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K-ras4B and Prenylated Proteins Lacking “Second Signals” Associate Dynamically with Cellular Membranes

We have used fluorescence microscopy and the technique of rapamycin-regulated protein heterodimerization to examine the dynamics of the subcellular localizations of fluorescent proteins fused to lipid-modified protein sequences and to wild-type and mutated forms of full-length K-ras4B. Singly prenyl...

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Autori principali: Silvius, John R., Bhagatji, Pinkesh, Leventis, Rania, Terrone, Donato
Natura: Artigo
Lingua:Inglês
Pubblicazione: The American Society for Cell Biology 2006
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC1345658/
https://ncbi.nlm.nih.gov/pubmed/16236799
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1091/mbc.E05-05-0408
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