| ID: | 4.2.1.128 |
|---|---|
| Description: | Lupan-3-beta,20-diol 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 4.2.1.128 |
| BRENDA Enzyme Link: | BRENDA 4.2.1.128 |
| KEGG Enzyme Link: | KEGG4.2.1.128 |
| BioCyc Enzyme Link: | BioCyc 4.2.1.128 |
| ExPASy Enzyme Link: | ExPASy4.2.1.128 |
| EC2PDB Enzyme Link: | EC2PDB 4.2.1.128 |
| ExplorEnz Enzyme Link: | ExplorEnz 4.2.1.128 |
| PRIAM enzyme-specific profiles Link: | PRIAM 4.2.1.128 |
| IntEnz Enzyme Link: | IntEnz 4.2.1.128 |
| MEDLINE Enzyme Link: | MEDLINE 4.2.1.128 |
| MSA: | |
|---|---|
| Phylogenetic Tree: | |
| Uniprot: | |
| M-CSA: |
| RHEA:31351 | lupan-3beta,20-diol = (S)-2,3-epoxysqualene + H2O |
| RULE(radius=1) | ([*:1]-[C;H0;+0:2](-[*:3]-[*:4]-[CH;+0:5]=[C;H0;+0:6](-[*:7])-[*:8])=[CH;+0:9]-[*:10]-[CH2;+0:11]-[C;H0;+0:12](-[CH3;+0:13])=[CH;+0:14]-[*:15]-[*:16]-[CH;+0:17]=[C;H0;+0:18](-[*:19])-[*:20]-[*:21]-[CH;+0:22]=[C;H0;+0:23](-[*:24])-[*:25].[*:26]-[C;H0;+0:27]1(-[*:28])-[*:29]-[O;H0;+0:30]-1).[OH2;+0:31]>>[*:1]-[C;H0;+0:2]12-[*:3]-[*:4]-[C;H0;+0:5]3(-[CH3;+0:13])-[CH;+0:14](-[*:15]-[*:16]-[CH;+0:17]4-[C;H0;+0:23](-[*:24])(-[*:25])-[CH;+0:22](-[C;H0;+0:27](-[*:26])(-[*:28])-[*:29]-[OH;+0:30])-[*:21]-[*:20]-[C;H0;+0:18]-4-3-[*:19])-[CH;+0:12]-1-[CH;+0:11](-[C;H0;+0:6](-[*:7])(-[*:8])-[OH;+0:31])-[*:10]-[CH2;+0:9]-2 |
| Reaction | ![]() |
| Core-to-Core |
| Title | Authors | Date | PubMed ID |
|---|---|---|---|
| Stereochemical course in water addition during LUP1-catalyzed triterpene cyclization. | Kushiro T, Hoshino M, Tsutsumi T, Kawai K, Shiro M, Shibuya M, Ebizuka Y | 2006 Nov 23 | 17107079 |
| Arabidopsis thaliana LUP1 converts oxidosqualene to multiple triterpene alcohols and a triterpene diol. | Segura MJ, Meyer MM, Matsuda SP | 2000 Jul 27 | 10930257 |