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Yorodumi- PDB-6pyv: Crystal Structure of HLA-B*2703-P47G in complex with LRN, a self-... -
+Open data
-Basic information
Entry | Database: PDB / ID: 6pyv | ||||||
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Title | Crystal Structure of HLA-B*2703-P47G in complex with LRN, a self-peptide | ||||||
Components |
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Keywords | IMMUNE SYSTEM / Ankylosing spondylitis / HLA-B27 / HLA-B*27:05 / HLA-B*27:03 / HLA | ||||||
Function / homology | Function and homology information farnesyl diphosphate metabolic process / squalene synthase / squalene synthase [NAD(P)H] activity / : / Cholesterol biosynthesis / farnesyltranstransferase activity / steroid biosynthetic process / regulation of interleukin-12 production / regulation of dendritic cell differentiation / regulation of T cell anergy ...farnesyl diphosphate metabolic process / squalene synthase / squalene synthase [NAD(P)H] activity / : / Cholesterol biosynthesis / farnesyltranstransferase activity / steroid biosynthetic process / regulation of interleukin-12 production / regulation of dendritic cell differentiation / regulation of T cell anergy / regulation of interleukin-6 production / cholesterol biosynthetic process / TAP binding / protection from natural killer cell mediated cytotoxicity / detection of bacterium / Activation of gene expression by SREBF (SREBP) / positive regulation of ferrous iron binding / positive regulation of transferrin receptor binding / secretory granule membrane / positive regulation of receptor binding / early endosome lumen / Nef mediated downregulation of MHC class I complex cell surface expression / negative regulation of receptor binding / DAP12 interactions / antigen processing and presentation of endogenous peptide antigen via MHC class Ib / antigen processing and presentation of endogenous peptide antigen via MHC class I via ER pathway, TAP-independent / cellular response to iron ion / Endosomal/Vacuolar pathway / Antigen Presentation: Folding, assembly and peptide loading of class I MHC / lumenal side of endoplasmic reticulum membrane / cellular response to iron(III) ion / antigen processing and presentation of exogenous protein antigen via MHC class Ib, TAP-dependent / negative regulation of forebrain neuron differentiation / regulation of erythrocyte differentiation / peptide antigen assembly with MHC class I protein complex / ER to Golgi transport vesicle membrane / regulation of iron ion transport / response to molecule of bacterial origin / MHC class I peptide loading complex / HFE-transferrin receptor complex / PPARA activates gene expression / T cell mediated cytotoxicity / positive regulation of T cell cytokine production / antigen processing and presentation of endogenous peptide antigen via MHC class I / MHC class I protein complex / defense response / negative regulation of neurogenesis / positive regulation of receptor-mediated endocytosis / peptide antigen assembly with MHC class II protein complex / multicellular organismal-level iron ion homeostasis / MHC class II protein complex / cellular response to nicotine / specific granule lumen / positive regulation of cellular senescence / positive regulation of T cell mediated cytotoxicity / recycling endosome membrane / phagocytic vesicle membrane / peptide antigen binding / antigen processing and presentation of exogenous peptide antigen via MHC class II / negative regulation of epithelial cell proliferation / Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell / positive regulation of immune response / Interferon gamma signaling / Modulation by Mtb of host immune system / positive regulation of T cell activation / Interferon alpha/beta signaling / sensory perception of smell / negative regulation of neuron projection development / positive regulation of protein binding / tertiary granule lumen / DAP12 signaling / MHC class II protein complex binding / late endosome membrane / protein-folding chaperone binding / iron ion transport / ER-Phagosome pathway / T cell differentiation in thymus / early endosome membrane / protein refolding / protein homotetramerization / intracellular iron ion homeostasis / adaptive immune response / amyloid fibril formation / learning or memory / immune response / Amyloid fiber formation / endoplasmic reticulum lumen / lysosomal membrane / Golgi membrane / external side of plasma membrane / innate immune response / signaling receptor binding / focal adhesion / Neutrophil degranulation / endoplasmic reticulum membrane / SARS-CoV-2 activates/modulates innate and adaptive immune responses / structural molecule activity / Golgi apparatus / cell surface / endoplasmic reticulum Similarity search - Function | ||||||
Biological species | Homo sapiens (human) | ||||||
Method | X-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / molecular replacement / Resolution: 1.45 Å | ||||||
Authors | Gras, S. | ||||||
