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Structure of class B GPCR corticotropin-releasing factor receptor 1

Nature (London), 2013-07, Vol.499 (7459), p.438-443

2013

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Structure of class C GPCR metabotropic glutamate receptor 5 transmembrane domain

Nature (London), 2014-07, Vol.511 (7511), p.557-562

2014

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Structure of the complement C5a receptor bound to the extra-helical antagonist NDT9513727

Nature (London), 2018-01, Vol.553 (7686), p.111-114

2018

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Serial millisecond crystallography for routine room-temperature structure determination at synchrotrons

Nature communications, 2017-09, Vol.8 (1), p.542-11, Article 542

2017

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Controlling the Dissociation of Ligands from the Adenosine A2A Receptor through Modulation of Salt Bridge Strength

Journal of medicinal chemistry, 2016-07, Vol.59 (13), p.6470-6479

2016

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Crystal structure of the GLP-1 receptor bound to a peptide agonist

Nature (London), 2017-06, Vol.546 (7657), p.254-258

2017

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Extra-helical binding site of a glucagon receptor antagonist

Nature (London), 2016-05, Vol.533 (7602), p.274-277

2016

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Structural insight into allosteric modulation of protease-activated receptor 2

Nature (London), 2017-05, Vol.545 (7652), p.112-115

2017

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Crystal structures of the human neurokinin 1 receptor in complex with clinically used antagonists

Nature communications, 2019-01, Vol.10 (1), p.17-11, Article 17

2019

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Structure-Based Optimization Strategies for G Protein-Coupled Receptor (GPCR) Allosteric Modulators: A Case Study from Analyses of New Metabotropic Glutamate Receptor 5 (mGlu5) X‑ray Structures

Journal of medicinal chemistry, 2019-01, Vol.62 (1), p.207-222

2019

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Towards high throughput GPCR crystallography: In Meso soaking of Adenosine A2A Receptor crystals

Scientific reports, 2018-01, Vol.8 (1), p.1-41, Article 41

2018

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Biophysical Fragment Screening of the β1‑Adrenergic Receptor: Identification of High Affinity Arylpiperazine Leads Using Structure-Based Drug Design

Journal of medicinal chemistry, 2013-05, Vol.56 (9), p.3446-3455

2013

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Fragment and Structure-Based Drug Discovery for a Class C GPCR: Discovery of the mGlu5 Negative Allosteric Modulator HTL14242 (3-Chloro-5-[6-(5-fluoropyridin-2-yl)pyrimidin-4-yl]benzonitrile)

Journal of medicinal chemistry, 2015-08, Vol.58 (16), p.6653-6664

2015

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X‐Ray Crystallography and Free Energy Calculations Reveal the Binding Mechanism of A2A Adenosine Receptor Antagonists

Angewandte Chemie International Edition, 2020-09, Vol.59 (38), p.16536-16543

International ed. in English, 2020

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Outrunning free radicals in room-temperature macromolecular crystallography

Acta crystallographica. Section D, Biological crystallography., 2012-07, Vol.68 (7), p.810-818

2012

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SARS-CoV-2 Mpro responds to oxidation by forming disulfide and NOS/SONOS bonds

Nature communications, 2024-05, Vol.15 (1), p.3827-3827, Article 3827

2024

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Molecular basis for high-affinity agonist binding in GPCRs

Science (American Association for the Advancement of Science), 2019-05, Vol.364 (6442), p.775-778

2019

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Structures of Human A1 and A2A Adenosine Receptors with Xanthines Reveal Determinants of Selectivity

Structure (London), 2017-08, Vol.25 (8), p.1275-1285.e4

2017

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Intracellular allosteric antagonism of the CCR9 receptor

Nature (London), 2016-12, Vol.540 (7633), p.462-465

2016

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High-resolution crystal structure of parathyroid hormone 1 receptor in complex with a peptide agonist

Nature structural & molecular biology, 2018-12, Vol.25 (12), p.1086-1092

2018

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Structure of Class B GPCRs: new horizons for drug discovery

British journal of pharmacology, 2014-07, Vol.171 (13), p.3132-3145

2014

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Electron microscopy of Xrcc4 and the DNA ligase IV–Xrcc4 DNA repair complex

DNA repair, 2009-12, Vol.8 (12), p.1380-1389

2009

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Advancing structural biology through breakthroughs in AI

Current opinion in structural biology, 2023-06, Vol.80, p.102601-102601, Article 102601

2023

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Discovery of 1,2,4-Triazine Derivatives as Adenosine A2A Antagonists using Structure Based Drug Design

Journal of medicinal chemistry, 2012-03, Vol.55 (5), p.1898-1903

2012

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Structure of class B GPCR corticotropin-releasing factor receptor 1

Structure of class C GPCR metabotropic glutamate receptor 5 transmembrane domain

Structure of the complement C5a receptor bound to the extra-helical antagonist NDT9513727

Serial millisecond crystallography for routine room-temperature structure determination at synchrotrons

Controlling the Dissociation of Ligands from the Adenosine A2A Receptor through Modulation of Salt Bridge Strength

Crystal structure of the GLP-1 receptor bound to a peptide agonist

Extra-helical binding site of a glucagon receptor antagonist

Structural insight into allosteric modulation of protease-activated receptor 2

Crystal structures of the human neurokinin 1 receptor in complex with clinically used antagonists

Structure-Based Optimization Strategies for G Protein-Coupled Receptor (GPCR) Allosteric Modulators: A Case Study from Analyses of New Metabotropic Glutamate Receptor 5 (mGlu5) X‑ray Structures

Towards high throughput GPCR crystallography: In Meso soaking of Adenosine A2A Receptor crystals

Biophysical Fragment Screening of the β1‑Adrenergic Receptor: Identification of High Affinity Arylpiperazine Leads Using Structure-Based Drug Design

Fragment and Structure-Based Drug Discovery for a Class C GPCR: Discovery of the mGlu5 Negative Allosteric Modulator HTL14242 (3-Chloro-5-[6-(5-fluoropyridin-2-yl)pyrimidin-4-yl]benzonitrile)

X‐Ray Crystallography and Free Energy Calculations Reveal the Binding Mechanism of A2A Adenosine Receptor Antagonists

Outrunning free radicals in room-temperature macromolecular crystallography

Advances in long-wavelength native phasing at X-ray free-electron lasers

SARS-CoV-2 Mpro responds to oxidation by forming disulfide and NOS/SONOS bonds

Molecular basis for high-affinity agonist binding in GPCRs

Structures of Human A1 and A2A Adenosine Receptors with Xanthines Reveal Determinants of Selectivity

Intracellular allosteric antagonism of the CCR9 receptor

High-resolution crystal structure of parathyroid hormone 1 receptor in complex with a peptide agonist

Structure of Class B GPCRs: new horizons for drug discovery

Electron microscopy of Xrcc4 and the DNA ligase IV–Xrcc4 DNA repair complex

Advancing structural biology through breakthroughs in AI

Discovery of 1,2,4-Triazine Derivatives as Adenosine A2A Antagonists using Structure Based Drug Design

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