| Literature DB >> 19029121 |
Petra C Kienesberger1, Monika Oberer, Achim Lass, Rudolf Zechner.
Abstract
The human genome expresses nine patatin-like phospholipase domain containing proteins (PNPLA1-9). Members of this family share a protein domain discovered initially in patatin, the most abundant protein of the potato tuber. Patatin is a lipid hydrolase with an unusual folding topology that differs from classical lipases. Mammalian PNPLAs include lipid hydrolases with specificities for diverse substrates such as triacylglycerols, phospholipids, and retinol esters. Analysis of induced mutant mouse models and the clinical phenotype of patients with mutations revealed important insights into the physiological role of several members of the PNPLA family. This review aims to summarize current knowledge of PNPLA proteins and to document their emerging importance in lipid and energy homeostasis.Entities:
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Year: 2008 PMID: 19029121 PMCID: PMC2674697 DOI: 10.1194/jlr.R800082-JLR200
Source DB: PubMed Journal: J Lipid Res ISSN: 0022-2275 Impact factor: 5.922