6L1R
Crystal structure of N-terminal domain of human SSRP1
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | ROTATING ANODE |
Source details | RIGAKU MICROMAX-002+ |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2014-05-23 |
Detector | AGILENT EOS CCD |
Wavelength(s) | 1.5418 |
Spacegroup name | P 43 |
Unit cell lengths | 37.825, 37.825, 68.089 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 16.417 - 1.798 |
R-factor | 0.1764664673 |
Rwork | 0.173 |
R-free | 0.21000 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4khb |
RMSD bond length | 0.008 |
RMSD bond angle | 1.057 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | PHENIX (1.11.1_2575) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 16.417 | 1.880 |
High resolution limit [Å] | 1.798 | 1.800 |
Number of reflections | 8686 | 873 |
<I/σ(I)> | 18.16 | |
Completeness [%] | 95.7 | |
Redundancy | 3.4 | |
CC(1/2) | 0.423 | 0.360 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 287 | 30%(w/v) PEG 1500, 40% 1,2-Butanediol |