1MP8
Crystal structure of Focal Adhesion Kinase (FAK)
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ALS BEAMLINE 5.0.3 |
Synchrotron site | ALS |
Beamline | 5.0.3 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2002-01-12 |
Detector | ADSC QUANTUM 4 |
Wavelength(s) | 1.0 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 45.189, 46.636, 62.225 |
Unit cell angles | 90.00, 80.57, 90.00 |
Refinement procedure
Resolution | 46.000 - 1.700 * |
R-factor | 0.18182 |
Rwork | 0.179 |
R-free | 0.23000 * |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.015 |
RMSD bond angle | 1.660 * |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | AMoRE |
Refinement software | REFMAC (5.0) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 46.000 | 1.700 |
High resolution limit [Å] | 1.700 * | 1.600 |
Rmerge | 0.071 * | 0.255 * |
Number of reflections | 24650 * | |
Completeness [%] | 91.1 * | 65 * |
Redundancy | 3.8 * |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 7.6 * | 4 * | PEG 2000, citrate, pH 5, VAPOR DIFFUSION, SITTING DROP, temperature 293K |
Crystallization Reagents in Literatures
ID | crystal ID | solution | reagent name | concentration (unit) | details |
1 | 1 | drop | protein | 6.1 (mg/ml) | |
2 | 1 | drop | Tris-HCl | 50 (mM) | pH7.6 |
3 | 1 | drop | 250 (mM) | ||
4 | 1 | drop | EDTA | 1 (mM) | |
5 | 1 | drop | dithiothreitol | 1 (mM) | |
6 | 1 | reservoir | citrate/acetate | 0.1 (M) | pH5. |
7 | 1 | reservoir | PEG2000 MME | 24 (%) |