a Dipartimento di Chimica , Università di Firenze , Sesto Fiorentino (FI) , Italia.
b Istituto Italiano di Tecnologia , Genova , Italia.
J Enzyme Inhib Med Chem. 2018 Dec;33(1):999-1005. doi: 10.1080/14756366.2018.1475371.
Carbonic anhydrases (CAs, EC 4.2.1.1) are ubiquitous metalloenzymes, grouped into seven different classes, which catalyze the reaction of CO 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 O.
碳酸酐酶(CA,EC 4.2.1.1)是广泛存在的金属酶,分为 7 个不同的类别,它们催化 CO2 水合反应生成碳酸氢根和质子。迄今为止报道的 15 个人类同工酶都属于α类,含有锌作为辅助因子。已解析出人 Zn,Cu-CA II 的结构,其中包含一个结合在其 N 端的铜离子,与 His4 和 His64 配位。在活性位点,一个氧气分子与锌离子配位。由于氧气是一种相当出乎意料的 CA 配体,因此进行了分子动力学(MD)模拟,结果表明锌结合的 O 具有超氧化物的特征。