8II1
Crystal structure of V30M-TTR in complex with BID
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SLS BEAMLINE X06SA |
Synchrotron site | SLS |
Beamline | X06SA |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2020-10-09 |
Detector | DECTRIS EIGER X 16M |
Wavelength(s) | 1 |
Spacegroup name | P 21 21 2 |
Unit cell lengths | 43.066, 85.529, 63.640 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 38.465 - 1.907 |
R-factor | 0.1963 |
Rwork | 0.195 |
R-free | 0.23060 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.010 |
RMSD bond angle | 1.182 |
Data reduction software | XDS |
Data scaling software | XSCALE |
Phasing software | PHENIX |
Refinement software | PHENIX ((1.12_2829: ???)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 42.760 | 1.980 |
High resolution limit [Å] | 1.907 | 1.910 |
Rmeas | 0.107 | 0.704 |
Number of reflections | 18912 | 1856 |
<I/σ(I)> | 9.4 | 2.6 |
Completeness [%] | 99.7 | |
Redundancy | 5.5 | |
CC(1/2) | 0.994 | 0.834 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 293 | PEG 400, CaCl2, Sodium acetate |