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- PDB-3lh2: Crystal structure of HIV epitope-scaffold 4E10_1VI7A_S0_002_N 4E1... -
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Open data
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Basic information
Entry | Database: PDB / ID: 3lh2 | ||||||
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Title | Crystal structure of HIV epitope-scaffold 4E10_1VI7A_S0_002_N 4E10 Fv complex | ||||||
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![]() | IMMUNE SYSTEM / EPITOPE-SCAFFOLD | ||||||
Function / homology | Alpha-Beta Plaits - #240 / Alpha-Beta Plaits / Immunoglobulins / Immunoglobulin-like / Sandwich / 2-Layer Sandwich / Mainly Beta / Alpha Beta![]() | ||||||
Biological species | ARTIFICIAL GENE (others)![]() | ||||||
Method | ![]() ![]() | ||||||
![]() | Holmes, M.A. | ||||||
![]() | ![]() Title: Computational Design of Epitope-Scaffolds Allows Induction of Antibodies Specific for a Poorly Immunogenic HIV Vaccine Epitope. Authors: Correia, B.E. / Ban, Y.E. / Holmes, M.A. / Xu, H. / Ellingson, K. / Kraft, Z. / Carrico, C. / Boni, E. / Sather, D.N. / Zenobia, C. / Burke, K.Y. / Bradley-Hewitt, T. / Bruhn-Johannsen, J.F. ...Authors: Correia, B.E. / Ban, Y.E. / Holmes, M.A. / Xu, H. / Ellingson, K. / Kraft, Z. / Carrico, C. / Boni, E. / Sather, D.N. / Zenobia, C. / Burke, K.Y. / Bradley-Hewitt, T. / Bruhn-Johannsen, J.F. / Kalyuzhniy, O. / Baker, D. / Strong, R.K. / Stamatatos, L. / Schief, W.R. | ||||||
History |
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Structure visualization
Structure viewer | Molecule: ![]() ![]() |
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Downloads & links
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Download
PDBx/mmCIF format | ![]() | 231.6 KB | Display | ![]() |
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PDB format | ![]() | 186.3 KB | Display | ![]() |
PDBx/mmJSON format | ![]() | Tree view | ![]() | |
Others | ![]() |
-Validation report
Summary document | ![]() | 510.1 KB | Display | ![]() |
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Full document | ![]() | 522 KB | Display | |
Data in XML | ![]() | 42.1 KB | Display | |
Data in CIF | ![]() | 58.9 KB | Display | |
Arichive directory | ![]() ![]() | HTTPS FTP |
-Related structure data
Related structure data | ![]() 3lefC ![]() 3lf6C ![]() 3lf9C ![]() 3lg7C ![]() 3lhpC ![]() 1tzgS C: citing same article ( S: Starting model for refinement |
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Similar structure data |
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Links
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Assembly
Deposited unit | ![]()
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1 | ![]()
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2 | ![]()
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Unit cell |
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Components
#1: Protein | Mass: 8455.588 Da / Num. of mol.: 4 Source method: isolated from a genetically manipulated source Details: The author states that THE EPITOPE-SCAFFOLD IS BASED on the ribosome recycling factor from Vibrio parahaemolyticus (PDB ID 1IS1). Source: (gene. exp.) ARTIFICIAL GENE (others) / Plasmid: PET29 / Production host: ![]() ![]() #2: Antibody | Mass: 14712.454 Da / Num. of mol.: 4 / Mutation: W104A Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() ![]() ![]() #3: Antibody | Mass: 12304.698 Da / Num. of mol.: 4 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() ![]() ![]() #4: Water | ChemComp-HOH / | |
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-Experimental details
-Experiment
Experiment | Method: ![]() |
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Sample preparation
Crystal | Density Matthews: 3.06 Å3/Da / Density % sol: 59.82 % |
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Crystal grow | Temperature: 298 K / Method: vapor diffusion, hanging drop / pH: 8 Details: Na acetate, imidazole, pH 8, VAPOR DIFFUSION, HANGING DROP, temperature 298K |
-Data collection
Diffraction | Mean temperature: 107 K |
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Diffraction source | Source: ![]() |
Detector | Type: RIGAKU SATURN 944+ / Detector: CCD / Date: Oct 22, 2008 / Details: Rigaku Varimax HF |
Radiation | Monochromator: Mirrors / Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
Radiation wavelength | Wavelength: 1.54 Å / Relative weight: 1 |
Reflection | Resolution: 2.65→28.01 Å / Num. all: 49017 / Num. obs: 49017 / % possible obs: 98.9 % / Redundancy: 3.88 % / Biso Wilson estimate: 62.3 Å2 / Rmerge(I) obs: 0.095 / Net I/σ(I): 9.4 |
Reflection shell | Resolution: 2.65→2.74 Å / Redundancy: 3.68 % / Rmerge(I) obs: 0.376 / Mean I/σ(I) obs: 2.7 / Num. unique all: 4883 / % possible all: 98.6 |
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Processing
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Refinement | Method to determine structure: ![]() Starting model: Computationally-derived model of the epitope-scaffold Fv complex, with the Fv based on PDB ID 1TZG. Resolution: 2.65→26.7 Å / Cor.coef. Fo:Fc: 0.921 / Cor.coef. Fo:Fc free: 0.878 / SU B: 11.214 / SU ML: 0.24 / Isotropic thermal model: Isotropic / Cross valid method: THROUGHOUT / ESU R: 0.578 / ESU R Free: 0.325 / Stereochemistry target values: Engh & Huber / Details: HYDROGENS HAVE BEEN ADDED IN THE RIDING POSITIONS
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Solvent computation | Ion probe radii: 0.8 Å / Shrinkage radii: 0.8 Å / VDW probe radii: 1.4 Å / Solvent model: BABINET MODEL WITH MASK | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Displacement parameters | Biso mean: 47.111 Å2
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Refinement step | Cycle: LAST / Resolution: 2.65→26.7 Å
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Refine LS restraints |
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LS refinement shell | Resolution: 2.647→2.715 Å / Total num. of bins used: 20
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