A minor groove RNA triple helix within the catalytic core of a group I intron.
about
Dissecting RNA folding by nucleotide analog interference mapping (NAIM)Solution structure of an RNA fragment with the P7/P9.0 region and the 3'-terminal guanosine of the tetrahymena group I intronBackbone and nucleobase contacts to glucosamine-6-phosphate in the glmS ribozymeThree metal ions at the active site of the Tetrahymena group I ribozymeIn vivo selection of better self-splicing introns in Escherichia coli: the role of the P1 extension helix of the Tetrahymena intron.Comparative analysis of hairpin ribozyme structures and interference dataA mutate-and-map strategy accurately infers the base pairs of a 35-nucleotide model RNAA tertiary interaction that links active-site domains to the 5' splice site of a group II intron.Enthalpy-driven RNA folding: single-molecule thermodynamics of tetraloop-receptor tertiary interaction.An unconventional origin of metal-ion rescue and inhibition in the Tetrahymena group I ribozyme reaction.Extraordinarily slow binding of guanosine to the Tetrahymena group I ribozyme: implications for RNA preorganization and functionStructure-function analysis from the outside in: long-range tertiary contacts in RNA exhibit distinct catalytic roles.An important base triple anchors the substrate helix recognition surface within the Tetrahymena ribozyme active site.Communication between RNA folding domains revealed by folding of circularly permuted ribozymes.Probing RNA structure and function by nucleotide analog interference mapping.The structure and function of catalytic RNAs.Potential in vivo roles of nucleic acid triple-helices.Two conserved structural components, A-rich bulge and P4 XJ6/7 base-triples, in activating the group I ribozymes.Progress and Current Challenges in Modeling Large RNAs.The contribution of 2'-hydroxyls to the cleavage activity of the Neurospora VS ribozyme.Monitoring intermediate folding states of the td group I intron in vivoThe functional anatomy of an intrinsic transcription terminatorProbing the role of a secondary structure element at the 5'- and 3'-splice sites in group I intron self-splicing: the tetrahymena L-16 ScaI ribozyme reveals a new role of the G.U pair in self-splicingCrystal structure of a group I intron splicing intermediate.Molecular basis for RNA kink-turn recognition by the h15.5K small RNP protein.A base triple in the Tetrahymena group I core affects the reaction equilibrium via a threshold effect.Understanding catalysis of phosphate-transfer reactions by the large ribozymes.
P2860
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P2860
A minor groove RNA triple helix within the catalytic core of a group I intron.
description
1998 nî lūn-bûn
@nan
1998 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
A minor groove RNA triple helix within the catalytic core of a group I intron.
@ast
A minor groove RNA triple helix within the catalytic core of a group I intron.
@en
A minor groove RNA triple helix within the catalytic core of a group I intron.
@nl
type
label
A minor groove RNA triple helix within the catalytic core of a group I intron.
@ast
A minor groove RNA triple helix within the catalytic core of a group I intron.
@en
A minor groove RNA triple helix within the catalytic core of a group I intron.
@nl
prefLabel
A minor groove RNA triple helix within the catalytic core of a group I intron.
@ast
A minor groove RNA triple helix within the catalytic core of a group I intron.
@en
A minor groove RNA triple helix within the catalytic core of a group I intron.
@nl
P2093
P2860
P356
P1476
A minor groove RNA triple helix within the catalytic core of a group I intron.
@en
P2093
Moncoeur E
Ortoleva-Donnelly L
Strobel SA
Szewczak AA
P2860
P2888
P304
P356
10.1038/4146
P577
1998-12-01T00:00:00Z
P5875
P6179
1017208320