Substrate-Trapped Interactors of PHD3 and FIH Cluster in Distinct Signaling Pathways
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文摘

The proteomic screen for FIH and PHD3 substrates identifies numerous interactors

Potential substrates are enriched in numerous hypoxia-regulated pathways

FIH regulates RIPK4 kinase activity by direct hydroxylation

Hydroxylation of Pro25 by PHD3 regulates MAPK6 (Erk3) protein stability

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