4ihb

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
m (Protected "4ihb" [edit=sysop:move=sysop])
Line 1: Line 1:
-
'''Unreleased structure'''
+
{{STRUCTURE_4ihb| PDB=4ihb | SCENE= }}
 +
===X-RAY STRUCTURE OF THE canonical C2A DOMAIN FROM HUMAN DYSFERLIN===
 +
{{ABSTRACT_PUBMED_24239457}}
-
The entry 4ihb is ON HOLD
+
==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.
-
Authors: Sutton, R.B., Fuson, K.L.
+
==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).
-
Description: X-RAY STRUCTURE OF THE canonical C2A DOMAIN FROM HUMAN DYSFERLIN
+
==About this Structure==
 +
[[4ihb]] is a 6 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4IHB OCA].
 +
 
 +
==Reference==
 +
<ref group="xtra">PMID:024239457</ref><references group="xtra"/><references/>
 +
[[Category: Fuson, K L.]]
 +
[[Category: Sutton, R B.]]
 +
[[Category: Beta sandwich]]
 +
[[Category: Membrane protein]]
 +
[[Category: Membrane repair]]
 +
[[Category: Muscular dystrophy]]
 +
[[Category: Plasma membrane]]
 +
[[Category: Type ii c2 domain]]

Revision as of 10:20, 18 December 2013

Template:STRUCTURE 4ihb

Contents

X-RAY STRUCTURE OF THE canonical C2A DOMAIN FROM HUMAN DYSFERLIN

Template:ABSTRACT PUBMED 24239457

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

4ihb is a 6 chain structure. Full crystallographic information is available from OCA.

Reference

  • Fuson K, Rice A, Mahling R, Snow A, Nayak K, Shanbhogue P, Meyer AG, Redpath GM, Hinderliter A, Cooper ST, Sutton RB. Alternate Splicing of Dysferlin C2A Confers Ca-Dependent and Ca-Independent Binding for Membrane Repair. Structure. 2013 Nov 13. pii: S0969-2126(13)00392-4. doi:, 10.1016/j.str.2013.10.001. PMID:24239457 doi:http://dx.doi.org/10.1016/j.str.2013.10.001

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools