Targeted genetic and small molecule disruption of N-Ras CaaX cleavage alters its localization and oncogenic potential-Reference-Cited by-同舟云学术

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Targeted genetic and small molecule disruption of N-Ras CaaX cleavage alters its localization and oncogenic potential

Published:2024-06 Issue: Volume:147 Page:107316
ISSN:0045-2068
Container-title:Bioorganic Chemistry
language:en
Short-container-title:Bioorganic Chemistry

Author:

Hildebrandt Emily R.,Hussain Shaneela A.,Sieburg Michelle A.,Ravishankar Rajani,Asad Nadeem,Gore Sangram,Ito Takahiro,Hougland James L.,Dore Timothy M.,Schmidt Walter K.

Funder

National Institutes of Health

Publisher

Elsevier BV

Reference72 articles.

1. RAS isoforms and mutations in cancer at a glance;Hobbs;J. Cell Sci.,2016

2. The yeast Saccharomyces cerevisiae as a model for understanding RAS proteins and their role in human tumorigenesis;Cazzanelli;Cells,2018

3. Regulating the regulator: post-translational modification of RAS;Ahearn;Nat. Rev. Mol. Cell Biol.,2011

4. The Saccharomyces cerevisiae prenylcysteine carboxyl methltransferase Ste14p is in the endoplasmic reticulum membrane;Romano;Mol. Biol. Cell,1998

5. Endoplasmic reticulum membrane localization of Rce1p and Ste24p, yeast proteases involved in carboxyl-terminal CAAX protein processing and amino-terminal a-factor cleavage;Schmidt;PNAS,1998

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Evaluating protein prenylation of human and viral CaaX sequences using a humanized yeast system;Disease Models & Mechanisms;2024-05-01

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