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3NE7

Crystal structure of paia n-acetyltransferase from thermoplasma acidophilum in complex with coenzyme a

Experimental procedure
Experimental methodMOLECULAR REPLACEMENT
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 21-ID-G
Synchrotron siteAPS
Beamline21-ID-G
Temperature [K]100
Detector technologyCCD
Collection date2009-11-25
Wavelength(s)0.97872
Spacegroup nameP 43 21 2
Unit cell lengths69.224, 69.224, 90.628
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution55.010 - 2.300
R-factor0.187
Rwork0.184
R-free0.23800
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)3f0a
RMSD bond length0.017
RMSD bond angle1.601
Data reduction softwareHKL-2000
Data scaling softwareHKL-2000
Phasing softwareMOLREP
Refinement softwareREFMAC (5.5.0051)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]55.0102.340
High resolution limit [Å]2.3002.300
Rmerge0.1510.832
Number of reflections10296
<I/σ(I)>33.474
Completeness [%]100.098.4
Redundancy13.912.7
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP8.529412% GLYCEROL, 1.5 M AMMONIUM SULFATE, 0.1 M TRIS, pH 8.5, VAPOR DIFFUSION, SITTING DROP, temperature 294K

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