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Yorodumi- PDB-4l1h: Bence-Jones immunoglobulin REI variable portion with seven point ... -
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Open data
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Basic information
| Entry | Database: PDB / ID: 4l1h | ||||||
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| Title | Bence-Jones immunoglobulin REI variable portion with seven point mutations | ||||||
 Components | Ig kappa chain V-I region Rei | ||||||
 Keywords | IMMUNE SYSTEM / immunoglobulin kappa-chains / recombinant | ||||||
| Function / homology |  Function and homology informationCD22 mediated BCR regulation / Fc epsilon receptor (FCERI) signaling / Classical antibody-mediated complement activation / Initial triggering of complement / immunoglobulin complex / FCGR activation / Role of LAT2/NTAL/LAB on calcium mobilization / Role of phospholipids in phagocytosis / Scavenging of heme from plasma / antigen binding ...CD22 mediated BCR regulation / Fc epsilon receptor (FCERI) signaling / Classical antibody-mediated complement activation / Initial triggering of complement / immunoglobulin complex / FCGR activation / Role of LAT2/NTAL/LAB on calcium mobilization / Role of phospholipids in phagocytosis / Scavenging of heme from plasma / antigen binding / FCERI mediated Ca+2 mobilization / FCGR3A-mediated IL10 synthesis / Antigen activates B Cell Receptor (BCR) leading to generation of second messengers / Regulation of Complement cascade / Cell surface interactions at the vascular wall / FCGR3A-mediated phagocytosis / FCERI mediated MAPK activation / Regulation of actin dynamics for phagocytic cup formation / FCERI mediated NF-kB activation / Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell / blood microparticle / adaptive immune response / Potential therapeutics for SARS / immune response / extracellular exosome / extracellular region / plasma membrane Similarity search - Function  | ||||||
| Biological species |  Homo sapiens (human) | ||||||
| Method |  X-RAY DIFFRACTION /  SYNCHROTRON /  MOLECULAR REPLACEMENT / Resolution: 1.68 Å  | ||||||
 Authors | Uson, I. | ||||||
 Citation |  Journal: To be PublishedTitle: Bence-Jones immunoglobulin REI variable portion with seven point mutations Authors: Uson, I.  | ||||||
| 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 |  4l1h.cif.gz | 31.2 KB | Display |  PDBx/mmCIF format | 
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| PDB format |  pdb4l1h.ent.gz | 20.9 KB | Display |  PDB format | 
| PDBx/mmJSON format |  4l1h.json.gz | Tree view |  PDBx/mmJSON format | |
| Others |  Other downloads | 
-Validation report
| Summary document |  4l1h_validation.pdf.gz | 407.2 KB | Display |  wwPDB validaton report | 
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| Full document |  4l1h_full_validation.pdf.gz | 410.6 KB | Display | |
| Data in XML |  4l1h_validation.xml.gz | 6.8 KB | Display | |
| Data in CIF |  4l1h_validation.cif.gz | 7.8 KB | Display | |
| Arichive directory |  https://data.pdbj.org/pub/pdb/validation_reports/l1/4l1h ftp://data.pdbj.org/pub/pdb/validation_reports/l1/4l1h | HTTPS FTP  | 
-Related structure data
| Related structure data | |
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| 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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Components
| #1: Antibody |   Mass: 11751.089 Da / Num. of mol.: 1 / Mutation: Q24R,N34A,T39K,Y71F,F73L,I83F,Q105E Source method: isolated from a genetically manipulated source Source: (gene. exp.)  Homo sapiens (human) / References: UniProt: P01607, UniProt: P01593*PLUS | 
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| Has protein modification | Y | 
-Experimental details
-Experiment
| Experiment | Method:  X-RAY DIFFRACTION | 
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Sample preparation
| Crystal | Density Matthews: 3.42 Å3/Da / Density % sol: 64.05 % | 
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-Data collection
| Diffraction source | Source:  SYNCHROTRON / Site:  EMBL/DESY, HAMBURG   / Beamline: X11 / Wavelength: 0.98 Å | 
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| Detector | Type: MAR555 FLAT PANEL / Detector: IMAGE PLATE | 
| Radiation | Monochromator: Si(111) / Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray | 
| Radiation wavelength | Wavelength: 0.98 Å / Relative weight: 1 | 
| Reflection | Resolution: 1.68→52.61 Å / Num. all: 19267 / Num. obs: 15847 / % possible obs: 99.8 % / Observed criterion σ(F): 4 | 
| Reflection shell | Highest resolution: 1.68 Å | 
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Processing
| Software | Name: SHELXL-97 / Classification: refinement | ||||||||||||||||||||
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| Refinement | Method to determine structure:  MOLECULAR REPLACEMENT / Resolution: 1.68→52.61 Å / σ(F): 4  / Stereochemistry target values: Engh & Huber
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| Refinement step | Cycle: LAST / Resolution: 1.68→52.61 Å
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Homo sapiens (human)
X-RAY DIFFRACTION
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