(Q57376833)

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Robust Synthesis and Crystal-Structure Analysis of 7-Cyano-7-deazaguanine (PreQ0 Base) and 7-(Aminomethyl)-7-deazaguanine (PreQ1 Base)

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Robust Synthesis and Crystal-Structure Analysis of 7-Cyano-7-deazaguanine (PreQ0 Base) and 7-(Aminomethyl)-7-deazaguanine (PreQ1 Base) (English)

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Thomas Carell

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author name string

Florian Klepper

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1

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Kurt Polborn

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2

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publication date

October 2005

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Helvetica Chimica Acta

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88

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issue

10

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page(s)

2610-2616

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Summary: the modified nucleosides of RNA.

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The role of modifications in codon discrimination by tRNA(Lys)UUU.

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Three-dimensional structure of hyper-modified nucleoside Q located in the wobbling position of tRNA

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Possible anticodon sequences of tRNAHis, tRNAAsn, and tRNAAsp from Escherichia coli. Universal presence of nucleoside O in the first position of the anticodons of these transfer ribonucleic acid

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Biosynthesis of the 7-deazaguanosine hypermodified nucleosides of transfer RNA.

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Chemical trapping and crystal structure of a catalytic tRNA guanine transglycosylase covalent intermediate

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From cyclohydrolase to oxidoreductase: discovery of nitrile reductase activity in a common fold

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Queuosine modification of tRNA: a case for convergent evolution

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Synthesis of queuine, the base of naturally occurring hypermodified nucleoside (queuosine), and its analogues

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Synthesis, antifolate, and antitumor activities of classical and nonclassical 2-amino-4-oxo-5-substituted-pyrrolo[2,3-d]pyrimidines

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Water-mediated association provides an ion pair receptor

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10.1002/HLCA.200590201

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(Q57376833)

Robust Synthesis and Crystal-Structure Analysis of 7-Cyano-7-deazaguanine (PreQ0 Base) and 7-(Aminomethyl)-7-deazaguanine (PreQ1 Base)

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