4EQE
Crystal structure of histidine triad nucleotide-binding protein 1 (HINT1) from human complexed with Lys-AMS
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 21-ID-D |
Synchrotron site | APS |
Beamline | 21-ID-D |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2011-07-06 |
Detector | MARMOSAIC 300 mm CCD |
Wavelength(s) | 1.033 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 79.001, 46.409, 64.225 |
Unit cell angles | 90.00, 95.46, 90.00 |
Refinement procedure
Resolution | 24.396 - 1.520 |
R-factor | 0.1431 |
Rwork | 0.142 |
R-free | 0.16220 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 6rhn |
RMSD bond length | 0.008 |
RMSD bond angle | 1.189 |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Phasing software | MOLREP |
Refinement software | PHENIX (1.7.1_743) |
Data quality characteristics
Overall | Inner shell | Outer shell | |
Low resolution limit [Å] | 25.000 | 25.000 | 1.570 |
High resolution limit [Å] | 1.520 | 3.270 | 1.520 |
Rmerge | 0.048 | 0.026 | 0.299 |
Number of reflections | 35542 | ||
<I/σ(I)> | 13.2 | ||
Completeness [%] | 99.3 | 99.9 | 98.2 |
Redundancy | 7.5 | 7.4 | 6.5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 7.5 | 291 | 25-28% PEG3350, 0.1 M HEPES, pH 7.5, VAPOR DIFFUSION, SITTING DROP, temperature 291K |