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 locations published in Biophys. J.
| PMID | Journal | Published Date | Author | Title |
|---|---|---|---|---|
| 26536266 | Biophys. J. | 2015 | Lee TY et al. | Tuning the Photocycle Kinetics of Bacteriorhodopsin in Lipid Nanodiscs. |
| 25564843 | Biophys. J. | 2015 | Marek A et al. | Nanotube array method for studying lipid-induced conformational changes of a membrane protein by solid-state NMR. |
| 27705768 | Biophys. J. | 2016 | Steinkühler J et al. | Modulating Vesicle Adhesion by Electric Fields. |
| 27288275 | Biophys. J. | 2016 | Kubsch B et al. | Solution Asymmetry and Salt Expand Fluid-Fluid Coexistence Regions of Charged Membranes. |