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Open data
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Basic information
| Entry | Database: PDB / ID: 3at4 | ||||||
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| Title | Crystal structure of CK2alpha with pyradine derivertive | ||||||
Components | Casein kinase II subunit alpha | ||||||
Keywords | TRANSFERASE/TRANSFERASE INHIBITOR / CK2 / kinase / TRANSFERASE-TRANSFERASE INHIBITOR complex | ||||||
| Function / homology | Function and homology informationregulation of chromosome separation / positive regulation of aggrephagy / WNT mediated activation of DVL / Condensation of Prometaphase Chromosomes / protein kinase CK2 complex / symbiont-mediated disruption of host cell PML body / Receptor Mediated Mitophagy / Synthesis of PC / Sin3-type complex / Maturation of hRSV A proteins ...regulation of chromosome separation / positive regulation of aggrephagy / WNT mediated activation of DVL / Condensation of Prometaphase Chromosomes / protein kinase CK2 complex / symbiont-mediated disruption of host cell PML body / Receptor Mediated Mitophagy / Synthesis of PC / Sin3-type complex / Maturation of hRSV A proteins / RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known / negative regulation of signal transduction by p53 class mediator / negative regulation of apoptotic signaling pathway / positive regulation of Wnt signaling pathway / negative regulation of double-strand break repair via homologous recombination / : / negative regulation of proteasomal ubiquitin-dependent protein catabolic process / Signal transduction by L1 / Hsp90 protein binding / PML body / Regulation of PTEN stability and activity / Wnt signaling pathway / positive regulation of protein catabolic process / KEAP1-NFE2L2 pathway / kinase activity / rhythmic process / Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding / double-strand break repair / positive regulation of cell growth / Regulation of TP53 Activity through Phosphorylation / non-specific serine/threonine protein kinase / regulation of cell cycle / negative regulation of translation / protein stabilization / protein serine kinase activity / protein serine/threonine kinase activity / positive regulation of cell population proliferation / apoptotic process / DNA damage response / signal transduction / nucleoplasm / ATP binding / identical protein binding / nucleus / plasma membrane / cytosol Similarity search - Function | ||||||
| Biological species | Homo sapiens (human) | ||||||
| Method | X-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 2.2 Å | ||||||
Authors | Kinoshita, T. | ||||||
Citation | Journal: Mol.Cell.Biochem. / Year: 2011Title: A detailed thermodynamic profile of cyclopentyl and isopropyl derivatives binding to CK2 kinase Authors: Kinoshita, T. / Sekiguchi, Y. / Fukada, H. / Nakaniwa, T. / Tada, T. / Nakamura, S. / Kitaura, K. / Ohno, H. / Suzuki, Y. / Hirasawa, A. / Nakanishi, I. / Tsujimoto, G. | ||||||
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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 | 3at4.cif.gz | 85.7 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb3at4.ent.gz | 63.1 KB | Display | PDB format |
| PDBx/mmJSON format | 3at4.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 3at4_validation.pdf.gz | 737.6 KB | Display | wwPDB validaton report |
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| Full document | 3at4_full_validation.pdf.gz | 751.5 KB | Display | |
| Data in XML | 3at4_validation.xml.gz | 17.7 KB | Display | |
| Data in CIF | 3at4_validation.cif.gz | 24.5 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/at/3at4 ftp://data.pdbj.org/pub/pdb/validation_reports/at/3at4 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 3at2C ![]() 3at3C ![]() 2zjwS C: citing same article ( S: Starting model for refinement |
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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: Protein | Mass: 40478.191 Da / Num. of mol.: 1 / Fragment: residues 1-335 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: CSNK2A1 / Plasmid: pGEX-6p1 / Production host: ![]() References: UniProt: P68400, non-specific serine/threonine protein kinase |
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| #2: Chemical | ChemComp-CCK / [ |
| #3: Water | ChemComp-HOH / |
-Experimental details
-Experiment
| Experiment | Method: X-RAY DIFFRACTION / Number of used crystals: 1 |
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Sample preparation
| Crystal | Density Matthews: 1.94 Å3/Da / Density % sol: 36.57 % |
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| Crystal grow | Temperature: 277 K / Method: vapor diffusion, sitting drop / pH: 8 Details: 25% ethyleneglycol, pH 8, VAPOR DIFFUSION, SITTING DROP, temperature 277K |
-Data collection
| Diffraction | Mean temperature: 95 K |
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| Diffraction source | Source: SYNCHROTRON / Site: Photon Factory / Beamline: BL-17A / Wavelength: 1 Å |
| Detector | Type: ADSC QUANTUM 4 / Detector: CCD / Date: Nov 11, 2008 |
| Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
| Radiation wavelength | Wavelength: 1 Å / Relative weight: 1 |
| Reflection | Resolution: 2.2→38.66 Å / Num. all: 16481 / Num. obs: 16647 / % possible obs: 99 % |
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Processing
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| Refinement | Method to determine structure: MOLECULAR REPLACEMENTStarting model: 2ZJW Resolution: 2.2→38.66 Å / Stereochemistry target values: Engh & Huber
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| Refinement step | Cycle: LAST / Resolution: 2.2→38.66 Å
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Homo sapiens (human)
X-RAY DIFFRACTION
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