TRIM40
E3 ubiquitin ligase TRIM40
Also known as: RNF35, TRI40_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q6P9F5
- Gene
- TRIM40
- Ensembl
- ENSG00000204614
- Chromosome
- 6
- Canonical length
- 258 aa
- Protein class
- Enzymes, Predicted intracellular proteins
- Subcellular location
- Cytosol
OverviewNCBI Gene
This gene encodes a member of the tripartite motif (TRIM) protein family. The encoded protein may play a role as a negative regulator against inflammation and carcinogenesis in the gastrointestinal tract. Alternatively spliced transcript variants that encode different protein isoforms have been described. [provided by RefSeq, Feb 2014]
Canonical amino-acid sequenceUniProt
258 residues, UniProt reviewed canonical sequence.
>Q6P9F5|TRIM40
1 MIPLQKDNQE EGVCPICQES LKEAVSTNCG HLFCRVCLTQ HVEKASASGV FCCPLCRKPC
61 SEEVLGTGYI CPNHQKRVCR FCEESRLLLC VECLVSPEHM SHHELTIENA LSHYKERLNR
121 RSRKLRKDIA ELQRLKAQQE KKLQALQFQV DHGNHRLEAG PESQHQTREQ LGALPQQWLG
181 QLEHMPAEAA RILDISRAVT QLRSLVIDLE RTAKELDTNT LKNAGDLLNR SAPQKLEVIY
241 PQLEKGVSEL LLQPPQKLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TRIM40 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
- 2.9 nTPM
Expression across tissuesHPA
Tissue
- small intestine: 2.9 nTPM
- colon: 2 nTPM
- liver: 1.4 nTPM
- testis: 1.4 nTPM
- appendix: 0.2 nTPM
- kidney: 0.2 nTPM
Single-cell type
- proximal tubule cells: 0.3 nCPM
- enteric transient amplifying cells: 0.2 nCPM
- colonocytes: 0.1 nCPM
- loop of henle epithelial cells: 0.1 nCPM
- microglia: 0.1 nCPM
- adipocytes: 0 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- amygdala: 0 nTPM
- basal ganglia: 0 nTPM
- cerebellum: 0 nTPM
- cerebral cortex: 0 nTPM
- choroid plexus: 0 nTPM
- hippocampal formation: 0 nTPM
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)
- 1.83
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.15
- DepMap mean gene effect
- -0.08
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- innate immune response
- negative regulation of cell growth
- negative regulation of NF-kappaB transcription factor activity
- negative regulation of non-canonical NF-kappaB signal transduction
- negative regulation of protein catabolic process
- negative regulation of protein localization to nucleus
- protein neddylation
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TRIM40 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 TRIM40 as an antibody target. Whether an autoantibody or antibody against TRIM40 could matter depends on whether native TRIM40 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TRIM40 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 TRIM40 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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