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6DAR

Discovery of Potent 2-Aryl-6,7-Dihydro-5HPyrrolo[ 1,2-a]imidazoles as WDR5 WIN-site Inhibitors Using Fragment-Based Methods and Structure-Based Design

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 21-ID-G
Synchrotron siteAPS
Beamline21-ID-G
Temperature [K]100
Detector technologyCCD
Collection date2014-03-08
DetectorMARMOSAIC 300 mm CCD
Wavelength(s)0.98
Spacegroup nameC 2 2 21
Unit cell lengths78.550, 99.466, 80.460
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution30.823 - 1.880
R-factor0.1615
Rwork0.158
R-free0.19480
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)4y7r
RMSD bond length0.005
RMSD bond angle1.008
Data reduction softwareHKL-2000
Data scaling softwareHKL-2000
Phasing softwarePHASER
Refinement softwarePHENIX (dev_1760)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0001.920
High resolution limit [Å]1.8801.880
Number of reflections259741183
<I/σ(I)>10.112.07
Completeness [%]99.898.3
Redundancy4.372.77
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP62930.1 M Bis-Tris pH 6.0, 0.2 M ammonium acetate, 28% to 32% PEG3350

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