7B66
Structure of NUDT15 R139H Mutant in complex with TH7755
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | MAX IV BEAMLINE BioMAX |
Synchrotron site | MAX IV |
Beamline | BioMAX |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2019-11-21 |
Detector | DECTRIS EIGER X 16M |
Wavelength(s) | 0.97622 |
Spacegroup name | P 1 |
Unit cell lengths | 41.276, 60.215, 69.303 |
Unit cell angles | 100.08, 104.10, 90.25 |
Refinement procedure
Resolution | 40.590 - 1.600 |
Rwork | 0.185 |
R-free | 0.22010 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 5lpg |
RMSD bond length | 0.013 |
RMSD bond angle | 1.703 |
Data reduction software | DIALS |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | REFMAC (5.8.0258) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 40.590 | 1.630 |
High resolution limit [Å] | 1.600 | 1.600 |
Number of reflections | 81339 | 3976 |
<I/σ(I)> | 11.5 | |
Completeness [%] | 96.8 | |
Redundancy | 3.6 | |
CC(1/2) | 0.998 | 0.976 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 294 | 0.1 M MMT pH 5.0, 25.4% PEG 1500 |