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Characterisation of the effect of electrostatic interaction on the structure of Trp-cage using molecular dynamics simulation
- Source :
- Molecular Simulation. 36:1086-1095
- Publication Year :
- 2010
- Publisher :
- Informa UK Limited, 2010.
-
Abstract
- A mutated variant of 20 amino acid miniprotein Trp-cage (TC5b), called TC5c (Asp9 replaced by Asn9), was designed to demonstrate the effect of a salt bridge. As a result of strong electrostatic interaction, the distance distribution between Asp9 and Arg16 exhibited a larger probability in the range of the salt bridge for TC5b compared to TC5c. The probability of α-helix formation for residues 3–8, as well as for residues 11–14, was high for TC5b. The salt bridge formation between Asp9 and Arg16 in TC5b was indicated by (a) a strong correlation of their distance of separation with the subtended angle with the centre and (b) a step decrease in the distance between Gly11O and Arg16H at 12 ns. Replica exchange molecular dynamics simulation at different temperatures in the range of 270–590 K indicated that the average distance between Asp9 and Arg16, end-to-end distance, root mean square deviation with respect to a reference NMR structure of TC5b did not change significantly with temperature below 370 K for TC...
- Subjects :
- Range (particle radiation)
Chemistry
General Chemical Engineering
Subtended angle
General Chemistry
Salt bridge (protein and supramolecular)
Condensed Matter Physics
Crystallography
Molecular dynamics
Modeling and Simulation
General Materials Science
Protein folding
Cage
Root-mean-square deviation
Information Systems
Electrostatic interaction
Subjects
Details
- ISSN :
- 10290435 and 08927022
- Volume :
- 36
- Database :
- OpenAIRE
- Journal :
- Molecular Simulation
- Accession number :
- edsair.doi...........eb078e08cb4699ab98e561c50a5f573a
- Full Text :
- https://doi.org/10.1080/08927022.2010.504774