+Open data
-Basic information
Entry | Database: PDB / ID: 8v99 | ||||||
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Title | GII.26 Leon 4509 norovirus protruding domain | ||||||
Components | Capsid protein VP1 | ||||||
Keywords | VIRAL PROTEIN / norovirus | ||||||
Function / homology | Calicivirus coat protein C-terminal / Calicivirus coat protein C-terminal / Calicivirus coat protein / Calicivirus coat protein / Picornavirus/Calicivirus coat protein / Viral coat protein subunit / ACETATE ION / DI(HYDROXYETHYL)ETHER / Major capsid protein Function and homology information | ||||||
Biological species | Norovirus GII | ||||||
Method | X-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 1.47 Å | ||||||
Authors | Kher, G. / Reese, T. / Pancera, M. / Hansman, G. | ||||||
Funding support | Germany, 1items
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Citation | Journal: J.Virol. / Year: 2024 Title: Development of a broad-spectrum therapeutic Fc-nanobody for human noroviruses. Authors: Hansman, G.S. / Kher, G. / Svirina, A.D. / Tame, J.R.H. / Hartley-Tassell, L. / Irie, H. / Haselhorst, T. / von Itzstein, M. / Rudd, P.A. / Pancera, M. | ||||||
History |
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-Structure visualization
Structure viewer | Molecule: MolmilJmol/JSmol |
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-Downloads & links
-Download
PDBx/mmCIF format | 8v99.cif.gz | 369 KB | Display | PDBx/mmCIF format |
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PDB format | pdb8v99.ent.gz | 303.9 KB | Display | PDB format |
PDBx/mmJSON format | 8v99.json.gz | Tree view | PDBx/mmJSON format | |
Others | Other downloads |
-Validation report
Summary document | 8v99_validation.pdf.gz | 486.9 KB | Display | wwPDB validaton report |
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Full document | 8v99_full_validation.pdf.gz | 492.9 KB | Display | |
Data in XML | 8v99_validation.xml.gz | 30.2 KB | Display | |
Data in CIF | 8v99_validation.cif.gz | 45 KB | Display | |
Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/v9/8v99 ftp://data.pdbj.org/pub/pdb/validation_reports/v9/8v99 | HTTPS FTP |
-Related structure data
Related structure data | 8v95C 8v96C 8v97C 8v98C 8v9aC C: citing same article (ref.) |
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Similar structure data | Similarity search - Function & homologyF&H Search |
-Links
-Assembly
Deposited unit |
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1 |
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Unit cell |
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-Components
#1: Protein | Mass: 59535.848 Da / Num. of mol.: 2 / Fragment: GII.26 Leon 4509 P domain Source method: isolated from a genetically manipulated source Source: (gene. exp.) Norovirus GII / Production host: Escherichia coli (E. coli) / References: UniProt: A0A142KD02 #2: Chemical | ChemComp-EDO / #3: Chemical | #4: Chemical | #5: Water | ChemComp-HOH / | Has ligand of interest | N | |
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-Experimental details
-Experiment
Experiment | Method: X-RAY DIFFRACTION / Number of used crystals: 1 |
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-Sample preparation
Crystal grow | Temperature: 291.15 K / Method: vapor diffusion, hanging drop Details: 0.1M Ammonium acetate 0.1 M BIS-Tris (pH 5.5) 17% w/v PEG 10,000 |
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-Data collection
Diffraction | Mean temperature: 100 K / Serial crystal experiment: N |
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Diffraction source | Source: SYNCHROTRON / Site: Australian Synchrotron / Beamline: MX2 / Wavelength: 0.95372 Å |
Detector | Type: ADSC QUANTUM 315r / Detector: CCD / Date: Mar 3, 2023 |
Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
Radiation wavelength | Wavelength: 0.95372 Å / Relative weight: 1 |
Reflection | Resolution: 1.47→43.69 Å / Num. obs: 111573 / % possible obs: 98.8 % / Redundancy: 2.9 % / CC1/2: 0.995 / Rmerge(I) obs: 0.09 / Rpim(I) all: 0.062 / Rrim(I) all: 0.11 / Χ2: 0.47 / Net I/σ(I): 6.1 / Num. measured all: 322323 |
Reflection shell | Resolution: 1.47→1.5 Å / % possible obs: 93.9 % / Redundancy: 2.8 % / Rmerge(I) obs: 0.817 / Num. measured all: 14540 / Num. unique obs: 5215 / CC1/2: 0.476 / Rpim(I) all: 0.569 / Rrim(I) all: 1 / Χ2: 0.36 / Net I/σ(I) obs: 0.9 |
-Processing
Software |
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Refinement | Method to determine structure: MOLECULAR REPLACEMENT / Resolution: 1.47→40.66 Å / SU ML: 0.18 / Cross valid method: FREE R-VALUE / σ(F): 1.36 / Phase error: 18.43 / Stereochemistry target values: ML
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Solvent computation | Shrinkage radii: 0.9 Å / VDW probe radii: 1.11 Å / Solvent model: FLAT BULK SOLVENT MODEL | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Refinement step | Cycle: LAST / Resolution: 1.47→40.66 Å
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Refine LS restraints |
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LS refinement shell |
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