4wj7 | pdb_00004wj7
From Proteopedia
CCM2 PTB domain in complex with KRIT1 NPxY/F3
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Structural highlights
Disease[CCM2_HUMAN] Hereditary cerebral cavernous malformation. The disease is caused by mutations affecting the gene represented in this entry. Function[CCM2_HUMAN] Component of the CCM signaling pathway which is a crucial regulator of heart and vessel formation and integrity. May act through the stabilization of endothelial cell junctions (By similarity). May function as a scaffold protein for MAP2K3-MAP3K3 signaling. Seems to play a major role in the modulation of MAP3K3-dependent p38 activation induced by hyperosmotic shock (By similarity). Contents | ||||||||||||||||
This page was last modified 11:15, 24 December 2014.