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Yorodumi- PDB-5niu: Structure of human Programmed cell death 1 ligand 1 (PD-L1) with ... -
+Open data
-Basic information
Entry | Database: PDB / ID: 5niu | ||||||||||||||||||||||||
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Title | Structure of human Programmed cell death 1 ligand 1 (PD-L1) with low molecular mass inhibitor | ||||||||||||||||||||||||
Components | Programmed cell death 1 ligand 1 | ||||||||||||||||||||||||
Keywords | IMMUNE SYSTEM / PD-L1 / PD-1 / immune checkpoint | ||||||||||||||||||||||||
Function / homology | Function and homology information negative regulation of tumor necrosis factor superfamily cytokine production / positive regulation of activated CD8-positive, alpha-beta T cell apoptotic process / negative regulation of CD8-positive, alpha-beta T cell activation / negative regulation of T cell mediated immune response to tumor cell / TRIF-dependent toll-like receptor signaling pathway / negative regulation of CD4-positive, alpha-beta T cell proliferation / STAT3 nuclear events downstream of ALK signaling / negative regulation of interleukin-10 production / negative regulation of activated T cell proliferation / positive regulation of interleukin-10 production ...negative regulation of tumor necrosis factor superfamily cytokine production / positive regulation of activated CD8-positive, alpha-beta T cell apoptotic process / negative regulation of CD8-positive, alpha-beta T cell activation / negative regulation of T cell mediated immune response to tumor cell / TRIF-dependent toll-like receptor signaling pathway / negative regulation of CD4-positive, alpha-beta T cell proliferation / STAT3 nuclear events downstream of ALK signaling / negative regulation of interleukin-10 production / negative regulation of activated T cell proliferation / positive regulation of interleukin-10 production / negative regulation of type II interferon production / PD-1 signaling / positive regulation of T cell proliferation / T cell costimulation / response to cytokine / recycling endosome membrane / actin cytoskeleton / early endosome membrane / cellular response to lipopolysaccharide / adaptive immune response / transcription coactivator activity / cell surface receptor signaling pathway / receptor ligand activity / positive regulation of cell migration / immune response / external side of plasma membrane / signal transduction / extracellular exosome / nucleoplasm / plasma membrane Similarity search - Function | ||||||||||||||||||||||||
Biological species | Homo sapiens (human) | ||||||||||||||||||||||||
Method | X-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 2.01 Å | ||||||||||||||||||||||||
Authors | Zak, K.M. / Grudnik, P. / Skalniak, L. / Dubin, G. / Holak, T.A. | ||||||||||||||||||||||||
Funding support | Poland, 7items
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Citation | Journal: Oncotarget / Year: 2017 Title: Small-molecule inhibitors of PD-1/PD-L1 immune checkpoint alleviate the PD-L1-induced exhaustion of T-cells. Authors: Skalniak, L. / Zak, K.M. / Guzik, K. / Magiera, K. / Musielak, B. / Pachota, M. / Szelazek, B. / Kocik, J. / Grudnik, P. / Tomala, M. / Krzanik, S. / Pyrc, K. / Domling, A. / Dubin, G. / Holak, T.A. | ||||||||||||||||||||||||
History |
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-Structure visualization
Structure viewer | Molecule: MolmilJmol/JSmol |
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-Downloads & links
-Download
PDBx/mmCIF format | 5niu.cif.gz | 122.7 KB | Display | PDBx/mmCIF format |
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PDB format | pdb5niu.ent.gz | 94.3 KB | Display | PDB format |
PDBx/mmJSON format | 5niu.json.gz | Tree view | PDBx/mmJSON format | |
Others | Other downloads |
-Validation report
Summary document | 5niu_validation.pdf.gz | 997.5 KB | Display | wwPDB validaton report |
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Full document | 5niu_full_validation.pdf.gz | 1004.9 KB | Display | |
Data in XML | 5niu_validation.xml.gz | 25.5 KB | Display | |
Data in CIF | 5niu_validation.cif.gz | 35.8 KB | Display | |
Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/ni/5niu ftp://data.pdbj.org/pub/pdb/validation_reports/ni/5niu | HTTPS FTP |
-Related structure data
Related structure data | 5c3tS S: Starting model for refinement |
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Similar structure data |
-Links
-Assembly
Deposited unit |
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1 |
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2 |
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Unit cell |
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-Components
#1: Protein | Mass: 14678.759 Da / Num. of mol.: 4 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: CD274, B7H1, PDCD1L1, PDCD1LG1, PDL1 / Production host: Escherichia coli (E. coli) / References: UniProt: Q9NZQ7 #2: Chemical | #3: Chemical | #4: Water | ChemComp-HOH / | |
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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: 2.39 Å3/Da / Density % sol: 48.46 % |
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Crystal grow | Temperature: 298 K / Method: vapor diffusion, sitting drop Details: 0.1 M Tris pH 8.5 containing 0.2 M magnesium chloride and 30% (w/v) PEG 4000 |
-Data collection
Diffraction | Mean temperature: 100 K |
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Diffraction source | Source: SYNCHROTRON / Site: PETRA III, DESY / Beamline: P11 / Wavelength: 0.9795 Å |
Detector | Type: DECTRIS PILATUS3 6M / Detector: PIXEL / Date: Jul 25, 2016 |
Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
Radiation wavelength | Wavelength: 0.9795 Å / Relative weight: 1 |
Reflection | Resolution: 2.01→46.01 Å / Num. obs: 37778 / % possible obs: 99.8 % / Redundancy: 12.7 % / Rmerge(I) obs: 0.065 / Net I/σ(I): 22.3 |
Reflection shell | Resolution: 2.014→2.086 Å / Redundancy: 12.7 % / Rmerge(I) obs: 0.452 / Mean I/σ(I) obs: 5.3 / % possible all: 97.7 |
-Processing
Software |
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Refinement | Method to determine structure: MOLECULAR REPLACEMENT Starting model: 5C3T Resolution: 2.01→46.01 Å / Cross valid method: FREE R-VALUE / Details: HYDROGENS HAVE BEEN ADDED IN THE RIDING POSITIONS
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Displacement parameters | Biso mean: 42.19 Å2
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Refinement step | Cycle: LAST / Resolution: 2.01→46.01 Å
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