Cargando…
Discovery of Fragment Molecules That Bind the Human Peroxiredoxin 5 Active Site
The search for protein ligands is a crucial step in the inhibitor design process. Fragment screening represents an interesting method to rapidly find lead molecules, as it enables the exploration of a larger portion of the chemical space with a smaller number of compounds as compared to screening ba...
Autores principales: | Barelier, Sarah, Linard, Dominique, Pons, Julien, Clippe, André, Knoops, Bernard, Lancelin, Jean-Marc, Krimm, Isabelle |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2840032/ https://www.ncbi.nlm.nih.gov/pubmed/20305821 http://dx.doi.org/10.1371/journal.pone.0009744 |
Ejemplares similares
-
The curious case of peroxiredoxin-5: what its absence in aves can tell us and how it can be used
por: Pirson, Marc, et al.
Publicado: (2018) -
Abolition of Peroxiredoxin-5 Mitochondrial Targeting during Canid Evolution
por: Van der Eecken, Valérie, et al.
Publicado: (2013) -
Role of the Redox State of Human Peroxiredoxin-5 on Its TLR4-Activating DAMP Function
por: Poncin, Mégane A., et al.
Publicado: (2021) -
1D NMR WaterLOGSY as an efficient method for fragment-based lead discovery
por: Raingeval, Claire, et al.
Publicado: (2019) -
Fragment-based discovery of a new family of non-peptidic small-molecule cyclophilin inhibitors with potent antiviral activities
por: Ahmed-Belkacem, Abdelhakim, et al.
Publicado: (2016)