6CBT
DnaG Primase C-terminal domain complex with SSB C-terminal peptide
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | AUSTRALIAN SYNCHROTRON BEAMLINE MX2 |
| Synchrotron site | Australian Synchrotron |
| Beamline | MX2 |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2009-08-29 |
| Detector | ADSC QUANTUM 315r |
| Wavelength(s) | 0.953715 |
| Spacegroup name | P 21 21 2 |
| Unit cell lengths | 70.284, 115.841, 45.742 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 45.742 - 2.100 |
| R-factor | 0.2017 |
| Rwork | 0.200 |
| R-free | 0.22900 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 1t3w |
| RMSD bond length | 0.002 |
| RMSD bond angle | 0.546 |
| Data reduction software | MOSFLM (7.0.4) |
| Data scaling software | SCALA (3.3.15) |
| Phasing software | MOLREP (9.4.09) |
| Refinement software | PHENIX ((1.13_2998: ???)) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 70.000 | 2.210 |
| High resolution limit [Å] | 2.100 | 2.100 |
| Rmerge | 0.133 | 0.560 |
| Rmeas | 0.146 | 0.610 |
| Rpim | 0.057 | 0.230 |
| Number of reflections | 21786 | 3075 |
| <I/σ(I)> | 9 | 3.1 |
| Completeness [%] | 96.8 | 95.7 |
| Redundancy | 6.3 | 6.4 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 4.6 | 294 | 9.5% w/v PEG3000, 10 mM zinc acetate, 100 mM sodium acetate, pH 4.6 |






