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Yorodumi- PDB-9gd7: DNA-PK Ku80 mediated dimer bound to DNA polymerase Lambda and DNA... -
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Open data
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Basic information
| Entry | Database: PDB / ID: 9gd7 | ||||||||||||||||||||||||||||||
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| Title | DNA-PK Ku80 mediated dimer bound to DNA polymerase Lambda and DNA ligase 4/XRCC4 | ||||||||||||||||||||||||||||||
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Keywords | DNA BINDING PROTEIN / Kinase / complex / DNA-binding | ||||||||||||||||||||||||||||||
| Function / homology | Function and homology informationFHA domain binding / positive regulation of chromosome organization / positive regulation of ligase activity / DNA ligase IV complex / positive regulation of platelet formation / DNA ligase activity / Ku70:Ku80 complex / DN2 thymocyte differentiation / DNA ligase (ATP) / negative regulation of t-circle formation ...FHA domain binding / positive regulation of chromosome organization / positive regulation of ligase activity / DNA ligase IV complex / positive regulation of platelet formation / DNA ligase activity / Ku70:Ku80 complex / DN2 thymocyte differentiation / DNA ligase (ATP) / negative regulation of t-circle formation / T cell receptor V(D)J recombination / DNA end binding / pro-B cell differentiation / small-subunit processome assembly / positive regulation of lymphocyte differentiation / DNA ligase (ATP) activity / DNA-dependent protein kinase activity / DNA-dependent protein kinase complex / histone H2AXS139 kinase activity / DNA-dependent protein kinase-DNA ligase 4 complex / immunoglobulin V(D)J recombination / nonhomologous end joining complex / nucleotide-excision repair, DNA gap filling / immature B cell differentiation / single strand break repair / regulation of smooth muscle cell proliferation / cellular response to X-ray / V(D)J recombination / nuclear telomere cap complex / double-strand break repair via alternative nonhomologous end joining / regulation of epithelial cell proliferation / double-strand break repair via classical nonhomologous end joining / telomere capping / isotype switching / Cytosolic sensors of pathogen-associated DNA / protein localization to site of double-strand break / IRF3-mediated induction of type I IFN / regulation of hematopoietic stem cell differentiation / positive regulation of neurogenesis / recombinational repair / regulation of telomere maintenance / protein localization to chromosome, telomeric region / U3 snoRNA binding / DNA biosynthetic process / maturation of 5.8S rRNA / T cell lineage commitment / cellular response to lithium ion / cellular hyperosmotic salinity response / negative regulation of cGAS/STING signaling pathway / positive regulation of double-strand break repair via nonhomologous end joining / 2-LTR circle formation / B cell lineage commitment / telomeric DNA binding / hematopoietic stem cell proliferation / ligase activity / negative regulation of protein phosphorylation / positive regulation of protein kinase activity / Lyases; Carbon-oxygen lyases; Other carbon-oxygen lyases / site of DNA damage / peptidyl-threonine phosphorylation / 5'-deoxyribose-5-phosphate lyase activity / somatic stem cell population maintenance / hematopoietic stem cell differentiation / response to X-ray / chromosome organization / ectopic germ cell programmed cell death / ATP-dependent activity, acting on DNA / telomere maintenance via telomerase / somitogenesis / SUMOylation of DNA damage response and repair proteins / somatic hypermutation of immunoglobulin genes / base-excision repair, gap-filling / condensed chromosome / DNA polymerase binding / mitotic G1 DNA damage checkpoint signaling / neurogenesis / telomere maintenance / activation of innate immune response / DNA helicase activity / cyclin binding / positive regulation of erythrocyte differentiation / positive regulation of translation / cellular response to leukemia inhibitory factor / central nervous system development / stem cell proliferation / response to gamma radiation / cellular response to ionizing radiation / nucleotide-excision repair / small-subunit processome / Nonhomologous End-Joining (NHEJ) / enzyme activator activity / cellular response to gamma radiation / protein-DNA complex / double-strand break repair via homologous recombination / base-excision repair / regulation of circadian rhythm / brain development / peptidyl-serine phosphorylation / protein destabilization / protein modification process Similarity search - Function | ||||||||||||||||||||||||||||||
| Biological species | Homo sapiens (human) | ||||||||||||||||||||||||||||||
| Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 4.25 Å | ||||||||||||||||||||||||||||||
Authors | Chaplin, A.K. / Amin, H. / Zahid, S. / Hardwick, S.W. | ||||||||||||||||||||||||||||||
| Funding support | United Kingdom, 2items
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Citation | Journal: To Be PublishedTitle: Ku70/80 anchors DNA polymerase Lambda at sites of DNA synapsis during NHEJ Authors: Chaplin, A.K. / Amin, H. / Zahid, S. / Hardwick, S.W. | ||||||||||||||||||||||||||||||
| 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 | 9gd7.cif.gz | 990.8 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb9gd7.ent.gz | 759.2 KB | Display | PDB format |
