Ontology highlight
ABSTRACT:
SUBMITTER: Cronan JE
PROVIDER: S-EPMC7253636 | biostudies-literature | 2020
REPOSITORIES: biostudies-literature
Frontiers in genetics 20200521
Three human mitochondrial diseases that directly affect lipoic acid metabolism result from heterozygous missense and nonsense mutations in the <i>LIAS</i>, <i>LIPT1</i>, and <i>LIPT2</i> genes. However, the functions of the proteins encoded by these genes in lipoic acid metabolism remained uncertain due to a lack of biochemical analysis at the enzyme level. An exception was the LIPT1 protein for which a perplexing property had been reported, a ligase lacking the ability to activate its substrate ...[more]