| EC Tree |
| 1. Oxidoreductases |
| 1.14 Acting on paired donors, with incorporation or reduction of molecular oxygen |
| 1.14.13 With NADH or NADPH as one donor, and incorporation of one atom of oxygen into the other donor |
| ID: | 1.14.13.69 |
|---|---|
| Description: | Alkene monooxygenase. |
| Alternative Name: |
Alkene epoxygenase. |
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 1.14.13.69 |
| BRENDA Enzyme Link: | BRENDA 1.14.13.69 |
| KEGG Enzyme Link: | KEGG1.14.13.69 |
| BioCyc Enzyme Link: | BioCyc 1.14.13.69 |
| ExPASy Enzyme Link: | ExPASy1.14.13.69 |
| EC2PDB Enzyme Link: | EC2PDB 1.14.13.69 |
| ExplorEnz Enzyme Link: | ExplorEnz 1.14.13.69 |
| PRIAM enzyme-specific profiles Link: | PRIAM 1.14.13.69 |
| IntEnz Enzyme Link: | IntEnz 1.14.13.69 |
| MEDLINE Enzyme Link: | MEDLINE 1.14.13.69 |
| MSA: | |
|---|---|
| Phylogenetic Tree: | |
| Uniprot: | |
| M-CSA: |
| RHEA:11792 | H(+) + NADH + O2 + propene = 1,2-epoxypropane + H2O + NAD(+) |
| RULE(radius=1) | [*:1]-[CH;+0:2]=[CH2;+0:3].[*:4]-[N;H0;+0:5]1-[CH;+0:6]=[C;H0;+0:7](-[*:8])-[CH2;+0:9]-[CH;+0:10]=[CH;+0:11]-1.[H+;H0:12].[O;H0;+0:13]=[O;H0;+0:14]>>[*:1]-[CH;+0:2]1-[CH2;+0:3]-[O;H0;+0:13]-1.[*:4]-[n+;H0:5]1:[cH;+0:6]:[c;H0;+0:7](-[*:8]):[cH;+0:9]:[cH;+0:10]:[cH;+0:11]:1.[OH2;+0:14] |
| Reaction | ![]() |
| Core-to-Core |
| Title | Authors | Date | PubMed ID |
|---|---|---|---|
| Alkene monooxygenase from Xanthobacter strain Py2. Purification and characterization of a four-component system central to the bacterial metabolism of aliphatic alkenes. | Small FJ, Ensign SA | 1997 Oct 3 | 9312093 |
| Cometabolic degradation of chlorinated alkenes by alkene monooxygenase in a propylene-grown Xanthobacter strain. | Ensign SA, Hyman MR, Arp DJ | 1992 Sep | 1444418 |
| The alkene monooxygenase from Xanthobacter strain Py2 is closely related to aromatic monooxygenases and catalyzes aromatic monohydroxylation of benzene, toluene, and phenol. | Zhou NY, Jenkins A, Chan Kwo Chion CK, Leak DJ | 1999 Apr | 10103255 |