DTX3L
E3 ubiquitin-protein ligase DTX3L
Also known as: BBAP, DTX3L_HUMAN, RNF143
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8TDB6
- Gene
- DTX3L
- Ensembl
- ENSG00000163840
- Chromosome
- 3
- Canonical length
- 740 aa
- Protein class
- Enzymes, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytosol
- Quaternary structure
- Homodimer
OverviewNCBI Gene
Enables several functions, including STAT family protein binding activity; histone H4K91 ubiquitin ligase activity; and protein ADP-ribosyltransferase-substrate adaptor activity. Involved in several processes, including positive regulation of protein localization; protein ubiquitination; and regulation of macromolecule metabolic process. Located in several cellular components, including early endosome; lysosome; and nucleoplasm. Part of protein-containing complex. [provided by Alliance of Genome Resources, Apr 2025]
Canonical amino-acid sequenceUniProt
740 residues, UniProt reviewed canonical sequence.
>Q8TDB6|DTX3L
1 MASHLRPPSP LLVRVYKSGP RVRRKLESYF QSSKSSGGGE CTVSTQEHEA PGTFRVEFSE
61 RAAKERVLKK GEHQILVDEK PVPIFLVPTE NSIKKNTRPQ ISSLTQSQAE TPSGDMHQHE
121 GHIPNAVDSC LQKIFLTVTA DLNCNLFSKE QRAYITTLCP SIRKMEGHDG IEKVCGDFQD
181 IERIHQFLSE QFLESEQKQQ FSPSMTERKP LSQQERDSCI SPSEPETKAE QKSNYFEVPL
241 PYFEYFKYIC PDKINSIEKR FGVNIEIQES SPNMVCLDFT SSRSGDLEAA RESFASEFQK
301 NTEPLKQECV SLADSKQANK FKQELNHQFT KLLIKEKGGE LTLLGTQDDI SAAKQKISEA
361 FVKIPVKLFA ANYMMNVIEV DSAHYKLLET ELLQEISEIE KRYDICSKVS EKGQKTCILF
421 ESKDRQVDLS VHAYASFIDA FQHASCQLMR EVLLLKSLGK ERKHLHQTKF ADDFRKRHPN
481 VHFVLNQESM TLTGLPNHLA KAKQYVLKGG GMSSLAGKKL KEGHETPMDI DSDDSKAASP
541 PLKGSVSSEA SELDKKEKGI CVICMDTISN KKVLPKCKHE FCAPCINKAM SYKPICPTCQ
601 TSYGIQKGNQ PEGSMVFTVS RDSLPGYESF GTIVITYSMK AGIQTEEHPN PGKRYPGIQR
661 TAYLPDNKEG RKVLKLLYRA FDQKLIFTVG YSRVLGVSDV ITWNDIHHKT SRFGGPEMYG
721 YPDPSYLKRV KEELKAKGIELocalizationUniProt · AlphaFold · HPA
Whether an antibody against DTX3L 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
- Other membrane
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.39
- Highest tissue expression
- 30 nTPM
Expression across tissuesHPA
Tissue
- liver: 30 nTPM
- spleen: 25 nTPM
- appendix: 23 nTPM
- lymph node: 20 nTPM
- lung: 20 nTPM
- tonsil: 20 nTPM
Single-cell type
- alveolar cells type 1: 80 nCPM
- hepatocytes: 67 nCPM
- kupffer cells: 66 nCPM
- neutrophils: 61 nCPM
- monocyte progenitors: 59 nCPM
- foveolar cells: 56 nCPM
Immune cell
- neutrophil: 30 nTPM
- basophil: 22 nTPM
- non-classical monocyte: 20 nTPM
- intermediate monocyte: 19 nTPM
- MAIT T-cell: 13 nTPM
- memory CD8 T-cell: 13 nTPM
Brain region
- medulla oblongata: 24 nTPM
- thalamus: 18 nTPM
- spinal cord: 18 nTPM
- pons: 16 nTPM
- white matter: 15 nTPM
- midbrain: 13 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about DTX3L.
Disease | ImmuneIEDB
Conditions an epitope on DTX3L was assayed in.
- skin melanoma T cell
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)
- 0.78
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.33
- DepMap mean gene effect
- -0.01
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 8% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- defense response to virus
- DNA damage checkpoint signaling
- DNA repair-dependent chromatin remodeling
- double-strand break repair
- endosome to lysosome transport
- innate immune response
- negative regulation of ubiquitin-protein transferase activity
- Notch signaling pathway
- positive regulation of chromatin binding
- positive regulation of defense response to virus by host
- positive regulation of DNA-templated transcription
- positive regulation of protein binding
- positive regulation of protein localization to early endosome
- positive regulation of protein localization to nucleus
- positive regulation of receptor catabolic process
- protein autoubiquitination
- protein K48-linked ubiquitination
- protein transport
- protein ubiquitination
- ubiquitin-dependent protein catabolic process
Molecular functions
- enzyme binding
- enzyme inhibitor activity
- histone binding
- histone ubiquitin ligase activity
- protein ADP-ribosyltransferase-substrate adaptor activity
- STAT family protein binding
- ubiquitin protein ligase activity
- ubiquitin-like protein ligase binding
- ubiquitin-protein transferase activity
- zinc ion binding
- histone H4K91 ubiquitin ligase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Zinc finger, RING-type
- Nucleotide-binding alpha-beta plait domain superfamily
- Zinc finger, RING/FYVE/PHD-type
- Zinc finger, RING-type, conserved site
- Deltex, C-terminal
- Deltex family
- Deltex, C-terminal domain superfamily
- PAR14-like, first RRM domain
- Zinc finger, C3HC4 type (RING finger)
- Deltex C-terminal domain
- PAR14-like, first RRM domain
- DTX3L, RING-HC finger
- DTX3L, KH-like domain
- DTX3L, alpha/beta domain
- DTX3L, alpha/beta domain
- DTX3L, KH-like domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of DTX3L 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 DTX3L as an antibody target. Whether an autoantibody or antibody against DTX3L could matter depends on whether native DTX3L is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
DTX3L 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 DTX3L as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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