4YL9
Crystal Structure of wild-type of hsp14.1 from Sulfolobus solfatataricus P2
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL17U |
Synchrotron site | SSRF |
Beamline | BL17U |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2014-06-05 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 0.97915 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 65.733, 39.108, 119.674 |
Unit cell angles | 90.00, 91.64, 90.00 |
Refinement procedure
Resolution | 39.875 - 2.353 |
R-factor | 0.2335 |
Rwork | 0.233 |
R-free | 0.25150 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3aab |
RMSD bond length | 0.009 |
RMSD bond angle | 0.931 |
Phasing software | PHASER |
Refinement software | PHENIX ((phenix.refine: 1.8.4_1496)) |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 50.000 |
High resolution limit [Å] | 2.350 |
Number of reflections | 25552 |
<I/σ(I)> | 13.6 |
Completeness [%] | 99.3 |
Redundancy | 3.6 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | EVAPORATION | 293 | calcium chloride dehydrate, 2-methyl-2,4-pentanediol, bis-tris (pH 6.5), ethylenediaminetetraacetic acid disodium salt dihydrate |