Crystal structures of Mycobacterium tuberculosis GlgE and complexes with non-covalent inhibitors
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/srep12830.pdf
Reference33 articles.
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2. Ford, C. B. et al. Use of whole genome sequencing to estimate the mutation rate of Mycobacterium tuberculosis during latent infection. Nature genetics 43, 482–486 (2011).
3. Moonan, P. K. et al. Does directly observed therapy (DOT) reduce drug resistant tuberculosis? Bmc Public Health 11, 19 (2011).
4. Udwadia, Z. F., Amale, R. A., Ajbani, K. K. & Rodrigues, C. Totally drug-resistant tuberculosis in India. Clinical infectious diseases: an official publication of the Infectious Diseases Society of America 54, 579–581 (2012).
5. Kalscheuer, R. et al. Self-poisoning of Mycobacterium tuberculosis by targeting GlgE in an alpha-glucan pathway. Nature chemical biology 6, 376–384 (2010).
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