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7P41

Crystal Structure of human mARC1 A165T Variant

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsPETRA III, EMBL c/o DESY BEAMLINE P14 (MX2)
Synchrotron sitePETRA III, EMBL c/o DESY
BeamlineP14 (MX2)
Temperature [K]100
Detector technologyPIXEL
Collection date2021-05-15
DetectorDECTRIS PILATUS 6M
Wavelength(s)0.976200
Spacegroup nameP 21 21 21
Unit cell lengths61.063, 74.887, 111.164
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution31.920 - 1.600
R-factor0.1613
Rwork0.160
R-free0.18630
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)6fw2
Data reduction softwareXDS
Data scaling softwareAimless (0.7.4)
Phasing softwarePHASER (2.8.3)
Refinement softwarePHENIX (1.19.2_4158)
Data quality characteristics
 OverallInner shellOuter shell
Low resolution limit [Å]53.52053.5201.630
High resolution limit [Å]1.6008.7601.600
Rmerge0.0920.0890.239
Rmeas0.0960.0940.248
Rpim0.0260.0270.067
Total number of observations910173526944210
Number of reflections669114383234
<I/σ(I)>21289.1
Completeness [%]98.693.597.3
Redundancy13.61213.7
CC(1/2)0.9970.9930.986
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION6.5291100 mM bis-tris-propane, 5 mM sodium molybdate, 27.5 % PEG3350

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PDB entries from 2024-05-15

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