4MZG
Crystal structure of human Spindlin1 bound to histone H3K4me3 peptide
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | SSRF BEAMLINE BL17U |
| Synchrotron site | SSRF |
| Beamline | BL17U |
| Temperature [K] | 77 |
| Detector technology | CCD |
| Collection date | 2012-06-28 |
| Detector | ADSC QUANTUM 315r |
| Wavelength(s) | 0.9794 |
| Spacegroup name | P 1 21 1 |
| Unit cell lengths | 43.168, 122.037, 49.837 |
| Unit cell angles | 90.00, 91.71, 90.00 |
Refinement procedure
| Resolution | 32.144 - 1.698 |
| R-factor | 0.184 |
| Rwork | 0.183 |
| R-free | 0.20710 |
| Structure solution method | MOLECULAR REPLACEMENT |
| RMSD bond length | 0.007 |
| RMSD bond angle | 1.168 |
| Data reduction software | HKL-2000 |
| Data scaling software | HKL-2000 |
| Phasing software | MOLREP |
| Refinement software | PHENIX ((phenix.refine: 1.8.2_1309)) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 50.000 | 2.220 | 1.730 |
| High resolution limit [Å] | 1.698 | 2.140 | 1.698 |
| Rmerge | 0.057 | 0.088 | 0.645 |
| Number of reflections | 56230 | ||
| <I/σ(I)> | 24.8 | 19.3 | 2.64 |
| Completeness [%] | 99.6 | 100 | 99.6 |
| Redundancy | 4.4 | 4.4 | 4.4 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 8.5 | 291.15 | 37.5% MPD_P1K_P3350, 0.1M bicine/Trizma, pH 8.5, 0.06M MgCl2/CaCl2, VAPOR DIFFUSION, SITTING DROP, temperature 291.15K |






