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4MNR

Crystal Structure of D,D-Transpeptidase Domain of Peptidoglycan Glycosyltransferase from Eggerthella lenta

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 19-ID
Synchrotron siteAPS
Beamline19-ID
Temperature [K]100
Detector technologyCCD
Collection date2012-12-18
DetectorADSC QUANTUM 315r
Wavelength(s)0.97895
Spacegroup nameP 21 21 21
Unit cell lengths48.060, 69.159, 119.975
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution28.091 - 1.653
R-factor0.165
Rwork0.164
R-free0.18400
Structure solution methodSAD
RMSD bond length0.007
RMSD bond angle1.079
Data reduction softwareHKL-3000
Data scaling softwareHKL-3000
Phasing softwareHKL-3000
Refinement softwarePHENIX ((phenix.refine: dev_1367))
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0001.680
High resolution limit [Å]1.6301.630
Number of reflections48312
<I/σ(I)>10.11.9
Completeness [%]99.596.2
Redundancy3.93
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP82890.2 M calcium acetate, 0.1 M imidazole pH 8.0, 20 %(w/v) PEG1000, VAPOR DIFFUSION, SITTING DROP, temperature 289K

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