| Literature DB >> 33613463 |
David Rotella1, John Siekierka1, Purnima Bhanot2.
Abstract
The primary effector of cGMP signaling in Plasmodium is the cGMP-dependent protein kinase (PKG). Work in human-infective Plasmodium falciparum and rodent-infective Plasmodium berghei has provided biological validation of P. falciparum PKG (PfPKG) as a drug target for treating and/or protecting against malaria. PfPKG is essential in the asexual erythrocytic and sexual cycles as well as the pre-erythrocytic cycle. Medicinal chemistry efforts, both target-based and phenotype-based, have targeted PfPKG in the past few years. This review provides a brief overview of their results and challenges.Entities:
Keywords: Plasmodium; cGMP signaling; kinase; malaria; second messenger
Year: 2021 PMID: 33613463 PMCID: PMC7886688 DOI: 10.3389/fmicb.2020.610408
Source DB: PubMed Journal: Front Microbiol ISSN: 1664-302X Impact factor: 5.640