7SSI
CRYSTAL STRUCTURE OF THE DESK:DESR-Q10A COMPLEX IN THE PHOSPHOTRANSFER STATE
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | ROTATING ANODE |
Source details | RIGAKU MICROMAX-007 HF |
Temperature [K] | 100 |
Detector technology | IMAGE PLATE |
Collection date | 2016-02-14 |
Detector | MAR scanner 345 mm plate |
Wavelength(s) | 1.5418 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 88.067, 115.634, 91.374 |
Unit cell angles | 90.00, 116.74, 90.00 |
Refinement procedure
Resolution | 34.410 - 3.410 |
R-factor | 0.2534 |
Rwork | 0.252 |
R-free | 0.28340 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 5iuk |
RMSD bond length | 0.008 |
RMSD bond angle | 1.050 |
Data scaling software | Aimless (0.7.4) |
Phasing software | PHASER (2.5.7) |
Refinement software | BUSTER (2.10.4) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 34.410 | 3.460 |
High resolution limit [Å] | 3.410 | 3.410 |
Rmeas | 0.172 | 1.599 |
Number of reflections | 22186 | 1046 |
<I/σ(I)> | 7.5 | 0.8 |
Completeness [%] | 99.6 | 93.8 |
Redundancy | 3.6 | 3.3 |
CC(1/2) | 0.446 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 8 | 291 | PEG3350, tri-potassium citrate |