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 |






