8DOM
Structure of the N358Y single variant ofserine hydroxymethyltransferase 8 from Glycine max cultivar Essex complexed with PLP
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | APS BEAMLINE 24-ID-E |
| Synchrotron site | APS |
| Beamline | 24-ID-E |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2019-07-12 |
| Detector | DECTRIS EIGER X 16M |
| Wavelength(s) | 0.979180 |
| Spacegroup name | P 2 21 21 |
| Unit cell lengths | 55.967, 128.599, 128.629 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 64.310 - 1.890 |
| R-factor | 0.1822 |
| Rwork | 0.180 |
| R-free | 0.21770 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 6uxh |
| RMSD bond length | 0.008 |
| RMSD bond angle | 1.040 |
| Data reduction software | XDS |
| Data scaling software | Aimless |
| Phasing software | PHASER |
| Refinement software | PHENIX (1.19.1_4122) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 128.630 | 1.930 |
| High resolution limit [Å] | 1.890 | 1.890 |
| Rmerge | 0.069 | 4.323 |
| Rmeas | 0.075 | |
| Rpim | 0.027 | 1.678 |
| Number of reflections | 75185 | 33413 |
| <I/σ(I)> | 17 | 0.5 |
| Completeness [%] | 99.9 | 99.9 |
| Redundancy | 7.4 | 7.6 |
| CC(1/2) | 0.999 | 0.339 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 293 | 0.18 - 0.25 TMAO 0.1 M Tris (ph 8.5) 21-23 (w/v) % PEG MME 2000 |






