(Q40183981)

18 September 2017

Mutations in calpain 3 associated with limb girdle muscular dystrophy: analysis by molecular modeling and by mutation in m-calpain (English)

1 reference

18 September 2017

1 reference

Jia Z

1

1 reference

18 September 2017

Petrounevitch V

2

1 reference

18 September 2017

Wong A

3

1 reference

18 September 2017

Moldoveanu T

4

1 reference

18 September 2017

Davies PL

5

1 reference

18 September 2017

Elce JS

6

1 reference

18 September 2017

Beckmann JS

7

1 reference

18 September 2017

language of work or name

English

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publication date

1 June 2001

1 reference

18 September 2017

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18 September 2017

80

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18 September 2017

6

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18 September 2017

2590-2596

1 reference

describes a project that uses

18 September 2017

1 reference

New aspect of the research on limb-girdle muscular dystrophy 2A: a molecular biologic and biochemical approach to pathology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1301447

The crystal structure of calcium-free human m-calpain suggests an electrostatic switch mechanism for activation by calcium

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1301447

Crystal structure of calpain reveals the structural basis for Ca(2+)-dependent protease activity and a novel mode of enzyme activation

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1301447

Functional defects of a muscle-specific calpain, p94, caused by mutations associated with limb-girdle muscular dystrophy type 2A

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1301447

Structure and physiological function of calpains

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1301447

Multiple independent molecular etiology for limb-girdle muscular dystrophy type 2A patients from various geographical origins

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1301447

ProMod and Swiss-Model: Internet-based tools for automated comparative protein modelling

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1301447

Juvenile limb-girdle muscular dystrophy. Clinical, histopathological and genetic data from a small community living in the Reunion Island

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1301447

Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1301447

Roles of individual EF-hands in the activation of m-calpain by calcium

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1301447

Purification of native p94, a muscle-specific calpain, and characterization of its autolysis

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1301447

Exercise-induced muscle injury: a calpain hypothesis

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1301447

Recombinant calpain II: improved expression systems and production of a C105A active-site mutant for crystallography.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1301447

Mutations of calpain 3 gene in patients with sporadic limb-girdle muscular dystrophy in Japan.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1301447

Calpainopathy-a survey of mutations and polymorphisms

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1301447

Calpain: a protease in search of a function?

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1301447

Muscle-specific calpain, p94, is degraded by autolysis immediately after translation, resulting in disappearance from muscle.

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1301447

Active site residues in m-calpain: identification by site-directed mutagenesis.

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1301447

Calpain III mutation analysis of a heterogeneous limb-girdle muscular dystrophy population

20 August 2018

1 reference

Crossref

https://api.crossref.org/works/10.1016%2FS0006-3495%2801%2976229-7

MOLSCRIPT: a program to produce both detailed and schematic plots of protein structures

7 January 2021

1 reference

Crossref

https://api.crossref.org/works/10.1016%2FS0006-3495%2801%2976229-7

PROCHECK: a program to check the stereochemical quality of protein structures

7 January 2021

1 reference

Crossref

https://api.crossref.org/works/10.1016%2FS0006-3495%2801%2976229-7

10.1016/S0006-3495(01)76229-7

7 January 2021

Identifiers

DOI

1 reference

18 September 2017

1 reference

18 September 2017

1 reference