Naturally occurring mutations in the largest extracellular loops of ABCA1 can disrupt its direct interaction with apolipoprotein A-I (Q24300380)

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Language	Label	Description	Also known as
English	Naturally occurring mutations in the largest extracellular loops of ABCA1 can disrupt its direct interaction with apolipoprotein A-I	scientific article

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scholarly article

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Naturally occurring mutations in the largest extracellular loops of ABCA1 can disrupt its direct interaction with apolipoprotein A-I (English)

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ATP binding cassette subfamily A member 1

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GOA release 2020-03-11

cholesterol transfer activity

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GOA release 2020-03-11

Mason W. Freeman

6

object named as

Mason W Freeman

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author name string

Michael L Fitzgerald

1

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Andrea L Morris

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Jeongmi S Rhee

3

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Lorna P Andersson

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Armando J Mendez

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language of work or name

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publication date

6 September 2002

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Journal of Biological Chemistry

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277

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36

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33178-87

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Apolipoprotein specificity for lipid efflux by the human ABCAI transporter

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Human ABCA1 contains a large amino-terminal extracellular domain homologous to an epitope of Sjögren's Syndrome

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based on heuristic

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Cloning of two novel ABC transporters mapping on human chromosome 9

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Nuclear hormone receptors and cholesterol trafficking: the orphans find a new home

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A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease

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Decreased cellular cholesterol efflux is a common cause of familial hypoalphalipoproteinemia: role of the ABCA1 gene mutations

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Homogeneous assay based on 52 primer sets to scan for mutations of the ABCA1 gene and its application in genetic analysis of a new patient with familial high-density lipoprotein deficiency syndrome

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Novel mutations in ABCA1 gene in Japanese patients with Tangier disease and familial high density lipoprotein deficiency with coronary heart disease

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Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency

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based on heuristic

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The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier disease

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based on heuristic

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Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1

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based on heuristic

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ABC1 promotes engulfment of apoptotic cells and transbilayer redistribution of phosphatidylserine

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Transport of lipids from golgi to plasma membrane is defective in tangier disease patients and Abc1-deficient mice

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Cholesterol efflux to apolipoprotein AI involves endocytosis and resecretion in a calcium-dependent pathway

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High density lipoprotein deficiency and foam cell accumulation in mice with targeted disruption of ATP-binding cassette transporter-1

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Cell toxicity induced by inhibition of acyl coenzyme A:cholesterol acyltransferase and accumulation of unesterified cholesterol

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Functional changes in scavenger receptor binding conformation are induced by charge mutants spanning the entire collagen domain

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Specific binding of ApoA-I, enhanced cholesterol efflux, and altered plasma membrane morphology in cells expressing ABC1.

1 reference

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ABCA1 is the cAMP-inducible apolipoprotein receptor that mediates cholesterol secretion from macrophages

1 reference

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based on heuristic

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Specific docking of apolipoprotein A-I at the cell surface requires a functional ABCA1 transporter

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based on heuristic

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ATP-binding cassette transporter A1 contains an NH2-terminal signal anchor sequence that translocates the protein's first hydrophilic domain to the exoplasmic space.

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High density lipoprotein (HDL) particle uptake mediated by scavenger receptor class B type 1 results in selective sorting of HDL cholesterol from protein and polarized cholesterol secretion

1 reference

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Membrane topology of the ATP binding cassette transporter ABCR and its relationship to ABC1 and related ABCA transporters: identification of N-linked glycosylation sites

1 reference

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based on heuristic

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ATP-binding cassette transporter A1 (ABCA1) functions as a cholesterol efflux regulatory protein

1 reference

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based on heuristic

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Evaluation of the role of phosphatidylserine translocase activity in ABCA1-mediated lipid efflux

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The E. coli BtuCD structure: a framework for ABC transporter architecture and mechanism

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Regulation of absorption and ABC1-mediated efflux of cholesterol by RXR heterodimers

1 reference

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How cells handle cholesterol.

1 reference

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Decreased reverse cholesterol transport from Tangier disease fibroblasts. Acceptor specificity and effect of brefeldin on lipid efflux

1 reference

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based on heuristic

inferred from DOI database lookup

Common and rare ABCA1 variants affecting plasma HDL cholesterol

1 reference

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based on heuristic

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Age and residual cholesterol efflux affect HDL cholesterol levels and coronary artery disease in ABCA1 heterozygotes.

1 reference

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7 January 2021

based on heuristic

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Defective removal of cellular cholesterol and phospholipids by apolipoprotein A-I in Tangier Disease

1 reference

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7 January 2021

based on heuristic

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Defective HDL particle uptake in ob/ob hepatocytes causes decreased recycling, degradation, and selective lipid uptake

1 reference

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based on heuristic

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The Tangier disease gene product ABC1 controls the cellular apolipoprotein-mediated lipid removal pathway

1 reference

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based on heuristic

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10.1074/JBC.M204996200

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