+
Open data
-
Basic information
Entry | Database: PDB / ID: 8xvl | ||||||
---|---|---|---|---|---|---|---|
Title | Cryo-EM structure of ETAR bound with Zibotentan | ||||||
![]() |
| ||||||
![]() | SIGNALING PROTEIN / GPCR / COMPLEX / ETA / ZIBOTENTAN | ||||||
Function / homology | ![]() regulation of protein localization to cell leading edge / endothelin receptor activity / cellular response to human chorionic gonadotropin stimulus / meiotic cell cycle process involved in oocyte maturation / semaphorin-plexin signaling pathway involved in axon guidance / neural crest cell fate commitment / glomerular endothelium development / sympathetic neuron axon guidance / noradrenergic neuron differentiation / atrial cardiac muscle tissue development ...regulation of protein localization to cell leading edge / endothelin receptor activity / cellular response to human chorionic gonadotropin stimulus / meiotic cell cycle process involved in oocyte maturation / semaphorin-plexin signaling pathway involved in axon guidance / neural crest cell fate commitment / glomerular endothelium development / sympathetic neuron axon guidance / noradrenergic neuron differentiation / atrial cardiac muscle tissue development / vascular associated smooth muscle cell development / cardiac chamber formation / heparin proteoglycan metabolic process / pharyngeal arch artery morphogenesis / regulation of D-glucose transmembrane transport / endothelin receptor signaling pathway involved in heart process / cardiac neural crest cell migration involved in outflow tract morphogenesis / endothelin receptor signaling pathway / response to acetylcholine / podocyte differentiation / podocyte apoptotic process / developmental pigmentation / left ventricular cardiac muscle tissue morphogenesis / renal sodium ion absorption / embryonic skeletal system development / sodium ion homeostasis / enteric nervous system development / mesenchymal cell apoptotic process / positive regulation of cation channel activity / axonogenesis involved in innervation / glomerular filtration / protein transmembrane transport / artery smooth muscle contraction / cellular response to follicle-stimulating hormone stimulus / cellular response to luteinizing hormone stimulus / cranial skeletal system development / renal albumin absorption / respiratory gaseous exchange by respiratory system / sympathetic nervous system development / phosphatidylinositol-4,5-bisphosphate phospholipase C activity / norepinephrine metabolic process / vasoconstriction / embryonic heart tube development / axon extension / establishment of endothelial barrier / cellulase / aorta development / middle ear morphogenesis / cellulase activity / neuromuscular process / neuron remodeling / beta-glucosidase activity / branching involved in blood vessel morphogenesis / face development / thyroid gland development / cAMP/PKA signal transduction / smooth muscle contraction / blood vessel remodeling / canonical Wnt signaling pathway / cellulose catabolic process / activation of adenylate cyclase activity / response to amphetamine / regulation of heart rate / Peptide ligand-binding receptors / mitochondrion organization / electron transport chain / adenylate cyclase-inhibiting G protein-coupled receptor signaling pathway / calcium ion transmembrane transport / regulation of blood pressure / response to wounding / intracellular calcium ion homeostasis / mitotic cell cycle / positive regulation of cytosolic calcium ion concentration / cellular response to oxidative stress / phospholipase C-activating G protein-coupled receptor signaling pathway / gene expression / G alpha (q) signalling events / in utero embryonic development / positive regulation of canonical NF-kappaB signal transduction / periplasmic space / electron transfer activity / response to hypoxia / cell population proliferation / G protein-coupled receptor signaling pathway / iron ion binding / heme binding / cell surface / signal transduction / extracellular region / plasma membrane Similarity search - Function | ||||||
Biological species | ![]() synthetic construct (others) ![]() ![]() ![]() | ||||||
Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 3.22 Å | ||||||
![]() | Hou, J.Y. / Liu, S.H. / Wu, L.J. / Liu, Z.J. / Hua, T. | ||||||
Funding support | ![]()
| ||||||
