6L26
Neutron crystal structure of the mutant green fluorescent protein (EGFP)
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | NUCLEAR REACTOR |
Source details | FRM II BEAMLINE BIODIFF |
Synchrotron site | FRM II |
Beamline | BIODIFF |
Temperature [K] | 100 |
Detector technology | IMAGE PLATE |
Collection date | 2017-11-14 |
Detector | BIODIFF |
Wavelength(s) | 2.668 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 50.857, 62.160, 69.202 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 24.764 - 1.444 |
R-factor | 0.1696 |
Rwork | 0.168 |
R-free | 0.20650 |
Structure solution method | FOURIER SYNTHESIS |
Starting model (for MR) | 2wur |
RMSD bond length | 0.012 |
RMSD bond angle | 1.389 |
Data reduction software | HKL-2000 |
Data scaling software | SCALEPACK |
Phasing software | PHENIX |
Refinement software | PHENIX (1.9_1692) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 24.800 | 1.490 |
High resolution limit [Å] | 1.450 | 1.450 |
Rmerge | 0.098 | 0.177 |
Number of reflections | 90310 | 25594 |
<I/σ(I)> | 7.9 | 1.9 |
Completeness [%] | 88.9 | 73.8 |
Redundancy | 2.5 | 1.9 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 293 | 0.1 M MES-NaOD (pD 7.0), 5.0 % w/v PEG 2000 and 50 mM NDSB |