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3D‐SHOTGUN: A novel, cooperative, fold‐recognition meta‐predictor
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| Zeitschriftentitel: | Proteins: Structure, Function, and Bioinformatics |
|---|---|
| Personen und Körperschaften: | |
| In: | Proteins: Structure, Function, and Bioinformatics, 51, 2003, 3, S. 434-441 |
| Format: | E-Article |
| Sprache: | Englisch |
| veröffentlicht: |
Wiley
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| Schlagwörter: |
| author_facet |
Fischer, Daniel Fischer, Daniel |
|---|---|
| author |
Fischer, Daniel |
| spellingShingle |
Fischer, Daniel Proteins: Structure, Function, and Bioinformatics 3D‐SHOTGUN: A novel, cooperative, fold‐recognition meta‐predictor Molecular Biology Biochemistry Structural Biology |
| author_sort |
fischer, daniel |
| spelling |
Fischer, Daniel 0887-3585 1097-0134 Wiley Molecular Biology Biochemistry Structural Biology http://dx.doi.org/10.1002/prot.10357 <jats:title>Abstract</jats:title><jats:p>To gain a better understanding of the biological role of proteins encoded in genome sequences, knowledge of their three‐dimensional (3D) structure and function is required. The computational assignment of folds is becoming an increasingly important complement to experimental structure determination. In particular, fold‐recognition methods aim to predict approximate 3D models for proteins bearing no sequence similarity to any protein of known structure. However, fully automated structure‐prediction methods can currently produce reliable models for only a fraction of these sequences. Using a number of semiautomated procedures, human expert predictors are often able to produce more and better predictions than automated methods. We describe a novel, fully automatic, fold‐recognition meta‐predictor, named 3D‐SHOTGUN, which incorporates some of the strategies human predictors have successfully applied. This new method is reminiscent of the so‐called cooperative algorithms of Computer Vision. The input to 3D‐SHOTGUN are the top models predicted by a number of independent fold‐recognition servers. The meta‐predictor consists of three steps: (i) assembly of hybrid models, (ii) confidence assignment, and (iii) selection. We have applied 3D‐SHOTGUN to an unbiased test set of 77 newly released protein structures sharing no sequence similarity to proteins previously released. Forty‐six correct rank‐1 predictions were obtained, 30 of which had scores higher than that of the first incorrect prediction—a significant improvement over the performance of all individual servers. Furthermore, the predicted hybrid models were, on average, more similar to their corresponding native structures than those produced by the individual servers. This opens the possibility of generating more accurate, full‐atom homology models for proteins with no sequence similarity to proteins of known structure. These improvements represent a step forward toward the wider applicability of fully automated structure‐prediction methods at genome scales. Proteins 2003;51:434–441. © 2003 Wiley‐Liss, Inc.</jats:p> 3D‐SHOTGUN: A novel, cooperative, fold‐recognition meta‐predictor Proteins: Structure, Function, and Bioinformatics |
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Proteins: Structure, Function, and Bioinformatics |
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3D‐SHOTGUN: A novel, cooperative, fold‐recognition meta‐predictor |
| title_unstemmed |
3D‐SHOTGUN: A novel, cooperative, fold‐recognition meta‐predictor |
| title_full |
3D‐SHOTGUN: A novel, cooperative, fold‐recognition meta‐predictor |
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3D‐SHOTGUN: A novel, cooperative, fold‐recognition meta‐predictor |
| title_full_unstemmed |
3D‐SHOTGUN: A novel, cooperative, fold‐recognition meta‐predictor |
| title_short |
3D‐SHOTGUN: A novel, cooperative, fold‐recognition meta‐predictor |
| title_sort |
3d‐shotgun: a novel, cooperative, fold‐recognition meta‐predictor |
| topic |
Molecular Biology Biochemistry Structural Biology |
| url |
http://dx.doi.org/10.1002/prot.10357 |
| publishDate |
2003 |
| physical |
434-441 |
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<jats:title>Abstract</jats:title><jats:p>To gain a better understanding of the biological role of proteins encoded in genome sequences, knowledge of their three‐dimensional (3D) structure and function is required. The computational assignment of folds is becoming an increasingly important complement to experimental structure determination. In particular, fold‐recognition methods aim to predict approximate 3D models for proteins bearing no sequence similarity to any protein of known structure. However, fully automated structure‐prediction methods can currently produce reliable models for only a fraction of these sequences. Using a number of semiautomated procedures, human expert predictors are often able to produce more and better predictions than automated methods. We describe a novel, fully automatic, fold‐recognition meta‐predictor, named 3D‐SHOTGUN, which incorporates some of the strategies human predictors have successfully applied. This new method is reminiscent of the so‐called cooperative algorithms of Computer Vision. The input to 3D‐SHOTGUN are the top models predicted by a number of independent fold‐recognition servers. The meta‐predictor consists of three steps: (i) assembly of hybrid models, (ii) confidence assignment, and (iii) selection. We have applied 3D‐SHOTGUN to an unbiased test set of 77 newly released protein structures sharing no sequence similarity to proteins previously released. Forty‐six correct rank‐1 predictions were obtained, 30 of which had scores higher than that of the first incorrect prediction—a significant improvement over the performance of all individual servers. Furthermore, the predicted hybrid models were, on average, more similar to their corresponding native structures than those produced by the individual servers. This opens the possibility of generating more accurate, full‐atom homology models for proteins with no sequence similarity to proteins of known structure. These improvements represent a step forward toward the wider applicability of fully automated structure‐prediction methods at genome scales. Proteins 2003;51:434–441. © 2003 Wiley‐Liss, Inc.</jats:p> |
