Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1981 Apr;78(4):2213-7.
doi: 10.1073/pnas.78.4.2213.

Molecuar model of the DNA interaction site for the cyclic AMP receptor protein

Molecuar model of the DNA interaction site for the cyclic AMP receptor protein

M C O'Neill et al. Proc Natl Acad Sci U S A. 1981 Apr.

Abstract

A topological model of the DNA binding site for the cyclic AMP receptor protein (CRP) is presented. A consensus sequence drawn from the known CRP binding sites has several symmetrical subregions that are spatially resolved onto different faces of the DNA helix. Consideration of available biochemical and genetic data suggest one particular choice among the possible symmetrical arrangements. In this case, the sequence of its helical form presents nearly the same pattern of exposed base pairs on two faces of the helix. These two faces are separated by a helix angle of 72 degrees; the similar sequences that are exposed in the grooves occur in opposite orientations on the two faces. We propose that this inverted symmetry arrangement provides each of the identical subunits of the CRP with a similar recognition region within the overall site. In gal and ara, the site appears to accommodate a single molecule of the CRP; in lac, the site repeats the symmetrical arrangement and should accommodate two molecules of the CRP.

PubMed Disclaimer

References

    1. J Biol Chem. 1969 Nov 10;244(21):5828-35 - PubMed
    1. Proc Natl Acad Sci U S A. 1970 Jun;66(2):480-7 - PubMed
    1. Annu Rev Biochem. 1974;43(0):721-75 - PubMed
    1. Nature. 1975 Aug 21;256(5519):672-4 - PubMed
    1. J Mol Biol. 1976 Jul 5;104(3):557-66 - PubMed

Publication types