S100A7
Protein S100-A7
Also known as: PSOR1, S100A7c, S10A7_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P31151
- Gene
- S100A7
- Ensembl
- ENSG00000143556
- Chromosome
- 1
- Canonical length
- 101 aa
- Protein class
- Cancer-related genes, Plasma proteins, Predicted intracellular proteins, Predicted secreted proteins
- Subcellular location
- Cytosol
- Secretome location
- Secreted in other tissues
OverviewNCBI Gene
The protein encoded by this gene is a member of the S100 family of proteins containing 2 EF-hand calcium-binding motifs. S100 proteins are localized in the cytoplasm and/or nucleus of a wide range of cells, and involved in the regulation of a number of cellular processes such as cell cycle progression and differentiation. S100 genes include at least 13 members which are located as a cluster on chromosome 1q21. This protein differs from the other S100 proteins of known structure in its lack of calcium binding ability in one EF-hand at the N-terminus. The protein is overexpressed in hyperproliferative skin diseases, exhibits antimicrobial activities against bacteria and induces immunomodulatory activities. [provided by RefSeq, Nov 2014]
Canonical amino-acid sequenceUniProt
101 residues, UniProt reviewed canonical sequence.
>P31151|S100A7
1 MSNTQAERSI IGMIDMFHKY TRRDDKIEKP SLLTMMKENF PNFLSACDKK GTNYLADVFE
61 KKDKNEDKKI DFSEFLSLLG DIATDYHKQS HGAAPCSGGS QLocalizationUniProt · AlphaFold · HPA
Whether an antibody against S100A7 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)
- 0.34
- Highest tissue expression
- 1,901 nTPM
Expression across tissuesHPA
Tissue
- cervix: 1,901 nTPM
- vagina: 1,369 nTPM
- esophagus: 1,264 nTPM
- tonsil: 1,159 nTPM
- skin: 433 nTPM
- salivary gland: 78 nTPM
Single-cell type
- esophageal apical cells: 11,224 nCPM
- esophageal suprabasal cells: 5,422 nCPM
- suprabasal keratinocytes: 1,889 nCPM
- esophageal basal cells: 605 nCPM
- mast cells: 160 nCPM
- basal keratinocytes: 133 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
- cerebellum: 1.5 nTPM
- white matter: 0.9 nTPM
- cerebral cortex: 0.7 nTPM
- medulla oblongata: 0.5 nTPM
- basal ganglia: 0.4 nTPM
- hypothalamus: 0.3 nTPM
ReferencesPubMed · IEDB
Publications for S100A7 from three distinct lines of evidence, kept separate because they answer different questions: whether antibodies are directed at the protein, whether a B-cell epitope has been mapped on it, and whether a T-cell epitope has. Each is labelled with its source.
Reference: AutoantibodyPubMed
1 publication
- Use of a combination of approaches to identify and validate relevant tumor-associated antigens and their corresponding autoantibodies in ovarian cancer patients.
2008 · Clin Cancer Res · RCR 1.2 · 49 citations
Sources: PubMed — antigen-level antibody evidence from a custom retrieval. Records matching a controlled set of autoantibody terms (the MeSH descriptors Autoantibodies and Autoantigens, with title and abstract term variants) were obtained through NCBI E-utilities, and their titles and abstracts parsed for constructions that direct an antibody at a named protein rather than for co-occurrence. Captured names were resolved against UniProt nomenclature and each antigen adjudicated individually against the source text. Bibliographic records from PubMed and MeSH, U.S. National Library of Medicine; citation metrics from NIH iCite (Hutchins et al., PLoS Biology 2016). Titles link to PubMed; abstracts are not reproduced here. The NLM does not endorse this analysis.
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)
- 1.55
- gnomAD pLI
- 0.45
- gnomAD missense Z
- -0.49
- DepMap mean gene effect
- 0.13
- DepMap dependency class
- none
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
- angiogenesis
- antimicrobial humoral immune response mediated by antimicrobial peptide
- endothelial cell migration
- epidermis development
- keratinocyte differentiation
- positive regulation of ERK1 and ERK2 cascade
- positive regulation of granulocyte chemotaxis
- positive regulation of monocyte chemotaxis
- positive regulation of T cell chemotaxis
- response to lipopolysaccharide
- response to reactive oxygen species
Molecular functions
- calcium ion binding
- calcium-dependent protein binding
- RAGE receptor binding
- zinc ion binding
- zinc ion sequestering activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of S100A7 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 S100A7 as an antibody target. Whether an autoantibody or antibody against S100A7 could matter depends on whether native S100A7 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
S100A7 is annotated as secreted, so native S100A7 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 S100A7 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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