1K8J

NMR STRUCTURE OF THE CK14 DNA DUPLEX: A PORTION OF THE KNOWN NF-kB SEQUENCE CK1

1K8J の概要

• エントリーDOI: 10.2210/pdb1k8j/pdb
• 関連するPDBエントリー: 1K8L 1K8N
• NMR情報: BMRB: 5716,5717,5718
• 分子名称: FIRST STRAND OF CK14 DNA DUPLEX, SECOND STRAND OF CK14 DNA DUPLEX (2 entities in total)
• 機能のキーワード: dna duplex, ck14, ck1, nf-kb, dna
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 8561.58

構造登録者

Volk, D.E.,Yang, X.,Fennewald, S.M.,King, D.J.,Bassett, S.E.,Venkitachalam, S.,Herzog, N.,Luxon, B.A.,Gorenstein, D.G. (登録日: 2001-10-24, 公開日: 2003-04-15, 最終更新日: 2024-05-22)

主引用文献

Volk, D.E.,Yang, X.,Fennewald, S.M.,King, D.J.,Bassett, S.E.,Venkitachalam, S.,Herzog, N.,Luxon, B.A.,Gorenstein, D.G.
Solution structure and design of dithiophosphate backbone aptamers targeting transcription factor NF-kappaB
Bioorg.Chem., 30:396-419, 2002

PubMed Abstract: A variety of monothio- and dithiosubstituted duplex aptamers targeting NF-kappaB have been synthesized and designed. The specificity and affinity of the dithioate aptamers of p50 and RelA(p65) NF-kappaB homodimers was determined by gel shift experiments. The NMR solution structures for several unmodified and dithioate backbone modified 14-base paired duplex aptamers have been determined by a hybrid, complete matrix (MORASS)/restrained molecular dynamics method. Structural perturbations of the dithioate substitutions support our hypothesis that the dithioate binds cations less tightly than phosphoryl groups. This increases the electrostatic repulsion across the B-form narrow minor groove and enlarges the minor groove, similar to that found in A-form duplexes. Structural analysis of modeled aptamer complexes with NF-kappaB homo- and heterodimers suggests that the dithioate backbone substitution can increase the aptamer's relative affinity to basic groups in proteins such as NF-kappaB by helping to "strip" the cations from the aptamer backbone.

PubMed: 12642125
DOI: 10.1016/S0045-2068(02)00510-2

実験手法

SOLUTION NMR