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Yorodumi- PDB-4xcj: N-terminal domain of Hsp90 from Dictyostelium discoideum in compl... -
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Basic information
| Entry | Database: PDB / ID: 4xcj | ||||||
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| Title | N-terminal domain of Hsp90 from Dictyostelium discoideum in complex with ADP | ||||||
Components | Heat shock cognate 90 kDa protein | ||||||
Keywords | CHAPERONE / Hsp90 / ADP | ||||||
| Function / homology | Function and homology informationregulation of aggregation involved in sorocarp development / Tetrahydrobiopterin (BH4) synthesis, recycling, salvage and regulation / eNOS activation / HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of ligand / HSF1 activation / HSF1-dependent transactivation / Sema3A PAK dependent Axon repulsion / VEGFR2 mediated vascular permeability / The NLRP3 inflammasome / Aryl hydrocarbon receptor signalling ...regulation of aggregation involved in sorocarp development / Tetrahydrobiopterin (BH4) synthesis, recycling, salvage and regulation / eNOS activation / HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of ligand / HSF1 activation / HSF1-dependent transactivation / Sema3A PAK dependent Axon repulsion / VEGFR2 mediated vascular permeability / The NLRP3 inflammasome / Aryl hydrocarbon receptor signalling / Extra-nuclear estrogen signaling / Regulation of actin dynamics for phagocytic cup formation / Neutrophil degranulation / phagocytic vesicle / extracellular matrix / ATP-dependent protein folding chaperone / unfolded protein binding / protein folding / cellular response to heat / protein stabilization / perinuclear region of cytoplasm / protein-containing complex / ATP hydrolysis activity / ATP binding / plasma membrane / cytosol Similarity search - Function | ||||||
| Biological species | ![]() | ||||||
| Method | X-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 1.75 Å | ||||||
Authors | Raman, S. / Suguna, K. | ||||||
Citation | Journal: Sci Rep / Year: 2015Title: First Structural View of a Peptide Interacting with the Nucleotide Binding Domain of Heat Shock Protein 90 Authors: Raman, S. / Singh, M. / Tatu, U. / Suguna, K. | ||||||
| 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 | 4xcj.cif.gz | 62 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb4xcj.ent.gz | 42 KB | Display | PDB format |
| PDBx/mmJSON format | 4xcj.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/xc/4xcj ftp://data.pdbj.org/pub/pdb/validation_reports/xc/4xcj | HTTPS FTP |
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-Related structure data
| Related structure data | ![]() 4xc0C ![]() 4xclC ![]() 4xd8C ![]() 4xdmC ![]() 4xe2C ![]() 4xkaC ![]() 4xkoC ![]() 1yesS 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: 29226.871 Da / Num. of mol.: 1 / Fragment: N-terminal domain, UNP residues 1-223 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() ![]() |
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| #2: Chemical | ChemComp-ADP / |
| #3: Chemical | ChemComp-MG / |
| #4: Water | ChemComp-HOH / |
-Experimental details
-Experiment
| Experiment | Method: X-RAY DIFFRACTION |
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Sample preparation
| Crystal | Density Matthews: 1.9 Å3/Da / Density % sol: 35.26 % |
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| Crystal grow | Temperature: 290 K / Method: vapor diffusion, hanging drop / pH: 7.5 / Details: 0.1M TRIS, PEG3350 / PH range: 7-8.5 |
-Data collection
| Diffraction | Mean temperature: 100 K |
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| Diffraction source | Source: SYNCHROTRON / Site: ESRF / Beamline: BM14 / Wavelength: 0.97625 Å |
| Detector | Type: MARMOSAIC 225 mm CCD / Detector: CCD / Date: Oct 23, 2010 |
| Radiation | Monochromator: Si(111) / Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
| Radiation wavelength | Wavelength: 0.97625 Å / Relative weight: 1 |
| Reflection | Resolution: 1.75→56.89 Å / Num. obs: 22298 / % possible obs: 99.9 % / Redundancy: 7.4 % / Rmerge(I) obs: 0.082 / Net I/σ(I): 14.7 |
| Reflection shell | Resolution: 1.75→1.84 Å / Redundancy: 7.4 % / Rmerge(I) obs: 0.499 / Mean I/σ(I) obs: 3.8 / % possible all: 100 |
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Processing
| Software | Name: REFMAC / Version: 5.5.0109 / Classification: refinement | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Refinement | Method to determine structure: MOLECULAR REPLACEMENTStarting model: 1YES Resolution: 1.75→56.89 Å / Cor.coef. Fo:Fc: 0.953 / Cor.coef. Fo:Fc free: 0.939 / SU B: 2.585 / SU ML: 0.084 / Cross valid method: FREE R-VALUE / ESU R: 0.13 / ESU R Free: 0.124 / Stereochemistry target values: MAXIMUM LIKELIHOOD / Details: HYDROGENS HAVE BEEN ADDED IN THE RIDING POSITIONS
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| Solvent computation | Ion probe radii: 0.8 Å / Shrinkage radii: 0.8 Å / VDW probe radii: 1.4 Å / Solvent model: MASK | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Displacement parameters | Biso mean: 24.168 Å2
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| Refinement step | Cycle: LAST / Resolution: 1.75→56.89 Å
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| Refine LS restraints |
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