5TZM

59th Ig domain of human obscurin (OBSCN Ig59)

5TZM の概要

• エントリーDOI: 10.2210/pdb5tzm/pdb
• 分子名称: Obscurin (2 entities in total)
• 機能のキーワード: ig-like fold, cytoskeleton, muscle, muscular dystrophy, transferase, structural protein
• 由来する生物種: Homo sapiens (Human)
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 10708.93

構造登録者

Wright, N.T.,Berndsen, C.E.,Policke, R.A. (登録日: 2016-11-21, 公開日: 2017-11-08, 最終更新日: 2024-10-16)

主引用文献

Rossi, D.,Palmio, J.,Evila, A.,Galli, L.,Barone, V.,Caldwell, T.A.,Policke, R.A.,Aldkheil, E.,Berndsen, C.E.,Wright, N.T.,Malfatti, E.,Brochier, G.,Pierantozzi, E.,Jordanova, A.,Guergueltcheva, V.,Romero, N.B.,Hackman, P.,Eymard, B.,Udd, B.,Sorrentino, V.
A novel FLNC frameshift and an OBSCN variant in a family with distal muscular dystrophy.
PLoS ONE, 12:e0186642-e0186642, 2017

PubMed Abstract: A novel FLNC c.5161delG (p.Gly1722ValfsTer61) mutation was identified in two members of a French family affected by distal myopathy and in one healthy relative. This FLNC c.5161delG mutation is one nucleotide away from a previously reported FLNC mutation (c.5160delC) that was identified in patients and in asymptomatic carriers of three Bulgarian families with distal muscular dystrophy, indicating a low penetrance of the FLNC frameshift mutations. Given these similarities, we believe that the two FLNC mutations alone can be causative of distal myopathy without full penetrance. Moreover, comparative analysis of the clinical manifestations indicates that patients of the French family show an earlier onset and a complete segregation of the disease. As a possible explanation of this, the two French patients also carry a OBSCN c.13330C>T (p.Arg4444Trp) mutation. The p.Arg4444Trp variant is localized within the OBSCN Ig59 domain that, together with Ig58, binds to the ZIg9/ZIg10 domains of titin at Z-disks. Structural and functional studies indicate that this OBSCN p.Arg4444Trp mutation decreases titin binding by ~15-fold. On this line, we suggest that the combination of the OBSCN p.Arg4444Trp variant and of the FLNC c.5161delG mutation, can cooperatively affect myofibril stability and increase the penetrance of muscular dystrophy in the French family.

PubMed: 29073160
DOI: 10.1371/journal.pone.0186642

実験手法

X-RAY DIFFRACTION (1.177 Å)