6PT9
Crystal structure of PsS1_NC C84S in complex with k-neocarrabiose
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRL BEAMLINE BL11-1 |
Synchrotron site | SSRL |
Beamline | BL11-1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2014-02-17 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 0.97945 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 57.692, 101.793, 170.544 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 38.200 - 1.660 |
R-factor | 0.1764 |
Rwork | 0.175 |
R-free | 0.20200 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 6pt4 |
RMSD bond length | 0.011 |
RMSD bond angle | 1.654 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | REFMAC (5.8.0253) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 39.330 | 1.750 |
High resolution limit [Å] | 1.660 | 1.660 |
Rmerge | 0.076 | 0.603 |
Number of reflections | 119231 | 17125 |
<I/σ(I)> | 20.5 | |
Completeness [%] | 99.9 | |
Redundancy | 8.3 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7.5 | 291 | PEG 4000, Hepes, Na acetate trihydrate, arginine, glycerol |