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4cai

From Proteopedia

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'''Unreleased structure'''
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{{STRUCTURE_4cai| PDB=4cai | SCENE= }}
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===Structure of inner DysF domain of human dysferlin===
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{{ABSTRACT_PUBMED_24438169}}
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The entry 4cai is ON HOLD until Paper Publication
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==Disease==
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[[http://www.uniprot.org/uniprot/DYSF_HUMAN DYSF_HUMAN]] Miyoshi myopathy;Distal myopathy with anterior tibial onset;Congenital myopathy, Paradas type;Autosomal recessive limb-girdle muscular dystrophy type 2B. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry.
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Authors: Sula, A., Cole, A.R., Yeats, C., Orengo, C., Keep, N.H.
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==Function==
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[[http://www.uniprot.org/uniprot/DYSF_HUMAN DYSF_HUMAN]] Key calcium ion sensor involved in the Ca(2+)-triggered synaptic vesicle-plasma membrane fusion. Plays a role in the sarcolemma repair mechanism of both skeletal muscle and cardiomyocytes that permits rapid resealing of membranes disrupted by mechanical stress (By similarity).
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Description: Structure of inner DysF domain of human dysferlin
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==About this Structure==
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[[4cai]] is a 3 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4CAI OCA].
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==Reference==
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<ref group="xtra">PMID:024438169</ref><references group="xtra"/><references/>
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[[Category: Cole, A R.]]
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[[Category: Keep, N H.]]
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[[Category: Orengo, C.]]
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[[Category: Sula, A.]]
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[[Category: Yeats, C.]]
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[[Category: Dysf domain]]
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[[Category: Limb-girdle muscular dystrophy]]
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[[Category: Membrane protein]]
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[[Category: Membrane repair]]

Revision as of 07:39, 29 January 2014

Template:STRUCTURE 4cai

Contents

Structure of inner DysF domain of human dysferlin

Template:ABSTRACT PUBMED 24438169

Disease

[DYSF_HUMAN] Miyoshi myopathy;Distal myopathy with anterior tibial onset;Congenital myopathy, Paradas type;Autosomal recessive limb-girdle muscular dystrophy type 2B. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry.

Function

[DYSF_HUMAN] Key calcium ion sensor involved in the Ca(2+)-triggered synaptic vesicle-plasma membrane fusion. Plays a role in the sarcolemma repair mechanism of both skeletal muscle and cardiomyocytes that permits rapid resealing of membranes disrupted by mechanical stress (By similarity).

About this Structure

4cai is a 3 chain structure. Full crystallographic information is available from OCA.

Reference

Proteopedia Page Contributors and Editors (what is this?)

OCA

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