Cargando…
Increased Conformational Flexibility of a Macrocycle–Receptor Complex Contributes to Reduced Dissociation Rates
Constraining a peptide in its bioactive conformation by macrocyclization represents a powerful strategy to design modulators of challenging biomolecular targets. This holds particularly true for the development of inhibitors of protein‐protein interactions which often involve interfaces lacking defi...
Autores principales: | Glas, Adrian, Wamhoff, Eike‐Christian, Krüger, Dennis M., Rademacher, Christoph, Grossmann, Tom N. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5724689/ https://www.ncbi.nlm.nih.gov/pubmed/28777495 http://dx.doi.org/10.1002/chem.201702776 |
Ejemplares similares
-
Adapting free energy perturbation simulations for large macrocyclic ligands: how to dissect contributions from direct binding and free ligand flexibility
por: Wallraven, Kerstin, et al.
Publicado: (2020) -
Structure-Based
Design of Non-natural Macrocyclic
Peptides That Inhibit Protein–Protein Interactions
por: Krüger, Dennis M., et al.
Publicado: (2017) -
Computational and Experimental Prediction of Human C-Type Lectin Receptor Druggability
por: Aretz, Jonas, et al.
Publicado: (2014) -
Protein Macrocyclization for Tertiary Structure Stabilization
por: Haim, Anissa, et al.
Publicado: (2021) -
Navigating complex peptide structures using macrocycle conformational maps
por: McTiernan, Timothy J., et al.
Publicado: (2022)