TRAF5
TNF receptor-associated factor 5
Also known as: RNF84, TRAF5_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O00463
- Gene
- TRAF5
- Ensembl
- ENSG00000082512
- Chromosome
- 1
- Canonical length
- 557 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Centrosome,Cytosol
- Quaternary structure
- Homotrimer
OverviewNCBI Gene
The scaffold protein encoded by this gene is a member of the tumor necrosis factor receptor-associated factor (TRAF) protein family and contains a meprin and TRAF homology (MATH) domain, a RING-type zinc finger, and two TRAF-type zinc fingers. TRAF proteins are associated with, and mediate signal transduction from members of the TNF receptor superfamily. This protein is one of the components of a multiple protein complex which binds to tumor necrosis factor (TNF) receptor cytoplasmic domains and mediates TNF-induced activation. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2016]
Canonical amino-acid sequenceUniProt
557 residues, UniProt reviewed canonical sequence.
>O00463|TRAF5
1 MAYSEEHKGM PCGFIRQNSG NSISLDFEPS IEYQFVERLE ERYKCAFCHS VLHNPHQTGC
61 GHRFCQHCIL SLRELNTVPI CPVDKEVIKS QEVFKDNCCK REVLNLYVYC SNAPGCNAKV
121 ILGRYQDHLQ QCLFQPVQCS NEKCREPVLR KDLKEHLSAS CQFRKEKCLY CKKDVVVINL
181 QNHEENLCPE YPVFCPNNCA KIILKTEVDE HLAVCPEAEQ DCPFKHYGCA VTDKRRNLQQ
241 HEHSALREHM RLVLEKNVQL EEQISDLHKS LEQKESKIQQ LAETIKKLEK EFKQFAQLFG
301 KNGSFLPNIQ VFASHIDKSA WLEAQVHQLL QMVNQQQNKF DLRPLMEAVD TVKQKITLLE
361 NNDQRLAVLE EETNKHDTHI NIHKAQLSKN EERFKLLEGT CYNGKLIWKV TDYKMKKREA
421 VDGHTVSIFS QSFYTSRCGY RLCARAYLNG DGSGRGSHLS LYFVVMRGEF DSLLQWPFRQ
481 RVTLMLLDQS GKKNIMETFK PDPNSSSFKR PDGEMNIASG CPRFVAHSVL ENAKNAYIKD
541 DTLFLKVAVD LTDLEDLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TRAF5 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)
- 0.38
- Highest tissue expression
- 28 nTPM
Expression across tissuesHPA
Tissue
- lymph node: 28 nTPM
- tonsil: 26 nTPM
- blood vessel: 21 nTPM
- pancreas: 20 nTPM
- smooth muscle: 19 nTPM
- fallopian tube: 18 nTPM
Single-cell type
- choroid plexus epithelial cells: 163 nCPM
- b-cells: 159 nCPM
- thymocytes: 122 nCPM
- podocytes: 111 nCPM
- tuft cells: 104 nCPM
- mast cells: 96 nCPM
Immune cell
- memory B-cell: 22 nTPM
- NK-cell: 21 nTPM
- naive B-cell: 20 nTPM
- T-reg: 18 nTPM
- MAIT T-cell: 17 nTPM
- basophil: 14 nTPM
Brain region
- choroid plexus: 55 nTPM
- basal ganglia: 8.6 nTPM
- hippocampal formation: 6.6 nTPM
- amygdala: 6.4 nTPM
- cerebral cortex: 5.4 nTPM
- thalamus: 5.4 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about TRAF5.
Disease | GeneticClinVar
1 pathogenic / likely-pathogenic of 95 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
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)
- 1.09
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.96
- DepMap mean gene effect
- 0.01
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- apoptotic process
- CD40 signaling pathway
- cell surface receptor signaling pathway
- interleukin-17-mediated signaling pathway
- mRNA stabilization
- positive regulation of canonical NF-kappaB signal transduction
- positive regulation of cell population proliferation
- positive regulation of NF-kappaB transcription factor activity
- regulation of apoptotic process
- regulation of canonical NF-kappaB signal transduction
- signal transduction
- signal transduction involved in regulation of gene expression
- tumor necrosis factor-mediated signaling pathway
Molecular functions
- identical protein binding
- signaling adaptor activity
- thioesterase binding
- tumor necrosis factor receptor binding
- ubiquitin protein ligase activity
- ubiquitin protein ligase binding
- zinc ion binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Zinc finger, TRAF-type
- Zinc finger, RING-type
- MATH/TRAF domain
- TRAF-like
- TNF receptor-associated factor TRAF, metazoa
- Zinc finger, RING/FYVE/PHD-type
- Zinc finger, RING-type, conserved site
- TRAF1-6, MATH domain
- TNF receptor-associated factor 3/5, RING domain
- TRAF-type zinc finger
- TRAF/meprin, MATH domain
- TNF receptor-associated factor 2/3/5, RING domain
- TNF receptor-associated factor 5, C3HC3D-type RING-HC finger
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TRAF5 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 TRAF5 as an antibody target. Whether an autoantibody or antibody against TRAF5 could matter depends on whether native TRAF5 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TRAF5 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 TRAF5 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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