Protein Backbone <sup>1</sup>H<sup>N</sup>−<sup>13</sup>C<sup>α</sup> and <sup>15</sup>N−<sup>13</sup>C<sup>α</sup> Residual Dipolar and <i>J</i> Couplings:  New Constraints for NMR Structure Determination

Keyang Ding, Angela M. Gronenborn

Journal of the American Chemical Society · 2004 · 49 citations · 14 references

Concepts

Abstract

A simple, sensitivity-enhanced experiment was devised for accurate measurement of backbone 15N-13Calpha and 1HN-13Calpha couplings in proteins. The measured residual dipolar couplings 2DHCA, 1DNCA, 3DHCA, and 2DNCA for protein GB1 display very good agreement with the refined NMR structure (PDB code: 3GB1). A Karplus-type relationship between the one-bond 1JNCA couplings and the backbone dihedral psi angles holds, and on the basis of the two-bond 2JNCA couplings a secondary structure index can be established.

References

14