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Yorodumi- EMDB-7294: Cryo-EM Structure of Hepatitis B virus T=4 capsid in complex with... -
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Basic information
| Entry | Database: EMDB / ID: EMD-7294 | |||||||||
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| Title | Cryo-EM Structure of Hepatitis B virus T=4 capsid in complex with the fluorescent allosteric modulator HAP-TAMRA | |||||||||
|  Map data | A Hepatitis B virus capsid with T=4 symmetry, bound to HAP-TAMRA. HAP-TAMRA is a fluorescent probe derived from the Heteroaryldihydropyrimidine (HAP) class of capsid-directed antivirals. | |||||||||
|  Sample | Hepatitis B virus T=4 capsid !=  Hepatitis B virus genotype D subtype adw Hepatitis B virus T=4 capsid 
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|  Keywords | capsid / CpAM / antiviral / fluorescent / VIRUS LIKE PARTICLE | |||||||||
| Function / homology |  Function and homology information microtubule-dependent intracellular transport of viral material towards nucleus / T=4 icosahedral viral capsid / viral penetration into host nucleus / host cell / host cell cytoplasm / symbiont entry into host cell / structural molecule activity / DNA binding / RNA binding / identical protein binding Similarity search - Function | |||||||||
| Biological species |  Hepatitis B virus genotype D subtype adw | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 4.0 Å | |||||||||
|  Authors | Schlicksup C / Wang JC | |||||||||
| Funding support |  United States, 1 items 
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|  Citation |  Journal: Elife / Year: 2018 Title: Hepatitis B virus core protein allosteric modulators can distort and disrupt intact capsids. Authors: Christopher John Schlicksup / Joseph Che-Yen Wang / Samson Francis / Balasubramanian Venkatakrishnan / William W Turner / Michael VanNieuwenhze / Adam Zlotnick /  Abstract: Defining mechanisms of direct-acting antivirals facilitates drug development and our understanding of virus function. Heteroaryldihydropyrimidines (HAPs) inappropriately activate assembly of ...Defining mechanisms of direct-acting antivirals facilitates drug development and our understanding of virus function. Heteroaryldihydropyrimidines (HAPs) inappropriately activate assembly of hepatitis B virus (HBV) core protein (Cp), suppressing formation of virions. We examined a fluorophore-labeled HAP, HAP-TAMRA. HAP-TAMRA induced Cp assembly and also bound pre-assembled capsids. Kinetic and spectroscopic studies imply that HAP-binding sites are usually not available but are bound cooperatively. Using cryo-EM, we observed that HAP-TAMRA asymmetrically deformed capsids, creating a heterogeneous array of sharp angles, flat regions, and outright breaks. To achieve high resolution reconstruction (<4 Å), we introduced a disulfide crosslink that rescued particle symmetry. We deduced that HAP-TAMRA caused quasi-sixfold vertices to become flatter and fivefold more angular. This transition led to asymmetric faceting. That a disordered crosslink could rescue symmetry implies that capsids have tensegrity properties. Capsid distortion and disruption is a new mechanism by which molecules like the HAPs can block HBV infection. | |||||||||
| History | 
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- Structure visualization
Structure visualization
| Movie | 
 
 
  Movie viewer | 
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| Structure viewer | EM map:  SurfView  Molmil  Jmol/JSmol | 
| Supplemental images | 
- Downloads & links
Downloads & links
-EMDB archive
| Map data |  emd_7294.map.gz | 195.7 MB |  EMDB map data format | |
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| Header (meta data) |  emd-7294-v30.xml  emd-7294.xml | 12.6 KB 12.6 KB | Display Display |  EMDB header | 
| FSC (resolution estimation) |  emd_7294_fsc.xml | 13.1 KB | Display |  FSC data file | 
| Images |  emd_7294.png | 212.5 KB | ||
| Filedesc metadata |  emd-7294.cif.gz | 5.8 KB | ||
| Archive directory |  http://ftp.pdbj.org/pub/emdb/structures/EMD-7294  ftp://ftp.pdbj.org/pub/emdb/structures/EMD-7294 | HTTPS FTP | 
-Validation report
| Summary document |  emd_7294_validation.pdf.gz | 769 KB | Display |  EMDB validaton report | 
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| Full document |  emd_7294_full_validation.pdf.gz | 768.5 KB | Display | |
| Data in XML |  emd_7294_validation.xml.gz | 13.3 KB | Display | |
| Data in CIF |  emd_7294_validation.cif.gz | 18.1 KB | Display | |
