ID: | 4.2.3.51 |
---|---|
Description: | Beta-phellandrene synthase (neryl-diphosphate-cyclizing). |
Alternative Name: |
Phellandrene synthase 1. |
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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 4.2.3.51 |
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 |
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 |
Title | Authors | Date | PubMed 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 E | 2009 Jun 30 | 19487664 |