5JTC

Aspartyl/Asparaginyl beta-hydroxylase (AspH)oxygenase and TPR domains in complex with manganese, 2,4-pyridine dicarboxylate and factor X substrate peptide fragment(39mer-4Ser)

5JTC の概要

• エントリーDOI: 10.2210/pdb5jtc/pdb
• 分子名称: Aspartyl/asparaginyl beta-hydroxylase, Coagulation factor X, MANGANESE (II) ION, ... (7 entities in total)
• 機能のキーワード: 2-oxoglutarate dependent oxygenase, aspartyl/asparaginyl beta-hydroxylase, egf-like domain hydroxylase, double stranded beta-helix, tetratricopeptide repeat, oxidoreductase
• 由来する生物種: Homo sapiens (Human); 詳細
• 細胞内の位置: Isoform 1: Endoplasmic reticulum membrane; Single-pass type II membrane protein . Isoform 4: Sarcoplasmic reticulum membrane; Single-pass type II membrane protein . Isoform 8: Endoplasmic reticulum membrane; Single-pass type II membrane protein : Q12797; Secreted: P00742
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 53989.78

構造登録者

McDonough, M.A.,Pfeffer, I. (登録日: 2016-05-09, 公開日: 2017-05-24, 最終更新日: 2024-10-16)

主引用文献

Brewitz, L.,Tumber, A.,Pfeffer, I.,McDonough, M.A.,Schofield, C.J.
Aspartate/asparagine-beta-hydroxylase: a high-throughput mass spectrometric assay for discovery of small molecule inhibitors.
Sci Rep, 10:8650-8650, 2020

PubMed Abstract: The human 2-oxoglutarate dependent oxygenase aspartate/asparagine-β-hydroxylase (AspH) catalyses the hydroxylation of Asp/Asn-residues in epidermal growth factor-like domains (EGFDs). AspH is upregulated on the surface of malign cancer cells; increased AspH levels correlate with tumour invasiveness. Due to a lack of efficient assays to monitor the activity of isolated AspH, there are few reports of studies aimed at identifying small-molecule AspH inhibitors. Recently, it was reported that AspH substrates have a non-canonical EGFD disulfide pattern. Here we report that a stable synthetic thioether mimic of AspH substrates can be employed in solid phase extraction mass spectrometry based high-throughput AspH inhibition assays which are of excellent robustness, as indicated by high Z'-factors and good signal-to-noise/background ratios. The AspH inhibition assay was applied to screen approximately 1500 bioactive small-molecules, including natural products and active pharmaceutical ingredients of approved human therapeutics. Potent AspH inhibitors were identified from both compound classes. Our AspH inhibition assay should enable the development of potent and selective small-molecule AspH inhibitors and contribute towards the development of safer inhibitors for other 2OG oxygenases, e.g. screens of the hypoxia-inducible factor prolyl-hydroxylase inhibitors revealed that vadadustat inhibits AspH with moderate potency.

PubMed: 32457455
DOI: 10.1038/s41598-020-65123-9

実験手法

X-RAY DIFFRACTION (2.24 Å)