(Q35103528)

6 August 2017

1 reference

title

Alanine:glyoxylate aminotransferase peroxisome-to-mitochondrion mistargeting in human hereditary kidney stone disease (English)

1 reference

6 August 2017

1 reference

Graeme M Birdsey

3

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author name string

Christopher J Danpure

series ordinal

1

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6 August 2017

Michael J Lumb

series ordinal

2

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6 August 2017

Xiaoxuan Zhang

series ordinal

4

1 reference

6 August 2017

language of work or name

English

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publication date

1 April 2003

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Biochimica et Biophysica Acta

6 August 2017

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6 August 2017

1647

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6 August 2017

70-75

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6 August 2017

1-2

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A glycine-to-glutamate substitution abolishes alanine:glyoxylate aminotransferase catalytic activity in a subset of patients with primary hyperoxaluria type 1

6 August 2017

1 reference

https://api.crossref.org/works/10.1016%2FS1570-9639%2803%2900055-4

7 January 2021

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%2FS1570-9639%2803%2900055-4

7 January 2021

Primary hyperoxaluria type I due to a point mutation of T to C in the coding region of the serine:pyruvate aminotransferase gene

1 reference

https://api.crossref.org/works/10.1016%2FS1570-9639%2803%2900055-4

7 January 2021

ATP-dependent degradation of a mutant serine: pyruvate/alanine:glyoxylate aminotransferase in a primary hyperoxaluria type 1 case

1 reference

https://api.crossref.org/works/10.1016%2FS1570-9639%2803%2900055-4

7 January 2021

An enzyme trafficking defect in two patients with primary hyperoxaluria type 1: peroxisomal alanine/glyoxylate aminotransferase rerouted to mitochondria

1 reference

https://api.crossref.org/works/10.1016%2FS1570-9639%2803%2900055-4

7 January 2021

Immunocytochemical localization of human hepatic alanine: glyoxylate aminotransferase in control subjects and patients with primary hyperoxaluria type 1

1 reference

https://api.crossref.org/works/10.1016%2FS1570-9639%2803%2900055-4

7 January 2021

Human peroxisomal L-alanine: glyoxylate aminotransferase. Evolutionary loss of a mitochondrial targeting signal by point mutation of the initiation codon

1 reference

https://api.crossref.org/works/10.1016%2FS1570-9639%2803%2900055-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1570-9639%2803%2900055-4

7 January 2021

Molecular characterization and clinical use of a polymorphic tandem repeat in an intron of the human alanine:glyoxylate aminotransferase gene.

1 reference

https://api.crossref.org/works/10.1016%2FS1570-9639%2803%2900055-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1570-9639%2803%2900055-4

7 January 2021

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

https://api.crossref.org/works/10.1016%2FS1570-9639%2803%2900055-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1570-9639%2803%2900055-4

7 January 2021

Context dependency of the PTS1 motif in human alanine: glyoxylate aminotransferase 1

1 reference

https://api.crossref.org/works/10.1016%2FS1570-9639%2803%2900055-4

7 January 2021

The peroxisomal targeting sequence type 1 receptor, Pex5p, and the peroxisomal import efficiency of alanine:glyoxylate aminotransferase

1 reference

https://api.crossref.org/works/10.1016%2FS1570-9639%2803%2900055-4

7 January 2021

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%2FS1570-9639%2803%2900055-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1570-9639%2803%2900055-4

7 January 2021

NMR identification of the Tom20 binding segment in mitochondrial presequences

1 reference

https://api.crossref.org/works/10.1016%2FS1570-9639%2803%2900055-4

7 January 2021

An oligomeric protein is imported into peroxisomes in vivo

1 reference

https://api.crossref.org/works/10.1016%2FS1570-9639%2803%2900055-4

7 January 2021

Saccharomyces cerevisiae peroxisomal thiolase is imported as a dimer.

