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8CWC

20ns Temperature-Jump (Light) XFEL structure of Lysozyme Bound to N,N'-diacetylchitobiose

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeFREE ELECTRON LASER
Source detailsSACLA BEAMLINE BL3
Synchrotron siteSACLA
BeamlineBL3
Temperature [K]291
Detector technologyCCD
Collection date2018-07-24
DetectorMPCCD
Wavelength(s)1.2468
Spacegroup nameP 43 21 2
Unit cell lengths77.061, 77.061, 37.223
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution30.740 - 1.480
R-factor0.1338
Rwork0.132
R-free0.16870
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1iee
RMSD bond length0.016
RMSD bond angle1.215
Data reduction softwarecctbx.xfel
Data scaling softwarecxi.merge
Phasing softwarePHASER
Refinement softwarePHENIX (1.19.2_4158)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]30.7401.510
High resolution limit [Å]1.4801.480
Number of reflections381538330777
<I/σ(I)>12.251
Completeness [%]100.0
Redundancy198.25
CC(1/2)0.9960.787
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1BATCH MODE3291Lysozyme-inhibitor complex [20 mg/ml lysozyme plus 10 mg/ml N,N'-diacetylchitobiose dissolved in 0.1 M sodium acetate at pH 3.0] mixed with precipitant [28% (w/v) NaCl, 8% (w/v) PEG6000 and 0.1 M sodium acetate at pH 3.0] in a 1:1 ratio

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