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Search Count: 40

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6E22 image
Displacement Of Wdr5 From Chromatin By A Pharmacological Win Site Inhibitor With Picomolar Affinity

6E1Z image
Displacement Of Wdr5 From Chromatin By A Pharmacological Win Site Inhibitor With Picomolar Affinity

6E23 image
Displacement Of Wdr5 From Chromatin By A Pharmacological Win Site Inhibitor With Picomolar Affinity

6E1Y image
Discovery Of Potent 2-Aryl-6,7-Dihydro-5Hpyrrolo[ 1,2-A]Imidazoles As Wdr5 Win-Site Inhibitors Using Fragment-Based Methods And Structure-Based Design

8F93 image
Wdr5 Covalently Modified At Y228 By (R)-2-Sf

6UFX image
Wd Repeat-Containing Protein 5 Complexed With N-[(3,5-Dimethoxyphenyl)Methyl]-4'-Fluoro-5-{[(2E)-2-Imino-3-Methyl-2,3-Dihydro-1H-Imidazol-1-Yl]Methyl}-2'-Methyl[1,1'-Biphenyl]-3-Carboxamide (Compound 13)

7LP0 image
Crystal Structure Of Bptf Bromodomain In Complex With Inhibitor Pdy-3-077

7LRO image
Crystal Structure Of Bptf Bromodomain In Complex With Inhibitor Hz-01-105

7LPK image
Crystal Structure Of Bptf Bromodomain In Complex With Inhibitor Hz-03-112

7LRK image
Crystal Structure Of Bptf Bromodomain In Complex With Inhibitor Pdy-3-093

6WVX image
Crystal Structure Of The First Bromodomain Of Human Brd4 With Benzodiazepine Inhibitor

6WGX image
Cocrystal Of Brd4(D1) With A Selective Inhibitor

8XV4 image
Crystal Structure Of Ttd-Phd Domain Of Uhrf1 In Complex With Mstella Peptide (Residues 85-119)

6UVM image
Cocrystal Of Brd4(D1) With A Methyl Carbamate Thiazepane Inhibitor

6UWX image
Cocrystal Of Brd4(D1) With A Ethyl Carbamate Thiazepane Inhibitor

6UVJ image
Cocrystal Of Brd4(D1) With A Methyl Carbamate Thiazepane Inhibitor

7LAZ image
Crystal Structure Of The First Bromodomain (Bd1) Of Human Brd3 Bound To Erk5-In-1

7LBT image
Crystal Structure Of The Second Bromodomain (Bd2) Of Human Brd3 Bound To Erk5-In-1

7LAY image
Crystal Structure Of The First Bromodomain (Bd1) Of Human Brd3 Bound To Sg3-179

7LAK image
Crystal Structure Of The First Bromodomain (Bd1) Of Human Brd2 Bound To Volasertib
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