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Volumn 18, Issue 16, 2008, Pages 4554-4557
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Crystal structure of chemically synthesized HIV-1 protease and a ketomethylene isostere inhibitor based on the p2/NC cleavage site
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Author keywords
Aspartic proteases; Chemical protein synthesis; HIV 1 protease; Ketomethylene isostere
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Indexed keywords
AMINO ACID DERIVATIVE;
CARBENE;
KETOMETHYLENE ISOSTERE;
PROTEIN P2;
PROTEINASE;
UNCLASSIFIED DRUG;
ARTICLE;
CATALYSIS;
CRYSTAL STRUCTURE;
ENZYME DEGRADATION;
ENZYME STRUCTURE;
ENZYME SYNTHESIS;
HUMAN IMMUNODEFICIENCY VIRUS 1;
HYDRATION;
HYDROGEN BOND;
MOLECULAR MECHANICS;
REVERSED PHASE HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;
STRUCTURE ANALYSIS;
X RAY CRYSTALLOGRAPHY;
CATALYTIC DOMAIN;
CHEMISTRY, PHYSICAL;
CRYSTALLOGRAPHY, X-RAY;
DRUG DESIGN;
GAG GENE PRODUCTS, HUMAN IMMUNODEFICIENCY VIRUS;
HIV PROTEASE;
HIV PROTEASE INHIBITORS;
HIV-1;
MODELS, CHEMICAL;
MOLECULAR CONFORMATION;
MOLECULAR STRUCTURE;
NUCLEOCAPSID;
PEPTIDE FRAGMENTS;
PEPTIDE HYDROLASES;
PROTEIN CONFORMATION;
HUMAN IMMUNODEFICIENCY VIRUS 1;
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EID: 48649102960
PISSN: 0960894X
EISSN: None
Source Type: Journal
DOI: 10.1016/j.bmcl.2008.07.039 Document Type: Article |
Times cited : (11)
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References (19)
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