3ZLH
Structure of group A Streptococcal enolase
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 | 2009-03-31 |
Detector | ADSC QUANTUM 210r |
Spacegroup name | P 4 |
Unit cell lengths | 185.795, 185.795, 56.324 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 19.750 - 2.900 |
R-factor | 0.15528 |
Rwork | 0.153 |
R-free | 0.20540 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1w6t |
RMSD bond length | 0.016 |
RMSD bond angle | 1.730 |
Data reduction software | XDS |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | REFMAC (5.7.0032) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 19.750 | 3.000 |
High resolution limit [Å] | 2.900 | 2.900 |
Rmerge | 0.430 | 1.130 |
Number of reflections | 43076 | |
<I/σ(I)> | 4.6 | 1.91 |
Completeness [%] | 99.7 | 98.8 |
Redundancy | 6 | 5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 6 | 1-3.5 M SODIUM/POTASSIUM PHOSPHATE BUFFER (PH 5-7.5); 2% PEG 400 |