Literature DB >> 16737770

Low-frequency normal modes in horse liver alcohol dehydrogenase and motions of residues involved in the enzymatic reaction.

Jia Luo1, Thomas C Bruice.   

Abstract

Normal mode analysis using the elastic network model has provided characteristics and directions of the low-frequency large domain motions of horse liver alcohol dehydrogenase. Three normal modes (mode 1, mode 7, and mode 8) were identified as representative domain motions that may promote the onset of Near Attack Conformers or facilitate the product to be released. The pattern of the atomic displacement for some key residues (such as Val292 and Val203) revealed in this study is in line with experimental structural and kinetic studies and theoretical simulations.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16737770     DOI: 10.1016/j.bpc.2006.05.009

Source DB:  PubMed          Journal:  Biophys Chem        ISSN: 0301-4622            Impact factor:   2.352


  7 in total

1.  Atomic-resolution structures of horse liver alcohol dehydrogenase with NAD(+) and fluoroalcohols define strained Michaelis complexes.

Authors:  Bryce V Plapp; S Ramaswamy
Journal:  Biochemistry       Date:  2012-05-01       Impact factor: 3.162

Review 2.  Hydrogen tunneling in enzymes and biomimetic models.

Authors:  Joshua P Layfield; Sharon Hammes-Schiffer
Journal:  Chem Rev       Date:  2013-12-20       Impact factor: 60.622

3.  Contribution of buried distal amino acid residues in horse liver alcohol dehydrogenase to structure and catalysis.

Authors:  Karthik K Shanmuganatham; Rachel S Wallace; Ann Ting-I Lee; Bryce V Plapp
Journal:  Protein Sci       Date:  2018-01-25       Impact factor: 6.725

Review 4.  Conformational changes and catalysis by alcohol dehydrogenase.

Authors:  Bryce V Plapp
Journal:  Arch Biochem Biophys       Date:  2009-07-05       Impact factor: 4.013

5.  Hydride Transfer Mechanism of Enzymatic Sugar Nucleotide C2 Epimerization Probed with a Loose-Fit CDP-Glucose Substrate.

Authors:  Christian Rapp; Bernd Nidetzky
Journal:  ACS Catal       Date:  2022-05-25       Impact factor: 13.700

6.  Dependence of crystallographic atomic displacement parameters on temperature (25-150 K) for complexes of horse liver alcohol dehydrogenase.

Authors:  Bryce V Plapp; Lokesh Gakhar; Ramaswamy Subramanian
Journal:  Acta Crystallogr D Struct Biol       Date:  2022-09-27       Impact factor: 5.699

7.  Effects of cavities at the nicotinamide binding site of liver alcohol dehydrogenase on structure, dynamics and catalysis.

Authors:  Atsushi Yahashiri; Jon K Rubach; Bryce V Plapp
Journal:  Biochemistry       Date:  2014-01-30       Impact factor: 3.162

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.