(Q28363923)

4 July 2017

title

Missense mutations in the N-terminal domain of human phenylalanine hydroxylase interfere with binding of regulatory phenylalanine (English)

1 reference

4 July 2017

Gjetting T

1

1 reference

4 July 2017

Petersen M

series ordinal

2

1 reference

4 July 2017

Guldberg P

series ordinal

3

1 reference

4 July 2017

Güttler F

series ordinal

4

1 reference

4 July 2017

language of work or name

English

0 references

publication date

20 April 2001

1 reference

American Journal of Human Genetics

4 July 2017

published in

1 reference

4 July 2017

volume

68

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4 July 2017

issue

6

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4 July 2017

page(s)

1353-1360

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Structural basis of autoregulation of phenylalanine hydroxylase

4 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226122

Structure of tetrameric human phenylalanine hydroxylase and its implications for phenylketonuria

20 March 2017

1 reference

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SWISS-MODEL and the Swiss-PdbViewer: an environment for comparative protein modeling

20 March 2017

1 reference

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Crystal structure of the catalytic domain of human phenylalanine hydroxylase reveals the structural basis for phenylketonuria

20 March 2017

1 reference

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Crystal structure of tyrosine hydroxylase at 2.3 A and its implications for inherited neurodegenerative diseases

20 March 2017

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Expression of recombinant human phenylalanine hydroxylase as fusion protein in Escherichia coli circumvents proteolytic degradation by host cell proteases. Isolation and characterization of the wild-type enzyme

20 March 2017

1 reference

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Mutagenesis of the regulatory domain of phenylalanine hydroxylase

20 March 2017

1 reference

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Essential role of the N-terminal autoregulatory sequence in the regulation of phenylalanine hydroxylase

29 September 2017

1 reference

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In vitro expression of 34 naturally occurring mutant variants of phenylalanine hydroxylase: correlation with metabolic phenotypes and susceptibility toward protein aggregation

29 September 2017

1 reference

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Characterization of phenylketonuria missense substitutions, distant from the phenylalanine hydroxylase active site, illustrates a paradigm for mechanism and potential modulation of phenotype

29 September 2017

1 reference

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The structural basis of phenylketonuria

29 September 2017

1 reference

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Monogenic traits are not simple: lessons from phenylketonuria

29 September 2017

1 reference

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Partial characterization and three-dimensional-structural localization of eight mutations in exon 7 of the human phenylalanine hydroxylase gene associated with phenylketonuria.

29 September 2017

1 reference

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Alterations in protein aggregation and degradation due to mild and severe missense mutations (A104D, R157N) in the human phenylalanine hydroxylase gene (PAH).

29 September 2017

1 reference

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A European multicenter study of phenylalanine hydroxylase deficiency: classification of 105 mutations and a general system for genotype-based prediction of metabolic phenotype

29 September 2017

1 reference

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In vitro expression analysis of mutations in phenylalanine hydroxylase: linking genotype to phenotype and structure to function

29 September 2017

1 reference

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The role of phenylalanine in structure-function relationships of phenylalanine hydroxylase revealed by radiation target analysis

29 September 2017

1 reference

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PKU mutation (D143G) associated with an apparent high residual enzyme activity: expression of a kinetic variant form of phenylalanine hydroxylase in three different systems

29 September 2017

1 reference

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PKU mutation G46S is associated with increased aggregation and degradation of the phenylalanine hydroxylase enzyme

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226122

The phenylalanine hydroxylating system.

29 September 2017

1 reference

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Structure and function of the aromatic amino acid hydroxylases.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226122

Molecular basis of phenotypic heterogeneity in phenylketonuria

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226122

Novel mutations in the pheA gene of Escherichia coli K-12 which result in highly feedback inhibition-resistant variants of chorismate mutase/prephenate dehydratase

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226122

PAHdb: a locus-specific knowledgebase.

29 September 2017

1 reference

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Human phenylalanine hydroxylase mutations and hyperphenylalaninemia phenotypes: a metanalysis of genotype-phenotype correlations

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226122

Mechanism of phenylalanine regulation of phenylalanine hydroxylase.

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226122

A single locus encodes both phenylalanine hydroxylase and tryptophan hydroxylase activities in Drosophila.

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226122

Structural interpretation of mutations in phenylalanine hydroxylase protein aids in identifying genotype–phenotype correlations in phenylketonuria

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226122

Urea-induced denaturation of human phenylalanine hydroxylase

27 November 2018

1 reference

12 December 2020

Relationship between the substrate activation site and catalytic site of phenylalanine hydroxylase

1 reference

12 December 2020

Chorismate Mutase-Prephenate Dehydratase fromEscherichia coli

1 reference

12 December 2020

Missense mutations in the phenylalanine hydroxylase gene (PAH) can cause accelerated proteolytic turnover of PAH enzyme: a mechanism underlying phenylketonuria

1 reference

12 December 2020

Regulation of Phenylalanine Biosynthesis. Studies on the Mechanism of Phenylalanine Binding and Feedback Inhibition in theEscherichia coliP-Protein†

1 reference

12 December 2020

Identifiers

DOI

10.1086/320604

1 reference

release_3xnxkox5hjhehegk2xn5zs5r7e

4 July 2017

Fatcat ID

0 references

OpenCitations bibliographic resource ID

2461183

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

4 July 2017

1 reference