1BUX
3'-PHOSPHORYLATED NUCLEOTIDES BINDING TO NUCLEOSIDE DIPHOSPHATE KINASE
Experimental procedure
Source type | ROTATING ANODE |
Source details | RIGAKU |
Temperature [K] | 277 |
Detector technology | IMAGE PLATE |
Collection date | 1997-04 |
Detector | RIGAKU |
Spacegroup name | P 31 2 1 |
Unit cell lengths | 71.500, 71.500, 153.900 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 10.000 - 2.800 |
R-factor | 0.204 |
Rwork | 0.204 |
R-free | 0.31200 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.013 |
RMSD bond angle | 1.530 * |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Phasing software | X-PLOR |
Refinement software | X-PLOR |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 15.000 | 2.900 |
High resolution limit [Å] | 2.800 | 2.800 |
Rmerge | 0.073 | |
Number of reflections | 10703 | |
<I/σ(I)> | 18 | 3.3 |
Completeness [%] | 91.5 | 95.7 |
Redundancy | 2.8 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | Vapor diffusion, hanging drop * | 8.5 * | pH 7.5 |
Crystallization Reagents in Literatures
ID | crystal ID | solution | reagent name | concentration (unit) | details |
1 | 1 | reservoir | PEG550 | 30-32 (%) | |
2 | 1 | reservoir | Tris-HCl | 50 (mM) | |
3 | 1 | reservoir | 20 (mM) | ||
4 | 1 | drop | protein | 5 (mg/ml) | |
5 | 1 | drop | PEG550 | 15-16 (%) | |
6 | 1 | drop | Tris-HCl | 50 (mM) | |
7 | 1 | drop | 20 (mM) | ||
8 | 1 | drop | 3'-amino-ADP | 17 (mM) |