Literature DB >> 17085431

Dividing the large glycoside hydrolase family 13 into subfamilies: towards improved functional annotations of alpha-amylase-related proteins.

Mark R Stam1, Etienne G J Danchin, Corinne Rancurel, Pedro M Coutinho, Bernard Henrissat.   

Abstract

Family GH13, also known as the alpha-amylase family, is the largest sequence-based family of glycoside hydrolases and groups together a number of different enzyme activities and substrate specificities acting on alpha-glycosidic bonds. This polyspecificity results in the fact that the simple membership of this family cannot be used for the prediction of gene function based on sequence alone. In order to establish robust groups that show an improved correlation between sequence and enzymatic specificity, we have performed a large-scale analysis of 1691 family GH13 sequences by combining clustering, similarity search and phylogenetic methods. About 80% of the sequences could be reliably classified into 35 subfamilies. Most subfamilies appear monofunctional (i.e. contain enzymes with the same substrate and the same product). The close examination of the other, apparently polyspecific, subfamilies revealed that they actually group together enzymes with strongly related (or even sometimes virtually identical) activities. Overall our subfamily assignment allows to set the limits for genomic function prediction on this large family of biologically and industrially important enzymes.

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Year:  2006        PMID: 17085431     DOI: 10.1093/protein/gzl044

Source DB:  PubMed          Journal:  Protein Eng Des Sel        ISSN: 1741-0126            Impact factor:   1.650


  162 in total

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2.  Cloning and characterization of two new thermostable and alkalitolerant α-amylases from the Anoxybacillus species that produce high levels of maltose.

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3.  Sequence fingerprints of enzyme specificities from the glycoside hydrolase family GH57.

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4.  Thermus thermophilus glycoside hydrolase family 57 branching enzyme: crystal structure, mechanism of action, and products formed.

Authors:  Marta Palomo; Tjaard Pijning; Thijs Booiman; Justyna M Dobruchowska; Jeroen van der Vlist; Slavko Kralj; Antoni Planas; Katja Loos; Johannis P Kamerling; Bauke W Dijkstra; Marc J E C van der Maarel; Lubbert Dijkhuizen; Hans Leemhuis
Journal:  J Biol Chem       Date:  2010-11-19       Impact factor: 5.157

5.  Characterization of maltase clusters in the genus Drosophila.

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Journal:  J Mol Evol       Date:  2010-11-17       Impact factor: 2.395

6.  Structural insight into the bifunctional mechanism of the glycogen-debranching enzyme TreX from the archaeon Sulfolobus solfataricus.

Authors:  Eui-Jeon Woo; Seungjae Lee; Hyunju Cha; Jong-Tae Park; Sei-Mee Yoon; Hyung-Nam Song; Kwan-Hwa Park
Journal:  J Biol Chem       Date:  2008-08-14       Impact factor: 5.157

7.  Novel Maltogenic Amylase CoMA from Corallococcus sp. Strain EGB Catalyzes the Conversion of Maltooligosaccharides and Soluble Starch to Maltose.

Authors:  Jie Zhou; Zhoukun Li; Han Zhang; Jiale Wu; Xianfeng Ye; Weiliang Dong; Min Jiang; Yan Huang; Zhongli Cui
Journal:  Appl Environ Microbiol       Date:  2018-07-02       Impact factor: 4.792

8.  Role of glycoside phosphorylases in mannose foraging by human gut bacteria.

Authors:  Simon Ladevèze; Laurence Tarquis; Davide A Cecchini; Juliette Bercovici; Isabelle André; Christopher M Topham; Sandrine Morel; Elisabeth Laville; Pierre Monsan; Vincent Lombard; Bernard Henrissat; Gabrielle Potocki-Véronèse
Journal:  J Biol Chem       Date:  2013-09-16       Impact factor: 5.157

9.  An alpha-amylase is a novel receptor for Bacillus thuringiensis ssp. israelensis Cry4Ba and Cry11Aa toxins in the malaria vector mosquito Anopheles albimanus (Diptera: Culicidae).

Authors:  Maria Teresa Fernandez-Luna; Humberto Lanz-Mendoza; Sarjeet S Gill; Alejandra Bravo; Mario Soberon; Juan Miranda-Rios
Journal:  Environ Microbiol       Date:  2009-12-04       Impact factor: 5.491

10.  Introduction of novel thermostable α-amylases from genus Anoxybacillus and proposing to group the Bacillaceae related α-amylases under five individual GH13 subfamilies.

Authors:  Arzu Coleri Cihan; Emine Derebay Yildiz; Ergin Sahin; Ozal Mutlu
Journal:  World J Microbiol Biotechnol       Date:  2018-06-15       Impact factor: 3.312

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