Homo sapiens Protein: TRIM32
Summary
InnateDB Protein IDBP-378852.4
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol TRIM32
Protein Name tripartite motif containing 32
Synonyms BBS11; HT2A; LGMD2H; TATIP;
Species Homo sapiens
Ensembl Protein ENSP00000408292
InnateDB Gene IDBG-82716 (TRIM32)
Protein Structure
UniProt Annotation
Function Has an E3 ubiquitin ligase activity. Ubiquitinates DTNBP1 (dysbindin) and promotes its degradation. May ubiquitinate BBS2. May play a significant role in mediating the biological activity of the HIV-1 Tat protein in vivo. Binds specifically to the activation domain of HIV-1 Tat and can also interact with the HIV-2 and EIAV Tat proteins in vivo. {ECO:0000269PubMed:19349376, ECO:0000269PubMed:22500027}.
Subcellular Localization Cytoplasm. Note=Localized in cytoplasmic bodies, often located around the nucleus.
Disease Associations Limb-girdle muscular dystrophy 2H (LGMD2H) [MIM:254110]: An autosomal recessive degenerative myopathy characterized by pelvic girdle, shoulder girdle and quadriceps muscle weakness. Clinical phenotype and severity are highly variable. Disease progression is slow and most patients remain ambulatory into the sixth decade of life. {ECO:0000269PubMed:11822024, ECO:0000269PubMed:17994549}. Note=The disease is caused by mutations affecting the gene represented in this entry.Bardet-Biedl syndrome 11 (BBS11) [MIM:209900]: A syndrome characterized by usually severe pigmentary retinopathy, early- onset obesity, polydactyly, hypogenitalism, renal malformation and mental retardation. Secondary features include diabetes mellitus, hypertension and congenital heart disease. Bardet-Biedl syndrome inheritance is autosomal recessive, but three mutated alleles (two at one locus, and a third at a second locus) may be required for clinical manifestation of some forms of the disease. {ECO:0000269PubMed:16606853}. Note=The disease is caused by mutations affecting the gene represented in this entry. It has been suggested that TRIM32 might be the E3 ubiquitin ligase for BBS2, a component of the BBSome complex involved in ciliogenesis, that is ubiquitinated and degraded by the proteasome (PubMed:22500027). {ECO:0000269PubMed:22500027}.
Tissue Specificity Spleen, thymus, prostate, testis, ovary, intestine, colon and skeletal muscle. {ECO:0000269PubMed:11822024}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 77 experimentally validated interaction(s) in this database.
They are also associated with 7 interaction(s) predicted by orthology.
Experimentally validated
Total 77 [view]
Protein-Protein 77 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 7 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003713 transcription coactivator activity
GO:0003723 RNA binding
GO:0004842 ubiquitin-protein transferase activity
GO:0005515 protein binding
GO:0008270 zinc ion binding
GO:0016874 ligase activity
GO:0017022 myosin binding
GO:0030957 Tat protein binding
GO:0031369 translation initiation factor binding
GO:0043130 ubiquitin binding
GO:0043621 protein self-association
GO:0046872 metal ion binding
Biological Process
GO:0000209 protein polyubiquitination
GO:0009411 response to UV
GO:0016567 protein ubiquitination
GO:0030307 positive regulation of cell growth
GO:0030335 positive regulation of cell migration
GO:0032479 regulation of type I interferon production
GO:0032481 positive regulation of type I interferon production
GO:0032897 negative regulation of viral transcription
GO:0034612 response to tumor necrosis factor
GO:0042787 protein ubiquitination involved in ubiquitin-dependent protein catabolic process
GO:0043123 positive regulation of I-kappaB kinase/NF-kappaB signaling
GO:0045087 innate immune response (InnateDB)
GO:0045444 fat cell differentiation
GO:0045666 positive regulation of neuron differentiation
GO:0045732 positive regulation of protein catabolic process
GO:0045787 positive regulation of cell cycle
GO:0045862 positive regulation of proteolysis
GO:0048147 negative regulation of fibroblast proliferation
GO:0050769 positive regulation of neurogenesis
GO:0051091 positive regulation of sequence-specific DNA binding transcription factor activity
GO:0051092 positive regulation of NF-kappaB transcription factor activity
GO:1902187 negative regulation of viral release from host cell
GO:1902230 negative regulation of intrinsic apoptotic signaling pathway in response to DNA damage
GO:2000147 positive regulation of cell motility
Cellular Component
GO:0005622 intracellular
GO:0005634 nucleus
GO:0005737 cytoplasm
GO:0005829 cytosol
GO:0005863 striated muscle myosin thick filament
Protein Structure and Domains
PDB ID
InterPro IPR000315 Zinc finger, B-box
IPR001258 NHL repeat
IPR001841 Zinc finger, RING-type
IPR013017 NHL repeat, subgroup
IPR018957 Zinc finger, C3HC4 RING-type
PFAM PF00643
PF01436
PF13639
PF14634
PF00097
PRINTS
PIRSF
SMART SM00336
SM00184
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q13049
PhosphoSite PhosphoSite-Q13049
TrEMBL Q5JVY0
UniProt Splice Variant
Entrez Gene 22954
UniGene Hs.591910
RefSeq NP_036342
HUGO HGNC:16380
OMIM 602290
CCDS CCDS6817
HPRD 03797
IMGT
EMBL AL133284 BC003154 CH471090 U18543
GenPept AAA86474 AAH03154 CAB92723 EAW87446 EAW87447