5P8S
Automated refinement of diffraction data obtained from an endothiapepsin crystal treated with fragment 361
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 | 2013-12-14 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 0.918409 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 45.324, 73.029, 52.821 |
Unit cell angles | 90.00, 109.56, 90.00 |
Refinement procedure
Resolution | 39.625 - 1.109 |
R-factor | 0.1313 |
Rwork | 0.131 |
R-free | 0.14350 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4y5l |
RMSD bond length | 0.006 |
RMSD bond angle | 1.190 |
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] | 42.708 | 1.180 | |
High resolution limit [Å] | 1.110 | 3.320 | 1.110 |
Rmerge | 0.047 | 0.027 | 0.469 |
Rmeas | 0.055 | 0.032 | 0.548 |
Total number of observations | 470047 | ||
Number of reflections | 123969 | 4832 | 19248 |
<I/σ(I)> | 12.84 | 46.24 | 2.41 |
Completeness [%] | 96.9 | 98.9 | 93.3 |
Redundancy | 3.791 | ||
CC(1/2) | 0.999 | 0.998 | 0.811 |
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 361 with the SMILES code FC(F)(F)C1=CC(=C)NS(=O)(=O)N1 |