PPP1R15B
Protein phosphatase 1 regulatory subunit 15B
Also known as: FLJ14744, PR15B_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q5SWA1
- Gene
- PPP1R15B
- Ensembl
- ENSG00000158615
- Chromosome
- 1
- Canonical length
- 713 aa
- Protein class
- Disease related genes, Human disease related genes, Predicted intracellular proteins
- Subcellular location
- Golgi apparatus
OverviewNCBI Gene
This gene encodes a protein phosphatase I-interacting protein that promotes the dephosphorylation of eukaryotic translation initiation factor 2A to regulate translation under conditions of cellular stress. The transcribed messenger RNA contains two upstream open reading frames (ORFs) that repress translation of the main protein coding ORF under normal conditions, while the protein coding ORF is expressed at high levels in response to stress. Continual translation of the mRNA under conditions of eukaryotic translation initiation factor 2A inactivation is thought to create a feedback loop for reactivation of the gene during recovery from stress. In addition, it has been shown that this protein plays a role in membrane traffic that is independent of translation and that it is required for exocytosis from erythroleukemia cells. Allelic variants of this gene are associated with microcephaly, short stature, and impaired glucose metabolism. [provided by RefSeq, Feb 2016]
Canonical amino-acid sequenceUniProt
713 residues, UniProt reviewed canonical sequence.
>Q5SWA1|PPP1R15B
1 MEPGTGGSRK RLGPRAGFRF WPPFFPRRSQ AGSSKFPTPL GPENSGNPTL LSSAQPETRV
61 SYWTKLLSQL LAPLPGLLQK VLIWSQLFGG MFPTRWLDFA GVYSALRALK GREKPAAPTA
121 QKSLSSLQLD SSDPSVTSPL DWLEEGIHWQ YSPPDLKLEL KAKGSALDPA AQAFLLEQQL
181 WGVELLPSSL QSRLYSNREL GSSPSGPLNI QRIDNFSVVS YLLNPSYLDC FPRLEVSYQN
241 SDGNSEVVGF QTLTPESSCL REDHCHPQPL SAELIPASWQ GCPPLSTEGL PEIHHLRMKR
301 LEFLQQASKG QDLPTPDQDN GYHSLEEEHS LLRMDPKHCR DNPTQFVPAA GDIPGNTQES
361 TEEKIELLTT EVPLALEEES PSEGCPSSEI PMEKEPGEGR ISVVDYSYLE GDLPISARPA
421 CSNKLIDYIL GGASSDLETS SDPEGEDWDE EAEDDGFDSD SSLSDSDLEQ DPEGLHLWNS
481 FCSVDPYNPQ NFTATIQTAA RIVPEEPSDS EKDLSGKSDL ENSSQSGSLP ETPEHSSGEE
541 DDWESSADEA ESLKLWNSFC NSDDPYNPLN FKAPFQTSGE NEKGCRDSKT PSESIVAISE
601 CHTLLSCKVQ LLGSQESECP DSVQRDVLSG GRHTHVKRKK VTFLEEVTEY YISGDEDRKG
661 PWEEFARDGC RFQKRIQETE DAIGYCLTFE HRERMFNRLQ GTCFKGLNVL KQCLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PPP1R15B 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)
- 0.67
- Highest tissue expression
- 111 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 111 nTPM
- urinary bladder: 48 nTPM
- liver: 44 nTPM
- adipose tissue: 36 nTPM
- pancreas: 33 nTPM
- placenta: 30 nTPM
Single-cell type
- neutrophils: 421 nCPM
- monocytes: 256 nCPM
- urothelial cells: 218 nCPM
- endometrial glandular cells: 188 nCPM
- endometrial luminal cells: 162 nCPM
- monocyte progenitors: 160 nCPM
Immune cell
- neutrophil: 14 nTPM
- basophil: 10 nTPM
- non-classical monocyte: 5.8 nTPM
- eosinophil: 5.4 nTPM
- classical monocyte: 5.2 nTPM
- myeloid DC: 4.9 nTPM
Brain region
- white matter: 46 nTPM
- cerebellum: 43 nTPM
- choroid plexus: 41 nTPM
- thalamus: 38 nTPM
- basal ganglia: 37 nTPM
- midbrain: 36 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about PPP1R15B.
Disease | AllUniProt
Conditions PPP1R15B is implicated in, by any mechanism.
- Microcephaly, short stature, and impaired glucose metabolism 2 (MSSGM2) MIM:616817
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)
- 0.51
- gnomAD pLI
- 0.15
- gnomAD missense Z
- -1.35
- DepMap mean gene effect
- -0.82
- DepMap dependency class
- common
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 10% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- ER overload response
- negative regulation of PERK-mediated unfolded protein response
- negative regulation of protein phosphorylation
- regulation of translation
- response to endoplasmic reticulum stress
- response to hydrogen peroxide
Molecular functions
- eukaryotic initiation factor eIF2 binding
- molecular adaptor activity
- protein phosphatase 1 binding
- protein phosphatase regulator activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Protein phosphatase 1, regulatory subunit 15A/B, C-terminal
- Protein Phosphatase 1 Regulatory Subunit 15
- Phosphatase-1 catalytic subunit binding region
- Protein phosphatase 1, regulatory subunit 15B, N-terminal
- eIF2-alpha phosphatase phosphorylation constitutive repressor
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PPP1R15B 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 PPP1R15B as an antibody target. Whether an autoantibody or antibody against PPP1R15B could matter depends on whether native PPP1R15B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PPP1R15B 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 PPP1R15B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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