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 |