8GSV
Crystal structure of human BAK in complex with the Pxt1 BH3 domain
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | PAL/PLS BEAMLINE 5C (4A) |
| Synchrotron site | PAL/PLS |
| Beamline | 5C (4A) |
| Temperature [K] | 93 |
| Detector technology | PIXEL |
| Collection date | 2021-05-18 |
| Detector | DECTRIS EIGER X 9M |
| Wavelength(s) | 0.987 |
| Spacegroup name | P 1 |
| Unit cell lengths | 69.997, 108.365, 108.416 |
| Unit cell angles | 120.03, 90.02, 89.98 |
Refinement procedure
| Resolution | 46.942 - 2.200 |
| R-factor | 0.2153 |
| Rwork | 0.211 |
| R-free | 0.26600 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 5vwz |
| RMSD bond length | 0.011 |
| RMSD bond angle | 1.097 |
| Data reduction software | HKL-2000 |
| Data scaling software | HKL-2000 |
| Phasing software | PHASER |
| Refinement software | PHENIX ((1.10.1_2155: ???)) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 50.000 | 2.240 |
| High resolution limit [Å] | 2.200 | 2.200 |
| Rmerge | 0.069 | 0.288 |
| Number of reflections | 136032 | 6695 |
| <I/σ(I)> | 14.4 | |
| Completeness [%] | 97.4 | |
| Redundancy | 3.6 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION | 291 | 0.1 M Sodium citrate(pH 4.8) and 17 % PEG 3000 |






