGGCCGGACGTCATCGAGATTTCCAAGACCAACAAA
GCTCTGCCGGAAGCGGCTCAACGTCTTGCCCATGATTTCTTCAAGGAACAGCCTGTCAAAGGAGCCAAGGCCTAC
TTCCTACGGCAGATCATTCACGACTATTCGGACGCCATGAGCGTCAAGATTCTCTCTCATCTAGCTGCTGCCATG
GCTCCAGATTCGCGCGTTCTAATCTTCGAAACTGTGCTTCCGCCACAACTAGGCGAGGCCAACATTCCGGCAGTA
GTGATTGATCATGGTGTCATGGCCATTGGTGGAAAGGAACGGACGGAGCAGGCCTTTTCCGCAATTCTCAATGAG
GCAGGCCTTGAGCTGGTTAGAGTGTGGCGAGCTCCCGGAAATCCTACAGCTGGGGCGTGTGTCGAGGGTAAACTG
AGAGGCCAGTCCGTGTGA
Transcript >Ophun1|6630
ATGACGCTGATCGCCGCCTTAGACCACCGTGGCTGGCCCTCCCCAGCTGCCTTCTCGGGCTCGTCGCCCCACCGC
GCTCCCCGACTCCCCCAGCGGCGTGGAGACGATCCCTCCGGCTTTCACATGGGCGAATCGAAGCCGACCGTCTCT
TCCAGTACCTCGGTAAGCGTGGCAACCGGCATAGCCTCACATGTCGCCTCGGGCGTCGTCACGCCCGGGCTGTCT
CCCTTGGCCGAGTCACCCCTGGCCGAGTCCGAGTCGCCGCCGCCGCCCGAGTACGTGAACCCCCTGGAAGCCAGC
TCGCGATGGTATCTCTCCGCTCGTGCCTCGGCCGTACGCTACGCCGCGAGCCTGGGTTTCAGCCTCTCCAACCGG
TCCGACTCGACGGCTCCATCCCCCACGCGCGATCTTTGGCTCGACTCGACCTTGTCTCGCTGGAGCGGACGTCGG
AAGATCAAGGTTGACGTCTGGGTGCCGACCCGAATGTCGGCCGGGCCTCGCCCCGCCGTCATTGATCTTCACGGC
GGTGGATGGATCCTCGGCCAGGGCACCGACGATGCCCGCTGGGCAGGCGCCGTAATGGAAGCCCTCGATGCCGTC
GTCTTCTCCGTCAACTACCGGCTGGCCCCGAGCTACCCCTTTCCAACTCCCATCGAAGACTGTGTCGATGCCGTG
CTGCAGATTGCCAACCGTGCTAACGAGCTGGGCATCGATCCGAACAACCTCTTCCTCTCGGGTTTCTCAGCCGGC
GCCACCAACGCTCTCACCAGCTGGCTCATGATTCAGGATCCATCACGCTGGGGCTACGACCTGCCTTCTGCGCCC
CCAACCGTCGCCGGCCTTATACTCTTCTATCCTACGCTCGACATCACCATCTCGCGGCCGGAGAAGCGGCAGATG
TGTGCCCGTCCTGAGCTGACGCTGTCTCCCAGCCTAACGGATCTCATCGACGCCTCATATGTCTACCCGCCCATC
CCCCGTGATCAGCGGACCGATCCTCGGCTGTCCCCTGGCCTCATGTCGGATGAGCTTTTGCAGAAGCTGCCTCCG
CTGCATCTCTGCCTCTGCGAGTATGACATGCTCTTGGCCGAGGGCTTCCGATTCGCTCAGCGCCTGCAATACCAT
CATAAGCACTTCTCCATGCGTGTCGTCAAGGGCGAAGCCCACGGTTGGGACAAACCTCCGCCTCTTGTGCCCAAG
GAGAGCGTGGTTATCGAGTACGGCGAGGCGACGCGTGCCGTGGCCGGGTGGTTGGGTCGAGACTGTGAAACGGAC
