2CIM
Crystal structure of Methanosarcina barkeri seryl-tRNA synthetase
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SLS BEAMLINE X06SA |
Synchrotron site | SLS |
Beamline | X06SA |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2004-07-24 |
Detector | MARRESEARCH |
Spacegroup name | P 32 2 1 |
Unit cell lengths | 97.150, 97.150, 268.500 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 19.940 - 2.510 |
R-factor | 0.202 |
Rwork | 0.199 |
R-free | 0.25200 |
Structure solution method | MAD |
RMSD bond length | 0.008 |
RMSD bond angle | 1.115 |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Phasing software | SHARP |
Refinement software | REFMAC (5.2.0005) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.590 |
High resolution limit [Å] | 2.500 | 2.500 |
Rmerge | 0.080 | 0.380 |
Number of reflections | 51404 | |
<I/σ(I)> | 27.9 | 4.3 |
Completeness [%] | 99.9 | 99.8 |
Redundancy | 9.7 | 8.1 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 5.9 | 294 | PROTEIN WAS CRYSTALLIZED FROM 5-9% MPD, 50 MM MES, PH 5.9; 294 K; HANGING DROP VAPOR DIFFUSION |