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The DEXD/H-box RNA Helicase DDX19 Is Regulated by an α-Helical Switch

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JOURNAL OF BIOLOGICAL CHEMISTRY
卷 284, 期 16, 页码 10296-10300

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DOI: 10.1074/jbc.C900018200

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DEXD/H-box RNA helicases couple ATP hydrolysis to RNA remodeling by an unknown mechanism. We used x-ray crystallography and biochemical analysis of the human DEXD/H-box protein DDX19 to investigate its regulatory mechanism. The crystal structures of DDX19, in its RNA-bound prehydrolysis and free posthydrolysis state, reveal an alpha-helix that inserts between the conserved domains of the free protein to negatively regulate ATPase activity. This finding was corroborated by biochemical data that confirm an autoregulatory function of the N-terminal region of the protein. This is the first study describing crystal structures of a DEXD/H-box protein in its open and closed cleft conformations.

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