ID: | 4.2.1.128 |
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Description: | Lupan-3-beta,20-diol synthase. |
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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 4.2.1.128 |
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: | |
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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 |