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9P0L

Composite map of CXCL10-CXCR3-Gi-scFv16

Summary for 9P0L
Entry DOI10.2210/pdb9p0l/pdb
EMDB information71080
DescriptorC-X-C chemokine receptor type 3,GFP-like fluorescent chromoprotein FP506, related, C-X-C motif chemokine 10, Guanine nucleotide-binding protein G(i) subunit alpha-1, ... (6 entities in total)
Functional Keywordsgpcr, chemokine receptor, membrane protein
Biological sourceHomo sapiens (human)
More
Total number of polymer chains6
Total formula weight203772.31
Authors
Sun, D.,Masureel, M.,Johnson, M. (deposition date: 2025-06-06, release date: 2026-04-29)
Primary citationBouyssou, A.,Sun, D.,Zhou, T.,Smith, S.,Ho, H.,Johnson, M.,Azumaya, C.,Noreng, S.,Liu, P.,Ti, S.,Joshi, P.,Tam, C.,Yang, Y.,Janezic, E.,Comps-Agrar, L.,Masureel, M.
Molecular basis of CXC chemokine receptor 3 ligand multispecificity.
Sci Adv, 12:eadz3767-eadz3767, 2026
Cited by
PubMed Abstract: C-X-C motif chemokine receptor 3 (CXCR3) is essential for immune cell functions and pivotal in T helper 1 cell infiltration in autoimmune and chronic inflammatory diseases and in tumor proliferation and metastasis, but the mechanisms by which the endogenous ligands CXCL9, CXCL10, and CXCL11 differentially recognize and activate CXCR3 are not fully understood. Here, we present cryo-electron microscopy structures of all three chemokine-CXCR3-G complexes, complemented by cell binding studies and functional mutagenesis data. We systematically compare the pharmacological and interaction profiles of CXCL9, CXCL10, and CXCL11 to rationalize their varying efficacies and potencies and to reveal the critical role of the membrane-distal CXCR3 N terminus in ligand binding and signaling. Using chimeric chemokines and molecular dynamics, we reveal the signaling plasticity of chemokine ligands and signaling determinants. Together, these insights enable us to propose a multimodal binding and activation framework that explains CXCR3 chemokine ligand multispecificity and signaling versatility and offer tools to interrogate and modulate CXCR3 biology.
PubMed: 41996512
DOI: 10.1126/sciadv.adz3767
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.1 Å)
Structure validation

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