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5OCI

Human Heat Shock Protein 90 bound to 6-Hydroxy-3-(3-methyl-benzyl)-1H-indazole-5-carboxylic acid methyl-(4-morpholin-4-yl-phenyl)-amide

5OCI の概要
エントリーDOI10.2210/pdb5oci/pdb
分子名称Heat shock protein HSP 90-alpha, 6-Hydroxy-3-(3-methyl-benzyl)-1H-indazole-5-carboxylic acid methyl-(4-morpholin-4-yl-phenyl)-amide (3 entities in total)
機能のキーワードheat-shock protein complex, hsp90, atpase, pyrazole, chaperone, atp-binding, heat shock, nucleotide-binding, phosphorylation
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26170.36
構造登録者
Schuetz, D.A.,Richter, L.,Amaral, M.,Grandits, M.,Musil, D.,Graedler, U.,Frech, M.,Ecker, G.F. (登録日: 2017-07-03, 公開日: 2018-05-23, 最終更新日: 2024-05-08)
主引用文献Schuetz, D.A.,Richter, L.,Amaral, M.,Grandits, M.,Gradler, U.,Musil, D.,Buchstaller, H.P.,Eggenweiler, H.M.,Frech, M.,Ecker, G.F.
Ligand Desolvation Steers On-Rate and Impacts Drug Residence Time of Heat Shock Protein 90 (Hsp90) Inhibitors.
J. Med. Chem., 61:4397-4411, 2018
Cited by
PubMed Abstract: Residence time and more recently the association rate constant k are increasingly acknowledged as important parameters for in vivo efficacy and safety of drugs. However, their broader consideration in drug development is limited by a lack of knowledge of how to optimize these parameters. In this study on a set of 176 heat shock protein 90 inhibitors, structure-kinetic relationships, X-ray crystallography, and molecular dynamics simulations were combined to retrieve a concrete scheme of how to rationally slow down on-rates. We discovered that an increased ligand desolvation barrier by introducing polar substituents resulted in a significant k decrease. The slowdown was accomplished by introducing polar moieties to those parts of the ligand that point toward a hydrophobic cavity. We validated this scheme by increasing polarity of three Hsp90 inhibitors and observed a 9-, 13-, and 45-fold slowdown of on-rates and a 9-fold prolongation in residence time. This prolongation was driven by transition state destabilization rather than ground state stabilization.
PubMed: 29701469
DOI: 10.1021/acs.jmedchem.8b00080
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.62 Å)
構造検証レポート
Validation report summary of 5oci
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2026-04-15に公開中

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