1. Gene
  2. PARP2 - poly(ADP-ribose) polymerase 2 Gene

PARP2 - poly(ADP-ribose) polymerase 2 Gene

Homo sapiens

Also known as ARTD2; ADPRT2; PARP-2; ADPRTL2; ADPRTL3; pADPRT-2

Gene ID: 10038 | Gene type: protein coding

About PARP2

Cytogenetic location: 14q11.2 Genomic coordinates (GRCh38): 14:20,343,635-20,357,904 (from NCBI)

This gene has 11 transcripts (splice variants), 185 orthologues and 2 paralogues. Ubiquitous expression in brain (RPKM 14.3), testis (RPKM 13.0) and 25 other tissues.

Summary

This gene encodes poly(ADP-ribosyl)transferase-like 2 protein, which contains a catalytic domain and is capable of catalyzing a poly(ADP-ribosyl)ation reaction. This protein has a catalytic domain which is homologous to that of poly (ADP-ribosyl) transferase, but lacks an N-terminal DNA binding domain which activates the C-terminal catalytic domain of poly (ADP-ribosyl) transferase. The basic residues within the N-terminal region of this protein may bear potential DNA-binding properties, and may be involved in the nuclear and/or nucleolar targeting of the protein. Two alternatively spliced transcript variants encoding distinct isoforms have been found. [provided by RefSeq, Jul 2008]

PARP2 Products(5)

mRNA Protein Name
NM_005484.4 NP_005475.2 poly [ADP-ribose] polymerase 2 isoform 1
XM_005267247.4 XP_005267304.1 poly [ADP-ribose] polymerase 2 isoform X1
XM_047430869.1 XP_047286825.1 poly [ADP-ribose] polymerase 2 isoform X3
XM_017020912.2 XP_016876401.1 poly [ADP-ribose] polymerase 2 isoform X2
NM_001042618.2 NP_001036083.1 poly [ADP-ribose] polymerase 2 isoform 2
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables NAD DNA ADP-ribosyltransferase activity IDA
IDA: Inferred from direct assay
27471034 GOA
enables NAD+-protein ADP-ribosyltransferase activity IDA
IDA: Inferred from direct assay
25043379 GOA
enables NAD+-protein poly-ADP-ribosyltransferase activity IDA
IDA: Inferred from direct assay
30104678 GOA
enables NAD+-protein-aspartate ADP-ribosyltransferase activity IDA
IDA: Inferred from direct assay
25043379 GOA
enables NAD+-protein-glutamate ADP-ribosyltransferase activity IDA
IDA: Inferred from direct assay
25043379 GOA
enables NAD+-protein-serine ADP-ribosyltransferase activity IDA
IDA: Inferred from direct assay
28190768 GOA
enables chromatin binding IDA
IDA: Inferred from direct assay
32939087 GOA
enables damaged DNA binding IDA
IDA: Inferred from direct assay
34108479 GOA
enables nucleosome binding IDA
IDA: Inferred from direct assay
32939087 GOA
enables poly-ADP-D-ribose binding IDA
IDA: Inferred from direct assay
30104678 GOA
enables poly-ADP-D-ribose modification-dependent protein binding IDA
IDA: Inferred from direct assay
30104678 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
21812934 GOA
Biological Process GO Annotation Evidence Reference Source
involved in DNA ADP-ribosylation IDA
IDA: Inferred from direct assay
27471034 GOA
involved in DNA damage response IDA
IDA: Inferred from direct assay
34108479 GOA
involved in DNA repair IDA
IDA: Inferred from direct assay
30104678 GOA
involved in DNA repair-dependent chromatin remodeling IDA
IDA: Inferred from direct assay
32939087 GOA
involved in protein auto-ADP-ribosylation IDA
IDA: Inferred from direct assay
32939087 GOA
involved in protein poly-ADP-ribosylation IDA
IDA: Inferred from direct assay
25043379 GOA
Cellular Component GO Annotation Evidence Reference Source
located in nucleolus IDA
IDA: Inferred from direct assay
15615785 GOA
located in nucleoplasm IDA
IDA: Inferred from direct assay
15615785 GOA
located in nucleus IDA
IDA: Inferred from direct assay
26704974 GOA
is active in site of DNA damage IDA
IDA: Inferred from direct assay
30104678 GOA
located in site of DNA damage IDA
IDA: Inferred from direct assay
26704974 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

