Literature DB >> 3340545

Analysis of conformational parameters in nucleic acid fragments. II. Co-crystal complexes of nucleic acid bases.

C C Wilson1.   

Abstract

Studies have been made of conformational parameters in co-crystal complexes and compounds of nucleic acid bases in which there is the possibility of formation of hetero-base-pairs. Using published data extracted from the Cambridge structural database, a total of 37 base-pairs were found, of which 25 were hetero-pairs and 12 homo-pairs. These base-pairs were subject to analysis to reveal hydrogen bond parameters, propeller twist, buckle and C1'-C1' separation (or a similar parameter if C1' atoms were not present). Hetero-pairs were found to show larger twists than homo-pairs, the magnitude of twist being unrelated to hydrogen bond parameters or buckle value. The propeller twisting is less pronounced in these nucleic acid bases than in nucleosides, but still has a significant magnitude. Propeller twisting in hetero-pairs is found to be larger than in homo-pairs. Hetero-pairs appear to be formed preferentially in competitive situations.

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Year:  1988        PMID: 3340545      PMCID: PMC334667          DOI: 10.1093/nar/16.2.385

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  7 in total

1.  Base-pairing configurations between purines and pyrimidines in the solid state. II. Crystal and molecular structure of 9-ethyl-8-bromoadenine-1-methyl-5-bromouracil.

Authors:  S S Tavale; T D Sakore; H M Sobell
Journal:  J Mol Biol       Date:  1969-08-14       Impact factor: 5.469

2.  Base-pairing configurations between purines and pyrimidines in the solid state. I. Crystal and molecular structure of a 1:2 purine-pyrimidine hydrogen-bonded complex: 9-ethyladenine-1-methyl-5-iodouracil.

Authors:  T D Sakore; S S Tavale; H M Sobell
Journal:  J Mol Biol       Date:  1969-08-14       Impact factor: 5.469

3.  Crystal structure of the intermolecular complex 9-ethyladenine: 1-methyl-5-fluorouracil.

Authors:  K Tomita; L Katz; A Rich
Journal:  J Mol Biol       Date:  1967-12-28       Impact factor: 5.469

4.  Base sequence and helix structure variation in B and A DNA.

Authors:  R E Dickerson
Journal:  J Mol Biol       Date:  1983-05-25       Impact factor: 5.469

5.  Base-pairing configurations between purines and pyrimidines in the solid state. V. Crystal and molecular structure of two 1:1 hydrogen-bonded complexes, 1-methyluracil: 9-ethyl-8-bromo-2,6-diaminopurine and 1-ethylthymine: 9-ethyl-8-bromo-2,6--diaminopurine.

Authors:  G Simundza; T D Sakore; H M Sobell
Journal:  J Mol Biol       Date:  1970-03-14       Impact factor: 5.469

6.  Base-pairing configurations between purines and pyrimidines in the solid state. 3. Crystal and molecular structure of two 2:1 hydrogen-bonded complexes, 1-methylthymine: 9-ethyl-2,6-diaminopurine and 1-methyl-5-iodouracil: 9-ethyl-2,6-diaminopurine.

Authors:  T D Sakore; H M Sobell; F Mazza; G Kartha
Journal:  J Mol Biol       Date:  1969-08-14       Impact factor: 5.469

7.  Base-pairing configurations between purines and pyrimidines in the solid state. IV. Crystal and molecular structure of two 1:1 hydrogen-bonded complexes, 1-methyl-5-bromouracil: 9-ethyl-2-aminopurine and 1-methyl-5-fluorouracil: 9-ethyl-2-aminopurine.

Authors:  F Mazza; H M Sobell; G Kartha
Journal:  J Mol Biol       Date:  1969-08-14       Impact factor: 5.469

  7 in total
  3 in total

1.  On Spectral Identification of DNA-Base Pairs Polymorphism.

Authors:  V M Komarov
Journal:  J Biol Phys       Date:  1999-06       Impact factor: 1.365

2.  Analysis of conformational parameters in nucleic acid fragments. III. Very short chain oligonucleotides. The effect of base stacking.

Authors:  C C Wilson
Journal:  Nucleic Acids Res       Date:  1988-06-10       Impact factor: 16.971

3.  Analysis of conformational parameters in nucleic acid fragments. IV. Intercalating drug complexes of very short chain oligonucleotides.

Authors:  C C Wilson
Journal:  Nucleic Acids Res       Date:  1988-06-24       Impact factor: 16.971

  3 in total

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