PDB ID: 4E92
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Code | Name | Style | Show | Link | |
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0OE | 4-{2-[5-(3-chlorophenyl)-1h-pyrazol-4-yl]-1-[3-(1h-imidazol-1-yl)propyl]-1h-benzimidazol-5-yl}benzoic acid | PoSSuM | |||
0OG | 3-{5-[3-ethyl-5-(5-methylfuran-2-yl)-1h-pyrazol-1-yl]-1-[(6-oxo-1,6-dihydropyridin-3-yl)methyl]-1h-benzimidazol-2-yl}-4-hydroxybenzoic acid | PoSSuM |
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Download interaction data: 4E92
Structure summary
Code : | 4E92 PDBj RCSB PDB PDBe | ||||||||||||
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Header : | STRUCTURAL PROTEIN/INHIBITOR | ||||||||||||
Title : | Crystal Structure of the N-Terminal Domain of HIV-1 Capsid in Complex With Inhibitor BM4 | ||||||||||||
Release Data : | 2012-04-25 | ||||||||||||
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Authors : | Lemke, C.T. | ||||||||||||
Keywords : | Structural protein Capsid, STRUCTURAL PROTEIN-INHIBITOR complex | ||||||||||||
Exp. method : | X-RAY DIFFRACTION ( 1.800 Å ) | ||||||||||||
Citation : |
Distinct Effects of Two HIV-1 Capsid Assembly Inhibitor Families That Bind the Same Site within the N-Terminal Domain of the Viral CA Protein.
Lemke, C.T.,Titolo, S.,von Schwedler, U.
et al.
PubMed: 22496222 A novel inhibitor-binding site on the HIV-1 capsid N-terminal domain leads to improved crystallization via compound-mediated dimerization.
Lemke, C.T.,Titolo, S.,Goudreau, N.
et al.
PubMed: 23695256 |
Reaction
Chain : | A, B |
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UniProt : | Q79791 (Q79791_9HIV1) |
Reaction : | - |