Protein ID | Hirsu2|4216 |
Gene name | |
Location | Contig_217:18198..20162 |
Strand | - |
Gene length (bp) | 1964 |
Transcript length (bp) | 1674 |
Coding sequence length (bp) | 1674 |
Protein length (aa) | 558 |
PFAM Domain ID | Short name | Long name | E-value | Start | End |
---|---|---|---|---|---|
PF00067 | p450 | Cytochrome P450 | 7.4E-25 | 328 | 520 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|P46634|CP7A1_CRIGR | Cholesterol 7-alpha-monooxygenase OS=Cricetulus griseus GN=CYP7A1 PE=3 SV=1 | 201 | 556 | 6.0E-21 |
sp|Q64505|CP7A1_MOUSE | Cholesterol 7-alpha-monooxygenase OS=Mus musculus GN=Cyp7a1 PE=2 SV=2 | 201 | 556 | 2.0E-20 |
sp|P18125|CP7A1_RAT | Cholesterol 7-alpha-monooxygenase OS=Rattus norvegicus GN=Cyp7a1 PE=1 SV=1 | 201 | 556 | 2.0E-19 |
sp|P51542|CP7A1_RABIT | Cholesterol 7-alpha-monooxygenase OS=Oryctolagus cuniculus GN=CYP7A1 PE=1 SV=1 | 196 | 554 | 3.0E-18 |
sp|P22680|CP7A1_HUMAN | Cholesterol 7-alpha-monooxygenase OS=Homo sapiens GN=CYP7A1 PE=1 SV=2 | 201 | 554 | 8.0E-17 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|P46634|CP7A1_CRIGR | Cholesterol 7-alpha-monooxygenase OS=Cricetulus griseus GN=CYP7A1 PE=3 SV=1 | 201 | 556 | 6.0E-21 |
sp|Q64505|CP7A1_MOUSE | Cholesterol 7-alpha-monooxygenase OS=Mus musculus GN=Cyp7a1 PE=2 SV=2 | 201 | 556 | 2.0E-20 |
sp|P18125|CP7A1_RAT | Cholesterol 7-alpha-monooxygenase OS=Rattus norvegicus GN=Cyp7a1 PE=1 SV=1 | 201 | 556 | 2.0E-19 |
sp|P51542|CP7A1_RABIT | Cholesterol 7-alpha-monooxygenase OS=Oryctolagus cuniculus GN=CYP7A1 PE=1 SV=1 | 196 | 554 | 3.0E-18 |
sp|P22680|CP7A1_HUMAN | Cholesterol 7-alpha-monooxygenase OS=Homo sapiens GN=CYP7A1 PE=1 SV=2 | 201 | 554 | 8.0E-17 |
sp|O46491|CP7A1_PIG | Cholesterol 7-alpha-monooxygenase OS=Sus scrofa GN=CYP7A1 PE=3 SV=1 | 277 | 556 | 4.0E-16 |
sp|Q9UNU6|CP8B1_HUMAN | 7-alpha-hydroxycholest-4-en-3-one 12-alpha-hydroxylase OS=Homo sapiens GN=CYP8B1 PE=1 SV=2 | 310 | 554 | 1.0E-15 |
sp|O35074|PTGIS_MOUSE | Prostacyclin synthase OS=Mus musculus GN=Ptgis PE=1 SV=1 | 324 | 556 | 3.0E-15 |
sp|O02766|CP8B1_RABIT | 7-alpha-hydroxycholest-4-en-3-one 12-alpha-hydroxylase OS=Oryctolagus cuniculus GN=CYP8B1 PE=1 SV=3 | 321 | 556 | 9.0E-15 |
sp|O75881|CP7B1_HUMAN | 25-hydroxycholesterol 7-alpha-hydroxylase OS=Homo sapiens GN=CYP7B1 PE=1 SV=2 | 39 | 556 | 3.0E-14 |
sp|Q62969|PTGIS_RAT | Prostacyclin synthase OS=Rattus norvegicus GN=Ptgis PE=2 SV=1 | 324 | 556 | 8.0E-14 |
sp|Q29626|PTGIS_BOVIN | Prostacyclin synthase OS=Bos taurus GN=PTGIS PE=1 SV=1 | 299 | 556 | 8.0E-14 |
sp|Q60991|CP7B1_MOUSE | 25-hydroxycholesterol 7-alpha-hydroxylase OS=Mus musculus GN=Cyp7b1 PE=2 SV=2 | 332 | 517 | 4.0E-13 |
sp|Q7YRB2|CP8B1_PIG | 5-beta-cholestane-3-alpha,7-alpha-diol 12-alpha-hydroxylase OS=Sus scrofa GN=CYP8B1 PE=2 SV=1 | 299 | 556 | 7.0E-13 |
