5AQS
Fragment-based screening of HSP70 sheds light on the functional role of ATP-binding site residues
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | ROTATING ANODE |
Source details | BRUKER AXS MICROSTAR |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2011-02-08 |
Detector | BRUKER PT135 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 230.369, 40.538, 116.618 |
Unit cell angles | 90.00, 90.51, 90.00 |
Refinement procedure
Resolution | 58.310 - 2.000 |
R-factor | 0.2105 |
Rwork | 0.208 |
R-free | 0.26050 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1hx1 |
RMSD bond length | 0.009 |
RMSD bond angle | 1.080 |
Data reduction software | SAINT |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | BUSTER (2.10.2) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 58.310 | 2.050 |
High resolution limit [Å] | 2.000 | 2.000 |
Rmerge | 0.190 | 0.820 |
Number of reflections | 47003 | |
<I/σ(I)> | 3.6 | 0.6 |
Completeness [%] | 63.7 | 17.9 |
Redundancy | 2.6 | 1 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 8.5 | 16-26% (W/V) PEG3350, 0.1 M K-NA TARTRATE, 0.1 M TRIS.HCL PH 8.5 AND 25% (V/V) GLYCEROL |