6W30
Protein Tyrosine Phosphatase 1B Bound to Amorphadiene
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | ALS BEAMLINE 8.2.1 |
| Synchrotron site | ALS |
| Beamline | 8.2.1 |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2019-11-05 |
| Detector | ADSC QUANTUM 315r |
| Wavelength(s) | 1.00003 |
| Spacegroup name | P 31 2 1 |
| Unit cell lengths | 89.033, 89.033, 105.559 |
| Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
| Resolution | 44.520 - 2.100 |
| R-factor | 0.1994 |
| Rwork | 0.197 |
| R-free | 0.23880 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 3a5j |
| RMSD bond length | 0.007 |
| RMSD bond angle | 0.957 |
| Data reduction software | DIALS (1.12.5-gf509b3367-release) |
| Data scaling software | xia2 (0.5.769-ga0b6e151-dials-1.12) |
| Phasing software | PHENIX (1.14_3260) |
| Refinement software | PHENIX (1.14_3260) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 62.340 | 2.130 |
| High resolution limit [Å] | 2.100 | 2.100 |
| Number of reflections | 28751 | 1314 |
| <I/σ(I)> | 0.442 | |
| Completeness [%] | 99.8 | 93.9 |
| Redundancy | 10.7 | 5.6 |
| CC(1/2) | 0.985 | 0.324 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 7.5 | 277.15 | 140 g/L PEG8000, 100 mM HEPES, 200 mM magnesium acetate, pH 7.5 |






