PXYLP1
2-phosphoxylose phosphatase 1
Also known as: ACPL2, FLJ23751, PXYP1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8TE99
- Gene
- PXYLP1
- Ensembl
- ENSG00000155893
- Chromosome
- 3
- Canonical length
- 480 aa
- Protein class
- Metabolic proteins, Predicted intracellular proteins
- Secretome location
- Intracellular and membrane
OverviewNCBI Gene
Enables phosphatase activity. Involved in chondroitin sulfate proteoglycan biosynthetic process and positive regulation of heparan sulfate proteoglycan biosynthetic process. Located in Golgi apparatus. [provided by Alliance of Genome Resources, Apr 2025]
Canonical amino-acid sequenceUniProt
480 residues, UniProt reviewed canonical sequence.
>Q8TE99|PXYLP1
1 MLFRNRFLLL LALAALLAFV SLSLQFFHLI PVSTPKNGMS SKSRKRIMPD PVTEPPVTDP
61 VYEALLYCNI PSVAERSMEG HAPHHFKLVS VHVFIRHGDR YPLYVIPKTK RPEIDCTLVA
121 NRKPYHPKLE AFISHMSKGS GASFESPLNS LPLYPNHPLC EMGELTQTGV VQHLQNGQLL
181 RDIYLKKHKL LPNDWSADQL YLETTGKSRT LQSGLALLYG FLPDFDWKKI YFRHQPSALF
241 CSGSCYCPVR NQYLEKEQRR QYLLRLKNSQ LEKTYGEMAK IVDVPTKQLR AANPIDSMLC
301 HFCHNVSFPC TRNGCVDMEH FKVIKTHQIE DERERREKKL YFGYSLLGAH PILNQTIGRM
361 QRATEGRKEE LFALYSAHDV TLSPVLSALG LSEARFPRFA ARLIFELWQD REKPSEHSVR
421 ILYNGVDVTF HTSFCQDHHK RSPKPMCPLE NLVRFVKRDM FVALGGSGTN YYDACHREGFLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PXYLP1 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
- Other membrane
- Secreted
- No
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.28
- Highest tissue expression
- 140 nTPM
Expression across tissuesHPA
Tissue
- epididymis: 140 nTPM
- thymus: 50 nTPM
- seminal vesicle: 27 nTPM
- placenta: 17 nTPM
- retina: 17 nTPM
- parathyroid gland: 15 nTPM
Single-cell type
- late primary spermatocytes: 288 nCPM
- epididymal principal cells: 276 nCPM
- early spermatids: 177 nCPM
- late spermatids: 165 nCPM
- renal collecting duct principal cells: 119 nCPM
- neutrophils: 76 nCPM
Immune cell
- naive CD4 T-cell: 22 nTPM
- NK-cell: 19 nTPM
- naive CD8 T-cell: 18 nTPM
- basophil: 15 nTPM
- gdT-cell: 14 nTPM
- eosinophil: 9.4 nTPM
Brain region
- cerebral cortex: 39 nTPM
- hypothalamus: 26 nTPM
- white matter: 25 nTPM
- basal ganglia: 24 nTPM
- amygdala: 23 nTPM
- hippocampal formation: 23 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)
- 0.77
- gnomAD pLI
- 0
- DepMap mean gene effect
- -0.07
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 8% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- chondroitin sulfate proteoglycan biosynthetic process
- glycosaminoglycan biosynthetic process
- positive regulation of heparan sulfate proteoglycan biosynthetic process
- positive regulation of proteoglycan biosynthetic process
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PXYLP1 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 PXYLP1 as an antibody target. Whether an autoantibody or antibody against PXYLP1 could matter depends on whether native PXYLP1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PXYLP1 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 PXYLP1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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