Roussel_1999_J.Biol.Chem_274_16995

Reference

Title : Crystal structure of human gastric lipase and model of lysosomal acid lipase, two lipolytic enzymes of medical interest - Roussel_1999_J.Biol.Chem_274_16995
Author(s) : Roussel A , Canaan S , Egloff MP , Riviere M , Dupuis L , Verger R , Cambillau C
Ref : Journal of Biological Chemistry , 274 :16995 , 1999
Abstract :

Fat digestion in humans requires not only the classical pancreatic lipase but also gastric lipase, which is stable and active despite the highly acidic stomach environment. We report here the structure of recombinant human gastric lipase at 3.0-A resolution, the first structure to be described within the mammalian acid lipase family. This globular enzyme (379 residues) consists of a core domain belonging to the alpha/beta hydrolase-fold family and a "cap" domain, which is analogous to that present in serine carboxypeptidases. It possesses a classical catalytic triad (Ser-153, His-353, Asp-324) and an oxyanion hole (NH groups of Gln-154 and Leu-67). Four N-glycosylation sites were identified on the electron density maps. The catalytic serine is deeply buried under a segment consisting of 30 residues, which can be defined as a lid and belonging to the cap domain. The displacement of the lid is necessary for the substrates to have access to Ser-153. A phosphonate inhibitor was positioned in the active site that clearly suggests the location of the hydrophobic substrate binding site. The lysosomal acid lipase was modeled by homology, and possible explanations for some previously reported mutations leading to the cholesterol ester storage disease are given based on the present model.

PubMedSearch : Roussel_1999_J.Biol.Chem_274_16995
PubMedID: 10358049
Gene_locus related to this paper: human-LIPF

Related information

Gene_locus human-LIPF
Family human-LIPF    Acidic_Lipase
Structure human-LIPF    Acidic_Lipase    1HLG

Citations formats

Roussel A, Canaan S, Egloff MP, Riviere M, Dupuis L, Verger R, Cambillau C (1999)
Crystal structure of human gastric lipase and model of lysosomal acid lipase, two lipolytic enzymes of medical interest
Journal of Biological Chemistry 274 :16995

Roussel A, Canaan S, Egloff MP, Riviere M, Dupuis L, Verger R, Cambillau C (1999)
Journal of Biological Chemistry 274 :16995