DENR
Density-regulated protein
Also known as: DENR_HUMAN, DRP, DRP1, SMAP-3
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O43583
- Gene
- DENR
- Ensembl
- ENSG00000139726
- Chromosome
- 12
- Canonical length
- 198 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Cytosol
OverviewNCBI Gene
This gene encodes a protein whose expression was found to increase in cultured cells at high density but not during growth arrest. This gene was also shown to have increased expression in cells overexpressing HER-2/neu proto-oncogene. The protein contains an SUI1 domain. In budding yeast, SUI1 is a translation initiation factor that along with eIF-2 and the initiator tRNA-Met, directs the ribosome to the proper translation start site. Proteins similar to SUI have been found in mammals, insects, and plants. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
198 residues, UniProt reviewed canonical sequence.
>O43583|DENR
1 MAADISESSG ADCKGDPRNS AKLDADYPLR VLYCGVCSLP TEYCEYMPDV AKCRQWLEKN
61 FPNEFAKLTV ENSPKQEAGI SEGQGTAGEE EEKKKQKRGG RGQIKQKKKT VPQKVTIAKI
121 PRAKKKYVTR VCGLATFEID LKEAQRFFAQ KFSCGASVTG EDEIIIQGDF TDDIIDVIQE
181 KWPEVDDDSI EDLGEVKKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against DENR 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
- 56 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 56 nTPM
- parathyroid gland: 55 nTPM
- tongue: 42 nTPM
- thymus: 36 nTPM
- lymph node: 34 nTPM
- tonsil: 33 nTPM
Single-cell type
- esophageal apical cells: 215 nCPM
- early primary spermatocytes: 204 nCPM
- extravillous trophoblasts: 174 nCPM
- differentiating spermatogonia: 164 nCPM
- esophageal suprabasal cells: 141 nCPM
- megakaryocyte progenitors: 122 nCPM
Immune cell
- basophil: 229 nTPM
- non-classical monocyte: 70 nTPM
- eosinophil: 58 nTPM
- intermediate monocyte: 53 nTPM
- T-reg: 49 nTPM
- naive CD4 T-cell: 49 nTPM
Brain region
- cerebral cortex: 41 nTPM
- midbrain: 40 nTPM
- hypothalamus: 36 nTPM
- pons: 35 nTPM
- basal ganglia: 34 nTPM
- amygdala: 30 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)
- 0.43
- gnomAD pLI
- 0.88
- gnomAD missense Z
- 1.58
- DepMap mean gene effect
- -0.78
- DepMap dependency class
- common
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 7% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- formation of translation preinitiation complex
- IRES-dependent viral translational initiation
- ribosome disassembly
- translation reinitiation
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- SUI1 domain
- SUI1 domain superfamily
- Translation initiation factor SUI1
- DENR, eukaryotes
- DENR, C-terminal domain
- DENR, N-terminal domain
- DENR/SUI1 Translation Initiation Factor
- DENR, N-terminal
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of DENR 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 DENR as an antibody target. Whether an autoantibody or antibody against DENR could matter depends on whether native DENR is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
DENR 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 DENR as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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