Literature DB >> 34727710

Ancestral sequences of a large promiscuous enzyme family correspond to bridges in sequence space in a network representation.

Patrick C F Buchholz1, Bert van Loo2,3, Bernard D G Eenink3, Erich Bornberg-Bauer3,4, Jürgen Pleiss1.   

Abstract

Evolutionary relationships of protein families can be characterized either by networks or by trees. Whereas trees allow for hierarchical grouping and reconstruction of the most likely ancestral sequences, networks lack a time axis but allow for thresholds of pairwise sequence identity to be chosen and, therefore, the clustering of family members with presumably more similar functions. Here, we use the large family of arylsulfatases and phosphonate monoester hydrolases to investigate similarities, strengths and weaknesses in tree and network representations. For varying thresholds of pairwise sequence identity, values of betweenness centrality and clustering coefficients were derived for nodes of the reconstructed ancestors to measure the propensity to act as a bridge in a network. Based on these properties, ancestral protein sequences emerge as bridges in protein sequence networks. Interestingly, many ancestral protein sequences appear close to extant sequences. Therefore, reconstructed ancestor sequences might also be interpreted as yet-to-be-identified homologues. The concept of ancestor reconstruction is compared to consensus sequences, too. It was found that hub sequences in a network, e.g. reconstructed ancestral sequences that are connected to many neighbouring sequences, share closer similarity with derived consensus sequences. Therefore, some reconstructed ancestor sequences can also be interpreted as consensus sequences.

Entities:  

Keywords:  ancestor reconstruction; consensus sequence; network biology; phylogeny; protein evolution

Mesh:

Substances:

Year:  2021        PMID: 34727710      PMCID: PMC8564622          DOI: 10.1098/rsif.2021.0389

Source DB:  PubMed          Journal:  J R Soc Interface        ISSN: 1742-5662            Impact factor:   4.118


  61 in total

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Review 2.  Enzyme promiscuity: a mechanistic and evolutionary perspective.

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3.  A minimal sequence code for switching protein structure and function.

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4.  Balancing Specificity and Promiscuity in Enzyme Evolution: Multidimensional Activity Transitions in the Alkaline Phosphatase Superfamily.

Authors:  Bert van Loo; Christopher D Bayer; Gerhard Fischer; Stefanie Jonas; Eugene Valkov; Mark F Mohamed; Anastassia Vorobieva; Celine Dutruel; Marko Hyvönen; Florian Hollfelder
Journal:  J Am Chem Soc       Date:  2018-12-20       Impact factor: 15.419

5.  Natural selection and the concept of a protein space.

Authors:  J M Smith
Journal:  Nature       Date:  1970-02-07       Impact factor: 49.962

6.  A general method applicable to the search for similarities in the amino acid sequence of two proteins.

Authors:  S B Needleman; C D Wunsch
Journal:  J Mol Biol       Date:  1970-03       Impact factor: 5.469

7.  Matching the Diversity of Sulfated Biomolecules: Creation of a Classification Database for Sulfatases Reflecting Their Substrate Specificity.

Authors:  Tristan Barbeyron; Loraine Brillet-Guéguen; Wilfrid Carré; Cathelène Carrière; Christophe Caron; Mirjam Czjzek; Mark Hoebeke; Gurvan Michel
Journal:  PLoS One       Date:  2016-10-17       Impact factor: 3.240

8.  Historical contingency and its biophysical basis in glucocorticoid receptor evolution.

Authors:  Michael J Harms; Joseph W Thornton
Journal:  Nature       Date:  2014-06-15       Impact factor: 49.962

9.  Database resources of the National Center for Biotechnology Information.

Authors: 
Journal:  Nucleic Acids Res       Date:  2015-11-28       Impact factor: 16.971

10.  Structural and Mechanistic Analysis of the Choline Sulfatase from Sinorhizobium melliloti: A Class I Sulfatase Specific for an Alkyl Sulfate Ester.

Authors:  Bert van Loo; Markus Schober; Eugene Valkov; Magdalena Heberlein; Erich Bornberg-Bauer; Kurt Faber; Marko Hyvönen; Florian Hollfelder
Journal:  J Mol Biol       Date:  2018-02-17       Impact factor: 5.469

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