5XOP
Crystal Structure of N-terminal domain EhCaBP1 EF-2 mutant
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE BM14 |
Synchrotron site | ESRF |
Beamline | BM14 |
Temperature [K] | 77.15 |
Detector technology | CCD |
Collection date | 2013-04-20 |
Detector | MARRESEARCH |
Wavelength(s) | 0.97 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 44.690, 101.359, 107.475 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 73.740 - 1.900 |
R-factor | 0.2122 |
Rwork | 0.210 |
R-free | 0.24980 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2nxq |
RMSD bond length | 0.019 |
RMSD bond angle | 1.881 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | REFMAC (5.8.0131) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 73.740 | 1.930 |
High resolution limit [Å] | 1.900 | 1.900 |
Rmerge | 0.888 | |
Number of reflections | 39381 | 39381 |
<I/σ(I)> | 33 | 1.9 |
Completeness [%] | 98.7 | 92.3 |
Redundancy | 7.7 | 7.7 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 289 | 58%-63% MPD, 5mM Cacl2 |