Protein ID | Ophun1|286 |
Gene name | |
Location | Contig_1070:2100..3702 |
Strand | - |
Gene length (bp) | 1602 |
Transcript length (bp) | 1257 |
Coding sequence length (bp) | 1257 |
Protein length (aa) | 419 |
PFAM Domain ID | Short name | Long name | E-value | Start | End |
---|---|---|---|---|---|
PF00891 | Methyltransf_2 | O-methyltransferase domain | 1.9E-23 | 188 | 386 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
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 | 1 | 386 | 5.0E-36 |
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 | 105 | 386 | 1.0E-33 |
sp|B9WZX2|FTMD_ASPFM | 6-hydroxytryprostatin B O-methyltransferase OS=Neosartorya fumigata GN=ftmMT PE=1 SV=1 | 105 | 386 | 8.0E-33 |
sp|Q9P900|OMTB_ASPFL | Demethylsterigmatocystin 6-O-methyltransferase OS=Aspergillus flavus GN=omtB PE=3 SV=1 | 47 | 410 | 1.0E-18 |
sp|Q9UQY0|OMTB_ASPPA | Demethylsterigmatocystin 6-O-methyltransferase OS=Aspergillus parasiticus GN=omtB PE=1 SV=2 | 47 | 410 | 1.0E-18 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
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 | 1 | 386 | 5.0E-36 |
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 | 105 | 386 | 1.0E-33 |
sp|B9WZX2|FTMD_ASPFM | 6-hydroxytryprostatin B O-methyltransferase OS=Neosartorya fumigata GN=ftmMT PE=1 SV=1 | 105 | 386 | 8.0E-33 |
sp|Q9P900|OMTB_ASPFL | Demethylsterigmatocystin 6-O-methyltransferase OS=Aspergillus flavus GN=omtB PE=3 SV=1 | 47 | 410 | 1.0E-18 |
sp|Q9UQY0|OMTB_ASPPA | Demethylsterigmatocystin 6-O-methyltransferase OS=Aspergillus parasiticus GN=omtB PE=1 SV=2 | 47 | 410 | 1.0E-18 |
sp|C6TAY1|SOMT2_SOYBN | Flavonoid 4'-O-methyltransferase OS=Glycine max PE=1 SV=1 | 69 | 386 | 5.0E-16 |
sp|O95671|ASML_HUMAN | N-acetylserotonin O-methyltransferase-like protein OS=Homo sapiens GN=ASMTL PE=1 SV=3 | 84 | 394 | 5.0E-16 |
sp|Q12120|OMTA_ASPPA | Sterigmatocystin 8-O-methyltransferase OS=Aspergillus parasiticus GN=omtA PE=1 SV=1 | 68 | 384 | 6.0E-16 |
sp|P55790|OMTA_ASPFL | Sterigmatocystin 8-O-methyltransferase OS=Aspergillus flavus GN=omtA PE=3 SV=1 | 68 | 397 | 1.0E-15 |
sp|B6VJS4|ROMT_VITVI | Trans-resveratrol di-O-methyltransferase OS=Vitis vinifera GN=ROMT PE=1 SV=2 | 228 | 386 | 5.0E-14 |
sp|Q54B59|OMT12_DICDI | O-methyltransferase 12 OS=Dictyostelium discoideum GN=omt12 PE=1 SV=1 | 235 | 386 | 1.0E-12 |
sp|Q8GSN1|MOMT_CATRO | Myricetin O-methyltransferase OS=Catharanthus roseus PE=1 SV=1 | 49 | 386 | 2.0E-12 |
