BioCyc:RXN-18117
ActVI-ORF1 catalyzes the reduction of |FRAME: CPD1A0-6104| at C-3 via two active amino acids, Glu141 and His129,and NAD(P)H to yield a secondary alcohol |CITS: [7929165]||CITS: [10091691]||CITS: [10805574]||CITS: [15498668]|.It was also discovered that the likely substrate for ActVI-ORF1 is the β-keto acid form of the bicyclic intermediate,thus indicating that the ACP is released prior to this reaction |CITS: [15645472]|.
CPD-19414 + OXYGEN-MOLECULE + FMNH2 --> CPD-19415 + WATER + FMN + PROTON
Medermycin[C24H27NO8] + Oxygen[O2] + Reduced FMN[C17H23N4O9P] = Mederrhodin A[C24H27NO9] + H2O[H2O] + FMN(3-)[C17H18N4O9P] + H+[H]
DB Links
- BioCyc: RXN-18117
- EC Number: 1.14.14.-
Alias
Metabolites
Substrates
| metabolite | compartment | Structure |
|---|---|---|
| Medermycin Formula: C24H27NO8 |
Cytoplasm | |
| Oxygen Formula: O2 |
Cytoplasm | |
| Reduced FMN Formula: C17H23N4O9P |
Cytoplasm |
Products
| metabolite | compartment | Structure |
|---|---|---|
| Mederrhodin A Formula: C24H27NO9 |
Cytoplasm | |
| H2O Formula: H2O |
Cytoplasm | |
| FMN(3-) Formula: C17H18N4O9P |
Cytoplasm | |
| H+ Formula: H |
Cytoplasm |