1F3P
FERREDOXIN REDUCTASE (BPHA4)-NADH COMPLEX
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | PHOTON FACTORY BEAMLINE BL-18B |
Synchrotron site | Photon Factory |
Beamline | BL-18B |
Temperature [K] | 100 |
Detector technology | DIFFRACTOMETER |
Collection date | 1998-12-11 |
Detector | WEISSENBERG |
Spacegroup name | P 61 2 2 |
Unit cell lengths | 98.900, 98.900, 170.900 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 38.000 - 2.400 |
R-factor | 0.206 * |
Rwork | 0.205 |
R-free | 0.29100 |
RMSD bond length | 0.009 |
RMSD bond angle | 1.400 * |
Data reduction software | DENZO |
Data scaling software | CCP4 ((SCALA)) |
Phasing software | AMoRE |
Refinement software | X-PLOR (3.851) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 38.000 | 2.530 |
High resolution limit [Å] | 2.400 | 2.400 |
Rmerge | 0.085 | 0.478 |
Total number of observations | 133802 * | |
Number of reflections | 19786 * | |
<I/σ(I)> | 8.9 | |
Completeness [%] | 99.6 | 99.2 |
Redundancy | 6.7 | 6 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 5.4 * | 20 * | Yamada, T., (2000) Protein Pept.Lett., 7, 277. * |
Crystallization Reagents in Literatures
ID | crystal ID | solution | reagent name | concentration (unit) | details |
1 | 1 | drop | protein | 14.0 (mg/ml) | |
2 | 1 | reservoir | sodium formate | 2.0 (M) | |
3 | 1 | reservoir | sodium acetate | 100 (mM) |