6E4O
Structure of apo T. brucei RRM: P4(1)2(1)2 form
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | ALS BEAMLINE 8.3.1 |
| Synchrotron site | ALS |
| Beamline | 8.3.1 |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2010-02-24 |
| Detector | ADSC QUANTUM 210r |
| Wavelength(s) | 1 |
| Spacegroup name | P 41 21 2 |
| Unit cell lengths | 72.100, 72.100, 118.724 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 38.676 - 1.800 |
| R-factor | 0.1674 |
| Rwork | 0.165 |
| R-free | 0.19680 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 6e4n |
| RMSD bond length | 0.006 |
| RMSD bond angle | 0.890 |
| Data reduction software | MOSFLM |
| Data scaling software | SCALA |
| Phasing software | MOLREP |
| Refinement software | PHENIX (1.6.4_486) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 38.676 | 1.970 |
| High resolution limit [Å] | 1.800 | 1.800 |
| Rpim | 0.035 | 0.208 |
| Number of reflections | 28420 | |
| <I/σ(I)> | 12.5 | 2.3 |
| Completeness [%] | 96.0 | 80.3 |
| Redundancy | 2.6 | 1.4 |
| CC(1/2) | 0.997 | 0.977 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 298 | 1.2-1.4 M trisodium citrate, HEPES buffer |






