Big-data approaches to protein structure prediction

2017 | journal article

Jump to: Cite & Linked | Documents & Media | Details | Version history

Cite this publication

​Söding, Johannes. "Big-data approaches to protein structure prediction​." ​Science, vol. 355, no. 6322, ​2017, pp. 248​-249​, ​doi: 10.1126/science.aal4512. 

Documents & Media

License

GRO License GRO License

Details

Authors
Söding, Johannes 
Abstract
Metagenomics sequence data give protein structure prediction a boost
A protein's structure determines its function. Experimental protein structure determination is cumbersome and costly, which has driven the search for methods that can predict protein structure from sequence information ( 1 ). About half of the known proteins are amenable to comparative modeling; that is, an evolutionarily related protein of known structure can be used as a template for modeling the unknown structure. For the remaining proteins, no satisfactory solution had been found. On page 294 of this issue, Ovchinnikov et al. ( 2 ) used recently developed methodology for predicting intraprotein amino acid contacts in combination with protein sequences from metagenomics of microbial DNA to compute reliable models for 622 protein families, and discovered more than 100 new folds along the way. The fast-paced growth of metagenomics data should enable reliable structure prediction of many more protein families.
Metagenomics sequence data give protein structure prediction a boost
A protein's structure determines its function. Experimental protein structure determination is cumbersome and costly, which has driven the search for methods that can predict protein structure from sequence information ( 1 ). About half of the known proteins are amenable to comparative modeling; that is, an evolutionarily related protein of known structure can be used as a template for modeling the unknown structure. For the remaining proteins, no satisfactory solution had been found. On page 294 of this issue, Ovchinnikov et al. ( 2 ) used recently developed methodology for predicting intraprotein amino acid contacts in combination with protein sequences from metagenomics of microbial DNA to compute reliable models for 622 protein families, and discovered more than 100 new folds along the way. The fast-paced growth of metagenomics data should enable reliable structure prediction of many more protein families.
Issue Date
2017
Journal
Science 
ISSN
0036-8075
eISSN
1095-9203
Language
English

Reference

Citations


Social Media