9N4A
Wild-type RhoA GTPase bound to GppNHp
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | ROTATING ANODE |
| Source details | RIGAKU MICROMAX-007 HF |
| Temperature [K] | 100 |
| Detector technology | IMAGE PLATE |
| Collection date | 2015-08-17 |
| Detector | RIGAKU RAXIS IV++ |
| Wavelength(s) | 1.54 |
| Spacegroup name | C 1 2 1 |
| Unit cell lengths | 119.100, 60.778, 70.031 |
| Unit cell angles | 90.00, 123.71, 90.00 |
Refinement procedure
| Resolution | 45.886 - 1.947 |
| R-factor | 0.1808 |
| Rwork | 0.178 |
| R-free | 0.22120 |
| Structure solution method | MOLECULAR REPLACEMENT |
| RMSD bond length | 0.008 |
| RMSD bond angle | 1.219 |
| Data reduction software | HKL-2000 |
| Data scaling software | HKL-2000 |
| Phasing software | PHENIX |
| Refinement software | PHENIX (1.8.4) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 45.886 | 2.020 |
| High resolution limit [Å] | 1.947 | 1.950 |
| Rmerge | 0.042 | |
| Rmeas | 0.059 | 0.514 |
| Rpim | 0.046 | 0.276 |
| Number of reflections | 30326 | 2661 |
| <I/σ(I)> | 12.2 | 2.47 |
| Completeness [%] | 98.5 | 83.43 |
| Redundancy | 3.6 | 3.3 |
| CC(1/2) | 0.995 | 0.828 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 291.18 | 2 uL protein (10 mg/mL RhoA-GppNHp, 25 mM Tris-HCl pH 8.0, 2 mM MgCl2, 10 mM BME) + 2 uL of crystallization solution over 500 uL reservoir of crystallization solution. Crystallization solution: 25% dioxane, 17% PEG 8000, and 100 mM HEPES pH 6.9 |