Citation | Journal: J.Biol.Chem. / Year: 2019 Title: Allelic association with ankylosing spondylitis fails to correlate with human leukocyte antigen B27 homodimer formation. Authors: Lim Kam Sian, T.C.C. / Indumathy, S. / Halim, H. / Greule, A. / Cryle, M.J. / Bowness, P. / Rossjohn, J. / Gras, S. / Purcell, A.W. / Schittenhelm, R.B. | ||||||
History |
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-Structure visualization
Structure viewer | Molecule: MolmilJmol/JSmol |
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-Downloads & links
-Download
PDBx/mmCIF format | 6pyv.cif.gz | 110.1 KB | Display | PDBx/mmCIF format |
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PDB format | pdb6pyv.ent.gz | 82 KB | Display | PDB format |
PDBx/mmJSON format | 6pyv.json.gz | Tree view | PDBx/mmJSON format | |
Others | Other downloads |
-Validation report
Summary document | 6pyv_validation.pdf.gz | 249.8 KB | Display | wwPDB validaton report |
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Full document | 6pyv_full_validation.pdf.gz | 249.7 KB | Display | |
Data in XML | 6pyv_validation.xml.gz | 925 B | Display | |
Data in CIF | 6pyv_validation.cif.gz | 8 KB | Display | |
Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/py/6pyv ftp://data.pdbj.org/pub/pdb/validation_reports/py/6pyv | HTTPS FTP |
-Related structure data
Related structure data | 6pyjC 6pylC 6pywC 6pz5C 4g9dS S: Starting model for refinement C: citing same article (ref.) |
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Similar structure data |
-Links
-Assembly
Deposited unit |
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1 |
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Unit cell |
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-Components
#1: Protein | Mass: 31863.070 Da / Num. of mol.: 1 / Mutation: P47G Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: HLA-B, HLAB / Plasmid: pET30 / Production host: Escherichia coli BL21 (bacteria) / References: UniProt: P03989, UniProt: P01889*PLUS |
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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: pET30 / Production host: Escherichia coli BL21 (bacteria) / References: UniProt: P61769 |
#3: Protein/peptide | Mass: 1125.257 Da / Num. of mol.: 1 / Source method: obtained synthetically / Details: synthesized / Source: (synth.) Homo sapiens (human) / References: UniProt: P37268*PLUS |
#4: Water | ChemComp-HOH / |
Has protein modification | Y |
Sequence details | Y83H IN ALLELE B*27:03 |
-Experimental details
-Experiment
Experiment | Method: X-RAY DIFFRACTION / Number of used crystals: 1 |
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-Sample preparation
Crystal | Density Matthews: 2.59 Å3/Da / Density % sol: 52.55 % / Mosaicity: 0.21 ° |
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Crystal grow | Temperature: 277 K / Method: vapor diffusion, hanging drop / pH: 5.6 Details: 20-30% PEG 4K, 0.2M Na Acetate and 0.1M Na Citrate pH 5.6 |
-Data collection
Diffraction | Mean temperature: 100 K / Serial crystal experiment: N | ||||||||||||||||||||||||
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Diffraction source | Source: SYNCHROTRON / Site: Australian Synchrotron / Beamline: MX1 / Wavelength: 0.954 Å | ||||||||||||||||||||||||
Detector | Type: ADSC QUANTUM 210 / Detector: CCD / Date: Mar 27, 2018 | ||||||||||||||||||||||||
Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray | ||||||||||||||||||||||||
Radiation wavelength | Wavelength: 0.954 Å / Relative weight: 1 | ||||||||||||||||||||||||
Reflection | Resolution: 1.45→28 Å / Num. obs: 82939 / % possible obs: 99.8 % / Redundancy: 6 % / Biso Wilson estimate: 17.8 Å2 / CC1/2: 0.999 / Rmerge(I) obs: 0.057 / Net I/σ(I): 18.3 / Num. measured all: 499862 / Scaling rejects: 6 | ||||||||||||||||||||||||
Reflection shell | Diffraction-ID: 1
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-Phasing
Phasing | Method: molecular replacement |
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-Processing
Software |
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Refinement | Method to determine structure: MOLECULAR REPLACEMENT Starting model: 4g9d Resolution: 1.45→21.23 Å / Cor.coef. Fo:Fc: 0.946 / Cor.coef. Fo:Fc free: 0.92 / SU R Cruickshank DPI: 0.065 / Cross valid method: THROUGHOUT / σ(F): 0 / SU R Blow DPI: 0.072 / SU Rfree Blow DPI: 0.078 / SU Rfree Cruickshank DPI: 0.072
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Displacement parameters | Biso max: 86.05 Å2 / Biso mean: 21.89 Å2 / Biso min: 6.28 Å2
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Refine analyze | Luzzati coordinate error obs: 0.21 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Refinement step | Cycle: final / Resolution: 1.45→21.23 Å
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Refine LS restraints |
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LS refinement shell | Resolution: 1.45→1.49 Å / Rfactor Rfree error: 0 / Total num. of bins used: 20
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