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The structure and function of the glucagon‐like peptide‐1 receptor and its ligands

British journal of pharmacology, 2012-05, Vol.166 (1), p.27-41

Donnelly, Dan

2012

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Glucagon-Like Peptide-1 and Its Class B G Protein-Coupled Receptors: A Long March to Therapeutic Successes

Pharmacological reviews, 2016-10, Vol.68 (4), p.954-1013

2016

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The GIP receptor displays higher basal activity than the GLP-1 receptor but does not recruit GRK2 or arrestin3 effectively

PloS one, 2014-09, Vol.9 (9), p.e106890

2014

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A model for receptor–peptide binding at the glucagon‐like peptide‐1 (GLP‐1) receptor through the analysis of truncated ligands and receptors

British journal of pharmacology, 2003-09, Vol.140 (2), p.339-346

2003

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Mapping interaction sites within the N-terminus of the calcitonin gene-related peptide receptor; the role of residues 23–60 of the calcitonin receptor-like receptor

Peptides (New York, N.Y. : 1980), 2010-01, Vol.31 (1), p.170-176

2010

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Ligand-Receptor Interactions at the Parathyroid Hormone Receptors: Subtype Binding Selectivity Is Mediated via an Interaction between Residue 23 on the Ligand and Residue 41 on the Receptor

Molecular pharmacology, 2008-09, Vol.74 (3), p.605-613

2008

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The Isolated N-terminal Domain of the Glucagon-like Peptide-1 (GLP-1) Receptor Binds Exendin Peptides with Much Higher Affinity than GLP-1

The Journal of biological chemistry, 2003-03, Vol.278 (12), p.10195-10200

2003

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The structure and function of the glucagon-like peptide-1 receptor and its ligands : Secretin Family (Class B) G Protein-Coupled Receptors - from Molecular to Clinical Perspectives

British journal of pharmacology, 2012, Vol.166 (1), p.27-41

DONNELLY, Dan

2012

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A mechanism for agonist activation of the glucagon-like peptide-1 (GLP-1) receptor through modelling & molecular dynamics

Biochemical and biophysical research communications, 2018-03, Vol.498 (2), p.359-365

2018

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The Conformational Change Responsible for AT1 Receptor Activation Is Dependent upon Two Juxtaposed Asparagine Residues on Transmembrane Helices III and VII

The Journal of biological chemistry, 1997-02, Vol.272 (7), p.4245-4251

1997

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The peptide agonist-binding site of the glucagon-like peptide-1 (GLP-1) receptor based on site-directed mutagenesis and knowledge-based modelling

Bioscience reports, 2016-02, Vol.36 (1), p.e00285-e00285

2016

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The primary ligand-binding interaction at the GLP-1 receptor is via the putative helix of the peptide agonists

Protein and peptide letters, 2004-02, Vol.11 (1), p.9

2004

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N‑Terminal Phosphorylation of Parathyroid Hormone (PTH) Abolishes Its Receptor Activity

ACS chemical biology, 2014-11, Vol.9 (11), p.2465-2470

2014

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High affinity binding of the peptide agonist TIP-39 to the parathyroid hormone 2 (PTH2) receptor requires the hydroxyl group of Tyr-318 on transmembrane helix 5

Biochemical pharmacology, 2017-03, Vol.127, p.71-81

2017

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Met-204 and Tyr-205 are together important for binding GLP-1 receptor agonists but not their N-terminally truncated analogues

Protein and peptide letters, 2004-02, Vol.11 (1), p.15

2004

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Cover, Volume 42, Issue 2

Human mutation, 2021-02, Vol.42 (2), p.ii-ii

2021

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A salt bridge between Arg-20 on parathyroid hormone (PTH) and Asp-137 on the PTH sub(1) receptor is essential for full affinity

Peptides (New York, N.Y. : 1980), 2014-01, Vol.61, p.83-87

2014

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A salt bridge between Arg-20 on parathyroid hormone (PTH) and Asp-137 on the PTH1 receptor is essential for full affinity

Peptides (New York, N.Y. : 1980), 2014-11, Vol.61, p.83-87

2014

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The arrangement of the transmembrane helices in the secretin receptor family of G-protein-coupled receptors

FEBS letters, 1997-06, Vol.409 (3), p.431-436

Donnelly, Dan

1997

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Non-peptidic antagonists of the CGRP receptor, BIBN4096BS and MK-0974, interact with the calcitonin receptor-like receptor via methionine-42 and RAMP1 via tryptophan-74

