CTU1
Cytoplasmic tRNA 2-thiolation protein 1
Also known as: ATPBD3, CTU1_HUMAN, MGC17332, NCS6
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q7Z7A3
- Gene
- CTU1
- Ensembl
- ENSG00000142544
- Chromosome
- 19
- Canonical length
- 348 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Cytosol
OverviewNCBI Gene
Predicted to enable tRNA binding activity. Predicted to be involved in tRNA wobble position uridine thiolation. Located in cytosol. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
348 residues, UniProt reviewed canonical sequence.
>Q7Z7A3|CTU1
1 MPAPPCASCH AARAALRRPL SGQALCGACF CAAFEAEVLH TVLAGRLLPP GAVVAVGASG
61 GKDSTVLAHV LRALAPRLGI SLQLVAVDEG IGGYRDAALA AVRRQAARWE LPLTVVAYED
121 LFGGWTMDAV ARSTAGSGRS RSCCTFCGVL RRRALEEGAR RVGATHIVTG HNADDMAETV
181 LMNFLRGDAG RLARGGGLGS PGEGGALPRC RPLQFASQKE VVLYAHFRRL DYFSEECVYA
241 PEAFRGHARD LLKRLEAARP SAVLDLVHSA ERLALAPAAR PPRPGACSRC GALASRALCQ
301 ACALLDGLNR GRPRLAIGKG RRGLDEEATP GTPGDPARPP ASKAVPTFLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CTU1 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)
- 0.32
- Highest tissue expression
- 6.2 nTPM
Expression across tissuesHPA
Tissue
- ovary: 6.2 nTPM
- cerebellum: 4.4 nTPM
- esophagus: 4.4 nTPM
- pancreas: 4.1 nTPM
- endometrium: 4 nTPM
- kidney: 3.9 nTPM
Single-cell type
- alveolar cells type 1: 35 nCPM
- suprabasal keratinocytes: 35 nCPM
- basal keratinocytes: 25 nCPM
- fallopian secretory cells: 19 nCPM
- pancreatic acinar cells: 17 nCPM
- breast secretory cells: 17 nCPM
Immune cell
- classical monocyte: 0.1 nTPM
- eosinophil: 0.1 nTPM
- MAIT T-cell: 0.1 nTPM
- memory CD8 T-cell: 0.1 nTPM
- naive CD4 T-cell: 0.1 nTPM
- naive CD8 T-cell: 0.1 nTPM
Brain region
- medulla oblongata: 8.4 nTPM
- white matter: 7.9 nTPM
- cerebral cortex: 7.3 nTPM
- pons: 7 nTPM
- basal ganglia: 6.4 nTPM
- midbrain: 6.3 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)
- 1.51
- gnomAD pLI
- 0.07
- gnomAD missense Z
- 1.7
- DepMap mean gene effect
- -0.36
- 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
- protein urmylation
- tRNA thio-modification
- tRNA wobble position uridine thiolation
- tRNA wobble uridine modification
Molecular functions
Cellular components
- cytosol
- cytosolic tRNA wobble base thiouridylase complex
Protein domainsUniProt · Pfam · InterPro
- Rossmann-like alpha/beta/alpha sandwich fold
- Cytoplasmic tRNA 2-thiolation protein 1
- tRNA(Ile)-lysidine/2-thiocytidine synthase, N-terminal
- Cytoplasmic tRNA 2-thiolation protein 1, C-terminal
- tRNA thiolation protein, TtcA/Ctu1 type
- Cytoplasmic tRNA 2-thiolation protein 1-like, ATP-binding domain
- PP-loop domain
- Zinc-ribbon
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CTU1 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 CTU1 as an antibody target. Whether an autoantibody or antibody against CTU1 could matter depends on whether native CTU1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CTU1 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 CTU1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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