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| description | <jats:title>Abstract</jats:title><jats:p>To gain a better understanding of the biological role of proteins encoded in genome sequences, knowledge of their three‐dimensional (3D) structure and function is required. The computational assignment of folds is becoming an increasingly important complement to experimental structure determination. In particular, fold‐recognition methods aim to predict approximate 3D models for proteins bearing no sequence similarity to any protein of known structure. However, fully automated structure‐prediction methods can currently produce reliable models for only a fraction of these sequences. Using a number of semiautomated procedures, human expert predictors are often able to produce more and better predictions than automated methods. We describe a novel, fully automatic, fold‐recognition meta‐predictor, named 3D‐SHOTGUN, which incorporates some of the strategies human predictors have successfully applied. This new method is reminiscent of the so‐called cooperative algorithms of Computer Vision. The input to 3D‐SHOTGUN are the top models predicted by a number of independent fold‐recognition servers. The meta‐predictor consists of three steps: (i) assembly of hybrid models, (ii) confidence assignment, and (iii) selection. We have applied 3D‐SHOTGUN to an unbiased test set of 77 newly released protein structures sharing no sequence similarity to proteins previously released. Forty‐six correct rank‐1 predictions were obtained, 30 of which had scores higher than that of the first incorrect prediction—a significant improvement over the performance of all individual servers. Furthermore, the predicted hybrid models were, on average, more similar to their corresponding native structures than those produced by the individual servers. This opens the possibility of generating more accurate, full‐atom homology models for proteins with no sequence similarity to proteins of known structure. These improvements represent a step forward toward the wider applicability of fully automated structure‐prediction methods at genome scales. Proteins 2003;51:434–441. © 2003 Wiley‐Liss, Inc.</jats:p> |
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| spelling | Fischer, Daniel 0887-3585 1097-0134 Wiley Molecular Biology Biochemistry Structural Biology http://dx.doi.org/10.1002/prot.10357 <jats:title>Abstract</jats:title><jats:p>To gain a better understanding of the biological role of proteins encoded in genome sequences, knowledge of their three‐dimensional (3D) structure and function is required. The computational assignment of folds is becoming an increasingly important complement to experimental structure determination. In particular, fold‐recognition methods aim to predict approximate 3D models for proteins bearing no sequence similarity to any protein of known structure. However, fully automated structure‐prediction methods can currently produce reliable models for only a fraction of these sequences. Using a number of semiautomated procedures, human expert predictors are often able to produce more and better predictions than automated methods. We describe a novel, fully automatic, fold‐recognition meta‐predictor, named 3D‐SHOTGUN, which incorporates some of the strategies human predictors have successfully applied. This new method is reminiscent of the so‐called cooperative algorithms of Computer Vision. The input to 3D‐SHOTGUN are the top models predicted by a number of independent fold‐recognition servers. The meta‐predictor consists of three steps: (i) assembly of hybrid models, (ii) confidence assignment, and (iii) selection. We have applied 3D‐SHOTGUN to an unbiased test set of 77 newly released protein structures sharing no sequence similarity to proteins previously released. Forty‐six correct rank‐1 predictions were obtained, 30 of which had scores higher than that of the first incorrect prediction—a significant improvement over the performance of all individual servers. Furthermore, the predicted hybrid models were, on average, more similar to their corresponding native structures than those produced by the individual servers. This opens the possibility of generating more accurate, full‐atom homology models for proteins with no sequence similarity to proteins of known structure. These improvements represent a step forward toward the wider applicability of fully automated structure‐prediction methods at genome scales. Proteins 2003;51:434–441. © 2003 Wiley‐Liss, Inc.</jats:p> 3D‐SHOTGUN: A novel, cooperative, fold‐recognition meta‐predictor Proteins: Structure, Function, and Bioinformatics |
| spellingShingle | Fischer, Daniel, Proteins: Structure, Function, and Bioinformatics, 3D‐SHOTGUN: A novel, cooperative, fold‐recognition meta‐predictor, Molecular Biology, Biochemistry, Structural Biology |
| title | 3D‐SHOTGUN: A novel, cooperative, fold‐recognition meta‐predictor |
| title_full | 3D‐SHOTGUN: A novel, cooperative, fold‐recognition meta‐predictor |
| title_fullStr | 3D‐SHOTGUN: A novel, cooperative, fold‐recognition meta‐predictor |
| title_full_unstemmed | 3D‐SHOTGUN: A novel, cooperative, fold‐recognition meta‐predictor |
| title_short | 3D‐SHOTGUN: A novel, cooperative, fold‐recognition meta‐predictor |
| title_sort | 3d‐shotgun: a novel, cooperative, fold‐recognition meta‐predictor |
| title_unstemmed | 3D‐SHOTGUN: A novel, cooperative, fold‐recognition meta‐predictor |
| topic | Molecular Biology, Biochemistry, Structural Biology |
| url | http://dx.doi.org/10.1002/prot.10357 |