(Q24300662)

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The N-terminal extension is essential for the formation of the active dimeric structure of liver peroxisomal alanine:glyoxylate aminotransferase

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The N-terminal extension is essential for the formation of the active dimeric structure of liver peroxisomal alanine:glyoxylate aminotransferase (English)

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Alanine--glyoxylate and serine--pyruvate aminotransferase

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GOA release 2020-03-11

L-alanine catabolic process

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GOA release 2020-03-11

2

object named as

Sonia Fargue

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author name string

Riccardo Montioli

1

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Jackie Lewin

3

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Carlotta Zamparelli

4

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Christopher J Danpure

5

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Carla Borri Voltattorni

6

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Barbara Cellini

7

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language of work or name

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publication date

March 2012

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International Journal of Biochemistry & Cell Biology

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44

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536-46

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3

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Variable peroxisomal and mitochondrial targeting of alanine: glyoxylate aminotransferase in mammalian evolution and disease

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Crystal structure of phosphoserine aminotransferase from Escherichia coli at 2.3 A resolution: comparison of the unligated enzyme and a complex with alpha-methyl-l-glutamate

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NMR identification of the Tom20 binding segment in mitochondrial presequences

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An intronic duplication in the alanine: glyoxylate aminotransferase gene facilitates identification of mutations in compound heterozygote patients with primary hyperoxaluria type 1.

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Peroxisomal alanine:glyoxylate aminotransferase deficiency in primary hyperoxaluria type I

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Crystalline mitochondrial aspartate aminotransferase exists in only two conformations

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Primary hyperoxaluria type 1: AGT mistargeting highlights the fundamental differences between the peroxisomal and mitochondrial protein import pathways

1 reference

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

1 reference

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Treponema denticola cystalysin catalyzes β‐desulfination of L‐cysteine sulfinic acid and β‐decarboxylation of L‐aspartate and oxalacetate

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Crystal structure of IscS, a cysteine desulfurase from Escherichia coli

1 reference

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

1 reference

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Structural basis of presequence recognition by the mitochondrial protein import receptor Tom20

1 reference

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The crystal structure of human cytosolic serine hydroxymethyltransferase: a target for cancer chemotherapy

1 reference

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Molecular aetiology of primary hyperoxaluria and its implications for clinical management

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Degradation pathway of the phosphonate ciliatine: crystal structure of 2-aminoethylphosphonate transaminase

1 reference

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Biochemical and Structural Characterization of a Ureidoglycine Aminotransferase in the Klebsiella pneumoniae Uric Acid Catabolic Pathway

1 reference

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Reconstruction of human hepatocyte glyoxylate metabolic pathways in stably transformed Chinese-hamster ovary cells.

1 reference

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

1 reference

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

1 reference

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Mistargeting of peroxisomal L-alanine:glyoxylate aminotransferase to mitochondria in primary hyperoxaluria patients depends upon activation of a cryptic mitochondrial targeting sequence by a point mutation

1 reference

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Characterization of human type X procollagen and its NC-1 domain expressed as recombinant proteins in HEK293 cells.

1 reference

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Effect of N-terminal alpha-helix formation on the dimerization and intracellular targeting of alanine:glyoxylate aminotransferase

1 reference

https://api.crossref.org/works/10.1016%2FJ.BIOCEL.2011.12.007

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based on heuristic

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Functional synergism between the most common polymorphism in human alanine:glyoxylate aminotransferase and four of the most common disease-causing mutations

1 reference

https://api.crossref.org/works/10.1016%2FJ.BIOCEL.2011.12.007

7 January 2021

based on heuristic

inferred from DOI database lookup

Peroxisomal import of human alanine:glyoxylate aminotransferase requires ancillary targeting information remote from its C terminus

1 reference

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

1 reference

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Identification of mutations associated with peroxisome-to-mitochondrion mistargeting of alanine/glyoxylate aminotransferase in primary hyperoxaluria type 1

1 reference

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Mammalian alanine/glyoxylate aminotransferase 1 is imported into peroxisomes via the PTS1 translocation pathway. Increased degeneracy and context specificity of the mammalian PTS1 motif and implications for the peroxisome-to-mitochondrion mistargeti

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Inhibition of alanine:glyoxylate aminotransferase 1 dimerization is a prerequisite for its peroxisome-to-mitochondrion mistargeting in primary hyperoxaluria type 1.

1 reference

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Domain structure of secretin PulD revealed by limited proteolysis and electron microscopy.

1 reference

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Truncated aspartate aminotransferase from alkalophilic Bacillus circulans with deletion of N-terminal 32 amino acids is a non-functional monomer in a partially structured state

1 reference

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A comparative analysis of the evolutionary relationship between diet and enzyme targeting in bats, marsupials and other mammals

1 reference

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Structural implications of a G170R mutation of alanine:glyoxylate aminotransferase that is associated with peroxisome-to-mitochondrion mistargeting

1 reference

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10.1016/J.BIOCEL.2011.12.007

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