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4JVI image
Crystal Structure Of Pqsr Co-Inducer Binding Domain Of Pseudomonas Aeruginosa With Inhibitor 3Nh2-7Cl-C9Qzn

5U28 image
Brd4 First Bromodomain (Bd1) In Complex With Dual Pi3 Kinase Inhibitor Sf2523

5U2F image
Brd4 First Bromodomain (Bd1) In Complex With Dual Pi3 Kinase (Pi3K) Inhibitor Sf2558Ha

5U2E image
Brd4 First Bromodomain (Bd1) In Complex With Dual Pi3 Kinase (Pi3K) Inhibitor Sf2535

5U2C image
Brd4 Second Bromodomain (Bd2) In Complex With Dual Pi3 Kinase (Pi3K) Inhibitor Sf2558Ha

4FLP image
Crystal Structure Of The First Bromodomain Of Human Brdt In Complex With The Inhibitor Jq1

5W0F image
Crebbp Bromodomain In Complex With Cpd3 ((S)-1-(3-(6-(1-Methyl-1H-Pyrazol-4-Yl)-3,4-Dihydroquinolin-1(2H)-Yl)-1-(Tetrahydrofuran-3-Yl)-1,4,6,7-Tetrahydro-5H-Pyrazolo[4,3-C]Pyridin-5-Yl)Ethan-1-One)

5W0Q image
Crebbp Bromodomain In Complex With Cpd17 (N,2,7-Trimethyl-2,3-Dihydro-4H-Benzo[B][1,4]Oxazine-4-Carboxamide)

5TTW image
Crystal Structure Of Eed In Complex With Unc4859

5W0E image
Crebbp Bromodomain In Complex With Cpd19 (3-(7-(Difluoromethyl)-6-(1-Methyl-1H-Pyrazol-4-Yl)-3,4-Dihydroquinolin-1(2H)-Yl)-N-Methyl-1-(Tetrahydro-2H-Pyran-4-Yl)-1,4,6,7-Tetrahydro-5H-Pyrazolo[4,3-C]Pyridine-5-Carboxamide)

4LR6 image
Structure Of Brd4 Bromodomain 1 With A 3-Methyl-4-Phenylisoxazol-5-Amine Fragment

4LRG image
Structure Of Brd4 Bromodomain 1 With A Dimethyl Thiophene Isoxazole Azepine Carboxamide

5VZS image
Brd4-Bd1 In Complex With Cpd19 (3-(7-(Difluoromethyl)-6-(1-Methyl-1H-Pyrazol-4-Yl)-3,4-Dihydroquinolin-1(2H)-Yl)-N-Methyl-1-(Tetrahydro-2H-Pyran-4-Yl)-1,4,6,7-Tetrahydro-5H-Pyrazolo[4,3-C]Pyridine-5-Carboxamide)

5W0L image
Crebbp Bromodomain In Complex With Cpd10 (1-(3-(7-(Difluoromethyl)-6-(1-Methyl-1H-Pyrazol-4-Yl)-3,4-Dihydroquinolin-1(2H)-Yl)-1-(Tetrahydro-2H-Pyran-4-Yl)-1,4,6,7-Tetrahydro-5H-Pyrazolo[4,3-C]Pyridin-5-Yl)Ethan-1-One)

9NN5 image
Bet Brd4-Bd1 In Complex With Peptide 9.2
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