8ELB
CTX-M-14 beta-lactamase mutant- N132A
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ALS BEAMLINE 8.2.1 |
Synchrotron site | ALS |
Beamline | 8.2.1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2019-09-11 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 1.00001 |
Spacegroup name | C 2 2 21 |
Unit cell lengths | 59.230, 60.410, 264.100 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 42.290 - 1.500 |
R-factor | 0.19101 |
Rwork | 0.189 |
R-free | 0.22212 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1ylt |
RMSD bond length | 0.035 |
RMSD bond angle | 2.122 |
Data reduction software | iMOSFLM |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | REFMAC (5) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 42.290 | 1.520 |
High resolution limit [Å] | 1.500 | 1.500 |
Rmerge | 0.183 | 0.118 |
Rmeas | 0.132 | |
Rpim | 0.084 | 0.058 |
Number of reflections | 69726 | 2475 |
<I/σ(I)> | 6 | 7.9 |
Completeness [%] | 95.3 | 95.3 |
Redundancy | 5.9 | |
CC(1/2) | 0.975 | 0.975 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 8.5 | 296 | 0.1 M Tris-HCl, PEG 10,000 (20% w/v) |