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Dioxygen, an unexpected carbonic anhydrase ligand.

Authors :
Ferraroni, Marta
Gaspari, Roberto
Scozzafava, Andrea
Cavalli, Andrea
Supuran, Claudiu T.
Source :
Journal of Enzyme Inhibition & Medicinal Chemistry. Dec2018, Vol. 33 Issue 1, p999-1005. 7p.
Publication Year :
2018

Abstract

Carbonic anhydrases (CAs, EC 4.2.1.1) are ubiquitous metalloenzymes, grouped into seven different classes, which catalyze the reaction of CO2 hydration to bicarbonate and protons. All of the fifteen human isoforms reported to date belong to the α-class and contain zinc as a cofactor. The structure of human Zn,Cu-CA II has been solved which contains a copper ion bound at its N-terminal, coordinated to His4 and His64. In the active site a dioxygen molecule is coordinated to the zinc ion. Since dioxygen is a rather unexpected CA ligand, molecular dynamics (MD) simulations were performed which suggested a superoxide character of the zinc bound O2. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14756366
Volume :
33
Issue :
1
Database :
Academic Search Index
Journal :
Journal of Enzyme Inhibition & Medicinal Chemistry
Publication Type :
Academic Journal
Accession number :
132616383
Full Text :
https://doi.org/10.1080/14756366.2018.1475371