3OOO
The structure of a proline dipeptidase from Streptococcus agalactiae 2603V
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 19-ID |
Synchrotron site | APS |
Beamline | 19-ID |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2010-06-27 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 0.9792 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 43.744, 58.325, 101.995 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 50.000 - 1.570 |
R-factor | 0.18788 |
Rwork | 0.186 |
R-free | 0.21473 |
Structure solution method | SAD |
RMSD bond length | 0.007 |
RMSD bond angle | 1.039 |
Data reduction software | HKL-3000 |
Data scaling software | HKL-3000 |
Phasing software | SHELXD |
Refinement software | REFMAC (5.5.0109) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 1.600 |
High resolution limit [Å] | 1.570 | 1.570 |
Rmerge | 0.050 | 0.142 |
Number of reflections | 37273 | |
<I/σ(I)> | 40.6 | |
Completeness [%] | 99.3 | 90.8 |
Redundancy | 4.7 | 3.8 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 7.5 | 297 | 0.2M sodium chloride, 0.1M HEPES pH7.5, 20%v/v 1,4-butanediol, VAPOR DIFFUSION, SITTING DROP, temperature 297K |