Your browser doesn't support javascript.
loading
Identification of csk tyrosine phosphorylation sites and a tyrosine residue important for kinase domain structure.
Joukov, V; Vihinen, M; Vainikka, S; Sowadski, J M; Alitalo, K; Bergman, M.
Afiliación
  • Joukov V; Molecular/Cancer Biology Laboratory, Haartman Institute, P.O. Box 21 (Haartmaninkatu 3), FIN-00014, Finland.
Biochem J ; 322 ( Pt 3): 927-35, 1997 Mar 15.
Article en En | MEDLINE | ID: mdl-9148770
The lack of a conserved tyrosine autophosphorylation site is a unique feature of the C-terminal Src-kinase, Csk, although this protein tyrosine kinase can be autophosphorylated on tyrosine residues in vitro and in bacteria. Here we show that human Csk is tyrosine phosphorylated in HeLa cells treated with sodium pervanadate. Phosphorylation in vivo occurs mainly at Tyr-184 and in vitro mainly at Tyr-304. A Y304F mutation strongly decreased Csk phosphorylation in vitro, and a Y184F mutation abolished tyrosine phosphorylation in vivo. A catalytically inactive form of Csk was also phosphorylated on Tyr-184 in vivo, suggesting that this is not a site of autophosphorylation. The kinase activity of the Y184F protein was not changed, while the Y304F protein showed one-third of wild-type activity. Three-dimensional modelling of the Csk kinase domain indicated that the Y304F mutation abolishes one of two conserved hydrogen bonds between the upper and the lower lobes in the open conformation of the kinase domain. Phosphopeptide binding studies suggested that phosphorylation of Tyr-184 creates a binding site for low-molecular-mass proteins. Cellular Csk was associated with several phosphoproteins, some of which were interacting with the Csk SH2 domain. Taken together these results indicate that Csk can be phosphorylated in vivo at Tyr-184 by an as yet unknown tyrosine kinase, and that autophosphorylation of Tyr-304 occurs only at abnormally high Csk concentrations in vitro. Furthermore, Tyr-304 is required for the maintenance of the structure of the Csk kinase domain.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Tirosina / Proteínas Tirosina Quinasas Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Biochem J Año: 1997 Tipo del documento: Article País de afiliación: Finlandia Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Tirosina / Proteínas Tirosina Quinasas Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Biochem J Año: 1997 Tipo del documento: Article País de afiliación: Finlandia Pais de publicación: Reino Unido