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8F0B

Lysozyme Anomalous Dataset at 240 K and 7.1 keV

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSSRL BEAMLINE BL14-1
Synchrotron siteSSRL
BeamlineBL14-1
Temperature [K]240
Detector technologyPIXEL
Collection date2020-01-19
DetectorDECTRIS EIGER X 16M
Wavelength(s)1.7462
Spacegroup nameP 43 21 2
Unit cell lengths77.106, 77.106, 37.042
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution34.507 - 1.900
Rwork0.137
R-free0.19810
Structure solution methodSAD
RMSD bond length0.007
RMSD bond angle1.475
Data reduction softwareXDS
Data scaling softwareAimless
Phasing softwareSHELXCD
Refinement softwareREFMAC (5.8.0352)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]37.0401.940
High resolution limit [Å]1.9001.900
Rmerge0.0530.169
Rpim0.0180.067
Number of reflections9246590
<I/σ(I)>35.412.6
Completeness [%]100.0100
Redundancy15.812.5
CC(1/2)0.9990.993
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP4.52935 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.

220113

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