4NVC
Predicting protein conformational response in prospective ligand discovery
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ALS BEAMLINE 8.3.1 |
Synchrotron site | ALS |
Beamline | 8.3.1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2011-10-25 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 1.11587 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 50.840, 73.930, 104.400 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 31.500 - 1.600 |
R-factor | 0.1444 |
Rwork | 0.142 |
R-free | 0.18470 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.015 |
RMSD bond angle | 1.434 |
Data scaling software | XSCALE |
Phasing software | PHASER |
Refinement software | PHENIX (1.8.2_1309) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 31.500 | 1.650 |
High resolution limit [Å] | 1.600 | 1.600 |
Rmerge | 0.040 | 0.100 |
Number of reflections | 44139 | |
<I/σ(I)> | 20 | 6.3 |
Completeness [%] | 84.8 | 84.8 |
Redundancy | 3.6 | 2.1 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 6 | 283 | Compound soaked into crystal grown in equal volume of 500mM MES buffer (pH 6.0) and 25% MPD, VAPOR DIFFUSION, HANGING DROP, temperature 283K |