Molecular basis for the unusual ring reconstruction in fungal meroterpenoid biogenesis-Reference-Cited by-同舟云学术

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Molecular basis for the unusual ring reconstruction in fungal meroterpenoid biogenesis

Published:2017-07-31 Issue:10 Volume:13 Page:1066-1073
ISSN:1552-4450
Container-title:Nature Chemical Biology
language:en
Short-container-title:Nat Chem Biol

Author:

Mori Takahiro,Iwabuchi Taiki,Hoshino Shotaro,Wang Hang,Matsuda Yudai,Abe Ikuro

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Molecular Biology

Link

http://www.nature.com/articles/nchembio.2443.pdf

Reference35 articles.

1. Geris, R. & Simpson, T.J. Meroterpenoids produced by fungi. Nat. Prod. Rep. 26, 1063–1094 (2009).

2. Matsuda, Y. & Abe, I. Biosynthesis of fungal meroterpenoids. Nat. Prod. Rep. 33, 26–53 (2016).

3. Sintchak, M.D. et al. Structure and mechanism of inosine monophosphate dehydrogenase in complex with the immunosuppressant mycophenolic acid. Cell 85, 921–930 (1996).

4. McCowen, M.C., Callender, M.E. & Lawlis, J.F. Fumagillin (H-3), a new antibiotic with amebicidal properties. Science 113, 202–203 (1951).

5. Tomoda, H. et al. Relative and Absolute stereochemistry of pyripyropene A, a potent, bioavailable inhibitor of acyl-CoA:cholesterol acyltransferase (ACAT). J. Am. Chem. Soc. 116, 12097–12098 (1994).

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