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9BBI

Co-crystal structure of human DDB1 bound to fragment UB028669

This is a non-PDB format compatible entry.
Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 24-ID-C
Synchrotron siteAPS
Beamline24-ID-C
Temperature [K]100
Detector technologyPIXEL
Collection date2021-09-25
DetectorDECTRIS EIGER2 X 16M
Wavelength(s)0.97911
Spacegroup nameP 21 21 21
Unit cell lengths63.039, 125.742, 169.937
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution47.010 - 1.900
R-factor0.18998
Rwork0.188
R-free0.22060
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.005
RMSD bond angle1.395
Data scaling softwareAimless
Phasing softwarePHASER
Refinement softwareREFMAC (5.8.0425)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]47.0101.930
High resolution limit [Å]1.9001.900
Rmerge0.1250.726
Rmeas0.1350.786
Rpim0.0520.298
Total number of observations35004
Number of reflections1065485233
<I/σ(I)>7.21.7
Completeness [%]99.4
Redundancy6.46.7
CC(1/2)0.9950.755
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP29120% (v/w) PEG 3350, 0.2 M di-NH4tart

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