PDB ID: 1IDA
Hetero Atom Contents
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0PO | N-[(1r)-1-{[(1s,2s)-1-benzyl-3-{(2r,4s)-2-(tert-butylcarbamoyl)-4-[(pyridin-3-ylmethyl)sulfanyl]piperidin-1-yl}-2-hydroxypropyl]carbamoyl}-2-methylpropyl]quinoline-2-carboxamide | PoSSuM |
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Download interaction data: 1IDA
Structure summary
Code : | 1IDA PDBj RCSB PDB PDBe | ||||||||||||
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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 | ||||||||||||
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Authors : | Tong, L., Anderson, P.C. | ||||||||||||
Keywords : | ACID PROTEINASE, AIDS, Protease, HYDROLASE-HYDROLASE INHIBITOR complex | ||||||||||||
Exp. method : | X-RAY DIFFRACTION ( 1.7 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.
PubMed: 7743130 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.
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Reaction
Chain : | A, B | ||||||||||||||||||||||||
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UniProt : | P04584 (POL_HV2RO) | ||||||||||||||||||||||||
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