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  • Chiral auxiliaries  (1)
  • DYANA  (1)
  • 2000-2004  (1)
  • 1995-1999  (1)
  • 1940-1944
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  • 2000-2004  (1)
  • 1995-1999  (1)
  • 1940-1944
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  • 1
    ISSN: 1573-5001
    Schlagwort(e): AIDS ; DYANA ; HIV-1 ; NMR structure ; ribonuclease H ; RNA-DNA hybrid ; torsion angle dynamics
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie , Chemie und Pharmazie
    Notizen: Abstract A high-quality NMR solution structure of the chimeric hybrid duplex r(gcaguggc)⋅r(gcca)d(CTGC) was determined using the program DYANA with its recently implemented new module FOUND, which performs exhaustive conformational grid searches for dinucleotides. To ensure conservative data interpretation, the use of 1H-1H lower distance limit constraints was avoided. The duplex comprises the tRNA–DNA junction formed during the initiation of HIV-1 reverse transcription. It forms an A-type double helix that exhibits distinct structural deviations from a standard A-conformation. In particular, the minor groove is remarkably narrow, and its width decreases from about 7.5 Å in the RNA/RNA stem to about 4.5 Å in the RNA/DNA segment. This is unexpected, since minor groove widths for A-RNA and RNA/DNA hybrid duplexes of ∼11 Å and ∼8.5 Å, respectively, were previously reported. The present, new structure supports that reverse transcriptase-associated RNaseH specificity is related primarily to conformational adaptability of the nucleic acid in 'induced-fit'-type interactions, rather than the minor groove width of a predominantly static nucleic acid duplex.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 2000 (2000), S. 837-840 
    ISSN: 1434-193X
    Schlagwort(e): Chiral auxiliaries ; Analytical methods ; Through-space interactions ; Lactic acid ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: ---The enantiomeric purity of a chiral compound is determined by NMR spectroscopic analysis of the diastereomers formed with a chiral derivatizing agent. Fluorinated O-aryllactic acids (FAC) 1 are efficient chiral reporters, whose spectacular remote anisotropic effects allow an easy identification and measurement of diastereomers. The remote effects are attributed to the particular design of FAC esters relative to other CDAs.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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