In silico analysis of class I adenylate-forming enzymes reveals family and group-specific conservations.

Autor: Clark L; Department of Biology, Franciscan University of Steubenville, Steubenville, OH, United States of America., Leatherby D; Department of Biology, Franciscan University of Steubenville, Steubenville, OH, United States of America., Krilich E; Department of Biology, Franciscan University of Steubenville, Steubenville, OH, United States of America., Ropelewski AJ; Pittsburgh Supercomputing Center, Carnegie Mellon University, Pittsburgh, PA, United States of America., Perozich J; Department of Biology, Franciscan University of Steubenville, Steubenville, OH, United States of America.
Jazyk: angličtina
Zdroj: PloS one [PLoS One] 2018 Sep 04; Vol. 13 (9), pp. e0203218. Date of Electronic Publication: 2018 Sep 04 (Print Publication: 2018).
DOI: 10.1371/journal.pone.0203218
Abstrakt: Luciferases, aryl- and fatty-acyl CoA synthetases, and non-ribosomal peptide synthetase proteins belong to the class I adenylate-forming enzyme superfamily. The reaction catalyzed by the adenylate-forming enzymes is categorized by a two-step process of adenylation and thioesterification. Although all of these proteins perform a similar two-step process, each family may perform the process to yield completely different results. For example, luciferase proteins perform adenylation and oxidation to produce the green fluorescent light found in fireflies, while fatty-acyl CoA synthetases perform adenylation and thioesterification with coenzyme A to assist in metabolic processes involving fatty acids. This study aligned a total of 374 sequences belonging to the adenylate-forming superfamily. Analysis of the sequences revealed five fully conserved residues throughout all sequences, as well as 78 more residues conserved in at least 60% of sequences aligned. Conserved positions are involved in magnesium and AMP binding and maintaining enzyme structure. Also, ten conserved sequence motifs that included most of the conserved residues were identified. A phylogenetic tree was used to assign sequences into nine different groups. Finally, group entropy analysis identified novel conservations unique to each enzyme group. Common group-specific positions identified in multiple groups include positions critical to coordinating AMP and the CoA-bound product, a position that governs active site shape, and positions that help to maintain enzyme structure through hydrogen bonds and hydrophobic interactions. These positions could serve as excellent targets for future research.
Competing Interests: The authors have declared that no competing interests exist.
Databáze: MEDLINE
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