2A5F
Cholera toxin A1 subunit bound to its substrate, NAD+, and its human protein activator, ARF6
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 32-ID |
Synchrotron site | APS |
Beamline | 32-ID |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2004-11-08 |
Detector | CUSTOM-MADE |
Wavelength(s) | 0.97943 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 44.905, 90.925, 98.001 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 43.150 - 2.020 |
R-factor | 0.18369 |
Rwork | 0.181 |
R-free | 0.23075 |
Structure solution method | Isomorphous replacement |
Starting model (for MR) | CTA1:ARF6-GTP |
RMSD bond length | 0.014 |
RMSD bond angle | 1.561 |
Data reduction software | HKL-2000 |
Data scaling software | CCP4 ((SCALA)) |
Refinement software | REFMAC (5.2.0005) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.090 |
High resolution limit [Å] | 2.020 | 2.020 |
Number of reflections | 25861 | |
Completeness [%] | 97.5 | 81.7 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 6.5 | 298 | PEG2000mme, cacodylate, pH 6.5, VAPOR DIFFUSION, SITTING DROP, temperature 298K |