3Q93
Crystal Structure of Human 8-oxo-dGTPase (MTH1)
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | BESSY BEAMLINE 14.1 |
Synchrotron site | BESSY |
Beamline | 14.1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2010-12-16 |
Detector | RAYONIX MX-225 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 59.544, 67.681, 82.678 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 33.960 - 1.800 |
R-factor | 0.203 |
Rwork | 0.201 |
R-free | 0.23300 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1iry |
RMSD bond length | 0.007 |
RMSD bond angle | 1.066 |
Data reduction software | XDS |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | PHENIX ((phenix.refine: 1.6.4_486)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 33.960 | 1.900 |
High resolution limit [Å] | 1.800 | 1.800 |
Rmerge | 0.108 | 0.701 |
Number of reflections | 31366 | |
<I/σ(I)> | 4.4 | 2.3 |
Completeness [%] | 99.2 | 99.2 |
Redundancy | 7.7 | 7.3 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 7.4 | 277 | 0.26 M AMMONIUM SULFATE, 22 % w/v PEG4000, 13 % GLYCEROL, pH 7.4, VAPOR DIFFUSION, SITTING DROP, temperature 277K |