Title : A flexible-protein molecular docking study of the binding of ruthenium complex compounds to PIM1, GSK-3β, and CDK2/Cyclin A protein kinases.

Pub. Date : 2013 Jan

PMID : 22926267






1 Functional Relationships(s)
Download
Sentence
Compound Name
Protein Name
Organism
1 We employ ensemble docking simulations to characterize the interactions of two enantiomeric forms of a Ru-complex compound (1-R and 1-S) with three protein kinases, namely PIM1, GSK-3beta, and CDK2/cyclin A. Ruthenium Pim-1 proto-oncogene, serine/threonine kinase Homo sapiens