| Literature DB >> 15376558 |
Hidetaka Hatori1, Tatsuya Zenkoh, Motoo Kobayashi, Yoshihiro Ohtsu, Nobuharu Shigematsu, Hiroyuki Setoi, Motohiro Hino, Hiroshi Handa.
Abstract
FR225659 was originally isolated as a novel gluconeogenesis inhibitor produced by fungal strain Helicomyces sp. No. 19353. To identify the target protein of FR225659, we synthesized high-performance affinity latex beads that immobilized FR225659 derivative FR253761 or FR259383. Using these beads, we identified FR225659 binding proteins as serine/threonine protein phosphatase type1 (PP1) and type2A (PP2A) from rat hepatocyte crude extract. FR225659 and its synthetic derivatives were strongly inhibited the enzyme activities of purified catalytic subunits of PP1 and PP2A in vitro.Entities:
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Year: 2004 PMID: 15376558 DOI: 10.7164/antibiotics.57.456
Source DB: PubMed Journal: J Antibiot (Tokyo) ISSN: 0021-8820 Impact factor: 2.649