| PDBx/mmJSON format | 9gd7.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 9gd7_validation.pdf.gz | 1.5 MB | Display | wwPDB validaton report |
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| Full document | 9gd7_full_validation.pdf.gz | 1.7 MB | Display | |
| Data in XML | 9gd7_validation.xml.gz | 150.7 KB | Display | |
| Data in CIF | 9gd7_validation.cif.gz | 229 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/gd/9gd7 ftp://data.pdbj.org/pub/pdb/validation_reports/gd/9gd7 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 51249MC ![]() 9g9lC 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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| 1 |
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Components
-Protein , 5 types, 6 molecules EMPQSA
| #1: Protein | Mass: 104124.953 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: LIG4 / Production host: ![]() | ||||
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| #3: Protein | Mass: 21663.498 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: PAXX, C9orf142, XLS / Production host: ![]() | ||||
| #4: Protein | Mass: 38337.703 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: XRCC4 / Production host: ![]() #5: Protein | | Mass: 469673.219 Da / Num. of mol.: 1 / Source method: isolated from a natural source / Source: (natural) Homo sapiens (human) / Cell line: HELAReferences: UniProt: P78527, non-specific serine/threonine protein kinase #9: Protein | | Mass: 63571.238 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: POLL / Production host: ![]() References: UniProt: Q9UGP5, DNA-directed DNA polymerase, Lyases; Carbon-oxygen lyases; Other carbon-oxygen lyases |
-X-ray repair cross-complementing protein ... , 2 types, 2 molecules LT
| #2: Protein | Mass: 82812.438 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: XRCC5, G22P2Production host: Insect cell expression vector pTIE1 (others) References: UniProt: P13010, Hydrolases; Acting on acid anhydrides; Acting on acid anhydrides to facilitate cellular and subcellular movement |
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| #6: Protein | Mass: 69945.039 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: XRCC6, G22P1Production host: Insect cell expression vector pTIE1 (others) References: UniProt: P12956, Hydrolases; Acting on acid anhydrides; Acting on acid anhydrides to facilitate cellular and subcellular movement, Lyases; Carbon-oxygen lyases; Other carbon-oxygen lyases |
-DNA chain , 2 types, 2 molecules ij
| #7: DNA chain | Mass: 7632.012 Da / Num. of mol.: 1 / Source method: obtained synthetically / Source: (synth.) Homo sapiens (human) |
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| #8: DNA chain | Mass: 7748.026 Da / Num. of mol.: 1 / Source method: obtained synthetically / Source: (synth.) Homo sapiens (human) |
-Details
| Has protein modification | N |
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-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: Ku80 mediated dimer of DNA-PK bound to Polymerase Lambda and XRCC4/DNA ligase IV Type: COMPLEX / Entity ID: all / Source: NATURAL |
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| Molecular weight | Value: 0.8 MDa / Experimental value: NO |
| Source (natural) | Organism: Homo sapiens (human) |
| Buffer solution | pH: 7.5 |
| Specimen | Conc.: 2 mg/ml / Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES |
| Specimen support | Grid type: Quantifoil R1.2/1.3 |
| Vitrification | Instrument: FEI VITROBOT MARK IV / Cryogen name: ETHANE |
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Electron microscopy imaging
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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| Microscopy | Model: FEI TITAN KRIOS |
| Electron gun | Electron source: FIELD EMISSION GUN / Accelerating voltage: 300 kV / Illumination mode: FLOOD BEAM |
| Electron lens | Mode: BRIGHT FIELD / Nominal magnification: 130000 X / Nominal defocus max: 2200 nm / Nominal defocus min: 800 nm / Cs: 2.7 mm / C2 aperture diameter: 100 µm |
| Specimen holder | Cryogen: NITROGEN / Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER |
| Image recording | Average exposure time: 1.04 sec. / Electron dose: 51.96 e/Å2 / Film or detector model: GATAN K3 BIOQUANTUM (6k x 4k) / Num. of grids imaged: 1 / Num. of real images: 11487 |
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Processing
| EM software |
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| CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION | |||||||||||||||||||||||||||
| Particle selection | Num. of particles selected: 603711 | |||||||||||||||||||||||||||
| Symmetry | Point symmetry: C1 (asymmetric) | |||||||||||||||||||||||||||
| 3D reconstruction | Resolution: 4.25 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 14964 / Symmetry type: POINT | |||||||||||||||||||||||||||
| Refinement | Cross valid method: NONE Stereochemistry target values: GeoStd + Monomer Library + CDL v1.2 | |||||||||||||||||||||||||||
| Displacement parameters | Biso mean: 386.83 Å2 | |||||||||||||||||||||||||||
| Refine LS restraints |
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About Yorodumi



Homo sapiens (human)
United Kingdom, 2items
Citation


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