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9H9O image
Crystal Structure Of Nedd4 Hect Domain In Complex With Norclomipramine
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.12 Å Release Date: 2025-06-04
Classification: LIGASE
Ligands: EDO, A1ITH

9H9T image
Crystal Structure Of Nedd4 Hect Domain In Complex With Covalent Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.17 Å Release Date: 2025-06-04
Classification: LIGASE
Ligands: A1ITT

6TE1 image
Structure Of The Kdm1A/Corest Complex With The Inhibitor 2-[3-{4-Chloro-3-[(4-Chlorophenyl)Ethynyl]Phenyl}-1-(3-Morpholin-4-Ylpropyl)-1,4,6,7-Tetrahydro-5H-Pyrazolo[4,3-C]Pyridin-5-Yl]-2-Oxoethanol

5LGN image
Thieno[3,2-B]Pyrrole-5-Carboxamides As Novel Reversible Inhibitors Of Histone Lysine Demethylase Kdm1A/Lsd1: Compound 19

5LGT image
Thieno[3,2-B]Pyrrole-5-Carboxamides As Novel Reversible Inhibitors Of Histone Lysine Demethylase Kdm1A/Lsd1: Compound 15

5LGU image
Thieno[3,2-B]Pyrrole-5-Carboxamides As Novel Reversible Inhibitors Of Histone Lysine Demethylase Kdm1A/Lsd1: Compound 34

5LHG image
Structure Of The Kdm1A/Corest Complex With The Inhibitor 4-Methyl-N-[4-[[4-(1-Methylpiperidin-4-Yl)Oxyphenoxy]Methyl]Phenyl]Thieno[3,2-B]Pyrrole-5-Carboxamide

5LHH image
Structure Of The Kdm1A/Corest Complex With The Inhibitor 4-Ethyl-N-[3-(Methoxymethyl)-2-[[4-[[(3R)-Pyrrolidin-3-Yl]Methoxy]Phenoxy]Methyl]Phenyl]Thieno[3,2-B]Pyrrole-5-Carboxamide

5LHI image
Structure Of The Kdm1A/Corest Complex With The Inhibitor N-[3-(Ethoxymethyl)-2-[[4-[[(3R)-Pyrrolidin-3-Yl]Methoxy]Phenoxy]Methyl]Phenyl]-4-Methylthieno[3,2-B]Pyrrole-5-Carboxamide

4UXN image
Lsd1(Kdm1A)-Corest In Complex With Z-Pro Derivative Of Mc2580

4UV8 image
Lsd1(Kdm1A)-Corest In Complex With 1-Benzyl-Tranylcypromine

4UV9 image
Lsd1(Kdm1A)-Corest In Complex With 1-Ethyl-Tranylcypromine

4UVA image
Lsd1(Kdm1A)-Corest In Complex With 1-Methyl-Tranylcypromine (1R,2S)

4UVB image
Lsd1(Kdm1A)-Corest In Complex With 1-Methyl-Tranylcypromine (1S,2R)

4UVC image
Lsd1(Kdm1A)-Corest In Complex With 1-Phenyl-Tranylcypromine

2WPA image
Optimisation Of 6,6-Dimethyl Pyrrolo 3,4-C Pyrazoles: Identification Of Pha-793887, A Potent Cdk Inhibitor Suitable For Intravenous Dosing
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.51 Å Release Date: 2010-02-23
Classification: CELL CYCLE
Ligands: SO4, 889

2WXV image
Structure Of Cdk2-Cyclin A With A Pyrazolo(4,3-H) Quinazoline-3- Carboxamide Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.60 Å Release Date: 2010-02-23
Classification: TRANSFERASE
Ligands: WXV, SO4

2WIH image
Structure Of Cdk2-Cyclin A With Pha-848125
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.50 Å Release Date: 2009-07-28
Classification: TRANSFERASE
Ligands: P48, SO4

2WIP image
Structure Of Cdk2-Cyclin A Complexed With 8-Anilino-1-Methyl-4,5-Dihydro- 1H-Pyrazolo[4,3-H] Quinazoline-3-Carboxylic Acid
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.80 Å Release Date: 2009-07-28
Classification: TRANSFERASE
Ligands: P49, SO4

3FT8 image
Structure Of Hsp90 Bound With A Noval Fragment.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.00 Å Release Date: 2009-06-30
Classification: CHAPERONE
Ligands: MOJ
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