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8PN4

transcription factor BARHL2 bound to DNA sequences

Summary for 8PN4
Entry DOI10.2210/pdb8pn4/pdb
Related8PM5 8PM7 8PMC 8PMF 8PMV 8PNA 8PNC
DescriptorBarH-like 2 homeobox protein, DNA, ACETATE ION, ... (5 entities in total)
Functional Keywordstranscription, transcription factor, dna-binding, protein-dna complex, dna-binding domain
Biological sourceHomo sapiens (human)
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Total number of polymer chains13
Total formula weight66909.67
Authors
Morgunova, E.,Yin, Y.,Popov, A.,Taipale, J. (deposition date: 2023-06-29, release date: 2024-07-10, Last modification date: 2025-01-15)
Primary citationMorgunova, E.,Nagy, G.,Yin, Y.,Zhu, F.,Nayak, S.P.,Xiao, T.,Sokolov, I.,Popov, A.,Laughton, C.,Grubmuller, H.,Taipale, J.
Interfacial water confers transcription factors with dinucleotide specificity.
Nat.Struct.Mol.Biol., 2025
Cited by
PubMed Abstract: Transcription factors (TFs) recognize specific bases within their DNA-binding motifs, with each base contributing nearly independently to total binding energy. However, the energetic contributions of particular dinucleotides can deviate strongly from the additive approximation, indicating that some TFs can specifically recognize DNA dinucleotides. Here we solved high-resolution (<1 Å) structures of MYF5 and BARHL2 bound to DNAs containing sets of dinucleotides that have different affinities to the proteins. The dinucleotides were recognized either enthalpically, by an extensive water network that connects the adjacent bases to the TF, or entropically, by a hydrophobic patch that maintained interfacial water mobility. This mechanism confers differential temperature sensitivity to the optimal sites, with implications for thermal regulation of gene expression. Our results uncover the enigma of how TFs can recognize more complex local features than mononucleotides and demonstrate that water-mediated recognition is important for predicting affinities of macromolecules from their sequence.
PubMed: 39753777
DOI: 10.1038/s41594-024-01449-6
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.6 Å)
Structure validation

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