4MFQ
The crystal structure of acyltransferase in complex with CoA and 10C-Teicoplanin
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | NSRRC BEAMLINE BL15A |
Synchrotron site | NSRRC |
Beamline | BL15A |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2013-03-19 |
Detector | RAYONIX MX300HE |
Wavelength(s) | 1.00000 |
Spacegroup name | P 65 |
Unit cell lengths | 133.471, 133.471, 49.196 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 30.000 - 2.000 |
R-factor | 0.17501 |
Rwork | 0.173 |
R-free | 0.21653 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4mfj |
RMSD bond length | 0.011 |
RMSD bond angle | 1.456 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER (for MR) |
Refinement software | REFMAC (5.6.0117) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 30.000 | 2.070 |
High resolution limit [Å] | 2.000 | 2.000 |
Number of reflections | 32571 | |
Completeness [%] | 100.0 | 100 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 6.5 | 293 | 0.1mM MES, 0.2M ammonium sulphate, 30%(V/V) PEG5000 MME, pH 6.5, VAPOR DIFFUSION, HANGING DROP, temperature 293K |