Cargando…
Precise Probing of Residue Roles by Post-Translational β,γ-C,N Aza-Michael Mutagenesis in Enzyme Active Sites
[Image: see text] Biomimicry valuably allows the understanding of the essential chemical components required to recapitulate biological function, yet direct strategies for evaluating the roles of amino acids in proteins can be limited by access to suitable, subtly-altered unnatural variants. Here we...
Autores principales: | Dadová, Jitka, Wu, Kuan-Jung, Isenegger, Patrick G., Errey, James C., Bernardes, Gonçalo J. L., Chalker, Justin M., Raich, Lluís, Rovira, Carme, Davis, Benjamin G. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2017
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5704290/ https://www.ncbi.nlm.nih.gov/pubmed/29202018 http://dx.doi.org/10.1021/acscentsci.7b00341 |
Ejemplares similares
-
Chemoselective
Installation of Amine Bonds on Proteins
through Aza-Michael Ligation
por: Freedy, Allyson M., et al.
Publicado: (2017) -
Synthesis of highly substituted tetrahydroquinolines using ethyl cyanoacetate via aza-Michael–Michael addition
por: Palanimuthu, Arunan, et al.
Publicado: (2020) -
Recent advances in organocatalytic asymmetric aza-Michael reactions of amines and amides
por: Sharma, Pratibha, et al.
Publicado: (2021) -
The complete conformational free energy landscape of β-xylose reveals a two-fold catalytic itinerary for β-xylanases
por: Iglesias-Fernández, Javier, et al.
Publicado: (2015) -
Aza-Michael Mono-addition Using Acidic Alumina under Solventless Conditions
por: Bosica, Giovanna, et al.
Publicado: (2016)