sp|Q63688|CP7B1_RAT | 25-hydroxycholesterol 7-alpha-hydroxylase (Fragment) OS=Rattus norvegicus GN=Cyp7b1 PE=1 SV=1 | 332 | 556 | 2.0E-12 |
sp|Q16647|PTGIS_HUMAN | Prostacyclin synthase OS=Homo sapiens GN=PTGIS PE=1 SV=1 | 324 | 556 | 3.0E-12 |
sp|O81972|C82A2_SOYBN | Cytochrome P450 82A2 OS=Glycine max GN=CYP82A2 PE=2 SV=1 | 321 | 514 | 6.0E-12 |
sp|P93149|C93B1_GLYEC | Licodione synthase OS=Glycyrrhiza echinata GN=CYP93B1 PE=1 SV=2 | 317 | 529 | 2.0E-11 |
sp|O49342|C71AD_ARATH | Indoleacetaldoxime dehydratase OS=Arabidopsis thaliana GN=CYP71A13 PE=1 SV=1 | 310 | 513 | 5.0E-11 |
sp|Q42799|C93A2_SOYBN | Cytochrome P450 93A2 OS=Glycine max GN=CYP93A2 PE=2 SV=1 | 309 | 522 | 2.0E-10 |
sp|Q9SXS3|C93C2_GLYEC | 2-hydroxyisoflavanone synthase OS=Glycyrrhiza echinata GN=CYP93C2 PE=1 SV=1 | 317 | 517 | 3.0E-10 |
sp|Q42798|C93A1_SOYBN | 3,9-dihydroxypterocarpan 6A-monooxygenase OS=Glycine max GN=CYP93A1 PE=1 SV=1 | 317 | 532 | 6.0E-10 |
sp|Q6Z5I7|C76M6_ORYSJ | Oryzalexin E synthase OS=Oryza sativa subsp. japonica GN=CYP76M6 PE=1 SV=1 | 308 | 513 | 7.0E-10 |
sp|G4XV71|C93C2_GLYUR | 2-hydroxyisoflavanone synthase OS=Glycyrrhiza uralensis GN=CYP93C2 PE=2 SV=2 | 317 | 517 | 9.0E-10 |
sp|Q6WNQ8|C81E8_MEDTR | Cytochrome P450 81E8 OS=Medicago truncatula GN=CYP81E8 PE=2 SV=1 | 324 | 513 | 1.0E-09 |
sp|L7X3S1|MSH_PAPSO | Methyltetrahydroprotoberberine 14-monooxygenase OS=Papaver somniferum GN=CYP82N4 PE=1 SV=1 | 327 | 518 | 1.0E-09 |
sp|Q9SAB6|C71AI_ARATH | Cytochrome P450 71A18 OS=Arabidopsis thaliana GN=CYP71A18 PE=2 SV=2 | 310 | 513 | 2.0E-09 |
sp|P48416|CP10_LYMST | Cytochrome P450 10 OS=Lymnaea stagnalis GN=CYP10 PE=2 SV=1 | 327 | 556 | 2.0E-09 |
sp|Q9XHC6|C93E1_SOYBN | Beta-amyrin 24-hydroxylase OS=Glycine max GN=CYP93E1 PE=1 SV=1 | 311 | 524 | 2.0E-09 |
sp|P49602|CP51_USTMA | Lanosterol 14-alpha demethylase OS=Ustilago maydis (strain 521 / FGSC 9021) GN=ERG11 PE=3 SV=1 | 200 | 512 | 3.0E-09 |
sp|Q9CA60|C98A9_ARATH | Cytochrome P450 98A9 OS=Arabidopsis thaliana GN=CYP98A9 PE=1 SV=1 | 326 | 507 | 3.0E-09 |
sp|Q9T0K2|C71AK_ARATH | Cytochrome P450 71A20 OS=Arabidopsis thaliana GN=CYP71A20 PE=2 SV=2 | 328 | 513 | 3.0E-09 |
sp|Q7XHW5|C14B1_ORYSJ | Cytochrome P450 714B1 OS=Oryza sativa subsp. japonica GN=CYP714B1 PE=1 SV=2 | 333 | 518 | 3.0E-09 |
sp|O49340|C71AC_ARATH | Cytochrome P450 71A12 OS=Arabidopsis thaliana GN=CYP71A12 PE=2 SV=1 | 307 | 513 | 5.0E-09 |
sp|Q9VVR9|C12C1_DROME | Probable cytochrome P450 12c1, mitochondrial OS=Drosophila melanogaster GN=Cyp12c1 PE=2 SV=2 | 234 | 522 | 5.0E-09 |
sp|Q9SWR5|C93C1_SOYBN | 2-hydroxyisoflavanone synthase OS=Glycine max GN=IFS2 PE=2 SV=1 | 329 | 517 | 1.0E-08 |
sp|Q0DS59|C14B2_ORYSJ | Cytochrome P450 714B2 OS=Oryza sativa subsp. japonica GN=CYP714B2 PE=1 SV=2 | 326 | 516 | 1.0E-08 |
