Blocking Plasmodium falciparum development via dual inhibition of hemoglobin degradation and the ubiquitin proteasome system by MG132.

Blocking Plasmodium falciparum development via dual inhibition of hemoglobin degradation and the ubiquitin proteasome system by MG132.

Among key potential drug target proteolytic systems in the malaria parasite Plasmodium falciparum are falcipains, a family of hemoglobin-degrading cysteine proteases, and the ubiquitin proteasomal system (UPS), which has fundamental importance in cellular protein turnover. Inhibition of falcipains b...

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Bibliographic Details
Main Authors: Rajesh Prasad, Atul, Venkata Karunakar Kolla, Jennifer Legac, Neha Singhal, Rahul Navale, Philip J Rosenthal, Puran Singh Sijwali
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3759421?pdf=render

Internet

http://europepmc.org/articles/PMC3759421?pdf=render

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