7R8X
Crystal Structure of the LNK SH2 Domain in Complex with an EPOR pY454 Phosphopeptide
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | AUSTRALIAN SYNCHROTRON BEAMLINE MX2 |
| Synchrotron site | Australian Synchrotron |
| Beamline | MX2 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2018-06-21 |
| Detector | DECTRIS EIGER X 16M |
| Wavelength(s) | 0.953740 |
| Spacegroup name | P 61 |
| Unit cell lengths | 86.157, 86.157, 38.052 |
| Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
| Resolution | 33.900 - 2.300 |
| R-factor | 0.1998 |
| Rwork | 0.197 |
| R-free | 0.23050 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 2hdv |
| Data reduction software | XDS |
| Data scaling software | XDS |
| Phasing software | PHENIX |
| Refinement software | PHENIX (1.19.2_4158) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 33.900 | 2.383 |
| High resolution limit [Å] | 2.300 | 2.301 |
| Rmerge | 0.044 | 0.492 |
| Rmeas | 0.047 | 0.539 |
| Rpim | 0.015 | |
| Number of reflections | 7318 | 724 |
| <I/σ(I)> | 31 | 2.81 |
| Completeness [%] | 99.8 | 99.45 |
| Redundancy | 9.6 | |
| CC(1/2) | 1.000 | 0.904 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 9.5 | 277.15 | 20% PEG8000, 0.05 M magnesium acetate, 0.1 M Tris, ph 8.5 |






