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Open data
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Basic information
| Entry | Database: PDB / ID: 9dqh | ||||||||||||||||||||||||
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| Title | CryoEM structure of Gq-coupled MRGPRD with a new agonist EP-2825 | ||||||||||||||||||||||||
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Keywords | SIGNALING PROTEIN / GPCR | ||||||||||||||||||||||||
| Function / homology | Function and homology informationangiotensin-mediated vasodilation involved in regulation of systemic arterial blood pressure / G protein-coupled peptide receptor activity / G protein-coupled receptor activity / Olfactory Signaling Pathway / Activation of the phototransduction cascade / adenylate cyclase-activating G protein-coupled receptor signaling pathway / G beta:gamma signalling through PLC beta / Presynaptic function of Kainate receptors / Thromboxane signalling through TP receptor / G protein-coupled acetylcholine receptor signaling pathway ...angiotensin-mediated vasodilation involved in regulation of systemic arterial blood pressure / G protein-coupled peptide receptor activity / G protein-coupled receptor activity / Olfactory Signaling Pathway / Activation of the phototransduction cascade / adenylate cyclase-activating G protein-coupled receptor signaling pathway / G beta:gamma signalling through PLC beta / Presynaptic function of Kainate receptors / Thromboxane signalling through TP receptor / G protein-coupled acetylcholine receptor signaling pathway / Activation of G protein gated Potassium channels / Inhibition of voltage gated Ca2+ channels via Gbeta/gamma subunits / G-protein activation / Prostacyclin signalling through prostacyclin receptor / G beta:gamma signalling through CDC42 / Glucagon signaling in metabolic regulation / G beta:gamma signalling through BTK / Synthesis, secretion, and inactivation of Glucagon-like Peptide-1 (GLP-1) / ADP signalling through P2Y purinoceptor 12 / photoreceptor disc membrane / Sensory perception of sweet, bitter, and umami (glutamate) taste / Glucagon-type ligand receptors / Adrenaline,noradrenaline inhibits insulin secretion / Vasopressin regulates renal water homeostasis via Aquaporins / Glucagon-like Peptide-1 (GLP1) regulates insulin secretion / G alpha (z) signalling events / cellular response to catecholamine stimulus / ADORA2B mediated anti-inflammatory cytokines production / ADP signalling through P2Y purinoceptor 1 / G beta:gamma signalling through PI3Kgamma / adenylate cyclase-activating dopamine receptor signaling pathway / Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding / GPER1 signaling / Inactivation, recovery and regulation of the phototransduction cascade / cellular response to prostaglandin E stimulus / G-protein beta-subunit binding / heterotrimeric G-protein complex / G alpha (12/13) signalling events / sensory perception of taste / extracellular vesicle / signaling receptor complex adaptor activity / Thrombin signalling through proteinase activated receptors (PARs) / retina development in camera-type eye / GTPase binding / Ca2+ pathway / fibroblast proliferation / High laminar flow shear stress activates signaling by PIEZO1 and PECAM1:CDH5:KDR in endothelial cells / G alpha (i) signalling events / G alpha (s) signalling events / phospholipase C-activating G protein-coupled receptor signaling pathway / G alpha (q) signalling events / Ras protein signal transduction / Extra-nuclear estrogen signaling / cell population proliferation / G protein-coupled receptor signaling pathway / lysosomal membrane / GTPase activity / synapse / protein-containing complex binding / signal transduction / extracellular space / extracellular exosome / membrane / plasma membrane / cytoplasm / cytosol Similarity search - Function | ||||||||||||||||||||||||
| Biological species | Homo sapiens (human)![]() | ||||||||||||||||||||||||
| Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 2.92 Å | ||||||||||||||||||||||||
Authors | Cao, C. / Wang, C. / Liu, Y. / Fay, J.F. / Roth, B.L. | ||||||||||||||||||||||||
| Funding support | United States, 2items
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Citation | Journal: Cell Rep / Year: 2024Title: High-affinity agonists reveal recognition motifs for the MRGPRD GPCR. Authors: Chunyu Wang / Yongfeng Liu / Marion Lanier / Adam Yeager / Isha Singh / Ryan H Gumpper / Brian E Krumm / Chelsea DeLeon / Shicheng Zhang / Marcus Boehm / Richard Pittner / Alain Baron / Lisa ...Authors: Chunyu Wang / Yongfeng Liu / Marion Lanier / Adam Yeager / Isha Singh / Ryan H Gumpper / Brian E Krumm / Chelsea DeLeon / Shicheng Zhang / Marcus Boehm / Richard Pittner / Alain Baron / Lisa Dvorak / Corinne Bacon / Brian K Shoichet / Esther Martinborough / Jonathan F Fay / Can Cao / Bryan L Roth / ![]() Abstract: The human MRGPRD protein is a member of the Mas-related G protein-coupled receptors (MRGPRs) that is involved in the sensing of pain, itch, and other inflammatory stimuli. As with other MRGPRs, ...The human MRGPRD protein is a member of the Mas-related G protein-coupled receptors (MRGPRs) that is involved in the sensing of pain, itch, and other inflammatory stimuli. As