6JG9
Crystal structure of AimR in complex with arbitrium peptide
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL19U1 |
Synchrotron site | SSRF |
Beamline | BL19U1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2017-04-29 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 0.9778 |
Spacegroup name | P 21 21 2 |
Unit cell lengths | 120.926, 213.996, 33.590 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 46.123 - 1.998 |
R-factor | 0.2151 |
Rwork | 0.213 |
R-free | 0.24880 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 5xyb |
RMSD bond length | 0.010 |
RMSD bond angle | 1.094 |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | PHENIX ((1.14rc3_3206: ???)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 46.123 | 2.070 |
High resolution limit [Å] | 2.000 | 2.000 |
Number of reflections | 60685 | |
<I/σ(I)> | 39.1 | |
Completeness [%] | 100.0 | |
Redundancy | 25.7 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 291.15 | sodium cacodylate, PEG 8000, NaBr, DTT |