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Search Count: 20

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9PW6 image
Myeloid Cell Leukemia-1 (Mcl-1) Complexed With Compound 8
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.07 Å Release Date: 2025-09-17
Classification: APOPTOSIS
Ligands: A1CL3

9PW7 image
Myeloid Cell Leukemia-1 (Mcl-1) Complexed With Compound 13
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:1.95 Å Release Date: 2025-09-17
Classification: APOPTOSIS
Ligands: A1CL6

9BCG image
Myeloid Cell Leukemia-1 (Mcl-1) Complexed With Compound
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:1.90 Å Release Date: 2024-08-07
Classification: APOPTOSIS
Ligands: A1ALT

6D5W image
Ras:Sos:Ras In Complex With A Small Molecule Activator

6D55 image
Ras:Sos:Ras In Complex With A Small Molecule Activator

6D56 image
Ras:Sos:Ras In Complex With A Small Molecule Activator

6D59 image
Ras:Sos:Ras In Complex With A Small Molecule Activator

6D5E image
Ras:Sos:Ras In Complex With A Small Molecule Activator

6D5G image
Ras:Sos:Ras In Complex With A Small Molecule Activator

6D5H image
Ras:Sos:Ras In Complex With A Small Molecule Activator

6D5J image
Ras:Sos:Ras In Complex With A Small Molecule Activator

6D5L image
Ras:Sos:Ras In Complex With A Small Molecule Activator

6D5M image
Ras:Sos:Ras In Complex With A Small Molecule Activator

6D5V image
Ras:Sos:Ras In Complex With A Small Molecule Activator

6D9X 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

6DAI 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

6DAK 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

6DAR 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

6DAS 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

3EOC image
Cdk2/Cyclina Complexed With A Imidazo Triazin-2-Amine
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