7ED6
Crystal structure of Thermus thermophilus FakA ATP-binding domain
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SPRING-8 BEAMLINE BL26B1 |
Synchrotron site | SPring-8 |
Beamline | BL26B1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2020-11-17 |
Detector | DECTRIS EIGER X 4M |
Wavelength(s) | 0.9788 |
Spacegroup name | P 43 21 2 |
Unit cell lengths | 90.190, 90.190, 111.620 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 45.095 - 1.929 |
R-factor | 0.20945075519 |
Rwork | 0.208 |
R-free | 0.23641 |
Structure solution method | SAD |
RMSD bond length | 0.003 |
RMSD bond angle | 0.753 |
Data reduction software | XDS |
Data scaling software | XDS |
Phasing software | PHENIX (1.10.1_2155) |
Refinement software | PHENIX (1.10.1_2155) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 45.095 | 2.000 |
High resolution limit [Å] | 1.928 | 1.928 |
Number of reflections | 35300 | 3455 |
<I/σ(I)> | 13 | 1.04 |
Completeness [%] | 99.9 | 99.4 |
Redundancy | 14.2 | 14.2 |
CC(1/2) | 0.999 | 0.671 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 8.5 | 293 | 2.2M sodium chloride, 0.1M tris-HCl |