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]
<references />
External links[edit]
- TAP1 at the US National Library of Medicine Medical Subject Headings (MeSH)
