| Autor: |
Liu Y; Department of Chemistry & Chemical Biology, McMaster University, Hamilton, Ontario, Canada., Patel AHG; Department of Chemistry & Chemical Biology, McMaster University, Hamilton, Ontario, Canada., Burger SK; Department of Chemistry & Chemical Biology, McMaster University, Hamilton, Ontario, Canada., Ayers PW; Department of Chemistry & Chemical Biology, McMaster University, Hamilton, Ontario, Canada. ayers@mcmaster.ca. |
| Jazyk: |
angličtina |
| Zdroj: |
Journal of molecular modeling [J Mol Model] 2017 May; Vol. 23 (5), pp. 155. Date of Electronic Publication: 2017 Apr 05. |
| DOI: |
10.1007/s00894-017-3324-x |
| Abstrakt: |
Three different pK a prediction methods were used to calculate the pK a of Lys115 in acetoacetate decarboxylase (AADase): the empirical method PROPKA, the multiconformation continuum electrostatics (MCCE) method, and the molecular dynamics/thermodynamic integration (MD/TI) method with implicit solvent. As expected, accurate pK a prediction of Lys115 depends on the protonation patterns of other ionizable groups, especially the nearby Glu76. However, since the prediction methods do not explicitly sample the protonation patterns of nearby residues, this must be done manually. When Glu76 is deprotonated, all three methods give an incorrect pK a value for Lys115. If protonated, Glu76 is used in an MD/TI calculation, the pK a of Lys115 is predicted to be 5.3, which agrees well with the experimental value of 5.9. This result agrees with previous site-directed mutagenesis studies, where the mutation of Glu76 (negative charge when deprotonated) to Gln (neutral) causes no change in K m , suggesting that Glu76 has no effect on the pK a shift of Lys115. Thus, we postulate that the pK a of Glu76 is also shifted so that Glu76 is protonated (neutral) in AADase. Graphical abstract Simulated abundances of protonated species as pH is varied. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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