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PMID: 6390433 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Molecular basis of DNA sequence recognition by the catabolite gene activator protein: detailed inferences from three mutations that alter DNA sequence specificity.

Ebright RH, Cossart P, Gicquel-Sanzey B, Beckwith J

Abstract

Previously, we reported that substitution of Glu-181 of the catabolite gene activator protein (CAP) by lysine, leucine, or valine results in a protein that has specificity for A X T base pairs at positions 7 and 16 of the DNA recognition site, rather than G X C base pairs as is the case with the wild-type CAP. In this paper, we deduce from these genetic data both (i) the specific chemical interactions by which amino acid side chains at position 181 interact with base pairs 7 and 16 and (ii) the precise alignment between the structures of the CAP and DNA in the intermolecular CAP-DNA complex. Our analysis supports the idea that the two symmetry-related F alpha-helices of the CAP dimer interact with successive major grooves of right-handed B-type DNA [Pabo, C. & Lewis, M. (1982) Nature (London) 298, 443-447; and Steitz, T., Weber, I. & Matthew, J. (1983) Cold Spring Harbor Symp. Quant. Biol. 47, 419-426].

MeSH Terms
Base Composition Base Sequence DNA, Bacterial/genetics Escherichia coli/genetics Genes Genes, Bacterial Hydrogen Bonding Models, Molecular Mutation Nucleic Acid Conformation Protein Binding Protein Conformation Receptors, Cyclic AMP/genetics
Chemicals
DNA, Bacterial Receptors, Cyclic AMP
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Ebright R H
Cossart P
Gicquel-Sanzey B
Beckwith J
References (35)
35 references, click to expand
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1984-12-00
Pages
7274-8
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC392128
Subset
IM
Grants
NIGMS NIH HHS · GM13017 · United States
NCRR NIH HHS · RR-01032 · United States
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