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2O53

Crystal structure of apo-Aspartoacylase from human brain

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 23-ID-B
Synchrotron siteAPS
Beamline23-ID-B
Temperature [K]100
Detector technologyCCD
Collection date2006-10-13
DetectorMARMOSAIC 300 mm CCD
Wavelength(s)1.033
Spacegroup nameP 42 21 2
Unit cell lengths143.794, 143.794, 104.076
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution50.000 - 2.700
R-factor0.21891
Rwork0.216
R-free0.26867
Structure solution methodFOURIER SYNTHESIS
Starting model (for MR)2o4h
RMSD bond length0.013
RMSD bond angle1.469
Data reduction softwareHKL-2000
Data scaling softwareSCALEPACK
Phasing softwareCCP4
Refinement softwareREFMAC (5.2.0019)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0002.800
High resolution limit [Å]2.7002.700
Number of reflections26648
<I/σ(I)>17.82.8
Completeness [%]87.347.2
Redundancy3.92.5
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP6293Protein concentration 8-10 mg/ml, 0.05 M Sodium citrate pH 6.0, 0.3 M K2HPO4, 19% PEG 3350, VAPOR DIFFUSION, HANGING DROP, temperature 293K

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