6RNR
The crystal structure of a complex between the LlFpg protein, a THF-DNA and an inhibitor
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | ESRF BEAMLINE MASSIF-3 |
| Synchrotron site | ESRF |
| Beamline | MASSIF-3 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2016-07-11 |
| Detector | DECTRIS EIGER X 4M |
| Wavelength(s) | 0.96770 |
| Spacegroup name | P 41 21 2 |
| Unit cell lengths | 91.813, 91.813, 141.617 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 45.907 - 2.003 |
| R-factor | 0.175 |
| Rwork | 0.174 |
| R-free | 0.19500 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 1pm5 |
| RMSD bond length | 0.008 |
| RMSD bond angle | 0.979 |
| Data reduction software | XDS |
| Data scaling software | autoPROC |
| Phasing software | PHASER |
| Refinement software | PHENIX (1.10.1_2155) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 47.210 | 2.040 |
| High resolution limit [Å] | 2.000 | 2.000 |
| Rmerge | 0.056 | |
| Number of reflections | 41111 | 2048 |
| <I/σ(I)> | 18.7 | 2.1 |
| Completeness [%] | 98.8 | 99.9 |
| Redundancy | 7.1 | |
| CC(1/2) | 0.999 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 293 | HEPES, CITRATE |






