Plasmodium falciparum cGMP-Dependent Protein Kinase - A Novel Chemotherapeutic Target.

Plasmodium falciparum cGMP-Dependent Protein Kinase - A Novel Chemotherapeutic Target.
复制标题

DOI:
10.3389/fmicb.2020.610408
复制
发表时间:
2020
影响因子:
5.2
通讯作者:
Bhanot P
Bhanot P
中科院分区:
生物学2区
文献类型:
--
作者:
Rotella D;Siekierka J;Bhanot P

文献摘要

参考文献

相似文献

在疟原虫中,cGMP信号的主要效应者是cGMP依赖的蛋白激酶(PKG)。对人类感染的恶性疟原虫和啮齿动物感染的伯氏疟原虫的研究为恶性疟原虫PKG(PfPKG)作为治疗和/或预防疟疾的药物靶标提供了生物学验证。PfPKG在无性红细胞周期和有性周期以及前红细胞周期中是必不可少的。在过去的几年里,基于靶点和基于表型的药物化学努力一直以PfPKG为目标。本审查简要概述了它们的成果和挑战。
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.
DOI: 10.1016/j.jmb.2007.11.053
发表时间: 2008-02-01
影响因子: 5.6
作者:
Alverdi, Vera;Mazon, Hortense;Heck, Albert J. R.
通讯作者: Heck, Albert J. R.
DOI: 10.1021/acsinfecdis.7b00222
发表时间: 2018-03-01
影响因子: 5.3
作者:
Franz, Eugen;Knape, Matthias J.;Herberg, Friedrich W.
通讯作者: Herberg, Friedrich W.
DOI: 10.1371/journal.ppat.1003344
发表时间: 2013-05
期刊: PLoS pathogens
影响因子: 6.7
作者:
Collins CR;Hackett F;Strath M;Penzo M;Withers-Martinez C;Baker DA;Blackman MJ
通讯作者: Blackman MJ
DOI: 10.1128/aac.00519-09
发表时间: 2009-10-01
影响因子: 4.9
作者:
Belen Jimenez-Diaz, Maria;Mulet, Teresa;Angulo-Barturen, Inigo
通讯作者: Angulo-Barturen, Inigo
DOI: 10.1016/j.molbiopara.2005.10.020
发表时间: 2006-03-01
影响因子: 1.5
作者:
Diaz, CA;Allocco, J;Liberator, PA
通讯作者: Liberator, PA