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pubmed-article:15780623pubmed:abstractTextTyropeptin A, a new potent proteasome inhibitor, was produced by Kitasatospora sp. MK993-dF2. To enhance the inhibitory potency of tyropeptin A, we constructed the structural model of tyropeptin A bound to the site responsible for the chymotrypsin-like activity of mammalian 20S proteasome. Based on these modeling experiments, we designed and synthesized several derivatives of tyropeptin A. Among them, the most potent compound, TP-104, exhibited a 20-fold enhancement in its inhibitory potency compared to tyropeptin A. Additionally, TP-110 specifically inhibited the chymotrypsin-like activity, but did not inhibit the PGPH and the trypsin-like activities.lld:pubmed
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pubmed-article:15780623pubmed:authorpubmed-author:MomoseIsaoIlld:pubmed
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pubmed-article:15780623pubmed:pagination1867-71lld:pubmed
pubmed-article:15780623pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:15780623pubmed:articleTitleStructure-based design of derivatives of tyropeptin A as the potent and selective inhibitors of mammalian 20S proteasome.lld:pubmed
pubmed-article:15780623pubmed:affiliationNumazu Bio-Medical Research Institute, Microbial Chemistry Research Center, 18-24 Miyamoto, Numazu City, Shizuoka 410-0301, Japan. imomose@bikaken.or.jplld:pubmed
pubmed-article:15780623pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:15780623pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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