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8Z1D

Cryo-EM structure of the panda P2X7 receptor in complex with PSFL1191

This is a non-PDB format compatible entry.
Summary for 8Z1D
Entry DOI10.2210/pdb8z1d/pdb
EMDB information39723
DescriptorP2X purinoceptor, 2-acetamido-2-deoxy-beta-D-glucopyranose, PSFL1191 (3 entities in total)
Functional Keywordschannel, transport protein
Biological sourceAiluropoda melanoleuca (giant panda)
Total number of polymer chains3
Total formula weight118614.30
Authors
Sheng, D.,Hattori, M. (deposition date: 2024-04-11, release date: 2025-04-16, Last modification date: 2026-05-06)
Primary citationGuo, C.R.,Sheng, D.,Li, J.Y.,Li, T.T.,Yao, J.B.,Zhang, R.,Huang, Y.,Zhao, Y.Y.,Wang, D.P.,Chen, J.,Li, J.,Wang, J.,Zhou, Y.,Shen, C.,Jin, F.,Cao, P.,Hattori, M.,Liu, H.,Yu, Y.
Understanding interspecies drug response variations between human and rodent P2X7 receptors.
Nat Commun, 16:10827-10827, 2025
Cited by
PubMed Abstract: Despite intensive development, P2X7 modulators have struggled in translation due to human genetic variability and species-dependent drug responses. Here, we identify PSFL1191, a portal-of-central-pocket (PCP)-site inhibitor selective for human and panda P2X7, but inactive against rodents. Cryo-EM structures revealed two distinct PCP sub-pockets: PCP1, a rigid base pocket demanding precise steric complementarity with PSFL1191, and PCP2, a conserved middle cavity targeted by JNJ-54175446, a clinical candidate unaffected by species differences. Species selectivity maps to a deep PCP1 motif (V312-Y295-M105-F103-P96). In P2rx7 mice, PSFL1191 markedly altered macrophage-mediated bacterial clearance and wound healing while preserving basal physiology, effects absent in wild-type animals. Our findings establish the structural basis for interspecies pharmacological divergence in P2X7 modulation and highlight transgenic models as powerful tools for predicting therapeutic efficacy, thereby enabling more precise and efficient drug discovery.
PubMed: 41330895
DOI: 10.1038/s41467-025-65847-0
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (4 Å)
Structure validation

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