Literature DB >> 22819817

In silico identification of catalytic residues and domain fold of the family GH119 sharing the catalytic machinery with the α-amylase family GH57.

Stefan Janeček1, Andrea Kuchtová.   

Abstract

The glycoside hydrolase family 119 (GH119) contains the α-amylase from Bacillus circulans and five other hypothetical proteins. Until now, nothing has been reported on the catalytic residues and catalytic-domain fold of GH119. Based on a detailed in silico analysis involving sequence comparison in combination with BLAST searches and structural modelling, an unambiguous relationship was revealed between the families GH119 and GH57. This includes sharing the catalytic residues, i.e. Glu231 and Asp373 as catalytic nucleophile and proton donor, respectively, in the predicted catalytic (β/α)(7)-barrel domain of GH119 B. circulans α-amylase. The GH57 and GH119 families may thus define a new CAZy clan.
Copyright © 2012 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22819817     DOI: 10.1016/j.febslet.2012.07.020

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  11 in total

Review 1.  Aspects and Recent Trends in Microbial α-Amylase: a Review.

Authors:  Jai Shankar Paul; Nisha Gupta; Esmil Beliya; Shubhra Tiwari; Shailesh Kumar Jadhav
Journal:  Appl Biochem Biotechnol       Date:  2021-03-14       Impact factor: 2.926

Review 2.  α-Amylase: an enzyme specificity found in various families of glycoside hydrolases.

Authors:  Štefan Janeček; Birte Svensson; E Ann MacGregor
Journal:  Cell Mol Life Sci       Date:  2013-06-27       Impact factor: 9.261

Review 3.  Remarkable evolutionary relatedness among the enzymes and proteins from the α-amylase family.

Authors:  Štefan Janeček; Marek Gabriško
Journal:  Cell Mol Life Sci       Date:  2016-05-06       Impact factor: 9.261

4.  A new GH13 subfamily represented by the α-amylase from the halophilic archaeon Haloarcula hispanica.

Authors:  Štefan Janeček; Barbora Zámocká
Journal:  Extremophiles       Date:  2019-11-16       Impact factor: 2.395

5.  A putative novel starch-binding domain revealed by in silico analysis of the N-terminal domain in bacterial amylomaltases from the family GH77.

Authors:  Filip Mareček; Marie Sofie Møller; Birte Svensson; Štefan Janeček
Journal:  3 Biotech       Date:  2021-04-21       Impact factor: 2.406

6.  Phylogenomic relationships between amylolytic enzymes from 85 strains of fungi.

Authors:  Wanping Chen; Ting Xie; Yanchun Shao; Fusheng Chen
Journal:  PLoS One       Date:  2012-11-15       Impact factor: 3.240

7.  Aspergillus Oryzae S2 α-Amylase Domain C Involvement in Activity and Specificity: In Vivo Proteolysis, Molecular and Docking Studies.

Authors:  Mouna Sahnoun; Sonia Jemli; Sahar Trabelsi; Leila Ayadi; Samir Bejar
Journal:  PLoS One       Date:  2016-04-21       Impact factor: 3.240

8.  Complete Genome of the Starch-Degrading Myxobacteria Sandaracinus amylolyticus DSM 53668T.

Authors:  Gaurav Sharma; Indu Khatri; Srikrishna Subramanian
Journal:  Genome Biol Evol       Date:  2016-08-29       Impact factor: 3.416

9.  A new group of glycoside hydrolase family 13 α-amylases with an aberrant catalytic triad.

Authors:  Fean D Sarian; Štefan Janeček; Tjaard Pijning; Zeily Nurachman; Ocky K Radjasa; Lubbert Dijkhuizen; Dessy Natalia; Marc J E C van der Maarel
Journal:  Sci Rep       Date:  2017-03-13       Impact factor: 4.379

10.  In silico analysis of the α-amylase family GH57: eventual subfamilies reflecting enzyme specificities.

Authors:  Mária Martinovičová; Štefan Janeček
Journal:  3 Biotech       Date:  2018-07-09       Impact factor: 2.406

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.