6K02
Crystal structure of ceNAP1 core
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 | 2018-07-08 |
Detector | DECTRIS PILATUS3 6M |
Wavelength(s) | 0.9789 |
Spacegroup name | C 2 2 21 |
Unit cell lengths | 95.733, 126.747, 118.192 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 37.196 - 2.162 |
R-factor | 0.2517 |
Rwork | 0.250 |
R-free | 0.27920 |
Structure solution method | MOLECULAR REPLACEMENT |
Data reduction software | HKL-2000 |
Data scaling software | SCALA |
Phasing software | MOLREP |
Refinement software | PHENIX ((1.14_3260: ???)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 37.200 | 2.240 |
High resolution limit [Å] | 2.160 | 2.160 |
Rmerge | 0.845 | |
Number of reflections | 38052 | 38052 |
<I/σ(I)> | 20 | |
Completeness [%] | 99.2 | |
Redundancy | 9.9 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 291 | 0.2M Zinc acetate dihydrate, 0.1M Sodium cacodylate tridydrate pH=6.5, 18% PEG 8000 |