Literature DB >> 2208277

A polybasic domain or palmitoylation is required in addition to the CAAX motif to localize p21ras to the plasma membrane.

J F Hancock1, H Paterson, C J Marshall.   

Abstract

The C-terminal CAAX motif of ras proteins undergoes a triplet of posttranslational modifications that are required for membrane association. The CAAX motif lies immediately C-terminal to the hypervariable domain, a region of 20 amino acids that distinguishes the ras proteins from each other. The hypervariable domains of p21H-ras, p21N-ras, and p21K-ras(A) contain sites for palmitoylation, which we now show must combine with the CAAX motif to target specific plasma membrane localization. Within the hypervariable domain of p21K-ras(B), which is not palmitoylated, we have identified a novel plasma membrane targeting signal consisting of a polybasic domain that also acts in combination with the CAAX motif. One function of the hypervariable domains of p21ras is therefore to provide different signals for plasma membrane localization.

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Year:  1990        PMID: 2208277     DOI: 10.1016/0092-8674(90)90294-o

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  338 in total

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Authors:  E M Fitzgerald
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8.  Association of prenylated proteins with the plasma membrane and the inner nuclear membrane is mediated by the same membrane-targeting motifs.

Authors:  H Hofemeister; K Weber; R Stick
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Authors:  June Chunqiu Hou; Jeffrey E Pessin
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10.  Plasma membrane localization of Ras requires class C Vps proteins and functional mitochondria in Saccharomyces cerevisiae.

Authors:  Geng Wang; Robert J Deschenes
Journal:  Mol Cell Biol       Date:  2006-04       Impact factor: 4.272

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