6IUH
Crystal structure of GIT1 PBD domain in complex with Liprin-alpha2
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | SSRF BEAMLINE BL18U1 |
| Synchrotron site | SSRF |
| Beamline | BL18U1 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2017-05-22 |
| Detector | DECTRIS PILATUS3 6M |
| Wavelength(s) | 0.98 |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 88.200, 38.617, 99.134 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 49.567 - 1.800 |
| R-factor | 0.2285 |
| Rwork | 0.227 |
| R-free | 0.26680 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 2jx0 |
| RMSD bond length | 0.003 |
| RMSD bond angle | 0.618 |
| Data reduction software | HKL-3000 |
| Data scaling software | HKL-3000 |
| Phasing software | PHASER |
| Refinement software | PHENIX (1.9_1692) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 50.000 | 50.000 | 1.830 |
| High resolution limit [Å] | 1.800 | 4.880 | 1.800 |
| Rmerge | 0.098 | 0.066 | 0.842 |
| Rmeas | 0.110 | 0.076 | 0.930 |
| Rpim | 0.050 | 0.036 | 0.390 |
| Number of reflections | 32467 | 1785 | 1606 |
| <I/σ(I)> | 5.7 | ||
| Completeness [%] | 99.2 | 98.5 | 100 |
| Redundancy | 5.3 | 4.7 | 5.6 |
| CC(1/2) | 0.994 | 0.865 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 6.5 | 289 | 0.2M Potassium iodide, 0.1M MES pH 6.5, 25% w/v PEG 4000 |






