PPP1CB
Serine/threonine-protein phosphatase PP1-beta catalytic subunit
Also known as: MP, PP-1B, PP1B, PP1B_HUMAN, PP1beta, PP1c, PPP1beta
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P62140
- Gene
- PPP1CB
- Ensembl
- ENSG00000213639
- Chromosome
- 2
- Canonical length
- 327 aa
- Protein class
- Disease related genes, Enzymes, Human disease related genes, Metabolic proteins, Plasma proteins, Potential drug targets, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytosol
OverviewNCBI Gene
The protein encoded by this gene is one of the three catalytic subunits of protein phosphatase 1 (PP1). PP1 is a serine/threonine specific protein phosphatase known to be involved in the regulation of a variety of cellular processes, such as cell division, glycogen metabolism, muscle contractility, protein synthesis, and HIV-1 viral transcription. Mouse studies suggest that PP1 functions as a suppressor of learning and memory. Two alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
327 residues, UniProt reviewed canonical sequence.
>P62140|PPP1CB
1 MADGELNVDS LITRLLEVRG CRPGKIVQMT EAEVRGLCIK SREIFLSQPI LLELEAPLKI
61 CGDIHGQYTD LLRLFEYGGF PPEANYLFLG DYVDRGKQSL ETICLLLAYK IKYPENFFLL
121 RGNHECASIN RIYGFYDECK RRFNIKLWKT FTDCFNCLPI AAIVDEKIFC CHGGLSPDLQ
181 SMEQIRRIMR PTDVPDTGLL CDLLWSDPDK DVQGWGENDR GVSFTFGADV VSKFLNRHDL
241 DLICRAHQVV EDGYEFFAKR QLVTLFSAPN YCGEFDNAGG MMSVDETLMC SFQILKPSEK
301 KAKYQYGGLN SGRPVTPPRT ANPPKKRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PPP1CB 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)
- 0.25
- Highest tissue expression
- 377 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 377 nTPM
- tongue: 289 nTPM
- esophagus: 280 nTPM
- blood vessel: 222 nTPM
- heart muscle: 200 nTPM
- smooth muscle: 179 nTPM
Single-cell type
- neutrophils: 974 nCPM
- hematopoietic stem cells: 505 nCPM
- salivary acinar cells: 366 nCPM
- cdc: 301 nCPM
- innate lymphoid cells: 296 nCPM
- endometrial ciliated cells: 295 nCPM
Immune cell
- non-classical monocyte: 115 nTPM
- neutrophil: 107 nTPM
- intermediate monocyte: 98 nTPM
- eosinophil: 84 nTPM
- T-reg: 75 nTPM
- basophil: 72 nTPM
Brain region
- white matter: 183 nTPM
- hypothalamus: 165 nTPM
- spinal cord: 163 nTPM
- basal ganglia: 162 nTPM
- medulla oblongata: 161 nTPM
- thalamus: 147 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about PPP1CB.
Disease | AllUniProt
Conditions PPP1CB is implicated in, by any mechanism.
- Noonan syndrome-like disorder with loose anagen hair 2 (NSLH2) MIM:617506
Disease | GeneticClinVar
14 pathogenic / likely-pathogenic of 370 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Noonan syndrome-like disorder with loose anagen hair 2
- RASopathy
- Cardiovascular phenotype
- Noonan syndrome
- Inborn genetic diseases
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)
- 0.15
- gnomAD pLI
- 1
- gnomAD missense Z
- 4.33
- DepMap mean gene effect
- -1.21
- DepMap dependency class
- common
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 7% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cell division
- circadian regulation of gene expression
- entrainment of circadian clock by photoperiod
- glycogen metabolic process
- MAPK cascade
- protein dephosphorylation
- regulation of cell adhesion
- regulation of circadian rhythm
Molecular functions
- metal ion binding
- myosin phosphatase activity
- phosphatase activity
- protein kinase binding
- protein serine/threonine phosphatase activity
- myosin-light-chain-phosphatase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Calcineurin-like, phosphoesterase domain
- Serine/threonine-specific protein phosphatase/bis(5-nucleosyl)-tetraphosphatase
- Metallo-dependent phosphatase-like
- Serine-threonine protein phosphatase, N-terminal
- Serine/threonine-protein phosphatase PP1 catalytic subunit
- Calcineurin-like phosphoesterase
- Serine-threonine protein phosphatase N-terminal domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PPP1CB 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 PPP1CB as an antibody target. Whether an autoantibody or antibody against PPP1CB could matter depends on whether native PPP1CB is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PPP1CB 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 PPP1CB as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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