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29AJ

Crystal Structure of the human mARC1 M187K variant

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsPETRA III, EMBL c/o DESY BEAMLINE P13 (MX1)
Synchrotron sitePETRA III, EMBL c/o DESY
BeamlineP13 (MX1)
Temperature [K]100
Detector technologyPIXEL
Collection date2025-11-24
DetectorDECTRIS EIGER X 16M
Wavelength(s)0.9762
Spacegroup nameP 21 21 21
Unit cell lengths60.986, 75.072, 110.659
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution62.120 - 1.630
R-factor0.1889
Rwork0.188
R-free0.21530
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.010
RMSD bond angle1.054
Data reduction softwareXDS
Data scaling softwareXDS
Phasing softwarePHENIX
Refinement softwarePHENIX (2.0_5936)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]62.1201.660
High resolution limit [Å]1.6301.630
Rmerge0.1901.148
Rmeas0.1981.185
Rpim0.0540.313
Number of reflections640432850
<I/σ(I)>8.52.2
Completeness [%]99.999.8
Redundancy13.6
CC(1/2)0.9890.790
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP8291100 mM Bis-TRIS propane, 20 mM Na2MoO4, 10 mM TCEP, 27.5 % PEG3350

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