6FKR
Crystal structure of the dolphin proline-rich antimicrobial peptide Tur1A bound to the Thermus thermophilus 70S ribosome
This is a non-PDB format compatible entry.
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID23-1 |
Synchrotron site | ESRF |
Beamline | ID23-1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2016-12-09 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 0.972422 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 209.680, 449.250, 621.900 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 49.757 - 3.200 |
R-factor | 0.1929 |
Rwork | 0.190 |
R-free | 0.25160 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 5f8k |
RMSD bond length | 0.030 |
RMSD bond angle | 1.978 |
Data reduction software | XDS |
Data scaling software | XSCALE |
Phasing software | PHENIX |
Refinement software | PHENIX (1.8.1_1168) |
Data quality characteristics
Overall | Inner shell | Outer shell | |
Low resolution limit [Å] | 49.757 | 49.757 | 3.280 |
High resolution limit [Å] | 3.200 | 14.310 | 3.200 |
Rmerge | 0.393 | 0.117 | 1.902 |
Rmeas | 0.423 | 0.126 | 2.045 |
Total number of observations | 6646089 | ||
Number of reflections | 941634 | 10701 | 69402 |
<I/σ(I)> | 4.08 | 13.04 | 1 |
Completeness [%] | 98.6 | 93.7 | 98.6 |
Redundancy | 7.058 | 6.981 | 7.246 |
CC(1/2) | 0.980 | 0.988 | 0.323 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 7.6 | 293 | Tris-HCl pH 7.6, PEG 20,000, 2-methyl-2,4-pentanediol, L-arginine |