Literature DB >> 1351295

Coupling of ras p21 signalling and GTP hydrolysis by GTPase activating proteins.

F McCormick1.   

Abstract

Ras p21 proteins cycle between inactive, GDP-bound forms and active GTP-bound forms. Hydrolysis of bound GTP to GDP is mediated by proteins referred to as GAPs, two forms of which have been described. The first, p120-GAP, contains regions of homologies with tyrosine kinase oncogenes, and interacts with tyrosine phosphoproteins as well as with ras proteins; p120-GAP may therefore connect signalling pathways that involve tyrosine kinase and ras p21 proteins. The second type of GAP is the product of the neurofibromatosis type 1 gene (NF1-GAP). This is a protein of 325,000 Da that is defective in patients with NF1; NF1-GAP is regulated by signalling lipids, and may serve to connect ras p21 with phospholipid second messenger systems. The significance of ras p21 interaction with distinct GAPs is discussed.

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Year:  1992        PMID: 1351295     DOI: 10.1098/rstb.1992.0042

Source DB:  PubMed          Journal:  Philos Trans R Soc Lond B Biol Sci        ISSN: 0962-8436            Impact factor:   6.237


  3 in total

Review 1.  MicroRNA-Based Therapeutic Strategies for Targeting Mutant and Wild Type RAS in Cancer.

Authors:  Sriganesh B Sharma; John Michael Ruppert
Journal:  Drug Dev Res       Date:  2015-08-18       Impact factor: 4.360

2.  Ab initio study of the role of lysine 16 for the molecular switching mechanism of Ras protein p21.

Authors:  N Futatsugi; M Hata; T Hoshino; M Tsuda
Journal:  Biophys J       Date:  1999-12       Impact factor: 4.033

3.  Effects of mutant Ran/TC4 proteins on cell cycle progression.

Authors:  M Ren; E Coutavas; P D'Eustachio; M G Rush
Journal:  Mol Cell Biol       Date:  1994-06       Impact factor: 4.272

  3 in total

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