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1T2U

Structural basis of phosphopeptide recognition by the BRCT domain of BRCA1: structure of BRCA1 missense variant V1809F

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsALS BEAMLINE 5.0.3
Synchrotron siteALS
Beamline5.0.3
Temperature [K]100
Detector technologyCCD
Collection date2003-08-15
DetectorADSC QUANTUM 4
Spacegroup nameP 61 2 2
Unit cell lengths113.924, 113.924, 120.906
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution20.000 - 2.800
R-factor0.277
Rwork0.275
R-free0.29400
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.019
RMSD bond angle1.636
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareMOLREP
Refinement softwareREFMAC (5.1.24)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]20.0002.900
High resolution limit [Å]2.8002.800
Rmerge0.0510.434
Number of reflections11803
<I/σ(I)>37.93
Completeness [%]99.396.3
Redundancy9.8
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
16.7298Ammounium sulphate, cobaltous chloride, MES, pH 6.7, VAPOR DIFFUSION, HANGING DROP, temperature 298K, pH 6.70

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