The calcium-dependent protein kinase 1 from Toxoplasma gondii as target for structure-based drug design

Parasitology. 2018 Feb;145(2):210-218. doi: 10.1017/S0031182017001901. Epub 2017 Dec 1.

Abstract

The apicomplexan protozoan parasites include the causative agents of animal and human diseases ranging from malaria (Plasmodium spp.) to toxoplasmosis (Toxoplasma gondii). The complex life cycle of T. gondii is regulated by a unique family of calcium-dependent protein kinases (CDPKs) that have become the target of intensive efforts to develop new therapeutics. In this review, we will summarize structure-based strategies, recent successes and future directions in the pursuit of specific and selective inhibitors of T. gondii CDPK1.

Keywords: Toxoplasma gondii; CDPK1; Calcium-dependent protein kinase; drug design; protein structure.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Drug Design*
  • Humans
  • Life Cycle Stages / drug effects
  • Malaria / drug therapy
  • Models, Molecular
  • Plasmodium / drug effects
  • Protein Kinases / chemistry
  • Protein Kinases / drug effects*
  • Protozoan Proteins / metabolism
  • Toxoplasma / drug effects*
  • Toxoplasma / enzymology*
  • Toxoplasmosis / parasitology

Substances

  • Protozoan Proteins
  • Protein Kinases
  • calcium-dependent protein kinase