4Y7I
Crystal Structure of MTMR8
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | PAL/PLS BEAMLINE 7A (6B, 6C1) |
Synchrotron site | PAL/PLS |
Beamline | 7A (6B, 6C1) |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2012-06-15 |
Detector | ADSC QUANTUM 210r |
Wavelength(s) | 1.00 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 69.573, 77.188, 197.793 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 41.637 - 2.802 |
R-factor | 0.1803 |
Rwork | 0.177 |
R-free | 0.24670 |
RMSD bond length | 0.009 |
RMSD bond angle | 1.163 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | REFMAC |
Refinement software | PHENIX ((phenix.refine: 1.8.4_1496)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.850 |
High resolution limit [Å] | 2.800 | 2.800 |
Rmerge | 0.489 | |
Number of reflections | 26992 | |
<I/σ(I)> | 17 | 2.65 |
Completeness [%] | 100.0 | 100 |
Redundancy | 5.8 | 6 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION | 293 | 10mM N-(2-Acetamido)iminodiacetic acid, 1.0M ammonium phosphate dibasic |