7ODD

Crystal structure of bovine Hsc70(aa1-554)E213A/D214A in complex with tricine

7ODD の概要

• エントリーDOI: 10.2210/pdb7odd/pdb
• 関連するPDBエントリー: 7O6R 7ODB 7ODI 7PLK
• 分子名称: Heat shock cognate 71 kDa protein, GLYCEROL, N-[1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl]glycine, ... (6 entities in total)
• 機能のキーワード: chaperone
• 由来する生物種: Bos taurus (Bovine)
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 61750.82

構造登録者

Zehe, M.,Grimm, C.,Sotriffer, C. (登録日: 2021-04-29, 公開日: 2022-06-01, 最終更新日: 2024-02-14)

主引用文献

Zehe, M.,Kehrein, J.,Schollmayer, C.,Plank, C.,Kovacs, H.,Merino Asumendi, E.,Holzgrabe, U.,Grimm, C.,Sotriffer, C.
Combined In-Solution Fragment Screening and Crystallographic Binding-Mode Analysis with a Two-Domain Hsp70 Construct.
Acs Chem.Biol., 2024

PubMed Abstract: Heat shock protein 70 (Hsp70) isoforms are key players in the regulation of protein homeostasis and cell death pathways and are therefore attractive targets in cancer research. Developing nucleotide-competitive inhibitors or allosteric modulators, however, has turned out to be very challenging for this protein family, and no Hsp70-directed therapeutics have so far become available. As the field could profit from alternative starting points for inhibitor development, we present the results of a fragment-based screening approach on a two-domain Hsp70 construct using in-solution NMR methods, together with X-ray-crystallographic investigations and mixed-solvent molecular dynamics simulations. The screening protocol resulted in hits on both domains. In particular, fragment binding in a deeply buried pocket at the substrate-binding domain could be detected. The corresponding site is known to be important for communication between the nucleotide-binding and substrate-binding domains of Hsp70 proteins. The main fragment identified at this position also offers an interesting starting point for the development of a dual Hsp70/Hsp90 inhibitor.

PubMed: 38317495
DOI: 10.1021/acschembio.3c00589

実験手法

X-RAY DIFFRACTION (1.984 Å)