5DF1
Iridoid synthase from Catharanthus roseus - ternary complex with NADP+ and geranic acid
Summary for 5DF1
Entry DOI | 10.2210/pdb5df1/pdb |
Descriptor | Iridoid synthase, NADP NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE, (2E)-3,7-dimethylocta-2,6-dienoic acid, ... (6 entities in total) |
Functional Keywords | oxidoreductase, iridoid synthase, short chain dehydrogenase, nadph-dependent, catharanthus roseus |
Biological source | Catharanthus roseus (Madagascar periwinkle) |
Cellular location | Cytoplasm, cytosol : K7WDL7 |
Total number of polymer chains | 2 |
Total formula weight | 85051.78 |
Authors | Caputi, L.,Kries, H.,Stevenson, C.E.M.,Kamileen, M.O.,Sherden, N.H.,Geu-Flores, F.,Lawson, D.M.,O'Connor, S.E. (deposition date: 2015-08-26, release date: 2015-10-28, Last modification date: 2024-01-10) |
Primary citation | Kries, H.,Caputi, L.,Stevenson, C.E.,Kamileen, M.O.,Sherden, N.H.,Geu-Flores, F.,Lawson, D.M.,O'Connor, S.E. Structural determinants of reductive terpene cyclization in iridoid biosynthesis. Nat.Chem.Biol., 12:6-8, 2016 Cited by PubMed Abstract: The carbon skeleton of ecologically and pharmacologically important iridoid monoterpenes is formed in a reductive cyclization reaction unrelated to canonical terpene cyclization. Here we report the crystal structure of the recently discovered iridoid cyclase (from Catharanthus roseus) bound to a mechanism-inspired inhibitor that illuminates substrate binding and catalytic function of the enzyme. Key features that distinguish iridoid synthase from its close homolog progesterone 5β-reductase are highlighted. PubMed: 26551396DOI: 10.1038/nchembio.1955 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.75 Å) |
Structure validation
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