TRUB2
Pseudouridylate synthase TRUB2, mitochondrial
Also known as: CLONE24922, TRUB2_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O95900
- Gene
- TRUB2
- Ensembl
- ENSG00000167112
- Chromosome
- 9
- Canonical length
- 331 aa
- Protein class
- Enzymes, Predicted intracellular proteins
OverviewNCBI Gene
Pseudouridine is an abundant component of rRNAs and tRNAs and is enzymatically generated by isomerization of uridine by pseudouridine synthase (Zucchini et al., 2003 [PubMed 12736709]).[supplied by OMIM, Mar 2008]
Canonical amino-acid sequenceUniProt
331 residues, UniProt reviewed canonical sequence.
>O95900|TRUB2
1 MGSAGLSRLH GLFAVYKPPG LKWKHLRDTV ELQLLKGLNA RKPPAPKQRV RFLLGPMEGS
61 EEKELTLTAT SVPSFINHPL VCGPAFAHLK VGVGHRLDAQ ASGVLVLGVG HGCRLLTDMY
121 NAHLTKDYTV RGLLGKATDD FREDGRLVEK TTYDHVTREK LDRILAVIQG SHQKALVMYS
181 NLDLKTQEAY EMAVRGLIRP MNKSPMLITG IRCLYFAPPE FLLEVQCMHE TQKELRKLVH
241 EIGLELKTTA VCTQVRRTRD GFFTLDSALL RTQWDLTNIQ DAIRAATPQV AAELEKSLSP
301 GLDTKQLPSP GWSWDSQGPS STLGLERGAG QLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TRUB2 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)
- 0.34
- Highest tissue expression
- 13 nTPM
Expression across tissuesHPA
Tissue
- liver: 13 nTPM
- midbrain: 9.5 nTPM
- choroid plexus: 9.4 nTPM
- cerebral cortex: 9.1 nTPM
- tongue: 9.1 nTPM
- amygdala: 9 nTPM
Single-cell type
- esophageal basal cells: 77 nCPM
- esophageal suprabasal cells: 75 nCPM
- cytotrophoblasts: 63 nCPM
- hepatocytes: 62 nCPM
- extravillous trophoblasts: 54 nCPM
- migrating cytotrophoblasts: 53 nCPM
Immune cell
- NK-cell: 6.4 nTPM
- memory B-cell: 6.3 nTPM
- T-reg: 6.2 nTPM
- MAIT T-cell: 5.7 nTPM
- memory CD8 T-cell: 5.7 nTPM
- naive CD8 T-cell: 5.7 nTPM
Brain region
- pons: 20 nTPM
- white matter: 19 nTPM
- midbrain: 19 nTPM
- thalamus: 19 nTPM
- medulla oblongata: 19 nTPM
- cerebral cortex: 19 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)
- 1.25
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.05
- DepMap mean gene effect
- -0.35
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- mitochondrial tRNA pseudouridine synthesis
- mRNA modification
- mRNA processing
- mRNA pseudouridine synthesis
- positive regulation of mitochondrial translation
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Pseudouridine synthase II, N-terminal
- Pseudouridine synthase, catalytic domain superfamily
- TruB family pseudouridylate synthase (N terminal domain)
- Mitochondrial pseudouridylate synthase Trub2
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TRUB2 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 TRUB2 as an antibody target. Whether an autoantibody or antibody against TRUB2 could matter depends on whether native TRUB2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TRUB2 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 TRUB2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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