sp|O24529|7OMT8_MEDSA | Isoflavone-7-O-methyltransferase 8 OS=Medicago sativa PE=1 SV=1 | 65 | 386 | 4.0E-12 |
sp|O22308|7OMT6_MEDSA | Isoflavone-7-O-methyltransferase 6 OS=Medicago sativa PE=2 SV=1 | 65 | 386 | 5.0E-12 |
sp|Q8HZJ0|ASMT_MACMU | Acetylserotonin O-methyltransferase OS=Macaca mulatta GN=ASMT PE=2 SV=1 | 188 | 385 | 7.0E-12 |
sp|Q93WU3|CVMT1_OCIBA | Chavicol O-methyltransferase OS=Ocimum basilicum GN=CVOMT1 PE=1 SV=1 | 216 | 408 | 7.0E-12 |
sp|Q6WUC1|6OMT_PAPSO | (RS)-norcoclaurine 6-O-methyltransferase OS=Papaver somniferum GN=6OMT PE=1 SV=1 | 235 | 384 | 1.0E-11 |
sp|A8QW53|OMT3_SORBI | 5-pentadecatrienyl resorcinol O-methyltransferase OS=Sorghum bicolor GN=OMT3 PE=1 SV=1 | 235 | 386 | 1.0E-11 |
sp|Q54S95|OMT7_DICDI | O-methyltransferase 7 OS=Dictyostelium discoideum GN=omt7 PE=3 SV=1 | 235 | 383 | 1.0E-11 |
sp|O22309|7OMT9_MEDSA | Isoflavone-7-O-methyltransferase 9 OS=Medicago sativa PE=2 SV=1 | 65 | 386 | 1.0E-11 |
sp|Q9LEL6|6OMT_COPJA | (RS)-norcoclaurine 6-O-methyltransferase OS=Coptis japonica PE=1 SV=1 | 227 | 408 | 2.0E-11 |
sp|P10950|ASMT_BOVIN | Acetylserotonin O-methyltransferase OS=Bos taurus GN=ASMT PE=1 SV=2 | 188 | 385 | 2.0E-11 |
sp|P46597|ASMT_HUMAN | Acetylserotonin O-methyltransferase OS=Homo sapiens GN=ASMT PE=1 SV=1 | 188 | 385 | 2.0E-11 |
sp|B0CN39|SFMM3_STRLA | O-methyltransferase SfmM3 OS=Streptomyces lavendulae GN=sfmM3 PE=3 SV=1 | 210 | 406 | 4.0E-11 |
sp|Q54527|RDMB_STREF | Aclacinomycin 10-hydroxylase RdmB OS=Streptomyces purpurascens GN=rdmB PE=1 SV=1 | 124 | 342 | 5.0E-11 |
sp|O24305|M3OM1_PEA | (+)-6a-hydroxymaackiain 3-O-methyltransferase 1 OS=Pisum sativum GN=HMM1 PE=1 SV=1 | 187 | 386 | 1.0E-10 |
sp|B0EXJ8|HTOMT_CATRO | Tabersonine 16-O-methyltransferase OS=Catharanthus roseus GN=16OMT PE=1 SV=1 | 228 | 386 | 1.0E-10 |
sp|Q54GZ0|OMT9_DICDI | O-methyltransferase 9 OS=Dictyostelium discoideum GN=omt9 PE=3 SV=1 | 221 | 409 | 1.0E-10 |
sp|Q8T638|DMTA_DICDI | Des-methyl DIF-1 methyltransferase A OS=Dictyostelium discoideum GN=dmtA PE=1 SV=1 | 82 | 386 | 2.0E-10 |
sp|P16559|TCMN_STRGA | Multifunctional cyclase-dehydratase-3-O-methyl transferase TcmN OS=Streptomyces glaucescens GN=tcmN PE=1 SV=2 | 233 | 395 | 2.0E-10 |
sp|D3KU67|ASMT_MUSMM | Acetylserotonin O-methyltransferase OS=Mus musculus molossinus GN=Asmt PE=2 SV=1 | 167 | 352 | 2.0E-10 |
sp|D3KU66|ASMT_MOUSE | Acetylserotonin O-methyltransferase OS=Mus musculus GN=Asmt PE=2 SV=1 | 167 | 352 | 2.0E-10 |
sp|Q92056|ASMT_CHICK | Acetylserotonin O-methyltransferase OS=Gallus gallus GN=ASMT PE=2 SV=1 | 253 | 392 | 3.0E-10 |
