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Open data
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Basic information
| Entry | Database: PDB / ID: 7q6c | ||||||
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| Title | complement C6 FIM1-2 bound to CP010 antibody | ||||||
Components |
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Keywords | IMMUNE SYSTEM / complement antibody terminal pathway | ||||||
| Function / homology | Function and homology informationTerminal pathway of complement / membrane attack complex / complement activation / complement activation, classical pathway / Regulation of Complement cascade / positive regulation of immune response / killing of cells of another organism / in utero embryonic development / innate immune response / extracellular space ...Terminal pathway of complement / membrane attack complex / complement activation / complement activation, classical pathway / Regulation of Complement cascade / positive regulation of immune response / killing of cells of another organism / in utero embryonic development / innate immune response / extracellular space / extracellular exosome / extracellular region / plasma membrane Similarity search - Function | ||||||
| Biological species | Homo sapiens (human)![]() ![]() | ||||||
| Method | X-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 2.29274 Å | ||||||
Authors | Olesen, H.G. / Andersen, G.R. | ||||||
| Funding support | 1items
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Citation | Journal: J Innate Immun / Year: 2022Title: Development, Characterization, and in vivo Validation of a Humanized C6 Monoclonal Antibody that Inhibits the Membrane Attack Complex. Authors: Gytz Olesen, H. / Michailidou, I. / Zelek, W.M. / Vreijling, J. / Ruizendaal, P. / de Klein, F. / Marquart, J.A. / Kuipers, T.B. / Mei, H. / Zhang, Y. / Ahasan, M. / Johnson, K.K. / Wang, Y. ...Authors: Gytz Olesen, H. / Michailidou, I. / Zelek, W.M. / Vreijling, J. / Ruizendaal, P. / de Klein, F. / Marquart, J.A. / Kuipers, T.B. / Mei, H. / Zhang, Y. / Ahasan, M. / Johnson, K.K. / Wang, Y. / Morgan, B.P. / van Dijk, M. / Fluiter, K. / Andersen, G.R. / Baas, F. | ||||||
| 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 | 7q6c.cif.gz | 489.5 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb7q6c.ent.gz | 337.7 KB | Display | PDB format |
| PDBx/mmJSON format | 7q6c.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 7q6c_validation.pdf.gz | 455.2 KB | Display | wwPDB validaton report |
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| Full document | 7q6c_full_validation.pdf.gz | 458.4 KB | Display | |
| Data in XML | 7q6c_validation.xml.gz | 26.3 KB | Display | |
| Data in CIF | 7q6c_validation.cif.gz | 37.2 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/q6/7q6c ftp://data.pdbj.org/pub/pdb/validation_reports/q6/7q6c | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 6andS S: Starting model for refinement |
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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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| 1 |
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| Unit cell |
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Components
-Protein , 1 types, 1 molecules A
| #1: Protein | Mass: 18478.031 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: C6 / Cell line (production host): HEK293F / Production host: Homo sapiens (human) / References: UniProt: P13671 |
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-Antibody , 3 types, 3 molecules HKL
| #2: Antibody | Mass: 23490.137 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Homo sapiens (human) |
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| #3: Antibody | Mass: 13375.629 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() ![]() |
| #4: Antibody | Mass: 23851.471 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Homo sapiens (human) |
-Non-polymers , 2 types, 129 molecules 


| #5: Chemical | ChemComp-ACT / |
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| #6: Water | ChemComp-HOH / |
-Details
| Has ligand of interest | N |
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| Has protein modification | Y |
-Experimental details
-Experiment
| Experiment | Method: X-RAY DIFFRACTION / Number of used crystals: 1 |
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Sample preparation
| Crystal | Density Matthews: 3.27 Å3/Da / Density % sol: 62.37 % |
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| Crystal grow | Temperature: 291 K / Method: vapor diffusion / pH: 6.4 Details: 112 mM calcium acetate, 56 mM sodium cacodylate pH 6.4, 8.5% PEG8000 and 16% glycerol |
-Data collection
| Diffraction | Mean temperature: 100 K / Serial crystal experiment: N |
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| Diffraction source | Source: SYNCHROTRON / Site: MAX IV / Beamline: BioMAX / Wavelength: 0.9762 Å |
| Detector | Type: DECTRIS EIGER X 16M / Detector: PIXEL / Date: Feb 20, 2020 |
| Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
| Radiation wavelength | Wavelength: 0.9762 Å / Relative weight: 1 |
| Reflection | Resolution: 2.29274→100.826 Å / Num. obs: 45105 / % possible obs: 97.2 % / Redundancy: 3.46 % / Biso Wilson estimate: 49.63 Å2 / CC1/2: 0.999 / Rmerge(I) obs: 0.063 / Rrim(I) all: 0.075 / Net I/σ(I): 12.08 |
| Reflection shell | Resolution: 2.29274→2.43 Å / Num. unique obs: 6899 / CC1/2: 0.399 |
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Processing
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| Refinement | Method to determine structure: MOLECULAR REPLACEMENTStarting model: 6AND Resolution: 2.29274→44.45 Å / SU ML: 0.3214 / Cross valid method: FREE R-VALUE / σ(F): 1.46 / Phase error: 25.6852 Stereochemistry target values: GeoStd + Monomer Library + CDL v1.2
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| Solvent computation | Shrinkage radii: 0.9 Å / VDW probe radii: 1.11 Å / Solvent model: FLAT BULK SOLVENT MODEL | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Displacement parameters | Biso mean: 60.62 Å2 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Refinement step | Cycle: LAST / Resolution: 2.29274→44.45 Å
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| Refine LS restraints |
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| LS refinement shell |
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| Refinement TLS params. | Method: refined / Refine-ID: X-RAY DIFFRACTION
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| Refinement TLS group |
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Homo sapiens (human)
X-RAY DIFFRACTION
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