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Yorodumi- PDB-5v5l: Crystal structure of HLA-B*5801 complex with HIV-1 gag derived pe... -
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Basic information
| Entry | Database: PDB / ID: 5v5l | ||||||
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| Title | Crystal structure of HLA-B*5801 complex with HIV-1 gag derived peptide TW10 | ||||||
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Keywords | IMMUNE SYSTEM / HLA / HIV / gag / TW10 | ||||||
| Function / homology | Function and homology informationregulation of interleukin-12 production / regulation of dendritic cell differentiation / regulation of T cell anergy / regulation of interleukin-6 production / TAP binding / protection from natural killer cell mediated cytotoxicity / antigen processing and presentation of endogenous peptide antigen via MHC class Ib / antigen processing and presentation of endogenous peptide antigen via MHC class I via ER pathway, TAP-independent / detection of bacterium / negative regulation of receptor binding ...regulation of interleukin-12 production / regulation of dendritic cell differentiation / regulation of T cell anergy / regulation of interleukin-6 production / TAP binding / protection from natural killer cell mediated cytotoxicity / antigen processing and presentation of endogenous peptide antigen via MHC class Ib / antigen processing and presentation of endogenous peptide antigen via MHC class I via ER pathway, TAP-independent / detection of bacterium / negative regulation of receptor binding / secretory granule membrane / early endosome lumen / Nef mediated downregulation of MHC class I complex cell surface expression / DAP12 interactions / transferrin transport / cellular response to iron ion / Endosomal/Vacuolar pathway / HIV-1 retropepsin / Antigen Presentation: Folding, assembly and peptide loading of class I MHC / symbiont-mediated activation of host apoptosis / retroviral ribonuclease H / peptide antigen assembly with MHC class II protein complex / lumenal side of endoplasmic reticulum membrane / exoribonuclease H / cellular response to iron(III) ion / exoribonuclease H activity / MHC class II protein complex / negative regulation of forebrain neuron differentiation / antigen processing and presentation of exogenous protein antigen via MHC class Ib, TAP-dependent / ER to Golgi transport vesicle membrane / peptide antigen assembly with MHC class I protein complex / regulation of iron ion transport / regulation of erythrocyte differentiation / HFE-transferrin receptor complex / defense response / response to molecule of bacterial origin / MHC class I peptide loading complex / T cell mediated cytotoxicity / positive regulation of T cell cytokine production / antigen processing and presentation of endogenous peptide antigen via MHC class I / antigen processing and presentation of exogenous peptide antigen via MHC class II / DNA integration / positive regulation of immune response / MHC class I protein complex / positive regulation of T cell activation / peptide antigen binding / positive regulation of receptor-mediated endocytosis / negative regulation of neurogenesis / viral genome integration into host DNA / cellular response to nicotine / positive regulation of T cell mediated cytotoxicity / multicellular organismal-level iron ion homeostasis / RNA-directed DNA polymerase / establishment of integrated proviral latency / RNA stem-loop binding / specific granule lumen / viral penetration into host nucleus / host multivesicular body / phagocytic vesicle membrane / RNA-directed DNA polymerase activity / recycling endosome membrane / Interferon gamma signaling / RNA-DNA hybrid ribonuclease activity / Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell / negative regulation of epithelial cell proliferation / Transferases; Transferring phosphorus-containing groups; Nucleotidyltransferases / MHC class II protein complex binding / Interferon alpha/beta signaling / Modulation by Mtb of host immune system / late endosome membrane / sensory perception of smell / positive regulation of cellular senescence / tertiary granule lumen / DAP12 signaling / T cell differentiation in thymus / host cell / negative regulation of neuron projection development / protein-folding chaperone binding / ER-Phagosome pathway / protein refolding / viral nucleocapsid / early endosome membrane / DNA recombination / protein homotetramerization / amyloid fibril formation / DNA-directed DNA polymerase / adaptive immune response / aspartic-type endopeptidase activity / Hydrolases; Acting on ester bonds / intracellular iron ion homeostasis / DNA-directed DNA polymerase activity / learning or memory / immune response / endoplasmic reticulum lumen / Amyloid fiber formation / symbiont-mediated suppression of host gene expression / signaling receptor binding / viral translational frameshifting / Golgi membrane / innate immune response Similarity search - Function | ||||||
| Biological species | Homo sapiens (human)![]() Human immunodeficiency virus 1 | ||||||
| Method | X-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 2.002 Å | ||||||
Authors | Li, X. / Wang, J.-H. | ||||||
Citation | Journal: Cell. Mol. Immunol. / Year: 2017Title: Crystal structure of HLA-B*5801 with a TW10 HIV Gag epitope reveals a novel mode of peptide presentation. Authors: Li, X. / Lamothe, P.A. / Walker, B.D. / Wang, J.H. | ||||||
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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 | 5v5l.cif.gz | 181.3 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb5v5l.ent.gz | 142.5 KB | Display | PDB format |
| PDBx/mmJSON format | 5v5l.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 5v5l_validation.pdf.gz | 459 KB | Display | wwPDB validaton report |
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| Full document | 5v5l_full_validation.pdf.gz | 463.6 KB | Display | |
| Data in XML | 5v5l_validation.xml.gz | 33.8 KB | Display | |
| Data in CIF | 5v5l_validation.cif.gz | 49.2 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/v5/5v5l ftp://data.pdbj.org/pub/pdb/validation_reports/v5/5v5l | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 5v5mC ![]() 1a1mS C: citing same article ( S: Starting model for refinement |
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| Similar structure data |
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Assembly
| Deposited unit | ![]()
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| 2 | ![]()
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| Unit cell |
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Components
| #1: Protein | Mass: 32098.465 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: HLA-B, HLAB / Production host: ![]() #2: Protein | Mass: 11879.356 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: B2M, CDABP0092, HDCMA22P / Production host: ![]() #3: Protein/peptide | Mass: 1162.249 Da / Num. of mol.: 2 / Source method: obtained synthetically / Source: (synth.) ![]() Human immunodeficiency virus 1 / References: UniProt: P03366*PLUS#4: Water | ChemComp-HOH / | 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: 2.6 Å3/Da / Density % sol: 52.72 % |
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| Crystal grow | Temperature: 290 K / Method: vapor diffusion, sitting drop / pH: 6.5 Details: 15-20% w/v PEG 4000, 20% w/v 2-propanol, 0.1 M MES pH 6.5 |
-Data collection
| Diffraction | Mean temperature: 100 K |
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| Diffraction source | Source: SYNCHROTRON / Site: APS / Beamline: 19-ID / Wavelength: 0.9792 Å |
| Detector | Type: ADSC QUANTUM 315r / Detector: CCD / Date: Oct 21, 2016 |
| Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
| Radiation wavelength | Wavelength: 0.9792 Å / Relative weight: 1 |
| Reflection | Resolution: 2→50 Å / Num. obs: 63127 / % possible obs: 98.22 % / Redundancy: 6.6 % / Rmerge(I) obs: 0.07 |
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Processing
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| Refinement | Method to determine structure: MOLECULAR REPLACEMENTStarting model: 1A1M Resolution: 2.002→42.816 Å / SU ML: 0.2 / Cross valid method: FREE R-VALUE / σ(F): 1.35 / Phase error: 21.31
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| Solvent computation | Shrinkage radii: 0.9 Å / VDW probe radii: 1.11 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Refinement step | Cycle: LAST / Resolution: 2.002→42.816 Å
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| Refine LS restraints |
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| LS refinement shell |
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Homo sapiens (human)
Human immunodeficiency virus 1
X-RAY DIFFRACTION
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