5P4B
Automated refinement of diffraction data obtained from an endothiapepsin crystal treated with fragment 200
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 | 2013-04-04 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 0.918409 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 45.281, 73.161, 52.656 |
Unit cell angles | 90.00, 109.25, 90.00 |
Refinement procedure
Resolution | 42.748 - 1.199 |
R-factor | 0.1375 |
Rwork | 0.137 |
R-free | 0.15050 |
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] | 42.749 | 1.270 | |
High resolution limit [Å] | 1.200 | 3.580 | 1.200 |
Rmerge | 0.067 | 0.046 | 0.347 |
Rmeas | 0.078 | 0.054 | 0.429 |
Total number of observations | 354706 | ||
Number of reflections | 98242 | 3862 | 13494 |
<I/σ(I)> | 10.57 | 29.26 | 2.42 |
Completeness [%] | 96.8 | 99.2 | 82.7 |
Redundancy | 3.61 | ||
CC(1/2) | 0.997 | 0.995 | 0.818 |
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 200 with the SMILES code O=C1NC2=CC=CC=C2N=C1\C=C\C1=CC=CS1 |