8v0j
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Structure of the complex between Human LIAS and H-protein in the presence of s-adenosyl-l-methionine
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Structural highlights
DiseaseLIAS_HUMAN Lipoic acid synthetase deficiency. The disease is caused by variants affecting the gene represented in this entry. FunctionLIAS_HUMAN Catalyzes the radical-mediated insertion of two sulfur atoms into the C-6 and C-8 positions of the octanoyl moiety bound to the lipoyl domains of lipoate-dependent enzymes, thereby converting the octanoylated domains into lipoylated derivatives.[HAMAP-Rule:MF_03123] Contents | ||||||||||||||||||||
This page was last modified 06:07, 20 August 2025.