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Environment and coordination of FeMo-co in the nitrogenase metallochaperone NafY.

Aaron H PhillipsJose A HernandezLucı A Payá-TormoStefan BurénBruno Cuevas-ZuviríaLuis F PaciosisJeffrey G PeltonDavid E WemmerLuis Manuel Rubio
Published in: RSC chemical biology (2021)
In nitrogenase biosynthesis, the iron-molybdenum cofactor (FeMo-co) is externally assembled at scaffold proteins and delivered to the NifDK nitrogenase component by the NafY metallochaperone. Here we have used nuclear magnetic resonance, molecular dynamics, and functional analysis to elucidate the environment and coordination of FeMo-co in NafY. H121 stands as the key FeMo-co ligand. Regions near FeMo-co diverge from H121 and include the η1, α1, α2 helical lobe and a narrow path between H121 and C196.
Keyphrases
  • molecular dynamics
  • magnetic resonance
  • density functional theory
  • magnetic resonance imaging
  • tissue engineering
  • iron deficiency