4.7 Article Proceedings Paper

Acetylcholinesterase: How is structure related to function?

Journal

CHEMICO-BIOLOGICAL INTERACTIONS
Volume 175, Issue 1-3, Pages 3-10

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.cbi.2008.05.035

Keywords

Acetylcholinesterase; Butyrylcholinesterase; pi-cation interaction; Transition state; Molecular dynamics

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In accordance with its biological role, termination of neurotransmission at cholinergic synapses by rapid hydrolysis of the neurotransmitter, acetylcholine, acetylcholinesterase is one of nature's most efficient enzymes. Solution of its three-dimensional structure revealed that its active site is located at the bottom of a deep and narrow gorge. Such an architecture was unanticipated in view of its high turnover number. The present review examines how the highly specialized Structure of acetylcholinesterase, with its sequestered active site, contributes to its catalytic efficacy, and discusses how the traffic of substrate and products to and from the active site is controlled. (C) 2008 Elsevier Ireland Ltd. All rights reserved.

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