PDB ID: 6D0E
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FQ1 | (3as,4s,7ar)-hexahydro-4h-furo[2,3-B]pyran-4-yl [(2s,3r)-1-(3,5-difluorophenyl)-3-hydroxy-4-{[(4-methoxyphenyl)sulfonyl](2-methylpropyl)amino}butan-2-yl]carbamate | PoSSuM |
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Download interaction data: 6D0E
Structure summary
Code : | 6D0E PDBj RCSB PDB PDBe | ||||||||
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Header : | HYDROLASE/INHIBITOR | ||||||||
Title : | X-ray crystal structure of wild type HIV-1 protease in complex with GRL-084-13 | ||||||||
Release Data : | 2019-05-01 | ||||||||
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Authors : | Yedidi, R.S., Hayashi, H., Ghosh, A.K., Mitsuya, H. | ||||||||
Keywords : | HIV-1 protease, protease inhibitor, darunavir, difluorophenyl, nonpeptidic, TMC-126, HYDROLASE, HYDROLASE-INHIBITOR complex | ||||||||
Exp. method : | X-RAY DIFFRACTION ( 1.950 Å ) | ||||||||
Citation : |
Novel Central Nervous System (CNS)-Targeting Protease Inhibitors for Drug-Resistant HIV Infection and HIV-Associated CNS Complications.
Amano, M.,Salcedo-Gomez, P.M.,Yedidi, R.S.
et al.
PubMed: 31061155 |
Reaction
Chain : | A, B |
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UniProt : | C8B467 (C8B467_9HIV1) |
Reaction : | - |