2Q9Z
Trichodiene synthase: Complex with inorganic pyrophosphate resulting from the reaction with 2-fluorofarnesyl diphosphate
Summary for 2Q9Z
Entry DOI | 10.2210/pdb2q9z/pdb |
Related | 1JFA 1JFG |
Descriptor | Trichodiene synthase, 1,2-ETHANEDIOL, MAGNESIUM ION, ... (5 entities in total) |
Functional Keywords | terpenoid synthase fold, 2-fluorofarnesyl diphosphate, inorganic pyrophosphate, lyase |
Biological source | Fusarium sporotrichioides |
Total number of polymer chains | 2 |
Total formula weight | 88474.21 |
Authors | Vedula, L.S.,Zhao, Y.,Coates, R.M.,Koyama, T.,Cane, D.E.,Christianson, D.W. (deposition date: 2007-06-14, release date: 2007-10-30, Last modification date: 2023-08-30) |
Primary citation | Vedula, L.S.,Zhao, Y.,Coates, R.M.,Koyama, T.,Cane, D.E.,Christianson, D.W. Exploring biosynthetic diversity with trichodiene synthase. Arch.Biochem.Biophys., 466:260-266, 2007 Cited by PubMed Abstract: Trichodiene synthase is a terpenoid cyclase that catalyzes the cyclization of farnesyl diphosphate (FPP) to form the bicyclic sesquiterpene hydrocarbon trichodiene (89%), at least five sesquiterpene side products (11%), and inorganic pyrophosphate (PP(i)). Incubation of trichodiene synthase with 2-fluorofarnesyl diphosphate or 4-methylfarnesyl diphosphate similarly yields sesquiterpene mixtures despite the electronic effects or steric bulk introduced by substrate derivatization. The versatility of the enzyme is also demonstrated in the 2.85A resolution X-ray crystal structure of the complex with Mg(2+) (3)-PP(i) and the benzyl triethylammonium cation, which is a bulkier mimic of the bisabolyl carbocation intermediate in catalysis. Taken together, these findings show that the active site of trichodiene synthase is sufficiently flexible to accommodate bulkier and electronically-diverse substrates and intermediates, which could indicate additional potential for the biosynthetic utility of this terpenoid cyclase. PubMed: 17678871DOI: 10.1016/j.abb.2007.06.016 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.95 Å) |
Structure validation
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