9DHE
The crystal structure on the heme/hemoglobin transporter ChuA, in complex with heme
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 | 2018-06-11 |
Detector | DECTRIS EIGER X 4M |
Wavelength(s) | 0.987 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 78.200, 116.112, 123.289 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 48.410 - 3.200 |
R-factor | 0.253 |
Rwork | 0.251 |
R-free | 0.29920 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.003 |
RMSD bond angle | 0.647 |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | PHENIX (1.20.1_4487) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 48.430 | 2.950 |
High resolution limit [Å] | 2.800 | 2.800 |
Rmerge | 0.187 | 3.670 |
Rpim | 0.065 | 1.286 |
Number of reflections | 28374 | 4040 |
<I/σ(I)> | 8.9 | |
Completeness [%] | 99.9 | |
Redundancy | 10 | |
CC(1/2) | 0.999 | 0.442 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 7 | 298 | 20 % PEG 1500, 0.1 M MIB Buffer |