4M8B
Fungal Protein
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ALS BEAMLINE 8.3.1 |
Synchrotron site | ALS |
Beamline | 8.3.1 |
Temperature [K] | 80 |
Detector technology | CCD |
Collection date | 2013-01-10 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 1.115869 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 90.293, 103.401, 73.178 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 38.250 - 2.610 |
Rwork | 0.198 |
R-free | 0.23540 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | The starting model was a poor initial model built from MAD phases of a SeMet derivative. |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | SOLVE |
Refinement software | PHENIX |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 68.012 | 2.750 |
High resolution limit [Å] | 2.610 | 2.610 |
Rmerge | 0.512 | |
Number of reflections | 19969 | |
<I/σ(I)> | 9.7 | 1.5 |
Completeness [%] | 93.6 | 87.9 |
Redundancy | 3.6 | 3.4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7.5 | 298 | 2 uL drops were a 1 to 1 mixture of protein with a well solution of 9 mM Calcium chloride, 10 mM Spermine, 50 mM Sodium cacodylate pH 7, 4.5% Isopropanol, 3.5% Ethylene glycol. Cryoprotection involved a 4 to 6 mixture of 25% Glucose/Ethylene Glycol and well solution., VAPOR DIFFUSION, HANGING DROP, temperature 298K |