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7Q75

Room temperature structure of RNase A at atmospheric pressure

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsPETRA III, DESY BEAMLINE P11
Synchrotron sitePETRA III, DESY
BeamlineP11
Temperature [K]295
Detector technologyPIXEL
Collection date2019-09-26
DetectorDECTRIS PILATUS3 X CdTe 2M
Wavelength(s)0.477
Spacegroup nameP 32 2 1
Unit cell lengths64.520, 64.520, 65.140
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution28.140 - 1.640
R-factor0.1573
Rwork0.155
R-free0.18890
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)2e3w
RMSD bond length0.008
RMSD bond angle1.070
Data reduction softwareXDS
Data scaling softwareXSCALE
Phasing softwarePHASER
Refinement softwarePHENIX (1.13-2998_9999)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]28.1401.690
High resolution limit [Å]1.6401.640
Rmerge0.1692.139
Rpim0.0510.668
Number of reflections196111936
<I/σ(I)>7.761.02
Completeness [%]99.899.38
Redundancy11.2
CC(1/2)0.9950.334
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP4.529510-20 mg/ml protein dissolved in 0.1 M sodium acetate pH 4.5 was mixed in a 1:1 ratio with precipitant containing 0.1 M sodium acetate pH 4.5, 1.2-1.5 M ammonium sulphate and 2-2.5 M sodium chloride and equilibrated for one to two days at room-temperature.

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