5E1D
NTMT1 in complex with YPKRIA peptide
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 24-ID-E |
Synchrotron site | APS |
Beamline | 24-ID-E |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2015-07-11 |
Detector | ADSC QUANTUM 315 |
Wavelength(s) | 0.97921 |
Spacegroup name | P 65 2 2 |
Unit cell lengths | 107.082, 107.082, 205.946 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 29.610 - 1.450 |
R-factor | 0.1541 |
Rwork | 0.154 |
R-free | 0.16880 |
Structure solution method | FOURIER SYNTHESIS |
Starting model (for MR) | isomorphous crystal structure of same protein |
RMSD bond length | 0.017 |
RMSD bond angle | 1.825 |
Data reduction software | XDS |
Data scaling software | Aimless (0.5.12) |
Refinement software | REFMAC (5.8.0131) |
Data quality characteristics
Overall | Inner shell | Outer shell | |
Low resolution limit [Å] | 29.610 | 29.610 | 1.470 |
High resolution limit [Å] | 1.450 | 7.940 | 1.450 |
Rmerge | 0.095 | 0.038 | 1.249 |
Rmeas | 0.097 | 0.040 | 1.278 |
Rpim | 0.021 | 0.010 | 0.268 |
Total number of observations | 2648646 | 13746 | 129181 |
Number of reflections | 122141 | ||
<I/σ(I)> | 25.1 | 69.3 | 3.1 |
Completeness [%] | 99.3 | 92.7 | 98.3 |
Redundancy | 21.7 | 16.5 | 22 |
CC(1/2) | 1.000 | 0.999 | 0.838 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 277 | 26% PEG3350, 16% tacsimate |