DCPS
m7GpppX diphosphatase
Also known as: DCPS_HUMAN, HINT-5, HINT5, HSL1, HSPC015
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96C86
- Gene
- DCPS
- Ensembl
- ENSG00000110063
- Chromosome
- 11
- Canonical length
- 337 aa
- Protein class
- Disease related genes, Enzymes, Human disease related genes, Potential drug targets, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytosol
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene encodes a member of the histidine triad family of pyrophosphatases that removes short mRNA fragments containing the 5′ mRNA cap structure, which appear in the 3′ → 5′ mRNA decay pathway, following deadenylation and exosome-mediated turnover. This enzyme hydrolyzes the triphosphate linkage of the cap structure (7-methylguanosine nucleoside triphosphate) to yield 7-methylguanosine monophosphate and nucleoside diphosphate. It protects the cell from the potentially toxic accumulation of these short, capped mRNA fragments, and regulates the activity of other cap-binding proteins, which are inhibited by their accumulation. It also acts as a transcript-specific modulator of pre-mRNA splicing and microRNA turnover. [provided by RefSeq, Apr 2017]
Canonical amino-acid sequenceUniProt
337 residues, UniProt reviewed canonical sequence.
>Q96C86|DCPS
1 MADAAPQLGK RKRELDVEEA HAASTEEKEA GVGNGTCAPV RLPFSGFRLQ KVLRESARDK
61 IIFLHGKVNE ASGDGDGEDA VVILEKTPFQ VEQVAQLLTG SPELQLQFSN DIYSTYHLFP
121 PRQLNDVKTT VVYPATEKHL QKYLRQDLRL IRETGDDYRN ITLPHLESQS LSIQWVYNIL
181 DKKAEADRIV FENPDPSDGF VLIPDLKWNQ QQLDDLYLIA ICHRRGIRSL RDLTPEHLPL
241 LRNILHQGQE AILQRYRMKG DHLRVYLHYL PSYYHLHVHF TALGFEAPGS GVERAHLLAE
301 VIENLECDPR HYQQRTLTFA LRADDPLLKL LQEAQQSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against DCPS 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
- 80 nTPM
Expression across tissuesHPA
Tissue
- liver: 80 nTPM
- kidney: 28 nTPM
- gallbladder: 15 nTPM
- choroid plexus: 14 nTPM
- lymph node: 11 nTPM
- bone marrow: 10 nTPM
Single-cell type
- pdcs: 93 nCPM
- plasma cells: 87 nCPM
- cholangiocytes: 63 nCPM
- migrating cytotrophoblasts: 55 nCPM
- extravillous trophoblasts: 54 nCPM
- cytotrophoblasts: 51 nCPM
Immune cell
- plasmacytoid DC: 47 nTPM
- myeloid DC: 17 nTPM
- non-classical monocyte: 15 nTPM
- intermediate monocyte: 15 nTPM
- T-reg: 15 nTPM
- memory B-cell: 13 nTPM
Brain region
- choroid plexus: 19 nTPM
- cerebellum: 13 nTPM
- basal ganglia: 10 nTPM
- cerebral cortex: 10 nTPM
- hippocampal formation: 10 nTPM
- hypothalamus: 9.9 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about DCPS.
Disease | AllUniProt
Conditions DCPS is implicated in, by any mechanism.
- Al-Raqad syndrome (ARS) MIM:616459
Disease | GeneticClinVar
7 pathogenic / likely-pathogenic of 120 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Al-Raqad syndrome
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
- gnomAD missense Z
- -0.49
- DepMap mean gene effect
- -0.08
- 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
- deadenylation-dependent decapping of nuclear-transcribed mRNA
- mRNA cis splicing, via spliceosome
- mRNA methylguanosine-cap decapping
- nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay
Molecular functions
- 5'-(N(7)-methyl 5'-triphosphoguanosine)-[mRNA] diphosphatase activity
- identical protein binding
- RNA 7-methylguanosine cap binding
- RNA exonuclease activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Histidine triad, conserved site
- HIT-like superfamily
- Scavenger mRNA decapping enzyme C-term binding
- Scavenger mRNA decapping enzyme DcpS/DCS2
- Scavenger mRNA decapping enzyme, N-terminal
- Scavenger mRNA decapping enzyme (DcpS) N-terminal
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of DCPS 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 DCPS as an antibody target. Whether an autoantibody or antibody against DCPS could matter depends on whether native DCPS is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
DCPS 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 DCPS as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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