6KY8
Crystal structure of ASFV dUTPase
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL19U1 |
Synchrotron site | SSRF |
Beamline | BL19U1 |
Temperature [K] | 100 |
Detector technology | CMOS |
Collection date | 2019-04-07 |
Detector | RDI CMOS_8M |
Wavelength(s) | 1.03923 |
Spacegroup name | I 21 3 |
Unit cell lengths | 97.855, 97.855, 97.855 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 39.949 - 2.301 |
R-factor | 0.2236 |
Rwork | 0.222 |
R-free | 0.25470 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1vyq |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | PHENIX (1.14_3260) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.380 |
High resolution limit [Å] | 2.300 | 2.300 |
Number of reflections | 7082 | 690 |
<I/σ(I)> | 53.9 | |
Completeness [%] | 100.0 | |
Redundancy | 38.6 | |
CC(1/2) | 1.000 | 0.999 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 291 | 0.1 M ammonium citrate tribasic pH 7.0, 12% w/v Polyethylene glycol 3,350 |