27AF
Crystal structure of protein PF1862 from Pyrococcus furiosus crystallized at 04 degree Celsius
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 | 2026-05-08 |
| Detector | MARMOSAIC 225 mm CCD |
| Wavelength(s) | 0.997 |
| Spacegroup name | P 1 21 1 |
| Unit cell lengths | 38.483, 39.574, 64.933 |
| Unit cell angles | 90.00, 100.53, 90.00 |
Refinement procedure
| Resolution | 35.520 - 1.520 |
| R-factor | 0.1857 |
| Rwork | 0.184 |
| R-free | 0.21990 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | AlphaFold |
| RMSD bond length | 0.011 |
| RMSD bond angle | 1.142 |
| Data scaling software | XDS |
| Phasing software | PHENIX |
| Refinement software | PHENIX (1.21.2_5419) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 39.570 | 1.550 |
| High resolution limit [Å] | 1.520 | 1.520 |
| Rmerge | 0.087 | 0.502 |
| Rmeas | 0.095 | 0.546 |
| Rpim | 0.036 | 0.213 |
| Number of reflections | 29688 | 1345 |
| <I/σ(I)> | 11.4 | 2 |
| Completeness [%] | 99.6 | 92.2 |
| Redundancy | 7 | 6.3 |
| CC(1/2) | 0.998 | 0.927 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | MICROBATCH | 5.5 | 277 | 0.1 M Bis-Tris (pH 5.5) and 17% PEG 10000; protein PF1862 at 20 mg/mL |






