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Yorodumi- PDB-1dlh: CRYSTAL STRUCTURE OF THE HUMAN CLASS II MHC PROTEIN HLA-DR1 COMPL... -
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Basic information
| Entry | Database: PDB / ID: 1dlh | |||||||||
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| Title | CRYSTAL STRUCTURE OF THE HUMAN CLASS II MHC PROTEIN HLA-DR1 COMPLEXED WITH AN INFLUENZA VIRUS PEPTIDE | |||||||||
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Keywords | HISTOCOMPATIBILITY ANTIGEN | |||||||||
| Function / homology | Function and homology informationregulation 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 ...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 / 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 / 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 / clathrin-dependent endocytosis of virus by host cell / adaptive immune response / positive regulation of viral entry into host cell / lysosome / positive regulation of ERK1 and ERK2 cascade / positive regulation of canonical NF-kappaB signal transduction / positive regulation of MAPK cascade / host cell surface receptor binding / immune response / Golgi membrane / lysosomal membrane / fusion of virus membrane with host plasma membrane / external side of plasma membrane / fusion of virus membrane with host endosome membrane / viral envelope / positive regulation of DNA-templated transcription / virion attachment to host cell / host cell plasma membrane / virion membrane / cell surface / signal transduction / extracellular space / extracellular exosome / membrane / plasma membrane Similarity search - Function | |||||||||
| Biological species | Homo sapiens (human) | |||||||||
| Method | X-RAY DIFFRACTION / Resolution: 2.8 Å | |||||||||
Authors | Stern, L.J. | |||||||||
Citation | Journal: Nature / Year: 1994Title: Crystal structure of the human class II MHC protein HLA-DR1 complexed with an influenza virus peptide. Authors: Stern, L.J. / Brown, J.H. / Jardetzky, T.S. / Gorga, J.C. / Urban, R.G. / Strominger, J.L. / Wiley, D.C. #1: Journal: Nature / Year: 1993Title: Three-Dimensional Structure of the Human Class II Histocompatibility Antigen Hla-Dr1 Authors: Brown, J.H. / Jardetzky, T.S. / Gorga, J.C. / Stern, L.J. / Urban, R.G. / Strominger, J.L. / Wiley, D.C. | |||||||||
| 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 | 1dlh.cif.gz | 172.8 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb1dlh.ent.gz | 137.5 KB | Display | PDB format |
| PDBx/mmJSON format | 1dlh.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 1dlh_validation.pdf.gz | 579.8 KB | Display | wwPDB validaton report |
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| Full document | 1dlh_full_validation.pdf.gz | 619.7 KB | Display | |
| Data in XML | 1dlh_validation.xml.gz | 23.5 KB | Display | |
| Data in CIF | 1dlh_validation.cif.gz | 34.5 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/dl/1dlh ftp://data.pdbj.org/pub/pdb/validation_reports/dl/1dlh | HTTPS FTP |
-Related structure data
| Similar structure data |
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Links
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Assembly
| Deposited unit | ![]()
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| Unit cell |
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| Atom site foot note | 1: CIS PROLINE - PRO A 16 / 2: CIS PROLINE - PRO A 114 / 3: CIS PROLINE - PRO B 124 / 4: CIS PROLINE - PRO D 16 / 5: CIS PROLINE - PRO D 114 / 6: CIS PROLINE - PRO E 124 7: AMBIGUOUS DENSITY FOR SIDE CHAINS OF RESIDUES: ARG A 50, ARG D 50 GLU A 55, GLU D 55 GLU B 59, GLU E 59 GLU B 187, GLU E 187 ARG B 189, ARG E 189 | ||||||||
| Noncrystallographic symmetry (NCS) | NCS oper: (Code: given Matrix: (0.2889, -0.5925, 0.752), Vector: Details | TWO MOLECULES IN THE ASYMMETRIC UNIT ARE RELATED BY AN APPROXIMATE TWO-FOLD AXIS. THE TRANSFORMATION PRESENTED ON *MTRIX* RECORDS BELOW WILL YIELD APPROXIMATE COORDINATES FOR CHAINS *D* AND *E* WHEN APPLIED TO CHAINS *A* AND *B*, RESPECTIVELY. MOLECULE 1 : ALPHA CHAIN - RESIDUES A 3 THROUGH A 182 : BETA CHAIN - RESIDUES B 3 THROUGH B 190 : PEPTIDE - RESIDUES C 306 THROUGH C 318 : SUGARS - RESIDUES A 501, B 511, B 512, B 521 MOLECULE 2 : ALPHA CHAIN - RESIDUES D 3 THROUGH D 182 : BETA CHAIN - RESIDUES E 3 THROUGH E 190 : PEPTIDE - RESIDUES F 306 THROUGH F 318 : SUGARS - RESIDUES D 501, E 511, E 512, E 521 WATERS : MOL1 + MOL2 - RESIDUES 1 THROUGH 153 | |
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Components
-CLASS II HISTOCOMPATIBILITY ANTIGEN (HLA-DR1) ... , 2 types, 4 molecules ADBE
| #1: Protein | Mass: 20913.568 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Production host: Spodoptera (butterflies/moths) / References: UniProt: P01903#2: Protein | Mass: 21908.523 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Production host: Spodoptera (butterflies/moths) / References: UniProt: P13758, UniProt: P01911*PLUS |
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-Protein/peptide / Non-polymers , 2 types, 155 molecules CF

| #3: Protein/peptide | Mass: 1506.807 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source References: UniProt: P11133, UniProt: P04664*PLUS #6: Water | ChemComp-HOH / | |
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-Sugars , 2 types, 6 molecules 
| #4: Polysaccharide | Source method: isolated from a genetically manipulated source #5: Sugar | ChemComp-NAG / |
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-Details
| Has protein modification | Y |
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-Experimental details
-Experiment
| Experiment | Method: X-RAY DIFFRACTION |
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Sample preparation
| Crystal | Density Matthews: 3.12 Å3/Da / Density % sol: 60.59 % | |||||||||||||||
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| Crystal grow | *PLUS Method: vapor diffusion, hanging dropDetails: referred to 'Stern, L.J.', (1992) Cell, 68, 465-477 | |||||||||||||||
| Components of the solutions | *PLUS
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-Data collection
| Radiation | Scattering type: x-ray |
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| Radiation wavelength | Relative weight: 1 |
| Reflection | *PLUS Highest resolution: 2.75 Å / Lowest resolution: 20 Å / Num. obs: 29857 / % possible obs: 94.5 % / Num. measured all: 88058 / Rmerge(I) obs: 0.067 |
| Reflection shell | *PLUS Highest resolution: 2.75 Å / Lowest resolution: 3 Å / % possible obs: 89.8 % / Rmerge(I) obs: 0.231 |
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Processing
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| Refinement | Resolution: 2.8→7 Å / σ(F): 2
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| Refinement step | Cycle: LAST / Resolution: 2.8→7 Å
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| Refine LS restraints |
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| Software | *PLUS Name: X-PLOR / Classification: refinement | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Refinement | *PLUS Rfactor Rfree: 0.304 / Rfactor Rwork: 0.205 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Solvent computation | *PLUS | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Displacement parameters | *PLUS | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Refine LS restraints | *PLUS Type: x_angle_d / Dev ideal: 2.13 |
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Homo sapiens (human)
X-RAY DIFFRACTION
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Spodoptera (butterflies/moths)