5PWU
PanDDA analysis group deposition -- Crystal Structure of SP100 after initial refinement with no ligand modelled (structure 18)
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | DIAMOND BEAMLINE I04-1 |
| Synchrotron site | Diamond |
| Beamline | I04-1 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2015-04-02 |
| Detector | DECTRIS PILATUS 2M |
| Wavelength(s) | 0.9200 |
| Spacegroup name | C 1 2 1 |
| Unit cell lengths | 127.690, 45.340, 83.360 |
| Unit cell angles | 90.00, 102.35, 90.00 |
Refinement procedure
| Resolution | 36.670 - 1.440 |
| R-factor | 0.1761 |
| Rwork | 0.175 |
| R-free | 0.20320 |
| Structure solution method | FOURIER SYNTHESIS |
| Starting model (for MR) | 4ptb |
| RMSD bond length | 0.028 |
| RMSD bond angle | 2.340 |
| Data reduction software | XDS |
| Data scaling software | Aimless (0.3.11) |
| Phasing software | REFMAC |
| Refinement software | REFMAC (5.8.0135) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 36.670 | 36.670 | 1.480 |
| High resolution limit [Å] | 1.440 | 6.440 | 1.440 |
| Rmerge | 0.055 | 0.045 | 0.529 |
| Rmeas | 0.065 | 0.054 | 0.631 |
| Rpim | 0.035 | 0.029 | 0.338 |
| Total number of observations | 283092 | 3454 | 20623 |
| Number of reflections | 82819 | ||
| <I/σ(I)> | 12.7 | 32.4 | 2.2 |
| Completeness [%] | 98.1 | 97.6 | 98.5 |
| Redundancy | 3.4 | 3.5 | 3.4 |
| CC(1/2) | 0.997 | 0.994 | 0.750 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 7 | 277 | 0.1M MES pH 6.1 -- 20% PEG20K |
