TRIM55 - tripartite motif containing 55 Gene

Also Known as RNF29; muRF2; MURF-2

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 84675

About TRIM55

Cytogenetic location: 8q13.1 Genomic coordinates (GRCh38): 8:66,113,351-66,175,485 (from NCBI)

This gene has 5 transcripts (splice variants), 272 orthologues and 80 paralogues. Biased expression in heart (RPKM 14.3), liver (RPKM 6.5) and 2 other tissues.

Summary

The protein encoded by this gene contains a RING zinc finger, a motif known to be involved in protein-protein interactions. This protein associates transiently with microtubules, Myosin, and titin during muscle sarcomere assembly. It may act as a transient adaptor and plays a regulatory role in the assembly of sarcomeres. Four alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2008]

TRIM55 Products (4)

mRNA Protein Name
NM_033058.3 NP_149047.2 tripartite motif-containing protein 55 isoform 2
NM_184085.2 NP_908973.1 tripartite motif-containing protein 55 isoform 1
NM_184086.2 NP_908974.1 tripartite motif-containing protein 55 isoform 3
NM_184087.2 NP_908975.1 tripartite motif-containing protein 55 isoform 4
Molecular Function GO Annotation Evidence References Source
enables identical protein binding IPI
IPI: Inferred from physical interaction
22493164 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
22493164 GOA
enables protein-macromolecule adaptor activity IDA
IDA: Inferred from direct assay
37816088 GOA
enables ubiquitin protein ligase activity IDA
IDA: Inferred from direct assay
37816088 GOA
Biological Process GO Annotation Evidence References Source
involved in positive regulation of non-canonical NF-kappaB signal transduction IDA
IDA: Inferred from direct assay
37816088 GOA
involved in protein K48-linked ubiquitination IDA
IDA: Inferred from direct assay
37816088 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

TRIM55 Protein Structure

zf-C3HC4_2

zf-C3HC4_2: Zinc finger, C3HC4 type (RING finger) (26 - 81)

zf-B_box

zf-B_box: B-box zinc finger (120 - 155)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 500
  • 548 a.a.
Protein Preferred Names Protein Names

tripartite motif-containing protein 55

  • muscle specific ring finger 2

TRIM55 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
TRIM55 Q9BYV6 USP13 Homo sapiens Q92995 31391242
Intra
TRIM55 Q9BYV6 USP35 Homo sapiens Q9P2H5 31391242
Intra
TRIM55 Q9BYV6 USP13 Homo sapiens Q92995 31391242
Intra
TRIM55 Q9BYV6 AEBP2 Homo sapiens Q6ZN18-2 31391242
Intra
TRIM55 Q9BYV6 acbd4 Homo sapiens EBI-21999915 31391242
Intra
TRIM55 Q9BYV6 TRIM55 Homo sapiens Q9BYV6 22493164
Intra
TRIM55 Q9BYV6 ADAMTSL4 Homo sapiens Q6UY14-3 31391242
Intra
TRIM55 Q9BYV6 znf767-5 Homo sapiens EBI-22023041 31391242
Intra
TRIM55 Q9BYV6 SERPINB3 Homo sapiens P29508 33961781
Intra
TRIM55 Q9BYV6 TRIM55 Homo sapiens Q9BYV6 22493164
Intra
TRIM55 Q9BYV6 TRIM23 Homo sapiens P36406 31391242
Intra
TRIM55 Q9BYV6 MYLK2 Homo sapiens Q9H1R3 31391242
Intra
TRIM55 Q9BYV6 ypel3-5 Homo sapiens EBI-22021574 31391242
Intra
TRIM55 Q9BYV6 ACD Homo sapiens Q96AP0 31391242
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Hyaline Body Myopathy
  • Myosin Storage Myopathy

  • Autosomal Dominant Hyaline Body Myopathy

  • Myopathy, Myosin Storage

Hypertrophic Cardiomyopathy
  • Hypertrophic Obstructive Cardiomyopathy

  • Cardiomyopathy, Hypertrophic

  • Cardiomyopathy Hypertrophic Obstructive

  • Cardiomyopathy, Hypertrophic, Familial

  • Idiopathic Myocardial Hypertrophy

  • Idiopathic Hypertrophic Cardiomyopathy

  • Obstructive Idiopathic Hypertrophic Cardiomyopathy

  • Obstructive Cardiomyopathy

  • Idiopathic Hypertrophic Subaortic Stenosis

  • Muscular Subaortic Stenosis

  • Hypertrophic Obstructive Subaortic Stenosis

Noonan Syndrome 8
  • NS8

  • Noonan Syndrome, Type 8

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Macaca mulatta TRIM55 VGNC VGNC:78951
Rattus norvegicus TRIM55 RGD RGD:1306943
Bos taurus TRIM55 VGNC VGNC:36341
Mus musculus TRIM55 MGD MGI:3036269
Felis catus TRIM55 VGNC VGNC:66545
Canis familiaris TRIM55 VGNC VGNC:47827
Others TRIM55 NCBI