5FGN
Integral membrane protein lipooligosaccharide phosphoethanolamine transferase A (EptA) from Neisseria meningitidis
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | AUSTRALIAN SYNCHROTRON BEAMLINE MX2 |
Synchrotron site | Australian Synchrotron |
Beamline | MX2 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2013-08-09 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 0.9537 |
Spacegroup name | I 4 2 2 |
Unit cell lengths | 187.285, 187.285, 205.125 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 46.821 - 2.750 |
R-factor | 0.2155 |
Rwork | 0.214 |
R-free | 0.24140 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4kav |
RMSD bond length | 0.010 |
RMSD bond angle | 1.033 |
Data reduction software | XDS |
Data scaling software | SCALA (3.3.20) |
Phasing software | PHASER |
Refinement software | PHENIX (1.9_1692) |
Data quality characteristics
Overall | Inner shell | Outer shell | |
Low resolution limit [Å] | 138.308 | 46.821 | 2.900 |
High resolution limit [Å] | 2.750 | 8.700 | 2.750 |
Rmerge | 0.034 | 2.366 | |
Rmeas | 0.278 | 0.037 | 2.488 |
Rpim | 0.086 | 0.013 | 0.762 |
Total number of observations | 487530 | 15544 | 70794 |
Number of reflections | 47424 | ||
<I/σ(I)> | 9.3 | 34.4 | 1.3 |
Completeness [%] | 100.0 | 99.3 | 100 |
Redundancy | 10.3 | 9.5 | 10.4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 293 | Ammonium Sulphate, Hepes, Beta octylglucoside |