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Michael J.E. Sternberg

Researcher at Imperial College London

Publications -  337
Citations -  43070

Michael J.E. Sternberg is an academic researcher from Imperial College London. The author has contributed to research in topics: Protein structure & Inductive logic programming. The author has an hindex of 93, co-authored 327 publications receiving 39429 citations. Previous affiliations of Michael J.E. Sternberg include University of Cambridge & National Institutes of Health.

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The Phyre2 web portal for protein modeling, prediction and analysis

TL;DR: An updated protocol for Phyre2, which uses advanced remote homology detection methods to build 3D models, predict ligand binding sites and analyze the effect of amino acid variants for a user's protein sequence.
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Protein structure prediction on the Web: a case study using the Phyre server.

TL;DR: This protocol provides a guide to interpreting the output of structure prediction servers in general and one such tool in particular, the protein homology/analogy recognition engine (Phyre), which can reliably detect up to twice as many remote homologies as standard sequence-profile searching.
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Enhanced genome annotation using structural profiles in the program 3D-PSSM.

TL;DR: Three-dimensional position-specific scoring matrix, 3D-PSSM, combines the power of multiple sequence profiles with knowledge of protein structure to provide enhanced recognition and thus functional assignment of newly sequenced genomes.
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A large-scale evaluation of computational protein function prediction

Predrag Radivojac, +107 more
- 01 Mar 2013 - 
TL;DR: Today's best protein function prediction algorithms substantially outperform widely used first-generation methods, with large gains on all types of targets, and there is considerable need for improvement of currently available tools.
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Modelling protein docking using shape complementarity, electrostatics and biochemical information

TL;DR: A protein docking study was performed for two classes of biomolecular complexes: six enzyme/inhibitor and four antibody/antigen and tested the native rather than the complexed forms of the proteins to address the more scientifically interesting problem of predictive docking.