2X65
Crystal structure of T. maritima GDP-mannose pyrophosphorylase in complex with mannose-1-phosphate.
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SOLEIL BEAMLINE PROXIMA 1 |
Synchrotron site | SOLEIL |
Beamline | PROXIMA 1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2009-01-29 |
Detector | ADSC CCD |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 63.933, 91.738, 69.730 |
Unit cell angles | 90.00, 110.75, 90.00 |
Refinement procedure
Resolution | 65.210 - 2.100 |
R-factor | 0.18837 |
Rwork | 0.187 |
R-free | 0.23010 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2x5s |
RMSD bond length | 0.013 |
RMSD bond angle | 1.335 |
Data reduction software | XDS |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | REFMAC (5.5.0088) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 65.200 | 2.210 |
High resolution limit [Å] | 2.100 | 2.100 |
Rmerge | 0.040 | 0.470 |
Number of reflections | 43388 | |
<I/σ(I)> | 17.3 | 2.5 |
Completeness [%] | 98.7 | 98.8 |
Redundancy | 3.1 | 3.1 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 35% (V/V) MPD |