Sousa Filipa L, Parente Daniel J, Shis David L, Hessman Jacob A, Chazelle Allen, Bennett Matthew R, Teichmann Sarah A, Swint-Kruse Liskin
Institute of Molecular Evolution, Heinrich-Heine Universität Düsseldorf, Universitätstrasse 1, 40225 Düsseldorf, Germany.
Department of Biochemistry and Molecular Biology, University of Kansas Medical Center, Kansas City, KS 66160, USA.
J Mol Biol. 2016 Feb 22;428(4):671-678. doi: 10.1016/j.jmb.2015.09.015. Epub 2015 Sep 25.
Protein families evolve functional variation by accumulating point mutations at functionally important amino acid positions. Homologs in the LacI/GalR family of transcription regulators have evolved to bind diverse DNA sequences and allosteric regulatory molecules. In addition to playing key roles in bacterial metabolism, these proteins have been widely used as a model family for benchmarking structural and functional prediction algorithms. We have collected manually curated sequence alignments for >3000 sequences, in vivo phenotypic and biochemical data for >5750 LacI/GalR mutational variants, and noncovalent residue contact networks for 65 LacI/GalR homolog structures. Using this rich data resource, we compared the noncovalent residue contact networks of the LacI/GalR subfamilies to design and experimentally validate an allosteric mutant of a synthetic LacI/GalR repressor for use in biotechnology. The AlloRep database (freely available at www.AlloRep.org) is a key resource for future evolutionary studies of LacI/GalR homologs and for benchmarking computational predictions of functional change.
蛋白质家族通过在功能重要的氨基酸位置积累点突变来进化功能变异。转录调节因子LacI/GalR家族中的同源物已经进化到能够结合多种DNA序列和变构调节分子。除了在细菌代谢中发挥关键作用外,这些蛋白质还被广泛用作基准结构和功能预测算法的模型家族。我们已经收集了超过3000个序列的人工整理序列比对、超过5750个LacI/GalR突变变体的体内表型和生化数据,以及65个LacI/GalR同源结构的非共价残基接触网络。利用这一丰富的数据资源,我们比较了LacI/GalR亚家族的非共价残基接触网络,以设计并通过实验验证一种用于生物技术的合成LacI/GalR阻遏物的变构突变体。AlloRep数据库(可在www.AlloRep.org免费获取)是未来LacI/GalR同源物进化研究以及功能变化计算预测基准测试的关键资源。