PDB ID: 3H5B
Hetero Atom Contents
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Code | Name | Style | Show | Link | |
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031 | (3as,5r,6ar)-hexahydro-2h-cyclopenta[B]furan-5-yl [(1s,2r)-1-benzyl-2-hydroxy-3-([(4-methoxyphenyl)sulfonyl]{[(2r)-5-oxopyrrolidin-2-yl]methyl}amino)propyl]carbamate | PoSSuM | |||
CL | Chloride ion | PoSSuM | |||
GOL | Glycerol | PoSSuM | |||
NA | Sodium ion | PoSSuM |
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Download interaction data: 3H5B
Structure summary
Code : | 3H5B PDBj RCSB PDB PDBe | ||||||||||||
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Header : | HYDROLASE | ||||||||||||
Title : | Crystal structure of wild type HIV-1 protease with novel P1'-ligand GRL-02031 | ||||||||||||
Release Data : | 2009-06-16 | ||||||||||||
Compound : |
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Authors : | Tie, Y., Wang, Y.F., Weber, I.T. | ||||||||||||
Keywords : | HIV-1, wild type protease, protease inhibitor, P1'-ligand, AIDS, Hydrolase | ||||||||||||
Exp. method : | X-RAY DIFFRACTION ( 1.29 Å ) | ||||||||||||
Citation : |
Design of HIV-1 protease inhibitors with pyrrolidinones and oxazolidinones as novel P1'-ligands to enhance backbone-binding interactions with protease: synthesis, biological evaluation, and protein-ligand X-ray studies.
Ghosh, A.K.,Leshchenko-Yashchuk, S.,Anderson, D.D.
et al.
PubMed: 19473017 |
Reaction
Chain : | A, B | ||||||||||||||||||||||||
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UniProt : | P03367 (POL_HV1BR) | ||||||||||||||||||||||||
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