4FIH
Catalytic domain of human PAK4 with QKFTGLPRQW peptide
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | NSLS BEAMLINE X6A |
Synchrotron site | NSLS |
Beamline | X6A |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2011-12-02 |
Detector | ADSC QUANTUM 270 |
Wavelength(s) | 0.97550 |
Spacegroup name | P 41 21 2 |
Unit cell lengths | 61.673, 61.673, 181.452 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 50.000 - 1.970 |
R-factor | 0.18085 |
Rwork | 0.178 |
R-free | 0.22527 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2cdz |
RMSD bond length | 0.019 |
RMSD bond angle | 2.014 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | REFMAC (5.6.0117) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.040 |
High resolution limit [Å] | 1.970 | 1.970 |
Rmerge | 0.072 | 0.593 |
<I/σ(I)> | 36.8 | 3.9 |
Completeness [%] | 99.5 | 96.1 |
Redundancy | 11.4 | 10.3 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7.5 | 295 | 0.1M Tris-HCl, 1.5M Na acetate, pH 7.5, VAPOR DIFFUSION, HANGING DROP, temperature 295K |