TBCA
Tubulin-specific chaperone A
Also known as: TBCA_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O75347
- Gene
- TBCA
- Ensembl
- ENSG00000171530
- Chromosome
- 5
- Canonical length
- 108 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoli,Microtubules
OverviewNCBI Gene
The product of this gene is one of four proteins (cofactors A, D, E, and C) involved in the pathway leading to correctly folded beta-tubulin from folding intermediates. Cofactors A and D are believed to play a role in capturing and stabilizing beta-tubulin intermediates in a quasi-native confirmation. Cofactor E binds to the cofactor D/beta-tubulin complex; interaction with cofactor C then causes the release of beta-tubulin polypeptides that are committed to the native state. This gene encodes chaperonin cofactor A. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]
Canonical amino-acid sequenceUniProt
108 residues, UniProt reviewed canonical sequence.
>O75347|TBCA
1 MADPRVRQIK IKTGVVKRLV KEKVMYEKEA KQQEEKIEKM RAEDGENYDI KKQAEILQES
61 RMMIPDCQRR LEAAYLDLQR ILENEKDLEE AEEYKEARLV LDSVKLEALocalizationUniProt · AlphaFold · HPA
Whether an antibody against TBCA 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)
- 0.35
- Highest tissue expression
- 267 nTPM
Expression across tissuesHPA
Tissue
- liver: 267 nTPM
- adrenal gland: 253 nTPM
- epididymis: 232 nTPM
- hypothalamus: 208 nTPM
- blood vessel: 202 nTPM
- ovary: 193 nTPM
Single-cell type
- parietal cells: 1,775 nCPM
- hepatocytes: 1,394 nCPM
- esophageal apical cells: 1,091 nCPM
- epididymal efferent duct ciliated cells: 884 nCPM
- epididymal principal cells: 672 nCPM
- epididymal efferent duct absorptive cells: 666 nCPM
Immune cell
- plasmacytoid DC: 255 nTPM
- T-reg: 243 nTPM
- memory B-cell: 220 nTPM
- naive B-cell: 197 nTPM
- naive CD8 T-cell: 196 nTPM
- myeloid DC: 173 nTPM
Brain region
- hypothalamus: 116 nTPM
- midbrain: 116 nTPM
- pons: 113 nTPM
- medulla oblongata: 100 nTPM
- cerebral cortex: 92 nTPM
- white matter: 89 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)
- 1.02
- gnomAD pLI
- 0.16
- gnomAD missense Z
- 0.6
- DepMap mean gene effect
- -0.9
- DepMap dependency class
- common
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 binding cofactor A
- Tubulin binding cofactor A superfamily
- Tubulin binding cofactor A
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TBCA 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 TBCA as an antibody target. Whether an autoantibody or antibody against TBCA could matter depends on whether native TBCA is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TBCA 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 TBCA as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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