5C8I

Joint X-ray/neutron structure of Human Carbonic Anhydrase II in complex with Methazolamide

5C8I の概要

• エントリーDOI: 10.2210/pdb5c8i/pdb
• 関連するPDBエントリー: 4G0C
• 分子名称: Carbonic anhydrase 2, ZINC ION, N-(3-methyl-5-sulfamoyl-1,3,4-thiadiazol-2(3H)-ylidene)acetamide, ... (4 entities in total)
• 機能のキーワード: methazolamide, acetazolamide, water displacement, lyase
• 由来する生物種: Homo sapiens (Human)
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 29590.74

構造登録者

Aggarwal, M.,Kovalevsky, A.Y.,Fisher, S.Z.,McKenna, R. (登録日: 2015-06-25, 公開日: 2016-07-20, 最終更新日: 2025-11-12)

主引用文献

Aggarwal, M.,Kovalevsky, A.Y.,Velazquez, H.,Fisher, S.Z.,Smith, J.C.,McKenna, R.
Neutron structure of human carbonic anhydrase II in complex with methazolamide: mapping the solvent and hydrogen-bonding patterns of an effective clinical drug.
IUCrJ, 3:319-325, 2016

PubMed Abstract: Carbonic anhydrases (CAs; EC 4.2.1.1) catalyze the interconversion of CO and HCO, and their inhibitors have long been used as diuretics and as a therapeutic treatment for many disorders such as glaucoma and epilepsy. Acetazolamide (AZM) and methazolamide (MZM, a methyl derivative of AZM) are two of the classical CA inhibitory drugs that have been used clinically for decades. The jointly refined X-ray/neutron structure of MZM in complex with human CA isoform II (hCA II) has been determined to a resolution of 2.2 Å with an of ∼16.0%. Presented in this article, along with only the second neutron structure of a clinical drug-bound hCA, is an in-depth structural comparison and analyses of differences in hydrogen-bonding network, water-molecule orientation and solvent displacement that take place upon the binding of AZM and MZM in the active site of hCA II. Even though MZM is slightly more hydrophobic and displaces more waters than AZM, the overall binding affinity () for both of the drugs against hCA II is similar (∼10 n). The plausible reasons behind this finding have also been discussed using molecular dynamics and X-ray crystal structures of hCA II-MZM determined at cryotemperature and room temperature. This study not only allows a direct comparison of the hydrogen bonding, protonation states and solvent orientation/displacement of AZM and MZM, but also shows the significant effect that the methyl derivative has on the solvent organization in the hCA II active site.

PubMed: 28461893
DOI: 10.1107/S2052252516010514

実験手法

NEUTRON DIFFRACTION (2.2 Å)
X-RAY DIFFRACTION (1.56 Å)