5FLO
Native state mass spectrometry, surface plasmon resonance and X-ray crystallography correlate strongly as a fragment screening combination
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | AUSTRALIAN SYNCHROTRON BEAMLINE MX1 |
Synchrotron site | Australian Synchrotron |
Beamline | MX1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2015-04-08 |
Detector | ADSC CCD |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 42.753, 41.493, 71.660 |
Unit cell angles | 90.00, 104.60, 90.00 |
Refinement procedure
Resolution | 69.350 - 1.660 |
R-factor | 0.16101 |
Rwork | 0.158 |
R-free | 0.21513 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4cq0 |
RMSD bond length | 0.020 |
RMSD bond angle | 1.974 |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | REFMAC (5.8.0135) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 41.500 | 1.690 |
High resolution limit [Å] | 1.660 | 1.660 |
Rmerge | 0.090 | 0.640 |
Number of reflections | 28587 | |
<I/σ(I)> | 16.2 | 2.7 |
Completeness [%] | 99.4 | 92.4 |
Redundancy | 7.4 | 6.5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 8.5 | 15 MG/ML PROTEIN WITH 2.7 M AMMONIUM SULFATE, 100 MM TRIS PH 8.5 AT 8 C IN SITTING DROPS. |