5TQS
Phospholipase C gamma-1 C-terminal SH2 domain bound to a phosphopeptide derived from the receptor tyrosine kinase ErbB2
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ALS BEAMLINE 8.2.1 |
Synchrotron site | ALS |
Beamline | 8.2.1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2016-08-04 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 1.000 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 65.320, 30.620, 104.570 |
Unit cell angles | 90.00, 100.12, 90.00 |
Refinement procedure
Resolution | 51.472 - 1.876 |
R-factor | 0.1909 |
Rwork | 0.189 |
R-free | 0.23700 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4k44 |
RMSD bond length | 0.007 |
RMSD bond angle | 0.820 |
Data reduction software | MOSFLM |
Data scaling software | SCALA (3.3.22) |
Phasing software | PHASER (2.6.1) |
Refinement software | PHENIX (1.10.1_2155) |
Data quality characteristics
Overall | Inner shell | Outer shell | |
Low resolution limit [Å] | 64.304 | 64.304 | 1.980 |
High resolution limit [Å] | 1.876 | 5.930 | 1.876 |
Rmerge | 0.057 | 0.433 | |
Rmeas | 0.102 | ||
Rpim | 0.055 | ||
Total number of observations | 112903 | ||
Number of reflections | 33698 | ||
<I/σ(I)> | 9.1 | 8.6 | 1.5 |
Completeness [%] | 99.0 | 99 | 96.3 |
Redundancy | 3.4 | 3.2 | 2.8 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 277 | 0.1 M sodium acetate (pH 5.5), 22% PEG MME 5000 |