Identification of proteins binding to decursinol by chemical proteomics = 화학단백질체학을 이용한 디커시놀 결합 단백질의 발굴

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dc.contributor.authorHyo Jin Kang-
dc.contributor.authorTae-Sung Yoon-
dc.contributor.authorDae Gwin Jeong-
dc.contributor.authorYongmo Kim-
dc.contributor.authorJin Woong Chung-
dc.contributor.authorJong Seong Ha-
dc.contributor.authorSung Sup Park-
dc.contributor.authorSeong Eon Ryu-
dc.contributor.authorS Kim-
dc.contributor.authorKwang-Hee Bae-
dc.contributor.authorSang Jeon Chung-
dc.date.accessioned2017-04-19T09:11:32Z-
dc.date.available2017-04-19T09:11:32Z-
dc.date.issued2008-
dc.identifier.issn1017-7825-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/8564-
dc.description.abstractDecursinol, found in the roots of Angelica gigas Nakai, has been traditionally used to treat anemia and other various diseases. Recently, numerous biological activities such as cytotoxic effect on leukemia cells, and antitumor, neuroprotection, and antibacterial activities have been reported for this compound. Although a number of proteins including protein kinase C, androgen receptor, and acetylcholinesterase were proposed as molecular targets responsible for the activities of decursinol, they are not enough to explain such a diverse biological activity mentioned above. In this study, we employed a chemical proteomic approach, leading to identification of seven proteins as potential proteins interacting with decursinol. Most of the proteins contain a defined ATP or nucleic acid binding domain and have been implied to be involved in the pathogenesis and progression of various human diseases including cancer, autoimmune disorders, or neurodegenerative diseases. The present results may provide clues to understand the molecular mechanism of the biological activities shown by decursinol, an anticancer natural product.-
dc.publisherKorea Soc-Assoc-Inst-
dc.titleIdentification of proteins binding to decursinol by chemical proteomics = 화학단백질체학을 이용한 디커시놀 결합 단백질의 발굴-
dc.title.alternativeIdentification of proteins binding to decursinol by chemical proteomics-
dc.typeArticle-
dc.citation.titleJournal of Microbiology and Biotechnology-
dc.citation.number8-
dc.citation.endPage1430-
dc.citation.startPage1427-
dc.citation.volume18-
dc.contributor.affiliatedAuthorHyo Jin Kang-
dc.contributor.affiliatedAuthorTae-Sung Yoon-
dc.contributor.affiliatedAuthorDae Gwin Jeong-
dc.contributor.affiliatedAuthorYongmo Kim-
dc.contributor.affiliatedAuthorJin Woong Chung-
dc.contributor.affiliatedAuthorJong Seong Ha-
dc.contributor.affiliatedAuthorSung Sup Park-
dc.contributor.affiliatedAuthorSeong Eon Ryu-
dc.contributor.affiliatedAuthorKwang-Hee Bae-
dc.contributor.affiliatedAuthorSang Jeon Chung-
dc.contributor.alternativeName강효진-
dc.contributor.alternativeName윤태성-
dc.contributor.alternativeName정대균-
dc.contributor.alternativeName김용모-
dc.contributor.alternativeName정진웅-
dc.contributor.alternativeName하종성-
dc.contributor.alternativeName박성섭-
dc.contributor.alternativeName류성언-
dc.contributor.alternativeName김상희-
dc.contributor.alternativeName배광희-
dc.contributor.alternativeName정상전-
dc.identifier.bibliographicCitationJournal of Microbiology and Biotechnology, vol. 18, no. 8, pp. 1427-1430-
dc.subject.keywordanticancer-
dc.subject.keywordchemical proteomics-
dc.subject.keyworddecursinol-
dc.subject.keywordenolase-
dc.subject.keywordHsp90-
dc.subject.localAnti-cancer-
dc.subject.localAnticancer-
dc.subject.localanti-cancer-
dc.subject.localanticancer-
dc.subject.localAnti-Cancer-
dc.subject.localchemical proteomics-
dc.subject.localChemical proteomics-
dc.subject.localDecursinol-
dc.subject.localdecursinol-
dc.subject.localenolase-
dc.subject.localHsp90-
dc.subject.localHSP90-
dc.description.journalClassY-
Appears in Collections:
Critical Diseases Diagnostics Convergence Research Center > 1. Journal Articles
Division of Research on National Challenges > Bionanotechnology Research Center > 1. Journal Articles
Aging Convergence Research Center > 1. Journal Articles
Division of A.I. & Biomedical Research > Metabolic Regulation Research Center > 1. Journal Articles
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