3BXX
Binding of two substrate analogue molecules to dihydroflavonol 4-reductase alters the functional geometry of the catalytic site
Summary for 3BXX
Entry DOI | 10.2210/pdb3bxx/pdb |
Related | 2IOD 3C1T |
Descriptor | dihydroflavonol 4-reductase, NADP NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE, 3,5,7,3',4'-PENTAHYDROXYFLAVONE, ... (4 entities in total) |
Functional Keywords | rossmann fold, oxidoreductase |
Biological source | Vitis vinifera (wine grape) |
Total number of polymer chains | 6 |
Total formula weight | 233346.62 |
Authors | Trabelsi, N.,Petit, P.,Granier, T.,Langlois d'Estaintot, B.,Delrot, S.,Gallois, B. (deposition date: 2008-01-15, release date: 2008-10-21, Last modification date: 2024-02-21) |
Primary citation | Trabelsi, N.,Petit, P.,Manigand, C.,Langlois d'Estaintot, B.,Granier, T.,Chaudiere, J.,Gallois, B. Structural evidence for the inhibition of grape dihydroflavonol 4-reductase by flavonols Acta Crystallogr.,Sect.D, D64:883-891, 2008 Cited by PubMed Abstract: Dihydroflavonol 4-reductase (DFR) is a key enzyme of the flavonoid biosynthesis pathway which catalyses the NADPH-dependent reduction of 2R,3R-trans-dihydroflavonols to leucoanthocyanidins. The latter are the precursors of anthocyans and condensed tannins, two major classes of phenolic compounds that strongly influence the organoleptic properties of wine. DFR has been investigated in many plant species, but little was known about its structural properties until the three-dimensional structure of the Vitis vinifera enzyme complexed with NADP(+) and its natural substrate dihydroquercetin (DHQ) was described. In the course of the study of substrate specificity, crystals of DFR-NADP(+)-flavonol (myricetin and quercetin) complexes were obtained. Their structures exhibit major changes with respect to that of the abortive DFR-NADP(+)-DHQ complex. Two flavonol molecules bind to the catalytic site in a stacking arrangement and alter its geometry, which becomes incompatible with enzymatic activity. The X-ray structures of both DFR-NADP(+)-myricetin and DFR-NADP(+)-quercetin are reported together with preliminary spectroscopic data. The results suggest that flavonols could be inhibitors of the activity of DFR towards dihydroflavonols. PubMed: 18645237DOI: 10.1107/S0907444908017769 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.9 Å) |
Structure validation
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