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5JLW

AntpHD with 15bp DNA duplex R-monothioated at Cytidine-8

Summary for 5JLW
Entry DOI10.2210/pdb5jlw/pdb
Related5JLX
DescriptorHomeotic protein antennapedia, DNA (5'-D(*AP*GP*AP*AP*AP*GP*CP*(C7R)P*AP*TP*TP*AP*GP*AP*G)-3'), DNA (5'-D(*TP*CP*TP*CP*TP*AP*AP*TP*GP*GP*CP*TP*TP*TP*C)-3'), ... (6 entities in total)
Functional Keywordshomeodomain, dna-binding protein, complex (homeodomain-dna), transcription-dna complex, transcription regulator-dna complex, monothiolated dna, transcription regulator/dna
Biological sourceDrosophila melanogaster (Fruit fly)
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Total number of polymer chains6
Total formula weight35015.42
Authors
White, M.A.,Zandarashvili, L.,Iwahara, J.,Nguyen, D. (deposition date: 2016-04-27, release date: 2016-06-22, Last modification date: 2023-09-27)
Primary citationNguyen, D.,Zandarashvili, L.,White, M.A.,Iwahara, J.
Stereospecific Effects of Oxygen-to-Sulfur Substitution in DNA Phosphate on Ion Pair Dynamics and Protein-DNA Affinity.
Chembiochem, 17:1636-1642, 2016
Cited by
PubMed Abstract: Oxygen-to-sulfur substitutions in DNA phosphate often enhance affinity for DNA-binding proteins. Our previous studies have suggested that this effect of sulfur substitution of both OP1 and OP2 atoms is due to an entropic gain associated with enhanced ion pair dynamics. In this work, we studied stereospecific effects of single sulfur substitution of either the OP1 or OP2 atom in DNA phosphate at the Lys57 interaction site of the Antennapedia homeodomain-DNA complex. Using crystallography, we obtained structural information on the RP and SP diastereomers of the phosphoromonothioate and their interaction with Lys57. Using fluorescence-based assays, we found significant affinity enhancement upon sulfur substitution of the OP2 atom. Using NMR spectroscopy, we found significant mobilization of the Lys57 side-chain NH3 (+) group upon sulfur substitution of the OP2 atom. These data provide further mechanistic insights into the affinity enhancement by oxygen-to-sulfur substitution in DNA phosphate.
PubMed: 27271797
DOI: 10.1002/cbic.201600265
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.088 Å)
Structure validation

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