1GS0

Crystal structure of the catalytic fragment of murine poly(ADP-ribose) polymerase-2

1GS0 の概要

• エントリーDOI: 10.2210/pdb1gs0/pdb
• 分子名称: POLY (ADP-RIBOSE) POLYMERASE-2 (2 entities in total)
• 機能のキーワード: transferase, catalytic fragment, polymerase transferase, nuclear protein, dna-binding
• 由来する生物種: MUS MUSCULUS (MOUSE)
• 細胞内の位置: Nucleus: O88554
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 79395.41

構造登録者

Oliver, A.W.,Roe, S.M.,Pearl, L.H. (登録日: 2001-12-19, 公開日: 2002-12-19, 最終更新日: 2023-12-13)

主引用文献

Oliver, A.W.,Ame, J.C.,Roe, S.M.,Good, V.,De Murcia, G.,Pearl, L.H.
Crystal Structure of the Catalytic Fragment of Murine Poly(Adp-Ribose) Polymerase-2
Nucleic Acids Res., 32:456-, 2004

PubMed Abstract: Poly(ADP-ribose) polymerase-1 (PARP-1) has become an important pharmacological target in the treatment of cancer due to its cellular role as a 'DNA-strand break sensor', which leads in part to resistance to some existing chemo- and radiological treatments. Inhibitors have now been developed which prevent PARP-1 from synthesizing poly(ADP-ribose) in response to DNA-breaks and potentiate the cytotoxicity of DNA damaging agents. However, with the recent discoveries of PARP-2, which has a similar DNA-damage dependent catalytic activity, and additional members containing the 'PARP catalytic' signature, the isoform selectivity and resultant pharmacological effects of existing inhibitors are brought into question. We present here the crystal structure of the catalytic fragment of murine PARP-2, at 2.8 A resolution, and compare this to the catalytic fragment of PARP-1, with an emphasis on providing a possible framework for rational drug design in order to develop future isoform-specific inhibitors.

PubMed: 14739238
DOI: 10.1093/NAR/GKH215

実験手法

X-RAY DIFFRACTION (2.8 Å)