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Search Count: 14

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9Z6T image
Human Hcn1 In Complex With Camp In Nanodisc

5JON image
Crystal Structure Of The Unliganded Form Of Hcn2 Cnbd

4RFM image
Itk Kinase Domain In Complex With Compound 1 N-{1-[(1,1-Dioxo-1-Thian-2-Yl)(Phenyl)Methyl]-1H- Pyrazol-4-Yl}-5,5-Difluoro-5A-Methyl-1H,4H,4Ah,5H,5Ah,6H-Cyclopropa[F]Indazole-3-Carboxamide

4HLE image
Compound 21 (1-Alkyl-Substituted 1,2,4-Triazoles)

3T8M image
Rational Design Of Pi3K-Alpha Inhibitors That Exhibit Selectivity Over The Pi3K-Beta Isoform

3TL5 image
Discovery Of Gdc-0980: A Potent, Selective, And Orally Available Class I Phosphatidylinositol 3-Kinase (Pi3K)/Mammalian Target Of Rapamycin (Mtor) Kinase Inhibitor For The Treatment Of Cancer

3R7Q image
Structure-Based Design Of Thienobenzoxepin Inhibitors Of Pi3- Kinase

3R7R image
Structure-Based Design Of Thienobenzoxepin Inhibitors Of Pi3-Kinase

3L13 image
Crystal Structures Of Pan-Pi3-Kinase And Dual Pan-Pi3-Kinase/Mtor Inhibitors
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:3.00 Å Release Date: 2010-02-16
Classification: TRANSFERASE
Ligands: JZW

3L16 image
Discovery Of (Thienopyrimidin-2-Yl)Aminopyrimidines As Potent, Selective, And Orally Available Pan-Pi3-Kinase And Dual Pan-Pi3-Kinase/Mtor Inhibitors For The Treatment Of Cancer
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.90 Å Release Date: 2010-02-16
Classification: TRANSFERASE
Ligands: JZX

3L17 image
Discovery Of (Thienopyrimidin-2-Yl)Aminopyrimidines As Potent, Selective, And Orally Available Pan-Pi3-Kinase And Dual Pan-Pi3-Kinase/Mtor Inhibitors For The Treatment Of Cancer
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:3.00 Å Release Date: 2010-02-16
Classification: TRANSFERASE
Ligands: JZY

2HJI image
Structural Model For The Fe-Containing Isoform Of Acireductone Dioxygenase

1YGC image
Short Factor Viia With A Small Molecule Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.00 Å Release Date: 2005-01-18
Classification: HYDROLASE
Ligands: CA, SO4, 905
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