pKa Calculations of Key Ionizable Protein Residues in Acetylcholinesterase

Investor logo

Warning

This publication doesn't include Faculty of Education. It includes Faculty of Science. Official publication website can be found on muni.cz.
Authors

WIESNER Jiří KŘÍŽ Zdeněk KOČA Jaroslav

Year of publication 2010
Type Article in Proceedings
Conference UF5 - Book of Contributions
MU Faculty or unit

Faculty of Science

Citation
Web http://indico.cern.ch/conferenceDisplay.py?confId=69338%20[+]
Field Physical chemistry and theoretical chemistry
Description One of the most abundant quantities characterising proteins is its isoelectric point, which is directly dependent on the number of charged ionizable residues, on the pKa of all ionizable residues more exactly. In this work, the pKa of buried protein aminoacids are estimated using method based on molecular dynamics called thermodynamic integration. The main scope is to compute pKa in acetylcholinesterase, but the computations on a small protein, thioredoxin, will be also presented as benchmark calculations.
Related projects:

You are running an old browser version. We recommend updating your browser to its latest version.