Abstract
Confined by the Boltzmann distribution of the energies of the states, a multitude of structural states are inherent to biomolecules. For a detailed understanding of a protein's function, its entire structural landscape at atomic resolution and insight into the interconversion between all the structural states (i.e. dynamics) are required. Whereas dedicated trickery with NMR relaxation provides aspects of local dynamics, and 3D structure determination by NMR is well established, only recently have several attempts been made to formulate a more comprehensive description of the dynamics and the structural landscape of a protein. Here, a perspective is given on the use of exact NOEs (eNOEs) for the elucidation of structural ensembles of a protein describing the covered conformational space.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 53-59 |
| Number of pages | 7 |
| Journal | Journal of Magnetic Resonance |
| Volume | 241 |
| Issue number | 1 |
| DOIs | |
| State | Published - Apr 2014 |
| Externally published | Yes |
Keywords
- Biological macromolecules
- Correlated dynamics
- Dynamics
- eNOE
- NMR
- NOE
- Nuclear Overhauser effect
- Proteins
- Structure calculation
- Structure ensemble
ASJC Scopus subject areas
- Biophysics
- Biochemistry
- Nuclear and High Energy Physics
- Condensed Matter Physics
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