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5T72

Human carboanhydrase F131C_C206S double mutant in complex with 2

5T72 の概要
エントリーDOI10.2210/pdb5t72/pdb
関連するPDBエントリー2VVA
分子名称Carbonic anhydrase 2, ZINC ION, 4-(HYDROXYMERCURY)BENZOIC ACID, ... (6 entities in total)
機能のキーワードphotopharmacology; carbonic anhydrase; photochromic tethered ligand; azobenzene; computational screening, transferase
由来する生物種Homo sapiens (Human)
細胞内の位置Cytoplasm : P00918
タンパク質・核酸の鎖数1
化学式量合計30031.54
構造登録者
DuBay, K.H.,Iwan, K.,Osorio-Planes, L.,Geissler, P.,Groll, M.,Trauner, D.,Broichhagen, J. (登録日: 2016-09-02, 公開日: 2017-09-06, 最終更新日: 2024-01-17)
主引用文献DuBay, K.H.,Iwan, K.,Osorio-Planes, L.,Geissler, P.L.,Groll, M.,Trauner, D.,Broichhagen, J.
A Predictive Approach for the Optical Control of Carbonic Anhydrase II Activity.
ACS Chem. Biol., 13:793-800, 2018
Cited by
PubMed Abstract: Optogenetics and photopharmacology are powerful approaches to investigating biochemical systems. While the former is based on genetically encoded photoreceptors that utilize abundant chromophores, the latter relies on synthetic photoswitches that are either freely diffusible or covalently attached to specific bioconjugation sites, which are often native or engineered cysteines. The identification of suitable cysteine sites and appropriate linkers for attachment is generally a lengthy and cumbersome process. Herein, we describe an in silico screening approach that is designed to propose a small number of optimal combinations. By applying this computational approach to human carbonic anhydrase and a set of three photochromic tethered ligands, the number of potential site-ligand combinations was narrowed from over 750 down to 6, which we then evaluated experimentally. Two of these six combinations resulted in light-responsive human Carbonic Anhydrases (LihCAs), which were characterized with enzymatic activity assays, mass spectrometry, and X-ray crystallography. Our study also provides insights into the reactivity of cysteines toward maleimides and the hydrolytic stability of the adducts obtained.
PubMed: 29357237
DOI: 10.1021/acschembio.7b00862
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.3 Å)
構造検証レポート
Validation report summary of 5t72
検証レポート(詳細版)ダウンロードをダウンロード

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件を2025-12-31に公開中

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