5IFP
STRUCTURE OF BETA-GALACTOSIDASE FROM ASPERGILLUS NIGER
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | ALBA BEAMLINE XALOC |
| Synchrotron site | ALBA |
| Beamline | XALOC |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2013-09-26 |
| Detector | DECTRIS PILATUS3 6M |
| Wavelength(s) | 0.97948 |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 85.570, 111.421, 126.730 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 83.680 - 1.710 |
| R-factor | 0.15127 |
| Rwork | 0.150 |
| R-free | 0.17136 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 4iug |
| RMSD bond length | 0.006 |
| RMSD bond angle | 1.272 |
| Data reduction software | MOSFLM (7.0.9) |
| Data scaling software | Aimless (0.5.21) |
| Phasing software | MOLREP (11.4.04) |
| Refinement software | REFMAC (5.8.0135) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 83.680 | 1.740 |
| High resolution limit [Å] | 1.710 | 1.710 |
| Rmerge | 0.115 | 0.599 |
| Number of reflections | 131079 | |
| <I/σ(I)> | 11.5 | 3.7 |
| Completeness [%] | 99.9 | 99.9 |
| Redundancy | 6.8 | 6.2 |
| CC(1/2) | 0.997 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 5.5 | 291 | 21% (W/V) PEG 3350, 0.1M BIS-TRIS BUFFER PH 5.5 , 0.2M LITHIUM SULPHATE |






