6IKT
K1U complex structure of peptide deformylase from Xanthomonas oryzae pv. oryzae
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | PAL/PLS BEAMLINE 5C (4A) |
Synchrotron site | PAL/PLS |
Beamline | 5C (4A) |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2018-03-09 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 0.97940 |
Spacegroup name | P 61 2 2 |
Unit cell lengths | 58.880, 58.880, 265.292 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 49.900 - 1.900 |
R-factor | 0.2048 |
Rwork | 0.203 |
R-free | 0.23920 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 5e5d |
RMSD bond length | 0.019 |
RMSD bond angle | 2.187 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Refinement software | REFMAC (5.8.0158) |
Data quality characteristics
Overall | Inner shell | Outer shell | |
Low resolution limit [Å] | 50.000 | 50.000 | 1.930 |
High resolution limit [Å] | 1.900 | 5.160 | 1.900 |
Rmerge | 0.161 | 0.099 | 0.516 |
Rmeas | 0.169 | 0.103 | 0.588 |
Rpim | 0.049 | 0.027 | 0.269 |
Number of reflections | 21949 | 1310 | 982 |
<I/σ(I)> | 16.6 | ||
Completeness [%] | 96.6 | 96.1 | 91.6 |
Redundancy | 8.7 | 12.8 | 4 |
CC(1/2) | 0.996 | 0.057 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | EVAPORATION | 7.5 | 287 | 0.05M cadmium sulfate, 0.1M HEPES pH 7.5, 2.0M sodium acetate trihydrate |