6Q5A
Crystal structure of Cryptosporidium hominis CPSF3 in the apo form
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | ESRF BEAMLINE ID30B |
| Synchrotron site | ESRF |
| Beamline | ID30B |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2017-04-14 |
| Detector | DECTRIS PILATUS3 6M |
| Wavelength(s) | 0.97625 |
| Spacegroup name | P 65 2 2 |
| Unit cell lengths | 90.360, 90.360, 238.660 |
| Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
| Resolution | 47.490 - 1.550 |
| R-factor | 0.13969 |
| Rwork | 0.138 |
| R-free | 0.17931 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 6q55 |
| RMSD bond length | 0.008 |
| RMSD bond angle | 1.293 |
| Data reduction software | XDS |
| Data scaling software | XSCALE |
| Phasing software | PHASER |
| Refinement software | REFMAC (5.8.0230) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 48.000 | 1.660 |
| High resolution limit [Å] | 1.550 | 1.550 |
| Rmeas | 0.070 | 0.900 |
| Number of reflections | 82588 | 14867 |
| <I/σ(I)> | 15.7 | 2.6 |
| Completeness [%] | 98.0 | 96.8 |
| Redundancy | 10.1 | 9.3 |
| CC(1/2) | 0.990 | 0.840 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 7.5 | 273 | 17% (v/v) Poly Ethylene Glycol 4000, 10% (v/v) Isopropanol, 100 mM HEPES pH 7.5 |






