FPR1
fMet-Leu-Phe receptor
Also known as: FMLP, FPR, FPR1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P21462
- Gene
- FPR1
- Ensembl
- ENSG00000171051
- Chromosome
- 19
- Canonical length
- 350 aa
- Protein class
- G-protein coupled receptors, Predicted membrane proteins
- Subcellular location
- Nucleoplasm,Nucleoli,Golgi apparatus
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene encodes a G protein-coupled receptor of mammalian phagocytic cells that is a member of the G-protein coupled receptor 1 family. The protein mediates the response of phagocytic cells to invasion of the host by microorganisms and is important in host defense and inflammation.[provided by RefSeq, Jul 2010]
Canonical amino-acid sequenceUniProt
350 residues, UniProt reviewed canonical sequence.
>P21462|FPR1
1 METNSSLPTN ISGGTPAVSA GYLFLDIITY LVFAVTFVLG VLGNGLVIWV AGFRMTHTVT
61 TISYLNLAVA DFCFTSTLPF FMVRKAMGGH WPFGWFLCKF VFTIVDINLF GSVFLIALIA
121 LDRCVCVLHP VWTQNHRTVS LAKKVIIGPW VMALLLTLPV IIRVTTVPGK TGTVACTFNF
181 SPWTNDPKER INVAVAMLTV RGIIRFIIGF SAPMSIVAVS YGLIATKIHK QGLIKSSRPL
241 RVLSFVAAAF FLCWSPYQVV ALIATVRIRE LLQGMYKEIG IAVDVTSALA FFNSCLNPML
301 YVFMGQDFRE RLIHALPASL ERALTEDSTQ TSDTATNSTL PSAEVELQAKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against FPR1 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)
- 0.33
- Highest tissue expression
- 179 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 179 nTPM
- spleen: 175 nTPM
- appendix: 154 nTPM
- lung: 66 nTPM
- adipose tissue: 64 nTPM
- urinary bladder: 62 nTPM
Single-cell type
- neutrophils: 3,551 nCPM
- monocytes: 454 nCPM
- neutrophil progenitors: 341 nCPM
- hofbauer cells: 222 nCPM
- cdc: 203 nCPM
- macrophages: 177 nCPM
Immune cell
- neutrophil: 4,198 nTPM
- classical monocyte: 759 nTPM
- total PBMC: 420 nTPM
- intermediate monocyte: 319 nTPM
- basophil: 318 nTPM
- eosinophil: 204 nTPM
Brain region
- white matter: 32 nTPM
- medulla oblongata: 27 nTPM
- thalamus: 17 nTPM
- spinal cord: 16 nTPM
- cerebral cortex: 16 nTPM
- pons: 15 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 missense Z
- 0.55
- DepMap mean gene effect
- 0.08
- 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
- adenylate cyclase-modulating G protein-coupled receptor signaling pathway
- chemotaxis
- complement receptor mediated signaling pathway
- G protein-coupled receptor signaling pathway
- inflammatory response
- nitric oxide mediated signal transduction
- phospholipase C-activating G protein-coupled receptor signaling pathway
- positive regulation of cytosolic calcium ion concentration
- signal transduction
Molecular functions
- complement receptor activity
- G protein-coupled receptor activity
- G protein-coupled receptor binding
- N-formyl peptide receptor activity
- RAGE receptor binding
- scavenger receptor binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads FPR1 as an antibody target. Whether an autoantibody or antibody against FPR1 could matter depends on whether native FPR1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
FPR1 is annotated at the cell surface, where native FPR1 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 FPR1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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