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2OO6

Crystal structure of putative L-alanine-DL-glutamate epimerase from Burkholderia xenovorans strain LB400

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsNSLS BEAMLINE X29A
Synchrotron siteNSLS
BeamlineX29A
Temperature [K]100
Detector technologyCCD
Collection date2007-01-20
DetectorADSC QUANTUM 315
Wavelength(s)0.97958
Spacegroup nameI 4 2 2
Unit cell lengths104.906, 104.906, 145.658
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution20.000 - 1.800
R-factor0.157
Rwork0.156
R-free0.19200
Structure solution methodSAD
RMSD bond length0.015
RMSD bond angle1.331
Data reduction softwareHKL-2000
Data scaling softwareSCALA
Phasing softwareSHELXD
Refinement softwareREFMAC
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]85.1301.900
High resolution limit [Å]1.8001.800
Rmerge0.1090.825
Total number of observations7055
Number of reflections35232
<I/σ(I)>16.80.9
Completeness [%]93.256.8
Redundancy8.82.3
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION8.5294100mM Tris-HCl pH 8.5, 12% Glycerol, 1.5M Ammonium sulfate, VAPOR DIFFUSION, temperature 294K

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