| 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: | 1.14.13.216 |
|---|---|
| Description: | Asperlicin C monooxygenase. |
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 1.14.13.216 |
| BRENDA Enzyme Link: | BRENDA 1.14.13.216 |
| KEGG Enzyme Link: | KEGG1.14.13.216 |
| BioCyc Enzyme Link: | BioCyc 1.14.13.216 |
| ExPASy Enzyme Link: | ExPASy1.14.13.216 |
| EC2PDB Enzyme Link: | EC2PDB 1.14.13.216 |
| ExplorEnz Enzyme Link: | ExplorEnz 1.14.13.216 |
| PRIAM enzyme-specific profiles Link: | PRIAM 1.14.13.216 |
| IntEnz Enzyme Link: | IntEnz 1.14.13.216 |
| MEDLINE Enzyme Link: | MEDLINE 1.14.13.216 |
| MSA: | |
|---|---|
| Phylogenetic Tree: | |
| Uniprot: | |
| M-CSA: |
| RHEA:49056 | asperlicin C + H(+) + NADPH + O2 = asperlicin E + H2O + NADP(+) |
| RULE(radius=1) | [*:1]-[N;H0;+0:2]1-[CH;+0:3]=[C;H0;+0:4](-[*:5])-[CH2;+0:6]-[CH;+0:7]=[CH;+0:8]-1.[*:9]-[NH;+0:10]-[*:11]-[*:12]-[c;H0;+0:13]1:[*:14]:[*:15]:[nH;+0:16]:[cH;+0:17]:1.[H+;H0:18].[O;H0;+0:19]=[O;H0;+0:20]>>[*:9]-[N;H0;+0:10]1-[*:11]-[*:12]-[C;H0;+0:13]2(-[OH;+0:19])-[*:14]:[*:15]-[NH;+0:16]-[CH;+0:17]-1-2.[*:1]-[n+;H0:2]1:[cH;+0:3]:[c;H0;+0:4](-[*:5]):[cH;+0:6]:[cH;+0:7]:[cH;+0:8]:1.[OH2;+0:20] |
| Reaction | ![]() |
| Core-to-Core | |
| Core-to-Core |
| Title | Authors | Date | PubMed ID |
|---|---|---|---|
| Assembly of asperlicin peptidyl alkaloids from anthranilate and tryptophan: a two-enzyme pathway generates heptacyclic scaffold complexity in asperlicin E. | Haynes SW, Gao X, Tang Y, Walsh CT | 2012 Oct 24 | 23030663 |
| RHEA:49052 | asperlicin C + H(+) + NADH + O2 = asperlicin E + H2O + NAD(+) |
| RULE(radius=1) | [*:1]-[N;H0;+0:2]1-[CH;+0:3]=[C;H0;+0:4](-[*:5])-[CH2;+0:6]-[CH;+0:7]=[CH;+0:8]-1.[*:9]-[NH;+0:10]-[*:11]-[*:12]-[c;H0;+0:13]1:[*:14]:[*:15]:[nH;+0:16]:[cH;+0:17]:1.[H+;H0:18].[O;H0;+0:19]=[O;H0;+0:20]>>[*:9]-[N;H0;+0:10]1-[*:11]-[*:12]-[C;H0;+0:13]2(-[OH;+0:19])-[*:14]:[*:15]-[NH;+0:16]-[CH;+0:17]-1-2.[*:1]-[n+;H0:2]1:[cH;+0:3]:[c;H0;+0:4](-[*:5]):[cH;+0:6]:[cH;+0:7]:[cH;+0:8]:1.[OH2;+0:20] |
| Reaction | ![]() |
| Core-to-Core | |
| Core-to-Core |
| Title | Authors | Date | PubMed ID |
|---|---|---|---|
| Assembly of asperlicin peptidyl alkaloids from anthranilate and tryptophan: a two-enzyme pathway generates heptacyclic scaffold complexity in asperlicin E. | Haynes SW, Gao X, Tang Y, Walsh CT | 2012 Oct 24 | 23030663 |