List of works - Cheng Zhang

An inactive receptor-G protein complex maintains the dynamic range of agonist-induced signaling

scientific article published on 16 November 2020

Cholesterol increases kinetic, energetic, and mechanical stability of the human β2-adrenergic receptor.

scientific article

Conformational Plasticity of Human Protease-Activated Receptor 1 upon Antagonist- and Agonist-Binding

scientific article published on 15 August 2019

Covalent agonists for studying G protein-coupled receptor activation

scientific article

Cryo-EM Structure of the Human Cannabinoid Receptor CB2-Gi Signaling Complex

scientific article published on 30 January 2020

Cryo-EM structure of oxysterol-bound human Smoothened coupled to a heterotrimeric Gi

scientific article published on 05 June 2019

Crystal structure of Human ASB9-2 and substrate-recognition of CKB.

scientific article published in April 2012

Crystal structure of the C-terminal domain of the ɛ subunit of human translation initiation factor eIF2B.

scientific article published on June 2010

Crystal structures of human IPP isomerase: new insights into the catalytic mechanism

scientific article

Development of "Plug and Play" Fiducial Marks for Structural Studies of GPCR Signaling Complexes by Single-Particle Cryo-EM

scientific article published on 25 October 2019

Effective application of bicelles for conformational analysis of G protein-coupled receptors by hydrogen/deuterium exchange mass spectrometry

scientific article published on 5 March 2015

G Protein-Coupled Receptors in Asthma Therapy: Pharmacology and Drug Action

scientific article published on 01 January 2020

High-resolution crystal structure of human protease-activated receptor 1

scientific article

Identifying and quantifying two ligand-binding sites while imaging native human membrane receptors by AFM.

scientific article

Imaging G protein-coupled receptors while quantifying their ligand-binding free-energy landscape

scientific article published on 13 July 2015

Membrane binding of the insertion sequence of Proteus vulgaris L-amino acid deaminase stabilizes protein structure and increases catalytic activity

scientific article published on 20 October 2017

Molecular recognition of formylpeptides and diverse agonists by the formylpeptide receptors FPR1 and FPR2

scientific article published on 25 February 2022

Orthosteric and allosteric action of the C5a receptor antagonists

scientific article published on 04 June 2018

Publisher Correction: Structural insights into binding specificity, efficacy and bias of a β2AR partial agonist

scientific article published on 01 February 2019

Single-molecule force spectroscopy of G-protein-coupled receptors.

scientific article

Structural insights into binding specificity, efficacy and bias of a βAR partial agonist

scientific article

Structure and function of an irreversible agonist-β(2) adrenoceptor complex

scientific article

Structure of formylpeptide receptor 2-Gi complex reveals insights into ligand recognition and signaling

scientific article published on 14 February 2020

Structure of human steroid 5α-reductase 2 with anti-androgen drug finasteride

scientific article published on 15 July 2020

Structure of human steroid 5α-reductase 2 with the anti-androgen drug finasteride

scientific article published on 27 October 2020

Structure of the human M2 muscarinic acetylcholine receptor bound to an antagonist

scientific article

Structures of the Human PGD Receptor CRTH2 Reveal Novel Mechanisms for Ligand Recognition

scientific article published on 13 September 2018

Trypsin inhibitory loop is an excellent lead structure to design serine protease inhibitors and antimicrobial peptides

scientific article published on 23 March 2007

Versatile and multivalent nanobodies efficiently neutralize SARS-CoV-2

scientific article

List of works by Cheng Zhang

An inactive receptor-G protein complex maintains the dynamic range of agonist-induced signaling

Cholesterol increases kinetic, energetic, and mechanical stability of the human β2-adrenergic receptor.

Conformational Plasticity of Human Protease-Activated Receptor 1 upon Antagonist- and Agonist-Binding

Covalent agonists for studying G protein-coupled receptor activation

Cryo-EM Structure of the Human Cannabinoid Receptor CB2-Gi Signaling Complex

Cryo-EM structure of oxysterol-bound human Smoothened coupled to a heterotrimeric Gi

Crystal structure of Human ASB9-2 and substrate-recognition of CKB.

Crystal structure of the C-terminal domain of the ɛ subunit of human translation initiation factor eIF2B.

Crystal structures of human IPP isomerase: new insights into the catalytic mechanism

Development of "Plug and Play" Fiducial Marks for Structural Studies of GPCR Signaling Complexes by Single-Particle Cryo-EM

Effective application of bicelles for conformational analysis of G protein-coupled receptors by hydrogen/deuterium exchange mass spectrometry

G Protein-Coupled Receptors in Asthma Therapy: Pharmacology and Drug Action

High-resolution crystal structure of human protease-activated receptor 1

Identifying and quantifying two ligand-binding sites while imaging native human membrane receptors by AFM.

Imaging G protein-coupled receptors while quantifying their ligand-binding free-energy landscape

Membrane binding of the insertion sequence of Proteus vulgaris L-amino acid deaminase stabilizes protein structure and increases catalytic activity

Molecular recognition of formylpeptides and diverse agonists by the formylpeptide receptors FPR1 and FPR2

Orthosteric and allosteric action of the C5a receptor antagonists

Publisher Correction: Structural insights into binding specificity, efficacy and bias of a β2AR partial agonist

Single-molecule force spectroscopy of G-protein-coupled receptors.

Structural insights into binding specificity, efficacy and bias of a βAR partial agonist

Structure and function of an irreversible agonist-β(2) adrenoceptor complex

Structure of formylpeptide receptor 2-Gi complex reveals insights into ligand recognition and signaling

Structure of human steroid 5α-reductase 2 with anti-androgen drug finasteride

Structure of human steroid 5α-reductase 2 with the anti-androgen drug finasteride

Structure of the human M2 muscarinic acetylcholine receptor bound to an antagonist

Structures of the Human PGD Receptor CRTH2 Reveal Novel Mechanisms for Ligand Recognition

Trypsin inhibitory loop is an excellent lead structure to design serine protease inhibitors and antimicrobial peptides

Versatile and multivalent nanobodies efficiently neutralize SARS-CoV-2