Function
Secretory calcium-dependent phospholipase A2 that primarily targets extracellular phospholipids. Hydrolyzes the ester bond of the fatty acyl group attached at sn-2 position of phospholipids (phospholipase A2 activity), preferentially releasing fatty acyl groups with a low degree of unsaturation such as oleoyl (C18:1) and linoleoyl (C18:2) groups. Hydrolyzes low-density lipoprotein (LDL) phospholipids releasing unsaturated fatty acids that drive macrophage polarization toward an M2 phenotype.
Biological Context
Subcellular Location: Secreted; Cell membrane; Cytoplasmic vesicle, phagosome; Recycling endosome; Golgi apparatus, cis-Golgi network; Golgi apparatus, trans-Golgi network
Tissue Specificity: Heart, placenta and less abundantly, in lung. Detected in the outer and inner plexiform layers of the retina (at protein level). Expressed in monocytes and macrophages
Disease Association: 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. [The disease is caused by variants affecting the gene represented in this entry]
Pathway: Lipid metabolism; leukotriene C4 biosynthesis
Product Specifications
Recombinant Human Phospholipase A2 group V (PLA2G5) is a recombinant protein from Homo sapiens (Human), expressed in Yeast, covering amino acids 21-138aa, with N-terminal 6xHis-tagged tag, molecular weight 15.6kDa, purity Greater than 90% as determined by SDS-PAGE.. Suitable for ELISA and Western Blot applications.
