Protein-Derived Cofactors. Expanding the Scope of Post-Translational Modifications
- 17 April 2007
- journal article
- review article
- Published by American Chemical Society (ACS) in Biochemistry
- Vol. 46 (18) , 5283-5292
- https://doi.org/10.1021/bi700468t
Abstract
Recent advances in enzymology, structural biology, and protein chemistry have extended the scope of the field of cofactor-dependent enzyme catalysis. It has been documented that catalytic and redox-active prosthetic groups may be derived from post-translational modification of amino acid residues of proteins. These protein-derived cofactors typically arise from the oxygenation of aromatic residues, covalent cross-linking of amino acid residues, or cyclization or cleavage of internal amino acid residues. In some cases, the post-translation modification is a self-processing event, whereas in others, another processing enzyme is required. The characterization of protein-derived cofactors and their mechanisms of biogenesis introduce a new dimension to our current views about protein evolution and protein structure−function relationships.Keywords
This publication has 21 references indexed in Scilit:
- Probing the structure and bifunctionality of catalase-peroxidase (KatG)Journal of Inorganic Biochemistry, 2006
- Unusual Cys-Tyr Covalent Bond in a Large CatalaseJournal of Molecular Biology, 2004
- Cu(I)-dependent Biogenesis of the Galactose Oxidase Redox CofactorJournal of Biological Chemistry, 2003
- Lysyl oxidase: Properties, specificity, and biological roles inside and outside of the cellJournal of Cellular Biochemistry, 2002
- Identification of d-Proline Reductase fromClostridium sticklandiias a Selenoenzyme and Indications for a Catalytically Active Pyruvoyl Group Derived from a Cysteine Residue by Cleavage of a ProproteinPublished by Elsevier ,1999
- Crystal Structures of the Copper-Containing Amine Oxidase from Arthrobacter globiformis in the Holo and Apo Forms: Implications for the Biogenesis of Topaquinone,Biochemistry, 1997
- Direct Detection by 15N NMR of the Tryptophan Tryptophylquinone Aminoquinol Reaction Intermediate of Methylamine DehydrogenaseJournal of the American Chemical Society, 1996
- Generation of the topa quinone cofactor in bacterial monoamine oxidase by cupric ion‐dependent autooxidation of a specific tyrosyl residueFEBS Letters, 1994
- Erratum: Orbits of shepherd satellites deduced from the structure of the rings of UranusNature, 1991
- Mutagenesis of the gene encoding amicyanin of Paracoccus denitrificans and the resultant effect on methylamine oxidationFEBS Letters, 1990