Literature DB >> 2115210

Identification of small clusters of divergent amino acids that mediate the opposing effects of ras and Krev-1.

K Zhang1, M Noda, W C Vass, A G Papageorge, D R Lowy.   

Abstract

Krev-1 is an anti-oncogene that was originally identified by its ability to induce morphologic reversion of ras-transformed cells that continue to express the ras gene. The Krev-1-encoded protein is structurally related to Ras proteins. The biological activities of a series of ras-Krev-1 chimeras were studied to test the hypothesis that Krev-1 may directly interfere with a ras function. The ras-specific and Krev-1-specific amino acids immediately surrounding residues 32 to 44, which are identical between the two proteins, determined whether the protein induced cellular transformation or suppressed ras transformation. Because this region in Ras proteins has been implicated in effector function, the results suggest that Krev-1 suppresses ras-induced transformation by interfering with interaction of Ras with its effector.

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Year:  1990        PMID: 2115210     DOI: 10.1126/science.2115210

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  20 in total

1.  The small GTP-binding protein R-Ras can influence integrin activation by antagonizing a Ras/Raf-initiated integrin suppression pathway.

Authors:  T Sethi; M H Ginsberg; J Downward; P E Hughes
Journal:  Mol Biol Cell       Date:  1999-06       Impact factor: 4.138

2.  Isolation of rsp-1, a novel cDNA capable of suppressing v-Ras transformation.

Authors:  M L Cutler; R H Bassin; L Zanoni; N Talbot
Journal:  Mol Cell Biol       Date:  1992-09       Impact factor: 4.272

3.  A ras effector domain mutant which is temperature sensitive for cellular transformation: interactions with GTPase-activating protein and NF-1.

Authors:  J E DeClue; J C Stone; R A Blanchard; A G Papageorge; P Martin; K Zhang; D R Lowy
Journal:  Mol Cell Biol       Date:  1991-06       Impact factor: 4.272

4.  Mitogenic and oncogenic properties of the small G protein Rap1b.

Authors:  D L Altschuler; F Ribeiro-Neto
Journal:  Proc Natl Acad Sci U S A       Date:  1998-06-23       Impact factor: 11.205

5.  Insulin regulates the dynamic balance between Ras and Rap1 signaling by coordinating the assembly states of the Grb2-SOS and CrkII-C3G complexes.

Authors:  S Okada; M Matsuda; M Anafi; T Pawson; J E Pessin
Journal:  EMBO J       Date:  1998-05-01       Impact factor: 11.598

Review 6.  Biology of the Rap proteins, members of the ras superfamily of GTP-binding proteins.

Authors:  G M Bokoch
Journal:  Biochem J       Date:  1993-01-01       Impact factor: 3.857

Review 7.  Cellular consequences of thrombin-receptor activation.

Authors:  R J Grand; A S Turnell; P W Grabham
Journal:  Biochem J       Date:  1996-01-15       Impact factor: 3.857

8.  Comparison of the low energy conformations of an oncogenic and a non-oncogenic p21 protein, neither of which binds GTP or GDP.

Authors:  A Liwo; K D Gibson; H A Scheraga; P W Brandt-Rauf; R Monaco; M R Pincus
Journal:  J Protein Chem       Date:  1994-02

9.  Identification of amino acid residues required for Ras p21 target activation.

Authors:  M S Marshall; L J Davis; R D Keys; S D Mosser; W S Hill; E M Scolnick; J B Gibbs
Journal:  Mol Cell Biol       Date:  1991-08       Impact factor: 4.272

10.  Identification of Rap1 as a target for the Crk SH3 domain-binding guanine nucleotide-releasing factor C3G.

Authors:  T Gotoh; S Hattori; S Nakamura; H Kitayama; M Noda; Y Takai; K Kaibuchi; H Matsui; O Hatase; H Takahashi
Journal:  Mol Cell Biol       Date:  1995-12       Impact factor: 4.272

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