Literature DB >> 17439161

Protein-derived cofactors. Expanding the scope of post-translational modifications.

Victor L Davidson1.   

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.

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Year:  2007        PMID: 17439161     DOI: 10.1021/bi700468t

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  37 in total

1.  Functional importance of tyrosine 294 and the catalytic selectivity for the bis-Fe(IV) state of MauG revealed by replacement of this axial heme ligand with histidine .

Authors:  Nafez Abu Tarboush; Lyndal M R Jensen; Manliang Feng; Hiroyasu Tachikawa; Carrie M Wilmot; Victor L Davidson
Journal:  Biochemistry       Date:  2010-10-20       Impact factor: 3.162

Review 2.  Tryptophan tryptophylquinone biosynthesis: a radical approach to posttranslational modification.

Authors:  Victor L Davidson; Aimin Liu
Journal:  Biochim Biophys Acta       Date:  2012-01-28

3.  Roles of Copper and a Conserved Aspartic Acid in the Autocatalytic Hydroxylation of a Specific Tryptophan Residue during Cysteine Tryptophylquinone Biogenesis.

Authors:  Heather R Williamson; Esha Sehanobish; Alan M Shiller; Antonio Sanchez-Amat; Victor L Davidson
Journal:  Biochemistry       Date:  2017-02-10       Impact factor: 3.162

4.  Roles of Conserved Residues of the Glycine Oxidase GoxA in Controlling Activity, Cooperativity, Subunit Composition, and Cysteine Tryptophylquinone Biosynthesis.

Authors:  Esha Sehanobish; Heather R Williamson; Victor L Davidson
Journal:  J Biol Chem       Date:  2016-09-16       Impact factor: 5.157

Review 5.  Metals and Methanotrophy.

Authors:  Jeremy D Semrau; Alan A DiSpirito; Wenyu Gu; Sukhwan Yoon
Journal:  Appl Environ Microbiol       Date:  2018-03-01       Impact factor: 4.792

6.  Roles of active site residues in LodA, a cysteine tryptophylquinone dependent ε-lysine oxidase.

Authors:  Esha Sehanobish; María Dolores Chacón-Verdú; Antonio Sanchez-Amat; Victor L Davidson
Journal:  Arch Biochem Biophys       Date:  2015-06-03       Impact factor: 4.013

7.  Formation and Reactivity of New Isoporphyrins: Implications for Understanding the Tyr-His Cross-Link Cofactor Biogenesis in Cytochrome c Oxidase.

Authors:  Melanie A Ehudin; Laura Senft; Alicja Franke; Ivana Ivanović-Burmazović; Kenneth D Karlin
Journal:  J Am Chem Soc       Date:  2019-06-26       Impact factor: 15.419

8.  A catalytic di-heme bis-Fe(IV) intermediate, alternative to an Fe(IV)=O porphyrin radical.

Authors:  Xianghui Li; Rong Fu; Sheeyong Lee; Carsten Krebs; Victor L Davidson; Aimin Liu
Journal:  Proc Natl Acad Sci U S A       Date:  2008-06-18       Impact factor: 11.205

9.  Characterization of PlGoxB, a flavoprotein required for cysteine tryptophylquinone biosynthesis in glycine oxidase from Pseudoalteromonas luteoviolacea.

Authors:  Kyle J Mamounis; Zhongxin Ma; Antonio Sanchez-Amat; Victor L Davidson
Journal:  Arch Biochem Biophys       Date:  2019-09-18       Impact factor: 4.013

10.  Roles of multiple-proton transfer pathways and proton-coupled electron transfer in the reactivity of the bis-FeIV state of MauG.

Authors:  Zhongxin Ma; Heather R Williamson; Victor L Davidson
Journal:  Proc Natl Acad Sci U S A       Date:  2015-08-17       Impact factor: 11.205

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