7AAA: Catalytic domain of human PARP1

Crystal structure of the catalytic domain of human PARP1 (apo). Determined by X-ray diffraction at 1.74 Å resolution. Released 13 Jan 2021.

Method
X-ray diffraction
Resolution
1.74 Å
Organism
Homo sapiens
Chains
2
Atoms
5,841
Mol. weight
79.13 kDa
Released
13 Jan 2021

Explore 7AAA in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

7AAA contains 46 α-helices and 40 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: 23 helices, 20 β-strands

ElementResiduesLengthSheet
α-helix667-67610
α-helix679-68810
β-strand69111
α-helix698-7003
α-helix703-72119
α-helix726-73914
β-strand74211
α-helix748-7514
α-helix755-77925
α-helix789-7968
β-strand799-80352
α-helix804-8052
α-helix809-82012
α-helix824-8263
β-strand829-841132
α-helix844-8485
α-helix849-8513
β-strand857-86482
α-helix866-8683
α-helix869-8757
α-helix879-8813
α-helix886-8883
β-strand895-89733
β-strand89812
α-helix901-9055
α-helix906-9083
β-strand91114
β-strand91414
β-strand916-925102
β-strand929-93243
β-strand93615
α-helix941-9422
β-strand947-95043
β-strand952-95656
α-helix958-9603
β-strand962-96432
β-strand967-96932
α-helix9731
β-strand974-97636
β-strand984-98636
β-strand988-99143
α-helix994-9963
β-strand997-1009132
Chain B: 23 helices, 20 β-strands
ElementResiduesLengthSheet
α-helix667-67610
α-helix679-68810
β-strand69117
α-helix698-7003
α-helix703-72220
α-helix726-73914
β-strand74217
α-helix748-7514
α-helix755-77925
α-helix789-7968
β-strand799-80358
α-helix804-8052
α-helix809-82012
α-helix824-8263
β-strand829-841138
α-helix844-8485
α-helix849-8513
β-strand857-86488
α-helix866-8683
α-helix869-8757
α-helix879-8813
α-helix886-8883
β-strand895-89739
β-strand89818
α-helix901-9055
α-helix906-9083
β-strand911110
β-strand914110
β-strand916-925108
β-strand929-93249
β-strand93615
α-helix941-9422
β-strand947-95049
β-strand954-956311
α-helix958-9603
β-strand962-96438
β-strand967-96938
α-helix972-9732
β-strand974-976311
β-strand986111
β-strand988-99149
α-helix994-9963
β-strand997-1009138

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Poly [ADP-ribose] polymerase 1A, Bprotein352Homo sapiensP09874 (AlphaFold model)
Sequence of entity 1 (A, B), FASTA
>7AAA_1 Poly [ADP-ribose] polymerase 1 (chains A, B)
GSKSKLPKPVQDLIKMIFDVESMKKAMVEYEIDLQKMPLGKLSKRQIQAAYSILSEVQQA
VSQGSSDSQILDLSNRFYTLIPHDFGMKKPPLLNNADSVQAKAEMLDNLLDIEVAYSLLR
GGSDDSSKDPIDVNYEKLKTDIKVVDRDSEEAEIIRKYVKNTHATTHNAYDLEVIDIFKI
EREGECQRYKPFKQLHNRRLLWHGSRTTNFAGILSQGLRIAPPEAPVTGYMFGKGIYFAD
MVSKSANYCHTSQGDPIGLILLGEVALGNMYELKHASHISKLPKGKHSVKGLGKTTPDPS
ANISLDGVDVPLGTGISSGVNDTSLLYNEYIVYDIAQVNLKYLLKLKFNFKT

Primary citation

Dynamics of the HD regulatory subdomain of PARP-1; substrate access and allostery in PARP activation and inhibition. Ogden, T.E.H., Yang, J.C., Schimpl, M. et al. Nucleic Acids Res (2021) 49:2266-2288. DOI 10.1093/nar/gkab020 · PubMed

Other PDB entries of the same protein (UniProt P09874 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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