7r89
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The structure of human ABCG5/ABCG8 purified from yeast
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Structural highlights
DiseaseABCG5_HUMAN Sitosterolemia. The disease is caused by mutations affecting the gene represented in this entry. FunctionABCG5_HUMAN Transporter that appears to play an indispensable role in the selective transport of the dietary cholesterol in and out of the enterocytes and in the selective sterol excretion by the liver into bile. See Also | ||||||||||||||||||||
This page was last modified 08:54, 4 June 2025.