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Organisms Homo sapiens Communities Inherited Metabolic Disorders (IMD) Pathways ONTOX Rare Diseases Annotations Disease Ontology autosomal recessive disease metabolic acidosis gamma-glutamyl transpeptidase deficiency hemolytic anemia Pathway Ontology glutathione metabolic pathway glutathione biosynthetic pathway disease pathway amino acid metabolic pathway glutathionuria disease pathway References Glutathionuria: inborn error of metabolism due to tissue deficiency of gamma-glutamyl transpeptidase

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TB-500, an actin binding protein, helps to sequester actin in areas where it is most useful for building filaments from actin to allow for cell movement [2]

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