sp|O49394|C82C2_ARATH | Cytochrome P450 82C2 OS=Arabidopsis thaliana GN=CYP82C2 PE=2 SV=2 | 325 | 517 | 1.0E-08 |
sp|B6SSW8|C14B3_MAIZE | Cytochrome P450 714B3 OS=Zea mays GN=CYP714B3 PE=2 SV=1 | 326 | 516 | 2.0E-08 |
sp|H1A988|C7254_GLYUR | 11-oxo-beta-amyrin 30-oxidase OS=Glycyrrhiza uralensis GN=CYP72A154 PE=1 SV=1 | 307 | 516 | 2.0E-08 |
sp|O81973|C93A3_SOYBN | Cytochrome P450 93A3 OS=Glycine max GN=CYP93A3 PE=2 SV=1 | 317 | 512 | 2.0E-08 |
sp|Q50EK4|C75A1_PINTA | Cytochrome P450 750A1 OS=Pinus taeda GN=CYP750A1 PE=2 SV=1 | 337 | 513 | 2.0E-08 |
sp|O65790|C81F1_ARATH | Cytochrome P450 81F1 OS=Arabidopsis thaliana GN=CYP81F1 PE=2 SV=2 | 324 | 530 | 2.0E-08 |
sp|E3W9C4|C71A1_ZINZE | Alpha-humulene 10-hydroxylase OS=Zingiber zerumbet GN=CYP71BA1 PE=1 SV=1 | 315 | 513 | 3.0E-08 |
sp|D1MI46|C76BA_SWEMU | Geraniol 8-hydroxylase OS=Swertia mussotii GN=CYP76B10 PE=1 SV=1 | 328 | 541 | 3.0E-08 |
sp|Q9FG65|C81D1_ARATH | Cytochrome P450 81D1 OS=Arabidopsis thaliana GN=CYP81D1 PE=2 SV=1 | 314 | 532 | 3.0E-08 |
sp|P93531|C71D7_SOLCH | Cytochrome P450 71D7 OS=Solanum chacoense GN=CYP71D7 PE=3 SV=1 | 324 | 513 | 4.0E-08 |
sp|Q07973|CP24A_HUMAN | 1,25-dihydroxyvitamin D(3) 24-hydroxylase, mitochondrial OS=Homo sapiens GN=CYP24A1 PE=1 SV=2 | 288 | 515 | 4.0E-08 |
sp|D5JBW8|GAO_CICIN | Germacrene A oxidase OS=Cichorium intybus PE=1 SV=1 | 324 | 539 | 6.0E-08 |
sp|P29980|CPXN_NOSS1 | Probable cytochrome P450 110 OS=Nostoc sp. (strain PCC 7120 / UTEX 2576) GN=cyp110 PE=3 SV=3 | 323 | 514 | 6.0E-08 |
sp|Q94FM7|C71DK_TOBAC | 5-epiaristolochene 1,3-dihydroxylase OS=Nicotiana tabacum GN=CYP71D20 PE=1 SV=2 | 329 | 513 | 7.0E-08 |
sp|Q12664|CP51_PENIT | Eburicol 14-alpha-demethylase OS=Penicillium italicum GN=CYP51 PE=3 SV=1 | 47 | 556 | 7.0E-08 |
sp|Q6YTF5|C76M5_ORYSJ | Cytochrome P450 76M5 OS=Oryza sativa subsp. japonica GN=CYP76M5 PE=1 SV=1 | 313 | 513 | 8.0E-08 |
sp|S4UX02|CYPH1_SALMI | Ferruginol synthase OS=Salvia miltiorrhiza GN=CYP76AH1 PE=1 SV=1 | 331 | 513 | 8.0E-08 |
sp|Q9Y8G7|C505_FUSOX | Bifunctional P-450:NADPH-P450 reductase OS=Fusarium oxysporum GN=CYP505 PE=1 SV=1 | 319 | 514 | 9.0E-08 |
sp|O48921|C97B2_SOYBN | Cytochrome P450 97B2, chloroplastic OS=Glycine max GN=CYP97B2 PE=2 SV=1 | 324 | 516 | 1.0E-07 |
sp|Q9NYL5|CP39A_HUMAN | 24-hydroxycholesterol 7-alpha-hydroxylase OS=Homo sapiens GN=CYP39A1 PE=2 SV=2 | 332 | 556 | 1.0E-07 |
sp|O64635|C76C4_ARATH | Cytochrome P450 76C4 OS=Arabidopsis thaliana GN=CYP76C4 PE=3 SV=1 | 320 | 535 | 2.0E-07 |
sp|Q9T0K0|C71AJ_ARATH | Cytochrome P450 71A19 OS=Arabidopsis thaliana GN=CYP71A19 PE=2 SV=1 | 275 | 513 | 2.0E-07 |
sp|Q9CA61|C98A8_ARATH | Cytochrome P450 98A8 OS=Arabidopsis thaliana GN=CYP98A8 PE=1 SV=1 | 333 | 507 | 2.0E-07 |
