PSMB6
Proteasome subunit beta type-6
Also known as: DELTA, PSB6_HUMAN, Y
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P28072
- Gene
- PSMB6
- Ensembl
- ENSG00000142507
- Chromosome
- 17
- Canonical length
- 239 aa
- Protein class
- Enzymes, Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Mitochondria,Cytosol
OverviewNCBI Gene
The proteasome is a multicatalytic proteinase complex with a highly ordered ring-shaped 20S core structure. The core structure is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. The encoded protein is a member of the proteasome B-type family, also known as the T1B family, and is a 20S core beta subunit in the proteasome. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012]
Canonical amino-acid sequenceUniProt
239 residues, UniProt reviewed canonical sequence.
>P28072|PSMB6
1 MAATLLAARG AGPAPAWGPE AFTPDWESRE VSTGTTIMAV QFDGGVVLGA DSRTTTGSYI
61 ANRVTDKLTP IHDRIFCCRS GSAADTQAVA DAVTYQLGFH SIELNEPPLV HTAASLFKEM
121 CYRYREDLMA GIIIAGWDPQ EGGQVYSVPM GGMMVRQSFA IGGSGSSYIY GYVDATYREG
181 MTKEECLQFT ANALALAMER DGSSGGVIRL AAIAESGVER QVLLGDQIPK FAVATLPPALocalizationUniProt · AlphaFold · HPA
Whether an antibody against PSMB6 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)
- 0.31
- Highest tissue expression
- 362 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 362 nTPM
- tongue: 317 nTPM
- heart muscle: 200 nTPM
- choroid plexus: 196 nTPM
- liver: 172 nTPM
- parathyroid gland: 163 nTPM
Single-cell type
- esophageal suprabasal cells: 751 nCPM
- syncytiotrophoblasts: 740 nCPM
- esophageal apical cells: 729 nCPM
- cytotrophoblasts: 694 nCPM
- esophageal basal cells: 582 nCPM
- migrating cytotrophoblasts: 568 nCPM
Immune cell
- total PBMC: 818 nTPM
- memory B-cell: 672 nTPM
- naive B-cell: 645 nTPM
- myeloid DC: 626 nTPM
- classical monocyte: 605 nTPM
- intermediate monocyte: 591 nTPM
Brain region
- white matter: 75 nTPM
- pons: 72 nTPM
- hypothalamus: 70 nTPM
- cerebellum: 70 nTPM
- choroid plexus: 69 nTPM
- medulla oblongata: 66 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)
- 0.83
- gnomAD pLI
- 0.02
- gnomAD missense Z
- 1.46
- DepMap mean gene effect
- -1.72
- 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
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PSMB6 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 PSMB6 as an antibody target. Whether an autoantibody or antibody against PSMB6 could matter depends on whether native PSMB6 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PSMB6 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 PSMB6 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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