8EU4
Escherichia coli pyruvate kinase A301S
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | AUSTRALIAN SYNCHROTRON BEAMLINE MX1 |
Synchrotron site | Australian Synchrotron |
Beamline | MX1 |
Temperature [K] | 110 |
Detector technology | CCD |
Collection date | 2012-12-17 |
Detector | ADSC QUANTUM 210r |
Wavelength(s) | 0.9537 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 129.334, 74.473, 240.826 |
Unit cell angles | 90.00, 90.04, 90.00 |
Refinement procedure
Resolution | 48.170 - 2.100 |
R-factor | 0.2037 |
Rwork | 0.202 |
R-free | 0.22360 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4yng |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | PHENIX (1.19.2_4158) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 48.170 | 2.175 |
High resolution limit [Å] | 2.100 | 2.100 |
Rmerge | 0.060 | |
Number of reflections | 267878 | 26557 |
<I/σ(I)> | 11.61 | 2.16 |
Completeness [%] | 100.0 | 100 |
Redundancy | 2 | |
CC(1/2) | 0.997 | 0.734 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 293 | 0.1M (Malic acid, MES, Tris), 25 % w/v PEG 1500 |