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1BD8

STRUCTURE OF CDK INHIBITOR P19INK4D

1BD8 の概要
エントリーDOI10.2210/pdb1bd8/pdb
分子名称P19INK4D CDK4/6 INHIBITOR (2 entities in total)
機能のキーワードtumor suppressor, cdk4/6 inhibitor, ankyrin motif
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16627.81
構造登録者
Baumgartner, R.,Fernandez-Catalan, C.,Winoto, A.,Huber, R.,Engh, R.,Holak, T.A. (登録日: 1998-05-12, 公開日: 1998-10-14, 最終更新日: 2024-02-07)
主引用文献Baumgartner, R.,Fernandez-Catalan, C.,Winoto, A.,Huber, R.,Engh, R.A.,Holak, T.A.
Structure of human cyclin-dependent kinase inhibitor p19INK4d: comparison to known ankyrin-repeat-containing structures and implications for the dysfunction of tumor suppressor p16INK4a.
Structure, 6:1279-1290, 1998
Cited by
PubMed Abstract: The four members of the INK4 gene family (p16(INK4a), p15(INK4b), p18(INK4c) and p19(INK4d)) inhibit the closely related cyclin-dependent kinases CDK4 and CDK6 as part of the regulation of the G1-->S transition in the cell-division cycle. Loss of INK4 gene product function, particularly that of p16(INK4a), is found in 10-60% of human tumors, suggesting that broadly applicable anticancer therapies might be based on restoration of p16(INK4a) CDK inhibitory function. Although much less frequent, defects of p19(INK4d) have also been associated with human cancer (osteosarcomas). The protein structures of some INK4 family members, determined by nuclear magnetic resonance (NMR) spectroscopy and X-ray techniques, have begun to clarify the functional role of p16(INK4a) and the dysfunction introduced by the mutations associated with human tumors.
PubMed: 9782052
DOI: 10.1016/S0969-2126(98)00128-2
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.8 Å)
構造検証レポート
Validation report summary of 1bd8
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2026-02-04に公開中

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