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6E1Y

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-F
Synchrotron siteAPS
Beamline21-ID-F
Temperature [K]100
Detector technologyCCD
Collection date2018-07-06
DetectorMARMOSAIC 300 mm CCD
Wavelength(s)0.98
Spacegroup nameP 1
Unit cell lengths46.971, 61.573, 64.668
Unit cell angles110.47, 91.22, 112.27
Refinement procedure
Resolution29.016 - 1.219
R-factor0.1699
Rwork0.170
R-free0.18160
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)6d9x
RMSD bond length0.008
RMSD bond angle1.113
Data reduction softwareHKL-2000
Data scaling softwareSCALEPACK
Phasing softwareAMoRE
Refinement softwarePHENIX ((dev_3139: ???))
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0001.240
High resolution limit [Å]1.2191.220
Rmerge0.0400.292
Number of reflections173496
<I/σ(I)>14.68
Completeness [%]94.1
Redundancy3.3
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP7.52930.1 M Bis-Tris pH 6.0 or Hepes pH 7.5, 0.2 M ammonium acetate, 28% to 32% PEG3350

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