Enzyme

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EC Tree
     4. Lyases
        4.2 Carbon-oxygen lyases
            4.2.3 Acting on phosphates
ID:4.2.3.122
Description:(+)-beta-pinene synthase.
Alternative Name: (+)-pinene cyclase.
Cath: 1.10.600.10; 1.50.10.130;

3D structure

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References

External Links

UniProtKB Enzyme Link: UniProtKB 4.2.3.122
BRENDA Enzyme Link: BRENDA 4.2.3.122
KEGG Enzyme Link: KEGG4.2.3.122
BioCyc Enzyme Link: BioCyc 4.2.3.122
ExPASy Enzyme Link: ExPASy4.2.3.122
EC2PDB Enzyme Link: EC2PDB 4.2.3.122
ExplorEnz Enzyme Link: ExplorEnz 4.2.3.122
PRIAM enzyme-specific profiles Link: PRIAM 4.2.3.122
IntEnz Enzyme Link: IntEnz 4.2.3.122
MEDLINE Enzyme Link: MEDLINE 4.2.3.122
MSA:

4.2.3.122;

Phylogenetic Tree:

4.2.3.122;

Uniprot:
M-CSA:
RHEA:32579 (2E)-geranyl diphosphate = (+)-beta-pinene + diphosphate
RULE(radius=1) [*:1]-[C;H0;+0:2](-[*:3])=[CH;+0:4]-[*:5]-[*:6]-[C;H0;+0:7](-[CH3;+0:8])=[CH;+0:9]-[CH2;+0:10]-[O;H0;+0:11]-[*:12]>>[*:1]-[C;H0;+0:2]1(-[*:3])-[CH;+0:9]2-[CH2;+0:10]-[CH;+0:4]-1-[*:5]-[*:6]-[C;H0;+0:7]-2=[CH2;+0:8].[*:12]-[OH;+0:11]
Reaction
Core-to-Core No scaffolds atoms were exchanged as a result of the reaction

References

TitleAuthorsDatePubMed ID
Monoterpene biosynthesis: isotope effects associated with bicyclic olefin formation catalyzed by pinene synthases from sage (Salvia officinalis).Wagschal KC, Pyun HJ, Coates RM, Croteau R1994 Feb 18109978
Stereochemistry of the proton elimination in the formation of (+)- and (-)-alpha-pinene by monoterpene cyclases from sage (Salvia officinalis).Pyun HJ, Wagschal KC, Jung DI, Coates RM, Croteau R1994 Feb 18109979