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Systematic exploration of multiple drug binding sites
BACKGROUND: Targets with multiple (prerequisite or allosteric) binding sites have an increasing importance in drug design. Experimental determination of atomic resolution structures of ligands weakly bound to multiple binding sites is often challenging. Blind docking has been widely used for fast ma...
Autores principales: | Bálint, Mónika, Jeszenői, Norbert, Horváth, István, van der Spoel, David, Hetényi, Csaba |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5745209/ https://www.ncbi.nlm.nih.gov/pubmed/29282592 http://dx.doi.org/10.1186/s13321-017-0255-6 |
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