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2WE4

Carbamate kinase from Enterococcus faecalis bound to a sulfate ion and two water molecules, which mimic the substrate carbamyl phosphate

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsESRF BEAMLINE ID14-2
Synchrotron siteESRF
BeamlineID14-2
Temperature [K]100
Detector technologyCCD
Collection date1999-11-20
DetectorMARRESEARCH
Spacegroup nameP 21 21 21
Unit cell lengths80.888, 172.600, 98.627
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution20.000 - 2.020
R-factor0.195
Rwork0.195
R-free0.23400
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1b7b
RMSD bond length0.005
RMSD bond angle1.150
Data reduction softwareMOSFLM
Data scaling softwareSCALA
Refinement softwareCNS (1.0)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0002.120
High resolution limit [Å]2.0202.020
Rmerge0.0900.440
Number of reflections88372
<I/σ(I)>6.61.6
Completeness [%]93.082
Redundancy6.35.2
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP277CRYSTALS WERE OBTAINED AT 4 DEGREES USING THE HANGING DROP VAPOUR DIFFUSION METHOD BY MIXING 1.5 MICROLITERS OF A 10 MG/ML PROTEIN SOLUTION IN 5 MM SODIUM CACODYLATE PH 6.5 AND 1.5 MICROLITERS OF THE RESERVOIR BUFFER CONTAINING 16-20% PEG 8000, 25-100 MM AMMONIUM SULFATE AND 0.1 M SODIUM CACODYLATE PH 6.5

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