Molecular Modeling Studies ofYersinia pestisDihydrofolate Reductase-Reference-Cited by-同舟云学术

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Molecular Modeling Studies ofYersinia pestisDihydrofolate Reductase

Published:2011-10 Issue:2 Volume:29 Page:351-367
ISSN:0739-1102
Container-title:Journal of Biomolecular Structure and Dynamics
language:en
Short-container-title:Journal of Biomolecular Structure and Dynamics

Author:

Oliveira Aline A.,Rennó Magdalena N.,de Matos César A. S.,Bertuzzi Morena D.,Ramalho Teodorico C.,Fraga Carlos A.M.,França Tanos C. C.

Publisher

Informa UK Limited

Subject

Molecular Biology,General Medicine,Structural Biology

Link

http://www.tandfonline.com/doi/pdf/10.1080/10256018808623883

Reference93 articles.

1. Yersinia pestis, the cause of plague, is a recently emerged clone of Yersinia pseudotuberculosis

2. Yersinia pestis--etiologic agent of plague

3. Protein regions important for plasminogen activation and inactivation of alpha2-antiplasmin in the surface protease Pla of Yersinia pestis

4. Zoonotic Focus of Plague, Algeria

5. Fleas and flea-borne diseases

Cited by 15 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. Dihydrofolate Reductase (DHFR) Inhibitors: A Comprehensive Review;Current Medicinal Chemistry;2024-02

2. Microwave-assisted Synthesis and Docking Studies of Phenylureas as Candidates for the Drug Design Against the Biological Warfare Agent Yersinia Pestis;Letters in Drug Design & Discovery;2020-05-18

3. A multilayer screening approach toward the discovery of novel Pf -DHFR inhibitors;Computational Biology and Chemistry;2016-06

4. Analyses of the Binding between Water Soluble C60 Derivatives and Potential Drug Targets through a Molecular Docking Approach;PLOS ONE;2016-02-01

5. Virtual screening, docking, and dynamics of potential new inhibitors of dihydrofolate reductase from Yersinia pestis;Journal of Biomolecular Structure and Dynamics;2016-01-11

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