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2BR1

Structure-based Design of Novel Chk1 Inhibitors: Insights into Hydrogen Bonding and Protein-Ligand Affinity

2BR1 の概要
エントリーDOI10.2210/pdb2br1/pdb
関連するPDBエントリー1IA8 1NVQ 1NVR 1NVS 2BRB 2BRG 2BRH 2BRM 2BRN 2BRO
分子名称SERINE/THREONINE-PROTEIN KINASE CHK1, 2-[5,6-BIS-(4-METHOXY-PHENYL)-FURO[2,3-D]PYRIMIDIN-4-YLAMINO]-ETHANOL, SULFATE ION, ... (4 entities in total)
機能のキーワードtransferase, drug design, furanopyrimidine, molecular recognition, oncology, pyrrolopyrimidine, kinase
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34731.69
構造登録者
Foloppe, N.,Fisher, L.M.,Howes, R.,Kierstan, P.,Potter, A.,Robertson, A.G.S.,Surgenor, A.E. (登録日: 2005-04-29, 公開日: 2005-05-12, 最終更新日: 2023-12-13)
主引用文献Foloppe, N.,Fisher, L.M.,Howes, R.,Kierstan, P.,Potter, A.,Robertson, A.G.S.,Surgenor, A.E.
Structure-Based Design of Novel Chk1 Inhibitors: Insights Into Hydrogen Bonding and Protein-Ligand Affinity.
J.Med.Chem., 48:4332-, 2005
Cited by
PubMed: 15974586
DOI: 10.1021/JM049022C
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2 Å)
構造検証レポート
Validation report summary of 2br1
検証レポート(詳細版)ダウンロードをダウンロード

217705

件を2024-03-27に公開中

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