sp|Q9FI39|THAD_ARATH | Cytochrome P450 705A5 OS=Arabidopsis thaliana GN=CYP705A5 PE=2 SV=1 | 340 | 527 | 2.0E-07 |
sp|P58046|C71AF_ARATH | Cytochrome P450 71A15 OS=Arabidopsis thaliana GN=CYP71A15 PE=3 SV=1 | 307 | 513 | 3.0E-07 |
sp|Q6IV13|C7D95_MENSP | Cytochrome P450 71D95 OS=Mentha spicata GN=CYP71D95 PE=1 SV=1 | 329 | 513 | 3.0E-07 |
sp|Q9LSF8|C82G1_ARATH | Cytochrome P450 82G1 OS=Arabidopsis thaliana GN=CYP82G1 PE=1 SV=1 | 324 | 532 | 3.0E-07 |
sp|D5J9U8|GAO_LACSA | Germacrene A oxidase OS=Lactuca sativa GN=GAO1 PE=1 SV=1 | 324 | 539 | 3.0E-07 |
sp|Q93Z79|C14A1_ARATH | Cytochrome P450 714A1 OS=Arabidopsis thaliana GN=CYP714A1 PE=2 SV=1 | 304 | 513 | 3.0E-07 |
sp|Q6WKY9|C7D95_MENGR | Cytochrome P450 71D95 OS=Mentha gracilis GN=CYP71D95 PE=1 SV=1 | 329 | 513 | 4.0E-07 |
sp|I3PFJ5|C76AD_BETVU | Cytochrome P450 76AD1 OS=Beta vulgaris GN=CYP76AD1 PE=2 SV=1 | 319 | 497 | 5.0E-07 |
sp|Q9XHE7|C71DD_MENPI | Cytochrome P450 71D13 OS=Mentha piperita GN=CYP71D13 PE=1 SV=1 | 213 | 513 | 5.0E-07 |
sp|Q09J78|ABAH2_ORYSI | Abscisic acid 8'-hydroxylase 2 OS=Oryza sativa subsp. indica GN=CYP707A6 PE=2 SV=1 | 327 | 522 | 6.0E-07 |
sp|Q6ZDE3|ABAH2_ORYSJ | Abscisic acid 8'-hydroxylase 2 OS=Oryza sativa subsp. japonica GN=CYP707A6 PE=2 SV=1 | 327 | 522 | 6.0E-07 |
sp|Q947B7|MFS_MENPI | (+)-menthofuran synthase OS=Mentha piperita PE=1 SV=1 | 322 | 513 | 6.0E-07 |
sp|H1A981|C7263_MEDTR | 11-oxo-beta-amyrin 30-oxidase OS=Medicago truncatula GN=CYP72A63 PE=1 SV=1 | 296 | 516 | 7.0E-07 |
sp|Q9XHE8|C71DI_MENSP | Cytochrome P450 71D18 OS=Mentha spicata GN=CYP71D18 PE=1 SV=1 | 322 | 513 | 7.0E-07 |
sp|Q6WKZ1|C71DI_MENGR | Cytochrome P450 71D18 OS=Mentha gracilis GN=CYP71D18 PE=1 SV=1 | 322 | 513 | 7.0E-07 |
sp|B9G934|C14C3_ORYSJ | Cytochrome P450 714C3 OS=Oryza sativa subsp. japonica GN=CYP714C3 PE=3 SV=2 | 333 | 512 | 8.0E-07 |
sp|O64636|C76C1_ARATH | Cytochrome P450 76C1 OS=Arabidopsis thaliana GN=CYP76C1 PE=2 SV=1 | 266 | 552 | 8.0E-07 |
sp|E1B2Z9|C7AV8_CICIN | Cytochrome P450 71AV8 OS=Cichorium intybus GN=CYP71AV8 PE=2 SV=1 | 340 | 539 | 9.0E-07 |
sp|P47195|C80A1_BERST | Berbamunine synthase OS=Berberis stolonifera GN=CYP80A1 PE=1 SV=1 | 331 | 512 | 1.0E-06 |
sp|Q6YTF1|C76M8_ORYSJ | Oryzalexin D synthase OS=Oryza sativa subsp. japonica GN=CYP76M8 PE=1 SV=1 | 340 | 516 | 1.0E-06 |
sp|D5JBX0|GAO_HELAN | Germacrene A oxidase OS=Helianthus annuus PE=1 SV=1 | 324 | 539 | 1.0E-06 |
sp|Q8VWZ7|C76B6_CATRO | Geraniol 8-hydroxylase OS=Catharanthus roseus GN=CYP76B6 PE=1 SV=1 | 328 | 513 | 1.0E-06 |
sp|P93147|C81E1_GLYEC | Isoflavone 2'-hydroxylase OS=Glycyrrhiza echinata GN=CYP81E1 PE=1 SV=2 | 300 | 518 | 1.0E-06 |
sp|Q759W0|CP51_ASHGO | Lanosterol 14-alpha demethylase OS=Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) GN=ERG11 PE=3 SV=1 | 319 | 556 | 1.0E-06 |
