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Open data
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Basic information
| Entry | Database: PDB / ID: 8yqn | ||||||||||||||||||||||||
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| Title | Torpedo acetylcholine receptor in complex with Erabutoxin A | ||||||||||||||||||||||||
Components |
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Keywords | MEMBRANE PROTEIN / Nicotinic acetylcholine receptor / short-chain alpha-neurotoxin / three-finger toxin / torpedo / cys-loop receptor / pentameric ligand-gated ion channel | ||||||||||||||||||||||||
| Function / homology | Function and homology informationacetylcholine receptor inhibitor activity / acetylcholine-gated monoatomic cation-selective channel activity / ion channel regulator activity / transmitter-gated monoatomic ion channel activity involved in regulation of postsynaptic membrane potential / transmembrane signaling receptor activity / toxin activity / postsynaptic membrane / extracellular region Similarity search - Function | ||||||||||||||||||||||||
| Biological species | Laticauda semifasciata (broad-banded blue sea krait)![]() | ||||||||||||||||||||||||
| Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 2.27 Å | ||||||||||||||||||||||||
Authors | Chan, C.Y.L. / Li, H.H. / Hibbs, R.E. / Kini, R.M. | ||||||||||||||||||||||||
| Funding support | Singapore, 1items
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Citation | Journal: To Be PublishedTitle: Structure of Erabutoxin bound to Torpedo acetylcholine receptor gives insight to intramolecular selectivity Authors: Chan, C.Y.L. / Li, H.H. / Hibbs, R.E. / Kini, R.M. | ||||||||||||||||||||||||
| 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 | 8yqn.cif.gz | 459.6 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb8yqn.ent.gz | 367.8 KB | Display | PDB format |
| PDBx/mmJSON format | 8yqn.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 8yqn_validation.pdf.gz | 1.7 MB | Display | wwPDB validaton report |
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| Full document | 8yqn_full_validation.pdf.gz | 1.7 MB | Display | |
| Data in XML | 8yqn_validation.xml.gz | 71.9 KB | Display | |
| Data in CIF | 8yqn_validation.cif.gz | 109.4 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/yq/8yqn ftp://data.pdbj.org/pub/pdb/validation_reports/yq/8yqn | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 39500MC 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
-Acetylcholine receptor subunit ... , 4 types, 5 molecules ADBCE
| #1: Protein | Mass: 50168.164 Da / Num. of mol.: 2 / Source method: isolated from a natural source Source: (natural) ![]() References: UniProt: P02710 #2: Protein | | Mass: 57625.711 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural) ![]() References: UniProt: P02718 #3: Protein | | Mass: 53731.773 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural) ![]() References: UniProt: P02712 #4: Protein | | Mass: 56335.684 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural) ![]() References: UniProt: P02714 |
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-Protein , 1 types, 2 molecules FG
| #5: Protein | Mass: 6853.715 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Laticauda semifasciata (broad-banded blue sea krait)Production host: ![]() |
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-Sugars , 4 types, 8 molecules 
| #6: Polysaccharide | Source method: isolated from a genetically manipulated source #7: Polysaccharide | #8: Polysaccharide | alpha-D-mannopyranose-(1-6)-alpha-D-mannopyranose-(1-6)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1- ...alpha-D-mannopyranose-(1-6)-alpha-D-mannopyranose-(1-6)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose | Type: oligosaccharide / Mass: 951.875 Da / Num. of mol.: 1 / Source method: obtained synthetically #10: Sugar | |
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-Non-polymers , 3 types, 6 molecules 




| #9: Chemical | ChemComp-POV / ( #11: Chemical | ChemComp-OCT / | #12: Chemical | ChemComp-PLM / | |
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-Details
| Has ligand of interest | N |
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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: Torpedo acetylcholine receptor in complex with Erabutoxin A Type: COMPLEX / Entity ID: #1-#5 / Source: MULTIPLE SOURCES |
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| Molecular weight | Value: 0.292 MDa / Experimental value: NO |
| Source (natural) | Organism: ![]() |
| Buffer solution | pH: 7.4 |
| Specimen | Conc.: 0.2 mg/ml / Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES |
| Specimen support | Grid material: COPPER / Grid mesh size: 200 divisions/in. / Grid type: Quantifoil R2/1 |
| Vitrification | Instrument: FEI VITROBOT MARK IV / Cryogen name: ETHANE / Humidity: 100 % |
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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: 2400 nm / Nominal defocus min: 1000 nm |
| Image recording | Electron dose: 50 e/Å2 / Film or detector model: FEI FALCON IV (4k x 4k) / Num. of grids imaged: 1 / Num. of real images: 2149 |
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Processing
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| CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION | ||||||||||||||||
| 3D reconstruction | Resolution: 2.27 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 369101 / Symmetry type: POINT |
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Laticauda semifasciata (broad-banded blue sea krait)

Singapore, 1items
Citation
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FIELD EMISSION GUN