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Titlebook: G Protein-Coupled Receptors - Modeling and Simulation; Marta Filizola Book 2014 The Editor(s) (if applicable) and The Author(s), under exc

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楼主: CLIP
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Erratum to: B. Seehäfen und Seekanäle with their ligands, and to assess their applicability the rational discovery of GPCR modulators. Given the current state of the art and the pace of the field, the future of GPCR structural studies is likely to be characterized by a landscape populated by an increasingly higher number of experimental and theoretical structures.
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The GPCR Crystallography Boom: Providing an Invaluable Source of Structural Information and Expandin with their ligands, and to assess their applicability the rational discovery of GPCR modulators. Given the current state of the art and the pace of the field, the future of GPCR structural studies is likely to be characterized by a landscape populated by an increasingly higher number of experimental and theoretical structures.
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,Berichte der Arbeitsausschüsse,he use of homology modeling techniques for building three-dimensional models of homologous G protein–coupled receptors, higher order oligomers, and their complexes with ligands and signaling proteins.
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Modeling of G Protein-Coupled Receptors Using Crystal Structures: From Monomers to Signaling Complexhe use of homology modeling techniques for building three-dimensional models of homologous G protein–coupled receptors, higher order oligomers, and their complexes with ligands and signaling proteins.
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Beyond Standard Molecular Dynamics: Investigating the Molecular Mechanisms of G Protein-Coupled Receing mechanistic details of complex receptor processes such as ligand recognition, activation, and oligomerization. We provide here an overview of these methods in their most recent application to the field.
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Structure and Dynamics of G-Protein Coupled Receptors kink angle on the transmembrane helix6. The activation mechanism of the β.-adrenergic receptor has been studied using multiscale computational methods. The results of these studies showed that the receptor without any ligand bound, samples conformations that resemble some of the structural characte
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