5TQ1
Phospholipase C gamma-1 C-terminal SH2 domain bound to a phosphopeptide derived from the insulin receptor
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | ALS BEAMLINE 8.2.2 |
| Synchrotron site | ALS |
| Beamline | 8.2.2 |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2014-12-10 |
| Detector | ADSC QUANTUM 315r |
| Wavelength(s) | 1.000 |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 34.010, 55.140, 58.665 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 29.332 - 1.485 |
| R-factor | 0.1736 |
| Rwork | 0.172 |
| R-free | 0.20990 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 4k44 |
| RMSD bond length | 0.004 |
| RMSD bond angle | 0.834 |
| Data reduction software | MOSFLM |
| Data scaling software | SCALA (3.3.20) |
| Phasing software | PHASER (2.3.0) |
| Refinement software | PHENIX (1.10.1_2155) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 58.665 | 58.665 | 1.560 |
| High resolution limit [Å] | 1.485 | 4.690 | 1.485 |
| Rmerge | 0.041 | 0.223 | |
| Rmeas | 0.064 | ||
| Rpim | 0.024 | ||
| Total number of observations | 104032 | ||
| Number of reflections | 18758 | ||
| <I/σ(I)> | 16.5 | 14.6 | 2.2 |
| Completeness [%] | 99.5 | 98.7 | 97.5 |
| Redundancy | 5.5 | 7.1 | 3.3 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 9 | 277 | 0.1M Tris (pH 9.0), 30% PEG MME 2000 |






