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3K3N

Crystal structure of the catalytic core domain of human PHF8

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSSRF BEAMLINE BL17U
Synchrotron siteSSRF
BeamlineBL17U
Temperature [K]200
Detector technologyCCD
Collection date2009-05-31
DetectorMARMOSAIC 225 mm CCD
Wavelength(s)0.97939
Spacegroup nameP 21 21 21
Unit cell lengths52.238, 52.583, 134.930
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution20.000 - 2.400
R-factor0.224
Rwork0.222
R-free0.26100
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)2yu2
RMSD bond length0.007
RMSD bond angle1.019
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwarePHASER
Refinement softwareREFMAC (5.5.0072)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0002.440
High resolution limit [Å]2.4002.400
Rmerge0.0550.426
Number of reflections14988
<I/σ(I)>312.6
Completeness [%]98.04.1
Redundancy5.73.7
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION6.5298200mM KCl, 100mM Mes, 20% PEG5K, pH 6.5, VAPOR DIFFUSION, temperature 298K

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