7V1L
Structure of sNASP core in complex with H3 alpha3 helix peptide
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 | 2018-12-15 |
| Detector | DECTRIS PILATUS3 S 6M |
| Wavelength(s) | 0.9766 |
| Spacegroup name | C 2 2 21 |
| Unit cell lengths | 66.902, 177.051, 65.892 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 36.742 - 2.849 |
| R-factor | 0.2031 |
| Rwork | 0.201 |
| R-free | 0.24600 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 4nq0 |
| RMSD bond length | 0.008 |
| RMSD bond angle | 0.935 |
| Data reduction software | HKL-3000 |
| Data scaling software | HKL-2000 |
| Phasing software | PHASER |
| Refinement software | PHENIX (1.19) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 40.000 | 40.000 | 2.950 |
| High resolution limit [Å] | 2.849 | 6.130 | 2.850 |
| Rmerge | 0.142 | 0.059 | |
| Rmeas | 0.149 | 0.062 | |
| Rpim | 0.045 | 0.018 | 0.390 |
| Number of reflections | 9497 | 1030 | 926 |
| <I/σ(I)> | 2.9 | ||
| Completeness [%] | 99.8 | 99.9 | 98.4 |
| Redundancy | 12 | 12.1 | 10 |
| CC(1/2) | 0.998 | 0.475 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 293 | 1.4M Na-K phosphate, pH 8.2 |






