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8DQR

Crystal structure of Arabidopsis thaliana COSY in complex with scopoletin

Summary for 8DQR
Entry DOI10.2210/pdb8dqr/pdb
DescriptorCoumarin Synthase, COENZYME A, GLYCEROL, ... (5 entities in total)
Functional Keywordscoumarin synthase, trans/cis isomerase, bahd acyltransferase, plant protein
Biological sourceArabidopsis thaliana (thale cress)
Total number of polymer chains1
Total formula weight50647.96
Authors
Kim, C.Y.,Mitchell, A.J.,Gutierrez, M.,Weng, J.K. (deposition date: 2022-07-19, release date: 2023-01-11, Last modification date: 2024-10-23)
Primary citationKim, C.Y.,Mitchell, A.J.,Kastner, D.W.,Albright, C.E.,Gutierrez, M.A.,Glinkerman, C.M.,Kulik, H.J.,Weng, J.K.
Emergence of a proton exchange-based isomerization and lactonization mechanism in the plant coumarin synthase COSY.
Nat Commun, 14:597-597, 2023
Cited by
PubMed Abstract: Plants contain rapidly evolving specialized enzymes that support the biosynthesis of functionally diverse natural products. In coumarin biosynthesis, a BAHD acyltransferase-family enzyme COSY was recently discovered to accelerate coumarin formation as the only known BAHD enzyme to catalyze an intramolecular acyl transfer reaction. Here we investigate the structural and mechanistic basis for COSY's coumarin synthase activity. Our structural analyses reveal an unconventional active-site configuration adapted to COSY's specialized activity. Through mutagenesis studies and deuterium exchange experiments, we identify a unique proton exchange mechanism at the α-carbon of the o-hydroxylated trans-hydroxycinnamoyl-CoA substrates during the catalytic cycle of COSY. Quantum mechanical cluster modeling and molecular dynamics further support this key mechanism for lowering the activation energy of the rate-limiting trans-to-cis isomerization step in coumarin production. This study unveils an unconventional catalytic mechanism mediated by a BAHD-family enzyme, and sheds light on COSY's evolutionary origin and its recruitment to coumarin biosynthesis in eudicots.
PubMed: 36737607
DOI: 10.1038/s41467-023-36299-1
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.26 Å)
Structure validation

227344

數據於2024-11-13公開中

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