5P44
Automated refinement of diffraction data obtained from an endothiapepsin crystal treated with fragment 193
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 | 45.345, 73.063, 52.778 |
Unit cell angles | 90.00, 109.48, 90.00 |
Refinement procedure
Resolution | 41.127 - 1.180 |
R-factor | 0.1188 |
Rwork | 0.118 |
R-free | 0.13050 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4y5l |
RMSD bond length | 0.006 |
RMSD bond angle | 1.225 |
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] | 42.750 | 1.250 | |
High resolution limit [Å] | 1.180 | 3.530 | 1.180 |
Rmerge | 0.034 | 0.029 | 0.122 |
Rmeas | 0.040 | 0.033 | 0.151 |
Total number of observations | 362726 | ||
Number of reflections | 100679 | 4049 | 12002 |
<I/σ(I)> | 21.18 | 47.64 | 6.77 |
Completeness [%] | 94.5 | 99.2 | 70 |
Redundancy | 3.602 | ||
CC(1/2) | 0.999 | 0.998 | 0.975 |
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 193 with the SMILES code COC(=O)C1=C(N)C=C(S1)C(C)(C)C |