| ID: | 4.2.3.136 |
|---|---|
| Description: | Alpha-isocomene 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 4.2.3.136 |
| BRENDA Enzyme Link: | BRENDA 4.2.3.136 |
| KEGG Enzyme Link: | KEGG4.2.3.136 |
| BioCyc Enzyme Link: | BioCyc 4.2.3.136 |
| ExPASy Enzyme Link: | ExPASy4.2.3.136 |
| EC2PDB Enzyme Link: | EC2PDB 4.2.3.136 |
| ExplorEnz Enzyme Link: | ExplorEnz 4.2.3.136 |
| PRIAM enzyme-specific profiles Link: | PRIAM 4.2.3.136 |
| IntEnz Enzyme Link: | IntEnz 4.2.3.136 |
| MEDLINE Enzyme Link: | MEDLINE 4.2.3.136 |
| MSA: | |
|---|---|
| Phylogenetic Tree: | |
| Uniprot: | |
| M-CSA: |
| RHEA:34699 | (2E,6E)-farnesyl diphosphate = (-)-alpha-isocomene + diphosphate |
| RULE(radius=1) | [*:1]-[C;H0;+0:2](-[*:3]-[*:4]-[CH;+0:5]=[C;H0;+0:6](-[CH3;+0:7])-[*:8]-[*:9]-[CH;+0:10]=[C;H0;+0:11](-[*:12])-[CH3;+0:13])=[CH;+0:14]-[CH2;+0:15]-[O;H0;+0:16]-[*:17]>>[*:1]-[C;H0;+0:2]12-[*:3]-[*:4]-[CH;+0:5](-[CH3;+0:7])-[C;H0;+0:6]-13-[*:8]-[*:9]-[CH2;+0:10]-[C;H0;+0:11]-3(-[*:12])-[CH;+0:13]=[C;H0;+0:14]-2-[CH3;+0:15].[*:17]-[OH;+0:16] |
| Reaction | ![]() |
| Core-to-Core | No scaffolds atoms were exchanged as a result of the reaction |
| Title | Authors | Date | PubMed ID |
|---|---|---|---|
| The organ-specific expression of terpene synthase genes contributes to the terpene hydrocarbon composition of chamomile essential oils. | Irmisch S, Krause ST, Kunert G, Gershenzon J, Degenhardt J, Köllner TG | 2012 Jun 8 | 22682202 |
| Theoretical and experimental analysis of the reaction mechanism of MrTPS2, a triquinane-forming sesquiterpene synthase from chamomile. | Hong YJ, Irmisch S, Wang SC, Garms S, Gershenzon J, Zu L, Köllner TG, Tantillo DJ | 2013 Sep 27 | 23963956 |