Reconstitution of ATP-dependent aminophospholipid translocation in proteoliposomes
about
Chilling tolerance in Arabidopsis involves ALA1, a member of a new family of putative aminophospholipid translocasesP4-ATPases as Phospholipid Flippases-Structure, Function, and EnigmasMammalian P4-ATPases and ABC transporters and their role in phospholipid transportP-type ATPase TAT-2 negatively regulates monomethyl branched-chain fatty acid mediated function in post-embryonic growth and development in C. elegansEndocytic sorting and recycling require membrane phosphatidylserine asymmetry maintained by TAT-1/CHAT-1Role for Drs2p, a P-type ATPase and potential aminophospholipid translocase, in yeast late Golgi functionAn essential subfamily of Drs2p-related P-type ATPases is required for protein trafficking between Golgi complex and endosomal/vacuolar systemDrs2p-coupled aminophospholipid translocase activity in yeast Golgi membranes and relationship to in vivo function.Requirement for neo1p in retrograde transport from the Golgi complex to the endoplasmic reticulumManipulation of the phosphatidylethanolamine pool in the human red cell membrane affects its Mg2+-ATPase activityHuman Type IV P-type ATPases That Work as Plasma Membrane Phospholipid Flippases and Their Regulation by Caspase and CalciumEnergy-dependent flip of fluorescence-labeled phospholipids is regulated by nutrient starvation and transcription factors, PDR1 and PDR3.Age-related loss of phospholipid asymmetry in APP(NLh)/APP(NLh) x PS-1(P264L)/PS-1(P264L) human double mutant knock-in mice: relevance to Alzheimer disease.Mice deficient in the putative phospholipid flippase ATP11C exhibit altered erythrocyte shape, anemia, and reduced erythrocyte life span.Cloning and characterization of an atypical Type IV P-type ATPase that binds to the RING motif of RUSH transcription factors.Identification of a functional role for lipid asymmetry in biological membranes: Phosphatidylserine-skeletal protein interactions modulate membrane stabilityAn aminophospholipid translocase associated with body fat and type 2 diabetes phenotypes.Lipid traffic: the ABC of transbilayer movement.Regulation of transbilayer plasma membrane phospholipid asymmetry.Chemical control of phospholipid distribution across bilayer membranes.Scott syndrome: an inherited defect of the procoagulant activity of platelets.mGluRI targets microglial activation and selectively prevents neuronal cell engulfment through Akt and caspase dependent pathwaysPhospholipid flippases: building asymmetric membranes and transport vesicles.ATP dependence of Na+/H+ exchange. Nucleotide specificity and assessment of the role of phospholipidsDiseases of intramembranous lipid transport.Loss of phospholipid asymmetry and elevated brain apoptotic protein levels in subjects with amnestic mild cognitive impairment and Alzheimer disease.ATP11B mediates platinum resistance in ovarian cancer.Cdc50p plays a vital role in the ATPase reaction cycle of the putative aminophospholipid transporter Drs2p.Scott syndrome erythrocytes contain a membrane protein capable of mediating Ca2+-dependent transbilayer migration of membrane phospholipidsReconstitution of phospholipid translocase activity with purified Drs2p, a type-IV P-type ATPase from budding yeast.Localization, purification, and functional reconstitution of the P4-ATPase Atp8a2, a phosphatidylserine flippase in photoreceptor disc membranes.Screening for the drug-phospholipid interaction: correlation to phospholipidosis.Critical roles of isoleucine-364 and adjacent residues in a hydrophobic gate control of phospholipid transport by the mammalian P4-ATPase ATP8A2.Where do they come from and where do they go: candidates for regulating extracellular vesicle formation in fungi.Regulatory mechanisms in maintenance and modulation of transmembrane lipid asymmetry: pathophysiological implications.Increased vesicle endocytosis due to an increase in the plasma membrane phosphatidylserine concentrationEnergy requirements for two aspects of phospholipid metabolism in mammalian brain.Rapid kinetics of insertion and accessibility of spin-labeled phospholipid analogs in lipid membranes: a stopped-flow electron paramagnetic resonance approach.A mitochondrial membrane protein is required for translocation of phosphatidylserine from mitochondria-associated membranes to mitochondria.Functional cloning of the miltefosine transporter. A novel P-type phospholipid translocase from Leishmania involved in drug resistance.
P2860
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P2860
Reconstitution of ATP-dependent aminophospholipid translocation in proteoliposomes
description
1994 nî lūn-bûn
@nan
1994 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1994 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
name
Reconstitution of ATP-dependent aminophospholipid translocation in proteoliposomes
@ast
Reconstitution of ATP-dependent aminophospholipid translocation in proteoliposomes
@en
Reconstitution of ATP-dependent aminophospholipid translocation in proteoliposomes
@nl
type
label
Reconstitution of ATP-dependent aminophospholipid translocation in proteoliposomes
@ast
Reconstitution of ATP-dependent aminophospholipid translocation in proteoliposomes
@en
Reconstitution of ATP-dependent aminophospholipid translocation in proteoliposomes
@nl
prefLabel
Reconstitution of ATP-dependent aminophospholipid translocation in proteoliposomes
@ast
Reconstitution of ATP-dependent aminophospholipid translocation in proteoliposomes
@en
Reconstitution of ATP-dependent aminophospholipid translocation in proteoliposomes
@nl
P2093
P2860
P3181
P356
P1476
Reconstitution of ATP-dependent aminophospholipid translocation in proteoliposomes
@en
P2093
A Zachowski
M E Auland
P F Devaux
P2860
P304
10938-10942
P3181
P356
10.1073/PNAS.91.23.10938
P407
P577
1994-11-01T00:00:00Z