Unknown

Dataset Information

0

Prediction of ligand binding sites using homologous structures and conservation at CASP8.


ABSTRACT: The critical assessment of protein structure prediction experiment is a blind assessment of the prediction of protein structure and related topics including function prediction. We present our results in the function/binding site prediction category. Our approach to identify binding sites combined the use of the predicted structure of the targets with both residue conservation and the location of ligands bound to homologous structures. We obtained an average coverage of 83% and 56% accuracy. Analysis of our predictions suggests that over-prediction reduces the accuracy obtained due to large areas of conservation around the binding site that do not bind the ligand. In some proteins such conserved residues may have a functional role. A server version of our method will soon be available.

SUBMITTER: Wass MN 

PROVIDER: S-EPMC2814558 | biostudies-literature | 2009

REPOSITORIES: biostudies-literature

altmetric image

Publications

Prediction of ligand binding sites using homologous structures and conservation at CASP8.

Wass Mark N MN   Sternberg Michael J E MJ  

Proteins 20090101


The critical assessment of protein structure prediction experiment is a blind assessment of the prediction of protein structure and related topics including function prediction. We present our results in the function/binding site prediction category. Our approach to identify binding sites combined the use of the predicted structure of the targets with both residue conservation and the location of ligands bound to homologous structures. We obtained an average coverage of 83% and 56% accuracy. Ana  ...[more]

Similar Datasets

| S-EPMC2896164 | biostudies-literature
| S-EPMC1601958 | biostudies-literature
| S-EPMC8424938 | biostudies-literature
| S-EPMC3287474 | biostudies-literature
| S-EPMC3204792 | biostudies-literature
| S-EPMC4731830 | biostudies-literature
| S-EPMC9847135 | biostudies-literature
| S-EPMC3692107 | biostudies-literature
| S-EPMC9252821 | biostudies-literature
| S-EPMC2785799 | biostudies-literature