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Light-Activatable, 2,5-Disubstituted Tetrazoles for the Proteome-wide Profiling of Aspartates and Glutamates in Living Bacteria

[Image: see text] Covalent inhibitors have recently seen a resurgence of interest in drug development. Nevertheless, compounds, which do not rely on an enzymatic activity, have almost exclusively been developed to target cysteines. Expanding the scope to other amino acids would be largely facilitate...

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Detalles Bibliográficos
Autores principales: Bach, Kathrin, Beerkens, Bert L. H., Zanon, Patrick R. A., Hacker, Stephan M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7181327/
https://www.ncbi.nlm.nih.gov/pubmed/32342004
http://dx.doi.org/10.1021/acscentsci.9b01268

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