5NOU
Structure of cyclophilin A in complex with hexahydropyrimidin-2-one
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | DIAMOND BEAMLINE I02 |
Synchrotron site | Diamond |
Beamline | I02 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2015-05-18 |
Detector | DECTRIS PILATUS 6M-F |
Wavelength(s) | 0.97949 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 41.720, 52.680, 89.180 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 45.360 - 1.300 |
R-factor | 0.1336 |
Rwork | 0.132 |
R-free | 0.16324 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 5lud |
RMSD bond length | 0.028 |
RMSD bond angle | 2.343 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | REFMAC (5.8.0103) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 45.360 | 1.320 |
High resolution limit [Å] | 1.300 | 1.300 |
Rmerge | 0.070 | 0.620 |
Number of reflections | 48076 | |
<I/σ(I)> | 12.7 | 1.7 |
Completeness [%] | 98.1 | 84.1 |
Redundancy | 5 | 3.2 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 8 | 279.15 | PEG 8000, Tris-HCl |