APCS
Serum amyloid P-component
Also known as: MGC88159, PTX2, SAMP_HUMAN, SAP
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P02743
- Gene
- APCS
- Ensembl
- ENSG00000132703
- Chromosome
- 1
- Canonical length
- 223 aa
- Protein class
- Disease related genes, Plasma proteins, Potential drug targets, Predicted secreted proteins, Transporters
- Secretome location
- Secreted to blood
- Quaternary structure
- Homopentamer
OverviewNCBI Gene
The protein encoded by this gene is a glycoprotein, belonging to the pentraxin family of proteins, which has a characteristic pentameric organization. These family members have considerable sequence homology which is thought to be the result of gene duplication. The binding of the encoded protein to proteins in the pathological amyloid cross-beta fold suggests its possible role as a chaperone. This protein is also thought to control the degradation of chromatin. It has been demonstrated that this protein binds to apoptotic cells at an early stage, which raises the possibility that it is involved in dealing with apoptotic cells in vivo. [provided by RefSeq, Sep 2008]
Canonical amino-acid sequenceUniProt
223 residues, UniProt reviewed canonical sequence.
>P02743|APCS
1 MNKPLLWISV LTSLLEAFAH TDLSGKVFVF PRESVTDHVN LITPLEKPLQ NFTLCFRAYS
61 DLSRAYSLFS YNTQGRDNEL LVYKERVGEY SLYIGRHKVT SKVIEKFPAP VHICVSWESS
121 SGIAEFWING TPLVKKGLRQ GYFVEAQPKI VLGQEQDSYG GKFDRSQSFV GEIGDLYMWD
181 SVLPPENILS AYQGTPLPAN ILDWQALNYE IRGYVIIKPL VWVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against APCS 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)
- 0.27
- Highest tissue expression
- 3,389 nTPM
Expression across tissuesHPA
Tissue
- liver: 3,389 nTPM
- gallbladder: 45 nTPM
- pancreas: 8.9 nTPM
- kidney: 2.3 nTPM
- spleen: 1.5 nTPM
- adipose tissue: 0.4 nTPM
Single-cell type
- hepatocytes: 4,781 nCPM
- cholangiocytes: 379 nCPM
- hepatic stellate cells: 58 nCPM
- pancreatic duct cells: 47 nCPM
- kupffer cells: 45 nCPM
- loop of henle epithelial cells: 11 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
- amygdala: 0 nTPM
- basal ganglia: 0 nTPM
- cerebellum: 0 nTPM
- cerebral cortex: 0 nTPM
- choroid plexus: 0 nTPM
- hippocampal formation: 0 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)
- 1.83
- gnomAD pLI
- 0.03
- gnomAD missense Z
- -0.23
- DepMap mean gene effect
- -0.09
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 2% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- acute-phase response
- chaperone-mediated protein complex assembly
- host-mediated suppression of symbiont invasion
- innate immune response
- negative regulation by host of viral glycoprotein metabolic process
- negative regulation of acute inflammatory response
- negative regulation of glycoprotein metabolic process
- negative regulation of monocyte differentiation
- negative regulation of viral process
- negative regulation of wound healing
- protein folding
Molecular functions
- calcium ion binding
- carbohydrate binding
- complement component C1q complex binding
- identical protein binding
- unfolded protein binding
- virion binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of APCS 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 APCS as an antibody target. Whether an autoantibody or antibody against APCS could matter depends on whether native APCS is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
APCS is annotated as secreted, so native APCS 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 APCS as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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