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Open data
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Basic information
| Entry | Database: PDB / ID: 9l1l | ||||||||||||||||||||||||
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| Title | Structure of anti-HEL AiTab | ||||||||||||||||||||||||
Components |
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Keywords | PROTEIN BINDING / Major histocompatibility complex class II(MHC-II) / T cell receptor (TCR) / antigen-induced TCR-like antibodies (AiTabs) | ||||||||||||||||||||||||
| Function / homology | Function and homology informationPhosphorylation of CD3 and TCR zeta chains / Translocation of ZAP-70 to Immunological synapse / Co-inhibition by PD-1 / Generation of second messenger molecules / Downstream TCR signaling / antigen processing and presentation of peptide antigen / MHC class II antigen presentation / positive regulation of T cell differentiation / antigen processing and presentation / negative regulation of T cell proliferation ...Phosphorylation of CD3 and TCR zeta chains / Translocation of ZAP-70 to Immunological synapse / Co-inhibition by PD-1 / Generation of second messenger molecules / Downstream TCR signaling / antigen processing and presentation of peptide antigen / MHC class II antigen presentation / positive regulation of T cell differentiation / antigen processing and presentation / negative regulation of T cell proliferation / multivesicular body / Lactose synthesis / Antimicrobial peptides / Neutrophil degranulation / beta-N-acetylglucosaminidase activity / peptide antigen assembly with MHC class II protein complex / MHC class II protein complex / peptide antigen binding / antigen processing and presentation of exogenous peptide antigen via MHC class II / positive regulation of immune response / positive regulation of T cell activation / cell wall macromolecule catabolic process / lysozyme / lysozyme activity / MHC class II protein complex binding / late endosome membrane / killing of cells of another organism / defense response to Gram-negative bacterium / adaptive immune response / early endosome / lysosome / defense response to bacterium / defense response to Gram-positive bacterium / external side of plasma membrane / lysosomal membrane / protein-containing complex binding / cell surface / endoplasmic reticulum / Golgi apparatus / extracellular space / identical protein binding / plasma membrane / cytoplasm Similarity search - Function | ||||||||||||||||||||||||
| Biological species | ![]() ![]() | ||||||||||||||||||||||||
| Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 3.09 Å | ||||||||||||||||||||||||
Authors | Kawakami, K. / Yonekura, K. | ||||||||||||||||||||||||
| Funding support | Japan, 1items
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Citation | Journal: To Be PublishedTitle: Antigen-specific immune regulation mediated by self TCR-like antibodies Authors: Kishida, K. / Kawakami, K. / Yonekura, K. / Arase, H. | ||||||||||||||||||||||||
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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 | 9l1l.cif.gz | 168.2 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb9l1l.ent.gz | 130.6 KB | Display | PDB format |
| PDBx/mmJSON format | 9l1l.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/l1/9l1l ftp://data.pdbj.org/pub/pdb/validation_reports/l1/9l1l | HTTPS FTP |
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-Related structure data
| Related structure data | ![]() 62748MC M: map data used to model this data C: citing same article ( |
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| Similar structure data | Similarity search - Function & homology F&H Search |
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Links
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Assembly
| Deposited unit | ![]()
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Components
| #1: Protein | Mass: 20431.785 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() |
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| #2: Protein | Mass: 22124.916 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() |
| #3: Antibody | Mass: 23637.178 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() |
| #4: Antibody | Mass: 23418.830 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() |
| #5: Protein/peptide | Mass: 1810.984 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Details: HEL peptide / Source: (gene. exp.) ![]() |
| Has protein modification | Y |
-Experimental details
-Experiment
| Experiment | Method: ELECTRON MICROSCOPY |
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| EM experiment | Aggregation state: PARTICLE / 3D reconstruction method: single particle reconstruction |
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Sample preparation
| Component | Name: anti-HEL AiTab / Type: COMPLEX / Entity ID: all / Source: RECOMBINANT |
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| Source (natural) | Organism: ![]() |
| Source (recombinant) | Organism: unidentified plasmid (others) |
| Buffer solution | pH: 8 |
| Specimen | Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES |
| Vitrification | Cryogen name: NITROGEN |
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Electron microscopy imaging
| Microscopy | Model: JEOL CRYO ARM 300 |
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| Electron gun | Electron source: FIELD EMISSION GUN / Accelerating voltage: 300 kV / Illumination mode: FLOOD BEAM |
| Electron lens | Mode: BRIGHT FIELD / Nominal defocus max: 1800 nm / Nominal defocus min: 800 nm / Cs: 2.7 mm |
| Image recording | Electron dose: 98.95 e/Å2 / Film or detector model: GATAN K3 (6k x 4k) |
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Processing
| CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION |
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| 3D reconstruction | Resolution: 3.09 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 50032 / Symmetry type: POINT |
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Japan, 1items
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FIELD EMISSION GUN