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6D9X

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 nameP 21 21 2
Unit cell lengths81.291, 86.273, 40.288
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution29.443 - 1.830
R-factor0.2003
Rwork0.198
R-free0.24130
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)4y7r
RMSD bond length0.007
RMSD bond angle1.023
Data reduction softwareHKL-2000
Data scaling softwareSCALEPACK
Phasing softwarePHASER
Refinement softwarePHENIX (dev_1645)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0001.860
High resolution limit [Å]1.8301.830
Rpim0.0270.264
Number of reflections256851192
<I/σ(I)>19
Completeness [%]99.193.9
Redundancy86.5
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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