1SUS
Crystal structure of alfalfa feruoyl coenzyme A 3-O-methyltransferase
Experimental procedure
Experimental method | MAD |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE BM30A |
Synchrotron site | ESRF |
Beamline | BM30A |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2001-04-18 |
Detector | MARRESEARCH |
Wavelength(s) | 0.97966, 0.97927, 0.97549 |
Spacegroup name | C 2 2 21 |
Unit cell lengths | 60.854, 136.486, 332.778 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 25.000 - 2.700 |
Rwork | 0.245 |
R-free | 0.28900 |
Structure solution method | MAD |
RMSD bond length | 0.008 |
RMSD bond angle | 1.700 |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Phasing software | SnB |
Refinement software | CNS |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 25.000 | 2.760 |
High resolution limit [Å] | 2.700 | 2.700 |
Number of reflections | 37858 | |
<I/σ(I)> | 19.6 | 0.92 |
Completeness [%] | 94.2 | 61.8 |
Redundancy | 2 | 1.44 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 8.5 | 288 | PEG 8000, TAPS, calcium acetate, pH 8.5, VAPOR DIFFUSION, HANGING DROP, temperature 288K |