Pluramycins. Old Drugs Having Modern Friends in Structural Biology
Authors:
- 14 May 1996
- journal article
- research article
- Published by American Chemical Society (ACS) in Accounts of Chemical Research
- Vol. 29 (5) , 249-258
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Hedamycin intercalates the DNA helix and, through carbohydrate-mediated recognition in the minor groove, directs N7-alkylation of guanine in the major groove in a sequence-specific mannerChemistry & Biology, 1995
- Comparison of the sequence selectivity of the DNA-alkylating pluramycin antitumour antibiotics DC92-B and hedamycinChemico-Biological Interactions, 1995
- Altromycin B Threads the DNA Helix Interacting with Both the Major and the Minor Grooves To Position Itself for Site-Directed Alkylation and Guanine N7Journal of the American Chemical Society, 1995
- Acid-Dependent Electrophilicity of Cyclopropylpyrroloindoles. Nature's Masking Strategy for a Potent DNA AlkylatorJournal of the American Chemical Society, 1994
- Co-crystal structure of TBP recognizing the minor groove of a TATA elementNature, 1993
- The complexities of eukaryotic transcription initiation: regulation of preinitiation complex assemblyTrends in Biochemical Sciences, 1991
- Sequence specificity of DNA alkylation by the unnatural enantiomer of CC-1065 and its synthetic analogsJournal of the American Chemical Society, 1990
- Sequence selectivity of DNA covalent modificationChemical Research in Toxicology, 1988
- Molecular basis for sequence-specific DNA alkylation by CC-1065Biochemistry, 1988
- Hedamycin and rubiflavin complexes with deoxyribonucleic acid and other polynucleotidesBiochemistry, 1969