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6O6Y

Crystal structure of Csm6 in complex with cyclic-tetraadenylates (cA4) by cocrystallization of Csm6 and cA4

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 24-ID-C
Synchrotron siteAPS
Beamline24-ID-C
Temperature [K]100
Detector technologyPIXEL
Collection date2018-11-19
DetectorDECTRIS PILATUS 6M
Wavelength(s)0.9791
Spacegroup nameC 2 2 21
Unit cell lengths103.451, 163.963, 111.105
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution48.370 - 1.960
R-factor0.21083
Rwork0.206
R-free0.25510
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.004
RMSD bond angle1.323
Data reduction softwareHKL-2000
Data scaling softwareHKL-2000
Phasing softwarePHENIX
Refinement softwareREFMAC (5.8.0238)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0002.020
High resolution limit [Å]1.9501.950
Rpim0.036
Number of reflections674416657
<I/σ(I)>17.2
Completeness [%]99.5
Redundancy9.9
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP6.229310% PEG 8K, 0.2 M NaCl, 0.1 M Na/K phosphate pH 6.2

219869

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