5P6N
Automated refinement of diffraction data obtained from an endothiapepsin crystal treated with fragment 284
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | BESSY BEAMLINE 14.1 |
Synchrotron site | BESSY |
Beamline | 14.1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2013-07-18 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 0.91841 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 45.298, 72.891, 52.905 |
Unit cell angles | 90.00, 109.46, 90.00 |
Refinement procedure
Resolution | 19.167 - 1.109 |
R-factor | 0.1276 |
Rwork | 0.127 |
R-free | 0.14130 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4y5l |
RMSD bond length | 0.006 |
RMSD bond angle | 1.197 |
Data reduction software | XDS |
Data scaling software | XDS |
Phasing software | PHASER (2.5.7) |
Refinement software | PHENIX |
Data quality characteristics
Overall | Inner shell | Outer shell | |
Low resolution limit [Å] | 19.167 | 1.180 | |
High resolution limit [Å] | 1.110 | 3.280 | 1.110 |
Rmerge | 0.040 | 0.017 | 0.487 |
Rmeas | 0.047 | 0.020 | 0.571 |
Total number of observations | 467856 | ||
Number of reflections | 127133 | 4976 | 20178 |
<I/σ(I)> | 16.94 | 67.22 | 2.53 |
Completeness [%] | 99.4 | 98.7 | 98.1 |
Redundancy | 3.68 | ||
CC(1/2) | 1.000 | 0.999 | 0.799 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 4.6 | 290 | 0.1 M ammonium acetate, 0.1 M sodium acetate, 24-30% PEG 4000; crystal obtained by streak-seeding and soaked with 90 mM of fragment 284 with the SMILES code O[C@@H](COCC1=CC=CC=C1F)CN1CCCC1 |