sp|Q7XB10|4OMT2_PAPSO | 3'-hydroxy-N-methyl-(S)-coclaurine 4'-O-methyltransferase 2 OS=Papaver somniferum GN=4'OMT2 PE=1 SV=1 | 235 | 384 | 2.0E-09 |
sp|B3GSH5|ASMT_RAT | Acetylserotonin O-methyltransferase OS=Rattus norvegicus GN=Asmt PE=1 SV=1 | 167 | 353 | 2.0E-09 |
sp|Q9LEL5|4OMT_COPJA | 3'-hydroxy-N-methyl-(S)-coclaurine 4'-O-methyltransferase OS=Coptis japonica PE=1 SV=1 | 235 | 384 | 3.0E-09 |
sp|C7SDN9|N7OMT_PAPSO | Norreticuline-7-O-methyltransferase OS=Papaver somniferum PE=1 SV=1 | 228 | 384 | 3.0E-09 |
sp|Q84KK4|I4OMT_LOTJA | Isoflavone 4'-O-methyltransferase OS=Lotus japonicus GN=HI4'OMT PE=1 SV=1 | 59 | 371 | 3.0E-09 |
sp|Q93WU2|EOMT1_OCIBA | Eugenol O-methyltransferase OS=Ocimum basilicum GN=EOMT1 PE=1 SV=1 | 216 | 408 | 4.0E-09 |
sp|P42712|DMPM_STRAD | O-demethylpuromycin-O-methyltransferase OS=Streptomyces alboniger GN=dmpM PE=3 SV=1 | 229 | 386 | 6.0E-09 |
sp|Q86I40|OMT4_DICDI | O-methyltransferase 4 OS=Dictyostelium discoideum GN=omt4 PE=3 SV=1 | 73 | 383 | 8.0E-09 |
sp|Q7XB11|4OMT1_PAPSO | 3'-hydroxy-N-methyl-(S)-coclaurine 4'-O-methyltransferase 1 OS=Papaver somniferum GN=4'OMT1 PE=2 SV=1 | 223 | 384 | 2.0E-08 |
sp|P0DH60|M3OM2_PEA | (+)-6a-hydroxymaackiain 3-O-methyltransferase 2 OS=Pisum sativum GN=HMM2 PE=1 SV=1 | 235 | 386 | 2.0E-08 |
sp|Q6VMW0|Q8OMT_MENPI | 8-hydroxyquercetin 8-O-methyltransferase OS=Mentha piperita GN=OMT2 PE=1 SV=1 | 227 | 408 | 3.0E-08 |
sp|Q6WUC2|7OMT_PAPSO | (R,S)-reticuline 7-O-methyltransferase OS=Papaver somniferum GN=7OMT PE=1 SV=1 | 230 | 384 | 4.0E-08 |
sp|B1P123|BX7_MAIZE | TRIBOA-glucoside O-methyltransferase BX7 OS=Zea mays GN=BX7 PE=1 SV=1 | 129 | 384 | 4.0E-08 |
sp|A8QW51|OMT2_SORBI | Probable O-methyltransferase 2 OS=Sorghum bicolor GN=OMT2 PE=2 SV=1 | 240 | 408 | 9.0E-08 |
sp|Q8H9A8|COOMT_COPJA | Columbamine O-methyltransferase OS=Coptis japonica PE=1 SV=1 | 82 | 393 | 3.0E-07 |
sp|P39896|TCMO_STRGA | Tetracenomycin polyketide synthesis 8-O-methyl transferase TcmO OS=Streptomyces glaucescens GN=tcmO PE=3 SV=1 | 197 | 345 | 2.0E-06 |
sp|Q06528|DNRK_STRPE | Carminomycin 4-O-methyltransferase DnrK OS=Streptomyces peucetius GN=dnrK PE=1 SV=2 | 186 | 385 | 6.0E-06 |
sp|Q54FP4|OMT10_DICDI | O-methyltransferase 10 OS=Dictyostelium discoideum GN=omt10 PE=3 SV=2 | 185 | 393 | 7.0E-06 |
sp|P47917|ZRP4_MAIZE | O-methyltransferase ZRP4 OS=Zea mays GN=ZRP4 PE=2 SV=1 | 227 | 408 | 1.0E-05 |
GO Term | Description | Terminal node |
---|---|---|
