PG(18:1(9Z)/18:1(9Z))

PG(18:1(9Z)/18:1(9Z)) is a lipid of Glycerophospholipids (GP) class. Pg(18:1(9z)/18:1(9z)) is associated with abnormalities such as Neonatal hemochromatosis, Renal tubular disorder, Hereditary pancreatitis and UDPglucose 4-epimerase deficiency disease. The involved functions are known as Genetic Translation Process, Regulation, Saturated, enzyme activity and Cytokinesis. Pg(18:1(9z)/18:1(9z)) often locates in Membrane, soluble, Tissue membrane, membrane fraction and Thylakoid Membrane. The associated genes with PG(18:1(9Z)/18:1(9Z)) are COIL gene, P4HTM gene, GRAP2 gene, Integral Membrane Proteins and synthetic peptide. The related lipids are Liposomes, Fatty Acids, Sphingolipids, DOPE and 1,2-oleoylphosphatidylcholine.

References related to genes published in Biochim. Biophys. Acta


PMIDJournalPublished DateAuthorTitle
27806910Biochim. Biophys. Acta2017McDonald C et al.Structure and function of PspA and Vipp1 N-terminal peptides: Insights into the membrane stress sensing and mitigation.
27085977Biochim. Biophys. Acta2016Shinoda WPermeability across lipid membranes.
25306964Biochim. Biophys. Acta2015Tavano R et al.The peculiar N- and (-termini of trichogin GA IV are needed for membrane interaction and human cell death induction at doses lacking antibiotic activity.