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6AO5

Crystal structure of human MST2 in complex with SAV1 SARAH domain

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 19-ID
Synchrotron siteAPS
Beamline19-ID
Temperature [K]100
Detector technologyCCD
Collection date2015-10-12
DetectorADSC QUANTUM 315r
Wavelength(s)0.97918
Spacegroup nameH 3 2
Unit cell lengths223.678, 223.678, 79.645
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution42.271 - 2.955
R-factor0.2357
Rwork0.235
R-free0.25640
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)4lgd
RMSD bond length0.009
RMSD bond angle0.600
Data reduction softwareHKL-3000
Data scaling softwareHKL-3000
Phasing softwarePHASER
Refinement softwarePHENIX (1.12_2829)
Data quality characteristics
 OverallInner shellOuter shell
Low resolution limit [Å]50.00050.0003.000
High resolution limit [Å]2.9508.0002.950
Rmerge0.1240.0511.715
Rmeas0.1280.0531.788
Rpim0.0290.0120.483
Total number of observations303392
Number of reflections15976839763
<I/σ(I)>7
Completeness [%]99.999.398.5
Redundancy1918.412
CC(1/2)0.9990.841
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP2930.05 M NaCl, 0.1 M Hepes, 0.19 mM CYMAL-7, 1 mM TCEP, 40% PEG 400

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