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Hinge Atlas: relating protein sequence to sites of structural flexibility

BACKGROUND: Relating features of protein sequences to structural hinges is important for identifying domain boundaries, understanding structure-function relationships, and designing flexibility into proteins. Efforts in this field have been hampered by the lack of a proper dataset for studying chara...

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Autores principales: Flores, Samuel C, Lu, Long J, Yang, Julie, Carriero, Nicholas, Gerstein, Mark B
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1913541/
https://www.ncbi.nlm.nih.gov/pubmed/17519025
http://dx.doi.org/10.1186/1471-2105-8-167
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author Flores, Samuel C
Lu, Long J
Yang, Julie
Carriero, Nicholas
Gerstein, Mark B
author_facet Flores, Samuel C
Lu, Long J
Yang, Julie
Carriero, Nicholas
Gerstein, Mark B
author_sort Flores, Samuel C
collection PubMed
description BACKGROUND: Relating features of protein sequences to structural hinges is important for identifying domain boundaries, understanding structure-function relationships, and designing flexibility into proteins. Efforts in this field have been hampered by the lack of a proper dataset for studying characteristics of hinges. RESULTS: Using the Molecular Motions Database we have created a Hinge Atlas of manually annotated hinges and a statistical formalism for calculating the enrichment of various types of residues in these hinges. CONCLUSION: We found various correlations between hinges and sequence features. Some of these are expected; for instance, we found that hinges tend to occur on the surface and in coils and turns and to be enriched with small and hydrophilic residues. Others are less obvious and intuitive. In particular, we found that hinges tend to coincide with active sites, but unlike the latter they are not at all conserved in evolution. We evaluate the potential for hinge prediction based on sequence. Motions play an important role in catalysis and protein-ligand interactions. Hinge bending motions comprise the largest class of known motions. Therefore it is important to relate the hinge location to sequence features such as residue type, physicochemical class, secondary structure, solvent exposure, evolutionary conservation, and proximity to active sites. To do this, we first generated the Hinge Atlas, a set of protein motions with the hinge locations manually annotated, and then studied the coincidence of these features with the hinge location. We found that all of the features have bearing on the hinge location. Most interestingly, we found that hinges tend to occur at or near active sites and yet unlike the latter are not conserved. Less surprisingly, we found that hinge residues tend to be small, not hydrophobic or aliphatic, and occur in turns and random coils on the surface. A functional sequence based hinge predictor was made which uses some of the data generated in this study. The Hinge Atlas is made available to the community for further flexibility studies.
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spelling pubmed-19135412007-07-10 Hinge Atlas: relating protein sequence to sites of structural flexibility Flores, Samuel C Lu, Long J Yang, Julie Carriero, Nicholas Gerstein, Mark B BMC Bioinformatics Research Article BACKGROUND: Relating features of protein sequences to structural hinges is important for identifying domain boundaries, understanding structure-function relationships, and designing flexibility into proteins. Efforts in this field have been hampered by the lack of a proper dataset for studying characteristics of hinges. RESULTS: Using the Molecular Motions Database we have created a Hinge Atlas of manually annotated hinges and a statistical formalism for calculating the enrichment of various types of residues in these hinges. CONCLUSION: We found various correlations between hinges and sequence features. Some of these are expected; for instance, we found that hinges tend to occur on the surface and in coils and turns and to be enriched with small and hydrophilic residues. Others are less obvious and intuitive. In particular, we found that hinges tend to coincide with active sites, but unlike the latter they are not at all conserved in evolution. We evaluate the potential for hinge prediction based on sequence. Motions play an important role in catalysis and protein-ligand interactions. Hinge bending motions comprise the largest class of known motions. Therefore it is important to relate the hinge location to sequence features such as residue type, physicochemical class, secondary structure, solvent exposure, evolutionary conservation, and proximity to active sites. To do this, we first generated the Hinge Atlas, a set of protein motions with the hinge locations manually annotated, and then studied the coincidence of these features with the hinge location. We found that all of the features have bearing on the hinge location. Most interestingly, we found that hinges tend to occur at or near active sites and yet unlike the latter are not conserved. Less surprisingly, we found that hinge residues tend to be small, not hydrophobic or aliphatic, and occur in turns and random coils on the surface. A functional sequence based hinge predictor was made which uses some of the data generated in this study. The Hinge Atlas is made available to the community for further flexibility studies. BioMed Central 2007-05-22 /pmc/articles/PMC1913541/ /pubmed/17519025 http://dx.doi.org/10.1186/1471-2105-8-167 Text en Copyright © 2007 Flores et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Flores, Samuel C
Lu, Long J
Yang, Julie
Carriero, Nicholas
Gerstein, Mark B
Hinge Atlas: relating protein sequence to sites of structural flexibility
title Hinge Atlas: relating protein sequence to sites of structural flexibility
title_full Hinge Atlas: relating protein sequence to sites of structural flexibility
title_fullStr Hinge Atlas: relating protein sequence to sites of structural flexibility
title_full_unstemmed Hinge Atlas: relating protein sequence to sites of structural flexibility
title_short Hinge Atlas: relating protein sequence to sites of structural flexibility
title_sort hinge atlas: relating protein sequence to sites of structural flexibility
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1913541/
https://www.ncbi.nlm.nih.gov/pubmed/17519025
http://dx.doi.org/10.1186/1471-2105-8-167
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