5FI0
Crystal Structure of the P-Rex1 DH/PH tandem in complex with Rac1
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 21-ID-D |
Synchrotron site | APS |
Beamline | 21-ID-D |
Temperature [K] | 110 |
Detector technology | CCD |
Collection date | 2013-07-12 |
Detector | MARMOSAIC 300 mm CCD |
Wavelength(s) | 1.127 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 81.373, 107.053, 323.568 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 34.847 - 3.282 |
R-factor | 0.1924 |
Rwork | 0.190 |
R-free | 0.23550 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2DFK and 5D3W |
RMSD bond length | 0.005 |
RMSD bond angle | 1.048 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | PHENIX |
Data quality characteristics
Overall | Inner shell | Outer shell | |
Low resolution limit [Å] | 35.000 | 35.000 | 3.310 |
High resolution limit [Å] | 3.250 | 8.780 | 3.250 |
Rmerge | 0.173 | 0.066 | 0.870 |
Rmeas | 0.190 | 0.072 | 0.952 |
Rpim | 0.076 | 0.029 | 0.377 |
Total number of observations | 247146 | ||
Number of reflections | 42862 | ||
<I/σ(I)> | 5.6 | ||
Completeness [%] | 98.0 | 98.7 | 91.9 |
Redundancy | 5.8 | 6 | 5.5 |
CC(1/2) | 0.996 | 0.775 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 6.5 | 294 | Sodium dihydrogen phosphate, PEG 8000 |