6DWF

Crystal structure of complex of BBKI mutant, L55R with Bovine Trypsin

6DWF の概要

• エントリーDOI: 10.2210/pdb6dwf/pdb
• 分子名称: Cationic trypsin, Kunitz-type inihibitor (3 entities in total)
• 機能のキーワード: hydrolase
• 由来する生物種: Bauhinia bauhinioides; 詳細
• タンパク質・核酸の鎖数: 12
• 化学式量合計: 252218.81

構造登録者

Li, M.,Wlodawer, A.,Gustchina, A. (登録日: 2018-06-26, 公開日: 2019-01-30, 最終更新日: 2024-10-16)

主引用文献

Li, M.,Srp, J.,Gustchina, A.,Dauter, Z.,Mares, M.,Wlodawer, A.
Crystal structures of the complex of a kallikrein inhibitor from Bauhinia bauhinioides with trypsin and modeling of kallikrein complexes.
Acta Crystallogr D Struct Biol, 75:56-69, 2019

PubMed Abstract: Structures of a recombinant Kunitz-type serine protease inhibitor from Bauhinia bauhinioides (BbKI) complexed with bovine trypsin were determined in two crystal forms. The crystal structure with the L55R mutant of BbKI was determined in space group P6 at 1.94 Å resolution and that with native BbKI in the monoclinic space group P2 at 3.95 Å resolution. The asymmetric unit of the latter crystals contained 44 independent complexes, thus representing one of the largest numbers of independent objects deposited in the Protein Data Bank. Additionally, the structure of the complex with native BbKI was determined at 2.0 Å resolution from P6 crystals isomorphous to those of the mutant. Since BbKI has previously been found to be a potent inhibitor of the trypsin-like plasma kallikrein, it was also tested against several tissue kallikreins. It was found that BbKI is a potent inhibitor of human tissue kallikrein 4 (KLK4) and the chymotrypsin-like human tissue kallikrein 7 (KLK7). Structures of BbKI complexed with the catalytic domain of human plasma kallikrein were modeled, as well as those with KLK4 and KLK7, and the structures were analyzed in order to identify the interactions that are responsible for inhibitory potency.

PubMed: 30644845
DOI: 10.1107/S2059798318016492

実験手法

X-RAY DIFFRACTION (1.94 Å)