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7HBW

PanDDA analysis group deposition -- Crystal structure of HSP90N in complex with PS-4774

This is a non-PDB format compatible entry.
Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSSRF BEAMLINE BL02U1
Synchrotron siteSSRF
BeamlineBL02U1
Temperature [K]100
Detector technologyPIXEL
Collection date2023-09-04
DetectorDECTRIS EIGER2 S 9M
Wavelength(s)0.97918
Spacegroup nameI 2 2 2
Unit cell lengths66.550, 89.330, 100.520
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution31.370 - 1.910
R-factor0.2058
Rwork0.205
R-free0.22180
Structure solution methodFOURIER SYNTHESIS
RMSD bond length0.002
RMSD bond angle0.525
Data reduction softwareXDS
Data scaling softwareAimless (0.7.7)
Phasing softwareDIMPLE
Refinement softwarePHENIX (1.20.1_4487)
Data quality characteristics
 OverallInner shellOuter shell
Low resolution limit [Å]33.39033.3901.960
High resolution limit [Å]1.9108.5401.910
Rmerge0.1410.0480.912
Rmeas0.1480.0511.027
Rpim0.0450.0160.454
Total number of observations25926032387106
Number of reflections229562991346
<I/σ(I)>14.237.92.2
Completeness [%]97.297.979
Redundancy11.310.85.3
CC(1/2)0.9930.9960.829
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP8.5277100mM Tris-HCl pH 8.5, 22% PEG4000, 200mM MgCl2

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