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7OKE

Crystal structure of human BCL6 BTB domain in complex with compound 2

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsESRF BEAMLINE MASSIF-1
Synchrotron siteESRF
BeamlineMASSIF-1
Temperature [K]100
Detector technologyPIXEL
Collection date2016-05-01
DetectorDECTRIS PILATUS3 2M
Wavelength(s)0.966
Spacegroup nameP 61 2 2
Unit cell lengths67.125, 67.125, 164.890
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution39.940 - 1.480
R-factor0.169
Rwork0.168
R-free0.18700
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)3bim
RMSD bond length0.010
RMSD bond angle0.980
Data reduction softwareXDS
Data scaling softwareAimless (0.5.25)
Phasing softwarePHASER
Refinement softwareBUSTER (2.10.3)
Data quality characteristics
 OverallInner shellOuter shell
Low resolution limit [Å]47.51047.5101.530
High resolution limit [Å]1.4805.7301.480
Rmerge0.1130.0452.660
Rmeas0.1160.0472.736
Rpim0.0260.0110.633
Total number of observations7181881341466900
Number of reflections376517993631
<I/σ(I)>17.760.61.3
Completeness [%]100.099.9100
Redundancy19.116.818.4
CC(1/2)0.9990.9990.511
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION72912 microliter of the BCL6-BTB/WVIP complex at 4 mg/mL plus 1 microliter of a crystallisation solution consisting of 1 M K2HPO4, 0.7 M NaH2PO4, 75 mM sodium acetate buffer pH 4.5 and 2 % DMSO, against 350 microliter of crystallisation solution.

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