Pairing geometry of the hydrophobic thymine analogue 2,4-difluorotoluene in duplex DNA as analyzed by X-ray crystallography

Journal of the American Chemical Society

Volumn 131, Issue 35, 2009, Pages 12548-12549

  Pallan, Pradeep S ^a   Egli, Martin ^a  

^a VANDERBILT UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACTIVE SITE; AMINO GROUP; CHEMICAL EQUATIONS; DNA POLYMERASE; DNA REPLICATIONS; DUPLEX DNA; H-BONDING; STERIC CONSTRAINT;

AMINES; CHEMICAL REACTIONS; DNA; FLUORINE; GENES; HYDROPHOBICITY; MINERALOGY; NUCLEIC ACIDS; SELF ASSEMBLY;

X RAY CRYSTALLOGRAPHY;

2,4 DIFLUOROTOLUENE; DNA B; DOUBLE STRANDED DNA; THYMIDINE TRIPHOSPHATE; THYMINE DERIVATIVE; TOLUENE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CONFORMATION; CRYSTAL STRUCTURE; GEOMETRY; HYDROGEN BOND; HYDROPHOBICITY; X RAY CRYSTALLOGRAPHY;

BACILLUS; BASE PAIRING; BASE SEQUENCE; CRYSTALLOGRAPHY, X-RAY; DNA; HYDROPHOBICITY; MODELS, MOLECULAR; RIBONUCLEASE H; THYMINE; TOLUENE;

EID: 69849102641     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja905739j     Document Type: Article

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