![]() | ![]() Title: Structural basis of antagonist selectivity in endothelin receptors. Authors: Junyi Hou / Shenhui Liu / Xiaodan Zhang / Guowei Tu / Lijie Wu / Yijie Zhang / Hao Yang / Xiangcheng Li / Junlin Liu / Longquan Jiang / Qiwen Tan / Fang Bai / Zhijie Liu / Changhong Miao / Tian Hua / Zhe Luo / ![]() Abstract: Endothelins and their receptors, ET and ET, play vital roles in maintaining vascular homeostasis. Therapeutically targeting endothelin receptors, particularly through ET antagonists, has shown ...Endothelins and their receptors, ET and ET, play vital roles in maintaining vascular homeostasis. Therapeutically targeting endothelin receptors, particularly through ET antagonists, has shown efficacy in treating pulmonary arterial hypertension (PAH) and other cardiovascular- and renal-related diseases. Here we present cryo-electron microscopy structures of ET in complex with two PAH drugs, macitentan and ambrisentan, along with zibotentan, a selective ET antagonist, respectively. Notably, a specialized anti-ET antibody facilitated the structural elucidation. These structures, together with the active-state structures of ET-1-bound ET and ET, and the agonist BQ3020-bound ET, in complex with G, unveil the molecular basis of agonist/antagonist binding modes in endothelin receptors. Key residues that confer antagonist selectivity to endothelin receptors were identified along with the activation mechanism of ET. Furthermore, our results suggest that ECL2 in ET can serve as an epitope for antibody-mediated receptor antagonism. Collectively, these insights establish a robust theoretical framework for the rational design of small-molecule drugs and antibodies with selective activity against endothelin receptors. | ||||||
History |
|
-
Structure visualization
Structure viewer | Molecule: ![]() ![]() |
---|
-
Downloads & links
-
Download
PDBx/mmCIF format | ![]() | 208.6 KB | Display | ![]() |
---|---|---|---|---|
PDB format | ![]() | Display | ![]() | |
PDBx/mmJSON format | ![]() | Tree view | ![]() | |
Others | ![]() |
-Validation report
Arichive directory | ![]() ![]() | HTTPS FTP |
---|
-Related structure data
Related structure data | ![]() 38708MC ![]() 8xveC ![]() 8xvhC ![]() 8xviC ![]() 8xvjC ![]() 8xvkC M: map data used to model this data C: citing same article ( |
---|---|
Similar structure data | Similarity search - Function & homology ![]() |
-
Links
-
Assembly
Deposited unit | ![]()
|
---|---|
1 |
|
-
Components
#1: Antibody | Mass: 28577.918 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Production host: Mammalian expression vector Flag-MCS-pcDNA3.1 (others) |
---|---|
#2: Antibody | Mass: 15071.431 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) synthetic construct (others) / Production host: ![]() ![]() |
#3: Antibody | Mass: 25575.604 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Production host: Mammalian expression vector Flag-MCS-pcDNA3.1 (others) |
#4: Protein | Mass: 89090.867 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Acetivibrio thermocellus (strain ATCC 27405 / DSM 1237 / JCM 9322 / NBRC 103400 / NCIMB 10682 / NRRL B-4536 / VPI 7372) (bacteria), (gene. exp.) Homo sapiens (human), (gene. exp.) ...Source: (gene. exp.) ![]() ![]() ![]() ![]() Gene: celH, Cthe_1472, EDNRA, ETA, ETRA, cybC / Production host: ![]() ![]() References: UniProt: P16218, UniProt: P25101, UniProt: P0ABE7, cellulase |
#5: Chemical | ChemComp-A1D5L / Mass: 424.433 Da / Num. of mol.: 1 / Source method: obtained synthetically / Formula: C19H16N6O4S / Feature type: SUBJECT OF INVESTIGATION |
Has ligand of interest | Y |
Has protein modification | Y |
-Experimental details
-Experiment
Experiment | Method: ELECTRON MICROSCOPY |
---|---|
EM experiment | Aggregation state: PARTICLE / 3D reconstruction method: single particle reconstruction |
-
Sample preparation
Component | Name: Complex of Endothelin receptor type A with Zibotentan / Type: COMPLEX / Entity ID: #1-#4 / Source: RECOMBINANT |
---|---|
Source (natural) | Organism: ![]() |
Source (recombinant) | Organism: ![]() ![]() |
Buffer solution | pH: 7.4 |
Specimen | Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES |
Vitrification | Cryogen name: ETHANE |
-
Electron microscopy imaging
Microscopy | Model: FEI TITAN |
---|---|
Electron gun | Electron source: ![]() |
Electron lens | Mode: BRIGHT FIELD / Nominal defocus max: 2000 nm / Nominal defocus min: 1000 nm |
Image recording | Electron dose: 60 e/Å2 / Film or detector model: FEI FALCON IV (4k x 4k) |
-
Processing
CTF correction | Type: NONE |
---|---|
3D reconstruction | Resolution: 3.22 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 644807 / Symmetry type: POINT |