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4Q18

Human dCK C4S-S74E mutant in complex with UDP and the inhibitor 4 [1-[5-(4-{[(2,6-diaminopyrimidin-4-yl)sulfanyl]methyl}-5-propyl-1,3-thiazol-2-yl)-2-methoxyphenoxy]-2-methylpropan-2-ol]

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 21-ID-G
Synchrotron siteAPS
Beamline21-ID-G
Temperature [K]100
Detector technologyCCD
Collection date2012-11-20
DetectorMARMOSAIC 300 mm CCD
Wavelength(s)0.9785
Spacegroup nameP 41
Unit cell lengths68.750, 68.750, 122.450
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution27.970 - 2.000
R-factor0.18485
Rwork0.183
R-free0.21613
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)4jln
RMSD bond length0.012
RMSD bond angle1.656
Data reduction softwareXDS
Data scaling softwareXDS
Phasing softwareMOLREP
Refinement softwareREFMAC (5.8.0049)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]30.0002.100
High resolution limit [Å]2.0002.000
Number of reflections38119
<I/σ(I)>13.62.75
Completeness [%]99.499.9
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP7.52851.5 M trisodium citrate dehydrate and 25 mM HEPES pH 7.5, VAPOR DIFFUSION, HANGING DROP, temperature 285K

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