PDB ID: 6E9A
Hetero Atom Contents
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Data format:
Color scheme of protein:
Code | Name | Style | Show | Link | |
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CL | Chloride ion | PoSSuM | |||
FMT | Formic acid | PoSSuM | |||
J0S | (3as,5r,6ar)-2-oxohexahydro-2h-cyclopenta[D][1,3]oxazol-5-yl [(2s,3r)-3-hydroxy-4-{[(4-methoxyphenyl)sulfonyl](2-methylpropyl)amino}-1-phenylbutan-2-yl]carbamate | PoSSuM | |||
NA | Sodium ion | PoSSuM |
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Download interaction data: 6E9A
Structure summary
Code : | 6E9A PDBj RCSB PDB PDBe | ||||||||||||
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Header : | HYDROLASE/HYDROLASE INHIBITOR | ||||||||||||
Title : | HIV-1 WILD TYPE PROTEASE WITH GRL-034-17A, (3aS, 5R, 6aR)-2-OXOHEXAHYD CYCLOPENTA[D]-5-OXAZOLYL URETHANE WITH A BICYCLIC OXAZOLIDINONE SCAFF AS THE P2 LIGAND | ||||||||||||
Release Data : | 2018-11-07 | ||||||||||||
Compound : |
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Source : |
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Authors : | Wang, Y.-F., Agniswamy, J., Weber, I.T. | ||||||||||||
Keywords : | ANTIVIRAL, HIV-1 PROTEASE INHIBITOR OF GRL-034-17A, P2 LIGAND, MULTIDRUG-RESISTANT, OXAZOLIDINONE, VIRAL PROTEIN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX, HYDROLASE | ||||||||||||
Exp. method : | X-RAY DIFFRACTION ( 1.22 Å ) | ||||||||||||
Citation : |
Design and Synthesis of Potent HIV-1 Protease Inhibitors Containing Bicyclic Oxazolidinone Scaffold as the P2 Ligands: Structure-Activity Studies and Biological and X-ray Structural Studies.
Ghosh, A.K.,Williams, J.N.,Ho, R.Y.
et al.
PubMed: 30354121 |
Reaction
Chain : | A, B |
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UniProt : | Q5RZ08 (Q5RZ08_9HIV1) |
Reaction : | - |