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Organic Letters|October 24, 2003
Stereochemical control of skeletal diversityJason K Sello, Peter R Andreana, Daesung Lee, et al.
ACS Chemical Biology|September 20, 2013
Antibacterial activity of and resistance to small molecule inhibitors of the ClpP peptidaseCorey L Compton, Karl R Schmitz, Robert T Sauer, et al.
ACS Infectious Diseases|September 14, 2016
Fragment-Based Strategy for Investigating and Suppressing the Efflux of Bioactive Small MoleculesCorey L Compton, Daniel W Carney, Patrice V Groomes, et al.
Bioorganic & Medicinal Chemistry|September 14, 2010
Diversity-oriented synthesis of cyclic acyldepsipeptides leads to the discovery of a potent antibacterial agentAaron M Socha, Nicholas Y Tan, Kerry L LaPlante, et al.
Organic Letters|June 6, 2025
Total Syntheses of Stereoisomeric Congeners of Rufomycin Natural Products Having Anti-Mycobacterial ActivityFan Fei, Shichun Lun, Alexander Pacheco, et al.
Journal of Bacteriology|June 3, 2015
Genetic and Proteomic Analyses of Pupylation in Streptomyces coelicolorCorey L Compton, Michael S Fernandopulle, Rohith T Nagari, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 2014
Crystal structure of Mycobacterium tuberculosis ClpP1P2 suggests a model for peptidase activation by AAA+ partner binding and substrate deliveryKarl R Schmitz, Daniel W Carney, Jason K Sello, et al.
Bioorganic & Medicinal Chemistry|August 23, 2015
Substrate-guided optimization of the syringolins yields potent proteasome inhibitors with activity against leukemia cell linesKyle A Totaro, Dominik Barthelme, Peter T Simpson, et al.
Nucleic Acids Research|December 15, 2017
A peculiar IclR family transcription factor regulates para-hydroxybenzoate catabolism in Streptomyces coelicolorRui Zhang, Dana M Lord, Rakhi Bajaj, et al.
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