sp|A3A871|C71Z6_ORYSJ | Ent-isokaurene C2-hydroxylase OS=Oryza sativa subsp. japonica GN=CYP71Z6 PE=1 SV=1 | 320 | 513 | 1.0E-06 |
sp|O65782|C83B1_ARATH | Cytochrome P450 83B1 OS=Arabidopsis thaliana GN=CYP83B1 PE=1 SV=1 | 314 | 513 | 1.0E-06 |
sp|Q9UVC3|CP51_CUNEL | Lanosterol 14-alpha demethylase OS=Cunninghamella elegans GN=CYP51 PE=3 SV=1 | 310 | 553 | 2.0E-06 |
sp|O48923|C71DA_SOYBN | Cytochrome P450 71D10 OS=Glycine max GN=CYP71D10 PE=2 SV=1 | 328 | 513 | 2.0E-06 |
sp|Q9LUC6|C7A14_ARATH | Cytochrome P450 72A14 OS=Arabidopsis thaliana GN=CYP72A14 PE=2 SV=1 | 328 | 516 | 2.0E-06 |
sp|D5JBW9|GAO_SAUCO | Germacrene A oxidase OS=Saussurea costus PE=1 SV=1 | 324 | 539 | 2.0E-06 |
sp|Q69X58|C76M7_ORYSJ | Ent-cassadiene C11-alpha-hydroxylase 1 OS=Oryza sativa subsp. japonica GN=CYP76M7 PE=1 SV=1 | 340 | 513 | 2.0E-06 |
sp|O49396|C82C3_ARATH | Cytochrome P450 82C3 OS=Arabidopsis thaliana GN=CYP82C3 PE=2 SV=3 | 325 | 517 | 2.0E-06 |
sp|P37124|C77A2_SOLME | Cytochrome P450 77A2 OS=Solanum melongena GN=CYP77A2 PE=2 SV=1 | 330 | 513 | 2.0E-06 |
sp|Q9STL1|C71AM_ARATH | Cytochrome P450 71A22 OS=Arabidopsis thaliana GN=CYP71A22 PE=2 SV=1 | 272 | 513 | 3.0E-06 |
sp|Q9LVD2|C71BA_ARATH | Cytochrome P450 71B10 OS=Arabidopsis thaliana GN=CYP71B10 PE=3 SV=1 | 304 | 513 | 3.0E-06 |
sp|A2Z212|ABAH3_ORYSI | Abscisic acid 8'-hydroxylase 3 OS=Oryza sativa subsp. indica GN=CYP707A7 PE=3 SV=1 | 305 | 535 | 3.0E-06 |
sp|Q64441|CP24A_MOUSE | 1,25-dihydroxyvitamin D(3) 24-hydroxylase, mitochondrial OS=Mus musculus GN=Cyp24a1 PE=2 SV=1 | 328 | 514 | 3.0E-06 |
sp|O81970|C71A9_SOYBN | Cytochrome P450 71A9 OS=Glycine max GN=CYP71A9 PE=2 SV=1 | 265 | 516 | 3.0E-06 |
sp|P58051|C71BE_ARATH | Cytochrome P450 71B14 OS=Arabidopsis thaliana GN=CYP71B14 PE=2 SV=1 | 265 | 513 | 3.0E-06 |
sp|Q6YV88|C71Z7_ORYSJ | Ent-cassadiene C2-hydroxylase OS=Oryza sativa subsp. japonica GN=CYP71Z7 PE=1 SV=1 | 332 | 535 | 4.0E-06 |
sp|Q9SZ46|C82C4_ARATH | Cytochrome P450 82C4 OS=Arabidopsis thaliana GN=CYP82C4 PE=2 SV=1 | 317 | 517 | 4.0E-06 |
sp|P48421|C83A1_ARATH | Cytochrome P450 83A1 OS=Arabidopsis thaliana GN=CYP83A1 PE=1 SV=2 | 327 | 530 | 4.0E-06 |
sp|Q9LW27|C71BF_ARATH | Bifunctional dihydrocamalexate synthase/camalexin synthase OS=Arabidopsis thaliana GN=CYP71B15 PE=1 SV=1 | 337 | 513 | 4.0E-06 |
sp|Q0J185|ABAH3_ORYSJ | Abscisic acid 8'-hydroxylase 3 OS=Oryza sativa subsp. japonica GN=CYP707A7 PE=2 SV=1 | 305 | 522 | 5.0E-06 |
sp|Q09128|CP24A_RAT | 1,25-dihydroxyvitamin D(3) 24-hydroxylase, mitochondrial OS=Rattus norvegicus GN=Cyp24a1 PE=1 SV=1 | 328 | 514 | 5.0E-06 |
sp|O49858|C82A3_SOYBN | Cytochrome P450 82A3 OS=Glycine max GN=CYP82A3 PE=2 SV=1 | 325 | 540 | 5.0E-06 |
