3GXB
Crystal structure of VWF A2 domain
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 24-ID-E |
Synchrotron site | APS |
Beamline | 24-ID-E |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2008-10-15 |
Detector | ADSC QUANTUM 315 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 55.110, 60.810, 56.350 |
Unit cell angles | 90.00, 99.09, 90.00 |
Refinement procedure
Resolution | 27.820 - 1.900 |
R-factor | 0.185 |
Rwork | 0.183 |
R-free | 0.22400 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1fe8 |
RMSD bond length | 0.006 |
RMSD bond angle | 1.010 |
Data scaling software | XSCALE |
Phasing software | MOLREP |
Refinement software | REFMAC |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 27.820 | 2.000 |
High resolution limit [Å] | 1.900 | 1.900 |
Rmerge | 0.104 | 0.801 |
Number of reflections | 28792 | |
<I/σ(I)> | 2 | |
Completeness [%] | 98.8 | 98.3 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 7.2 | 277 | 0.1 M Bis-Tris pH 7.2, 0.2 M lithium sulfate, 25 % PEG3350, vapor diffusion, hanging drop, temperature 277K |