PARP2 Protein Structure

WGR

WGR: WGR domain (112 - 194)

PARP_reg

PARP_reg: Poly(ADP-ribose) polymerase, regulatory domain (231 - 363)

PARP

PARP: Poly(ADP-ribose) polymerase catalytic domain (365 - 577)

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  • 583 a.a.
Protein Preferred Names Protein Names

poly [ADP-ribose] polymerase 2

ADP-ribosyltransferase (NAD+

poly(ADP-ribose) polymerase)-like 2

ADP-ribosyltransferase diphtheria toxin-like 2

ADPRT-2

DNA ADP-ribosyltransferase PARP2

NAD(+) ADP-ribosyltransferase 2

hPARP-2

poly (ADP-ribose) polymerase family, member 2

poly (ADP-ribosyl) transferase-like 2

poly[ADP-ribose] synthase 2

poly[ADP-ribose] synthetase 2

protein poly-ADP-ribosyltransferase PARP2

PARP2 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
PARP2 Q9UGN5 FKBP3 Homo sapiens Q00688 21812934
Intra
PARP2 Q9UGN5 FKBP3 Homo sapiens Q00688 21812934
Intra
PARP2 Q9UGN5 APLF Homo sapiens Q8IW19 21812934
Intra
PARP2 Q9UGN5 HMGN2 Homo sapiens P05204 21812934
Intra
PARP2 Q9UGN5 STAC Homo sapiens Q99469 21812934
Intra
PARP2 Q9UGN5 STAC Homo sapiens Q99469 21812934
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Fanconi Anemia, Complementation Group A

Fanconi Anemia

Fanconi Pancytopenia

Fanconi Anemia Complementation Group A

FANCA

Fa

Fanconi Panmyelopathy

Fanconi'S Anemia

Fanconi Anaemia

Fanconi'S Anaemia

Fanconi Hypoplastic Anemia

Estren-Dameshek Variant Of Fanconi Anemia

Estren-Dameshek Variant Of Fanconi Pancytopenia

Fanconi Anemia Estren-Dameshek Variant

Fanconis Anemia

Fallopian Tube Carcinoma

Fallopian Tube Cancer

Cancer Of The Fallopian Tube

Carcinoma Of Fallopian Tube

Neoplasm Of Fallopian Tube

Fallopian Tube Neoplasms

Fallopian Tube Ca

Fallopian Tube Neoplasm

Malignant Neoplasm Of Uterine Tube

Malignant Tumor Of Fallopian Tube

Malignant Tumour Of Fallopian Tube

Tumor Of The Fallopian Tube

Tumor, Fallopian Tube, Malignant

Malignant Tumor Of Fallopian Tubes

Cancer Of Fallopian Tubes

Malignant Tubal Tumor

Tubal Cancer

Malignant Neoplasm Of Fallopian Tube

Primary Malignant Neoplasm Of Fallopian Tube

Cancer Of The Oviduct

Hereditary Breast Ovarian Cancer Syndrome

Hereditary Breast And Ovarian Cancer Syndrome

Brca1- And Brca2-Associated Hereditary Breast And Ovarian Cancer

Breast And/Or Ovarian Cancer

Breast And Ovarian Cancer Syndrome

Hboc Syndrome

Hereditary Breast And Ovarian Cancer

Brca1- Brca2-Associated Hboc

Osebold-Remondini Syndrome

Brachydactyly Type A6

Brachymesophalangy With Mesomelic Short Limbs And Carpal And Tarsal Osseous Abnormalities

Bda6

Brachydactyly, Type A6

Neurodegeneration, Childhood-Onset, Stress-Induced, With Variable Ataxia And Seizures

CONDSIAS

Stress-Induced Childhood-Onset Neurodegeneration With Variable Ataxia And Seizures

Fallopian Tube Disease

Fallopian Tube Diseases

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Bos taurus PARP2 VGNC VGNC:53577
Felis catus PARP2 VGNC VGNC:80893
Rattus norvegicus PARP2 RGD RGD:1310568
Macaca mulatta PARP2 VGNC VGNC:84417
Canis familiaris PARP2 VGNC VGNC:54219
Mus musculus PARP2 MGD MGI:1341112
Others PARP2 NCBI