Enzyme

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EC Tree
     4. Lyases
        4.2 Carbon-oxygen lyases
            4.2.3 Acting on phosphates
ID:4.2.3.190
Description:Manoyl oxide synthase.

3D structure

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References

External Links

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:

4.2.3.190;

Phylogenetic Tree:

4.2.3.190;

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
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References

TitleAuthorsDatePubMed 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 J2014 Sep24990389
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 B2014 Mar24481136
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 J2013 Jun23613273