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6VKO

Crystal Structure of human PARP-1 CAT domain bound to inhibitor UKTT15

Summary for 6VKO
Entry DOI10.2210/pdb6vko/pdb
DescriptorPoly [ADP-ribose] polymerase 1, methyl 2-{4-[4-(7-carbamoyl-1H-benzimidazol-2-yl)benzene-1-carbonyl]piperazin-1-yl}pyrimidine-5-carboxylate, SULFATE ION, ... (4 entities in total)
Functional Keywordsparp-1, poly(adp-ribose) polymerase, parp inhibitor, parp1, artd1, transferase, transferase-inhibitor complex, transferase/inhibitor
Biological sourceHomo sapiens (Human)
Total number of polymer chains4
Total formula weight169384.58
Authors
Langelier, M.F.,Pascal, J.M. (deposition date: 2020-01-21, release date: 2020-06-17, Last modification date: 2023-10-11)
Primary citationZandarashvili, L.,Langelier, M.F.,Velagapudi, U.K.,Hancock, M.A.,Steffen, J.D.,Billur, R.,Hannan, Z.M.,Wicks, A.J.,Krastev, D.B.,Pettitt, S.J.,Lord, C.J.,Talele, T.T.,Pascal, J.M.,Black, B.E.
Structural basis for allosteric PARP-1 retention on DNA breaks.
Science, 368:-, 2020
Cited by
PubMed: 32241924
DOI: 10.1126/science.aax6367
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.8 Å)
Structure validation

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