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Search Count: 40

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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

6E22 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)

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

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

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

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

7LB4 image
Crystal Structure Of The Second Bromodomain (Bd2) Of Human Brd3 Bound To Bromosporine

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

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