5T3D
Crystal structure of holo-EntF a nonribosomal peptide synthetase in the thioester-forming conformation
Replaces: 4ZXJExperimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 23-ID-B |
Synchrotron site | APS |
Beamline | 23-ID-B |
Temperature [K] | 113.15 |
Detector technology | CCD |
Collection date | 2015-03-14 |
Detector | MARMOSAIC 300 mm CCD |
Wavelength(s) | 1.0332 |
Spacegroup name | P 41 21 2 |
Unit cell lengths | 127.711, 127.711, 186.940 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 60.427 - 2.800 |
R-factor | 0.1877 |
Rwork | 0.185 |
R-free | 0.23190 |
Structure solution method | SAD |
RMSD bond length | 0.012 |
RMSD bond angle | 1.307 |
Data reduction software | iMOSFLM |
Data scaling software | SCALA (0.3.8) |
Phasing software | PHASER |
Refinement software | PHENIX (1.10.1_2155) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 60.427 | 2.920 |
High resolution limit [Å] | 2.800 | 2.800 |
Rmerge | 0.098 | 0.635 |
Number of reflections | 38818 | |
<I/σ(I)> | 9.85 | 2.1 |
Completeness [%] | 100.0 | 100 |
Redundancy | 4.5 | 4.5 |
CC(1/2) | 0.997 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7.5 | 293.15 | 100 MM BTP PH 7.5, 125-150 MM MGCL2, AND 22-28% PEG 4000, |