AATCACAGCACCGGCTCCAAAGGTCATCGGGTTATGCGGCTCCTCAAGCGTCCCAGTTACCTCTCGTTCCGGTCG
AGAAGCCAAACACTGCCTTCACTTTGGACGGCGATGACGACGATATCATCAAAAGCCGAGGTCGAAGAGGCCGTT
CAGGAGCTGGTGGAAGCAGCAAAGAGCTACTCGGAAGATGCTGGACCAGCAGGTCAAGCAGTGAGAGCCGAGATA
CTTGCTCAGACTCGCAAGTTGACCAAGGTTCTCCTGACGCCGGATATGATGCCCTTCTATCACGGACTCAACATG
TCTGAGATTGTCAACATTCACGCCTTTATGAAGCTTCGGGTGCTGCAAGCTATTCCTGAACAGGGATCCATCTCT
CTCGGCAAGCTTTCGCAGGCAACAGGCGTTCAAGAGTCGTTGCTTGAACGCATGGCCCGCAGTCTCGTCATGTCC
GGCTTTCTAGAGCAGACGCGGCGCGAGGGAGGCGAGTACCGGCACTCCAAGTTCTCTCATGCCTATCGTCTAGAC
AGCATGAGTCAAGGCCACCTATTCCTCGTCCTCTACGACTTCATACTAGAACCCTTCATCCACTTCGATGGCTAC
TTACAGAAACGGGACCAGTTGCAGCACGCCCGCGAGCCGGAGGACGGCCACAACAGCCCATACTCCTTCAGCAAA
GGGCAATTCGGGACCGATCCATGGATCATCATGAGTCAAGATCCGGAACGGGTGCGCAGCTTCCAGATGAGCATG
GCAGTTAACAAGAAGGCCGTTCCTGCGGTTGGCGCCTTCGACTTCGACTGCCTTCGCAACACAGCAGAAGAGGCG
GCCGCTGGACGGGTTCAGCTGGTGGACGTGGGAGGCGGTCAAGGCAACGTTCTCGGCGAGATCATCAGCGCCCAT
CCTGACGCGTTGAGGCCTGAGACTTGCGTCCTCGAAGATAGGCCGGACGTCATCGAGATTTCCAAGACCAACAAA
GCTCTGCCGGAAGCGGCTCAACGTCTTGCCCATGATTTCTTCAAGGAACAGCCTGTCAAAGGAGCCAAGGCCTAC
TTCCTACGGCAGATCATTCACGACTATTCGGACGCCATGAGCGTCAAGATTCTCTCTCATCTAGCTGCTGCCATG
GCTCCAGATTCGCGCGTTCTAATCTTCGAAACTGTGCTTCCGCCACAACTAGGCGAGGCCAACATTCCGGCAGTA
GTGATTGATCATGGTGTCATGGCCATTGGTGGAAAGGAACGGACGGAGCAGGCCTTTTCCGCAATTCTCAATGAG
GCAGGCCTTGAGCTGGTTAGAGTGTGGCGAGCTCCCGGAAATCCTACAGCTGGGGCGTGTGTCGAGGGTAAACTG
AGAGGCCAGTCCGTGTGA
Gene >Ophun1|6630
ATGACGCTGATCGCCGCCTTAGACCACCGTGGCTGGCCCTCCCCAGCTGCCTTCTCGGGCTCGTCGCCCCACCGC
GCTCCCCGACTCCCCCAGCGGCGTGGAGACGATCCCTCCGGCTTTCACATGGGCGAATCGAAGCCGACCGTCTCT
TCCAGTACCTCGGTAAGCGTGGCAACCGGCATAGCCTCACATGTCGCCTCGGGCGTCGTCACGCCCGGGCTGTCT
CCCTTGGCCGAGTCACCCCTGGCCGAGTCCGAGTCGCCGCCGCCGCCCGAGTACGTGAACCCCCTGGAAGCCAGC
