HSPB6
Heat shock protein beta-6
Also known as: FLJ32389, Hsp20, HSPB6_HUMAN, PPP1R91
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O14558
- Gene
- HSPB6
- Ensembl
- ENSG00000004776
- Chromosome
- 19
- Canonical length
- 160 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nuclear speckles,Mitochondria,Cytosol
- Secretome location
- Intracellular and membrane
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This locus encodes a heat shock protein. The encoded protein likely plays a role in smooth muscle relaxation. [provided by RefSeq, Jan 2012]
Canonical amino-acid sequenceUniProt
160 residues, UniProt reviewed canonical sequence.
>O14558|HSPB6
1 MEIPVPVQPS WLRRASAPLP GLSAPGRLFD QRFGEGLLEA ELAALCPTTL APYYLRAPSV
61 ALPVAQVPTD PGHFSVLLDV KHFSPEEIAV KVVGEHVEVH ARHEERPDEH GFVAREFHRR
121 YRLPPGVDPA AVTSALSPEG VLSIQAAPAS AQAPPPAAAKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against HSPB6 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
- Secreted
- Secreted
- Yes
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.45
- Highest tissue expression
- 2,832 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 2,832 nTPM
- tongue: 1,642 nTPM
- heart muscle: 1,367 nTPM
- colon: 668 nTPM
- blood vessel: 634 nTPM
- adipose tissue: 610 nTPM
Single-cell type
- decidual stromal cells: 734 nCPM
- thymic myoid cells: 311 nCPM
- smooth muscle cells: 265 nCPM
- hepatic stellate cells: 265 nCPM
- leydig cells: 254 nCPM
- vascular smooth muscle cells: 241 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- medulla oblongata: 125 nTPM
- pons: 119 nTPM
- thalamus: 75 nTPM
- spinal cord: 71 nTPM
- white matter: 67 nTPM
- midbrain: 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)
- 1.35
- gnomAD pLI
- 0.09
- gnomAD missense Z
- 1.28
- DepMap mean gene effect
- -0.03
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- negative regulation of apoptotic process
- negative regulation of cardiac muscle cell apoptotic process
- positive regulation of angiogenesis
- protein folding
- protein refolding
- response to heat
Molecular functions
- protein folding chaperone
- protein homodimerization activity
- protein kinase binding
- protein-folding chaperone binding
- structural constituent of eye lens
- unfolded protein binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of HSPB6 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 HSPB6 as an antibody target. Whether an autoantibody or antibody against HSPB6 could matter depends on whether native HSPB6 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
HSPB6 is annotated as secreted, so native HSPB6 circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.
Annotation status
The present source text does not explicitly label HSPB6 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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