1LG5
Crystal Structure Analysis of the HCA II Mutant T199P in complex with beta-mercaptoethanol
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | ROTATING ANODE |
Source details | ENRAF-NONIUS FR591 |
Temperature [K] | 298 |
Detector technology | IMAGE PLATE |
Collection date | 1997-12-01 |
Detector | MAC Science DIP-2030H |
Wavelength(s) | 1.5418 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 72.840, 44.803, 76.457 |
Unit cell angles | 90.00, 92.51, 90.00 |
Refinement procedure
Resolution | 20.000 - 1.750 |
R-factor | 0.20648 |
Rwork | 0.205 |
R-free | 0.22700 * |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.010 |
RMSD bond angle | 1.420 |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Phasing software | X-PLOR |
Refinement software | REFMAC (5.0) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 20.000 | 1.810 |
High resolution limit [Å] | 1.750 | 1.750 |
Rmerge | 0.066 | 0.360 |
Total number of observations | 52605 * | |
Number of reflections | 22169 | |
Completeness [%] | 93.1 | 94.5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7.8 | 4 * | PEG 2000 or 3350, Tris-HCl, BME, pH 7.8, VAPOR DIFFUSION, HANGING DROP, temperature 293K |
Crystallization Reagents in Literatures
ID | crystal ID | solution | reagent name | concentration (unit) | details |
1 | 1 | reservoir | PEG2000 | 20-22 (%) | or PEG3350 |
2 | 1 | reservoir | Tris | 50 (mM) | pH7.8 |
3 | 1 | reservoir | beta-mercaptoethanol | 3 (mM) | |
4 | 1 | drop | protein | 13 (mg/ml) | |
5 | 1 | drop | Tris | 25 (mM) | pH8.0 |
6 | 1 | drop | PEG2000 | 13 (%) | or PEG3350 |
7 | 1 | drop | Tris | 50 (mM) | pH7.8 |
8 | 1 | drop | beta-mercaptoethanol | 3 (mM) |