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 The multifunctional GIT family of proteins Hoefen RJ; Berk BCJ Cell Sci  2006[Apr]; 119 (Pt 8): 1469-75The G-protein-coupled receptor (GPCR)-kinase-interacting proteins 1 and 2 (GIT1  and GIT2) are ubiquitous multidomain proteins involved in diverse cellular  processes. They traffic between three distinct cellular compartments (cytoplasmic  complexes, focal adhesions and the cell periphery) through interactions with  proteins including ARF, Rac1 and Cdc42 GTPases, p21-activated kinase (PAK),  PAK-interacting exchange factor (PIX), the kinase MEK1, phospholipase Cgamma  (PLCgamma) and paxillin. GITs and PIX cooperate to form large oligomeric  complexes to which other proteins are transiently recruited. Activation of Rac1  and Cdc42 drives association of PAK with these oligomers, which unmasks the  paxillin-binding site in GITs that recruits them to focal complexes. There, they  regulate cytoskeletal dynamics by feedback inhibition of Rac1. GITs also  participate in receptor internalization by regulating membrane trafficking  between the plasma membrane and endosomes, targeting ARF GTPases through their  ARF GTPase-activating protein (ARF-GAP) activity. Furthermore, GITs act as  scaffolds to control spatial activation of several signaling molecules. Finally,  recent results suggest pathogenic roles for GIT proteins in Huntington's disease  and HIV infection.|*Protein Structure, Tertiary[MESH]|*Protein Transport[MESH]|Adaptor Proteins, Signal Transducing/genetics/*metabolism/physiology[MESH]|Binding Sites[MESH]|Cell Cycle Proteins/genetics/*metabolism/physiology[MESH]|Cytoskeleton/metabolism[MESH]|GTP Phosphohydrolases/*metabolism[MESH]|GTPase-Activating Proteins/genetics/*metabolism/physiology[MESH]|Humans[MESH]|Phosphorylation[MESH]|Protein Binding[MESH]|Signal Transduction[MESH]
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