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. 2022 Sep 15;13:5417. doi: 10.1038/s41467-022-33121-2

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© The Author(s) 2022

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 3 — a, b Superimposition of the agonist-bound LPA₁, S1P₃ (PDB 7C4S), and CB₁ (PDB 5XRA) structures, viewed from the membrane plane (a) and the extracellular side (b). Cross sections of the ligand binding pockets in LPA₁ (c), S1P₃ (d), and CB₁ (e). Superimposition of the LPA₁ and S1P₃ structures, focused on the phosphate recognition site (f) and the bottom of the hydrophobic pocket (g).