| Entry | Q66QH3 |
Entry Name | KSL4_ORYSI |
| Sequence Status | reviewed |
| Protein Name | Syn-pimara-7,15-diene synthase (EC 4.2.3.35) (9-beta-pimara-7,15-diene synthase) (Ent-kaurene synthase-like 4) (OsKS4) (OsKSL4) (OsDTS2) |
| Sequence Length | 840 |
| Gene Name | KSL4 DTS2 OsI_014459 |
| Organism | Oryza sativa subsp. indica (Rice) |
| EC Number | 4.2.3.35 |
Protein Function | FUNCTION: Involved in the momilactone phytoalexins biosynthesis. Catalyzes the conversion of syn-copalyl diphosphate to the phytoalexin precursor syn-pimara-7,15-diene. {ECO:0000269|PubMed:15299118}. |
Pathway | |
Protein Active Site | |
Reference | 15299118; 15685292 |
Domain | DOMAIN: The Asp-Asp-Xaa-Xaa-Asp/Glu (DDXXD/E) motif is important for the catalytic activity, presumably through binding to Mg(2+). |
Motif | MOTIF 589 593 DDXXD motif. |
Protein Family | Terpene synthase family |
Ensembl ID | BGIOSGA015980-TA; |
Biocyc ID | PF01397;PF03936; |
Protein Existence | Evidence at transcript level |
Subunit Structure | |
Gene Ontology Biological Process | defense response [GO:0006952]; metabolic process [GO:0008152] |
Gene Ontology Cellular Component | |
Gene Ontology | magnesium ion binding [GO:0000287]; syn-pimara-7,15-diene synthase activity [GO:0034279]; terpene synthase activity [GO:0010333]; defense response [GO:0006952]; metabolic process [GO:0008152] |
Gene Ontology Molecular Function | magnesium ion binding [GO:0000287]; syn-pimara-7,15-diene synthase activity [GO:0034279]; terpene synthase activity [GO:0010333] |
GO ID | GO:0000287; GO:0006952; GO:0008152; GO:0010333; GO:0034279 |
String Database | 39946.BGIOSGA015980-PA; |
PDB | |
RefSeq | |
KEGG | ag:AAU05906; |
InterPro | IPR008949;IPR001906;IPR036965;IPR005630;IPR008930; |
Protein Sequence | MASPMEAVARSSLVLAPRRRRALGLLPAAAAPFVLDCRRRHNGGMRRPHVSFACSAELDTGRRQLPSTGTRAVMSSCPGYVEGRMVGENTSQINMGREARIRRHLENPEFLPSSYDIAWVAMVPLPGTDHLQAPCFPECVEWILQNQHSNGSWGVNEFDSSASKDILLSTLACIIALEKWNVGSEQIRRGLHFIAKNFSIVIDDQIAAPIGFNLTFPAMVNLAIKMGLEFPASEISIDQILHLRDMELKRLSGEESLGKEAYFAYIAEGLEESMVDWSEVMKFQGKNGSLFNSPAATAAALVHRYDDKALGYLYSVVNKFGGEVPTVYPLNIFSQLSMVDTLVNIGISRHFSSDIKRILDKTYILWSQRDEEVMLDLPTCAMAFRLLRMNGYGVSSDDLSHVAEASTFHNSVEGYLDDTKSLLELYKASKVSLSENEPILEKMGCWSGSLLKEKLCSDDIRGTPILGEVEYALKFPFYATLEPLDHKWNIENFDARAYQKIKTKNMPCHVNEDLLALAAEDFSFCQSTYQNEIQHLESWEKENKLDQLEFTRKNLINSYLSAAATISPYELSDARIACAKSIALTLVADDFFDVGSSKEEQENLISLVEKWDQYHKVEFYSENVKAVFFALYSTVNQLGAMASAVQNRDVTKYNVESWLDYLRSLATDAEWQRSKYVPTMEEYMKNSIVTFALGPTILIALYFMGQNLWEDIVKNAEYDELFRLMNTCGRLQNDIQSFERECKDGKLNSVSLLVLDSKDVMSVEEAKEAINESISSCRRELLRLVVREDGVIPKSCKEMFWNLYKTSHVFYSQADGFSSPKEMMGAMNGVIFEPLKTRGN |
