7MYS
Crystal structure of a tRNA (guanine-N1)-methyltransferase from Acinetobacter baumannii AB5075-UW bound to S-adenosyl homocysteine
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 | 2021-02-25 |
| Detector | RAYONIX MX-300 |
| Wavelength(s) | 0.9787 |
| Spacegroup name | P 41 |
| Unit cell lengths | 65.960, 65.960, 132.590 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 46.640 - 2.400 |
| R-factor | 0.185 |
| Rwork | 0.181 |
| R-free | 0.22520 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 1ual |
| Data reduction software | XDS |
| Data scaling software | XSCALE |
| Phasing software | MOLREP |
| Refinement software | PHENIX (dev-4224-000) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 46.640 | 46.640 | 2.460 |
| High resolution limit [Å] | 2.400 | 10.730 | 2.400 |
| Rmerge | 0.040 | 0.023 | 0.524 |
| Rmeas | 0.043 | 0.026 | 0.571 |
| Total number of observations | 140392 | ||
| Number of reflections | 22187 | 259 | 1654 |
| <I/σ(I)> | 25.84 | 57.93 | 3.69 |
| Completeness [%] | 100.0 | 97 | 100 |
| Redundancy | 6.328 | 5.521 | 6.387 |
| CC(1/2) | 1.000 | 0.999 | 0.910 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 6.5 | 287 | AcbaC.00054.a.B1.PW38905 at 26 mg/mL with 6 mM GMP and 6 mM SAH against Morpheus condition F2 with 10% PEG 8000, 20% ethylene glycol, 0.1 M MES/imidazole pH 6.5, 0.02 M each glucose, mannose, galactose, fucose, xylose, acetyl-glucosamine, direct cryo, unique puck ID okj1-10, crystal tracking ID 319640f2 |






