Penicisulfuranol A, a novel C-terminal inhibitor disrupting molecular chaperone function of Hsp90 independent of ATP binding domain-Reference-Cited by-同舟云学术

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Penicisulfuranol A, a novel C-terminal inhibitor disrupting molecular chaperone function of Hsp90 independent of ATP binding domain

Published:2019-05 Issue: Volume:163 Page:404-415
ISSN:0006-2952
Container-title:Biochemical Pharmacology
language:en
Short-container-title:Biochemical Pharmacology

Author:

Dai Jiajia,Chen Ao,Zhu Meilin,Qi Xin,Tang Wei,Liu Ming,Li Dehai,Gu Qianqun,Li Jing

Funder

National Natural Science Foundation of China

NSFC

Publisher

Elsevier BV

Subject

Pharmacology,Biochemistry

Reference55 articles.

1. Quantitative analysis of Hsp90-client interactions reveals principles of substrate recognition;Taipale;Cell,2012

2. Hsp90: structure and function;Jackson,2013

3. HSP90 as a platform for the assembly of more effective cancer chemotherapy;Whitesell;Biochim. Biophys. Acta (BBA) – Mol. Cell Res.,2012

4. Protein chaperones: a composition of matter review (2008–2013);Taldone;Expert Opin. Therap. Patents,2014

5. Crystal structure of an Hsp90–nucleotide–p23/Sba1 closed chaperone complex;Ali;Nature,2006

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