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1U0U

An Aldol Switch Discovered in Stilbene Synthases Mediates Cyclization Specificity of Type III Polyketide Synthases: Pine stilbene synthase structure

Summary for 1U0U
Entry DOI10.2210/pdb1u0u/pdb
Related1BI5 1U0V 1U0W
DescriptorDihydropinosylvin synthase (2 entities in total)
Functional Keywordspks, type iii polyketide synthase, condensing enzyme, thiolase fold, alpha-beta-alpha-beta-alpha fold, aldol switch, catalytic triad, transferase
Biological sourcePinus sylvestris (Scots pine)
Cellular locationCytoplasm: Q02323
Total number of polymer chains6
Total formula weight258733.87
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 citationAustin, 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: 15380179
DOI: 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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