1EJM
CRYSTAL STRUCTURE OF THE BPTI ALA16LEU MUTANT IN COMPLEX WITH BOVINE TRYPSIN
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF |
Synchrotron site | ESRF |
Temperature [K] | 120 |
Detector technology | CCD |
Collection date | 1999-06-18 |
Detector | ADSC QUANTUM 4 |
Spacegroup name | I 41 2 2 |
Unit cell lengths | 180.870, 180.870, 170.510 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 15.000 - 1.850 |
R-factor | 0.211 * |
Rwork | 0.211 |
R-free | 0.23300 |
RMSD bond length | 0.005 |
RMSD bond angle | 24.800 * |
Data scaling software | SCALA |
Phasing software | CNS |
Refinement software | CNS |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 15.000 | 1.950 |
High resolution limit [Å] | 1.850 | 1.850 |
Rmerge | 0.071 | 0.412 |
Total number of observations | 1360301 * | |
Number of reflections | 119391 | |
<I/σ(I)> | 5.4 | |
Completeness [%] | 99.4 | 99.3 |
Redundancy | 7.4 | 1.8 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7.5 | 310 | Helland, R., (1999) J. Mol. Biol., 287, 923. * |
Crystallization Reagents in Literatures
ID | crystal ID | solution | reagent name | concentration (unit) | details |
1 | 1 | drop | protein | 27 (mg/ml) | |
2 | 1 | reservoir | ammonium sulfate | 48-50 (%sat) | |
3 | 1 | reservoir | HEPES | 0.1 (M) |