6UW3
The crystal structure of FbiA from Mycobacterium Smegmatis, GDP Bound form
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 | 2019-09-29 |
Detector | DECTRIS EIGER X 16M |
Wavelength(s) | 0.987 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 46.067, 73.629, 90.931 |
Unit cell angles | 90.00, 95.38, 90.00 |
Refinement procedure
Resolution | 45.864 - 2.400 |
R-factor | 0.1959 |
Rwork | 0.193 |
R-free | 0.25860 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3c3d |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | PHENIX |
Refinement software | PHENIX (1.14_3260) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 46.070 | 2.490 |
High resolution limit [Å] | 2.400 | 2.400 |
Rmerge | 0.139 | 0.740 |
Rpim | 0.106 | 0.644 |
Number of reflections | 23704 | 2453 |
<I/σ(I)> | 6.7 | 1.7 |
Completeness [%] | 99.6 | |
Redundancy | 3.3 | |
CC(1/2) | 0.986 | 0.644 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 8.5 | 298 | 18 % PEG6000, 0.1 M Tris, 0.2 M calcium acetate |