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3ZIB

Rap2a protein (SMA2265) from Serratia marcescens

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsDIAMOND BEAMLINE I03
Synchrotron siteDiamond
BeamlineI03
Temperature [K]287
Detector technologyPIXEL
Collection date2012-09-22
DetectorDECTRIS PILATUS 6M
Spacegroup nameP 1 21 1
Unit cell lengths39.650, 81.350, 58.450
Unit cell angles90.00, 91.54, 90.00
Refinement procedure
Resolution58.430 - 1.900
R-factor0.18566
Rwork0.183
R-free0.23358
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)4b6i
RMSD bond length0.019
RMSD bond angle1.745
Data reduction softwareiMOSFLM
Data scaling softwareSCALA (CCP4)
Phasing softwarePHASER
Refinement softwareREFMAC (5.6.0117)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]40.6002.000
High resolution limit [Å]1.9001.900
Rmerge0.1000.520
Number of reflections29067
<I/σ(I)>15.34
Completeness [%]99.498.9
Redundancy7.47.5
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP6.5SITTING DROP VAPOUR DIFFUSION. PROTEIN BUFFER: 10 MM SODIUM PHOSPHATE, PH 6.4 RESERVOIR CONDITION: 25% W/V POLYETHYLENE GLYCOL 1000, 0.1 M MES, PH6.5. CRYOPROTECTANT USED: 20% GLYCEROL WITH MOTHER LIQUOR.

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