|
|
||||||||
Department of Biochemistry and Biophysics, School of Medicine, University of North Carolina, Chapel Hill, North Carolina 27599-7260, USA
Reprint requests to: Jan Hermans, Department of Biochemistry and Biophysics, University of North Carolina, Chapel Hill, NC 27599-7260, USA; e-mail: hermans{at}med.unc.edu; fax: (919) 843-9244.
We analyze packing imperfections in globular proteins as reflected in deviations of torsion angles from the equilibrium values for the isolated side chains. The distribution of conformations of methionine and lysine residues in a database of high-resolution structures is compared with energies of model compounds calculated with high-level quantum-mechanics. The distribution of the CC and CS torsion angles (
3) correlates well with the Boltzmann factor of the torsion energy, exp(-ßE) of the model compounds C2H5C2H5 and C2H5SCH3. An exponential relation was again found between the relative occurrence of g+, g- and t conformations for C
Cß bonds in long side chains and the energy differences of rotamers of
-amino n-butyric acid, when dependence on backbone conformation was taken into account. The distribution of all 27 rotamers of methionine was correlated with the energy differences between the models rotamers, corrected for clashes with nearby residues, the correlation being good for a set with backbone in the ß-conformation, but less clear for backbone
-conformation. In all correlations, the value of the coefficient ß corresponds to a temperature of circa 300 K. These results can be interpreted with a model that considers the structure of a folded protein as resulting from packing imperfectly complementary parts, with a requirement of an overall low energy. Compromises are required to optimize the fit of nonbonded contacts with surrounding groups, and side chains assume conformations away from the energy minimum. An exponential distribution is a most probable distribution, and this can be established easily under conditions other than thermal equilibrium.
Keywords: Torsion angle distribution; relation between distribution and energy; Boltzmann-type distribution; exponential distribution; methionine side chains; small molecules as models
![]()
CiteULike
Connotea
Del.icio.us
Digg
Reddit
Technorati What's this?
This article has been cited by other articles:
![]() |
M. Persson, J. A. Letts, B. Hosseini-Maaf, S. N. Borisova, M. M. Palcic, S. V. Evans, and M. L. Olsson Structural Effects of Naturally Occurring Human Blood Group B Galactosyltransferase Mutations Adjacent to the DXD Motif J. Biol. Chem., March 30, 2007; 282(13): 9564 - 9570. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. Avbelj, S. G. Grdadolnik, J. Grdadolnik, and R. L. Baldwin Intrinsic backbone preferences are fully present in blocked amino acids PNAS, January 31, 2006; 103(5): 1272 - 1277. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. J. Fleming and G. D. Rose Do all backbone polar groups in proteins form hydrogen bonds? Protein Sci., July 1, 2005; 14(7): 1911 - 1917. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. Avbelj and R. L. Baldwin Origin of the neighboring residue effect on peptide backbone conformation PNAS, July 27, 2004; 101(30): 10967 - 10972. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |