PARP11
Protein mono-ADP-ribosyltransferase PARP11
Also known as: ARTD11, C12orf6, PAR11_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NR21
- Gene
- PARP11
- Ensembl
- ENSG00000111224
- Chromosome
- 12
- Canonical length
- 338 aa
- Protein class
- Metabolic proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nuclear bodies,Cytosol
OverviewNCBI Gene
Enables NAD+ poly-ADP-ribosyltransferase activity and NAD+-protein mono-ADP-ribosyltransferase activity. Involved in protein auto-ADP-ribosylation. Located in cytosol; nuclear body; and nuclear envelope. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
338 residues, UniProt reviewed canonical sequence.
>Q9NR21|PARP11
1 MWEANPEMFH KAEELFSKTT NNEVDDMDTS DTQWGWFYLA ECGKWHMFQP DTNSQCSVSS
61 EDIEKSFKTN PCGSISFTTS KFSYKIDFAE MKQMNLTTGK QRLIKRAPFS ISAFSYICEN
121 EAIPMPPHWE NVNTQVPYQL IPLHNQTHEY NEVANLFGKT MDRNRIKRIQ RIQNLDLWEF
181 FCRKKAQLKK KRGVPQINEQ MLFHGTSSEF VEAICIHNFD WRINGIHGAV FGKGTYFARD
241 AAYSSRFCKD DIKHGNTFQI HGVSLQQRHL FRTYKSMFLA RVLIGDYING DSKYMRPPSK
301 DGSYVNLYDS CVDDTWNPKI FVVFDANQIY PEYLIDFHLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PARP11 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)
- 0.34
- Highest tissue expression
- 9.6 nTPM
Expression across tissuesHPA
Tissue
- thymus: 9.6 nTPM
- lymph node: 9.5 nTPM
- tonsil: 8.8 nTPM
- testis: 8.7 nTPM
- thyroid gland: 8.5 nTPM
- prostate: 8.1 nTPM
Single-cell type
- sertoli cells: 136 nCPM
- early spermatids: 99 nCPM
- pituitary stem cells: 89 nCPM
- thymocytes: 76 nCPM
- prostatic glandular cells: 73 nCPM
- hematopoietic stem cells: 71 nCPM
Immune cell
- basophil: 21 nTPM
- MAIT T-cell: 10 nTPM
- memory B-cell: 10 nTPM
- naive CD4 T-cell: 9.3 nTPM
- eosinophil: 9.2 nTPM
- myeloid DC: 9 nTPM
Brain region
- white matter: 11 nTPM
- hypothalamus: 11 nTPM
- medulla oblongata: 11 nTPM
- midbrain: 11 nTPM
- pons: 10 nTPM
- basal ganglia: 9.9 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)
- 1.19
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.7
- DepMap mean gene effect
- 0.03
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cell differentiation
- mRNA transport
- nuclear envelope organization
- protein auto-ADP-ribosylation
- protein transport
- spermatogenesis
Molecular functions
- NAD+ poly-ADP-ribosyltransferase activity
- NAD+-protein mono-ADP-ribosyltransferase activity
- NAD+-protein-aspartate ADP-ribosyltransferase activity
- NAD+-protein-cysteine ADP-ribosyltransferase activity
- NAD+-protein-glutamate ADP-ribosyltransferase activity
- NAD+-protein-lysine ADP-ribosyltransferase activity
- nucleotidyltransferase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PARP11 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 PARP11 as an antibody target. Whether an autoantibody or antibody against PARP11 could matter depends on whether native PARP11 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PARP11 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 PARP11 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...