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ATP-binding cassette sub-family A member 3

Domain

Multifunctional polypeptide with two homologous halves, each containing a hydrophobic membrane-anchoring domain and an ATP binding cassette (ABC) domain.

Function

Catalyzes the ATP-dependent transport of phospholipids such as phosphatidylcholine and phosphoglycerol from the cytoplasm into the lumen side of lamellar bodies, in turn participates in the lamellar bodies biogenesis and homeostasis of pulmonary surfactant (PubMed:17142808, PubMed:17267394, PubMed:17540762, PubMed:17577581, PubMed:20190032, PubMed:28034695). Transports preferentially phosphatidylcholine containing short acyl chains (PubMed:17142808). In addition plays a role as an efflux transporter of miltefosine across macrophage membranes and free cholesterol (FC) through intralumenal vesicles by removing FC from the cell as a component of surfactant and protects cells from free cholesterol toxicity (By similarity).

Post-translational modifications

N-glycosylated. Localization at intracellular vesicles is accompanied by processing of oligosaccharide from high mannose type to complex type. N-linked glycosylation at Asn-124 and Asn-140 is required for stability and efficient anterograde trafficking and prevents from proteasomal degradation.

Proteolytically cleaved by CTSL and to a lower extent by CTSB within multivesicular bodies (MVB) and lamellar bodies (LB) leading to a mature form of 150 kDa.

Sequence similarities

Belongs to the ABC transporter superfamily. ABCA family.

Tissue specificity

Highly expressed in the lung and moderately expressed in the kidney, adipose, macrophage, and spleen.

Cellular localization

  • Endosome
  • Multivesicular body membrane
  • Multi-pass membrane protein
  • Cytoplasmic vesicle membrane
  • Late endosome membrane
  • Lysosome membrane
  • Localized in the limiting membrane of lamellar bodies in lung alveolar type II cells (PubMed:11940594). Trafficks via the Golgi, sorting vesicles (SVs) and late endosome/multivesicular body network directly to the outer membrane of lamellar bodies in AT2 lung epithelial cells or to lysosomes and lysosomal-related organelles (LROs) in other cells where undergoes proteolytic cleavage and oligosaccharide processing from high mannose type to complex type. Oligomers formation takes place in a post-endoplasmic reticulum compartment (By similarity).

Alternative names

Phospholipid-transporting ATPase ABCA3, ATP-binding cassette sub-family A member 3, Xenobiotic-transporting ATPase ABCA3, Abca3

Target type

Proteins

Primary research area

Immunology & Infectious Disease

Molecular weight

191971Da

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Primary Antibodies

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