3SYV
Crystal structure of mPACSIN 3 F-BAR domain mutant
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | BSRF BEAMLINE 1W2B |
Synchrotron site | BSRF |
Beamline | 1W2B |
Temperature [K] | 298 |
Detector technology | CCD |
Collection date | 2011-07-02 |
Detector | MAR CCD 165 mm |
Wavelength(s) | 1.0000 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 120.570, 108.901, 222.319 |
Unit cell angles | 90.00, 90.05, 90.00 |
Refinement procedure
Resolution | 48.900 - 3.100 |
R-factor | 0.28345 |
Rwork | 0.281 |
R-free | 0.33683 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.024 |
RMSD bond angle | 2.038 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | MOLREP |
Refinement software | REFMAC (5.5.0110) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 48.900 | 3.180 |
High resolution limit [Å] | 3.100 | 3.100 |
Number of reflections | 99512 | |
Completeness [%] | 98.7 | 98 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 5.6 | 290 | 0.5M Ammonium sulfate, 0.1M Sodium citrate tribasic dihydrate pH 5.6, 1.0M Lithium sulfate monohydrate, VAPOR DIFFUSION, HANGING DROP, temperature 290K |