PDAP1
28 kDa heat- and acid-stable phosphoprotein
Also known as: HAP28_HUMAN, HASPP28, PAP, PAP1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q13442
- Gene
- PDAP1
- Ensembl
- ENSG00000106244
- Chromosome
- 7
- Canonical length
- 181 aa
- Protein class
- Cancer-related genes, Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Plasma membrane,Cytosol
OverviewNCBI Gene
The protein encoded by this gene is a phosphoprotein that may upregulate the PDGFA-stimulated growth of fibroblasts and also downregulate the mitogenicity of PDGFB. The encoded protein in rodents has been shown to bind PDGFA with a low affinity. [provided by RefSeq, Dec 2010]
Canonical amino-acid sequenceUniProt
181 residues, UniProt reviewed canonical sequence.
>Q13442|PDAP1
1 MPKGGRKGGH KGRARQYTSP EEIDAQLQAE KQKAREEEEQ KEGGDGAAGD PKKEKKSLDS
61 DESEDEEDDY QQKRKGVEGL IDIENPNRVA QTTKKVTQLD LDGPKELSRR EREEIEKQKA
121 KERYMKMHLA GKTEQAKADL ARLAIIRKQR EEAARKKEEE RKAKDDATLS GKRMQSLSLN
181 KLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PDAP1 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.58
- Highest tissue expression
- 98 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 98 nTPM
- tongue: 56 nTPM
- choroid plexus: 38 nTPM
- heart muscle: 37 nTPM
- esophagus: 34 nTPM
- colon: 30 nTPM
Single-cell type
- esophageal suprabasal cells: 310 nCPM
- esophageal basal cells: 307 nCPM
- esophageal apical cells: 293 nCPM
- extravillous trophoblasts: 255 nCPM
- cytotrophoblasts: 252 nCPM
- migrating cytotrophoblasts: 249 nCPM
Immune cell
- neutrophil: 33 nTPM
- NK-cell: 28 nTPM
- plasmacytoid DC: 21 nTPM
- T-reg: 21 nTPM
- intermediate monocyte: 17 nTPM
- memory B-cell: 16 nTPM
Brain region
- midbrain: 36 nTPM
- spinal cord: 35 nTPM
- pons: 35 nTPM
- medulla oblongata: 34 nTPM
- thalamus: 34 nTPM
- white matter: 32 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)
- 0.81
- gnomAD pLI
- 0.05
- gnomAD missense Z
- 1.37
- DepMap mean gene effect
- -0.8
- DepMap dependency class
- common
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 14% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Casein kinase substrate, phosphoprotein PP28
- 28kDa heat- and acid-stable phosphoprotein
- Casein kinase substrate phosphoprotein PP28
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PDAP1 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 PDAP1 as an antibody target. Whether an autoantibody or antibody against PDAP1 could matter depends on whether native PDAP1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PDAP1 is annotated at the cell surface, where native PDAP1 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label PDAP1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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