7D6C
Crystal structure of CcmM N-terminal domain in complex with CcmN
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | SSRF BEAMLINE BL19U1 |
| Synchrotron site | SSRF |
| Beamline | BL19U1 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2019-11-10 |
| Detector | DECTRIS PILATUS3 S 6M |
| Wavelength(s) | 0.978530 |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 84.180, 92.330, 125.380 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 44.160 - 2.890 |
| R-factor | 0.2117 |
| Rwork | 0.209 |
| R-free | 0.27200 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 3kwc |
| RMSD bond length | 0.011 |
| RMSD bond angle | 1.239 |
| Data reduction software | XDS |
| Data scaling software | SCALA |
| Phasing software | MOLREP |
| Refinement software | PHENIX (1.18.2_3874) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 44.160 | 3.060 |
| High resolution limit [Å] | 2.890 | 2.890 |
| Number of reflections | 22669 | 3594 |
| <I/σ(I)> | 12 | |
| Completeness [%] | 99.9 | |
| Redundancy | 6.6 | |
| CC(1/2) | 0.998 | 0.858 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 287.15 | PEG 8000, N-(2-acetamido) iminodiacetic acid |






