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Yorodumi- PDB-8rbv: SARS-CoV-2 Spike-derived peptide S976-984 S982A mutant (VLNDILARL... -
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Open data
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Basic information
| Entry | Database: PDB / ID: 8rbv | ||||||
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| Title | SARS-CoV-2 Spike-derived peptide S976-984 S982A mutant (VLNDILARL) presented by HLA-A*02:01 | ||||||
Components |
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Keywords | IMMUNE SYSTEM / human leukocyte antigen / major histocompatibility complex / HLA-A2 / HLA-A*02:01 / SARS-CoV-2 / Spike | ||||||
| Function / homology | Function and homology informationantigen processing and presentation of peptide antigen via MHC class I / negative regulation of receptor binding / early endosome lumen / Nef mediated downregulation of MHC class I complex cell surface expression / DAP12 interactions / transferrin transport / cellular response to iron ion / lumenal side of endoplasmic reticulum membrane / Endosomal/Vacuolar pathway / Antigen Presentation: Folding, assembly and peptide loading of class I MHC ...antigen processing and presentation of peptide antigen via MHC class I / negative regulation of receptor binding / early endosome lumen / Nef mediated downregulation of MHC class I complex cell surface expression / DAP12 interactions / transferrin transport / cellular response to iron ion / lumenal side of endoplasmic reticulum membrane / Endosomal/Vacuolar pathway / Antigen Presentation: Folding, assembly and peptide loading of class I MHC / peptide antigen assembly with MHC class II protein complex / cellular response to iron(III) ion / 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 / 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 / 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 / cellular response to nicotine / positive regulation of T cell mediated cytotoxicity / multicellular organismal-level iron ion homeostasis / specific granule lumen / phagocytic vesicle membrane / recycling endosome membrane / Interferon gamma signaling / Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell / negative regulation of epithelial cell proliferation / MHC class II protein complex binding / 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 / negative regulation of neuron projection development / ER-Phagosome pathway / protein refolding / early endosome membrane / protein homotetramerization / amyloid fibril formation / intracellular iron ion homeostasis / learning or memory / immune response / endoplasmic reticulum lumen / Amyloid fiber formation / Golgi membrane / lysosomal membrane / external side of plasma membrane / focal adhesion / Neutrophil degranulation / SARS-CoV-2 activates/modulates innate and adaptive immune responses / structural molecule activity / cell surface / endoplasmic reticulum / Golgi apparatus / protein homodimerization activity / extracellular space / extracellular exosome / extracellular region / metal ion binding / identical protein binding / membrane / plasma membrane / cytosol Similarity search - Function | ||||||
| Biological species | Homo sapiens (human)![]() | ||||||
| Method | X-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / molecular replacement / Resolution: 1.8 Å | ||||||
Authors | Ahn, Y.M. / Maddumage, J.C. / Szeto, C. / Gras, S. | ||||||
| Funding support | Australia, 1items
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Citation | Journal: Curr Res Struct Biol / Year: 2024Title: The impact of SARS-CoV-2 spike mutation on peptide presentation is HLA allomorph-specific. Authors: Ahn, Y.M. / Maddumage, J.C. / Grant, E.J. / Chatzileontiadou, D.S.M. / Perera, W.W.J.G. / Baker, B.M. / Szeto, C. / Gras, S. | ||||||
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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 | 8rbv.cif.gz | 105.2 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb8rbv.ent.gz | 75.7 KB | Display | PDB format |
| PDBx/mmJSON format | 8rbv.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 8rbv_validation.pdf.gz | 3 MB | Display | wwPDB validaton report |
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| Full document | 8rbv_full_validation.pdf.gz | 3 MB | Display | |
| Data in XML | 8rbv_validation.xml.gz | 18.4 KB | Display | |
| Data in CIF | 8rbv_validation.cif.gz | 26.2 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/rb/8rbv ftp://data.pdbj.org/pub/pdb/validation_reports/rb/8rbv | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 8rbuC ![]() 8rcvC ![]() 8refC ![]() 8rh6C ![]() 8rhqC ![]() 1ogaS S: Starting model for refinement C: citing same article ( |
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| Similar structure data | Similarity search - Function & homology F&H Search |
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Links
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Assembly
| Deposited unit | ![]()
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| Unit cell |
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Components
-Protein , 2 types, 2 molecules AB
| #1: Protein | Mass: 40974.797 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: HLA-AProduction host: ![]() References: UniProt: Q53Z42 |
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| #2: Protein | Mass: 11879.356 Da / Num. of mol.: 1 / Fragment: UNP residues 21-119 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: B2M, CDABP0092, HDCMA22PProduction host: ![]() References: UniProt: P61769 |
-Protein/peptide , 1 types, 1 molecules C
| #3: Protein/peptide | Mass: 1027.239 Da / Num. of mol.: 1 / Source method: obtained synthetically Source: (synth.) ![]() |
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-Non-polymers , 5 types, 225 molecules 








| #4: Chemical | | #5: Chemical | #6: Chemical | #7: Chemical | ChemComp-PEG / | #8: Water | ChemComp-HOH / | |
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-Details
| Has ligand of interest | Y |
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| Has protein modification | Y |
-Experimental details
-Experiment
| Experiment | Method: X-RAY DIFFRACTION / Number of used crystals: 1 |
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Sample preparation
| Crystal | Density Matthews: 2.41 Å3/Da / Density % sol: 48.89 % |
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| Crystal grow | Temperature: 293 K / Method: vapor diffusion, hanging drop / Details: 13% P3350; 0.1M NaFlu; 2% EG; 1 mM CdCl2 |
-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: 0.953732 Å | ||||||||||||||||||||||||||||||
| Detector | Type: DECTRIS EIGER X 16M / Detector: PIXEL / Date: Sep 22, 2021 | ||||||||||||||||||||||||||||||
| Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray | ||||||||||||||||||||||||||||||
| Radiation wavelength | Wavelength: 0.953732 Å / Relative weight: 1 | ||||||||||||||||||||||||||||||
| Reflection | Resolution: 1.8→47.51 Å / Num. obs: 49032 / % possible obs: 100 % / Redundancy: 7.3 % / Biso Wilson estimate: 29.38 Å2 / CC1/2: 0.998 / Rmerge(I) obs: 0.091 / Rpim(I) all: 0.036 / Rrim(I) all: 0.099 / Net I/σ(I): 12 / Num. measured all: 359908 / Scaling rejects: 9 | ||||||||||||||||||||||||||||||
| Reflection shell | Diffraction-ID: 1
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-Phasing
| Phasing | Method: molecular replacement | |||||||||
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| Phasing MR | Model details: Phaser MODE: MR_AUTO
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Processing
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| Refinement | Method to determine structure: MOLECULAR REPLACEMENTStarting model: 1OGA Resolution: 1.8→43.67 Å / SU ML: 0.21 / Cross valid method: THROUGHOUT / σ(F): 1.34 / Phase error: 20.9 / Stereochemistry target values: ML
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| Solvent computation | Shrinkage radii: 0.9 Å / VDW probe radii: 1.1 Å / Solvent model: FLAT BULK SOLVENT MODEL | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Refinement step | Cycle: LAST / Resolution: 1.8→43.67 Å
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| Refine LS restraints |
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| LS refinement shell |
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About Yorodumi



Homo sapiens (human)
X-RAY DIFFRACTION
Australia, 1items
Citation





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