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J Biosci ; 2000 Dec; 25(4): 339-46
Article in English | IMSEAR | ID: sea-111272

ABSTRACT

Tyrosine phosphorylation events are key components of several cellular signal transduction pathways. This study describes a novel method for identification of substrates for tyrosine kinases. Co-expression of the tyrosine kinase EphB1 with the intracellular domain of guanylyl cyclase C (GCC) in Escherichia coli cells resulted in tyrosine phosphorylation of GCC, indicating that GCC is a potential substrate for tyrosine kinases. Indeed, GCC expressed in mammalian cells is tyrosine phosphorylated, suggesting that tyrosine phosphorylation may play a role in regulation of GCC signalling. This is the first demonstration of tyrosine phosphorylation of any member of the family of membrane-associated guanylyl cyclases.


Subject(s)
Animals , Blotting, Western , Cell Line , Chromatography, Thin Layer , Ephrin-B1 , Escherichia coli/enzymology , Guanylate Cyclase/metabolism , Humans , Immunoglobulin G/metabolism , Membrane Proteins/metabolism , Mice , Peptide Mapping , Phosphorylation , Plasmids/metabolism , Precipitin Tests , Protein Structure, Tertiary , Receptors, Cell Surface/metabolism , Receptors, Peptide/metabolism , Recombinant Fusion Proteins/metabolism , Signal Transduction , Tyrosine/metabolism
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