TCGCGATGGTATCTCTCCGCTCGTGCCTCGGCCGTACGCTACGCCGCGAGCCTGGGTTTCAGCCTCTCCAACCGG
TCCGACTCGACGGCTCCATCCCCCACGCGCGATCTTTGGCTCGACTCGACCTTGTCTCGCTGGAGCGGACGTCGG
AAGATCAAGGTTGACGTCTGGGTGCCGACCCGAATGTCGGCCGGGCCTCGCCCCGCCGTCATTGATCTTCACGGC
GGTGGATGGATCCTCGGCCAGGGCACCGACGATGCCCGCTGGGCAGGCGCCGTAATGGAAGCCCTCGATGCCGTC
GTCTTCTCCGTCAACTACCGGCTGGCCCCGAGCTACCCCTTTCCAACTCCCATCGAAGACTGTGTCGATGCCGTG
CTGCAGATTGCCAACCGTGCTAACGAGCTGGGCATCGATCCGAACAACCTCTTCCTCTCGGGTTTCTCAGCCGGC
GCCACCAACGCTCTCACCAGCTGGCTCATGATTCAGGATCCATCACGCTGGGGCTACGACCTGCCTTCTGCGCCC
CCAACCGTCGCCGGCCTTATACTCTTCTATCCTACGCTCGACATCACCATCTCGCGGCCGGAGAAGCGGCAGATG
TGTGCCCGTCCTGAGCTGACGCTGTCTCCCAGCCTAACGGATCTCATCGACGCCTCATATGTCTACCCGCCCATC
CCCCGTGATCAGCGGACCGATCCTCGGCTGTCCCCTGGCCTCATGTCGGATGAGCTTTTGCAGAAGCTGCCTCCG
CTGCATCTCTGCCTCTGCGAGTATGACATGCTCTTGGCCGAGGGCTTCCGATTCGCTCAGCGCCTGCAATACCAT
CATAAGCACTTCTCCATGCGTGTCGTCAAGGGCGAAGCCCACGGTTGGGACAAACCTCCGCCTCTTGTGCCCAAG
GAGAGCGTGGTTATCGAGTACGGCGAGGCGACGCGTGCCGTGGCCGGGTGGTTGGGTCGAGACTGTGAAACGGAC
AATCACAGCACCGGCTCCAAAGGTCATCGGGTTATGCGGCTCCTCAAGCGTCCCAGTTACCTCTCGTTCCGGTCG
AGAAGCGTGAGATAACTTTGTCACGTGTTTGTTCACTTTGGAGGAAAAGGATGGGGGTTTCTATTCCCCTTCATA
TGTGGTGCTCTCGTCCCATCAATAATATGATGATATTTATCGGCAGATAACGTCCACGTTGGTGACCCCAACGCA
GAGAAATGTCACCATCAAAGCTCACGTAGTAGCGCTAGAGAGATGGCTGAATCAGCCCAAAGCAAATTATCCCGG
CCGTGATGCAACTCGGTTGTCCGTCCATGGTGGTCTAGCGGAACTCTGTACTTCGTACACGAAGTCCGCAAGTGA
AGACTCTGCACTGCAAGAGCTAACACGTCGTCGCTGCGTGCTGACGGCTCTTGGCTCAGCAAACACTGCCTTCAC
TTTGGACGGCGGTGAGTTACTAGCTACAGATCTAGCAGCGGTCCTGGCGGAGACTTTTGGAGGCGAGGGACGGCA
CGGAGATCCGATCTGCGCTTCATCATCATCTGAGCTGCATGTCCTCGTGTCGGGCCGTTGAGTGGAGGTTGCAAG
ACTATACTGTTAGCGGATAGACTCATGAGACGACCAATATTGATCCCTGATGGCGGTGCAACATGATGTTAGTCT
TACGGGAAGCAAAGAAGGATGTCTACTCCTCTCTCCGCATTTTTTTTCTCGCACCTTGGTTGGCGGCTGTGTTCT
CTTTCTGTTGATCTTGTGTCCTCGTCGTCCGCGCATTGACGAAAGATGACGACGATATCATCAAAAGCCGAGGTC
