Loading
PDBj
MenuPDBj@FacebookPDBj@X(formerly Twitter)PDBj@BlueSkyPDBj@YouTubewwPDB FoundationwwPDBDonate
RCSB PDBPDBeBMRBAdv. SearchSearch help

6ISW

Structure of human telomeric DNA with 5-selenophene-modified deoxyuridine at residue 12

Summary for 6ISW
Entry DOI10.2210/pdb6isw/pdb
DescriptorDNA (22-MER), POTASSIUM ION (2 entities in total)
Functional Keywordshuman telomere, parallel g-quadruplex, dna
Biological sourceHomo sapiens
Total number of polymer chains1
Total formula weight7199.78
Authors
Saikrishnan, K.,Nuthanakanti, A.,Srivatsan, S.G.,Ahmad, I. (deposition date: 2018-11-19, release date: 2019-05-15, Last modification date: 2023-11-22)
Primary citationNuthanakanti, A.,Ahmed, I.,Khatik, S.Y.,Saikrishnan, K.,Srivatsan, S.G.
Probing G-quadruplex topologies and recognition concurrently in real time and 3D using a dual-app nucleoside probe.
Nucleic Acids Res., 47:6059-6072, 2019
Cited by
PubMed Abstract: Comprehensive understanding of structure and recognition properties of regulatory nucleic acid elements in real time and atomic level is highly important to devise efficient therapeutic strategies. Here, we report the establishment of an innovative biophysical platform using a dual-app nucleoside analog, which serves as a common probe to detect and correlate different GQ structures and ligand binding under equilibrium conditions and in 3D by fluorescence and X-ray crystallography techniques. The probe (SedU) is composed of a microenvironment-sensitive fluorophore and an excellent anomalous X-ray scatterer (Se), which is assembled by attaching a selenophene ring at 5-position of 2'-deoxyuridine. SedU incorporated into the loop region of human telomeric DNA repeat fluorescently distinguished subtle differences in GQ topologies and enabled quantify ligand binding to different topologies. Importantly, anomalous X-ray dispersion signal from Se could be used to determine the structure of GQs. As the probe is minimally perturbing, a direct comparison of fluorescence data and crystal structures provided structural insights on how the probe senses different GQ conformations without affecting the native fold. Taken together, our dual-app probe represents a new class of tool that opens up new experimental strategies to concurrently investigate nucleic acid structure and recognition in real time and 3D.
PubMed: 31106340
DOI: 10.1093/nar/gkz419
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.3 Å)
Structure validation

237735

数据于2025-06-18公开中

PDB statisticsPDBj update infoContact PDBjnumon