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Tripeptides as selective inhibitors of src-SH2 phosphoprotein interactions
Authors:Marc Rodriguez   Renae Crosby   Krystal Alligood   Tona Gilmer  Judd Berman
Affiliation:(1) Glaxo Wellcome Research Institute, 5 Moore Drive, 27709 Research Triangle Park, NC, U.S.A.;(2) Present address: Neosystems, 7 rue de Boulogne, F-67100 Strasbourg, France
Abstract:Summary This paper describes the synthesis of phosphorylated peptides of the general structural Ac-Tyr(PO3H2)-Glu-Xaa_NH2, where Xaa represents a hydrophobic gamma-amino acid of d-configuration. These peptides displayed activities in the micromolar range in inhibiting src-SH2 domain/epidermal growth factor receptor interactions.
Keywords:Phosphotyrosine  SH2
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