Journal of Enzyme Inhibition and Medicinal Chemistry (Jan 2018)

Dioxygen, an unexpected carbonic anhydrase ligand

  • Marta Ferraroni,
  • Roberto Gaspari,
  • Andrea Scozzafava,
  • Andrea Cavalli,
  • Claudiu T. Supuran

DOI
https://doi.org/10.1080/14756366.2018.1475371
Journal volume & issue
Vol. 33, no. 1
pp. 999 – 1005

Abstract

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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.

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