PDB ID: 4DJR
Hetero Atom Contents
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0KJ | [(2s)-5-oxopyrrolidin-2-yl]methyl [(2s,3r)-4-{(1,3-benzothiazol-6-ylsulfonyl)[(2s)-2-methylbutyl]amino}-3-hydroxy-1-phenylbutan-2-yl]carbamate | PoSSuM | |||
PO4 | Phosphate ion | PoSSuM |
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Download interaction data: 4DJR
Structure summary
Code : | 4DJR PDBj RCSB PDB PDBe | ||||||||||||
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Header : | HYDROLASE/HYDROLASE inhibitor | ||||||||||||
Title : | Crystal Structure of wild-type HIV-1 Protease in Complex with MKP97 | ||||||||||||
Release Data : | 2012-08-01 | ||||||||||||
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Authors : | Schiffer, C.A., Nalam, M.N.L. | ||||||||||||
Keywords : | HIV-1 protease, drug resistance, drug design, Protease inhibitors, AIDS, Aspartyl protease, HYDROLASE-HYDROLASE inhibitor complex | ||||||||||||
Exp. method : | X-RAY DIFFRACTION ( 1.5500 Å ) | ||||||||||||
Citation : |
Design, synthesis, and biological and structural evaluations of novel HIV-1 protease inhibitors to combat drug resistance.
Parai, M.K.,Huggins, D.J.,Cao, H.
et al.
PubMed: 22708897 |
Reaction
Chain : | A, B | ||||||||
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UniProt : | Q90K99 (Q90K99_9HIV1) | ||||||||
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