6X39
Crystal structure of the FN5 domain of Mouse Lar
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 22-BM |
Synchrotron site | APS |
Beamline | 22-BM |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2014-02-08 |
Detector | MARMOSAIC 225 mm CCD |
Wavelength(s) | 1.00 |
Spacegroup name | P 32 2 1 |
Unit cell lengths | 86.110, 86.110, 29.344 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 28.190 - 1.700 |
R-factor | 0.1663 |
Rwork | 0.164 |
R-free | 0.19030 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | Dlar FN5 |
RMSD bond length | 0.011 |
RMSD bond angle | 1.155 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHENIX (1.17_3644) |
Refinement software | PHENIX (1.17_3644) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 1.760 |
High resolution limit [Å] | 1.700 | 1.700 |
Rmerge | 0.119 | 0.492 |
Number of reflections | 13907 | 1337 |
<I/σ(I)> | 27.7 | 4.2 |
Completeness [%] | 99.5 | |
Redundancy | 21.3 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 293 | 100mM Na-cacodylate pH 6.5, 1.4 M Na-citrate tribasic dehydrate |