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7ZEK

Structure of a hybrid-type G-quadruplex with a snapback loop (hybrid 1R')

Summary for 7ZEK
Entry DOI10.2210/pdb7zek/pdb
NMR InformationBMRB: 34721
DescriptorDNA (5'-D(*(DG5)P*GP*CP*TP*AP*(BG)P*GP*GP*TP*CP*AP*GP*GP*GP*TP*GP*GP*GP*TP*CP*AP*(DG3))-3') (1 entity in total)
Functional Keywordshybrid g-quadruplex, snapback loop, dna
Biological sourcesynthetic construct
Total number of polymer chains1
Total formula weight6928.37
Authors
Jana, J.,Vianney, Y.M.,Schroeder, N.,Weisz, K. (deposition date: 2022-03-31, release date: 2022-06-22, Last modification date: 2024-06-19)
Primary citationJana, J.,Vianney, Y.M.,Schroder, N.,Weisz, K.
Guiding the folding of G-quadruplexes through loop residue interactions.
Nucleic Acids Res., 50:7161-7175, 2022
Cited by
PubMed Abstract: A G-rich sequence was designed to allow folding into either a stable parallel or hybrid-type topology. With the parent sequence featuring coexisting species, various related sequences with single and double mutations and with a shortened central propeller loop affected the topological equilibrium. Two simple modifications, likewise introduced separately to all sequences, were employed to lock folds into one of the topologies without noticeable structural alterations. The unique combination of sequence mutations, high-resolution NMR structural information, and the thermodynamic stability for both topological competitors identified critical loop residue interactions. In contrast to first loop residues, which are mostly disordered and exposed to solvent in both propeller and lateral loops bridging a narrow groove, the last loop residue in a lateral three-nucleotide loop is engaged in stabilizing stacking interactions. The propensity of single-nucleotide loops to favor all-parallel topologies by enforcing a propeller-like conformation of an additional longer loop is shown to result from their preference in linking two outer tetrads of the same tetrad polarity. Taken together, the present studies contribute to a better structural and thermodynamic understanding of delicate loop interactions in genomic and artificially designed quadruplexes, e.g. when employed as therapeutics or in other biotechnological applications.
PubMed: 35758626
DOI: 10.1093/nar/gkac549
PDB entries with the same primary citation
Experimental method
SOLUTION NMR
Structure validation

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