Prediction and characterization of enzymatic activities guided by sequence similarity and genome neighborhood networks

Author:

Zhao Suwen1,Sakai Ayano2,Zhang Xinshuai2,Vetting Matthew W3,Kumar Ritesh2,Hillerich Brandan3,San Francisco Brian2,Solbiati Jose2,Steves Adam4,Brown Shoshana4,Akiva Eyal4,Barber Alan4,Seidel Ronald D3,Babbitt Patricia C4,Almo Steven C3,Gerlt John A256,Jacobson Matthew P1

Affiliation:

1. Department of Pharmaceutical Chemistry, University of California, San Francisco, San Francisco, United States

2. Institute for Genomic Biology, University of Illinois at Urbana-Champaign, Urbana, United States

3. Department of Biochemistry, Albert Einstein College of Medicine, New York, United States

4. Department of Bioengineering and Therapeutic Sciences, University of California, San Francisco, San Francisco, United States

5. Department of Biochemistry, University of Illinois at Urbana-Champaign, Urbana, United States

6. Department of Chemistry, University of Illinois at Urbana-Champaign, Urbana, United States

Abstract

Metabolic pathways in eubacteria and archaea often are encoded by operons and/or gene clusters (genome neighborhoods) that provide important clues for assignment of both enzyme functions and metabolic pathways. We describe a bioinformatic approach (genome neighborhood network; GNN) that enables large scale prediction of the in vitro enzymatic activities and in vivo physiological functions (metabolic pathways) of uncharacterized enzymes in protein families. We demonstrate the utility of the GNN approach by predicting in vitro activities and in vivo functions in the proline racemase superfamily (PRS; InterPro IPR008794). The predictions were verified by measuring in vitro activities for 51 proteins in 12 families in the PRS that represent ~85% of the sequences; in vitro activities of pathway enzymes, carbon/nitrogen source phenotypes, and/or transcriptomic studies confirmed the predicted pathways. The synergistic use of sequence similarity networks3 and GNNs will facilitate the discovery of the components of novel, uncharacterized metabolic pathways in sequenced genomes.

Funder

National Institute of General Medical Sciences

Argonne National Laboratory, Office of Science

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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