F2R
Proteinase-activated receptor 1
Also known as: CF2R, PAR-1, PAR1, PAR1_HUMAN, TR
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P25116
- Gene
- F2R
- Ensembl
- ENSG00000181104
- Chromosome
- 5
- Canonical length
- 425 aa
- Protein class
- FDA approved drug targets, G-protein coupled receptors, Predicted intracellular proteins, Predicted membrane proteins, Transporters
OverviewNCBI Gene
Coagulation factor II receptor is a 7-transmembrane receptor involved in the regulation of thrombotic response. Proteolytic cleavage leads to the activation of the receptor. F2R is a G-protein coupled receptor family member. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2015]
Canonical amino-acid sequenceUniProt
425 residues, UniProt reviewed canonical sequence.
>P25116|F2R
1 MGPRRLLLVA ACFSLCGPLL SARTRARRPE SKATNATLDP RSFLLRNPND KYEPFWEDEE
61 KNESGLTEYR LVSINKSSPL QKQLPAFISE DASGYLTSSW LTLFVPSVYT GVFVVSLPLN
121 IMAIVVFILK MKVKKPAVVY MLHLATADVL FVSVLPFKIS YYFSGSDWQF GSELCRFVTA
181 AFYCNMYASI LLMTVISIDR FLAVVYPMQS LSWRTLGRAS FTCLAIWALA IAGVVPLLLK
241 EQTIQVPGLN ITTCHDVLNE TLLEGYYAYY FSAFSAVFFF VPLIISTVCY VSIIRCLSSS
301 AVANRSKKSR ALFLSAAVFC IFIICFGPTN VLLIAHYSFL SHTSTTEAAY FAYLLCVCVS
361 SISCCIDPLI YYYASSECQR YVYSILCCKE SSDPSSYNSS GQLMASKMDT CSSNLNNSIY
421 KKLLTLocalizationUniProt · AlphaFold · HPA
Whether an antibody against F2R 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 7
- Mean surface accessibility (rSASA)
- 0.37
- Highest tissue expression
- 65 nTPM
Expression across tissuesHPA
Tissue
- spleen: 65 nTPM
- blood vessel: 45 nTPM
- skin: 43 nTPM
- gallbladder: 37 nTPM
- salivary gland: 29 nTPM
- heart muscle: 29 nTPM
Single-cell type
- platelets: 557 nCPM
- megakaryocyte progenitors: 126 nCPM
- hepatic stellate cells: 116 nCPM
- podocytes: 108 nCPM
- megakaryocytes: 99 nCPM
- decidual stromal cells: 66 nCPM
Immune cell
- gdT-cell: 26 nTPM
- memory CD8 T-cell: 18 nTPM
- naive CD8 T-cell: 13 nTPM
- total PBMC: 11 nTPM
- NK-cell: 7 nTPM
- MAIT T-cell: 6.5 nTPM
Brain region
- midbrain: 7 nTPM
- medulla oblongata: 6.6 nTPM
- thalamus: 5.3 nTPM
- spinal cord: 5.1 nTPM
- hypothalamus: 4.8 nTPM
- choroid plexus: 4.7 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)
- 0.96
- gnomAD pLI
- 0.01
- gnomAD missense Z
- 1.19
- DepMap mean gene effect
- -0.13
- DepMap dependency class
- selective
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
- anatomical structure morphogenesis
- cell-cell junction maintenance
- connective tissue replacement involved in inflammatory response wound healing
- dendritic cell homeostasis
- establishment of synaptic specificity at neuromuscular junction
- G protein-coupled receptor signaling pathway
- homeostasis of number of cells within a tissue
- inflammatory response
- negative regulation of cell population proliferation
- negative regulation of glomerular filtration
- negative regulation of neuron apoptotic process
- phospholipase C-activating G protein-coupled receptor signaling pathway
- platelet activation
- platelet dense granule organization
- positive regulation of apoptotic process
- positive regulation of blood coagulation
- positive regulation of calcium ion transport
- positive regulation of canonical NF-kappaB signal transduction
- positive regulation of cell migration
- positive regulation of cell population proliferation
- positive regulation of collagen biosynthetic process
- positive regulation of cytosolic calcium ion concentration
- positive regulation of DNA-templated transcription
- positive regulation of ERK1 and ERK2 cascade
- positive regulation of interleukin-6 production
- positive regulation of interleukin-8 production
- positive regulation of MAPK cascade
- positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction
- positive regulation of receptor signaling pathway via JAK-STAT
- positive regulation of release of sequestered calcium ion into cytosol
- positive regulation of Rho protein signal transduction
- positive regulation of smooth muscle contraction
- positive regulation of vasoconstriction
- regulation of blood coagulation
- regulation of interleukin-1 beta production
- regulation of synaptic plasticity
- release of sequestered calcium ion into cytosol
- response to lipopolysaccharide
- response to wounding
- thrombin-activated receptor signaling pathway
- trans-synaptic signaling by endocannabinoid, modulating synaptic transmission
- negative regulation of renin secretion into blood stream
Molecular functions
- G protein-coupled receptor activity
- G-protein alpha-subunit binding
- G-protein beta-subunit binding
- signaling receptor binding
- thrombin-activated receptor activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of F2R 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 F2R as an antibody target. Whether an autoantibody or antibody against F2R could matter depends on whether native F2R is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
F2R is annotated at the cell surface, where native F2R is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label F2R as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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