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      Rho, rac, and cdc42 GTPases regulate the assembly of multimolecular focal complexes associated with actin stress fibers, lamellipodia, and filopodia.

      Cell
      3T3 Cells, cytology, Actins, metabolism, Animals, Cell Adhesion, physiology, Cell Adhesion Molecules, Cell Movement, Cytoskeletal Proteins, Cytoskeleton, Focal Adhesion Kinase 1, Focal Adhesion Protein-Tyrosine Kinases, Fungal Proteins, GTP Phosphohydrolases, pharmacology, GTP-Binding Proteins, antagonists & inhibitors, Membrane Proteins, Mice, Microinjections, Paxillin, Phosphoproteins, Phosphotyrosine, Protein-Tyrosine Kinases, Pseudopodia, Recombinant Fusion Proteins, biosynthesis, isolation & purification, Signal Transduction, Tyrosine, analogs & derivatives, Vinculin, cdc42 GTP-Binding Protein, Saccharomyces cerevisiae, rac GTP-Binding Proteins, rhoB GTP-Binding Protein

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          Abstract

          Rho and rac, two members of the ras-related superfamily of small GTPases, regulate the polymerization of actin to produce stress fibers and lamellipodia, respectively. We report here that cdc42, another member of the rho family, triggers the formation of a third type of actin-based structure found at the cell periphery, filopodia. In addition to stress fibers, rho controls the assembly of focal adhesion complexes. We now show that rac and cdc42 also stimulate the assembly of multimolecular focal complexes at the plasma membrane. These complexes, which are associated with lamellipodia and filopodia, contain vinculin, paxillin, and focal adhesion kinase, but are distinct from and formed independently of rho-induced focal adhesions. Activation of cdc42 in Swiss 3T3 cells leads to the sequential activation of rac and then rho, suggesting a molecular model for the coordinated control of cell motility by members of the rho family of GTPases.

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          A brain serine/threonine protein kinase activated by Cdc42 and Rac1.

          A new brain serine/threonine protein kinase may be a target for the p21ras-related proteins Cdc42 and Rac1. The kinase sequence is related to that of the yeast protein STE20, implicated in pheromone-response pathways. The kinase complexes specifically with activated (GTP-bound) p21, inhibiting p21 GTPase activity and leading to kinase autophosphorylation and activation. Autophosphorylated kinase has a decreased affinity for Cdc42/Rac, freeing the p21 for further stimulatory activities or downregulation by GTPase-activating proteins. This bimolecular interaction provides a model for studying p21 regulation of mammalian phosphorylation signalling pathways.
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            Proteins regulating Ras and its relatives.

            GTPases of the Ras superfamily regulate many aspects of cell growth, differentiation and action. Their functions depend on their ability to alternate between inactive and active forms, and on their cellular localization. Numerous proteins affecting the GTPase activity, nucleotide exchange rates and membrane localization of Ras superfamily members have now been identified. Many of these proteins are much larger and more complex than their targets, containing multiple domains capable of interacting with an intricate network of cellular enzymes and structures.
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              Focal adhesions: transmembrane junctions between the extracellular matrix and the cytoskeleton.

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