| Arichive directory |  https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-7294  ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-7294 | HTTPS FTP | 
-Related structure data
| Related structure data |  6bvfMC  7295C  6bvnC C: citing same article ( M: atomic model generated by this map | 
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| Similar structure data | 
- Links
Links
| EMDB pages |  EMDB (EBI/PDBe) /  EMDataResource | 
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| Related items in Molecule of the Month | 
- Map
Map
| File |  Download / File: emd_7294.map.gz / Format: CCP4 / Size: 209.3 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Annotation | A Hepatitis B virus capsid with T=4 symmetry, bound to HAP-TAMRA. HAP-TAMRA is a fluorescent probe derived from the Heteroaryldihydropyrimidine (HAP) class of capsid-directed antivirals. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Projections & slices | Image control
 
 Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 1.285 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Density | 
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Details | EMDB XML: 
 CCP4 map header: 
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-Supplemental data
- Sample components
Sample components
-Entire : Hepatitis B virus T=4 capsid
| Entire | Name: Hepatitis B virus T=4 capsid | 
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| Components | 
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-Supramolecule #1: Hepatitis B virus genotype D subtype adw
| Supramolecule | Name: Hepatitis B virus genotype D subtype adw / type: virus / ID: 1 / Parent: 0 / Macromolecule list: #1 / NCBI-ID: 10419 / Sci species name: Hepatitis B virus genotype D subtype adw / Sci species strain: isolate United Kingdom/adyw/1979 / Virus type: VIRUS-LIKE PARTICLE / Virus isolate: OTHER / Virus enveloped: No / Virus empty: Yes | 
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-Macromolecule #1: Capsid protein
| Macromolecule | Name: Capsid protein / type: protein_or_peptide / ID: 1 / Number of copies: 4 / Enantiomer: LEVO | 
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| Source (natural) | Organism:  Hepatitis B virus genotype D subtype adw | 
| Molecular weight | Theoretical: 16.791104 KDa | 
| Recombinant expression | Organism:   Escherichia coli (E. coli) | 
| Sequence | String: MDIDPYKEFG ATVELLSFLP SDFFPSVRDL LDTAAALYRD ALESPEHASP HHTALRQAIL AWGDLMTLAT WVGTNLEDPA  SRDLVVSYV NTNVGLKFRQ LLWFHISALT FGRETVLEYL VSFGVWIRTP PAYRPPNAPI LSTLPETTVV C UniProtKB: Capsid protein | 
-Macromolecule #2: Heteroaryldihydropyrimidine tetramethylrodamine
| Macromolecule | Name: Heteroaryldihydropyrimidine tetramethylrodamine / type: ligand / ID: 2 / Number of copies: 2 / Formula: E9D | 
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| Molecular weight | Theoretical: 939.428 Da | 
| Chemical component information |  ChemComp-E9D:  | 
-Experimental details
-Structure determination
| Method | cryo EM | 
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|  Processing | single particle reconstruction | 
| Aggregation state | particle | 
- Sample preparation
Sample preparation
| Concentration | 10 mg/mL | |||||||||
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| Buffer | pH: 7.5 Component: 
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| Grid | Model: Quantifoil R2/2 / Material: COPPER / Mesh: 300 | |||||||||
| Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 295.15 K / Instrument: FEI VITROBOT MARK III | 
- Electron microscopy
Electron microscopy
| Microscope | FEI TITAN KRIOS | 
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| Image recording | Film or detector model: GATAN K2 SUMMIT (4k x 4k) / Detector mode: SUPER-RESOLUTION / Number grids imaged: 1 / Number real images: 679 / Average electron dose: 33.0 e/Å2 | 
| Electron beam | Acceleration voltage: 300 kV / Electron source:  FIELD EMISSION GUN | 
| Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD | 
| Experimental equipment |  Model: Titan Krios / Image courtesy: FEI Company | 
+ Image processing
Image processing
-Atomic model buiding 1
| Initial model | PDB ID: Chain - Chain ID: A / Chain - Residue range: 1-143 / Chain - Source name: PDB / Chain - Initial model type: experimental model | 
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| Refinement | Space: REAL / Protocol: FLEXIBLE FIT / Target criteria: Correlation Coefficient | 
| Output model |  PDB-6bvf:  | 
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