6UCR
Structure of ClpC1-NTD L92S L96P
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | APS BEAMLINE 21-ID-F |
| Synchrotron site | APS |
| Beamline | 21-ID-F |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2019-06-04 |
| Detector | MARMOSAIC 225 mm CCD |
| Wavelength(s) | .97872 |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 38.137, 63.350, 68.305 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 40.000 - 2.300 |
| R-factor | 0.18899 |
| Rwork | 0.186 |
| R-free | 0.23697 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 6cn8 |
| RMSD bond length | 0.014 |
| RMSD bond angle | 1.797 |
| Data reduction software | HKL-2000 |
| Data scaling software | HKL-2000 |
| Phasing software | MOLREP |
| Refinement software | PHENIX |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 40.000 | 2.340 |
| High resolution limit [Å] | 2.300 | 2.300 |
| Rmeas | 0.100 | 0.253 |
| Rpim | 0.028 | 0.068 |
| Number of reflections | 7594 | 376 |
| <I/σ(I)> | 56.1 | 27.2 |
| Completeness [%] | 96.4 | |
| Redundancy | 12.7 | |
| CC(1/2) | 0.995 | 0.990 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 289 | 0.1 M HEPES, pH 7.5, 10% PEG8000, 8% ethylene glycol |






