Binds alpha-tocopherol, enhances its transfer between separate membranes, and stimulates its release from liver cells. Binds both phosphatidylinol 3,4-bisphosphate and phosphatidylinol 4,5-bisphosphate; the resulting conformation change is important for the release of the bound alpha-tocopherol (By similarity).
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Alpha-tocopherol transfer protein Recombinant
Alpha-tocopherol transfer protein Antibody
TTPA: Binds alpha-tocopherol and enhances its transfer between separate membranes. Defects in TTPA are the cause of ataxia with isolated vitamin E deficiency (AVED). AVED is an autosomal recessive disease characterized by spinocerebellar degeneration. It causes ataxia and peripheral neuropathy that resembles Friedreich ataxia. AVED patients have markedly reduced plasma levels of vitamin E.
Protein type: Lipid-binding
Cellular Component: cytosol; late endosome
Molecular Function: phosphatidylinositol-3,4-bisphosphate binding; phosphatidylinositol-4,5-bisphosphate binding; vitamin binding; vitamin E binding
Biological Process: developmental process; embryonic placenta development; intermembrane transport; intracellular pH reduction; placenta development; response to nutrient; response to pH; response to toxin; vitamin E metabolic process; vitamin transport