Molecular docking and ligand specificity in fragment-based inhibitor discovery
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cell Biology,Molecular Biology
Link
http://www.nature.com/articles/nchembio.155.pdf
Reference41 articles.
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3. Murray, C.W. et al. Application of fragment screening by X-ray crystallography to beta-secretase. J. Med. Chem. 50, 1116–1123 (2007).
4. Haydon, D.J. et al. An inhibitor of FtsZ with potent and selective anti-staphylococcal activity. Science 321, 1673–1675 (2008).
5. Card, G.L. et al. A family of phosphodiesterase inhibitors discovered by cocrystallography and scaffold-based drug design. Nat. Biotechnol. 23, 201–207 (2005).
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