UniProt P03369
HIV-1 protease (P03369)
HIV-1 protease (UniProt P03369): 162 experimental structures on GenesisL1, 1 ligand bound. Binding sites, pockets, druggability and 3D structures in GL1X.
- UniProt
- P03369
- Protein
- HIV-1 protease
- Experimental structures
- 162
- Predicted models
- 0
- Ligands
- 1
Structures
162 records of P03369 in the MolNFT archive: 162 experimental, 0 predicted.
| Entry | Title | Method | Chains | Ligands | Pockets |
|---|---|---|---|---|---|
| 1AID | Structure of a non-peptide inhibitor complexed with HIV-1 protease: developing a cycle of… | x-ray diffraction | A, B | — | — |
| 1AID | Structure of a non-peptide inhibitor complexed with HIV-1 protease: developing a cycle of… | x-ray diffraction | A, B | — | — |
| 1B6J | HIV-1 protease complexed with macrocyclic peptidomimetic inhibitor 1 | x-ray diffraction | A, B | — | — |
| 1B6J | HIV-1 protease complexed with macrocyclic peptidomimetic inhibitor 1 | x-ray diffraction | A, B | — | — |
| 1B6K | HIV-1 protease complexed with macrocyclic peptidomimetic inhibitor 5 | x-ray diffraction | A, B | — | — |
| 1B6K | HIV-1 protease complexed with macrocyclic peptidomimetic inhibitor 5 | x-ray diffraction | A, B | — | — |
| 1B6L | HIV-1 protease complexed with macrocyclic peptidomimetic inhibitor 4 | x-ray diffraction | A, B | — | — |
| 1B6L | HIV-1 protease complexed with macrocyclic peptidomimetic inhibitor 4 | x-ray diffraction | A, B | — | — |
| 1B6M | HIV-1 protease complexed with macrocyclic peptidomimetic inhibitor 6 | x-ray diffraction | A, B | — | — |
| 1B6M | HIV-1 protease complexed with macrocyclic peptidomimetic inhibitor 6 | x-ray diffraction | A, B | — | — |
| 1B6P | HIV-1 protease complexed with macrocyclic peptidomimetic inhibitor 7 | x-ray diffraction | A, B | — | — |
| 1B6P | HIV-1 protease complexed with macrocyclic peptidomimetic inhibitor 7 | x-ray diffraction | A, B | — | — |
| 1CPI | Regioselective structural and functional mimicry of peptides. design of hydrolytically stable… | x-ray diffraction | A, B | — | — |
| 1CPI | Regioselective structural and functional mimicry of peptides. design of hydrolytically stable… | x-ray diffraction | A, B | — | — |
| 1D4K | HIV-1 protease complexed with a macrocyclic peptidomimetic inhibitor | x-ray diffraction | A, B | — | — |
| 1D4K | HIV-1 protease complexed with a macrocyclic peptidomimetic inhibitor | x-ray diffraction | A, B | — | — |
| 1D4L | HIV-1 protease complexed with a macrocyclic peptidomimetic inhibitor | x-ray diffraction | A, B | — | — |
| 1D4L | HIV-1 protease complexed with a macrocyclic peptidomimetic inhibitor | x-ray diffraction | A, B | — | — |
| 1F7A | How does a symmetric dimer recognize an asymmetric substrate? a substrate complex of HIV-1 protease. | x-ray diffraction | A, B | — | — |
| 1F7A | How does a symmetric dimer recognize an asymmetric substrate? a substrate complex of HIV-1 protease. | x-ray diffraction | A, B | — | — |
| 1KJ4 | Substrate shape determines specificity of recognition recognition for HIV-1 protease: analysis of… | x-ray diffraction | A, B, C, D | — | — |
| 1KJ4 | Substrate shape determines specificity of recognition recognition for HIV-1 protease: analysis of… | x-ray diffraction | A, B, C, D | — | — |
| 1KJ7 | Substrate shape determines specificity of recognition recognition for HIV-1 protease: analysis of… | x-ray diffraction | A, B | — | — |
| 1KJ7 | Substrate shape determines specificity of recognition recognition for HIV-1 protease: analysis of… | x-ray diffraction | A, B | — | — |
| 1KJF | Substrate shape determines specificity of recognition recognition for HIV-1 protease: analysis of… | x-ray diffraction | A, B | — | — |
| 1KJF | Substrate shape determines specificity of recognition recognition for HIV-1 protease: analysis of… | x-ray diffraction | A, B | — | — |
| 1KJG | Substrate shape determines specificity of recognition recognition for HIV-1 protease: analysis of… | x-ray diffraction | A, B | — | — |
| 1KJG | Substrate shape determines specificity of recognition recognition for HIV-1 protease: analysis of… | x-ray diffraction | A, B | — | — |
