3P72
structure of platelet Glycoprotein 1b alpha with a bound peptide inhibitor
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID23-2 |
Synchrotron site | ESRF |
Beamline | ID23-2 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2008-11-15 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 0.87300 |
Spacegroup name | P 31 2 1 |
Unit cell lengths | 58.817, 58.817, 163.027 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 54.300 - 1.900 |
R-factor | 0.22061 |
Rwork | 0.217 |
R-free | 0.28627 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.022 |
RMSD bond angle | 1.938 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | REFMAC (5.5.0102) |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 54.300 |
High resolution limit [Å] | 1.900 |
Rmerge | 0.105 |
Number of reflections | 25267 |
<I/σ(I)> | 12.4 |
Completeness [%] | 100.0 |
Redundancy | 7.6 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 8.2 | 298 | 1.9M ammonium sulfate, 80mM lithium sulfate, 100mM N-cyclohexyl-3-aminopropanesulfonic acid buffer. 1:1 mix buffer with 4mg/mL protein. lyophilised peptide added directly to crystallised protein drops., pH 8.2, VAPOR DIFFUSION, SITTING DROP, temperature 298K |