5jym | pdb_00005jym
From Proteopedia
Human P-cadherin EC12 with scFv TSP11 bound
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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 16:24, 2 January 2017.