Homo sapiens Protein: TLE2
Summary
InnateDB Protein IDBP-16682.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol TLE2
Protein Name transducin-like enhancer of split 2 (E(sp1) homolog, Drosophila)
Synonyms ESG; ESG2; GRG2;
Species Homo sapiens
Ensembl Protein ENSP00000262953
InnateDB Gene IDBG-16680 (TLE2)
Protein Structure
UniProt Annotation
Function Transcriptional corepressor that binds to a number of transcription factors. Inhibits the transcriptional activation mediated by CTNNB1 and TCF family members in Wnt signaling. The effects of full-length TLE family members may be modulated by association with dominant-negative AES (By similarity). {ECO:0000250}.
Subcellular Localization Nucleus.
Disease Associations
Tissue Specificity In all tissues examined, mostly in heart, brain, and muscle.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 19 experimentally validated interaction(s) in this database.
Experimentally validated
Total 19 [view]
Protein-Protein 19 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0003714 transcription corepressor activity
GO:0005515 protein binding
Biological Process
GO:0006351 transcription, DNA-templated
GO:0007165 signal transduction
GO:0007219 Notch signaling pathway
GO:0009887 organ morphogenesis
GO:0016055 Wnt signaling pathway
GO:0045892 negative regulation of transcription, DNA-templated
GO:0090090 negative regulation of canonical Wnt signaling pathway
Cellular Component
GO:0005615 extracellular space
GO:0005634 nucleus
GO:0005654 nucleoplasm
Protein Structure and Domains
PDB ID
InterPro IPR001680 WD40 repeat
IPR005617 Groucho/TLE, N-terminal Q-rich domain
IPR009146 Groucho/transducin-like enhancer
IPR017986 WD40-repeat-containing domain
PFAM PF00400
PF03920
PRINTS PR01850
PIRSF
SMART SM00320
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q04725
PhosphoSite PhosphoSite-Q04725
TrEMBL
UniProt Splice Variant
Entrez Gene 7089
UniGene Hs.332173
RefSeq NP_003251
HUGO HGNC:11838
OMIM 601041
CCDS CCDS45911
HPRD 03025
IMGT
EMBL AC007766 AC011549 AC093053 AK293407 AK308137 BC017364 M99436
GenPept AAA61193 AAD38075 AAH17364 BAG56914