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Volumn 39, Issue 31, 2000, Pages 9597-9603
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Kinetics and crystal structure of the wild-type and the engineered Y101F mutant of Herpes simplex virus type 1 thymidine kinase interacting with (North)-methanocarba-thymidine
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Author keywords
[No Author keywords available]
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Indexed keywords
2' EXOMETHANOCARBATHYMIDINE;
ANTIVIRUS AGENT;
THYMIDINE KINASE;
UNCLASSIFIED DRUG;
ARTICLE;
BINDING AFFINITY;
CATALYSIS;
CRYSTAL STRUCTURE;
DRUG CONFORMATION;
DRUG PROTEIN BINDING;
ENZYME KINETICS;
ENZYME SPECIFICITY;
ENZYME STRUCTURE;
HERPES SIMPLEX VIRUS 1;
HYDROGEN BOND;
PRIORITY JOURNAL;
PROTEIN EXPRESSION;
STRUCTURE ANALYSIS;
AMINO ACID SUBSTITUTION;
BICYCLO COMPOUNDS;
BINDING, COMPETITIVE;
CRYSTALLIZATION;
CRYSTALLOGRAPHY, X-RAY;
ENZYME INHIBITORS;
HERPESVIRUS 1, HUMAN;
HUMANS;
KINETICS;
MACROMOLECULAR SUBSTANCES;
MODELS, MOLECULAR;
MOLECULAR SEQUENCE DATA;
MUTAGENESIS, SITE-DIRECTED;
PHENYLALANINE;
PHOSPHORYLATION;
PROTEIN CONFORMATION;
THYMIDINE;
THYMIDINE KINASE;
TYROSINE;
FELIS CATUS;
HERPES;
HUMAN HERPESVIRUS 1;
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EID: 0034622629
PISSN: 00062960
EISSN: None
Source Type: Journal
DOI: 10.1021/bi000668q Document Type: Article |
Times cited : (48)
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References (61)
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