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2QEC

Crystal structure of histone acetyltransferase HPA2 and related acetyltransferase (NP_600742.1) from Corynebacterium glutamicum ATCC 13032 at 1.90 A resolution

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSSRL BEAMLINE BL11-1
Synchrotron siteSSRL
BeamlineBL11-1
Temperature [K]100
Detector technologyCCD
Collection date2007-01-18
DetectorMARMOSAIC 325 mm CCD
Wavelength(s)0.91162
Spacegroup nameP 65 2 2
Unit cell lengths79.070, 79.070, 181.260
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution27.640 - 1.900
R-factor0.195
Rwork0.193
R-free0.24200
Structure solution methodMAD, MOLECULAR REPLACEMENT
RMSD bond length0.016
RMSD bond angle1.609
Data reduction softwareXDS
Data scaling softwareXSCALE
Phasing softwareSHELXD
Refinement softwareREFMAC (5.2.0005)
Data quality characteristics
 OverallInner shellOuter shell
Low resolution limit [Å]27.64027.6401.970
High resolution limit [Å]1.9004.0801.900
Rmerge0.0710.0360.905
Number of reflections27197
<I/σ(I)>17.3651.72
Completeness [%]99.599.599.3
Redundancy17.62
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP4.6277NANODROP, 8.0% PEG 4000, 0.1M Acetate pH 4.6, VAPOR DIFFUSION, SITTING DROP, temperature 277K
2VAPOR DIFFUSION, SITTING DROP8.5277NANODROP, 0.2M Li2SO4, 40.0% PEG 400, 0.1M Tris-HCl pH 8.5, VAPOR DIFFUSION, SITTING DROP, temperature 277K

220113

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