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PMID: 15994296 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, P.H.S.

Mechanism of redox-mediated guanine nucleotide exchange on redox-active Rho GTPases.

The Journal of biological chemistry ·Vol. 280 ·No. 35 ·2005-09-02 ·Pages 31003-10

Heo J, Campbell SL

Abstract

Rho GTPases regulate multiple cellular processes including actin cytoskeletal rearrangements, transcriptional regulation, and oxidant production. The studies described herein demonstrate that small molecule redox agents, in addition to protein regulatory factors, can regulate the activity of redox-active Rho GTPases. A novel (GXXXXGK(S/T)C) motif, conserved in a number of Rho GTPases, appears critical for redox-mediated guanine nucleotide dissociation in vitro. A detailed molecular mechanism for redox regulation of GXXXXGK(S/T)C motif-containing Rho GTPases is proposed.

MeSH Terms
Amino Acid Motifs Guanine Nucleotides/chemistry,metabolism Molecular Structure Molecular Weight Oxidation-Reduction Reactive Nitrogen Species Reactive Oxygen Species/chemistry,metabolism rho GTP-Binding Proteins/chemistry,genetics,metabolism
Chemicals
Guanine Nucleotides Reactive Nitrogen Species Reactive Oxygen Species rho GTP-Binding Proteins
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Heo Jongyun
Department of Biochemistry and Biophysics, University of North Carolina, Chapel Hill, North Carolina 27599-7260, USA.
Campbell Sharon L
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
2005-09-02
Epub
2005-00-30
Pages
31003-10
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NHLBI NIH HHS · P01 HL45100 · United States
NCI NIH HHS · R01CA89614-O1A1 · United States
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