6O0L
crystal structure of BCL-2 G101V mutation with venetoclax
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 | 2018-07-25 |
Detector | DECTRIS EIGER X 16M |
Wavelength(s) | 0.9537 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 33.147, 82.005, 47.508 |
Unit cell angles | 90.00, 90.08, 90.00 |
Refinement procedure
Resolution | 47.508 - 2.200 |
R-factor | 0.197 |
Rwork | 0.195 |
R-free | 0.22680 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 6o0g |
RMSD bond length | 0.003 |
RMSD bond angle | 0.589 |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | PHENIX ((1.14_3260) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 47.510 | 2.280 |
High resolution limit [Å] | 2.200 | 2.200 |
Rmeas | 0.143 | |
Number of reflections | 12909 | 1270 |
<I/σ(I)> | 7.6 | 1.56 |
Completeness [%] | 99.8 | 99.53 |
Redundancy | 3.8 | 3.7 |
CC(1/2) | 0.991 | 0.646 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION | 291 | 4% PEG4K, 35% PEG400, 0.08M MES pH 6.0 |