Structure of limonene synthase, a simple model for terpenoid cyclase catalysis

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Abstract

The crystal structure of (4S)-limonene synthase from Mentha spicata, a metal ion-dependent monoterpene cyclase that catalyzes the coupled isomerization and cyclization of geranyl diphosphate, is reported at 2.7-Å resolution in two forms liganded to the substrate and intermediate analogs, 2-fluorogeranyl diphosphate and 2-fluorolinalyl diphosphate, respectively. The implications of these findings are described for domain interactions in the homodimer and for changes in diphosphate-metal ion coordination and substrate binding conformation in the course of the multistep reaction. © 2007 by The National Academy of Sciences of the USA.

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Hyatt, D. C., Youn, B., Zhao, Y., Santhamma, B., Coates, R. M., Croteau, R. B., & Kang, C. (2007). Structure of limonene synthase, a simple model for terpenoid cyclase catalysis. Proceedings of the National Academy of Sciences of the United States of America, 104(13), 5360–5365. https://doi.org/10.1073/pnas.0700915104

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