4MGK
Selective activation of Epac1 and Epac2
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | ESRF BEAMLINE ID14-1 |
| Synchrotron site | ESRF |
| Beamline | ID14-1 |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2009-06-13 |
| Detector | ADSC QUANTUM 315r |
| Wavelength(s) | 0.972 |
| Spacegroup name | I 21 21 21 |
| Unit cell lengths | 125.040, 144.550, 227.840 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 19.900 - 2.700 |
| R-factor | 0.24995 |
| Rwork | 0.249 |
| R-free | 0.26441 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 3cf6 |
| RMSD bond length | 0.006 |
| RMSD bond angle | 0.942 |
| Data reduction software | XDS |
| Data scaling software | XSCALE |
| Phasing software | MOLREP |
| Refinement software | REFMAC (5.5.0109) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 20.000 | 2.800 |
| High resolution limit [Å] | 2.700 | 2.700 |
| Number of reflections | 56554 | |
| <I/σ(I)> | 3.03 | |
| Completeness [%] | 99.3 | 99.8 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 5.6 | 277 | 0.4M (NH4)2SO4, 1.2M LI2SO4, 0.1M CITRATE, pH 5.6, VAPOR DIFFUSION, SITTING DROP, temperature 277K |
