Title : Targeting the trypanosome kinetochore with CLK1 protein kinase inhibitors.

Pub. Date : 2020 Oct

PMID : 32661312






3 Functional Relationships(s)
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1 Biochemical studies and the co-crystal structure of CLK1 in complex with AB1 show that the irreversible competitive inhibition of CLK1 is dependent on a Michael acceptor forming an irreversible bond with Cys 215 in the ATP-binding pocket, a residue that is not present in human CLK1, thereby providing selectivity. Adenosine Triphosphate CDC like kinase 1 Homo sapiens
2 Biochemical studies and the co-crystal structure of CLK1 in complex with AB1 show that the irreversible competitive inhibition of CLK1 is dependent on a Michael acceptor forming an irreversible bond with Cys 215 in the ATP-binding pocket, a residue that is not present in human CLK1, thereby providing selectivity. Adenosine Triphosphate CDC like kinase 1 Homo sapiens
3 Biochemical studies and the co-crystal structure of CLK1 in complex with AB1 show that the irreversible competitive inhibition of CLK1 is dependent on a Michael acceptor forming an irreversible bond with Cys 215 in the ATP-binding pocket, a residue that is not present in human CLK1, thereby providing selectivity. Adenosine Triphosphate CDC like kinase 1 Homo sapiens