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2RL3

Crystal structure of the OXA-10 W154H mutant at pH 7

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsESRF BEAMLINE BM30A
Synchrotron siteESRF
BeamlineBM30A
Temperature [K]100
Detector technologyCCD
Collection date2007-09-02
DetectorADSC QUANTUM 315
Wavelength(s)0.978872
Spacegroup nameP 21 21 21
Unit cell lengths48.680, 97.060, 125.680
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution48.680 - 1.900
R-factor0.17109
Rwork0.169
R-free0.21815
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1k4f
RMSD bond length0.015
RMSD bond angle1.497
Data reduction softwareXDS
Data scaling softwareSCALA
Phasing softwareAMoRE
Refinement softwareREFMAC (5.2.0019)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]48.6802.000
High resolution limit [Å]1.9001.900
Rmerge0.1230.762
Number of reflections47547
<I/σ(I)>10.91.7
Completeness [%]99.496.2
Redundancy5.33.5
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP72931.6M AS, 0.1M HEPES, PEG 30%, pH 7, VAPOR DIFFUSION, HANGING DROP, temperature 293K

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