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Yorodumi- EMDB-66832: The Gi protein local map of Leu-enkephalin-BMS-986187-bound DOR-G... -
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Basic information
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| Title | The Gi protein local map of Leu-enkephalin-BMS-986187-bound DOR-Gi complex | |||||||||
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Keywords | Complex / PAM / Agonist / MEMBRANE PROTEIN | |||||||||
| Biological species | Homo sapiens (human) | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 2.87 Å | |||||||||
Authors | Zhao C / Fu H / Tian XW / Cheng L / Yan W / Shao ZH | |||||||||
| Funding support | China, 2 items
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Citation | Journal: Signal Transduct Target Ther / Year: 2026Title: Molecular mechanism of allosteric modulation of opioid receptors. Authors: Heli Wang / Zhuang Miao / Chang Zhao / Hong Fu / Xiaowen Tian / Xinlei Liu / Lei Wang / Yuan Liu / Xingyu Liu / Xihao Yong / Lantian Su / Wei Yan / Lin Cheng / Renjie Chai / Zhenhua Shao / Bowen Ke / ![]() Abstract: Opioid analgesics provide potent pain relief but are limited by severe adverse effects, tolerance, and interindividual genetic variability in response. Poly-pharmacology and allosteric modulation of ...Opioid analgesics provide potent pain relief but are limited by severe adverse effects, tolerance, and interindividual genetic variability in response. Poly-pharmacology and allosteric modulation of opioid receptors offer promising strategies to enhance analgesic efficacy while mitigating these limitations. Pan-positive allosteric modulators (pan-PAMs), which simultaneously potentiate multiple opioid receptor subtypes, integrate the advantages of both approaches and represent an emerging therapeutic paradigm for pain management. However, the molecular mechanisms underlying pan-PAM activity at opioid receptors remain poorly understood. Here, we characterize BMS-986187 as a pan-PAM of opioid receptors and report the cryo-electron microscopy (cryo-EM) structures of multiple opioid receptor subtypes bound to this modulator, revealing a previously unidentified allosteric pocket. Structural and functional analyses revealed a conserved binding motif that mediates PAM recognition across the opioid receptor family and revealed the essential contributions of key opioid receptor residues to allosteric modulation by BMS-986187. Functionally, BMS-986187 enhances analgesic efficacy through an opioid-sparing effect, allowing lower opioid doses and reducing side effects, while restoring activity in loss-of-function (LOF) μ-opioid receptor variants. These findings define a previously unrecognized allosteric site in opioid receptors and establish a structural framework for the rational design of safer and more effective opioid therapeutics through allosteric modulation. | |||||||||
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Structure visualization
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Downloads & links
-EMDB archive
| Header (meta data) | emd-66832-v30.xml emd-66832.xml | 14.5 KB 14.5 KB | Display Display | EMDB header |
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| Images | emd_66832.png | 39.1 KB | ||
| Map data | emd_66832.map.gz | 97 MB | EMDB map data format | |
| Filedesc metadata | emd-66832.cif.gz | 4.1 KB | ||
| Others | emd_66832_half_map_1.map.gz emd_66832_half_map_2.map.gz | 95.7 MB 95.7 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-66832 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-66832 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 66723 ![]() 66725 ![]() 66726 ![]() 66730 ![]() 66771 ![]() 66773 ![]() 66801 ![]() 66825 ![]() 66826 ![]() 66827 ![]() 66828 ![]() 66829 ![]() 66830 ![]() 66831 ![]() 66833 ![]() 9xc6C ![]() 9xdqC ![]() 9xdrC ![]() 9xf4C C: citing same article ( |
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Links
| EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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Map
-Supplemental data
-Half map: #1
| File | emd_66832_half_map_1.map | ||||||||||||
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-Half map: #2
| File | emd_66832_half_map_2.map | ||||||||||||
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Sample components
-Entire : DOR in complex with Gi heterotrimer
| Entire | Name: DOR in complex with Gi heterotrimer |
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| Components |
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-Supramolecule #1: DOR in complex with Gi heterotrimer
| Supramolecule | Name: DOR in complex with Gi heterotrimer / type: complex / ID: 1 / Parent: 0 / Macromolecule list: #4, #1-#3 |
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| Source (natural) | Organism: Homo sapiens (human) |
-Experimental details
-Structure determination
| Method | cryo EM |
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Processing | single particle reconstruction |
| Aggregation state | particle |
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Sample preparation
| Buffer | pH: 7.5 |
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| Vitrification | Cryogen name: ETHANE |
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Electron microscopy
| Microscope | TFS KRIOS |
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| Image recording | Film or detector model: FEI FALCON IV (4k x 4k) / Average electron dose: 50.0 e/Å2 |
| Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm / Nominal defocus max: 1.4000000000000001 µm / Nominal defocus min: 0.8 µm |
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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About Yorodumi



Keywords
Homo sapiens (human)
Authors
China, 2 items
Citation



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Processing
FIELD EMISSION GUN
