9c19 | pdb_00009c19

Structure of human LIAS

spinqualitylabelsall models 9c19, resolution 2.58Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Structural highlights 9c19 is a 6 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance. Method: X-ray diffraction, Resolution 2.58Å Ligands: PO4, SAM, YVI Resources: FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT Disease LIAS_HUMAN Lipoic acid synthetase deficiency. The disease is caused by variants affecting the gene represented in this entry. Function LIAS_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]

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