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Andrew H.-J. Wang

Researcher at Academia Sinica

Publications -  494
Citations -  28088

Andrew H.-J. Wang is an academic researcher from Academia Sinica. The author has contributed to research in topics: DNA & Base pair. The author has an hindex of 81, co-authored 490 publications receiving 26260 citations. Previous affiliations of Andrew H.-J. Wang include University of Texas Medical Branch & Argonne National Laboratory.

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Molecular structure of a left-handed double helical DNA fragment at atomic resolution

TL;DR: The DNA fragment d(CpGpCpC pGp CpG pG) crystallises as a left-handed double helical molecule with Watson–Crick base pairs and an antiparallel organisation of the sugar phosphate chains.
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The chemistry and biology of left-handed z-dna

TL;DR: Z-DNA in Other Naturally Occurring Sequences, e.g. d(CA/GT}n, Drosophilia and Chironomus, and Other Species : 831.
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Three-dimensional tertiary structure of yeast phenylalanine transfer RNA.

TL;DR: The 3-angstrom electron density map of crystalline yeast phenylalanine transfer RNA has provided us with a complete three-dimensional model which defines the positions of all of the nucleotide residues in the moleclule, which explains, in a simple and direct fashion, chemical modification studies of transfer RNA.
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A bifurcated hydrogen-bonded conformation in the d(A.T) base pairs of the DNA dodecamer d(CGCAAATTTGCG) and its complex with distamycin.

TL;DR: The crystal structures of d(CGCA3T3GCG) complex to the antitumor drug distamycin and the DNA fragment alone were solved by x-ray diffraction at 2.2 and 2.5 A resolution, respectively, suggesting a model to explain the unusual properties of poly-(dA).poly(dT) in which a modified B conformation is associated with a large propeller twist of the bases and a set of continuous bifurcating hydrogen bonds
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Structural comparison of anticancer drug-DNA complexes: adriamycin and daunomycin.

TL;DR: The observed changes in the overall structures of the ternary complexes amplify the small chemical differences between these two antibiotics and provide a possible explanation for the significantly different clinical activities of these important drugs.