5T39
Crystal Structure of the N-terminal domain of EvdMO1 in the presence of SAH and D-fucose
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 21-ID-F |
Synchrotron site | APS |
Beamline | 21-ID-F |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2016-06-03 |
Detector | MARMOSAIC 225 mm CCD |
Wavelength(s) | 0.97872 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 50.222, 41.270, 58.504 |
Unit cell angles | 90.00, 98.58, 90.00 |
Refinement procedure
Resolution | 22.472 - 1.100 |
R-factor | 0.1378 |
Rwork | 0.137 |
R-free | 0.15390 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3mgg |
RMSD bond length | 0.006 |
RMSD bond angle | 1.009 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | PHENIX |
Data quality characteristics
Overall | Inner shell | Outer shell | |
Low resolution limit [Å] | 50.000 | 50.000 | 1.120 |
High resolution limit [Å] | 1.100 | 2.990 | 1.100 |
Rmerge | 0.060 | 0.042 | 0.434 |
Rmeas | 0.068 | ||
Rpim | 0.031 | ||
Total number of observations | 421834 | ||
Number of reflections | 94601 | ||
<I/σ(I)> | 9.2 | ||
Completeness [%] | 98.5 | 96.4 | 95.3 |
Redundancy | 4.5 | 4.3 | 3.7 |
CC(1/2) | 0.996 | 0.868 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7.4 | 293 | 40% Tacsimate, pH 7.4 |