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Yorodumi- PDB-7kgo: Crystal Structure of HLA-A*0201in complex with SARS-CoV-2 N351-359 -
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Open data
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Basic information
| Entry | Database: PDB / ID: 7kgo | |||||||||
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| Title | Crystal Structure of HLA-A*0201in complex with SARS-CoV-2 N351-359 | |||||||||
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Keywords | IMMUNE SYSTEM / HLA-A*0201 / T cell / SARS-CoV-2 / COVID-19 / viral peptide / TCR | |||||||||
| Function / homology | Function and homology information: / response to host immune response / viral RNA genome packaging / negative regulation of interferon-beta production / Maturation of nucleoprotein / poly(U) RNA binding / intracellular membraneless organelle / positive regulation of NLRP3 inflammasome complex assembly / antigen processing and presentation of peptide antigen via MHC class I / MHC class I protein binding ...: / response to host immune response / viral RNA genome packaging / negative regulation of interferon-beta production / Maturation of nucleoprotein / poly(U) RNA binding / intracellular membraneless organelle / positive regulation of NLRP3 inflammasome complex assembly / antigen processing and presentation of peptide antigen via MHC class I / MHC class I protein binding / CD28 dependent PI3K/Akt signaling / SARS-CoV-2 targets host intracellular signalling and regulatory pathways / protein sequestering activity / negative regulation of receptor binding / early endosome lumen / Nef mediated downregulation of MHC class I complex cell surface expression / DAP12 interactions / transferrin transport / VEGFR2 mediated vascular permeability / 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 / molecular condensate scaffold activity / 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 / NOD1/2 Signaling Pathway / TAK1-dependent IKK and NF-kappa-B activation / T cell mediated cytotoxicity / positive regulation of T cell cytokine production / antigen processing and presentation of endogenous peptide antigen via MHC class I / DDX58/IFIH1-mediated induction of interferon-alpha/beta / 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 / RNA stem-loop binding / specific granule lumen / Interleukin-1 signaling / 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 / Interferon alpha/beta signaling / Modulation by Mtb of host immune system / late endosome membrane / sensory perception of smell / viral capsid / positive regulation of cellular senescence / tertiary granule lumen / DAP12 signaling / T cell differentiation in thymus / PIP3 activates AKT signaling / negative regulation of neuron projection development / ER-Phagosome pathway / protein refolding / viral nucleocapsid / Transcription of SARS-CoV-2 sgRNAs / host cell endoplasmic reticulum-Golgi intermediate compartment / early endosome membrane / protein homotetramerization / Translation of Structural Proteins / Virion Assembly and Release / host extracellular space / host cell Golgi apparatus / amyloid fibril formation / Induction of Cell-Cell Fusion / intracellular iron ion homeostasis / Attachment and Entry / learning or memory / host cell perinuclear region of cytoplasm / immune response / endoplasmic reticulum lumen / Amyloid fiber formation / ribonucleoprotein complex / 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 Similarity search - Function | |||||||||
| Biological species | Homo sapiens (human)![]() | |||||||||
| Method | X-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / molecular replacement / Resolution: 2.15 Å | |||||||||
Authors | Szeto, C. / Chatzileontiadou, D.S.M. / Riboldi-Tunnicliffe, A. / Gras, S. | |||||||||
| Funding support | Australia, 2items
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Citation | Journal: Iscience / Year: 2021Title: The presentation of SARS-CoV-2 peptides by the common HLA-A * 02:01 molecule. Authors: Szeto, C. / Chatzileontiadou, D.S.M. / Nguyen, A.T. / Sloane, H. / Lobos, C.A. / Jayasinghe, D. / Halim, H. / Smith, C. / Riboldi-Tunnicliffe, A. / Grant, E.J. / Gras, S. | |||||||||
| 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 | 7kgo.cif.gz | 98.7 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb7kgo.ent.gz | 73.9 KB | Display | PDB format |
| PDBx/mmJSON format | 7kgo.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 7kgo_validation.pdf.gz | 436.1 KB | Display | wwPDB validaton report |
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| Full document | 7kgo_full_validation.pdf.gz | 438.5 KB | Display | |
| Data in XML | 7kgo_validation.xml.gz | 17.8 KB | Display | |
| Data in CIF | 7kgo_validation.cif.gz | 25.6 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/kg/7kgo ftp://data.pdbj.org/pub/pdb/validation_reports/kg/7kgo | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 7kgpC ![]() 7kgqC ![]() 7kgrC ![]() 7kgsC ![]() 7kgtC ![]() 3gsoS S: Starting model for refinement C: citing same article ( |
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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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| Unit cell |
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Components
-Protein , 2 types, 2 molecules AB
| #1: Protein | Mass: 32125.473 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: HLA-A / Plasmid: pET / Production host: ![]() |
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| #2: Protein | Mass: 11748.160 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: B2M, CDABP0092, HDCMA22P / Plasmid: pET / Production host: ![]() |
-Protein/peptide , 1 types, 1 molecules C
| #3: Protein/peptide | Mass: 1038.241 Da / Num. of mol.: 1 / Fragment: residues 351-359 / Source method: obtained synthetically / Details: synthesized Source: (synth.) ![]() References: UniProt: P0DTC9 |
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-Non-polymers , 4 types, 194 molecules 






| #4: Chemical | | #5: Chemical | #6: Chemical | ChemComp-CD / | #7: Water | ChemComp-HOH / | |
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-Details
| Has ligand of interest | N |
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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: 2.91 Å3/Da / Density % sol: 57.79 % / Mosaicity: 0.13 ° |
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| Crystal grow | Temperature: 277 K / Method: vapor diffusion, hanging drop / pH: 8 / Details: 20% PEG3350 w/v, 0.2 M NaFormate, 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: 0.95373 Å | ||||||||||||||||||||||||||||||
| Detector | Type: DECTRIS EIGER X 16M / Detector: PIXEL / Date: Jun 6, 2020 | ||||||||||||||||||||||||||||||
| Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray | ||||||||||||||||||||||||||||||
| Radiation wavelength | Wavelength: 0.95373 Å / Relative weight: 1 | ||||||||||||||||||||||||||||||
| Reflection | Resolution: 2.15→47.51 Å / Num. obs: 29202 / % possible obs: 100 % / Redundancy: 7.8 % / CC1/2: 0.997 / Rmerge(I) obs: 0.147 / Rpim(I) all: 0.056 / Rrim(I) all: 0.158 / Net I/σ(I): 10.5 / Num. measured all: 226686 / Scaling rejects: 1 | ||||||||||||||||||||||||||||||
| Reflection shell | Diffraction-ID: 1
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-Phasing
| Phasing | Method: molecular replacement |
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Processing
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| Refinement | Method to determine structure: MOLECULAR REPLACEMENTStarting model: 3GSO Resolution: 2.15→47.51 Å / SU ML: 0.25 / Cross valid method: THROUGHOUT / σ(F): 1.34 / Phase error: 23.17 / 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 | ||||||||||||||||||||||||
| Displacement parameters | Biso max: 95.18 Å2 / Biso mean: 38.5353 Å2 / Biso min: 14.64 Å2 | ||||||||||||||||||||||||
| Refinement step | Cycle: final / Resolution: 2.15→47.51 Å
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About Yorodumi



Homo sapiens (human)
X-RAY DIFFRACTION
Australia, 2items
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