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9CDY

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 5.0.3
Synchrotron siteALS
Beamline5.0.3
Temperature [K]100
Detector technologyCCD
Collection date2021-06-10
DetectorADSC QUANTUM 315r
Wavelength(s)0.98
Spacegroup nameP 1 21 1
Unit cell lengths57.429, 39.775, 62.471
Unit cell angles90.00, 106.05, 90.00
Refinement procedure
Resolution47.730 - 1.500
Rwork0.206
R-free0.24000
Structure solution methodMOLECULAR REPLACEMENT
Data reduction softwareXDS
Data scaling softwareAimless (0.7.4)
Phasing softwarePHASER
Refinement softwarePRIME-X
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]47.7301.530
High resolution limit [Å]1.5001.500
Rmerge0.0561.336
Rmeas0.075
Rpim0.049
Number of reflections437362168
<I/σ(I)>12.20.9
Completeness [%]99.999.9
Redundancy4.13.8
CC(1/2)0.9990.326
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP7.529315.9% PEG 3350, 0.1M Magnesium Acetate, 0.1M HEPES

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