ACS Medicinal Chemistry Letters · 2010 · 142 citations · 13 references
Life SciencesMedicinal ChemistryMolecular BiologyDrug DiscoveryHost-pathogen InteractionsSignal TransductionEnzyme InhibitionParasitic Disease PathogenesisParasitic PathogenesisProtozoal InfectionsProtozoan Host-parasite InteractionsTyrosine Kinase InhibitorsCell Invasion MechanismsHost-protozoan InteractionsParasite Invasion MechanismsSelective Tyrosine Kinase InhibitorsSrc Family Kinases
The protozoans Cryptosporidium parvum and Toxoplasma gondii are parasites of major health concern to humans. Both parasites contain a group of calcium-dependent protein kinases (CDPKs), which are found in plants and ciliates but not in humans or fungi. Here we describe a series of potent inhibitors that target CDPK1 in C. parvum (CpCDPK1) and T. gondii (TgCDPK1). These inhibitors are highly selective for CpCDPK1 and TgCDPK1 over the mammalian kinases SRC and ABL. Furthermore, they are able to block an early stage of C. parvum invasion of HCT-8 host cells, which is similar to their effects on T. gondii invasion of human fibroblasts.
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A chemical switch for inhibitor-sensitive alleles of any protein kinase
Anthony C. Bishop, Jeffrey A. Ubersax, Dejah T. Petsch et al. · Nature · 2000 · 1.1K citations
Structural Bioinformatics-Based Design of Selective, Irreversible Kinase Inhibitors
Michael S. Cohen, Chao Zhang, Kevan M. Shokat et al. · Science · 2005 · 508 citations · Full text
Design of allele-specific inhibitors to probe protein kinase signaling
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