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5T39

Crystal Structure of the N-terminal domain of EvdMO1 in the presence of SAH and D-fucose

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 21-ID-F
Synchrotron siteAPS
Beamline21-ID-F
Temperature [K]100
Detector technologyCCD
Collection date2016-06-03
DetectorMARMOSAIC 225 mm CCD
Wavelength(s)0.97872
Spacegroup nameP 1 21 1
Unit cell lengths50.222, 41.270, 58.504
Unit cell angles90.00, 98.58, 90.00
Refinement procedure
Resolution22.472 - 1.100
R-factor0.1378
Rwork0.137
R-free0.15390
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)3mgg
RMSD bond length0.006
RMSD bond angle1.009
Data reduction softwareHKL-2000
Data scaling softwareHKL-2000
Phasing softwarePHASER
Refinement softwarePHENIX
Data quality characteristics
 OverallInner shellOuter shell
Low resolution limit [Å]50.00050.0001.120
High resolution limit [Å]1.1002.9901.100
Rmerge0.0600.0420.434
Rmeas0.068
Rpim0.031
Total number of observations421834
Number of reflections94601
<I/σ(I)>9.2
Completeness [%]98.596.495.3
Redundancy4.54.33.7
CC(1/2)0.9960.868
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP7.429340% Tacsimate, pH 7.4

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