Brand  (β version)

PDB ID: 1IDB

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Ligands
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0DO (2r,4s)-N-tert-butyl-1-[(2s,3s)-3-{[(2,6-dimethylphenoxy)acetyl]amino}-2-hydroxy-4-phenylbutyl]-4-(pyridin-4-ylsulfonyl)piperidine-2-carboxamide PoSSuM
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Structure summary

Code : 1IDB   PDBj   RCSB PDB   PDBe
Header : HYDROLASE/HYDROLASE INHIBITOR
Title : Crystal structures of HIV-2 protease in complex with inhibitors containing the hydroxyethylamine dipeptide isostere
Release Data : 1995-01-26
Compound :
mol_id molecule chains
1 Protease A,B
Source :
mol_id organism_scientific expression_system
1 Human immunodeficiency virus 2  (taxid:11709) Escherichia coli  (taxid:562)
gene: pol
Authors : Tong, L., Anderson, P.C.
Keywords : HYDROLASE-HYDROLASE INHIBITOR COMPLEX
Exp. method : X-RAY DIFFRACTION ( 2.2 Å )
Citation :

Crystal structures of HIV-2 protease in complex with inhibitors containing the hydroxyethylamine dipeptide isostere.

Tong, L.,Pav, S.,Mui, S.  et al.
(1995)  Structure  3 : 33 - 40

PubMed: 7743130
DOI: 10.1016/S0969-2126(01)00133-2

Crystal Structure of Human Immunodeficiency Virus (HIV) Type 2 Protease in Complex with a Reduced Amide Inhibitor and Comparison with HIV-1 Protease Structures

Tong, L.,Pav, S.,Pargellis, C.  et al.
(1993)  Proc.Natl.Acad.Sci.USA  90 : 8387

Reaction

Chain : A, B
UniProt : Q9W9R3 (Q9W9R3_9HIV2)
Reaction : -