7IFM
Crystal structure of Endothiapepsin in complex with follow-up compound EOS12514 from ECBL
This is a non-PDB format compatible entry.
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | BESSY BEAMLINE 14.2 |
| Synchrotron site | BESSY |
| Beamline | 14.2 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2021-09-28 |
| Detector | DECTRIS PILATUS3 2M |
| Wavelength(s) | 0.9184 |
| Spacegroup name | P 1 21 1 |
| Unit cell lengths | 45.300, 72.910, 52.680 |
| Unit cell angles | 90.00, 109.51, 90.00 |
Refinement procedure
| Resolution | 49.660 - 1.140 |
| R-factor | 0.16751 |
| Rwork | 0.167 |
| R-free | 0.18279 |
| Structure solution method | MOLECULAR REPLACEMENT |
| RMSD bond length | 0.012 |
| RMSD bond angle | 1.736 |
| Data reduction software | XDS |
| Data scaling software | XDS |
| Phasing software | PHASER |
| Refinement software | REFMAC (5.8.0238) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 49.660 | 3.410 | 1.210 |
| High resolution limit [Å] | 1.140 | 2.410 | 1.140 |
| Rmerge | 0.075 | 0.033 | 1.020 |
| Rmeas | 0.085 | 0.038 | 1.177 |
| Total number of observations | 509623 | ||
| Number of reflections | 117149 | 7978 | 18503 |
| <I/σ(I)> | 11.2 | 38.13 | 1.25 |
| Completeness [%] | 99.3 | ||
| CC(1/2) | 0.999 | 0.998 | 0.607 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 4.6 | 293 | 29 % (w/v) PEG 4000, 0.1 M ammonium acetate and 0.1 M sodium acetate, pH 4.6 |






