Protein ID | Ophun1|6630 |
Gene name | |
Location | Contig_74:17089..20765 |
Strand | + |
Gene length (bp) | 3676 |
Transcript length (bp) | 2643 |
Coding sequence length (bp) | 2643 |
Protein length (aa) | 881 |
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 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 |
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 |
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 |
Orthofinder run ID | 4 |
Orthogroup | 616 |
Change Orthofinder run |
Type of sequence | Sequence |
---|---|
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 |