Calcium-sensitive phospholipid binding properties of normal and mutant ferlin C2 domains (Q24294673)

GOA release 2020-03-11

Myoferlin

1 reference

GOA release 2020-03-11

author name string

Dawn Belt Davis

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Katherine R Doherty

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Anthony J Delmonte

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Elizabeth M McNally

Journal of Biological Chemistry

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language of work or name

English

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publication date

21 June 2002

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published in

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volume

277

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issue

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page(s)

22883-8

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cites work

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The C2 domain calcium-binding motif: structural and functional diversity

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Splicing mutation in dysferlin produces limb-girdle muscular dystrophy with inflammation

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The third human FER-1-like protein is highly similar to dysferlin.

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Differentiation-related differences in the plasma membrane phospholipid asymmetry of myogenic and fibrogenic cells

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Tandem events in myoblast fusion

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Myoblast aminophospholipid asymmetry differs from that of fibroblasts.

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Structure of the first C2 domain of synaptotagmin I: A novel Ca2+/phospholipid-binding fold

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Sustained overexpression of IGF-1 prevents age-dependent decrease in charge movement and intracellular Ca(2+) in mouse skeletal muscle

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Phenotypic variation in a large Japanese family with Miyoshi myopathy with nonsense mutation in exon 19 of dysferlin gene

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A practical guide to the preparation of Ca2+ buffers

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Synaptotagmin VII as a plasma membrane Ca(2+) sensor in exocytosis

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Three-dimensional structure of the synaptotagmin 1 C2B-domain: synaptotagmin 1 as a phospholipid binding machine

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Lipid structure and not membrane structure is the major determinant in the regulation of protein kinase C by phosphatidylserine.

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Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy

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Ca2+ regulates the interaction between synaptotagmin and syntaxin 1.

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Genetic mapping to 10q23.3-q24.2, in a large Italian pedigree, of a new syndrome showing bilateral cataracts, gastroesophageal reflux, and spastic paraparesis with amyotrophy

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The sarcolemmal proteins dysferlin and caveolin-3 interact in skeletal muscle

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Identical mutation in patients with limb girdle muscular dystrophy type 2B or Miyoshi myopathy suggests a role for modifier gene(s)

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Plasticity of the differentiated state

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Bipartite Ca2+-binding motif in C2 domains of synaptotagmin and protein kinase C

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Identical dysferlin mutation in limb-girdle muscular dystrophy type 2B and distal myopathy

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The earliest pathologic alterations in dysferlinopathy

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Identifiers

DOI

10.1074/JBC.M201858200

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

11959863

1 reference

Consolidated OpenCitations Corpus – April 2017