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6RXI

In-flow serial synchrotron crystallography using a 3D-printed microfluidic device (3D-MiXD): Lysozyme

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsESRF BEAMLINE MASSIF-3
Synchrotron siteESRF
BeamlineMASSIF-3
Temperature [K]293
Detector technologyPIXEL
Collection date2018-02-13
DetectorDECTRIS EIGER X 4M
Wavelength(s)0.9686
Spacegroup nameP 43 21 2
Unit cell lengths79.700, 79.700, 38.550
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution56.360 - 2.000
R-factor0.15984
Rwork0.158
R-free0.20117
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)6h79
RMSD bond length0.009
RMSD bond angle1.584
Data reduction softwareCrystFEL (0.8.0)
Data scaling softwareCrystFEL (0.8.0)
Phasing softwareMOLREP (11.7.01)
Refinement softwareREFMAC (5.8.0238)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]56.3602.080
High resolution limit [Å]2.0002.000
Number of reflections8876869
<I/σ(I)>6.211.83
Completeness [%]100.0100
Redundancy625448
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1BATCH MODE329330 mg/mL lysozyme in 100 mM NaAc (pH3.0) rapidly mixed in a 1:1 ratio with precipitant (100 mM NaAc pH 3.0, 20% NaCl, 6% PEG 6000)

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