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6MIA

Crystal structure of CTX-M-14 with compound 6

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 19-BM
Synchrotron siteAPS
Beamline19-BM
Temperature [K]100
Detector technologyCCD
Collection date2018-04-18
DetectorADSC QUANTUM 210r
Wavelength(s)1
Spacegroup nameP 1 21 1
Unit cell lengths45.340, 107.185, 47.881
Unit cell angles90.00, 101.33, 90.00
Refinement procedure
Resolution22.754 - 1.399
R-factor0.1258
Rwork0.125
R-free0.16330
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1ylt
Data reduction softwareHKL-2000
Data scaling softwareHKL-2000
Phasing softwarePHASER (2.6.0)
Refinement softwarePHENIX (1.14_3228)
Data quality characteristics
 OverallInner shellOuter shell
Low resolution limit [Å]50.00050.0001.420
High resolution limit [Å]1.4003.8001.400
Rmerge0.0250.0270.047
Rmeas0.0290.0330.058
Rpim0.0150.0190.033
Total number of observations315169
Number of reflections8699737254374
<I/σ(I)>37.1
Completeness [%]98.883.299.8
Redundancy3.63.22.9
CC(1/2)0.9960.995
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP8.32931.0 M potassium phosphate

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