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5JZV

The structure of D77G hCINAP-ADP

5JZV の概要
エントリーDOI10.2210/pdb5jzv/pdb
分子名称Adenylate kinase isoenzyme 6, ADENOSINE-5'-DIPHOSPHATE (3 entities in total)
機能のキーワードatpase, adenylate kinase, transferase
由来する生物種Homo sapiens (Human)
細胞内の位置Nucleus, nucleoplasm: Q9Y3D8
タンパク質・核酸の鎖数1
化学式量合計24004.52
構造登録者
Liu, Y.,Yang, Z.,Yang, Y.,Cai, X.,Zheng, X. (登録日: 2016-05-17, 公開日: 2016-08-10, 最終更新日: 2023-11-08)
主引用文献Bai, D.,Zhang, J.,Li, T.,Hang, R.,Liu, Y.,Tian, Y.,Huang, D.,Qu, L.,Cao, X.,Ji, J.,Zheng, X.
The ATPase hCINAP regulates 18S rRNA processing and is essential for embryogenesis and tumour growth.
Nat Commun, 7:12310-12310, 2016
Cited by
PubMed Abstract: Dysfunctions in ribosome biogenesis cause developmental defects and increased cancer susceptibility; however, the connection between ribosome assembly and tumorigenesis remains unestablished. Here we show that hCINAP (also named AK6) is required for human 18S rRNA processing and 40S subunit assembly. Homozygous CINAP(-/-) mice show embryonic lethality. The heterozygotes are viable and show defects in 18S rRNA processing, whereas no delayed cell growth is observed. However, during rapid growth, CINAP haploinsufficiency impairs protein synthesis. Consistently, hCINAP depletion in fast-growing cancer cells inhibits ribosome assembly and abolishes tumorigenesis. These data demonstrate that hCINAP reduction is a specific rate-limiting controller during rapid growth. Notably, hCINAP is highly expressed in cancers and correlated with a worse prognosis. Genome-wide polysome profiling shows that hCINAP selectively modulates cancer-associated translatome to promote malignancy. Our results connect the role of hCINAP in ribosome assembly with tumorigenesis. Modulation of hCINAP expression may be a promising target for cancer therapy.
PubMed: 27477389
DOI: 10.1038/ncomms12310
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.07 Å)
構造検証レポート
Validation report summary of 5jzv
検証レポート(詳細版)ダウンロードをダウンロード

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件を2026-04-22に公開中

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