DCTN3
Dynactin subunit 3
Also known as: DCTN-22, DCTN3_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O75935
- Gene
- DCTN3
- Ensembl
- ENSG00000137100
- Chromosome
- 9
- Canonical length
- 186 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoli,Cytosol,Perinuclear theca,Calyx,Mid piece,Principal piece
OverviewNCBI Gene
This gene encodes the smallest subunit of dynactin, a macromolecular complex consisting of 10 subunits ranging in size from 22 to 150 kD. Dynactin binds to both microtubules and cytoplasmic dynein. It is involved in a diverse array of cellular functions, including ER-to-Golgi transport, the centripetal movement of lysosomes and endosomes, spindle formation, cytokinesis, chromosome movement, nuclear positioning, and axonogenesis. This subunit, like most other dynactin subunits, exists only as a part of the dynactin complex. It is primarily an alpha-helical protein with very little coiled coil, and binds directly to the largest subunit (p150) of dynactin. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]
Canonical amino-acid sequenceUniProt
186 residues, UniProt reviewed canonical sequence.
>O75935|DCTN3
1 MAGLTDLQRL QARVEELERW VYGPGGARGS RKVADGLVKV QVALGNISSK RERVKILYKK
61 IEDLIKYLDP EYIDRIAIPD ASKLQFILAE EQFILSQVAL LEQVNALVPM LDSAHIKAVP
121 EHAARLQRLA QIHIQQQDQC VEITEESKAL LEEYNKTTML LSKQFVQWDE LLCQLEAATQ
181 VKPAEELocalizationUniProt · AlphaFold · HPA
Whether an antibody against DCTN3 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)
- 0.49
- Highest tissue expression
- 143 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 143 nTPM
- cerebral cortex: 128 nTPM
- heart muscle: 118 nTPM
- basal ganglia: 118 nTPM
- amygdala: 116 nTPM
- choroid plexus: 108 nTPM
Single-cell type
- esophageal apical cells: 385 nCPM
- esophageal suprabasal cells: 357 nCPM
- esophageal basal cells: 261 nCPM
- decidual stromal cells: 258 nCPM
- suprabasal keratinocytes: 174 nCPM
- hofbauer cells: 172 nCPM
Immune cell
- basophil: 236 nTPM
- eosinophil: 188 nTPM
- T-reg: 180 nTPM
- total PBMC: 153 nTPM
- non-classical monocyte: 151 nTPM
- intermediate monocyte: 140 nTPM
Brain region
- cerebral cortex: 91 nTPM
- basal ganglia: 88 nTPM
- hypothalamus: 88 nTPM
- pons: 86 nTPM
- hippocampal formation: 80 nTPM
- midbrain: 76 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)
- 1.54
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.35
- DepMap mean gene effect
- -0.73
- DepMap dependency class
- common
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
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Dynactin subunit 3
- Dynactin subunit p22
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of DCTN3 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 DCTN3 as an antibody target. Whether an autoantibody or antibody against DCTN3 could matter depends on whether native DCTN3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
DCTN3 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 DCTN3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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