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Open data
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Basic information
| Entry | Database: PDB / ID: 8hbd | ||||||
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| Title | Cryo-EM structure of IRL1620-bound ETBR-Gi complex | ||||||
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Keywords | MEMBRANE PROTEIN / IRL1620 / ETBR / Gi | ||||||
| Function / homology | Function and homology informationenteric smooth muscle cell differentiation / response to endothelin / negative regulation of neuron maturation / chordate pharynx development / neuroblast migration / endothelin receptor activity / aldosterone metabolic process / regulation of fever generation / vein smooth muscle contraction / positive regulation of penile erection ...enteric smooth muscle cell differentiation / response to endothelin / negative regulation of neuron maturation / chordate pharynx development / neuroblast migration / endothelin receptor activity / aldosterone metabolic process / regulation of fever generation / vein smooth muscle contraction / positive regulation of penile erection / heparin proteoglycan metabolic process / posterior midgut development / epithelial fluid transport / endothelin receptor signaling pathway / podocyte differentiation / developmental pigmentation / response to sodium phosphate / renal sodium excretion / enteric nervous system development / renal sodium ion absorption / protein transmembrane transport / renin secretion into blood stream / renal albumin absorption / regulation of pH / melanocyte differentiation / vasoconstriction / peripheral nervous system development / type 1 angiotensin receptor binding / negative regulation of adenylate cyclase activity / positive regulation of urine volume / regulation of epithelial cell proliferation / establishment of endothelial barrier / neural crest cell migration / negative regulation of protein metabolic process / : / response to pain / macrophage chemotaxis / peptide hormone binding / canonical Wnt signaling pathway / adenylate cyclase inhibitor activity / positive regulation of protein localization to cell cortex / Adenylate cyclase inhibitory pathway / T cell migration / D2 dopamine receptor binding / response to prostaglandin E / adenylate cyclase regulator activity / G protein-coupled serotonin receptor binding / adenylate cyclase-inhibiting serotonin receptor signaling pathway / Transcriptional and post-translational regulation of MITF-M expression and activity / cellular response to forskolin / regulation of heart rate / regulation of mitotic spindle organization / Peptide ligand-binding receptors / Regulation of insulin secretion / positive regulation of cholesterol biosynthetic process / calcium-mediated signaling / negative regulation of insulin secretion / G protein-coupled receptor binding / response to peptide hormone / adenylate cyclase-inhibiting G protein-coupled receptor signaling pathway / calcium ion transmembrane transport / adenylate cyclase-modulating G protein-coupled receptor signaling pathway / G-protein beta/gamma-subunit complex binding / centriolar satellite / vasodilation / Olfactory Signaling Pathway / Activation of the phototransduction cascade / 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 / GDP binding / Glucagon-like Peptide-1 (GLP1) regulates insulin secretion / G alpha (z) signalling events / cellular response to catecholamine stimulus / ADP signalling through P2Y purinoceptor 1 / ADORA2B mediated anti-inflammatory cytokines production / 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 / nervous system development / heterotrimeric G-protein complex Similarity search - Function | ||||||
| Biological species | Homo sapiens (human)![]() | ||||||
| Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 2.99 Å | ||||||
Authors | Yuan, Q. / Ji, Y. / Jiang, Y. / Duan, J. / Xu, H.E. | ||||||
| Funding support | China, 1items
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Citation | Journal: Nat Commun / Year: 2023Title: Structural basis of peptide recognition and activation of endothelin receptors. Authors: Yujie Ji / Jia Duan / Qingning Yuan / Xinheng He / Gong Yang / Shengnan Zhu / Kai Wu / Wen Hu / Tianyu Gao / Xi Cheng / Hualiang Jiang / H Eric Xu / Yi Jiang / ![]() Abstract: Endothelin system comprises three endogenous 21-amino-acid peptide ligands endothelin-1, -2, and -3 (ET-1/2/3), and two G protein-coupled receptor (GPCR) subtypes-endothelin receptor A (ETR) and B ...Endothelin system comprises three endogenous 21-amino-acid peptide ligands endothelin-1, -2, and -3 (ET-1/2/3), and two G protein-coupled receptor (GPCR) subtypes-endothelin receptor A (ETR) and B (ETR). Since ET-1, the first endothelin, was identified in 1988 as one of the most potent endothelial cell-derived vasoconstrictor peptides with long-lasting actions, the endothelin system has attracted extensive attention due to its critical role in vasoregulation and close relevance in cardiovascular-related diseases. Here we present three cryo-electron microscopy structures of ETR and ETR bound to ET-1 and ETR bound to the selective peptide IRL1620. These structures reveal a highly conserved recognition mode of ET-1 and characterize the ligand selectivity by ETRs. They also present several conformation features of the active ETRs, thus revealing a specific activation mechanism. Together, these findings deepen our understanding of endothelin system regulation and offer an opportunity to design selective drugs targeting specific ETR subtypes. | ||||||
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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 | 8hbd.cif.gz | 245.2 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb8hbd.ent.gz | 183.7 KB | Display | PDB format |
| PDBx/mmJSON format | 8hbd.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 8hbd_validation.pdf.gz | 1.1 MB | Display | wwPDB validaton report |
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| Full document | 8hbd_full_validation.pdf.gz | 1.2 MB | Display | |
| Data in XML | 8hbd_validation.xml.gz | 42.3 KB | Display | |
| Data in CIF | 8hbd_validation.cif.gz | 62.5 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/hb/8hbd ftp://data.pdbj.org/pub/pdb/validation_reports/hb/8hbd | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 34619MC ![]() 8hcqC ![]() 8hcxC 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
-Guanine nucleotide-binding protein ... , 3 types, 3 molecules ABG
| #1: Protein | Mass: 40445.059 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: GNAI1 / Production host: ![]() |
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| #2: Protein | Mass: 41055.867 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: GNB1 / Production host: ![]() |
| #3: 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 / Protein/peptide / Protein , 3 types, 3 molecules HLR
| #4: Antibody | Mass: 30363.043 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() ![]() |
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| #5: Protein/peptide | Mass: 1836.970 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Production host: ![]() |
| #6: Protein | Mass: 67882.320 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: EDNRB, ETRB / Production host: ![]() References: UniProt: P24530, Oplophorus-luciferin 2-monooxygenase |
-Details
| Has protein modification | Y |
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-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: IRL1620-bound ETBR-Gi complex / Type: COMPLEX / Entity ID: all / Source: MULTIPLE SOURCES | ||||||||||||
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| Source (natural) |
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| Source (recombinant) | Organism: ![]() | ||||||||||||
| Buffer solution | pH: 7.04 | ||||||||||||
| Specimen | Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES | ||||||||||||
| Vitrification | Cryogen name: ETHANE |
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Electron microscopy imaging
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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| Microscopy | Model: FEI TITAN KRIOS |
| Electron gun | Electron source: FIELD EMISSION GUN / Accelerating voltage: 300 kV / Illumination mode: FLOOD BEAM |
| Electron lens | Mode: BRIGHT FIELD / Nominal defocus max: 18000 nm / Nominal defocus min: 800 nm |
| Image recording | Electron dose: 50 e/Å2 / Film or detector model: GATAN K3 (6k x 4k) |
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Processing
| Software | Name: PHENIX / Version: 1.20.1_4487: / Classification: refinement | ||||||||||||||||||||||||
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| CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION | ||||||||||||||||||||||||
| 3D reconstruction | Resolution: 2.99 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 191493 / Symmetry type: POINT | ||||||||||||||||||||||||
| Refine LS restraints |
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Homo sapiens (human)

China, 1items
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gel filtration

