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LOMETS2: improved meta-threading server for fold-recognition and structure-based function annotation for

Wei Zheng1, Chengxin Zhang1, Qiqige Wuyun2

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Summary

The LOMETS2 server enhances protein structure prediction using advanced threading programs and deep sequence profiles. This update significantly improves template detection for difficult targets, aiding biological research.

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Area of Science:

  • Computational biology
  • Structural bioinformatics
  • Bioinformatics tools

Background:

  • The LOMETS server, a widely used online system for template-based protein structure prediction, has become outdated.
  • Aging algorithms and poor performance in identifying distant-homology templates necessitate an updated system.

Purpose of the Study:

  • To report advancements in the LOMETS2 server, integrating state-of-the-art methods for improved protein structure prediction.
  • To enhance template identification and introduce structure-based function annotations.

Main Methods:

  • Implemented new state-of-the-art threading programs, including contact-map-based approaches.
  • Utilized deep sequence search for improved sequence profile construction.
  • Redesigned the web interface with structure-based function annotations.

Main Results:

  • LOMETS2 demonstrated significantly improved structure modeling quality and template detection compared to the previous LOMETS server.
  • Detected 176% more templates (TM-scores >0.5) for difficult targets lacking homologous templates.
  • Incorporated structure-based function prediction to broaden the server's utility.

Conclusions:

  • The updated LOMETS2 server represents a significant advancement in template-based protein structure prediction.
  • Enhanced template detection and added functional annotation capabilities increase the server's value for the biological community.