Comparative theoretical study of the binding of potential cancer-treatment drugs to Checkpoint kinase 1

This Letter focuses the binding between Checkpoint kinase 1 and two molecules with known inhibition potential, C39 and C40. In order to find the most relevant residues the structures were submitted to an optimization process. As expected C39 presented the highest inhibitory power towards Chk1, being this inhibition mode highly dependent on the interactions with Lys38 and Glu91. Glu55 and Asp148 exhibit unfavorable interactions to C39. Glu91 was the most important residues in the binding of C40 to Chk1, while interaction with Lys38, Glu55 and Gly90 resulted in repulsion.