Tyrosine 1213 of Flt-1 is a major binding site of Nck and SHP-2.

Article Details

Citation

Igarashi K, Isohara T, Kato T, Shigeta K, Yamano T, Uno I

Tyrosine 1213 of Flt-1 is a major binding site of Nck and SHP-2.

Biochem Biophys Res Commun. 1998 May 8;246(1):95-9.

PubMed ID
9600074 [ View in PubMed
]
Abstract

Vascular endothelial growth factor (VEGF) binds to its receptor tyrosine kinase Flt-1 and KDR/Flk-1 and stimulates their autophosphorylation. However, little is known about their downstream signal transduction properties. We examined the interactions of certain proteins with a SH2-domain with Flt-1 and KDR using the yeast two-hybrid system and found that Nck, SHP-2, PLC gamma, and PI3K p85 bind to Flt-1. Extensive site-directed mutagenesis of Flt-1 revealed their major binding sites. Nck, SHP-2, and PI3K bind to Y1213 of Flt-1. Nck also binds to Y1333 of Flt-1. These results suggest that Nck, SHP-2, PLC gamma, and PI3K play important roles in Flt-1 signal transduction and that Y1213 of Flt-1 is a major binding site of PI3K, Nck, and SHP-2.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Vascular endothelial growth factor receptor 1P17948Details
Tyrosine-protein phosphatase non-receptor type 11Q06124Details
Phosphatidylinositol 3-kinase regulatory subunit betaO00459Details