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Yorodumi- PDB-4h26: TCR interaction with peptide mimics of nickel offers structure in... -
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Open data
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Basic information
| Entry | Database: PDB / ID: 4h26 | |||||||||
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| Title | TCR interaction with peptide mimics of nickel offers structure insight to nickel contact allergy | |||||||||
Components |
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Keywords | IMMUNE SYSTEM / protein-protein complex / immunoglobulin fold / antigen presentation / TCR / cell surface | |||||||||
| Function / homology | Function and homology informationmyeloid dendritic cell antigen processing and presentation / antigen processing and presentation of endogenous peptide antigen via MHC class II / autolysosome membrane / regulation of T-helper cell differentiation / positive regulation of CD4-positive, CD25-positive, alpha-beta regulatory T cell differentiation / MHC class II receptor activity / positive regulation of CD4-positive, alpha-beta T cell activation / antigen processing and presentation of peptide or polysaccharide antigen via MHC class II / positive regulation of memory T cell differentiation / transport vesicle membrane ...myeloid dendritic cell antigen processing and presentation / antigen processing and presentation of endogenous peptide antigen via MHC class II / autolysosome membrane / regulation of T-helper cell differentiation / positive regulation of CD4-positive, CD25-positive, alpha-beta regulatory T cell differentiation / MHC class II receptor activity / positive regulation of CD4-positive, alpha-beta T cell activation / antigen processing and presentation of peptide or polysaccharide antigen via MHC class II / positive regulation of memory T cell differentiation / transport vesicle membrane / Translocation of ZAP-70 to Immunological synapse / Phosphorylation of CD3 and TCR zeta chains / polysaccharide binding / Generation of second messenger molecules / immunological synapse / Co-inhibition by PD-1 / T cell receptor binding / MHC class II antigen presentation / trans-Golgi network membrane / lumenal side of endoplasmic reticulum membrane / peptide antigen assembly with MHC class II protein complex / MHC class II protein complex / clathrin-coated endocytic vesicle membrane / ER to Golgi transport vesicle membrane / antigen processing and presentation of exogenous peptide antigen via MHC class II / positive regulation of immune response / positive regulation of T cell activation / peptide antigen binding / positive regulation of T cell mediated cytotoxicity / cognition / Interferon gamma signaling / MHC class II protein complex binding / endocytic vesicle membrane / late endosome membrane / Downstream TCR signaling / early endosome membrane / adaptive immune response / lysosome / endosome membrane / immune response / Golgi membrane / lysosomal membrane / cell surface / extracellular exosome / plasma membrane Similarity search - Function | |||||||||
| Biological species | Homo sapiens (human) | |||||||||
| Method | X-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 2.5 Å | |||||||||
Authors | Kappler, J.W. / Yin, L. / Dai, S. / Marrack, P. / Crawford, F. | |||||||||
Citation | Journal: Proc.Natl.Acad.Sci.USA / Year: 2012Title: T-cell receptor (TCR) interaction with peptides that mimic nickel offers insight into nickel contact allergy. Authors: Yin, L. / Crawford, F. / Marrack, P. / Kappler, J.W. / Dai, 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 | 4h26.cif.gz | 169.7 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb4h26.ent.gz | 135.1 KB | Display | PDB format |
| PDBx/mmJSON format | 4h26.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/h2/4h26 ftp://data.pdbj.org/pub/pdb/validation_reports/h2/4h26 | HTTPS FTP |
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-Related structure data
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Links
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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: 20842.490 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: HLA-DRA, HLA-DRA1 / Production host: HOMO SAPIENS (human) / References: UniProt: P01903#2: Protein | Mass: 21936.555 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: HLA-DRB3 / Production host: HOMO SAPIENS (human) / References: UniProt: B8YAC7#3: Protein/peptide | Mass: 1425.743 Da / Num. of mol.: 2 / Source method: obtained synthetically #4: Polysaccharide | Source method: isolated from a genetically manipulated source #5: 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: 2.75 Å3/Da / Density % sol: 55.32 % |
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| Crystal grow | Temperature: 298 K / Method: vapor diffusion, hanging drop / pH: 8 Details: 16% PEG4000, 100mM Tris-HCL, pH 8, VAPOR DIFFUSION, HANGING DROP, temperature 298K |
-Data collection
| Diffraction | Mean temperature: 100 K |
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| Diffraction source | Source: SYNCHROTRON / Site: ALS / Beamline: 8.2.2 / Wavelength: 1 Å |
| Detector | Type: ADSC QUANTUM 315 / Detector: CCD |
| Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
| Radiation wavelength | Wavelength: 1 Å / Relative weight: 1 |
| Reflection | Resolution: 2.5→50 Å / Num. obs: 30552 |
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Processing
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| Refinement | Method to determine structure: MOLECULAR REPLACEMENT / Resolution: 2.5→50 ÅDetails: THE RFREE VALUE PROVIDED BY AUTHORS CAN NOT BE REPRODUCED BASED ON THE RFREE FLAGS PROVIDED BY AUTHORS
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| Refinement step | Cycle: LAST / Resolution: 2.5→50 Å
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Homo sapiens (human)
X-RAY DIFFRACTION
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