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Search Count: 21

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9PCA image
Human Prmt5:Mep50 Complex In Complex With Ligand 18

8T09 image
Co-Crystal Structure Of Krit1 With A 1-Hydroxy 2-Naphthaldehyde Derivative (6-Ethynyl-2-Hydroxy-1-Naphthaldehyde)

8SU8 image
Co-Crystal Structure Of Krit1 With A 1-Hydroxy 2-Naphthaldehyde Derivative (6-(Furan-2-Yl)-2-Hydroxy-1-Naphthaldehyde).

8T7V image
Co-Crystal Structure Of Krit1 With A 1-Hydroxy 2-Naphthaldehyde Derivative (6-(Furan-2-Yl)-2-Hydroxy-1-Naphthaldehyde)

7N5O image
Fragment-Based Discovery Of A Novel Bruton'S Tyrosine Kinase Inhibitor

7N5R image
Fragment-Based Discovery Of A Novel Bruton'S Tyrosine Kinase Inhibitor

7N5X image
Fragment-Based Discovery Of A Novel Bruton'S Tyrosine Kinase Inhibitor

7N5Y image
Fragment-Based Drug Design Of A Novel, Covalent Bruton'S Tyrosine Kinase Inhibitor

6UBW image
Met Tyrosine Kinase Inhibition Enhances The Antitumor Efficacy Of An Hgf Antibody

5UAB image
Met Tyrosine Kinase Inhibition Enhances The Antitumor Efficacy Of An Hgf Antibody

5UAD image
Met Tyrosine Kinase Inhibition Enhances The Antitumor Efficacy Of An Hgf Antibody

5USQ image
Alk-5 Kinase Inhibitor Complex

5INH image
Crystal Structure Of Autotaxin/Enpp2 With A Covalent Fragment

4P58 image
Crystal Structure Of Mouse Comt Bound To An Inhibitor

4L6S image
Parp Complexed With Benzo[1,4]Oxazin-3-One Inhibitor

3VHK image
Crystal Structure Of The Vegfr2 Kinase Domain In Complex With A Back Pocket Binder
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.49 Å Release Date: 2012-09-05
Classification: TRANSFERASE
Ligands: BPK, EDO

3VID image
Crystal Structure Of Human Vegfr2 Kinase Domain With Compound A.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.30 Å Release Date: 2012-08-15
Classification: TRANSFERASE
Ligands: 4TT

2ILP image
Clostridium Botulinum Serotype A Light Chain Inhibited By 4-Chlorocinnamic Hydroxamate

2IMA image
Clostridium Botulinum Neurotoxin Serotype A Light Chain Inhibited By 2,4-Dichlorocinnamic Hydroxamate

2IMB image
Clostridium Botulinum Neurotoxin Serotype A Light Chain Inhibited By L-Arginine Hydroxamate
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