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 |






