PPP1R3E
Protein phosphatase 1 regulatory subunit 3E
Also known as: FLJ00089, PPR3E_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9H7J1
- Gene
- PPP1R3E
- Ensembl
- ENSG00000235194
- Chromosome
- 14
- Canonical length
- 279 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Microtubules,Mitotic spindle,Mitochondria
OverviewNCBI Gene
Predicted to enable [phosphorylase] phosphatase activity; glycogen binding activity; and protein phosphatase 1 binding activity. Predicted to be involved in positive regulation of glycogen biosynthetic process. Predicted to be located in glycogen granule. Predicted to be part of protein phosphatase type 1 complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
279 residues, UniProt reviewed canonical sequence.
>Q9H7J1|PPP1R3E
1 MSRERPPGTD IPRNLSFIAA LTERAYYRSQ RPSLEEEPEE EPGEGGTRFG ARSRAHAPSR
61 GRRARSAPAG GGGARAPRSR SPDTRKRVRF ADALGLELAV VRRFRPGELP RVPRHVQIQL
121 QRDALRHFAP CQPRARGLQE ARAALEPASE PGFAARLLTQ RICLERAEAG PLGVAGSARV
181 VDLAYEKRVS VRWSADGWRS QREAPAAYAG PAPPPPRADR FAFRLPAPPI GGALLFALRY
241 RVTGHEFWDN NGGRDYALRG PEHPGSGGAP EPQGWIHFILocalizationUniProt · AlphaFold · HPA
Whether an antibody against PPP1R3E can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.49
- Highest tissue expression
- 43 nTPM
Expression across tissuesHPA
Tissue
- retina: 43 nTPM
- cerebellum: 35 nTPM
- midbrain: 23 nTPM
- spinal cord: 22 nTPM
- cerebral cortex: 19 nTPM
- pituitary gland: 19 nTPM
Single-cell type
- early spermatids: 105 nCPM
- adrenal cortex cells: 73 nCPM
- late spermatids: 60 nCPM
- retinal bipolar cells: 48 nCPM
- oligodendrocytes: 44 nCPM
- cone photoreceptor cells: 39 nCPM
Immune cell
- non-classical monocyte: 1.8 nTPM
- intermediate monocyte: 1.4 nTPM
- memory B-cell: 1 nTPM
- MAIT T-cell: 0.6 nTPM
- naive B-cell: 0.6 nTPM
- gdT-cell: 0.5 nTPM
Brain region
- white matter: 39 nTPM
- pons: 32 nTPM
- medulla oblongata: 29 nTPM
- cerebellum: 29 nTPM
- thalamus: 28 nTPM
- basal ganglia: 28 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.39
- gnomAD pLI
- 0.24
- gnomAD missense Z
- 0.62
- DepMap mean gene effect
- -0.19
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- glycogen metabolic process
- positive regulation of glycogen biosynthetic process
- regulation of glycogen biosynthetic process
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PPP1R3E in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads PPP1R3E as an antibody target. Whether an autoantibody or antibody against PPP1R3E could matter depends on whether native PPP1R3E is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PPP1R3E is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label PPP1R3E as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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