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3ZFI

Rap1a protein (SMA2260) from Serratia marcescens

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsDIAMOND BEAMLINE I04
Synchrotron siteDiamond
BeamlineI04
Temperature [K]287
Detector technologyCCD
Collection date2011-08-01
DetectorADSC QUANTUM 315r
Spacegroup nameC 2 2 21
Unit cell lengths82.650, 93.000, 51.260
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution61.780 - 1.980
R-factor0.19416
Rwork0.192
R-free0.23396
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.018
RMSD bond angle1.925
Data reduction softwareiMOSFLM
Data scaling softwareSCALA (CCP4)
Phasing softwarePHASER
Refinement softwareREFMAC (5.6.0117)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]46.5002.090
High resolution limit [Å]1.9801.980
Rmerge0.0700.490
Number of reflections14089
<I/σ(I)>13.42.7
Completeness [%]99.9100
Redundancy4.54.4
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP5.5SITTING DROP VAPOUR DIFFUSION. PROTEIN CONCENTRATION AT 9MG/ML, IN 150 MM SODIUM CHLORIDE, 25MM TRIS-HCL, PH 7.5 (SAMPLE BUFFER) RESERVOIR: 25% W/V POLYETHYLENE GLYCOL 3350, 0.1M BIS-TRIS, PH 5.5 2:1 SAMPLE TO RESERVOIR RATIO.

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