DUSP19
Dual specificity protein phosphatase 19
Also known as: DUS19_HUMAN, DUSP17, SKRP1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8WTR2
- Gene
- DUSP19
- Ensembl
- ENSG00000162999
- Chromosome
- 2
- Canonical length
- 217 aa
- Protein class
- Enzymes, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
Dual-specificity phosphatases (DUSPs) constitute a large heterogeneous subgroup of the type I cysteine-based protein-tyrosine phosphatase superfamily. DUSPs are characterized by their ability to dephosphorylate both tyrosine and serine/threonine residues. They have been implicated as major modulators of critical signaling pathways. DUSP19 contains a variation of the consensus DUSP C-terminal catalytic domain, with the last serine residue replaced by alanine, and lacks the N-terminal CH2 domain found in the MKP (mitogen-activated protein kinase phosphatase) class of DUSPs (see MIM 600714) (summary by Patterson et al., 2009 [PubMed 19228121]).[supplied by OMIM, Dec 2009]
Canonical amino-acid sequenceUniProt
217 residues, UniProt reviewed canonical sequence.
>Q8WTR2|DUSP19
1 MYSLNQEIKA FSRNNLRKQC TRVTTLTGKK IIETWKDARI HVVEEVEPSS GGGCGYVQDL
61 SSDLQVGVIK PWLLLGSQDA AHDLDTLKKN KVTHILNVAY GVENAFLSDF TYKSISILDL
121 PETNILSYFP ECFEFIEEAK RKDGVVLVHC NAGVSRAAAI VIGFLMNSEQ TSFTSAFSLV
181 KNARPSICPN SGFMEQLRTY QEGKESNKCD RIQENSSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against DUSP19 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)
- 0.35
- Highest tissue expression
- 3.7 nTPM
Expression across tissuesHPA
Tissue
- stomach: 3.7 nTPM
- testis: 3.4 nTPM
- epididymis: 3.3 nTPM
- fallopian tube: 3 nTPM
- heart muscle: 2.9 nTPM
- blood vessel: 2.4 nTPM
Single-cell type
- parietal cells: 110 nCPM
- late primary spermatocytes: 32 nCPM
- fallopian tube ciliated cells: 29 nCPM
- respiratory ciliated cells: 27 nCPM
- megakaryocytes: 25 nCPM
- endometrial ciliated cells: 20 nCPM
Immune cell
- memory B-cell: 1.1 nTPM
- T-reg: 1 nTPM
- memory CD8 T-cell: 0.8 nTPM
- basophil: 0.7 nTPM
- naive CD4 T-cell: 0.7 nTPM
- naive CD8 T-cell: 0.7 nTPM
Brain region
- hippocampal formation: 13 nTPM
- cerebral cortex: 11 nTPM
- basal ganglia: 10 nTPM
- amygdala: 8 nTPM
- white matter: 5.9 nTPM
- hypothalamus: 5.3 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)
- 1.24
- gnomAD pLI
- 0.01
- gnomAD missense Z
- -0.09
- DepMap mean gene effect
- 0
- 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
- negative regulation of JNK cascade
- positive regulation of JNK cascade
- positive regulation of MAPK cascade
- regulation of JNK cascade
Molecular functions
- MAP-kinase scaffold activity
- mitogen-activated protein kinase kinase kinase binding
- protein kinase activator activity
- protein kinase inhibitor activity
- protein serine/threonine phosphatase activity
- protein tyrosine phosphatase activity
- protein tyrosine/serine/threonine phosphatase activity
- JUN kinase phosphatase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of DUSP19 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 DUSP19 as an antibody target. Whether an autoantibody or antibody against DUSP19 could matter depends on whether native DUSP19 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
DUSP19 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 DUSP19 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...