Literature DB >> 9162034

Direct demonstration of geranylgeranylation and farnesylation of Ki-Ras in vivo.

C A Rowell1, J J Kowalczyk, M D Lewis, A M Garcia.   

Abstract

It has recently been reported that Ki-Ras protein can be modified in vitro by farnesylation or geranylgeranylation. However, a previous analysis of Ki-Ras prenylation in vivo found only farnesylated Ki-Ras. In this report it is shown that under normal conditions, Ki-Ras is farnesylated in vivo and when cells are treated with the farnesyl transferase inhibitors B956 or B957, farnesylation is inhibited and Ki-Ras becomes geranylgeranylated in a dose dependent manner. These results have strong implications in the design of anticancer drugs based on inhibition of prenylation.

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Year:  1997        PMID: 9162034     DOI: 10.1074/jbc.272.22.14093

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  81 in total

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4.  Amide-modified prenylcysteine based Icmt inhibitors: Structure-activity relationships, kinetic analysis and cellular characterization.

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Review 8.  RAS inhibitors in hematologic cancers: biologic considerations and clinical applications.

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Review 9.  Targeting RAS Membrane Association: Back to the Future for Anti-RAS Drug Discovery?

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Journal:  Clin Cancer Res       Date:  2015-04-15       Impact factor: 12.531

10.  Synthesis and screening of a CaaL peptide library versus FTase reveals a surprising number of substrates.

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