1U0U
An Aldol Switch Discovered in Stilbene Synthases Mediates Cyclization Specificity of Type III Polyketide Synthases: Pine stilbene synthase structure
Summary for 1U0U
Entry DOI | 10.2210/pdb1u0u/pdb |
Related | 1BI5 1U0V 1U0W |
Descriptor | Dihydropinosylvin synthase (2 entities in total) |
Functional Keywords | pks, type iii polyketide synthase, condensing enzyme, thiolase fold, alpha-beta-alpha-beta-alpha fold, aldol switch, catalytic triad, transferase |
Biological source | Pinus sylvestris (Scots pine) |
Cellular location | Cytoplasm: Q02323 |
Total number of polymer chains | 6 |
Total formula weight | 258733.87 |
Authors | Austin, M.B.,Bowman, M.E.,Ferrer, J.-L.,Schroder, J.,Noel, J.P. (deposition date: 2004-07-14, release date: 2004-10-12, Last modification date: 2023-08-23) |
Primary citation | Austin, M.B.,Bowman, M.E.,Ferrer, J.-L.,Schroder, J.,Noel, J.P. An Aldol Switch Discovered in Stilbene Synthases Mediates Cyclization Specificity of Type III Polyketide Synthases Chem.Biol., 11:1179-1194, 2004 Cited by PubMed Abstract: Stilbene synthase (STS) and chalcone synthase (CHS) each catalyze the formation of a tetraketide intermediate from a CoA-tethered phenylpropanoid starter and three molecules of malonyl-CoA, but use different cyclization mechanisms to produce distinct chemical scaffolds for a variety of plant natural products. Here we present the first STS crystal structure and identify, by mutagenic conversion of alfalfa CHS into a functional stilbene synthase, the structural basis for the evolution of STS cyclization specificity in type III polyketide synthase (PKS) enzymes. Additional mutagenesis and enzymatic characterization confirms that electronic effects rather than steric factors balance competing cyclization specificities in CHS and STS. Finally, we discuss the problematic in vitro reconstitution of plant stilbenecarboxylate pathways, using insights from existing biomimetic polyketide cyclization studies to generate a novel mechanistic hypothesis to explain stilbenecarboxylate biosynthesis. PubMed: 15380179DOI: 10.1016/j.chembiol.2004.05.024 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.11 Å) |
Structure validation
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