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The Dynamic Process of Drug-GPCR Binding at Either Orthosteric or Allosteric Sites Evaluated by Metadynamics

Major advances in G Protein-Coupled Receptor (GPCR) structural biology over the past few years have yielded a significant number of high-resolution crystal structures for several different receptor subtypes. This dramatic increase in GPCR structural information has underscored the use of automated d...

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Vydáno v:Methods Mol Biol
Hlavní autoři: Schneider, Sebastian, Provasi, Davide, Filizola, Marta
Médium: Artigo
Jazyk:Inglês
Vydáno: 2015
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On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4703114/
https://ncbi.nlm.nih.gov/pubmed/26260607
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/978-1-4939-2914-6_18
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