Herpes simplex virus 1 primase employs Watson-Crick hydrogen bonding to identify cognate nucleoside triphosphates

Biochemistry

Volumn 44, Issue 47, 2005, Pages 15585-15593

  Ramirez Aguilar, Kathryn A ^a   Moore, Chad L ^a   Kuchta, Robert D ^a  

^a UNIVERSITY OF COLORADO   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; ENZYMES; FREQUENCIES; HYDROGEN BONDS; POLYMERIZATION;

DNA-DEPENDENT NTPASE ACTIVITY; NATURAL BASES; NTP ANALOGUES; NTP SELECTION; WATSON-CRICK HYDROGEN BONDING;

VIRUSES;

1 DEAZAPURINE NUCLEOSIDE TRIPHOSPHATE; 2 CHLOROADENOSINE 5' TRIPHOSPHATE; 2 FLUOROADENOSINE 5' TRIPHOSPHATE; 3 DEAZAADENOSINE 5' TRIPHOSPHATE; 4 AMINOBENZIMIDAZOLE NUCLEOSIDE TRIPHOSPHATE; 4 NITROBENZIMIDAZOLE NUCLEOSIDE TRIPHOSPHATE; 4 TRIFLUOROMETHYLBENZIMIDAZOLE; 4 TRIFLUOROMETHYLBENZIMIDAZOLE NUCLEOSIDE TRIPHOSPHATE; 4,6 DIFLUOROBENZIMIDAZOLE NUCLEOSIDE TRIPHOSPHATE; 5 TRIFLUOROMETHYLBENZIMIDAZOLE NUCLEOSIDE TRIPHOSPHATE; 6 TRIFLUOROMETHYLBENZIMIDAZOLE NUCLEOSIDE TRIPHOSPHATE; 7 BETA GUANINE; 7 BETA GUANOSINE TRIPHOSPHATE; 7 TRIFLUOROMETHYLBENZIMIDAZOLE; 7 TRIFLUOROMETHYLBENZIMIDAZOLE NUCLEOSIDE TRIPHOSPHATE; BENZIMIDAZOLE DERIVATIVE; BENZIMIDAZOLE NUCLEOSIDE TRIPHOSPHATE; DNA PRIMASE; GUANINE DERIVATIVE; GUANOSINE TRIPHOSPHATE DERIVATIVE; HELICASE; INOSINE TRIPHOSPHATE; NUCLEOSIDE TRIPHOSPHATE; NUCLEOSIDE TRIPHOSPHATE DERIVATIVE; PURINE DERIVATIVE; PURINE NUCLEOSIDE TRIPHOSPHATE; UNCLASSIFIED DRUG;

ARTICLE; BINDING AFFINITY; COMPLEX FORMATION; ENZYME ACTIVITY; ENZYME BINDING; FREQUENCY ANALYSIS; HERPES SIMPLEX VIRUS 1; HYDROGEN BOND; HYDROPHOBICITY; MOLECULAR MECHANICS; MOLECULAR MODEL; NONHUMAN; POLYMERIZATION; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN MODIFICATION; PROTEIN PROTEIN INTERACTION; REGULATORY MECHANISM;

ANIMALS; CELL LINE; DNA HELICASES; DNA PRIMASE; HERPESVIRUS 1, HUMAN; HYDROGEN BONDING; HYDROPHOBICITY; NUCLEOTIDES; PROTEIN BINDING; SUBSTRATE SPECIFICITY; TRANSFECTION; VIRAL PROTEINS;

HERPES; HUMAN HERPESVIRUS 1;

EID: 28244441232     PISSN: 00062960     EISSN: None     Source Type: Journal    
DOI: 10.1021/bi0513711     Document Type: Article

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