6UHL
Crystal Structure of C148 mGFP-scDNA-1
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 21-ID-F |
Synchrotron site | APS |
Beamline | 21-ID-F |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2018-07-03 |
Detector | RAYONIX MX-300 |
Wavelength(s) | 0.97872 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 64.870, 52.290, 86.800 |
Unit cell angles | 90.00, 94.13, 90.00 |
Refinement procedure
Resolution | 43.290 - 1.910 |
R-factor | 0.2304 |
Rwork | 0.228 |
R-free | 0.27300 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4eul |
RMSD bond length | 0.009 |
RMSD bond angle | 1.776 |
Data reduction software | xia2 |
Data scaling software | Aimless |
Phasing software | PHENIX |
Refinement software | REFMAC (5.8.0257) |
Data quality characteristics
Overall | Inner shell | Outer shell | |
Low resolution limit [Å] | 43.290 | 43.290 | 1.960 |
High resolution limit [Å] | 1.910 | 8.540 | 1.910 |
Rmerge | 0.122 | 0.051 | 1.313 |
Rmeas | 0.128 | 0.054 | 1.444 |
Rpim | 0.040 | 0.017 | 0.579 |
Total number of observations | 435564 | ||
Number of reflections | 43945 | 547 | 2202 |
<I/σ(I)> | 12.1 | 29.4 | 1.3 |
Completeness [%] | 96.9 | 98.6 | 67.2 |
Redundancy | 9.9 | 9.2 | 5.8 |
CC(1/2) | 0.998 | 0.998 | 0.492 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 295 | 1 microliter C148 mGFP-scDNA-1 (5 mg/mL (protein concentration) in 10 mM Tris Buffer pH 7.4, 137 mM NaCl) + 1 microliter crystallization condition (0.1 M SPG Buffer pH 8, 25% (w/v) PEG 1500) in a sitting drop with a 70 microliter reservoir (0.1 M SPG Buffer pH 8, 25% (w/v) PEG 1500) |