4LPQ
Crystal structure of the L,D-transpeptidase (residues 123-326) from Xylanimonas cellulosilytica DSM 15894
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 | 2013-02-25 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 0.9794 |
Spacegroup name | P 43 21 2 |
Unit cell lengths | 62.849, 62.849, 167.210 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 23.610 - 1.370 |
R-factor | 0.1231 |
Rwork | 0.122 |
R-free | 0.14555 |
Structure solution method | SAD |
RMSD bond length | 0.024 |
RMSD bond angle | 2.176 |
Data reduction software | HKL-3000 |
Data scaling software | HKL-3000 |
Phasing software | HKL-3000 |
Refinement software | REFMAC (5.7.0029) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 23.620 | 1.390 |
High resolution limit [Å] | 1.370 | 1.370 |
Rmerge | 0.086 | |
Number of reflections | 69682 | |
<I/σ(I)> | 29 | |
Completeness [%] | 97.6 | 87 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 7 | 289 | 30% Peg6000, 1M Lithium Chloride, 0.1 M Sodium acetate, pH 7.0, VAPOR DIFFUSION, SITTING DROP, temperature 289K |