Prolyl oligopeptidase:: An unusual β-propeller domain regulates proteolysis

被引:462
作者
Fülöp, V
Böcskei, Z
Polgár, L
机构
[1] Univ Oxford, Oxford Ctr Mol Sci, Dept Biochem, Lab Mol Biophys, Oxford OX1 3QU, England
[2] Univ Warwick, Dept Biol Sci, Coventry CV4 7AL, W Midlands, England
[3] Eotvos Lorand Univ, Dept Theoret Chem, H-117 Budapest, Hungary
[4] Chinoin Chem & Pharmaceut Works Ltd, H-1325 Budapest, Hungary
[5] Hungarian Acad Sci, Biol Res Ctr, Inst Enzymol, H-1518 Budapest, Hungary
基金
英国惠康基金;
关键词
D O I
10.1016/S0092-8674(00)81416-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Prolyl oligopeptidase is a large cytosolic enzyme that belongs to a new class of serine peptidases. The enzyme is involved in the maturation and degradation of peptide hormones and neuropeptides, which relate to the induction of amnesia. The 1.4 Angstrom resolution crystal structure is presented here. The enzyme contains a peptidase domain with an alpha/beta hydrolase fold, and its catalytic triad (Ser554, His680, Asp641) is covered by. the central tunnel of an unusual beta propeller. This domain makes prolyl oligopeptidase an oligopeptidase by excluding large structured peptides from the active. site. In this way, the propeller protects larger peptides and proteins from proteolysis in the cytosol. The structure is also obtained with a transition state inhibitor, which may facilitate drug design to treat memory disorders.
引用
收藏
页码:161 / 170
页数:10
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