镍(II)牛碳酸酐酶及其抑制剂衍生物的表征

I. Bertini, E. Borghi, C. Luchinat
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引用次数: 12

摘要

利用电子波谱和核磁共振(nmr)研究了碳酸酐酶的镍(II)衍生物及其抑制剂加合物。纯酶中的金属离子是六配位的,有证据表明配位球中至少有一个水分子。抑制剂取代水分子,仍然产生六配位加合物。抑制剂的亲和力在碱性pH下降低,但与活性部位腔内的单一电离无关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Characterization of nickel(II) bovine carbonic anhydrase and its inhibitor derivatives

The nickel(II) derivative of carbonic anhydrase and its adducts with inhibitors have been investigated through electronic and nuclear magnetic resonance (nmr) spectroscopy. The metal ion in the pure enzyme is six-coordinated, and there is evidence for at least one water molecule in the coordination sphere. Inhibitors replace the water molecule, still giving rise to six-coordinated adducts. The affinity of the inhibitors is decreased at alkaline pH but cannot be related to a single ionization in the active site cavity.

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