7r89

Structural highlights

Disease

ABCG5_HUMAN Sitosterolemia. The disease is caused by mutations affecting the gene represented in this entry.

Function

ABCG5_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

• ABC transporter 3D structures