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Yorodumi- PDB-1jbj: CD3 Epsilon and gamma Ectodomain Fragment Complex in Single-Chain... -
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Open data
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Basic information
| Entry | Database: PDB / ID: 1jbj | ||||||
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| Title | CD3 Epsilon and gamma Ectodomain Fragment Complex in Single-Chain Construct | ||||||
Components | CD3 Epsilon and gamma Ectodomain Fragment Complex | ||||||
Keywords | IMMUNE SYSTEM / beta-sheet / C2-set IMMUNOGLOBULIN SUPERFAMILY / H-bonded G strand pair / single-chain | ||||||
| Function / homology | Function and homology informationlymphocyte activation / Phosphorylation of CD3 and TCR zeta chains / Translocation of ZAP-70 to Immunological synapse / Co-inhibition by PD-1 / Generation of second messenger molecules / FCGR activation / Role of phospholipids in phagocytosis / regulation of lymphocyte apoptotic process / Downstream TCR signaling / T cell anergy ...lymphocyte activation / Phosphorylation of CD3 and TCR zeta chains / Translocation of ZAP-70 to Immunological synapse / Co-inhibition by PD-1 / Generation of second messenger molecules / FCGR activation / Role of phospholipids in phagocytosis / regulation of lymphocyte apoptotic process / Downstream TCR signaling / T cell anergy / positive regulation of cell-cell adhesion mediated by integrin / Cargo recognition for clathrin-mediated endocytosis / Regulation of actin dynamics for phagocytic cup formation / positive regulation of T cell anergy / Clathrin-mediated endocytosis / CD4-positive, alpha-beta T cell proliferation / negative thymic T cell selection / positive regulation of CD4-positive, alpha-beta T cell proliferation / alpha-beta T cell receptor complex / Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell / positive regulation of cell-matrix adhesion / smoothened signaling pathway / T cell receptor complex / positive regulation of interleukin-4 production / establishment or maintenance of cell polarity / dendrite development / immunological synapse / T cell proliferation / T cell costimulation / positive regulation of T cell proliferation / positive regulation of interleukin-2 production / positive regulation of calcium-mediated signaling / T cell activation / cerebellum development / negative regulation of smoothened signaling pathway / apoptotic signaling pathway / calcium-mediated signaling / positive regulation of T cell activation / SH3 domain binding / positive regulation of type II interferon production / cell-cell junction / transmembrane signaling receptor activity / T cell receptor signaling pathway / protein transport / cell body / dendritic spine / adaptive immune response / cell surface receptor signaling pathway / negative regulation of gene expression / external side of plasma membrane / endoplasmic reticulum / Golgi apparatus / identical protein binding / plasma membrane / cytosol Similarity search - Function | ||||||
| Biological species | ![]() | ||||||
| Method | SOLUTION NMR / simulated annealing | ||||||
Authors | Sun, Z.-Y.J. / Kim, K.S. / Wagner, G. / Reinherz, E.L. | ||||||
Citation | Journal: Cell(Cambridge,Mass.) / Year: 2001Title: Mechanisms contributing to T cell receptor signaling and assembly revealed by the solution structure of an ectodomain fragment of the CD3 epsilon gamma heterodimer. Authors: Sun, Z.J. / Kim, K.S. / Wagner, G. / Reinherz, E.L. #1: Journal: J.Mol.Biol. / Year: 2000Title: Heterodimeric CD3epsilongamma Extracellular Domain Fragments: Production, Purification and Structural Analysis Authors: Kim, K.S. / Sun, Z.Y. / Wagner, G. / Reinherz, E.L. | ||||||
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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 | 1jbj.cif.gz | 1007.1 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb1jbj.ent.gz | 841.6 KB | Display | PDB format |
| PDBx/mmJSON format | 1jbj.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 1jbj_validation.pdf.gz | 346.9 KB | Display | wwPDB validaton report |
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| Full document | 1jbj_full_validation.pdf.gz | 529.4 KB | Display | |
| Data in XML | 1jbj_validation.xml.gz | 74.8 KB | Display | |
| Data in CIF | 1jbj_validation.cif.gz | 95.9 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/jb/1jbj ftp://data.pdbj.org/pub/pdb/validation_reports/jb/1jbj | HTTPS FTP |
-Related structure data
| Similar structure data |
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Assembly
| Deposited unit | ![]()
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| 1 |
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| NMR ensembles |
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Components
| #1: Protein | Mass: 20632.842 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Details: RESIDUES 1-79 ARE a fragment of T-CELL SURFACE GLYCOPROTEIN CD3 EPSILON CHAIN, RESIDUES 80-105 ARE AN ENGINEERED LINKER MODELED FROM A SINGLE CHAIN T CELL RECEPTOR CONSTRUCT, RESIDUES 106- ...Details: RESIDUES 1-79 ARE a fragment of T-CELL SURFACE GLYCOPROTEIN CD3 EPSILON CHAIN, RESIDUES 80-105 ARE AN ENGINEERED LINKER MODELED FROM A SINGLE CHAIN T CELL RECEPTOR CONSTRUCT, RESIDUES 106-186 ARE a fragment of T-CELL SURFACE GLYCOPROTEIN CD3 GAMMA CHAIN Source: (gene. exp.) ![]() ![]() References: UniProt: P22646, GenBank: 1531627, UniProt: P11942 |
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| Has protein modification | Y |
-Experimental details
-Experiment
| Experiment | Method: SOLUTION NMR | ||||||||||||||||||||||||||||||||
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| NMR experiment |
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| NMR details | Text: The structure was determined using triple-resonance NMR spectroscopy. Structures are superimposed based on backbone atoms from residues 7 to 79 and 113 to 184. |
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Sample preparation
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| Crystal grow | *PLUS Method: other / Details: NMR |
-NMR measurement
| Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M | ||||||||||||||||||||
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| Radiation wavelength | Relative weight: 1 | ||||||||||||||||||||
| NMR spectrometer |
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Processing
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| Refinement | Method: simulated annealing / Software ordinal: 1 Details: calculated using 1623 NOE restraints, 105 H-bond restraints, and 194 dihedral angle restrints | ||||||||||||||||||||||||
| NMR representative | Selection criteria: lowest energy | ||||||||||||||||||||||||
| NMR ensemble | Conformer selection criteria: structures with the least restraint violations Conformers calculated total number: 20 / Conformers submitted total number: 18 |
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