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9H24

Crystal structure of MtCERK1 extracellular domain

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsMAX IV BEAMLINE BioMAX
Synchrotron siteMAX IV
BeamlineBioMAX
Temperature [K]100
Detector technologyPIXEL
Collection date2024-10-09
DetectorDECTRIS EIGER2 XE CdTe 16M
Wavelength(s)0.97
Spacegroup nameP 43 21 2
Unit cell lengths70.669, 70.669, 95.205
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution44.250 - 2.980
R-factor0.2333
Rwork0.231
R-free0.28420
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.003
RMSD bond angle0.596
Data reduction softwareXDS
Data scaling softwarepointless
Phasing softwarePHASER
Refinement softwarePHENIX (1.21.2_5419)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]44.2503.760
High resolution limit [Å]2.9802.984
Rpim0.1820.697
Number of reflections52822560
<I/σ(I)>4.97
Completeness [%]99.9
Redundancy14.2
CC(1/2)0.9790.470
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP8.5292.150.2 M Lithium sulfate, 0.1 M Tris 8.5, 40 % v/v PEG 400

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