GO:0008171 | O-methyltransferase 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 |
SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
---|---|---|
No | 1 - 12 | 0.45 |
Type of sequence | Sequence |
---|---|
Locus | Download genbank file of locus
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|286 MTQLSSLARRLGRLADEIDAHGSIAGVTHVPGRIEAARRELLELADEIQIRVRDGPLFLEEHQYHVFACLRWLLH FNIFQHIPQDSTPITYPQLATLASVPAGRLRSVVRMAMTSGLFVEQQPGCVSHNQLSLSFAQDESLGDWATFIIR YGQPSAAAFTEATARWGDSQALDQTAQNIALDTDLPYFEAIKQREGAVDEFARYMSAIQKGSCLRHDHVVRGIDW VKLFGEKAHVVDVGGSTGGVSASLAEAYPFFTFTVQDLPETTRLGPAAMASLPEDLSRRISFQEHDFFTAQPTPA DVYLVRLILHDWPREEAILILSHLSSSLQTQCKPGSRILIMDTVLPAPGAVPLSREAKLRCRDMTMLASFNSGER ELEEWEALLAELSKVQVVNSRLVKATGVNVVLERRIMETGSNM* |
Coding | >Ophun1|286 ATGACGCAGCTCTCGTCGCTCGCCCGGCGTCTAGGCCGTCTGGCAGACGAGATTGACGCCCACGGCTCTATCGCT GGCGTCACGCACGTGCCGGGGAGGATTGAGGCGGCGAGGAGGGAGTTGCTTGAGCTGGCGGACGAGATTCAGATT CGTGTTCGGGACGGGCCTCTCTTCTTGGAGGAGCATCAGTATCATGTCTTTGCCTGTCTGCGCTGGCTGCTTCAC TTCAACATCTTCCAGCACATCCCCCAAGACTCAACCCCCATCACCTACCCCCAACTCGCAACCCTCGCCTCCGTC CCAGCAGGAAGGCTCCGATCGGTAGTGCGCATGGCCATGACATCCGGCCTCTTCGTCGAGCAGCAACCAGGATGC GTCTCCCACAACCAACTCTCCCTCTCCTTCGCACAAGATGAATCCCTCGGCGACTGGGCCACCTTCATCATCCGC TACGGCCAGCCCTCAGCCGCGGCCTTTACCGAAGCAACCGCCCGCTGGGGCGACAGCCAGGCCCTCGACCAGACG GCGCAGAACATTGCTCTCGACACTGACCTTCCCTACTTTGAGGCCATCAAGCAGCGTGAAGGGGCCGTCGACGAG TTCGCGAGGTACATGAGCGCCATTCAGAAGGGGAGCTGTCTGCGTCACGACCATGTTGTCAGGGGCATCGACTGG GTGAAGCTGTTTGGCGAGAAGGCTCATGTTGTTGACGTGGGGGGTTCGACGGGGGGAGTCAGTGCCTCGTTGGCT GAGGCTTACCCTTTCTTTACCTTTACGGTTCAGGATCTTCCCGAGACGACGAGGTTGGGGCCTGCTGCTATGGCT TCGTTACCGGAAGATCTAAGTCGACGGATTTCGTTTCAGGAGCATGATTTCTTCACGGCACAGCCTACACCGGCA GACGTATACCTCGTCCGACTCATCCTGCACGACTGGCCCCGCGAAGAAGCCATCCTAATCCTCTCCCATCTATCC TCATCCCTACAGACGCAATGCAAGCCCGGATCACGCATCCTCATCATGGACACGGTTCTCCCAGCGCCGGGCGCG GTGCCGCTTTCACGGGAGGCGAAGCTGCGGTGTCGCGACATGACGATGCTGGCGAGCTTCAATAGCGGGGAGAGG GAGTTGGAGGAGTGGGAGGCGTTGTTGGCGGAGTTGTCGAAGGTTCAAGTTGTCAACAGCAGACTGGTCAAGGCA ACTGGAGTGAATGTCGTGCTTGAGCGCAGAATCATGGAGACTGGTTCTAACATGTAG |
Transcript | >Ophun1|286 ATGACGCAGCTCTCGTCGCTCGCCCGGCGTCTAGGCCGTCTGGCAGACGAGATTGACGCCCACGGCTCTATCGCT GGCGTCACGCACGTGCCGGGGAGGATTGAGGCGGCGAGGAGGGAGTTGCTTGAGCTGGCGGACGAGATTCAGATT CGTGTTCGGGACGGGCCTCTCTTCTTGGAGGAGCATCAGTATCATGTCTTTGCCTGTCTGCGCTGGCTGCTTCAC TTCAACATCTTCCAGCACATCCCCCAAGACTCAACCCCCATCACCTACCCCCAACTCGCAACCCTCGCCTCCGTC CCAGCAGGAAGGCTCCGATCGGTAGTGCGCATGGCCATGACATCCGGCCTCTTCGTCGAGCAGCAACCAGGATGC GTCTCCCACAACCAACTCTCCCTCTCCTTCGCACAAGATGAATCCCTCGGCGACTGGGCCACCTTCATCATCCGC