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

Cellini B, Montioli R, Paiardini A, Lorenzetto A, Voltattorni CB.

J Biol Chem. 2009 Mar 27;284(13):8349-58. doi: 10.1074/jbc.M808965200. Epub 2009 Jan 20.


Human liver peroxisomal alanine:glyoxylate aminotransferase: characterization of the two allelic forms and their pathogenic variants.

Cellini B, Montioli R, Voltattorni CB.

Biochim Biophys Acta. 2011 Nov;1814(11):1577-84. doi: 10.1016/j.bbapap.2010.12.005. Epub 2010 Dec 20. Review.


Human liver peroxisomal alanine:glyoxylate aminotransferase: Different stability under chemical stress of the major allele, the minor allele, and its pathogenic G170R variant.

Cellini B, Lorenzetto A, Montioli R, Oppici E, Voltattorni CB.

Biochimie. 2010 Dec;92(12):1801-11. doi: 10.1016/j.biochi.2010.08.005. Epub 2010 Aug 14.


Human wild-type alanine:glyoxylate aminotransferase and its naturally occurring G82E variant: functional properties and physiological implications.

Cellini B, Bertoldi M, Montioli R, Paiardini A, Borri Voltattorni C.

Biochem J. 2007 Nov 15;408(1):39-50.


Gly161 mutations associated with Primary Hyperoxaluria Type I induce the cytosolic aggregation and the intracellular degradation of the apo-form of alanine:glyoxylate aminotransferase.

Oppici E, Roncador A, Montioli R, Bianconi S, Cellini B.

Biochim Biophys Acta. 2013 Dec;1832(12):2277-88. doi: 10.1016/j.bbadis.2013.09.002. Epub 2013 Sep 17.


Oxalate synthesis in mammals: properties and subcellular distribution of serine:pyruvate/alanine:glyoxylate aminotransferase in the liver.

Ichiyama A, Xue HH, Oda T, Uchida C, Sugiyama T, Maeda-Nakai E, Sato K, Nagai E, Watanabe S, Takayama T.

Mol Urol. 2000 Winter;4(4):333-40.


Molecular defects of the glycine 41 variants of alanine glyoxylate aminotransferase associated with primary hyperoxaluria type I.

Cellini B, Montioli R, Paiardini A, Lorenzetto A, Maset F, Bellini T, Oppici E, Voltattorni CB.

Proc Natl Acad Sci U S A. 2010 Feb 16;107(7):2896-901. doi: 10.1073/pnas.0908565107. Epub 2010 Feb 1.


Crystal structure of alanine:glyoxylate aminotransferase and the relationship between genotype and enzymatic phenotype in primary hyperoxaluria type 1.

Zhang X, Roe SM, Hou Y, Bartlam M, Rao Z, Pearl LH, Danpure CJ.

J Mol Biol. 2003 Aug 15;331(3):643-52.


The AGT gene in Africa: a distinctive minor allele haplotype, a polymorphism (V326I), and a novel PH1 mutation (A112D) in Black Africans.

Coulter-Mackie MB, Tung A, Henderson HE, Toone JR, Applegarth DA.

Mol Genet Metab. 2003 Jan;78(1):44-50.


Enzymological and mutational analysis of a complex primary hyperoxaluria type 1 phenotype involving alanine:glyoxylate aminotransferase peroxisome-to-mitochondrion mistargeting and intraperoxisomal aggregation.

Danpure CJ, Purdue PE, Fryer P, Griffiths S, Allsop J, Lumb MJ, Guttridge KM, Jennings PR, Scheinman JI, Mauer SM, et al.

Am J Hum Genet. 1993 Aug;53(2):417-32.


S81L and G170R mutations causing Primary Hyperoxaluria type I in homozygosis and heterozygosis: an example of positive interallelic complementation.

Montioli R, Roncador A, Oppici E, Mandrile G, Giachino DF, Cellini B, Borri Voltattorni C.

Hum Mol Genet. 2014 Nov 15;23(22):5998-6007. doi: 10.1093/hmg/ddu329. Epub 2014 Jul 2.


Crystal structure of the S187F variant of human liver alanine: glyoxylate [corrected] aminotransferase associated with primary hyperoxaluria type I and its functional implications.

Oppici E, Fodor K, Paiardini A, Williams C, Voltattorni CB, Wilmanns M, Cellini B.

Proteins. 2013 Aug;81(8):1457-65. doi: 10.1002/prot.24300. Epub 2013 Jun 1. Erratum in: Proteins. 2014 Jan;82(1):171.


A unique molecular basis for enzyme mistargeting in primary hyperoxaluria type 1.

Leiper JM, Danpure CJ.

Clin Chim Acta. 1997 Oct 9;266(1):39-50.

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