Biochemical and biophysical research communications, 2010-01, Vol.391 (1), p.437-442

2010

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The positive charge at Lys-288 of the glucagon-like peptide-1 (GLP-1) receptor is important for binding the N-terminus of peptide agonists

FEBS letters, 2003-10, Vol.553 (3), p.342-346

2003

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Interactions of the Melanocortin-4 Receptor with the Peptide Agonist NDP-MSH

Journal of molecular biology, 2010-08, Vol.401 (3), p.433-450

2010

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The glucagon-like peptide-1 receptor binding site for the N-terminus of GLP-1 requires polarity at Asp198 rather than negative charge

FEBS letters, 2002-10, Vol.530 (1), p.244-248

2002

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Aneuploidy and copy number breakpoints in the genome of lager yeasts mapped by microarray hybridisation

Current genetics, 2004-06, Vol.45 (6), p.360-370

2004

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Functional coupling of Cys-226 and Cys-296 in the glucagon-like peptide-1 (GLP-1) receptor indicates a disulfide bond that is close to the activation pocket

Peptides (New York, N.Y. : 1980), 2010-12, Vol.31 (12), p.2289-2293

2010

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The structure and function of the glucagon‐like peptide‐1 receptor and its ligands

Glucagon-Like Peptide-1 and Its Class B G Protein-Coupled Receptors: A Long March to Therapeutic Successes

The GIP receptor displays higher basal activity than the GLP-1 receptor but does not recruit GRK2 or arrestin3 effectively

A model for receptor–peptide binding at the glucagon‐like peptide‐1 (GLP‐1) receptor through the analysis of truncated ligands and receptors

Mapping interaction sites within the N-terminus of the calcitonin gene-related peptide receptor; the role of residues 23–60 of the calcitonin receptor-like receptor

Ligand-Receptor Interactions at the Parathyroid Hormone Receptors: Subtype Binding Selectivity Is Mediated via an Interaction between Residue 23 on the Ligand and Residue 41 on the Receptor

The Isolated N-terminal Domain of the Glucagon-like Peptide-1 (GLP-1) Receptor Binds Exendin Peptides with Much Higher Affinity than GLP-1

The structure and function of the glucagon-like peptide-1 receptor and its ligands : Secretin Family (Class B) G Protein-Coupled Receptors - from Molecular to Clinical Perspectives

A mechanism for agonist activation of the glucagon-like peptide-1 (GLP-1) receptor through modelling & molecular dynamics

The Conformational Change Responsible for AT1 Receptor Activation Is Dependent upon Two Juxtaposed Asparagine Residues on Transmembrane Helices III and VII

The peptide agonist-binding site of the glucagon-like peptide-1 (GLP-1) receptor based on site-directed mutagenesis and knowledge-based modelling

The primary ligand-binding interaction at the GLP-1 receptor is via the putative helix of the peptide agonists

N‑Terminal Phosphorylation of Parathyroid Hormone (PTH) Abolishes Its Receptor Activity

High affinity binding of the peptide agonist TIP-39 to the parathyroid hormone 2 (PTH2) receptor requires the hydroxyl group of Tyr-318 on transmembrane helix 5

Met-204 and Tyr-205 are together important for binding GLP-1 receptor agonists but not their N-terminally truncated analogues

Cover, Volume 42, Issue 2

A salt bridge between Arg-20 on parathyroid hormone (PTH) and Asp-137 on the PTH sub(1) receptor is essential for full affinity

A salt bridge between Arg-20 on parathyroid hormone (PTH) and Asp-137 on the PTH1 receptor is essential for full affinity

The arrangement of the transmembrane helices in the secretin receptor family of G-protein-coupled receptors

Non-peptidic antagonists of the CGRP receptor, BIBN4096BS and MK-0974, interact with the calcitonin receptor-like receptor via methionine-42 and RAMP1 via tryptophan-74

The positive charge at Lys-288 of the glucagon-like peptide-1 (GLP-1) receptor is important for binding the N-terminus of peptide agonists

Interactions of the Melanocortin-4 Receptor with the Peptide Agonist NDP-MSH

The glucagon-like peptide-1 receptor binding site for the N-terminus of GLP-1 requires polarity at Asp198 rather than negative charge

Aneuploidy and copy number breakpoints in the genome of lager yeasts mapped by microarray hybridisation

Functional coupling of Cys-226 and Cys-296 in the glucagon-like peptide-1 (GLP-1) receptor indicates a disulfide bond that is close to the activation pocket

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