ISSN:
0192-8651
Keywords:
protein structure prediction
;
united-residue representation of a polypeptide chain
;
potential of mean force
;
inverse folding
;
Z-score
;
Chemistry
;
Theoretical, Physical and Computational Chemistry
Source:
Wiley InterScience Backfile Collection 1832-2000
Topics:
Chemistry and Pharmacology
,
Computer Science
Notes:
Continuing our work on the determination of an off-lattice united-residue force field for protein-structure simulations, we determined and parameterized appropriate functional forms for the local-interaction terms, corresponding to the rotation about the virtual bonds (Utor), the bending of virtual-bond angles (Ub), and the energy of different rotameric states of side chains (Urot). These terms were determined by applying the Boltzmann principle to the distributions of virtual-bond torsional and virtual-bond angles and side-chain rotameric states, respectively, calculated from a data base of 195 high-resolution nonhomologous proteins. The complete energy function was constructed by combining the individual energy terms with appropriate weights. The weights were determined by optimizing the so-called Z-score value (which is the normalized difference between the energy of the native structure and the mean energy of non-native structures) of the histidine-containing phosphocarrier protein from Streptococcus faecalis (1PTF; an 88-residue α + β protein). To accomplish this, a database of Cα patterns was created using high-resolution nonhomologous protein structures from the Protein Data Bank, and the distributions of energy components of 1PTF were obtained by threading its sequence through ∼500 randomly chosen Cα-patterns from the X-ray structures in the PDB, followed by energy minimization, with the energy function incorporating initially guessed weights. The resulting minimized energies were used to optimize the Z-score value of 1PTF as a function of the weights of the various energy terms, and the new weights were used to generate new energy-component distributions. The process was iterated, until the weights used to generate the distributions and the optimized weights were self-consistent. The potential function with the weights of the various energy terms obtained by optimizing the Z-score value for 1PTF was found to locate the native structures of other test proteins (within an average RMS deviation of 3 Å): calcium-binding protein (4ICB), ubiquitin (1UBQ), α-spectrin (1SHG), major cold-shock protein (1MJC), and cytochrome b5 (3B5C) (which included α and β structures) as distinctively lowest in energy in similar threading experiments. © 1997 by John Wiley & Sons, Inc. J Comput Chem 18: 874-887, 1997
Additional Material:
5 Ill.
Type of Medium:
Electronic Resource
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