Curated Information
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Home > Curated Information Page > PubMed Id: 32054729
Jin S, et al. (2020) 5-Azacitidine Induces NOXA to Prime AML Cells for Venetoclax-Mediated Apoptosis. Clin Cancer Res 32054729
This page summarizes selected information from the record referenced above and curated into PhosphoSitePlus®, a comprehensive online resource for the study of protein post-translational modifications (NAR, 2015, 43:D512-20). To learn more about the scope of PhosphoSitePlus®, click here.
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S52-p - eIF2-alpha (human)
Modsite: MILLsELsRRRIRsI SwissProt Entrez-Gene
Orthologous residues
eIF2‑alpha (human): S52‑p, eIF2‑alpha (mouse): S52‑p, eIF2‑alpha (rat): S52‑p, eIF2‑alpha (rabbit): S51‑p, eIF2‑alpha (fruit fly): S51‑p
Characterization
Methods used to characterize site in vivo phospho-antibody, western blotting
Disease tissue studied:  leukemia, acute myelogenous leukemia, acute monoblastic leukemia (M5a) or acute monocytic leukemia (M5b), acute myeloblastic leukemia, with granulocytic maturation (M2)
Relevant cell lines - cell types - tissues:  Kasumi-1 (myeloid), MV4-11 (macrophage), OCI-AML5 (myeloid)
Cellular systems studied:  cell lines
Species studied:  human
Upstream Regulation
Treatments, proteins and their effect on site modification: 
Treatments Referenced Treatments Manipulated Protein Referenced Protein Effect Notes
AzaC increase
Downstream Regulation
Effect of modification (process):  apoptosis, induced, transcription, induced