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3CGE

Pyridine Nucleotide Complexes with Bacillus anthracis Coenzyme A-Disulfide Reductase: A Structural Analysis of Dual NAD(P)H Specificity

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsNSLS BEAMLINE X26C
Synchrotron siteNSLS
BeamlineX26C
Temperature [K]100
Detector technologyCCD
Collection date2006-04-27
DetectorADSC QUANTUM 4
Wavelength(s)1.10
Spacegroup nameC 1 2 1
Unit cell lengths169.332, 81.601, 98.384
Unit cell angles90.00, 104.11, 90.00
Refinement procedure
Resolution42.110 - 2.262
R-factor0.17884
Rwork0.177
R-free0.21371
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)3cgc
RMSD bond length0.007
RMSD bond angle1.155
Data reduction softwareHKL-2000
Data scaling softwareHKL-2000
Phasing softwareREFMAC (5.2.0019)
Refinement softwareREFMAC (5.2.0019)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0002.340
High resolution limit [Å]2.2602.260
Rmerge0.0580.240
Number of reflections60599
<I/σ(I)>23.15.5
Completeness [%]99.293.2
Redundancy43.6
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP6.528816-26% 2-methyl-2,4-pentanediol, 0.2 M magnesium acetate, 0.1 M sodium cacodylate, pH 6.5, and 2 mM NAD(P)+. Crystal soaked in NADPH prior to data collection., VAPOR DIFFUSION, SITTING DROP, temperature 288K

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