4oy9 | pdb_00004oy9
From Proteopedia
Crystal structure of human P-Cadherin EC1-EC2 in closed conformation
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Structural highlights
Disease[CADH3_HUMAN] Hypotrichosis with juvenile macular degeneration;EEM syndrome. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. Function[CADH3_HUMAN] Cadherins are calcium-dependent cell adhesion proteins. They preferentially interact with themselves in a homophilic manner in connecting cells; cadherins may thus contribute to the sorting of heterogeneous cell types. Contents | ||||||||||||||||||
This page was last modified 13:18, 1 April 2015.