5CH4
Peptide-Bound State of Thermus thermophilus SecYEG
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SPRING-8 BEAMLINE BL32XU |
Synchrotron site | SPring-8 |
Beamline | BL32XU |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2014-07-18 |
Detector | RAYONIX MX225HE |
Wavelength(s) | 1.0 |
Spacegroup name | C 2 2 21 |
Unit cell lengths | 97.829, 138.007, 115.974 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 44.393 - 3.640 |
R-factor | 0.2567 |
Rwork | 0.254 |
R-free | 0.27900 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2zjs |
RMSD bond length | 0.002 |
RMSD bond angle | 0.577 |
Data scaling software | XDS |
Phasing software | PHASER |
Refinement software | PHENIX (1.9_1692) |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 50.000 |
High resolution limit [Å] | 3.600 |
Number of reflections | 9099 |
<I/σ(I)> | 5.9 |
Completeness [%] | 99.8 |
Redundancy | 7.4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | LIPIDIC CUBIC PHASE | 7.5 | 293 | PEG 500DME, ZnSO4 |