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Identification of Mediators of T-cell Receptor Signaling via the Screening of Chemical Inhibitor Libraries
Published on: January 22, 2019
Selective bisubstrate inhibitors with sub-nanomolar affinity for protein kinase Pim-1
Ramesh Ekambaram1, Erki Enkvist, Angela Vaasa
1Institute of Chemistry, University of Tartu, Tartu, Estonia.
Abstract:
Potent and selective: The unique nature of the ATP binding pocket structure of Pim family protein kinases (PKs) was used for the development of bisubstrate inhibitors and a fluorescent probe with sub-nanomolar affinity. Conjugates of arginine-rich peptides with two ATP mimetic scaffolds were synthesized and tested as inhibitors of Pim-1. Against a panel of 124 protein kinases, a novel ARC-PIM conjugate selectively inhibited PKs of the Pim family.
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