6PBC
Structural basis for the activation of PLC-gamma isozymes by phosphorylation and cancer-associated mutations
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 22-BM |
Synchrotron site | APS |
Beamline | 22-BM |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2015-08-19 |
Detector | MARMOSAIC 225 mm CCD |
Wavelength(s) | 1.000 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 70.766, 82.441, 228.318 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 41.220 - 2.460 |
R-factor | 0.2049 |
Rwork | 0.202 |
R-free | 0.24470 |
Structure solution method | SAD |
RMSD bond length | 0.003 |
RMSD bond angle | 0.586 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER (2.6.0) |
Refinement software | PHENIX (1.10.1_2155) |
Data quality characteristics
Overall | Inner shell | Outer shell | |
Low resolution limit [Å] | 50.000 | 50.000 | 2.500 |
High resolution limit [Å] | 2.460 | 6.670 | 2.460 |
Rmerge | 0.123 | 0.038 | 0.691 |
Rmeas | 0.132 | 0.041 | 0.748 |
Rpim | 0.046 | 0.014 | 0.281 |
Total number of observations | 400272 | ||
Number of reflections | 49513 | 2718 | 2257 |
<I/σ(I)> | 6.8 | ||
Completeness [%] | 99.6 | 99.6 | 92.3 |
Redundancy | 8.1 | 7.5 | 6.8 |
CC(1/2) | 0.999 | 0.808 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 293 | 12.5% w/v PEG 3,350, 50 mM di-sodium tartrate, 5% v/v glycerol |