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FATCAT 2.0:深入理解蛋白质结构多样性

FATCAT 2.0: towards a better understanding of the structural diversity of proteins.

机构信息

Division of Biomedical Sciences, University of California Riverside School of Medicine, Riverside, CA 92521, USA.

Graduate School of Biomedical Sciences, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA 92037, USA.

出版信息

Nucleic Acids Res. 2020 Jul 2;48(W1):W60-W64. doi: 10.1093/nar/gkaa443.

DOI:10.1093/nar/gkaa443
PMID:32469061
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7319568/
Abstract

FATCAT 2.0 server (http://fatcat.godziklab.org/), provides access to a flexible protein structure alignment algorithm developed in our group. In such an alignment, rotations and translations between elements in the structure are allowed to minimize the overall root mean square deviation (RMSD) between the compared structures. This allows to effectively compare protein structures even if they underwent structural rearrangements in different functional forms, different crystallization conditions or as a result of mutations. The major update for the server introduces a new graphical interface, much faster database searches and several new options for visualization of the structural differences between proteins.

摘要

FATCAT 2.0 服务器(http://fatcat.godziklab.org/)提供了我们小组开发的灵活蛋白质结构比对算法的访问权限。在这种比对中,允许结构中元素的旋转和平移,以最小化比较结构之间的整体均方根偏差(RMSD)。这使得即使在不同的功能形式、不同的结晶条件或突变的情况下,也能够有效地比较蛋白质结构。服务器的主要更新引入了一个新的图形界面,更快的数据库搜索以及几个用于蛋白质结构差异可视化的新选项。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d3b/7319568/7df5bc44ec2c/gkaa443fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d3b/7319568/6559a5a78795/gkaa443fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d3b/7319568/7df5bc44ec2c/gkaa443fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d3b/7319568/6559a5a78795/gkaa443fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d3b/7319568/7df5bc44ec2c/gkaa443fig2.jpg

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