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The DEXD/H-box RNA Helicase DDX19 Is Regulated by an α-Helical Switch
- Source :
- The Journal of Biological Chemistry
- Publication Year :
- 2009
- Publisher :
- Elsevier BV, 2009.
-
Abstract
- 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.
- Subjects :
- Models, Molecular
Nucleocytoplasmic Transport Proteins
Molecular Sequence Data
Accelerated Publication
Biology
Crystallography, X-Ray
Biochemistry
Protein Structure, Secondary
DEAD-box RNA Helicases
03 medical and health sciences
ATP hydrolysis
Humans
Amino Acid Sequence
Binding site
Molecular Biology
Peptide sequence
030304 developmental biology
0303 health sciences
Binding Sites
030302 biochemistry & molecular biology
RNA
Cell Biology
Non-coding RNA
RNA Helicase A
Protein tertiary structure
Protein Structure, Tertiary
eIF4A
Biophysics
Subjects
Details
- ISSN :
- 00219258
- Volume :
- 284
- Database :
- OpenAIRE
- Journal :
- Journal of Biological Chemistry
- Accession number :
- edsair.doi.dedup.....d03c167cce1623e48a508438f560dc27
- Full Text :
- https://doi.org/10.1074/jbc.c900018200