PARP9
Protein mono-ADP-ribosyltransferase PARP9
Also known as: ARTD9, BAL, BAL1, PARP9_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8IXQ6
- Gene
- PARP9
- Ensembl
- ENSG00000138496
- Chromosome
- 3
- Canonical length
- 854 aa
- Protein class
- Disease related genes, Metabolic proteins, Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Mitochondria,Cytosol
OverviewNCBI Gene
Enables several functions, including ADP-D-ribose binding activity; STAT family protein binding activity; and pentosyltransferase activity. Involved in several processes, including DNA damage checkpoint signaling; regulation of defense response; and regulation of macromolecule metabolic process. Located in several cellular components, including mitochondrion; nucleoplasm; and site of DNA damage. Part of protein-containing complex. [provided by Alliance of Genome Resources, Apr 2025]
Canonical amino-acid sequenceUniProt
854 residues, UniProt reviewed canonical sequence.
>Q8IXQ6|PARP9
1 MDFSMVAGAA AYNEKSGRIT SLSLLFQKVF AQIFPQWRKG NTEECLPYKC SETGALGENY
61 SWQIPINHND FKILKNNERQ LCEVLQNKFG CISTLVSPVQ EGNSKSLQVF RKMLTPRIEL
121 SVWKDDLTTH AVDAVVNAAN EDLLHGGGLA LALVKAGGFE IQEESKQFVA RYGKVSAGEI
181 AVTGAGRLPC KQIIHAVGPR WMEWDKQGCT GKLQRAIVSI LNYVIYKNTH IKTVAIPALS
241 SGIFQFPLNL CTKTIVETIR VSLQGKPMMS NLKEIHLVSN EDPTVAAFKA ASEFILGKSE
301 LGQETTPSFN AMVVNNLTLQ IVQGHIEWQT ADVIVNSVNP HDITVGPVAK SILQQAGVEM
361 KSEFLATKAK QFQRSQLVLV TKGFNLFCKY IYHVLWHSEF PKPQILKHAM KECLEKCIEQ
421 NITSISFPAL GTGNMEIKKE TAAEILFDEV LTFAKDHVKH QLTVKFVIFP TDLEIYKAFS
481 SEMAKRSKML SLNNYSVPQS TREEKRENGL EARSPAINLM GFNVEEMYEA HAWIQRILSL
541 QNHHIIENNH ILYLGRKEHD ILSQLQKTSS VSITEIISPG RTELEIEGAR ADLIEVVMNI
601 EDMLCKVQEE MARKKERGLW RSLGQWTIQQ QKTQDEMKEN IIFLKCPVPP TQELLDQKKQ
661 FEKCGLQVLK VEKIDNEVLM AAFQRKKKMM EEKLHRQPVS HRLFQQVPYQ FCNVVCRVGF
721 QRMYSTPCDP KYGAGIYFTK NLKNLAEKAK KISAADKLIY VFEAEVLTGF FCQGHPLNIV
781 PPPLSPGAID GHDSVVDNVS SPETFVIFSG MQAIPQYLWT CTQEYVQSQD YSSGPMRPFA
841 QHPWRGFASG SPVDLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PARP9 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)
- 0.32
- Highest tissue expression
- 65 nTPM
Expression across tissuesHPA
Tissue
- liver: 65 nTPM
- spleen: 42 nTPM
- salivary gland: 38 nTPM
- lung: 35 nTPM
- appendix: 34 nTPM
- thymus: 29 nTPM
Single-cell type
- neutrophils: 165 nCPM
- esophageal apical cells: 86 nCPM
- prostatic glandular cells: 83 nCPM
- alveolar cells type 2: 76 nCPM
- alveolar cells type 1: 74 nCPM
- pancreatic islet cells: 73 nCPM
Immune cell
- neutrophil: 89 nTPM
- non-classical monocyte: 46 nTPM
- basophil: 42 nTPM
- intermediate monocyte: 42 nTPM
- eosinophil: 38 nTPM
- NK-cell: 31 nTPM
Brain region
- medulla oblongata: 26 nTPM
- thalamus: 18 nTPM
- spinal cord: 18 nTPM
- pons: 16 nTPM
- white matter: 15 nTPM
- midbrain: 13 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)
- 0.81
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.01
- DepMap mean gene effect
- 0.03
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 7% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cell migration
- defense response to virus
- DNA damage checkpoint signaling
- double-strand break repair
- innate immune response
- negative regulation of catalytic activity
- negative regulation of gene expression
- negative regulation of transcription by RNA polymerase II
- nicotinate metabolic process
- positive regulation of chromatin binding
- positive regulation of defense response to virus by host
- positive regulation of DNA-templated transcription
- positive regulation of protein localization to nucleus
- positive regulation of type II interferon-mediated signaling pathway
- positive regulation of tyrosine phosphorylation of STAT protein
- post-transcriptional regulation of gene expression
- viral protein processing
- regulation of response to type II interferon
Molecular functions
- ADP-D-ribose binding
- enzyme binding
- enzyme inhibitor activity
- histone binding
- NAD+ poly-ADP-ribosyltransferase activity
- nucleotidyltransferase activity
- STAT family protein binding
- transcription corepressor activity
- ubiquitin-like protein ligase binding
- NAD+-protein-C-terminal glycine ADP-ribosyltransferase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PARP9 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 PARP9 as an antibody target. Whether an autoantibody or antibody against PARP9 could matter depends on whether native PARP9 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PARP9 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 PARP9 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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