ID: | 4.2.3.190 |
---|---|
Description: | Manoyl oxide synthase. |
Click one PDB to see exact 3D structure provided by NGL.
Note: Use your mouse to drag, rotate, and zoom in and out of the structure. Mouse-over to identify atoms and bonds. Mouse controls documentation.UniProtKB Enzyme Link: | UniProtKB 4.2.3.190 |
BRENDA Enzyme Link: | BRENDA 4.2.3.190 |
KEGG Enzyme Link: | KEGG4.2.3.190 |
BioCyc Enzyme Link: | BioCyc 4.2.3.190 |
ExPASy Enzyme Link: | ExPASy4.2.3.190 |
EC2PDB Enzyme Link: | EC2PDB 4.2.3.190 |
ExplorEnz Enzyme Link: | ExplorEnz 4.2.3.190 |
PRIAM enzyme-specific profiles Link: | PRIAM 4.2.3.190 |
IntEnz Enzyme Link: | IntEnz 4.2.3.190 |
MEDLINE Enzyme Link: | MEDLINE 4.2.3.190 |
MSA: | |
---|---|
Phylogenetic Tree: | |
Uniprot: | |
M-CSA: |
RHEA:54516 | 8-hydroxycopalyl diphosphate = (13R)-manoyl oxide + diphosphate |
RULE(radius=1) | ([*:1]-[C;H0;+0:2](-[*:3])=[CH;+0:4]-[CH2;+0:5]-[O;H0;+0:6]-[*:7].[*:8]-[OH;+0:9])>>[*:1]-[C;H0;+0:2](-[*:3])(-[CH;+0:4]=[CH2;+0:5])-[O;H0;+0:9]-[*:8].[*:7]-[OH;+0:6] |
Reaction | ![]() |
Core-to-Core |
Title | Authors | Date | PubMed ID |
---|---|---|---|
Diterpene synthases of the biosynthetic system of medicinally active diterpenoids in Marrubium vulgare. | Zerbe P, Chiang A, Dullat H, O'Neil-Johnson M, Starks C, Hamberger B, Bohlmann J | 2014 Sep | 24990389 |
Manoyl oxide (13R), the biosynthetic precursor of forskolin, is synthesized in specialized root cork cells in Coleus forskohlii. | Pateraki I, Andersen-Ranberg J, Hamberger B, Heskes AM, Martens HJ, Zerbe P, Bach SS, Møller BL, Bohlmann J, Hamberger B | 2014 Mar | 24481136 |
Gene discovery of modular diterpene metabolism in nonmodel systems. | Zerbe P, Hamberger B, Yuen MM, Chiang A, Sandhu HK, Madilao LL, Nguyen A, Hamberger B, Bach SS, Bohlmann J | 2013 Jun | 23613273 |