5YQO
Crystal structure of Sirt2 in complex with selective inhibitor L5C
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL19U1 |
Synchrotron site | SSRF |
Beamline | BL19U1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2017-06-29 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 0.979 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 35.938, 73.918, 55.635 |
Unit cell angles | 90.00, 95.24, 90.00 |
Refinement procedure
Resolution | 44.332 - 1.483 |
R-factor | 0.1703 |
Rwork | 0.169 |
R-free | 0.19280 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 5mat |
RMSD bond length | 0.006 |
RMSD bond angle | 1.079 |
Data reduction software | HKL-3000 |
Data scaling software | HKL-3000 |
Phasing software | PHASER |
Refinement software | PHENIX (1.8.4_1496) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | |
High resolution limit [Å] | 1.483 | 1.483 |
Rpim | 0.080 | 0.243 |
Number of reflections | 47551 | |
<I/σ(I)> | 8.9 | |
Completeness [%] | 99.5 | |
Redundancy | 5.9 | |
CC(1/2) | 0.768 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 293 | 2.1M DL-malic acid PH7.0 |