9N3R
Crystal structure of PRMT5:MEP50 in complex with MTA and TNG462
This is a non-PDB format compatible entry.
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | APS BEAMLINE 23-ID-B |
| Synchrotron site | APS |
| Beamline | 23-ID-B |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2022-02-16 |
| Detector | DECTRIS EIGER X 16M |
| Wavelength(s) | 1.03317 |
| Spacegroup name | P 21 21 2 |
| Unit cell lengths | 98.210, 136.600, 178.010 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 29.700 - 2.470 |
| R-factor | 0.2116 |
| Rwork | 0.210 |
| R-free | 0.24290 |
| Structure solution method | FOURIER SYNTHESIS |
| RMSD bond length | 0.002 |
| RMSD bond angle | 0.512 |
| Data reduction software | XDS |
| Data scaling software | STARANISO |
| Phasing software | REFMAC |
| Refinement software | PHENIX (1.20.1_4487) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 29.700 | 2.540 |
| High resolution limit [Å] | 2.470 | 2.470 |
| Rmerge | 0.156 | 0.778 |
| Number of reflections | 52173 | 219 |
| <I/σ(I)> | 13.3 | 3.5 |
| Completeness [%] | 59.4 | 2.7 |
| Redundancy | 13.7 | 13.9 |
| CC(1/2) | 0.998 | 0.931 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION | 6 | 291 | 10% PEG 4000, 0.1 M sodium citrate (pH 6.0), 0.2 M magnesium chloride, 1 mM methylthioadenosine |






