6T4P

Human Carbonic anhydrase II bound by napthalene-1-sulfonamide

6T4P の概要

• エントリーDOI: 10.2210/pdb6t4p/pdb
• 関連するPDBエントリー: 6T4N 6T4O
• 分子名称: carbonic anhydrase 2, ZINC ION, DIMETHYL SULFOXIDE, ... (7 entities in total)
• 機能のキーワード: drug design, carbonic anhydrase, benzenesulfonamide, metal-binding, lyase-lyase inhibitor complex, 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: 29936.21

構造登録者

Smirnov, A.,Manakova, E.,Grazulis, S. (登録日: 2019-10-14, 公開日: 2020-10-14, 最終更新日: 2024-01-24)

主引用文献

Dudutiene, V.,Zubriene, A.,Kairys, V.,Smirnov, A.,Smirnoviene, J.,Leitans, J.,Kazaks, A.,Tars, K.,Manakova, L.,Grazulis, S.,Matulis, D.
Isoform-Selective Enzyme Inhibitors by Exploring Pocket Size According to the Lock-and-Key Principle.
Biophys.J., 119:1513-1524, 2020

PubMed Abstract: In the design of high-affinity and enzyme isoform-selective inhibitors, we applied an approach of augmenting the substituents attached to the benzenesulfonamide scaffold in three ways, namely, substitutions at the 3,5- or 2,4,6-positions or expansion of the condensed ring system. The increased size of the substituents determined the spatial limitations of the active sites of the 12 catalytically active human carbonic anhydrase (CA) isoforms until no binding was observed because of the inability of the compounds to fit in the active site. This approach led to the discovery of high-affinity and high-selectivity compounds for the anticancer target CA IX and antiobesity target CA VB. The x-ray crystallographic structures of compounds bound to CA IX showed the positions of the bound compounds, whereas computational modeling confirmed that steric clashes prevent the binding of these compounds to other isoforms and thus avoid undesired side effects. Such an approach, based on the Lock-and-Key principle, could be used for the development of enzyme-specific drug candidate compounds.

PubMed: 32971003
DOI: 10.1016/j.bpj.2020.08.037

実験手法

X-RAY DIFFRACTION (1.75 Å)