GAAGAGGCCGTTCAGGAGCTGGTGGAAGCAGCAAAGAGCTACTCGGAAGATGCTGGACCAGCAGGTCAAGCAGTG
AGAGCCGAGATACTTGCTCAGACTCGCAAGTTGACCAAGGTTCTCCTGACGCCGGATATGATGCCCTTCTATCAC
GGACTCAACGTACGCCTCCGCCTCCCCTTTCGTCTGAAAGCAGACTGCAGTGGAGACTGAGGTGCGGACTTGGCG
TTGCTGTGTAGATGTCTGAGATTGTCAACATTCACGCCTTTATGAAGCTTCGGGTGCTGCAAGCTATTCCTGAAC
AGGGATCCATCTCTCTCGGCAAGCTTTCGCAGGCAACAGGCGTTCAAGAGTCGTTGCTTGGTGCGGCTTTCACTT
CTGCTGTTATTCTGTTTCCATATCTGGAGGCTGACATGGACTGGTAACATGTGCGAGGTAGAACGCATGGCCCGC
AGTCTCGGTACGTTAACTTCACTCTTGATGCTTGGCTCTCGTTGATAGCTTCGTTGTGAACCAGTCATGTCCGGC
TTTCTAGAGCAGACGCGGCGCGAGGGAGGCGAGTACCGGCACTCCAAGTTCTCTCATGCCTATCGTCTAGACAGC
ATGAGTCAAGGCCACCTATTCCTCGTCCTGTAAGCGCAAGATTAGAATGAACCCCCCTCATCAGGACTCTCACTC
ATCTCTCGTCTCAGCTACGACTTCATACTAGAACCCTTCATCCACTTCGATGGCTACTTACAGAAACGGGACCAG
TTGCAGCACGCCCGCGAGCCGGAGGACGGCCACAACAGCCCATACTCCTTCAGCAAAGGGCAATTCGGGACCGAT
CCATGGATCATCATGAGTCAAGATCCGGAACGGGTGCGCAGCTTCCAGATGAGCATGGCAGTTAACAAGAAGGCC
GTTCCTGCGGTTGGCGCCTTCGACTTCGACTGCCTTCGCAACACAGCAGAAGAGGCGGCCGCTGGACGGGTTCAG
CTGGTGGACGTGGGAGGCGGTCAAGGCAACGTTCTCGGCGAGATCATCAGCGCCCATCCTGACGCGTTGAGGCCT
GAGACTTGCGTCCTCGAAGATAGGCCGGACGTCATCGAGATTTCCAAGACCAACAAAGCTCTGCCGGAAGCGGCT
CAACGTCTTGCCCATGATTTCTTCAAGGAACAGCCTGTCAAAGGTACCTAAGCTTTGAACAGATATATGCTTCCC
TCCGGAAGACCATGTAAATGGCTGACAGTTCTCTCCACCCGCAGGAGCCAAGGCCTACTTCCTACGGCAGATCAT
TCACGACTATTCGGACGCCATGAGCGTCAAGATTCTCTCTCATCTAGCTGCTGCCATGGCTCCAGATTCGCGCGT
TCTAATCTTCGAAACTGTGCTTCCGCCACAACTAGGCGAGGCCAACATTCCGGCAGTAGTGATTGATCATGGTGT
CATGGCCATTGGTGGAAAGGAACGGACGGAGCAGGCCTTTTCCGCAATTCTCAATGAGGCAGGCCTTGAGCTGGT
TAGAGTGTGGCGAGCTCCCGGAAATCCTACAGCTGGGGCGTGTGTCGAGGGTAAACTGAGAGGCCAGTCCGTGTG
A

© 2023 - Robin Ohm - Utrecht University - The Netherlands

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