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 J. Biol. Chem.
| PMID | Journal | Published Date | Author | Title |
|---|---|---|---|---|
| 9038182 | J. Biol. Chem. | 1997 | Vécsey-Semjén B et al. | Conformational changes due to membrane binding and channel formation by staphylococcal alpha-toxin. |
| 15572363 | J. Biol. Chem. | 2005 | Wang G et al. | Correlation of three-dimensional structures with the antibacterial activity of a group of peptides designed based on a nontoxic bacterial membrane anchor. |