| Literature DB >> 11120586 |
R Bhandari1, R Mathew, K Vijayachandra, S Visweswariah.
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.Entities:
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Year: 2000 PMID: 11120586 DOI: 10.1007/bf02703787
Source DB: PubMed Journal: J Biosci ISSN: 0250-5991 Impact factor: 1.826