4cah: Difference between revisions
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{{STRUCTURE_4cah| PDB=4cah | SCENE= }} | |||
===Structure of inner DysF domain of human dysferlin=== | |||
{{ABSTRACT_PUBMED_24438169}} | |||
The entry | ==Disease== | ||
[[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. | |||
==Function== | |||
[[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). | |||
==About this Structure== | |||
[[4cah]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4CAH OCA]. | |||
==Reference== | |||
<ref group="xtra">PMID:024438169</ref><references group="xtra"/><references/> | |||
[[Category: Cole, A R.]] | |||
[[Category: Keep, N H.]] | |||
[[Category: Orengo, C.]] | |||
[[Category: Sula, A.]] | |||
[[Category: Yeats, C.]] | |||
[[Category: Dysf domain]] | |||
[[Category: Limb-girdle muscular dystrophy]] | |||
[[Category: Membrane protein]] | |||
[[Category: Membrane repair]] | |||
Revision as of 07:35, 29 January 2014
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
4cah is a 1 chain structure. Full crystallographic information is available from OCA.
Reference
- Sula A, Cole AR, Yeats C, Orengo C, Keep NH. Crystal structures of the human Dysferlin inner DysF domain. BMC Struct Biol. 2014 Jan 17;14(1):3. doi: 10.1186/1472-6807-14-3. PMID:24438169 doi:https://dx.doi.org/10.1186/1472-6807-14-3
