1AUI
HUMAN CALCINEURIN HETERODIMER
Experimental procedure
| Source type | SYNCHROTRON |
| Source details | CHESS BEAMLINE F1 |
| Synchrotron site | CHESS |
| Beamline | F1 |
| Temperature [K] | 87 |
| Detector technology | IMAGE PLATE |
| Collection date | 1994-10 |
| Detector | FUJI |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 48.810, 104.340, 177.770 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 10.000 - 2.100 |
| R-factor | 0.187 |
| Rwork | 0.187 |
| Structure solution method | MULTIPLE ISOMORPHOUS REPLACEMENT PLUS ANOMALOUS SCATTERING |
| RMSD bond length | 0.019 |
| RMSD bond angle | 23.320 * |
| Data reduction software | DENZO |
| Data scaling software | SCALEPACK |
| Phasing software | MLPHARE |
| Refinement software | XTALVIEW |
Data quality characteristics
| Overall | |
| Low resolution limit [Å] | 30.000 |
| High resolution limit [Å] | 2.100 |
| Rmerge | 0.069 * |
| Number of reflections | 50007 |
| Completeness [%] | 92.5 |
| Redundancy | 4 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | unknown * | 7.5 | PROTEIN WAS CRYSTALLIZED FROM 8% PEG 6000, 0.1M CACL2, 0.1M TES PH 7.5, 1 MM DTT. |
Crystallization Reagents in Literatures
| ID | crystal ID | solution | reagent name | concentration (unit) | details |
| 1 | 1 | 1 | PEG6000 |






