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6CHA

STRUCTURE OF A TETRAHEDRAL TRANSITION STATE COMPLEX OF ALPHA-*CHYMOTRYPSIN AT 1.8-*ANGSTROMS RESOLUTION

6CHA の概要
エントリーDOI10.2210/pdb6cha/pdb
分子名称ALPHA-CHYMOTRYPSIN A, PHENYLETHANE BORONIC ACID, ... (5 entities in total)
機能のキーワードhydrolase (serine proteinase)
由来する生物種Bos taurus (cattle)
詳細
細胞内の位置Secreted, extracellular space: P00766 P00766 P00766
タンパク質・核酸の鎖数6
化学式量合計50825.09
構造登録者
Tulinsky, A.,Blevins, R.A. (登録日: 1987-02-06, 公開日: 1987-04-16, 最終更新日: 2024-10-16)
主引用文献Tulinsky, A.,Blevins, R.A.
Structure of a tetrahedral transition state complex of alpha-chymotrypsin dimer at 1.8-A resolution.
J.Biol.Chem., 262:7737-7743, 1987
Cited by
PubMed Abstract: A 1.8-A resolution x-ray crystallographic restrained least squares refinement has been carried out on the phenylethane boronic acid (PEBA) complex of alpha-chymotrypsin dimer (alpha-CHT), and it has been compared to the 1.67-A resolution structure of the native enzyme. PEBA has a high binding affinity for alpha-CHT, and the boronate forms a tetrahedral complex with Ser-195 OG of one molecule of the dimer; the boronate in the other molecule is severely disordered and does not form a tetrahedral complex. The former could be a model of the transition state of catalysis. The complex of PEBA X alpha-CHT displays significant nonequivalence in conformation of side chains between the independent molecules comparable to the native enzyme, but, like the latter, shows a high degree of fidelity in the folding of the main chain. The orientation of the phenyl ring, CA and CB of PEBA, in the specificity sites of the two molecules is similar, suggesting that recognition is fairly insensitive to small departures from local symmetry; the same does not apply to the boronate functionalities suggesting that greater precision is required for catalysis. The folding of the molecule remains the same upon PEBA binding, but some of the side chains respond nonequivalently. The latter is a consequence of the inherent nonequivalence of the native dimer and the asymmetrical nature of the PEBA binding.
PubMed: 3584139
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.8 Å)
構造検証レポート
Validation report summary of 6cha
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2026-01-28に公開中

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