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Open data
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Basic information
| Entry | Database: PDB / ID: 9yiw | |||||||||
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| Title | PC94-A.15 Fab in complex with BG505 SOSIP trimer and RM20A3 Fab | |||||||||
Components |
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Keywords | VIRAL PROTEIN / HIV / broadly neutralizing antibody / bnAb / V3-glycan / N332 / Env | |||||||||
| Biological species | Homo sapiens (human)![]() ![]() Human immunodeficiency virus 1 | |||||||||
| Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 3.6 Å | |||||||||
Authors | Phulera, S. / Omorodion, O. / Ward, A.B. / Ozorowski, G. | |||||||||
| Funding support | United States, 1items
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Citation | Journal: To Be PublishedTitle: Tolerance of multiple glycan conformations by an N332-directed HIV bnAb lineage provides a roadmap to broad neutralization Authors: Nemoz, B. / Rouzeau, R. | |||||||||
| 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 | 9yiw.cif.gz | 497.8 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb9yiw.ent.gz | 404.6 KB | Display | PDB format |
| PDBx/mmJSON format | 9yiw.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/yi/9yiw ftp://data.pdbj.org/pub/pdb/validation_reports/yi/9yiw | HTTPS FTP |
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-Related structure data
| Related structure data | ![]() 73000MC ![]() 9yj0C ![]() 9yj1C ![]() 9yj2C ![]() 9yj3C M: map data used to model this data C: citing same article ( |
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Links
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Assembly
| Deposited unit | ![]()
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Components
-BG505 SOSIP.664 ... , 2 types, 6 molecules ACEBDF
| #5: Protein | Mass: 57945.977 Da / Num. of mol.: 3 / Fragment: UNP residues 30-505 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Human immunodeficiency virus 1 / Production host: Homo sapiens (human)#6: Protein | Mass: 17146.482 Da / Num. of mol.: 3 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Human immunodeficiency virus 1 / Production host: Homo sapiens (human) |
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-Antibody , 4 types, 8 molecules HIKQLMOS
| #1: Antibody | Mass: 25094.072 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Production host: Homo sapiens (human) | ||||
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| #2: Antibody | Mass: 24194.145 Da / Num. of mol.: 3 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Homo sapiens (human)#3: Antibody | | Mass: 23513.094 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Production host: Homo sapiens (human)#4: Antibody | Mass: 22827.150 Da / Num. of mol.: 3 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Homo sapiens (human) |
-Sugars , 6 types, 61 molecules 
| #7: Polysaccharide | 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose Source method: isolated from a genetically manipulated source #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 | alpha-D-mannopyranose-(1-2)-alpha-D-mannopyranose-(1-2)-alpha-D-mannopyranose-(1-3)-[alpha-D- ...alpha-D-mannopyranose-(1-2)-alpha-D-mannopyranose-(1-2)-alpha-D-mannopyranose-(1-3)-[alpha-D-mannopyranose-(1-2)-alpha-D-mannopyranose-(1-6)-[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 #10: Polysaccharide | Source method: isolated from a genetically manipulated source #11: Polysaccharide | Source method: isolated from a genetically manipulated source #12: Sugar | ChemComp-NAG / |
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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: PC94-A.15 Fab in complex with BG505 SOSIP trimer and RM20A3 Fab Type: COMPLEX / Entity ID: #1-#6 / Source: RECOMBINANT |
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| Molecular weight | Experimental value: NO |
| Source (natural) | Organism: Homo sapiens (human) |
| Source (recombinant) | Organism: Homo sapiens (human) |
| Buffer solution | pH: 7.4 |
| Specimen | Conc.: 6.7 mg/ml / Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES |
| Specimen support | Grid material: GOLD / Grid mesh size: 300 divisions/in. / Grid type: UltrAuFoil R1.2/1.3 |
| Vitrification | Instrument: FEI VITROBOT MARK IV / Cryogen name: ETHANE / Humidity: 100 % / Chamber temperature: 277 K |
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Electron microscopy imaging
| Microscopy | Model: TFS GLACIOS |
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| Electron gun | Electron source: FIELD EMISSION GUN / Accelerating voltage: 200 kV / Illumination mode: FLOOD BEAM |
| Electron lens | Mode: BRIGHT FIELD / Nominal defocus max: 1700 nm / Nominal defocus min: 800 nm / Alignment procedure: COMA FREE |
| Image recording | Electron dose: 45 e/Å2 / Film or detector model: TFS FALCON 4i (4k x 4k) |
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Processing
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| CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION | ||||||||||||||||||||||||
| Symmetry | Point symmetry: C1 (asymmetric) | ||||||||||||||||||||||||
| 3D reconstruction | Resolution: 3.6 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 16931 / Symmetry type: POINT | ||||||||||||||||||||||||
| Refinement | Highest resolution: 3.6 Å Stereochemistry target values: REAL-SPACE (WEIGHTED MAP SUM AT ATOM CENTERS) | ||||||||||||||||||||||||
| Refine LS restraints |
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Movie
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About Yorodumi




Homo sapiens (human)

Human immunodeficiency virus 1
United States, 1items
Citation








PDBj




FIELD EMISSION GUN