8AXJ
Crystal structure of the N-terminal domain of Trypanosoma brucei CFAP410
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID23-1 |
Synchrotron site | ESRF |
Beamline | ID23-1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2020-11-06 |
Detector | PSI PILATUS 6M |
Wavelength(s) | 0.97242 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 39.799, 52.960, 61.433 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 19.900 - 1.000 |
R-factor | 0.1512 |
Rwork | 0.151 |
R-free | 0.16230 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 6l4p |
RMSD bond length | 0.010 |
RMSD bond angle | 1.221 |
Data reduction software | xia2 |
Data scaling software | xia2 |
Phasing software | PHASER |
Refinement software | PHENIX (1.18_3845) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 19.900 | 1.040 |
High resolution limit [Å] | 1.000 | 1.000 |
Number of reflections | 69889 | 5835 |
<I/σ(I)> | 10.84 | |
Completeness [%] | 98.2 | 83.75 |
Redundancy | 11.4 | |
CC(1/2) | 0.998 | 0.386 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | EVAPORATION | 5.5 | 293 | 0.1 M sodium citrate, 1 M ammonium dihydrogen phosphate |