High-Affinity Inhibition of a Family of Plasmodium falciparum Proteases by a Designed Adaptive Inhibitor-Reference-Cited by-同舟云学术

High-Affinity Inhibition of a Family of Plasmodium falciparum Proteases by a Designed Adaptive Inhibitor

Published:2003-06-21 Issue:28 Volume:42 Page:8459-8464
ISSN:0006-2960
Container-title:Biochemistry
language:en
Short-container-title:Biochemistry

Author:

Nezami Azin¹,Kimura Tooru¹,Hidaka Koushi¹,Kiso Aiko¹,Liu Jun¹,Kiso Yoshiaki¹,Goldberg Daniel E.¹,Freire Ernesto¹

Affiliation:

1. Department of Biology, The Johns Hopkins University, Baltimore, Maryland 21218, Department of Medicinal Chemistry, Center for Frontier Research in Medicinal Science, Kyoto Pharmaceutical University, Yamashina-ku, Kyoto 607-8412, Japan, and Howard Hughes Medical Institute, Departments of Medicine and Molecular Microbiology, Washington University School of Medicine, St. Louis, Missouri 63110

Publisher

American Chemical Society (ACS)

Subject

Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/bi034131z

Reference16 articles.

1. A distinct member of the aspartic proteinase gene family from the human malaria parasite Plasmodium falciparum

2. Designing drugs against heterogeneous targets

Cited by 108 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Dual effects of Pepstatin A on Plasmodium falciparum asexual blood-stage and early gametocyte development;2024-07-12

2. Trends of antimalarial marine natural products: progresses, challenges and opportunities;Natural Product Reports;2022

3. Investigation of the Effect of Loratadine and Calcium Ions on Oxidoreductase Activity of Catalase Enzyme;Current Enzyme Inhibition;2021-01

4. Plasmepsin Inhibitors in Antimalarial Drug Discovery: Medicinal Chemistry and Target Validation (2000 to Present);Journal of Medicinal Chemistry;2020-01-08

5. Plasmepsins as targets for antimalarial agents;Antimalarial Agents;2020