ACP7
Acid phosphatase type 7
Also known as: ACP7_HUMAN, FLJ16165, PAPL, PAPL1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q6ZNF0
- Gene
- ACP7
- Ensembl
- ENSG00000183760
- Chromosome
- 19
- Canonical length
- 438 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins, Predicted secreted proteins
- Secretome location
- Secreted - unknown location
OverviewNCBI Gene
Purple acid phosphatases (PAPs), including PAPL, are a family of binuclear metallohydrolases that have been identified in plants, animals, and fungi (Flanagan et al., 2006 [PubMed 16793224]).[supplied by OMIM, Mar 2008]
Canonical amino-acid sequenceUniProt
438 residues, UniProt reviewed canonical sequence.
>Q6ZNF0|ACP7
1 MHPLPGYWSC YCLLLLFSLG VQGSLGAPSA APEQVHLSYP GEPGSMTVTW TTWVPTRSEV
61 QFGLQPSGPL PLRAQGTFVP FVDGGILRRK LYIHRVTLRK LLPGVQYVYR CGSAQGWSRR
121 FRFRALKNGA HWSPRLAVFG DLGADNPKAV PRLRRDTQQG MYDAVLHVGD FAYNLDQDNA
181 RVGDRFMRLI EPVAASLPYM TCPGNHEERY NFSNYKARFS MPGDNEGLWY SWDLGPAHII
241 SFSTEVYFFL HYGRHLVQRQ FRWLESDLQK ANKNRAARPW IITMGHRPMY CSNADLDDCT
301 RHESKVRKGL QGKLYGLEDL FYKYGVDLQL WAHEHSYERL WPIYNYQVFN GSREMPYTNP
361 RGPVHIITGS AGCEERLTPF AVFPRPWSAV RVKEYGYTRL HILNGTHIHI QQVSDDQDGK
421 IVDDVWVVRP LFGRRMYLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ACP7 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
- Secreted
- Secreted
- Yes
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.23
- Highest tissue expression
- 10 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 10 nTPM
- skin: 5.6 nTPM
- tonsil: 2.4 nTPM
- spinal cord: 1.9 nTPM
- basal ganglia: 1.8 nTPM
- hippocampal formation: 1.7 nTPM
Single-cell type
- esophageal apical cells: 19 nCPM
- oligodendrocytes: 11 nCPM
- brain excitatory neurons: 7 nCPM
- respiratory ciliated cells: 2.8 nCPM
- foveolar cells: 2.7 nCPM
- salivary duct cells: 2.4 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- cerebellum: 14 nTPM
- white matter: 8.7 nTPM
- medulla oblongata: 8.4 nTPM
- pons: 8.1 nTPM
- midbrain: 8 nTPM
- basal ganglia: 7.2 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)
- 0.96
- gnomAD pLI
- 0
- DepMap mean gene effect
- -0.16
- 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
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Calcineurin-like, phosphoesterase domain
- Metallo-dependent phosphatase-like
- Calcineurin-like phosphoesterase
- Purple acid phosphatase-like, N-terminal
- Purple acid phosphatase, N-terminal
- Purple acid phosphatase, C-terminal domain
- Purple acid phosphatase, metallophosphatase domain
- Iron/zinc purple acid phosphatase-like protein C
- Purple acid Phosphatase, N-terminal domain
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ACP7 as an antibody target. Whether an autoantibody or antibody against ACP7 could matter depends on whether native ACP7 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ACP7 is annotated as secreted, so native ACP7 circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.
Annotation status
The present source text does not explicitly label ACP7 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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