PPP1R8
Nuclear inhibitor of protein phosphatase 1
Also known as: ard-1, ARD1, NIPP-1, NIPP1, PP1R8_HUMAN, PRO2047
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q12972
- Gene
- PPP1R8
- Ensembl
- ENSG00000117751
- Chromosome
- 1
- Canonical length
- 351 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nuclear speckles
OverviewNCBI Gene
This gene, through alternative splicing, encodes three different isoforms. Two of the protein isoforms encoded by this gene are specific inhibitors of type 1 serine/threonine protein phosphatases and can bind but not cleave RNA. The third protein isoform lacks the phosphatase inhibitory function but is a single-strand endoribonuclease comparable to RNase E of E. coli. This isoform requires magnesium for its function and cleaves specific sites in A+U-rich regions of RNA. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
351 residues, UniProt reviewed canonical sequence.
>Q12972|PPP1R8
1 MAAAANSGSS LPLFDCPTWA GKPPPGLHLD VVKGDKLIEK LIIDEKKYYL FGRNPDLCDF
61 TIDHQSCSRV HAALVYHKHL KRVFLIDLNS THGTFLGHIR LEPHKPQQIP IDSTVSFGAS
121 TRAYTLREKP QTLPSAVKGD EKMGGEDDEL KGLLGLPEEE TELDNLTEFN TAHNKRISTL
181 TIEEGNLDIQ RPKRKRKNSR VTFSEDDEII NPEDVDPSVG RFRNMVQTAV VPVKKKRVEG
241 PGSLGLEESG SRRMQNFAFS GGLYGGLPPT HSEAGSQPHG IHGTALIGGL PMPYPNLAPD
301 VDLTPVVPSA VNMNPAPNPA VYNPEAVNEP KKKKYAKEAW PGKKPTPSLL ILocalizationUniProt · AlphaFold · HPA
Whether an antibody against PPP1R8 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)
- 0.55
- Highest tissue expression
- 38 nTPM
Expression across tissuesHPA
Tissue
- thymus: 38 nTPM
- bone marrow: 37 nTPM
- tongue: 35 nTPM
- tonsil: 34 nTPM
- ovary: 34 nTPM
- lymph node: 33 nTPM
Single-cell type
- cytotrophoblasts: 60 nCPM
- oocytes: 60 nCPM
- syncytiotrophoblasts: 56 nCPM
- migrating cytotrophoblasts: 55 nCPM
- differentiating spermatogonia: 54 nCPM
- extravillous trophoblasts: 54 nCPM
Immune cell
- basophil: 17 nTPM
- MAIT T-cell: 14 nTPM
- NK-cell: 14 nTPM
- memory CD8 T-cell: 14 nTPM
- total PBMC: 13 nTPM
- gdT-cell: 12 nTPM
Brain region
- white matter: 43 nTPM
- basal ganglia: 35 nTPM
- spinal cord: 35 nTPM
- cerebellum: 35 nTPM
- medulla oblongata: 34 nTPM
- hypothalamus: 33 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)
- 0.22
- gnomAD pLI
- 0.99
- gnomAD missense Z
- 2.91
- DepMap mean gene effect
- -1.11
- DepMap dependency class
- common
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
Molecular functions
- DNA binding
- molecular function inhibitor activity
- mRNA binding
- protein serine/threonine phosphatase inhibitor activity
- RNA binding
- RNA endonuclease activity
- ribonuclease E activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PPP1R8 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 PPP1R8 as an antibody target. Whether an autoantibody or antibody against PPP1R8 could matter depends on whether native PPP1R8 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PPP1R8 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 PPP1R8 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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