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Discovery of New HIV Protease Inhibitors with Potential for Convenient Dosing and Reduced Side Effects: A-790742 and A-792611[HYDROLASE/HYDROLASE INHIBITOR]
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HIV protease complexed with compound 10b[TRANSFERASE]
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Crystal Structure of HIV-1 protease complexed with PL-100[HYDROLASE]
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THREE-DIMENSIONAL STRUCTURE OF ASPARTYL PROTEASE FROM HUMAN IMMUNODEFICIENCY VIRUS HIV-1[HYDROLASE(ACID PROTEINASE)]
View in iCn3D Similar StructuresPubMedProteinsConserved Domains
Design, activity and 2.8 Angstroms crystal structure of a C2 symmetric inhibitor complexed to HIV-1 protease[HYDROLASE/HYDROLASE INHIBITOR]
Inhibitor of HIV protease with unusual binding mode potently inhibiting multi-resistant protease mutants[HYDROLASE]
HIV-1 protease in complex with the inhibitor BEA369[HYDROLASE/HYDROLASE INHIBITOR]
HIV-1 PROTEASE COMPLEXED WITH THE INHIBITOR HOE/BAY 793 HEXAGONAL FORM[ASPARTYL PROTEASE]
HIV-1 PROTEASE COMPLEXED WITH THE INHIBITOR HOE/BAY 793 ORTHORHOMBIC FORM[ASPARTYL PROTEASE]
HIV-1 PROTEASE DIMER COMPLEXED WITH A-98881[HYDROLASE (ASPARTIC PROTEASE)]
X-RAY CRYSTAL STRUCTURE OF THE HIV PROTEASE COMPLEX WITH L-700,417, AN INHIBITOR WITH PSEUDO C2 SYMMETRY[HYDROLASE(ASPARTIC PROTEINASE)]
AN ORALLY-BIOAVAILABLE HIV-1 PROTEASE INHIBITOR CONTAINING AN IMIDAZOLE-DERIVED PEPTIDE BOND REPLACEMENT. CRYSTALLOGRAPHIC AND PHARMACOKINETIC ANALYSIS[HYDROLASE(ACID PROTEASE)]
Native HIV-1 Proteinase[Hydrolase/Hydrolase Inhibitor]
HIV-1 proteinase complexed with RO 31-8959[HYDROLASE/HYDROLASE INHIBITOR]
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