(Q24313539)

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

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

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crystal structure

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Alanine--glyoxylate and serine--pyruvate aminotransferase

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GOA release 2020-03-11

protein homodimerization activity

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GOA release 2020-03-11

primary hyperoxaluria

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based on heuristic

inferred from title

primary hyperoxaluria type I

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based on heuristic

inferred from title

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based on heuristic

inferred from title

4

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5

object named as

Zihe Rao

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author name string

Xiaoxuan Zhang

1

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S Mark Roe

2

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Yanwen Hou

3

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Laurence H Pearl

6

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Christopher J Danpure

7

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language of work or name

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publication date

15 August 2003

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Journal of Molecular Biology

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331

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3

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643-52

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

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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

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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

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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

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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

1 reference

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

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

1 reference

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An oligomeric protein is imported into peroxisomes in vivo

1 reference

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Saccharomyces cerevisiae peroxisomal thiolase is imported as a dimer.

1 reference

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Protein unfolding and the energetics of protein translocation across biological membranes

1 reference

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

1 reference

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Structure of a NifS homologue: X-ray structure analysis of CsdB, an Escherichia coli counterpart of mammalian selenocysteine lyase

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Crystal structure of a NifS-like protein from Thermotoga maritima: implications for iron sulphur cluster assembly

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Crystal structure of the cystine C-S lyase from Synechocystis: stabilization of cysteine persulfide for FeS cluster biosynthesis

1 reference

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Crystallization and preliminary X-ray analysis of phosphoserine aminotransferase from Bacillus circulans subsp. alkalophilus

1 reference

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Crystal structure at 2.4 A resolution of E. coli serine hydroxymethyltransferase in complex with glycine substrate and 5-formyl tetrahydrofolate

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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Pyridoxal 5'-phosphate binding of a recombinant rat serine: pyruvate/alanine:glyoxylate aminotransferase.

1 reference

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7 January 2021

Molecular analysis of hyperoxaluria type 1 in Italian patients reveals eight new mutations in the alanine: glyoxylate aminotransferase gene

1 reference

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

1 reference

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NMR identification of the Tom20 binding segment in mitochondrial presequences

1 reference

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

1 reference

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Protein unfolding by mitochondria. The Hsp70 import motor

1 reference

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

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

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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

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Setting the standards: quality control in the secretory pathway

1 reference

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ER protein quality control and proteasome-mediated protein degradation

1 reference

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

1 reference

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Correction of an enzyme trafficking defect in hereditary kidney stone disease in vitro

1 reference

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

1 reference

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Automated MAD and MIR structure solution

1 reference

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Maximum-likelihood density modification

1 reference

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Improved methods for building protein models in electron density maps and the location of errors in these models

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Crystallography & NMR System: A New Software Suite for Macromolecular Structure Determination

1 reference

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The CCP4 suite: programs for protein crystallography

1 reference

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Mitochondrial targeting sequences may form amphiphilic helices

1 reference

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10.1016/S0022-2836(03)00791-5

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30 July 2022

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https://api.fatcat.wiki/v0/release/p3nfpd4d3jbjlo2meep36kcdze

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OpenCitations bibliographic resource ID

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Consolidated OpenCitations Corpus – April 2017

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