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Search Count: 34

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6E0E image
Crystal Structure Of Glucokinase In Complex With Compound 6

6E0I image
Crystal Structure Of Glucokinase In Complex With Compound 72

4RCH image
Discovery Of 2-Pyridyl Ureas As Glucokinase Activators
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.30 Å Release Date: 2014-10-08
Classification: TRANSFERASE
Ligands: GLC, 3LZ

4PP7 image
Highly Potent And Selective 3-N-Methylquinazoline-4(3H)-One Based Inhibitors Of B-Rafv600E Kinase

4MBJ image
Human B-Raf Kinase Domain In Complex With An Imidazopyridine-Based Inhibitor

4MLE image
Human Glucokinase In Complex With Novel Amino Thiazole Activator

4MLH image
Human Glucokinase In Complex With A Novel Amino Thiazole Allosteric Activator

4EHE image
B-Raf Kinase Domain In Complex With An Aminothienopyrimidine-Based Inhibitor

4EHG image
B-Raf Kinase Domain In Complex With An Aminopyridimine-Based Inhibitor

4G9C image
Human B-Raf Kinase Domain Bound To A Type Ii Pyrazolopyridine Inhibitor

4G9R image
B-Raf V600E Kinase Domain Bound To A Type Ii Dihydroquinazoline Inhibitor

4E4X image
Crystal Structure Of B-Raf Kinase Domain In Complex With A Dihydropyrido[2,3-D]Pyrimidinone-Based Inhibitor

3TV4 image
Human B-Raf Kinase Domain In Complex With An Bromopyridine Benzamide Inhibitor

3TV6 image
Human B-Raf Kinase Domain In Complex With A Methoxypyrazolopyridinyl Benzamide Inhibitor

3SKC image
Human B-Raf Kinase In Complex With An Amide Linked Pyrazolopyridine Inhibitor

3PPJ image
Human B-Raf Kinase In Complex With A Furopyridine Inhibitor

3PPK image
Human B-Raf Kinase In Complex With A Non-Oxime Furopyridine Inhibitor

3PRF image
Crystal Structure Of Human B-Raf Kinase Domain In Complex With A Non-Oxime Furopyridine Inhibitor

3PRI image
Crystal Structure Of Human B-Raf Kinase In Complex With A Non-Oxime Furopyridine Inhibitor

3O96 image
Crystal Structure Of Human Akt1 With An Allosteric Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.70 Å Release Date: 2010-10-13
Classification: TRANSFERASE
Ligands: IQO
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