1XYA
X-RAY CRYSTALLOGRAPHIC STRUCTURES OF D-XYLOSE ISOMERASE-SUBSTRATE COMPLEXES POSITION THE SUBSTRATE AND PROVIDE EVIDENCE FOR METAL MOVEMENT DURING CATALYSIS
Replaces: 3XIAExperimental procedure
Spacegroup name | P 21 21 2 |
Unit cell lengths | 87.600, 99.340, 94.180 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 10.000 - 1.810 |
R-factor | 0.161 |
Rwork | 0.161 |
RMSD bond length | 0.014 |
RMSD bond angle | 2.700 |
Phasing software | X-PLOR |
Refinement software | X-PLOR |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 9999.000 * |
High resolution limit [Å] | 1.810 * |
Rmerge | 0.051 * |
Total number of observations | 243152 * |
Number of reflections | 56756 * |
Completeness [%] | 75.0 * |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | Vapor diffusion, sitting drop * | 7.5 * | taken from Farber, G.K. et al (1987). Protein Eng., 1, 459-466. * |
Crystallization Reagents in Literatures
ID | crystal ID | solution | reagent name | concentration (unit) | details |
1 | 1 | reservoir | ammonium sulfate | 45 (%sat) | |
2 | 1 | drop | enzyme | 43 (mg/ml) | |
3 | 1 | drop | PIPES | 0.025 (M) | |
4 | 1 | drop | 0.010 (M) | ||
5 | 1 | drop | 0.001 (M) |