PBLD
Phenazine biosynthesis-like domain-containing protein
Also known as: FLJ14767, MAWBP, MAWDBP, PBLD_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P30039
- Gene
- PBLD
- Ensembl
- ENSG00000108187
- Chromosome
- 10
- Canonical length
- 288 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Vesicles
OverviewNCBI Gene
Enables identical protein binding activity. Involved in maintenance of gastrointestinal epithelium. Acts upstream of or within with a positive effect on negative regulation of transforming growth factor beta receptor signaling pathway. Located in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
288 residues, UniProt reviewed canonical sequence.
>P30039|PBLD
1 MKLPIFIADA FTARAFRGNP AAVCLLENEL DEDMHQKIAR EMNLSETAFI RKLHPTDNFA
61 QSSCFGLRWF TPASEVPLCG HATLASAAVL FHKIKNMNST LTFVTLSGEL RARRAEDGIV
121 LDLPLYPAHP QDFHEVEDLI KTAIGNTLVQ DICYSPDTQK LLVRLSDVYN RSFLENLKVN
181 TENLLQVENT GKVKGLILTL KGEPGGQTQA FDFYSRYFAP WVGVAEDPVT GSAHAVLSSY
241 WSQHLGKKEM HAFQCSHRGG ELGISLRPDG RVDIRGGAAV VLEGTLTALocalizationUniProt · AlphaFold · HPA
Whether an antibody against PBLD 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
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.24
- Highest tissue expression
- 313 nTPM
Expression across tissuesHPA
Tissue
- liver: 313 nTPM
- kidney: 252 nTPM
- duodenum: 161 nTPM
- small intestine: 138 nTPM
- pancreas: 59 nTPM
- stomach: 52 nTPM
Single-cell type
- enterocytes: 396 nCPM
- hepatocytes: 271 nCPM
- parietal cells: 179 nCPM
- epicardial cells: 139 nCPM
- epididymal efferent duct absorptive cells: 128 nCPM
- cardiomyocytes: 125 nCPM
Immune cell
- neutrophil: 3.3 nTPM
- classical monocyte: 2.8 nTPM
- myeloid DC: 2.8 nTPM
- basophil: 2.5 nTPM
- NK-cell: 1.8 nTPM
- eosinophil: 1.5 nTPM
Brain region
- white matter: 30 nTPM
- cerebellum: 24 nTPM
- basal ganglia: 24 nTPM
- cerebral cortex: 24 nTPM
- medulla oblongata: 23 nTPM
- hypothalamus: 22 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)
- 1.57
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.35
- DepMap mean gene effect
- 0.02
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- antiviral innate immune response
- apoptotic process
- maintenance of gastrointestinal epithelium
- negative regulation of transforming growth factor beta receptor signaling pathway
- positive regulation of canonical NF-kappaB signal transduction
- positive regulation of type I interferon production
- regulation of type I interferon production
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Phenazine biosynthesis PhzF-like
- Phenazine biosynthesis-like protein
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PBLD 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 PBLD as an antibody target. Whether an autoantibody or antibody against PBLD could matter depends on whether native PBLD is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PBLD is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label PBLD as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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