1G0F
SITE-SPECIFIC MUTANT (HIS64 REPLACED WITH ALA) OF HUMAN CARBONIC ANHYDRASE II
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | ROTATING ANODE |
Source details | RIGAKU |
Temperature [K] | 300 |
Detector technology | IMAGE PLATE |
Collection date | 2000-03-03 |
Detector | RIGAKU RAXIS |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 42.484, 41.616, 72.658 |
Unit cell angles | 90.00, 104.52, 90.00 |
Refinement procedure
Resolution | 25.000 - 1.600 |
R-factor | 0.179 |
Rwork | 0.179 |
R-free | 0.19800 |
RMSD bond length | 0.005 |
RMSD bond angle | 1.300 |
Data scaling software | SCALEPACK |
Phasing software | CNS |
Refinement software | CNS |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 25.000 | 25.000 |
High resolution limit [Å] | 1.600 | 1.600 |
Rmerge | 0.052 | 0.169 * |
Total number of observations | 139667 * | |
Number of reflections | 27019 | 1979 * |
<I/σ(I)> | 19.5 | |
Completeness [%] | 82.6 | 61.5 * |
Redundancy | 5.17 | 5.17 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7.8 | 4 * | Ammonium Sulfate, Mercury Chloride, Tris HCl, pH 7.8, VAPOR DIFFUSION, HANGING DROP, temperature 277K |
Crystallization Reagents in Literatures
ID | crystal ID | solution | reagent name | concentration (unit) | details |
1 | 1 | drop | protein | 10 (M) | |
2 | 1 | drop | Tris-HCl | 50 (mM) | |
3 | 1 | drop | 1 (mM) | ||
4 | 1 | reservoir | ammonium sulfate | 2.3-2.5 (M) | |
5 | 1 | reservoir | Tris-HCl | 50 (mM) | |
6 | 1 | reservoir | 1 (mM) |