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2VWC

STRUCTURE OF THE HSP90 INHIBITOR MACBECIN BOUND TO THE N-TERMINUS OF YEAST HSP90.

2VLS」から置き換えられました
2VWC の概要
エントリーDOI10.2210/pdb2vwc/pdb
関連するPDBエントリー1A4H 1AH6 1AH8 1AM1 1AMW 1BGQ 1HK7 1US7 1USU 1USV 1ZW9 1ZWH 2AKP 2BRC 2BRE 2CG9 2CGE 2CGF 2IWS 2IWU 2IWX 2VW5
分子名称ATP-DEPENDENT MOLECULAR CHAPERONE HSP82, MACBECIN, GLYCEROL, ... (4 entities in total)
機能のキーワードchaperone, chaperone-complex, inhibitor, heat shock, atp-binding, stress response, multigene family, nucleotide-binding
由来する生物種SACCHAROMYCES CEREVISIAE (BAKER'S YEAST)
細胞内の位置Cytoplasm: P02829
タンパク質・核酸の鎖数1
化学式量合計25427.04
構造登録者
Roe, S.M.,Prodromou, C.,Pearl, L.H. (登録日: 2008-06-20, 公開日: 2008-07-01, 最終更新日: 2023-12-13)
主引用文献Martin, C.J.,Gaisser, S.,Challis, I.R.,Carletti, I.,Wilkinson, B.,Gregory, M.,Prodromou, C.,Roe, S.M.,Pearl, L.H.,Boyd, S.M.,Zhang, M.Q.
Molecular Characterisation of Macbecin as an Hsp90 Inhibitor
J.Med.Chem., 51:2853-, 2008
Cited by
PubMed Abstract: Macbecin compares favorably to geldanamycin as an Hsp90 inhibitor, being more soluble, stable, more potently inhibiting ATPase activity (IC50 = 2 microM) and binding with higher affinity (Kd = 0.24 microM). Structural studies reveal significant differences in their Hsp90 binding characteristics, and macbecin-induced tumor cell growth inhibition is accompanied by characteristic degradation of Hsp90 client proteins. Macbecin significantly reduced tumor growth rates (minimum T/C: 32%) in a DU145 murine xenograft. Macbecin thus represents an attractive lead for further optimization.
PubMed: 18357975
DOI: 10.1021/JM701558C
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.4 Å)
構造検証レポート
Validation report summary of 2vwc
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2025-06-18に公開中

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