2QL6
human nicotinamide riboside kinase (NRK1)
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | NSLS BEAMLINE X29A |
Synchrotron site | NSLS |
Beamline | X29A |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2007-02-18 |
Detector | ADSC QUANTUM 315 |
Wavelength(s) | 1.0808 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 145.710, 99.960, 145.590 |
Unit cell angles | 90.00, 91.57, 90.00 |
Refinement procedure
Resolution | 30.000 - 2.700 |
R-factor | 0.207 |
Rwork | 0.207 |
R-free | 0.23500 |
Structure solution method | MOLECULAR REPLACEMENT |
Data reduction software | DENZO (package) |
Data scaling software | SCALEPACK (package) |
Phasing software | MOLREP |
Refinement software | CNS |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 30.000 | 2.800 |
High resolution limit [Å] | 2.700 | 2.700 |
Rmerge | 0.095 | 0.280 |
Number of reflections | 116539 | |
<I/σ(I)> | 13.2 | 2.98 |
Completeness [%] | 94.9 | 74.3 |
Redundancy | 3.1 | 2.3 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 7.8 | 298 | 8% (w/v) PEG 3350, 200 mM NH4Cl, 5 mM DTT, 5 mM Na2HPO, pH 7.8, VAPOR DIFFUSION, SITTING DROP, temperature 298K |