6P1A
Transcription antitermination factor Q21 in complex with Q21-binding-element DNA
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | NSLS-II BEAMLINE 17-ID-1 |
| Synchrotron site | NSLS-II |
| Beamline | 17-ID-1 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2018-10-02 |
| Detector | DECTRIS EIGER X 9M |
| Wavelength(s) | 0.97 |
| Spacegroup name | P 21 21 2 |
| Unit cell lengths | 69.573, 263.224, 56.770 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 47.808 - 2.837 |
| R-factor | 0.2353 |
| Rwork | 0.231 |
| R-free | 0.27490 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 6p1b |
| Data reduction software | DENZO |
| Data scaling software | SCALEPACK |
| Phasing software | PHASER |
| Refinement software | PHENIX (1.14_3260) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 50.000 | 50.000 | 2.900 |
| High resolution limit [Å] | 2.837 | 7.730 | 2.850 |
| Rmerge | 0.077 | 0.034 | 0.919 |
| Rmeas | 0.084 | 0.038 | 1.009 |
| Rpim | 0.033 | 0.015 | 0.409 |
| Number of reflections | 25517 | 1428 | 1247 |
| <I/σ(I)> | 9.9 | ||
| Completeness [%] | 99.6 | 99.1 | 99.8 |
| Redundancy | 6.3 | 6.5 | 5.9 |
| CC(1/2) | 0.967 | 0.646 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 6.5 | 291 | 0.2 M Sodium chloride, 0.1 M BIS-TRIS pH 6.5, 25% PEG 3,350 |