with other MRGPRs, MRGPRD is a relatively understudied receptor with few known agonists. The most potent small-molecule agonist of MRGPRD reported so far is β-alanine, with an affinity in the micromole range, which largely restricts its functional study. Here, we report two MRGPRD agonists, EP-2825 and EP-3945, that are approximately 100-fold more potent than β-alanine and determine the structures of MRGPRD-Gq in complex with EP-2825 and EP-3945, respectively. The structures reveal distinct agonist binding modes of MRGPRD and large conformational plasticity of the orthosteric pocket. Collectively, the discovery of high-affinity MRGPRD agonists and their distinct binding modes will facilitate the functional study and the structure-based design of ligands targeting this understudied receptor. | ||||||||||||||||||||||||
| History |
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Structure visualization
| Structure viewer | Molecule: Molmil Jmol/JSmol |
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Downloads & links
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Download
| PDBx/mmCIF format | 9dqh.cif.gz | 198.9 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb9dqh.ent.gz | Display | PDB format | |
| PDBx/mmJSON format | 9dqh.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 9dqh_validation.pdf.gz | 1.2 MB | Display | wwPDB validaton report |
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| Full document | 9dqh_full_validation.pdf.gz | 1.2 MB | Display | |
| Data in XML | 9dqh_validation.xml.gz | 47.1 KB | Display | |
| Data in CIF | 9dqh_validation.cif.gz | 71.1 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/dq/9dqh ftp://data.pdbj.org/pub/pdb/validation_reports/dq/9dqh | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 47113MC ![]() 9dqjC M: map data used to model this data C: citing same article ( |
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| Similar structure data | Similarity search - Function & homology F&H Search |
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Links
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Assembly
| Deposited unit | ![]()
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Components
-Protein , 2 types, 2 molecules AB
| #1: Protein | Mass: 36171.523 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: MRGPRD, MRGD / Production host: ![]() |
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| #2: Protein | Mass: 28084.832 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Production host: ![]() |
-Guanine nucleotide-binding protein ... , 2 types, 2 molecules CD
| #3: Protein | Mass: 37728.152 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: GNB1 / Production host: ![]() |
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| #4: Protein | Mass: 7861.143 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: GNG2 / Production host: ![]() |
-Antibody / Non-polymers , 2 types, 2 molecules E
| #5: Antibody | Mass: 27409.588 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() ![]() |
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| #6: Chemical | ChemComp-A1BE2 / Mass: 428.955 Da / Num. of mol.: 1 / Source method: obtained synthetically / Formula: C23H29ClN4O2 / Feature type: SUBJECT OF INVESTIGATION |
-Details
| Has ligand of interest | Y |
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| Has protein modification | Y |
-Experimental details
-Experiment
| Experiment | Method: ELECTRON MICROSCOPY |
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| EM experiment | Aggregation state: PARTICLE / 3D reconstruction method: single particle reconstruction |
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Sample preparation
| Component | Name: EP-2825-bound MRGPRD-Gq complex / Type: COMPLEX / Entity ID: #1-#5 / Source: MULTIPLE SOURCES |
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| Molecular weight | Value: 0.137 MDa / Experimental value: NO |
| Buffer solution | pH: 7.4 |
| Specimen | Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES |
| Vitrification | Cryogen name: ETHANE-PROPANE |
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Electron microscopy imaging
| Experimental equipment | ![]() Model: Talos Arctica / Image courtesy: FEI Company |
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| Microscopy | Model: FEI TALOS ARCTICA |
| Electron gun | Electron source: FIELD EMISSION GUN / Accelerating voltage: 200 kV / Illumination mode: FLOOD BEAM |
| Electron lens | Mode: BRIGHT FIELD / Nominal defocus max: 11000 nm / Nominal defocus min: 200 nm |
| Image recording | Electron dose: 55.8 e/Å2 / Film or detector model: GATAN K3 (6k x 4k) |
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Processing
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| CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION | ||||||||||||
| Symmetry | Point symmetry: C1 (asymmetric) | ||||||||||||
| 3D reconstruction | Resolution: 2.92 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 158802 / Symmetry type: POINT |
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Homo sapiens (human)

United States, 2items
Citation



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FIELD EMISSION GUN