Illuminating the Path to Target GPCR Structures and Functions-Reference-Cited by-同舟云学术

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Illuminating the Path to Target GPCR Structures and Functions

Published:2020-09-21 Issue:40 Volume:59 Page:3783-3795
ISSN:0006-2960
Container-title:Biochemistry
language:en
Short-container-title:Biochemistry

Author:

Nielsen Christian D.-T.¹,Dhasmana Divya²,Floresta Giuseppe³,Wohland Thorsten²⁴,Cilibrizzi Agostino³^ORCID

Affiliation:

1. Imperial College London, White City Campus, Molecular Sciences Research Hub, 80 Wood Lane, London W12 0BZ, U.K.

2. Department of Biological Sciences, National University of Singapore, 14 Science Drive 4, Singapore 117543

3. Institute of Pharmaceutical Science, King’s College London, London SE1 9NH, U.K.

4. Department of Chemistry, National University of Singapore, 3 Science Drive 3, Singapore 117543

Funder

Ministry of Education - Singapore

National University of Singapore

Publisher

American Chemical Society (ACS)

Subject

Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.biochem.0c00606

Reference162 articles.

1. How and why do GPCRs dimerize?

2. Methodological advances: the unsung heroes of the GPCR structural revolution

3. Nuclear G-protein-coupled receptors as putative novel pharmacological targets

4. A ternary complex model explains the agonist-specific binding properties of the adenylate cyclase-coupled beta-adrenergic receptor.

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2. Illuminating the structural basis of human neurokinin 1 receptor (NK1R) antagonism through classical all‐atoms molecular dynamics simulations;Journal of Cellular Biochemistry;2023-11

3. A dual-targeting peptide for glioblastoma screened by phage display peptide library biopanning combined with affinity-adaptability analysis;International Journal of Pharmaceutics;2023-09

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