6E4N
Structure of the T. brucei TbRGG2 RRM domain: apo R3 crystal 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 | 2011-02-20 |
Detector | ADSC QUANTUM 210r |
Wavelength(s) | 1.0 |
Spacegroup name | H 3 |
Unit cell lengths | 59.871, 59.871, 57.571 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 19.264 - 1.801 |
R-factor | 0.1533 |
Rwork | 0.152 |
R-free | 0.18750 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2m8d |
RMSD bond length | 0.004 |
RMSD bond angle | 0.763 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | MOLREP |
Refinement software | PHENIX (1.8.4_1496) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 19.264 | 1.990 |
High resolution limit [Å] | 1.800 | 1.800 |
Rpim | 0.040 | 0.161 |
Number of reflections | 7045 | |
<I/σ(I)> | 11.3 | |
Completeness [%] | 99.0 | 91.3 |
Redundancy | 1.7 | 1.7 |
CC(1/2) | 0.994 | 0.960 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 298 | 1.4 M citrate, 0.1 M Bis-Tris pH 7 or HEPES |