8DSK
Structure of the N358Y variant of serine hydroxymethyltransferase 8 in complex with PLP, glycine, and formyl tetrahydrofolate
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 24-ID-C |
Synchrotron site | APS |
Beamline | 24-ID-C |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2019-07-06 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 0.979180 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 87.106, 90.798, 147.441 |
Unit cell angles | 90.00, 90.55, 90.00 |
Refinement procedure
Resolution | 74.680 - 1.630 |
R-factor | 0.186 |
Rwork | 0.184 |
R-free | 0.21380 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 6uxj |
RMSD bond length | 0.007 |
RMSD bond angle | 0.962 |
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] | 90.800 | 1.650 |
High resolution limit [Å] | 1.630 | 1.630 |
Rmerge | 0.088 | 1.336 |
Rmeas | 0.102 | 1.656 |
Rpim | 0.052 | 0.801 |
Number of reflections | 281201 | 12043 |
<I/σ(I)> | 8.1 | 0.8 |
Completeness [%] | 97.8 | 84.9 |
Redundancy | 3.8 | 3.6 |
CC(1/2) | 0.997 | 0.381 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 8.5 | 293 | 0.18-0.25 triethylamine oxide, 0.1 M Tris, pH 8.5, 21-23 % w/v PEG MME 2000 |