1OZM
Y106F mutant of Z. mobilis TGT
Experimental procedure
| Experimental method | SINGLE WAVELENGTH | 
| Source type | ROTATING ANODE | 
| Source details | RIGAKU RU300 | 
| Temperature [K] | 100 | 
| Detector technology | IMAGE PLATE | 
| Collection date | 2001-05-28 | 
| Detector | RIGAKU RAXIS IV | 
| Wavelength(s) | 1.54 | 
| Spacegroup name | C 1 2 1 | 
| Unit cell lengths | 90.390, 64.720, 71.880 | 
| Unit cell angles | 90.00, 97.02, 90.00 | 
Refinement procedure
| Resolution | 40.000 - 1.950 | 
| Rwork | 0.184 | 
| R-free | 0.19800 | 
| Structure solution method | FOURIER SYNTHESIS | 
| Starting model (for MR) | 1pud | 
| RMSD bond length | 0.005 | 
| RMSD bond angle | 1.200 | 
| Data reduction software | DENZO | 
| Data scaling software | SCALEPACK | 
| Phasing software | CNS | 
| Refinement software | CNS | 
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 40.000 | 2.020 | 
| High resolution limit [Å] | 1.950 | 1.950 | 
| Rmerge | 0.070 *  | 0.294 *  | 
| Total number of observations | 109129 *  | |
| Number of reflections | 29077 | |
| Completeness [%] | 96.4 | 94 | 
| Redundancy | 3.8 | 
Crystallization Conditions
| crystal ID | method | pH | temperature | details | 
| 1 | VAPOR DIFFUSION, HANGING DROP | 7.5  *  | 25  *  | Romier, C., (1996) Proteins: Struct.,Funct., Genet., 24, 516.  *  | 
Crystallization Reagents in Literatures
| ID | crystal ID | solution | reagent name | concentration (unit) | details | 
| 1 | 1 | reservoir | Tris-HCl | 100 (mM) | |
| 2 | 1 | reservoir | PEG8000 | 13 (%) | |
| 3 | 1 | reservoir | dithiothreitol | 1 (mM) | |
| 4 | 1 | reservoir | agarose | 0.2 (%) | |
| 5 | 1 | drop | HEPES | 10 (mM) | pH7.5 | 
| 6 | 1 | drop | 2 (M) | ||
| 7 | 1 | drop | dithiothreitol | 1 (mM) | |
| 8 | 1 | drop | protein | 12 (mg/ml) | 






