PI3K/Akt/mTOR · target hub

PPP2R5E

Serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit (PPP2R5E)

PPP2R5E is a PIP₃ / Akt phosphatase or PP2A regulation on the PI3K/Akt/mTOR axis. The B regulatory subunit might modulate substrate selectivity and catalytic activity, and also might direct the localization of the catalytic enzyme to a particular subcellular compartment It is indexed under "Akt / mTOR-directed phosphatases & PP2A subunits (selected)" on our pathway page for antibodies, inhibitors, and assay guidance.

Back to pathway overviewSearch: PPP2R5EUniProt (Q562F2)

Research notes

  • Combine with other genes in the same hub block via genetics or pharmacology to test non-redundant roles of PPP2R5E.
  • Annotate PIK3CA/PTEN and upstream RTK–Ras context when reading p-AKT, mTORC1/2, or lipid outputs.
  • Verify antibody clone, phospho-site, and stimulation; include KD/KO or inhibitor controls.

On the pathway hub (sections)

Genetic lesions & expression context (quick reference)

Type / exampleDomain / context (brief)
Expression contextTissue/cell-type–dependent expression
Rare variantsSporadic variants—require functional validation
Pathway couplingCo-occurs with neighboring nodes on the hub

Naming and prevalence vary by cohort and assay—annotate clinically with COSMIC, ClinVar, OncoKB, and datasheets; research context only.

Assay readouts for PPP2R5E

  • Lipid pools: PIP₃, PI(3,4)P₂, or substrates relevant to PPP2R5E.
  • Loss-of-function: CRISPR/siRNA often elevates p-AKT and growth readouts (context-dependent).
  • Tumor specimens: matched tumor/adjacent with mutation/expression annotation.
  • Inhibitor controls: PI3K/mTOR inhibitors to test phenotypic reversibility.

PPP2R5E experimental notes

Examples below reflect common literature and public resources (e.g., CCLE, DepMap)—validate genotypes, expression, and passage in your own stocks before committing assays.

[1] Cell lines commonly used for PPP2R5E studies (examples)

  • Tool lines: MCF-7, U87, PC-3, HEK293T, A549—screen by PPP2R5E expression and pathway context (CCLE/DepMap).
  • Combine with neighbors (PHLPP1, PHLPP2, PPP2CA, PPP2CB) via KD/pharmacology to test non-redundancy.
  • Overexpression/rescue in HEK293T supports mechanism and IP workflows.
  • Isogenic/CRISPR models separate pathway dependency from bypass survival.

[2] Cell samples for PPP2R5E Western blot

  • Whole-cell lysates—optimize RIPA/NP-40 per antibody; phosphatase inhibitors for phospho blots.
  • Stimulation: serum starvation ± insulin/EGF or amino-acid withdrawal/refeed as relevant.
  • Controls: siRNA/shRNA, CRISPR KO, or inhibitors to validate band specificity.
  • Loading: BCA normalization; subcellular fractionation when needed.

[3] Tissue samples for PPP2R5E Western blot

  • Matched tumor/adjacent frozen tissues after pathology review.
  • Mouse GEMM or xenografts—mind species antibody cross-reactivity.
  • Primary cells/PDCs when ethically approved.
  • FFPE needs specialized extraction; frozen tissue preferred for phospho work.

[4] Cell samples for PPP2R5E immunoprecipitation

  • Tagged overexpression: HEK293T FLAG/HA-PPP2R5E for complex capture.
  • Endogenous IP: high-expression lines; often ≥1–5×10⁶ cells per IP.
  • Stimulation: ligand or nutrient treatments enrich interactions—pilot time courses.
  • Controls: isotype IgG, empty vector, KD/KO negatives.

Human tissues and primary cells require ethics/IRB approval; tumors are heterogeneous—record histotype, site, and preservation conditions.

Bypass & related pathways

Models & genetics note

Overexpression vs endogenous PPP2R5E can differ in dosage, splicing, and compartmentation—in organoids/PDX, record passage, matrix, and drug history.

Quick search presets

PPP2R5EPPP2R5E antibodyPI3K inhibitormTOR inhibitor

PPP2R5E-related antibodies (keyword-biased)

Adds PPP2R5E keyword bias atop the PI3K/Akt/mTOR antibody pool—if sparse, use presets above or global search.

Neighboring targets (same hub)

PHLPP1PHLPP2PPP2CAPPP2CBPPP2R1APPP2R1BPPP2R2APPP2R2B

External databases & resources

FAQ

This content supports research reagents and pathway education—not medical advice. Annotate mutations, drug indications, and protocols with authoritative databases, datasheets, and institutional oversight.

Last reviewed: 2026-05-18

Related on this site

See the PI3K/Akt/mTOR hub for neighboring nodes and assay guidance—cross-check MAPK, RTK, metabolism, and autophagy pages as needed.

PI3K/Akt/mTOR·MAPK/ERK·Receptor tyrosine kinase·Metabolism