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Open data
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Basic information
| Entry | Database: PDB / ID: 1t5w | ||||||
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| Title | HLA-DR1 in complex with a synthetic peptide (AAYSDQATPLLLSPR) | ||||||
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Keywords | IMMUNE SYSTEM / MHC class II / najor histocompatibility complex protein / HLA-DR1 / antigen / peptide | ||||||
| Function / homology | Function and homology informationpositive regulation of filamentous growth of a population of unicellular organisms in response to starvation / regulation of interleukin-4 production / regulation of interleukin-10 production / 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 ...positive regulation of filamentous growth of a population of unicellular organisms in response to starvation / regulation of interleukin-4 production / regulation of interleukin-10 production / 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 T cell mediated immune response to tumor cell / positive regulation of kinase activity / positive regulation of memory T cell differentiation / positive regulation of monocyte differentiation / inflammatory response to antigenic stimulus / CD4 receptor binding / intermediate filament / T-helper 1 type immune response / transport vesicle membrane / Translocation of ZAP-70 to Immunological synapse / nuclear envelope lumen / Phosphorylation of CD3 and TCR zeta chains / polysaccharide binding / negative regulation of type II interferon production / humoral immune response / macrophage differentiation / Generation of second messenger molecules / immunological synapse / Co-inhibition by PD-1 / epidermis development / positive regulation of insulin secretion involved in cellular response to glucose stimulus / detection of bacterium / T cell receptor binding / negative regulation of T cell proliferation / MHC class II antigen presentation / trans-Golgi network membrane / lumenal side of endoplasmic reticulum membrane / protein tetramerization / peptide antigen assembly with MHC class II protein complex / negative regulation of inflammatory response to antigenic stimulus / 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 / structural constituent of cytoskeleton / positive regulation of T cell mediated cytotoxicity / DNA-binding transcription repressor activity, RNA polymerase II-specific / cognition / positive regulation of protein phosphorylation / Interferon gamma signaling / MHC class II protein complex binding / endocytic vesicle membrane / late endosome membrane / Downstream TCR signaling / T cell receptor signaling pathway / early endosome membrane / adaptive immune response / sequence-specific DNA binding / positive regulation of viral entry into host cell / positive regulation of ERK1 and ERK2 cascade / lysosome / positive regulation of canonical NF-kappaB signal transduction / positive regulation of MAPK cascade / immune response / RNA polymerase II cis-regulatory region sequence-specific DNA binding / Golgi membrane / lysosomal membrane / external side of plasma membrane / positive regulation of DNA-templated transcription / cell surface / negative regulation of transcription by RNA polymerase II / signal transduction / positive regulation of transcription by RNA polymerase II / extracellular space / extracellular exosome / zinc ion binding / nucleus / membrane / plasma membrane / cytoplasm Similarity search - Function | ||||||
| Biological species | Homo sapiens (human) | ||||||
| Method | X-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 2.4 Å | ||||||
Authors | Zavala-Ruiz, Z. / Strug, I. / Anderson, M.W. / Gorski, J. / Stern, L.J. | ||||||
Citation | Journal: Chem.Biol. / Year: 2004Title: A Polymorphic Pocket at the P10 Position Contributes to Peptide Binding Specificity in Class II MHC Proteins Authors: Zavala-Ruiz, Z. / Strug, I. / Anderson, M.W. / Gorski, J. / Stern, L.J. | ||||||
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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 | 1t5w.cif.gz | 165.4 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb1t5w.ent.gz | 131.9 KB | Display | PDB format |
| PDBx/mmJSON format | 1t5w.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 1t5w_validation.pdf.gz | 470.1 KB | Display | wwPDB validaton report |
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| Full document | 1t5w_full_validation.pdf.gz | 487.9 KB | Display | |
| Data in XML | 1t5w_validation.xml.gz | 31.4 KB | Display | |
| Data in CIF | 1t5w_validation.cif.gz | 43.2 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/t5/1t5w ftp://data.pdbj.org/pub/pdb/validation_reports/t5/1t5w | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 1t5xC ![]() 1aqdS S: Starting model for refinement C: citing same article ( |
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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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| Details | Tow molecules in the asymteric unit are related by an approximate 2-fold axis |
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Components
| #1: Protein | Mass: 20971.670 Da / Num. of mol.: 2 / Fragment: Extracellular domain Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: HLA-DRA / Plasmid: pRMAHA-3 / Cell line (production host): S2 / Production host: ![]() #2: Protein | Mass: 22080.664 Da / Num. of mol.: 2 / Fragment: Extracellular domain Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: HLA-DRB1 / Plasmid: pRMHA-3 / Cell line (production host): S2 / Production host: ![]() #3: Protein/peptide | Mass: 1603.795 Da / Num. of mol.: 2 / Fragment: Synthetic peptide / Source method: obtained synthetically Details: Synthetic peptide desinged to study the P10 side chain specificity of HLA-DR1 References: UniProt: P27705 #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: 3.21 Å3/Da / Density % sol: 59.15 % |
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| Crystal grow | Temperature: 298 K / Method: vapor diffusion, hanging drop / pH: 4 Details: PEG 6000, pH 4.0, VAPOR DIFFUSION, HANGING DROP, temperature 298K |
-Data collection
| Diffraction | Mean temperature: 100 K |
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| Diffraction source | Source: SYNCHROTRON / Site: NSLS / Beamline: X25 / Wavelength: 1.1 Å |
| Detector | Type: ADSC QUANTUM 315 / Detector: CCD / Date: Apr 5, 2001 / Details: Cylindrical platinum-coated silicon mirror |
| Radiation | Monochromator: Cylindrical platinum-coated silicon mirror / Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
| Radiation wavelength | Wavelength: 1.1 Å / Relative weight: 1 |
| Reflection | Resolution: 2.4→23.9 Å / Num. all: 46428 / Num. obs: 44505 / % possible obs: 99.8 % / Observed criterion σ(F): 0 / Observed criterion σ(I): 0 / Redundancy: 6 % / Biso Wilson estimate: 34.1 Å2 / Rmerge(I) obs: 0.053 / Rsym value: 0.065 / Net I/σ(I): 11 |
| Reflection shell | Resolution: 2.4→2.55 Å / Redundancy: 5 % / Rmerge(I) obs: 0.312 / Mean I/σ(I) obs: 3.5 / Num. unique all: 4384 / Rsym value: 0.378 / % possible all: 99.9 |
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Processing
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| Refinement | Method to determine structure: MOLECULAR REPLACEMENTStarting model: PDB Entry 1AQD Resolution: 2.4→23.9 Å / Isotropic thermal model: Restrained / Cross valid method: THROUGHOUT / σ(F): 0 / σ(I): 0 / Stereochemistry target values: Engh & Huber
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| Displacement parameters | Biso mean: 45.1 Å2
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| Refine analyze |
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| Refinement step | Cycle: LAST / Resolution: 2.4→23.9 Å
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| Refine LS restraints |
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| LS refinement shell | Resolution: 2.4→2.55 Å / Rfactor Rfree error: 0.015
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Homo sapiens (human)
X-RAY DIFFRACTION
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