Pharmacophore modeling, molecular docking and molecular dynamics simulations toward identifying lead compounds for Chk1

Comput Biol Chem. 2018 Oct:76:53-60. doi: 10.1016/j.compbiolchem.2018.06.001. Epub 2018 Jun 4.

Abstract

Checkpoint kinase 1 (Chk1), a serine/threonine protein kinase, plays an important role in G2/M checkpoint, which is a key regulator in response to DNA damage. In this study, the structure-based drug design approach and molecular dynamics (MD) simulations were used to explore potent Chk1 inhibitors. A series of the best fitting candidates were picked out from the Specs database. Out of these, five candidates were submitted for MD simulations to explore the stability of complex. The result indicates that these five candidates could be considered potential Chk1 inhibitors and represents a promising starting point for developing potent inhibitors of Chk1 for the treatment of tumor.

Keywords: Checkpoint kinase 1 inhibitor; Molecular docking; Molecular dynamics simulations; Pharmacophore modeling; Virtual screening.

MeSH terms

  • Checkpoint Kinase 1 / antagonists & inhibitors*
  • Checkpoint Kinase 1 / metabolism
  • Drug Discovery
  • Humans
  • Hydrogen Bonding
  • Ligands
  • Molecular Docking Simulation
  • Molecular Dynamics Simulation
  • Protein Binding
  • Protein Kinase Inhibitors / chemistry*
  • Protein Kinase Inhibitors / metabolism

Substances

  • Ligands
  • Protein Kinase Inhibitors
  • CHEK1 protein, human
  • Checkpoint Kinase 1