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5QDC

Crystal structure of BACE complex with BMC019 hydrolyzed

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSLS BEAMLINE X10SA
Synchrotron siteSLS
BeamlineX10SA
Temperature [K]100
Detector technologyCCD
Collection date2006-05-12
DetectorMARMOSAIC 225 mm CCD
Spacegroup nameP 1 21 1
Unit cell lengths82.008, 102.635, 100.500
Unit cell angles90.00, 104.20, 90.00
Refinement procedure
Resolution41.530 - 2.100
R-factor0.172
Rwork0.171
R-free0.19500
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.008
RMSD bond angle0.875
Data scaling softwareSCALEPACK
Phasing softwareCNX
Refinement softwarePHENIX (1.12_2829)
Data quality characteristics
 Overall
Low resolution limit [Å]41.525
High resolution limit [Å]2.100
Rmerge0.052
Number of reflections93941
Completeness [%]99.8
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1hanging drop5292CRYSTALS WERE GROWN AT 19C BY VAPOUR DIFFUSION IN HANGING DROPS FROM 1.0M AMMONIUM PHOSPHATE, 0.1M SODIUM CITRATE PH 5.0. PROTEIN STOCK WAS BACE MUT46B BATCH XIV 7.4MG/ML IN 10MM TRIS-HCL PH 7.4, 25MM NACL, WITH A 6-FOLD EXCESS OF BMC019 ADDED FROM A 50MM STOCK SOLUTION IN DMSO. CRYO-PROTECTANT WAS 1.0M AMMONIUM PHOSPHATE, 0.1M SODIUM CITRATE, 25%(V/V)GLYCEROL, 2.0% DMSO, 1MM BMC019.

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