| 1KJH | Substrate shape determines specificity of recognition recognition for HIV-1 protease: analysis of… | x-ray diffraction | A, B | — | — |
| 1KJH | Substrate shape determines specificity of recognition recognition for HIV-1 protease: analysis of… | x-ray diffraction | A, B | — | — |
| 1KZK | JE-2147-HIV Protease Complex | x-ray diffraction | A, B | — | — |
| 1KZK | Je-2147-HIV protease complex | x-ray diffraction | A, B | — | — |
| 1MT7 | Viability of a drug-resistant HIV-1 protease mutant: structural insights for better antiviral… | x-ray diffraction | A, B | — | — |
| 1MT7 | Viability of a drug-resistant HIV-1 protease mutant: structural insights for better antiviral… | x-ray diffraction | A, B | — | — |
| 1MT8 | Viability of a drug-resistant HIV-1 protease mutant: structural insights for better antiviral… | x-ray diffraction | A, B | — | — |
| 1MT8 | Viability of a drug-resistant HIV-1 protease mutant: structural insights for better antiviral… | x-ray diffraction | A, B | — | — |
| 1MT9 | Viability of a drug-resistant HIV-1 protease mutant: structural insights for better antiviral… | x-ray diffraction | A, B | — | — |
| 1MT9 | Viability of a drug-resistant HIV-1 protease mutant: structural insights for better antiviral… | x-ray diffraction | A, B | — | — |
| 1MTB | Viability of a drug-resistant HIV-1 protease mutant: structural insights for better antiviral… | x-ray diffraction | A, B | — | — |
| 1MTB | Viability of a drug-resistant HIV-1 protease mutant: structural insights for better antiviral… | x-ray diffraction | A, B | — | — |
| 1MTR | HIV-1 protease complexed with a cyclic phe-ile-val peptidomimetic inhibitor | x-ray diffraction | A, B | — | — |
| 1MTR | HIV-1 protease complexed with a cyclic phe-ile-val peptidomimetic inhibitor | x-ray diffraction | A, B | — | — |
| 1N49 | Viability of a Drug-Resistant HIV-1 Protease Variant: Structural Insights for Better Anti-Viral… | x-ray diffraction | A, B, C, D | — | — |
| 1N49 | Viability of a drug-resistant HIV-1 protease variant: structural insights for better anti-viral… | x-ray diffraction | A, B, C, D | — | — |
| 1T3R | HIV protease wild-type in complex with TMC114 inhibitor | x-ray diffraction | A, B | — | — |
| 1T3R | HIV protease wild-type in complex with TMC114 inhibitor | x-ray diffraction | A, B | — | — |
| 1TSQ | Crystal structure of AP2V substrate variant of nc-P1 decamer peptide in complex with V82A/D25N… | x-ray diffraction | A, B | — | — |
| 1TSQ | Crystal structure of AP2V substrate variant of nc-P1 decamer peptide in complex with V82A/D25N… | x-ray diffraction | A, B | — | — |
| 1TSU | Crystal structure of decamer NCP1 substrate peptide in complex with wild-type D25N HIV-1 protease… | x-ray diffraction | A, B | — | — |
| 1TSU | Crystal structure of decamer NCP1 substrate peptide in complex with wild-type D25N HIV-1 protease… | x-ray diffraction | A, B | — | — |
| 1YTG | SIV protease crystallized with peptide product | x-ray diffraction | A, B | — | — |
| 1YTG | SIV protease crystallized with peptide product | x-ray diffraction | A, B | — | — |
| 1YTH | SIV protease crystallized with peptide product | x-ray diffraction | A, B | — | — |
| 1YTH | SIV protease crystallized with peptide product | x-ray diffraction | A, B | — | — |
| 1Z1H | HIV-1 protease complexed with macrocyclic peptidomimetic inhibitor 3 | x-ray diffraction | A, B | — | — |
| 1Z1H | HIV-1 protease complexed with macrocyclic peptidomimetic inhibitor 3 | x-ray diffraction | A, B | — | — |
| 1Z1R | HIV-1 protease complexed with Macrocyclic peptidomimetic inhibitor 2 | x-ray diffraction | A, B | — | — |
| 1Z1R | HIV-1 protease complexed with macrocyclic peptidomimetic inhibitor 2 | x-ray diffraction | A, B | — | — |
| 2AID | Structure of a non-peptide inhibitor complexed with HIV-1 protease: developing a cycle of… | x-ray diffraction | A, B | — | — |
| 2AID | Structure of a non-peptide inhibitor complexed with HIV-1 protease: developing a cycle of… | x-ray diffraction | A, B | — | — |
102 records more on the page itself.
Ligands
- ACE · Acetyl group · in 1 record
Elsewhere
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