Carregant...
Miniatura

Tipus de document

Article

Versió

Versió publicada

Data de publicació

Llicència de publicació

cc-by (c) Majewski, Meciej et al., 2019
Si us plau utilitzeu sempre aquest identificador per citar o enllaçar aquest document: https://hdl.handle.net/2445/163382

An investigation of structural stability in protein-ligand complexes reveals the balance between order and disorder

Títol de la revista

Director/Tutor

ISSN de la revista

Títol del volum

Resum

The predominant view in structure-based drug design is that small-molecule ligands, once bound to their target structures, display a well-defined binding mode. However, structural stability (robustness) is not necessary for thermodynamic stability (binding affinity). In fact, it entails an entropic penalty that counters complex formation. Surprisingly, little is known about the causes, consequences and real degree of robustness of protein-ligand complexes. Since hydrogen bonds have been described as essential for structural stability, here we investigate 469 such interactions across two diverse structure sets, comprising of 79 drug-like and 27 fragment ligands, respectively. Completely constricted protein-ligand complexes are rare and may fulfill a functional role. Most complexes balance order and disorder by combining a single anchoring point with looser regions. 25% do not contain any robust hydrogen bond and may form loose structures. Structural stability analysis reveals a hidden layer of complexity in protein-ligand complexes that should be considered in ligand design.

Citació

Citació

MAJEWSKI, Maciej, RUIZ CARMONA, Sergio, BARRIL ALONSO, Xavier. An investigation of structural stability in protein-ligand complexes reveals the balance between order and disorder. _Communications Chemistry_. 2019. Vol. 2, núm. 110. [consulta: 21 de gener de 2026]. ISSN: 2399-3669. [Disponible a: https://hdl.handle.net/2445/163382]

Exportar metadades

JSON - METS

Compartir registre