1UTI
Mona/Gads SH3C in complex with HPK derived peptide
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE BM14 |
Synchrotron site | ESRF |
Beamline | BM14 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2003-08-15 |
Detector | MARRESEARCH |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 71.456, 27.442, 33.043 |
Unit cell angles | 90.00, 104.22, 90.00 |
Refinement procedure
Resolution | 34.710 - 1.500 |
R-factor | 0.208 |
Rwork | 0.207 |
R-free | 0.22100 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1oeb |
RMSD bond length | 0.012 |
RMSD bond angle | 1.113 |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Phasing software | AMoRE |
Refinement software | REFMAC (5.1.24) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 20.000 | 1.550 |
High resolution limit [Å] | 1.500 | 1.500 |
Rmerge | 0.030 | 0.065 |
Number of reflections | 9855 | |
<I/σ(I)> | 25.2 | 14.7 |
Completeness [%] | 97.4 | 98.2 |
Redundancy | 3.4 | 3 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 7.5 | 2M AMMONIUM SULFATE, 0.05M HEPES PH7.5, pH 7.50 |