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4CP8

Structure of the amidase domain of allophanate hydrolase from Pseudomonas sp strain ADP

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAUSTRALIAN SYNCHROTRON BEAMLINE MX2
Synchrotron siteAustralian Synchrotron
BeamlineMX2
Temperature [K]100
Detector technologyCCD
Collection date2012-07-25
DetectorADSC QUANTUM 315
Spacegroup nameP 1 21 1
Unit cell lengths82.447, 179.232, 112.610
Unit cell angles90.00, 106.63, 90.00
Refinement procedure
Resolution40.000 - 2.500
R-factor0.22577
Rwork0.224
R-free0.25883
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)2dqn
RMSD bond length0.009
RMSD bond angle1.315
Data reduction softwareXDS
Data scaling softwareSCALA
Phasing softwarePHASER
Refinement softwareREFMAC (5.7.0032)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]179.2002.640
High resolution limit [Å]2.5002.500
Rmerge0.1500.810
Number of reflections107970
<I/σ(I)>12.62.8
Completeness [%]100.0100
Redundancy7.77.7
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
15PROTEIN AT 5.5 MG/ML WAS ADDED TO THE RESERVOIR CONDITION OF 11-14% (W/V) PEG 3350, 2% TACSIMATE PH 5. MICROSEEDS WERE ALSO ADDED TO THESE DROPS FOR REPRODUCIBLE CRYSTALS.

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