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Yorodumi- PDB-5wdu: HIV-1 Env BG505 SOSIP.664 H72C-H564C trimer in complex with bNAbs... -
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Open data
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Basic information
| Entry | Database: PDB / ID: 5wdu | |||||||||||||||
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| Title | HIV-1 Env BG505 SOSIP.664 H72C-H564C trimer in complex with bNAbs PGT122 Fab, 35O22 Fab and NIH45-46 scFv | |||||||||||||||
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Keywords | IMMUNE SYSTEM / HIV-1 Env / broadly neutralizing antibodies / viral glycoprotein | |||||||||||||||
| Function / homology | Function and homology informationsymbiont-mediated perturbation of host defense response / positive regulation of plasma membrane raft polarization / positive regulation of receptor clustering / host cell endosome membrane / clathrin-dependent endocytosis of virus by host cell / viral protein processing / fusion of virus membrane with host plasma membrane / fusion of virus membrane with host endosome membrane / viral envelope / virion attachment to host cell ...symbiont-mediated perturbation of host defense response / positive regulation of plasma membrane raft polarization / positive regulation of receptor clustering / host cell endosome membrane / clathrin-dependent endocytosis of virus by host cell / viral protein processing / fusion of virus membrane with host plasma membrane / fusion of virus membrane with host endosome membrane / viral envelope / virion attachment to host cell / host cell plasma membrane / virion membrane / structural molecule activity / identical protein binding / membrane Similarity search - Function | |||||||||||||||
| Biological species | ![]() Human immunodeficiency virus 1 Homo sapiens (human) | |||||||||||||||
| Method | X-RAY DIFFRACTION / SYNCHROTRON / Resolution: 7 Å | |||||||||||||||
Authors | Julien, J.-P. / Torrents de la Pena, A. / Sanders, R.W. / Wilson, I.A. | |||||||||||||||
| Funding support | United States, 3items
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Citation | Journal: Cell Rep / Year: 2017Title: Improving the Immunogenicity of Native-like HIV-1 Envelope Trimers by Hyperstabilization. Authors: Torrents de la Pena, A. / Julien, J.P. / de Taeye, S.W. / Garces, F. / Guttman, M. / Ozorowski, G. / Pritchard, L.K. / Behrens, A.J. / Go, E.P. / Burger, J.A. / Schermer, E.E. / Sliepen, K. ...Authors: Torrents de la Pena, A. / Julien, J.P. / de Taeye, S.W. / Garces, F. / Guttman, M. / Ozorowski, G. / Pritchard, L.K. / Behrens, A.J. / Go, E.P. / Burger, J.A. / Schermer, E.E. / Sliepen, K. / Ketas, T.J. / Pugach, P. / Yasmeen, A. / Cottrell, C.A. / Torres, J.L. / Vavourakis, C.D. / van Gils, M.J. / LaBranche, C. / Montefiori, D.C. / Desaire, H. / Crispin, M. / Klasse, P.J. / Lee, K.K. / Moore, J.P. / Ward, A.B. / Wilson, I.A. / Sanders, R.W. | |||||||||||||||
| 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 | 5wdu.cif.gz | 1 MB | Display | PDBx/mmCIF format |
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| PDB format | pdb5wdu.ent.gz | 867 KB | Display | PDB format |
| PDBx/mmJSON format | 5wdu.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 5wdu_validation.pdf.gz | 5.4 MB | Display | wwPDB validaton report |
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| Full document | 5wdu_full_validation.pdf.gz | 5.5 MB | Display | |
| Data in XML | 5wdu_validation.xml.gz | 176.9 KB | Display | |
| Data in CIF | 5wdu_validation.cif.gz | 235.3 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/wd/5wdu ftp://data.pdbj.org/pub/pdb/validation_reports/wd/5wdu | HTTPS FTP |
-Related structure data
| Similar structure data |
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Links
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Assembly
| Deposited unit | ![]()
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| Unit cell |
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Components
-Envelope glycoprotein ... , 2 types, 6 molecules GFQAJR
