Fulop_1998_Cell_94_161

Reference

Title : Prolyl oligopeptidase: an unusual beta-propeller domain regulates proteolysis - Fulop_1998_Cell_94_161
Author(s) : Fulop V , Bocskei Z , Polgar L
Ref : Cell , 94 :161 , 1998
Abstract :

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 A 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.

PubMedSearch : Fulop_1998_Cell_94_161
PubMedID: 9695945
Gene_locus related to this paper: pig-ppce

Related information

Inhibitor Z-Pro-Prolinal
Gene_locus pig-ppce
Family S9N_PPCE_Peptidase_S9    S9N_PREPL_Peptidase_S9
Structure 1QFM    1QFS

Citations formats

Fulop V, Bocskei Z, Polgar L (1998)
Prolyl oligopeptidase: an unusual beta-propeller domain regulates proteolysis
Cell 94 :161

Fulop V, Bocskei Z, Polgar L (1998)
Cell 94 :161