TAP1: Difference between revisions

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Latest revision as of 01:34, 18 March 2025

TAP1 (Transporter 1, ATP-binding cassette sub-family B) is a protein that in humans is encoded by the TAP1 gene. It is a member of the ABC transporter family, which are integral membrane proteins that utilize ATP to drive the transport of various molecules across the cell membrane.

Function[edit]

TAP1 is involved in the transport of antigens from the cytoplasm to the endoplasmic reticulum for association with MHC class I molecules. It also interacts with the viral proteins of certain viruses, preventing the transport of the antigenic peptides into the endoplasmic reticulum.

Clinical significance[edit]

Mutations in the TAP1 gene can lead to bare lymphocyte syndrome, a type of MHC class I deficiency. This can result in a variety of immune disorders, including increased susceptibility to viral infections.

Structure[edit]

The TAP1 protein is composed of two subunits, each of which has six transmembrane domains. The protein also contains an ATP-binding domain, which is responsible for the energy-dependent transport of antigens.

Interactions[edit]

TAP1 has been shown to interact with:

See also[edit]

References[edit]

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External links[edit]

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