BDKRB1
B1 bradykinin receptor
Also known as: B1BKR, BKR1, BKRB1_HUMAN, bradyb1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P46663
- Gene
- BDKRB1
- Ensembl
- ENSG00000100739
- Chromosome
- 14
- Canonical length
- 353 aa
- Protein class
- G-protein coupled receptors, Predicted membrane proteins
OverviewNCBI Gene
Bradykinin, a 9 aa peptide, is generated in pathophysiologic conditions such as inflammation, trauma, burns, shock, and allergy. The protein encoded by this gene belongs to the G-protein coupled receptor 1 family. Two types of G-protein coupled receptors have been found which bind bradykinin and mediate responses to these pathophysiologic conditions. The protein encoded by this gene is one of these receptors and is synthesized de novo following tissue injury. Receptor binding leads to an increase in the cytosolic calcium ion concentration, ultimately resulting in chronic and acute inflammatory responses. [provided by RefSeq, Aug 2020]
Canonical amino-acid sequenceUniProt
353 residues, UniProt reviewed canonical sequence.
>P46663|BDKRB1
1 MASSWPPLEL QSSNQSQLFP QNATACDNAP EAWDLLHRVL PTFIISICFF GLLGNLFVLL
61 VFLLPRRQLN VAEIYLANLA ASDLVFVLGL PFWAENIWNQ FNWPFGALLC RVINGVIKAN
121 LFISIFLVVA ISQDRYRVLV HPMASRRQQR RRQARVTCVL IWVVGGLLSI PTFLLRSIQA
181 VPDLNITACI LLLPHEAWHF ARIVELNILG FLLPLAAIVF FNYHILASLR TREEVSRTRC
241 GGRKDSKTTA LILTLVVAFL VCWAPYHFFA FLEFLFQVQA VRGCFWEDFI DLGLQLANFF
301 AFTNSSLNPV IYVFVGRLFR TKVWELYKQC TPKSLAPISS SHRKEIFQLF WRNLocalizationUniProt · AlphaFold · HPA
Whether an antibody against BDKRB1 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
- 22 nTPM
Expression across tissuesHPA
Tissue
- urinary bladder: 22 nTPM
- esophagus: 13 nTPM
- gallbladder: 13 nTPM
- adipose tissue: 10 nTPM
- vagina: 7.5 nTPM
- kidney: 6.8 nTPM
Single-cell type
- esophageal apical cells: 94 nCPM
- basal keratinocytes: 37 nCPM
- esophageal suprabasal cells: 25 nCPM
- fibroblasts: 23 nCPM
- epicardial cells: 23 nCPM
- esophageal basal cells: 19 nCPM
Immune cell
- T-reg: 0.2 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
Brain region
- cerebellum: 2.2 nTPM
- cerebral cortex: 1 nTPM
- white matter: 0.8 nTPM
- pons: 0.5 nTPM
- basal ganglia: 0.4 nTPM
- hippocampal formation: 0.4 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)
- 1.1
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.11
- DepMap mean gene effect
- 0.14
- 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
- cell migration
- G protein-coupled receptor signaling pathway
- inflammatory response
- negative regulation of blood pressure
- negative regulation of cell growth
- positive regulation of cytosolic calcium ion concentration
- positive regulation of leukocyte migration
- positive regulation of release of sequestered calcium ion into cytosol
- response to lipopolysaccharide
- response to mechanical stimulus
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads BDKRB1 as an antibody target. Whether an autoantibody or antibody against BDKRB1 could matter depends on whether native BDKRB1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
BDKRB1 is annotated at the cell surface, where native BDKRB1 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 BDKRB1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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