6i2k | pdb_00006i2k
From Proteopedia
Structure of EV71 complexed with its receptor SCARB2
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Structural highlights
Disease[SCRB2_HUMAN] Unverricht-Lundborg disease;Gaucher disease type 1;Action myoclonus - renal failure syndrome. The disease is caused by mutations affecting the gene represented in this entry. Genetic variants in SCARB2 can act as modifier of the phenotypic expression and severity of Gaucher disease. Function[SCRB2_HUMAN] Acts as a lysosomal receptor for glucosylceramidase (GBA) targeting.[1] References
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This page was last modified 20:34, 2 December 2018.