Cellularly active N -hydroxyurea FEN1 inhibitors block substrate entry to the active site
Nature chemical biology(2016)
摘要
Structural, enzymatic and cellular target engagement studies reveal the mechanism of action by N -hydroxyurea small molecule inhibitors of the DNA repair enzyme, human flap endonuclease-1 (FEN1) that prevent cleavage of DNA flaps in cancer cells.
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关键词
Enzyme mechanisms,DNA damage and repair,X-ray crystallography,Small molecules
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