5TEB
Crystal Structure of the TIR domain from the Arabidopsis Thaliana disease resistance protein RPP1
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | AUSTRALIAN SYNCHROTRON BEAMLINE MX1 |
Synchrotron site | Australian Synchrotron |
Beamline | MX1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2015-10-27 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 0.9537 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 81.890, 84.330, 122.750 |
Unit cell angles | 90.00, 90.10, 90.00 |
Refinement procedure
Resolution | 40.945 - 2.796 |
R-factor | 0.2203 |
Rwork | 0.218 |
R-free | 0.26850 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.006 |
RMSD bond angle | 0.988 |
Phasing software | PHENIX (1.11rc2_2531) |
Refinement software | PHENIX (1.11rc2_2531) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 40.945 | 2.660 |
High resolution limit [Å] | 2.550 | 2.580 |
Number of reflections | 41428 | |
<I/σ(I)> | 14.5 | 1.3 |
Completeness [%] | 99.6 | 95.6 |
Redundancy | 7.6 | 6.9 |
CC(1/2) | 0.590 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 5.5 | 291 | 15% PEG 6000, 0.2 M citrate pH 5.5 |