6TFA
Structure of the engineered retro-aldolase RA95.5-8F F112L
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SLS BEAMLINE X06SA |
Synchrotron site | SLS |
Beamline | X06SA |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2019-07-04 |
Detector | DECTRIS EIGER X 16M |
Wavelength(s) | 1.000 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 75.098, 101.865, 120.527 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 47.001 - 2.163 |
R-factor | 0.2304 |
Rwork | 0.229 |
R-free | 0.27850 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 5an7 |
Data reduction software | XDS |
Data scaling software | Aimless (0.7.4) |
Phasing software | PHASER (2.8.1) |
Refinement software | PHENIX (1.16_3549) |
Data quality characteristics
Overall | Inner shell | Outer shell | |
Low resolution limit [Å] | 49.920 | 47.000 | 2.230 |
High resolution limit [Å] | 2.160 | 8.920 | 2.160 |
Rmerge | 0.177 | 0.128 | 2.447 |
Rmeas | 0.140 | 2.697 | |
Rpim | 0.056 | 1.109 | |
Total number of observations | 4996 | 22607 | |
Number of reflections | 49820 | 827 | 4164 |
<I/σ(I)> | 5.7 | 13.8 | 1.3 |
Completeness [%] | 99.4 | 99.4 | 97.5 |
Redundancy | 6 | 6 | 5.4 |
CC(1/2) | 0.977 | 0.380 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 6.14 | 293.15 | 200 mM sodium chloride 22.91 %w/v PEG 3350 100 mM BIS-TRIS pH 6.14 |