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6CQV

Crystal Structure of Recombinant Human Acetylcholinesterase in Complex with VX(+) and HI-6

Summary for 6CQV
Entry DOI10.2210/pdb6cqv/pdb
Related6CQT 6CQU 6CQW 6CQX 6CQY 6CQZ
DescriptorAcetylcholinesterase, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-[alpha-L-fucopyranose-(1-6)]2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ... (7 entities in total)
Functional Keywordshydrolase
Biological sourceHomo sapiens (Human)
Total number of polymer chains2
Total formula weight121505.66
Authors
Bester, S.M.,Guelta, M.A.,Pegan, S.D.,Height, J.J. (deposition date: 2018-03-16, release date: 2018-12-05, Last modification date: 2024-10-09)
Primary citationBester, S.M.,Guelta, M.A.,Cheung, J.,Winemiller, M.D.,Bae, S.Y.,Myslinski, J.,Pegan, S.D.,Height, J.J.
Structural Insights of Stereospecific Inhibition of Human Acetylcholinesterase by VX and Subsequent Reactivation by HI-6.
Chem. Res. Toxicol., 31:1405-1417, 2018
Cited by
PubMed Abstract: Over 50 years ago, the toxicity of irreversible organophosphate inhibitors targeting human acetylcholinesterase (hAChE) was observed to be stereospecific. The therapeutic reversal of hAChE inhibition by reactivators has also been shown to depend on the stereochemistry of the inhibitor. To gain clarity on the mechanism of stereospecific inhibition, the X-ray crystallographic structures of hAChE inhibited by a racemic mixture of VX (P ) and its enantiomers were obtained. Beyond identifying hAChE structural features that lend themselves to stereospecific inhibition, structures of the reactivator HI-6 bound to hAChE inhibited by VX enantiomers of varying toxicity, or in its uninhibited state, were obtained. Comparison of hAChE in these pre-reactivation and post-reactivation states along with enzymatic data reveals the potential influence of unproductive reactivator poses on the efficacy of these types of therapeutics. The recognition of structural features related to hAChE's stereospecificity toward VX shed light on the molecular influences of toxicity and their effect on reactivators. In addition to providing a better understanding of the innate issues with current reactivators, an avenue for improvement of reactivators is envisioned.
PubMed: 30462502
DOI: 10.1021/acs.chemrestox.8b00294
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.601 Å)
Structure validation

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