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5O2E

Crystal structure of NDM-1 in complex with hydrolyzed cefuroxime - new refinement

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSSRF BEAMLINE BL17B1
Synchrotron siteSSRF
BeamlineBL17B1
Temperature [K]100
Detector technologyCCD
Collection date2012-04-12
DetectorADSC QUANTUM 315r
Wavelength(s)0.9791
Spacegroup nameP 21 21 21
Unit cell lengths39.180, 78.890, 133.060
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution29.360 - 1.300
R-factor0.10251
Rwork0.101
R-free0.13265
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.013
RMSD bond angle1.625
Data reduction softwareMOSFLM
Data scaling softwareSCALA
Phasing softwarePHASER
Refinement softwareREFMAC (5.8.0135)
Data quality characteristics
 Overall
Low resolution limit [Å]29.360
High resolution limit [Å]1.300
Number of reflections93575
Completeness [%]98.8
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP629530% (w/v) PEG3350, 0.1M Bis-Tris pH 6.0 and 0.2 M lithium sulfate, VAPOR DIFFUSION, HANGING DROP, temperature 295K

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