The Salmonella Typhimurium effector SteC inhibits Cdc42-mediated signaling through binding to the exchange factor Cdc24 in Saccharomyces cerevisiae
Expression of the Salmonella effector SteC in yeast leads to down-regulation of the mating and HOG pathways by Cdc42 inhibition. This is mediated by the SteC N-terminal domain through binding to the GEF Cdc24. SteC alters Cdc24 localization and also interacts with human GEF Vav1, suggesting that Ste...
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The American Society for Cell Biology
2012
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Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3496616/ |
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pubmed-34966162013-01-30 The Salmonella Typhimurium effector SteC inhibits Cdc42-mediated signaling through binding to the exchange factor Cdc24 in Saccharomyces cerevisiae Fernandez-Piñar, Pablo Alemán, Ainel Sondek, John Dohlman, Henrik G. Molina, María Martín, Humberto Articles Expression of the Salmonella effector SteC in yeast leads to down-regulation of the mating and HOG pathways by Cdc42 inhibition. This is mediated by the SteC N-terminal domain through binding to the GEF Cdc24. SteC alters Cdc24 localization and also interacts with human GEF Vav1, suggesting that SteC could target Cdc42 function in host cells. The American Society for Cell Biology 2012-11-15 /pmc/articles/PMC3496616/ /pubmed/23015760 http://dx.doi.org/10.1091/mbc.E12-03-0243 Text en © 2012 Fernandez-Piñar et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0). “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society of Cell BD; are registered trademarks of The American Society of Cell Biology. |
repository_type |
Open Access Journal |
institution_category |
Foreign Institution |
institution |
US National Center for Biotechnology Information |
building |
NCBI PubMed |
collection |
Online Access |
language |
English |
format |
Online |
author |
Fernandez-Piñar, Pablo Alemán, Ainel Sondek, John Dohlman, Henrik G. Molina, María Martín, Humberto |
spellingShingle |
Fernandez-Piñar, Pablo Alemán, Ainel Sondek, John Dohlman, Henrik G. Molina, María Martín, Humberto The Salmonella Typhimurium effector SteC inhibits Cdc42-mediated signaling through binding to the exchange factor Cdc24 in Saccharomyces cerevisiae |
author_facet |
Fernandez-Piñar, Pablo Alemán, Ainel Sondek, John Dohlman, Henrik G. Molina, María Martín, Humberto |
author_sort |
Fernandez-Piñar, Pablo |
title |
The Salmonella Typhimurium effector SteC inhibits Cdc42-mediated signaling through binding to the exchange factor Cdc24 in Saccharomyces cerevisiae |
title_short |
The Salmonella Typhimurium effector SteC inhibits Cdc42-mediated signaling through binding to the exchange factor Cdc24 in Saccharomyces cerevisiae |
title_full |
The Salmonella Typhimurium effector SteC inhibits Cdc42-mediated signaling through binding to the exchange factor Cdc24 in Saccharomyces cerevisiae |
title_fullStr |
The Salmonella Typhimurium effector SteC inhibits Cdc42-mediated signaling through binding to the exchange factor Cdc24 in Saccharomyces cerevisiae |
title_full_unstemmed |
The Salmonella Typhimurium effector SteC inhibits Cdc42-mediated signaling through binding to the exchange factor Cdc24 in Saccharomyces cerevisiae |
title_sort |
salmonella typhimurium effector stec inhibits cdc42-mediated signaling through binding to the exchange factor cdc24 in saccharomyces cerevisiae |
description |
Expression of the Salmonella effector SteC in yeast leads to down-regulation of the mating and HOG pathways by Cdc42 inhibition. This is mediated by the SteC N-terminal domain through binding to the GEF Cdc24. SteC alters Cdc24 localization and also interacts with human GEF Vav1, suggesting that SteC could target Cdc42 function in host cells. |
publisher |
The American Society for Cell Biology |
publishDate |
2012 |
url |
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3496616/ |
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1611923781251497984 |