9VYR
Crystal structure of UPF0235 protein PF1765 from Pyrococcus furiosus at pH 6
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 | 2025-03-12 |
| Detector | MARMOSAIC 225 mm CCD |
| Wavelength(s) | 0.978930 |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 44.405, 59.266, 79.408 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 35.540 - 1.130 |
| R-factor | 0.1862 |
| Rwork | 0.186 |
| R-free | 0.19880 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 9unt |
| RMSD bond length | 0.013 |
| RMSD bond angle | 1.395 |
| Data reduction software | XDS |
| Data scaling software | Aimless |
| Phasing software | PHASER |
| Refinement software | PHENIX (1.21.2_5419) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 47.500 | 1.150 |
| High resolution limit [Å] | 1.130 | 1.130 |
| Rmerge | 0.034 | 0.358 |
| Rmeas | 0.396 | |
| Rpim | 0.014 | 0.166 |
| Number of reflections | 74461 | 2512 |
| <I/σ(I)> | 29.3 | 4.3 |
| Completeness [%] | 94.4 | 65.4 |
| Redundancy | 7 | 5.4 |
| CC(1/2) | 0.999 | 0.919 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | BATCH MODE | 6 | 294 | 0.1 M PIPES CACODYLATE BIS-TRIS (PCB) buffer pH 6, 25% PEG 1500 |






