5T38
Crystal Structure of the N-terminal domain of EvdMO1 with SAH bound
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 | 2016-04-09 |
| Detector | MARMOSAIC 225 mm CCD |
| Wavelength(s) | 0.97872 |
| Spacegroup name | P 1 21 1 |
| Unit cell lengths | 51.427, 41.272, 56.465 |
| Unit cell angles | 90.00, 99.80, 90.00 |
Refinement procedure
| Resolution | 32.002 - 1.150 |
| R-factor | 0.1536 |
| Rwork | 0.153 |
| R-free | 0.16820 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 3mgg |
| RMSD bond length | 0.006 |
| RMSD bond angle | 0.984 |
| Data reduction software | HKL-2000 |
| Data scaling software | HKL-2000 |
| Phasing software | PHASER |
| Refinement software | PHENIX (1.10_2155) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 50.000 | 50.000 | 1.170 |
| High resolution limit [Å] | 1.150 | 3.120 | 1.150 |
| Rmerge | 0.052 | 0.029 | 0.347 |
| Number of reflections | 79855 | ||
| <I/σ(I)> | 9.5 | ||
| Completeness [%] | 96.3 | 95.7 | 70 |
| Redundancy | 3.5 | 3.5 | 2.3 |
| CC(1/2) | 0.998 | 0.836 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 7.4 | 293 | 40% Tacsimate, pH 7.4 |






