Exploring structural requirements for the inhibition of Plasmodium falciparum calcium-dependent protein kinase-4 (PfCDPK-4) using multiple in silico approaches
Author:
Affiliation:
1. Drug Theoretics and Cheminformatics Laboratory
2. Department of Pharmaceutical Technology
3. Jadavpur University
4. Kolkata 700032
5. India
Abstract
Plasmodial protein kinases represent one of the most important thrust areas for antimalarial drug discovery.
Funder
University Grants Commission
Indian Council of Medical Research
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemical Engineering,General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2016/RA/C6RA05692J
Reference31 articles.
1. World Health Organization , World Malaria Report 2012, World Health Organization, Geneva, 2012, available at: http://www.who.int/malaria/publications/world_malaria_report_2012/en, accessed 22 Feb. 2016
2. First report on exploring classification and regression based QSAR modelling ofPlasmodium falciparumglycogen synthase kinase (PfGSK-3) inhibitors
3. Development of potent and selective Plasmodium falciparum calcium-dependent protein kinase 4 (PfCDPK4) inhibitors that block the transmission of malaria to mosquitoes
4. Characteristics of the Plasmodium falciparum PK5 ATP-binding site: implications for the design of novel antimalarial agents
5. Selective inhibition of Pfmrk, a Plasmodium falciparum CDK, by antimalarial 1,3-diaryl-2-propenones
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