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3LY1

Crystal structure of Putative histidinol-phosphate aminotransferase (YP_050345.1) from Erwinia carotovora atroseptica SCRI1043 at 1.80 A resolution

Experimental procedure
Experimental methodMAD
Source typeSYNCHROTRON
Source detailsSSRL BEAMLINE BL9-2
Synchrotron siteSSRL
BeamlineBL9-2
Temperature [K]100
Detector technologyCCD
Collection date2009-11-07
DetectorMARMOSAIC 325 mm CCD
Wavelength(s)0.96109,0.97946,0.97936
Spacegroup nameP 1 21 1
Unit cell lengths58.625, 150.477, 100.092
Unit cell angles90.00, 94.38, 90.00
Refinement procedure
Resolution29.564 - 1.800
R-factor0.178
Rwork0.176
R-free0.20600
Structure solution methodMAD
RMSD bond length0.017
RMSD bond angle1.533
Data reduction softwareXDS
Data scaling softwareXSCALE
Phasing softwareSHELX
Refinement softwareREFMAC (5.5.0102)
Data quality characteristics
 OverallInner shellOuter shell
Low resolution limit [Å]29.56429.5641.850
High resolution limit [Å]1.8003.8501.790
Rmerge0.0590.0220.675
Number of reflections1585473134824110
<I/σ(I)>8.3624.71.4
Completeness [%]96.59779.8
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP5.627720.0000% iso-Propanol, 20.0000% PEG-4000, 0.1M Citrate pH 5.6, NANODROP, VAPOR DIFFUSION, SITTING DROP, temperature 277K

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