2H5G
Crystal structure of human pyrroline-5-carboxylate synthetase
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SLS BEAMLINE X10SA |
Synchrotron site | SLS |
Beamline | X10SA |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2005-05-06 |
Detector | MARRESEARCH |
Wavelength(s) | 0.97925 |
Spacegroup name | P 21 21 2 |
Unit cell lengths | 122.022, 137.402, 72.057 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 46.560 - 2.250 |
R-factor | 0.23248 |
Rwork | 0.230 |
R-free | 0.27211 |
Structure solution method | SAD |
RMSD bond length | 0.020 |
RMSD bond angle | 1.478 |
Data scaling software | SCALEPACK |
Phasing software | SOLVE |
Refinement software | REFMAC (5.2.0019) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 91.290 | 2.350 |
High resolution limit [Å] | 2.250 | 2.250 |
Rmerge | 0.056 | 0.261 |
Number of reflections | 57217 | |
<I/σ(I)> | 4.39 | |
Completeness [%] | 98.2 | 88.3 |
Redundancy | 6.89 | 3.67 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 5.5 | 293 | 1% PEG 3350, 1.0M (NH4)2SO4, 0.1M BIS-TRIS, pH 5.5, VAPOR DIFFUSION, SITTING DROP, temperature 293K |