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PDBsum entry 4ond

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Top Page protein dna_rna metals Protein-protein interface(s) links
Transcription/DNA PDB id
4ond
Contents
Protein chains
72 a.a.
DNA/RNA
Metals
_ZN ×8
Waters ×132

References listed in PDB file
Key reference
Title Evolution of DNA specificity in a transcription factor family produced a new gene regulatory module.
Authors A.N.Mckeown, J.T.Bridgham, D.W.Anderson, M.N.Murphy, E.A.Ortlund, J.W.Thornton.
Ref. Cell, 2014, 159, 58-68. [DOI no: 10.1016/j.cell.2014.09.003]
PubMed id 25259920
Abstract
Complex gene regulatory networks require transcription factors (TFs) to bind distinct DNA sequences. To understand how novel TF specificity evolves, we combined phylogenetic, biochemical, and biophysical approaches to interrogate how DNA recognition diversified in the steroid hormone receptor (SR) family. After duplication of the ancestral SR, three mutations in one copy radically weakened binding to the ancestral estrogen response element (ERE) and improved binding to a new set of DNA sequences (steroid response elements, SREs). They did so by establishing unfavorable interactions with ERE and abolishing unfavorable interactions with SRE; also required were numerous permissive substitutions, which nonspecifically improved cooperativity and affinity of DNA binding. Our findings indicate that negative determinants of binding play key roles in TFs' DNA selectivity and-with our prior work on the evolution of SR ligand specificity during the same interval-show how a specific new gene regulatory module evolved without interfering with the integrity of the ancestral module.
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