sp|Q9XHE6|C71DF_MENPI | Cytochrome P450 71D15 OS=Mentha piperita GN=CYP71D15 PE=1 SV=1 | 314 | 513 | 5.0E-06 |
sp|O04164|C71A6_NEPRA | Cytochrome P450 71A6 (Fragment) OS=Nepeta racemosa GN=CYP71A6 PE=2 SV=1 | 330 | 520 | 6.0E-06 |
sp|O88962|CP8B1_MOUSE | 7-alpha-hydroxycholest-4-en-3-one 12-alpha-hydroxylase OS=Mus musculus GN=Cyp8b1 PE=1 SV=1 | 310 | 556 | 7.0E-06 |
sp|Q9V676|CP6T3_DROME | Probable cytochrome P450 6t3 OS=Drosophila melanogaster GN=Cyp6t3 PE=3 SV=1 | 325 | 515 | 7.0E-06 |
sp|P48522|TCMO_CATRO | Trans-cinnamate 4-monooxygenase OS=Catharanthus roseus GN=CYP73A4 PE=2 SV=1 | 340 | 514 | 7.0E-06 |
sp|P58049|C71BB_ARATH | Cytochrome P450 71B11 OS=Arabidopsis thaliana GN=CYP71B11 PE=2 SV=1 | 337 | 513 | 8.0E-06 |
sp|Q9STK8|C71AP_ARATH | Cytochrome P450 71A25 OS=Arabidopsis thaliana GN=CYP71A25 PE=2 SV=1 | 305 | 513 | 8.0E-06 |
sp|P58050|C71BD_ARATH | Cytochrome P450 71B13 OS=Arabidopsis thaliana GN=CYP71B13 PE=2 SV=1 | 339 | 513 | 8.0E-06 |
sp|Q6WNR0|C81E7_MEDTR | Isoflavone 2'-hydroxylase OS=Medicago truncatula GN=CYP81E7 PE=1 SV=1 | 325 | 513 | 8.0E-06 |
sp|Q9LHA1|C8D11_ARATH | Cytochrome P450 81D11 OS=Arabidopsis thaliana GN=CYP81D11 PE=2 SV=1 | 324 | 518 | 9.0E-06 |
sp|Q949P1|ABAH1_ARATH | Abscisic acid 8'-hydroxylase 1 OS=Arabidopsis thaliana GN=CYP707A1 PE=2 SV=1 | 233 | 533 | 9.0E-06 |
GO Term | Description | Terminal node |
---|---|---|
GO:0004497 | monooxygenase activity | Yes |
GO:0016705 | oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen | Yes |
GO:0005506 | iron ion binding | Yes |
GO:0020037 | heme binding | Yes |
GO:0016491 | oxidoreductase activity | No |
GO:0046906 | tetrapyrrole binding | No |
GO:0003824 | catalytic activity | No |
GO:0046872 | metal ion binding | No |
GO:0046914 | transition metal ion binding | No |
GO:0097159 | organic cyclic compound binding | No |
GO:0005488 | binding | No |
GO:0043167 | ion binding | No |
GO:1901363 | heterocyclic compound binding | No |
GO:0043169 | cation binding | No |
GO:0003674 | molecular_function | No |
SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
---|---|---|
No | 1 - 39 | 0.5 |
Domain # | Start | End | Length |
---|---|---|---|
1 | 20 | 42 | 22 |
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 | >Hirsu2|4216 MAQFIDWRPAAGRMVDLAKGHWLVTAACLGLAVAFACAARLGRRADEPPSLPEWLPFVVNTYRYMSDRKKLMDRI RPLVSRHKVAMLWIIGKPVYVVSGDIVRMMFRSSESMNADNLSLLILKNLQGLSAEDVAKFANDKSGRLKTPGRG HEHVPADQRYWAANHDLHHDHLLPAEATAQLARSYETFFTQRLEMQPLGRWVTLGIHDVLKRDMVWAATSSLCGT LLLDMYPDFIAAFWDLDSVIDKLLWGLPRWLYPGPLRVREKVFGMCGRYLEEAFKRFDWDGPDATAGWEPIFGSR YARERAKSTRDAGFTWQSRISFHMISIIALNSNTTPVTAWAMFELIKDPSLFEALRAEVETSLVSDPETGCRRFD TSRLLTLPLLQSVYVETLRLHVAVLITRQLIEPIHVGPYQLRKGAWLQAPPNFSHLDDALWGADSSHPASEFWAK RHVVEEETEEAVTGQRIQKQKFVMEARPSEFFPFGGGHTMCPGRNLARQEIMMTIAMIVSRFDIEFVHWVDKNGG ISTGLPRDDTKYYGFGAMPPDRDARIRWRRRW* |
