Pages that link to "Q27682443"
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The following pages link to The 2.1 Å Resolution Structure of Cyanopindolol-Bound β1-Adrenoceptor Identifies an Intramembrane Na+ Ion that Stabilises the Ligand-Free Receptor (Q27682443):
Displaying 50 items.
- Membrane potentials regulating GPCRs: insights from experiments and molecular dynamics simulations (Q26740438) (← links)
- Large-scale production and protein engineering of G protein-coupled receptors for structural studies (Q26866010) (← links)
- Molecular switches of the κ opioid receptor triggered by 6'-GNTI and 5'-GNTI. (Q27302413) (← links)
- Sequence, structure and ligand binding evolution of rhodopsin-like G protein-coupled receptors: a crystal structure-based phylogenetic analysis (Q28649590) (← links)
- How Do Short Chain Nonionic Detergents Destabilize G-Protein-Coupled Receptors? (Q30831488) (← links)
- Allosteric sodium in class A GPCR signaling (Q33931569) (← links)
- Mechanistic insights into the allosteric modulation of opioid receptors by sodium ions (Q34041202) (← links)
- Structural insights into µ-opioid receptor activation (Q34488374) (← links)
- Disruption of the Na+ ion binding site as a mechanism for positive allosteric modulation of the mu-opioid receptor (Q34793269) (← links)
- Allosteric effects of sodium ion binding on activation of the m3 muscarinic g-protein-coupled receptor (Q35333859) (← links)
- Stabilization of G protein-coupled receptors by point mutations (Q35486811) (← links)
- The purification and characterization of ATP synthase complexes from the mitochondria of four fungal species (Q35576179) (← links)
- Eukaryotic G protein-coupled receptors as descendants of prokaryotic sodium-translocating rhodopsins (Q35809744) (← links)
- GPCR structure, function, drug discovery and crystallography: report from Academia-Industry International Conference (UK Royal Society) Chicheley Hall, 1-2 September 2014. (Q35830953) (← links)
- Fusion-protein-assisted protein crystallization (Q35841518) (← links)
- Structural prerequisites for G-protein activation by the neurotensin receptor (Q35891222) (← links)
- Structural dynamics and thermostabilization of neurotensin receptor 1 (Q36044571) (← links)
- Pharmacological Analysis and Structure Determination of 7-Methylcyanopindolol-Bound β1-Adrenergic Receptor. (Q36316813) (← links)
- Structural features embedded in G protein-coupled receptor co-crystal structures are key to their success in virtual screening (Q36336103) (← links)
- Molecular Determinants of CGS21680 Binding to the Human Adenosine A2A Receptor (Q36482631) (← links)
- Structural basis for Na(+)-sensitivity in dopamine D2 and D3 receptors (Q37585111) (← links)
- The receptor concept in 3D: from hypothesis and metaphor to GPCR-ligand structures (Q38237899) (← links)
- Modulation of GPCRs by monovalent cations and anions. (Q38272337) (← links)
- Signaling within Allosteric Machines: Signal Transmission Pathways Inside G Protein-Coupled Receptors. (Q38675922) (← links)
- Allosteric Modulators of the Class A G Protein Coupled Receptors (Q38847270) (← links)
- Quality control in eukaryotic membrane protein overproduction (Q38934286) (← links)
- Molecular Modelling Approaches for the Analysis of Histamine Receptors and Their Interaction with Ligands (Q39007384) (← links)
- New approaches towards the understanding of integral membrane proteins: A structural perspective on G protein-coupled receptors (Q39332114) (← links)
- Structure of the adenosine A(2A) receptor bound to an engineered G protein. (Q39555371) (← links)
- Engineering a minimal G protein to facilitate crystallisation of G protein-coupled receptors in their active conformation. (Q39768399) (← links)
- Backbone NMR reveals allosteric signal transduction networks in the β1-adrenergic receptor (Q40028443) (← links)
- Catestatin Gly364Ser Variant Alters Systemic Blood Pressure and the Risk for Hypertension in Human Populations via Endothelial Nitric Oxide Pathway (Q40690975) (← links)
- Conformational thermostabilisation of corticotropin releasing factor receptor 1. (Q41151319) (← links)
- Biased Gs versus Gq proteins and β-arrestin signaling in the NK1 receptor determined by interactions in the water hydrogen bond network (Q41455641) (← links)
- A mutagenesis and screening strategy to generate optimally thermostabilized membrane proteins for structural studies (Q42327908) (← links)
- Sodium ion binding pocket mutations and adenosine A2A receptor function. (Q42469733) (← links)
- Homology modeling of a Class A GPCR in the inactive conformation: A quantitative analysis of the correlation between model/template sequence identity and model accuracy (Q42806068) (← links)
- Propagation of the Allosteric Modulation Induced by Sodium in the δ-Opioid Receptor (Q44343199) (← links)
- D4 dopamine receptor high-resolution structures enable the discovery of selective agonists. (Q46445025) (← links)
- Insight into partial agonism by observing multiple equilibria for ligand-bound and Gs-mimetic nanobody-bound β1-adrenergic receptor (Q47118886) (← links)
- Na+-mimicking ligands stabilize the inactive state of leukotriene B4 receptor BLT1. (Q47194753) (← links)
- Intracellular Transfer of Na+ in an Active-State G-Protein-Coupled Receptor. (Q47241989) (← links)
- Molecular modeling and docking studies of the oxytocin receptor (Q47298705) (← links)
- Exploring GPCR-Ligand Interactions with the Fragment Molecular Orbital (FMO) Method (Q47348707) (← links)
- The action of a negative allosteric modulator at the dopamine D2 receptor is dependent upon sodium ions (Q47722639) (← links)
- X-ray structures of endothelin ETB receptor bound to clinical antagonist bosentan and its analog (Q47929318) (← links)
- Activation processes in ligand-activated G protein-coupled receptors: A case study of the adenosine A2A receptor (Q47979078) (← links)
- In silico studies targeting G-protein coupled receptors for drug research against Parkinson's disease. (Q52665081) (← links)
- Mechanistic insights into allosteric regulation of the A2A adenosine G protein-coupled receptor by physiological cations. (Q53831234) (← links)
- Synthesis and Characterization of a Bidirectional Photoswitchable Antagonist Toolbox for Real-Time GPCR Photopharmacology. (Q55232052) (← links)