7VFC
Crystal structure of cPMO2
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL18U1 |
Synchrotron site | SSRF |
Beamline | BL18U1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2021-07-13 |
Detector | DECTRIS EIGER X 16M |
Wavelength(s) | 0.979 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 39.392, 51.223, 57.133 |
Unit cell angles | 90.00, 99.34, 90.00 |
Refinement procedure
Resolution | 29.820 - 1.210 |
R-factor | 0.1564 |
Rwork | 0.155 |
R-free | 0.17880 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 6h1z |
RMSD bond length | 0.005 |
RMSD bond angle | 0.808 |
Data reduction software | HKL-3000 |
Data scaling software | HKL-3000 |
Phasing software | PHENIX |
Refinement software | PHENIX (1.16_3549) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 29.820 | 1.254 |
High resolution limit [Å] | 1.210 | 1.210 |
Number of reflections | 67508 | 67522 |
<I/σ(I)> | 9.9 | |
Completeness [%] | 98.8 | |
Redundancy | 6.6 | |
CC(1/2) | 0.928 | 0.928 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION | 291 | 25% PEG3350,0.1 M Tris-HCl, pH8.5,0.2M ammonium acetate |