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The human and mouse complement of SH2 domain proteins-establishing the boundaries of phosphotyrosine signaling.
Liu, Bernard A; Jablonowski, Karl; Raina, Monica; Arcé, Michael; Pawson, Tony; Nash, Piers D.
Afiliación
  • Liu BA; Ben May Institute for Cancer Research and the Committee on Cancer Biology, The University of Chicago, Chicago, Illinois 60637.
  • Jablonowski K; Ben May Institute for Cancer Research and the Committee on Cancer Biology, The University of Chicago, Chicago, Illinois 60637.
  • Raina M; Samuel Lunenfeld Research Institute, Mount Sinai Hospital, Toronto M5G 1X5, Canada.
  • Arcé M; Ben May Institute for Cancer Research and the Committee on Cancer Biology, The University of Chicago, Chicago, Illinois 60637.
  • Pawson T; Samuel Lunenfeld Research Institute, Mount Sinai Hospital, Toronto M5G 1X5, Canada. Electronic address: pawson@mshri.on.ca.
  • Nash PD; Ben May Institute for Cancer Research and the Committee on Cancer Biology, The University of Chicago, Chicago, Illinois 60637. Electronic address: pdnash@uchicago.edu.
Mol Cell ; 22(6): 851-868, 2006 Jun 23.
Article en En | MEDLINE | ID: mdl-16793553
ABSTRACT
SH2 domains are interaction modules uniquely dedicated to the recognition of phosphotyrosine sites and are embedded in proteins that couple protein-tyrosine kinases to intracellular signaling pathways. Here, we report a comprehensive bioinformatics, structural, and functional view of the human and mouse complement of SH2 domain proteins. This information delimits the set of SH2-containing effectors available for PTK signaling and will facilitate the systems-level analysis of pTyr-dependent protein-protein interactions and PTK-mediated signal transduction. The domain-based architecture of SH2-containing proteins is of more general relevance for understanding the large family of protein interaction domains and the modular organization of the majority of human proteins.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteínas Tirosina Quinasas / Transducción de Señal / Modelos Moleculares / Dominios Homologos src / Fosfotirosina / Modelos Biológicos Límite: Animals / Humans Idioma: En Revista: Mol Cell Asunto de la revista: BIOLOGIA MOLECULAR Año: 2006 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteínas Tirosina Quinasas / Transducción de Señal / Modelos Moleculares / Dominios Homologos src / Fosfotirosina / Modelos Biológicos Límite: Animals / Humans Idioma: En Revista: Mol Cell Asunto de la revista: BIOLOGIA MOLECULAR Año: 2006 Tipo del documento: Article