6KSH
Crystal structure of pyruvate kinase (PYK) from Plasmodium falciparum in complex with oxalate and ATP
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | AUSTRALIAN SYNCHROTRON BEAMLINE MX2 |
Synchrotron site | Australian Synchrotron |
Beamline | MX2 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2016-02-01 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 0.9537 |
Spacegroup name | P 65 2 2 |
Unit cell lengths | 139.410, 139.410, 453.156 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 37.990 - 2.600 |
R-factor | 0.154 |
Rwork | 0.151 |
R-free | 0.20700 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3khd |
RMSD bond length | 0.010 |
RMSD bond angle | 1.250 |
Data reduction software | MOSFLM |
Data scaling software | SCALA (3.3.22) |
Phasing software | PHASER |
Refinement software | BUSTER (2.10.3) |
Data quality characteristics
Overall | Inner shell | Outer shell | |
Low resolution limit [Å] | 120.733 | 59.838 | 2.740 |
High resolution limit [Å] | 2.600 | 8.220 | 2.600 |
Rmerge | 0.051 | 1.319 | |
Rmeas | 0.194 | 0.052 | 1.350 |
Rpim | 0.042 | 0.012 | 0.288 |
Total number of observations | 1695738 | 56437 | 251897 |
Number of reflections | 81169 | 2932 | 11640 |
<I/σ(I)> | 15.4 | 42.2 | 3.1 |
Completeness [%] | 100.0 | 99.7 | 100 |
Redundancy | 20.9 | 19.2 | 21.6 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7.2 | 277 | 12% PEG 8000, 20% glycerol, 50 mM triethanolamine-HCl (TEA) buffer pH 7.2, 100 mM KCl, 50 mM MgCl2, 5 mM oxalate, 5 mM ATP, 5 mM G6P |