7F2W
TbUox in complex with uric acid
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | NSRRC BEAMLINE BL13B1 |
Synchrotron site | NSRRC |
Beamline | BL13B1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2019-03-19 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 1.00000 |
Spacegroup name | I 4 2 2 |
Unit cell lengths | 146.362, 146.362, 132.407 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 28.580 - 2.160 |
R-factor | 0.1598 |
Rwork | 0.158 |
R-free | 0.19890 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 6oe8 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | PHENIX (1.17.1_3660) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 28.580 | 2.230 |
High resolution limit [Å] | 2.160 | 2.160 |
Number of reflections | 38278 | 3502 |
<I/σ(I)> | 92.3 | |
Completeness [%] | 99.8 | |
Redundancy | 6.7 | |
CC(1/2) | 0.970 | 0.907 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 283 | sodium cacodylate trihydrate, magnesium acetate tetrahydrate, PEG8000 |