6AR5
Structure of a Thermostable Group II Intron Reverse Transcriptase with Template-Primer and Its Functional and Evolutionary Implications (Duplex Only)
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | ALS BEAMLINE 5.0.3 |
| Synchrotron site | ALS |
| Beamline | 5.0.3 |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2017-04-01 |
| Detector | ADSC QUANTUM 315r |
| Wavelength(s) | 0.9765 |
| Spacegroup name | P 31 2 1 |
| Unit cell lengths | 46.428, 46.428, 82.195 |
| Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
| Resolution | 36.118 - 2.413 |
| R-factor | 0.187 |
| Rwork | 0.185 |
| R-free | 0.21210 |
| Structure solution method | MOLECULAR REPLACEMENT |
| RMSD bond length | 0.007 |
| RMSD bond angle | 0.948 |
| Data reduction software | XDS (May 1, 2016) |
| Data scaling software | Aimless (0.5.31) |
| Phasing software | PHASER (2.7.16) |
| Refinement software | PHENIX (1.11.1) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 36.118 | 41.100 | 2.500 |
| High resolution limit [Å] | 2.410 | 9.020 | 2.410 |
| Rmerge | 0.053 | 0.021 | 0.531 |
| Rmeas | 0.055 | 0.022 | 0.544 |
| Rpim | 0.012 | 0.006 | 0.117 |
| Total number of observations | 88698 | ||
| Number of reflections | 4275 | 106 | 436 |
| <I/σ(I)> | 48 | ||
| Completeness [%] | 100.0 | 98.8 | 100 |
| Redundancy | 20.7 | 16 | 21.3 |
| CC(1/2) | 1.000 | 1.000 | 0.983 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 293 | sodium malonate, ammonium citrate tribasic |






