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4K0W

X-ray crystal structure of OXA-23 A220 duplication clinical variant

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 21-ID-G
Synchrotron siteAPS
Beamline21-ID-G
Temperature [K]100
Detector technologyIMAGE PLATE
Collection date2012-07-28
DetectorMAR scanner 300 mm plate
Wavelength(s)1.1
Spacegroup nameP 21 2 21
Unit cell lengths44.116, 46.662, 137.018
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution137.000 - 1.200
R-factor0.18335
Rwork0.182
R-free0.20212
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.016
RMSD bond angle1.800
Data reduction softwareHKL-3000
Data scaling softwareHKL-3000
Phasing softwarePHASER
Refinement softwareREFMAC (5.6.0117)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]137.0001.140
High resolution limit [Å]1.1001.100
Number of reflections103356
Completeness [%]94.794
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP4.22960.2M sodium chloride, 0.1M phosphate, 0.1M citrate 20% w/v PEG 8000 , pH 4.2, VAPOR DIFFUSION, HANGING DROP, temperature 296K

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