5KAB
Protein Tyrosine Phosphatase 1B Delta helix 7, P185G mutant in complex with TCS401, open state
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | ROTATING ANODE |
Source details | RIGAKU FR-E+ SUPERBRIGHT |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2015-07-21 |
Detector | RIGAKU SATURN 944+ |
Wavelength(s) | 1.54 |
Spacegroup name | P 32 2 1 |
Unit cell lengths | 88.170, 88.170, 71.908 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 38.179 - 1.968 |
R-factor | 0.1796 |
Rwork | 0.178 |
R-free | 0.20920 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1c88 |
RMSD bond length | 0.010 |
RMSD bond angle | 1.042 |
Data reduction software | HKL-3000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER (2.5.6) |
Refinement software | PHENIX |
Data quality characteristics
Overall | Inner shell | Outer shell | |
Low resolution limit [Å] | 38.179 | 50.000 | 2.000 |
High resolution limit [Å] | 1.970 | 5.350 | 1.970 |
Rmerge | 0.051 | 0.026 | 0.224 |
Total number of observations | 233517 | ||
Number of reflections | 23190 | ||
<I/σ(I)> | 12.9 | ||
Completeness [%] | 99.6 | 99.9 | 93.8 |
Redundancy | 10.1 | 10.2 | 5.4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 8 | 277 | 0.1 M Tris, pH 8.0, 0.2 M MgCl2, 22% PEG8000 |