2BSP
BACILLUS SUBTILIS PECTATE LYASE R279K MUTANT
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SRS BEAMLINE PX9.6 |
Synchrotron site | SRS |
Beamline | PX9.6 |
Temperature [K] | 290 |
Detector technology | IMAGE PLATE |
Collection date | 1996-02-15 |
Detector | MARRESEARCH |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 51.430, 69.710, 60.230 |
Unit cell angles | 90.00, 112.65, 90.00 |
Refinement procedure
Resolution | 10.000 - 1.800 |
Rwork | 0.196 |
R-free | 0.22500 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | WILD TYPE STRUCTURE |
RMSD bond length | 0.005 |
RMSD bond angle | 0.020 |
Data reduction software | DENZO |
Data scaling software | CCP4 ((AGROVATA) |
Phasing software | X-PLOR |
Refinement software | REFMAC |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 56.000 | 1.850 |
High resolution limit [Å] | 1.800 | 1.800 |
Rmerge | 0.085 | 0.152 |
Number of reflections | 35454 | |
<I/σ(I)> | 12 | 4 |
Completeness [%] | 96.0 | 99 |
Redundancy | 2.6 | 2.6 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 4.6 | 30 % PEG 4000 0.2 M AMMONIUM SULPHATE 0.1 M SODIUM ACETATE AT PH 4.6 |