TPGS1
Tubulin polyglutamylase complex subunit 1
Also known as: C19orf20, GTRGEO22, PGs1, TPGS1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q6ZTW0
- Gene
- TPGS1
- Ensembl
- ENSG00000141933
- Chromosome
- 19
- Canonical length
- 290 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
Predicted to enable microtubule binding activity and tubulin-glutamic acid ligase activity. Predicted to be involved in sperm axoneme assembly. Predicted to act upstream of or within several processes, including adult behavior; chemical synaptic transmission; and protein polyglutamylation. Located in centrosome. [provided by Alliance of Genome Resources, Apr 2025]
Canonical amino-acid sequenceUniProt
290 residues, UniProt reviewed canonical sequence.
>Q6ZTW0|TPGS1
1 MAAVEKRRQA VPPPAGFTDS GRQSVSRAAG AAESEEDFLR QVGVTEMLRA ALLKVLEARP
61 EEPIAFLAHY FENMGLRSPV NGGAGEPPGQ LLLQQQRLGR ALWHLRLAHH SQRAAFNNNV
121 SVAYECLSAG GRRKRPGLDG RTYSELLRRI CRDGQAPEEV VAPLLRKVQC RDHEAVPLSV
181 FRAGTLTCFV LLEFVARAGA LFQLLEDSAA AVADRRVGQA VLDTLEGALQ ASDAAAPARF
241 LEAGSRLGPD SLALALDRAV GGRRPSAPMT REEFLERAAA LFIAKVKPVGLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TPGS1 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
- 23 nTPM
Expression across tissuesHPA
Tissue
- hippocampal formation: 23 nTPM
- cerebral cortex: 21 nTPM
- amygdala: 19 nTPM
- blood vessel: 19 nTPM
- basal ganglia: 17 nTPM
- kidney: 17 nTPM
Single-cell type
- epididymal principal cells: 84 nCPM
- enterocytes: 69 nCPM
- epididymal efferent duct absorptive cells: 69 nCPM
- esophageal apical cells: 66 nCPM
- esophageal suprabasal cells: 66 nCPM
- epididymal clear cells: 61 nCPM
Immune cell
- naive B-cell: 5.3 nTPM
- eosinophil: 3.9 nTPM
- T-reg: 3.7 nTPM
- memory B-cell: 2.7 nTPM
- memory CD8 T-cell: 1.7 nTPM
- naive CD4 T-cell: 1 nTPM
Brain region
- medulla oblongata: 28 nTPM
- white matter: 26 nTPM
- midbrain: 26 nTPM
- thalamus: 25 nTPM
- cerebellum: 25 nTPM
- hippocampal formation: 25 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about TPGS1.
Disease | ImmuneIEDB
Conditions an epitope on TPGS1 was assayed in.
- psoriasis T cell
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)
- 1.56
- gnomAD pLI
- 0.06
- gnomAD missense Z
- 1.33
- DepMap mean gene effect
- -0.11
- 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
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Tubulin polyglutamylase complex subunit 1
- Tubulin polyglutamylase complex subunit 1, dimerization/docking domain
- Tubulin polyglutamylase complex subunit 1-like, C-terminal
- Tubulin polyglutamylase complex subunit 1-like, C-terminal
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TPGS1 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 TPGS1 as an antibody target. Whether an autoantibody or antibody against TPGS1 could matter depends on whether native TPGS1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TPGS1 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 TPGS1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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