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8S2V

SSX structure of Lysozyme grown in microfluidic droplets

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsESRF BEAMLINE ID29
Synchrotron siteESRF
BeamlineID29
Temperature [K]293
Detector technologyPIXEL
Collection date2023-01-23
DetectorPSI JUNGFRAU 4M
Wavelength(s)1.07
Spacegroup nameP 43 21 2
Unit cell lengths78.900, 78.900, 37.900
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution55.853 - 1.800
Rwork0.146
R-free0.18970
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.008
RMSD bond angle1.767
Data reduction softwareCrystFEL (0.10.2)
Data scaling softwareCrystFEL (0.10.2)
Phasing softwareMOLREP
Refinement softwareREFMAC (5.8.0425)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]78.9001.830
High resolution limit [Å]1.8001.800
Number of reflections11607663
<I/σ(I)>17.20.9
Completeness [%]100.0100
Redundancy46451.94
CC(1/2)0.9900.440
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1MICROFLUIDIC329420 mg/mL Lysozyme dissolved in 20 mM sodium acetate pH 4.6 Precipitant: 6% PEG 6000 (W/V), 3.4M NaCl and 1M sodium acetate pH 3.0

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