(Q40494868)

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An activating mutant of Cdc42 that fails to interact with Rho GDP-dissociation inhibitor localizes to the plasma membrane and mediates actin reorganization

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21 September 2017

An activating mutant of Cdc42 that fails to interact with Rho GDP-dissociation inhibitor localizes to the plasma membrane and mediates actin reorganization (English)

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Europe PubMed Central

PubMed publication ID

21 September 2017

author name string

Richard M Gibson

1

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21 September 2017

Payal N Gandhi

2

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21 September 2017

Xiaofeng Tong

3

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21 September 2017

Jun Miyoshi

4

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21 September 2017

Yoshimi Takai

5

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21 September 2017

Martha Konieczkowski

6

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21 September 2017

John R Sedor

7

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21 September 2017

Amy L Wilson-Delfosse

8

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21 September 2017

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publication date

1 December 2004

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21 September 2017

Experimental Cell Research

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21 September 2017

301

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21 September 2017

2

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21 September 2017

211-222

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21 September 2017

A novel Cdc42Hs mutant induces cellular transformation

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.07.033

7 January 2021

The gamma-subunit of the coatomer complex binds Cdc42 to mediate transformation

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.07.033

7 January 2021

The Ras-related protein Cdc42Hs and bradykinin promote formation of peripheral actin microspikes and filopodia in Swiss 3T3 fibroblasts

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.07.033

7 January 2021

An essential role for Rho, Rac, and Cdc42 GTPases in cell cycle progression through G1

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.07.033

7 January 2021

Wiskott-Aldrich syndrome protein, a novel effector for the GTPase CDC42Hs, is implicated in actin polymerization

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.07.033

7 January 2021

Scar1 and the related Wiskott-Aldrich syndrome protein, WASP, regulate the actin cytoskeleton through the Arp2/3 complex

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.07.033

7 January 2021

Role of protein modification reactions in programming interactions between ras-related GTPases and cell membranes

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.07.033

7 January 2021

All ras proteins are polyisoprenylated but only some are palmitoylated

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.07.033

7 January 2021

Characterization of the interaction between RhoGDI and Cdc42Hs using fluorescence spectroscopy.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.07.033

7 January 2021

RhoGDI-binding-defective mutant of Cdc42Hs targets to membranes and activates filopodia formation but does not cycle with the cytosol of mammalian cells

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.07.033

7 January 2021

Structure of the Rho family GTP-binding protein Cdc42 in complex with the multifunctional regulator RhoGDI

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.07.033

7 January 2021

Protein-DNA interactions at a drug-responsive element of the human apolipoprotein A-I gene

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.07.033

7 January 2021

Maintenance of CDC42 GDP-bound state by Rho-GDI inhibits MAP kinase activation by the exchange factor Ras-GRF. evidence for Ras-GRF function being inhibited by Cdc42-GDP but unaffected by CDC42-GTP.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.07.033

7 January 2021

RhoGDI is required for Cdc42-mediated cellular transformation

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.07.033

7 January 2021

Epidermal Growth Factor-dependent Regulation of Cdc42 Is Mediated by the Src Tyrosine Kinase

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.07.033

7 January 2021

Rho GTPases and the actin cytoskeleton

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.07.033

7 January 2021

Association of Rab1B with GDP-dissociation inhibitor (GDI) is required for recycling but not initial membrane targeting of the Rab protein

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.07.033

7 January 2021

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.07.033

7 January 2021

Mutational analysis of CDC42Sc, a Saccharomyces cerevisiae gene that encodes a putative GTP-binding protein involved in the control of cell polarity

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.07.033

7 January 2021

A GDP dissociation inhibitor that serves as a GTPase inhibitor for the Ras-like protein CDC42Hs

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.07.033

7 January 2021

C-terminal binding domain of Rho GDP-dissociation inhibitor directs N-terminal inhibitory peptide to GTPases

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.07.033

7 January 2021

Kinetics of Cdc42 membrane extraction by Rho-GDI monitored by real-time fluorescence resonance energy transfer

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.07.033

7 January 2021

The human Arp2/3 complex is composed of evolutionarily conserved subunits and is localized to cellular regions of dynamic actin filament assembly

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.07.033

7 January 2021

Regulation of cell-cell adhesion by rac and rho small G proteins in MDCK cells

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.07.033

7 January 2021

Progressive impairment of kidneys and reproductive organs in mice lacking Rho GDIalpha

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.07.033

7 January 2021

Characterization of rac and cdc42 activation in chemoattractant-stimulated human neutrophils using a novel assay for active GTPases

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.07.033

7 January 2021

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10.1016/J.YEXCR.2004.07.033

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

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