4uzq | pdb_00004uzq
From Proteopedia
STRUCTURE OF A WNT SIGNAL REGULATOR COMPLEX - CRYSTAL FORM IX - 1.5A
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Structural highlights
Disease[WNT7A_HUMAN] Phocomelia, Schinzel type;Fuhrmann 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[NOTUM_HUMAN] May deacetylate GlcNAc residues on cell surface glycans. [WNT7A_HUMAN] Ligand for members of the frizzled family of seven transmembrane receptors. Probable developmental protein. Signaling by Wnt-7a allows sexually dimorphic development of the mullerian ducts (By similarity). Contents | ||||||||||||||||||||||
This page was last modified 14:05, 25 February 2015.