Enzyme

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EC Tree
     4. Lyases
        4.2 Carbon-oxygen lyases
            4.2.3 Acting on phosphates
ID:4.2.3.51
Description:Beta-phellandrene synthase (neryl-diphosphate-cyclizing).
Alternative Name: Phellandrene synthase 1.

3D structure

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References

External Links

UniProtKB Enzyme Link: UniProtKB 4.2.3.51
BRENDA Enzyme Link: BRENDA 4.2.3.51
KEGG Enzyme Link: KEGG4.2.3.51
BioCyc Enzyme Link: BioCyc 4.2.3.51
ExPASy Enzyme Link: ExPASy4.2.3.51
EC2PDB Enzyme Link: EC2PDB 4.2.3.51
ExplorEnz Enzyme Link: ExplorEnz 4.2.3.51
PRIAM enzyme-specific profiles Link: PRIAM 4.2.3.51
IntEnz Enzyme Link: IntEnz 4.2.3.51
MEDLINE Enzyme Link: MEDLINE 4.2.3.51
MSA:

4.2.3.51;

Phylogenetic Tree:

4.2.3.51;

Uniprot:
M-CSA:
RHEA:27830 neryl diphosphate = beta-phellandrene + 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]-[CH;+0:2](-[*:3])-[CH;+0:4]1-[*:5]-[*:6]-[C;H0;+0:7](=[CH2;+0:8])-[CH;+0:9]=[CH;+0:10]-1.[*:12]-[OH;+0:11]
Reaction
Core-to-Core No scaffolds atoms were exchanged as a result of the reaction

References

TitleAuthorsDatePubMed ID
Monoterpenes in the glandular trichomes of tomato are synthesized from a neryl diphosphate precursor rather than geranyl diphosphate.Schilmiller AL, Schauvinhold I, Larson M, Xu R, Charbonneau AL, Schmidt A, Wilkerson C, Last RL, Pichersky E2009 Jun 3019487664