Literature DB >> 17649971

ProtSqueeze: simple and effective automated tool for setting up membrane protein simulations.

Semen O Yesylevskyy1.   

Abstract

The major challenge in setting up membrane protein simulations is embedding the protein into the pre-equilibrated lipid bilayer. Several techniques were proposed to achieve optimal packing of the lipid molecules around the protein. However, all of them possess serious disadvantages, which limit their applicability and discourage the users of simulation packages from using them. In the present work, we analyzed existing approaches and proposed a new procedure of protein insertion into the lipid bilayer, which is implemented in the ProtSqueeze software. The advantages of ProtSqueeze are as follows: (1) the insertion algorithm is simple, understandable, and controllable; (2) the software can work with virtually any simulation package on virtually any platform; (3) no modification of the source code of the simulation package is needed; (4) the procedure of insertion is as automated as possible; (5) ProtSqueeze is distributed for free under a general public license. In this work, we present the architecture and the algorithm of ProtSqueeze and demonstrate its usage in case studies.

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Year:  2007        PMID: 17649971     DOI: 10.1021/ci600553y

Source DB:  PubMed          Journal:  J Chem Inf Model        ISSN: 1549-9596            Impact factor:   4.956


  8 in total

1.  An internal water-retention site in the rhomboid intramembrane protease GlpG ensures catalytic efficiency.

Authors:  Yanzi Zhou; Syed M Moin; Sinisa Urban; Yingkai Zhang
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Review 2.  Membrane Packing Problems: A short Review on computational Membrane Modeling Methods and Tools.

Authors:  Björn Sommer
Journal:  Comput Struct Biotechnol J       Date:  2013-04-07       Impact factor: 7.271

3.  Temperature dependence of protein-water interactions in a gated yeast aquaporin.

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Journal:  Sci Rep       Date:  2017-06-21       Impact factor: 4.379

4.  High-resolution experimental and computational electrophysiology reveals weak β-lactam binding events in the porin PorB.

Authors:  Annika Bartsch; Salomé Llabrés; Florian Pein; Christof Kattner; Markus Schön; Manuel Diehn; Mikio Tanabe; Axel Munk; Ulrich Zachariae; Claudia Steinem
Journal:  Sci Rep       Date:  2019-02-04       Impact factor: 4.379

5.  An antibiotic-resistance conferring mutation in a neisserial porin: Structure, ion flux, and ampicillin binding.

Authors:  Annika Bartsch; Callum M Ives; Christof Kattner; Florian Pein; Manuel Diehn; Mikio Tanabe; Axel Munk; Ulrich Zachariae; Claudia Steinem; Salomé Llabrés
Journal:  Biochim Biophys Acta Biomembr       Date:  2021-03-03       Impact factor: 3.747

6.  Rotational Dynamics of The Transmembrane Domains Play an Important Role in Peptide Dynamics of Viral Fusion and Ion Channel Forming Proteins-A Molecular Dynamics Simulation Study.

Authors:  Chia-Wen Wang; Wolfgang B Fischer
Journal:  Viruses       Date:  2022-03-28       Impact factor: 5.818

7.  Modulation of the Neisseria gonorrhoeae drug efflux conduit MtrE.

Authors:  Giulia Tamburrino; Salomé Llabrés; Owen N Vickery; Samantha J Pitt; Ulrich Zachariae
Journal:  Sci Rep       Date:  2017-12-06       Impact factor: 4.379

8.  In silico assessment of the conduction mechanism of the Ryanodine Receptor 1 reveals previously unknown exit pathways.

Authors:  Leonard P Heinz; Wojciech Kopec; Bert L de Groot; Rainer H A Fink
Journal:  Sci Rep       Date:  2018-05-02       Impact factor: 4.379

  8 in total

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