4K7X
Crystal structure of a 4-hydroxyproline epimerase from burkholderia multivorans, target efi-506479, with bound phosphate, closed domains
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 31-ID |
Synchrotron site | APS |
Beamline | 31-ID |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2012-04-06 |
Detector | RAYONIX 225 HE |
Wavelength(s) | 0.9793 |
Spacegroup name | I 41 2 2 |
Unit cell lengths | 114.885, 114.885, 173.699 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 28.779 - 1.750 |
R-factor | 0.138 |
Rwork | 0.137 |
R-free | 0.15640 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4j9w |
RMSD bond length | 0.009 |
RMSD bond angle | 1.268 |
Data reduction software | MOSFLM |
Data scaling software | SCALA (3.3.20) |
Phasing software | AMoRE |
Refinement software | PHENIX (1.8.1_1168) |
Data quality characteristics
Overall | Inner shell | Outer shell | |
Low resolution limit [Å] | 95.823 | 28.779 | 1.840 |
High resolution limit [Å] | 1.750 | 5.530 | 1.750 |
Rmerge | 0.130 | 0.041 | 0.699 |
Total number of observations | 27683 | 113790 | |
Number of reflections | 58608 | ||
<I/σ(I)> | 14.1 | 14.6 | 1.1 |
Completeness [%] | 100.0 | 99.4 | 100 |
Redundancy | 14.3 | 13.7 | 13.5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 4.2 | 298 | Protein (10 mM Tris, 150 mM NaCl, 5% glycerol, 5 mM BME, 20 mM pyrrole 2-carboxylate); Reservoir (0.1 M Phosphate-citrate, 1.6 M NaH2PO4/0.4 M K2HPO4 (MCSG2 E10)); Cryoprotection (Reservoir+20% glycerol), pH 4.2, VAPOR DIFFUSION, HANGING DROP, temperature 298K |