PDB ID: 1ZPK
Hetero Atom Contents
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Color scheme of protein:
| Code | Name | Style | Show | Link | |
|---|---|---|---|---|---|
| 0ZS | N-{(2r,3s)-3-[(tert-butoxycarbonyl)amino]-2-hydroxy-4-phenylbutyl}-L-phenylalanyl-L-alpha-glutamyl-L-phenylalaninamide | PoSSuM | |||
| CL | Chloride ion | PoSSuM | |||
| NA | Sodium ion | PoSSuM |
| Code | Name | Show |
|---|---|---|
| CME | S,S-(2-hydroxyethyl)thiocysteine |
| Code | Name | Emphasize |
|---|
| Code | Name | Show |
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Download interaction data: 1ZPK
Structure summary
| Code : | 1ZPK PDBj RCSB PDB PDBe | ||||||||||||
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| Header : | HYDROLASE/HYDROLASE INHIBITOR | ||||||||||||
| Title : | Crystal structure of the complex of mutant HIV-1 protease (A71V, V82T, I84V) with a hydroxyethylamine peptidomimetic inhibitor BOC-PHE-PSI[R-CH(OH)CH2NH]-PHE-GLU-PHE-NH2 | ||||||||||||
| Release Data : | 2006-04-25 | ||||||||||||
| Compound : |
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| Source : |
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| Authors : | Duskova, J., Skalova, T., Dohnalek, J., Petrokova, H., Hasek, J. | ||||||||||||
| Keywords : | HIV, PROTEASE, PEPTIDOMIMETIC INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX | ||||||||||||
| Exp. method : | X-RAY DIFFRACTION ( 1.65 Å ) | ||||||||||||
| Citation : |
Mutational Study of Pseudopeptide Inhibitor Binding to HIV-1 Protease; Analysis of Four X-ray Structures
Duskova, J.,Skalova, T.,Dohnalek, J.
et al.
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Reaction
| Chain : | A, B | ||||||||||||||||||||||||||||||||||||
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| UniProt : | P03367 (POL_HV1BR) | ||||||||||||||||||||||||||||||||||||
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