6JEV
K2U bound crystal structure of class I type a peptide deformylase from Acinetobacter baumanii
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 | 2017-10-18 | 
| Detector | ADSC QUANTUM 315r | 
| Wavelength(s) | 0.97950 | 
| Spacegroup name | P 32 | 
| Unit cell lengths | 40.062, 40.062, 188.271 | 
| Unit cell angles | 90.00, 90.00, 120.00 | 
Refinement procedure
| Resolution | 32.580 - 1.900 | 
| R-factor | 0.2014 | 
| Rwork | 0.199 | 
| R-free | 0.25630 | 
| Structure solution method | MOLECULAR REPLACEMENT | 
| Starting model (for MR) | 6jer | 
| RMSD bond length | 0.009 | 
| RMSD bond angle | 1.696 | 
| Data reduction software | HKL-2000 | 
| Data scaling software | HKL-2000 | 
| Phasing software | MOLREP | 
| Refinement software | REFMAC (5.8.0238) | 
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 | 0.176 | 0.111 | 0.494 | 
| Rmeas | 0.202 | 0.125 | 0.611 | 
| Rpim | 0.098 | 0.058 | 0.353 | 
| Total number of observations | 89131 | ||
| Number of reflections | 25998 | 1304 | 1216 | 
| <I/σ(I)> | 18.1 | ||
| Completeness [%] | 97.8 | 96.2 | 92.7 | 
| Redundancy | 3.4 | 4.4 | 2.5 | 
| CC(1/2) | 0.983 | 0.128 | 
Crystallization Conditions
| crystal ID | method | pH | temperature | details | 
| 1 | EVAPORATION | 8.5 | 287 | 0.03 M MgCl2, 0.03 M CaCl2, 15% (v/v) PEGMME, 15% (w/v) PEG 20000, 0.1 M Tris (base)/ Bicine pH 8.5 | 






