Homo sapiens Protein: TRIM37 | |||||||||||||||||||
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Summary | |||||||||||||||||||
InnateDB Protein | IDBP-244363.6 | ||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||
Gene Symbol | TRIM37 | ||||||||||||||||||
Protein Name | tripartite motif containing 37 | ||||||||||||||||||
Synonyms | MUL; POB1; TEF3; | ||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||
Ensembl Protein | ENSP00000376785 | ||||||||||||||||||
InnateDB Gene | IDBG-61551 (TRIM37) | ||||||||||||||||||
Protein Structure |
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UniProt Annotation | |||||||||||||||||||
Function | E3 ubiquitin-protein ligase required to prevent centriole reduplication. Probably acts by ubiquitinating positive regulators of centriole reduplication. {ECO:0000269PubMed:15885686, ECO:0000269PubMed:23769972}. | ||||||||||||||||||
Subcellular Localization | Cytoplasm, perinuclear region. Peroxisome. Note=Found in vesicles of the peroxisome. Aggregates as aggresomes, a perinuclear region where certain misfolded or aggregated proteins are sequestered for proteasomal degradation. | ||||||||||||||||||
Disease Associations | Mulibrey nanism (MUL) [MIM:253250]: Autosomal recessive disorder that involves several tissues of mesodermal origin, implying a defect in a highly pleiotropic gene. Characteristic features include severe growth failure of prenatal onset and constrictive pericardium with consequent hepatomegaly. In addition, muscle hypotonia, J-shaped sella turcica, yellowish dots in the ocular fundi, typical dysmorphic features and hypoplasia of various endocrine glands causing hormonal deficiency are common. {ECO:0000269PubMed:15108285, ECO:0000269PubMed:15885686, ECO:0000269PubMed:17100991}. Note=The disease is caused by mutations affecting the gene represented in this entry. | ||||||||||||||||||
Tissue Specificity | Ubiquitous. {ECO:0000269PubMed:10888877}. | ||||||||||||||||||
Comments | |||||||||||||||||||
Interactions | |||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 53 experimentally validated interaction(s) in this database.
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Gene Ontology | |||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Protein Structure and Domains | |||||||||||||||||||
PDB ID | |||||||||||||||||||
InterPro |
IPR000315
Zinc finger, B-box IPR001841 Zinc finger, RING-type IPR002083 MATH IPR003649 B-box, C-terminal IPR008974 TRAF-like |
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PFAM |
PF00643
PF13639 PF14634 PF00917 |
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PRINTS | |||||||||||||||||||
PIRSF | |||||||||||||||||||
SMART |
SM00336
SM00184 SM00061 SM00502 |
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TIGRFAMs | |||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||
Modification | |||||||||||||||||||
Cross-References | |||||||||||||||||||
SwissProt | O94972 | ||||||||||||||||||
PhosphoSite | PhosphoSite-O94972 | ||||||||||||||||||
TrEMBL | B3KMU3 | ||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||
Entrez Gene | 4591 | ||||||||||||||||||
UniGene | Hs.605697 | ||||||||||||||||||
RefSeq | NP_001005207 | ||||||||||||||||||
HUGO | HGNC:7523 | ||||||||||||||||||
OMIM | 605073 | ||||||||||||||||||
CCDS | CCDS45746 | ||||||||||||||||||
HPRD | 05463 | ||||||||||||||||||
IMGT | |||||||||||||||||||
EMBL | AB020705 AF213365 AK022701 AK289674 BC036012 BX537955 CH471109 | ||||||||||||||||||
GenPept | AAH36012 AAL36460 BAA74921 BAF82363 BAG51105 CAD97922 EAW94425 EAW94426 | ||||||||||||||||||