DCTD
Deoxycytidylate deaminase
Also known as: DCTD_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P32321
- Gene
- DCTD
- Ensembl
- ENSG00000129187
- Chromosome
- 4
- Canonical length
- 178 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytosol
- Quaternary structure
- Homohexamer
OverviewNCBI Gene
The protein encoded by this gene catalyzes the deamination of dCMP to dUMP, the nucleotide substrate for thymidylate synthase. The encoded protein is allosterically activated by dCTP and inhibited by dTTP, and is found as a homohexamer. This protein uses zinc as a cofactor for its activity. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
178 residues, UniProt reviewed canonical sequence.
>P32321|DCTD
1 MSEVSCKKRD DYLEWPEYFM AVAFLSAQRS KDPNSQVGAC IVNSENKIVG IGYNGMPNGC
61 SDDVLPWRRT AENKLDTKYP YVCHAELNAI MNKNSTDVKG CSMYVALFPC NECAKLIIQA
121 GIKEVIFMSD KYHDSDEATA ARLLFNMAGV TFRKFIPKCS KIVIDFDSIN SRPSQKLQLocalizationUniProt · AlphaFold · HPA
Whether an antibody against DCTD 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
- 94 nTPM
Expression across tissuesHPA
Tissue
- thyroid gland: 94 nTPM
- adrenal gland: 80 nTPM
- liver: 75 nTPM
- choroid plexus: 74 nTPM
- ovary: 65 nTPM
- esophagus: 59 nTPM
Single-cell type
- esophageal suprabasal cells: 114 nCPM
- esophageal basal cells: 100 nCPM
- parietal cells: 96 nCPM
- adrenal cortex cells: 84 nCPM
- esophageal apical cells: 84 nCPM
- gastric chief cells: 82 nCPM
Immune cell
- MAIT T-cell: 77 nTPM
- NK-cell: 74 nTPM
- memory B-cell: 71 nTPM
- basophil: 69 nTPM
- memory CD8 T-cell: 63 nTPM
- gdT-cell: 61 nTPM
Brain region
- choroid plexus: 64 nTPM
- white matter: 52 nTPM
- spinal cord: 49 nTPM
- hypothalamus: 49 nTPM
- midbrain: 47 nTPM
- medulla oblongata: 47 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)
- 1.27
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.18
- DepMap mean gene effect
- -0.02
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- dTMP biosynthetic process
- dUMP biosynthetic process
- nucleoside salvage
- pyrimidine nucleotide metabolic process
Molecular functions
- 5-hydroxymethyl-dUMP N-hydrolase activity
- dCMP deaminase activity
- identical protein binding
- zinc ion binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of DCTD 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 DCTD as an antibody target. Whether an autoantibody or antibody against DCTD could matter depends on whether native DCTD is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
DCTD 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 DCTD as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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