EIF4EBP2
Eukaryotic translation initiation factor 4E-binding protein 2
Also known as: 4EBP2_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q13542
- Gene
- EIF4EBP2
- Ensembl
- ENSG00000148730
- Chromosome
- 10
- Canonical length
- 120 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Mitochondria
OverviewNCBI Gene
This gene encodes a member of the eukaryotic translation initiation factor 4E binding protein family. The gene products of this family bind eIF4E and inhibit translation initiation. However, insulin and other growth factors can release this inhibition via a phosphorylation-dependent disruption of their binding to eIF4E. Regulation of protein production through these gene products have been implicated in cell proliferation, cell differentiation and viral infection. [provided by RefSeq, Oct 2008]
Canonical amino-acid sequenceUniProt
120 residues, UniProt reviewed canonical sequence.
>Q13542|EIF4EBP2
1 MSSSAGSGHQ PSQSRAIPTR TVAISDAAQL PHDYCTTPGG TLFSTTPGGT RIIYDRKFLL
61 DRRNSPMAQT PPCHLPNIPG VTSPGTLIED SKVEVNNLNN LNNHDRKHAV GDDAQFEMDILocalizationUniProt · AlphaFold · HPA
Whether an antibody against EIF4EBP2 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)
- 0.59
- Highest tissue expression
- 64 nTPM
Expression across tissuesHPA
Tissue
- adipose tissue: 64 nTPM
- tongue: 63 nTPM
- skeletal muscle: 60 nTPM
- kidney: 54 nTPM
- liver: 47 nTPM
- small intestine: 45 nTPM
Single-cell type
- esophageal apical cells: 422 nCPM
- enterocytes: 227 nCPM
- thymic myoid cells: 201 nCPM
- hepatocytes: 201 nCPM
- extravillous trophoblasts: 192 nCPM
- neutrophil progenitors: 189 nCPM
Immune cell
- eosinophil: 29 nTPM
- non-classical monocyte: 23 nTPM
- neutrophil: 21 nTPM
- basophil: 21 nTPM
- classical monocyte: 19 nTPM
- total PBMC: 19 nTPM
Brain region
- thalamus: 79 nTPM
- medulla oblongata: 66 nTPM
- choroid plexus: 65 nTPM
- amygdala: 63 nTPM
- midbrain: 62 nTPM
- basal ganglia: 57 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)
- 1.16
- gnomAD pLI
- 0.31
- gnomAD missense Z
- 0.07
- DepMap mean gene effect
- -0.18
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- insulin receptor signaling pathway
- memory
- modulation of chemical synaptic transmission
- negative regulation of translational initiation
- regulation of synaptic plasticity
- social behavior
- TOR signaling
- translation
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of EIF4EBP2 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 EIF4EBP2 as an antibody target. Whether an autoantibody or antibody against EIF4EBP2 could matter depends on whether native EIF4EBP2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
EIF4EBP2 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 EIF4EBP2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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