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1C8K

FLAVOPIRIDOL INHIBITS GLYCOGEN PHOSPHORYLASE BY BINDING AT THE INHIBITOR SITE

1C8K の概要
エントリーDOI10.2210/pdb1c8k/pdb
分子名称PROTEIN (GLYCOGEN PHOSPHORYLASE), PYRIDOXAL-5'-PHOSPHATE, 2-(2-CHLORO-PHENYL)-5,7-DIHYDROXY-8-(3-HYDROXY-1-METHYL-PIPERIDIN-4-YL)-4H-BENZOPYRAN-4-ONE, ... (4 entities in total)
機能のキーワードglycogen metabolism, glycogen phosphorylase b, inhibition, inhibitor binding site, antitumour agent, transferase
由来する生物種Oryctolagus cuniculus (rabbit)
タンパク質・核酸の鎖数1
化学式量合計97940.18
構造登録者
Oikonomakos, N.G.,Zographos, S.E.,Skamnaki, V.T.,Tsitsanou, K.E.,Johnson, L.N. (登録日: 2000-05-11, 公開日: 2000-05-24, 最終更新日: 2023-12-27)
主引用文献Oikonomakos, N.G.,Schnier, J.B.,Zographos, S.E.,Skamnaki, V.T.,Tsitsanou, K.E.,Johnson, L.N.
Flavopiridol inhibits glycogen phosphorylase by binding at the inhibitor site.
J.Biol.Chem., 275:34566-34573, 2000
Cited by
PubMed: 10924512
DOI: 10.1074/jbc.M004485200
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.76 Å)
構造検証レポート
Validation report summary of 1c8k
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2024-04-17に公開中

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