Missense polymorphism in the human carboxypeptidase E gene alters enzymatic activity. (Q40791331)

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9 November 2019

title

Missense polymorphism in the human carboxypeptidase E gene alters enzymatic activity (English)

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11

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9 November 2019

author name string

Chen H

1

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9 November 2019

Jawahar S

2

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Qian Y

3

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Duong Q

4

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Chan G

5

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Parker A

6

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Meyer JM

7

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Moore KJ

8

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Chayen S

9

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Gross DJ

10

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Permutt MA

12

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Fricker LD

13

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publication date

1 August 2001

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9 November 2019

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volume

18

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issue

2

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page(s)

120-131

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Sequence diversity in 36 candidate genes for cardiovascular disorders

9 November 2019

cites work

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Characterization of single-nucleotide polymorphisms in coding regions of human genes

21 January 2018

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Proinsulin radioimmunoassay in the evaluation of insulinomas and familial hyperproinsulinemia

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Posttranslational processing of carboxypeptidase E, a neuropeptide-processing enzyme, in AtT-20 cells and bovine pituitary secretory granules

21 January 2018

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Peptides, enzymes and obesity: new insights from a 'dead' enzyme

21 January 2018

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Crystal structure of avian carboxypeptidase D domain II: a prototype for the regulatory metallocarboxypeptidase subfamily

21 January 2018

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Regulation of carboxypeptidase E. Effect of pH, temperature and Co2+ on kinetic parameters of substrate hydrolysis

21 January 2018

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Assignment of the human carboxypeptidase E (CPE) gene to chromosome 4

21 January 2018

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Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis

21 January 2018

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Obesity and impaired prohormone processing associated with mutations in the human prohormone convertase 1 gene

21 January 2018

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Hyperproinsulinaemia in obese fat/fat mice associated with a carboxypeptidase E mutation which reduces enzyme activity

21 January 2018

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Characterization of the enzymatic properties of the first and second domains of metallocarboxypeptidase D.

21 January 2018

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Human prohormone convertase 3 gene: exon-intron organization and molecular scanning for mutations in Japanese subjects with NIDDM.

21 January 2018

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A Genome Scan for Type 2 Diabetes Susceptibility Loci in a Genetically Isolated Population

21 January 2018

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Hyperproinsulinemia and amyloid in NIDDM. Clues to etiology of islet beta-cell dysfunction?

21 January 2018

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Banting lecture 1990. Beta-cells in type II diabetes mellitus

21 January 2018

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Glu300 of rat carboxypeptidase E is essential for enzymatic activity but not substrate binding or routing to the regulated secretory pathway

21 January 2018

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The future of genetic studies of complex human diseases

21 January 2018

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Catalysis of slow C-terminal processing reactions by carboxypeptidase H.

21 January 2018

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Cloning and expression of human carboxypeptidase Z, a novel metallocarboxypeptidase

21 January 2018

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Sequence of human carboxypeptidase D reveals it to be a member of the regulatory carboxypeptidase family with three tandem active site domains

21 January 2018

1 reference

A pre-Columbian Y chromosome-specific transition and its implications for human evolutionary history

21 January 2018

1 reference

Organization of the human carboxypeptidase E gene and molecular scanning for mutations in Japanese subjects with NIDDM or obesity

21 January 2018

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Induced and spontaneous mutations at Ser202 of carboxypeptidase E. Effect on enzyme expression, activity, and intracellular routing

21 January 2018

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Protein sorting and secretion granule formation in regulated secretory cells

21 January 2018

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7 January 2021

Mechanism of acidification of the trans-Golgi network (TGN). In situ measurements of pH using retrieval of TGN38 and furin from the cell surface

1 reference

7 January 2021

Comparison of a spectrophotometric, a fluorometric, and a novel radiometric assay for carboxypeptidase E (EC 3.4.17.10) and other carboxypeptidase B-like enzymes

1 reference

7 January 2021

Increased susceptibility of islets from diabetes-prone Psammomys obesus to the deleterious effects of chronic glucose exposure

1 reference

7 January 2021

Prohormone Convertase 1 in Obesity, Gestational Diabetes Mellitus, and NIDDM: No Evidence for a Major Susceptibility Role

1 reference

7 January 2021

Association of the Prohormone Convertase 2 Gene (PCSK2) on Chromosome 20 with NIDDM in Japanese Subjects

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7 January 2021

Identifiers

DOI

10.1002/HUMU.1161

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9 November 2019

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