5X49
Crystal Structure of Human mitochondrial X-prolyl Aminopeptidase (XPNPEP3)
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | RRCAT INDUS-2 BEAMLINE PX-BL21 |
| Synchrotron site | RRCAT INDUS-2 |
| Beamline | PX-BL21 |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2016-07-29 |
| Detector | MARMOSAIC 225 mm CCD |
| Wavelength(s) | 0.97947 |
| Spacegroup name | P 1 21 1 |
| Unit cell lengths | 62.897, 135.103, 67.205 |
| Unit cell angles | 90.00, 99.87, 90.00 |
Refinement procedure
| Resolution | 30.983 - 1.650 |
| R-factor | 0.1552 |
| Rwork | 0.154 |
| R-free | 0.17750 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 1wl9 |
| RMSD bond length | 0.010 |
| RMSD bond angle | 1.069 |
| Phasing software | PHASER |
| Refinement software | PHENIX ((1.10_2152)) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 47.280 | 1.680 |
| High resolution limit [Å] | 1.650 | 1.650 |
| Rmerge | 0.062 | 0.636 |
| Number of reflections | 130822 | |
| <I/σ(I)> | 12.9 | 2.2 |
| Completeness [%] | 98.8 | 99.8 |
| Redundancy | 3.7 | 3.7 |
| CC(1/2) | 0.998 | 0.742 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | MICROBATCH | 294 | 10 mM TrisCl, 100 mM NaCl, 50 mM HEPES, 10% PEG 3350, 2.5 mM Apstatin |






