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2HW6

Crystal structure of Mnk1 catalytic domain

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSLS BEAMLINE X10SA
Synchrotron siteSLS
BeamlineX10SA
Temperature [K]100
Detector technologyCCD
Collection date2005-04-04
DetectorMAR CCD 165 mm
Wavelength(s)0.98008
Spacegroup nameP 43 21 2
Unit cell lengths93.468, 93.468, 175.181
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution30.000 - 2.500
R-factor0.20911
Rwork0.207
R-free0.25701
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)2ac3
RMSD bond length0.010
RMSD bond angle1.174
Data reduction softwareHKL-2000
Data scaling softwareHKL-2000
Phasing softwareMOLREP
Refinement softwareREFMAC (5.2.0005)
Data quality characteristics
 Overall
Low resolution limit [Å]30.000
High resolution limit [Å]2.500
Number of reflections18256
Completeness [%]92.1
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION5.629320% PEG3350, 0.2M Ammonium sulfate, pH 5.6, VAPOR DIFFUSION, temperature 293K

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