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 |