A diiron protein autogenerates a valine-phenylalanine cross-link

Science. 2011 May 20;332(6032):929. doi: 10.1126/science.1205687.

Abstract

All known internal covalent cross-links in proteins involve functionalized groups having oxygen, nitrogen, or sulfur atoms present to facilitate their formation. Here, we report a carbon-carbon cross-link between two unfunctionalized side chains. This valine-phenyalanine cross-link, produced in an oxygen-dependent reaction, is generated by its own carboxylate-bridged diiron center and serves to stabilize the metallocenter. This finding opens the door to new types of posttranslational modifications, and it demonstrates new catalytic potential of diiron centers.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Binding Sites
  • Crystallography, X-Ray
  • Cyanophora / chemistry*
  • Cyanophora / metabolism
  • Iron / chemistry*
  • Metalloproteins / chemistry*
  • Metalloproteins / metabolism
  • Oxygen / chemistry
  • Phenylalanine / chemistry*
  • Plant Proteins / chemistry
  • Plant Proteins / metabolism
  • Protein Conformation
  • Protein Structure, Secondary
  • Valine / chemistry*

Substances

  • Metalloproteins
  • Plant Proteins
  • Phenylalanine
  • Iron
  • Valine
  • Oxygen

Associated data

  • PDB/3QHB