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Search Count: 31

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9YMN image
Crystal Structure Of Human Kras G12D In Complex With Gdp And Compound 7

9YMO image
Crystal Structure Of Human Kras G12D In Complex With Gdp And Am-2383

9YMP image
Crystal Structure Of Human Kras G12D In Complex With Gmppcp And Am-2383

9YMQ image
Crystal Structure Of Human Kras G12V In Complex With Gdp And Am-2383

9YMR image
Crystal Structure Of Human Kras G12V In Complex With Gmppcp And Am-2383

9E9H image
Crystal Structure Of Human Kras G12C Covalently Bound To Del Triazine Compound 5

9E9I image
Crystal Structure Of Human Kras G12C Covalently Bound To Nopinone-Derived Naphthol Compound 21

6PGO image
Crystal Structure Of Human Kras G12C Covalently Bound To A Phthalazine Inhibitor

6PGP image
Crystal Structure Of Human Kras G12C Covalently Bound To A Quinazolinone Inhibitor

6OIM image
Crystal Structure Of Human Kras G12C Covalently Bound To Amg 510

6MT0 image
Crystal Structure Of Human Pim-1 Kinase In Complex With A Quinazolinone-Pyrrolodihydropyrrolone Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.20 Å Release Date: 2019-01-16
Classification: TRANSFERASE
Ligands: JYG, GOL

5IPJ image
Crystal Structure Of Human Pim-1 Kinase In Complex With A Quinazolinone-Pyrrolopyrrolone Inhibitor.

5EOL image
Crystal Structure Of Human Pim-1 Kinase In Complex With A Macrocyclic Quinoxaline-Pyrrolodihydropiperidinone Inhibitor

5EYC image
Crystal Structure Of C-Met In Complex With Naphthyridinone Inhibitor 5

5EYD image
Crystal Structure Of C-Met In Complex With Amg 337

4XMO image
Crystal Structure Of C-Met In Complex With (R)-5-(8-Fluoro-3-(1-Fluoro-1-(3-Methoxyquinolin-6-Yl)Ethyl)-[1,2,4]Triazolo[4,3-A]Pyridin-6-Yl)-3-Methylisoxazole

4XYF image
Crystal Structure Of C-Met In Complex With (S)-5-(8-Fluoro-3-(1-(3-(2-Methoxyethoxy)Quinolin-6-Yl)Ethyl)-[1,2,4]Triazolo[4,3-A]Pyridin-6-Yl)-3-Methylisoxazole

4L02 image
Crystal Structure Of Sphk1 With Inhibitor

4DEG image
Crystal Structure Of C-Met In Complex With Triazolopyridazine Inhibitor 2

4DEH image
Crystal Structure Of C-Met In Complex With Triazolopyridinone Inhibitor 3
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