Nitrogenase MoFe-Protein at 1.16 Å Resolution: A Central Ligand in the FeMo-Cofactor
California Institute of Technology · Howard Hughes Medical Institute · +1 more institution
Abstract
A high-resolution crystallographic analysis of the nitrogenase MoFe-protein reveals a previously unrecognized ligand coordinated to six iron atoms in the center of the catalytically essential FeMo-cofactor. The electron density for this ligand is masked in structures with resolutions lower than 1.55 angstroms, owing to Fourier series termination ripples from the surrounding iron and sulfur atoms in the cofactor. The central atom completes an approximate tetrahedral coordination for the six iron atoms, instead of the trigonal coordination proposed on the basis of lower resolution structures. The crystallographic refinement at 1.16 angstrom resolution is consistent with this newly detected component being a…
Citation impact
- FWCI
- 77.72
- Percentile
- 100%
- References
- 25
Authors
7- OEOliver Einsle
California Institute of Technology, Howard Hughes Medical Institute
- FAF. Akif Tezcan
California Institute of Technology
- SLSusana L. A. Andrade
California Institute of Technology, Howard Hughes Medical Institute
- BSBenedikt Schmid
California Institute of Technology
- MYMika Yoshida
California Institute of Technology, Howard Hughes Medical Institute
Topics & keywords
- Nitrogenase
- Crystallography
- Chemistry
- Ligand (biochemistry)
- Cofactor
- Resolution (logic)
- Atom (system on chip)
- Sulfur
- Clean water and sanitation