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6DJE

Crystal structure of Tdp1 catalytic domain in complex with Sigma Aldrich compound CDS010292

Summary for 6DJE
Entry DOI10.2210/pdb6dje/pdb
DescriptorTyrosyl-DNA phosphodiesterase 1, 1,2-ETHANEDIOL, 4-hydroxy-8-(propan-2-yl)quinoline-3-carboxylic acid, ... (4 entities in total)
Functional Keywordsfragment-based drug design, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor
Biological sourceHomo sapiens (Human)
Total number of polymer chains2
Total formula weight104963.44
Authors
Lountos, G.T.,Zhao, X.Z.,Kiselev, E.,Tropea, J.E.,Needle, D.,Burke Jr., T.R.,Pommier, Y.,Waugh, D.S. (deposition date: 2018-05-25, release date: 2019-05-29, Last modification date: 2023-10-11)
Primary citationLountos, G.T.,Zhao, X.Z.,Kiselev, E.,Tropea, J.E.,Needle, D.,Pommier, Y.,Burke, T.R.,Waugh, D.S.
Identification of a ligand binding hot spot and structural motifs replicating aspects of tyrosyl-DNA phosphodiesterase I (TDP1) phosphoryl recognition by crystallographic fragment cocktail screening.
Nucleic Acids Res., 47:10134-10150, 2019
Cited by
PubMed: 31199869
DOI: 10.1093/nar/gkz515
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.705 Å)
Structure validation

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