PGP
Glycerol-3-phosphate phosphatase
Also known as: PGP_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- A6NDG6
- Gene
- PGP
- Ensembl
- ENSG00000184207
- Chromosome
- 16
- Canonical length
- 321 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins
- Subcellular location
- Nuclear bodies
- Quaternary structure
- Homodimer
OverviewNCBI Gene
Enables glycerol-3-phosphatase activity and phosphoglycolate phosphatase activity. Involved in glycerol biosynthetic process; glycerophospholipid metabolic process; and negative regulation of gluconeogenesis. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
321 residues, UniProt reviewed canonical sequence.
>A6NDG6|PGP
1 MAAAEAGGDD ARCVRLSAER AQALLADVDT LLFDCDGVLW RGETAVPGAP EALRALRARG
61 KRLGFITNNS SKTRAAYAEK LRRLGFGGPA GPGASLEVFG TAYCTALYLR QRLAGAPAPK
121 AYVLGSPALA AELEAVGVAS VGVGPEPLQG EGPGDWLHAP LEPDVRAVVV GFDPHFSYMK
181 LTKALRYLQQ PGCLLVGTNM DNRLPLENGR FIAGTGCLVR AVEMAAQRQA DIIGKPSRFI
241 FDCVSQEYGI NPERTVMVGD RLDTDILLGA TCGLKTILTL TGVSTLGDVK NNQESDCVSK
301 KKMVPDFYVD SIADLLPALQ GLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PGP 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)
- 0.26
- Highest tissue expression
- 60 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 60 nTPM
- testis: 44 nTPM
- skeletal muscle: 35 nTPM
- cerebral cortex: 32 nTPM
- heart muscle: 28 nTPM
- hippocampal formation: 19 nTPM
Single-cell type
- late spermatids: 2,429 nCPM
- early spermatids: 479 nCPM
- late primary spermatocytes: 402 nCPM
- cone photoreceptor cells: 197 nCPM
- cytotrophoblasts: 151 nCPM
- retinal ganglion cells: 147 nCPM
Immune cell
- eosinophil: 2.5 nTPM
- intermediate monocyte: 1.2 nTPM
- non-classical monocyte: 1.2 nTPM
- classical monocyte: 0.8 nTPM
- naive B-cell: 0.8 nTPM
- gdT-cell: 0.7 nTPM
Brain region
- pons: 53 nTPM
- cerebral cortex: 52 nTPM
- cerebellum: 36 nTPM
- medulla oblongata: 36 nTPM
- white matter: 32 nTPM
- basal ganglia: 32 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)
- 1.02
- gnomAD pLI
- 0.16
- gnomAD missense Z
- 1.3
- DepMap mean gene effect
- -0.09
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- glycerol biosynthetic process
- glycerophospholipid metabolic process
- negative regulation of gluconeogenesis
Molecular functions
- ADP phosphatase activity
- magnesium ion binding
- phosphoglycolate phosphatase activity
- protein tyrosine phosphatase activity
- sn-glycerol 1-phosphatase activity
- sn-glycerol 3-phosphatase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads PGP as an antibody target. Whether an autoantibody or antibody against PGP could matter depends on whether native PGP is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PGP 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 PGP as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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