Publication | Open Access
SM-20, EGL-9, and the EGLN Family of Hypoxia-inducible Factor Prolyl Hydroxylases
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Citations
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References
2003
Year
Aldo-keto ReductaseGlycobiologyRedox BiologyOxidative StressProtein ExpressionSignaling PathwayRedox RegulatorAutophagyNew MechanismProteomicsCell SignalingAldehyde DehydrogenaseBiochemistryHypoxia (Medicine)Protein InteractionsGene ExpressionCell BiologyProtein PhosphorylationSignal TransductionDevelopmental BiologyEgln FamilyNatural SciencesCellular BiochemistrySystems BiologyMedicine
Key to the transduction of signals from the environment to the cell nucleus are enzymes that post-translationally modify proteins. Modifications such as protein phosphorylation have long been known to regulate protein interactions, stability, and localization, as well as enzyme activity. Recent investigations into how cells respond to varying oxygen levels have identified a new mechanism for regulating signal transduction involving the post-translational hydroxylation of proline. The enzymes that catalyze this reaction comprise a novel family of prolyl hydroxylases, which include a growth-factor-responsive and cell-death-related protein (SM-20) in mammals, and a protein (EGL-9) in C. elegans important for normal egg laying.
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