TACGGCCAGCCCTCAGCCGCGGCCTTTACCGAAGCAACCGCCCGCTGGGGCGACAGCCAGGCCCTCGACCAGACG GCGCAGAACATTGCTCTCGACACTGACCTTCCCTACTTTGAGGCCATCAAGCAGCGTGAAGGGGCCGTCGACGAG TTCGCGAGGTACATGAGCGCCATTCAGAAGGGGAGCTGTCTGCGTCACGACCATGTTGTCAGGGGCATCGACTGG GTGAAGCTGTTTGGCGAGAAGGCTCATGTTGTTGACGTGGGGGGTTCGACGGGGGGAGTCAGTGCCTCGTTGGCT GAGGCTTACCCTTTCTTTACCTTTACGGTTCAGGATCTTCCCGAGACGACGAGGTTGGGGCCTGCTGCTATGGCT TCGTTACCGGAAGATCTAAGTCGACGGATTTCGTTTCAGGAGCATGATTTCTTCACGGCACAGCCTACACCGGCA GACGTATACCTCGTCCGACTCATCCTGCACGACTGGCCCCGCGAAGAAGCCATCCTAATCCTCTCCCATCTATCC TCATCCCTACAGACGCAATGCAAGCCCGGATCACGCATCCTCATCATGGACACGGTTCTCCCAGCGCCGGGCGCG GTGCCGCTTTCACGGGAGGCGAAGCTGCGGTGTCGCGACATGACGATGCTGGCGAGCTTCAATAGCGGGGAGAGG GAGTTGGAGGAGTGGGAGGCGTTGTTGGCGGAGTTGTCGAAGGTTCAAGTTGTCAACAGCAGACTGGTCAAGGCA ACTGGAGTGAATGTCGTGCTTGAGCGCAGAATCATGGAGACTGGTTCTAACATGTAG |
Gene | >Ophun1|286 ATGACGCAGCTCTCGTCGCTCGCCCGGCGTCTAGGCCGTCTGGCAGACGAGATTGACGCCCACGGCTCTATCGCT GGCGTCACGCACGTGCCGGGGAGGATTGAGGCGGCGAGGAGGGAGTTGCTTGAGCTGGCGGACGAGATTCAGATT CGTGTTCGGGACGGGCCTCTCTTCTTGGAGGAGCATCAGGTTCATGTAGGTTTCAGTTTCTACTCGATGGCCTCG TCATCTCTAATGTAGCAGTATCATGTCTTTGCCTGTCTGCGCTGGCTGCTTCACTTCAACATCTTCCAGCACATC CCCCAAGACTCAACCCCCATCACCTACCCCCAACTCGCAACCCTCGCCTCCGTCCCAGCAGGAAGGCTCCGATCG GTAGTGCGCATGGCCATGACATCCGGCCTCTTCGTCGAGCAGCAACCAGGATGCGTCTCCCACAACCAACTCTCC CTCTCCTTCGCACAAGATGAATCCCTCGGCGACTGGGCCACCTTCATCATCCGCTACGGCCAGCCCTCAGCCGCG GCCTTTACCGAAGCAACCGCCCGCTGGGGCGACAGCCAGGCCCTCGACCAGACGGCGCAGAACATTGCTCTCGAC ACTGACCTTCCCTACTTTGAGGCCATCAAGCAGCGTGAAGGGGCCGTCGACGAGTTCGCGAGGTACATGAGCGCC ATTCAGAAGGGGAGCTGTCTGCGTCACGACCATGTTGTCAGGGGCATCGACTGGGTGAAGCTGTTTGGCGAGAAG GCTCATGTTGTTGACGTGGGGGGTTCGACGGGGGGAGTCAGTGCCTCGTTGGCTGAGGCTTACCCTTTCTTTACC TTTACGGTTCAGGATCTTCCCGAGACGACGAGGTTGGGGCCTGCTGCTATGGCTTCGTTACCGGAAGATCTAAGT CGACGGATTTCGTTTCAGGAGCATGATTTCTTCACGGCACAGCCTACACCGGCAGACGTATACCTCGTCCGACTC ATCCTGCACGACTGGCCCCGCGAAGAAGCCATCCTAATCCTCTCCCATCTATCCTCATCCCTACAGACGCAATGC AAGCCCGGATCACGCATCCTCATCATGGACACGGTTCTCCCAGCGCCGGGCGCGGTGCCGCTTTCACGGGAGGCG AAGCTGCGGTGTCGCGACATGACGATGCTGGCGAGCTTCAATAGCGGGGAGAGGGAGTTGGAGGAGTGGGAGGCG TTGTTGGCGGAGGTGAGGCCGGAGTTGGTGCTGCTGGAGAGGGTGCAGCCTGCGGGGAGTGTGATGGATTTGATG GTTGTTGGGTTGAGGGGGGTGTAAGTGTTGTTGACGAACTTGAGACTAGTATATGTAGACTGGTGAGGTGTAAGT AGAGGTTGTGAGGTGAGTGGGAGAGTTGAGTTTGGGAGGGTTGAGGAGGAGATTGCTTTCAGGGTTACAAGTTTA TAAACAGCAGGGTGGAGATGACTTGGAGTGAGGATCTTGTCTTTAGAGACAAGGATCCTGACACTGGTGTTGCAT TAGTTGTCGAAGGTTCAAGTTGTCAACAGCAGACTGGTCAAGGCAACTGGAGTGAATGTCGTGCTTGAGCGCAGA ATCATGGAGACTGGTTCTAACATGTAG |