7CQ2
Crystal structure of Slx1-Slx4
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL17U |
Synchrotron site | SSRF |
Beamline | BL17U |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2011-07-19 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 0.9792 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 61.284, 75.960, 186.966 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 42.486 - 2.500 |
R-factor | 0.2044 |
Rwork | 0.201 |
R-free | 0.26230 |
Structure solution method | SAD |
RMSD bond length | 0.004 |
RMSD bond angle | 0.740 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHENIX |
Refinement software | PHENIX (1.7.3_928) |
Data quality characteristics
Overall | Inner shell | Outer shell | |
Low resolution limit [Å] | 50.000 | 50.000 | 2.590 |
High resolution limit [Å] | 2.500 | 5.380 | 2.500 |
Rmerge | 0.104 | 0.070 | 0.383 |
Number of reflections | 58698 | 3373 | 3076 |
<I/σ(I)> | 9.4 | ||
Completeness [%] | 99.3 | 98.9 | 98.3 |
Redundancy | 5.5 | 5.4 | 5.6 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 289 | 0.2 M potassium sodium tartrate tetrahydrate, 0.1M sodium cacodylate trihydrate, 20% PEG 3350 and 0.2 M NDSB-201 |