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Dioxygen, an unexpected carbonic anhydrase ligand.


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 ?-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.

SUBMITTER: Ferraroni M 

PROVIDER: S-EPMC6010096 | biostudies-literature | 2018 Dec

REPOSITORIES: biostudies-literature

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Dioxygen, an unexpected carbonic anhydrase ligand.

Ferraroni Marta M   Gaspari Roberto R   Scozzafava Andrea A   Cavalli Andrea A   Supuran Claudiu T CT  

Journal of enzyme inhibition and medicinal chemistry 20181201 1


Carbonic anhydrases (CAs, EC 4.2.1.1) are ubiquitous metalloenzymes, grouped into seven different classes, which catalyze the reaction of CO<sub>2</sub> 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  ...[more]

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