Molecular Insight into the Synergism between the Minor Allele of Human Liver Peroxisomal Alanine:Glyoxylate Aminotransferase and the F152I Mutation

Human liver peroxisomal alanine:glyoxylate aminotransferase (AGT) is a pyridoxal 5′-phosphate (PLP)-dependent enzyme that converts glyoxylate into glycine. AGT deficiency causes primary hyperoxaluria type 1 (PH1), a rare autosomal recessive disorder, due to a marked increase in hepatic oxalate produ...

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Detalhes bibliográficos
Main Authors: Cellini, Barbara, Montioli, Riccardo, Paiardini, Alessandro, Lorenzetto, Antonio, Voltattorni, Carla Borri
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Biochemistry and Molecular Biology 2009
Assuntos:
Enzyme Catalysis and Regulation
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2659193/
https://ncbi.nlm.nih.gov/pubmed/19155213
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M808965200
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