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基本情報
登録情報 | データベース: PDB / ID: 9oyo | |||||||||||||||||||||||||||
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タイトル | Structure of R15L D10-NT amyloid fibrils | |||||||||||||||||||||||||||
![]() | Coiled-coil-helix-coiled-coil-helix domain-containing protein 10, mitochondrial | |||||||||||||||||||||||||||
![]() | PROTEIN FIBRIL / CHCHD10 / R15L / Amyloid Fibril | |||||||||||||||||||||||||||
機能・相同性 | ![]() : / MICOS complex / mitochondria-nucleus signaling pathway / positive regulation of cristae formation / positive regulation of mitochondrial transcription / stabilization of membrane potential / maintenance of synapse structure / Mitochondrial protein import / maintenance of protein location in nucleus / positive regulation of mitochondrial outer membrane permeabilization involved in apoptotic signaling pathway ...: / MICOS complex / mitochondria-nucleus signaling pathway / positive regulation of cristae formation / positive regulation of mitochondrial transcription / stabilization of membrane potential / maintenance of synapse structure / Mitochondrial protein import / maintenance of protein location in nucleus / positive regulation of mitochondrial outer membrane permeabilization involved in apoptotic signaling pathway / oxidative phosphorylation / mitochondrion organization / mitochondrial intermembrane space / protein-containing complex assembly / mitochondrion / nucleus 類似検索 - 分子機能 | |||||||||||||||||||||||||||
生物種 | ![]() | |||||||||||||||||||||||||||
手法 | 電子顕微鏡法 / らせん対称体再構成法 / クライオ電子顕微鏡法 / 解像度: 3.15 Å | |||||||||||||||||||||||||||
![]() | Lv, G. / Eliezer, D. | |||||||||||||||||||||||||||
資金援助 | ![]()
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![]() | ![]() タイトル: Amyloid fibril structures link CHCHD10 and CHCHD2 to neurodegeneration. 著者: Guohua Lv / Nicole M Sayles / Yun Huang / Chiara Mancinelli / Kevin McAvoy / Neil A Shneider / Giovanni Manfredi / Hibiki Kawamata / David Eliezer / ![]() 要旨: Mitochondrial proteins CHCHD10 and CHCHD2 are mutated in rare cases of heritable FTD, ALS and PD and aggregate in tissues affected by these diseases. Here, we show that both proteins form amyloid ...Mitochondrial proteins CHCHD10 and CHCHD2 are mutated in rare cases of heritable FTD, ALS and PD and aggregate in tissues affected by these diseases. Here, we show that both proteins form amyloid fibrils and report cryo-EM structures of fibrils formed from their disordered N-terminal domains. The ordered cores of these fibrils are comprised of a region highly conserved between the two proteins, and a subset of the CHCHD10 and CHCHD2 fibril structures share structural similarities and appear compatible with sequence variations in this region. In contrast, disease-associated mutations p.S59L in CHCHD10 and p.T61I in CHCHD2, situated within the ordered cores of these fibrils, cannot be accommodated by the wildtype structures and promote different protofilament folds and fibril structures. These results link CHCHD10 and CHCHD2 amyloid fibrils to neurodegeneration and further suggest that fibril formation by the WT proteins could also be involved in disease etiology. | |||||||||||||||||||||||||||
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-関連構造データ
関連構造データ | ![]() 71028MC ![]() 9cwwC ![]() 9oyqC ![]() 9oyrC ![]() 9oysC ![]() 9oytC ![]() 9oywC C: 同じ文献を引用 ( M: このデータのモデリングに利用したマップデータ |
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非結晶学的対称性 (NCS) | NCSドメイン:
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