Annual review of biochemistry · 2016
Radical S-Adenosylmethionine Enzymes in Human Health and Disease.
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Landgraf Bradley J, McCarthy Erin L, Booker Squire J
Аннотация
Radical S-adenosylmethionine (SAM) enzymes catalyze an astonishing array of complex and chemically challenging reactions across all domains of life. Of approximately 114,000 of these enzymes, 8 are known to be present in humans: MOCS1, molybdenum cofactor biosynthesis; LIAS, lipoic acid biosynthesis; CDK5RAP1, 2-methylthio-N(6)-isopentenyladenosine biosynthesis; CDKAL1, methylthio-N(6)-threonylcarbamoyladenosine biosynthesis; TYW1, wybutosine biosynthesis; ELP3, 5-methoxycarbonylmethyl uridine; and RSAD1 and viperin, both of unknown function. Aberrations in the genes encoding these proteins result in a variety of diseases. In this review, we summarize the biochemical characterization of these 8 radical S-adenosylmethionine enzymes and, in the context of human health, describe the deleterious effects that result from such genetic mutations.
Предметные рубрики MeSH
Carbon-Carbon LyasesDiabetes Mellitus, Type 2Gene ExpressionHeart Defects, CongenitalHistone AcetyltransferasesHumansIntracellular Signaling Peptides and ProteinsIron-Sulfur ProteinsMetal Metabolism, Inborn ErrorsMutationNerve Tissue ProteinsNeurodegenerative DiseasesNuclear ProteinsOxidoreductasesOxidoreductases Acting on CH-CH Group DonorsProteinsS-AdenosylmethionineThioctic AcidtRNA MethyltransferasesViperin ProteinSulfur Group TransferasesMitochondrial Proteins