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9CDX

Crystal structure of DLK with inhibitor bound

This is a non-PDB format compatible entry.
Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsALS BEAMLINE 5.0.2
Synchrotron siteALS
Beamline5.0.2
Temperature [K]100
Detector technologyPIXEL
Collection date2018-11-29
DetectorDECTRIS PILATUS3 S 6M
Wavelength(s)1.00
Spacegroup nameP 1 21 1
Unit cell lengths57.619, 39.960, 62.503
Unit cell angles90.00, 106.50, 90.00
Refinement procedure
Resolution47.970 - 2.380
Rwork0.234
R-free0.28400
Structure solution methodMOLECULAR REPLACEMENT
Data reduction softwareXDS
Data scaling softwareAimless (0.7.2)
Phasing softwarePHASER
Refinement softwarePRIME-X
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]47.9702.470
High resolution limit [Å]2.3802.380
Rmerge0.1871.249
Rmeas0.248
Rpim0.161
Number of reflections111621176
<I/σ(I)>4.2
Completeness [%]99.699.9
Redundancy3.94
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP7.529315.9% PEG 3350, 0.1M Magnesium Acetate, 0.1M HEPES

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