Cargando…
3-Fluoro-4-hydroxyprolines: Synthesis, Conformational Analysis, and Stereoselective Recognition by the VHL E3 Ubiquitin Ligase for Targeted Protein Degradation
[Image: see text] Hydroxylation and fluorination of proline alters the pyrrolidine ring pucker and the trans:cis amide bond ratio in a stereochemistry-dependent fashion, affecting molecular recognition of proline-containing molecules by biological systems. While hydroxyprolines and fluoroprolines ar...
Autores principales: | Testa, Andrea, Lucas, Xavier, Castro, Guilherme V., Chan, Kwok-Ho, Wright, Jane E., Runcie, Andrew C., Gadd, Morgan S., Harrison, William T. A., Ko, Eun-Jung, Fletcher, Daniel, Ciulli, Alessio |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2018
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6430500/ https://www.ncbi.nlm.nih.gov/pubmed/29949369 http://dx.doi.org/10.1021/jacs.8b05807 |
Ejemplares similares
-
Correction
to “3-Fluoro-4-hydroxyprolines:
Synthesis, Conformational Analysis, and Stereoselective Recognition
by the VHL E3 Ubiquitin Ligase for Targeted Protein Degradation”
por: Testa, Andrea, et al.
Publicado: (2019) -
Crystal Structure of the Cul2-Rbx1-EloBC-VHL Ubiquitin Ligase Complex
por: Cardote, Teresa A.F., et al.
Publicado: (2017) -
Thioamide substitution to probe the hydroxyproline recognition of VHL ligands
por: Soares, Pedro, et al.
Publicado: (2018) -
Homo-PROTACs: bivalent small-molecule dimerizers of the VHL E3 ubiquitin ligase to induce self-degradation
por: Maniaci, Chiara, et al.
Publicado: (2017) -
Cereblon versus VHL: Hijacking E3 ligases against each other using PROTACs
por: Girardini, Miriam, et al.
Publicado: (2019)