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3HP1

Crystal structure of human dCK R104M/D133A in complex with L-dT and ADP

Replaces:  3EXK
Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 22-BM
Synchrotron siteAPS
Beamline22-BM
Temperature [K]100
Detector technologyCCD
Collection date2008-08-28
DetectorMARMOSAIC 225 mm CCD
Wavelength(s)1.0000
Spacegroup nameP 43 21 2
Unit cell lengths79.780, 79.780, 93.700
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution30.000 - 2.310
R-factor0.21041
Rwork0.205
R-free0.26108
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1p5z
RMSD bond length0.012
RMSD bond angle1.402
Data reduction softwareXDS
Data scaling softwareXDS
Phasing softwareMOLREP
Refinement softwareREFMAC (5.2.0019)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]30.0002.450
High resolution limit [Å]2.3002.300
Rmerge0.0890.298
Number of reflections13710
<I/σ(I)>14.426.93
Completeness [%]99.398.2
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP7.52951 microliter of protein-nucleoside-nucleotide mix and 1 microliter reservoir solution containing 0.9-1.5 M Trisodium citrate dihydrate and 100 mM HEPES pH 7.5, VAPOR DIFFUSION, HANGING DROP, temperature 295K

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