Myotilin

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Current revision (08:15, 17 August 2017) (edit) (undo)
 
Line 1: Line 1:
-
{{STRUCTURE_2kdg| PDB=2kdg | SIZE=400| SCENE= |right|CAPTION=Human myotilin 1st Ig domain NMR structure [[2kdg]] }}
+
 
 +
<StructureSection load='2kdg' size='350' side='right' caption='Human myotilin 1st Ig domain NMR structure (PDB entry [[2kdg]])' scene=''>
== Function ==
== Function ==
'''Myotilin''' is a cytoskeletal protein expressed in skeletal and cardiac muscles. Myotilin C-terminal contails two Ig-like domains similar to titin<ref>PMID:10369880</ref>. See details in [[Group:MUZIC:Myotilin]].
'''Myotilin''' is a cytoskeletal protein expressed in skeletal and cardiac muscles. Myotilin C-terminal contails two Ig-like domains similar to titin<ref>PMID:10369880</ref>. See details in [[Group:MUZIC:Myotilin]].
Line 6: Line 7:
Mutations in myotilin cause myofibrillar myopathy<ref>PMID:15111675</ref> and spheroid body myopathy<ref>PMID:16380616</ref>.
Mutations in myotilin cause myofibrillar myopathy<ref>PMID:15111675</ref> and spheroid body myopathy<ref>PMID:16380616</ref>.
-
 
+
</StructureSection>
== 3D Structures of myotilin ==
== 3D Structures of myotilin ==

Current revision

Human myotilin 1st Ig domain NMR structure (PDB entry 2kdg)

Drag the structure with the mouse to rotate

3D Structures of myotilin

Updated on 17-August-2017

2kkq - hMyotilin Ig-like C2-type 2 domain - human - NMR
2kdg - hMyotilin 1st Ig domain - NMR

References

  1. Salmikangas P, Mykkanen OM, Gronholm M, Heiska L, Kere J, Carpen O. Myotilin, a novel sarcomeric protein with two Ig-like domains, is encoded by a candidate gene for limb-girdle muscular dystrophy. Hum Mol Genet. 1999 Jul;8(7):1329-36. PMID:10369880
  2. Selcen D, Engel AG. Mutations in myotilin cause myofibrillar myopathy. Neurology. 2004 Apr 27;62(8):1363-71. PMID:15111675
  3. Foroud T, Pankratz N, Batchman AP, Pauciulo MW, Vidal R, Miravalle L, Goebel HH, Cushman LJ, Azzarelli B, Horak H, Farlow M, Nichols WC. A mutation in myotilin causes spheroid body myopathy. Neurology. 2005 Dec 27;65(12):1936-40. PMID:16380616 doi:10.1212/01.wnl.0000188872.28149.9a

Proteopedia Page Contributors and Editors (what is this?)

Michal Harel

Personal tools