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9IXR

Crystal structure of OXA-10 variant A124T in the complex with ceftazidime

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsPAL/PLS BEAMLINE 11C
Synchrotron sitePAL/PLS
Beamline11C
Temperature [K]100
Detector technologyPIXEL
Collection date2023-02-18
DetectorDECTRIS PILATUS 6M
Wavelength(s)0.97942
Spacegroup nameP 21 21 21
Unit cell lengths48.510, 99.040, 127.100
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution29.300 - 2.190
R-factor0.16909
Rwork0.167
R-free0.20926
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1fof
RMSD bond length0.007
RMSD bond angle1.769
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareHKL-3000
Refinement softwareREFMAC (5.8.0415)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]29.3002.270
High resolution limit [Å]2.1902.190
Rmerge0.144
Rmeas0.151
Rpim0.0420.317
Number of reflections322113169
<I/σ(I)>15.63
Completeness [%]99.6
Redundancy12.6
CC(1/2)0.999
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP28820% PEG 3350, 0.2 M Sodium formate, 0.1 M Tris-HCl pH 7.0

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