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5M4W

Structure of DNA AGCGA-quadruplex adopted by 15-mer oligonucleotide found in regulatory region of the PLEKHG3 human gene with G11 to I11 mutation, d(GCGAGGGAGCIAGGG),VK34_I11

Summary for 5M4W
Entry DOI10.2210/pdb5m4w/pdb
NMR InformationBMRB: 34056
DescriptorDNA (5'-D(*GP*CP*GP*AP*GP*GP*GP*AP*GP*CP*IP*AP*GP*GP*G)-3') (1 entity in total)
Functional Keywordsagcga-quadruplex, agcga-quadruplex family, g-g n1-carboniyl symmetric base pair, plekhg3 gene, dna, inosine
Biological sourceHomo sapiens
Total number of polymer chains2
Total formula weight9500.14
Authors
Kocman, V.,Plavec, J. (deposition date: 2016-10-19, release date: 2017-05-31, Last modification date: 2024-05-15)
Primary citationKocman, V.,Plavec, J.
Tetrahelical structural family adopted by AGCGA-rich regulatory DNA regions.
Nat Commun, 8:15355-15355, 2017
Cited by
PubMed Abstract: Here we describe AGCGA-quadruplexes, an unexpected addition to the well-known tetrahelical families, G-quadruplexes and i-motifs, that have been a focus of intense research due to their potential biological impact in G- and C-rich DNA regions, respectively. High-resolution structures determined by solution-state nuclear magnetic resonance (NMR) spectroscopy demonstrate that AGCGA-quadruplexes comprise four 5'-AGCGA-3' tracts and are stabilized by G-A and G-C base pairs forming GAGA- and GCGC-quartets, respectively. Residues in the core of the structure are connected with edge-type loops. Sequences of alternating 5'-AGCGA-3' and 5'-GGG-3' repeats could be expected to form G-quadruplexes, but are shown herein to form AGCGA-quadruplexes instead. Unique structural features of AGCGA-quadruplexes together with lower sensitivity to cation and pH variation imply their potential biological relevance in regulatory regions of genes responsible for basic cellular processes that are related to neurological disorders, cancer and abnormalities in bone and cartilage development.
PubMed: 28513602
DOI: 10.1038/ncomms15355
PDB entries with the same primary citation
Experimental method
SOLUTION NMR
Structure validation

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