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8EZO

Lysozyme Anomalous Dataset at 220 K and 7.1 keV

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSSRL BEAMLINE BL14-1
Synchrotron siteSSRL
BeamlineBL14-1
Temperature [K]220
Detector technologyPIXEL
Collection date2020-01-19
DetectorDECTRIS EIGER X 16M
Wavelength(s)1.7462
Spacegroup nameP 43 21 2
Unit cell lengths76.909, 76.909, 36.961
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution38.484 - 1.900
Rwork0.156
R-free0.19130
Structure solution methodSAD
RMSD bond length0.009
RMSD bond angle1.633
Data reduction softwareXDS
Data scaling softwareAimless
Phasing softwareSHELXDE
Refinement softwareREFMAC (5.8.0352)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]38.4841.940
High resolution limit [Å]1.9001.900
Rmerge0.0460.251
Rpim0.0150.102
Number of reflections9211580
<I/σ(I)>37.28.5
Completeness [%]99.998.2
Redundancy15.611.6
CC(1/2)0.9990.992
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP4.52985 uL of 0.6 M Sodium Chloride in 100 mM Sodium Acetate buffer pH 4.5 and 25% ethylene glycol were mixed with 5 uL 100 mg/mL lysozyme in 100 mM Sodium Acetate.

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