PGGHG
Protein-glucosylgalactosylhydroxylysine glucosidase
Also known as: ATHL1, FLJ22635, PGGHG_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q32M88
- Gene
- PGGHG
- Ensembl
- ENSG00000142102
- Chromosome
- 11
- Canonical length
- 737 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins
- Subcellular location
- Cytosol
OverviewNCBI Gene
Enables protein-glucosylgalactosylhydroxylysine glucosidase activity. Involved in carbohydrate metabolic process. Located in cytosol. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
737 residues, UniProt reviewed canonical sequence.
>Q32M88|PGGHG
1 MEDAGEDPTT FAAHSLPSDP RLLATVTNAY LGTRVFHDTL HVSGVYNGAG GDTHRAMLPS
61 PLNVRLEAPA GMGEQLTETF ALDTNTGSFL HTLEGPRFRA SQCIYAHRTL PHVLAFRVSI
121 ARLAPGSGPI TLLLRSAFSP ESPDLDLHQG PDFQGARYLY GHTLTPEQPG GPQQEVHMLW
181 TPAPPDLTLG EGEEARTWDF LTAVGGSQAE AQACLTEALQ LQARGALYTA HAQAWAQLWV
241 ECGLDVVGPL QLRQALRGSL YYLLSALPQP KAPGYICHGL SPGGLSNGSR EECYWGHVFW
301 DQDLWMFPSI LMFHPEAARA ILEYRIRTLD GALENAQNLG YQGAKFAWES ADSGLEVCPE
361 DIYGVQEVHV NGAVVLAFEL YYHTTQDLQL FREAGGWDVV RAVAEFWCSR VEWSPREEKY
421 HLRGVMSPDE YHSGVNNSVY TNVLVQNSLR FAAALAQDLG LPIPSQWLAV ADKIKVPFDV
481 EQNFHPEFDG YEPGEVVKQA DVVLLGYPVP FSLSPDVRRK NLEIYEAVTS PQGPAMTWSM
541 FAVGWMELKD AVRARGLLDR SFANMAEPFK VWTENADGSG AVNFLTGMGG FLQAVVFGCT
601 GFRVTRAGVT FDPVCLSGIS RVSVSGIFYQ GNKLNFSFSE DSVTVEVTAR AGPWAPHLEA
661 ELWPSQSRLS LLPGHKVSFP RSAGRIQMSP PKLPGSSSSE FPGRTFSDVR DPLQSPLWVT
721 LGSSSPTESL TVDPASELocalizationUniProt · AlphaFold · HPA
Whether an antibody against PGGHG 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)
- 0.23
- Highest tissue expression
- 623 nTPM
Expression across tissuesHPA
Tissue
- pancreas: 623 nTPM
- kidney: 146 nTPM
- spleen: 100 nTPM
- small intestine: 98 nTPM
- liver: 75 nTPM
- thyroid gland: 74 nTPM
Single-cell type
- renal collecting duct principal cells: 122 nCPM
- neutrophils: 105 nCPM
- pancreatic acinar cells: 91 nCPM
- papillary tip epithelial cells: 72 nCPM
- innate lymphoid cells: 62 nCPM
- loop of henle epithelial cells: 53 nCPM
Immune cell
- gdT-cell: 6.1 nTPM
- NK-cell: 5.6 nTPM
- MAIT T-cell: 5.2 nTPM
- naive CD8 T-cell: 4.6 nTPM
- neutrophil: 3.7 nTPM
- memory CD8 T-cell: 3.3 nTPM
Brain region
- cerebral cortex: 51 nTPM
- pons: 11 nTPM
- thalamus: 8.7 nTPM
- medulla oblongata: 8.1 nTPM
- choroid plexus: 7.5 nTPM
- midbrain: 6.9 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)
- 1.04
- gnomAD pLI
- 0
- DepMap mean gene effect
- -0.12
- DepMap dependency class
- selective
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
Molecular functions
- protein-glucosylgalactosylhydroxylysine glucosidase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Six-hairpin glycosidase superfamily
- Six-hairpin glycosidase-like superfamily
- Glycoside hydrolase, family 65, central catalytic
- Glycosyl hydrolase family 65 central catalytic domain
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads PGGHG as an antibody target. Whether an autoantibody or antibody against PGGHG could matter depends on whether native PGGHG is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PGGHG 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 PGGHG as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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