Coding | >Hirsu2|4216 ATGGCGCAGTTCATCGACTGGAGGCCGGCGGCCGGCCGAATGGTCGACTTGGCCAAGGGTCACTGGCTGGTGACG GCGGCGTGCCTCGGCTTGGCCGTCGCCTTCGCGTGCGCTGCTCGGCTCGGTCGCCGGGCGGACGAGCCGCCCTCG CTTCCCGAGTGGCTTCCCTTTGTCGTCAACACGTATCGGTACATGAGCGACCGGAAGAAACTCATGGACCGAATC AGGCCTCTCGTCAGTCGGCACAAAGTGGCCATGCTCTGGATCATTGGGAAGCCCGTGTACGTCGTTTCCGGCGAC ATTGTCCGAATGATGTTTCGTTCGTCCGAAAGCATGAACGCCGACAACTTGAGCTTGCTCATCCTCAAAAATCTC CAAGGCCTCAGCGCCGAGGACGTGGCCAAGTTCGCCAACGACAAATCCGGCCGGCTCAAGACGCCCGGACGAGGT CATGAGCACGTCCCCGCCGACCAGCGTTACTGGGCCGCAAACCACGACCTGCACCACGACCACCTGCTCCCGGCC GAGGCGACGGCCCAGCTGGCCCGCTCGTACGAAACCTTCTTCACCCAGAGGTTGGAGATGCAGCCGCTTGGGCGG TGGGTGACTCTGGGCATCCACGATGTCCTCAAGCGCGACATGGTATGGGCCGCCACCTCGTCGCTCTGCGGTACC CTTCTGCTGGACATGTACCCGGACTTCATCGCCGCTTTCTGGGACCTTGACAGCGTCATAGACAAGCTTCTGTGG GGCCTGCCGAGGTGGCTGTACCCCGGCCCGCTCAGGGTTAGAGAAAAGGTGTTTGGAATGTGTGGTAGGTATCTG GAAGAGGCCTTCAAGAGGTTCGACTGGGACGGACCTGATGCCACTGCCGGCTGGGAGCCCATCTTTGGGTCGAGG TATGCGCGCGAGCGGGCAAAGTCGACTCGTGATGCTGGATTCACCTGGCAGAGTCGCATTAGCTTCCACATGATC TCCATCATCGCACTCAACTCCAACACGACGCCCGTCACGGCGTGGGCCATGTTTGAATTAATCAAGGACCCTTCG CTCTTTGAGGCCCTACGGGCCGAGGTCGAGACGTCGCTCGTCTCCGATCCGGAGACTGGATGCCGTCGATTCGAT ACAAGTAGGCTTCTGACACTGCCACTGCTCCAGTCTGTCTACGTGGAGACCCTGAGACTGCACGTGGCCGTCCTC ATCACGCGGCAGCTCATCGAGCCCATCCATGTCGGGCCGTATCAGCTGCGCAAGGGCGCCTGGCTTCAGGCACCG CCCAACTTCAGCCATCTCGACGACGCGCTATGGGGAGCCGACTCAAGTCATCCTGCCTCAGAGTTTTGGGCCAAG CGTCATGTCGTCGAAGAGGAAACAGAAGAAGCCGTAACCGGGCAGAGGATCCAGAAACAGAAATTCGTCATGGAA GCGCGGCCCAGCGAATTCTTCCCGTTCGGCGGTGGACACACTATGTGTCCGGGTCGAAACCTCGCCAGGCAGGAG ATCATGATGACGATAGCCATGATCGTGTCGCGCTTCGACATCGAATTCGTTCACTGGGTCGACAAGAATGGCGGA ATATCGACCGGCCTACCGAGAGACGATACGAAGTATTACGGATTTGGCGCCATGCCTCCCGACCGAGATGCAAGA ATTCGTTGGAGACGTCGGTGGTGA |
Transcript | >Hirsu2|4216 ATGGCGCAGTTCATCGACTGGAGGCCGGCGGCCGGCCGAATGGTCGACTTGGCCAAGGGTCACTGGCTGGTGACG GCGGCGTGCCTCGGCTTGGCCGTCGCCTTCGCGTGCGCTGCTCGGCTCGGTCGCCGGGCGGACGAGCCGCCCTCG CTTCCCGAGTGGCTTCCCTTTGTCGTCAACACGTATCGGTACATGAGCGACCGGAAGAAACTCATGGACCGAATC AGGCCTCTCGTCAGTCGGCACAAAGTGGCCATGCTCTGGATCATTGGGAAGCCCGTGTACGTCGTTTCCGGCGAC ATTGTCCGAATGATGTTTCGTTCGTCCGAAAGCATGAACGCCGACAACTTGAGCTTGCTCATCCTCAAAAATCTC CAAGGCCTCAGCGCCGAGGACGTGGCCAAGTTCGCCAACGACAAATCCGGCCGGCTCAAGACGCCCGGACGAGGT CATGAGCACGTCCCCGCCGACCAGCGTTACTGGGCCGCAAACCACGACCTGCACCACGACCACCTGCTCCCGGCC GAGGCGACGGCCCAGCTGGCCCGCTCGTACGAAACCTTCTTCACCCAGAGGTTGGAGATGCAGCCGCTTGGGCGG TGGGTGACTCTGGGCATCCACGATGTCCTCAAGCGCGACATGGTATGGGCCGCCACCTCGTCGCTCTGCGGTACC CTTCTGCTGGACATGTACCCGGACTTCATCGCCGCTTTCTGGGACCTTGACAGCGTCATAGACAAGCTTCTGTGG GGCCTGCCGAGGTGGCTGTACCCCGGCCCGCTCAGGGTTAGAGAAAAGGTGTTTGGAATGTGTGGTAGGTATCTG GAAGAGGCCTTCAAGAGGTTCGACTGGGACGGACCTGATGCCACTGCCGGCTGGGAGCCCATCTTTGGGTCGAGG TATGCGCGCGAGCGGGCAAAGTCGACTCGTGATGCTGGATTCACCTGGCAGAGTCGCATTAGCTTCCACATGATC