Origin of pKa Shifts of Internal Lysine Residues in SNase Studied Via Equal-Molar VMMS Simulations in Explicit Water-Reference-Cited by-同舟云学术

Origin of pKa Shifts of Internal Lysine Residues in SNase Studied Via Equal-Molar VMMS Simulations in Explicit Water

Published:2016-10-18 Issue:15 Volume:121 Page:3318-3330
ISSN:1520-6106
Container-title:The Journal of Physical Chemistry B
language:en
Short-container-title:J. Phys. Chem. B

Author:

Wu Xiongwu¹,Lee Juyong¹,Brooks Bernard R.¹

Affiliation:

1. Laboratory of Computational Biology, National Heart, Lung, and Blood Institute (NHLBI), National Institutes of Health (NIH), Bethesda, Maryland 20892, United States

Funder

National Heart, Lung, and Blood Institute

Publisher

American Chemical Society (ACS)

Subject

Materials Chemistry,Surfaces, Coatings and Films,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.jpcb.6b08249

Reference97 articles.

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3. Structural Changes in Bacteriorhodopsin During Ion Transport at 2 Angstrom Resolution

4. Structure and dynamics of hydronium in the ion channel gramicidin A

5. The pKa of the General Acid/Base Carboxyl Group of a Glycosidase Cycles during Catalysis: A 13C-NMR Study of Bacillus circulans Xylanase

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