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1XJK

Structural mechanism of allosteric substrate specificity in a ribonucleotide reductase: dGTP-ADP complex

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsMAX II BEAMLINE I711
Synchrotron siteMAX II
BeamlineI711
Temperature [K]100
Detector technologyCCD
Collection date2003-02-27
DetectorMARRESEARCH
Wavelength(s)1.035
Spacegroup nameC 1 2 1
Unit cell lengths118.120, 122.860, 106.060
Unit cell angles90.00, 103.46, 90.00
Refinement procedure
Resolution22.700 - 2.120
R-factor0.20763
Rwork0.205
R-free0.25572
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1xje
RMSD bond length0.018
RMSD bond angle1.882
Data scaling softwareXDS
Refinement softwareREFMAC (5.1.24)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]25.0002.300
High resolution limit [Å]2.1502.150
Number of reflections77677
<I/σ(I)>8.92.48
Completeness [%]97.296.9
Redundancy2.152.15
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP4.5293PEG8000, sodium acetate, sodium chloride, dithiotreithol, pH 4.5, VAPOR DIFFUSION, HANGING DROP, temperature 293K

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