8HNA
Crystal structure of N-terminal fragment (20-221aa) of human SCARF1
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 | 2016-09-26 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 1.0 |
Spacegroup name | P 41 2 2 |
Unit cell lengths | 102.007, 102.007, 83.612 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 26.890 - 2.600 |
R-factor | 0.2305 |
Rwork | 0.229 |
R-free | 0.24560 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.007 |
RMSD bond angle | 1.068 |
Data reduction software | HKL-3000 |
Data scaling software | HKL-3000 |
Phasing software | PHENIX |
Refinement software | PHENIX (1.18.2-3874-000) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 30.000 | 2.690 |
High resolution limit [Å] | 2.600 | 2.600 |
Rmerge | 0.086 | 0.780 |
Number of reflections | 14015 | 1299 |
<I/σ(I)> | 32.125 | |
Completeness [%] | 99.1 | |
Redundancy | 12.7 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 289.15 | 0.1 M citric acid/sodium citrate (pH 3.6), 9% PEG8000 |