-CH2-lengthening of the internucleotide linkage in the ApA dimer can improve its conformational compatibility with its natural polynucleotide counterpart

Nucleic Acids Research

Volumn 29, Issue 24, 2001, Pages 5182-5194

  Hanus, J ^a,b   Barvik I ^a   Ruszova Chmelova K ^a,b   Stepanek J ^a   Turpin, P Y ^b   Bok, J ^a   Rosenberg, I ^c   Petrova Endova M ^c  

^a CHARLES UNIVERSITY   (Czech Republic)

^b SORBONNE UNIVERSITÉ   (France)

^c INSTITUTE OF ORGANIC CHEMISTRY AND BIOCHEMISTRY   (Czech Republic)

Author keywords

[No Author keywords available]

Indexed keywords

ADENINE; DIMER; METHYL GROUP; PHOSPHONIC ACID DERIVATIVE; POLYNUCLEOTIDE; POLYURIDYLIC ACID; DINUCLEOSIDE PHOSPHATE;

ARTICLE; CALCULATION; CHEMICAL INTERACTION; CHEMICAL MODIFICATION; CHEMICAL STRUCTURE; CONFORMATION; CONTROLLED STUDY; GENETIC LINKAGE; MOLECULAR DYNAMICS; MOLECULAR HYBRIDIZATION; PRIORITY JOURNAL; RAMAN SPECTROMETRY; ROOM TEMPERATURE; CHEMISTRY; HYDROGEN BOND; METHODOLOGY;

INSERTION SEQUENCES;

DINUCLEOSIDE PHOSPHATES; HYDROGEN BONDING; MODELS, MOLECULAR; NUCLEIC ACID CONFORMATION; POLYNUCLEOTIDES; SPECTRUM ANALYSIS, RAMAN;

EID: 0035944933     PISSN: 03051048     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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