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9N48

Crystal structure of PAK1 bound to compound C1

This is a non-PDB format compatible entry.
Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 21-ID-G
Synchrotron siteAPS
Beamline21-ID-G
Temperature [K]93
Detector technologyPIXEL
Collection date2013-11-20
DetectorDECTRIS PILATUS 6M
Wavelength(s)1
Spacegroup nameP 1 21 1
Unit cell lengths62.215, 80.961, 65.955
Unit cell angles90.00, 106.23, 90.00
Refinement procedure
Resolution34.110 - 1.850
R-factor0.1783
Rwork0.176
R-free0.21610
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.006
RMSD bond angle0.916
Data reduction softwareHKL-2000
Data scaling softwareHKL-2000
Phasing softwarePHASER
Refinement softwarePHENIX ((1.20.1_4487: ???))
Data quality characteristics
 OverallInner shellOuter shell
Low resolution limit [Å]50.00050.0001.920
High resolution limit [Å]1.8503.9901.850
Rmerge0.0570.0300.667
Total number of observations203038
Number of reflections5289554255219
<I/σ(I)>11.8
Completeness [%]98.398.897.5
Redundancy3.83.73.6
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP8.52910.2 M Lithium Sulfate, 0.1 M Tris pH8.5, 30% PEG4000

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