3BX9
Monomeric Far-red Fluorescent Protein mKate Crystallized at pH 2.0
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 22-ID |
Synchrotron site | APS |
Beamline | 22-ID |
Temperature [K] | 100 |
Detector technology | CCD |
Detector | MARMOSAIC 300 mm CCD |
Wavelength(s) | 1.0 |
Spacegroup name | P 65 2 2 |
Unit cell lengths | 67.852, 67.852, 413.030 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 30.000 - 1.800 |
R-factor | 0.205 |
Rwork | 0.205 |
R-free | 0.24700 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1uis |
RMSD bond length | 0.017 |
RMSD bond angle | 1.773 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | MOLREP |
Refinement software | REFMAC (5.2.0019) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 30.430 | 1.860 |
High resolution limit [Å] | 1.800 | 1.800 |
Rmerge | 0.061 | 0.556 |
Number of reflections | 52642 | |
<I/σ(I)> | 5.63 | |
Completeness [%] | 99.9 | 99.7 |
Redundancy | 14.1 | 14.4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 2 | 293 | 20% w/v PEG 3350, 0.2M ammonium citrate tribasic, 0.4M citric acid, pH 2.0, VAPOR DIFFUSION, HANGING DROP, temperature 293K |