4unk | pdb_00004unk
From Proteopedia
Crystal structure of human triosephosphate isomerase (mutant N15D)
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Structural highlights
Disease[TPIS_HUMAN] Defects in TPI1 are the cause of triosephosphate isomerase deficiency (TPI deficiency) [MIM:190450]. TPI deficiency is an autosomal recessive disorder. It is the most severe clinical disorder of glycolysis. It is associated with neonatal jaundice, chronic hemolytic anemia, progressive neuromuscular dysfunction, cardiomyopathy and increased susceptibility to infection. Contents | ||||||||||||||||||||
This page was last modified 15:59, 7 February 2015.