Riboflavin reductase (NAD(P)H)
| Riboflavin reductase (NAD(P)H) | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Identifiers | |||||||||
| EC no. | 1.5.1.41 | ||||||||
| Databases | |||||||||
| IntEnz | IntEnz view | ||||||||
| BRENDA | BRENDA entry | ||||||||
| ExPASy | NiceZyme view | ||||||||
| KEGG | KEGG entry | ||||||||
| MetaCyc | metabolic pathway | ||||||||
| PRIAM | profile | ||||||||
| PDB structures | RCSB PDB PDBe PDBsum | ||||||||
| |||||||||
Riboflavin reductase (NAD(P)H) (EC 1.5.1.41, NAD(P)H-FMN reductase, Fre) is an enzyme with systematic name riboflavin:NAD(P)+ oxidoreductase.[1][2][3] This enzyme catalyses the following chemical reaction
- reduced riboflavin + NAD(P)+ riboflavin + NAD(P)H + H+
This enzyme catalyses the reduction of soluble flavins.
The structure of the protein suggests that the enzymatic mechanism of flavin reductase is of a bisubstrate-biproduct nature3. Due to its structural features, the enzyme is not able to bind both NAD(P)H and flavin at the same time. Therefore, in the proposed mechanism the flavin reductase first binds NAD(P)H and stabilizes the release of a hydride3. Next, NAD(P)+ is released and the flavin mononucleotide binds to the enzyme. This is followed by further protonation when the hydride attacks a nitrogen atom on the flavin mononucleotide3. Finally, the reduced flavin is released from flavin reductase. If this mechanism is indeed correct, it suggests that the reduction of flavin by flavin reductase is dependent on the enzyme binding first to NAD(P)H3.
References
[edit]- ^ Fontecave M, Eliasson R, Reichard P (September 1987). "NAD(P)H:flavin oxidoreductase of Escherichia coli. A ferric iron reductase participating in the generation of the free radical of ribonucleotide reductase". The Journal of Biological Chemistry. 262 (25): 12325–31. PMID 3305505.
- ^ Spyrou G, Haggård-Ljungquist E, Krook M, Jörnvall H, Nilsson E, Reichard P (June 1991). "Characterization of the flavin reductase gene (fre) of Escherichia coli and construction of a plasmid for overproduction of the enzyme". Journal of Bacteriology. 173 (12): 3673–9. PMC 207994. PMID 2050627.
- ^ Ingelman M, Ramaswamy S, Nivière V, Fontecave M, Eklund H (June 1999). "Crystal structure of NAD(P)H:flavin oxidoreductase from Escherichia coli". Biochemistry. 38 (22): 7040–9. doi:10.1021/bi982849m. PMID 10353815.
External links
[edit]- Riboflavin+reductase+(NAD(P)H) at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
