4ZZX: PARP2 catalytic domain

Structure of PARP2 catalytic domain bound to an isoindolinone inhibitor. Determined by X-ray diffraction at 1.65 Å resolution. Released 12 Aug 2015.

Method
X-ray diffraction
Resolution
1.65 Å
Organism
HOMO SAPIENS
Chains
2
Atoms
5,927
Mol. weight
82.7 kDa
Ligands
FSU
Released
12 Aug 2015

Explore 4ZZX in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

4ZZX contains 42 α-helices and 34 β-strands across 2 chains. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.

Chain A: 20 helices, 17 β-strands

ElementResiduesLengthSheet
α-helix236-24510
α-helix248-25710
β-strand26011
α-helix267-2693
α-helix272-29019
α-helix296-30813
β-strand31111
α-helix317-3204
α-helix324-34623
α-helix348-3503
α-helix357-3659
β-strand367-37152
α-helix377-38812
β-strand397-409132
α-helix412-4154
β-strand423-42972
α-helix432-4343
α-helix435-4417
α-helix445-4473
α-helix452-4543
β-strand461-46333
β-strand46412
α-helix467-4715
α-helix472-4743
β-strand482-491102
β-strand495-49843
α-helix505-5084
β-strand514-51743
β-strand519-52354
α-helix525-5273
β-strand529-53132
β-strand534-53632
β-strand541-54334
β-strand554-55634
β-strand558-56143
α-helix564-5663
β-strand567-579132
Chain B: 22 helices, 17 β-strands
ElementResiduesLengthSheet
α-helix236-24510
α-helix248-25710
β-strand26015
α-helix267-2693
α-helix272-29019
α-helix296-30813
β-strand31115
α-helix317-3204
α-helix324-34623
α-helix348-3503
α-helix357-3659
β-strand367-37156
α-helix372-3732
α-helix377-38812
β-strand397-409136
α-helix412-4154
β-strand423-42976
α-helix432-4343
α-helix435-4417
α-helix445-4473
α-helix452-4543
β-strand461-46337
β-strand46416
α-helix467-4715
α-helix472-4743
β-strand482-491106
β-strand495-49847
α-helix505-5084
β-strand514-51747
α-helix5181
β-strand519-52358
α-helix525-5273
β-strand529-53136
β-strand534-53636
β-strand541-54338
β-strand554-55638
β-strand558-56147
α-helix564-5663
β-strand567-579136

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Poly [ADP-ribose] polymerase 2A, Bprotein363HOMO SAPIENSQ9UGN5 (AlphaFold model)
Sequence of entity 1 (A, B), FASTA
>4ZZX_1 POLY [ADP-RIBOSE] POLYMERASE 2 (chains A, B)
GPSLKSPLKPESQLDLRVQELIKLICNVQAMEEMMMEMKYNTKKAPLGKLTVAQIKAGYQ
SLKKIEDCIRAGQHGRALMEACNEFYTRIPHDFGLRTPPLIRTQKELSEKIQLLEALGDI
EIAIKLVKTELQSPEHPLDQHYRNLHCALRPLDHESYEFKVISQYLQSTHAPTHSDYTMT
LLDLFEVEKDGEKEAFREDLHNRMLLWHGSRMSNWVGILSHGLRIAPPEAPITGYMFGKG
IYFADMSSKSANYCFASRLKNTGLLLLSEVALGQCNELLEANPKAEGLLQGKHSTKGLGK
MAPSSAHFVTLNGSTVPLGPASDTGILNPDGYTLNYNEYIVYNPNQVRMRYLLKVQFNFL
QLW

Ligands and cofactors

IDNameFormulaCopies
FSU2-(3-methoxypropyl)-3-oxo-2,3-dihydro-1H-isoindole-4-carboxamideC13 H16 N2 O32

Primary citation

Discovery of 2-[1-(4,4-Difluorocyclohexyl)Piperidin-4-Yl]-6-Fluoro-3-Oxo-2,3-Dihydro-1H-Isoindole-4-Carboxamide (Nms-P118): A Potent, Orally Available and Highly Selective Parp- 1 Inhibitor for Cancer Therapy. Papeo, G.M.E., Posteri, H., Borghi, D. et al. J Med Chem (2015) 58:6875. DOI 10.1021/ACS.JMEDCHEM.5B00680 · PubMed

Other PDB entries of the same protein (UniProt Q9UGN5 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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