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9DU0

Crystal structure of the bromodomain of human BRM (SMARCA2) in complex with a SMARCA-BD binder

This is a non-PDB format compatible entry.
Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSSRF BEAMLINE BL17U1
Synchrotron siteSSRF
BeamlineBL17U1
Temperature [K]100
Detector technologyPIXEL
Collection date2020-04-24
DetectorDECTRIS EIGER X 16M
Wavelength(s)0.979183
Spacegroup nameP 31
Unit cell lengths64.558, 64.558, 89.083
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution47.400 - 3.000
R-factor0.2285
Rwork0.223
R-free0.33810
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.005
RMSD bond angle1.406
Data reduction softwareXDS
Data scaling softwareAimless
Phasing softwarePHASER
Refinement softwareREFMAC (5.8.0258)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]47.4003.180
High resolution limit [Å]3.0003.000
Rmerge0.1320.827
Rmeas0.1701.073
Rpim0.1050.674
Number of reflections81981331
<I/σ(I)>5.3
Completeness [%]98.4
Redundancy2.3
CC(1/2)0.9920.674
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP7.52910.025~0.1 M zinc acetate, 16~26% w/v PEG3350

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