1 reference

https://api.crossref.org/works/10.1016%2FS1570-9639%2803%2900055-4

7 January 2021

Oilseed isocitrate lyases lacking their essential type 1 peroxisomal targeting signal are piggybacked to glyoxysomes

1 reference

https://api.crossref.org/works/10.1016%2FS1570-9639%2803%2900055-4

7 January 2021

Protein unfolding and the energetics of protein translocation across biological membranes

1 reference

https://api.crossref.org/works/10.1016%2FS1570-9639%2803%2900055-4

7 January 2021

Protein folding causes an arrest of preprotein translocation into mitochondria in vivo

1 reference

https://api.crossref.org/works/10.1016%2FS1570-9639%2803%2900055-4

7 January 2021

Transport of proteins into mitochondria: translocational intermediates spanning contact sites between outer and inner membranes

1 reference

https://api.crossref.org/works/10.1016%2FS1570-9639%2803%2900055-4

7 January 2021

Protein unfolding by mitochondria. The Hsp70 import motor

1 reference

https://api.crossref.org/works/10.1016%2FS1570-9639%2803%2900055-4

7 January 2021

Competition of spontaneous protein folding and mitochondrial import causes dual subcellular location of major adenylate kinase

1 reference

https://api.crossref.org/works/10.1016%2FS1570-9639%2803%2900055-4

7 January 2021

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

https://api.crossref.org/works/10.1016%2FS1570-9639%2803%2900055-4

7 January 2021

Crystallization and preliminary crystallographic analysis of human alanine:glyoxylate aminotransferase and its polymorphic variants

1 reference

https://api.crossref.org/works/10.1016%2FS1570-9639%2803%2900055-4

7 January 2021

Pharmacological chaperones: a new twist on receptor folding.

1 reference

https://api.crossref.org/works/10.1016%2FS1570-9639%2803%2900055-4

7 January 2021

Aggregation of the inactive form of human alpha-galactosidase in the endoplasmic reticulum

1 reference

https://api.crossref.org/works/10.1016%2FS1570-9639%2803%2900055-4

7 January 2021

Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS1570-9639%2803%2900055-4

7 January 2021

Chemical chaperones mediate increased secretion of mutant alpha 1-antitrypsin (alpha 1-AT) Z: A potential pharmacological strategy for prevention of liver injury and emphysema in alpha 1-AT deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS1570-9639%2803%2900055-4

7 January 2021

Defective aquaporin-2 trafficking in nephrogenic diabetes insipidus and correction by chemical chaperones

1 reference

https://api.crossref.org/works/10.1016%2FS1570-9639%2803%2900055-4

7 January 2021

Setting the standards: quality control in the secretory pathway

1 reference

https://api.crossref.org/works/10.1016%2FS1570-9639%2803%2900055-4

7 January 2021

ER protein quality control and proteasome-mediated protein degradation

1 reference

https://api.crossref.org/works/10.1016%2FS1570-9639%2803%2900055-4

7 January 2021

Posttranslational quality control: folding, refolding, and degrading proteins.

1 reference

https://api.crossref.org/works/10.1016%2FS1570-9639%2803%2900055-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1570-9639%2803%2900055-4

7 January 2021

Processing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitive

1 reference

https://api.crossref.org/works/10.1016%2FS1570-9639%2803%2900055-4

7 January 2021

Chemical chaperones correct the mutant phenotype of the delta F508 cystic fibrosis transmembrane conductance regulator protein

1 reference

https://api.crossref.org/works/10.1016%2FS1570-9639%2803%2900055-4

7 January 2021

Glycerol reverses the misfolding phenotype of the most common cystic fibrosis mutation.

1 reference

https://api.crossref.org/works/10.1016%2FS1570-9639%2803%2900055-4

7 January 2021

Accelerated transport and maturation of lysosomal α–galactosidase A in Fabry lymphoblasts by an enzyme inhibitor

1 reference

https://api.crossref.org/works/10.1016%2FS1570-9639%2803%2900055-4

7 January 2021

Mitochondrial targeting sequences may form amphiphilic helices

1 reference

https://api.crossref.org/works/10.1016%2FS1570-9639%2803%2900055-4

7 January 2021

10.1016/S1570-9639(03)00055-4

Identifiers

DOI

1 reference

6 August 2017

1 reference