PDB ID: 3TH9
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9Y9 | Tert-butyl {(2s,3r)-4-[(4s)-7-fluoro-4-methyl-1,1-dioxido-4,5-dihydro-1,2-benzothiazepin-2(3h)-yl]-3-hydroxy-1-phenylbutan-2-yl}carbamate | PoSSuM |
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Download interaction data: 3TH9
Structure summary
Code : | 3TH9 PDBj RCSB PDB PDBe | ||||||||||||
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Header : | HYDROLASE/HYDROLASE INHIBITOR | ||||||||||||
Title : | Crystal Structure of HIV-1 Protease Mutant Q7K V32I L63I with a cyclic sulfonamide inhibitor | ||||||||||||
Release Data : | 2011-09-28 | ||||||||||||
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Authors : | Orth, P. | ||||||||||||
Keywords : | enzyme inhibition, aspartic protease, HIV/AIDS, conformational change, Amprenavir, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR complex | ||||||||||||
Exp. method : | X-RAY DIFFRACTION ( 1.3400 Å ) | ||||||||||||
Citation : |
Design, Synthesis, and X-ray Crystallographic Analysis of a Novel Class of HIV-1 Protease Inhibitors.
Ganguly, A.K.,Alluri, S.S.,Caroccia, D.
et al.
PubMed: 21916489 |
Reaction
Chain : | A, B | ||||||||||||||||||||||||
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UniProt : | P0C6F2 (POL_HV1LW) | ||||||||||||||||||||||||
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