Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10593533 | Bioorganic & Medicinal Chemistry Letters | 2013 | 4 Pages |
Abstract
Vialinin A, a small compound isolated from the Chinese mushroom Thelephora vialis, exhibits more effective anti-inflammatory activity than the widely used immunosuppressive drug tacrolimus (FK506). Here, we show that ubiquitin-specific peptidase 5/isopeptidase T (USP5/IsoT) is a target molecule of vialinin A, identified by using a beads-probe method. Vialinin A inhibited the peptidase activity of USP5/IsoT and also inhibited the enzymatic activities of USP4 among deubiquitinating enzymes tested. Although USPs are a member of thiol protease family, vialinin A exhibited no inhibitions for other thiol proteases, such as calpain and cathepsin.
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Authors
Kiyoshi Okada, Yue Qi Ye, Kayoko Taniguchi, Ayaka Yoshida, Tomonori Akiyama, Yasukiyo Yoshioka, Jun-ichi Onose, Hiroyuki Koshino, Shunya Takahashi, Arata Yajima, Naoki Abe, Shunsuke Yajima,