TCCATCATCGCACTCAACTCCAACACGACGCCCGTCACGGCGTGGGCCATGTTTGAATTAATCAAGGACCCTTCG CTCTTTGAGGCCCTACGGGCCGAGGTCGAGACGTCGCTCGTCTCCGATCCGGAGACTGGATGCCGTCGATTCGAT ACAAGTAGGCTTCTGACACTGCCACTGCTCCAGTCTGTCTACGTGGAGACCCTGAGACTGCACGTGGCCGTCCTC ATCACGCGGCAGCTCATCGAGCCCATCCATGTCGGGCCGTATCAGCTGCGCAAGGGCGCCTGGCTTCAGGCACCG CCCAACTTCAGCCATCTCGACGACGCGCTATGGGGAGCCGACTCAAGTCATCCTGCCTCAGAGTTTTGGGCCAAG CGTCATGTCGTCGAAGAGGAAACAGAAGAAGCCGTAACCGGGCAGAGGATCCAGAAACAGAAATTCGTCATGGAA GCGCGGCCCAGCGAATTCTTCCCGTTCGGCGGTGGACACACTATGTGTCCGGGTCGAAACCTCGCCAGGCAGGAG ATCATGATGACGATAGCCATGATCGTGTCGCGCTTCGACATCGAATTCGTTCACTGGGTCGACAAGAATGGCGGA ATATCGACCGGCCTACCGAGAGACGATACGAAGTATTACGGATTTGGCGCCATGCCTCCCGACCGAGATGCAAGA ATTCGTTGGAGACGTCGGTGGTGA |
Gene | >Hirsu2|4216 ATGGCGCAGTTCATCGACTGGAGGCCGGCGGCCGGCCGAATGGTCGACTTGGCCAAGGGTCACTGGCTGGTGACG GCGGCGTGCCTCGGCTTGGCCGTCGCCTTCGCGTGCGCTGCTCGGCTCGGTCGCCGGGCGGACGAGCCGCCCTCG CTTCCCGAGTGGCTTCCCTTTGTCGTCAACACGTATCGGTACATGAGCGACCGGAAGAAACTCATGGACCGAATC AGGTGGGCACTGCCTCTCCCGCTCTGTATGACGAGCAAAGCCGTGCCTGAGCACAGAGGAGGAGGAGGAAGAAAG GCGGCGAGAGGGTTGGAGAAGCGCGCTCACATCTGCTCGCCAGGCCTCTCGTCAGTCGGCACAAAGTGGCCATGC TCTGGATCATTGGGAAGCCCGTGTACGTCGTTTCCGGCGACATTGTCCGAATGATGTTTCGTTCGTCCGAAAGCA TGAACGCCGACAACTTGAGCTTGCTCATCCTCAAAAATCTCCAAGGCCTCAGCGCCGAGGACGTGGCCAAGTTCG CCAACGACAAATCCGGCCGGCTCAAGACGCCCGGACGAGGTCATGAGCACGTCCCCGCCGACCAGCGTTACTGGG CCGCAAACCACGACCTGCACCACGACCACCTGCTCCCGGCCGAGGCGACGGCCCAGCTGGCCCGCTCGTACGAAA CCTTCTTCACCCAGAGGTTGGAGATGCAGCCGCTTGGGCGGTGGGTGACTCTGGGCATCCACGATGTCCTCAAGC GCGACATGGTATGGGCCGCCACCTCGTCGCTCTGCGGTACCCTTCTGCTGGACATGTACCCGGACTTCATCGCCG CTTTCTGGGACCTTGACAGCGTCATAGACAAGCTTCTGTGGGGCCTGCCGAGGTGGCTGTACCCCGGCCCGCTCA GGGTTAGAGAAAAGGTGTTTGGAATGTGTGGTAGGTATCTGGAAGAGGCCTTCAAGAGGTTCGACTGGGACGGAC CTGATGCCACTGCCGGCTGGGAGCCCATCTTTGGGTCGAGGTATGCGCGCGAGCGGGCAAAGTCGACTCGTGATG CTGGATTCACCTGGCAGAGTCGCATTAGCTTCCACATGATCTCCATCATCGCGTACGTTCCAAGCCCGTGTCGCT GCGTCGCCGGCGCGAACAGGCGGTCCGTCTTGAGCACGCAACTCACAGGCCTGGCCGCAGACTCAACTCCAACAC GACGCCCGTCACGGCGTGGGCCATGTTTGAATTAATCAAGGACCCTTCGCTCTTTGAGGCCCTACGGGCCGAGGT CGAGACGTCGCTCGTCTCCGATCCGGAGACTGGATGCCGTCGATTCGATACAAGTAGGCTTCTGACACTGCCACT GCTCCAGTCTGTCTACGTGGAGACCCTGAGACTGCACGTGGCCGTCCTCATCACGCGGCAGCTCATCGAGCCCAT CCATGTCGGGCCGTATCAGCTGCGCAAGGGCGCCTGGCTTCAGGCACCGCCCAACTTCAGCCATCTCGACGACGC GCTATGGGGAGCCGACTCAAGTCATCCTGCCTCAGAGTTTTGGGCCAAGCGTCATGTCGTCGAAGAGGAAACAGA AGAAGCCGTAACCGGGCAGAGGATCCAGAAACAGAAATTCGTCATGGAAGCGCGGCCCAGCGAATTCTTCCCGTT CGGTACGTACGCCCGCGGTGCTATGCCGAGCAACCACCGTTTTGCAAGCCAATGCGTCCAGAGAGTTTACGAAAC TGACGGTTCTGGAAAAAGGCGGTGGACACACTATGTGTCCGGGTCGAAACCTCGCCAGGCAGGAGATCATGATGA CGATAGCCATGATCGTGTCGCGCTTCGACATCGAATTCGTTCACTGGGTCGACAAGAATGGCGGAATATCGACCG GCCTACCGAGAGACGATACGAAGTATTACGGATTTGGCGCCATGCCTCCCGACCGAGATGCAAGAATTCGTTGGA GACGTCGGTGGTGA |