4WX6
Crystal structure of human adenovirus 8 protease with an irreversible vinyl sulfone inhibitor
Summary for 4WX6
Entry DOI | 10.2210/pdb4wx6/pdb |
Descriptor | Protease, PVI, N-[(2S)-2-(3,5-dichlorophenyl)-2-(ethylamino)acetyl]-3-methyl-L-valyl-N-[3-(methylsulfonyl)propyl]glycinamide, ... (4 entities in total) |
Functional Keywords | cysteine protease, deubiquitinase, inhibitor, hydrolase |
Biological source | Human adenovirus D serotype 8 (HAdV-8) More |
Total number of polymer chains | 4 |
Total formula weight | 49803.01 |
Authors | Grosche, P.,Sirockin, F.,Mac Sweeney, A.,Ramage, P.,Erbel, P.,Melkko, S.,Bernardi, A.,Hughes, N.,Ellis, D.,Combrink, K.,Jarousse, N.,Altmann, E. (deposition date: 2014-11-13, release date: 2015-01-14, Last modification date: 2015-01-28) |
Primary citation | Grosche, P.,Sirockin, F.,Mac Sweeney, A.,Ramage, P.,Erbel, P.,Melkko, S.,Bernardi, A.,Hughes, N.,Ellis, D.,Combrink, K.D.,Jarousse, N.,Altmann, E. Structure-based design and optimization of potent inhibitors of the adenoviral protease. Bioorg.Med.Chem.Lett., 25:438-443, 2015 Cited by PubMed: 25571794DOI: 10.1016/j.bmcl.2014.12.057 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.15 Å) |
Structure validation
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