Structure-activity relationships in HIV-1 reverse transcriptase revealed by radiation target analysis

Protein Science

Volumn 12, Issue 9, 2003, Pages 2081-2086

  Sluis Cremer, Nicolas ^a   Kempner, Ellis ^b   Parniak, Michael A ^a  

^a UNIVERSITY OF PITTSBURGH   (United States)

^b NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES   (United States)

Author keywords

Dimer; HIV 1; Monomer; Radiation inactivation; Reverse transcriptase

Indexed keywords

DIMER; DNA; MONOMER; PRIMER DNA; PROTEIN P51; PROTEIN P66; RNA DIRECTED DNA POLYMERASE; UNCLASSIFIED DRUG; VIRUS ENZYME;

ANALYTIC METHOD; ARTICLE; DIMERIZATION; DNA TEMPLATE; ENZYME STRUCTURE; ENZYME SUBSTRATE; FUNCTIONAL ANATOMY; GENETIC RECOMBINATION; HUMAN IMMUNODEFICIENCY VIRUS 1; IONIZATION; MACROMOLECULE; MOLECULAR SIZE; MURINE LEUKEMIA VIRUS; NONHUMAN; PRIORITY JOURNAL; PROTEIN ISOLATION; PROTEIN TARGETING; RADIATION DETECTION; RADIATION INACTIVATION ANALYSIS; RADIATION TARGET ANALYSIS; STRUCTURE ACTIVITY RELATION; STRUCTURE ANALYSIS; VIRUS ISOLATION;

CHROMATOGRAPHY, HIGH PRESSURE LIQUID; DIMERIZATION; DNA-DIRECTED DNA POLYMERASE; DOSE-RESPONSE RELATIONSHIP, RADIATION; ELECTROPHORESIS, POLYACRYLAMIDE GEL; HIV-1 REVERSE TRANSCRIPTASE; RECOMBINANT PROTEINS; STRUCTURE-ACTIVITY RELATIONSHIP;

HUMAN IMMUNODEFICIENCY VIRUS; HUMAN IMMUNODEFICIENCY VIRUS 1; MURINAE; MURINE LEUKEMIA VIRUS; RNA VIRUSES;

EID: 0043011942     PISSN: 09618368     EISSN: None     Source Type: Journal    
DOI: 10.1110/ps.03130503     Document Type: Article

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