PLA2G5: PA2 catalyzes the calcium-dependent hydrolysis of the 2- acyl groups in 3-sn-phosphoglycerides. This isozyme hydrolyzes more efficiently L-alpha-1-palmitoyl-2-oleoyl phosphatidylcholine than L-alpha-1-palmitoyl-2-arachidonyl phosphatidylcholine, L- alpha-1-palmitoyl-2-arachidonyl phosphatidylethanolamine, or L- alpha-1-stearoyl-2-arachidonyl phosphatidylinositol. May be involved in the production of lung surfactant, the remodeling or regulation of cardiac muscle. Defects in PLA2G5 are the cause of fleck retina, familial benign (FRFB). An autosomal recessive condition associated with a distinctive retinal appearance and no apparent visual or electrophysiologic deficits. Affected individuals are asymptomatic, but fundus examination reveals a striking pattern of diffuse, yellow-white, fleck-like lesions extending to the far periphery of the retina but sparing the foveal region. Belongs to the phospholipase A2 family.
Protein type: EC 3.1.1.4; Secreted, signal peptide; Lipid Metabolism - glycerophospholipid; Lipid Metabolism - alpha-linolenic acid; Secreted; Lipid Metabolism - linoleic acid; Lipid Metabolism - ether lipid; Cell surface; Phospholipase; Lipid Metabolism - arachidonic acid
Chromosomal Location of Human Ortholog: 1p36-p34
Cellular Component: cell surface; extracellular region; Golgi apparatus; perinuclear region of cytoplasm; plasma membrane
Molecular Function: calcium ion binding; calcium-dependent phospholipase A2 activity; heparin binding
Biological Process: arachidonic acid secretion; glycerophospholipid biosynthetic process; leukotriene biosynthetic process; lipid catabolic process; phosphatidic acid biosynthetic process; phospholipid metabolic process; platelet activating factor biosynthetic process; response to cAMP; response to cytokine stimulus
Disease: Fleck Retina, Familial Benign
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