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Inhibition and termination of physiological responses by GTPase activating proteins.
Ligeti, Erzsébet; Welti, Stefan; Scheffzek, Klaus.
Afiliación
  • Ligeti E; Department of Physiology, Semmelweis University, Budapest, Hungary. Ligeti@puskin.sote.hu
Physiol Rev ; 92(1): 237-72, 2012 Jan.
Article en En | MEDLINE | ID: mdl-22298657
ABSTRACT
Physiological processes are strictly organized in space and time. However, in cell physiology research, more attention is given to the question of space rather than to time. To function as a signal, environmental changes must be restricted in time; they need not only be initiated but also terminated. In this review, we concentrate on the role of one specific protein family involved in biological signal termination. GTPase activating proteins (GAPs) accelerate the endogenously low GTP hydrolysis rate of monomeric guanine nucleotide-binding proteins (GNBPs), limiting thereby their prevalence in the active, GTP-bound form. We discuss cases where defective or excessive GAP activity of specific proteins causes significant alteration in the function of the nervous, endocrine, and hemopoietic systems, or contributes to development of infections and tumors. Biochemical and genetic data as well as observations from human pathology support the notion that GAPs represent vital elements in the spatiotemporal fine tuning of physiological processes.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas Activadoras de GTPasa / Sistema Endocrino / Hematopoyesis / Fenómenos Fisiológicos del Sistema Nervioso Tipo de estudio: Risk_factors_studies Límite: Animals / Humans Idioma: En Revista: Physiol Rev Año: 2012 Tipo del documento: Article País de afiliación: Hungria

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas Activadoras de GTPasa / Sistema Endocrino / Hematopoyesis / Fenómenos Fisiológicos del Sistema Nervioso Tipo de estudio: Risk_factors_studies Límite: Animals / Humans Idioma: En Revista: Physiol Rev Año: 2012 Tipo del documento: Article País de afiliación: Hungria