2XH7
Engineering the enolase active site pocket: Crystal structure of the D321A mutant of yeast enolase 1
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SLS BEAMLINE X10SA |
Synchrotron site | SLS |
Beamline | X10SA |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2009-07-27 |
Detector | DECTRIS PILATUS 6M |
Spacegroup name | P 1 |
Unit cell lengths | 61.973, 62.000, 64.320 |
Unit cell angles | 67.89, 78.33, 80.60 |
Refinement procedure
Resolution | 43.690 - 1.800 |
R-factor | 0.177 |
Rwork | 0.175 |
R-free | 0.21400 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2xh4 |
RMSD bond length | 0.007 |
RMSD bond angle | 1.071 |
Data reduction software | XDS |
Data scaling software | XDS |
Phasing software | MOLREP |
Refinement software | REFMAC (5.2.0019) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 1.910 |
High resolution limit [Å] | 1.800 | 1.800 |
Rmerge | 0.150 | 0.680 |
Number of reflections | 73622 | |
<I/σ(I)> | 11.43 | 3.12 |
Completeness [%] | 91.3 | 89.6 |
Redundancy | 1.81 | 1.75 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 8 | 18% PEG 6000, 0.2M MAGNESIUM CHLORIDE, 0.1M TRIS PH 8.0 |