6XVW: Catalytic domain of human PARP-1

Catalytic domain of human PARP-1 in complex with the inhibitor MC2050. Determined by X-ray diffraction at 2.0 Å resolution. Released 3 Jun 2020.

Method
X-ray diffraction
Resolution
2.0 Å
Organism
Homo sapiens
Chains
2
Atoms
5,908
Mol. weight
81.03 kDa
Ligands
NI, O3H
Released
3 Jun 2020

Explore 6XVW in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

6XVW contains 46 α-helices and 38 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: 22 helices, 19 β-strands

ElementResiduesLengthSheet
α-helix667-67610
α-helix679-68810
β-strand69111
α-helix703-72220
α-helix728-73912
β-strand74211
α-helix757-77822
α-helix789-7968
β-strand799-80352
α-helix804-8052
α-helix809-82012
α-helix823-8253
β-strand829-841132
α-helix844-8485
α-helix849-8535
β-strand857-86482
α-helix866-8683
α-helix869-8757
α-helix879-8813
α-helix886-8883
β-strand895-89733
β-strand89812
α-helix901-9044
α-helix905-9084
β-strand91114
β-strand91414
β-strand916-925102
β-strand929-93243
α-helix941-9422
β-strand947-95043
α-helix9511
β-strand952-95655
α-helix958-9603
β-strand962-96432
β-strand967-96932
α-helix972-9732
β-strand974-97635
β-strand984-98635
β-strand988-99143
α-helix994-9963
β-strand997-1009132
Chain B: 24 helices, 19 β-strands
ElementResiduesLengthSheet
α-helix667-67610
α-helix679-68810
β-strand69116
α-helix698-7003
α-helix703-71816
α-helix719-7235
α-helix728-73912
β-strand74216
α-helix757-77923
α-helix789-7968
β-strand799-80357
α-helix804-8052
α-helix809-82012
α-helix823-8253
β-strand829-841137
α-helix844-8485
α-helix849-8535
β-strand857-86487
α-helix866-8683
α-helix869-8757
α-helix879-8813
α-helix886-8883
β-strand895-89738
β-strand89817
α-helix901-9055
α-helix906-9083
β-strand91119
β-strand91419
β-strand916-925107
β-strand929-93248
α-helix941-9422
β-strand947-95048
α-helix9511
β-strand952-956510
α-helix958-9603
β-strand962-96437
β-strand967-96937
α-helix972-9732
β-strand974-976310
β-strand984-986310
β-strand988-99148
α-helix994-9963
β-strand997-1009137

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Poly [ADP-ribose] polymerase 1A, Bprotein354Homo sapiensP09874 (AlphaFold model)
Sequence of entity 1 (A, B), FASTA
>6XVW_1 Poly [ADP-ribose] polymerase 1 (chains A, B)
HMSKLPKPVQDLIKMIFDVESMKKAMVEYEIDLQKMPLGKLSKRQIQAAYSILSEVQQAV
SQGSSDSQILDLSNRFYTLIPHDFGMKKPPLLNNADSVQAKVEMLDNLLDIEVAYSLLRG
GSDDSSKDPIDVNYEKLKTDIKVVDRDSEEAEIIRKYVKNTHATTHNAYDLEVIDIFKIE
REGECQRYKPFKQLHNRRLLWHGSRTTNFAGILSQGLRIAPPEAPVTGYMFGKGIYFADM
VSKSANYCHTSQGDPIGLILLGEVALGNMYELKHASHISKLPKGKHSVKGLGKTTPDPSA
NISLDGVDVPLGTGISSGVNDTSLLYNEYIVYDIAQVNLKYLLKLKFNFKTSLW

Ligands and cofactors

IDNameFormulaCopies
NINickel (II) ionNi6
O3H2-[2-(4-pyridin-2-ylpiperazin-1-yl)ethylsulfanyl]-3~{H}-quinazolin-4-oneC19 H21 N5 O S2

Water and common crystallization additives (EDO) are not listed.

Primary citation

From PARP1 to TNKS2 Inhibition: A Structure-Based Approach. Tomassi, S., Pfahler, J., Mautone, N. et al. ACS Med Chem Lett (2020) 11:862-868. DOI 10.1021/acsmedchemlett.9b00654 · PubMed

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

Browse structure collections

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