GPCRdb in 2023: state-specific structure models using AlphaFold2 and new ligand resources

Author:

Pándy-Szekeres Gáspár12,Caroli Jimmy1,Mamyrbekov Alibek1,Kermani Ali A3,Keserű György M2,Kooistra Albert J1ORCID,Gloriam David E1ORCID

Affiliation:

1. Department of Drug Design and Pharmacology, University of Copenhagen , Universitetsparken 2, 2100 Copenhagen, Denmark

2. Medicinal Chemistry Research Group, Research Center for Natural Sciences , Budapest H-1117, Hungary

3. Department of Structural Biology, St. Jude Children's Research Hospital , Memphis, TN 38105, USA

Abstract

Abstract G protein-coupled receptors (GPCRs) are physiologically abundant signaling hubs routing hundreds of extracellular signal substances and drugs into intracellular pathways. The GPCR database, GPCRdb supports >5000 interdisciplinary researchers every month with reference data, analysis, visualization, experiment design and dissemination. Here, we present our fifth major GPCRdb release setting out with an overview of the many resources for receptor sequences, structures, and ligands. This includes recently published additions of class D generic residue numbers, a comparative structure analysis tool to identify functional determinants, trees clustering GPCR structures by 3D conformation, and mutations stabilizing inactive/active states. We provide new state-specific structure models of all human non-olfactory GPCRs built using AlphaFold2-MultiState. We also provide a new resource of endogenous ligands along with a larger number of surrogate ligands with bioactivity, vendor, and physiochemical descriptor data. The one-stop-shop ligand resources integrate ligands/data from the ChEMBL, Guide to Pharmacology, PDSP Ki and PubChem database. The GPCRdb is available at https://gpcrdb.org.

Funder

Lundbeck Foundation

Novo Nordisk Foundation

Hungarian Academy of Sciences

Publisher

Oxford University Press (OUP)

Subject

Genetics

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