| EC Tree |
| 5. Isomerases |
| 5.4 Intramolecular transferases |
| 5.4.99 Transferring other groups |
| ID: | 5.4.99.57 |
|---|---|
| Description: | Baruol synthase. |
| Alternative Name: |
BARS1. |
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 5.4.99.57 |
| BRENDA Enzyme Link: | BRENDA 5.4.99.57 |
| KEGG Enzyme Link: | KEGG5.4.99.57 |
| BioCyc Enzyme Link: | BioCyc 5.4.99.57 |
| ExPASy Enzyme Link: | ExPASy5.4.99.57 |
| EC2PDB Enzyme Link: | EC2PDB 5.4.99.57 |
| ExplorEnz Enzyme Link: | ExplorEnz 5.4.99.57 |
| PRIAM enzyme-specific profiles Link: | PRIAM 5.4.99.57 |
| IntEnz Enzyme Link: | IntEnz 5.4.99.57 |
| MEDLINE Enzyme Link: | MEDLINE 5.4.99.57 |
| MSA: | |
|---|---|
| Phylogenetic Tree: | |
| Uniprot: | |
| M-CSA: |
| RHEA:31987 | (S)-2,3-epoxysqualene = baruol |
| RULE(radius=1) | ([*:1]-[C;H0;+0:2](-[*:3]-[*:4]-[CH;+0:5]=[C;H0;+0:6](-[CH3;+0:7])-[*:8]-[CH2;+0:9]-[CH;+0:10]=[C;H0;+0:11](-[CH3;+0:12])-[CH3;+0:13])=[CH;+0:14]-[*:15]-[*:16]-[CH;+0:17]=[C;H0;+0:18](-[CH3;+0:19])-[*:20]-[CH2;+0:21]-[CH;+0:22]=[C;H0;+0:23](-[*:24])-[CH3;+0:25].[*:26]-[C;H0;+0:27]1(-[*:28])-[*:29]-[O;H0;+0:30]-1)>>[*:1]-[C;H0;+0:2]12-[*:3]-[*:4]-[C;H0;+0:5](-[CH3;+0:19])(-[CH2;+0:6]-[*:8]-[CH;+0:9]=[C;H0;+0:10](-[CH3;+0:11])-[CH3;+0:25])-[CH2;+0:13]-[C;H0;+0:14]-1(-[CH3;+0:12])-[*:15]-[*:16]-[C;H0;+0:17]1(-[CH3;+0:7])-[CH;+0:23](-[*:24])-[C;H0;+0:22](-[C;H0;+0:27](-[*:26])(-[*:28])-[*:29]-[OH;+0:30])=[CH;+0:21]-[*:20]-[CH;+0:18]-1-2 |
| Reaction | ![]() |
| Core-to-Core |
| Title | Authors | Date | PubMed ID |
|---|---|---|---|
| An oxidosqualene cyclase makes numerous products by diverse mechanisms: a challenge to prevailing concepts of triterpene biosynthesis. | Lodeiro S, Xiong Q, Wilson WK, Kolesnikova MD, Onak CS, Matsuda SP | 2007 Sep 12 | 17705488 |