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6SYE

Crystal structure of orthorhombic lysozyme in presence of the dye bromophenol blue at pH 7.0

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsALBA BEAMLINE XALOC
Synchrotron siteALBA
BeamlineXALOC
Temperature [K]100
Detector technologyPIXEL
Collection date2018-03-16
DetectorDECTRIS PILATUS 6M
Wavelength(s)0.979
Spacegroup nameP 21 21 21
Unit cell lengths30.206, 55.235, 71.576
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution19.600 - 0.970
R-factor0.1744
Rwork0.173
R-free0.19830
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)6f1m
RMSD bond length0.009
RMSD bond angle1.056
Data reduction softwareXDS
Data scaling softwareAimless (0.6.3)
Phasing softwarePHASER
Refinement softwarePHENIX (1.18.2_3874)
Data quality characteristics
 OverallInner shellOuter shell
Low resolution limit [Å]19.60019.6000.980
High resolution limit [Å]0.9705.2900.970
Rmerge0.0300.0220.916
Rmeas0.0330.0241.039
Rpim0.0130.0100.484
Total number of observations286815591
Number of reflections1370045123500
<I/σ(I)>23.772.21.6
Completeness [%]99.897.498.3
Redundancy65.64.5
CC(1/2)1.0000.9990.618
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP7298Crystals grew in 0.1 M sodium acetate, 0.3 M sodium chloride at pH 4.6 in the presence of 0.1 M Lithium sulfate. After growth, and before measurement, these crystals were soaked in the dye solution: saturated bromophenol blue, 0.3 M sodium chloride, 100 mM Lithium sulfate, 100 mM phosphate buffer at pH 7.0

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PDB entries from 2024-05-15

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