6EB6
Crystal structure of BAX W139A monomer
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | AUSTRALIAN SYNCHROTRON BEAMLINE MX2 |
| Synchrotron site | Australian Synchrotron |
| Beamline | MX2 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2018-03-21 |
| Detector | DECTRIS EIGER X 16M |
| Wavelength(s) | 0.9536 |
| Spacegroup name | P 31 2 1 |
| Unit cell lengths | 63.159, 63.159, 82.265 |
| Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
| Resolution | 32.870 - 2.023 |
| R-factor | 0.1729 |
| Rwork | 0.171 |
| R-free | 0.20130 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 5w61 |
| RMSD bond length | 0.007 |
| RMSD bond angle | 0.734 |
| Data reduction software | XDS |
| Data scaling software | Aimless (0.5.32) |
| Phasing software | PHASER (2.8.1) |
| Refinement software | PHENIX ((1.13_2998)) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 45.550 | 2.095 |
| High resolution limit [Å] | 2.023 | 2.023 |
| Rmerge | 0.063 | 0.526 |
| Number of reflections | 12611 | 1200 |
| <I/σ(I)> | 21.15 | |
| Completeness [%] | 98.4 | |
| Redundancy | 10.1 | |
| CC(1/2) | 0.999 | 0.952 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 293 | Sodium formate, TCEP |






