4.8 Review

Metal Fluorides as Analogues for Studies on Phosphoryl Transfer Enzymes

Journal

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 56, Issue 15, Pages 4110-4128

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201606474

Keywords

F-19 NMR spectroscopy; enzyme mechanisms; metal fluorides; phosphoryl transfer; transition; state analogues

Funding

  1. BBSRC
  2. Cardiff University
  3. University of Manchester
  4. University of Sheffield, UK
  5. ERC Advanced Grant [AdG-322942]
  6. Biotechnology and Biological Sciences Research Council [BB/M021637/1, 1090141, BB/K016245/1] Funding Source: researchfish
  7. BBSRC [BB/M021637/1, BB/K016245/1] Funding Source: UKRI

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The 1994 structure of a transition-state analogue with AlF4- and GDP complexed to G1 alpha, a small G protein, heralded a new field of research into the structure and mechanism of enzymes that manipulate the transfer of phosphoryl (PO3-) groups. The number of enzyme structures in the PDB containing metal fluorides (MFx) as ligands that imitate either a phosphoryl or a phosphate group was 357 at the end of 2016. They fall into three distinct geometrical classes: 1) Tetrahedral complexes based on BeF3- that mimic ground-state phosphates; 2) octahedral complexes, primarily based on AlF4-, which mimic in-line anionic transition states for phosphoryl transfer; and 3) trigonal bipyramidal complexes, represented by MgF3- and putative AlF30 moieties, which mimic the geometry of the transition state. The interpretation of these structures provides a deeper mechanistic understanding into the behavior and manipulation of phosphate monoesters in molecular biology. This Review provides a comprehensive overview of these structures, their uses, and their computational development.

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