| #1: Protein | Mass: 52756.711 Da / Num. of mol.: 3 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Human immunodeficiency virus 1 / Gene: env / Production host: Homo sapiens (human) / References: UniProt: Q2N0S6#3: Protein | Mass: 16693.975 Da / Num. of mol.: 3 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Human immunodeficiency virus 1 / Gene: env / Production host: Homo sapiens (human) / References: UniProt: Q2N0S8 |
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-Antibody , 5 types, 15 molecules DOWBKSCLTHMUINV
| #2: Antibody | Mass: 27420.459 Da / Num. of mol.: 3 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Production host: Homo sapiens (human)#4: Antibody | Mass: 22560.941 Da / Num. of mol.: 3 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Production host: Homo sapiens (human) / References: UniProt: Q2N0S6*PLUS#5: Antibody | Mass: 25115.289 Da / Num. of mol.: 3 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Production host: Homo sapiens (human)#6: Antibody | Mass: 26042.402 Da / Num. of mol.: 3 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Production host: Homo sapiens (human)#7: Antibody | Mass: 23000.473 Da / Num. of mol.: 3 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Production host: Homo sapiens (human) |
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-Sugars , 8 types, 60 molecules 
| #8: Polysaccharide | alpha-D-mannopyranose-(1-3)-[alpha-D-mannopyranose-(1-6)]beta-D-mannopyranose-(1-4)-2-acetamido-2- ...alpha-D-mannopyranose-(1-3)-[alpha-D-mannopyranose-(1-6)]beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose Source method: isolated from a genetically manipulated source #9: Polysaccharide | Source method: isolated from a genetically manipulated source #10: Polysaccharide | Source method: isolated from a genetically manipulated source #11: Polysaccharide | Source method: isolated from a genetically manipulated source #12: Polysaccharide | Source method: isolated from a genetically manipulated source #13: Polysaccharide | Source method: isolated from a genetically manipulated source #14: Polysaccharide | Source method: isolated from a genetically manipulated source #15: Sugar | ChemComp-NAG / |
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-Details
| Has protein modification | Y |
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-Experimental details
-Experiment
| Experiment | Method: X-RAY DIFFRACTION / Number of used crystals: 1 |
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Sample preparation
| Crystal | Density Matthews: 5.6 Å3/Da / Density % sol: 78.04 % |
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| Crystal grow | Temperature: 293 K / Method: vapor diffusion, sitting drop Details: 8% (w/v) polyethylene glycol 8000, 0.1 M Tris, pH 8.5 |
-Data collection
| Diffraction | Mean temperature: 100 K |
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| Diffraction source | Source: SYNCHROTRON / Site: APS / Beamline: 23-ID-D / Wavelength: 1.03317 Å |
| Detector | Type: DECTRIS PILATUS3 6M / Detector: PIXEL / Date: Feb 1, 2014 |
| Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
| Radiation wavelength | Wavelength: 1.03317 Å / Relative weight: 1 |
| Reflection | Resolution: 7→40 Å / Num. obs: 19551 / % possible obs: 99.3 % / Redundancy: 7.6 % / CC1/2: 0.994 / Rpim(I) all: 0.08 / Rsym value: 0.2 / Net I/σ(I): 7.2 |
| Reflection shell | Resolution: 7→7.1 Å / Redundancy: 8.1 % / Mean I/σ(I) obs: 1.7 / CC1/2: 0.448 / Rpim(I) all: 0.33 / Rsym value: 0.88 / % possible all: 99.9 |
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Processing
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| Refinement | Resolution: 7→39.707 Å / SU ML: 1.36 / Cross valid method: FREE R-VALUE / σ(F): 1.45 / Phase error: 42.99 / 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: 7→39.707 Å
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| Refine LS restraints |
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| LS refinement shell |
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About Yorodumi




Human immunodeficiency virus 1
Homo sapiens (human)
X-RAY DIFFRACTION
United States, 3items
Citation







PDBj





