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Multiple mechanisms control phosphorylation of PHAS-I in five (S/T)P sites that govern translational repression
Isabelle Mothe-Satney
, Daqing Yang
, Patrick Fadden
, Timothy A.J. Haystead
, John C. Lawrence
Research output
:
Contribution to journal
›
Article
›
peer-review
168
Scopus citations
Overview
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Dive into the research topics of 'Multiple mechanisms control phosphorylation of PHAS-I in five (S/T)P sites that govern translational repression'. Together they form a unique fingerprint.
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Keyphrases
Amino Acids
10%
Binding Affinity
10%
Dependent Processes
10%
Electrophoretic Properties
10%
Eukaryotic Translation Initiation Factor 4E (eIF4E)
30%
HEK293 Cells
10%
Insulin
10%
Mammalian Target of Rapamycin (mTOR)
10%
Mechanism Control
100%
Multiple Mechanisms
100%
One-site
10%
P-site
100%
Phosphorylation
100%
Phosphorylation Sites
10%
Site Influence
10%
Third Level
10%
Three-level
10%
Translational Repression
100%
Translational Repressor
10%
Biochemistry, Genetics and Molecular Biology
Amino Acids
33%
Binding Affinity
33%
Eukaryotic Initiation Factor
100%
Mammalian Target of Rapamycin
33%
P-Site
100%
Repressor
33%
RNA Translation
33%