PGBD4
PiggyBac transposable element-derived protein 4
Also known as: FLJ32638, FLJ37497, PGBD4_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96DM1
- Gene
- PGBD4
- Ensembl
- ENSG00000182405
- Chromosome
- 15
- Canonical length
- 585 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Centrosome
OverviewNCBI Gene
The piggyBac family of proteins, found in diverse animals, are transposases related to the transposase of the canonical piggyBac transposon from the moth, Trichoplusia ni. This family also includes genes in several genomes, including human, that appear to have been derived from the piggyBac transposons. This gene belongs to the subfamily of piggyBac transposable element derived (PGBD) genes. The PGBD proteins appear to be novel, with no obvious relationship to other transposases, or other known protein families. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
585 residues, UniProt reviewed canonical sequence.
>Q96DM1|PGBD4
1 MSNPRKRSIP MRDSNTGLEQ LLAEDSFDES DFSEIDDSDN FSDSALEADK IRPLSHLESD
61 GKSSTSSDSG RSMKWSARAM IPRQRYDFTG TPGRKVDVSD ITDPLQYFEL FFTEELVSKI
121 TRETNAQAAL LASKPPGPKG FSRMDKWKDT DNDELKVFFA VMLLQGIVQK PELEMFWSTR
181 PLLDTPYLRQ IMTGERFLLL FRCLHFVNNS SISAGQSKAQ ISLQKIKPVF DFLVNKFSTV
241 YTPNRNIAVD ESLMLFKGPL AMKQYLPTKR VRFGLKLYVL CESQSGYVWN ALVHTGPGMN
301 LKDSADGLKS SRIVLTLVND LLGQGYCVFL DNFNISPMLF RELHQNRTDA VGTARLNRKQ
361 IPNDLKKRIA KGTTVARFCG ELMALKWCDG KEVTMLSTFH NDTVIEVNNR NGKKTKRPRV
421 IVDYNENMGA VDSADQMLTS YPSERKRHKV WYKKFFHHLL HITVLNSYIL FKKDNPEHTM
481 SHINFRLALI ERMLEKHHKP GQQHLRGRPC SDDVTPLRLS GRHFPKSIPA TSGKQNPTGR
541 CKICCSQYDK DGKKIRKETR YFCAECDVPL CVVPCFEIYH TKKNYLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PGBD4 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
- Unknown
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.3
- Highest tissue expression
- 4.9 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 4.9 nTPM
- bone marrow: 2.6 nTPM
- retina: 2.2 nTPM
- cerebral cortex: 1.9 nTPM
- lymph node: 1.9 nTPM
- testis: 1.7 nTPM
Single-cell type
- late spermatids: 15 nCPM
- early spermatids: 12 nCPM
- adrenal medulla cells: 11 nCPM
- late primary spermatocytes: 11 nCPM
- thymic myoid cells: 8.2 nCPM
- bergmann glia: 8.1 nCPM
Immune cell
- basophil: 3.8 nTPM
- neutrophil: 1.1 nTPM
- naive CD4 T-cell: 0.9 nTPM
- naive B-cell: 0.8 nTPM
- naive CD8 T-cell: 0.8 nTPM
- eosinophil: 0.6 nTPM
Brain region
- pons: 12 nTPM
- cerebral cortex: 11 nTPM
- medulla oblongata: 10 nTPM
- hippocampal formation: 9.7 nTPM
- white matter: 9.5 nTPM
- cerebellum: 9.3 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)
- 1.83
- gnomAD pLI
- 0.34
- gnomAD missense Z
- 1.49
- DepMap mean gene effect
- 0.1
- 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).
Protein domainsUniProt · Pfam · InterPro
- PiggyBac transposable element-derived protein
- Transposase IS4
- PiggyBac transposable element-derived protein 4, C-terminal zinc-finger domain
- DDE_Tnp_1-like zinc finger
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads PGBD4 as an antibody target. Whether an autoantibody or antibody against PGBD4 could matter depends on whether native PGBD4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PGBD4 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 PGBD4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...