8UKY
Crystal structure of BAK in complex with inhibiting antibody 14G6
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 | 2021-02-12 |
Detector | DECTRIS EIGER X 16M |
Wavelength(s) | 0.9537 |
Spacegroup name | P 1 |
Unit cell lengths | 71.554, 72.622, 75.282 |
Unit cell angles | 103.01, 103.98, 112.15 |
Refinement procedure
Resolution | 45.379 - 2.398 |
R-factor | 0.2167 |
Rwork | 0.215 |
R-free | 0.25180 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | PDB entries 2YV6 & 5W5Z |
Data reduction software | XDS |
Data scaling software | XSCALE |
Phasing software | MOLREP |
Refinement software | PHENIX (1.16_3549) |
Data quality characteristics
Overall | Inner shell | Outer shell | |
Low resolution limit [Å] | 45.379 | 45.379 | 2.460 |
High resolution limit [Å] | 2.398 | 10.720 | 2.400 |
Rmerge | 0.066 | 0.021 | 0.447 |
Rmeas | 0.086 | 0.028 | 0.586 |
Number of reflections | 48280 | 509 | 3563 |
<I/σ(I)> | 9.55 | 33.46 | 1.76 |
Completeness [%] | 96.3 | 91.1 | 94.9 |
Redundancy | 2.205 | 2.32 | 2.258 |
CC(1/2) | 0.997 | 0.998 | 0.824 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 293 | 0.09 M Bis-Tris chloride, pH 5.5, 22.5% PEG3350, 4% acetonitrile |