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7Q7T

Crystal structure of human BCL6 BTB domain in complex with compound 7

Summary for 7Q7T
Entry DOI10.2210/pdb7q7t/pdb
DescriptorB-cell lymphoma 6 protein, ALA-TRP-VAL-ILE-PRO-ALA, 2-chloranyl-4-[[(2S)-2,7-dimethyl-5,6-bis(oxidanylidene)-2,3-dihydro-1H-[1,4]oxazepino[6,5-c]quinolin-10-yl]amino]pyridine-3-carbonitrile, ... (7 entities in total)
Functional Keywordstranscription, inhibitor
Biological sourceHomo sapiens (Human)
More
Total number of polymer chains2
Total formula weight16026.45
Authors
Rodrigues, M.J.,Le Bihan, Y.-V.,van Montfort, R.L.M. (deposition date: 2021-11-09, release date: 2022-06-15, Last modification date: 2024-01-31)
Primary citationDavis, O.A.,Cheung, K.J.,Brennan, A.,Lloyd, M.G.,Rodrigues, M.J.,Pierrat, O.A.,Collie, G.W.,Le Bihan, Y.V.,Huckvale, R.,Harnden, A.C.,Varela, A.,Bright, M.D.,Eve, P.,Hayes, A.,Henley, A.T.,Carter, M.D.,McAndrew, P.C.,Talbot, R.,Burke, R.,van Montfort, R.L.M.,Raynaud, F.I.,Rossanese, O.W.,Meniconi, M.,Bellenie, B.R.,Hoelder, S.
Optimizing Shape Complementarity Enables the Discovery of Potent Tricyclic BCL6 Inhibitors.
J.Med.Chem., 65:8169-8190, 2022
Cited by
PubMed: 35657291
DOI: 10.1021/acs.jmedchem.1c02174
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.46 Å)
Structure validation

221051

數據於2024-06-12公開中

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