1I1O
ROOM TEMPERATURE CRYSTAL STRUCTURE FLAVODOXIN D. VULGARIS MUTANT Y98H AT 2.0 ANG. RESOLUTION
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | ROTATING ANODE |
Source details | SIEMENS |
Temperature [K] | 293 |
Detector technology | AREA DETECTOR |
Collection date | 1991-02-04 |
Detector | XENTRONICS |
Wavelength(s) | 1.5418 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 41.960, 61.450, 57.040 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 8.000 - 2.000 |
R-factor | 0.172 |
Rwork | 0.172 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | Flavodoxin D.vulgaris p2a |
RMSD bond length | 0.013 * |
RMSD bond angle | 2.600 |
Data scaling software | X-GEN |
Phasing software | MERLOT |
Refinement software | PROFFT |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 8.000 | 8.000 |
High resolution limit [Å] | 2.000 | 2.000 |
Rmerge | 0.060 | 0.060 |
Number of reflections | 9294 | |
<I/σ(I)> | 5 | |
Completeness [%] | 90.0 | 98 |
Redundancy | 1.5 | 1.5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | unknown * | 7.5 * | 293 | 3.2 M Ammonium Sulfate, Tris.buffer, pH 7.3, VAPOR DIFFUSION, HANGING DROP, temperature 293K |
Crystallization Reagents in Literatures
ID | crystal ID | solution | reagent name | concentration (unit) | details |
1 | 1 | 1 | protein | 0.8-1.0 (%) | |
2 | 1 | 2 | ammonium sulfate | 3.1 (M) | |
3 | 1 | 2 | Tris-HCl | 0.1 (M) |