4H7W
Crystal Structure of Human C16orf57
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | DIAMOND BEAMLINE I02 |
Synchrotron site | Diamond |
Beamline | I02 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2011-05-13 |
Detector | ADSC |
Wavelength(s) | 0.97950 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 43.247, 51.070, 48.013 |
Unit cell angles | 90.00, 107.44, 90.00 |
Refinement procedure
Resolution | 45.810 - 1.100 |
R-factor | 0.13276 |
Rwork | 0.132 |
R-free | 0.15434 |
Structure solution method | SAD |
RMSD bond length | 0.027 |
RMSD bond angle | 2.225 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | SHARP |
Refinement software | REFMAC (5.6.0117) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 45.810 | 1.160 |
High resolution limit [Å] | 1.100 | 1.100 |
Rmerge | 0.076 | 0.324 |
Number of reflections | 79339 | |
<I/σ(I)> | 12 | 2.3 |
Completeness [%] | 99.0 | 99 |
Redundancy | 5.2 | 3.5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 5.6 | 291 | 25% PEG 4000, 0.2 M ammonium sulphate, 0.1 M Na citrate pH 5.6, VAPOR DIFFUSION, SITTING DROP, temperature 291K |