7jr7
From Proteopedia
Cryo-EM structure of ABCG5/G8 in complex with Fab 2E10 and 11F4
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
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Categories: Homo sapiens | Large Structures | Huang CS | Min X | Wang Z | Yu X | Zhang H