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

PA(18:1(9Z)/18:1(9Z)) is a lipid of Glycerophospholipids (GP) class. The involved functions are known as adenylate cyclase activity, inhibitors, Drug Interactions, Membrane Fluidity and Force. Pa(18:1(9z)/18:1(9z)) often locates in Cell membrane, Tissue membrane, Epidermis, Connective Tissue and Back. The associated genes with PA(18:1(9Z)/18:1(9Z)) are growth promoting activity and RAF1 gene. The related lipids are Phosphatidic Acid, Lysophospholipids, lysophosphatidic acid, Lysophosphatidylcholines and dioleoyl phosphate.

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Introduction

To understand associated biological information of PA(18:1(9Z)/18:1(9Z)), we collected biological information of abnormalities, associated pathways, cellular/molecular locations, biological functions, related genes/proteins, lipids and common seen animal/experimental models with organized paragraphs from literatures.

What diseases are associated with PA(18:1(9Z)/18:1(9Z))?

There are no associated biomedical information in the current reference collection.

No disease MeSH terms mapped to the current reference collection.

PubChem Associated disorders and diseases

What pathways are associated with PA(18:1(9Z)/18:1(9Z))

There are no associated biomedical information in the current reference collection.

PubChem Biomolecular Interactions and Pathways

Link to PubChem Biomolecular Interactions and Pathways

What cellular locations are associated with PA(18:1(9Z)/18:1(9Z))?

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What functions are associated with PA(18:1(9Z)/18:1(9Z))?


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What lipids are associated with PA(18:1(9Z)/18:1(9Z))?

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What genes are associated with PA(18:1(9Z)/18:1(9Z))?

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Gene Cross reference Weighted score Related literatures

What common seen animal models are associated with PA(18:1(9Z)/18:1(9Z))?

There are no associated biomedical information in the current reference collection.

NCBI Entrez Crosslinks

All references with PA(18:1(9Z)/18:1(9Z))

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Authors Title Published Journal PubMed Link
Raines DE and Krishnan NS Agonist binding and affinity state transitions in reconstituted nicotinic acetylcholine receptors revealed by single and sequential mixing stopped-flow fluorescence spectroscopies. 1998 Biochim. Biophys. Acta pmid:9814855
Dalton KA et al. Anionic lipids and accumulation of Ca2+ by a Ca(2+)-ATPase. 1998 Biochem. Soc. Trans. pmid:9765953
Hixon MS et al. Calcium-dependent and -independent interfacial binding and catalysis of cytosolic group IV phospholipase A2. 1998 Biochemistry pmid:9622504
Oja CD et al. Influence of dose on liposome clearance: critical role of blood proteins. 1996 Biochim. Biophys. Acta pmid:8652601
Farren SB et al. Polymorphic phase preferences of phosphatidic acid: A 31P and 2H NMR study. 1983 Biochem. Biophys. Res. Commun. pmid:6838577
Miner VW and Prestegard JH Structure of divalent cation-phosphatidic acid complexes as determined by 31P-NMR. 1984 Biochim. Biophys. Acta pmid:6743656
Brasseur R et al. Mode of organization of lipid aggregates: a conformational analysis. 1984 Biosci. Rep. pmid:6547066
Nayar R et al. Phosphatidic acid as a calcium ionophore in large unilamellar vesicle systems. 1984 Biochim. Biophys. Acta pmid:6435674
Smaal EB et al. Essential adaptation of the calcium influx assay into liposomes with entrapped arsenazo III for studies on the possible calcium translocating properties of acidic phospholipids. 1985 Biochim. Biophys. Acta pmid:3924100
Smaal EB et al. 2H-NMR, 31P-NMR and DSC characterization of a novel lipid organization in calcium-dioleoylphosphatidate membranes. Implications for the mechanism of the phosphatidate calcium transmembrane shuttle. 1987 Biochim. Biophys. Acta pmid:3814595
Nicolay K et al. Ethylene glycol causes acyl chain disordering in liquid-crystalline, unsaturated phospholipid model membranes, as measured by 2H NMR. 1986 FEBS Lett. pmid:3803574
Houslay MD et al. Acidic phospholipid species inhibit adenylate cyclase activity in rat liver plasma membranes. 1986 Biochem. J. pmid:3741383
Smaal EB et al. Consequences of the interaction of calcium with dioleoylphosphatidate-containing model membranes: changes in membrane permeability. 1986 Biochim. Biophys. Acta pmid:3730389
Woźniak M et al. The influence of phosphatidate bilayers on pig heart AMP deaminase. Crucial role of pH-dependent lipid-phase transition. 1988 Biochem. J. pmid:3214434
Smaal EB et al. Consequences of the interaction of calcium with dioleoylphosphatidate-containing model membranes: calcium-membrane and membrane-membrane interactions. 1987 Biochim. Biophys. Acta pmid:3099843
Mizuno S et al. Dioleoyl-phosphatidic acid selectively binds to α-synuclein and strongly induces its aggregation. 2017 FEBS Lett. pmid:28186641
Rivero Berti I et al. Delivery of fluorophores by calcium phosphate-coated nanoliposomes and interaction with Staphylococcus aureus biofilms. 2016 Colloids Surf B Biointerfaces pmid:26954088
Chen YF et al. Differential dependencies on [Ca2+] and temperature of the monolayer spontaneous curvatures of DOPE, DOPA and cardiolipin: effects of modulating the strength of the inter-headgroup repulsion. 2015 Soft Matter pmid:25907686
Li J et al. Calcium phosphate nanoparticles with an asymmetric lipid bilayer coating for siRNA delivery to the tumor. 2012 J Control Release pmid:22056915
Lebeau L et al. Two-dimensional crystallization of DNA gyrase B subunit on specifically designed lipid monolayers. 1990 FEBS Lett. pmid:2163898