8A3N
Geissoschizine synthase from Catharanthus roseus - binary complex with NADP+
Summary for 8A3N
Entry DOI | 10.2210/pdb8a3n/pdb |
Descriptor | Geissoschizine synthase, NADP NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE, ZINC ION, ... (4 entities in total) |
Functional Keywords | medium-chain alcohol dehydrogenase, oxidoreductase, iminium reduction, natural product biosynthesis |
Biological source | Catharanthus roseus (Madagascar periwinkle) |
Total number of polymer chains | 2 |
Total formula weight | 80923.59 |
Authors | Langley, C.,Tatsis, E.,Hong, B.,Nakamura, Y.,Kamileen, M.O.,Paetz, C.,Stevenson, C.E.M.,Basquin, J.,Lawson, D.M.,Caputi, L.,O'Connor, S.E. (deposition date: 2022-06-08, release date: 2022-10-19, Last modification date: 2024-01-31) |
Primary citation | Langley, C.,Tatsis, E.,Hong, B.,Nakamura, Y.,Paetz, C.,Stevenson, C.E.M.,Basquin, J.,Lawson, D.M.,Caputi, L.,O'Connor, S.E. Expansion of the Catalytic Repertoire of Alcohol Dehydrogenases in Plant Metabolism. Angew.Chem.Int.Ed.Engl., 61:e202210934-e202210934, 2022 Cited by PubMed Abstract: Medium-chain alcohol dehydrogenases (ADHs) comprise a highly conserved enzyme family that catalyse the reversible reduction of aldehydes. However, recent discoveries in plant natural product biosynthesis suggest that the catalytic repertoire of ADHs has been expanded. Here we report the crystal structure of dihydroprecondylocarpine acetate synthase (DPAS), an ADH that catalyses the non-canonical 1,4-reduction of an α,β-unsaturated iminium moiety. Comparison with structures of plant-derived ADHs suggest the 1,4-iminium reduction does not require a proton relay or the presence of a catalytic zinc ion in contrast to canonical 1,2-aldehyde reducing ADHs that require the catalytic zinc and a proton relay. Furthermore, ADHs that catalysed 1,2-iminium reduction required the presence of the catalytic zinc and the loss of the proton relay. This suggests how the ADH active site can be modified to perform atypical carbonyl reductions, providing insight into how chemical reactions are diversified in plant metabolism. PubMed: 36198083DOI: 10.1002/anie.202210934 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2 Å) |
Structure validation
Download full validation report