| Literature DB >> 19675644 |
Günter Schwarz1, Ralf R Mendel, Markus W Ribbe.
Abstract
The trace element molybdenum is essential for nearly all organisms and forms the catalytic centre of a large variety of enzymes such as nitrogenase, nitrate reductases, sulphite oxidase and xanthine oxidoreductases. Nature has developed two scaffolds holding molybdenum in place, the iron-molybdenum cofactor and pterin-based molybdenum cofactors. Despite the different structures and functions of molybdenum-dependent enzymes, there are important similarities, which we highlight here. The biosynthetic pathways leading to both types of cofactor have common mechanistic aspects relating to scaffold formation, metal activation and cofactor insertion into apoenzymes, and have served as an evolutionary 'toolbox' to mediate additional cellular functions in eukaryotic metabolism.Entities:
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Year: 2009 PMID: 19675644 DOI: 10.1038/nature08302
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 49.962