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3G8D

Crystal structure of the biotin carboxylase subunit, E296A mutant, of acetyl-COA carboxylase from Escherichia coli

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsNSLS BEAMLINE X29A
Synchrotron siteNSLS
BeamlineX29A
Temperature [K]100
Detector technologyCCD
Collection date2008-12-07
DetectorADSC QUANTUM 315
Wavelength(s)1.0809
Spacegroup nameP 21 21 21
Unit cell lengths81.331, 114.738, 122.148
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution30.000 - 1.900
R-factor0.2
Rwork0.198
R-free0.22600
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.009
RMSD bond angle1.121
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareCOMO
Refinement softwareREFMAC
Data quality characteristics
 OverallInner shellOuter shell
Low resolution limit [Å]83.62030.0001.970
High resolution limit [Å]1.9004.0901.900
Rmerge0.0690.0400.373
Number of reflections90912
<I/σ(I)>28.075
Completeness [%]99.999.999.8
Redundancy8.58.78.2
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP829823% PEG3350, 0.12M Li2SO4, 3.9% SORBITOL, pH 8.0, VAPOR DIFFUSION, SITTING DROP, temperature 298K

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