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Structure (London, England : 1993)|July 17, 2009
Crystal structures of Mycobacterium tuberculosis KasA show mode of action within cell wall biosynthesis and its inhibition by thiolactomycinSylvia R Luckner, Carl A Machutta, Peter J Tonge, et al.
Bioorganic Chemistry|February 7, 2006
A Raman-active competitive inhibitor of OMP decarboxylaseBrian P Callahan, Alasdair F Bell, Peter J Tonge, et al.
Biochemistry|January 24, 2007
Structure and mechanism of MbtI, the salicylate synthase from Mycobacterium tuberculosisJacque Zwahlen, Subramaniapillai Kolappan, Rong Zhou, et al.
Protein Science : a Publication of the Protein Society|June 30, 2007
Probing mechanisms of resistance to the tuberculosis drug isoniazid: Conformational changes caused by inhibition of InhA, the enoyl reductase from Mycobacterium tuberculosisNicole A Kruh, Richa Rawat, Béla P Ruzsicska, et al.
The Journal of Antimicrobial Chemotherapy|September 8, 2009
Substituted diphenyl ethers as a broad-spectrum platform for the development of chemotherapeutics for the treatment of tularaemiaKathleen England, Christopher am Ende, Hao Lu, et al.
Current Topics in Medicinal Chemistry|March 10, 2007
FtsZ: a novel target for tuberculosis drug discoveryQing Huang, Peter J Tonge, Richard A Slayden, et al.
Biochemistry|May 28, 2011
Elucidation of the protonation states of the catalytic residues in mtKasA: implications for inhibitor designWook Lee, Sylvia R Luckner, Caroline Kisker, et al.
Journal of the American Chemical Society|June 5, 2003
Light-driven decarboxylation of wild-type green fluorescent proteinAlasdair F Bell, Deborah Stoner-Ma, Rebekka M Wachter, et al.
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