1QF7
STRUCTURE OF THE MUTANT HIS392GLN OF CATALASE HPII FROM E. COLI
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | ROTATING ANODE |
Source details | RIGAKU RU200 |
Temperature [K] | 100 |
Detector technology | IMAGE PLATE |
Collection date | 1998-10-01 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 93.400, 132.920, 121.670 |
Unit cell angles | 90.00, 109.47, 90.00 |
Refinement procedure
Resolution | 20.000 - 2.200 |
R-factor | 0.144 * |
Rwork | 0.144 |
R-free | 0.21000 |
Structure solution method | OTHER |
Starting model (for MR) | 1iph |
RMSD bond length | 0.015 |
RMSD bond angle | 16.100 * |
Data reduction software | MOSFLM |
Data scaling software | CCP4 ((SCALA)) |
Phasing software | CCP4 |
Refinement software | REFMAC |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 20.000 | 2.200 |
High resolution limit [Å] | 2.120 | 2.120 |
Rmerge | 0.080 | 0.210 |
Number of reflections | 137604 | |
<I/σ(I)> | 10.4 | 5.1 |
Completeness [%] | 96.6 | 95 |
Redundancy | 3 | 2.5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | Vapor diffusion, hanging drop * | 9 | Bravo, J., (1995) Structure, 3, 491. * |
Crystallization Reagents in Literatures
ID | crystal ID | solution | reagent name | concentration (unit) | details |
1 | 1 | reservoir | PEG3350 | 15 (%(w/v)) | |
2 | 1 | reservoir | 1.5 (M) | ||
3 | 1 | reservoir | Tris-HCl | 0.2 (M) |