BPIFA1
BPI fold-containing family A member 1
Also known as: bA49G10.5, BPIA1_HUMAN, LUNX, PLUNC, SPLUNC1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NP55
- Gene
- BPIFA1
- Ensembl
- ENSG00000198183
- Chromosome
- 20
- Canonical length
- 256 aa
- Protein class
- Plasma proteins, Predicted secreted proteins
- Secretome location
- Secreted in other tissues
OverviewNCBI Gene
This gene is the human homolog of murine plunc, and like the mouse gene, is specifically expressed in the upper airways and nasopharyngeal regions. The encoded antimicrobial protein displays antibacterial activity against Gram-negative bacteria. It is thought to be involved in inflammatory responses to irritants in the upper airways and may also serve as a potential molecular marker for detection of micrometastasis in non-small-cell lung cancer. Multiple transcript variants resulting from alternative splicing in the 3' UTR have been detected, but the full-length nature of only three are known. [provided by RefSeq, Aug 2014]
Canonical amino-acid sequenceUniProt
256 residues, UniProt reviewed canonical sequence.
>Q9NP55|BPIFA1
1 MFQTGGLIVF YGLLAQTMAQ FGGLPVPLDQ TLPLNVNPAL PLSPTGLAGS LTNALSNGLL
61 SGGLLGILEN LPLLDILKPG GGTSGGLLGG LLGKVTSVIP GLNNIIDIKV TDPQLLELGL
121 VQSPDGHRLY VTIPLGIKLQ VNTPLVGASL LRLAVKLDIT AEILAVRDKQ ERIHLVLGDC
181 THSPGSLQIS LLDGLGPLPI QGLLDSLTGI LNKVLPELVQ GNVCPLVNEV LRGLDITLVH
241 DIVNMLIHGL QFVIKVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against BPIFA1 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)
- 0.38
- Highest tissue expression
- 19 nTPM
Expression across tissuesHPA
Tissue
- lung: 19 nTPM
- pituitary gland: 12 nTPM
- cervix: 5.8 nTPM
- salivary gland: 3.5 nTPM
- testis: 0.9 nTPM
- urinary bladder: 0.9 nTPM
Single-cell type
- conjunctival goblet cells: 23,186 nCPM
- respiratory deuterosomal cells: 1,648 nCPM
- respiratory secretory cells: 1,149 nCPM
- submucosal glandular cells: 896 nCPM
- transitional alveolar cells: 74 nCPM
- salivary duct cells: 41 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
- basal ganglia: 0.1 nTPM
- cerebral cortex: 0.1 nTPM
- hippocampal formation: 0.1 nTPM
- medulla oblongata: 0.1 nTPM
- amygdala: 0 nTPM
- cerebellum: 0 nTPM
ReferencesPubMed · IEDB
Publications for BPIFA1 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
2 publications
- Profiling Autoantibodies against Salivary Proteins in Sicca Conditions.
2019 · J Dent Res · RCR 0.8 · 18 citations - Anti-BPIFA1/SPLUNC1: a new autoantibody prevalent in patients with endstage cystic fibrosis.
2014 · J Cyst Fibros · RCR 0.2 · 5 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)
- 1.64
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.44
- DepMap mean gene effect
- 0.06
- DepMap dependency class
- none
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
- antibacterial humoral response
- antimicrobial humoral immune response mediated by antimicrobial peptide
- defense response to virus
- immune response in nasopharyngeal-associated lymphoid tissue
- innate immune response
- multicellular organismal-level water homeostasis
- negative regulation of single-species biofilm formation in or on host organism
- regulation of sodium ion transmembrane transport
- surfactant homeostasis
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of BPIFA1 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 BPIFA1 as an antibody target. Whether an autoantibody or antibody against BPIFA1 could matter depends on whether native BPIFA1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
BPIFA1 is annotated as secreted, so native BPIFA1 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 BPIFA1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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