5RP9
PanDDA analysis group deposition -- Proteinase K changed state model for fragment Frag Xtal Screen B7a
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | MAX IV BEAMLINE BioMAX |
Synchrotron site | MAX IV |
Beamline | BioMAX |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2019-03-23 |
Detector | DECTRIS EIGER X 16M |
Wavelength(s) | 0.954 |
Spacegroup name | P 43 21 2 |
Unit cell lengths | 68.290, 68.290, 103.040 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 29.280 - 1.480 |
R-factor | 0.1645 |
Rwork | 0.164 |
R-free | 0.18230 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.005 |
RMSD bond angle | 0.862 |
Data reduction software | XDS |
Data scaling software | Aimless (0.7.4) |
Phasing software | PHASER (2.8.3) |
Refinement software | PHENIX (1.19.1) |
Data quality characteristics
Overall | Inner shell | Outer shell | |
Low resolution limit [Å] | 29.280 | 29.280 | 1.510 |
High resolution limit [Å] | 1.480 | 8.130 | 1.480 |
Rmerge | 0.024 | 0.013 | 0.192 |
Rmeas | 0.034 | 0.018 | 0.271 |
Rpim | 0.024 | 0.013 | 0.192 |
Total number of observations | 76831 | 473 | 3572 |
Number of reflections | 40987 | 314 | 1893 |
<I/σ(I)> | 17.4 | 34.8 | 4 |
Completeness [%] | 99.7 | 98.2 | 94.7 |
Redundancy | 1.9 | 1.5 | 1.9 |
CC(1/2) | 0.999 | 0.999 | 0.933 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 8 | 290 | 1.2M ammonium sulfate, 0.1M Tris-HCl, pH 8.0 |