3O1Z
High resolution crystal structure of histidine triad nucleotide-binding protein 1 (Hint1) double cysteine mutant from rabbit
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | BESSY BEAMLINE 14.1 |
| Synchrotron site | BESSY |
| Beamline | 14.1 |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2009-09-17 |
| Detector | RAYONIX MX-225 |
| Wavelength(s) | 0.91841 |
| Spacegroup name | P 43 21 2 |
| Unit cell lengths | 39.790, 39.790, 142.630 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 26.170 - 1.300 |
| R-factor | 0.13002 |
| Rwork | 0.128 |
| R-free | 0.17612 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 3LLJ |
| RMSD bond length | 0.024 |
| RMSD bond angle | 2.039 |
| Data reduction software | MOSFLM |
| Data scaling software | SCALA |
| Phasing software | MOLREP (10.2.31) |
| Refinement software | REFMAC (5.5.0109) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 26.170 | 1.370 |
| High resolution limit [Å] | 1.300 | 1.300 |
| Rmerge | 0.103 | 0.680 |
| Number of reflections | 29103 | |
| <I/σ(I)> | 14.2 | 4.1 |
| Completeness [%] | 99.4 | 99 |
| Redundancy | 12.4 | 12.3 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 6.5 | 281 | 30% PEG 8000, 0.1M sodium cacodylate pH 6.5, protein concentration 10 mg/ml, VAPOR DIFFUSION, HANGING DROP, temperature 281K |






